This is a modern-English version of The Descent of Man and Selection in Relation to Sex, Vol. I, originally written by Darwin, Charles.
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THE
DESCENT OF MAN,
AND
SELECTION IN RELATION TO SEX.
By CHARLES DARWIN, M.A., F.R.S., &c.
IN TWO VOLUMES.—Vol. 1.
WITH ILLUSTRATIONS.
LONDON:
JOHN MURRAY, ALBEMARLE STREET.
1871.
[The right of Translation is reserved.]
BY THE SAME AUTHOR.
ON THE ORIGIN OF SPECIES BY MEANS OF NATURAL SELECTION; or, The Preservation of Favoured Races in the Struggle for Life; Fifth Edition (Tenth Thousand), with Additions and Corrections. 1869. Murray.
ON THE ORIGIN OF SPECIES BY MEANS OF NATURAL SELECTION; or, The Conservation of Preferred Races in the Fight for Survival; Fifth Edition (Tenth Thousand), with Additions and Corrections. 1869. Murray.
THE VARIATION OF ANIMALS AND PLANTS UNDER DOMESTICATION. In two vols. With Illustrations. 1868. Murray.
THE VARIATION OF ANIMALS AND PLANTS UNDER DOMESTICATION. In two volumes. With Illustrations. 1868. Murray.
ON THE VARIOUS CONTRIVANCES by which BRITISH AND FOREIGN ORCHIDS ARE FERTILISED BY INSECTS; and on the Good Effects of Crossing. With numerous Woodcuts. Murray.
ON THE DIFFERENT METHODS that BRITISH AND FOREIGN ORCHIDS ARE POLLINATED BY INSECTS; and on the Benefits of Hybridization. With many Illustrations. Murray.
A NATURALIST‘S VOYAGE ROUND THE WORLD; or, A Journal of Researches into the Natural History and Geology of the Countries visited during the voyage of H.M.S. ‘Beagle,’ under the command of Captain FitzRoy, R.N. Eleventh Thousand. Murray.
A NATURALIST'S VOYAGE AROUND THE WORLD; or, A Journal of Research on the Natural History and Geology of the Countries visited during the voyage of H.M.S. 'Beagle,' under the command of Captain FitzRoy, R.N. Eleventh Thousand. Murray.
ON THE STRUCTURE AND DISTRIBUTION OF CORAL REEFS. Smith, Elder, & Co.
ON THE STRUCTURE AND DISTRIBUTION OF CORAL REEFS. Smith, Elder, & Co.
GEOLOGICAL OBSERVATIONS ON VOLCANIC ISLANDS. Smith, Elder, & Co.
GEOLOGICAL OBSERVATIONS ON VOLCANIC ISLANDS. Smith, Elder, & Co.
GEOLOGICAL OBSERVATIONS ON SOUTH AMERICA. Smith, Elder & Co.
GEOLOGICAL OBSERVATIONS ON SOUTH AMERICA. Smith, Elder & Co.
A MONOGRAPH OF THE CIRRIPEDIA. With numerous Illustrations. 2 vols. 8vo. Hardwicke.
A MONOGRAPH OF THE CIRRIPEDIA. With many Illustrations. 2 vols. 8vo. Hardwicke.
ON THE MOVEMENTS AND HABITS OF CLIMBING PLANTS. With Woodcuts. Williams & Norgate.
ON THE MOVEMENTS AND HABITS OF CLIMBING PLANTS. With Illustrations. Williams & Norgate.
LONDON: PRINTED BY WILLIAM CLOWES AND SONS, STAMFORD STREET, AND CHARING CROSS.
CONTENTS. |
|
Intro | Page 1-5 |
PART I. |
|
ON THE DESCENT OF MAN |
|
CHAPTER I. | |
The Evidence of Humanity's Origin from Lower Forms. | |
Nature of the evidence bearing on the origin of man—Homologous structures in man and the lower animals—Miscellaneous points of correspondence—Development—Rudimentary structures, muscles, sense-organs, hair, bones, reproductive organs, &c.—The bearing of these three great classes of facts on the origin of man | 9-33 |
CHAPTER II. | |
Comparison of the Mental Abilities of Humans and Lower Animals. | |
The difference in mental power between the highest ape and the lowest savage, immense—Certain instincts in common—The emotions—Curiosity—Imitation—Attention—Memory—Imagination—Reason—Progressive improvement—Tools and weapons used by animals—Language—Self-consciousness—Sense of beauty—Belief in God, spiritual agencies, superstitions | 34-69 |
CHAPTER III. | |
Comparison of the Mental Abilities of Humans and Lower Animals—continued. | |
The difference in mental power between the highest ape and the lowest savage, immense—Certain instincts in common—The emotions—Curiosity—Imitation—Attention—Memory—Imagination—Reason—Progressive improvement—Tools and weapons used by animals—Language—Self-consciousness—Sense of beauty—Belief in God, spiritual agencies, superstitions | 70-106 |
CHAPTER IV. | |
On How Man Develops from a Lower Form. | |
Variability of body and mind in man—Inheritance—Causes of variability—Laws of variation the same in man as in the lower animals—Direct action of the conditions of life—Effects of the increased use and disuse of parts—Arrested development—Reversion—Correlated variation—Rate of increase—Checks to increase—Natural selection—Man the most dominant animal in the world—Importance of his corporeal structure—The causes which have led to his becoming erect—Consequent changes of structure—Decrease in size of the canine teeth—Increased size and altered shape of the skull—Nakedness—Absence of a tail—Defenceless condition of man | 107-157 |
CHAPTER V. | |
On the Development of Intellectual and Moral Abilities in Prehistoric and Civilized Times. | |
The advancement of the intellectual powers through natural selection—Importance of imitation—Social and moral faculties—Their development within the limits of the same tribe—Natural selection as affecting civilised nations—Evidence that civilised nations were once barbarous | 158-184 |
CHAPTER VI. | |
On the Connections and Ancestry of Humanity. | |
Position of man in the animal series—The natural system genealogical—Adaptive characters of slight value—Various small points of resemblance between man and the Quadrumana—Rank of man in the natural system—Birthplace and antiquity vii of man—Absence of fossil connecting-links—Lower stages in the genealogy of man, as inferred, firstly from his affinities and secondly from his structure—Early androgynous condition of the Vertebrata—Conclusion | 185-213 |
CHAPTER VII. | |
On Human Races. | |
The nature and value of specific characters—Application to the races of man—Arguments in favour of, and opposed to, ranking the so-called races of man as distinct species—Sub-species—Monogenists and polygenists—Convergence of character—Numerous points of resemblance in body and mind between the most distinct races of man—The state of man when he first spread over the earth—Each race not descended from a single pair—The extinction of races—The formation of races—The effects of crossing—Slight influence of the direct action of the conditions of life—Slight or no influence of natural selection—Sexual selection. | 214-250 |
PART II. |
|
CHAPTER VIII. | |
Principles of Sexual Selection. | |
Secondary sexual characters—Sexual selection—Manner of action—Excess of males—Polygamy—The male alone generally modified through sexual selection—Eagerness of the male—Variability of the male—Choice exerted by the female—Sexual compared with natural selection—Inheritance at corresponding periods of life, at corresponding seasons of the year, and as limited by sex—Relations between the several forms of inheritance—Causes why one sex and the young are not modified through sexual selection—Supplement on the proportional numbers of the two sexes throughout the animal kingdom—On the limitation of the numbers of the two sexes through natural selection | 253-320 |
CHAPTER IX. | |
Secondary Sexual Characteristics in the Lower Classes of the Animal Kingdom. | |
viii These characters absent in the lowest classes—Brilliant colours—Mollusca—Annelids—Crustacea, secondary sexual characters strongly developed; dimorphism; colour; characters not acquired before maturity—Spiders, sexual colours of; stridulation by the males—Myriapoda | 321-340 |
CHAPTER X. | |
Insect Secondary Sexual Characteristics. | |
Diversified structures possessed by the males for seizing the females—Differences between the sexes, of which the meaning is not understood—Difference in size between the sexes—Thysanura—Diptera—Hemiptera—Homoptera, musical powers possessed by the males alone—Orthoptera, musical instruments of the males, much diversified in structure; pugnacity; colours—Neuroptera, sexual differences in colour—Hymenoptera, pugnacity and colours—Coleoptera, colours; furnished with great horns, apparently as an ornament; battles; stridulating organs generally common to both sexes | 341-385 |
CHAPTER XI. | |
Bugs, continued.—Order Lepidoptera. | |
Courtship of butterflies—Battles—Ticking noise—Colours common to both sexes, or more brilliant in the males—Examples—Not due to the direct action of the conditions of life—Colours adapted for protection—Colours of moths—Display—Perceptive powers of the Lepidoptera—Variability—Causes of the difference in colour between the males and females—Mimickry, female butterflies more brilliantly coloured than the males—Bright colours of caterpillars—Summary and concluding remarks on the secondary sexual characters of insects—Birds and insects compared | 386-423 |
THE DESCENT OF MAN;
AND ON
SELECTION IN RELATION TO SEX.
INTRODUCTION.
The nature of the following work will be best understood by a brief account of how it came to be written. During many years I collected notes on the origin or descent of man, without any intention of publishing on the subject, but rather with the determination not to publish, as I thought that I should thus only add to the prejudices against my views. It seemed to me sufficient to indicate, in the first edition of my ‘Origin of Species,’ that by this work “light would be thrown on the origin of man and his history;” and this implies that man must be included with other organic beings in any general conclusion respecting his manner of appearance on this earth. Now the case wears a wholly different aspect. When a naturalist like Carl Vogt ventures to say in his address as President of the National Institution of Geneva (1869), “personne, en Europe au moins, n’ose plus soutenir la création indépendante et de toutes pièces, des espèces,” it is manifest that at least a large number of naturalists must admit that species are the modified descendants of other species;2 and this especially holds good with the younger and rising naturalists. The greater number accept the agency of natural selection; though some urge, whether with justice the future must decide, that I have greatly overrated its importance. Of the older and honoured chiefs in natural science, many unfortunately are still opposed to evolution in every form.
The nature of the following work will be best understood by a brief account of how it came to be written. For many years, I collected notes on the origin or descent of man, without any intention of publishing on the subject, and actually with the intention of not publishing, since I believed that doing so would only add to the prejudices against my views. I thought it was enough to indicate, in the first edition of my 'Origin of Species,' that this work would “shed light on the origin of man and his history;” which implies that man must be included with other living beings in any general conclusion about how he appeared on this earth. Now the situation looks completely different. When a naturalist like Carl Vogt dares to say in his speech as President of the National Institution of Geneva (1869), “nobody, in Europe at least, dares to claim the independent and complete creation of species,” it’s clear that at least a significant number of naturalists must acknowledge that species are the modified descendants of other species; and this is particularly true for the younger and emerging naturalists. The majority accept the role of natural selection, although some argue—whether justly or not will be determined in the future—that I have greatly exaggerated its significance. Unfortunately, many of the older respected leaders in natural science are still opposed to evolution in any form.2
In consequence of the views now adopted by most naturalists, and which will ultimately, as in every other case, be followed by other men, I have been led to put together my notes, so as to see how far the general conclusions arrived at in my former works were applicable to man. This seemed all the more desirable as I had never deliberately applied these views to a species taken singly. When we confine our attention to any one form, we are deprived of the weighty arguments derived from the nature of the affinities which connect together whole groups of organisms—their geographical distribution in past and present times, and their geological succession. The homological structure, embryological development, and rudimentary organs of a species, whether it be man or any other animal, to which our attention may be directed, remain to be considered; but these great classes of facts afford, as it appears to me, ample and conclusive evidence in favour of the principle of gradual evolution. The strong support derived from the other arguments should, however, always be kept before the mind.
As a result of the perspectives now taken by most naturalists, which will eventually be mirrored by others, I felt compelled to compile my notes to assess how the general conclusions from my earlier works apply to humans. This seemed especially necessary because I had never intentionally focused these views on a single species. When we focus on just one form, we miss out on the significant insights derived from the relationships that connect entire groups of organisms—their geographical distribution both in the past and present, and their geological succession. The homologous structure, embryological development, and rudimentary organs of a species, whether human or any other animal, still need to be examined; however, these major categories of facts provide, it seems to me, substantial and convincing evidence in support of the principle of gradual evolution. Nevertheless, the strong arguments derived from other sources should always remain in mind.
The sole object of this work is to consider, firstly, whether man, like every other species, is descended from some pre-existing form; secondly, the manner of3 his development; and thirdly, the value of the differences between the so-called races of man. As I shall confine myself to these points, it will not be necessary to describe in detail the differences between the several races—an enormous subject which has been fully discussed in many valuable works. The high antiquity of man has recently been demonstrated by the labours of a host of eminent men, beginning with M. Boucher de Perthes; and this is the indispensable basis for understanding his origin. I shall, therefore, take this conclusion for granted, and may refer my readers to the admirable treatises of Sir Charles Lyell, Sir John Lubbock, and others. Nor shall I have occasion to do more than to allude to the amount of difference between man and the anthropomorphous apes; for Prof. Huxley, in the opinion of most competent judges, has conclusively shewn that in every single visible character man differs less from the higher apes than these do from the lower members of the same order of Primates.
The main goal of this work is to explore, first, whether humans, like every other species, evolved from some earlier form; second, how this development occurred; and third, the significance of the differences between what are called the races of humans. Since I will focus on these points, it's unnecessary to detail the various differences among the races—an extensive topic that has been thoroughly addressed in many important works. The ancient history of humans has recently been proven by the work of many distinguished individuals, starting with M. Boucher de Perthes; this is essential for understanding human origins. Therefore, I will assume this conclusion and refer my readers to the excellent writings of Sir Charles Lyell, Sir John Lubbock, and others. I also won’t need to elaborate on the differences between humans and the anthropoid apes; because Prof. Huxley, according to most qualified experts, has convincingly shown that in every single visible trait, humans differ less from the higher apes than those apes do from the lower members of the same order of Primates.
This work contains hardly any original facts in regard to man; but as the conclusions at which I arrived, after drawing up a rough draft, appeared to me interesting, I thought that they might interest others. It has often and confidently been asserted, that man’s origin can never be known: but ignorance more frequently begets confidence than does knowledge: it is those who know little, and not those who know much, who so positively assert that this or that problem will never be solved by science. The conclusion that man is the co-descendant with other species of some ancient, lower, and extinct form, is not in any degree new. La4marck long ago came to this conclusion, which has lately been maintained by several eminent naturalists and philosophers; for instance by Wallace, Huxley, Lyell, Vogt, Lubbock, Büchner, Rolle, &c.,1 and especially by Häckel. This last naturalist, besides his great work, 'Generelle Morphologie ‘(1866), has recently (1868, with a second edit. in 1870), published his ‘Natürliche Schöpfungsgeschichte, ‘in which he fully discusses the genealogy of man. If this work had appeared before my essay had been written, I should probably never have completed it. Almost all the conclusions at which I have arrived I find confirmed by this naturalist, whose knowledge on many points is much fuller than mine. Wherever I have added any fact or view from Prof. Häckel’s writings, I give his authority in the text, other statements I leave as they originally stood in my manuscript, occasionally giving in the foot-notes references to his works, as a confirmation of the more doubtful or interesting points.
This work contains hardly any original facts about humans; however, as the conclusions I reached after creating a rough draft seemed interesting to me, I thought they might interest others as well. It has often and confidently been claimed that the origin of humans can never be understood: yet ignorance tends to generate more confidence than knowledge does. It's usually those who know little, not those with extensive knowledge, who assert so firmly that a specific problem will never be solved by science. The conclusion that humans share a common ancestor with other species from some ancient, lower, and extinct form is not at all new. Lamarck reached this conclusion long ago, and many distinguished naturalists and philosophers have supported it recently, including Wallace, Huxley, Lyell, Vogt, Lubbock, Büchner, Rolle, etc., and especially Häckel. This last naturalist, in addition to his significant work 'Generelle Morphologie' (1866), recently (1868, with a second edition in 1870) published 'Natürliche Schöpfungsgeschichte,' in which he thoroughly explores the genealogy of humans. If this work had been published before I finished my essay, I probably wouldn’t have completed it. Almost all the conclusions I've drawn are confirmed by this naturalist, whose knowledge on many topics is much broader than mine. Wherever I have included any fact or idea from Prof. Häckel’s writings, I cite his authority in the text; other statements remain as they were in my original manuscript, sometimes with footnotes referencing his works to substantiate the more questionable or intriguing points.
During many years it has seemed to me highly probable
that sexual selection has played an important
part in differentiating the races of man; but in my
5
6‘Origin of Species’ (first edition, p. 199) I contented
myself by merely alluding to this belief. When I came
to apply this view to man, I found it indispensable to
treat the whole subject in full detail.2 Consequently
the second part of the present work, treating of sexual
selection, has extended to an inordinate length, compared
with the first part; but this could not be
avoided.
For many years, I’ve thought it was very likely that sexual selection has played a significant role in differentiating human races; however, in my 5
6‘Origin of Species’ (first edition, p. 199), I only briefly mentioned this belief. When I tried to apply this idea to humans, I realized it was essential to discuss the entire subject in detail.2 As a result, the second part of this work, which focuses on sexual selection, has become disproportionately longer than the first part; but there was no way to avoid this.
I had intended adding to the present volumes an essay on the expression of the various emotions by man and the lower animals. My attention was called to this subject many years ago by Sir Charles Bell’s admirable work. This illustrious anatomist maintains that man is endowed with certain muscles solely for the sake of expressing his emotions. As this view is obviously opposed to the belief that man is descended from some other and lower form, it was necessary for me to consider it. I likewise wished to ascertain how far the emotions are expressed in the same manner by the different races of man. But owing to the length of the present work, I have thought it better to reserve my essay, which is partially completed, for separate publication.
I had planned to include an essay in the current volumes about how humans and lower animals express various emotions. I became interested in this topic many years ago after reading Sir Charles Bell’s excellent work. This renowned anatomist argues that humans have certain muscles specifically for expressing emotions. This perspective clearly contradicts the idea that humans evolved from some lower form, so I needed to consider it carefully. I also wanted to find out how different races of humans express emotions in similar or different ways. However, because of the length of this work, I decided it would be better to save my partially completed essay for a separate publication.
Part I.
THE DESCENT OR ORIGIN OF MAN.
Part I.—THE DESCENT OF MAN.
CHAPTER I.
The Evidence of Humanity's Evolution from a Lower Form.
Nature of the evidence bearing on the origin of man—Homologous structures in man and the lower animals—Miscellaneous points of correspondence—Development—Rudimentary structures, muscles, sense-organs, hair, bones, reproductive organs, &c.—The bearing of these three great classes of facts on the origin of man.
Nature of the evidence regarding human origins—Similar structures in humans and lower animals—Various points of comparison—Development—Underdeveloped structures, muscles, sense organs, hair, bones, reproductive organs, etc.—The significance of these three major categories of facts on the origin of humans.
He who wishes to decide whether man is the modified descendant of some pre-existing form, would probably first enquire whether man varies, however slightly, in bodily structure and in mental faculties; and if so, whether the variations are transmitted to his offspring in accordance with the laws which prevail with the lower animals; such as that of the transmission of characters to the same age or sex. Again, are the variations the result, as far as our ignorance permits us to judge, of the same general causes, and are they governed by the same general laws, as in the case of other organisms; for instance by correlation, the inherited effects of use and disuse, &c.? Is man subject to similar malconformations, the result of arrested development, of reduplication of parts, &c., and does he display in any of his anomalies reversion to some former and ancient type of structure? It might also naturally be enquired whether man, like so many other animals, has given rise to varieties and sub-races, differing but slightly from each other, or to10 races differing so much that they must be classed as doubtful species? How are such races distributed over the world; and how, when crossed, do they react on each other, both in the first and succeeding generations? And so with many other points.
Anyone who wants to determine whether humans are an evolved version of some earlier form would probably first ask if humans vary, even slightly, in physical build and mental abilities. If they do, then we need to see if these variations are passed on to offspring according to the same rules that apply to lower animals, like the transmission of traits based on age or sex. Additionally, are these variations caused by similar factors, as far as our limited understanding allows, and do they follow the same general principles as other organisms? For example, do they involve correlations, the inherited effects of use and disuse, etc.? Is humanity subject to similar deformities resulting from halted development, duplication of parts, etc.? And do we see any of these anomalies showing a return to an earlier and ancient structural type? It would also make sense to ask whether humans, like many other animals, have given rise to various types and subgroups that are only slightly different from one another or to races that differ so much they could be considered questionable species. How are these races spread around the world, and how do they interact when mixed, both in the first generation and later ones? There are many other questions to consider as well.
The enquirer would next come to the important point, whether man tends to increase at so rapid a rate, as to lead to occasional severe struggles for existence, and consequently to beneficial variations, whether in body or mind, being preserved, and injurious ones eliminated. Do the races or species of men, whichever term may be applied, encroach on and replace each other, so that some finally become extinct? We shall see that all these questions, as indeed is obvious in respect to most of them, must be answered in the affirmative, in the same manner as with the lower animals. But the several considerations just referred to may be conveniently deferred for a time; and we will first see how far the bodily structure of man shows traces, more or less plain, of his descent from some lower form. In the two succeeding chapters the mental powers of man, in comparison with those of the lower animals, will be considered.
The inquirer would next address the important point of whether humans tend to grow at such a rapid pace that it leads to significant struggles for survival, resulting in beneficial changes, whether in body or mind, being preserved while harmful ones are eliminated. Do different races or species of humans, whatever term you use, encroach on and replace one another, causing some to eventually go extinct? We will find that all these questions, as is obvious for many of them, must be answered with a yes, just like with lower animals. However, we can set aside these various considerations for now and first look at how far human bodily structure shows clear signs of descent from some lower form. In the next two chapters, we will examine the mental capabilities of humans in comparison to those of lower animals.
The Bodily Structure of Man.—It is notorious that man is constructed on the same general type or model with other mammals. All the bones in his skeleton can be compared with corresponding bones in a monkey, bat, or seal. So it is with his muscles, nerves, blood-vessels and internal viscera. The brain, the most important of all the organs, follows the same law, as shewn by Huxley and other anatomists. Bischoff,3 who is a hostile witness, admits that every chief fissure and fold 11in the brain of man has its analogy in that of the orang; but he adds that at no period of development do their brains perfectly agree; nor could this be expected, for otherwise their mental powers would have been the same. Vulpian4 remarks: “Les différences réelles qui existent entre l’encéphale de l’homme et celui des singes supérieurs, sont bien minimes. Il ne faut pas se faire d’illusions à cet égard. L’homme est bien plus près des singes anthropomorphes par les caractères anatomiques de son cerveau que ceux-ci ne le sont non-seulement des autres mammifères, mais mêmes de certains quadrumanes, des guenons et des macaques.” But it would be superfluous here to give further details on the correspondence between man and the higher mammals in the structure of the brain and all other parts of the body.
The Bodily Structure of Man.—It's well-known that humans are built similarly to other mammals. Every bone in our skeleton can be compared to corresponding bones in monkeys, bats, or seals. The same goes for our muscles, nerves, blood vessels, and internal organs. The brain, which is the most important organ, follows the same pattern, as shown by Huxley and other anatomists. Bischoff,3 who is a critical observer, acknowledges that every major groove and fold in the human brain has a counterpart in the orangutan; however, he adds that at no point in development do their brains match perfectly, which is to be expected, since otherwise, their mental abilities would be the same. Vulpian4 states: “The real differences that exist between the human brain and that of higher primates are quite minimal. We should not delude ourselves in this regard. Humans are much closer to anthropoid apes in the anatomical features of their brain than these apes are not only to other mammals but even to certain quadrumanous animals, such as guenons and macaques.” But it would be unnecessary to provide more details on the similarities between humans and higher mammals regarding brain structure and all other parts of the body.
It may, however, be worth while to specify a few points, not directly or obviously connected with structure, by which this correspondence or relationship is well shewn.
It might be helpful to point out a few details that aren't directly or obviously related to structure, which clearly demonstrate this correspondence or relationship.
Man is liable to receive from the lower animals, and to communicate to them, certain diseases as hydrophobia, variola, the glanders, &c.; and this fact proves the close similarity of their tissues and blood, both in minute structure and composition, far more plainly than does their comparison under the best microscope, or by the aid of the best chemical analysis. Monkeys are liable to many of the same non-contagious diseases as we are; thus Rengger,5 who carefully observed for a long time the Cebus Azaræ in its native land, found it liable to catarrh, with the usual symptoms, and which when 12often recurrent led to consumption. These monkeys suffered also from apoplexy, inflammation of the bowels, and cataract in the eye. The younger ones when shedding their milk-teeth often died from fever. Medicines produced the same effect on them as on us. Many kinds of monkeys have a strong taste for tea, coffee, and spirituous liquors: they will also, as I have myself seen, smoke tobacco with pleasure. Brehm asserts that the natives of north-eastern Africa catch the wild baboons by exposing vessels with strong beer, by which they are made drunk. He has seen some of these animals, which he kept in confinement, in this state; and he gives a laughable account of their behaviour and strange grimaces. On the following morning they were very cross and dismal; they held their aching heads with both hands and wore a most pitiable expression: when beer or wine was offered them, they turned away with disgust, but relished the juice of lemons.6 An American monkey, an Ateles, after getting drunk on brandy, would never touch it again, and thus was wiser than many men. These trifling facts prove how similar the nerves of taste must be in monkeys and man, and how similarly their whole nervous system is affected.
Humans can catch certain diseases from lower animals and can also pass them on, like rabies, smallpox, and glanders. This shows that our tissues and blood are very similar in structure and composition, even more so than what we can see under a microscope or analyze chemically. Monkeys can get many of the same non-contagious diseases that we do. For instance, Rengger,5 who closely studied the Cebus Azaræ in its natural habitat, found that it was prone to colds, which could lead to consumption if they became frequent. These monkeys also experienced strokes, bowel inflammation, and cataracts. Younger monkeys sometimes died from fever when losing their baby teeth. Medicines affected them the same way they do us. Many types of monkeys enjoy tea, coffee, and alcoholic drinks. I've even seen them smoke tobacco happily. Brehm claims that people in northeastern Africa catch wild baboons by putting out containers of strong beer, which intoxicates them. He has observed some of these monkeys in captivity while drunk and shares a funny account of their behavior and strange expressions. The next morning, they were moody and miserable, holding their aching heads and looking quite pitiful. When offered beer or wine, they turned away in disgust but enjoyed lemon juice.6 An American monkey, an Ateles, after getting drunk on brandy, refused to touch it again, showing it was wiser than many humans. These small details demonstrate how similar the taste nerves must be in both monkeys and humans, and how their entire nervous system reacts in similar ways.
Man is infested with internal parasites, sometimes causing fatal effects, and is plagued by external parasites, all of which belong to the same genera or families with those infesting other mammals. Man is subject like other mammals, birds, and even insects, to that mysterious law, which causes certain normal processes, such as gestation, as well as the maturation and duration of various diseases, to follow lunar periods.7 His wounds 13are repaired by the same process of healing; and the stumps left after the amputation of his limbs occasionally possess, especially during an early embryonic period, some power of regeneration, as in the lowest animals.8
Humans are affected by internal parasites, which can sometimes lead to serious health issues, as well as external parasites, all of which are related to those that infest other mammals. Like other mammals, birds, and even insects, humans are influenced by a mysterious law that causes certain normal processes, such as pregnancy, as well as the progression and duration of various diseases, to follow lunar cycles.7 Their wounds are healed through the same healing process; and the areas remaining after limb amputation can sometimes have, especially during early development, a degree of regenerative ability, similar to the simplest animals.8
The whole process of that most important function, the reproduction of the species, is strikingly the same in all mammals, from the first act of courtship by the male9 to the birth and nurturing of the young. Monkeys are born in almost as helpless a condition as our own infants; and in certain genera the young differ fully as much in appearance from the adults, as do our children from their full-grown parents.10 It has been urged by some writers as an important distinction, that with man the young arrive at maturity at a much later age than with any other animal; but if we look to the races of mankind which inhabit tropical countries the difference is not great, for the orang is believed not to be adult till the age of from ten to fifteen years.11 Man 14differs from woman in size, bodily strength, hairyness, &c., as well as in mind, in the same manner as do the two sexes of many mammals. It is, in short, scarcely possible to exaggerate the close correspondence in general structure, in the minute structure of the tissues, in chemical composition and in constitution, between man and the higher animals, especially the anthropomorphous apes.
The entire process of the most important function, the reproduction of the species, is remarkably similar in all mammals, from the first act of courtship by the male9 to the birth and care of their young. Monkeys are born in nearly as helpless a state as our own infants; and in certain species, the young look as different from the adults as our children do from their grown-up parents.10 Some writers have pointed out that an important distinction is that humans reach maturity at a much later age than other animals; however, if we consider the human races living in tropical regions, the difference isn't significant, since orangutans are believed not to reach adulthood until they are between ten and fifteen years old.11 Men 14 differ from women in size, physical strength, hairiness, etc., as well as in mental aspects, just like the two sexes of many mammals. In short, it's hardly possible to overstate the close resemblance in overall structure, detailed tissue structure, chemical makeup, and constitution between humans and higher animals, particularly the great apes.
Embryonic Development.—Man is developed from an ovule, about the 125th of an inch in diameter, which differs in no respect from the ovules of other animals. The embryo itself at a very early period can hardly be distinguished from that of other members of the vertebrate kingdom. At this period the arteries run in arch-like branches, as if to carry the blood to branchiæ which are not present in the higher vertebrata, though the slits on the sides of the neck still remain (f, g, fig. 1), marking their former position. At a somewhat later period, when the extremities are developed, “the feet of lizards and mammals,” as the illustrious Von Baer remarks, “the wings and feet of birds, no less than the hands and feet of man, all arise from the same fundamental form.” It is, says Prof. Huxley,12 “quite in the later stages of development that the young human being presents marked differences from the young ape, while the latter departs as much from the dog in its developments, as the man does. Startling as this last assertion may appear to be, it is demonstrably true.”
Embryonic Development.—Humans develop from an ovule, about the 125th of an inch in diameter, which is identical to the ovules of other animals. At a very early stage, the embryo is almost indistinguishable from those of other vertebrates. At this stage, the arteries branch out in arch-like shapes, as if to supply blood to gills that are not present in higher vertebrates, although the slits on the sides of the neck still exist (f, g, fig. 1), indicating their previous position. A bit later, when the limbs develop, “the feet of lizards and mammals,” as the notable Von Baer points out, “the wings and feet of birds, and the hands and feet of humans all originate from the same basic form.” It is, as Prof. Huxley says,12 “only in the later stages of development that the young human exhibits clear differences from the young ape, while the latter diverges as much from the dog in its development as humans do. As surprising as this claim might sound, it is undeniably true.”

Fig. 1. Upper figure human embryo, from Ecker. Lower figure that of a dog, from Bischoff.
Fig. 1. The upper figure shows a human embryo, from Ecker. The lower figure depicts that of a dog, from Bischoff.
a. Fore-brain, cerebral hemispheres, &c. | g. Second visceral arch. | |
b. Mid-brain, corpora quadrigemina. | H. Vertebral columns and muscles in process of development. | |
c. Hind-brain, cerebellum, medulla oblongata. | i. Anterior | ┐ │ extremities ┘ |
d. Eye. | K. Posterior | |
e. Ear. | L. Tail or os coccyx. | |
f. First visceral arch. |
After the foregoing statements made by such high authorities, it would be superfluous on my part to give a number of borrowed details, shewing that the embryo of man closely resembles that of other mammals. It may, however, be added that the human embryo likewise resembles in various points of structure certain low forms when adult. For instance, the heart at first exists as a simple pulsating vessel; the excreta are voided through a cloacal passage; and the os coccyx projects like a true tail, “extending considerably beyond the rudimentary legs.”14 In the embryos of all air-breathing vertebrates, certain glands called the corpora Wolffiana, correspond with and act like the kidneys of mature fishes.15 Even at a later embryonic period, some striking resemblances between man and the lower animals may be observed. Bischoff says that the convolutions of the brain in a human fœtus at the end of the seventh month reach about the same stage of development as in a baboon when adult.16 The great toe, as Prof. Owen remarks,17 “which forms the fulcrum when standing or walking, is perhaps the most characteristic 17peculiarity in the human structure;” but in an embryo, about an inch in length, Prof. Wyman18 found “that the great toe was shorter than the others, and, instead of being parallel to them, projected at an angle from the side of the foot, thus corresponding with the permanent condition of this part in the quadrumana.” I will conclude with a quotation from Huxley,19 who after asking, does man originate in a different way from a dog, bird, frog or fish? says, “the reply is not doubtful for a moment; without question, the mode of origin and the early stages of the development of man are identical with those of the animals immediately below him in the scale: without a doubt in these respects, he is far nearer to apes, than the apes are to the dog.”
After what has been said by such high authorities, it would be unnecessary for me to provide numerous borrowed details showing that the human embryo closely resembles those of other mammals. However, it's worth noting that the human embryo also shares various structural similarities with certain lower forms when they are fully developed. For example, the heart initially exists as a simple pulsating vessel; waste is expelled through a cloacal passage; and the tailbone protrudes like a real tail, "extending considerably beyond the rudimentary legs." 14 In the embryos of all air-breathing vertebrates, certain glands called the corpora Wolffiana correspond to and function like the kidneys of mature fish.15 Even at a later embryonic stage, some striking similarities between humans and lower animals can be observed. Bischoff notes that the brain folds in a human fetus at the end of the seventh month reach a developmental stage comparable to that of an adult baboon.16 The big toe, as Prof. Owen points out,17 "which acts as the lever when standing or walking, is perhaps the most distinctive feature in human structure;" but in an embryo about an inch long, Prof. Wyman18 found "that the big toe was shorter than the others, and instead of being parallel to them, projected at an angle from the side of the foot, thus resembling the permanent condition of this part in primates." I will conclude with a quote from Huxley,19 who, after asking whether humans originate differently from a dog, bird, frog, or fish, states, "the answer is not in doubt for a moment; without question, the way humans originate and the early stages of human development are identical to those of the animals immediately below them on the scale: without a doubt in these respects, they are much closer to apes than apes are to dogs."
Rudiments.—This subject, though not intrinsically more important than the two last, will for several reasons be here treated with more fullness.20 Not one of the higher animals can be named which does not bear some part in a rudimentary condition; and man forms no exception to the rule. Rudimentary organs must be distinguished from those that are nascent; though in some cases the distinction is not easy. The former are either absolutely useless, such as the mammæ of male quadrupeds, or the incisor teeth of ruminants which never cut through the gums; or they are of such slight service to their present possessors, that we cannot suppose that they were developed under the conditions 18which now exist. Organs in this latter state are not strictly rudimentary, but they are tending in this direction. Nascent organs, on the other hand, though not fully developed, are of high service to their possessors, and are capable of further development. Rudimentary organs are eminently variable; and this is partly intelligible, as they are useless or nearly useless, and consequently are no longer subjected to natural selection. They often become wholly suppressed. When this occurs, they are nevertheless liable to occasional reappearance through reversion; and this is a circumstance well worthy of attention.
Basics.—This topic, while not inherently more important than the previous two, will be discussed in more detail for several reasons.20 There is not a single higher animal that doesn’t have some part in a rudimentary state; humans are no exception. Rudimentary organs should be distinguished from those that are developing, although sometimes it's not easy to make that distinction. The former are either completely useless, like the mammary glands of male mammals, or the incisor teeth of ruminants that never break through the gums; or they are so minimally useful to their current owners that we can't assume they developed under the circumstances that exist now. Organs in this latter state aren’t strictly rudimentary, but are moving in that direction. Developing organs, on the other hand, while not fully formed, are very useful to their owners and can develop further. Rudimentary organs are very variable; this makes sense since they are useless or nearly useless and therefore aren't subject to natural selection anymore. They often become completely suppressed. When this happens, they can still reappear occasionally through reversion, which is an interesting point to note.
Disuse at that period of life, when an organ is chiefly used, and this is generally during maturity, together with inheritance at a corresponding period of life, seem to have been the chief agents in causing organs to become rudimentary. The term “disuse” does not relate merely to the lessened action of muscles, but includes a diminished flow of blood to a part or organ, from being subjected to fewer alternations of pressure, or from becoming in any way less habitually active. Rudiments, however, may occur in one sex of parts normally present in the other sex; and such rudiments, as we shall hereafter see, have often originated in a distinct manner. In some cases organs have been reduced by means of natural selection, from having become injurious to the species under changed habits of life. The process of reduction is probably often aided through the two principles of compensation and economy of growth; but the later stages of reduction, after disuse has done all that can fairly be attributed to it, and when the saving to be effected by the economy of growth would be very small,21 are difficult to understand. The final and com19plete suppression of a part, already useless and much reduced in size, in which case neither compensation nor economy can come into play, is perhaps intelligible by the aid of the hypothesis of pangenesis, and apparently in no other way. But as the whole subject of rudimentary organs has been fully discussed and illustrated in my former works,22 I need here say no more on this head.
Disuse during the stage of life when an organ is mostly used, which is typically during adulthood, along with inheritance at a similar life stage, seem to be the main reasons why organs become less developed. The term “disuse” doesn’t just refer to reduced muscle activity; it also includes a decreased blood flow to a part or organ due to fewer changes in pressure, or because it is less frequently used. However, rudimentary organs can appear in one sex for parts that are usually found in the other sex; and as we will explore later, these rudiments have often originated in different ways. In some cases, organs have diminished through natural selection because they became harmful to the species due to altered living conditions. The reduction process is likely often supported by the principles of compensation and growth efficiency; however, the later stages of reduction, after disuse has done all it reasonably can, and when the savings from growth efficiency would be minimal,21 are hard to explain. The complete and final loss of a part that is already useless and significantly reduced in size, where neither compensation nor efficiency can apply, might be understandable through the idea of pangenesis, and seemingly in no other way. But since the entire topic of rudimentary organs has been thoroughly discussed and illustrated in my earlier works,22 I won’t elaborate further on this matter.
Rudiments of various muscles have been observed in many parts of the human body;23 and not a few muscles, which are regularly present in some of the lower animals can occasionally be detected in man in a greatly reduced condition. Every one must have noticed the power which many animals, especially horses, possess of moving or twitching their skin; and this is effected by the panniculus carnosus. Remnants of this muscle in an efficient state are found in various parts of our bodies; for instance, on the forehead, by which the eyebrows are raised. The platysma myoides, which is well developed on the neck, belongs to this system, but cannot be voluntarily brought into action. Prof. Turner, of Edinburgh, has occasionally detected, as he informs me, muscular fasciculi in five different situations, namely in the axillæ, near the scapulæ, &c., all of which must be referred to the system of the panniculus. He has also shewn24 that the musculus sternalis or sternalis brutorum, which is not an extension of the rectus abdominalis, but is closely allied to the panniculus, oc20curred in the proportion of about 3 per cent. in upwards of 600 bodies: he adds, that this muscle affords “an excellent illustration of the statement that occasional and rudimentary structures are especially liable to variation in arrangement.”
Rudimentary versions of various muscles can be found in many parts of the human body;23 and several muscles that are regularly present in some lower animals can sometimes be found in humans, albeit in a much-reduced form. Most people must have noticed how many animals, especially horses, have the ability to move or twitch their skin; this is done by the panniculus carnosus. Remnants of this muscle in an active state are present in different areas of our bodies, like on the forehead, where it helps raise the eyebrows. The platysma myoides, which is well developed in the neck, is part of this system but can't be controlled voluntarily. Professor Turner from Edinburgh has occasionally found muscular bundles in five different locations, such as in the armpits and near the shoulder blades, all of which belong to the panniculus system. He has also shown24 that the musculus sternalis or sternalis brutorum, which isn't an extension of the rectus abdominalis but is closely related to the panniculus, occurs in about 3 percent of over 600 bodies: he adds that this muscle provides “an excellent illustration of the statement that occasional and rudimentary structures are especially prone to variation in arrangement.”
Some few persons have the power of contracting the superficial muscles on their scalps; and these muscles are in a variable and partially rudimentary condition. M. A. de Candolle has communicated to me a curious instance of the long-continued persistence or inheritance of this power, as well as of its unusual development. He knows a family, in which one member, the present head of a family, could, when a youth, pitch several heavy books from his head by the movement of the scalp alone; and he won wagers by performing this feat. His father, uncle, grandfather, and all his three children possess the same power to the same unusual degree. This family became divided eight generations ago into two branches; so that the head of the above-mentioned branch is cousin in the seventh degree to the head of the other branch. This distant cousin resides in another part of France, and on being asked whether he possessed the same faculty, immediately exhibited his power. This case offers a good illustration how persistently an absolutely useless faculty may be transmitted.
Some people have the ability to contract the superficial muscles on their scalps, and these muscles are in a variable and somewhat rudimentary state. M. A. de Candolle shared an interesting example of the long-lasting persistence or inheritance of this ability, as well as its unusual development. He knows a family where one member, the current head of the family, could, when he was younger, throw several heavy books off his head just by moving his scalp; he even won bets by doing this. His father, uncle, grandfather, and all three of his children have the same ability to an unusual degree. This family split into two branches eight generations ago, so the head of the mentioned branch is a seventh-degree cousin to the head of the other branch. This distant cousin lives in another part of France, and when asked if he had the same skill, he immediately demonstrated it. This case nicely illustrates how persistently a completely useless ability can be passed down.
The extrinsic muscles which serve to move the whole external ear, and the intrinsic muscles which move the different parts, all of which belong to the system of the panniculus, are in a rudimentary condition in man; they are also variable in development, or at least in function. I have seen one man who could draw his ears forwards, and another who could draw them backwards;25
The external muscles that move the entire outer ear and the internal muscles that adjust the various parts, all part of the panniculus system, are underdeveloped in humans. They also vary in how they develop or work. I've seen one person who could pull their ears forward and another who could pull them backward;25
21 and from what one of these persons told me, it is probable that most of us by often touching our ears and thus directing our attention towards them, could by repeated trials recover some power of movement. The faculty of erecting the ears and of directing them to different points of the compass, is no doubt of the highest service to many animals, as they thus perceive the point of danger; but I have never heard of a man who possessed the least power of erecting his ears,—the one movement which might be of use to him. The whole external shell of the ear may be considered a rudiment, together with the various folds and prominences (helix and anti-helix, tragus and anti-tragus, &c.) which in the lower animals strengthen and support the ear when erect, without adding much to its weight. Some authors, however, suppose that the cartilage of the shell serves to transmit vibrations to the acoustic nerve; but Mr. Toynbee,26 after collecting all the known evidence on this head, concludes that the external shell is of no distinct use. The ears of the chimpanzee and orang are curiously like those of man, and I am assured by the keepers in the Zoological Gardens that these animals never move or erect them; so that they are in an equally rudimentary condition, as far as function is concerned, as in man. Why these animals, as well as the progenitors of man, should have lost the power of erecting their ears we cannot say. It may be, though I am not quite satisfied with this view, that owing to their arboreal habits and great strength they were but little exposed to danger, and so during a lengthened period moved their ears but little, and thus gradually lost the power of moving them. This would be a parallel case with that of those large and heavy birds, 22which from inhabiting oceanic islands have not been exposed to the attacks of beasts of prey, and have consequently lost the power of using their wings for flight.
21 From what one of these individuals shared with me, it's likely that most of us could regain some ability to move our ears by frequently touching them and paying attention to that area. The ability to lift the ears and move them in different directions is undoubtedly very useful for many animals, as it helps them identify potential dangers. However, I've never heard of a human being who could lift their ears—an ability that could actually benefit them. The entire outer structure of the ear can be seen as a remnant, along with the various folds and shapes (like the helix and anti-helix, tragus and anti-tragus, etc.) that support and stabilize the ear when raised without adding much weight. Some writers argue that the cartilage of the ear helps transmit vibrations to the auditory nerve, but Mr. Toynbee,26 after reviewing all the evidence, concludes that the outer ear serves no specific purpose. The ears of chimpanzees and orangutans are strikingly similar to those of humans, and the caretakers at the Zoological Gardens have assured me that these animals never move or raise their ears, indicating they are in a similarly undeveloped state functionally, as in humans. Why these creatures, along with the ancestors of humans, have lost the ability to lift their ears is unclear. It may be, although I'm not entirely convinced by this explanation, that due to their tree-dwelling lifestyle and significant strength, they were less exposed to danger and, as a result, didn't move their ears much over time, eventually losing that ability. This situation is reminiscent of those large, heavy birds that, having lived on isolated oceanic islands, have not faced predators and consequently lost the ability to use their wings for flying. 22

Fig. 2. Human Ear, modelled
and drawn by Mr. Woolner.
a. The projecting point.
Fig. 2. Human Ear, modeled and drawn by Mr. Woolner.
a. The projecting point.
The celebrated sculptor, Mr. Woolner, informs me of one little peculiarity in the external ear, which he has often observed both in men and women, and of which he perceived the full signification. His attention was first called to the subject whilst at work on his figure of Puck, to which he had given pointed ears. He was thus led to examine the ears of various monkeys, and subsequently more carefully those of man. The peculiarity consists in a little blunt point, projecting from the inwardly folded margin, or helix. Mr. Woolner made an exact model of one such case, and has sent me the accompanying drawing. (Fig. 2.) These points not only project inwards, but often a little outwards, so that they are visible when the head is viewed from directly in front or behind. They are variable in size and somewhat in position, standing either a little higher or lower; and they sometimes occur on one ear and not on the other. Now the meaning of these projections is not, I think, doubtful; but it may be thought that they offer too trifling a character to be worth notice. This thought, however, is as false as it is natural. Every character, however slight, must be the result of some definite cause; and if it occurs in many individuals deserves consideration. The helix obviously consists of the extreme margin of the ear folded inwards; and this folding appears to be in some manner connected with the23 whole external ear being permanently pressed backwards. In many monkeys, which do not stand high in the order, as baboons and some species of macacus,27 the upper portion of the ear is slightly pointed, and the margin is not at all folded inwards; but if the margin were to be thus folded, a slight point would necessarily project inwards and probably a little outwards. This could actually be observed in a specimen of the Ateles beelzebuth in the Zoological Gardens; and we may safely conclude that it is a similar structure—a vestige of formerly pointed ears—which occasionally reappears in man.
The well-known sculptor, Mr. Woolner, tells me about a small quirk in the outer ear that he has frequently noticed in both men and women and understands its significance. He first became interested in this topic while working on his statue of Puck, to which he gave pointed ears. This prompted him to examine the ears of various monkeys, and later to look closely at human ears. The quirk is a small blunt point that sticks out from the inwardly folded edge, or helix. Mr. Woolner created an exact model of one such example and sent me the drawing that goes with it. (Fig. 2.) These points not only extend inwards but often a little outwards as well, making them visible when you look at the head from directly in front or behind. Their size and position can vary; they can be a bit higher or lower and may appear on one ear and not the other. I don't think the purpose of these projections is unclear, but some might consider them too minor to be noteworthy. However, that belief is as incorrect as it is common. Every trait, no matter how small, must have a specific cause, and if it shows up in many people, it merits attention. The helix clearly consists of the outer edge of the ear folded inward; this folding seems to be connected to the entire outer ear being permanently pushed backwards. In several monkeys that are lower on the evolutionary scale, like baboons and some species of macaques, the upper part of the ear is slightly pointed, and the edge is not folded inward at all; however, if the edge were to fold inward, a slight point would naturally extend inwards and possibly a little outwards as well. This was actually seen in a specimen of the Ateles beelzebuth in the Zoological Gardens, leading us to conclude that this kind of structure—a remnant of once pointed ears—occasionally reappears in humans.
The nictitating membrane, or third eyelid, with its accessory muscles and other structures, is especially well developed in birds, and is of much functional importance to them, as it can be rapidly drawn across the whole eye-ball. It is found in some reptiles and amphibians, and in certain fishes, as in sharks. It is fairly well developed in the two lower divisions of the mammalian series, namely, in the monotremata and marsupials, and in some few of the higher mammals, as in the walrus. But in man, the quadrumana, and most other mammals, it exists, as is admitted by all anatomists, as a mere rudiment, called the semilunar fold.28
The nictitating membrane, or third eyelid, along with its supporting muscles and other structures, is particularly well developed in birds and serves a significant functional purpose for them, as it can quickly sweep across the entire eyeball. It's also present in some reptiles, amphibians, and certain fish, like sharks. It is somewhat developed in the two lower groups of mammals, specifically in monotremes and marsupials, and in a few higher mammals, such as the walrus. However, in humans, primates, and most other mammals, it exists, as all anatomists agree, as a simple remnant known as the semilunar fold.28
The sense of smell is of the highest importance to the greater number of mammals—to some, as the ruminants, in warning them of danger; to others, as the 24carnivora, in finding their prey; to others, as the wild boar, for both purposes combined. But the sense of smell is of extremely slight service, if any, even to savages, in whom it is generally more highly developed than in the civilised races. It does not warn them of danger, nor guide them to their food; nor does it prevent the Esquimaux from sleeping in the most fetid atmosphere, nor many savages from eating half-putrid meat. Those who believe in the principle of gradual evolution, will not readily admit that this sense in its present state was originally acquired by man, as he now exists. No doubt he inherits the power in an enfeebled and so far rudimentary condition, from some early progenitor, to whom it was highly serviceable and by whom it was continually used. We can thus perhaps understand how it is, as Dr. Maudsley has truly remarked,29 that the sense of smell in man “is singularly effective in recalling vividly the ideas and images of forgotten scenes and places;” for we see in those animals, which have this sense highly developed, such as dogs and horses, that old recollections of persons and places are strongly associated with their odour.
The sense of smell is extremely important for most mammals. For some, like ruminants, it helps them detect danger; for others, like carnivores, it helps them hunt for food; and for animals like wild boars, it serves both purposes. However, the sense of smell is not very useful, if at all, even for primitive people, who typically have a more developed sense of smell than modern humans. It doesn’t warn them about danger or help them find food, nor does it stop the Eskimos from sleeping in very unpleasant environments, or many primitive people from eating meat that’s almost rotten. Those who believe in gradual evolution may find it hard to accept that our sense of smell, as it is now, was originally developed by humans as they exist today. It's likely that we inherit this ability, in a weakened and somewhat basic form, from some early ancestor for whom it was very useful and used frequently. This might explain why, as Dr. Maudsley observed, the sense of smell in humans “is particularly good at vividly bringing back memories and images of forgotten scenes and places.” We can see in animals with a highly developed sense of smell, like dogs and horses, that old memories of people and places are closely linked to their scents.
Man differs conspicuously from all the other Primates in being almost naked. But a few short straggling hairs are found over the greater part of the body in the male sex, and fine down on that of the female sex, In individuals belonging to the same race these hairs are highly variable, not only in abundance, but likewise in position: thus the shoulders in some Europeans are quite naked, whilst in others they bear thick tufts of hair.30 There can be little doubt that the hairs 25thus scattered over the body are the rudiments of the uniform hairy coat of the lower animals. This view is rendered all the more probable, as it is known that fine, short, and pale-coloured hairs on the limbs and other parts of the body occasionally become developed into “thickset, long, and rather coarse dark hairs,” when abnormally nourished near old-standing inflamed surfaces.31
Humans stand out from all other primates mainly because they're almost hairless. Most of the body only has a few scattered hairs in males and fine fuzz in females. Within the same race, these hairs vary greatly, not just in how much hair there is but also in where it grows: some European men have completely bare shoulders, while others have thick patches of hair. 30 It’s clear that the hairs spread across the body are remnants of the full fur coat found in lower animals. This idea is supported by the fact that fine, short, light-colored hairs on the limbs and elsewhere can turn into "thick, long, and somewhat coarse dark hairs" when they’re unusually nourished near old inflamed areas. 31
I am informed by Mr. Paget that persons belonging to the same family often have a few hairs in their eyebrows much longer than the others; so that this slight peculiarity seems to be inherited. These hairs apparently represent the vibrissæ, which are used as organs of touch by many of the lower animals. In a young chimpanzee I observed that a few upright, rather long, hairs, projected above the eyes, where the true eyebrows, if present, would have stood.
I was told by Mr. Paget that people from the same family often have a few longer hairs in their eyebrows compared to the others; this small trait seems to be inherited. These hairs likely serve a purpose similar to the whiskers, which many lower animals use as touch-sensitive organs. I noticed in a young chimpanzee that a few straight, somewhat long hairs stuck up above the eyes, where the actual eyebrows, if they existed, would be located.
The fine wool-like hair, or so-called lanugo, with which the human fœtus during the sixth month is thickly covered, offers a more curious case. It is first developed, during the fifth month, on the eyebrows and face, and especially round the mouth, where it is much longer than that on the head. A moustache of this kind was observed by Eschricht32 on a female fœtus; but this is not so surprising a circumstance as it may at first appear, for the two sexes generally resemble each other in all external characters during an early period of growth. The direction and arrangement of the hairs on all parts of the fœtal body are the same as in the adult, but are subject to much variability. The whole surface, including even the forehead and ears, is thus thickly clothed; but it is a significant fact that the palms of the hands and 26the soles of the feet are quite naked, like the inferior surfaces of all four extremities in most of the lower animals. As this can hardly be an accidental coincidence, we must consider the woolly covering of the fœtus to be the rudimental representative of the first permanent coat of hair in those mammals which are born hairy. This representation is much more complete, in accordance with the usual law of embryological development, than that afforded by the straggling hairs on the body of the adult.
The fine, wool-like hair, known as lanugo, that covers the human fetus during the sixth month is quite an interesting case. It first appears during the fifth month on the eyebrows and face, especially around the mouth, where it's longer than the hair on the head. Eschricht32 observed this kind of mustache on a female fetus, which might seem surprising at first, but it's not unusual because both sexes look quite similar in their external features during the early stages of development. The direction and arrangement of the hair on all parts of the fetal body are similar to adults, but they can vary a lot. The entire surface, including the forehead and ears, is covered, but notably, the palms of the hands and the soles of the feet are completely bare, like the undersides of limbs in many lower animals. Since this seems unlikely to be just a coincidence, we should view the fuzzy covering of the fetus as a rudimentary version of the first permanent coat of hair in mammals that are born with fur. This representation is much more developed, following the usual patterns of embryonic growth, than the scattered hairs found on the bodies of adults.
It appears as if the posterior molar or wisdom-teeth were tending to become rudimentary in the more civilised races of man. These teeth are rather smaller than the other molars, as is likewise the case with the corresponding teeth in the chimpanzee and orang; and they have only two separate fangs. They do not cut through the gums till about the seventeenth year, and I am assured by dentists that they are much more liable to decay, and are earlier lost, than the other teeth. It is also remarkable that they are much more liable to vary both in structure and in the period of their development than the other teeth.33 In the Melanian races, on the other hand, the wisdom-teeth are usually furnished with three separate fangs, and are generally sound: they also differ from the other molars in size less than in the Caucasian races.34 Prof. Schaaffhausen accounts for this difference between the races by “the posterior dental portion of the jaw being always shortened” in those that are civilised,35 and this shortening may, I presume, be safely attributed to civi27lised men habitually feeding on soft, cooked food, and thus using their jaws less. I am informed by Mr. Brace that it is becoming quite a common practice in the United States to remove some of the molar teeth of children, as the jaw does not grow large enough for the perfect development of the normal number.
It seems that the back molars, or wisdom teeth, are becoming less developed in more civilized populations. These teeth are smaller than the other molars, similar to those in chimpanzees and orangutans, and they typically have only two distinct roots. They usually don’t break through the gums until around the age of seventeen, and dentists tell me they tend to decay more easily and are lost sooner than other teeth. It's also notable that these teeth vary more in structure and development timing compared to other teeth. In Melanesian populations, however, wisdom teeth usually have three separate roots and are generally healthier; they also differ less in size from other molars than they do in Caucasian populations. Prof. Schaaffhausen explains this difference between the races by noting that “the back dental part of the jaw is always shorter” in those who are civilized, and this shortening can likely be linked to civilized humans typically eating soft, cooked foods, leading to less jaw usage. Mr. Brace informs me that it's becoming quite common in the United States to remove some of children's molars because their jaws don’t grow large enough for the normal amount to fully develop.
With respect to the alimentary canal I have met with an account of only a single rudiment, namely the vermiform appendage of the cæcum. The cæcum is a branch or diverticulum of the intestine, ending in a cul-de-sac, and it is extremely long in many of the lower vegetable-feeding mammals. In the marsupial koala it is actually more than thrice as long as the whole body.36 It is sometimes produced into a long gradually-tapering point, and is sometimes constricted in parts. It appears as if, in consequence of changed diet or habits, the cæcum had become much shortened in various animals, the vermiform appendage being left as a rudiment of the shortened part. That this appendage is a rudiment, we may infer from its small size, and from the evidence which Prof. Canestrini37 has collected of its variability in man. It is occasionally quite absent, or again is largely developed. The passage is sometimes completely closed for half or two-thirds of its length, with the terminal part consisting of a flattened solid expansion. In the orang this appendage is long and convoluted: in man it arises from the end of the short cæcum, and is commonly from four to five inches in length, being only about the third of an inch in diameter. Not only is it useless, but it is sometimes the cause of death, of which fact I have lately heard two instances: this is due to small hard bodies, 28such as seeds, entering the passage and causing inflammation.38
Regarding the digestive system, I’ve come across information about only one remnant, which is the vermiform appendix of the cecum. The cecum is a branch or pouch of the intestine that ends in a dead end, and it can be extremely long in many lower herbivorous mammals. In the marsupial koala, it's actually more than three times the length of its entire body.36 Sometimes, it ends in a long, gradually tapering point, while in other cases, it becomes constricted in certain areas. It seems that due to changes in diet or habits, the cecum has shortened in various animals, leaving the vermiform appendix as a remnant of the shortened section. We can infer that this appendix is a remnant because of its small size and from the evidence collected by Prof. Canestrini37 regarding its variability in humans. Sometimes it’s completely absent or can be quite developed. The passage may also be fully closed for half or two-thirds of its length, with the end part being a flattened solid expansion. In orangutans, this appendix is long and coiled; in humans, it originates from the end of the short cecum and typically measures about four to five inches in length, with a diameter of only about a third of an inch. Not only is it unnecessary, but it can sometimes lead to death; I've recently heard of two cases where this occurred because small hard objects, like seeds, entered the passage and caused inflammation.38
In the Quadrumana and some other orders of mammals, especially in the Carnivora, there is a passage near the lower end of the humerus, called the supra-condyloid foramen, through which the great nerve of the fore limb passes, and often the great artery. Now in the humerus of man, as Dr. Struthers39 and others have shewn, there is generally a trace of this passage, and it is sometimes fairly well developed, being formed by a depending hook-like process of bone, completed by a band of ligament. When present the great nerve invariably passes through it, and this clearly indicates that it is the homologue and rudiment of the supra-condyloid foramen of the lower animals. Prof. Turner estimates, as he informs me, that it occurs in about one per cent. of recent skeletons; but during ancient times it appears to have been much more common. Mr. Busk40 has collected the following evidence on this head: Prof. Broca “noticed the perforation in four and a half per cent. of the arm-bones collected in the ‘Cimetière du Sud’ at Paris; and in the Grotto of Orrony, the contents of which are referred to the Bronze period, as many as eight humeri out of thirty-two were perforated; but this extraordinary proportion, he thinks, might be due to the cavern having been a sort of 29 ‘family vault.’ Again, M. Dupont found 30 per cent. of perforated bones in the caves of the Valley of the Lesse, belonging to the Reindeer period; whilst M. Leguay, in a sort of dolmen at Argenteuil, observed twenty-five per cent. to be perforated; and M. Pruner-Bey found twenty-six per cent. in the same condition in bones from Vauréal. Nor should it be left unnoticed that M. Pruner-Bey states that this condition is common in Guanche skeletons.” The fact that ancient races, in this and several other cases, more frequently present structures which resemble those of the lower animals than do the modern races, is interesting. One chief cause seems to be that ancient races stand somewhat nearer than modern races in the long line of descent to their remote animal-like progenitors.
In the Quadrumana and some other groups of mammals, especially in the Carnivora, there’s an opening near the lower end of the humerus called the supra-condyloid foramen, through which the major nerve of the forelimb passes, and often the major artery as well. In the humerus of humans, as Dr. Struthers39 and others have shown, there is usually some trace of this passage, and it can sometimes be quite well-developed, formed by a downward hook-like bone process, completed by a band of ligament. When it’s present, the major nerve always passes through it, clearly indicating that it’s the homologue and remnant of the supra-condyloid foramen found in lower animals. Prof. Turner estimates, as he informed me, that it occurs in about one percent of recent skeletons; however, in ancient times, it seems to have been much more common. Mr. Busk40 has gathered the following evidence on this topic: Prof. Broca “observed the perforation in four and a half percent of the arm bones collected in the ‘Cimetière du Sud’ in Paris; and in the Grotto of Orrony, which dates back to the Bronze Age, as many as eight out of thirty-two humeri were perforated; but he thinks this extraordinary proportion might be due to the cavern serving as a sort of 29 ‘family vault.’ Additionally, M. Dupont found 30 percent of perforated bones in the caves of the Valley of the Lesse, from the Reindeer period; while M. Leguay, in a sort of dolmen at Argenteuil, noted that twenty-five percent were perforated; and M. Pruner-Bey discovered twenty-six percent in the same condition in bones from Vauréal. It’s also worth noting that M. Pruner-Bey states this condition is common in Guanche skeletons.” The fact that ancient races more frequently exhibit structures resembling those of lower animals, compared to modern races, is intriguing. One main reason seems to be that ancient races are somewhat closer in the long lineage of descent to their distant animal-like ancestors.
The os coccyx in man, though functionless as a tail, plainly represents this part in other vertebrate animals. At an early embryonic period it is free, and, as we have seen, projects beyond the lower extremities. In certain rare and anomalous cases it has been known, according to Isidore Geoffroy St.-Hilaire and others,41 to form a small external rudiment of a tail. The os coccyx is short, usually including only four vertebræ: and these are in a rudimental condition, for they consist, with the exception of the basal one, of the centrum alone.42 They are furnished with some small muscles; one of which, as I am informed by Prof. Turner, has been expressly described by Theile as a rudimentary repetition of the extensor of the tail, which is so largely developed in many mammals.
The coccyx in humans, although it doesn't function like a tail, clearly represents this part found in other vertebrate animals. During early embryonic development, it is free and, as we've seen, extends beyond the lower limbs. In some rare and unusual cases, it has been reported, according to Isidore Geoffroy St.-Hilaire and others,41 to form a small external remnant of a tail. The coccyx is short, usually consisting of only four vertebrae, which are in a rudimentary state, as they are composed, except for the base, of just the centrum.42 It is equipped with a few small muscles; one of which, as noted by Prof. Turner, has been specifically identified by Theile as a rudimentary version of the tail extensor, which is highly developed in many mammals.
The spinal cord in man extends only as far downwards as the last dorsal or first lumbar vertebra; but a 30thread-like structure (the filum terminale) runs down the axis of the sacral part of the spinal canal, and even along the back of the coccygeal bones. The upper part of this filament, as Prof. Turner informs me, is undoubtedly homologous with the spinal cord; but the lower part apparently consists merely of the pia mater, or vascular investing membrane. Even in this case the os coccyx may be said to possess a vestige of so important a structure as the spinal cord, though no longer enclosed within a bony canal. The following fact, for which I am also indebted to Prof. Turner, shews how closely the os coccyx corresponds with the true tail in the lower animals: Luschka has recently discovered at the extremity of the coccygeal bones a very peculiar convoluted body, which is continuous with the middle sacral artery; and this discovery led Krause and Meyer to examine the tail of a monkey (Macacus) and of a cat, in both of which they found, though not at the extremity, a similarly convoluted body.
The spinal cord in humans only extends down to the last thoracic or first lumbar vertebra; however, a 30thread-like structure (the filum terminale) runs along the sacral part of the spinal canal and even along the back of the tailbone. According to Prof. Turner, the upper part of this filament is definitely related to the spinal cord; but the lower part seems to consist mainly of the pia mater, or the vascular covering membrane. In this case, the coccyx can be said to have a remnant of such an important structure as the spinal cord, although it's no longer enclosed within a bony canal. Another fact that I also owe to Prof. Turner shows how closely the coccyx corresponds to the actual tail in lower animals: Luschka recently found at the end of the coccygeal bones a very unique convoluted body that connects with the middle sacral artery; this discovery prompted Krause and Meyer to study the tail of a monkey (Macacus) and a cat, where they discovered, although not at the very end, a similarly convoluted body.
The reproductive system offers various rudimentary structures; but these differ in one important respect from the foregoing cases. We are not here concerned with a vestige of a part which does not belong to the species in an efficient state; but with a part which is always present and efficient in the one sex, being represented in the other by a mere rudiment. Nevertheless, the occurrence of such rudiments is as difficult to explain on the belief of the separate creation of each species, as in the foregoing cases. Hereafter I shall have to recur to these rudiments, and shall shew that their presence generally depends merely on inheritance; namely, on parts acquired by one sex having been partially transmitted to the other. Here I will only give some instances of such rudiments. It is well known that in the males of all mammals, in31cluding man, rudimentary mammæ exist. These in several instances have become well developed, and have yielded a copious supply of milk. Their essential identity in the two sexes is likewise shewn by their occasional sympathetic enlargement in both during an attack of the measles. The vesicula prostratica, which has been observed in many male mammals, is now universally acknowledged to be the homologue of the female uterus, together with the connected passage. It is impossible to read Leuckart’s able description of this organ, and his reasoning, without admitting the justness of his conclusion. This is especially clear in the case of those mammals in which the true female uterus bifurcates, for in the males of these the vesicula likewise bifurcates.43 Some additional rudimentary structures belonging to the reproductive system might here have been adduced.44
The reproductive system has various basic structures; however, these differ in one important way from the previous cases. We are not dealing with a remnant of a part that doesn't belong to the species in a functional state; instead, we have a part that is always present and functional in one sex, while represented in the other by just a small remnant. Still, the existence of such remnants is as hard to explain under the idea of each species being created separately, as in the previous cases. Later, I will revisit these remnants and demonstrate that their presence generally depends solely on inheritance; specifically, that parts acquired by one sex have been partially passed down to the other. For now, I will just provide a few examples of such remnants. It is well known that in the males of all mammals, including humans, there are rudimentary mammary glands. In several cases, these have developed well and produced a significant amount of milk. Their essential similarity in both sexes is also shown by their occasional synchronized enlargement in both during measles outbreaks. The vesicula prostratica, observed in many male mammals, is now universally recognized as the counterpart of the female uterus and the related passage. It's impossible to read Leuckart’s excellent description of this organ and his reasoning without agreeing with his conclusion. This is especially evident in those mammals where the actual female uterus is bifurcated, as in the males, this vesicula also bifurcates.43 Some additional rudimentary structures related to the reproductive system could have been mentioned here. 44
The bearing of the three great classes of facts now given is unmistakeable. But it would be superfluous here fully to recapitulate the line of argument given in detail in my ‘Origin of Species.’ The homological construction of the whole frame in the members of the same class is intelligible, if we admit their descent from a common progenitor, together with their subsequent adaptation to diversified conditions. On any other view the similarity of pattern between the hand of a man or monkey, the foot of a horse, the flipper of a seal, the wing of a bat, &c., is utterly inexplicable. It is no scientific 32explanation to assert that they have all been formed on the same ideal plan. With respect to development, we can clearly understand, on the principle of variations supervening at a rather late embryonic period, and being inherited at a corresponding period, how it is that the embryos of wonderfully different forms should still retain, more or less perfectly, the structure of their common progenitor. No other explanation has ever been given of the marvellous fact that the embryo of a man, dog, seal, bat, reptile, &c., can at first hardly be distinguished from each other. In order to understand the existence of rudimentary organs, we have only to suppose that a former progenitor possessed the parts in question in a perfect state, and that under changed habits of life they became greatly reduced, either from simple disuse, or through the natural selection of those individuals which were least encumbered with a superfluous part, aided by the other means previously indicated.
The significance of the three major classes of facts presented is clear. However, there's no need to fully repeat the detailed argument I provided in my ‘Origin of Species.’ The similar structure of the limbs within the same class makes sense if we accept that they evolved from a common ancestor and adapted to different environments afterward. Any other explanation for the similarity between a human hand or monkey hand, a horse's foot, a seal's flipper, and a bat's wing, etc., is completely baffling. It’s not a scientific explanation to claim they were all created based on the same ideal model. Regarding development, we can easily understand, based on the principle of variations occurring at a relatively late embryonic stage and being inherited at a similar time, how embryos of vastly different species can still show, to some degree, the structure of their common ancestor. No other explanation has ever been provided for the amazing fact that the embryos of a human, dog, seal, bat, reptile, etc., are initially nearly indistinguishable from one another. To explain the existence of rudimentary organs, we only need to assume that a previous ancestor had those parts in a complete form, and that due to changes in lifestyle, they became significantly reduced, either due to simple disuse or through natural selection favoring individuals least burdened by unnecessary parts, supported by the other methods previously mentioned.
Thus we can understand how it has come to pass that man and all other vertebrate animals have been constructed on the same general model, why they pass through the same early stages of development, and why they retain certain rudiments in common. Consequently we ought frankly to admit their community of descent: to take any other view, is to admit that our own structure and that of all the animals around us, is a mere snare laid to entrap our judgment. This conclusion is greatly strengthened, if we look to the members of the whole animal series, and consider the evidence derived from their affinities or classification, their geographical distribution and geological succession. It is only our natural prejudice, and that arrogance which made our forefathers declare that they were descended from demi-gods, which leads us to demur to33 this conclusion. But the time will before long come when it will be thought wonderful, that naturalists, who were well acquainted with the comparative structure and development of man and other mammals, should have believed that each was the work of a separate act of creation.
So, we can see how it has happened that humans and all other vertebrate animals are built on the same general design, why they go through the same early stages of development, and why they share certain common features. Therefore, we should honestly acknowledge their shared ancestry: believing otherwise is to suggest that our own makeup, along with that of all the animals around us, is just a trick to confuse our understanding. This conclusion is even stronger when we examine the entire range of animals and look at the evidence based on their relationships or classification, their geographical spread, and their geological history. It's only our natural bias, and the pride that led our ancestors to claim descent from demi-gods, that causes us to hesitate about33 this conclusion. However, the time will soon come when it will seem incredible that naturalists, who were familiar with the comparative structure and development of humans and other mammals, believed that each was the result of a separate act of creation.
CHAPTER II.
Comparison of the Mental Abilities of Humans and Lower Animals.
The difference in mental power between the highest ape and the lowest savage, immense—Certain instincts in common—The emotions—Curiosity—Imitation—Attention—Memory—Imagination—Reason—Progressive improvement—Tools and weapons used by animals—Language—Self-consciousness—Sense of beauty—Belief in God, spiritual agencies, superstitions.
The gap in mental ability between the smartest ape and the most primitive human is huge—They share certain instincts—Emotions—Curiosity—Imitation—Attention—Memory—Imagination—Reason—Ongoing improvement—Tools and weapons used by animals—Language—Self-awareness—Appreciation of beauty—Belief in God, spiritual forces, superstitions.
We have seen in the last chapter that man bears in his bodily structure clear traces of his descent from some lower form; but it may be urged that, as man differs so greatly in his mental power from all other animals, there must be some error in this conclusion. No doubt the difference in this respect is enormous, even if we compare the mind of one of the lowest savages, who has no words to express any number higher than four, and who uses no abstract terms for the commonest objects or affections,45 with that of the most highly organised ape. The difference would, no doubt, still remain immense, even if one of the higher apes had been improved or civilised as much as a dog has been in comparison with its parent-form, the wolf or jackal. The Fuegians rank amongst the lowest barbarians; but I was continually struck with surprise how closely the three natives on board H.M.S. “Beagle,” who had lived some years in England and could talk a little English, resembled us in disposition and in most of our mental faculties. If no 35organic being excepting man had possessed any mental power, or if his powers had been of a wholly different nature from those of the lower animals, then we should never have been able to convince ourselves that our high faculties had been gradually developed. But it can be clearly shewn that there is no fundamental difference of this kind. We must also admit that there is a much wider interval in mental power between one of the lowest fishes, as a lamprey or lancelet, and one of the higher apes, than between an ape and man; yet this immense interval is filled up by numberless gradations.
We saw in the last chapter that humans exhibit clear signs of their descent from a lower form in their physical structure; however, some might argue that because humans are so different in mental ability from all other animals, there must be a mistake in this conclusion. The difference in this regard is huge, even when we compare the mind of one of the most basic savages, who has no words to express any number above four and doesn’t use abstract terms for even the simplest objects or feelings, with that of the most advanced ape. The gap would still be significant, even if one of the higher apes had been as modified or socialized as much as a dog has compared to its ancestor, the wolf or jackal. The Fuegians are considered among the most primitive barbarians, but I was often amazed by how closely the three natives on board H.M.S. “Beagle,” who had lived in England for a few years and could speak a little English, resembled us in temperament and most of our mental abilities. If no living being other than humans had any mental capacity, or if their capacities were completely different from those of lower animals, we would never have been able to convince ourselves that our advanced abilities developed gradually. However, it can be clearly demonstrated that there is no fundamental difference like that. We must also acknowledge that there is a much greater gap in mental ability between one of the lowest fish, like a lamprey or lancelet, and one of the higher apes, than there is between an ape and a human; yet this vast gap is filled with countless gradations.
Nor is the difference slight in moral disposition between a barbarian, such as the man described by the old navigator Byron, who dashed his child on the rocks for dropping a basket of sea-urchins, and a Howard or Clarkson; and in intellect, between a savage who does not use any abstract terms, and a Newton or Shakspeare. Differences of this kind between the highest men of the highest races and the lowest savages, are connected by the finest gradations. Therefore it is possible that they might pass and be developed into each other.
The difference in moral character is not small between a barbarian, like the man described by the old navigator Byron, who threw his child on the rocks for dropping a basket of sea urchins, and someone like Howard or Clarkson; and in intellect, between a savage who doesn’t use any abstract terms, and a Newton or Shakespeare. Differences of this kind between the most advanced individuals of the highest races and the lowest savages are connected by the finest gradations. So, it’s possible for them to transition into and develop into each other.
My object in this chapter is solely to shew that there is no fundamental difference between man and the higher mammals in their mental faculties. Each division of the subject might have been extended into a separate essay, but must here be treated briefly. As no classification of the mental powers has been universally accepted, I shall arrange my remarks in the order most convenient for my purpose; and will select those facts which have most struck me, with the hope that they may produce some effect on the reader.
My goal in this chapter is simply to show that there is no fundamental difference between humans and the higher mammals in their mental abilities. Each part of the topic could have been expanded into a separate essay, but I will address it briefly here. Since no classification of mental powers has been universally accepted, I will organize my comments in the way that is most convenient for my purpose; I'll choose the facts that have stood out to me the most, hoping they will have some impact on the reader.
With respect to animals very low in the scale, I shall have to give some additional facts under Sexual Selection, shewing that their mental powers are higher than36 might have been expected. The variability of the faculties in the individuals of the same species is an important point for us, and some few illustrations will here be given. But it would be superfluous to enter into many details on this head, for I have found on frequent enquiry, that it is the unanimous opinion of all those who have long attended to animals of many kinds, including birds, that the individuals differ greatly in every mental characteristic. In what manner the mental powers were first developed in the lowest organisms, is as hopeless an enquiry as how life first originated. These are problems for the distant future, if they are ever to be solved by man.
Regarding animals that are very low on the scale, I need to provide some additional facts under Sexual Selection, showing that their mental abilities are higher than36 one might expect. The variability in the abilities among individuals of the same species is a significant point for us, and a few examples will be provided here. However, it would be unnecessary to go into many details on this topic, as I've often found that it is the unanimous opinion of all who have closely studied various animals, including birds, that individuals vary greatly in every mental trait. How mental abilities first developed in the lowest organisms is as futile a question as how life first began. These are problems for the distant future, if they are ever to be solved by humans.
As man possesses the same senses with the lower animals, his fundamental intuitions must be the same. Man has also some few instincts in common, as that of self-preservation, sexual love, the love of the mother for her new-born offspring, the power possessed by the latter of sucking, and so forth. But man, perhaps, has somewhat fewer instincts than those possessed by the animals which come next to him in the series. The orang in the Eastern islands, and the chimpanzee in Africa, build platforms on which they sleep; and, as both species follow the same habit, it might be argued that this was due to instinct, but we cannot feel sure that it is not the result of both animals having similar wants and possessing similar powers of reasoning. These apes, as we may assume, avoid the many poisonous fruits of the tropics, and man has no such knowledge; but as our domestic animals, when taken to foreign lands and when first turned out in the spring, often eat poisonous herbs, which they afterwards avoid, we cannot feel sure that the apes do not learn from their own experience or from that of their parents what fruits to select. It is however certain, as we shall presently see, that apes have37 an instinctive dread of serpents, and probably of other dangerous animals.
As humans have the same senses as lower animals, their basic instincts must be the same. Humans also share a few instincts, like self-preservation, sexual attraction, a mother’s love for her newborn, and the newborn's ability to suck. However, humans likely have somewhat fewer instincts than the animals closest to them. The orangutans in the Eastern islands and chimpanzees in Africa build platforms to sleep on; since both species display this behavior, it could be argued that it’s instinctual. Still, we can’t be sure it’s not just because they have similar needs and reasoning abilities. These apes likely avoid many of the poisonous fruits found in the tropics, and humans don’t have that knowledge. However, when our domestic animals are taken to new lands and first let out in the spring, they often eat poisonous plants initially but learn to avoid them later. So, we can’t say for certain that the apes don’t learn from their own experiences or from their parents which fruits to eat. It is, however, clear, as we will see shortly, that apes have37an instinctive fear of snakes and probably other dangerous animals.
The fewness and the comparative simplicity of the instincts in the higher animals are remarkable in contrast with those of the lower animals. Cuvier maintained that instinct and intelligence stand in an inverse ratio to each other; and some have thought that the intellectual faculties of the higher animals have been gradually developed from their instincts. But Pouchet, in an interesting essay,46 has shewn that no such inverse ratio really exists. Those insects which possess the most wonderful instincts are certainly the most intelligent. In the vertebrate series, the least intelligent members, namely fishes and amphibians, do not possess complex instincts; and amongst mammals the animal most remarkable for its instincts, namely the beaver, is highly intelligent, as will be admitted by every one who has read Mr. Morgan’s excellent account of this animal.47
The few instincts and relative simplicity of the instincts in higher animals are striking compared to those in lower animals. Cuvier argued that instinct and intelligence are inversely related, and some believe that the intellectual abilities of higher animals have gradually evolved from their instincts. However, Pouchet, in an interesting essay,46 showed that no true inverse relationship exists. The insects with the most amazing instincts are definitely the most intelligent. Among vertebrates, the least intelligent groups, like fish and amphibians, lack complex instincts; and among mammals, the animal known for its impressive instincts, the beaver, is very intelligent, as anyone who has read Mr. Morgan’s outstanding account of this animal would agree.47
Although the first dawnings of intelligence, according to Mr. Herbert Spencer,48 have been developed through the multiplication and co-ordination of reflex actions, and although many of the simpler instincts graduate into actions of this kind and can hardly be distinguished from them, as in the case of young animals sucking, yet the more complex instincts seem to have originated independently of intelligence. I am, however, far from wishing to deny that instinctive actions may lose their fixed and untaught character, and be replaced by others performed by the aid of the free will. On the other hand, some intelligent actions—as when, birds on oceanic islands first learn to avoid man—after 38being performed during many generations, become converted into instincts and are inherited. They may then be said to be degraded in character, for they are no longer performed through reason or from experience. But the greater number of the more complex instincts appear to have been gained in a wholly different manner, through the natural selection of variations of simpler instinctive actions. Such variations appear to arise from the same unknown causes acting on the cerebral organisation, which induce slight variations or individual differences in other parts of the body; and these variations, owing to our ignorance, are often said to arise spontaneously. We can, I think, come to no other conclusion with respect to the origin of the more complex instincts, when we reflect on the marvellous instincts of sterile worker-ants and bees, which leave no offspring to inherit the effects of experience and of modified habits.
Although, according to Mr. Herbert Spencer, the early stages of intelligence have developed through the repetition and connection of reflex actions, and while many simpler instincts evolve into actions of this type and can barely be distinguished from them—like young animals sucking—more complex instincts seem to have emerged independently of intelligence. However, I don’t mean to deny that instinctive actions can lose their rigid and unlearned nature and be replaced by actions done with free will. On the other hand, some intelligent actions—like when birds on oceanic islands first learn to avoid humans—after being practiced over many generations, turn into instincts and are passed down. At that point, they can be seen as degraded in nature, as they are no longer performed through reasoning or experience. Yet, most of the more complex instincts appear to have developed in a completely different way, through natural selection of variations in simpler instinctive actions. These variations seem to come from the same unknown factors that influence the brain structure and cause slight variations or individual differences in other body parts; and because of our lack of knowledge, we often claim that these happen spontaneously. I believe we can only conclude that the origins of more complex instincts lie in this reasoning, especially when we consider the incredible instincts of sterile worker ants and bees, which have no offspring to inherit the effects of their experiences and modified behaviors.
Although a high degree of intelligence is certainly compatible with the existence of complex instincts, as we see in the insects just named and in the beaver, it is not improbable that they may to a certain extent interfere with each other’s development. Little is known about the functions of the brain, but we can perceive that as the intellectual powers become highly developed, the various parts of the brain must be connected by the most intricate channels of intercommunication; and as a consequence each separate part would perhaps tend to become less well fitted to answer in a definite and uniform, that is instinctive, manner to particular sensations or associations.
Although a high level of intelligence can definitely coexist with complex instincts, like we see in the insects mentioned earlier and in beavers, it's likely that these two aspects might somewhat interfere with each other's development. We don't know much about the functions of the brain, but we can see that as intellectual abilities become highly advanced, the different parts of the brain must be linked by very intricate communication channels. As a result, each separate part might become less effective at responding in a clear and consistent, or instinctive, way to specific sensations or associations.
I have thought this digression worth giving, because we may easily underrate the mental powers of the higher animals, and especially of man, when we compare their actions founded on the memory of past events, on foresight, reason, and imagination, with39 exactly similar actions instinctively performed by the lower animals; in this latter case the capacity of performing such actions having been gained, step by step, through the variability of the mental organs and natural selection, without any conscious intelligence on the part of the animal during each successive generation. No doubt, as Mr. Wallace has argued,49 much of the intelligent work done by man is due to imitation and not to reason; but there is this great difference between his actions and many of those performed by the lower animals, namely, that man cannot, on his first trial, make, for instance, a stone hatchet or a canoe, through his power of imitation. He has to learn his work by practice; a beaver, on the other hand, can make its dam or canal, and a bird its nest, as well, or nearly as well, the first time it tries, as when old and experienced.
I thought this digression was worth sharing because we often underestimate the mental abilities of higher animals, especially humans, when we compare their actions based on memory, foresight, reasoning, and imagination with39 similar actions instinctively carried out by lower animals. In the latter case, the ability to perform such actions was developed gradually through the variability of mental traits and natural selection, without any conscious intelligence from the animal over each successive generation. Certainly, as Mr. Wallace has pointed out,49 much of the intelligent work done by humans comes from imitation rather than reasoning. However, there's a significant difference between human actions and many performed by lower animals: humans can’t create a stone hatchet or a canoe on their first try just through imitation. They have to learn their skills through practice; whereas a beaver can build its dam or a bird can construct its nest almost as well the first time it tries as when it becomes experienced.
To return to our immediate subject: the lower animals, like man, manifestly feel pleasure and pain, happiness and misery. Happiness is never better exhibited than by young animals, such as puppies, kittens, lambs, &c., when playing together, like our own children. Even insects play together, as has been described by that excellent observer, P. Huber,50 who saw ants chasing and pretending to bite each other, like so many puppies.
To get back to our main topic: lower animals, like humans, clearly experience pleasure and pain, joy and suffering. The best examples of happiness can be seen in young animals, like puppies, kittens, lambs, etc., when they're playing together, just like our kids do. Even insects engage in play, as noted by the great observer, P. Huber,50 who observed ants chasing and pretending to bite one another, much like a group of puppies.
The fact that the lower animals are excited by the same emotions as ourselves is so well established, that it will not be necessary to weary the reader by many details. Terror acts in the same manner on them as on us, causing the muscles to tremble, the heart to palpitate, the sphincters to be relaxed, and the hair to stand on end. Suspicion, the offspring of fear, is eminently characteristic of most wild animals. Courage 40and timidity are extremely variable qualities in the individuals of the same species, as is plainly seen in our dogs. Some dogs and horses are ill-tempered and easily turn sulky; others are good-tempered; and these qualities are certainly inherited. Every one knows how liable animals are to furious rage, and how plainly they show it. Many anecdotes, probably true, have been published on the long-delayed and artful revenge of various animals. The accurate Rengger and Brehm51 state that the American and African monkeys which they kept tame, certainly revenged themselves. The love of a dog for his master is notorious; in the agony of death he has been known to caress his master, and every one has heard of the dog suffering under vivisection, who licked the hand of the operator; this man, unless he had a heart of stone, must have felt remorse to the last hour of his life. As Whewell52 has remarked, “who that reads the touching instances of maternal affection, related so often of the women of all nations, and of the females of all animals, can doubt that the principle of action is the same in the two cases?”
The fact that lower animals experience the same emotions as we do is so well established that it won’t be necessary to bore the reader with too many details. Fear affects them just like it does us, causing their muscles to tremble, their hearts to race, their sphincters to relax, and their hair to stand on end. Suspicion, which comes from fear, is very typical of most wild animals. Courage and timidity can vary greatly among individuals of the same species, as is clearly seen in our dogs. Some dogs and horses are bad-tempered and easily become sullen; others are friendly, and these traits are certainly inherited. Everyone knows how prone animals are to furious anger and how clearly they express it. Many stories, probably true, have been shared about the carefully plotted revenge of various animals. The precise Rengger and Brehm state that the American and African monkeys they kept in captivity certainly sought revenge. The love a dog has for its owner is well-known; in the agony of death, a dog has been known to comfort its owner, and everyone has heard of the dog suffering during vivisection that licked the hand of the operator; this man, unless he had a heart of stone, must have felt remorse for the rest of his life. As Whewell has said, “who that reads the touching instances of maternal affection, related so often of the women of all nations, and of the females of all animals, can doubt that the principle of action is the same in the two cases?”
We see maternal affection exhibited in the most trifling details; thus Rengger observed an American monkey (a Cebus) carefully driving away the flies which plagued her infant; and Duvaucel saw a Hylobates washing the faces of her young ones in a stream. So intense is the grief of female monkeys for the loss of their young, that it invariably caused the death of certain kinds kept under confinement by Brehm in N. 41Africa. Orphan-monkeys were always adopted and carefully guarded by the other monkeys, both males and females. One female baboon had so capacious a heart that she not only adopted young monkeys of other species, but stole young dogs and cats, which she continually carried about. Her kindness, however, did not go so far as to share her food with her adopted offspring, at which Brehm was surprised, as his monkeys always divided everything quite fairly with their own young ones. An adopted kitten scratched the above-mentioned affectionate baboon, who certainly had a fine intellect, for she was much astonished at being scratched, and immediately examined the kitten’s feet, and without more ado bit off the claws. In the Zoological Gardens, I heard from the keeper that an old baboon (C. chacma) had adopted a Rhesus monkey; but when a young drill and mandrill were placed in the cage, she seemed to perceive that these monkeys, though distinct species, were her nearer relatives, for she at once rejected the Rhesus and adopted both of them. The young Rhesus, as I saw, was greatly discontented at being thus rejected, and it would, like a naughty child, annoy and attack the young drill and mandrill whenever it could do so with safety; this conduct exciting great indignation in the old baboon. Monkeys will also, according to Brehm, defend their master when attacked by any one, as well as dogs to whom they are attached, from the attacks of other dogs. But we here trench on the subject of sympathy, to which I shall recur. Some of Brehm’s monkeys took much delight in teasing, in various ingenious ways, a certain old dog whom they disliked, as well as other animals.
We can see maternal love displayed in the smallest details. For example, Rengger noticed an American monkey (a Cebus) carefully shooing away the flies bothering her baby, and Duvaucel saw a Hylobates washing the faces of her young in a stream. Female monkeys feel such deep grief over losing their young that it often led to the death of certain species kept in captivity by Brehm in N. 41Africa. Orphaned monkeys were always taken in and protected by other monkeys, both males and females. One female baboon had such a big heart that she not only adopted young monkeys of different species but also stole young dogs and cats, which she carried around all the time. However, her kindness didn’t extend to sharing her food with her adopted offspring, which surprised Brehm since his monkeys typically shared everything fairly with their own young ones. An adopted kitten scratched the affectionate baboon, who was quite intelligent. She was shocked at being scratched and immediately checked the kitten’s paws, then simply bit off its claws. At the Zoological Gardens, I heard from the keeper that an old baboon (C. chacma) had adopted a Rhesus monkey. But when a young drill and mandrill were placed in the cage, she seemed to realize that these monkeys, although different species, were closer to her, so she immediately rejected the Rhesus and took in both of them. The young Rhesus, as I observed, was very unhappy about being rejected and would annoy and attack the young drill and mandrill whenever it could do so safely, which upset the old baboon greatly. According to Brehm, monkeys will also defend their owner when attacked, just like the dogs they are attached to, against other dogs. But here we touch on the topic of sympathy, which I will discuss further. Some of Brehm's monkeys took great pleasure in teasing a particular old dog they disliked, using various clever methods, as well as other animals.
Most of the more complex emotions are common to the higher animals and ourselves. Every one has seen42 how jealous a dog is of his master’s affection, if lavished on any other creature; and I have observed the same fact with monkeys. This shews that animals not only love, but have the desire to be loved. Animals manifestly feel emulation. They love approbation or praise; and a dog carrying a basket for his master exhibits in a high degree self-complacency or pride. There can, I think, be no doubt that a dog feels shame, as distinct from fear, and something very like modesty when begging too often for food. A great dog scorns the snarling of a little dog, and this may be called magnanimity. Several observers have stated that monkeys certainly dislike being laughed at; and they sometimes invent imaginary offences. In the Zoological Gardens I saw a baboon who always got into a furious rage when his keeper took out a letter or book and read it aloud to him; and his rage was so violent that, as I witnessed on one occasion, he bit his own leg till the blood flowed.
Most of the more complex emotions are shared by higher animals and us. Everyone has seen how jealous a dog can be of his owner's affection if it's given to another creature; I've noticed the same in monkeys. This shows that animals not only love but also want to be loved. Animals clearly experience competition. They love approval or praise; a dog carrying a basket for its owner shows noticeable pride or self-satisfaction. I believe there’s no doubt that a dog feels shame, distinct from fear, and something closely resembling modesty when it begs too often for food. A big dog looks down on the barking of a small dog, which could be called generosity. Several observers have noted that monkeys definitely dislike being laughed at, and they sometimes create imaginary offenses. At the Zoo, I saw a baboon who would get extremely angry whenever his keeper took out a letter or book and read it aloud to him; his rage was so intense that, as I witnessed once, he bit his own leg until it bled.
We will now turn to the more intellectual emotions and faculties, which are very important, as forming the basis for the development of the higher mental powers. Animals manifestly enjoy excitement and suffer from ennui, as may be seen with dogs, and, according to Rengger, with monkeys. All animals feel Wonder, and many exhibit Curiosity. They sometimes suffer from this latter quality, as when the hunter plays antics and thus attracts them; I have witnessed this with deer, and so it is with the wary chamois, and with some kinds of wild-ducks. Brehm gives a curious account of the instinctive dread which his monkeys exhibited towards snakes; but their curiosity was so great that they could not desist from occasionally satiating their horror in a most human fashion, by lifting up the lid of the box in which the snakes were kept. I was so much surprised at his account, that I took a stuffed and43 coiled-up snake into the monkey-house at the Zoological Gardens, and the excitement thus caused was one of the most curious spectacles which I ever beheld. Three species of Cercopithecus were the most alarmed; they dashed about their cages and uttered sharp signal-cries of danger, which were understood by the other monkeys. A few young monkeys and one old Anubis baboon alone took no notice of the snake. I then placed the stuffed specimen on the ground in one of the larger compartments. After a time all the monkeys collected round it in a large circle, and staring intently, presented a most ludicrous appearance. They became extremely nervous; so that when a wooden ball, with which they were familiar as a plaything, was accidently moved in the straw, under which it was partly hidden, they all instantly started away. These monkeys behaved very differently when a dead fish, a mouse, and some other new objects were placed in their cages; for though at first frightened, they soon approached, handled and examined them. I then placed a live snake in a paper bag, with the mouth loosely closed, in one of the larger compartments. One of the monkeys immediately approached, cautiously opened the bag a little, peeped in, and instantly dashed away. Then I witnessed what Brehm has described, for monkey after monkey, with head raised high and turned on one side, could not resist taking momentary peeps into the upright bag, at the dreadful object lying quiet at the bottom. It would almost appear as if monkeys had some notion of zoological affinities, for those kept by Brehm exhibited a strange, though mistaken, instinctive dread of innocent lizards and frogs. An orang, also, has been known to be much alarmed at the first sight of a turtle.53
We will now shift our focus to the more intellectual emotions and abilities, which are crucial as they lay the groundwork for developing higher cognitive skills. Animals clearly experience excitement and boredom, as seen in dogs and, as noted by Rengger, in monkeys. All animals feel wonder, and many show curiosity. They can suffer from this curiosity, such as when a hunter plays tricks to draw them in; I've seen this with deer, the cautious chamois, and certain species of wild ducks. Brehm provides an interesting account of his monkeys' instinctive fear of snakes; yet their curiosity was so strong that they couldn’t help but occasionally confront their fear in a very human way by lifting the lid of the box that held the snakes. I was so intrigued by his account that I brought a stuffed, coiled snake into the monkey house at the Zoological Gardens, and the reaction was one of the most fascinating sights I have ever witnessed. Three species of Cercopithecus were the most frightened; they ran around their cages, making sharp warning calls that the other monkeys recognized. A few young monkeys and one older Anubis baboon were the only ones that didn’t react to the snake. I then placed the stuffed specimen on the ground in one of the larger enclosures. After a while, all the monkeys gathered around it in a large circle, staring intently, and their appearance was quite comical. They became extremely nervous; when a wooden ball they were familiar with rolled slightly in the straw beneath which it was partially hidden, they all immediately jumped back. These monkeys acted very differently when a dead fish, a mouse, and some other new items were put in their cages; although they were initially scared, they soon approached and examined them. Then, I placed a live snake in a paper bag with the opening loosely closed in one of the larger compartments. One of the monkeys quickly approached, cautiously opened the bag a bit, peeked inside, and then ran away. What I saw next was just as Brehm described: one monkey after another, with their heads held high and tilted to one side, couldn’t resist taking quick glances into the upright bag at the frightening object lying still at the bottom. It almost seemed like the monkeys had some understanding of zoological relationships, as those kept by Brehm showed a strange, yet misplaced, instinctive fear of harmless lizards and frogs. An orangutan has also been known to become very alarmed at the first sight of a turtle.
The principle of Imitation is strong in man, and especially in man in a barbarous state. Desor54 has remarked that no animal voluntarily imitates an action performed by man, until in the ascending scale we come to monkeys, which are well-known to be ridiculous mockers. Animals, however, sometimes imitate each others’ actions: thus two species of wolves, which had been reared by dogs, learned to bark, as does sometimes the jackal,55 but whether this can be called voluntary imitation is another question. From one account which I have read, there is reason to believe that puppies nursed by cats sometimes learn to lick their feet and thus to clean their faces: it is at least certain, as I hear from a perfectly trustworthy friend, that some dogs behave in this manner. Birds imitate the songs of their parents, and sometimes those of other birds; and parrots are notorious imitators of any sound which they often hear.
The principle of Imitation is strong in humans, especially in those who are in a primitive state. Desor54 noted that no animal willingly mimics an action performed by humans, except when we look at monkeys, which are well-known for being silly imitators. However, animals do occasionally copy each other's actions: for instance, two species of wolves that were raised by dogs learned to bark, just as the jackal sometimes does,55 but whether this counts as voluntary imitation is a different matter. From one account I've read, there's reason to believe that puppies nursed by cats sometimes learn to lick their paws to clean their faces: it's at least certain, as I hear from a completely reliable friend, that some dogs act this way. Birds copy the songs of their parents and sometimes those of other birds; and parrots are famous for imitating any sounds they hear often.
Hardly any faculty is more important for the intellectual progress of man than the power of Attention. Animals clearly manifest this power, as when a cat watches by a hole and prepares to spring on its prey. Wild animals sometimes become so absorbed when thus engaged, that they may be easily approached. Mr. Bartlett has given me a curious proof how variable this faculty is in monkeys. A man who trains monkeys to act used to purchase common kinds from the Zoological Society at the price of five pounds for each; but he offered to give double the price, if he might keep three or four of them for a few days, in order to select one. When asked how he could possibly so soon learn whether 45a particular monkey would turn out a good actor, he answered that it all depended on their power of attention. If when he was talking and explaining anything to a monkey, its attention was easily distracted, as by a fly on the wall or other trifling object, the case was hopeless. If he tried by punishment to make an inattentive monkey act, it turned sulky. On the other hand, a monkey which carefully attended to him could always be trained.
Hardly any ability is more crucial for human intellectual growth than the power of Attention. Animals clearly display this ability, like when a cat sits by a hole, ready to pounce on its prey. Wild animals can become so focused during such moments that they can be easily approached. Mr. Bartlett has shown me an interesting example of how variable this ability is in monkeys. A man who trains monkeys for performances would buy common ones from the Zoological Society for five pounds each; however, he offered to pay double if he could keep three or four for a few days to choose one. When asked how he could quickly determine if a specific monkey would be a good actor, he replied that it all depended on their ability to pay attention. If, while he was speaking and explaining something to a monkey, its attention was easily distracted—like by a fly on the wall or other trivial object—the situation was hopeless. If he tried to make an inattentive monkey perform through punishment, it would just become sulky. On the other hand, a monkey that focused on him could always be trained.
It is almost superfluous to state that animals have excellent Memories for persons and places. A baboon at the Cape of Good Hope, as I have been informed by Sir Andrew Smith, recognised him with joy after an absence of nine months. I had a dog who was savage and averse to all strangers, and I purposely tried his memory after an absence of five years and two days. I went near the stable where he lived, and shouted to him in my old manner; he showed no joy, but instantly followed me out walking and obeyed me, exactly as if I had parted with him only half-an-hour before. A train of old associations, dormant during five years, had thus been instantaneously awakened in his mind. Even ants, as P. Huber56 has clearly shewn, recognised their fellow-ants belonging to the same community after a separation of four months. Animals can certainly by some means judge of the intervals of time between recurrent events.
It's almost obvious to say that animals have great Memories for people and places. A baboon at the Cape of Good Hope, as Sir Andrew Smith informed me, recognized him with joy after being apart for nine months. I had a dog who was aggressive and disliked all strangers, and I intentionally tested his memory after being away for five years and two days. I approached the stable where he lived and called out to him in my old way; he didn't show any excitement, but immediately followed me and obeyed me, just as if we had been apart for only half an hour. A stream of old memories, dormant for five years, was suddenly triggered in his mind. Even ants, as P. Huber56 has clearly demonstrated, recognized their fellow ants from the same colony after being separated for four months. Animals can definitely somehow gauge the time between repeated events.
The Imagination is one of the highest prerogatives of man. By this faculty he unites, independently of the will, former images and ideas, and thus creates brilliant and novel results. A poet, as Jean Paul Richter remarks,57 “who must reflect whether he shall make a 46character say yes or no—to the devil with him; he is only a stupid corpse.” Dreaming gives us the best notion of this power; as Jean Paul again says, “The dream is an involuntary art of poetry.” The value of the products of our imagination depends of course on the number, accuracy, and clearness of our impressions; on our judgment and taste in selecting or rejecting the involuntary combinations, and to a certain extent on our power of voluntarily combining them. As dogs, cats, horses, and probably all the higher animals, even birds, as is stated on good authority,58 have vivid dreams, and this is shewn by their movements and voice, we must admit that they possess some power of imagination.
The Imagination is one of humanity's greatest abilities. Through this ability, we can combine past images and ideas without relying on our will, resulting in exciting and original outcomes. A poet, as Jean Paul Richter points out,57 “who has to think about whether their character will say yes or no—forget about it; they’re just a mindless shell.” Dreaming gives us the clearest example of this power; as Jean Paul again notes, “A dream is an unintentional form of poetry.” The worth of what we create with our imagination depends, of course, on the number, accuracy, and clarity of our impressions; on our ability to judge and decide what to keep or discard from those involuntary combinations, and to some extent, on our skill in consciously combining them. Since dogs, cats, horses, and likely all higher animals, even birds, as credible sources suggest,58 experience vivid dreams, as shown by their movements and sounds, we must acknowledge that they have some degree of imagination.
Of all the faculties of the human mind, it will, I presume, be admitted that Reason stands at the summit. Few persons any longer dispute that animals possess some power of reasoning. Animals may constantly be seen to pause, deliberate, and resolve. It is a significant fact, that the more the habits of any particular animal are studied by a naturalist, the more he attributes to reason and the less to unlearnt instincts.59 In future chapters we shall see that some animals extremely low in the scale apparently display a certain amount of reason. No doubt it is often difficult to distinguish between the power of reason and that of instinct. Thus Dr. Hayes, in his work on ‘The Open Polar Sea,’ repeatedly remarks that his dogs, instead of continuing to draw the sledges in a compact body, diverged and separated when they came to thin ice, so that their weight might be more evenly distributed. This was often the first warn47ing and notice which the travellers received that the ice was becoming thin and dangerous. Now, did the dogs act thus from the experience of each individual, or from the example of the older and wiser dogs, or from an inherited habit, that is from an instinct? This instinct might possibly have arisen since the time, long ago, when dogs were first employed by the natives in drawing their sledges; or the Arctic wolves, the parent-stock of the Esquimaux dog, may have acquired this instinct, impelling them not to attack their prey in a close pack when on thin ice. Questions of this kind are most difficult to answer.
Of all the abilities of the human mind, I think it can be agreed that Reason is at the top. Few people still argue that animals have some level of reasoning. We can often see animals take a moment to pause, think, and make decisions. It’s noteworthy that the more a naturalist studies the behavior of a specific animal, the more he attributes actions to reason rather than just instinct.59 In upcoming chapters, we will find that some animals very low on the evolutionary scale seem to show a certain degree of reasoning. It's often tricky to tell the difference between reasoning and instinct. For example, Dr. Hayes, in his book ‘The Open Polar Sea,’ notes that his dogs, instead of sticking together while pulling sleds, spread out when they reached thin ice to distribute their weight more evenly. This was often the first sign the travelers got that the ice was becoming thin and unsafe. So, did the dogs do this based on their individual experiences, by following the example of older, wiser dogs, or from an inherited behavior, which is instinct? This instinct might have originated since the early days when dogs were first used by locals to pull sleds, or the Arctic wolves, which are the ancestors of the Inuit dog, may have developed this instinct, leading them not to attack their prey in a tight group on thin ice. Questions like these are really hard to answer.
So many facts have been recorded in various works shewing that animals possess some degree of reason, that I will here give only two or three instances, authenticated by Rengger, and relating to American monkeys, which stand low in their order. He states that when he first gave eggs to his monkeys, they smashed them and thus lost much of their contents; afterwards they gently hit one end against some hard body, and picked off the bits of shell with their fingers. After cutting themselves only once with any sharp tool, they would not touch it again, or would handle it with the greatest care. Lumps of sugar were often given them wrapped up in paper; and Rengger sometimes put a live wasp in the paper, so that in hastily unfolding it they got stung; after this had once happened, they always first held the packet to their ears to detect any movement within. Any one who is not convinced by such facts as these, and by what he may observe with his own dogs, that animals can reason, would not be convinced by anything that I could add. Nevertheless I will give one case with respect to dogs, as it rests on two distinct observers, and can hardly depend on the modification of any instinct.
So many facts have been recorded in various works showing that animals have some degree of reasoning that I will here provide just a couple of examples, verified by Rengger, concerning American monkeys, which are low on the evolutionary scale. He mentions that when he first gave eggs to his monkeys, they smashed them and lost a lot of the contents; later on, they gently tapped one end against a hard surface and removed the bits of shell with their fingers. After cutting themselves just once with a sharp tool, they wouldn’t touch it again or would handle it very carefully. They were often given lumps of sugar wrapped in paper; Rengger sometimes included a live wasp in the paper, so when they quickly unwrapped it, they got stung. After experiencing this once, they would always hold the packet to their ears first to check for any movement inside. Anyone who isn’t convinced by facts like these, or by what they can observe with their own dogs, that animals can reason, wouldn’t be convinced by anything else I could add. Still, I will share one case regarding dogs since it comes from two different observers and is unlikely to be just a modification of instinct.
48Mr. Colquhoun60 winged two wild-ducks, which fell on the opposite side of a stream; his retriever tried to bring over both at once, but could not succeed; she then, though never before known to ruffle a feather, deliberately killed one, brought over the other, and returned for the dead bird. Col. Hutchinson relates that two partridges were shot at once, one being killed, the other wounded; the latter ran away, and was caught by the retriever, who on her return came across the dead bird; “she stopped, evidently greatly puzzled, and after one or two trials, finding she could not take it up without permitting the escape of the winged bird, she considered a moment, then deliberately murdered it by giving it a severe crunch, and afterwards brought away both together. This was the only known instance of her ever having wilfully injured any game.” Here we have reason, though not quite perfect, for the retriever might have brought the wounded bird first and then returned for the dead one, as in the case of the two wild-ducks.
48Mr. Colquhoun60 shot two wild ducks, which landed on the other side of a stream. His retriever tried to bring both at once but couldn't manage it. Then, although she had never shown any aggressive behavior before, she deliberately killed one, brought back the other, and returned for the dead bird. Col. Hutchinson reports that two partridges were shot simultaneously, one killed and the other wounded. The wounded one ran off but was caught by the retriever. On her way back, she came across the dead bird; “she paused, clearly confused, and after one or two attempts, realizing she couldn't pick it up without letting the wounded bird escape, she thought for a moment, then intentionally killed it by giving it a hard crunch, and later brought both back together. This was the only known case of her ever intentionally harming any game.” Here we have some reasoning, though not entirely convincing, since the retriever might have brought the wounded bird first and then returned for the dead one, similar to what happened with the two wild ducks.
The muleteers in S. America say, “I will not give you the mule whose step is easiest, but la mas rational,—the one that reasons best;” and Humboldt61 adds, “this popular expression, dictated by long experience, combats the system of animated machines, better perhaps than all the arguments of speculative philosophy.”
The muleteers in South America say, “I won’t give you the mule with the easiest gait, but la mas rational,—the one that thinks best;” and Humboldt61 adds, “this common saying, shaped by extensive experience, counters the idea of animated machines, maybe better than all the arguments from speculative philosophy.”
It has, I think, now been shewn that man and the higher animals, especially the Primates, have some few instincts in common. All have the same senses, intuitions and sensations—similar passions, affections, and emotions, even the more complex ones; they feel 49wonder and curiosity; they possess the same faculties of imitation, attention, memory, imagination, and reason, though in very different degrees. Nevertheless many authors have insisted that man is separated through his mental faculties by an impassable barrier from all the lower animals. I formerly made a collection of above a score of such aphorisms, but they are not worth giving, as their wide difference and number prove the difficulty, if not the impossibility, of the attempt. It has been asserted that man alone is capable of progressive improvement; that he alone makes use of tools or fire, domesticates other animals, possesses property, or employs language; that no other animal is self-conscious, comprehends itself, has the power of abstraction, or possesses general ideas; that man alone has a sense of beauty, is liable to caprice, has the feeling of gratitude, mystery, &c.; believes in God, or is endowed with a conscience. I will hazard a few remarks on the more important and interesting of these points.
It has, I think, now been shown that humans and higher animals, especially primates, share some common instincts. They all have the same senses, intuitions, and sensations—similar passions, affections, and emotions, even the more complex ones; they experience wonder and curiosity; they have similar abilities in imitation, attention, memory, imagination, and reasoning, though to varying degrees. However, many authors have argued that humans are separated by an unbridgeable gap in mental faculties from all lower animals. I previously gathered over twenty of such statements, but they aren’t worth sharing, as their wide variety and number highlight the difficulty, if not the impossibility, of the attempt. It has been claimed that only humans can improve progressively; that only they use tools or fire, domesticate other animals, own property, or use language; that no other animal is self-aware, understands itself, has the ability to think abstractly, or possesses general ideas; that only humans have a sense of beauty, can act whimsically, feel gratitude, mystery, etc.; believe in God, or have a conscience. I will attempt to make a few comments on the more significant and intriguing of these points.
Archbishop Sumner formerly maintained62 that man alone is capable of progressive improvement. With animals, looking first to the individual, every one who has had any experience in setting traps knows that young animals can be caught much more easily than old ones; and they can be much more easily approached by an enemy. Even with respect to old animals, it is impossible to catch many in the same place and in the same kind of trap, or to destroy them by the same kind of poison; yet it is improbable that all should have partaken of the poison, and impossible that all should have been caught in the trap. They must learn caution by seeing their brethren caught or poisoned. In North America, where the fur-bearing animals have long been 50pursued, they exhibit, according to the unanimous testimony of all observers, an almost incredible amount of sagacity, caution, and cunning; but trapping has been there so long carried on that inheritance may have come into play.
Archbishop Sumner previously argued that humans are the only ones capable of making progressive improvements. When it comes to animals, anyone who's had experience with trapping knows that young animals can be caught much more easily than older ones; they also tend to be more easily approached by predators. Even regarding older animals, it's difficult to capture many in the same location and with the same type of trap, or to eliminate them with the same kind of poison; however, it's unlikely that all of them would have consumed the poison, and it's impossible that all would have been caught in the trap. They must learn caution by observing their peers being trapped or poisoned. In North America, where fur-bearing animals have been hunted for a long time, they show, according to the consensus of all observers, an almost unbelievable level of intelligence, caution, and cunning; but trapping has been practiced there for so long that inherited behaviors may have come into play.
If we look to successive generations, or to the race, there is no doubt that birds and other animals gradually both acquire and lose caution in relation to man or other enemies;63 and this caution is certainly in chief part an inherited habit or instinct, but in part the result of individual experience. A good observer, Leroy,64 states that in districts where foxes are much hunted, the young when they first leave their burrows are incontestably much more wary than the old ones in districts where they are not much disturbed.
If we look at successive generations or the species as a whole, it's clear that birds and other animals gradually gain and lose their caution towards humans or other threats; and this caution is mainly a learned habit or instinct, but also shaped by individual experiences. A keen observer, Leroy, points out that in areas where foxes are frequently hunted, the young foxes that first emerge from their burrows are undoubtedly much more cautious than the older ones in areas where they aren't frequently disturbed.
Our domestic dogs are descended from wolves and jackals,65 and though they may not have gained in cunning, and may have lost in waryness and suspicion, yet they have progressed in certain moral qualities, such as in affection, trust-worthiness, temper, and probably in general intelligence. The common rat has conquered and beaten several other species throughout Europe, in parts of North America, New Zealand, and recently in Formosa, as well as on the mainland of China. Mr. Swinhoe,66 who describes these latter cases, attributes the victory of the common rat over the large Mus coninga to its superior cunning; and this latter quality may be attributed to the habitual exercise of all its faculties in avoiding extirpation by man, as well 51as to nearly all the less cunning or weak-minded rats having been successively destroyed by him. To maintain, independently of any direct evidence, that no animal during the course of ages has progressed in intellect or other mental faculties, is to beg the question of the evolution of species. Hereafter we shall see that, according to Lartet, existing mammals belonging to several orders have larger brains than their ancient tertiary prototypes.
Our domestic dogs come from wolves and jackals,65 and while they might not have become more cunning, and may have lost some of their wariness and suspicion, they have developed certain moral qualities, like affection, trustworthiness, temperament, and probably general intelligence. The common rat has managed to outcompete several other species across Europe, parts of North America, New Zealand, and recently in Taiwan, as well as on the mainland of China. Mr. Swinhoe,66 who discusses these recent cases, attributes the common rat's success over the large Mus coninga to its superior cunning; this cunning may be due to the constant need to use all its skills to avoid extinction at the hands of humans, as well as the fact that most of the less cunning or weaker rats have been wiped out by him. To claim, without any direct evidence, that no animal has improved in intellect or other mental abilities over time is to overlook the question of species evolution. Later, we will see that, according to Lartet, existing mammals from various orders have larger brains than their ancient tertiary ancestors.
It has often been said that no animal uses any tool; but the chimpanzee in a state of nature cracks a native fruit, somewhat like a walnut, with a stone.67 Rengger68 easily taught an American monkey thus to break open hard palm-nuts, and afterwards of its own accord it used stones to open other kinds of nuts, as well as boxes. It thus also removed the soft rind of fruit that had a disagreeable flavour. Another monkey was taught to open the lid of a large box with a stick, and afterwards it used the stick as a lever to move heavy bodies; and I have myself seen a young orang put a stick into a crevice, slip his hand to the other end, and use it in the proper manner as a lever. In the cases just mentioned stones and sticks were employed as implements; but they are likewise used as weapons. Brehm69 states, on the authority of the well-known traveller Schimper, that in Abyssinia when the baboons belonging to one species (C. gelada) descend in troops from the mountains to plunder the fields, they sometimes encounter troops of another species (C. hamadryas), and then a fight ensues. The Geladas roll down great stones, which the Hamadryas try to avoid, and then, both species, 52making a great uproar, rush furiously against each other. Brehm, when accompanying the Duke of Coburg-Gotha, aided in an attack with fire-arms on a troop of baboons in the pass of Mensa in Abyssinia. The baboons in return rolled so many stones down the mountain, some as large as a man’s head, that the attackers had to beat a hasty retreat; and the pass was actually for a time closed against the caravan. It deserves notice that these baboons thus acted in concert. Mr. Wallace70 on three occasions saw female orangs, accompanied by their young, “breaking off branches and the great spiny fruit of the Durian tree, with every appearance of rage; causing such a shower of missiles as effectually kept us from approaching too near the tree.”
It’s often said that no animal uses tools, but chimpanzees in the wild crack open a native fruit, similar to a walnut, using a stone.67 Rengger68 easily taught an American monkey to break open hard palm nuts, and later it independently started using stones to open other types of nuts and boxes. It also removed the unpleasant outer layer of certain fruits. Another monkey learned to lift the lid of a large box with a stick, and afterwards used the stick as a lever to move heavy objects; I have personally seen a young orangutan put a stick into a crack, slip his hand to the other end, and use it as a lever in the right way. In these examples, stones and sticks were used as tools, but they can also serve as weapons. Brehm69 claims, citing the well-known traveler Schimper, that in Abyssinia, when troops of baboons from one species (C. gelada) come down from the mountains to raid the fields, they sometimes clash with troops from another species (C. hamadryas), leading to a fight. The Geladas roll down large stones that the Hamadryas try to dodge, and then both groups, 52creating a huge commotion, charge at each other. Brehm, while accompanying the Duke of Coburg-Gotha, participated in an armed attack on a troop of baboons in the Mensa pass in Abyssinia. In response, the baboons rolled down so many stones, some as big as a man’s head, that the attackers had to make a quick retreat, and the pass was actually blocked to the caravan for a time. It’s noteworthy that these baboons acted together like this. Mr. Wallace70 witnessed female orangutans on three occasions, accompanied by their young, “breaking off branches and the large spiny fruit of the Durian tree, appearing quite angry; creating such a rain of missiles that effectively kept us from getting too close to the tree.”
In the Zoological Gardens a monkey which had weak teeth used to break open nuts with a stone; and I was assured by the keepers that this animal, after using the stone, hid it in the straw, and would not let any other monkey touch it. Here, then, we have the idea of property; but this idea is common to every dog with a bone, and to most or all birds with their nests.
In the Zoo, there was a monkey with weak teeth that would crack open nuts using a stone. The keepers assured me that this monkey, after using the stone, would hide it in the straw and wouldn’t let any other monkey touch it. So, here we see a sense of ownership; but this concept is also seen in every dog with a bone and in most, if not all, birds with their nests.
The Duke of Argyll71 remarks, that the fashioning of an implement for a special purpose is absolutely peculiar to man; and he considers that this forms an immeasurable gulf between him and the brutes. It is no doubt a very important distinction, but there appears to me much truth in Sir J. Lubbock’s suggestion,72 that when primeval man first used flint-stones for any purpose, he would have accidentally splintered them, and would then have used the sharp fragments. From this step it would be a small one to intentionally break the 53flints, and not a very wide step to rudely fashion them. This latter advance, however, may have taken long ages, if we may judge by the immense interval of time which elapsed before the men of the neolithic period took to grinding and polishing their stone tools. In breaking the flints, as Sir J. Lubbock likewise remarks, sparks would have been emitted, and in grinding them heat would have been evolved: “thus the two usual methods of obtaining fire may have originated.” The nature of fire would have been known in the many volcanic regions where lava occasionally flows through forests. The anthropomorphous apes, guided probably by instinct, build for themselves temporary platforms; but as many instincts are largely controlled by reason, the simpler ones, such as this of building a platform, might readily pass into a voluntary and conscious act. The orang is known to cover itself at night with the leaves of the Pandanus; and Brehm states that one of his baboons used to protect itself from the heat of the sun by throwing a straw-mat over its head. In these latter habits, we probably see the first steps towards some of the simpler arts; namely rude architecture and dress, as they arose amongst the early progenitors of man.
The Duke of Argyll71 points out that creating a tool for a specific purpose is uniquely human, and he believes this creates a significant divide between humans and animals. While this is certainly an important distinction, I think there’s a lot of truth in Sir J. Lubbock’s observation,72 that when early humans first used flint stones for any task, they likely broke them by accident and then used the sharp pieces. From that point, it wouldn’t be a huge leap to start intentionally breaking flints, and it wouldn’t be a big step to shape them roughly. However, this latter progress might have taken a very long time, as the considerable gap before Neolithic people began grinding and polishing their stone tools suggests. When breaking the flints, as Sir J. Lubbock also notes, sparks would have flown, and grinding them would have produced heat: “so the two common methods of starting a fire may have originated this way.” People likely understood fire from the many volcanic areas where lava sometimes flows through forests. The great apes, probably guided by instinct, build temporary platforms; but since many instincts are largely governed by reasoning, simpler ones, like platform building, could easily become a deliberate and conscious action. It’s known that orangutans cover themselves at night with leaves from the Pandanus, and Brehm mentions that one of his baboons used to shield itself from the sun by throwing a straw mat over its head. In these behaviors, we likely see the initial steps towards some of the simpler arts, like primitive architecture and clothing, as they developed among early human ancestors.
Language.—This faculty has justly been considered as one of the chief distinctions between man and the lower animals. But man, as a highly competent judge, Archbishop Whately remarks, “is not the only animal that can make use of language to express what is passing in his mind, and can understand, more or less, what is so expressed by another.”73 In Paraguay the Cebus Azaræ when excited utters at least six distinct sounds, which 54excite in other monkeys similar emotions.74 The movements of the features and gestures of monkeys are understood by us, and they partly understand ours, as Rengger and others declare. It is a more remarkable fact that the dog, since being domesticated, has learnt to bark75 in at least four or five distinct tones. Although barking is a new art, no doubt the wild species, the parents of the dog, expressed their feelings by cries of various kinds. With the domesticated dog we have the bark of eagerness, as in the chase; that of anger; the yelping or howling bark of despair, as when shut up; that of joy, as when starting on a walk with his master; and the very distinct one of demand or supplication, as when wishing for a door or window to be opened.
Language.—This ability has rightly been seen as one of the main differences between humans and lower animals. However, man, as a knowledgeable judge, Archbishop Whately remarks, “is not the only animal that can use language to convey what is happening in his mind, and can understand, to some extent, what is expressed by another.”73 In Paraguay, the Cebus Azaræ emits at least six distinct sounds when excited, which trigger similar emotions in other monkeys.74 The expressions and gestures of monkeys are comprehensible to us, and they partially understand ours, as Rengger and others have noted. More remarkably, since being domesticated, dogs have learned to bark75 in at least four or five different tones. While barking is a new skill, it’s likely that wild ancestors of dogs expressed their feelings with various cries. With domesticated dogs, we have the bark of eagerness, like during a chase; the bark of anger; the yelping or howling bark of despair, as when confined; the bark of joy, like when going for a walk with their owner; and the very distinct bark of demand or pleading, as when wanting a door or window to be opened.
Articulate language is, however, peculiar to man; but he uses in common with the lower animals inarticulate cries to express his meaning, aided by gestures and the movements of the muscles of the face.76 This especially holds good with the more simple and vivid feelings, which are but little connected with our higher intelligence. Our cries of pain, fear, surprise, anger, together with their appropriate actions, and the murmur of a mother to her beloved child, are more expressive than any words. It is not the mere power of articulation that distinguishes man from other animals, for as every one knows, parrots can talk; but it is his large power of connecting definite sounds with definite ideas; and this obviously depends on the development of the mental faculties.
Articulate language is unique to humans; however, we share with lower animals the use of inarticulate cries to convey our meaning, supported by gestures and the movements of our facial muscles.76 This is particularly true for the simpler and more intense emotions, which are not closely tied to our higher reasoning. Our cries of pain, fear, surprise, and anger, along with our corresponding actions and a mother's soothing murmurs to her cherished child, are more expressive than any words. It’s not just the ability to articulate that sets humans apart from other animals—after all, everyone knows parrots can talk—but rather our greater capacity to associate specific sounds with specific ideas, which clearly relies on the development of our mental faculties.
As Horne Tooke, one of the founders of the noble science of philology, observes, language is an art, like brewing or baking; but writing would have been a much more appropriate simile. It certainly is not a true instinct, as every language has to be learnt. It differs, however, widely from all ordinary arts, for man has an instinctive tendency to speak, as we see in the babble of our young children; whilst no child has an instinctive tendency to brew, bake, or write. Moreover, no philologist now supposes that any language has been deliberately invented; each has been slowly and unconsciously developed by many steps. The sounds uttered by birds offer in several respects the nearest analogy to language, for all the members of the same species utter the same instinctive cries expressive of their emotions; and all the kinds that have the power of singing exert this power instinctively; but the actual song, and even the call-notes, are learnt from their parents or foster-parents. These sounds, as Daines Barrington77 has proved, “are no more innate than language is in man.” The first attempts to sing “may be compared to the imperfect endeavour in a child to babble.” The young males continue practising, or, as the bird-catchers say, recording, for ten or eleven months. Their first essays show hardly a rudiment of the future song; but as they grow older we can perceive what they are aiming at; and at last they are said “to sing their song round.” Nestlings which have learnt the song of a distinct species, as with the canary-birds educated in the Tyrol, teach and transmit their new song to their offspring. The slight natural differences of song in the same species inha56biting different districts may be appositely compared, as Barrington remarks, “to provincial dialects;” and the songs of allied, though distinct species may be compared with the languages of distinct races of man. I have given the foregoing details to shew that an instinctive tendency to acquire an art is not a peculiarity confined to man.
As Horne Tooke, one of the founders of the important field of philology, points out, language is an art, similar to brewing or baking; but writing would be a much better comparison. It certainly isn't a natural instinct, since every language has to be taught. However, it differs significantly from other common arts, because humans have a natural drive to speak, as evident in the babbling of young children; whereas no child has an innate drive to brew, bake, or write. Furthermore, no linguist today believes that any language has been purposely invented; each one has slowly and unconsciously evolved through many stages. The sounds made by birds provide a closer analogy to language, as all members of the same species produce the same instinctive calls that express their feelings; all species capable of singing do so instinctively, but the actual song and even the call notes are learned from their parents or guardians. As Daines Barrington77 has shown, “these sounds are no more innate than language is in humans.” The first attempts to sing “can be likened to a child's imperfect efforts to babble.” The young males keep practicing, or, as bird-catchers say, recording, for ten or eleven months. Their initial attempts rarely show any sign of the future song; but as they mature, we can see what they are aiming for; eventually, they are said “to sing their song completely.” Young birds that have learned the song of a different species, like canaries raised in Tyrol, teach and pass on their new song to their chicks. The slight natural variations in song among the same species in different regions can be aptly compared, as Barrington notes, “to regional dialects;” and the songs of related, though different species can be compared to the languages of distinct human races. I've included the details above to demonstrate that having an instinctive drive to master an art is not unique to humans.
With respect to the origin of articulate language, after having read on the one side the highly interesting works of Mr. Hensleigh Wedgwood, the Rev. F. Farrar, and Prof. Schleicher,78 and the celebrated lectures of Prof. Max Müller on the other side, I cannot doubt that language owes its origin to the imitation and modification, aided by signs and gestures, of various natural sounds, the voices of other animals, and man’s own instinctive cries. When we treat of sexual selection we shall see that primeval man, or rather some early progenitor of man, probably used his voice largely, as does one of the gibbon-apes at the present day, in producing true musical cadences, that is in singing; we may conclude from a widely-spread analogy that this power would have been especially exerted during the courtship of the sexes, serving to express various emotions, as love, jealousy, triumph, and serving as a challenge to their rivals. The imitation by articulate sounds of musical cries might have given rise to words expressive of various complex emotions. As bearing on the subject of imitation, the strong tendency in our nearest allies, the monkeys, in microcephalous 57idiots,79 and in the barbarous races of mankind, to imitate whatever they hear deserves notice. As monkeys certainly understand much that is said to them by man, and as in a state of nature they utter signal-cries of danger to their fellows,80 it does not appear altogether incredible, that some unusually wise ape-like animal should have thought of imitating the growl of a beast of prey, so as to indicate to his fellow monkeys the nature of the expected danger. And this would have been a first step in the formation of a language.
Regarding the origin of spoken language, after considering the fascinating works of Mr. Hensleigh Wedgwood, Rev. F. Farrar, and Prof. Schleicher,78 along with the famous lectures of Prof. Max Müller, I have no doubt that language originated from the imitation and modification, supported by signs and gestures, of various natural sounds, the calls of other animals, and humans' instinctive cries. When we discuss sexual selection, we will see that early humans, or perhaps some of their ancestors, likely used their voices a lot, similar to how gibbon apes do today, to create true musical sounds, that is, to sing; we can infer from broad similarities that this ability would have been particularly used during courtship, helping to express various feelings such as love, jealousy, and triumph, and to challenge rivals. The imitation of musical calls through speech may have led to words that express complex emotions. It’s noteworthy that our closest relatives, monkeys, as well as those with microcephaly and some primitive human communities, have a strong tendency to mimic what they hear. Since monkeys clearly understand much of what humans say to them and emit warning calls in their natural habitat,80 it doesn't seem far-fetched that a particularly clever ape-like creature could have tried to imitate the growl of a predator to signal to its fellow monkeys about the type of danger approaching. This would have marked an initial step in the development of language.
As the voice was used more and more, the vocal organs would have been strengthened and perfected through the principle of the inherited effects of use; and this would have reacted on the power of speech. But the relation between the continued use of language and the development of the brain has no doubt been far more important. The mental powers in some early progenitor of man must have been more highly developed than in any existing ape, before even the most imperfect form of speech could have come into use; but we may confidently believe that the continued use and advancement of this power would have reacted on the mind by enabling and encouraging it to carry on long trains of thought. A long and complex train of thought can no more be carried on without the aid of words, whether spoken or silent, than a long calculation without the use of figures or algebra. It appears, also, that even ordinary trains of thought almost require some form of language, for the dumb, deaf, and blind girl, Laura Bridgman, was observed to use her fingers whilst dream58ing.81 Nevertheless a long succession of vivid and connected ideas, may pass through the mind without the aid of any form of language, as we may infer from the prolonged dreams of dogs. We have, also, seen that retriever-dogs are able to reason to a certain extent; and this they manifestly do without the aid of language. The intimate connection between the brain, as it is now developed in us, and the faculty of speech, is well shewn by those curious cases of brain-disease, in which speech is specially affected, as when the power to remember substantives is lost, whilst other words can be correctly used.82 There is no more improbability in the effects of the continued use of the vocal and mental organs being inherited, than in the case of handwriting, which depends partly on the structure of the hand and partly on the disposition of the mind; and handwriting is certainly inherited.83
As people used their voices more often, their vocal organs would have become stronger and more refined through the principle of inherited effects of use; this would have also influenced their speaking abilities. However, the connection between the regular use of language and brain development has likely been even more significant. The mental capabilities in some early human ancestor must have been more advanced than in any current ape before even the most basic form of speech could have emerged; still, we can confidently assume that the consistent use and improvement of this ability would have impacted the mind by allowing and encouraging it to pursue extended lines of thought. A long and complex stream of thought can't be maintained without words, whether spoken or silent, just as a lengthy calculation can't be done without numbers or algebra. It also seems that even ordinary thought processes almost require some form of language, as seen with Laura Bridgman, a girl who was dumb, deaf, and blind, who was observed using her fingers while dreaming.58 Nevertheless, a continuous flow of vivid and connected ideas can pass through the mind without any form of language, as we can infer from the extended dreams of dogs. Additionally, we have observed that retriever dogs can reason to some extent, which they clearly do without relying on language. The close relationship between our advanced brains and the ability to speak is evident in those peculiar cases of brain disease where speech is specifically impacted, such as when someone loses the ability to remember nouns while still being able to use other words correctly.82 There's no more improbability in the idea that the continued use of vocal and mental abilities can be inherited than in the case of handwriting, which depends partly on hand structure and partly on the person's mindset; and handwriting is definitely inherited.83
Why the organs now used for speech should have been originally perfected for this purpose, rather than any other organs, it is not difficult to see. Ants have considerable powers of intercommunication by means of their antennæ, as shewn by Huber, who devotes a whole chapter to their language. We might have used our fingers as efficient instruments, for a person with practice can report to a deaf man every word of a speech rapidly delivered at a public meeting; but the loss of our hands, whilst thus employed, would have been a serious inconvenience. As all the higher mammals possess vocal organs constructed on the same general 59plan with ours, and which are used as a means of communication, it was obviously probable, if the power of communication had to be improved, that these same organs would have been still further developed; and this has been effected by the aid of adjoining and well-adapted parts, namely the tongue and lips.84 The fact of the higher apes not using their vocal organs for speech, no doubt depends on their intelligence not having been sufficiently advanced. The possession by them of organs, which with long-continued practice might have been used for speech, although not thus used, is paralleled by the case of many birds which possess organs fitted for singing, though they never sing. Thus, the nightingale and crow have vocal organs similarly constructed, these being used by the former for diversified song, and by the latter merely for croaking.85
Why the organs we use for speech were originally developed specifically for this purpose, rather than any other organs, is easy to understand. Ants have a strong ability to communicate through their antennae, as shown by Huber, who dedicates an entire chapter to their language. We might have been able to use our fingers effectively, since a trained person can convey every word of a speech quickly to a deaf individual at a public meeting; however, losing the use of our hands while doing so would be quite inconvenient. Since all higher mammals have vocal organs similar in structure to ours, which they use to communicate, it was likely that if communication needed to be enhanced, these same organs would have evolved further. This development has been aided by nearby and well-suited parts, namely the tongue and lips.84 The fact that higher apes do not use their vocal organs for speech likely stems from their intelligence not being advanced enough. The existence of organs in them that could potentially be used for speech, despite not being used as such, is similar to many birds that have organs suitable for singing, even though they never sing. For instance, both the nightingale and the crow have similarly structured vocal organs; the former uses them for a variety of songs, while the latter uses them simply for croaking.85
The formation of different languages and of distinct species, and the proofs that both have been developed through a gradual process, are curiously the same.86 But we can trace the origin of many words further back than in the case of species, for we can perceive that they have arisen from the imitation of various sounds, as in alliterative poetry. We find in distinct languages striking homologies due to community of descent, and analogies due to a similar process of 60formation. The manner in which certain letters or sounds change when others change is very like correlated growth. We have in both cases the reduplication of parts, the effects of long-continued use, and so forth. The frequent presence of rudiments, both in languages and in species, is still more remarkable. The letter m in the word am, means I; so that in the expression I am, a superfluous and useless rudiment has been retained. In the spelling also of words, letters often remain as the rudiments of ancient forms of pronunciation. Languages, like organic beings, can be classed in groups under groups; and they can be classed either naturally according to descent, or artificially by other characters. Dominant languages and dialects spread widely and lead to the gradual extinction of other tongues. A language, like a species, when once extinct, never, as Sir C. Lyell remarks, reappears. The same language never has two birthplaces. Distinct languages may be crossed or blended together.87 We see variability in every tongue, and new words are continually cropping up; but as there is a limit to the powers of the memory, single words, like whole languages, gradually become extinct. As Max Müller88 has well remarked:—“A struggle for life is constantly going on amongst the words and grammatical forms in each language. The better, the shorter, the easier forms are constantly gaining the upper hand, and they owe their success to their own inherent virtue.” To these more important causes of the survival of certain words, mere novelty may, I think, be added; for there is in the mind of man a strong love for slight changes in all things. The survival or 61preservation of certain favoured words in the struggle for existence is natural selection.
The development of different languages and distinct species, along with the evidence that both have evolved gradually, are surprisingly similar. But we can trace the origins of many words further back compared to species, as we can see they come from mimicking various sounds, similar to alliterative poetry. In distinct languages, we notice significant similarities because of shared ancestry, and parallels due to a similar process of formation. The way certain letters or sounds change when others do is quite similar to correlated growth. In both cases, there is a repetition of parts, the effects of prolonged use, and so on. The frequent presence of remnants, both in languages and in species, is even more remarkable. The letter m in the word am means I; thus, in the phrase I am, a redundant and unnecessary remnant has been kept. In the spelling of words, letters often remain as leftovers from ancient pronunciations. Languages, like living organisms, can be grouped together in larger categories; they can be organized either naturally by descent or artificially by other characteristics. Dominant languages and dialects spread widely, leading to the gradual disappearance of other languages. Once a language goes extinct, it never reappears, as Sir C. Lyell pointed out. No language has two original homes. Distinct languages can be mixed or blended together. We observe variability in every language, with new words constantly emerging; however, since the capacity of memory is limited, individual words, just like entire languages, gradually fade away. As Max Müller noted, “A struggle for survival is ongoing among the words and grammatical forms in each language. The better, shorter, and easier forms are consistently coming out on top, and their success is due to their inherent qualities.” Besides these significant reasons for the survival of certain words, I think we can also consider mere novelty as a factor, as humans have a strong affinity for slight changes in everything. The survival or preservation of certain favored words in the competition for existence is natural selection.
The perfectly regular and wonderfully complex construction of the languages of many barbarous nations has often been advanced as a proof, either of the divine origin of these languages, or of the high art and former civilisation of their founders. Thus F. von Schlegel writes: “In those languages which appear to be at the lowest grade of intellectual culture, we frequently observe a very high and elaborate degree of art in their grammatical structure. This is especially the case with the Basque and the Lapponian, and many of the American languages.”89 But it is assuredly an error to speak of any language as an art in the sense of its having been elaborately and methodically formed. Philologists now admit that conjugations, declensions, &c., originally existed as distinct words, since joined together; and as such words express the most obvious relations between objects and persons, it is not surprising that they should have been used by the men of most races during the earliest ages. With respect to perfection, the following illustration will best shew how easily we may err: a Crinoid sometimes consists of no less than 150,000 pieces of shell,90 all arranged with perfect symmetry in radiating lines; but a naturalist does not consider an animal of this kind as more perfect than a bilateral one with comparatively few parts, and with none of these alike, excepting on the opposite sides of the body. He justly considers the differentiation and specialisation of organs as the test of perfection. So with languages, the most symmetrical and complex ought not to be ranked above irregular, abbre62viated, and bastardised languages, which have borrowed expressive words and useful forms of construction from various conquering, or conquered, or immigrant races.
The perfectly regular and incredibly complex structure of the languages of many so-called primitive nations has often been cited as proof of either the divine origin of these languages or the advanced skill and former civilization of their creators. F. von Schlegel notes: “In those languages that seem to be at the lowest level of intellectual culture, we often see a very high and intricate level of artistry in their grammatical structure. This is particularly true for the Basque, the Lapponian, and many American languages.”89 However, it is certainly a mistake to refer to any language as an art in the sense of being intricately and systematically created. Linguists now acknowledge that conjugations, declensions, etc., originally existed as separate words that were later combined; and since these words express the most basic relationships between objects and people, it’s not surprising that they were utilized by early humans from various cultures. To illustrate the idea of perfection, consider this: a crinoid can consist of as many as 150,000 shell pieces,90 all perfectly arranged in radiating lines; yet a naturalist doesn’t view such an organism as more perfect than a bilateral one with relatively few parts, none of which are identical except on opposite sides of the body. He rightly views the differentiation and specialization of organs as the measure of perfection. Similarly, in languages, the most symmetrical and complex should not be considered superior to irregular, abbreviated, and mixed languages, which have borrowed expressive words and useful construction forms from various conquering, conquered, or immigrant cultures.
From these few and imperfect remarks I conclude that the extremely complex and regular construction of many barbarous languages, is no proof that they owe their origin to a special act of creation.91 Nor, as we have seen, does the faculty of articulate speech in itself offer any insuperable objection to the belief that man has been developed from some lower form.
From these brief and not entirely accurate comments, I conclude that the highly complex and structured nature of many primitive languages does not demonstrate that they originated from a specific act of creation.91 Nor, as we've seen, does the ability to speak clearly present any unresolvable challenge to the idea that humans evolved from some simpler form.
Self-consciousness, Individuality, Abstraction, General Ideas, &c.—It would be useless to attempt discussing these high faculties, which, according to several recent writers, make the sole and complete distinction between man and the brutes, for hardly two authors agree in their definitions. Such faculties could not have been fully developed in man until his mental powers had advanced to a high standard, and this implies the use of a perfect language. No one supposes that one of the lower animals reflects whence he comes or whither he goes,—what is death or what is life, and so forth. But can we feel sure that an old dog with an excellent memory and some power of imagination, as shewn by his dreams, never reflects on his past pleasures in the chase? and this would be a form of self-consciousness. On the other hand, as Büchner92 has remarked, how little can the hard-worked wife of a degraded Australian savage, who uses hardly any abstract words and cannot count above four, exert her self-consciousness, or reflect on the nature of her own existence.
Self-awareness, Individuality, Abstraction, General Ideas, etc.—It would be pointless to try to discuss these advanced faculties, which, according to several recent writers, are the only clear distinction between humans and animals, since hardly two authors agree on their definitions. These faculties couldn't have fully developed in humans until their mental capabilities reached a high level, which suggests the use of a sophisticated language. No one thinks that lower animals ponder where they come from or where they are going—what death is or what life means, and so on. But can we be certain that an older dog with a great memory and some imagination, as shown in his dreams, never reflects on his past pleasures during the chase? That could be a type of self-awareness. On the flip side, as Büchner92 pointed out, how little self-awareness can the overworked wife of a degraded Australian savage, who barely uses any abstract words and can't count past four, have or reflect on the nature of her own existence?
63That animals retain their mental individuality is unquestionable. When my voice awakened a train of old associations in the mind of the above-mentioned dog, he must have retained his mental individuality, although every atom of his brain had probably undergone change more than once during the interval of five years. This dog might have brought forward the argument lately advanced to crush all evolutionists, and said, “I abide amid all mental moods and all material changes.... The teaching that atoms leave their impressions as legacies to other atoms falling into the places they have vacated is contradictory of the utterance of consciousness, and is therefore false; but it is the teaching necessitated by evolutionism, consequently the hypothesis is a false one.”93
63It's undeniable that animals maintain their mental individuality. When my voice triggered a wave of old memories in the dog mentioned earlier, it showed that he held onto his mental identity, even though every part of his brain had likely changed several times over the five years. This dog could have used the recent argument meant to disprove all evolutionists and said, “I exist through all mental states and all physical changes.... The idea that atoms pass on their impressions as legacies to other atoms that move into their previous spaces contradicts what consciousness expresses, and thus it is false; but this is the theory required by evolutionism, so the hypothesis is incorrect.”93
Sense of Beauty.—This sense has been declared to be peculiar to man. But when we behold male birds elaborately displaying their plumes and splendid colours before the females, whilst other birds not thus decorated make no such display, it is impossible to doubt that the females admire the beauty of their male partners. As women everywhere deck themselves with these plumes, the beauty of such ornaments cannot be disputed. The Bower-birds by tastefully ornamenting their playing-passages with gaily-coloured objects, as do certain humming-birds their nests, offer additional evidence that they possess a sense of beauty. So with the song of birds, the sweet strains poured forth by the males during the season of love are certainly admired by the females, of which fact evidence will hereafter be given. If female birds had been incapable of appreciating the beautiful colours, the ornaments, and voices 64of their male partners, all the labour and anxiety exhibited by them in displaying their charms before the females would have been thrown away; and this it is impossible to admit. Why certain bright colours and certain sounds should excite pleasure, when in harmony, cannot, I presume, be explained any more than why certain flavours and scents are agreeable; but assuredly the same colours and the same sounds are admired by us and by many of the lower animals.
Sense of Beauty.—This sense is said to be unique to humans. However, when we see male birds showcasing their feathers and vivid colors to attract females, while other birds without such adornments don't, it's hard to believe that females aren't drawn to the beauty of their male counterparts. Women everywhere adorn themselves with such feathers, proving the appeal of these decorations. Bower-birds, by tastefully decorating their play areas with colorful items, much like certain hummingbirds do with their nests, provide more evidence that they have an appreciation for beauty. The singing of birds also illustrates this point; the melodious tunes sung by males during mating season are certainly enjoyed by females, as will be shown later. If female birds couldn't appreciate the brilliant colors, decorations, and songs of their male counterparts, all the effort and care that males put into showcasing their attractiveness would be pointless, which is hard to accept. The reasons why certain bright colors and sounds bring pleasure together can't be explained any more than why certain tastes and scents are enjoyable; yet it's clear that we and many lower animals share an admiration for the same colors and sounds.
The taste for the beautiful, at least as far as female beauty is concerned, is not of a special nature in the human mind; for it differs widely in the different races of man, as will hereafter be shewn, and is not quite the same even in the different nations of the same race. Judging from the hideous ornaments and the equally hideous music admired by most savages, it might be urged that their æsthetic faculty was not so highly developed as in certain animals, for instance, in birds. Obviously no animal would be capable of admiring such scenes as the heavens at night, a beautiful landscape, or refined music; but such high tastes, depending as they do on culture and complex associations, are not enjoyed by barbarians or by uneducated persons.
The appreciation for beauty, especially when it comes to female beauty, isn't something unique to the human mind; it varies greatly across different races, which will be discussed later, and even among different nations within the same race. Looking at the ugly decorations and equally unpleasant music favored by many indigenous groups, one could argue that their sense of aesthetics isn't as developed as that of some animals, like birds. Clearly, no animal can appreciate breathtaking sights like a starry night, a stunning landscape, or refined music; however, such advanced tastes, which rely on culture and intricate associations, are not typically found among those considered barbaric or uneducated.
Many of the faculties, which have been of inestimable service to man for his progressive advancement, such as the powers of the imagination, wonder, curiosity, an undefined sense of beauty, a tendency to imitation, and the love of excitement or novelty, could not fail to have led to the most capricious changes of customs and fashions. I have alluded to this point, because a recent writer94 has oddly fixed on Caprice “as one of the most remarkable and 65typical differences between savages and brutes.” But not only can we perceive how it is that roan is capricious, but the lower animals are, as we shall hereafter see, capricious in their affections, aversions, and sense of beauty. There is also good reason to suspect that they love novelty, for its own sake.
Many of the abilities that have been incredibly valuable to humanity's progress, like imagination, wonder, curiosity, a vague sense of beauty, a tendency to imitate, and a love for excitement or new experiences, inevitably lead to the most unpredictable changes in customs and trends. I mention this because a recent writer94 has strangely identified Caprice as one of the most significant and typical differences between humans and animals. However, we can see not only how humans are capricious, but also that lower animals can be capricious in their likes, dislikes, and sense of beauty, as we will explore later. There's also reason to believe that they enjoy novelty for its own sake.
Belief in God—Religion.—There is no evidence that man was aboriginally endowed with the ennobling belief in the existence of an Omnipotent God. On the contrary there is ample evidence, derived not from hasty travellers, but from men who have long resided with savages, that numerous races have existed and still exist, who have no idea of one or more gods, and who have no words in their languages to express such an idea.95 The question is of course wholly distinct from that higher one, whether there exists a Creator and Ruler of the universe; and this has been answered in the affirmative by the highest intellects that have ever lived.
Belief in God—Religion.—There’s no evidence that humans were originally given the noble belief in the existence of an all-powerful God. In fact, there’s plenty of evidence from people who have spent a long time living among indigenous groups, showing that many races have existed and still exist without any concept of one or more gods, and their languages lack the words to express such an idea.95 The question is obviously completely different from the deeper one of whether a Creator and Ruler of the universe exists, which has been affirmed by the greatest minds that have ever lived.
If, however, we include under the term “religion” the belief in unseen or spiritual agencies, the case is wholly different; for this belief seems to be almost universal with the less civilised races. Nor is it difficult to comprehend how it arose. As soon as the important faculties of the imagination, wonder, and curiosity, together with some power of reasoning, had become partially developed, man would naturally have craved to understand what was passing around him, and have vaguely speculated on his own existence. As 66Mr. M’Lennan96 has remarked, “Some explanation of the phenomena of life, a man must feign for himself; and to judge from the universality of it, the simplest hypothesis, and the first to occur to men, seems to have been that natural phenomena are ascribable to the presence in animals, plants, and things, and in the forces of nature, of such spirits prompting to action as men are conscious they themselves possess.” It is probable, as Mr. Tylor has clearly shewn, that dreams may have first given rise to the notion of spirits; for savages do not readily distinguish between subjective and objective impressions. When a savage dreams, the figures which appear before him are believed to have come from a distance and to stand over him; or “the soul of the dreamer goes out on its travels, and comes home with a remembrance of what it has seen.”97 But until the above-named faculties of imagination, curiosity, reason, &c., had been fairly well developed in the mind of man, his dreams would not have led him to believe in spirits, any more than in the case of a dog.
If we include the belief in unseen or spiritual forces under the term “religion,” the situation changes completely; this belief appears to be nearly universal among less developed cultures. It’s also easy to see how it came about. Once the key abilities of imagination, wonder, and curiosity, along with some reasoning skills, were somewhat developed, humans would naturally seek to understand what was happening around them and might have speculated about their own existence. As Mr. M’Lennan has noted, “Everyone must create some explanation for the phenomena of life; and judging by how widespread it is, the simplest idea seems to be that natural events can be attributed to spirits in animals, plants, and objects, as well as in the forces of nature, similar to the motivations that individuals are aware they possess.” It’s likely, as Mr. Tylor has demonstrated, that dreams may have initially sparked the idea of spirits; because primitive people often don't differentiate between subjective and objective experiences. When a primitive person dreams, they think that the images they see come from afar and are present with them; or “the soul of the dreamer goes out on its journey and returns with memories of what it has encountered.” However, until the previously mentioned faculties of imagination, curiosity, and reasoning were reasonably developed in humans, their dreams wouldn’t have led them to believe in spirits, just like a dog wouldn't.
The tendency in savages to imagine that natural objects and agencies are animated by spiritual or living essences, is perhaps illustrated by a little fact which I once noticed: my dog, a full-grown and very sensible animal, was lying on the lawn during a hot and still day; but at a little distance a slight breeze occasionally moved an open parasol, which would have been wholly disregarded by the dog, had any one stood near it. As it was, every time that the parasol slightly moved, the dog growled fiercely and barked. He must, I think, have reasoned to himself in a rapid and unconscious manner, that movement without any apparent cause indicated the presence of some strange living agent, and no stranger had a right to be on his territory.
The tendency for primitive people to believe that natural objects and forces are driven by spiritual or living beings is perhaps illustrated by a little incident I once observed: my dog, a fully grown and very sensible animal, was lying on the lawn during a hot and calm day; but a short distance away, a slight breeze occasionally moved an open parasol, which the dog would have completely ignored if anyone had been standing near it. As it was, every time the parasol moved slightly, the dog growled fiercely and barked. I think he must have quickly and unconsciously reasoned that movement without an obvious cause suggested the presence of some strange living entity, and no stranger had the right to be in his territory.
The belief in spiritual agencies would easily pass into the belief in the existence of one or more gods. For savages would naturally attribute to spirits the same passions, the same love of vengeance or simplest form of justice, and the same affections which they themselves experienced. The Fuegians appear to be in this respect in an intermediate condition, for when the surgeon on board the “Beagle” shot some young ducklings as specimens, York Minster declared in the most solemn manner, “Oh! Mr. Bynoe, much rain, much snow, blow much;” and this was evidently a retributive punishment for wasting human food. So again he related how, when his brother killed a “wild man,” storms long raged, much rain and snow fell. Yet we could never discover that the Fuegians believed in what we should call a God, or practised any religious rites; and Jemmy Button, with justifiable pride, stoutly maintained that there was no devil in his land. This latter assertion is the more remarkable, as with savages the belief in bad spirits is far more common than the belief in good spirits.68
The belief in spiritual beings would easily evolve into the belief in one or more gods. Indigenous people would naturally attribute to spirits the same passions, vengeance, and basic sense of justice, as well as the same feelings they experienced themselves. The Fuegians seem to be in a middle ground on this, as when the surgeon on the “Beagle” shot some young ducklings for samples, York Minster seriously stated, “Oh! Mr. Bynoe, much rain, much snow, blow much;” which was clearly seen as a punishment for wasting food. He also mentioned that when his brother killed a “wild man,” storms raged, and there was heavy rain and snow for a long time. However, we could never find that the Fuegians believed in what we would call a God or practiced any religious rituals; and Jemmy Button proudly insisted that there was no devil in his land. This last claim is particularly notable, as among Indigenous people, belief in evil spirits is typically much more common than belief in good spirits.68
The feeling of religious devotion is a highly complex one, consisting of love, complete submission to an exalted and mysterious superior, a strong sense of dependence,98 fear, reverence, gratitude, hope for the future, and perhaps other elements. No being could experience so complex an emotion until advanced in his intellectual and moral faculties to at least a moderately high level. Nevertheless we see some distant approach to this state of mind, in the deep love of a dog for his master, associated with complete submission, some fear, and perhaps other feelings. The behaviour of a dog when returning to his master after an absence, and, as I may add, of a monkey to his beloved keeper, is widely different from that towards their fellows. In the latter case the transports of joy appear to be somewhat less, and the sense of equality is shewn in every action. Professor Braubach99 goes so far as to maintain that a dog looks on his master as on a god.
The feeling of religious devotion is very complex. It includes love, total submission to a higher and mysterious power, a strong sense of dependence,98 fear, respect, gratitude, hope for the future, and possibly other elements. No one could feel such a complex emotion until their intellectual and moral faculties are developed to at least a moderately high level. Still, we can see some hint of this mindset in the deep love a dog has for its owner, which involves complete submission, some fear, and perhaps other emotions. A dog’s behavior when returning to its owner after being away, as well as that of a monkey towards its beloved caretaker, is very different from how they act towards others. In the latter case, expressions of joy seem to be somewhat less, and a sense of equality is shown in every action. Professor Braubach99 even goes so far as to claim that a dog views its owner as a god.
The same high mental faculties which first led man to believe in unseen spiritual agencies, then in fetishism, polytheism, and ultimately in monotheism, would infallibly lead him, as long as his reasoning powers remained poorly developed, to various strange superstitions and customs. Many of these are terrible to think of—such as the sacrifice of human beings to a blood-loving god; the trial of innocent persons by the ordeal of poison or fire; witchcraft, &c.—yet it is well occasionally to reflect on these superstitions, for they shew us what an infinite debt of gratitude we owe to the improvement of our reason, to science, and our 69accumulated knowledge.100 As Sir J. Lubbock has well observed, “it is not too much to say that the horrible dread of unknown evil hangs like a thick cloud over savage life, and embitters every pleasure.” These miserable and indirect consequences of our highest faculties may be compared with the incidental and occasional mistakes of the instincts of the lower animals.
The same advanced mental abilities that first led humans to believe in unseen spiritual forces, then in fetishism, polytheism, and eventually in monotheism, would inevitably lead them, as long as their reasoning skills remained underdeveloped, to various odd superstitions and customs. Many of these are horrifying to think about—like sacrificing humans to a bloodthirsty god; putting innocent people through trials by poison or fire; witchcraft, etc.—yet it's important to occasionally reflect on these superstitions because they show us how much we owe to the enhancement of our reasoning, to science, and to our accumulated knowledge. 69 As Sir J. Lubbock has aptly pointed out, “it is not too much to say that the horrible dread of unknown evil hangs like a thick cloud over savage life, and embitters every pleasure.” These unfortunate and indirect outcomes of our highest abilities can be compared to the occasional and incidental mistakes made by the instincts of lower animals.
CHAPTER III.
Comparison of the Mental Abilities of Humans and Lower Animals—continued.
The moral sense—Fundamental proposition—The qualities of social animals—Origin of sociability—Struggle between opposed instincts—Man a social animal—The more enduring social instincts conquer other less persistent instincts—The social virtues alone regarded by savages—The self-regarding virtues acquired at a later stage of development—The importance of the judgment of the members of the same community on conduct—Transmission of moral tendencies—Summary.
The moral sense—Core idea—Traits of social animals—Roots of sociability—Conflict between competing instincts—Humans as social beings—The stronger social instincts prevail over weaker ones—Social virtues seen as important by primitive societies—Self-focused virtues developed later—The significance of community judgment on behavior—Passing down of moral traits—Summary.
I fully subscribe to the judgment of those writers101 who maintain that of all the differences between man and the lower animals, the moral sense or conscience is by far the most important. This sense, as Mackintosh102 remarks, “has a rightful supremacy over every other principle of human action;” it is summed up in that short but imperious word ought, so full of high significance. It is the most noble of all the attributes of man, leading him without a moment’s hesitation to risk his life for that of a fellow-creature; or after due deliberation, impelled simply by the deep feeling of right or duty, to sacrifice it in some great cause. Immanuel Kant exclaims, “Duty! Wondrous thought, that workest neither by fond insinuation, flattery, nor by any threat, but merely by holding up thy naked law in the soul, and so extorting for thyself always 71reverence, if not always obedience; before whom all appetites are dumb, however secretly they rebel; whence thy original?”103
I completely agree with those writers101 who argue that the most significant difference between humans and lower animals is the moral sense or conscience. This sense, as Mackintosh102 points out, "has a rightful supremacy over every other principle of human action;" it is captured in the powerful word ought, which carries immense significance. It is the noblest of all human traits, prompting a person, without hesitation, to risk their life for another; or, after careful thought, to willingly give it up for a greater cause, driven solely by a strong sense of right or duty. Immanuel Kant declares, “Duty! Wondrous thought, that works neither through gentle persuasion, flattery, nor threats, but simply by laying bare your true law within the soul, demanding for yourself always reverence, if not always obedience; before whom all desires fall silent, no matter how secretly they resist; from where do you come?”103
This great question has been discussed by many writers104 of consummate ability; and my sole excuse for touching on it is the impossibility of here passing it over, and because, as far as I know, no one has approached it exclusively from the side of natural history. The investigation possesses, also, some independent interest, as an attempt to see how far the study of the lower animals can throw light on one of the highest psychical faculties of man.
This important question has been explored by many skilled writers104 of exceptional talent; and my only reason for bringing it up is that I cannot ignore it, and because, as far as I know, no one has specifically examined it from the perspective of natural history. The exploration also holds some independent interest, as it seeks to understand how studying lower animals can illuminate one of the greatest mental abilities of humans.
The following proposition seems to me in a high degree probable—namely, that any animal whatever, endowed with well-marked social instincts,105 would inevitably acquire a moral sense or conscience, as soon as 72its intellectual powers had become as well developed, or nearly as well developed, as in man. For, firstly, the social instincts lead an animal to take pleasure in the society of its fellows, to feel a certain amount of sympathy with them, and to perform various services for them. The services may be of a definite and evidently instinctive nature; or there may be only a wish and readiness, as with most of the higher social animals, to aid their fellows in certain general ways. But these feelings and services are by no means extended to all the individuals of the same species, only to those of the same association. Secondly, as soon as the mental faculties had become highly developed, images of all past actions and motives would be incessantly passing through the brain of each individual; and that feeling of dissatisfaction which invariably results, as we shall hereafter see, from any unsatisfied instinct, would arise, as often as it was perceived that the enduring and always present social instinct had yielded to some other instinct, at the time stronger, but neither enduring in its nature, nor leaving behind it a very vivid impression. It is clear that many instinctive desires, such as that of hunger, are in their nature of short duration; and after being satisfied are not readily or vividly recalled. Thirdly, after the power of language had been acquired and the wishes of the members of the same community could be distinctly expressed, the common opinion how each member ought to act for the public good, would naturally become to a large extent the guide to action. But the social instincts would still give the impulse to act for the good of the community, this impulse being strengthened, directed, and sometimes even deflected by public opinion, the power of which rests, as we shall presently see, on instinctive sympathy. Lastly, habit in the individual would ultimately play a very73 important part in guiding the conduct of each member; for the social instincts and impulses, like all other instincts, would be greatly strengthened by habit, as would obedience to the wishes and judgment of the community. These several subordinate propositions must now be discussed; and some of them at considerable length.
The following idea seems very likely to me—namely, that any animal with strong social instincts would inevitably develop a moral sense or conscience, as soon as its intellectual abilities were as well-developed, or nearly as well-developed, as those in humans. For, first, social instincts drive an animal to enjoy the company of others, to feel some level of sympathy for them, and to perform various services for them. These services can be clearly instinctive; or there may just be a willingness, as seen in most higher social animals, to help others in general ways. However, these feelings and actions are not directed towards all individuals of the same species, but only to those within the same group. Second, as soon as mental abilities were highly developed, memories of all past actions and motives would constantly flow through each individual's mind; and that feeling of dissatisfaction that always arises from any unfulfilled instinct would occur whenever it was noticed that the persistent and always-present social instinct had been overshadowed by another instinct that was stronger at the time, but neither enduring in nature nor leaving a vivid impression. It's clear that many instinctual desires, like hunger, are short-lived; and once satisfied, are not easily remembered. Third, once the ability to use language was acquired and the desires of community members could be clearly communicated, the shared understanding of how each member should act for the common good would largely guide actions. However, the social instincts would still motivate actions for the benefit of the community, with this motivation being strengthened, directed, and sometimes even redirected by public opinion, which we will see soon is based on instinctive sympathy. Lastly, habits in individuals would eventually play a significant role in guiding behavior; because social instincts and impulses, like all other instincts, would be greatly reinforced by habit, as would obedience to the wishes and judgments of the community. These various points need to be discussed now; and some of them in considerable detail.
It may be well first to premise that I do not wish to maintain that any strictly social animal, if its intellectual faculties were to become as active and as highly developed as in man, would acquire exactly the same moral sense as ours. In the same manner as various animals have some sense of beauty, though they admire widely different objects, so they might have a sense of right and wrong, though led by it to follow widely different lines of conduct. If, for instance, to take an extreme case, men were reared under precisely the same conditions as hive-bees, there can hardly be a doubt that our unmarried females would, like the worker-bees, think it a sacred duty to kill their brothers, and mothers would strive to kill their fertile daughters; and no one would think of interfering. Nevertheless the bee, or any other social animal, would in our supposed case gain, as it appears to me, some feeling of right and wrong, or a conscience. For each individual would have an inward sense of possessing certain stronger or more enduring instincts, and others less strong or enduring; so that there would often be a struggle which impulse should be followed; and satisfaction or dissatisfaction would be felt, as past impressions were compared during their incessant passage through the mind. In this case an inward monitor would tell the animal that it would have been better to have followed the one impulse rather than the other. The one course ought to have been followed: the one74 would have been right and the other wrong; but to these terms I shall have to recur.
It might be useful to start by saying that I don't believe that any purely social animal, if its thinking abilities were to become as active and developed as humans, would have the same moral sense we do. Just as different animals have a sense of beauty, even if they appreciate different things, they could also have a sense of right and wrong, even if it leads them down different paths. For example, if men were raised under the same conditions as hive-bees, there's a good chance our unmarried females would see it as a sacred duty to kill their brothers, and mothers would try to eliminate their fertile daughters; no one would think to intervene. Still, in this hypothetical situation, the bee or any other social animal would develop some sense of right and wrong, or a conscience. Each individual would feel an internal awareness of having stronger or more persistent instincts, versus those that are weaker or less enduring. This would lead to conflicts over which impulse to follow, and feelings of satisfaction or dissatisfaction as past experiences cycled through their minds. In this scenario, an internal guide would suggest that it would have been better to follow one impulse instead of the other. One choice should have been taken: one would be right while the other would be wrong; but I will need to revisit these terms.
Sociability.—Animals of many kinds are social; we find even distinct species living together, as with some American monkeys, and with the united flocks of rooks, jackdaws, and starlings. Man shows the same feeling in his strong love for the dog, which the dog returns with interest. Every one must have noticed how miserable horses, dogs, sheep, &c. are when separated from their companions; and what affection at least the two former kinds show on their reunion. It is curious to speculate on the feelings of a dog, who will rest peacefully for hours in a room with his master or any of the family, without the least notice being taken of him; but if left for a short time by himself, barks or howls dismally. We will confine our attention to the higher social animals, excluding insects, although these aid each other in many important ways. The most common service which the higher animals perform for each other, is the warning each other of danger by means of the united senses of all. Every sportsman knows, as Dr. Jaeger remarks,106 how difficult it is to approach animals in a herd or troop. Wild horses and cattle do not, I believe, make any danger-signal; but the attitude of any one who first discovers an enemy, warns the others. Rabbits stamp loudly on the ground with their hind-feet as a signal: sheep and chamois do the same, but with their fore-feet, uttering likewise a whistle. Many birds and some mammals post sentinels, which in the case of seals are said107 generally to be the females. The leader of a troop of monkeys acts as the sentinel, and utters cries expressive both of danger and of safety.108 Social 75animals perform many little services for each other: horses nibble, and cows lick each other, on any spot which itches: monkeys search for each other’s external parasites; and Brehm states that after a troop of the Cercopithecus griseo-viridis has rushed through a thorny brake, each monkey stretches itself on a branch, and another monkey sitting by “conscientiously” examines its fur and extracts every thorn or burr.
Sociability.—Many types of animals are social; we can even find different species living together, like some American monkeys, and the flocks of rooks, jackdaws, and starlings. Humans display a similar bond through their strong love for dogs, which dogs reciprocate wholeheartedly. Everyone has probably noticed how unhappy horses, dogs, sheep, etc. are when they're away from their companions, and the affection that at least the first two kinds show when they reunite. It's interesting to think about the feelings of a dog, who can rest contentedly for hours in a room with his owner or family members, without anyone paying attention to him; but if he's left alone for a little while, he barks or howls sadly. We will focus on the more advanced social animals, excluding insects, although these also help each other in important ways. The most common service that social animals provide each other is alerting one another to danger using the collective senses of the group. Every hunter knows, as Dr. Jaeger points out,106 how tough it is to sneak up on animals in a herd or troop. Wild horses and cattle, I believe, don’t send out danger signals, but the posture of the first animal that notices a threat warns the others. Rabbits stomp loudly on the ground with their hind feet to signal alarm: sheep and chamois do the same, but with their front feet, also letting out a whistle. Many birds and some mammals appoint sentinels, which, in the case of seals, are said107 to usually be the females. The leader of a monkey troop serves as the sentinel and makes calls that indicate both danger and safety.108 Social 75 animals do many small favors for each other: horses nibble, and cows lick each other on any spot that itches; monkeys groom each other for external parasites; and Brehm notes that after a troop of the Cercopithecus griseo-viridis has rushed through a thorny thicket, each monkey lays down on a branch, and another nearby monkey “conscientiously” examines its fur and removes every thorn or burr.
Animals also render more important services to each other: thus wolves and some other beasts of prey hunt in packs, and aid each other in attacking their victims. Pelicans fish in concert. The Hamadryas baboons turn over stones to find insects, &c.; and when they come to a large one, as many as can stand round, turn it over together and share the booty. Social animals mutually defend each other. The males of some ruminants come to the front when there is danger and defend the herd with their horns. I shall also in a future chapter give cases of two young wild bulls attacking an old one in concert, and of two stallions together trying to drive away a third stallion from a troop of mares. Brehm encountered in Abyssinia a great troop of baboons which were crossing a valley: some had already ascended the opposite mountain, and some were still in the valley: the latter were attacked by the dogs, but the old males immediately hurried down from the rocks, and with mouths widely opened roared so fearfully, that the dogs precipitately retreated. They were again encouraged to the attack; but by this time all the baboons had reascended the heights, excepting a young one, about six 76months old, who, loudly calling for aid, climbed on a block of rock and was surrounded. Now one of the largest males, a true hero, came down again from the mountain, slowly went to the young one, coaxed him, and triumphantly led him away—the dogs being too much astonished to make an attack. I cannot resist giving another scene which was witnessed by this same naturalist; an eagle seized a young Cercopithecus, which, by clinging to a branch, was not at once carried off; it cried loudly for assistance, upon which the other members of the troop with much uproar rushed to the rescue, surrounded the eagle, and pulled out so many feathers, that he no longer thought of his prey, but only how to escape. This eagle, as Brehm remarks, assuredly would never again attack a monkey in a troop.
Animals provide each other with important services: for example, wolves and some other predatory animals hunt in packs and help each other attack their prey. Pelicans fish together. Hamadryas baboons turn over stones to find insects, and when they come across a large stone, as many as can fit around it will turn it over together and share the find. Social animals protect one another. The males of some herbivores step forward in times of danger to defend the herd with their horns. In a future chapter, I will present examples of two young wild bulls attacking an older one together and of two stallions trying to drive away a third stallion from a group of mares. Brehm observed a large troop of baboons crossing a valley in Abyssinia: some had already climbed the opposite mountain, while others were still in the valley. The ones in the valley were attacked by dogs, but the older males rushed down from the rocks and roared fiercely, causing the dogs to retreat quickly. The dogs were encouraged to attack again, but by that time, all the baboons had moved up to higher ground, except for a young one, about six months old, who climbed onto a rock and called out for help. One of the largest males, a true hero, came down from the mountain, slowly approached the young baboon, coaxed him, and triumphantly led him away while the dogs were too astonished to attack. I can't help but share another scene witnessed by the same naturalist: an eagle grabbed a young Cercopithecus, which clung to a branch and wasn't immediately taken away. It cried out for help, and the other members of the troop rushed to the rescue with loud commotion, surrounding the eagle and pulling out so many feathers that the eagle gave up on its prey and focused only on escaping. As Brehm notes, this eagle would surely never attempt to attack a monkey within a troop again.
It is certain that associated animals have a feeling of love for each other which is not felt by adult and non-social animals. How far in most cases they actually sympathise with each other’s pains and pleasures is more doubtful, especially with respect to the latter. Mr. Buxton, however, who had excellent means of observation,109 states that his macaws, which lived free in Norfolk, took “an extravagant interest” in a pair with a nest, and whenever the female left it, she was surrounded by a troop “screaming horrible acclamations in her honour.” It is often difficult to judge whether animals have any feeling for each other’s sufferings. Who can say what cows feel, when they surround and stare intently on a dying or dead companion? That animals sometimes are far from feeling any sympathy is too certain; for they will expel a wounded animal from the herd, or gore or worry it to death. This is almost the blackest fact in natural 77history, unless indeed the explanation which has been suggested is true, that their instinct or reason leads them to expel an injured companion, lest beasts of prey, including man, should be tempted to follow the troop. In this case their conduct is not much worse than that of the North American Indians who leave their feeble comrades to perish on the plains, or the Feegeans, who, when their parents get old or fall ill, bury them alive.110
It's clear that social animals have a sense of love for one another that adult and unsocial animals lack. However, it's less certain how much they truly empathize with each other's joys and sorrows, especially the latter. Mr. Buxton, who had great observational skills,109 mentions that his macaws, living freely in Norfolk, showed "an extravagant interest" in a nesting pair, and whenever the female left the nest, she was surrounded by a group "screaming horrible cheers in her honor." It's often hard to determine whether animals care about each other's suffering. Who can say what cows feel when they gather around a dying or dead friend? It's also evident that animals can be quite unsympathetic; they will sometimes drive a wounded member out of the herd, or even gore it to death. This is one of the darkest truths in natural77 history, unless the suggested explanation is correct: that their instincts or reasoning tell them to expel an injured companion to avoid attracting predators, including humans. In this case, their behavior isn't much worse than that of North American Indians who abandon weak comrades to die on the plains, or the Feegeans, who bury their elderly or sick parents alive.110
Many animals, however, certainly sympathise with each other’s distress or danger. This is the case even with birds; Capt. Stansbury111 found on a salt lake in Utah an old and completely blind pelican, which was very fat, and must have been long and well fed by his companions. Mr. Blyth, as he informs me, saw Indian crows feeding two or three of their companions which were blind; and I have heard of an analogous case with the domestic cock. We may, if we choose, call these actions instinctive; but such cases are much too rare for the development of any special instinct.112 I have myself seen a dog, who never passed a great friend of his, a cat which lay sick in a basket, without giving her a few licks with his tongue, the surest sign of kind feeling in a dog.
Many animals certainly empathize with each other's pain or danger. This includes birds; Capt. Stansbury111 found an old, completely blind pelican on a salt lake in Utah, which was very overweight and must have been well-cared for by its companions for a long time. Mr. Blyth tells me he saw Indian crows feeding two or three of their blind friends; and I've heard about a similar situation involving a domestic rooster. We could label these actions as instinctive, but such cases are too rare to indicate the development of any specific instinct.112 I personally witnessed a dog who never passed by his great friend, a cat lying sick in a basket, without giving her a few licks with his tongue, which is the surest sign of affection in a dog.
It must be called sympathy that leads a courageous dog to fly at any one who strikes his master, as he certainly will. I saw a person pretending to beat a lady who had a very timid little dog on her lap, and the trial had never before been made. The little crea78ture instantly jumped away, but after the pretended beating was over, it was really pathetic to see how perseveringly he tried to lick his mistress’s face and comfort her. Brehm113 states that when a baboon in confinement was pursued to be punished, the others tried to protect him. It must have been sympathy in the cases above given which led the baboons and Cercopitheci to defend their young comrades from the dogs and the eagle. I will give only one other instance of sympathetic and heroic conduct in a little American monkey. Several years ago a keeper at the Zoological Gardens, showed me some deep and scarcely healed wounds on the nape of his neck, inflicted on him whilst kneeling on the floor by a fierce baboon. The little American monkey, who was a warm friend of this keeper, lived in the same large compartment, and was dreadfully afraid of the great baboon. Nevertheless, as soon as he saw his friend the keeper in peril, he rushed to the rescue, and by screams and bites so distracted the baboon that the man was able to escape, after running great risk, as the surgeon who attended him thought, of his life.
It can only be called sympathy that drives a brave dog to attack anyone who harms its owner, as it certainly will. I once saw someone pretending to hit a woman holding a very nervous little dog on her lap, and this situation had never happened before. The little creature immediately jumped away, but once the fake beating was over, it was truly heartbreaking to see how desperately he tried to lick his owner's face and comfort her. Brehm113 mentions that when a baboon in captivity was chased to be punished, the others tried to protect it. It must have been sympathy that led the baboons and Cercopitheci to defend their young peers from the dogs and the eagle. I'll share just one more example of sympathetic and heroic behavior from a little American monkey. Several years ago, a zookeeper at the Zoological Gardens showed me some deep and barely healed wounds on his neck, caused by a fierce baboon while he was kneeling on the floor. The little American monkey, who was a dear friend of this zookeeper, lived in the same large enclosure and was terrified of the big baboon. Still, as soon as he saw his friend in danger, he rushed to help, and by screaming and biting, he distracted the baboon enough for the man to escape, after facing great risk, as the surgeon who treated him believed he was close to losing his life.
Besides love and sympathy, animals exhibit other qualities which in us would be called moral; and I agree with Agassiz114 that dogs possess something very like a conscience. They certainly possess some power of self-command, and this does not appear to be wholly the result of fear. As Braubach115 remarks, a dog will refrain from stealing food in the absence of his master. Dogs have long been accepted as the very type of fidelity and obedience. All animals living in a body which defend each other or attack their enemies 79in concert, must be in some degree faithful to each other; and those that follow a leader must be in some degree obedient. When the baboons in Abyssinia116 plunder a garden, they silently follow their leader; and if an imprudent young animal makes a noise, he receives a slap from the others to teach him silence and obedience; but as soon as they are sure that there is no danger, all show their joy by much clamour.
Besides love and compassion, animals display other traits that we would consider moral; and I agree with Agassiz114 that dogs have something very similar to a conscience. They definitely have some ability to control themselves, and this doesn’t seem to be entirely due to fear. As Braubach115 points out, a dog will avoid stealing food when his owner isn’t around. Dogs have long been recognized as the ultimate symbol of loyalty and obedience. All animals living in groups that support each other or attack their foes together must be somewhat loyal to one another; and those that follow a leader must be somewhat obedient. When baboons in Abyssinia116 raid a garden, they quietly trail behind their leader; and if a careless young one makes a sound, the others will hit him to teach him to be quiet and obedient; but as soon as they are sure there’s no threat, they all express their excitement with loud noise.
With respect to the impulse which leads certain animals to associate together, and to aid each other in many ways, we may infer that in most cases they are impelled by the same sense of satisfaction or pleasure which they experience in performing other instinctive actions; or by the same sense of dissatisfaction, as in other cases of prevented instinctive actions. We see this in innumerable instances, and it is illustrated in a striking manner by the acquired instincts of our domesticated animals; thus a young shepherd-dog delights in driving and running round a flock of sheep, but not in worrying them; a young foxhound delights in hunting a fox, whilst some other kinds of dogs as I have witnessed, utterly disregard foxes. What a strong feeling of inward satisfaction must impel a bird, so full of activity, to brood day after day over her eggs. Migratory birds are miserable if prevented from migrating, and perhaps they enjoy starting on their long flight. Some few instincts are determined solely by painful feelings, as by fear, which leads to self-preservation, or is specially directed against certain enemies. No one, I presume, can analyse the sensations of pleasure or pain. In many cases, however, it is probable that instincts are persistently followed from the 80mere force of inheritance, without the stimulus of either pleasure or pain. A young pointer, when it first scents game, apparently cannot help pointing. A squirrel in a cage who pats the nuts which it cannot eat, as if to bury them in the ground, can hardly be thought to act thus either from pleasure or pain. Hence the common assumption that men must be impelled to every action by experiencing some pleasure or pain may be erroneous. Although a habit may be blindly and implicitly followed, independently of any pleasure or pain felt at the moment, yet if it be forcibly and abruptly checked, a vague sense of dissatisfaction is generally experienced; and this is especially true in regard to persons of feeble intellect.
Regarding the urge that drives some animals to gather and help each other in various ways, we can conclude that, in most cases, they are motivated by the same sense of satisfaction or pleasure they feel when doing other instinctive behaviors; or by a sense of dissatisfaction, as seen in instances of thwarted instinctive actions. This is evident in countless examples and is vividly demonstrated by the learned instincts of our domestic animals. For instance, a young shepherd dog enjoys herding and running around a flock of sheep, but not bothering them; a young foxhound loves chasing a fox, while some other dog breeds, as I've observed, completely ignore foxes. Consider the strong sense of inner satisfaction that drives a bird, full of energy, to sit on her eggs day after day. Migratory birds feel unhappy if they can't migrate, and they likely enjoy setting out on their long journeys. A few instincts are driven solely by painful feelings, like fear, which leads to self-preservation or is specifically aimed at certain threats. I assume no one can accurately analyze the feelings of pleasure or pain. However, it’s likely that instincts are often followed purely out of the force of inheritance, without being triggered by pleasure or pain. A young pointer, when it smells game for the first time, seemingly cannot help but point. A squirrel in a cage that taps the nuts it can't eat, as if to bury them, doesn't seem to do this for pleasure or pain. Therefore, the common belief that humans are driven to act by experiencing some form of pleasure or pain may be mistaken. Although a habit might be followed blindly and unthinkingly, regardless of any pleasure or pain felt at that moment, if it's suddenly interrupted, a general sense of dissatisfaction is usually felt, especially in individuals with weaker intellects.
It has often been assumed that animals were in the first place rendered social, and that they feel as a consequence uncomfortable when separated from each other, and comfortable whilst together; but it is a more probable view that these sensations were first developed, in order that those animals which would profit by living in society, should be induced to live together. In the same manner as the sense of hunger and the pleasure of eating were, no doubt, first acquired in order to induce animals to eat. The feeling of pleasure from society is probably an extension of the parental or filial affections; and this extension may be in chief part attributed to natural selection, but perhaps in part to mere habit. For with those animals which were benefited by living in close association, the individuals which took the greatest pleasure in society would best escape various dangers; whilst those that cared least for their comrades and lived solitary would perish in greater numbers. With respect to the origin of the parental and filial affections, which apparently lie at the basis of the social affections, it is hopeless to speculate; but we81 may infer that they have been to a large extent gained through natural selection. So it has almost certainly been with the unusual and opposite feeling of hatred between the nearest relations, as with the worker-bees which kill their brother-drones, and with the queen-bees which kill their daughter-queens; the desire to destroy, instead of loving, their nearest relations having been here of service to the community.
It's often assumed that animals are social by nature and feel uncomfortable when separated and comfortable when together. However, a more likely perspective is that these feelings developed so that animals that would benefit from living in groups would be encouraged to do so. Just like the sense of hunger and the enjoyment of eating likely evolved to motivate animals to feed, the pleasure derived from social interactions is probably an extension of parental or sibling bonds. This extension can mostly be attributed to natural selection, but possibly also to simple habit. Animals that thrived in close groups were more likely to find joy in socializing, helping them avoid various dangers, while those indifferent to companionship and more solitary tended to die off at higher rates. As for the origins of parental and sibling bonds, which seem to form the foundation of social feelings, it's futile to speculate; however, we81 might assume they have largely developed through natural selection. The same goes for the unusual and conflicting feelings of hatred among close relatives, such as worker bees that kill their brother drones and queen bees that eliminate their daughter queens; the drive to harm instead of love their closest kin has proved advantageous to the community.
The all-important emotion of sympathy is distinct from that of love. A mother may passionately love her sleeping and passive infant, but she can then hardly be said to feel sympathy for it. The love of a man for his dog is distinct from sympathy, and so is that of a dog for his master. Adam Smith formerly argued, as has Mr. Bain recently, that the basis of sympathy lies in our strong retentiveness of former states of pain or pleasure. Hence, “the sight of another person enduring hunger, cold, fatigue, revives in us some recollection of these states, which are painful even in idea.” We are thus impelled to relieve the sufferings of another, in order that our own painful feelings may be at the same time relieved. In like manner we are led to participate in the pleasures of others.117 But I cannot see how this view explains the fact that sympathy is excited in an immeasurably stronger degree by a beloved than by an indifferent person. The mere 82sight of suffering, independently of love, would suffice to call up in us vivid recollections and associations. Sympathy may at first have originated in the manner above suggested; but it seems now to have become an instinct, which is especially directed towards beloved objects, in the same manner as fear with animals is especially directed against certain enemies. As sympathy is thus directed, the mutual love of the members of the same community will extend its limits. No doubt a tiger or lion feels sympathy for the sufferings of its own young, but not for any other animal. With strictly social animals the feeling will be more or less extended to all the associated members, as we know to be the case. With mankind selfishness, experience, and imitation probably add, as Mr. Bain has shewn, to the power of sympathy; for we are led by the hope of receiving good in return to perform acts of sympathetic kindness to others; and there can be no doubt that the feeling of sympathy is much strengthened by habit. In however complex a manner this feeling may have originated, as it is one of high importance to all those animals which aid and defend each other, it will have been increased, through natural selection; for those communities, which included the greatest number of the most sympathetic members, would flourish best and rear the greatest number of offspring.
The crucial emotion of sympathy is different from love. A mother may deeply love her sleeping and passive baby, but it’s hard to say she feels sympathy for it. The love a man has for his dog is separate from sympathy, just like the bond between a dog and its owner. Adam Smith argued in the past, as Mr. Bain has recently, that the foundation of sympathy comes from our strong memory of past pains or pleasures. So, “seeing another person going through hunger, cold, or exhaustion brings back memories of those experiences, which are painful even to think about.” This compels us to help relieve someone else's suffering so that we can alleviate our own painful feelings at the same time. Similarly, we are drawn to share in the joys of others. But I don’t see how this viewpoint explains why sympathy is felt much more intensely for someone we love than for someone we don’t care about. Just seeing someone suffer, regardless of love, would still likely trigger vivid memories and associations in us. While sympathy may have originated in the way just described, it now seems to be more of an instinct that is particularly directed toward those we care about, much like how animals have specific fears directed at their enemies. As sympathy is directed this way, the mutual love among members of the same community will broaden its scope. It’s true that a tiger or lion feels sympathy for its own young but not for other animals. With genuinely social animals, this feeling tends to extend more or less to all related members, as we can see. Among humans, selfishness, experience, and imitation likely enhance sympathy’s effects, as Mr. Bain has shown, because we’re motivated by the hope of receiving something in return when we act kindly toward others; and it’s clear that the feeling of sympathy is much strengthened by habit. No matter how complex this feeling's origins may be, since it’s essential for animals that help and protect each other, it has likely been amplified through natural selection; communities with the most sympathetic members are more likely to thrive and raise the largest number of offspring.
In many cases it is impossible to decide whether certain social instincts have been acquired through natural selection, or are the indirect result of other instincts and faculties, such as sympathy, reason, experience, and a tendency to imitation; or again, whether they are simply the result of long-continued habit. So remarkable an instinct as the placing sentinels to warn the community of danger, can hardly have been83 the indirect result of any other faculty; it must therefore have been directly acquired. On the other hand, the habit followed by the males of some social animals, of defending the community and of attacking their enemies or their prey in concert, may perhaps have originated from mutual sympathy; but courage, and in most cases strength, must have been previously acquired, probably through natural selection.
In many instances, it's tough to determine whether certain social instincts developed through natural selection, or if they're just the byproducts of other instincts and abilities like empathy, reasoning, experience, and a tendency to copy others; or if they simply come from long-term habits. An instinct as significant as having sentinels to alert the community of danger probably wasn't just an indirect outcome of any other ability; it must have been directly developed. On the flip side, the behavior seen in male social animals, where they defend their community and attack enemies or prey together, might have started from mutual empathy; but courage, and generally strength, must have been developed first, likely through natural selection.
Of the various instincts and habits, some are much stronger than others, that is, some either give more pleasure in their performance and more distress in their prevention than others; or, which is probably quite as important, they are more persistently followed through inheritance without exciting any special feeling of pleasure or pain. We are ourselves conscious that some habits are much more difficult to cure or change than others. Hence a struggle may often be observed in animals between different instincts, or between an instinct and some habitual disposition; as when a dog rushes after a hare, is rebuked, pauses, hesitates, pursues again or returns ashamed to his master; or as between the love of a female dog for her young puppies and for her master, for she may be seen to slink away to them, as if half ashamed of not accompanying her master. But the most curious instance known to me of one instinct conquering another, is the migratory instinct conquering the maternal instinct. The former is wonderfully strong; a confined bird will at the proper season beat her breast against the wires of her cage, until it is bare and bloody. It causes young salmon to leap out of the fresh water, where they could still continue to live, and thus unintentionally to commit suicide. Every one knows how strong the maternal instinct is, leading even timid birds to face great danger, though with hesitation and in opposition to the instinct of self84preservation. Nevertheless the migratory instinct is so powerful that late in the autumn swallows and house-martins frequently desert their tender young, leaving them to perish miserably in their nests.118
Some instincts and habits are much stronger than others; that is, some provide more pleasure when fulfilled and more distress when resisted than others do. Or, which is probably just as important, they are more consistently followed due to inheritance without triggering a strong feeling of pleasure or pain. We are aware that certain habits are much harder to change or break than others. Thus, we often see a struggle in animals between conflicting instincts or between an instinct and a habitual behavior; for example, when a dog chases a hare, gets reprimanded, pauses, hesitates, chases again, or returns sheepishly to its owner. Or consider the conflict between a female dog's affection for her puppies and her owner, as she sometimes sneaks away to be with them, almost as if she feels guilty for not staying with her owner. However, one of the most intriguing examples I know of one instinct overpowering another is the migratory instinct overcoming the maternal instinct. The migratory instinct is incredibly strong; a caged bird will, during migration season, beat its breast against the bars of the cage until it's raw and bleeding. This instinct even drives young salmon to jump out of freshwater, where they could survive, leading to their own accidental deaths. Everyone knows how powerful the maternal instinct is, prompting even timid birds to confront great danger, albeit hesitantly and against their instinct for self-preservation. Yet, the migratory instinct is so intense that late in autumn, swallows and house-martins often abandon their delicate young, leaving them to suffer tragically in their nests.84118
We can perceive that an instinctive impulse, if it be in any way more beneficial to a species than some other or opposed instinct, would be rendered the more potent of the two through natural selection; for the individuals which had it most strongly developed would survive in larger numbers. Whether this is the case with the migratory in comparison with the maternal instinct, may well be doubted. The great persistence or steady action of the former at certain seasons of the year during the whole day, may give it for a time paramount force.
We can see that if a natural impulse benefits a species more than another conflicting instinct, it would become stronger through natural selection, as individuals with that impulse would survive in greater numbers. However, whether this is true for the migratory instinct compared to the maternal instinct is open to question. The strong and consistent presence of the migratory instinct at specific times of the year throughout the day might give it a temporary advantage.
Man a social animal.—Most persons admit that man is a social being. We see this in his dislike of solitude, and in his wish for society beyond that of his own family. Solitary confinement is one of the severest punishments which can be inflicted. Some authors suppose that man primevally lived in single families; but at the present day, though single families, or only two or three together, roam the solitudes of some savage lands, they are always, as far as I can discover, friendly with other families inhabiting the same district. Such families occasionally meet in council, and they unite 85for their common defence. It is no argument against savage man being a social animal, that the tribes inhabiting adjacent districts are almost always at war with each other; for the social instincts never extend to all the individuals of the same species. Judging from the analogy of the greater number of the Quadrumana, it is probable that the early ape-like progenitors of man were likewise social; but this is not of much importance for us. Although man, as he now exists, has few special instincts, having lost any which his early progenitors may have possessed, this is no reason why he should not have retained from an extremely remote period some degree of instinctive love and sympathy for his fellows. We are indeed all conscious that we do possess such sympathetic feelings;119 but our consciousness does not tell us whether they are instinctive, having originated long ago in the same manner as with the lower animals, or whether they have been acquired by each of us during our early years. As man is a social animal, it is also probable that he would inherit a tendency to be faithful to his comrades, for this quality is common to most social animals. He would in like manner possess some capacity for self-command, and perhaps of obedience to the leader of the community. He would from an inherited tendency still be willing to defend, in concert with others, his fellow-men, and would be ready to aid them in any way which did not too greatly interfere with his own welfare or his own strong desires.
Man is a social animal.—Most people agree that humans are social beings. We see this in our dislike of being alone and in our desire for companionship beyond just our own families. Solitary confinement is one of the harshest punishments that can be imposed. Some writers suggest that early humans lived in isolated families; however, today, even though single families, or just a few together, may roam the remote areas of some wild lands, they are usually friendly with other families living in the same area. These families sometimes meet for discussions, and they come together for their collective protection. It doesn’t disprove that primitive humans were social animals just because tribes in neighboring areas often fight with one another; social instincts don’t extend to every individual of the same species. Based on the behavior of many primates, it's likely that the early ape-like ancestors of humans were also social, but that’s not very important for our discussion. Even though modern humans have few specific instincts, having lost those that their early ancestors might have had, it doesn't mean that we haven't kept some instinctive feelings of love and sympathy for each other from a very long time ago. We are all aware that we have these empathetic feelings;119but we don’t know if they are instinctive, originating long ago like in lower animals, or if they were developed individually during our early years. Since humans are social animals, it's also likely that we inherit a tendency to stay loyal to our friends, a trait common in most social species. Similarly, we likely have some ability for self-control and perhaps for following the community leader. From inherited tendencies, we would still be inclined to defend our fellow humans alongside others and be ready to help them in ways that don't significantly compromise our own well-being or strong desires.
The social animals which stand at the bottom of the 86scale are guided almost exclusively, and those which stand higher in the scale are largely guided, in the aid which they give to the members of the same community, by special instincts; but they are likewise in part impelled by mutual love and sympathy, assisted apparently by some amount of reason. Although man, as just remarked, has no special instincts to tell him how to aid his fellow-men, he still has the impulse, and with his improved intellectual faculties would naturally be much guided in this respect by reason and experience. Instinctive sympathy would, also, cause him to value highly the approbation of his fellow-men; for, as Mr. Bain has clearly shewn,120 the love of praise and the strong feeling of glory, and the still stronger horror of scorn and infamy, “are due to the workings of sympathy.” Consequently man would be greatly influenced by the wishes, approbation, and blame of his fellow-men, as expressed by their gestures and language. Thus the social instincts, which must have been acquired by man in a very rude state, and probably even by his early ape-like progenitors, still give the impulse to many of his best actions; but his actions are largely determined by the expressed wishes and judgment of his fellow-men, and unfortunately still oftener by his own strong, selfish desires. But as the feelings of love and sympathy and the power of self-command become strengthened by habit, and as the power of reasoning becomes clearer so that man can appreciate the justice of the judgments of his fellow-men, he will feel himself impelled, independently of any pleasure or pain felt at the moment, to certain lines of conduct. He may then say, I am the supreme judge of my own conduct, and in the words of Kant, I will not in my own person violate the dignity of humanity.
The social animals at the bottom of the hierarchy are mainly driven by instincts, while those higher up are mostly guided by instincts as well, but they're also influenced by love and empathy, along with a bit of reasoning. While humans, like mentioned earlier, don't have specific instincts telling them how to help others, they do have the impulse to do so, and with their advanced thinking skills, they tend to rely on reason and experience in this area. An instinctive sense of empathy makes them value the approval of others; as Mr. Bain has clearly shown, the desire for praise, a strong sense of glory, and an even stronger aversion to disdain and disgrace are all linked to the effects of empathy. Therefore, humans are significantly influenced by the desires, approval, and criticism of their peers, conveyed through their expressions and words. The social instincts, which likely developed in humans while they were still quite primitive, and probably even in their early ape-like ancestors, still drive many of their best actions; however, their actions are often shaped more by the opinions of others and, unfortunately, frequently by their own intense, selfish wants. But as feelings of love and empathy and the ability to control oneself become stronger through practice, and as the power of reasoning becomes clearer, allowing humans to recognize the fairness in others' judgments, they will find themselves driven to follow certain paths of behavior, independently of any immediate pleasure or pain. They may then say, “I am the ultimate judge of my own actions,” and in Kant's words, “I will not, in my own person, violate the dignity of humanity.”
87The more enduring Social Instincts conquer the less Persistent Instincts.—We have, however, not as yet considered the main point, on which the whole question of the moral sense hinges. Why should a man feel that he ought to obey one instinctive desire rather than another? Why does he bitterly regret if he has yielded to the strong sense of self-preservation, and has not risked his life to save that of a fellow-creature; or why does he regret having stolen food from severe hunger?
87The more lasting social instincts take precedence over the less persistent ones.—However, we have not yet addressed the main issue that the entire question of moral sense depends on. Why does a person feel they should follow one instinctive urge over another? Why do they feel deep regret if they give in to the powerful instinct of self-preservation and don’t risk their life to save someone else; or why do they regret stealing food out of extreme hunger?
It is evident in the first place, that with mankind the instinctive impulses have different degrees of strength; a young and timid mother urged by the maternal instinct will, without a moment’s hesitation, run the greatest danger for her infant, but not for a mere fellow-creature. Many a man, or even boy, who never before risked his life for another, but in whom courage and sympathy were well developed, has, disregarding the instinct of self-preservation, instantaneously plunged into a torrent to save a drowning fellow-creature. In this case man is impelled by the same instinctive motive, which caused the heroic little American monkey, formerly described, to attack the great and dreaded baboon, to save his keeper. Such actions as the above appear to be the simple result of the greater strength of the social or maternal instincts than of any other instinct or motive; for they are performed too instantaneously for reflection, or for the sensation of pleasure or pain; though if prevented distress would be caused.
It’s clear from the start that humans have instinctive urges with varying degrees of intensity. A young, anxious mother driven by maternal instinct will, without hesitation, put herself in serious danger to protect her baby, but she might not do the same for a stranger. Many men or even boys who’ve never risked their lives for anyone before, but who possess a strong sense of courage and empathy, have jumped into raging waters to save someone drowning, ignoring their own self-preservation instinct. In these situations, humans are driven by the same instinctive urge that led the brave little American monkey, mentioned before, to confront the large, feared baboon to protect his caretaker. Actions like these seem to stem from the stronger influence of social or maternal instincts over any other drives; they occur so quickly that there’s no time for thought or feelings of pleasure or pain, although being stopped would certainly cause distress.
I am aware that some persons maintain that actions performed impulsively, as in the above cases, do not come under the dominion of the moral sense, and cannot be called moral. They confine this term to actions done deliberately, after a victory over opposing desires, or to actions prompted by some lofty motive. But it appears scarcely possible to draw any clear line88 of distinction of this kind; though the distinction may be real. As far as exalted motives are concerned, many instances have been recorded of barbarians, destitute of any feeling of general benevolence towards mankind, and not guided by any religious motive, who have deliberately as prisoners sacrificed their lives,121 rather than betray their comrades; and surely their conduct ought to be considered as moral. As far as deliberation and the victory over opposing motives are concerned, animals may be seen doubting between opposed instincts, as in rescuing their offspring or comrades from danger; yet their actions, though done for the good of others, are not called moral. Moreover, an action repeatedly performed by us, will at last be done without deliberation or hesitation, and can then hardly be distinguished from an instinct; yet surely no one will pretend that an action thus done ceases to be moral. On the contrary, we all feel that an act cannot be considered as perfect, or as performed in the most noble manner, unless it be done impulsively, without deliberation or effort, in the same manner as by a man in whom the requisite qualities are innate. He who is forced to overcome his fear or want of sympathy before he acts, deserves, however, in one way higher credit than the man whose innate disposition leads him to a good act without effort. As we cannot distinguish between motives, we rank all actions of a certain class as moral, when they are performed by a moral being. A moral being is one who is capable of comparing his past and future actions or motives, and of approving or disapproving of them. We have no reason to suppose that any of the lower animals have 89this capacity; therefore when a monkey faces danger to rescue its comrade, or takes charge of an orphan-monkey, we do not call its conduct moral. But in the case of man, who alone can with certainty be ranked as a moral being, actions of a certain class are called moral, whether performed deliberately after a struggle with opposing motives, or from the effects of slowly-gained habit, or impulsively through instinct.
I know some people argue that actions taken on impulse, like the ones mentioned above, aren’t governed by our moral sense and shouldn’t be considered moral. They limit the term "moral" to actions that are done intentionally, after overcoming conflicting desires, or actions driven by a noble motive. However, it seems difficult to define a clear distinction like this, even if the distinction might exist. Regarding noble motives, there are many recorded instances of people who, despite lacking general kindness towards humanity and not being driven by any religious motive, have willingly sacrificed their lives as prisoners rather than betray their friends; surely, their actions should be viewed as moral. In terms of intention and overcoming conflicting motives, animals can be seen hesitating between competing instincts, like when they save their young or peers from danger; yet their actions, even when aimed at helping others, aren’t labeled as moral. Furthermore, when we repeatedly perform an action, it eventually becomes automatic, making it hard to differentiate from instinct; yet no one would argue that an action performed this way stops being moral. On the contrary, we all feel that an act cannot be seen as perfect or performed in the most admirable way unless it’s done impulsively, without thought or struggle, like someone who inherently possesses the necessary qualities. Someone who has to overcome their fear or lack of empathy before acting deserves, in one way, more credit than someone whose natural tendency leads them to do good without effort. Since we can’t distinguish between motives, we classify all actions in a particular category as moral when they are carried out by a moral being. A moral being is someone who can reflect on their past and future actions or motives and judge them positively or negatively. We have no reason to think that lower animals possess this ability; therefore, when a monkey risks itself to save a friend or cares for an orphaned monkey, we don’t label its behavior as moral. But with humans, who can certainly be considered moral beings, actions in a certain category are referred to as moral, whether they are performed deliberately after wrestling with conflicting motives, as a result of developed habits, or impulsively out of instinct.
But to return to our more immediate subject; although some instincts are more powerful than others, thus leading to corresponding actions, yet it cannot be maintained that the social instincts are ordinarily stronger in man, or have become stronger through long-continued habit, than the instincts, for instance, of self-preservation, hunger, lust, vengeance, &c. Why then does man regret, even though he may endeavour to banish any such regret, that he has followed the one natural impulse, rather than the other; and why does he further feel that he ought to regret his conduct? Man in this respect differs profoundly from the lower animals. Nevertheless we can, I think, see with some degree of clearness the reason of this difference.
But to return to our more immediate subject; while some instincts are stronger than others, leading to corresponding actions, it can't be said that social instincts are generally stronger in humans, or have become stronger over time, compared to instincts like self-preservation, hunger, lust, revenge, etc. So why does a person feel regret, even if they try to push it away, for following one natural impulse over another? And why do they feel they should regret their actions? In this regard, humans are very different from lower animals. Still, I believe we can see the reason for this difference fairly clearly.
Man, from the activity of his mental faculties, cannot avoid reflection: past impressions and images are incessantly passing through his mind with distinctness. Now with those animals which live permanently in a body, the social instincts are ever present and persistent. Such animals are always ready to utter the danger-signal, to defend the community, and to give aid to their fellows in accordance with their habits; they feel at all times, without the stimulus of any special passion or desire, some degree of love and sympathy for them; they are unhappy if long separated from them, and always happy to be in their company. So it is with ourselves. A man who possessed no trace90 of such feelings would be an unnatural monster. On the other hand, the desire to satisfy hunger, or any passion, such as vengeance, is in its nature temporary, and can for a time be fully satisfied. Nor is it easy, perhaps hardly possible, to call up with complete vividness the feeling, for instance, of hunger; nor indeed, as has often been remarked, of any suffering. The instinct of self-preservation is not felt except in the presence of danger; and many a coward has thought himself brave until he has met his enemy face to face. The wish for another man’s property is perhaps as persistent a desire as any that can be named; but even in this case the satisfaction of actual possession is generally a weaker feeling than the desire: many a thief, if not an habitual one, after success has wondered why he stole some article.
Humans, by nature of their thinking, can't help but reflect: past experiences and images constantly flow through their minds with clarity. For animals that live together, social instincts are always present and strong. These animals are quick to sound the alarm, protect their group, and help their peers based on their habits; they feel a consistent level of love and sympathy for each other without needing a specific urge or desire. They are unhappy if they’re apart for too long and always content when they are together. The same goes for us. A person who has no trace of these feelings would be an unnatural monster. On the flip side, the urge to satisfy hunger or another passion, like revenge, is usually temporary and can be fully satisfied for a while. It’s also not easy, and maybe nearly impossible, to vividly recall feelings like hunger or any kind of suffering. The instinct for self-preservation only kicks in when there’s danger; many cowards have believed they were brave until they faced their enemy directly. The desire for someone else’s belongings is perhaps one of the most enduring desires, but even then, the feeling of actually possessing something is often weaker than the desire itself; a thief, especially if they don’t usually steal, may wonder why they took something after they succeeded.
Thus, as man cannot prevent old impressions continually repassing through his mind, he will be compelled to compare the weaker impressions of, for instance, past hunger, or of vengeance satisfied or danger avoided at the cost of other men, with the instinct of sympathy and good-will to his fellows, which is still present and ever in some degree active in his mind. He will then feel in his imagination that a stronger instinct has yielded to one which now seems comparatively weak; and then that sense of dissatisfaction will inevitably be felt with which man is endowed, like every other animal, in order that his instincts may be obeyed. The case before given, of the swallow, affords an illustration, though of a reversed nature, of a temporary though for the time strongly persistent instinct conquering another instinct which is usually dominant over all others. At the proper season these birds seem all day long to be impressed with the desire to migrate; their habits change; they become restless, are noisy,91 and congregate in flocks. Whilst the mother-bird is feeding or brooding over her nestlings, the maternal instinct is probably stronger than the migratory; but the instinct which is more persistent gains the victory, and at last, at a moment when her young ones are not in sight, she takes flight and deserts them. When arrived at the end of her long journey, and the migratory instinct ceases to act, what an agony of remorse each bird would feel, if, from being endowed with great mental activity, she could not prevent the image continually passing before her mind of her young ones perishing in the bleak north from cold and hunger.
So, since a person can’t stop old thoughts from constantly running through their mind, they end up comparing weaker memories—like past hunger, revenge fulfilled, or avoiding danger at the expense of others—with the instinct of empathy and goodwill towards others, which still exists and is always somewhat active in their mind. They will then imagine that a stronger instinct has given way to one that now seems relatively weak; and soon enough, they’ll feel that familiar sense of dissatisfaction, which is built into humans, like all animals, to ensure their instincts are followed. The case mentioned earlier, of the swallow, provides an example, although it’s the opposite: a temporary but forceful instinct overcoming another instinct that usually takes precedence over all others. At the right time, these birds appear to be driven by a strong desire to migrate all day long; their behavior changes—they become restless, noisy, and gather in flocks. While the mother bird is feeding or caring for her chicks, the maternal instinct likely is stronger than the migratory one; however, the more persistent instinct ultimately wins out, and finally, at a moment when her young are out of sight, she takes off and leaves them behind. Once she reaches the end of her long journey and the migratory instinct fades, what an agony of remorse each bird would feel if, due to their high mental engagement, they couldn’t shake the image of their chicks starving in the cold north from their mind.
At the moment of action, man will no doubt be apt to follow the stronger impulse; and though this may occasionally prompt him to the noblest deeds, it will far more commonly lead him to gratify his own desires at the expense of other men. But after their gratification, when past and weaker impressions are contrasted with the ever-enduring social instincts, retribution will surely come. Man will then feel dissatisfied with himself, and will resolve with more or less force to act differently for the future. This is conscience; for conscience looks backwards and judges past actions, inducing that kind of dissatisfaction, which if weak we call regret, and if severe remorse.
At the moment of action, a person will likely follow the strongest impulse; although this can sometimes lead to the best actions, it often drives them to satisfy their own desires at the expense of others. However, once those desires are fulfilled, and weaker feelings are compared with the lasting social instincts, consequences will inevitably follow. The person will then feel unhappy with themselves and will decide, with varying levels of determination, to behave differently in the future. This is conscience; because conscience reflects on the past and evaluates previous actions, creating a sense of dissatisfaction that, if mild, we call regret, and if intense, we call remorse.
These sensations are, no doubt, different from those experienced when other instincts or desires are left unsatisfied; but every unsatisfied instinct has its own proper prompting sensation, as we recognise with hunger, thirst, &c. Man thus prompted, will through long habit acquire such perfect self-command, that his desires and passions will at last instantly yield to his social sympathies, and there will no longer be a struggle between them. The still hungry, or the still revengeful man will not think of stealing food, or of wreaking his92 vengeance. It is possible, or, as we shall hereafter see, even probable, that the habit of self-command may, like other habits, be inherited. Thus at last man comes to feel, through acquired and perhaps inherited habit, that it is best for him to obey his more persistent instincts. The imperious word ought seems merely to imply the consciousness of the existence of a persistent instinct, either innate or partly acquired, serving him as a guide, though liable to be disobeyed. We hardly use the word ought in a metaphorical sense, when we say hounds ought to hunt, pointers to point, and retrievers to retrieve their game. If they fail thus to act, they fail in their duty and act wrongly.
These feelings are definitely different from those felt when other instincts or desires go unmet; however, every unfulfilled instinct has its unique prompting sensation, as we recognize with hunger, thirst, etc. A person, driven by this, will, through long practice, develop such strong self-control that their desires and emotions will eventually give way to their social instincts, eliminating the conflict between them. A person who is still hungry or still seeking revenge won’t think about stealing food or taking revenge. It’s possible, or as we’ll see later even likely, that the habit of self-control can be passed down just like other habits. Eventually, people come to realize, through developed and maybe inherited habits, that it’s best to follow their more persistent instincts. The strong word ought seems simply to reflect the awareness of the presence of a persistent instinct, either innate or partly learned, that serves as a guide, even though it can still be ignored. We rarely use the term ought in a metaphorical way when we say that hounds ought to hunt, pointers to point, and retrievers to retrieve their game. If they fail to do these things, they are not fulfilling their duty and are acting incorrectly.
If any desire or instinct, leading to an action opposed to the good of others, still appears to a man, when recalled to mind, as strong as, or stronger than, his social instinct, he will feel no keen regret at having followed it; but he will be conscious that if his conduct were known to his fellows, it would meet with their disapprobation; and few are so destitute of sympathy as not to feel discomfort when this is realised. If he has no such sympathy, and if his desires leading to bad actions are at the time strong, and when recalled are not overmastered by the persistent social instincts, then he is essentially a bad man;122 and the sole restraining motive left is the fear of punishment, and the conviction that in the long run it would be best for his own selfish interests to regard the good of others rather than his own.
If a person feels a desire or impulse to act in a way that harms others, and that feeling seems just as strong, or even stronger, than their social instincts, they won’t really regret acting on it. However, they’ll be aware that if their actions were known to others, they would be judged negatively, and most people wouldn’t lack enough empathy not to feel uncomfortable with that realization. If a person lacks this empathy, and their desires for harmful actions are strong at the moment and aren’t outweighed by their social instincts when they reflect on them, then they are fundamentally a bad person; and the only thing keeping them in check is the fear of getting punished and the belief that, in the long term, it’s better for their own selfish interests to consider the well-being of others over their own.
It is obvious that every one may with an easy conscience gratify his own desires, if they do not interfere 93with his social instincts, that is with the good of others; but in order to be quite free from self-reproach, or at least of anxiety, it is almost necessary for him to avoid the disapprobation, whether reasonable or not, of his fellow men. Nor must he break through the fixed habits of his life, especially if these are supported by reason; for if he does, he will assuredly feel dissatisfaction. He must likewise avoid the reprobation of the one God or gods, in whom according to his knowledge or superstition he may believe; but in this case the additional fear of divine punishment often supervenes.
It’s clear that anyone can easily satisfy their own desires without guilt, as long as those desires don't clash with their social instincts, meaning the welfare of others; however, to truly be free from self-reproach, or at least anxiety, it's almost essential to steer clear of the disapproval, whether justified or not, of other people. He also shouldn't disrupt the established patterns of his life, especially if those patterns are backed by reason; if he does, he will definitely experience dissatisfaction. Additionally, he should avoid the condemnation of the one God or gods he believes in based on his understanding or beliefs; in this case, the extra fear of divine punishment often comes into play.
The strictly Social Virtues at first alone regarded.—The above view of the first origin and nature of the moral sense, which tells us what we ought to do, and of the conscience which reproves us if we disobey it, accords well with what we see of the early and undeveloped condition of this faculty in mankind. The virtues which must be practised, at least generally, by rude men, so that they may associate in a body, are those which are still recognised as the most important. But they are practised almost exclusively in relation to the men of the same tribe; and their opposites are not regarded as crimes in relation to the men of other tribes. No tribe could hold together if murder, robbery, treachery, &c., were common; consequently such crimes within the limits of the same tribe “are branded with everlasting infamy;”123 but excite no such sentiment beyond these limits. A North-American Indian is well pleased with himself, and is honoured by others, when he scalps a man of another tribe; and a Dyak 94cuts off the head of an unoffending person and dries it as a trophy. The murder of infants has prevailed on the largest scale throughout the world,124 and has met with no reproach; but infanticide, especially of females, has been thought to be good for the tribe, or at least not injurious. Suicide during former times was not generally considered as a crime,125 but rather from the courage displayed as an honourable act; and it is still largely practised by some semi-civilised nations without reproach, for the loss to a nation of a single individual is not felt: whatever the explanation may be, suicide, as I hear from Sir J. Lubbock, is rarely practised by the lowest barbarians. It has been recorded that an Indian Thug conscientiously regretted that he had not strangled and robbed as many travellers as did his father before him. In a rude state of civilisation the robbery of strangers is, indeed, generally considered as honourable.
The strictly Social Virtues at first alone regarded.—The perspective on the origin and nature of our moral sense, which guides us on what we should do, and our conscience, which reprimands us when we fail to follow it, aligns well with what we observe in the early and undeveloped state of this faculty in humans. The virtues that must be practiced, at least broadly, by uncivilized people to maintain a group are those still deemed most important today. However, these virtues are mainly practiced in relation to people from the same tribe, and their opposites are not seen as wrong when it comes to people from other tribes. No tribe could remain unified if murder, theft, betrayal, etc., were common; thus, such crimes within the same tribe “are branded with everlasting infamy;” 123 but don't provoke the same feelings beyond those borders. A North-American Indian feels proud and is respected by others when he scalps a member of another tribe; and a Dyak 94decapitates an innocent person and preserves the head as a trophy. The murder of infants has occurred on a large scale around the world,124 and has faced little criticism; infanticide, especially of females, has often been seen as beneficial to the tribe, or at least not harmful. In the past, suicide was generally not viewed as a crime,125 but rather as an act of honor due to the courage displayed; it is still widely accepted among some semi-civilized nations without judgment, as the loss of a single individual is not felt by the nation. For whatever reasons, suicide, as noted by Sir J. Lubbock, is rarely practiced by the most primitive cultures. There's a record of an Indian Thug who sincerely lamented that he hadn't strangled and robbed as many travelers as his father did before him. In a primitive state of civilization, robbing strangers is often viewed as honorable.
The great sin of Slavery has been almost universal, and slaves have often been treated in an infamous manner. As barbarians do not regard the opinion of their women, wives are commonly treated like slaves. Most savages are utterly indifferent to the sufferings of strangers, or even delight in witnessing them. It is well known that the women and children of the North-American Indians aided in torturing their enemies. Some savages take a horrid pleasure in cruelty to animals,126 and humanity with them is an unknown virtue. Nevertheless, feelings of sympathy and kindness are common, especially 95during sickness, between the members of the same tribe, and are sometimes extended beyond the limits of the tribe. Mungo Park’s touching account of the kindness of the negro women of the interior to him is well known. Many instances could be given of the noble fidelity of savages towards each other, but not to strangers; common experience justifies the maxim of the Spaniard, “Never, never trust an Indian.” There cannot be fidelity without truth; and this fundamental virtue is not rare between the members of the same tribe: thus Mungo Park heard the negro women teaching their young children to love the truth. This, again, is one of the virtues which becomes so deeply rooted in the mind that it is sometimes practised by savages even at a high cost, towards strangers; but to lie to your enemy has rarely been thought a sin, as the history of modern diplomacy too plainly shews. As soon as a tribe has a recognised leader, disobedience becomes a crime, and even abject submission is looked at as a sacred virtue.
The terrible sin of slavery has been nearly universal, and slaves have often been treated in a disgraceful way. Just as barbarians disregard the views of their women, wives are often treated like property. Most savages are completely indifferent to the suffering of outsiders, or even take pleasure in seeing it. It's well known that the women and children of North American Indians participated in torturing their enemies. Some savages take a horrifying pleasure in cruelty to animals, and for them, compassion for humans is a foreign concept. However, feelings of sympathy and kindness are common, especially during times of illness, among members of the same tribe, and can sometimes extend beyond tribal boundaries. Mungo Park’s moving account of the generosity of the African women toward him is well known. Many examples could be provided of the loyalty of savages to one another, but not to outsiders; common experience supports the saying of the Spaniard, “Never, never trust an Indian.” There can be no loyalty without truth, and this basic virtue is not uncommon among members of the same tribe: Mungo Park noted the African women teaching their young children to value honesty. This is another virtue that can become so ingrained in a person’s mind that it is sometimes practiced by savages even at great personal cost toward outsiders; however, lying to your enemy has rarely been seen as a sin, as the history of modern diplomacy clearly shows. Once a tribe has a recognized leader, disobedience becomes a crime, and even total submission is viewed as a sacred virtue.
As during rude times no man can be useful or faithful to his tribe without courage, this quality has universally been placed in the highest rank; and although, in civilised countries, a good, yet timid, man may be far more useful to the community than a brave one, we cannot help instinctively honouring the latter above a coward, however benevolent. Prudence, on the other hand, which does not concern the welfare of others, though a very useful virtue, has never been highly esteemed. As no man can practise the virtues necessary for the welfare of his tribe without self-sacrifice, self-command, and the power of endurance, these qualities have been at all times highly and most justly valued. The American savage voluntarily submits without a groan to the most horrid tortures to prove and strengthen his fortitude and courage; and we cannot96 help admiring him, or even an Indian Fakir, who, from a foolish religious motive, swings suspended by a hook buried in his flesh.
As in tough times, no one can be useful or loyal to their community without courage, this trait has always been seen as the most important. Even though, in civilized societies, a good but timid person can be much more helpful to the community than a brave one, we still instinctively respect the brave person more than a coward, no matter how kind they may be. On the other hand, prudence, which doesn’t concern the well-being of others, though it's a very useful quality, has never been highly regarded. Since no one can practice the virtues needed for the welfare of their community without self-sacrifice, self-control, and resilience, these qualities have always been valued greatly and rightly so. The American Native willingly endures horrific tortures without a sound to test and strengthen his courage; and we can’t help but admire him, or even an Indian Fakir, who, for a misguided religious reason, hangs suspended by a hook embedded in his skin.
The other self-regarding virtues, which do not obviously, though they may really, affect the welfare of the tribe, have never been esteemed by savages, though now highly appreciated by civilised nations. The greatest intemperance with savages is no reproach. Their utter licentiousness, not to mention unnatural crimes, is something astounding.127 As soon, however, as marriage, whether polygamous or monogamous, becomes common, jealousy will lead to the inculcation of female virtue; and this being honoured will tend to spread to the unmarried females. How slowly it spreads to the male sex we see at the present day. Chastity eminently requires self-command; therefore it has been honoured from a very early period in the moral history of civilised man. As a consequence of this, the senseless practice of celibacy has been ranked from a remote period as a virtue.128 The hatred of indecency, which appears to us so natural as to be thought innate, and which is so valuable an aid to chastity, is a modern virtue, appertaining exclusively, as Sir G. Staunton remarks,129 to civilised life. This is shewn by the ancient religious rites of various nations, by the drawings on the walls of Pompeii, and by the practices of many savages.
The other self-focused virtues, which don’t obviously but may actually impact the well-being of the community, have never been valued by early societies, even though they are now highly regarded by modern nations. The greatest excesses among primitive people are not considered shameful. Their complete disregard for rules, not to mention unnatural behaviors, is quite shocking. As soon as marriage, whether it’s polygamous or monogamous, becomes common, jealousy will foster the idea of female virtue; and as this is respected, it will likely extend to unmarried women. We see how slowly this spreads to men even today. Chastity requires a lot of self-control, which is why it has been respected since the early moral history of civilized people. Consequently, the pointless practice of celibacy has been viewed as a virtue for a long time. The dislike of indecency, which seems so natural to us that we think it’s instinctual, and which is such an important support for chastity, is actually a modern virtue, exclusively related, as Sir G. Staunton points out, to civilized life. This is evident in the ancient religious rituals of different cultures, the illustrations on the walls of Pompeii, and the behaviors of many primitive peoples.
We have now seen that actions are regarded by savages, and were probably so regarded by primeval man, as good or bad, solely as they affect in an obvious manner the welfare of the tribe,—not that of the species, nor that of man as an individual member of the 97tribe. This conclusion agrees well with the belief that the so-called moral sense is aboriginally derived from the social instincts, for both relate at first exclusively to the community. The chief causes of the low morality of savages, as judged by our standard, are, firstly, the confinement of sympathy to the same tribe. Secondly, insufficient powers of reasoning, so that the bearing of many virtues, especially of the self-regarding virtues, on the general welfare of the tribe is not recognised. Savages, for instance, fail to trace the multiplied evils consequent on a want of temperance, chastity, &c. And, thirdly, weak power of self-command; for this power has not been strengthened through long-continued, perhaps inherited, habit, instruction and religion.
We have seen that people considered as savages, and likely early humans, viewed actions as good or bad mainly based on how they obviously impacted the tribe's welfare—not the species as a whole, nor the individual. This conclusion aligns with the idea that what we call the moral sense originally comes from social instincts, as both focus mainly on the community. The main reasons for the low morality of savages, when judged by our standards, are, first, that their sympathy is limited to their own tribe. Second, they have inadequate reasoning skills, meaning they often don’t recognize how many virtues, especially those related to self-interest, affect the tribe's overall welfare. For instance, they struggle to see the multiple problems that arise from a lack of temperance, chastity, etc. And third, they lack strong self-discipline; this ability has not been developed through long-term habits, education, and religion.
I have entered into the above details on the immorality of savages,130 because some authors have recently taken a high view of their moral nature, or have attributed most of their crimes to mistaken benevolence.131 These authors appear to rest their conclusion on savages possessing, as they undoubtedly do possess, and often in a high degree, those virtues which are serviceable, or even necessary, for the existence of a tribal community.
I have provided the details above on the immorality of savages,130 because some writers have recently taken an overly positive view of their moral character or have blamed most of their wrongdoings on misguided kindness.131 These writers seem to base their conclusions on the fact that savages have, and often exhibit to a significant degree, the virtues that are useful or even essential for the survival of a tribal community.
Concluding Remarks.—Philosophers of the derivative132 school of morals formerly assumed that the foundation of morality lay in a form of Selfishness; but more recently in the “Greatest Happiness principle.” According to the view given above, the moral sense is 98fundamentally identical with the social instincts; and in the case of the lower animals it would be absurd to speak of these instincts as having been developed from selfishness, or for the happiness of the community. They have, however, certainly been developed for the general good of the community. The term, general good, may be defined as the means by which the greatest possible number of individuals can be reared in full vigour and health, with all their faculties perfect, under the conditions to which they are exposed. As the social instincts both of man and the lower animals have no doubt been developed by the same steps, it would be advisable, if found practicable, to use the same definition in both cases, and to take as the test of morality, the general good or welfare of the community, rather than the general happiness; but this definition would perhaps require some limitation on account of political ethics.
Concluding Remarks.—Philosophers in the derivative132 school of morals once believed that the basis of morality was a type of Selfishness; however, more recently, this idea has shifted to the “Greatest Happiness principle.” According to the perspective outlined above, moral sense is fundamentally the same as social instincts; and when it comes to lower animals, it seems unreasonable to say these instincts evolved from selfishness or for the happiness of the community. They have, without a doubt, evolved for the overall benefit of the community. The term general good can be defined as the means by which the largest number of individuals can be nurtured in full vigor and health, with all their faculties intact, based on the conditions they face. Since the social instincts of both humans and lower animals have likely developed through similar processes, it would be wise, if feasible, to apply the same definition in both scenarios and to use the general good or welfare of the community as the standard for morality, rather than general happiness; however, this definition may require some adjustments due to political ethics.
When a man risks his life to save that of a fellow-creature, it seems more appropriate to say that he acts for the general good or welfare, rather than for the general happiness of mankind. No doubt the welfare and the happiness of the individual usually coincide; and a contented, happy tribe will flourish better than one that is discontented and unhappy. We have seen that at an early period in the history of man, the expressed wishes of the community will have naturally influenced to a large extent the conduct of each member; and as all wish for happiness, the “greatest happiness principle” will have become a most important secondary guide and object; the social instincts, including sympathy, always serving as the primary impulse and guide. Thus the reproach of laying the foundation of the most noble part of our nature in the base principle of selfishness is removed; unless indeed the satis99faction which every animal feels when it follows its proper instincts, and the dissatisfaction felt when prevented, be called selfish.
When a person risks their life to save another, it feels more appropriate to say they act for the common good or welfare, rather than just for the overall happiness of humanity. It's true that the welfare and happiness of individuals usually go hand in hand; a happy, content community will thrive better than one that is unhappy and discontented. We've seen that in early human history, the expressed desires of the community would significantly influence the behavior of each member; and since everyone desires happiness, the "greatest happiness principle" becomes a crucial secondary guide and goal, while social instincts, including sympathy, serve as the primary motivator and guide. This way, the criticism of grounding the most noble aspects of our nature in the basic principle of selfishness is countered, unless the satisfaction every being feels when following their instincts, and the dissatisfaction when they can't, is considered selfish.
The expression of the wishes and judgment of the members of the same community, at first by oral and afterwards by written language, serves, as just remarked, as a most important secondary guide of conduct, in aid of the social instincts, but sometimes in opposition to them. This latter fact is well exemplified by the Law of Honour, that is the law of the opinion of our equals, and not of all our countrymen. The breach of this law, even when the breach is known to be strictly accordant with true morality, has caused many a man more agony than a real crime. We recognise the same influence in the burning sense of shame which most of us have felt even after the interval of years, when calling to mind some accidental breach of a trifling though fixed rule of etiquette. The judgment of the community will generally be guided by some rude experience of what is best in the long run for all the members; but this judgment will not rarely err from ignorance and from weak powers of reasoning. Hence the strangest customs and superstitions, in complete opposition to the true welfare and happiness of mankind, have become all-powerful throughout the world. We see this in the horror felt by a Hindoo who breaks his caste, in the shame of a Mahometan woman who exposes her face, and in innumerable other instances. It would be difficult to distinguish between the remorse felt by a Hindoo who has eaten unclean food, from that felt after committing a theft; but the former would probably be the more severe.
The expression of the wishes and judgments of members of the same community, first through spoken language and later through written language, serves, as previously mentioned, as a very important secondary guide for behavior, supporting social instincts but sometimes contradicting them. This is clearly illustrated by the Law of Honour, which refers to the opinions of our peers rather than all our fellow citizens. Violating this law, even when the violation aligns with true moral values, has caused many people more distress than committing an actual crime. We recognize this influence in the intense sense of shame that many of us still feel, even years later, when recalling some accidental breach of a minor but established etiquette rule. The community's judgment is usually shaped by some rough understanding of what is best for all members in the long run; however, this judgment can often be misguided due to ignorance and weak reasoning skills. Consequently, the most bizarre customs and superstitions, which are completely against the genuine welfare and happiness of humanity, have become extremely powerful around the globe. We see this in the horror experienced by a Hindu who breaks his caste, in the shame felt by a Muslim woman who shows her face, and in countless other examples. It would be hard to differentiate between the remorse of a Hindu who has consumed unclean food and that of someone who has committed theft; however, the former would likely be felt more intensely.
How so many absurd rules of conduct, as well as so many absurd religious beliefs, have originated we do not know; nor how it is that they have become, in all100 quarters of the world, so deeply impressed on the mind of men; but it is worthy of remark that a belief constantly inculcated during the early years of life, whilst the brain is impressible, appears to acquire almost the nature of an instinct; and the very essence of an instinct is that it is followed independently of reason. Neither can we say why certain admirable virtues, such as the love of truth, are much more highly appreciated by some savage tribes than by others;133 nor, again, why similar differences prevail even amongst civilised nations. Knowing how firmly fixed many strange customs and superstitions have become, we need feel no surprise that the self-regarding virtues should now appear to us so natural, supported as they are by reason, as to be thought innate, although they were not valued by man in his early condition.
We don't know how so many ridiculous rules of behavior and strange religious beliefs originated, or why they've become so ingrained in the minds of people everywhere. However, it's worth noting that beliefs taught repeatedly during childhood, when the brain is highly impressionable, seem to take on almost instinctive qualities. The essence of an instinct is that it is followed without reasoning. We also can't explain why some admirable virtues, like the love of truth, are valued more by certain primitive tribes than by others, nor why similar differences exist among civilized nations. Given how deeply rooted many odd customs and superstitions have become, it's not surprising that the virtues related to self-interest now seem so natural to us, backed by reason, that we think they're innate, even though they weren't appreciated in early human societies.
Notwithstanding many sources of doubt, man can generally and readily distinguish between the higher and lower moral rules. The higher are founded on the social instincts, and relate to the welfare of others. They are supported by the approbation of our fellow-men and by reason. The lower rules, though some of them when implying self-sacrifice hardly deserve to be called lower, relate chiefly to self, and owe their origin to public opinion, when matured by experience and cultivated; for they are not practised by rude tribes.
Despite various doubts, people can usually and easily tell the difference between higher and lower moral principles. The higher ones are based on social instincts and concern the well-being of others. They gain support from the approval of others and from reason. The lower principles, although some of them, when involving self-sacrifice, hardly seem "lower," mainly focus on the self and originate from public opinion, shaped by experience and refinement; they aren’t practiced by primitive tribes.
As man advances in civilisation, and small tribes are united into larger communities, the simplest reason would tell each individual that he ought to extend his social instincts and sympathies to all the members of the same nation, though personally unknown to him. This point being once reached, there is only an arti101ficial barrier to prevent his sympathies extending to the men of all nations and races. If, indeed, such men are separated from him by great differences in appearance or habits, experience unfortunately shews us how long it is before we look at them as our fellow-creatures. Sympathy beyond the confines of man, that is humanity to the lower animals, seems to be one of the latest moral acquisitions. It is apparently unfelt by savages, except towards their pets. How little the old Romans knew of it is shewn by their abhorrent gladiatorial exhibitions. The very idea of humanity, as far as I could observe, was new to most of the Gauchos of the Pampas. This virtue, one of the noblest with which man is endowed, seems to arise incidentally from our sympathies becoming more tender and more widely diffused, until they are extended to all sentient beings. As soon as this virtue is honoured and practised by some few men, it spreads through instruction and example to the young, and eventually through public opinion.
As society progresses and small tribes come together to form larger communities, it seems obvious that each person should broaden their social instincts and compassion to include all members of their nation, even if they don’t know them personally. Once this recognition is made, there’s only an artificial barrier stopping those feelings from expanding to people of all nations and races. Unfortunately, if those people are very different in appearance or customs, it often takes a long time before we recognize them as fellow human beings. Compassion that extends beyond humans to include animals seems to be one of the last moral developments. It appears to be absent among primitive societies, except for their pets. The lack of understanding of this concept is evident in the ancient Romans’ gruesome gladiatorial games. Most of the Gauchos in the Pampas seemed unfamiliar with the idea of humanity. This virtue, one of the greatest qualities of humanity, appears to develop as our empathy grows more sensitive and widespread, eventually encompassing all sentient beings. Once a few individuals adopt and practice this virtue, it spreads to the young through teaching and example, and ultimately influences public opinion.
The highest stage in moral culture at which we can arrive, is when we recognise that we ought to control our thoughts, and “not even in inmost thought to think again the sins that made the past so pleasant to us.”134 Whatever makes any bad action familiar to the mind, renders its performance by so much the easier. As Marcus Aurelius long ago said, “Such as are thy habitual thoughts, such also will be the character of thy mind; for the soul is dyed by the thoughts.”135
The highest point we can reach in moral development is when we realize that we need to control our thoughts and “not even in our deepest thoughts dwell on the sins that once made the past so enjoyable.”134 Anything that makes bad actions feel familiar to us makes it easier to carry them out. As Marcus Aurelius said a long time ago, “Your habitual thoughts shape your character; for the soul is colored by your thoughts.”135
Our great philosopher, Herbert Spencer, has recently explained his views on the moral sense. He says,136 “I 102believe that the experiences of utility organised and consolidated through all past generations of the human race, have been producing corresponding modifications, which, by continued transmission and accumulation, have become in us certain faculties of moral intuition—certain emotions responding to right and wrong conduct, which have no apparent basis in the individual experiences of utility.” There is not the least inherent improbability, as it seems to me, in virtuous tendencies being more or less strongly inherited; for, not to mention the various dispositions and habits transmitted by many of our domestic animals, I have heard of cases in which a desire to steal and a tendency to lie appeared to run in families of the upper ranks; and as stealing is so rare a crime in the wealthy classes, we can hardly account by accidental coincidence for the tendency occurring in two or three members of the same family. If bad tendencies are transmitted, it is probable that good ones are likewise transmitted. Excepting through the principle of the transmission of moral tendencies, we cannot understand the differences believed to exist in this respect between the various races of mankind. We have, however, as yet, hardly sufficient evidence on this head.
Our great philosopher, Herbert Spencer, recently shared his thoughts on the moral sense. He says,136 “I 102believe that the experiences of utility, organized and strengthened through all past generations of the human race, have been creating corresponding changes that, through ongoing transmission and accumulation, have developed in us certain faculties of moral intuition—certain emotions that respond to right and wrong behavior, which don't seem to be based on individual experiences of utility.” It seems to me that there's no inherent unlikelihood in virtuous tendencies being more or less strongly inherited; for, aside from the various traits and habits passed down by many of our domesticated animals, I've heard of cases where a desire to steal and a tendency to lie seemed to run in families of the upper classes; and since stealing is such a rare crime among the wealthy, we can hardly explain it as mere coincidence when two or three members of the same family exhibit that tendency. If negative traits can be passed down, it's likely that positive traits can be too. Aside from the principle of the transmission of moral tendencies, we cannot fully understand the differences believed to exist in this regard between various races of humanity. However, we still don’t have enough evidence on this topic.
Even the partial transmission of virtuous tendencies would be an immense assistance to the primary impulse derived directly from the social instincts, and indirectly from the approbation of our fellow-men. Admitting for the moment that virtuous tendencies are inherited, it appears probable, at least in such cases as chastity, temperance, humanity to animals, &c., that they become first impressed on the mental organisation through habit, instruction, and example, continued during several generations in the same family, and in a quite subordinate degree, or not at all, by the individuals pos103sessing such virtues, having succeeded best in the struggle for life. My chief source of doubt with respect to any such inheritance, is that senseless customs, superstitions, and tastes, such as the horror of a Hindoo for unclean food, ought on the same principle to be transmitted. Although this in itself is perhaps not less probable than that animals should acquire inherited tastes for certain kinds of food or fear of certain foes, I have not met with any evidence in support of the transmission of superstitious customs or senseless habits.
Even the partial passing down of positive traits would greatly support the main drive coming directly from social instincts and, indirectly, from approval by others. Assuming for a moment that positive traits can be inherited, it seems likely—at least in cases like chastity, temperance, and compassion towards animals—that they first become ingrained in the mind through habit, lessons, and examples that persist over several generations within the same family, and to a much lesser extent, if at all, by the individuals who possess those traits succeeding in the struggle for survival. My main doubt about such inheritance stems from the observation that irrational customs, superstitions, and preferences, like a Hindoo's aversion to unclean food, should, by the same logic, also be passed down. While this possibility is perhaps just as likely as animals developing inherited preferences for certain foods or fears of particular enemies, I haven't encountered any evidence supporting the transmission of superstitious customs or irrational habits.
Finally, the social instincts which no doubt were acquired by man, as by the lower animals, for the good of the community, will from the first have given to him some wish to aid his fellows, and some feeling of sympathy. Such impulses will have served him at a very early period as a rude rule of right and wrong. But as man gradually advanced in intellectual power and was enabled to trace the more remote consequences of his actions; as he acquired sufficient knowledge to reject baneful customs and superstitions; as he regarded more and more not only the welfare but the happiness of his fellow-men; as from habit, following on beneficial experience, instruction, and example, his sympathies became more tender and widely diffused, so as to extend to the men of all races, to the imbecile, the maimed, and other useless members of society, and finally to the lower animals,—so would the standard of his morality rise higher and higher. And it is admitted by moralists of the derivative school and by some intuitionists, that the standard of morality has risen since an early period in the history of man.137
Finally, the social instincts that humans, like other animals, developed for the benefit of the community have, from the very beginning, given individuals a desire to help others and a sense of empathy. These impulses served as a basic guideline for distinguishing right from wrong in early human development. However, as humanity gradually progressed intellectually and learned to understand the further consequences of its actions, as knowledge increased allowing people to reject harmful customs and superstitions, and as individuals began to consider not just the welfare but also the happiness of others, their compassion naturally became deeper and more widespread. This sympathy grew to include people of every race, those with disabilities, the injured, and other marginalized members of society, and eventually even extended to animals. In turn, this evolution led to a continuously rising standard of morality. It is acknowledged by moralists from the derivative school and some intuitionists that the standard of morality has indeed improved since the early days of humanity.137
As a struggle may sometimes be seen going on 104between the various instincts of the lower animals, it is not surprising that there should be a struggle in man between his social instincts, with their derived virtues, and his lower, though at the moment, stronger impulses or desires. This, as Mr. Galton138 has remarked, is all the less surprising, as man has emerged from a state of barbarism within a comparatively recent period. After having yielded to some temptation we feel a sense of dissatisfaction, analogous to that felt from other unsatisfied instincts, called in this case conscience; for we cannot prevent past images and impressions continually passing through our minds, and these in their weakened state we compare with the ever-present social instincts, or with habits gained in early youth and strengthened during our whole lives, perhaps inherited, so that they are at last rendered almost as strong as instincts. Looking to future generations, there is no cause to fear that the social instincts will grow weaker, and we may expect that virtuous habits will grow stronger, becoming perhaps fixed by inheritance. In this case the struggle between our higher and lower impulses will be less severe, and virtue will be triumphant.
As we can sometimes see a struggle happening among the different instincts of lower animals, it's not surprising that humans also experience a struggle between their social instincts and their more immediate, stronger impulses or desires. As Mr. Galton has pointed out, this is even less surprising considering that humans have recently come out of a state of barbarism. After giving in to some temptation, we feel a sense of dissatisfaction, similar to what we feel from other unsatisfied instincts, known in this case as conscience; because we can't stop past images and impressions from continually running through our minds, and we compare these weakened memories with our ever-present social instincts or with habits formed in early youth and strengthened throughout our lives, possibly inherited, making them nearly as strong as instincts. Looking to future generations, there's no reason to worry that social instincts will weaken; instead, we can expect virtuous habits to become stronger, potentially fixed through inheritance. In that case, the struggle between our higher and lower impulses will be less intense, and virtue will prevail.
Summary of the two last Chapters.—There can be no doubt that the difference between the mind of the lowest man and that of the highest animal is immense. An anthropomorphous ape, if he could take a dispassionate view of his own case, would admit that though he could form an artful plan to plunder a garden—though he could use stones for fighting or for breaking open nuts, 105yet that the thought of fashioning a stone into a tool was quite beyond his scope. Still less, as he would admit, could he follow out a train of metaphysical reasoning, or solve a mathematical problem, or reflect on God, or admire a grand natural scene. Some apes, however, would probably declare that they could and did admire the beauty of the coloured skin and fur of their partners in marriage. They would admit, that though they could make other apes understand by cries some of their perceptions and simpler wants, the notion of expressing definite ideas by definite sounds had never crossed their minds. They might insist that they were ready to aid their fellow-apes of the same troop in many ways, to risk their lives for them, and to take charge of their orphans; but they would be forced to acknowledge that disinterested love for all living creatures, the most noble attribute of man, was quite beyond their comprehension.
Summary of the last two Chapters.—There is no doubt that the difference between the mind of the lowest human and that of the highest animal is huge. An anthropomorphous ape, if he could look at his situation objectively, would recognize that even though he could devise a clever plan to steal from a garden—though he could use stones for fighting or breaking open nuts, 105he would admit that the idea of creating a tool from a stone was completely beyond his capability. Even more so, he would acknowledge he couldn't engage in metaphysical reasoning, solve a math problem, reflect on God, or appreciate a beautiful natural scene. However, some apes might argue that they can and do admire the beauty of their partners' colorful skin and fur. They would concede that while they could communicate some of their feelings and basic needs to other apes with cries, the concept of expressing specific ideas with specific sounds had never occurred to them. They might claim they were willing to help their fellow apes in their troop in various ways, risking their lives for them and caring for their orphans; but they would have to admit that selfless love for all living beings, the most admirable trait of humans, is completely beyond their understanding.
Nevertheless the difference in mind between man and the higher animals, great as it is, is certainly one of degree and not of kind. We have seen that the senses and intuitions, the various emotions and faculties, such as love, memory, attention, curiosity, imitation, reason, &c., of which man boasts, may be found in an incipient, or even sometimes in a well-developed condition, in the lower animals. They are also capable of some inherited improvement, as we see in the domestic dog compared with the wolf or jackal. If it be maintained that certain powers, such as self-consciousness, abstraction, &c., are peculiar to man, it may well be that these are the incidental results of other highly-advanced intellectual faculties; and these again are mainly the result of the continued use of a highly developed language. At what age does the new-born infant possess the power of abstraction, or become self106conscious and reflect on its own existence? We cannot answer; nor can we answer in regard to the ascending organic scale. The half-art and half-instinct of language still bears the stamp of its gradual evolution. The ennobling belief in God is not universal with man; and the belief in active spiritual agencies naturally follows from his other mental powers. The moral sense perhaps affords the best and highest distinction between man and the lower animals; but I need not say anything on this head, as I have so lately endeavoured to shew that the social instincts,—the prime principle of man’s moral constitution139—with the aid of active intellectual powers and the effects of habit, naturally lead to the golden rule, “As ye would that men should do to you, do ye to them likewise;” and this lies at the foundation of morality.
Nevertheless, the difference in mindset between humans and higher animals, as significant as it is, is certainly one of degree rather than kind. We’ve observed that the senses and intuitions, along with various emotions and abilities like love, memory, attention, curiosity, imitation, reason, etc., that humans have can also be found in an early or sometimes well-developed state in lower animals. They are also capable of some inherited improvement, as seen in domestic dogs compared to wolves or jackals. If it’s argued that certain abilities, such as self-awareness and abstraction, are unique to humans, it’s possible these are just byproducts of other highly advanced cognitive abilities; and these, in turn, primarily result from the ongoing use of a well-developed language. At what age does a newborn have the ability for abstraction or become self-conscious and reflect on its own existence? We can't say; nor can we determine this regarding the evolutionary scale. The partially learned and partially instinctual nature of language still shows evidence of its gradual development. The uplifting belief in God is not universal among humans; and the belief in active spiritual forces naturally arises from their other mental abilities. The moral sense perhaps provides the best and highest distinction between humans and lower animals; but I won’t elaborate on this, as I've recently tried to demonstrate that social instincts—the fundamental principle of human moral structure—along with active intellectual abilities and the influence of habit, naturally lead to the golden rule, “Treat others as you would like to be treated;” and this is the foundation of morality.
In a future chapter I shall make some few remarks on the probable steps and means by which the several mental and moral faculties of man have been gradually evolved. That this at least is possible ought not to be denied, when we daily see their development in every infant; and when we may trace a perfect gradation from the mind of an utter idiot, lower than that of the lowest animal, to the mind of a Newton.
In a future chapter, I will share some thoughts on the likely steps and methods by which various mental and moral abilities in humans have gradually developed. This is certainly possible, as we observe their growth in every baby; we can also see a clear progression from the mind of a complete idiot, which is below the intelligence of the simplest animal, to the mind of someone like Newton.
CHAPTER IV.
On How Man Develops from a Lower Form.
Variability of body and mind in man—Inheritance—Causes of variability—Laws of variation the same in man as in the lower animals—Direct action of the conditions of life—Effects of the increased use and disuse of parts—Arrested development—Reversion—Correlated variation—Rate of increase—Checks to increase—Natural selection—Man the most dominant animal in the world—Importance of his corporeal structure—The causes which have led to his becoming erect—Consequent changes of structure—Decrease in size of the canine teeth—Increased size and altered shape of the skull—Nakedness—Absence of a tail—Defenceless condition of man.
Variability of body and mind in humans—Inheritance—Reasons for variability—The laws of variation are the same for humans as for lower animals—Direct impact of life conditions—Effects of increased use and disuse of body parts—Stunted development—Reversion—Related variation—Rate of growth—Limits to growth—Natural selection—Humans are the most dominant species on the planet—Importance of our physical structure—Reasons for our upright posture—Resulting changes in structure—Reduction in size of canine teeth—Larger size and changed shape of the skull—Hairlessness—Lack of a tail—Vulnerable state of humans.
We have seen in the first chapter that the homological structure of man, his embryological development and the rudiments which he still retains, all declare in the plainest manner that he is descended from some lower form. The possession of exalted mental powers is no insuperable objection to this conclusion. In order that an ape-like creature should have been transformed into man, it is necessary that this early form, as well as many successive links, should all have varied in mind and body. It is impossible to obtain direct evidence on this head; but if it can be shewn that man now varies—that his variations are induced by the same general causes, and obey the same general laws, as in the case of the lower animals—there can be little doubt that the preceding intermediate links varied in a like manner. The variations at each successive stage of descent must, also, have been in some manner accumulated and fixed.
We’ve seen in the first chapter that the biological structure of humans, their development in the womb, and the remnants they still have clearly show that we evolved from some lower form. Having advanced mental abilities doesn’t contradict this conclusion. For an ape-like creature to evolve into a human, it’s essential that this early form, along with many transitional species, all changed in their minds and bodies. Direct evidence for this is hard to get; however, if it can be shown that humans vary now—that their changes are caused by the same general factors and follow the same basic laws as those in lower animals—there’s little doubt that the earlier species also changed in similar ways. The variations at each stage of evolution must have also been somehow accumulated and stabilized.
108The facts and conclusions to be given in this chapter relate almost exclusively to the probable means by which the transformation of man has been effected, as far as his bodily structure is concerned. The following chapter will be devoted to the development of his intellectual and moral faculties. But the present discussion likewise bears on the origin of the different races or species of mankind, whichever term may be preferred.
108The facts and conclusions discussed in this chapter focus mainly on the likely ways that the transformation of humans has happened in terms of their physical structure. The next chapter will be dedicated to the evolution of their intellectual and moral abilities. However, this discussion also addresses the origins of the various races or species of humanity, depending on which term one prefers.
It is manifest that man is now subject to much variability. No two individuals of the same race are quite alike. We may compare millions of faces, and each will be distinct. There is an equally great amount of diversity in the proportions and dimensions of the various parts of the body; the length of the legs being one of the most variable points.140 Although in some quarters of the world an elongated skull, and in other quarters a short skull prevails, yet there is great diversity of shape even within the limits of the same race, as with the aborigines of America and South Australia,—the latter a race “probably as pure and homogeneous in blood, customs, and language as any in existence”—and even with the inhabitants of so confined an area as the Sandwich Islands.141 An eminent dentist assures me that there is nearly as much diversity in the teeth, as in the features. The chief arteries so frequently run in abnormal courses, that it has been found useful for surgical purposes to calculate 109from 12,000 corpses how often each course prevails.142 The muscles are eminently variable: thus those of the foot were found by Prof. Turner143 not to be strictly alike in any two out of fifty bodies; and in some the deviations were considerable. Prof. Turner adds that the power of performing the appropriate movements must have been modified in accordance with the several deviations. Mr. J. Wood has recorded144 the occurrence of 295 muscular variations in thirty-six subjects, and in another set of the same number no less than 558 variations, reckoning both sides of the body as one. In the last set, not one body out of the thirty-six was “found totally wanting in departures from the standard descriptions of the muscular system given in anatomical text-books.” A single body presented the extraordinary number of twenty-five distinct abnormalities. The same muscle sometimes varies in many ways: thus Prof. Macalister describes145 no less than twenty distinct variations in the palmaris accessorius.
It’s clear that people are now subject to a lot of variability. No two individuals of the same race are exactly alike. We could look at millions of faces, and each one would be unique. There’s also a huge variety in the proportions and dimensions of different body parts; the length of the legs is one of the most variable aspects.140 While some parts of the world have elongated skulls and others have shorter ones, there’s still a lot of shape diversity even within the same race, like among the indigenous people of America and South Australia—the latter being a group “probably as pure and homogeneous in blood, customs, and language as any in existence”—and even among the inhabitants of such a small area as the Sandwich Islands.141 A well-known dentist told me that there’s almost as much diversity in teeth as there is in facial features. The main arteries often follow unusual paths, so it’s been useful for surgical purposes to analyze 12,000 corpses to see how often each path is found.142 The muscles are highly variable: Prof. Turner143 found that those in the foot weren’t identical in any two out of fifty bodies; in some, the differences were significant. Prof. Turner adds that the ability to perform specific movements must have been affected by these variations. Mr. J. Wood recorded144 295 muscular variations in thirty-six subjects, and in another group of the same size, there were as many as 558 variations, counting both sides of the body as one. In the last group, every body out of the thirty-six showed “some departures from the standard descriptions of the muscular system found in anatomical textbooks.” One single body had an astonishing twenty-five distinct abnormalities. The same muscle can vary in multiple ways: for instance, Prof. Macalister describes145 no less than twenty distinct variations in the palmaris accessorius.
The famous old anatomist, Wolff,146 insists that the internal viscera are more variable than the external parts: Nulla particula est quæ non aliter et aliter in aliis se habeat hominibus. He has even written a treatise on the choice of typical examples of the viscera for representation. A discussion on the beau-ideal of the liver, lungs, kidneys, &c., as of the human face divine, sounds strange in our ears.
The renowned old anatomist, Wolff,146 argues that the internal organs are more varied than the external features: There is no part that does not behave differently in different people. He has even written a paper on selecting typical examples of the organs for representation. A conversation about the ideal appearance of the liver, lungs, kidneys, etc., just like the divine human face, sounds unusual to us.
The variability or diversity of the mental faculties in men of the same race, not to mention the greater 110differences between the men of distinct races, is so notorious that not a word need here be said. So it is with the lower animals, as has been illustrated by a few examples in the last chapter. All who have had charge of menageries admit this fact, and we see it plainly in our dogs and other domestic animals. Brehm especially insists that each individual monkey of those which he kept under confinement in Africa had its own peculiar disposition and temper: he mentions one baboon remarkable for its high intelligence; and the keepers in the Zoological Gardens pointed out to me a monkey, belonging to the New World division, equally remarkable for intelligence. Rengger, also, insists on the diversity in the various mental characters of the monkeys of the same species which he kept in Paraguay; and this diversity, as he adds, is partly innate, and partly the result of the manner in which they have been treated or educated.147
The variation or diversity of mental abilities among men of the same race, not to mention the larger differences between men of different races, is so well-known that it hardly needs to be discussed. The same applies to lower animals, as demonstrated by a few examples in the last chapter. Anyone who has managed a zoo recognizes this fact, and we can clearly see it in our dogs and other pets. Brehm particularly emphasizes that each individual monkey he kept in captivity in Africa had its own unique personality and temperament; he notes one baboon known for its high intelligence. The keepers in the Zoological Gardens pointed out to me a monkey from the New World that was also notable for its intelligence. Rengger similarly emphasizes the differences in the mental characteristics of monkeys of the same species that he kept in Paraguay; he adds that this diversity is partly innate and partly a result of how they have been treated or trained.147
I have elsewhere148 so fully discussed the subject of Inheritance that I need here add hardly anything. A greater number of facts have been collected with respect to the transmission of the most trifling, as well as of the most important characters in man than in any of the lower animals; though the facts are copious enough with respect to the latter. So in regard to mental qualities, their transmission is manifest in our dogs, horses, and other domestic animals. Besides special tastes and habits, general intelligence, courage, bad and good temper, &c., are certainly transmitted. With man we see similar facts in almost every family; and we 111now know through the admirable labours of Mr. Galton149 that genius, which implies a wonderfully complex combination of high faculties, tends to be inherited; and, on the other hand, it is too certain that insanity and deteriorated mental powers likewise run in the same families.
I have discussed the topic of inheritance in detail elsewhere148, so there’s not much more to add here. We've gathered more information about how both minor and major traits are passed down in humans compared to lower animals, even though there's still plenty of information available regarding them. When it comes to mental qualities, we can clearly see their transmission in our dogs, horses, and other pets. Along with specific preferences and habits, traits like general intelligence, courage, and personality—both positive and negative—are definitely passed down. With humans, we observe similar trends in nearly every family. Thanks to the excellent work of Mr. Galton149, we now understand that genius, which involves a highly intricate combination of abilities, tends to be inherited. At the same time, it's clear that insanity and diminished mental abilities can also run in the same families.
With respect to the causes of variability we are in all cases very ignorant; but we can see that in man as in the lower animals, they stand in some relation with the conditions to which each species has been exposed during several generations. Domesticated animals vary more than those in a state of nature; and this is apparently due to the diversified and changing nature of their conditions. The different races of man resemble in this respect domesticated animals, and so do the individuals of the same race when inhabiting a very wide area, like that of America. We see the influence of diversified conditions in the more civilised nations, the members of which belong to different grades of rank and follow different occupations, presenting a greater range of character than the members of barbarous nations. But the uniformity of savages has often been exaggerated, and in some cases can hardly be said to exist.150 It is nevertheless an error to speak of man, even if we look only to the conditions to which he has been subjected, as “far more domesticated”151 than 112any other animal. Some savage races, such as the Australians, are not exposed to more diversified conditions than are many species which have very wide ranges. In another and much more important respect, man differs widely from any strictly domesticated animal; for his breeding has not been controlled, either through methodical or unconscious selection. No race or body of men has been so completely subjugated by other men, that certain individuals have been preserved and thus unconsciously selected, from being in some way more useful to their masters. Nor have certain male and female individuals been intentionally picked out and matched, except in the well-known case of the Prussian grenadiers; and in this case man obeyed, as might have been expected, the law of methodical selection; for it is asserted that many tall men were reared in the villages inhabited by the grenadiers with their tall wives.
Regarding the causes of variability, we know very little; however, we can observe that, like lower animals, humans are affected by the conditions they have encountered over many generations. Domesticated animals show more variation than those in the wild, which seems to stem from the diverse and changing nature of their living conditions. The different races of humans, in this way, are similar to domesticated animals, as are individuals from the same race living across a large area, such as in America. We see the impact of varied conditions in more civilized nations, where people belong to different social classes and pursue different occupations, showcasing a broader range of characteristics than those in more primitive societies. However, the uniformity among savages has often been overstated, and in some instances, it can hardly be said to exist.150 Nonetheless, it is a mistake to claim that humans are “far more domesticated”151 than any other animal. Some indigenous races, like the Australians, experience no more varied conditions than numerous species that have extensive ranges. In another and much more crucial regard, humans differ significantly from completely domesticated animals; their breeding has not been managed through either planned or unintentional selection. No race or group of humans has been entirely dominated by others to the extent that certain individuals have been preserved simply for being more beneficial to their masters. Additionally, certain male and female individuals have not been specifically selected and paired, except in the well-known instance of the Prussian grenadiers; in that case, humans followed the law of systematic selection, as it is claimed that many tall men were raised in villages inhabited by grenadiers and their tall wives.
If we consider all the races of man, as forming a single species, his range is enormous; but some separate races, as the Americans and Polynesians, have very wide ranges. It is a well-known law that widely-ranging species are much more variable than species with restricted ranges; and the variability of man may with more truth be compared with that of widely-ranging species, than with that of domesticated animals.
If we think about all the human races as part of one species, their distribution is vast; however, some distinct races, like the Native Americans and Polynesians, have incredibly wide distributions. It's a well-known fact that species that cover large areas tend to be more variable than those with limited ranges; therefore, human variability can more accurately be compared to that of widely-ranging species than to that of domesticated animals.
Not only does variability appear to be induced in man and the lower animals by the same general causes, but in both the same characters are affected in a closely analogous manner. This has been proved in such full detail by Godron and Quatrefages, that I need here only refer to their works.152 Monstrosities, which gra113duate into slight variations, are likewise so similar in man and the lower animals, that the same classification and the same terms can be used for both, as may be seen in Isidore Geoffroy St.-Hilaire’s great work.153 This is a necessary consequence of the same laws of change prevailing throughout the animal kingdom. In my work on the variation of domestic animals, I have attempted to arrange in a rude fashion the laws of variation under the following heads:—The direct and definite action of changed conditions, as shewn by all or nearly all the individuals of the same species varying in the same manner under the same circumstances. The effects of the long-continued use or disuse of parts. The cohesion of homologous parts. The variability of multiple parts. Compensation of growth; but of this law I have found no good instances in the case of man. The effects of the mechanical pressure of one part on another; as of the pelvis on the cranium of the infant in the womb. Arrests of development, leading to the diminution or suppression of parts. The reappearance of long-lost characters through reversion. And lastly, correlated variation. All these so-called laws apply equally to man and the lower animals; and most of them even to plants. It would be superfluous here to discuss all of them;154 but several are so important for us, that they must be treated at considerable length.
Not only does variability seem to be caused in humans and other animals by the same general factors, but the same traits are similarly affected in both groups. This has been thoroughly demonstrated by Godron and Quatrefages, so I will just mention their works here.152 Monstrosities, which gradually develop into slight variations, are also so alike in humans and lower animals that the same classification and terminology can be applied to both, as shown in Isidore Geoffroy St.-Hilaire’s extensive research.153 This is a necessary outcome of the same laws of change that exist across the animal kingdom. In my research on the variation of domestic animals, I have tried to roughly categorize the laws of variation into the following categories:—The direct and specific impact of changed conditions, as shown by almost all individuals of the same species varying in the same way under similar circumstances. The effects of long-term use or disuse of certain parts. The connection between homologous parts. The variability of multiple parts. Compensation of growth; however, I haven't found good examples of this law in humans. The effects of mechanical pressure from one part on another; for instance, the effect of the pelvis on the cranium of an infant in the womb. Arrests of development, which lead to the reduction or loss of certain parts. The reappearance of long-lost traits through reversion. And finally, correlated variation. All these so-called laws apply equally to humans and lower animals, and most of them even to plants. It would be unnecessary to discuss all of them here;154 but several are so important for us that they need to be addressed in detail.
The direct and definite action of changed conditions.—This is a most perplexing subject. It cannot be denied 114that changed conditions produce some effect, and occasionally a considerable effect, on organisms of all kinds; and it seems at first probable that if sufficient time were allowed this would be the invariable result. But I have failed to obtain clear evidence in favour of this conclusion; and valid reasons may be urged on the other side, at least as far as the innumerable structures are concerned, which are adapted for special ends. There can, however, be no doubt that changed conditions induce an almost indefinite amount of fluctuating variability, by which the whole organisation is rendered in some degree plastic.
The direct and clear action of changed circumstances.—This is a very confusing topic. It's undeniable that changed circumstances have some effect, and sometimes a significant effect, on all types of organisms; and initially, it seems likely that if given enough time, this would always be the outcome. However, I haven't been able to find clear evidence supporting this conclusion, and there are solid arguments against it, at least regarding the countless structures that are designed for specific purposes. Nevertheless, there's no doubt that changed circumstances lead to an almost limitless amount of fluctuating variability, which makes the entire organism somewhat adaptable.
In the United States, above 1,000,000 soldiers, who served in the late war, were measured, and the States in which they were born and reared recorded.155 From this astonishing number of observations it is proved that local influences of some kind act directly on stature; and we further learn that “the State where the physical growth has in great measure taken place, and the State of birth, which indicates the ancestry, seem to exert a marked influence on the stature.” For instance it is established, “that residence in the Western States, during the years of growth, tends to produce increase of stature.” On the other hand, it is certain that with sailors, their manner of life delays growth, as shewn “by the great difference between the statures of soldiers and sailors at the ages of 17 and 18 years.” Mr. B. A. Gould endeavoured to ascertain the nature of the influences which thus act on stature; but he arrived only at negative results, namely, that they did not relate to climate, the elevation of the land, soil, nor even “in any controlling degree” to the abundance or need of the com115forts of life. This latter conclusion is directly opposed to that arrived at by Villermé from the statistics of the height of the conscripts in different parts of France. When we compare the differences in stature between the Polynesian chiefs and the lower orders within the same islands, or between the inhabitants of the fertile volcanic and low barren coral islands of the same ocean,156 or again between the Fuegians on the eastern and western shores of their country, where the means of subsistence are very different, it is scarcely possible to avoid the conclusion that better food and greater comfort do influence stature. But the preceding statements shew how difficult it is to arrive at any precise result. Dr. Beddoe has lately proved that, with the inhabitants of Britain, residence in towns and certain occupations have a deteriorating influence on height; and he infers that the result is to a certain extent inherited, as is likewise the case in the United States. Dr. Beddoe further believes that wherever a “race attains its maximum of physical development, it rises highest in energy and moral vigour.”157
In the United States, over 1,000,000 soldiers who served in the recent war were measured, and the states where they were born and raised were recorded.155 From this remarkable number of observations, it’s clear that local factors have a direct impact on height; we also learn that “the state where physical growth largely occurs and the state of birth, which reflects ancestry, seem to have a significant effect on height.” For example, it’s established that “living in the Western States during growth years tends to increase height.” Conversely, it’s evident that sailors experience a delay in growth due to their lifestyle, as shown by “the substantial difference in heights between soldiers and sailors at ages 17 and 18.” Mr. B. A. Gould tried to identify the factors affecting height, but he only found negative results, meaning they weren’t linked to climate, altitude, soil, or even “in any significant way” to the availability or scarcity of life's comforts.115 This conclusion contradicts that of Villermé, who based his findings on the height statistics of conscripts from different regions in France. When comparing the height differences between Polynesian chiefs and the lower classes on the same islands, or between residents of fertile volcanic islands and barren coral islands in the same ocean,156 or again between the Fuegians on the eastern and western coasts of their country, where food sources vary greatly, it’s hard to ignore the conclusion that better nutrition and greater comfort do affect height. However, the previous statements illustrate how challenging it is to reach definitive conclusions. Dr. Beddoe has recently demonstrated that, among the people of Britain, living in cities and certain jobs negatively impacts height; he concludes that this effect is inherited to some extent, similar to the situation in the United States. Dr. Beddoe also believes that wherever a “race reaches its peak of physical development, it rises highest in energy and moral strength.”157
Whether external conditions produce any other direct effect on man is not known. It might have been expected that differences of climate would have had a marked influence, as the lungs and kidneys are brought into fuller activity under a low temperature, and the liver and skin under a high one.158 It was formerly thought that the colour of the skin and the character 116of the hair were determined by light or heat; and although it can hardly be denied that some effect is thus produced, almost all observers now agree that the effect has been very small, even after exposure during many ages. But this subject will be more properly discussed when we treat of the different races of mankind. With our domestic animals there are grounds for believing that cold and damp directly affect the growth of the hair; but I have not met with any evidence on this head in the case of man.
Whether external conditions have any other direct effect on humans is unclear. One might have expected that differences in climate would have a significant impact, as the lungs and kidneys work harder in cold temperatures, while the liver and skin are more active in warm ones.158 It was previously believed that skin color and hair type were influenced by light or heat; and while it's hard to deny that there is some effect, almost all observers now agree that the impact has been minimal, even after exposure over many generations. However, this topic will be more appropriately addressed when we discuss the various races of humanity. With our domestic animals, there is reason to believe that cold and damp directly influence hair growth; but I have not found any evidence of this regarding humans.
Effects of the increased Use and Disuse of Parts.—It is well known that use strengthens the muscles in the individual, and complete disuse, or the destruction of the proper nerve, weakens them. When the eye is destroyed the optic nerve often becomes atrophied. When an artery is tied, the lateral channels increase not only in diameter, but in the thickness and strength of their coats. When one kidney ceases acting from disease, the other increases in size and does double work. Bones increase not only in thickness, but in length, from carrying a greater weight.159 Different occupations habitually followed lead to changed proportions in various parts of the body. Thus it was clearly ascertained by the United States Commission160 that the legs of the sailors employed in the late war were longer by 0.217 of an inch than those of the soldiers, though the sailors were on an average shorter men; whilst their arms were shorter by 1.09 of an inch, and therefore out of proportion shorter in relation to 117their lesser height. This shortness of the arms is apparently due to their greater use, and is an unexpected result; but sailors chiefly use their arms in pulling and not in supporting weights. The girth of the neck and the depth of the instep are greater, whilst the circumference of the chest, waist, and hips is less in sailors than in soldiers.
Effects of the Increased Use and Disuse of Parts.—It's well known that using muscles makes them stronger, while not using them, or damage to the proper nerve, weakens them. When the eye is lost, the optic nerve often shrinks. When an artery is tied off, the alternate pathways not only get bigger, but also thicker and stronger. When one kidney stops functioning due to illness, the other one grows larger and takes on extra work. Bones get thicker and longer when they bear more weight. 159 Different jobs that people do regularly result in changes in the size of different body parts. For example, the United States Commission160 found that the legs of sailors during the recent war were, on average, 0.217 inches longer than those of soldiers, even though sailors were generally shorter. Their arms, however, were shorter by 1.09 inches, which caused a disproportion in relation to their shorter stature. This shorter arm length seems to come from more frequent use, which is an unexpected finding, but sailors primarily use their arms for pulling rather than supporting weight. Additionally, sailors have a larger neck circumference and deeper instep, while their chest, waist, and hip measurements are smaller compared to soldiers.
Whether the several foregoing modifications would become hereditary, if the same habits of life were followed during many generations, is not known, but is probable. Rengger161 attributes the thin legs and thick arms of the Payaguas Indians to successive generations having passed nearly their whole lives in canoes, with their lower extremities motionless. Other writers have come to a similar conclusion in other analogous cases. According to Cranz,162 who lived for a long time with the Esquimaux, “the natives believe that ingenuity and dexterity in seal-catching (their highest art and virtue) is hereditary; there is really something in it, for the son of a celebrated seal-catcher will distinguish himself though he lost his father in childhood.” But in this case it is mental aptitude, quite as much as bodily structure, which appears to be inherited. It is asserted that the hands of English labourers are at birth larger than those of the gentry.163 From the correlation which exists, at least in some cases,164 between the development of the extremities and of the jaws, it is possible that in those classes which do not labour much with their hands and feet, the jaws would be reduced in size from this cause. That they are generally smaller in refined and civilised men than in hard-working men or savages, 118is certain. But with savages, as Mr. Herbert Spencer165 has remarked, the greater use of the jaws in chewing coarse, uncooked food, would act in a direct manner on the masticatory muscles and on the bones to which they are attached. In infants long before birth, the skin on the soles of the feet is thicker than on any other part of the body;166 and it can hardly be doubted that this is due to the inherited effects of pressure during a long series of generations.
Whether the various adaptations mentioned earlier would become hereditary if the same lifestyles were maintained over many generations is uncertain, but likely. Rengger161 attributes the thin legs and thick arms of the Payaguas Indians to many generations spending almost their entire lives in canoes, with their lower limbs remaining still. Other authors have reached similar conclusions in comparable situations. According to Cranz,162 who spent considerable time with the Esquimaux, “the natives believe that skill and dexterity in seal-catching (their highest art and virtue) is inherited; there is some truth to this, as the son of a renowned seal-catcher will excel even if he lost his father at a young age.” However, in this case, it appears that both mental ability and physical traits are inherited. It is claimed that English laborers have larger hands at birth than those from the upper class.163 From the relationship that exists, at least in some cases,164 between the development of limbs and jaws, it’s possible that in classes that do not engage much in physical labor, the jaws would be smaller as a result. It’s certainly true that jaws are generally smaller in refined and civilized individuals than in hardworking people or savages. 118As Mr. Herbert Spencer165 has noted, the increased use of jaws in chewing tough, uncooked food by savages may directly influence the chewing muscles and the bones they attach to. In infants long before birth, the skin on the bottoms of the feet is thicker than on any other part of the body;166 and it’s hard to doubt that this is a result of inherited pressure effects over many generations.
It is familiar to every one that watchmakers and engravers are liable to become short-sighted, whilst sailors and especially savages are generally long-sighted. Short-sight and long-sight certainly tend to be inherited.167 The inferiority of Europeans, in comparison with savages, in eyesight and in the other senses, is no doubt the accumulated and transmitted effect of lessened use during many generations; for Rengger168 states that he has repeatedly observed Europeans, who had been brought up and spent their whole lives with the wild Indians, who nevertheless did not equal them in the sharpness of their senses. The same naturalist observes that the cavities in the skull for the reception of the several sense-organs are larger in the American aborigines than in Europeans; and this no doubt indicates a corresponding difference in the dimensions of the organs themselves. Blumenbach has also remarked on the large size of the nasal cavities 119in the skulls of the American aborigines, and connects this fact with their remarkably acute power of smell. The Mongolians of the plains of Northern Asia, according to Pallas, have wonderfully perfect senses; and Prichard believes that the great breadth of their skulls across the zygomas follows from their highly-developed sense-organs.169
It's well known that watchmakers and engravers are prone to becoming nearsighted, while sailors and especially indigenous people are usually farsighted. Both nearsightedness and farsightedness tend to run in families.167 The disadvantage of Europeans compared to indigenous people in terms of eyesight and other senses is likely the result of less use over many generations. Rengger168 has noted that he has often seen Europeans who were raised and lived their entire lives with wild Indians, yet they still didn't match the sharpness of their senses. This naturalist also points out that the cavities in the skull for the various sense organs are larger in Native Americans than in Europeans, which likely indicates a corresponding difference in the size of the organs themselves. Blumenbach has also commented on the large nasal cavities in the skulls of Native Americans and links this observation to their exceptionally keen sense of smell. According to Pallas, the Mongolians of Northern Asia have remarkably acute senses, and Prichard believes that the broadness of their skulls across the cheekbones is a result of their highly developed sense organs.169
The Quechua Indians inhabit the lofty plateaux of Peru, and Alcide d’Orbigny states170 that from continually breathing a highly rarefied atmosphere they have acquired chests and lungs of extraordinary dimensions. The cells, also, of the lungs are larger and more numerous than in Europeans. These observations have been doubted; but Mr. D. Forbes carefully measured many Aymaras, an allied race, living at the height of between ten and fifteen thousand feet; and he informs me171 that they differ conspicuously from the men of all other races seen by him, in the circumference and length of their bodies. In his table of measurements, the stature of each man is taken at 1000, and the other measurements are reduced to this standard. It is here seen that the extended arms of the Aymaras are shorter than those of Europeans, and much shorter than those of Negroes. The legs are likewise shorter, and they present this remarkable peculiarity, that in every Aymara measured the femur is actually shorter than the tibia. On an average the length of the femur to that of the tibia is as 211 to 252; whilst in two Europeans measured at the same 120time, the femora to the tibiæ were as 244 to 230; and in three Negroes as 258 to 241. The humerus is likewise shorter relatively to the fore-arm. This shortening of that part of the limb which is nearest to the body, appears to be, as suggested to me by Mr. Forbes, a case of compensation in relation with the greatly increased length of the trunk. The Aymaras present some other singular points of structure, for instance, the very small projection of the heel.
The Quechua Indians live in the high plateaus of Peru, and Alcide d’Orbigny notes170 that by constantly breathing a very thin atmosphere, they have developed chests and lungs of remarkable size. Their lung cells are also larger and more numerous than those of Europeans. Some of these observations have been disputed; however, Mr. D. Forbes carefully measured many Aymaras, a related group living at elevations between ten and fifteen thousand feet, and he tells me171 that they are noticeably different from people of other races he has seen, in the circumference and length of their bodies. In his measurement table, the height of each man is taken as 1000, and other measurements are adjusted to this standard. It shows that the Aymaras' arms are shorter than those of Europeans, and much shorter than those of Black people. Their legs are also shorter, and they have this interesting peculiarity: in every Aymara measured, the femur is actually shorter than the tibia. On average, the ratio of the femur length to tibia length is 211 to 252; whereas in two Europeans measured at the same120time, the ratio was 244 to 230; and in three Black individuals, it was 258 to 241. The humerus is likewise shorter relative to the forearm. This shortening of the limb segment closest to the body seems to be, as Mr. Forbes suggested to me, a form of compensation for the significantly increased length of the trunk. The Aymaras also have some other unique structural features, such as a very small heel projection.
These men are so thoroughly acclimatised to their cold and lofty abode, that when formerly carried down by the Spaniards to the low Eastern plains, and when now tempted down by high wages to the gold-washings, they suffer a frightful rate of mortality. Nevertheless Mr. Forbes found a few pure families which had survived during two generations; and he observed that they still inherited their characteristic peculiarities. But it was manifest, even without measurement, that these peculiarities had all decreased; and on measurement their bodies were found not to be so much elongated as those of the men on the high plateau; whilst their femora had become somewhat lengthened, as had their tibiæ but in a less degree. The actual measurements may be seen by consulting Mr. Forbes‘ memoir. From these valuable observations, there can, I think, be no doubt that residence during many generations at a great elevation tends, both directly and indirectly, to induce inherited modifications in the proportions of the body.172
These men are so completely adapted to their cold and high home that when they were previously brought down by the Spaniards to the low Eastern plains, and when they are now lured down by high wages to the gold-washings, they face a terrifyingly high death rate. However, Mr. Forbes found a few pure families that had survived for two generations, and he noticed that they still retained their distinctive traits. But it was obvious, even without measurement, that these traits had all diminished; and when measured, their bodies were found to be not as elongated as those of the men on the high plateau; while their femurs had become somewhat longer, as had their tibiae but to a lesser extent. The actual measurements can be found in Mr. Forbes' memoir. From these valuable observations, I believe there can be no doubt that living at a high elevation for many generations tends to directly and indirectly induce inherited changes in body proportions.172
Although man may not have been much modified during the latter stages of his existence through the 121increased or decreased use of parts, the facts now given shew that his liability in this respect has not been lost; and we positively know that the same law holds good with the lower animals. Consequently we may infer, that when at a remote epoch the progenitors of man were in a transitional state, and were changing from quadrupeds into bipeds, natural selection would probably have been greatly aided by the inherited effects of the increased or diminished use of the different parts of the body.
Although humans may not have changed much during the later stages of their existence due to the increased or decreased use of body parts, the facts presented show that their vulnerability in this regard still exists; and we know for sure that the same principle applies to lower animals. Therefore, we can assume that when, long ago, the ancestors of humans were in a transitional phase, moving from four-legged to two-legged beings, natural selection would likely have been significantly influenced by the inherited effects of the increased or decreased use of various body parts.
Arrests of Development.—Arrested development differs from arrested growth, as parts in the former state continue to grow whilst still retaining their early condition. Various monstrosities come under this head, and some are known to be occasionally inherited, as a cleft-palate. It will suffice for our purpose to refer to the arrested brain-development of microcephalous idiots, as described in Vogt’s great memoir.173 Their skulls are smaller, and the convolutions of the brain are less complex than in normal men. The frontal sinus, or the projection over the eyebrows, is largely developed, and the jaws are prognathous to an “effrayant” degree; so that these idiots somewhat resemble the lower types of mankind. Their intelligence and most of their mental faculties are extremely feeble. They cannot acquire the power of speech, and are wholly incapable of prolonged attention, but are much given to imitation. They are strong and remarkably active, continually gamboling and jumping about, and making grimaces. They often ascend stairs on all-fours; and are curiously fond of climbing up furniture or trees. We are thus reminded of the delight 122shewn by almost all boys in climbing trees; and this again reminds us how lambs and kids, originally alpine animals, delight to frisk on any hillock, however small.
Arrests of Development.—Arrested development is different from arrested growth, as parts in the former continue to grow while still keeping their early condition. Various abnormalities fall into this category, and some are sometimes inherited, like a cleft palate. For our purpose, it's enough to mention the halted brain development in microcephalous individuals, as described in Vogt’s extensive study.173 Their skulls are smaller, and the brain's folds are less intricate than in typical individuals. The frontal sinus, or the bump over the eyebrows, is well-developed, and the jaws protrude to an “effrayant” degree, making these individuals somewhat resemble the more primitive types of humans. Their intelligence and most of their mental abilities are very weak. They cannot learn to speak and are completely unable to focus for long periods, but they frequently imitate others. They are strong and surprisingly active, often running and jumping around, and making faces. They often go up stairs on all fours and have a peculiar liking for climbing furniture or trees. This reminds us of the joy that almost all boys take in climbing trees, and it brings to mind how lambs and kids, originally mountain animals, love to play on any small hillock.
Reversion.—Many of the cases to be here given might have been introduced under the last heading. Whenever a structure is arrested in its development, but still continues growing until it closely resembles a corresponding structure in some lower and adult member of the same group, we may in one sense consider it as a case of reversion. The lower members in a group give us some idea how the common progenitor of the group was probably constructed; and it is hardly credible that a part arrested at an early phase of embryonic development should be enabled to continue growing so as ultimately to perform its proper function, unless it had acquired this power of continued growth during some earlier state of existence, when the present exceptional or arrested structure was normal. The simple brain of a microcephalous idiot, in as far as it resembles that of an ape, may in this sense be said to offer a case of reversion. There are other cases which come more strictly under our present heading of reversion. Certain structures, regularly occurring in the lower members of the group to which man belongs, occasionally make their appearance in him, though not found in the normal human embryo; or, if present in the normal human embryo, they become developed in an abnormal manner, though this manner of development is proper to the lower members of the same group. These remarks will be rendered clearer by the following illustrations.
Reversion.—Many of the examples we will discuss here could have been included under the previous heading. Whenever a structure stops developing but continues to grow until it closely resembles a similar structure in a lower, fully grown member of the same group, we can think of it as a case of reversion. The lower members in a group give us some insight into how the common ancestor of the group might have been structured; it’s hard to believe that a part that is halted in its early stages of embryonic development could still grow enough to eventually function properly, unless it had gained this ability to continue growing during some earlier phase of existence when the current unusual or stunted structure was normal. The simple brain of a person with microcephaly, especially as it resembles that of an ape, may be seen as a case of reversion in this context. There are other cases that more directly fit our current topic of reversion. Certain structures that normally occur in the lower members of the group to which humans belong sometimes appear in humans, even though they are not found in the typical human embryo; or if they are present in the normal human embryo, they develop in an unusual way, although this method of development is typical for the lower members of the same group. These points will be clearer with the following examples.
In various mammals the uterus graduates from a double organ with two distinct orifices and two passages, as in the marsupials, into a single organ, showing no signs of doubleness except a slight internal fold, as in123 the higher apes and man. The rodents exhibit a perfect series of gradations between these two extreme states. In all mammals the uterus is developed from two simple primitive tubes, the inferior portions of which form the cornua; and it is in the words of Dr. Farre “by the coalescence of the two cornua at their lower extremities that the body of the uterus is formed in man; while in those animals in which no middle portion or body exists, the cornua remain ununited. As the development of the uterus proceeds, the two cornua become gradually shorter, until at length they are lost, or, as it were, absorbed into the body of the uterus.” The angles of the uterus are still produced into cornua, even so high in the scale as in the lower apes, and their allies the lemurs.
In various mammals, the uterus evolves from a double organ with two separate openings and two passages, like in marsupials, into a single organ, showing no signs of duplicity except for a slight internal fold, as seen in123 higher apes and humans. Rodents display a complete range of variations between these two extremes. In all mammals, the uterus develops from two simple primitive tubes, the lower parts of which form the cornua; and it is, in the words of Dr. Farre, “through the merging of the two cornua at their lower ends that the body of the uterus is formed in humans; while in those animals where there is no middle portion or body, the cornua remain separate. As the uterus develops, the two cornua gradually shorten, until eventually they disappear, or, in a sense, get absorbed into the body of the uterus.” The angles of the uterus still extend into cornua, even at the higher end of the scale, as seen in lower apes and their relatives, the lemurs.
Now in women anomalous cases are not very infrequent, in which the mature uterus is furnished with cornua, or is partially divided into two organs; and such cases, according to Owen, repeat “the grade of concentrative development,” attained by certain rodents. Here perhaps we have an instance of a simple arrest of embryonic development, with subsequent growth and perfect functional development, for either side of the partially double uterus is capable of performing the proper office of gestation. In other and rarer cases, two distinct uterine cavities are formed, each having its proper orifice and passage.174 No such stage is passed through during the ordinary development of the embryo, and it is difficult to believe, though perhaps not impossible, that the two simple, minute, primitive tubes could know how (if such an expression may be used) to 124grow into two distinct uteri, each with a well-constructed orifice and passage, and each furnished with numerous muscles, nerves, glands and vessels, if they had not formerly passed through a similar course of development, as in the case of existing marsupials. No one will pretend that so perfect a structure as the abnormal double uterus in woman could be the result of mere chance. But the principle of reversion, by which long-lost dormant structures are called back into existence, might serve as the guide for the full development of the organ, even after the lapse of an enormous interval of time.
Now in women, unusual cases are not very rare, where the mature uterus has cornua or is partially split into two organs; and these cases, according to Owen, reflect “the grade of concentrative development” seen in certain rodents. This might be an example of a simple halt in embryonic development, followed by growth and full functional development, as either side of the partially double uterus can perform the proper role of gestation. In other, rarer cases, two distinct uterine cavities develop, each with its own opening and passage.174 No stage like this occurs during the typical development of the embryo, and it’s hard to believe, though perhaps not impossible, that the two simple, small, primitive tubes could somehow (if that’s the right way to say it) develop into two distinct uteri, each with a well-formed opening and passage, and each having numerous muscles, nerves, glands, and vessels if they hadn’t previously experienced a similar developmental process, as seen in current marsupials. No one would claim that such a well-formed structure as the abnormal double uterus in women could simply be the result of chance. However, the principle of reversion, where long-lost dormant structures are reactivated, could serve as a guide for the full development of the organ, even after a lengthy period has passed.
Professor Canestrini,175 after discussing the foregoing and various analogous cases, arrives at the same conclusion as that just given. He adduces, as another instance, the malar bone, which, in some of the Quadrumana and other mammals, normally consists of two portions. This is its condition in the two-months-old human fœtus; and thus it sometimes remains, through arrested development, in man when adult, more especially in the lower prognathous races. Hence Canestrini concludes that some ancient progenitor of man must have possessed this bone normally divided into two portions, which subsequently became fused together. In man the frontal bone consists of a single piece, but in the embryo and in children, and in almost all the lower mammals, it consists of two pieces separated by a distinct suture. This suture occasionally persists, more or less distinctly, in man after maturity, and more fre125quently in ancient than in recent crania, especially as Canestrini has observed in those exhumed from the Drift and belonging to the brachycephalic type. Here again he comes to the same conclusion as in the analogous case of the malar bones. In this and other instances presently to be given, the cause of ancient races approaching the lower animals in certain characters more frequently than do the modern races, appears to be that the latter stand at a somewhat greater distance in the long line of descent from their early semi-human progenitors.
Professor Canestrini,175 after discussing the previous points and various similar cases, arrives at the same conclusion mentioned earlier. He cites, as another example, the cheekbone, which, in some primates and other mammals, normally consists of two parts. This is its state in the two-month-old human fetus; and thus it sometimes remains, due to halted development, in adult humans, particularly in certain races with prominent jaws. Therefore, Canestrini concludes that some ancient ancestor of humans must have had this bone normally divided into two parts, which later fused together. In humans, the frontal bone is one piece, but in embryos, children, and nearly all lower mammals, it consists of two pieces separated by a clear suture. This suture sometimes persists, more or less distinctly, in adults, and is more common in ancient than in modern skulls, particularly as Canestrini has noted in those excavated from the Drift that belong to the brachycephalic type. Here again, he reaches the same conclusion as with the cheekbones. In this and other examples soon to be discussed, the reason ancient races resemble lower animals in certain aspects more often than modern races does, seems to be that modern races are positioned at a somewhat greater distance in the long line of descent from their early semi-human ancestors.
Various other anomalies in man, more or less analogous with the foregoing, have been advanced by different authors176 as cases of reversion; but these seem not a little doubtful, for we have to descend extremely low in the mammalian series before we find such structures normally present.177
Various other unusual traits in humans, somewhat similar to the ones mentioned earlier, have been suggested by different authors176 as examples of reversion; however, these claims seem quite uncertain, as we have to go very far down the mammal classification before we find these structures normally appearing.177
In man the canine teeth are perfectly efficient instruments for mastication. But their true canine character, as Owen178 remarks, “is indicated by the conical form of the crown, which terminates in an obtuse point, is convex outward and flat or sub-concave within, at the base of which surface there is a feeble prominence. The conical form is best expressed in the Melanian races, especially the Australian. The canine is more deeply implanted, and by a stronger fang than the incisors.” Nevertheless this tooth no longer serves man as a special weapon for tearing his enemies or prey; it may, therefore, as far as its proper function is concerned, be considered as rudimentary. In every large collection of human skulls some may be found, as Häckel179 observes, with the canine teeth projecting considerably beyond the others in the same manner, but in a less degree, as in the anthropomorphous apes. In these cases, open spaces between the teeth in the one jaw are left for the reception of the canines belonging to the opposite jaw. An interspace of this kind in a Kaffir skull, figured by Wagner, is surprisingly wide.180 Considering how few ancient skulls have been examined in comparison with recent skulls, it is an interesting fact that in at least three cases the canines project largely; and in the Naulette jaw they are spoken of as enormous.181
In humans, the canine teeth are very effective tools for chewing. However, their real canine nature, as Owen178 notes, “is shown by the cone-shaped crown, which ends in a blunt point, is rounded on the outside, and flat or slightly hollowed on the inside, at the base of which surface there is a slight bump. This cone shape is most pronounced in the Melanesian races, especially the Australians. The canine is rooted more deeply and has a stronger fang than the incisors.” Nonetheless, this tooth no longer functions as a specific weapon for tearing apart enemies or prey; thus, in terms of its original purpose, it can be seen as rudimentary. In any large collection of human skulls, some may show canines that project noticeably beyond the other teeth, similar to but to a lesser extent than in anthropoid apes. In these cases, there are gaps between the teeth in one jaw that allow space for the canines from the opposite jaw. A gap like this in a Kaffir skull, as illustrated by Wagner, is remarkably wide.180 Given how few ancient skulls have been examined compared to more recent ones, it is noteworthy that in at least three cases the canines project significantly; and in the Naulette jaw, they are described as enormous.181
The males alone of the anthropomorphous apes have their canines fully developed; but in the female gorilla, and in a less degree in the female orang, these teeth project considerably beyond the others; therefore the fact that women sometimes have, as I have been assured, considerably projecting canines, is no serious objection to the belief that their occasional great development in man is a case of reversion to an ape-like progenitor. He who rejects with scorn the belief that the shape of his own canines, and their occasional great development in other men, are due to our early progenitors having been provided with these formidable weapons, will probably reveal by sneering the line of his descent. For though he no longer intends, nor has the power, to use these teeth as weapons, he will unconsciously retract his “snarling muscles” (thus named by Sir C. Bell)182 so as to expose them ready for action, like a dog prepared to fight.
The male anthropoid apes have fully developed canine teeth, but in female gorillas, and to a lesser extent in female orangutans, these teeth are noticeably more prominent than the others. So, the fact that some women, as I've been told, have noticeably projecting canines doesn’t seriously challenge the idea that their occasional significant development in men is a throwback to an ape-like ancestor. Those who scoff at the idea that the shape of their own canines, and their sometimes significant growth in other men, is a result of our early ancestors having these intimidating teeth will likely reveal their lineage through their disdain. Even though he no longer intends to use these teeth as weapons and no longer has the ability to do so, he will involuntarily pull back his "snarling muscles" (as Sir C. Bell called them)182 to expose them as if ready for action, like a dog prepping for a fight.
Many muscles are occasionally developed in man, which are proper to the Quadrumana or other mammals. Professor Vlacovich183 examined forty male subjects, and found a muscle, called by him the ischiopubic, in nineteen of them; in three others there was a ligament which represented this muscle; and in the remaining eighteen no trace of it. Out of thirty female subjects this muscle was developed on both sides in only two, but in three others the rudimentary ligament was present. This muscle, therefore, appears to be much more common in the male than in the female sex; and on the principle of the descent of man from some lower form, its presence can be understood; for it has been detected in several of the lower animals, and in all of 128these it serves exclusively to aid the male in the act of reproduction.
Many muscles sometimes develop in humans that are typical of monkeys and other mammals. Professor Vlacovich183 studied forty male subjects and discovered a muscle he named the ischiopubic in nineteen of them. In three others, there was a ligament that represented this muscle, while the remaining eighteen showed no sign of it. Out of thirty female subjects, this muscle was developed on both sides in only two, but three others had the rudimentary ligament. Thus, this muscle seems to be much more common in males than in females. Based on the idea of humans evolving from a lower form, its presence makes sense; it has been found in several lower animals, and in all of these, it serves solely to assist the male in reproduction.
Mr. J. Wood, in his valuable series of papers,184 has minutely described a vast number of muscular variations in man, which resemble normal structures in the lower animals. Looking only to the muscles which closely resemble those regularly present in our nearest allies, the Quadrumana, they are too numerous to be here even specified. In a single male subject, having a strong bodily frame and well-formed skull, no less than seven muscular variations were observed, all of which plainly represented muscles proper to various kinds of apes. This man, for instance, had on both sides of his neck a true and powerful “levator claviculæ,” such as is found in all kinds of apes, and which is said to occur in about one out of sixty human subjects.185 Again, this man had “a special abductor of the metatarsal bone of the fifth digit, such as Professor Huxley and Mr. Flower have shewn to exist uniformly in the higher and lower apes.” The hands and arms of man are eminently characteristic structures, but their muscles are extremely liable to vary, so as to resemble the corresponding muscles in the lower animals.186 Such resemblances are either complete and per129fect or imperfect, yet in this latter case manifestly of a transitional nature. Certain variations are more common in man, and others in woman, without our being able to assign any reason. Mr. Wood, after describing numerous cases, makes the following pregnant remark: “Notable departures from the ordinary type of the muscular structures run in grooves or directions, which must be taken to indicate some unknown factor, of much importance to a comprehensive knowledge of general and scientific anatomy.”187
Mr. J. Wood, in his valuable series of papers,184 has detailed a significant number of muscular variations in humans that resemble normal structures found in lower animals. Focusing only on the muscles that closely resemble those typically found in our closest relatives, the primates, there are simply too many to list here. In one male subject, who had a strong physique and well-shaped skull, seven muscular variations were noted, all of which clearly corresponded to muscles found in various types of apes. For example, this man had a true and powerful “levator claviculæ” on both sides of his neck, a muscle seen in all types of apes, and which is reported to occur in about one out of every sixty humans.185 Additionally, this man had “a special abductor of the fifth metatarsal bone, as demonstrated by Professor Huxley and Mr. Flower to exist regularly in both higher and lower apes.” The hands and arms of humans are quite distinctive, but their muscles can vary significantly to resemble the corresponding muscles in lower animals.186 These similarities can either be complete and perfect or imperfect, with the latter clearly indicating a transitional nature. Certain variations are more commonly seen in men, while others are more frequent in women, though we can't determine a specific reason for this. After describing various cases, Mr. Wood makes this insightful observation: “Notable deviations from the usual type of muscular structures follow specific patterns or directions, which suggest some unknown factor of great significance for a thorough understanding of general and scientific anatomy.”187
That this unknown factor is reversion to a former state of existence may be admitted as in the highest degree probable. It is quite incredible that a man should through mere accident abnormally resemble, in no less than seven of his muscles, certain apes, if there had been no genetic connection between them. On the other hand, if man is descended from some ape-like creature, no valid reason can be assigned why certain muscles should not suddenly reappear after an interval of many thousand generations, in the same manner as with horses, asses, and mules, dark-coloured stripes suddenly reappear on the legs and shoulders, after an interval of hundreds, or more probably thousands, of generations.
That this unknown factor is returning to a previous state of existence seems highly likely. It's hard to believe that a person could accidentally resemble certain apes in seven of their muscles if there wasn't a genetic link between them. On the flip side, if humans evolved from some ape-like ancestor, there's no good reason why certain muscles couldn’t suddenly reappear after many thousands of generations, just like how dark stripes can unexpectedly show up on the legs and shoulders of horses, donkeys, and mules after hundreds, or more likely thousands, of generations.
These various cases of reversion are so closely related 130to those of rudimentary organs given in the first chapter, that many of them might have been indifferently introduced in either chapter. Thus a human uterus furnished with cornua may be said to represent in a rudimentary condition the same organ in its normal state in certain mammals. Some parts which are rudimental in man, as the os coccyx in both sexes and the mammæ in the male sex, are always present; whilst others, such as the supra-condyloid foramen, only occasionally appear, and therefore might have been introduced under the head of reversion. These several reversionary, as well as the strictly rudimentary, structures reveal the descent of man from some lower form in an unmistakeable manner.
These different cases of reversion are so closely related to those of rudimentary organs mentioned in the first chapter that many of them could have been included in either chapter. For example, a human uterus with cornua can be seen as a rudimentary version of the same organ in its normal form in some mammals. Some parts that are rudimentary in humans, like the coccyx in both males and females and the breasts in males, are always present; while others, like the supra-condyloid foramen, only sometimes appear and could have also been discussed in the context of reversion. These various reversionary and strictly rudimentary structures clearly show that humans descended from some lower form.
Correlated Variation.—In man, as in the lower animals, many structures are so intimately related, that when one part varies so does another, without our being able, in most cases, to assign any reason. We cannot say whether the one part governs the other, or whether both are governed by some earlier developed part. Various monstrosities, as I. Geoffroy repeatedly insists, are thus intimately connected. Homologous structures are particularly liable to change together, as we see on the opposite sides of the body, and in the upper and lower extremities. Meckel long ago remarked that when the muscles of the arm depart from their proper type, they almost always imitate those of the leg; and so conversely with the muscles of the legs. The organs of sight and hearing, the teeth and hair, the colour of the skin and hair, colour and constitution, are more or less correlated.188 Professor Schaaffhausen first drew attention to the rela131tion apparently existing between a muscular frame and strongly-pronounced supra-orbital ridges, which are so characteristic of the lower races of man.
Correlated Variation.—In humans, just like in lower animals, many structures are so closely connected that when one part changes, another does too, often without us being able to explain why. We can't determine if one part influences the other or if both are affected by some earlier developed structure. Various abnormalities, as I. Geoffroy often points out, are therefore closely linked. Homologous structures are particularly prone to change together, as seen on opposite sides of the body and in the upper and lower limbs. Meckel noted long ago that when the muscles of the arm deviate from their typical form, they often resemble those of the leg, and vice versa with the leg muscles. The organs of sight and hearing, teeth and hair, and skin and hair color, as well as other characteristics, tend to relate to one another.188 Professor Schaaffhausen was the first to highlight the apparent relationship between a muscular build and pronounced supra-orbital ridges, which are characteristic of lower human races.131
Besides the variations which can be grouped with more or less probability under the foregoing heads, there is a large class of variations which may be provisionally called spontaneous, for they appear, owing to our ignorance, to arise without any exciting cause. It can, however, be shewn that such variations, whether consisting of slight individual differences, or of strongly-marked and abrupt deviations of structure, depend much more on the constitution of the organism than on the nature of the conditions to which it has been subjected.189
Besides the variations that can be grouped with more or less certainty under the categories mentioned earlier, there's a large group of variations that we can temporarily call spontaneous, as they seem to occur without any identifiable trigger due to our lack of understanding. However, it can be demonstrated that these variations, whether they involve minor individual differences or significant and sudden changes in structure, are influenced much more by the organism's makeup than by the external conditions it has faced.189
Rate of Increase.—Civilised populations have been known under favourable conditions, as in the United States, to double their number in twenty-five years; and according to a calculation by Euler, this might occur in a little over twelve years.190 At the former rate the present population of the United States, namely, thirty millions, would in 657 years cover the whole terraqueous globe so thickly, that four men would have to stand on each square yard of surface. The primary or fundamental check to the continued increase of man is the difficulty of gaining subsistence and of living in comfort. We may infer that this is the case from what we see, for instance, in the United States, where subsistence is easy and there is plenty of room. If such means were suddenly doubled in Great Britain, our number would be quickly doubled. With civilised nations the 132above primary check acts chiefly by restraining marriages. The greater death-rate of infants in the poorest classes is also very important; as well as the greater mortality at all ages, and from various diseases, of the inhabitants of crowded and miserable houses. The effects of severe epidemics and wars are soon counterbalanced, and more than counterbalanced, in nations placed under favourable conditions. Emigration also comes in aid as a temporary check, but not to any great extent with the extremely poor classes.
Rate of Increase.—Civilized populations have been known, under favorable conditions like those in the United States, to double their numbers in twenty-five years; and based on a calculation by Euler, this could happen in just over twelve years.190 At the former rate, the current population of the United States, about thirty million, would, in 657 years, cover the entire globe so densely that four people would have to stand on every square yard of surface. The main check on the continued increase of the human population is the challenge of securing enough food and a decent standard of living. We can deduce this from what we observe, for instance, in the United States, where food is readily available and there is plenty of space. If such resources were suddenly doubled in Great Britain, our population would quickly double as well. In civilized nations, the primary check mainly limits marriages. The higher infant mortality rate in the poorest classes is also significant, along with the increased mortality at all ages and from various diseases among people living in overcrowded and poor housing. The impacts of severe epidemics and wars are quickly offset, and even surpassed, in nations with favorable conditions. Emigration also provides a temporary check, but it doesn't significantly affect the extremely poor classes.
There is reason to suspect, as Malthus has remarked, that the reproductive power is actually less in barbarous than in civilised races. We know nothing positively on this head, for with savages no census has been taken; but from the concurrent testimony of missionaries, and of others who have long resided with such people, it appears that their families are usually small, and large ones rare. This may be partly accounted for, as it is believed, by the women suckling their infants for a prolonged period; but it is highly probable that savages, who often suffer much hardship, and who do not obtain so much nutritious food as civilised men, would be actually less prolific. I have shewn in a former work,191 that all our domesticated quadrupeds and birds, and all our cultivated plants, are more fertile than the corresponding species in a state of nature. It is no valid objection to this conclusion that animals suddenly supplied with an excess of food, or when rendered very fat, and that most plants when suddenly removed from very poor to very rich soil, are rendered more or less sterile. We might, therefore, expect that civilised men, who in one sense are highly domesticated, would 133be more prolific than wild men. It is also probable that the increased fertility of civilised nations would become, as with our domestic animals, an inherited character: it is at least known that with mankind a tendency to produce twins runs in families.192
There’s reason to believe, as Malthus noted, that the reproductive rate is actually lower in primitive than in civilized societies. We don’t have solid evidence on this matter, since no census has been conducted among indigenous people; however, based on the consistent reports from missionaries and others who have lived with these communities for a long time, it seems that their families are generally small, with larger families being uncommon. This might partly be explained by the fact that women breastfeed their infants for extended periods; but it’s also likely that indigenous people, who often endure significant hardships and don’t have as much nutritious food as those in civilized societies, would be less fertile. I demonstrated in a previous work,191 that all our domesticated animals and birds, as well as all our cultivated plants, are more fertile than their wild counterparts. It doesn't invalidate this conclusion to argue that animals given too much food or that become very fat, and that most plants when suddenly moved from poor to rich soil, can become less fertile. Therefore, we could expect that civilized humans, who are in some ways highly domesticated, would be more fertile than those living in the wild. It’s also likely that the increased fertility of civilized nations would become, like that of our domesticated animals, an inherited trait: it’s at least known that within human families, there’s a tendency to have twins.192
Notwithstanding that savages appear to be less prolific than civilised people, they would no doubt rapidly increase if their numbers were not by some means rigidly kept down. The Santali, or hill-tribes of India, have recently afforded a good illustration of this fact; for they have increased, as shewn by Mr. Hunter,193 at an extraordinary rate since vaccination has been introduced, other pestilences mitigated, and war sternly repressed. This increase, however, would not have been possible had not these rude people spread into the adjoining districts and worked for hire. Savages almost always marry; yet there is some prudential restraint, for they do not commonly marry at the earliest possible age. The young men are often required to show that they can support a wife, and they generally have first to earn the price with which to purchase her from her parents. With savages the difficulty of obtaining subsistence occasionally limits their number in a much more direct manner than with civilised people, for all tribes periodically suffer from severe famines. At such times savages are forced to devour much bad food, and their health can hardly fail to be injured. Many accounts have been published of their protruding stomachs and emaciated limbs after and during famines. They are then, also, compelled to wander much about, and their infants, as I was assured in Australia, perish 134in large numbers. As famines are periodical, depending chiefly on extreme seasons, all tribes must fluctuate in number. They cannot steadily and regularly increase, as there is no artificial increase in the supply of food. Savages when hardly pressed encroach on each other’s territories, and war is the result; but they are indeed almost always at war with their neighbours. They are liable to many accidents on land and water in their search for food; and in some countries they must suffer much from the larger beasts of prey. Even in India, districts have been depopulated by the ravages of tigers.
Despite the fact that primitive groups seem to have fewer births than civilized people, they would likely grow in numbers quickly if their population wasn't strictly controlled in some way. The Santali, or hill tribes of India, recently provided a good example of this; they have been increasing at an astonishing rate since vaccination was introduced, other diseases were lessened, and warfare was significantly reduced, as shown by Mr. Hunter,193. However, this growth wouldn't have been achievable if these basic communities hadn’t expanded into nearby areas and taken jobs. Primitive societies generally marry, but there's some level of caution, as they don't usually marry at the earliest age possible. Young men often need to prove they can provide for a wife, and they usually first have to earn the money to pay her family for her hand. For these groups, the challenge of finding food sometimes directly limits their population more than it does for civilized people, as all tribes experience severe famines at times. During these periods, they are forced to eat poor-quality food, which inevitably harms their health. Many reports have documented their distended stomachs and thin limbs during and after famines. They also have to move around a lot, and, as I was told in Australia, their infants often die in large numbers. Since famines occur periodically, primarily due to extreme weather, all tribes experience fluctuations in their population. They can’t grow steadily or consistently because there’s no increase in food production. When facing pressure, these groups invade each other’s territories, leading to conflict; they are nearly always at war with their neighbors. They encounter various dangers on land and water while searching for food, and in some regions, they endure significant threats from larger predators. Even in India, some areas have been emptied due to tiger attacks.
Malthus has discussed these several checks, but he does not lay stress enough on what is probably the most important of all, namely infanticide, especially of female infants, and the habit of procuring abortion. These practices now prevail in many quarters of the world, and infanticide seems formerly to have prevailed, as Mr. M’Lennan194 has shewn, on a still more extensive scale. These practices appear to have originated in savages recognising the difficulty, or rather the impossibility of supporting all the infants that are born. Licentiousness may also be added to the foregoing checks; but this does not follow from failing means of subsistence; though there is reason to believe that in some cases (as in Japan) it has been intentionally encouraged as a means of keeping down the population.
Malthus has talked about various checks, but he doesn’t emphasize enough what is likely the most important one of all, which is infanticide, especially of female infants, and the practice of obtaining abortions. These practices are still common in many parts of the world today, and infanticide seems to have been even more widespread in the past, as Mr. M’Lennan194 has shown. These actions seem to have originated from early humans recognizing the difficulty—or rather the impossibility—of supporting all the infants that are born. We can also include licentiousness among these checks; however, this does not necessarily stem from insufficient resources. Still, there is reason to think that in some cases (like in Japan), it has been deliberately promoted as a way to control the population.
If we look back to an extremely remote epoch, before man had arrived at the dignity of manhood, he would have been guided more by instinct and less by reason than are savages at the present time. Our early semi-human progenitors would not have practised infanticide, for the instincts of the lower animals are never so perverted as to lead them regularly to destroy their own 135offspring. There would have been no prudential restraint from marriage, and the sexes would have freely united at an early age. Hence the progenitors of man would have tended to increase rapidly, but checks of some kind, either periodical or constant, must have kept down their numbers, even more severely than with existing savages. What the precise nature of these checks may have been, we cannot say, any more than with most other animals. We know that horses and cattle, which are not highly prolific animals, when first turned loose in South America, increased at an enormous rate. The slowest breeder of all known animals, namely the elephant, would in a few thousand years stock the whole world. The increase of every species of monkey must be checked by some means; but not, as Brehm remarks, by the attacks of beasts of prey. No one will assume that the actual power of reproduction in the wild horses and cattle of America, was at first in any sensible degree increased; or that, as each district became fully stocked, this same power was diminished. No doubt in this case and in all others, many checks concur, and different checks under different circumstances; periodical dearths, depending on unfavourable seasons, being probably the most important of all. So it will have been with the early progenitors of man.
If we look back to a very distant time, before humans had reached the status of being fully human, they would have relied more on instinct and less on reason than today's savages. Our early semi-human ancestors would not have practiced infanticide, since the instincts of lower animals are never so distorted as to lead them to regularly harm their own offspring. There would have been no cautious avoidance of marriage, and the sexes would have freely come together at a young age. As a result, the ancestors of humans would have increased rapidly, but some kind of checks, whether occasional or constant, must have kept their numbers lower than those of existing savages. We can't determine exactly what these checks were, just as with most other animals. We know that horses and cattle, which don’t reproduce frequently, when initially released in South America, grew in numbers significantly. The slowest reproducing animal, the elephant, could potentially populate the entire world in a few thousand years. The growth of every monkey species must be limited in some way, but not, as Brehm points out, by the attacks of predators. No one would suggest that the reproductive capacity of wild horses and cattle in America was significantly higher at the start, or that it decreased as each area became fully populated. Certainly, in this case and in all others, many checks work together, with different checks under different conditions; occasional shortages due to unfavorable seasons being likely the most significant. This would have been true for the early ancestors of humans.
Natural Selection.—We have now seen that man is variable in body and mind; and that the variations are induced, either directly or indirectly, by the same general causes, and obey the same general laws, as with the lower animals. Man has spread widely over the face of the earth, and must have been exposed, during his incessant migrations,195 to the most diversified con136ditions. The inhabitants of Tierra del Fuego, the Cape of Good Hope, and Tasmania in the one hemisphere, and of the Arctic regions in the other, must have passed through many climates and changed their habits many times, before they reached their present homes.196 The early progenitors of man must also have tended, like all other animals, to have increased beyond their means of subsistence; they must therefore occasionally have been exposed to a struggle for existence, and consequently to the rigid law of natural selection. Beneficial variations of all kinds will thus, either occasionally or habitually, have been preserved, and injurious ones eliminated. I do not refer to strongly-marked deviations of structure, which occur only at long intervals of time, but to mere individual differences. We know, for instance, that the muscles of our hands and feet, which determine our powers of movement, are liable, like those of the lower animals,197 to incessant variability. If then the ape-like progenitors of man which inhabited any district, especially one undergoing some change in its conditions, were divided into two equal bodies, the one half which included all the individuals best adapted by their powers of movement for gaining subsistence or for defending themselves, would on an average survive in greater number and procreate more offspring than the other and less well endowed half.
Natural Selection.—We’ve now seen that humans vary in both body and mind, and that these variations are caused, either directly or indirectly, by the same general factors, following the same general rules, as with lower animals. Humans have spread widely across the planet and must have faced a range of different conditions during their constant movements,195 encountering a variety of environments.136 The people of Tierra del Fuego, the Cape of Good Hope, and Tasmania in one hemisphere, and those in the Arctic regions in the other, must have experienced many climates and changed their lifestyles numerous times before reaching their current homes.196 The early ancestors of humans must have also tended, like all other animals, to grow beyond their resources; therefore, they must have occasionally faced a struggle for survival and, as a result, the strict law of natural selection. Favorable variations of all types would thus have been preserved, either sometimes or consistently, while harmful ones would have been eliminated. I’m not talking about significant structural changes that happen only over long periods, but rather small individual differences. For example, we know that the muscles in our hands and feet, which enable our movement, are subject, like those of lower animals,197 to constant variability. If the ape-like ancestors of humans living in any area, especially one going through changes, were split into two equal groups, the half that contained individuals best suited for moving around to find food or defend themselves would, on average, survive in larger numbers and produce more offspring than the other, less well-suited half.
Man in the rudest state in which he now exists is the most dominant animal that has ever appeared on the earth. He has spread more widely than any 137other highly organised form; and all others have yielded before him. He manifestly owes this immense superiority to his intellectual faculties, his social habits, which lead him to aid and defend his fellows, and to his corporeal structure. The supreme importance of these characters has been proved by the final arbitrament of the battle for life. Through his powers of intellect, articulate language has been evolved; and on this his wonderful advancement has mainly depended. He has invented and is able to use various weapons, tools, traps, &c., with which he defends himself, kills or catches prey, and otherwise obtains food. He has made rafts or canoes on which to fish or cross over to neighbouring fertile islands. He has discovered the art of making fire, by which hard and stringy roots can be rendered digestible, and poisonous roots or herbs innocuous. This last discovery, probably the greatest, excepting language, ever made by man, dates from before the dawn of history. These several inventions, by which man in the rudest state has become so preeminent, are the direct result of the development of his powers of observation, memory, curiosity, imagination, and reason. I cannot, therefore, understand how it is that Mr. Wallace198 maintains, that “natural selection could only have endowed the savage with a brain a little superior to that of an ape.”
Humans, even in their most primitive state, are the most dominant animals to ever inhabit the earth. They have spread farther than any other complex life forms, and all other species have given way to them. This significant superiority is clearly due to their intellectual abilities, social behaviors that promote helping and defending one another, and their physical structure. The crucial importance of these traits has been demonstrated through the harsh realities of survival. Thanks to their intellectual capabilities, humans have developed spoken language, which has largely contributed to their remarkable progress. They have invented and can use various weapons, tools, traps, etc., to defend themselves, hunt, and gather food. They've built rafts or canoes for fishing or crossing to nearby fertile islands. They have also learned how to create fire, which makes tough, fibrous roots edible and neutralizes poisonous plants. This last discovery, likely the greatest ever made by humans aside from language, predates written history. These inventions, which have elevated even the simplest humans to such prominence, are direct outcomes of enhanced observation, memory, curiosity, imagination, and reasoning skills. Therefore, I find it hard to grasp how Mr. Wallace maintains that “natural selection could only have endowed the savage with a brain a little superior to that of an ape.”
Although the intellectual powers and social habits of man are of paramount importance to him, we must not underrate the importance of his bodily structure, to which subject the remainder of this chapter will be devoted. The development of the intellectual and social or moral faculties will be discussed in the following chapter.
Although a person's intellectual abilities and social habits are extremely important, we shouldn't overlook the significance of their physical structure, which will be the focus of the rest of this chapter. The growth of intellectual and social or moral skills will be covered in the next chapter.
Even to hammer with precision is no easy matter, as every one who has tried to learn carpentry will admit. To throw a stone with as true an aim as can a Fuegian in defending himself, or in killing birds, requires the most consummate perfection in the correlated action of the muscles of the hand, arm, and shoulder, not to mention a fine sense of touch. In throwing a stone or spear, and in many other actions, a man must stand firmly on his feet; and this again demands the perfect coadaptation of numerous muscles. To chip a flint into the rudest tool, or to form a barbed spear or hook from a bone, demands the use of a perfect hand; for, as a most capable judge, Mr. Schoolcraft,199 remarks, the shaping fragments of stone into knives, lances, or arrow-heads, shews “extraordinary ability and long practice.” We have evidence of this in primeval men having practised a division of labour; each man did not manufacture his own flint tools or rude pottery; but certain individuals appear to have devoted themselves to such work, no doubt receiving in exchange the produce of the chase. Archæologists are convinced that an enormous interval of time 139elapsed before our ancestors thought of grinding chipped flints into smooth tools. A man-like animal who possessed a hand and arm sufficiently perfect to throw a stone with precision or to form a flint into a rude tool, could, it can hardly be doubted, with sufficient practice make almost anything, as far as mechanical skill alone is concerned, which a civilised man can make. The structure of the hand in this respect may be compared with that of the vocal organs, which in the apes are used for uttering various signal-cries, or, as in one species, musical cadences; but in man closely similar vocal organs have become adapted through the inherited effects of use for the utterance of articulate language.
Even being precise with a hammer isn't easy, as anyone who has tried to learn carpentry will agree. Throwing a stone with the same accuracy as a Fuegian defending himself or hunting birds requires incredible coordination among the muscles of the hand, arm, and shoulder, not to mention a keen sense of touch. When throwing a stone or spear, and in many other actions, a person must stand firmly on their feet; this also requires perfect coordination of many muscles. Chipping flint into a basic tool or shaping a barbed spear or hook from a bone requires skilled hands; as a knowledgeable expert, Mr. Schoolcraft,199 notes, shaping stone fragments into knives, lances, or arrowheads shows “extraordinary ability and long practice.” Evidence suggests that early humans practiced a division of labor; not everyone made their own flint tools or crude pottery; instead, certain individuals seemed to focus on these tasks, likely receiving food from hunters in return. Archaeologists believe a significant amount of time passed before our ancestors thought of grinding chipped flints into smooth tools. An ape-like creature with a hand and arm capable of throwing a stone with precision or shaping flint into a rudimentary tool could, with enough practice, likely create almost anything a skilled craftsman could make, purely from a mechanical standpoint. The structure of the hand can be compared to the vocal organs, which in apes are used for various calls or, in one species, musical sounds; however, in humans, similar vocal organs have adapted through inherited use to produce articulate language.
Turning now to the nearest allies of man, and therefore to the best representatives of our early progenitors, we find that the hands in the Quadrumana are constructed on the same general pattern as in us, but are far less perfectly adapted for diversified uses. Their hands do not serve so well as the feet of a dog for locomotion; as may be seen in those monkeys which walk on the outer margins of the palms, or on the backs of their bent fingers, as in the chimpanzee and orang.200 Their hands, however, are admirably adapted for climbing trees. Monkeys seize thin branches or ropes, with the thumb on one side and the fingers and palm on the other side, in the same manner as we do. They can thus also carry rather large objects, such as the neck of a bottle, to their mouths. Baboons turn over stones and scratch up roots with their hands. They seize nuts, insects, or other small objects with the thumb in opposition to the fingers, and no doubt they thus extract eggs and the young from the nests of birds. American monkeys beat the wild oranges on the 140branches until the rind is cracked, and then tear it off with the fingers of the two hands. Other monkeys open mussel-shells with the two thumbs. With their fingers they pull out thorns and burrs, and hunt for each other’s parasites. In a state of nature they break open hard fruits with the aid of stones. They roll down stones or throw them at their enemies; nevertheless, they perform these various actions clumsily, and they are quite unable, as I have myself seen, to throw a stone with precision.
Now, looking at the closest relatives of humans, and thus the best examples of our early ancestors, we see that the hands of primates are structured similarly to ours but aren't as well-suited for varied tasks. Their hands aren't as effective for movement as a dog's feet; you can observe this in monkeys that walk on the edges of their palms or the backs of their bent fingers, like chimpanzees and orangutans.200 However, their hands are excellently adapted for climbing trees. Monkeys grip thin branches or ropes with their thumb on one side and their fingers and palm on the other, just as we do. This allows them to carry relatively large items, like a bottle neck, to their mouths. Baboons flip over stones and dig up roots with their hands. They grasp nuts, insects, or other small things with their thumb opposing their fingers, and likely use this skill to take eggs and young from bird nests. American monkeys hit wild oranges against branches until the peel cracks, then tear it off using both hands. Other monkeys open mussel shells with their thumbs. With their fingers, they remove thorns and burrs and search for parasites on each other. In the wild, they use stones to break open hard fruits. They push down stones or throw them at their enemies; however, they do these various actions awkwardly and, as I have seen myself, they struggle to throw a stone accurately.
It seems to me far from true that because “objects are grasped clumsily” by monkeys, “a much less specialised organ of prehension” would have served them201 as well as their present hands. On the contrary, I see no reason to doubt that a more perfectly constructed hand would have been an advantage to them, provided, and it is important to note this, that their hands had not thus been rendered less well adapted for climbing trees. We may suspect that a perfect hand would have been disadvantageous for climbing; as the most arboreal monkeys in the world, namely Ateles in America and Hylobates in Asia, either have their thumbs much reduced in size and even rudimentary, or their fingers partially coherent, so that their hands are converted into mere grasping-hooks.202
It seems to me that the idea that monkeys' hands could be replaced by a "much less specialized organ of prehension" is far from accurate. In fact, I see no reason to believe that they wouldn’t benefit from having a better-designed hand, as long as it didn’t make them less capable of climbing trees. It’s possible that a perfect hand might actually hinder climbing; after all, the most tree-dwelling monkeys, like Ateles in America and Hylobates in Asia, have either very small or even rudimentary thumbs, or their fingers are partially fused, making their hands more like simple gripping hooks.
As soon as some ancient member in the great series of the Primates came, owing to a change in its manner of procuring subsistence, or to a change in the conditions of its native country, to live somewhat less on trees and more on the ground, its manner of progression would have been modified; and in this case it 141would have had to become either more strictly quadrupedal or bipedal. Baboons frequent hilly and rocky districts, and only from necessity climb up high trees;203 and they have acquired almost the gait of a dog. Man alone has become a biped; and we can, I think, partly see how he has come to assume his erect attitude, which forms one of the most conspicuous differences between him and his nearest allies. Man could not have attained his present dominant position in the world without the use of his hands which are so admirably adapted to act in obedience to his will. As Sir C. Bell204 insists “the hand supplies all instruments, and by its correspondence with the intellect gives him universal dominion.” But the hands and arms could hardly have become perfect enough to have manufactured weapons, or to have hurled stones and spears with a true aim, as long as they were habitually used for locomotion and for supporting the whole weight of the body, or as long as they were especially well adapted, as previously remarked, for climbing trees. Such rough treatment would also have blunted the sense of touch, on which their delicate use largely depends. From these causes alone it would have been an advantage to man to have become a biped; but for many actions it is almost necessary that both arms and the whole upper part of the body should be free; and he must for this end stand firmly on his feet. To gain this great advantage, the feet have been rendered flat, and the great toe peculiarly modified, though this has entailed the loss of the power of prehension. It accords with the principle of the division of physiological labour, which prevails throughout the animal kingdom, that 142as the hands became perfected for prehension, the feet should have become perfected for support and locomotion. With some savages, however, the foot has not altogether lost its prehensile power, as shewn by their manner of climbing trees and of using them in other ways.205
As soon as some ancient ancestor in the long line of Primates started to live a bit less in trees and more on the ground, due to changes in how it got food or shifts in its environment, its way of moving would have changed. In this situation, it would have had to become either more strictly four-legged or two-legged. Baboons often live in hilly and rocky areas and only climb high trees when necessary; they have developed a gait similar to that of a dog. Only humans have become fully bipedal, and we can see how they developed their upright posture, which is one of the most noticeable differences between them and their closest relatives. Humans wouldn't have achieved their current dominant role in the world without their hands, which are perfectly adapted to follow their will. As Sir C. Bell emphasizes, “the hand supplies all instruments, and through its connection to the mind, gives him universal control.” However, the hands and arms could hardly have evolved sufficiently to make tools or accurately throw stones and spears while they were mainly used for walking and supporting the body’s weight, or while they were very well suited for climbing trees. Such rough handling would also have diminished their sense of touch, which is crucial for their fine use. For these reasons alone, it would have been beneficial for humans to become bipedal; but for many actions, it is almost essential for both arms and the upper body to be free, requiring them to stand firmly on their feet. To achieve this advantage, the feet have become flat, and the big toe is specifically modified, although this has led to the loss of their grasping ability. According to the principle of the division of physiological labor, which is seen throughout the animal kingdom, as the hands perfected for grasping, the feet have become optimized for support and locomotion. However, some primitive tribes still show some grasping ability in their feet, as evidenced by how they climb trees and use them in various ways.
If it be an advantage to man to have his hands and arms free and to stand firmly on his feet, of which there can be no doubt from his preeminent success in the battle of life, then I can see no reason why it should not have been advantageous to the progenitors of man to have become more and more erect or bipedal. They would thus have been better able to have defended themselves with stones or clubs, or to have attacked their prey, or otherwise obtained food. The best constructed individuals would in the long run have succeeded best, and have survived in larger numbers. If the gorilla and a few allied forms had become extinct, it might have been argued with great force and apparent truth, that an animal could not have been gradually converted from a quadruped into a biped; as all the individuals in an intermediate condition would have been miserably ill-fitted for progression. But we know (and this is well worthy of reflection) that several kinds of apes are now actually in this intermediate condition; and no one doubts that they are on the whole well adapted for their conditions of life. Thus the gorilla runs with a sidelong shambling gait, but more commonly 143progresses by resting on its bent hands. The long-armed apes occasionally use their arms like crutches, swinging their bodies forward between them, and some kinds of Hylobates, without having been taught, can walk or run upright with tolerable quickness; yet they move awkwardly, and much less securely than man. We see, in short, with existing monkeys various gradations between a form of progression strictly like that of a quadruped and that of a biped or man.
If it's an advantage for humans to have their hands and arms free and to stand firmly on their feet, which is clearly shown by our success in life, then I see no reason why it wouldn't have been beneficial for our ancestors to become more upright and bipedal over time. This would have allowed them to defend themselves better with stones or clubs, hunt their prey more effectively, or find food in other ways. Over time, the individuals best suited for these conditions would have thrived and survived in greater numbers. If gorillas and some related species had gone extinct, it might have seemed convincingly true that an animal could not gradually transition from walking on four legs to two; all the intermediate forms would have been poorly suited for movement. However, we know (and it's important to consider) that several types of apes currently exist in this intermediate state, and no one doubts that they are generally well adapted to their environment. For example, the gorilla moves with a sidelong, awkward gait, but more often, it travels by resting on its bent hands. Long-armed apes sometimes use their arms like crutches, swinging their bodies forward between them, and some species of Hylobates, without any training, can walk or run upright with reasonable speed; yet they do so clumsily and far less securely than humans. In summary, we can observe various stages of movement among existing monkeys, ranging from a quadrupedal style to bipedalism, similar to humans.
As the progenitors of man became more and more erect, with their hands and arms more and more modified for prehension and other purposes, with their feet and legs at the same time modified for firm support and progression, endless other changes of structure would have been necessary. The pelvis would have had to be made broader, the spine peculiarly curved and the head fixed in an altered position, and all these changes have been attained by man. Prof. Schaaffhausen206 maintains that “the powerful mastoid processes of the human skull are the result of his erect position;” and these processes are absent in the orang, chimpanzee, &c., and are smaller in the gorilla than in man. Various other structures might here have been specified, which appear connected with man’s erect position. It is very difficult to decide how far all these correlated modifications are the result of natural selection, and how far of the inherited effects of the increased use of certain parts, or of the action of one part on another. No doubt these means of change act and react on each other: thus when certain muscles, and the crests of bone to which they are attached, become enlarged by 144habitual use, this shews that certain fictions are habitually performed and must be serviceable. Hence the individuals which performed them best, would tend to survive in greater numbers.
As the ancestors of humans became more upright, their hands and arms evolved to be better for grasping and other functions, while their feet and legs also adapted for stable support and movement, countless other structural changes were necessary. The pelvis needed to be wider, the spine needed to curve in a specific way, and the head had to be positioned differently—all of which humans have achieved. Prof. Schaaffhausen206 argues that "the robust mastoid processes of the human skull are a result of our upright posture;" these processes are absent in orangutans, chimpanzees, etc., and are smaller in gorillas than in humans. There are many other structures connected to humanity's upright stance that could be mentioned. It's challenging to determine how much of these related changes come from natural selection versus the inherited effects of increased use of certain body parts, or how one part influences another. These change mechanisms certainly interact: when specific muscles and the bone crests they attach to grow larger due to regular use, it indicates that certain actions are performed consistently and must be beneficial. Consequently, individuals who excelled in these actions would likely survive in greater numbers.
The free use of the arms and hands, partly the cause and partly the result of man’s erect position, appears to have led in an indirect manner to other modifications of structure. The early male progenitors of man were, as previously stated, probably furnished with great canine teeth; but as they gradually acquired the habit of using stones, clubs, or other weapons, for fighting with their enemies, they would have used their jaws and teeth less and less. In this case, the jaws, together with the teeth, would have become reduced in size, as we may feel sure from innumerable analogous cases. In a future chapter we shall meet with a closely-parallel case, in the reduction or complete disappearance of the canine teeth in male ruminants, apparently in relation with the development of their horns; and in horses, in relation with their habit of fighting with their incisor teeth and hoofs.
The free use of our arms and hands, which is partly caused by and partly a result of humans standing upright, seems to have indirectly led to other changes in our bodies. As previously mentioned, early male ancestors of humans likely had large canine teeth; however, as they gradually started using stones, clubs, or other weapons to fight their enemies, they would have relied less and less on their jaws and teeth. In this situation, the jaws and teeth would have likely become smaller over time, as seen in many similar cases. In a future chapter, we will look at a very similar example where male ruminants experience a reduction or complete loss of their canine teeth, likely linked to the growth of their horns; and in horses, this is related to their tendency to use their incisor teeth and hooves in fights.
In the adult male anthropomorphous apes, as Rütimeyer,207 and others have insisted, it is precisely the effect which the jaw-muscles by their great development have produced on the skull, that causes it to differ so greatly in many respects from that of man, and has given to it “a truly frightful physiognomy.” Therefore as the jaws and teeth in the progenitors of man gradually become reduced in size, the adult skull would have presented nearly the same characters which it offers in the young of the anthropomorphous apes, and would thus have come to resemble more nearly that of existing 145man. A great reduction of the canine teeth in the males would almost certainly, as we shall hereafter see, have affected through inheritance the teeth of the females.
In adult male apes, as Rütimeyer and others have pointed out, the significant development of the jaw muscles has greatly influenced the skull's shape, making it quite different from that of humans and giving it "a truly frightening appearance." As the jaws and teeth of human ancestors gradually got smaller, the adult skull would have shown characteristics similar to those seen in young anthropoid apes, thus resembling that of modern humans more closely. A significant reduction in the canine teeth of males would likely have, as we will see later, impacted the teeth of females through inheritance.
As the various mental faculties were gradually developed, the brain would almost certainly have become larger. No one, I presume, doubts that the large size of the brain in man, relatively to his body, in comparison with that of the gorilla or orang, is closely connected with his higher mental powers. We meet with closely analogous facts with insects, in which the cerebral ganglia are of extraordinary dimensions in ants; these ganglia in all the Hymenoptera being many times larger than in the less intelligent orders, such as beetles.208 On the other hand, no one supposes that the intellect of any two animals or of any two men can be accurately gauged by the cubic contents of their skulls. It is certain that there may be extraordinary mental activity with an extremely small absolute mass of nervous matter: thus the wonderfully diversified instincts, mental powers, and affections of ants are generally known, yet their cerebral ganglia are not so large as the quarter of a small pin’s head. Under this latter point of view, the brain of an ant is one of the most marvellous atoms of matter in the world, perhaps more marvellous than the brain of man.
As different mental abilities developed, the brain likely became larger. No one, I assume, doubts that a larger brain size in humans, relative to our bodies, compared to gorillas or orangutans, is closely linked to our superior mental abilities. We see similar cases in insects, where the brain ganglia are exceptionally large in ants; these ganglia in all Hymenoptera are many times bigger than in less intelligent groups, like beetles.208 On the other hand, no one thinks we can measure the intelligence of any two animals or two humans just by the size of their skulls. It's clear that extraordinary mental activity can occur with a very small amount of nervous tissue: for instance, the incredibly diverse instincts, mental capabilities, and emotions of ants are well-known, yet their brain ganglia are smaller than a quarter of a small pin’s head. From this perspective, an ant's brain is one of the most extraordinary pieces of matter in the world, perhaps even more remarkable than a human brain.
The belief that there exists in man some close relation between the size of the brain and the development of the intellectual faculties is supported by the comparison of the skulls of savage and civilised races, of ancient and modern people, and by the analogy of the whole verte146brate series. Dr. J. Barnard Davis has proved209 by many careful measurements, that the mean internal capacity of the skull in Europeans is 92·3 cubic inches; in Americans 87·5; in Asiatics 87·1; and in Australians only 81·9 inches. Professor Broca210 found that skulls from graves in Paris of the nineteenth century, were larger than those from vaults of the twelfth century, in the proportion of 1484 to 1426; and Prichard is persuaded that the present inhabitants of Britain have “much more capacious brain-cases” than the ancient inhabitants. Nevertheless it must be admitted that some skulls of very high antiquity, such as the famous one of Neanderthal, are well developed and capacious. With respect to the lower animals, M. E. Lartet,211 by comparing the crania of tertiary and recent mammals, belonging to the same groups, has come to the remarkable conclusion that the brain is generally larger and the convolutions more complex in the more recent form. On the other hand I have shewn212 that the brains of domestic rabbits are considerably reduced in bulk, in comparison with those of the wild rabbit or hare; and this may be attributed to their having been closely confined during many generations, so that they have exerted but little their intellect, instincts, senses, and voluntary movements.
The belief that there is a close relationship between brain size and intellectual development is supported by comparisons of the skulls of different races — both primitive and civilized, as well as ancient and modern — and by the analogies found throughout vertebrate evolution. Dr. J. Barnard Davis has demonstrated through careful measurements that the average internal capacity of the skull in Europeans is 92.3 cubic inches; in Americans, it's 87.5; in Asiatics, 87.1; and in Australians, it’s only 81.9 inches. Professor Broca found that skulls from 19th-century graves in Paris were larger than those from 12th-century vaults, with a ratio of 1484 to 1426. Additionally, Prichard believes that the current inhabitants of Britain have “much larger brain-cases” than the ancient people did. However, it's important to note that some very ancient skulls, like the well-known Neanderthal skull, are also quite developed and spacious. Regarding lower animals, M. E. Lartet has reached the interesting conclusion that the brains of more recent mammals from the same groups tend to be larger and have more complex folds compared to those from earlier periods. On the other hand, I have shown that the brains of domestic rabbits are significantly smaller compared to those of wild rabbits or hares, likely because they have been kept in captivity for many generations, resulting in less use of their intellect, instincts, senses, and voluntary movements.
The gradually increasing weight of the brain and skull in man must have influenced the development of the supporting spinal column, more especially whilst he was becoming erect. As this change of position was 147being brought about, the internal pressure of the brain, will, also, have influenced the form of the skull; for many facts shew how easily the skull is thus affected. Ethnologists believe that it is modified by the kind of cradle in which infants sleep. Habitual spasms of the muscles and a cicatrix from a severe burn have permanently modified the facial bones. In young persons whose heads from disease have become fixed either sideways or backwards, one of the eyes has changed its position, and the bones of the skull have been modified; and this apparently results from the brain pressing in a new direction.213 I have shewn that with long-eared rabbits, even so trifling a cause as the lopping forward of one ear drags forward on that side almost every bone of the skull; so that the bones on the opposite sides no longer strictly correspond. Lastly, if any animal were to increase or diminish much in general size, without any change in its mental powers; or if the mental powers were to be much increased or diminished without any great change in the size of the body; the shape of the skull would almost certainly be altered. I infer this from my observations on domestic rabbits, some kinds of which have become very much larger than the wild animal, whilst others have retained nearly the same size, but in both cases the brain has been much reduced relatively to the size of the body. Now I was at first much surprised by finding that in all these rabbits the skull had become elongated or dolicho148cephalic; for instance, of two skulls of nearly equal breadth, the one from a wild rabbit and the other from a large domestic kind, the former was only 3·15 and the latter 4·3 inches in length.214 One of the most marked distinctions in different races of man is that the skull in some is elongated, and in others rounded; and here the explanation suggested by the case of the rabbits may partially hold good; for Welcker finds that short “men incline more to brachycephaly, and tall men to dolichocephaly;”215 and tall men may be compared with the larger and longer-bodied rabbits, all of which have elongated skulls, or are dolichocephalic.
The gradually increasing weight of the brain and skull in humans must have influenced the development of the supporting spinal column, especially as we became upright. As this change in position occurred, the internal pressure of the brain would also have affected the shape of the skull; many facts show how easily the skull can be impacted this way. Ethnologists believe that it is modified by the type of cradle in which infants sleep. Chronic muscle spasms and a scar from a severe burn have permanently changed the facial bones. In young people whose heads have become fixed in either a sideways or backward position due to illness, one of the eyes has shifted, and the bones of the skull have been altered; this seemingly results from the brain pressing in a new direction. I have shown that with long-eared rabbits, even something as minor as one ear being bent forward pulls forward almost every bone on that side of the skull; thus, the bones on the opposite side no longer correspond exactly. Lastly, if any animal were to significantly increase or decrease in size without any change in its mental abilities, or if its mental abilities were to change significantly without a considerable alteration in body size, the shape of the skull would almost certainly be modified. I base this on my observations of domestic rabbits, some of which have become much larger than the wild counterparts, while others have remained nearly the same size, yet in both cases, the brain has been greatly reduced relative to body size. Initially, I was quite surprised to find that in all these rabbits, the skull had become elongated or dolichocephalic; for example, one skull from a wild rabbit was 3.15 inches long, while a skull from a large domestic rabbit was 4.3 inches long. One of the most notable differences among various human races is that some have elongated skulls while others have rounded ones; the explanation suggested by the case of the rabbits may partly apply here, as Welcker finds that short "men tend more towards brachycephaly, while tall men lean towards dolichocephaly;" and tall men can be compared to the larger and longer-bodied rabbits, all of which have elongated skulls or are dolichocephalic.
From these several facts we can to a certain extent understand the means through which the great size and more or less rounded form of the skull has been acquired by man; and these are characters eminently distinctive of him in comparison with the lower animals.
From these various facts, we can somewhat grasp the ways in which humans have developed a larger and more rounded skull shape; these traits are notably distinct when compared to lower animals.
Another most conspicuous difference between man and the lower animals is the nakedness of his skin. Whales and dolphins (Cetacea), dugongs (Sirenia) and the hippopotamus are naked; and this may be advantageous to them for gliding through the water; nor would it be injurious to them from the loss of warmth, as the species which inhabit the colder regions are protected by a thick layer of blubber, serving the same purpose as the fur of seals and otters. Elephants and rhinoceroses are almost hairless; and as certain extinct species which formerly lived under an arctic climate were covered with long wool or hair, it would almost appear as if the existing species of both genera had lost 149their hairy covering from exposure to heat. This appears the more probable, as the elephants in India which live on elevated and cool districts are more hairy216 than those on the lowlands. May we then infer that man became divested of hair from having aboriginally inhabited some tropical land? The fact of the hair being chiefly retained in the male sex on the chest and face, and in both sexes at the junction of all four limbs with the trunk, favours this inference, assuming that the hair was lost before man became erect; for the parts which now retain most hair would then have been most protected from the heat of the sun. The crown of the head, however, offers a curious exception, for at all times it must have been one of the most exposed parts, yet it is thickly clothed with hair. In this respect man agrees with the great majority of quadrupeds, which generally have their upper and exposed surfaces more thickly clothed than the lower surface. Nevertheless, the fact that the other members of the order of Primates, to which man belongs, although inhabiting various hot regions, are well clothed with hair, generally thickest on the upper surface,217 is strongly opposed to the supposition that man became naked through the action of the sun. I am inclined to believe, as we shall see under sexual selection, that man, or rather primarily woman, became divested of hair for ornamental purposes; and according to this belief it is not 150surprising that man should differ so greatly in hairiness from all his lower brethren, for characters gained through sexual selection often differ in closely-related forms to an extraordinary degree.
Another obvious difference between humans and lower animals is the bare skin. Whales and dolphins, dugongs, and hippopotamuses are hairless, which could help them move smoothly through water. They also don't lose warmth because species in cooler areas are protected by a thick layer of blubber, serving the same function as the fur of seals and otters. Elephants and rhinoceroses are nearly hairless, and since some extinct species that lived in arctic climates had long wool or hair, it seems like the existing species of both types have lost their fur due to heat exposure. This seems even more likely since elephants in India that live in cooler, elevated areas have more hair than those in lowlands. Can we then conclude that humans lost their hair because they originally lived in a tropical environment? The fact that hair is mainly retained in males on the chest and face, and in both sexes where the limbs meet the trunk, supports this idea, assuming hair was lost before humans became upright; the areas that currently have the most hair were probably the most protected from sunlight. However, the top of the head presents a strange exception since it has always been one of the most exposed areas, yet it’s covered in thick hair. In this way, humans are similar to most quadrupeds, which usually have their upper surfaces more densely covered than their lower surfaces. Still, the fact that other members of the Primates order, to which humans belong, are well-covered in hair despite living in various hot areas, strongly counters the idea that humans became hairless because of the sun. I tend to believe, as we’ll discuss under sexual selection, that humans, or rather primarily women, lost their hair for decorative reasons. According to this belief, it's not surprising that humans differ so much in hairiness from lower animals, as traits acquired through sexual selection can vary greatly even among closely related species.
According to a popular impression, the absence of a tail is eminently distinctive of man; but as those apes which come nearest to man are destitute of this organ, its disappearance does not especially concern us. Nevertheless it may be well to own that no explanation, as far as I am aware, has ever been given of the loss of the tail by certain apes and man. Its loss, however, is not surprising, for it sometimes differs remarkably in length in species of the same genera: thus in some species of Macacus the tail is longer than the whole body, consisting of twenty-four vertebræ; in others it consists of a scarcely visible stump, containing only three or four vertebræ. In some kinds of baboons there are twenty-five, whilst in the mandrill there are ten very small stunted caudal vertebræ, or, according to Cuvier,218 sometimes only five. This great diversity in the structure and length of the tail in animals belonging to the same genera, and following nearly the same habits of life, renders it probable that the tail is not of much importance to them; and if so, we might have expected that it would sometimes have become more or less rudimentary, in accordance with what we incessantly see with other structures. The tail almost always tapers towards the end whether it be long or short; and this, I presume, results from the atrophy, through disuse, of the terminal muscles together with their arteries and nerves, leading to the atrophy of the terminal bones. With respect 151to the os coccyx, which in man and the higher apes manifestly consists of the few basal and tapering segments of an ordinary tail, I have heard it asked how could these have become completely embedded within the body; but there is no difficulty in this respect, for in many monkeys the basal segments of the true tail are thus embedded. For instance, Mr. Murie informs me that in the skeleton of a not full-grown Macacus inornatus, he counted nine or ten caudal vertebræ, which altogether were only 1·8 inch in length. Of these the three basal ones appeared to have been embedded; the remainder forming the free part of the tail, which was only one inch in length, and half an inch in diameter. Here, then, the three embedded caudal vertebræ plainly correspond with the four coalesced vertebræ of the human os coccyx.
According to a common belief, not having a tail is a major characteristic of humans; however, since the apes most closely related to humans also lack this feature, its absence shouldn't concern us too much. Still, it’s important to note that no one, as far as I know, has ever really explained why some apes and humans lost their tails. But, it's not surprising, as tail length varies greatly among species within the same genera. For example, in some species of Macacus, the tail can be longer than the entire body, made up of twenty-four vertebrae; in others, it’s just a barely noticeable stump with only three or four vertebrae. In certain types of baboons, there are twenty-five vertebrae, while in the mandrill, there are ten tiny, stunted caudal vertebrae, or, according to Cuvier, sometimes only five. This significant variation in tail structure and length among animals of the same genera, which almost all have similar lifestyles, suggests that the tail might not be very important to them. If that’s the case, we might expect to see it become more or less rudimentary, as we often observe with other structures. The tail usually tapers at the end, whether it’s long or short, which I assume is due to the atrophy from not being used, affecting the terminal muscles as well as their arteries and nerves and leading to the shrinkage of the terminal bones. Regarding the coccyx, which in humans and higher apes clearly consists of the few base and tapering segments of an ordinary tail, I have heard people question how these could have become fully embedded in the body. But, this isn’t an issue, as many monkeys have the base segments of their true tails embedded. For instance, Mr. Murie told me that in the skeleton of a not fully grown Macacus inornatus, he counted nine or ten caudal vertebrae, which only measured 1.8 inches in total. Of these, the three basal ones appeared to be embedded, while the rest formed the free part of the tail, which was only one inch long and half an inch in diameter. So, here, the three embedded caudal vertebrae clearly correspond to the four fused vertebrae of the human coccyx.
I have now endeavoured to shew that some of the most distinctive characters of man have in all probability been acquired, either directly, or more commonly indirectly, through natural selection. We should bear in mind that modifications in structure or constitution, which are of no service to an organism in adapting it to its habits of life, to the food which it consumes, or passively to the surrounding conditions, cannot have been thus acquired. We must not, however, be too confident in deciding what modifications are of service to each being: we should remember how little we know about the use of many parts, or what changes in the blood or tissues may serve to fit an organism for a new climate or some new kind of food. Nor must we forget the principle of correlation, by which, as Isidore Geoffroy has shewn in the case of man, many fit-range deviations of structure are tied together. Independently of correlation, a change in one part often leads152 through the increased or decreased use of other parts, to other changes of a quite unexpected nature. It is also well to reflect on such facts, as the wonderful growth of galls on plants caused by the poison of an insect, and on the remarkable changes of colour in the plumage of parrots when fed on certain fishes, or inoculated with the poison of toads;219 for we can thus see that the fluids of the system, if altered for some special purpose, might induce other strange changes. We should especially bear in mind that modifications acquired and continually used during past ages for some useful purpose would probably become firmly fixed and might be long inherited.
I have now tried to show that some of the most distinctive traits of humans have probably been gained, either directly or more commonly indirectly, through natural selection. We should remember that changes in structure or function, which do not help an organism adapt to its lifestyle, the food it eats, or the surrounding conditions, cannot have been acquired this way. However, we shouldn't be overly certain when deciding which modifications are beneficial for each being: we should keep in mind how little we understand about the purpose of many parts, or what changes in blood or tissues might help an organism adapt to a new climate or a different kind of food. We also shouldn't forget the principle of correlation, where, as Isidore Geoffroy demonstrated for humans, many related structural variations are interconnected. Independently of correlation, a change in one part often leads, through increased or decreased use of other parts, to other unexpected changes. It's also worth considering facts like the amazing growth of galls on plants caused by insect poison, and the striking color changes in the feathers of parrots when they eat certain fish, or when exposed to toad poison; for we can see that if the body's fluids are altered for a specific purpose, they might trigger other unusual changes. We should especially keep in mind that modifications that have been acquired and consistently used over time for some beneficial purpose would likely become well-established and could be inherited for a long time.
Thus a very large yet undefined extension may safely be given to the direct and indirect results of natural selection; but I now admit, after reading the essay by Nägeli on plants, and the remarks by various authors with respect to animals, more especially those recently made by Professor Broca, that in the earlier editions of my ‘Origin of Species’ I probably attributed too much to the action of natural selection or the survival of the fittest. I have altered the fifth edition of the Origin so as to confine my remarks to adaptive changes of structure. I had not formerly sufficiently considered the existence of many structures which appear to be, as far as we can judge, neither beneficial nor injurious; and this I believe to be one of the greatest oversights as yet detected in my work. I may be permitted to say as some excuse, that I had two distinct objects in view, firstly, to shew that species had not been separately created, and secondly, that natural selection had been the chief agent of change, though largely aided by the 153inherited effects of habit, and slightly by the direct action of the surrounding conditions. Nevertheless I was not able to annul the influence of my former belief, then widely prevalent, that each species had been purposely created; and this led to my tacitly assuming that every detail of structure, excepting rudiments, was of some special, though unrecognised, service. Any one with this assumption in his mind would naturally extend the action of natural selection, either during past or present times, too far. Some of those who admit the principle of evolution, but reject natural selection, seem to forget, when criticising my book, that I had the above two objects in view; hence if I have erred in giving to natural selection great power, which I am far from admitting, or in having exaggerated its power, which is in itself probable, I have at least, as I hope, done good service in aiding to overthrow the dogma of separate creations.
So a very large but undefined scope can safely be given to the direct and indirect effects of natural selection; however, I now acknowledge, after reading the essay by Nägeli on plants and the comments from various authors regarding animals, especially those recently made by Professor Broca, that in the earlier editions of my ‘Origin of Species’, I probably gave too much weight to the role of natural selection or the survival of the fittest. I have revised the fifth edition of the Origin to focus my comments on adaptive changes in structure. I hadn’t previously considered enough the existence of many structures that seem to be, as far as we can tell, neither beneficial nor harmful; and I believe this to be one of the biggest oversights identified in my work so far. I should mention as some justification that I had two main goals in mind: first, to show that species were not created separately, and second, to argue that natural selection was the primary driver of change, although significantly supported by the inherited effects of habit and somewhat by the direct influence of the surrounding conditions. However, I couldn’t shake off the influence of my previous belief, which was widely accepted at the time, that each species had been intentionally created; and this led me to implicitly assume that every aspect of structure, except for rudimentary parts, served some specific, albeit unrecognized, purpose. Anyone with this assumption would naturally extend the action of natural selection—whether in the past or present—too far. Some who accept the principle of evolution but reject natural selection seem to overlook, when criticizing my book, that I had those two goals in mind; therefore, if I've made mistakes in attributing great power to natural selection, which I’m far from admitting, or in exaggerating its influence, which is quite likely, I hope I have at least contributed to undermining the doctrine of separate creations.
That all organic beings, including man, present many modifications of structure which are of no service to them at present, nor have been formerly, is, as I can now see, probable. We know not what produces the numberless slight differences between the individuals of each species, for reversion only carries the problem a few steps backwards; but each peculiarity must have had its own efficient cause. If these causes, whatever they may be, were to act more uniformly and energetically during a lengthened period (and no reason can be assigned why this should not sometimes occur), the result would probably be not mere slight individual differences, but well-marked, constant modifications. Modifications which are in no way beneficial cannot have been kept uniform through natural selection, though any which were injurious would have been thus eliminated. Uniformity of character would, however,154 naturally follow from, the assumed uniformity of the exciting causes, and likewise from the free intercrossing of many individuals. The same organism might acquire in this manner during successive periods successive modifications, and these would be transmitted in a nearly uniform state as long as the exciting causes remained the same and there was free intercrossing. With respect to the exciting causes we can only say, as when speaking of so-called spontaneous variations, that they relate much more closely to the constitution of the varying organism, than to the nature of the conditions to which it has been subjected.
That all living beings, including humans, show many changes in structure that are currently of no use to them, nor have been in the past, seems likely to me now. We don’t know what causes the countless slight differences between individuals of each species, since reversion only takes the problem a few steps back; however, each unique trait must have its own specific cause. If these causes, whatever they are, acted more consistently and forcefully over a long period (and there's no reason why this couldn't happen sometimes), the outcome would likely be not just minor individual differences, but distinct, consistent changes. Changes that aren't beneficial can't have been maintained by natural selection, though any that were harmful would have been eliminated. Consistency in these traits would, however, naturally result from the assumed consistency of the influencing causes and also from the free interbreeding of many individuals. The same organism might acquire successive changes over time, and these would be passed down in a nearly uniform way as long as the influencing causes remained the same and there was free interbreeding. Regarding the influencing causes, we can only say, as we do when discussing so-called spontaneous variations, that they relate much more closely to the makeup of the changing organism than to the nature of the conditions it encounters.154
Conclusion.—In this chapter we have seen that as man at the present day is liable, like every other animal, to multiform individual differences or slight variations, so no doubt were the early progenitors of man; the variations being then as now induced by the same general causes, and governed by the same general and complex laws. As all animals tend to multiply beyond their means of subsistence, so it must have been with the progenitors of man; and this will inevitably have led to a struggle for existence and to natural selection. This latter process will have been greatly aided by the inherited effects of the increased use of parts; these two processes incessantly reacting on each other. It appears, also, as we shall hereafter see, that various unimportant characters have been acquired by man through sexual selection. An unexplained residuum of change, perhaps a large one, must be left to the assumed uniform action of those unknown agencies, which occasionally induce strongly-marked and abrupt deviations of structure in our domestic productions.
Conclusion.—In this chapter, we have seen that today, humans, like every other animal, experience a variety of individual differences or slight variations. The early ancestors of humans likely experienced similar variations; these differences are caused by the same general factors and follow the same complex laws. Just as all animals tend to reproduce beyond their means of survival, so did the ancestors of humans, leading to competition for existence and natural selection. This process was likely enhanced by the inherited effects of increased use of certain traits, with these two processes continuously influencing each other. It also appears, as we will see later, that some minor traits have developed in humans through sexual selection. Additionally, there remains some unexplained changes, possibly significant, that must be attributed to the consistent influence of unknown factors, which occasionally cause noticeable and sudden changes in the structure of our domesticated species.
Judging from the habits of savages and of the greater number of the Quadrumana, primeval men, and even155 the ape-like progenitors of man, probably lived in society. With strictly social animals, natural selection sometimes acts indirectly on the individual, through the preservation of variations which are beneficial only to the community. A community including a large number of well-endowed individuals increases in number and is victorious over other and less well-endowed communities; although each separate member may gain no advantage over the other members of the same community. With associated insects many remarkable structures, which are of little or no service to the individual or its own offspring, such as the pollen-collecting apparatus, or the sting of the worker-bee, or the great jaws of soldier-ants, have been thus acquired. With the higher social animals, I am not aware that any structure has been modified solely for the good of the community, though some are of secondary service to it. For instance, the horns of ruminants and the great canine teeth of baboons appear to have been acquired by the males as weapons for sexual strife, but they are used in defence of the herd or troop. In regard to certain mental faculties the case, as we shall see in the following chapter, is wholly different; for these faculties have been chiefly, or even exclusively, gained for the benefit of the community; the individuals composing the community being at the same time indirectly benefited.
Judging by the behaviors of primitive peoples and most primates, early humans, and even155 the ape-like ancestors of humans likely lived in groups. In social animals, natural selection sometimes impacts individuals indirectly, through the preservation of traits that only benefit the community. A group with a large number of well-adapted individuals tends to grow and triumph over other, less adapted groups, even if individual members don’t gain advantages over each other. In social insects, many remarkable features, like the pollen-collecting equipment, the sting of a worker bee, or the large jaws of soldier ants, have developed even if they’re of little or no use to the individual or its offspring. With higher social animals, I haven’t seen any traits modified solely for the community's benefit, although some do provide secondary benefits to it. For example, the horns of grazing animals and the large canine teeth of baboons seem to have developed as weapons for mating competition, but are also used to defend the group. As for certain mental abilities, the situation is quite different, as we will explore in the next chapter; these abilities have been primarily, or even solely, developed for the community's benefit, indirectly benefiting the individuals within that community.
It has often been objected to such views as the foregoing, that man is one of the most helpless and defenceless creatures in the world; and that during his early and less well-developed condition he would have been still more helpless. The Duke of Argyll, for instance, insists220 that “the human frame has diverged from 156the structure of brutes, in the direction of greater physical helplessness and weakness. That is to say, it is a divergence which of all others it is most impossible to ascribe to mere natural selection.” He adduces the naked and unprotected state of the body, the absence of great teeth or claws for defence, the little strength of man, his small speed in running, and his slight power of smell, by which to discover food or to avoid danger. To these deficiencies there might have been added the still more serious loss of the power of quickly climbing trees, so as to escape from enemies. Seeing that the unclothed Fuegians can exist under their wretched climate, the loss of hair would not have been a great injury to primeval man, if he inhabited a warm country. When we compare defenceless man with the apes, many of which are provided with formidable canine teeth, we must remember that these in their fully-developed condition are possessed by the males alone, being chiefly used by them for fighting with their rivals; yet the females which are not thus provided, are able to survive.
It has often been argued against such views that humans are among the most vulnerable and defenseless creatures in the world; and that during their early and less developed stages, they would have been even more defenseless. The Duke of Argyll, for example, insists220 that “the human body has evolved away from the structure of animals, moving toward greater physical vulnerability and weakness. In other words, this is a divergence that cannot be simply explained by natural selection.” He points out the bare and unprotected condition of the body, the lack of large teeth or claws for defense, humans' limited strength, their slow running speed, and their weak sense of smell, which hampers their ability to find food or escape danger. Additionally, we could mention the even more significant loss of the ability to quickly climb trees to escape from predators. Given that the unclothed Fuegians can survive in their harsh climate, the loss of body hair wouldn’t have been a major disadvantage for early humans living in a warm environment. When comparing defenseless humans to apes, many of which have strong canine teeth, we must keep in mind that these teeth are primarily found in the males and are mainly used for fighting rivals; however, the females, who don’t have such teeth, are still able to survive.
In regard to bodily size or strength, we do not know whether man is descended from some comparatively small species, like the chimpanzee, or from one as powerful as the gorilla; and, therefore, we cannot say whether man has become larger and stronger, or smaller and weaker, in comparison with his progenitors. We should, however, bear in mind that an animal possessing great size, strength, and ferocity, and which, like the gorilla, could defend itself from all enemies, would probably, though not necessarily, have failed to become social; and this would most effectually have checked the acquirement by man of his higher mental qualities, such as sympathy and the love of his fellow-creatures. Hence it might have been an immense157 advantage to man to have sprung from some comparatively weak creature.
When it comes to body size or strength, we don’t know if humans evolved from a smaller species like the chimpanzee or from something as strong as the gorilla. So we can’t really say if humans have become larger and stronger or smaller and weaker compared to their ancestors. However, we should keep in mind that an animal with great size, strength, and ferocity, like the gorilla, would likely, though not necessarily, struggle to become social. This could have significantly hindered humans in developing higher mental traits, such as empathy and caring for others. Therefore, it might have been a huge advantage for humans to have evolved from a relatively weaker creature.
The slight corporeal strength of man, his little speed, his want of natural weapons, &c., are more than counterbalanced, firstly by his intellectual powers, through which he has, whilst still remaining in a barbarous state, formed for himself weapons, tools, &c., and secondly by his social qualities which lead him to give aid to his fellow-men and to receive it in return. No country in the world abounds in a greater degree with dangerous beasts than Southern Africa; no country presents more fearful physical hardships than the Arctic regions; yet one of the puniest races, namely, the Bushmen, maintain themselves in Southern Africa, as do the dwarfed Esquimaux in the Arctic regions. The early progenitors of man were, no doubt, inferior in intellect, and probably in social disposition, to the lowest existing savages; but it is quite conceivable that they might have existed, or even flourished, if, whilst they gradually lost their brute-like powers, such as climbing trees, &c., they at the same time advanced in intellect. But granting that the progenitors of man were far more helpless and defenceless than any existing savages, if they had inhabited some warm continent or large island, such as Australia or New Guinea, or Borneo (the latter island being now tenanted by the orang), they would not have been exposed to any special danger. In an area as large as one of these islands, the competition between tribe and tribe would have been sufficient, under favourable conditions, to have raised man, through the survival of the fittest, combined with the inherited effects of habit, to his present high position in the organic scale.
The slight physical strength of humans, their limited speed, and their lack of natural weapons, etc., are more than compensated for, firstly by their intellectual abilities, which have allowed them to create weapons and tools even while still in a primitive state, and secondly by their social traits that encourage them to help each other and receive help in return. No place in the world has more dangerous animals than Southern Africa; no area presents greater physical challenges than the Arctic regions; yet one of the smallest races, the Bushmen, survive in Southern Africa, just as the diminutive Eskimos do in the Arctic. Early human ancestors were likely less intelligent and probably less socially inclined than today's most primitive tribes; however, it's entirely possible that they could have existed or even thrived if, while gradually losing their animal-like abilities such as climbing trees, they simultaneously developed their intellect. But assuming that the ancestors of humans were far more helpless and defenseless than any current savages, if they had lived on a warm continent or large island, such as Australia or New Guinea, or Borneo (the latter now home to the orangutan), they wouldn’t have faced any specific dangers. In a space as large as one of those islands, competition among tribes would have been enough, given favorable conditions, to advance humanity through the survival of the fittest, along with the inherited effects of habit, to its current high standing in the biological hierarchy.
CHAPTER V.
On the Development of Intellectual and Moral Abilities during Ancient and Civilized Times.
The advancement of the intellectual powers through natural selection—Importance of imitation—Social and moral faculties—Their development within the limits of the same tribe—Natural selection as affecting civilised nations—Evidence that civilised nations were once barbarous.
The development of intellectual abilities through natural selection—The significance of imitation—Social and moral skills—Their growth within the boundaries of the same group—Natural selection's impact on civilized nations—Proof that civilized nations were once primitive.
The subjects to be discussed in this chapter are of the highest interest, but are treated by me in a most imperfect and fragmentary manner. Mr. Wallace, in an admirable paper before referred to,221 argues that man after he had partially acquired those intellectual and moral faculties which distinguish him from the lower animals, would have been but little liable to have had his bodily structure modified through natural selection or any other means. For man is enabled through his mental faculties “to keep with an unchanged body in harmony with the changing universe.” He has great power of adapting his habits to new conditions of life. He invents weapons, tools and various stratagems, by which he procures food and defends himself. When he migrates into a colder climate he uses clothes, builds sheds, and makes fires; and, by the aid of fire, cooks food otherwise indigestible. He aids his fellow-men in many ways, and anticipates future events. Even at a remote period he practised some subdivision of labour.
The topics discussed in this chapter are very interesting, but I approach them in a rather imperfect and fragmented way. Mr. Wallace, in a wonderful paper mentioned earlier,221 argues that once humans had partially developed the intellectual and moral traits that set them apart from lower animals, they were much less likely to have their physical structure changed through natural selection or any other means. This is because humans, thanks to their mental abilities, can "maintain an unchanged body in harmony with a changing universe." They have a great capacity to adjust their habits to new living conditions. They create weapons, tools, and various strategies to obtain food and protect themselves. When they move to a colder climate, they wear clothes, build shelters, and make fires; and with fire, they cook food that would otherwise be hard to digest. They help each other in many ways and can predict future events. Even in ancient times, they practiced some form of division of labor.
The lower animals, on the other hand, must have their bodily structure modified in order to survive under greatly changed conditions. They must be rendered stronger, or acquire more effective teeth or claws, in order to defend themselves from new enemies; or they must be reduced in size so as to escape detection and danger. When they migrate into a colder climate they must become clothed with thicker fur, or have their constitutions altered. If they fail to be thus modified, they will cease to exist.
The lower animals, on the other hand, need to change their physical structure to survive in significantly altered conditions. They must get stronger or develop more effective teeth or claws to protect themselves from new threats; or they may need to shrink in size to avoid detection and danger. When they move to a colder climate, they must grow thicker fur or adapt their bodies. If they don't make these changes, they will cease to exist.
The case, however, is widely different, as Mr. Wallace has with justice insisted, in relation to the intellectual and moral faculties of man. These faculties are variable; and we have every reason to believe that the variations tend to be inherited. Therefore, if they were formerly of high importance to primeval man and to his ape-like progenitors, they would have been perfected or advanced through natural selection. Of the high importance of the intellectual faculties there can be no doubt, for man mainly owes to them his preeminent position in the world. We can see that, in the rudest state of society, the individuals who were the most sagacious, who invented and used the best weapons or traps, and who were best able to defend themselves, would rear the greatest number of offspring. The tribes which included the largest number of men thus endowed would increase in number and supplant other tribes. Numbers depend primarily on the means of subsistence, and this, partly on the physical nature of the country, but in a much higher degree on the arts which are there practised. As a tribe increases and is victorious, it is often still further increased by the absorption of other tribes.222 The stature and strength of the men of a tribe 160are likewise of some importance for its success, and these depend in part on the nature and amount of the food which can be obtained. In Europe the men of the Bronze period were supplanted by a more powerful and, judging from their sword-handles, larger-handed race;223 but their success was probably due in a much higher degree to their superiority in the arts.
The situation is quite different, as Mr. Wallace rightly pointed out, when it comes to the intellectual and moral abilities of humans. These abilities are not fixed; and we have plenty of reasons to think that variations in them can be passed down through generations. So, if they were once very important to early humans and their ape-like ancestors, they must have been refined or improved through natural selection. There’s no doubt about the vital importance of intellectual faculties, as humans largely owe their top position in the world to them. We can observe that in the most primitive societies, the individuals who were the smartest, who invented and used the best tools or traps, and who were most capable of defending themselves, would have the most children. The tribes with the highest number of such skilled individuals would grow in population and replace other tribes. Population size mainly depends on the availability of resources, which is influenced not only by the physical environment but even more by the skills practiced there. As a tribe grows and wins battles, it often expands further by absorbing other tribes.222 The height and strength of a tribe's men are also significant for its success, and these factors depend partly on the quality and quantity of food available. In Europe, the Bronze Age men were replaced by a more powerful and, based on their sword handles, larger-handed people;223 but their success was likely due to their superior skills in various arts.
All that we know about savages, or may infer from their traditions and from old monuments, the history of which is quite forgotten by the present inhabitants, shew that from the remotest times successful tribes have supplanted other tribes. Relics of extinct or forgotten tribes have been discovered throughout the civilised regions of the earth, on the wild plains of America, and on the isolated islands in the Pacific Ocean. At the present day civilised nations are everywhere supplanting barbarous nations, excepting where the climate opposes a deadly barrier; and they succeed mainly, though not exclusively, through their arts, which are the products of the intellect. It is, therefore, highly probable that with mankind the intellectual faculties have been gradually perfected through natural selection; and this conclusion is sufficient for our purpose. Undoubtedly it would have been very interesting to have traced the development of each separate faculty from the state in which it exists in the lower animals to that in which it exists in man; but neither my ability nor knowledge permit the attempt.
All that we know about primitive people, or can guess from their traditions and forgotten monuments, shows that for a very long time, successful tribes have replaced other tribes. Remnants of extinct or forgotten tribes have been found throughout civilized areas of the world, on the open plains of America, and on remote islands in the Pacific Ocean. Nowadays, civilized nations are consistently replacing uncivilized ones, except where the climate creates a deadly barrier; and they succeed mainly, though not solely, through their skills, which come from intellect. It's highly likely that human intellectual abilities have gradually improved through natural selection, and this conclusion is enough for our purposes. It would certainly be fascinating to trace the development of each individual ability from its existence in lower animals to its level in humans, but neither my skills nor knowledge allow for that attempt.
It deserves notice that as soon as the progenitors of man became social (and this probably occurred at a very early period), the advancement of the intellectual faculties will have been aided and modified in an important manner, of which we see only traces in 161the lower animals, namely, through the principle of imitation, together with reason and experience. Apes are much given to imitation, as are the lowest savages; and the simple fact previously referred to, that after a time no animal can be caught in the same place by the same sort of trap, shews that animals learn by experience, and imitate each others’ caution. Now, if some one man in a tribe, more sagacious than the others, invented a new snare or weapon, or other means of attack or defence, the plainest self-interest, without the assistance of much reasoning power, would prompt the other members to imitate him; and all would thus profit. The habitual practice of each new art must likewise in some slight degree strengthen the intellect. If the new invention were an important one, the tribe would increase in number, spread, and supplant other tribes. In a tribe thus rendered more numerous there would always be a rather better chance of the birth of other superior and inventive members. If such men left children to inherit their mental superiority, the chance of the birth of still more ingenious members would be somewhat better, and in a very small tribe decidedly better. Even if they left no children, the tribe would still include their blood-relations; and it has been ascertained by agriculturists224 that by preserving and breeding from the family of an animal, which when slaughtered was found to be valuable, the desired character has been obtained.
It’s worth noting that as soon as humans became social (which probably happened quite early on), the development of intellectual abilities would have been significantly influenced and changed, of which we see only hints in 161 lower animals, specifically through the concepts of imitation, reason, and experience. Apes are very inclined to imitate, just like the earliest humans; and the simple fact mentioned earlier, that after a while no animal can be caught in the same trap repeatedly, shows that animals learn from experience and mimic each other's caution. Now, if one person in a group, who is smarter than the others, creates a new tool or a weapon, or another method of attack or defense, their obvious self-interest, even without much reasoning, would motivate the others to copy them; and everyone would benefit. Regularly practicing each new skill would also slightly enhance their intellect. If the new invention was significant, the group would grow in size, spread out, and replace other groups. In a group that has become larger, there would always be a better chance for the birth of other innovative and talented individuals. If such individuals had children who inherited their intelligence, the likelihood of having even more inventive members would be somewhat higher, and in a very small group, significantly higher. Even if they had no children, the group would still have their relatives; and it has been shown by farmers224 that by preserving and breeding from a line of an animal that was found to be valuable when killed, the desired traits have been achieved.
Turning now to the social and moral faculties. In order that primeval men, or the ape-like progenitors of man, should have become social, they must have 162acquired the same instinctive feelings which impel other animals to live in a body; and they no doubt exhibited the same general disposition. They would have felt uneasy when separated from their comrades, for whom they would have felt some degree of love; they would have warned each other of danger, and have given mutual aid in attack or defence. All this implies some degree of sympathy, fidelity, and courage. Such social qualities, the paramount importance of which to the lower animals is disputed by no one, were no doubt acquired by the progenitors of man in a similar manner, namely, through natural selection, aided by inherited habit. When two tribes of primeval man, living in the same country, came into competition, if the one tribe included (other circumstances being equal) a greater number of courageous, sympathetic, and faithful members, who were always ready to warn each other of danger, to aid and defend each other, this tribe would without doubt succeed best and conquer the other. Let it be borne in mind how all-important, in the never-ceasing wars of savages, fidelity and courage must be. The advantage which disciplined soldiers have over undisciplined hordes follows chiefly from the confidence which each man feels in his comrades. Obedience, as Mr. Bagehot has well shewn,225 is of the highest value, for any form of government is better than none. Selfish and contentious people will not cohere, and without coherence nothing can be effected. A tribe possessing the above qualities in a high degree would spread and be victorious over other tribes; but in the course of time it would, judging from all past history, be in its turn overcome by some other 163and still more highly endowed tribe. Thus the social and moral qualities would tend slowly to advance and be diffused throughout the world.
Turning now to social and moral traits. For early humans, or the ape-like ancestors of humans, to have become social, they must have developed the same instinctive feelings that drive other animals to live in groups; and they likely showed a similar overall disposition. They would have felt uneasy when separated from their companions, for whom they would have had some level of affection; they would have warned each other of danger, and offered mutual support in attack or defense. All of this suggests some degree of empathy, loyalty, and bravery. Such social traits, which are universally acknowledged as vital for lower animals, were likely developed by humanity's ancestors in a similar way, through natural selection, supported by inherited behaviors. When two tribes of early humans living in the same area competed against each other, if one tribe had, other factors being equal, a greater number of brave, empathetic, and loyal members who were always ready to warn one another of danger and to help and protect each other, that tribe would undoubtedly have been more successful and would have overcome the other. It's important to remember how crucial loyalty and bravery must be in the endless conflicts among savages. The advantage that well-trained soldiers have over untrained groups primarily comes from the trust that each individual has in their comrades. As Mr. Bagehot has shown well, obedience is extremely important, as any form of government is better than none. Selfish and argumentative people won't stick together, and without unity, nothing can be accomplished. A tribe with these qualities at a high level would expand and achieve victory over other tribes; but over time, based on all past history, it would eventually be defeated by another tribe with even greater qualities. Thus, social and moral traits would gradually advance and spread throughout the world.
But it may be asked, how within the limits of the same tribe did a large number of members first become endowed with these social and moral qualities, and how was the standard of excellence raised? It is extremely doubtful whether the offspring of the more sympathetic and benevolent parents, or of those which were the most faithful to their comrades, would be reared in greater number than the children of selfish and treacherous parents of the same tribe. He who was ready to sacrifice his life, as many a savage has been, rather than betray his comrades, would often leave no offspring to inherit his noble nature. The bravest men, who were always willing to come to the front in war, and who freely risked their lives for others, would on an average perish in larger number than other men. Therefore it seems scarcely possible (bearing in mind that we are not here speaking of one tribe being victorious over another) that the number of men gifted with such virtues, or that the standard of their excellence, could be increased through natural selection, that is, by the survival of the fittest.
But one might wonder how, within the same tribe, a large number of members initially developed these social and moral qualities, and how the standard of excellence was raised. It's highly questionable whether the children of the more compassionate and kind parents, or those who were most loyal to their friends, would be raised in greater numbers than the children of the selfish and deceitful parents from the same tribe. Those who were willing to sacrifice their lives, as many savages have been, rather than betray their comrades, would often leave no offspring to inherit their noble traits. The bravest individuals, who were always eager to take the lead in battle and who courageously risked their lives for others, would, on average, die in greater numbers than others. Therefore, it seems almost impossible (keeping in mind that we are not discussing one tribe defeating another) that the number of individuals endowed with such virtues, or that the standard of their excellence, could be increased through natural selection, meaning by the survival of the fittest.
Although the circumstances which lead to an increase in the number of men thus endowed within the same tribe are too complex to be clearly followed out, we can trace some of the probable steps. In the first place, as the reasoning powers and foresight of the members became improved, each man would soon learn from experience that if he aided his fellow-men, he would commonly receive aid in return. From this low motive he might acquire the habit of aiding his fellows; and the habit of performing benevolent actions certainly strengthens the feeling of sympathy, which gives the164 first impulse to benevolent actions. Habits, moreover, followed during many generations probably tend to be inherited.
Although the reasons behind the increase in the number of men with such qualities in the same tribe are too complicated to clearly understand, we can identify some likely steps. First, as the reasoning skills and foresight of the members improved, each man would quickly learn from experience that if he helped his fellow men, he would often receive help in return. From this basic motivation, he might develop a habit of helping others; and the habit of doing good deeds certainly strengthens the feeling of sympathy, which inspires the initial push for benevolent actions. Additionally, habits practiced over many generations are likely to be inherited.
But there is another and much more powerful stimulus to the development of the social virtues, namely, the praise and the blame of our fellow-men. The love of approbation and the dread of infamy, as well as the bestowal of praise or blame, are primarily due, as we have seen in the third chapter, to the instinct of sympathy; and this instinct no doubt was originally acquired, like all the other social instincts, through natural selection. At how early a period the progenitors of man, in the course of their development, became capable of feeling and being impelled by the praise or blame of their fellow-creatures, we cannot, of course, say. But it appears that even dogs appreciate encouragement, praise, and blame. The rudest savages feel the sentiment of glory, as they clearly show by preserving the trophies of their prowess, by their habit of excessive boasting, and even by the extreme care which they take of their personal appearance and decorations; for unless they regarded the opinion of their comrades, such habits would be senseless.
But there is another and much stronger drive for developing social virtues: the praise and criticism of others. The desire for approval and the fear of disgrace, along with receiving praise or blame, mainly stem, as we've discussed in the third chapter, from the instinct of sympathy; and this instinct was likely developed, like all other social instincts, through natural selection. We can’t precisely determine how early in their development humans’ ancestors became able to feel motivated by the praise or blame of others. However, it seems that even dogs understand encouragement, praise, and criticism. Even the most primitive societies have a sense of glory, as seen in how they keep trophies of their achievements, their tendency to boast, and the attention they pay to their appearance and decorations; if they didn't care about their peers' opinions, these behaviors would be pointless.
They certainly feel shame at the breach of some of their lesser rules; but how far they experience remorse is doubtful. I was at first surprised that I could not recollect any recorded instances of this feeling in savages; and Sir J. Lubbock226 states that he knows of none. But if we banish from our minds all cases given in novels and plays and in death-bed confessions made to priests, I doubt whether many of us have actually witnessed remorse; though we may have often seen shame and contrition for smaller offences. Remorse is 165a deeply hidden feeling. It is incredible that a savage, who will sacrifice his life rather than betray his tribe, or one who will deliver himself up as a prisoner rather than break his parole,227 would not feel remorse in his inmost soul, though he might conceal it, if he had failed in a duty which he held sacred.
They definitely feel shame for breaking some of their lesser rules, but how much they actually feel remorse is questionable. At first, I was surprised that I couldn't remember any documented instances of this feeling in primitive people, and Sir J. Lubbock226 says he doesn't know of any either. However, if we set aside all the examples found in novels, plays, and deathbed confessions to priests, I doubt many of us have actually seen true remorse; even though we may frequently observe shame and regret for smaller offenses. Remorse is a deeply buried feeling. It's hard to believe that a primitive person who would sacrifice his life rather than betray his group, or someone who would turn themselves in as a prisoner rather than break their word,227 wouldn't feel remorse deep down inside, even if they managed to hide it, if they failed in a duty they considered sacred.
We may therefore conclude that primeval man, at a very remote period, would have been influenced by the praise and blame of his fellows. It is obvious, that the members of the same tribe would approve of conduct which appeared to them to be for the general good, and would reprobate that which appeared evil. To do good unto others—to do unto others as ye would they should do unto you,—is the foundation-stone of morality. It is, therefore, hardly possible to exaggerate the importance during rude times of the love of praise and the dread of blame. A man who was not impelled by any deep, instinctive feeling, to sacrifice his life for the good of others, yet was roused to such actions by a sense of glory, would by his example excite the same wish for glory in other men, and would strengthen by exercise the noble feeling of admiration. He might thus do far more good to his tribe than by begetting offspring with a tendency to inherit his own high character.
We can conclude that early humans, a long time ago, were influenced by the opinions of their peers. It's clear that members of the same tribe would support behaviors they believed benefited everyone, and disapprove of actions they saw as harmful. Doing good for others—treating others how you want to be treated—is the foundation of morality. Therefore, it's hard to overstate the importance of the desire for praise and the fear of blame during primitive times. A person who wasn’t driven by a strong instinct to sacrifice for others, but was motivated by a sense of honor, could inspire others to seek that same respect and help foster a sense of admiration. In this way, he might do more good for his tribe than simply having children who might inherit his good qualities.
With increased experience and reason, man perceives the more remote consequences of his actions, and the self-regarding virtues, such as temperance, chastity, &c., which during early times are, as we have before seen, utterly disregarded, come to be highly esteemed or even held sacred. I need not, however, repeat what I have said on this head in the third chapter. Ultimately a highly complex sentiment, having its first origin in the 166social instincts, largely guided by the approbation of our fellow-men, ruled by reason, self-interest, and in later times by deep religious feelings, confirmed by instruction and habit, all combined, constitute our moral sense or conscience.
As people gain more experience and understanding, they begin to recognize the long-term effects of their actions. The self-focused virtues, like self-control and chastity, which were completely ignored in earlier times, come to be greatly valued or even revered. I don't need to restate what I discussed on this topic in the third chapter. In the end, a complex feeling, originating from our social instincts and largely shaped by the approval of others, along with reason, self-interest, and, more recently, strong religious beliefs reinforced by teaching and routine, all come together to form our moral sense or conscience.
It must not be forgotten that although a high standard of morality gives but a slight or no advantage to each individual man and his children over the other men of the same tribe, yet that an advancement in the standard of morality and an increase in the number of well-endowed men will certainly give an immense advantage to one tribe over another. There can be no doubt that a tribe including many members who, from possessing in a high degree the spirit of patriotism, fidelity, obedience, courage, and sympathy, were always ready to give aid to each other and to sacrifice themselves for the common good, would be victorious over most other tribes; and this would be natural selection. At all times throughout the world tribes have supplanted other tribes; and as morality is one element in their success, the standard of morality and the number of well-endowed men will thus everywhere tend to rise and increase.
It shouldn't be overlooked that while a high moral standard may offer little or no advantage to individual men and their children compared to others in the same tribe, an improvement in moral standards and a greater number of capable individuals will definitely provide a significant edge to one tribe over another. There's no doubt that a tribe made up of many members who possess a strong sense of patriotism, loyalty, obedience, courage, and empathy, and who are always willing to support one another and sacrifice for the common good, would triumph over most other tribes; this is what natural selection looks like. Throughout history, tribes have replaced other tribes, and since morality is a key factor in their success, the standards of morality and the number of capable individuals will inevitably rise and expand everywhere.
It is, however, very difficult to form any judgment why one particular tribe and not another has been successful and has risen in the scale of civilisation. Many savages are in the same condition as when first discovered several centuries ago. As Mr. Bagehot has remarked, we are apt to look at progress as the normal rule in human society; but history refutes this. The ancients did not even entertain the idea; nor do the oriental nations at the present day. According to another high authority, Mr. Maine,228 “the greatest part of mankind has never 167shewn a particle of desire that its civil institutions should be improved.” Progress seems to depend on many concurrent favourable conditions, far too complex to be followed out. But it has often been remarked, that a cool climate from leading to industry and the various arts has been highly favourable, or even indispensable for this end. The Esquimaux, pressed by hard necessity, have succeeded in many ingenious inventions, but their climate has been too severe for continued progress. Nomadic habits, whether over wide plains, or through the dense forests of the tropics, or along the shores of the sea, have in every case been highly detrimental. Whilst observing the barbarous inhabitants of Tierra del Fuego, it struck me that the possession of some property, a fixed abode, and the union of many families under a chief, were the indispensable requisites for civilisation. Such habits almost necessitate the cultivation of the ground; and the first steps in cultivation would probably result, as I have elsewhere shewn,229 from some such accident as the seeds of a fruit-tree falling on a heap of refuse and producing an unusually fine variety. The problem, however, of the first advance of savages towards civilisation is at present much too difficult to be solved.
It’s really tough to understand why one tribe succeeds and rises in civilization while others do not. Many groups are in the same state as when they were first discovered centuries ago. As Mr. Bagehot pointed out, we tend to view progress as the norm in human society, but history tells a different story. The ancients didn’t even consider the idea, and neither do many Eastern nations today. According to another respected figure, Mr. Maine,228 “most people have never shown any desire for their civil institutions to be improved.” Progress seems to rely on many favorable conditions that are too complex to fully understand. It has been noted that a cooler climate, which can promote industry and various arts, has been very helpful, if not essential, for progress. The Eskimos, pushed by necessity, have come up with many clever inventions, but their harsh climate has hindered sustained progress. Nomadic lifestyles, whether across vast plains, through dense tropical forests, or along seashores, have generally been very harmful. While observing the primitive people of Tierra del Fuego, I realized that having some property, a stable home, and the grouping of multiple families under a leader are essential for civilization. Such lifestyles almost require agricultural development; the first steps in farming could likely come from an incident like fruit tree seeds falling on a pile of waste and producing an unusually great variety. However, the question of how savages first move toward civilization is currently way too complicated to answer.
Natural Selection as affecting Civilised Nations.—In the last and present chapters I have considered the advancement of man from a former semi-human condition to his present state as a barbarian. But some remarks on the agency of natural selection on civilised nations may be here worth adding. This subject has been ably discussed by Mr. W. R. Greg,230 and previously 168by Mr. Wallace and Mr. Galton.231 Most of my remarks are taken from these three authors. With savages, the weak in body or mind are soon eliminated; and those that survive commonly exhibit a vigorous state of health. We civilised men, on the other hand, do our utmost to check the process of elimination; we build asylums for the imbecile, the maimed, and the sick; we institute poor-laws; and our medical men exert their utmost skill to save the life of every one to the last moment. There is reason to believe that vaccination has preserved thousands, who from a weak constitution would formerly have succumbed to small-pox. Thus the weak members of civilised societies propagate their kind. No one who has attended to the breeding of domestic animals will doubt that this must be highly injurious to the race of man. It is surprising how soon a want of care, or care wrongly directed, leads to the degeneration of a domestic race; but excepting in the case of man himself, hardly any one is so ignorant as to allow his worst animals to breed.
Natural Selection as Affecting Civilized Nations.—In the last and current chapters, I have looked at how humanity has progressed from a previous semi-human state to our current condition as a barbarian. However, it's worth adding some thoughts on how natural selection impacts civilized nations. This topic has been effectively explored by Mr. W. R. Greg,230 and earlier by Mr. Wallace and Mr. Galton.231 Most of my observations come from these three authors. Among savages, those who are weak in body or mind are quickly eliminated, and the survivors generally show a robust state of health. We civilized people, however, do everything we can to stop this process of elimination; we create asylums for the mentally impaired, disabled, and sick; we implement welfare laws; and our medical professionals do their very best to extend the life of everyone to the very end. There’s reason to believe that vaccinations have saved thousands who would have previously died from smallpox due to weak constitutions. As a result, the weaker members of civilized societies continue to reproduce. Anyone who has paid attention to breeding domestic animals knows that this must be highly detrimental to the human race. It's surprising how quickly a lack of care, or care that is misdirected, leads to the decline of a domestic breed; but aside from humans, hardly anyone is so negligent as to allow their worst animals to breed.
The aid which we feel impelled to give to the helpless is mainly an incidental result of the instinct of sympathy, which was originally acquired as part of the social instincts, but subsequently rendered, in the manner previously indicated, more tender and more widely diffused. Nor could we check our sympathy, if so urged by hard reason, without deterioration in the 169noblest part of our nature. The surgeon may harden himself whilst performing an operation, for he knows that he is acting for the good of his patient; but if we were intentionally to neglect the weak and helpless, it could only be for a contingent benefit, with a certain and great present evil. Hence we must bear without complaining the undoubtedly bad effects of the weak surviving and propagating their kind; but there appears to be at least one check in steady action, namely the weaker and inferior members of society not marrying so freely as the sound; and this check might be indefinitely increased, though this is more to be hoped for than expected, by the weak in body or mind refraining from marriage.
The help we feel compelled to give to those who can't help themselves mostly comes from our instinct to sympathize, which we developed as part of our social instincts. Over time, this instinct has become more compassionate and widespread. We couldn't suppress our sympathy, even if logic urged us to, without degrading the best parts of our nature. A surgeon might toughen up while doing a procedure because he understands he's acting for his patient's benefit; however, if we deliberately ignored the weak and helpless, it would only bring a potential future benefit at a significant current cost. Therefore, we must accept, without complaint, the undeniably negative consequences of the weak surviving and reproducing. But there seems to be at least one ongoing check: weaker and less capable members of society tend not to marry as easily as the strong do. This check could potentially be strengthened, although it's more of a hope than an expectation, if those who are physically or mentally weak choose to avoid marriage.
In all civilised countries man accumulates property and bequeaths it to his children. So that the children in the same country do not by any means start fair in the race for success. But this is far from an unmixed evil; for without the accumulation of capital the arts could not progress; and it is chiefly through their power that the civilised races have extended, and are now everywhere extending, their range, so as to take the place of the lower races. Nor does the moderate accumulation of wealth interfere with the process of selection. When a poor man becomes rich, his children enter trades or professions in which there is struggle enough, so that the able in body and mind succeed best. The presence of a body of well-instructed men, who have not to labour for their daily bread, is important to a degree which cannot be over-estimated; as all high intellectual work is carried on by them, and on such work material progress of all kinds mainly depends, not to mention other and higher advantages. No doubt wealth when very great tends to convert men into useless drones, but their number is never large; and some degree of elimi170nation here occurs, as we daily see rich men, who happen to be fools or profligate, squandering away all their wealth.
In all civilized countries, people accumulate wealth and pass it down to their children. As a result, children in the same country don’t exactly start off on equal footing in the competition for success. However, this isn’t entirely a bad thing; without the accumulation of capital, the arts couldn’t advance, and it’s largely through their influence that civilized societies have grown and continue to expand their influence, replacing less developed societies. Moreover, the moderate accumulation of wealth doesn’t hinder the process of selection. When a poor individual becomes wealthy, their children enter industries or professions where competition is strong, allowing the most capable physically and mentally to excel. The existence of a group of well-educated individuals who don’t need to work for their daily survival is extremely valuable; all advanced intellectual work is conducted by them, and this work is primarily what drives material progress of all kinds, not to mention other and greater benefits. Certainly, when wealth becomes excessive, it can sometimes turn individuals into unproductive leeches, but their numbers are never significant; a certain level of elimination occurs here, as we frequently observe wealthy individuals who are foolish or reckless wasting away all their money.
Primogeniture with entailed estates is a more direct evil, though it may formerly have been a great advantage by the creation of a dominant class, and any government is better than anarchy. The eldest sons, though they may be weak in body or mind, generally marry, whilst the younger sons, however superior in these respects, do not so generally marry. Nor can worthless eldest sons with entailed estates squander their wealth. But here, as elsewhere, the relations of civilised life are so complex that some compensatory checks intervene. The men who are rich through primogeniture are able to select generation after generation the more beautiful and charming women; and these must generally be healthy in body and active in mind. The evil consequences, such as they may be, of the continued preservation of the same line of descent, without any selection, are checked by men of rank always wishing to increase their wealth and power; and this they effect by marrying heiresses. But the daughters of parents who have produced single children, are themselves, as Mr. Galton has shewn,232 apt to be sterile; and thus noble families are continually cut off in the direct line, and their wealth flows into some side channel; but unfortunately this channel is not determined by superiority of any kind.
Primogeniture with entailed estates is a more direct issue, even though it may have once been a significant benefit by creating a dominant class, and any government is better than chaos. The oldest sons, even if they are weak in body or mind, usually get married, while younger sons, who are often superior in these areas, tend not to marry as often. Also, unworthy eldest sons with entailed estates can’t waste their wealth. However, like many things in civilized life, the situation is complex, and there are some balancing factors involved. Men who gain wealth through primogeniture can continuously choose the most beautiful and charming women for generations, and these women tend to be healthy and mentally active. The negative consequences, if any, of keeping the same line of descent without any selection are mitigated by men of rank who always want to increase their wealth and power; they do this by marrying heiresses. But, as Mr. Galton has shown,232 daughters of parents who only have one child often tend to be infertile, which leads to noble families being frequently cut off in the direct line, and their wealth ends up flowing into some alternative path; unfortunately, this alternative path is not based on any kind of superiority.
Although civilisation thus checks in many ways the action of natural selection, it apparently favours, by means of improved food and the freedom from occasional hardships, the better development of the body. This may be inferred from civilised men having been 171found, wherever compared, to be physically stronger than savages. They appear also to have equal powers of endurance, as has been proved in many adventurous expeditions. Even the great luxury of the rich can be but little detrimental; for the expectation of life of our aristocracy, at all ages and of both sexes, is very little inferior to that of healthy English lives in the lower classes.233
Even though civilization limits natural selection in many ways, it seems to promote better physical development due to improved nutrition and reduced hardships. This is suggested by the fact that civilized individuals, when compared, are generally stronger than those living in more primitive conditions. They also show comparable endurance, as evidenced by various adventurous expeditions. Even the considerable luxury enjoyed by the wealthy doesn't seem to have much negative impact; the life expectancy of our upper class, at all ages and for both genders, is only slightly lower than that of healthy individuals in the lower classes.
We will now look to the intellectual faculties alone. If in each grade of society the members were divided into two equal bodies, the one including the intellectually superior and the other the inferior, there can be little doubt that the former would succeed best in all occupations and rear a greater number of children. Even in the lowest walks of life, skill and ability must be of some advantage, though in many occupations, owing to the great division of labour, a very small one. Hence in civilised nations there will be some tendency to an increase both in the number and in the standard of the intellectually able. But I do not wish to assert that this tendency may not be more than counterbalanced in other ways, as by the multiplication of the reckless and improvident; but even to such as these, ability must be some advantage.
We will now focus on intellectual capabilities alone. If we were to divide the members of each social class into two equal groups, one consisting of the intellectually superior and the other of the inferior, it’s quite clear that the former would excel in all kinds of work and raise more children. Even in the most basic jobs, skills and abilities must offer some advantage, although in many fields, especially due to the high division of labor, that advantage might be minimal. Therefore, in developed nations, there will likely be a trend towards an increase both in the number and quality of intellectually capable individuals. However, I’m not claiming that this trend cannot be outweighed by other factors, like the growth of the careless and short-sighted; yet, even for these individuals, having some level of ability must still provide some benefit.
It has often been objected to views like the foregoing, that the most eminent men who have ever lived have left no offspring to inherit their great intellect. Mr. Galton says,234 “I regret I am unable to solve the simple question whether, and how far, men and women who are prodigies of genius are infertile. I have, however, shewn that men of eminence are by no means so.”
It has often been argued against views like the one above, that the greatest individuals who have ever lived left no descendants to inherit their remarkable intelligence. Mr. Galton says,234 “I regret that I cannot determine the straightforward question of whether, and to what extent, exceptional men and women are unable to have children. However, I have shown that eminent men are certainly not in that category.”
Great lawgivers, the founders of beneficent religions, great philosophers and discoverers in science, aid the progress of mankind in a far higher degree by their works than by leaving a numerous progeny. In the case of corporeal structures, it is the selection of the slightly better-endowed and the elimination of the slightly less well-endowed individuals, and not the preservation of strongly-marked and rare anomalies, that leads to the advancement of a species.235 So it will be with the intellectual faculties, namely from the somewhat more able men in each grade of society succeeding rather better than the less able, and consequently increasing in number, if not otherwise prevented. When in any nation the standard of intellect and the number of intellectual men have increased, we may expect from the law of the deviation from an average, as shewn by Mr. Galton, that prodigies of genius will appear somewhat more frequently than before.
Great lawgivers, founders of helpful religions, great philosophers, and pioneers in science contribute to human progress far more through their works than by having many children. In the case of physical structures, it's the selection of slightly better-equipped individuals and the removal of slightly less capable ones that drives the advancement of a species. So it will be with intellectual abilities; those who are somewhat more capable in each level of society will succeed better than the less capable, thus increasing in number unless something prevents it. When a nation's level of intelligence and the number of intelligent people increase, we can expect, according to the law of deviation from an average demonstrated by Mr. Galton, that extraordinary talents will emerge somewhat more frequently than before.
In regard to the moral qualities, some elimination of the worst dispositions is always in progress even in the most civilised nations. Malefactors are executed, or imprisoned for long periods, so that they cannot freely transmit their bad qualities. Melancholic and insane persons are confined, or commit suicide. Violent and quarrelsome men often come to a bloody end. Restless men who will not follow any steady occupation—and this relic of barbarism is a great check to civilisation236—emigrate to newly-settled countries, where they prove useful pioneers. Intemperance is so highly destructive, that the expectation of life of the intemperate, at the age, for instance, of thirty, is only 13.8 years; whilst for the rural labourers of England at the same age it is 17340·59 years.237 Profligate women bear few children, and profligate men rarely marry; both suffer from disease. In the breeding of domestic animals, the elimination of those individuals, though few in number, which are in any marked manner inferior, is by no means an unimportant element towards success. This especially holds good with injurious characters which tend to reappear through reversion, such as blackness in sheep; and with mankind some of the worst dispositions, which occasionally without any assignable cause make their appearance in families, may perhaps be reversions to a savage state, from which we are not removed by very many generations. This view seems indeed recognised in the common expression that such men are the black sheep of the family.
In terms of moral qualities, there is always an ongoing process of removing the worst traits, even in the most civilized nations. Criminals are executed or imprisoned for long periods so they can’t pass on their negative traits. Those who are depressed or mentally ill are often confined or take their own lives. Violent and contentious individuals frequently meet a violent end. Restless people who refuse to settle into any steady job—this remnant of barbarism is a major hindrance to civilization—move to newly-settled areas, where they end up being valuable pioneers. Alcoholism is incredibly destructive; for example, the life expectancy of someone who is alcoholic at the age of thirty is only 13.8 years, while rural laborers in England at the same age have a life expectancy of 40.59 years. Immoral women tend to have fewer children, and immoral men rarely marry; both are plagued by health issues. In breeding domestic animals, getting rid of individuals that are notably inferior, even if they are few, is a crucial factor for success. This is especially true for detrimental traits that tend to resurface due to genetics, such as blackness in sheep; similarly, some of the worst traits in humans, which can surface in families without any apparent reason, may be throwbacks to a savage state we aren’t separated from by many generations. This perspective is reflected in the saying that such individuals are the black sheep of the family.
With civilised nations, as far as an advanced standard of morality, and an increased number of fairly well-endowed men are concerned, natural selection apparently effects but little; though the fundamental social instincts were originally thus gained. But I have already said enough, whilst treating of the lower races, on the causes which lead to the advance of morality, namely, the approbation of our fellow-men—the strengthening of our sympathies by habit—example and imitation—reason—experience and even self-interest—instruction during youth, and religious feelings.
With civilized nations, when it comes to a high standard of morality and an increasing number of well-equipped individuals, natural selection seems to have minimal impact; although our basic social instincts were originally developed this way. However, I've already said enough about the lower races regarding the factors that contribute to the advancement of morality, such as the approval of others, the strengthening of our sympathies through habit, example, and imitation, reason, experience, and even self-interest, as well as education in youth and religious feelings.
A most important obstacle in civilised countries to an increase in the number of men of a superior class has been strongly urged by Mr. Greg and Mr. Galton,238 174namely, the fact that the very poor and reckless, who are often degraded by vice, almost invariably marry early, whilst the careful and frugal, who are generally otherwise virtuous, marry late in life, so that they may be able to support themselves and their children in comfort. Those who marry early produce within a given period not only a greater number of generations, but, as shewn by Dr. Duncan,239 they produce many more children. The children, moreover, that are born by mothers during the prime of life are heavier and larger, and therefore probably more vigorous, than those born at other periods. Thus the reckless, degraded, and often vicious members of society, tend to increase at a quicker rate than the provident and generally virtuous members. Or as Mr. Greg puts the case: “The careless, squalid, unaspiring Irishman multiplies like rabbits: the frugal, foreseeing, self-respecting, ambitious Scot, stern in his morality, spiritual in his faith, sagacious and disciplined in his intelligence, passes his best years in struggle and in celibacy, marries late, and leaves few behind him. Given a land originally peopled by a thousand Saxons and a thousand Celts—and in a dozen generations five-sixths of the population would be Celts, but five-sixths of the property, of the power, of the intellect, would belong to the one-sixth of Saxons that remained. In the eternal ‘struggle for existence,’ it would be the inferior and less favoured race that had prevailed—and prevailed by virtue not of its good qualities but of its faults.”
A significant barrier in developed countries to an increase in the number of high-class individuals has been strongly pointed out by Mr. Greg and Mr. Galton,238 174specifically, the fact that the very poor and reckless, who are often degraded by vice, tend to marry early, while the careful and frugal, who are generally virtuous, marry later in life so they can support themselves and their children comfortably. Those who marry early produce not only more generations in a given timeframe but, as shown by Dr. Duncan,239 they also have many more children. Additionally, babies born to mothers during their prime years are heavier and larger, and therefore likely more vigorous than those born at other times. Consequently, the reckless, degraded, and often vicious members of society tend to grow in number more quickly than the prudent and generally virtuous members. As Mr. Greg puts it: “The careless, squalid, unaspiring Irishman multiplies like rabbits: the frugal, foresighted, self-respecting, ambitious Scot, stern in his morality, spiritual in his faith, wise and disciplined in his intelligence, spends his best years struggling and remaining single, marries late, and leaves few behind. Given a land originally populated by a thousand Saxons and a thousand Celts—in just a dozen generations, five-sixths of the population would be Celts, but five-sixths of the property, power, and intelligence would still belong to the one-sixth of Saxons that remained. In the ongoing ‘struggle for existence,’ it would be the inferior and less favored race that prevailed—and prevailed not because of their virtues but because of their flaws.”
There are, however, some checks to this downward tendency. We have seen that the intemperate suffer 175from a high rate of mortality, and the extremely profligate leave few offspring. The poorest classes crowd into towns, and it has been proved by Dr. Stark from the statistics of ten years in Scotland,240 that at all ages the death-rate is higher in towns than in rural districts, “and during the first five years of life the town death-rate is almost exactly double that of the rural districts.” As these returns include both the rich and the poor, no doubt more than double the number of births would be requisite to keep up the number of the very poor inhabitants in the towns, relatively to those in the country. With women, marriage at too early an age is highly injurious; for it has been found in France that, “twice as many wives under twenty die in the year, as died out of the same number of the unmarried.” The mortality, also, of husbands under twenty is “excessively high,”241 but what the cause of this may be seems doubtful. Lastly, if the men who prudently delay marrying until they can bring up their families in comfort, were to select, as they often do, women in the prime of life, the rate of increase in the better class would be only slightly lessened.
There are, however, some limits to this downward trend. We have observed that excessive drinkers have a high mortality rate, and the extremely reckless usually have few children. The poorest populations flock to cities, and Dr. Stark has shown through ten years of statistics in Scotland that at all ages the death rate is higher in urban areas than in rural ones, “and during the first five years of life the town death rate is almost exactly double that of the rural areas.” Since these statistics include both the wealthy and the poor, it's clear that more than double the number of births would be needed to maintain the population of the very poor in cities compared to those in the countryside. For women, marrying too young is very harmful; in France, it has been found that “twice as many wives under twenty die in a year compared to the same number of unmarried women.” The mortality rate for husbands under twenty is also “excessively high,” but the reason for this remains uncertain. Lastly, if men who wisely wait to marry until they can support their families comfortably choose women in their prime, the growth rate among the better-off class would only be slightly reduced.
It was established from an enormous body of statistics, taken during 1853, that the unmarried men throughout France, between the ages of twenty and eighty, die in a much larger proportion than the married: for instance, out of every 1000 unmarried men, between the ages of twenty and thirty, 11·3 annually died, whilst of the married only 6·5 died.242 A similar law was proved to 176hold good, during the years 1863 and 1864, with the entire population above the age of twenty in Scotland: for instance, out of every 1000 unmarried men, between the ages of twenty and thirty, 14·97 annually died, whilst of the married only 7·24 died, that is less than half.243 Dr. Stark remarks on this, “Bachelorhood is more destructive to life than the most unwholesome trades, or than residence in an unwholesome house or district where there has never been the most distant attempt at sanitary improvement.” He considers that the lessened mortality is the direct result of “marriage, and the more regular domestic habits which attend that state.” He admits, however, that the intemperate, profligate, and criminal classes, whose duration of life is low, do not commonly marry; and it must likewise be admitted that men with a weak constitution, ill health, or any great infirmity in body or mind, will often not wish to marry, or will be rejected. Dr. Stark seems to have come to the conclusion that marriage in itself is a main cause of prolonged life, from finding that aged married men still have a considerable advantage in this respect over the unmarried of the same advanced age; but every one must have known instances of men, who with weak health during youth did not marry, and yet have survived to old age, though remaining weak and therefore always with a lessened chance of life. There is another remarkable circumstance which seems to support Dr. Stark’s conclusion, namely, that widows and widowers in France suffer in comparison with the married a very heavy rate of mortality; but Dr. Farr attributes this to the poverty and 177evil habits consequent on the disruption of the family, and to grief. On the whole we may conclude with Dr. Farr that the lesser mortality of married than of unmarried men, which seems to be a general law, “is mainly due to the constant elimination of imperfect types, and to the skilful selection of the finest individuals out of each successive generation;” the selection relating only to the marriage state, and acting on all corporeal, intellectual, and moral qualities. We may, therefore, infer that sound and good men who out of prudence remain for a time unmarried do not suffer a high rate of mortality.
It was determined from a large amount of data collected in 1853 that unmarried men in France, aged twenty to eighty, have a significantly higher mortality rate than married men. For example, out of every 1000 unmarried men aged twenty to thirty, 11.3 died each year, while only 6.5 married men died.242 A similar trend was observed during 1863 and 1864 among all individuals over twenty in Scotland: out of every 1000 unmarried men aged twenty to thirty, 14.97 died annually compared to just 7.24 married men, which is less than half.243 Dr. Stark comments on this, stating, “Bachelorhood is more harmful to life than the most unhealthy jobs or living in a bad neighborhood where there has never been any effort to improve conditions.” He believes that the lower mortality rate is directly related to “marriage and the more stable home life that comes with it.” He does acknowledge that the intemperate, immoral, and criminal classes, who generally have a shorter lifespan, tend not to marry, and it should also be noted that men with weak health or significant physical or mental disabilities often choose not to marry or are rejected. Dr. Stark seems to conclude that marriage is a key factor in extending life, noting that elderly married men have a considerable longevity advantage over their unmarried peers of the same age; however, many have seen instances of men with poor health in their youth who remained unmarried and still live to old age, even though they remained weak and thus always had a lower chance of survival. Another notable observation supporting Dr. Stark's conclusion is that widows and widowers in France experience much higher mortality rates compared to married individuals; however, Dr. Farr attributes this to the poverty and negative habits that follow the breakdown of a family, as well as to grief. Overall, we may agree with Dr. Farr that the lower mortality rate of married men compared to unmarried ones, which seems to be a widespread trend, “is mainly due to the continual elimination of weaker types and to the careful selection of the best individuals from each generation,” with this selection relating only to the marital state and impacting all physical, intellectual, and moral attributes. Therefore, we can conclude that decent and sensible men who choose to remain unmarried for a while due to prudence do not experience a high mortality rate.
If the various checks specified in the two last paragraphs, and perhaps others as yet unknown, do not prevent the reckless, the vicious and otherwise inferior members of society from increasing at a quicker rate than the better class of men, the nation will retrograde, as has occurred too often in the history of the world. We must remember that progress is no invariable rule. It is most difficult to say why one civilised nation rises, becomes more powerful, and spreads more widely, than another; or why the same nation progresses more at one time than at another. We can only say that it depends on an increase in the actual number of the population, on the number of the men endowed with high intellectual and moral faculties, as well as on their standard of excellence. Corporeal structure, except so far as vigour of body leads to vigour of mind, appears to have little influence.
If the various checks mentioned in the last two paragraphs, and maybe others that we haven't identified yet, don't stop the reckless, the immoral, and the less capable members of society from increasing at a faster rate than the more respectable individuals, the nation will decline, as has happened too often throughout history. We need to remember that progress is not guaranteed. It's hard to explain why one civilized nation advances, becomes more powerful, and spreads more widely than another, or why the same nation progresses more at certain times than at others. We can only say that it relies on a growth in the actual population, on the number of people with high intellectual and moral abilities, as well as their standard of excellence. Physical strength, except to the extent that physical vigor leads to mental vigor, seems to have little impact.
It has been urged by several writers that as high intellectual powers are advantageous to a nation, the old Greeks, who stood some grades higher in intellect than any race that has ever existed,244 ought to have 178risen, if the power of natural selection were real, still higher in the scale, increased in number, and stocked the whole of Europe. Here we have the tacit assumption, so often made with respect to corporeal structures, that there is some innate tendency towards continued development in mind and body. But development of all kinds depends on many concurrent favourable circumstances. Natural selection acts only in a tentative manner. Individuals and races may have acquired certain indisputable advantages, and yet have perished from failing in other characters. The Greeks may have retrograded from a want of coherence between the many small states, from the small size of their whole country, from the practice of slavery, or from extreme sensuality; for they did not succumb until “they were enervated and corrupt to the very core.”245 The western nations of Europe, who now so immeasurably surpass their former savage progenitors and stand at the summit of civilisation, owe little or none of their superiority to direct inheritance from the old Greeks; though they owe much to the written works of this wonderful people.
Several writers have argued that since high intellectual abilities benefit a nation, the ancient Greeks, who were intellectually superior to any race that has ever existed,244 should have advanced even further in development, increased in population, and populated all of Europe if natural selection truly worked. This implies an assumption, often applied to physical traits, that there is an inherent drive for ongoing development in both mind and body. However, all types of development depend on various favorable conditions happening at the same time. Natural selection only works sporadically. Individuals and groups might acquire certain clear advantages but still disappear due to lacking other important traits. The Greeks might have declined because of a lack of unity among their many small states, the limited size of their nation, the practice of slavery, or their excessive indulgence; they didn’t fall until they were “weakened and corrupt to the very core.”245 The western nations of Europe, which now far exceed their former savage ancestors and are at the peak of civilization, owe little or nothing of their superiority to direct inheritance from the ancient Greeks, though they do owe a lot to the written works of this remarkable culture.
Who can positively say why the Spanish nation, so dominant at one time, has been distanced in the race. The awakening of the nations of Europe from the dark ages is a still more perplexing problem. At this early period, as Mr. Galton246 has remarked, almost all the men of a gentle nature, those given to meditation or culture of the mind, had no refuge except in the bosom of the Church which demanded celibacy; 179and this could hardly fail to have had a deteriorating influence on each successive generation. During this same period the Holy Inquisition selected with extreme care the freest and boldest men in order to burn or imprison them. In Spain alone some of the best men—those who doubted and questioned, and without doubting there can be no progress—were eliminated during three centuries at the rate of a thousand a year. The evil which the Catholic Church has thus effected, though no doubt counterbalanced to a certain, perhaps large extent in other ways, is incalculable; nevertheless, Europe has progressed at an unparalleled rate.
Who can truly explain why the Spanish nation, once so powerful, has fallen behind in the race? The awakening of the nations of Europe from the dark ages is an even more confusing issue. At this early time, as Mr. Galton246 pointed out, almost all of the more gentle men, those inclined toward meditation and intellectual pursuits, found no refuge except within the Church, which required celibacy; 179 and this likely had a negative impact on each successive generation. During this same time, the Holy Inquisition meticulously targeted the most free-spirited and daring individuals for execution or imprisonment. In Spain alone, some of the finest minds—those who dared to question and doubt, and without questioning, there can be no progress—were eliminated at a rate of about a thousand a year over three centuries. The harm that the Catholic Church has caused, while perhaps offset by other factors to some extent, is immeasurable; yet, Europe has advanced at an unprecedented pace.
The remarkable success of the English as colonists over other European nations, which is well illustrated by comparing the progress of the Canadians of English and French extraction, has been ascribed to their “daring and persistent energy;” but who can say how the English gained their energy. There is apparently much truth in the belief that the wonderful progress of the United States, as well as the character of the people, are the results of natural selection; the more energetic, restless, and courageous men from all parts of Europe having emigrated during the last ten or twelve generations to that great country, and having there succeeded best.247 Looking to the distant future, I do not think that the Rev. Mr. Zincke takes an exaggerated view when he says:248 “All other series of events—as that which resulted in the culture of mind in Greece, and that which resulted in the empire of Rome—only appear to have purpose and value when viewed in connection with, or rather as subsidiary to ... the great stream of Anglo-Saxon emigration to the west.”
The impressive success of the English as colonizers compared to other European nations is clearly shown when we look at the development of Canadians of English and French descent. This success has been attributed to their "daring and persistent energy," but it’s hard to say exactly how the English developed this energy. There seems to be a lot of truth in the idea that the significant progress of the United States, along with the nature of its people, is due to natural selection. Over the last ten or twelve generations, the more energetic, restless, and brave individuals from various parts of Europe have emigrated to that vast country and thrived there. Looking ahead, I don’t believe the Rev. Mr. Zincke is being overly dramatic when he states: “All other series of events—as that which resulted in the culture of mind in Greece, and that which resulted in the empire of Rome—only appear to have purpose and value when viewed in connection with, or rather as subsidiary to ... the great stream of Anglo-Saxon emigration to the west.”
Obscure as is the problem of the advance of civilisation, we can at least see that a nation which produced during a lengthened period the greatest number of highly intellectual, energetic, brave, patriotic, and benevolent men, would generally prevail over less favoured nations.
Obscure as the issue of civilization's progress may be, we can at least see that a nation that consistently produces the most highly intelligent, energetic, brave, patriotic, and compassionate people would generally come out on top against less fortunate nations.
Natural selection follows from the struggle for existence; and this from a rapid rate of increase. It is impossible not bitterly to regret, but whether wisely is another question, the rate at which man tends to increase; for this leads in barbarous tribes to infanticide and many other evils, and in civilised nations to abject poverty, celibacy, and to the late marriages of the prudent. But as man suffers from the same physical evils with the lower animals, he has no right to expect an immunity from the evils consequent on the struggle for existence. Had he not been subjected to natural selection, assuredly he would never have attained to the rank of manhood. When we see in many parts of the world enormous areas of the most fertile land peopled by a few wandering savages, but which are capable of supporting numerous happy homes, it might be argued that the struggle for existence had not been sufficiently severe to force man upwards to his highest standard. Judging from all that we know of man and the lower animals, there has always been sufficient variability in the intellectual and moral faculties, for their steady advancement through natural selection. No doubt such advancement demands many favourable concurrent circumstances; but it may well be doubted whether the most favourable would have sufficed, had not the rate of increase been rapid, and the consequent struggle for existence severe to an extreme degree.
Natural selection comes from the struggle for survival; and this results from a rapid population growth. It’s hard not to feel a deep regret, though whether that's wise is another question, about how quickly humans tend to increase; this leads to infanticide and other negative issues in primitive tribes, and in more developed societies, it results in extreme poverty, singleness, and delayed marriages among those who are cautious. However, since humans face the same physical challenges as lower animals, they have no right to expect immunity from the struggles that come with survival. If humans hadn’t gone through natural selection, they would certainly not have achieved their current level of development. When we see vast fertile lands in many parts of the world inhabited by only a few nomadic peoples, lands that could easily support many thriving homes, one could argue that the struggle for existence hasn’t been severe enough to push humanity towards its highest potential. Based on everything we know about humans and lower animals, there has always been enough variability in intellectual and moral abilities for continuous progress through natural selection. Certainly, such progress requires many favorable conditions; but it's reasonable to question whether the best circumstances would have been enough without rapid population growth and an extremely severe struggle for survival.
On the evidence that all civilised nations were once barbarous.—As we have had to consider the steps by which181 some semi-human creature has been gradually raised to the rank of man in his most perfect state, the present subject cannot be quite passed over. But it has been treated in so full and admirable a manner by Sir J. Lubbock,249 Mr. Tylor, Mr. M’Lennan, and others, that I need here give only the briefest summary of their results. The arguments recently advanced by the Duke of Argyll250 and formerly by Archbishop Whately, in favour of the belief that man came into the world as a civilised being and that all savages have since undergone degradation, seem to me weak in comparison with those advanced on the other side. Many nations, no doubt, have fallen away in civilisation, and some may have lapsed into utter barbarism, though on this latter head I have not met with any evidence. The Fuegians were probably compelled by other conquering hordes to settle in their inhospitable country, and they may have become in consequence somewhat more degraded; but it would be difficult to prove that they have fallen much below the Botocudos who inhabit the finest parts of Brazil.
On the evidence that all civilized nations were once barbaric.—As we have had to consider the steps by which181 some semi-human creature has gradually evolved into man in his most perfect state, the current topic cannot be completely overlooked. However, it has already been addressed in such a comprehensive and impressive way by Sir J. Lubbock,249 Mr. Tylor, Mr. M’Lennan, and others, that I will only provide a brief summary of their findings. The arguments recently presented by the Duke of Argyll250 and previously by Archbishop Whately, suggesting that man entered the world as a civilized being and that all savages have since experienced degradation, seem to me weak compared to those put forward on the opposite side. Many nations have indeed declined in civilization, and some may have descended into complete barbarism, though I have not encountered any evidence to support this last point. The Fuegians were probably forced by other conquering groups to settle in their harsh environment, which may have led to them becoming somewhat more degraded; however, it would be challenging to prove that they have fallen significantly below the Botocudos who live in the finest regions of Brazil.
The evidence that all civilised nations are the descendants of barbarians, consists, on the one side, of clear traces of their former low condition in still-existing customs, beliefs, language, &c.; and on the other side, of proofs that savages are independently able to raise themselves a few steps in the scale of civilisation, and have actually thus risen. The evidence on the first head is extremely curious, but cannot be here given: I refer to such cases as that, for instance, of the art of enumeration, which, as Mr. Tylor clearly shews by the words still used in some places, originated in counting 182the fingers, first of one hand and then of the other, and lastly of the toes. We have traces of this in our own decimal system, and in the Roman numerals, which after reaching to the number V., change into VI., &c., when the other hand no doubt was used. So again, “when we speak of three-score and ten, we are counting by the vigesimal system, each score thus ideally made, standing for 20—for ‘one man’ as a Mexican or Carib would put it.”251 According to a large and increasing school of philologists, every language bears the marks of its slow and gradual evolution. So it is with the art of writing, as letters are rudiments of pictorial representations. It is hardly possible to read Mr. M’Lennan’s work252 and not admit that almost all civilised nations still retain some traces of such rude habits as the forcible capture of wives. What ancient nation, as the same author asks, can be named that was originally monogamous? The primitive idea of justice, as shewn by the law of battle and other customs of which traces still remain, was likewise most rude. Many existing superstitions are the remnants of former false religious beliefs. The highest form of religion—the grand idea of God hating sin and loving righteousness—was unknown during primeval times.
The proof that all civilized nations are descendants of barbarians comes from two sides: first, the clear signs of their earlier low status that still exist in customs, beliefs, language, etc.; and second, evidence that savages can independently improve their civilization and have actually done so. The evidence for the first point is quite fascinating but can't be provided here: I refer to examples like the art of counting, which, as Mr. Tylor clearly illustrates through words still in use in some places, started with counting on fingers—first one hand, then the other, and finally the toes. We can see this in our decimal system and in Roman numerals, which after reaching V., shift to VI., etc., indicating that the other hand was likely used. Additionally, when we talk about three-score and ten, we’re using a vigesimal counting system, where each score represents 20, or as a Mexican or Carib might say, "one man." According to a growing group of linguists, every language shows signs of its slow and gradual development. The same goes for writing, where letters are the basics of pictorial representations. It’s hard to read Mr. M’Lennan’s work without recognizing that nearly all civilized nations still hold traces of such primitive practices as the forceful taking of wives. What ancient nation, as he questions, can be identified as originally monogamous? The basic notion of justice, as demonstrated by the law of battle and other customs still evident, was also quite crude. Many current superstitions are leftover remnants of earlier false religious beliefs. The highest form of religion—the grand idea of God disapproving of sin and loving righteousness—was unknown in ancient times.
Turning to the other kind of evidence: Sir J. Lubbock has shewn that some savages have recently improved a little in some of their simpler arts. From the 183extremely curious account which he gives of the weapons, tools, and arts, used or practised by savages in various parts of the world, it cannot be doubted that these have nearly all been independent discoveries, excepting perhaps the art of making fire.253 The Australian boomerang is a good instance of one such independent discovery. The Tahitians when first visited had advanced in many respects beyond the inhabitants of most of the other Polynesian islands. There are no just grounds for the belief that the high culture of the native Peruvians and Mexicans was derived from any foreign source;254 many native plants were there cultivated, and a few native animals domesticated. We should bear in mind that a wandering crew from some semi-civilised land, if washed to the shores of America, would not, judging from the small influence of most missionaries, have produced any marked effect on the natives, unless they had already become somewhat advanced. Looking to a very remote period in the history of the world, we find, to use Sir J. Lubbock’s well-known terms, a paleolithic and neolithic period; and no one will pretend that the art of grinding rough flint tools was a borrowed one. In all parts of Europe, as far east as Greece, in Palestine, India, Japan, New Zealand, and Africa, including Egypt, flint tools have been discovered in abundance; and of their use the existing inhabitants retain no tradition. There is also indirect evidence of their former use by the Chinese and ancient Jews. Hence there can hardly be a doubt that the inhabitants of these many countries, which include nearly the whole civilised world, were once in a barbarous condition. To believe that man was aboriginally 184 civilised and then suffered utter degradation in so many regions, is to take a pitiably low view of human nature. It is apparently a truer and more cheerful view that progress has been much more general than retrogression; that man has risen, though by slow and interrupted steps, from a lowly condition to the highest standard as yet attained by him in knowledge, morals, and religion.
Turning to the other kind of evidence: Sir J. Lubbock has shown that some groups of people have recently made slight improvements in some of their simpler skills. From the extremely interesting account he provides of the weapons, tools, and skills used by various groups around the world, it's clear that these have mostly been independent discoveries, except perhaps the skill of making fire. The Australian boomerang is a good example of such an independent invention. The Tahitians, when first visited, were more advanced in many ways compared to the inhabitants of many other Polynesian islands. There’s no solid basis for believing that the advanced culture of the native Peruvians and Mexicans came from any foreign influence; many native plants were cultivated there, and a few native animals were domesticated. We should remember that a wandering group from some semi-civilized land, if washed ashore in America, likely wouldn’t have had a significant impact on the natives, judging by the minimal influence of most missionaries, unless the natives were already somewhat advanced. Looking back to a very early period in history, we see, using Sir J. Lubbock's well-known terms, a paleolithic and neolithic period; and no one would claim that the art of grinding rough flint tools was borrowed. Flint tools have been found in abundance all over Europe, as far east as Greece, in Palestine, India, Japan, New Zealand, and Africa, including Egypt; and the existing inhabitants have no traditions about their use. There’s also indirect evidence of their former use by the Chinese and ancient Jews. Thus, there is hardly any doubt that the people in these numerous countries, which encompass nearly the entire civilized world, were once in a barbaric state. To believe that humans were originally civilized and then fell into degradation across so many regions is to have a sadly low view of human nature. It appears to be a more accurate and optimistic view that progress has been much more widespread than regression; that humanity has risen, though through slow and intermittent steps, from a lowly state to the highest standards yet achieved in knowledge, morals, and religion.
CHAPTER VI.
On the Connections and Family Tree of Humanity.
Position of man in the animal series—The natural system genealogical—Adaptive characters of slight value—Various small points of resemblance between man and the Quadrumana—Rank of man in the natural system—Birthplace and antiquity of man—Absence of fossil connecting-links—Lower stages in the genealogy of man, as inferred, firstly from his affinities and secondly from his structure—Early androgynous condition of the Vertebrata—Conclusion.
Position of humans in the animal kingdom—The natural system genealogically—Adaptive traits of little significance—Various minor similarities between humans and the primates—The ranking of humans in the natural system—The origin and ancient history of humans—Lack of fossil evidence connecting links—Earlier stages in the evolution of humans, based on their relationships and structure—Early mixed-sex condition of vertebrates—Conclusion.
Even if it be granted that the difference between man and his nearest allies is as great in corporeal structure as some naturalists maintain, and although we must grant that the difference between them is immense in mental power, yet the facts given in the previous chapters declare, as it appears to me, in the plainest manner, that man is descended from some lower form, notwithstanding that connecting-links have not hitherto been discovered.
Even if we accept that the difference between humans and their closest relatives is as significant in physical structure as some naturalists argue, and while we have to acknowledge that the gap in mental capacity is enormous, the facts presented in the previous chapters indicate, to me, in the clearest way, that humans have evolved from some lower form, even though we haven't yet found any connecting links.
Man is liable to numerous, slight, and diversified variations, which are induced by the same general causes, are governed and transmitted in accordance with the same general laws, as in the lower animals. Man tends to multiply at so rapid a rate that his offspring are necessarily exposed to a struggle for existence, and consequently to natural selection. He has given rise to many races, some of which are so different that they have often been ranked by naturalists as distinct species. His body is constructed on the same homological plan as that of other mammals, independently of the uses to which the several parts may be put. He186 passes through the same phases of embryological development. He retains many rudimentary and useless structures, which no doubt were once serviceable. Characters occasionally make their reappearance in him, which we have every reason to believe were possessed by his early progenitors. If the origin of man had been wholly different from that of all other animals, these various appearances would be mere empty deceptions; but such an admission is incredible. These appearances, on the other hand, are intelligible, at least to a large extent, if man is the co-descendant with other mammals of some unknown and lower form.
Humans are subject to numerous, slight, and varied changes, which are caused by the same general factors, governed and passed down according to the same basic laws as in lower animals. Humans tend to reproduce at such a rapid pace that their offspring inevitably face a struggle for survival, and thus experience natural selection. Humans have given rise to many races, some of which are so different that naturalists have often classified them as distinct species. The human body is structured on the same basic plan as that of other mammals, regardless of how its various parts are used. He186 goes through the same stages of embryonic development. He retains many rudimentary and useless structures that were likely once functional. Traits occasionally resurface in him that we believe were present in his early ancestors. If the origin of humans were completely different from that of all other animals, these various traits would be nothing but illusions; however, that idea is hard to accept. On the other hand, these traits make sense, at least to a significant extent, if humans share a common ancestor with other mammals from some unknown and simpler form.
Some naturalists, from being deeply impressed with the mental and spiritual powers of man, have divided the whole organic world into three kingdoms, the Human, the Animal, and the Vegetable, thus giving to man a separate kingdom.255 Spiritual powers cannot be compared or classed by the naturalist; but he may endeavour to shew, as I have done, that the mental faculties of man and the lower animals do not differ in kind, although immensely in degree. A difference in degree, however great, does not justify us in placing man in a distinct kingdom, as will perhaps be best illustrated by comparing the mental powers of two insects, namely, a coccus or scale-insect and an ant, which undoubtedly belong to the same class. The difference is here greater, though of a somewhat different kind, than that between man and the highest mammal. The female coccus, whilst young, attaches itself by its proboscis to a plant; sucks the sap but never moves again; is fertilised and lays eggs; and this is its whole history. On the other hand, to describe the habits and mental 187powers of a female ant, would require, as Pierre Huber has shewn, a large volume; I may, however, briefly specify a few points. Ants communicate information to each other, and several unite for the same work, or games of play. They recognise their fellow-ants after months of absence. They build great edifices, keep them clean, close the doors in the evening, and post sentries. They make roads, and even tunnels under rivers. They collect food for the community, and when an object, too large for entrance, is brought to the nest, they enlarge the door, and afterwards build it up again.256 They go out to battle in regular bands, and freely sacrifice their lives for the common weal. They emigrate in accordance with a preconcerted plan. They capture slaves. They keep Aphides as milch-cows. They move the eggs of their aphides, as well as their own eggs and cocoons, into warm parts of the nest, in order that they may be quickly hatched; and endless similar facts could be given. On the whole, the difference in mental power between an ant and a coccus is immense; yet no one has ever dreamed of placing them in distinct classes, much less in distinct kingdoms. No doubt this interval is bridged over by the intermediate mental powers of many other insects; and this is not the case with man and the higher apes. But we have every reason to believe that breaks in the series are simply the result of many forms having become extinct.
Some naturalists, deeply impressed by the mental and spiritual abilities of humans, have divided the entire organic world into three kingdoms: Humans, Animals, and Plants, thus granting humans their own separate kingdom.255 Spiritual powers can't be compared or classified by naturalists; however, they can attempt to show, as I have, that the mental abilities of humans and lower animals differ not in kind, but in degree—though that degree is vast. A difference in degree, no matter how significant, doesn’t justify placing humans in a distinct kingdom, which can be illustrated by comparing the mental abilities of two insects: a coccus (scale insect) and an ant, both of which undoubtedly belong to the same class. The difference here is greater, albeit of a slightly different nature, than that between humans and the most advanced mammals. The female coccus, while young, attaches itself to a plant with its proboscis, sucks the sap, and then never moves again; it gets fertilized and lays eggs, and that’s its entire life story. In contrast, to describe the behaviors and mental abilities of a female ant would take, as Pierre Huber has shown, a large volume; I can, however, briefly point out a few key details. Ants share information with one another and often work together for tasks or play. They recognize their fellow ants after months apart. They construct impressive structures, keep them clean, close the entrances at night, and set up guards. They create paths and even tunnels under rivers. They gather food for their community, and when an object is too large to fit through the entrance, they enlarge the door and then rebuild it later.256 They go into battle in organized groups and willingly sacrifice their lives for the greater good. They migrate according to prearranged plans. They capture slaves. They tend to aphids like livestock. They move the eggs of their aphids, as well as their own eggs and cocoons, to warmer areas of the nest so they can hatch faster; and there are countless similar examples. Overall, the difference in mental abilities between an ant and a coccus is immense, yet no one has ever suggested placing them in separate classes, much less in separate kingdoms. This gap is undoubtedly filled by the intermediate mental abilities of many other insects; however, the same cannot be said for humans and higher apes. We have every reason to believe that gaps in the continuum are simply due to many forms becoming extinct.
Professor Owen, relying chiefly on the structure of the brain, has divided the mammalian series into four sub-classes. One of these he devotes to man; in another he places both the marsupials and the monotremata; so that he makes man as distinct from all other mam188mals as are these two latter groups conjoined. This view has not been accepted, as far as I am aware, by any naturalist capable of forming an independent judgment, and therefore need not here be further considered.
Professor Owen, mainly based on the structure of the brain, has categorized mammals into four subclasses. He devotes one of these to humans; in another, he includes both marsupials and monotremes. This means he views humans as being as distinct from all other mammals as these two groups are from each other. To my knowledge, this perspective hasn't been accepted by any naturalist who can form an independent judgment, so there's no need to discuss it further here.
We can understand why a classification founded on any single character or organ—even an organ so wonderfully complex and important as the brain—or on the high development of the mental faculties, is almost sure to prove unsatisfactory. This principle has indeed been tried with hymenopterous insects; but when thus classed by their habits or instincts, the arrangement proved thoroughly artificial.257 Classifications may, of course, be based on any character whatever, as on size, colour, or the element inhabited; but naturalists have long felt a profound conviction that there is a natural system. This system, it is now generally admitted, must be, as far as possible, genealogical in arrangement,—that is, the co-descendants of the same form must be kept together in one group, separate from the co-descendants of any other form; but if the parent-forms are related, so will be their descendants, and the two groups together will form a larger group. The amount of difference between the several groups—that is the amount of modification which each has undergone—will be expressed by such terms as genera, families, orders, and classes. As we have no record of the lines of descent, these lines can be discovered only by observing the degrees of resemblance between the beings which are to be classed. For this object numerous points of resemblance are of much more importance than the amount of similarity or dissimilarity in a few points. If two languages were found to resemble each other in a multitude of 189words and points of construction, they would be universally recognised as having sprung from a common source, notwithstanding that they differed greatly in some few words or points of construction. But with organic beings the points of resemblance must not consist of adaptations to similar habits of life: two animals may, for instance, have had their whole frames modified for living in the water, and yet they will not be brought any nearer to each other in the natural system. Hence we can see how it is that resemblances in unimportant structures, in useless and rudimentary organs, and in parts not as yet fully developed or functionally active, are by far the most serviceable for classification; for they can hardly be due to adaptations within a late period; and thus they reveal the old lines of descent or of true affinity.
We can see why a classification based on any single trait or organ—even one as complex and important as the brain—or on the advanced development of mental abilities is likely to be unsatisfactory. This idea has been tested with hymenopterous insects; however, when categorized by their behaviors or instincts, the classification turned out to be completely artificial.257 Classifications can, of course, be based on any characteristic, like size, color, or habitat; but naturalists have long believed there is a natural system. It’s now widely accepted that this system should ideally be organized genealogically—that is, the co-descendants of the same form should be grouped together, separate from the co-descendants of any other form; and if the parent forms are related, their descendants will be too, creating a larger group. The level of difference between the various groups—that is, how much each has changed—will be defined by terms like genera, families, orders, and classes. Since we don’t have records of the lines of descent, these lines can only be determined by looking at the degrees of similarity among the entities being classified. For this purpose, many points of resemblance are far more significant than the level of similarity or dissimilarity in just a few aspects. If two languages share many words and structural features, they would be widely recognized as having a common origin, even if they differ significantly in a few words or constructions. However, with living organisms, points of similarity shouldn’t come from adaptations to similar lifestyles: for instance, two animals might have evolved their entire bodies for aquatic living, yet they wouldn’t be classified any closer together in the natural system. This shows why similarities in less significant structures, in useless and rudimentary organs, and in parts that haven’t fully developed or aren’t functionally active are the most useful for classification; they’re unlikely to result from more recent adaptations and thus reveal the older lines of descent or true relationships.
We can further see why a great amount of modification in some one character ought not to lead us to separate widely any two organisms. A part which already differs much from the same part in other allied forms has already, according to the theory of evolution, varied much; consequently it would (as long as the organism remained exposed to the same exciting conditions) be liable to further variations of the same kind; and these, if beneficial, would be preserved, and thus continually augmented. In many cases the continued development of a part, for instance, of the beak of a bird, or of the teeth of a mammal, would not be advantageous to the species for gaining its food, or for any other object; but with man we can see no definite limit, as far as advantage is concerned, to the continued development of the brain and mental faculties. Therefore in determining the position of man in the natural or genealogical system, the extreme development of his brain ought not to outweigh a multitude of resem190blances in other less important or quite unimportant points.
We can also understand why significant changes in a single characteristic should not lead us to consider two organisms as completely separate. A part that already differs a lot from the same part in related species has already experienced considerable variation, according to evolutionary theory. Therefore, as long as the organism continues to face the same environmental pressures, it is likely to undergo further changes of the same type. If these changes are beneficial, they will be preserved and will continue to increase. In many cases, the ongoing development of a specific part, such as a bird's beak or a mammal's teeth, may not actually help the species in obtaining food or any other function. However, when it comes to humans, there doesn't seem to be a clear limit to how much the brain and mental abilities can develop in terms of benefit. So, when we're considering where humans fit in the natural or evolutionary classification, the highly developed brain shouldn't overshadow the many similarities in other less critical or even trivial traits.
The greater number of naturalists who have taken into consideration the whole structure of man, including his mental faculties, have followed Blumenbach and Cuvier, and have placed man in a separate Order, under the title of the Bimana, and therefore on an equality with the Orders of the Quadrumana, Carnivora, &c. Recently many of our best naturalists have recurred to the view first propounded by Linnæus, so remarkable for his sagacity, and have placed man in the same Order with the Quadrumana, under the title of the Primates. The justice of this conclusion will be admitted if, in the first place, we bear in mind the remarks just made on the comparatively small importance for classification of the great development of the brain in man; bearing, also, in mind that the strongly-marked differences between the skulls of man and the Quadrumana (lately insisted upon by Bischoff, Aeby, and others) apparently follow from their differently developed brains. In the second place, we must remember that nearly all the other and more important differences between man and the Quadrumana are manifestly adaptive in their nature, and relate chiefly to the erect position of man; such as the structure of his hand, foot, and pelvis, the curvature of his spine, and the position of his head. The family of seals offers a good illustration of the small importance of adaptive characters for classification. These animals differ from all other Carnivora in the form of their bodies and in the structure of their limbs, far more than does man from the higher apes; yet in every system, from that of Cuvier to the most recent one by Mr. Flower,258 seals are ranked as a mere family 191in the Order of the Carnivora. If man had not been his own classifier, he would never have thought of founding a separate order for his own reception.
The majority of naturalists who have looked at the complete structure of humans, including mental abilities, have followed Blumenbach and Cuvier, placing humans in a separate Order called Bimana, which puts them on the same level as the Orders of Quadrumana, Carnivora, etc. Recently, many top naturalists have returned to the perspective first suggested by Linnæus, known for his keen insight, and have categorized humans with the Quadrumana under the title of Primates. This conclusion seems fair if we consider, first, the earlier comments about the relative unimportance of brain size for classification; and second, that the significant differences in skull structure between humans and Quadrumana (recently emphasized by Bischoff, Aeby, and others) likely stem from the differences in their brain development. Additionally, we need to remember that most of the key differences between humans and Quadrumana are clearly adaptive and mainly relate to the upright posture of humans; this includes the structure of their hands, feet, and pelvis, the curvature of their spines, and the positioning of their heads. The seal family presents a good example of the limited significance of adaptive traits in classification. These animals differ from all other Carnivora in body shape and limb structure much more than humans differ from higher apes; yet, in every classification system, from Cuvier's to the latest by Mr. Flower,258 seals are categorized as just a family within the Order of Carnivora. If humans hadn't classified themselves, they would never have considered creating a separate order for their own classification.
It would be beyond my limits, and quite beyond my knowledge, even to name the innumerable points of structure in which man agrees with the other Primates. Our great anatomist and philosopher, Prof. Huxley, has fully discussed this subject,259 and has come to the conclusion that man in all parts of his organisation differs less from the higher apes, than these do from the lower members of the same group. Consequently there “is no justification for placing man in a distinct order.”
It would be beyond my limits and quite outside my knowledge to even name the countless aspects of structure in which humans are similar to other primates. Our renowned anatomist and philosopher, Prof. Huxley, has thoroughly explored this topic,259 and has concluded that humans differ less in all aspects of their organization from the higher apes than these apes do from the lower members of the same group. Therefore, there is “no justification for placing humans in a distinct order.”
In an early part of this volume I brought forward various facts, shewing how closely man agrees in constitution with the higher mammals; and this agreement, no doubt, depends on our close similarity in minute structure and chemical composition. I gave, as instances, our liability to the same diseases, and to the attacks of allied parasites; our tastes in common for the same stimulants, and the similar effects thus produced, as well as by various drugs; and other such facts.
In an earlier section of this book, I presented several facts showing how closely humans are similar in structure to higher mammals. This similarity undoubtedly comes from our comparable minute structures and chemical makeup. I provided examples, such as our susceptibility to the same diseases and attacks from related parasites; our shared preferences for the same stimulants and the similar effects they produce; along with various other related observations.
As small unimportant points of resemblance between man and the higher apes are not commonly noticed in systematic works, and as, when numerous, they clearly reveal our relationship, I will specify a few such points. The relative position of the features are manifestly the same in man and the Quadrumana; and the various emotions are displayed by nearly similar movements of the muscles and skin, chiefly above the eyebrows and round the mouth. Some few expressions are, indeed, almost the same, as in the weeping of certain kinds of monkeys, and in the laughing noise made by others, during which the corners of the mouth are drawn back192wards, and the lower eyelids wrinkled. The external ears are curiously alike. In man the nose is much more prominent than in most monkeys; but we may trace the commencement of an aquiline curvature in the nose of the Hoolock Gibbon; and this in the Semnopithecus nasica is carried to a ridiculous extreme.
As small, unimportant similarities between humans and higher apes aren't typically highlighted in systematic studies, and since they clearly show our connection when there are many, I’ll point out a few of these similarities. The arrangement of features is evidently the same in humans and the Quadrumana, and various emotions are expressed through nearly identical movements of the muscles and skin, especially above the eyebrows and around the mouth. Some expressions are indeed almost the same, like the crying of certain types of monkeys and the laughing sounds made by others, where the corners of the mouth are pulled back192and the lower eyelids wrinkle. The outer ears are surprisingly similar. In humans, the nose is much more prominent than in most monkeys; however, we can see the beginning of a hooked shape in the nose of the Hoolock Gibbon, and this is exaggerated to a comical degree in the Semnopithecus nasica.
The faces of many monkeys are ornamented with beards, whiskers, or moustaches. The hair on the head grows to a great length in some species of Semnopithecus;260 and in the Bonnet monkey (Macacus radiatus) it radiates from a point on the crown, with a parting down the middle, as in man. It is commonly said that the forehead gives to man his noble and intellectual appearance; but the thick hair on the head of the Bonnet monkey terminates abruptly downwards, and is succeeded by such short and fine hair, or down, that at a little distance the forehead, with the exception of the eyebrows, appears quite naked. It has been erroneously asserted that eyebrows are not present in any monkey. In the species just named the degree of nakedness of the forehead differs in different individuals; and Eschricht states261 that in our children the limit between the hairy scalp and the naked forehead is sometimes not well defined; so that here we seem to have a trifling case of reversion to a progenitor, in whom the forehead had not as yet become quite naked.
The faces of many monkeys are decorated with beards, whiskers, or mustaches. In some species of Semnopithecus, the hair on the head grows very long; and in the Bonnet monkey (Macacus radiatus), it spreads out from a point on the crown, with a part down the middle, just like humans. People often say that the forehead gives humans their noble and intellectual appearance, but the thick hair on the Bonnet monkey's head ends abruptly, followed by short and fine hair, or down, making it look like the forehead is almost completely bare from a distance, except for the eyebrows. It's a common mistake to say that monkeys don't have eyebrows. In the species mentioned, the degree of hairlessness on the forehead varies among individuals; and Eschricht notes that in our children, the division between the hairy scalp and the bare forehead is sometimes not very clear, suggesting a slight case of reversion to an ancestor where the forehead wasn’t fully bare yet.
It is well known that the hair on our arms tends to converge from above and below to a point at the elbow. This curious arrangement, so unlike that in most of the lower mammals, is common to the gorilla, chimpanzee, orang, some species of Hylobates, and even to some few American monkeys. But in Hylobates agilis the hair 193on the fore-arm is directed downwards or towards the wrist in the ordinary manner; and in H. lar it is nearly erect, with only a very slight forward inclination; so that in this latter species it is in a transitional state. It can hardly be doubted that with most mammals the thickness of the hair and its direction on the back is adapted to throw off the rain; even the transverse hairs on the fore-legs of a dog may serve for this end when he is coiled up asleep. Mr. Wallace remarks that the convergence of the hair towards the elbow on the arms of the orang (whose habits he has so carefully studied) serves to throw off the rain, when, as is the custom of this animal, the arms are bent, with the hands clasped round a branch or over its own head. We should, however, bear in mind that the attitude of an animal may perhaps be in part determined by the direction of the hair; and not the direction of the hair by the attitude. If the above explanation is correct in the case of the orang, the hair on our fore-arms offers a curious record of our former state; for no one supposes that it is now of any use in throwing off the rain, nor in our present erect condition is it properly directed for this purpose.
It’s well-known that the hair on our arms tends to come together from above and below at the elbow. This odd pattern, which is quite different from that of most lower mammals, is typical of gorillas, chimpanzees, orangutans, some species of gibbons, and even a few American monkeys. However, in Hylobates agilis, the hair on the forearm points downwards towards the wrist like normal; and in H. lar, it stands almost upright, with just a slight forward tilt, indicating that in this species it is in a transitional state. It’s hard to deny that for most mammals, the thickness of the hair and its direction on the back are designed to shed rain; even the crosswise hairs on a dog’s forelegs may help with this when it's curled up asleep. Mr. Wallace notes that the way the hair converges towards the elbow on the orang's arms (which he has studied thoroughly) works to repel rain when, as is typical for this animal, the arms are bent with the hands grasped around a branch or above its head. However, we should keep in mind that an animal's posture might partly be influenced by the hair's direction, rather than the other way around. If this explanation holds true for the orang, the hair on our forearms provides an interesting record of our past; since no one thinks it’s currently useful for shedding rain, and in our upright position, it isn't oriented properly for that purpose.
It would, however, be rash to trust too much to the principle of adaptation in regard to the direction of the hair in man or his early progenitors; for it is impossible to study the figures given by Eschricht of the arrangement of the hair on the human fœtus (this being the same as in the adult) and not agree with this excellent observer that other and more complex causes have intervened. The points of convergence seem to stand in some relation to those points in the embryo which are last closed in during development. There appears, also, to exist some relation between the arrangement194 of the hair on the limbs, and the course of the medullary arteries.262
It would be unwise to rely too much on the idea of adaptation when it comes to the direction of hair in humans or their early ancestors. It's impossible to look at Eschricht's diagrams of hair arrangement on human fetuses— which is the same as in adults— and not agree with this great observer that there are other, more complex factors at play. The points of convergence seem to be related to those areas in the embryo that close last during development. There also appears to be a connection between the hair arrangement on the limbs and the path of the medullary arteries.194262
It must not be supposed that the resemblances between man and certain apes in the above and many other points—such as in having a naked forehead, long tresses on the head, &c.—are all necessarily the result of unbroken inheritance from a common progenitor thus characterised, or of subsequent reversion. Many of these resemblances are more probably due to analogous variation, which follows, as I have elsewhere attempted to shew,263 from co-descended organisms having a similar constitution and having been acted on by similar causes inducing variability. With respect to the similar direction of the hair on the fore-arms of man and certain monkeys, as this character is common to almost all the anthropomorphous apes, it may probably be attributed to inheritance; but not certainly so, as some very distinct American monkeys are thus characterised. The same remark is applicable to the tailless condition of man; for the tail is absent in all the anthropomorphous apes. Nevertheless this character cannot with certainty be attributed to inheritance, as the tail, though not absent, is rudimentary in several other Old World and in some New World species, and is quite absent in several species belonging to the allied group of Lemurs.
It shouldn't be assumed that the similarities between humans and certain apes in the mentioned points—like having a bare forehead, long hair, etc.—are all necessarily the result of unbroken inheritance from a common ancestor with these traits or of later reversion. Many of these similarities are more likely due to analogous variation, which follows, as I have tried to show elsewhere, from co-descended organisms with a similar structure that have been influenced by similar factors causing variability. Regarding the similar direction of hair on the forearms of humans and certain monkeys, since this trait is common among almost all anthropoid apes, it might be attributed to inheritance; but this isn't certain, as some distinct American monkeys also exhibit this characteristic. The same observation applies to the lack of a tail in humans because the tail is absent in all anthropoid apes. However, this trait can't be definitively attributed to inheritance since the tail, although not absent, is rudimentary in several other Old World and some New World species, and is completely absent in several species in the related group of lemurs.
Although, as we have now seen, man has no just right to form a separate Order for his own reception, he may 195perhaps claim a distinct Sub-order or Family. Prof. Huxley, in his last work,264 divides the Primates into three Sub-orders; namely, the Anthropidæ with man alone, the Simiadæ including monkeys of all kinds, and the Lemuridæ with the diversified genera of lemurs. As far as differences in certain important points of structure are concerned, man may no doubt rightly claim the rank of a Sub-order; and this rank is too low, if we look chiefly to his mental faculties. Nevertheless, under a genealogical point of view it appears that this rank is too high, and that man ought to form merely a Family, or possibly even only a Sub-family. If we imagine three lines of descent proceeding from a common source, it is quite conceivable that two of them might after the lapse of ages be so slightly changed as still to remain as species of the same genus; whilst the third line might become so greatly modified as to deserve to rank as a distinct Sub-family, Family, or even Order. But in this case it is almost certain that the third line would still retain through inheritance numerous small points of resemblance with the other two lines. Here then would occur the difficulty, at present insoluble, how much weight we ought to assign in our classifications to strongly-marked differences in some few points,—that is to the amount of modification undergone; and how much to close resemblance in numerous unimportant points, as indicating the lines of descent or genealogy. The former alternative is the most obvious, and perhaps the safest, though the latter appears the most correct as giving a truly natural classification.
Even though, as we've seen, humans don't really have a valid claim to create a separate Order just for themselves, they might be able to argue for a distinct Sub-order or Family. Prof. Huxley, in his latest work, divides the Primates into three Sub-orders: the Anthropidæ, which includes only humans, the Simiadæ, which includes all kinds of monkeys, and the Lemuridæ, which consists of the diverse genera of lemurs. Regarding certain key structural differences, humans can certainly be considered a Sub-order; however, this classification seems too low when we focus mainly on their mental capabilities. On the other hand, from a genealogical perspective, this classification seems too high, and humans should really just be categorized as a Family, or maybe even just a Sub-family. If we think about three lines of descent coming from a common ancestor, it's entirely possible that two of them might change very little over time and remain as species within the same genus, while the third line could become so different that it deserves its own Sub-family, Family, or even Order. However, in this case, it's almost certain that the third line would still inherit many small similarities with the other two lines. This raises the current unsolvable issue of how much importance we should place in our classifications on striking differences in a few characteristics—that is, the extent of modification undergone—and how much we should consider close resemblance in many less significant traits, as indicators of descent or genealogy. The first option is the most straightforward and probably the safest, while the second seems more accurate for a truly natural classification.
To form a judgment on this head, with reference to man we must glance at the classification of the 196Simiadæ. This family is divided by almost all naturalists into the Catarhine group, or Old World monkeys, all of which are characterised (as their name expresses) by the peculiar structure of their nostrils and by having four premolars in each jaw; and into the Platyrhine group or New World monkeys (including two very distinct sub-groups), all of which are characterised by differently-constructed nostrils and by having six premolars in each jaw. Some other small differences might be mentioned. Now man unquestionably belongs in his dentition, in the structure of his nostrils, and some other respects, to the Catarhine or Old World division; nor does he resemble the Platyrhines more closely than the Catarhines in any characters, excepting in a few of not much importance and apparently of an adaptive nature. Therefore it would be against all probability to suppose that some ancient New World species had varied, and had thus produced a man-like creature with all the distinctive characters proper to the Old World division; losing at the same time all its own distinctive characters. There can consequently hardly be a doubt that man is an offshoot from the Old World Simian stem; and that under a genealogical point of view, he must be classed with the Catarhine division.265
To form a judgment on this topic regarding humans, we need to take a look at the classification of the 196Simiadæ. This family is divided by nearly all naturalists into the Catarhine group, or Old World monkeys, all of which are characterized (as their name suggests) by the unique structure of their nostrils and by having four premolars in each jaw; and into the Platyrhine group, or New World monkeys (which includes two very distinct sub-groups), all of which are characterized by differently-structured nostrils and by having six premolars in each jaw. There are some other minor differences to mention. Now, humans undoubtedly belong, in terms of their teeth, nostril structure, and a few other characteristics, to the Catarhine or Old World group; they do not resemble the Platyrhines more closely than the Catarhines in any features, except for a few that are not very significant and seem adaptive. Therefore, it would be highly unlikely to assume that some ancient New World species changed and thus produced a human-like creature with all the distinct traits typical of the Old World group while simultaneously losing all of its own unique features. Thus, there is hardly any doubt that humans are a branch of the Old World Simian lineage; and from a genealogical perspective, they must be classified with the Catarhine group.265
The anthropomorphous apes, namely the gorilla, chimpanzee, orang, and hylobates, are separated as a distinct sub-group from the other Old World monkeys by most naturalists. I am aware that Gratiolet, relying on the structure of the brain, does not admit the exist197ence of this sub-group, and no doubt it is a broken one; thus the orang, as Mr. St. G. Mivart remarks,266 “is one of the most peculiar and aberrant forms to be found in the Order.” The remaining, non-anthropomorphous, Old World monkeys, are again divided by some naturalists into two or three smaller sub-groups; the genus Semnopithecus, with its peculiar sacculated stomach, being the type of one such sub-group. But it appears from M. Gaudry’s wonderful discoveries in Attica, that during the Miocene period a form existed there, which connected Semnopithecus and Macacus; and this probably illustrates the manner in which the other and higher groups were once blended together.
The anthropomorphic apes, specifically the gorilla, chimpanzee, orangutan, and gibbons, are classified as a distinct subgroup from other Old World monkeys by most naturalists. I know that Gratiolet, based on brain structure, doesn’t recognize the existence of this subgroup, and it’s likely incomplete; as Mr. St. G. Mivart notes, “the orangutan is one of the most unique and unusual forms to be found in the Order.” The remaining non-anthropomorphic Old World monkeys are further divided by some naturalists into two or three smaller subgroups; the genus Semnopithecus, known for its unique sacculated stomach, is the type for one of these subgroups. However, M. Gaudry’s remarkable discoveries in Attica suggest that during the Miocene period, a form existed there that linked Semnopithecus and Macacus; and this likely shows how the other and higher groups were once interconnected.
If the anthropomorphous apes be admitted to form a natural sub-group, then as man agrees with them, not only in all those characters which he possesses in common with the whole Catarhine group, but in other peculiar characters, such as the absence of a tail and of callosities and in general appearance, we may infer that some ancient member of the anthropomorphous sub-group gave birth to man. It is not probable that a member of one of the other lower sub-groups should, through the law of analogous variation, have given rise to a man-like creature, resembling the higher anthropomorphous apes in so many respects. No doubt man, in comparison with most of his allies, has undergone an extraordinary amount of modification, chiefly in consequence of his greatly developed brain and erect position; nevertheless we should bear in mind that he “is but one of several exceptional forms of Primates.”267
If we accept that the anthropomorphous apes form a natural sub-group, then since humans share not only the traits common to the entire Catarhine group but also other unique features, like the absence of a tail and callosities, as well as general appearance, we can conclude that some ancient member of this anthropomorphous sub-group gave rise to humans. It's unlikely that a member of one of the other lower sub-groups could have given rise to a human-like creature that shares so many characteristics with the higher anthropomorphous apes through analogous variation. Certainly, humans have undergone remarkable changes compared to most of their relatives, mainly due to their highly developed brains and upright posture; however, we should remember that humans “are just one of several exceptional forms of Primates.”267
Every naturalist, who believes in the principle of 198evolution, will grant that the two main divisions of the Simiadæ, namely the Catarhine and Platyrhine monkeys, with their sub-groups, have all proceeded from some one extremely ancient progenitor. The early descendants of this progenitor, before they had diverged to any considerable extent from each other, would still have formed a single natural group; but some of the species or incipient genera would have already begun to indicate by their diverging characters the future distinctive marks of the Catarhine and Platyrhine divisions. Hence the members of this supposed ancient group would not have been so uniform in their dentition or in the structure of their nostrils, as are the existing Catarhine monkeys in one way and the Platyrhines in another way, but would have resembled in this respect the allied Lemuridæ which differ greatly from each other in the form of their muzzles,268 and to an extraordinary degree in their dentition.
Every naturalist who believes in the concept of evolution recognizes that the two main groups of Simiadæ, specifically the Catarhine and Platyrhine monkeys, along with their sub-groups, all originated from a single, very ancient ancestor. The early descendants of this ancestor, before they had significantly diverged from each other, would still have formed a single natural group; however, some species or early genera would have started to show diverging traits that hinted at the future differences between the Catarhine and Platyrhine groups. As a result, the members of this hypothetical ancient group would not have been as consistent in their dental structure or the shape of their nostrils as the current Catarhine monkeys are in one way and the Platyrhines in another, but would have more closely resembled the related Lemuridæ, which vary greatly in the shape of their muzzles and even more in their dental characteristics.
The Catarhine and Platyrhine monkeys agree in a multitude of characters, as is shewn by their unquestionably belonging to one and the same Order. The many characters which they possess in common can hardly have been independently acquired by so many distinct species; so that these characters must have been inherited. But an ancient form which possessed many characters common to the Catarhine and Platyrhine monkeys, and others in an intermediate condition, and some few perhaps distinct from those now present in either group, would undoubtedly have been ranked, if seen by a naturalist, as an ape or monkey. And as man under a genealogical point of view belongs to the Catarhine or Old World stock, we must conclude, how199ever much the conclusion may revolt our pride, that our early progenitors would have been properly thus designated.269 But we must not fall into the error of supposing that the early progenitor of the whole Simian stock, including man, was identical with, or even closely resembled, any existing ape or monkey.
The Catarhine and Platyrhine monkeys share many traits, clearly demonstrating that they belong to the same Order. The numerous traits they have in common likely weren’t developed independently by so many different species; instead, these traits must have been inherited. An ancient ancestor that had many shared traits with both Catarhine and Platyrhine monkeys, along with some that were intermediate and a few possibly unique to either group, would definitely have been classified as an ape or monkey if observed by a naturalist. And since humans belong to the Catarhine or Old World branch from a genealogical perspective, we must conclude, no matter how much it challenges our pride, that our early ancestors would rightfully be classified as such. However, we must avoid the mistake of thinking that the early ancestor of all Simians, including humans, was the same as, or even closely resembled, any existing ape or monkey.
On the Birthplace and Antiquity of Man.—We are naturally led to enquire where was the birthplace of man at that stage of descent when our progenitors diverged from the Catarhine stock. The fact that they belonged to this stock clearly shews that they inhabited the Old World; but not Australia nor any oceanic island, as we may infer from the laws of geographical distribution. In each great region of the world the living mammals are closely related to the extinct species of the same region. It is therefore probable that Africa was formerly inhabited by extinct apes closely allied to the gorilla and chimpanzee; and as these two species are now man’s nearest allies, it is somewhat more probable that our early progenitors lived on the African continent than elsewhere. But it is useless to speculate on this subject, for an ape nearly as large as a man, namely the Dryopithecus of Lartet, which was closely allied to the anthropomorphous Hylobates, existed in Europe during the Upper Miocene period; and since so remote a period the earth has certainly undergone many great revolutions, and there has been ample time for migration on the largest scale.
On the Birthplace and Antiquity of Man.—We naturally want to know where humanity originated at the time when our ancestors split from the Catarhine group. The fact that they were part of this group clearly indicates that they lived in the Old World; however, they were not in Australia or any oceanic island, as suggested by geographical distribution laws. In each major region of the world, the living mammals are closely linked to the extinct species from that same region. Therefore, it’s likely that Africa was once home to extinct apes closely related to the gorilla and chimpanzee; since these two species are currently humanity’s closest relatives, it makes it somewhat more plausible that our early ancestors lived on the African continent rather than elsewhere. However, speculating on this is pointless, because an ape almost as large as a human, known as Dryopithecus, which was closely related to the anthropoid Hylobates, existed in Europe during the Upper Miocene period; and since that time, the Earth has certainly experienced significant changes, allowing ample opportunity for large-scale migration.
At the period and place, whenever and wherever it may have been, when man first lost his hairy covering, he probably inhabited a hot country; and this would have been favourable for a frugiferous diet, on which, judging from analogy, he subsisted. We are far from knowing how long ago it was when man first diverged from the Catarhine stock; but this may have occurred at an epoch as remote as the Eocene period; for the higher apes had diverged from the lower apes as early as the Upper Miocene period, as shewn by the existence of the Dryopithecus. We are also quite ignorant at how rapid a rate organisms, whether high or low in the scale, may under favourable circumstances be modified: we know, however, that some have retained the same form during an enormous lapse of time. From what we see going on under domestication, we learn that within the same period some of the co-descendants of the same species may be not at all changed, some a little, and some greatly changed. Thus it may have been with man, who has undergone a great amount of modification in certain characters in comparison with the higher apes.
At the time and place, whenever and wherever it was, when humans first lost their body hair, they likely lived in a warm climate; this would have been suitable for a fruit-based diet, which, based on comparisons, they likely ate. We don't know exactly how long ago humans first separated from the Catarhine lineage, but this might have happened as far back as the Eocene period; the higher apes had already diverged from the lower apes by the Upper Miocene period, as evidenced by the existence of Dryopithecus. We also have no clear idea of how quickly organisms, whether highly developed or less so, can change under favorable conditions: however, we do know that some have remained unchanged for a very long time. Observing domestication shows us that within the same time frame, some descendants of the same species may not change at all, some may change a little, and some may change a lot. This could have also been true for humans, who have undergone significant modifications in certain traits compared to higher apes.
The great break in the organic chain between man and his nearest allies, which cannot be bridged over by any extinct or living species, has often been advanced as a grave objection to the belief that man is descended from some lower form; but this objection will not appear of much weight to those who, convinced by general reasons, believe in the general principle of evolution. Breaks incessantly occur in all parts of the series, some being wide, sharp and defined, others less so in various degrees; as between the orang and its nearest allies—between the Tarsius and the other Lemuridæ—between the elephant and in a more striking manner between the Ornithorhynchus or201 Echidna, and other mammals. But all these breaks depend merely on the number of related forms which have become extinct. At some future period, not very distant as measured by centuries, the civilised races of man will almost certainly exterminate and replace throughout the world the savage races. At the same time the anthropomorphous apes, as Professor Schaaffhausen has remarked,270 will no doubt be exterminated. The break will then be rendered wider, for it will intervene between man in a more civilised state, as we may hope, than the Caucasian, and some ape as low as a baboon, instead of as at present between the negro or Australian and the gorilla.
The significant gap in the evolutionary chain between humans and our closest relatives, which can't be filled by any extinct or living species, has often been raised as a serious argument against the idea that humans descended from some lower form. However, this argument may not seem very strong to those who, convinced by broader reasons, accept the general principle of evolution. Gaps frequently occur at various points in the series, some being wide, sharp, and clearly defined, while others are less obvious to varying degrees; for example, between the orangutan and its closest relatives, between the Tarsius and other lemurs, and between the elephant and, even more noticeably, between the platypus or echidna and other mammals. All these gaps simply reflect the number of related forms that have gone extinct. In the future, likely not too distant in terms of centuries, the more advanced human races will almost certainly wipe out and replace the primitive races worldwide. At the same time, as Professor Schaaffhausen has noted, the anthropoid apes will likely be exterminated as well. The gap will then be even wider, intervening between humans in a hopefully more advanced state than the Caucasian and some ape as low as a baboon, rather than, as it is now, between individuals like the African or Australian and the gorilla.
With respect to the absence of fossil remains, serving to connect man with his ape-like progenitors, no one will lay much stress on this fact, who will read Sir C. Lyell’s discussion,271 in which he shews that in all the vertebrate classes the discovery of fossil remains has been an extremely slow and fortuitous process. Nor should it be forgotten that those regions which are the most likely to afford remains connecting man with some extinct ape-like creature, have not as yet been searched by geologists.
Regarding the lack of fossil remains linking humans to their ape-like ancestors, no one who reads Sir C. Lyell’s discussion,271 will place much emphasis on this fact, as he demonstrates that in all vertebrate classes, the discovery of fossil remains has been a very slow and random process. It should also be noted that the areas most likely to yield remains connecting humans to some extinct ape-like species have not yet been explored by geologists.
Lower Stages in the Genealogy of Man.—We have seen that man appears to have diverged from the Catarhine or Old World division of the Simiadæ, after these had diverged from the New World division. We will now endeavour to follow the more remote traces of his genealogy, trusting in the first place to the mutual affinities between the various classes and orders, with some slight aid from the periods, as far as ascertained, 202of their successive appearance on the earth. The Lemuridæ stand below and close to the Simiadæ, constituting a very distinct family of the Primates, or, according to Häckel, a distinct Order. This group is diversified and broken to an extraordinary degree, and includes many aberrant forms. It has, therefore, probably suffered much extinction. Most of the remnants survive on islands, namely in Madagascar and in the islands of the Malayan archipelago, where they have not been exposed to such severe competition as they would have been on well-stocked continents. This group likewise presents many gradations, leading, as Huxley remarks,272 “insensibly from the crown and summit of the animal creation down to creatures from which there is but a step, as it seems, to the lowest, smallest, and least intelligent of the placental mammalia.” From these various considerations it is probable that the Simiadæ were originally developed from the progenitors of the existing Lemuridæ; and these in their turn from forms standing very low in the mammalian series.
Lower Stages in the Genealogy of Man.—We have seen that humans seem to have diverged from the Catarhine or Old World division of the Simiadæ, after they had separated from the New World division. Now, we will try to trace the more distant origins of their lineage, relying primarily on the connections between the different classes and orders, with a little help from the periods that we know, as far as we can determine, 202 of their successive appearances on Earth. The Lemuridæ are positioned just below and next to the Simiadæ, forming a very distinct family of Primates or, according to Häckel, a separate Order. This group is highly diverse and fragmented, including many unusual forms. It has likely experienced significant extinction, with most survivors found on islands, particularly in Madagascar and the islands of the Malayan archipelago, where they haven't faced as much competition as they would have on well-populated continents. This group also shows many variations, leading, as Huxley notes, 272 “gradually from the pinnacle of animal evolution down to creatures that seem just a step away from the lowest, smallest, and least intelligent of placental mammals.” Considering all of this, it's likely that the Simiadæ originally evolved from the ancestors of the current Lemuridæ; and these, in turn, came from forms that are very low on the mammalian hierarchy.
The Marsupials stand in many important characters below the placental mammals. They appeared at an earlier geological period, and their range was formerly much more extensive than what it now is. Hence the Placentata are generally supposed to have been derived from the Implacentata or Marsupials; not, however, from forms closely like the existing Marsupials, but from their early progenitors. The Monotremata are plainly allied to the Marsupials; forming a third and still lower division in the great mammalian series. They are represented at the present day solely by the Ornithorhynchus and Echidna; and these two forms may 203be safely considered as relics of a much larger group which have been preserved in Australia through some favourable concurrence of circumstances. The Monotremata are eminently interesting, as in several important points of structure they lead towards the class of reptiles.
The Marsupials are generally considered less advanced than placental mammals. They emerged during an earlier geological period and used to have a much broader range than they do now. Therefore, it's widely believed that placental mammals evolved from the Implacentata or Marsupials, but not from forms that closely resemble today's Marsupials—rather, from their early ancestors. The Monotremata are clearly related to the Marsupials and represent a third, even more primitive division in the mammal lineage. Today, they are only represented by the Ornithorhynchus and Echidna, and these two species can be viewed as remnants of a much larger group that has been preserved in Australia due to some favorable circumstances. The Monotremata are particularly fascinating, as several key structural features indicate a link to reptiles.
In attempting to trace the genealogy of the Mammalia, and therefore of man, lower down in the series, we become involved in greater and greater obscurity. He who wishes to see what ingenuity and knowledge can effect, may consult Prof. Häckel’s works.273 I will content myself with a few general remarks. Every evolutionist will admit that the five great vertebrate classes, namely, mammals, birds, reptiles, amphibians, and fishes, are all descended from some one prototype; for they have much in common, especially during their embryonic state. As the class of fishes is the most lowly organised and appeared before the others, we may conclude that all the members of the vertebrate kingdom are derived from some fish-like animal, less highly organised than any as yet found in the lowest known formations. The belief that animals so distinct as a monkey or elephant and a humming-bird, a snake, frog, and fish, &c., could all have sprung from the same parents, will appear monstrous to those who have not attended to the recent progress of natural history. For this belief implies the former existence of links closely binding together all these forms, now so utterly unlike.
In trying to trace the family tree of mammals, and thus of humans, further back in the sequence, we encounter increasing confusion. Anyone who wants to see what creativity and knowledge can achieve can look at Prof. Häckel’s works.273 I will limit myself to a few general observations. Every evolutionist will agree that the five main vertebrate classes—mammals, birds, reptiles, amphibians, and fish—are all derived from a single ancestor; they share a lot in common, especially during their early developmental stages. Since fish are the most primitively organized and appeared before the others, we can conclude that all vertebrates come from some fish-like creature that is less complex than any currently known from the earliest formations. The idea that such distinct animals as monkeys, elephants, hummingbirds, snakes, frogs, and fish could all have descended from the same ancestors seems outrageous to those who haven't kept up with the recent advancements in natural history. This idea suggests that there used to be connections that closely linked all these forms, which are now so completely different.
Nevertheless it is certain that groups of animals have existed, or do now exist, which serve to connect more or less closely the several great vertebrate classes. We have seen that the Ornithorhynchus graduates towards reptiles; and Prof. Huxley has made the remarkable discovery, confirmed by Mr. Cope and others, that the old Dinosaurians are intermediate in many important respects between certain reptiles and certain birds—the latter consisting of the ostrich-tribe (itself evidently a widely-diffused remnant of a larger group) and of the Archeopteryx, that strange Secondary bird having a long tail like that of the lizard. Again, according to Prof. Owen,274 the Ichthyosaurians—great sea-lizards furnished with paddles—present many affinities with fishes, or rather, according to Huxley, with amphibians. This latter class (including in its highest division frogs and toads) is plainly allied to the Ganoid fishes. These latter fishes swarmed during the earlier geological periods, and were constructed on what is called a highly generalised type, that is they presented diversified affinities with other groups of organisms. The amphibians and fishes are also so closely united by the Lepidosiren, that naturalists long disputed in which of these two classes it ought to be placed. The Lepidosiren and some few Ganoid fishes have been preserved from utter extinction by inhabiting our rivers, which are harbours of refuge, bearing the same relation to the great waters of the ocean that islands bear to continents.
However, it's clear that groups of animals have existed, or still exist, which link the various major vertebrate classes more or less closely. We’ve seen that the Ornithorhynchus is related to reptiles; and Professor Huxley has made the amazing discovery, supported by Mr. Cope and others, that the ancient Dinosaurians are in many important ways intermediate between certain reptiles and certain birds—the latter consisting of the ostrich tribe (which is clearly a widely-dispersed remnant of a larger group) and the Archeopteryx, a strange bird from the Secondary period with a long tail like that of a lizard. Additionally, according to Professor Owen,274 the Ichthyosaurians—large sea lizards with paddles—show many similarities with fish, or rather, according to Huxley, with amphibians. This latter class (which includes frogs and toads in its highest division) is clearly related to Ganoid fish. These fish were abundant during earlier geological periods and were built on what is known as a highly generalized type, meaning they had diverse connections with other groups of organisms. Amphibians and fish are also very closely linked by the Lepidosiren, which led naturalists to debate which of these two classes it should belong to. The Lepidosiren and a few Ganoid fish have avoided complete extinction by living in our rivers, which serve as safe havens, much like islands do in relation to continents.
Lastly, one single member of the immense and diversified class of fishes, namely the lancelet or amphioxus, is so different from all other fishes, that Häckel maintains that it ought to form a distinct class in the vertebrate kingdom. This fish is remarkable for its 205negative characters; it can hardly be said to possess a brain, vertebral column, or heart, &c.; so that it was classed by the older naturalists amongst the worms. Many years ago Prof. Goodsir perceived that the lancelet presented some affinities with the Ascidians, which are invertebrate, hermaphrodite, marine creatures permanently attached to a support. They hardly appear like animals, and consist of a simple, tough, leathery sack, with two small projecting orifices. They belong to the Molluscoida of Huxley—a lower division of the great kingdom of the Mollusca; but they have recently been placed by some naturalists amongst the Vermes or worms. Their larvæ somewhat resemble tadpoles in shape,275 and have the power of swimming freely about. Some observations lately made by M. Kowalevsky,276 since confirmed by Prof. Kuppfer, will form a discovery of extraordinary interest, if still further extended, as I hear from M. Kowalevsky in Naples he has now effected. The discovery is that the larvæ of Ascidians are related to the Vertebrata, in their manner of development, in the relative position of the nervous system, and in possessing a structure closely like the chorda dorsalis of vertebrate animals. It thus appears, if we may rely on embryology, which has always proved the safest guide in classification, that we have at last gained a clue to the source whence the Vertebrata have 206been derived. We should thus be justified in believing that at an extremely remote period a group of animals existed, resembling in many respects the larvæ of our present Ascidians, which diverged into two great branches—the one retrograding in development and producing the present class of Ascidians, the other rising to the crown and summit of the animal kingdom by giving birth to the Vertebrata.
Lastly, one single member of the vast and diverse class of fishes, the lancelet or amphioxus, is so different from all other fishes that Häckel argues it should form its own class in the vertebrate kingdom. This fish is notable for its unusual characteristics; it can barely be said to have a brain, backbone, or heart, etc.; thus, older naturalists classified it among worms. Many years ago, Prof. Goodsir noticed that the lancelet shares some similarities with the Ascidians, which are invertebrate, hermaphroditic marine creatures permanently attached to a support. They hardly look like animals and consist of a simple, tough, leathery sack with two small openings. They belong to the Molluscoida of Huxley—a lower division of the vast kingdom of Mollusca; however, some naturalists have recently classified them among the Vermes or worms. Their larvae somewhat resemble tadpoles in shape,275 and they can swim freely. Some recent observations by M. Kowalevsky,276 now confirmed by Prof. Kuppfer, could lead to a discovery of exceptional interest if further developed, as I hear from M. Kowalevsky in Naples he has now accomplished. The discovery is that the larvae of Ascidians are related to Vertebrates in their development, in the relative position of their nervous system, and in having structure closely resembling the chorda dorsalis of vertebrate animals. It seems, if we can trust embryology, which has always proven to be the most reliable guide in classification, that we have finally found a clue to the origin of Vertebrates. We should thus be justified in believing that a very long time ago, a group of animals existed resembling, in many ways, the larvae of our current Ascidians, which branched into two major lines—the first declining in development and resulting in the existing class of Ascidians, and the second advancing to the apex of the animal kingdom by giving rise to the Vertebrates.
We have thus far endeavoured rudely to trace the genealogy of the Vertebrata by the aid of their mutual affinities. We will now look to man as he exists; and we shall, I think, be able partially to restore during successive periods, but not in due order of time, the structure of our early progenitors. This can be effected by means of the rudiments which man still retains, by the characters which occasionally make their appearance in him through reversion, and by the aid of the principles of morphology and embryology. The various facts, to which I shall here allude, have been given in the previous chapters. The early progenitors of man were no doubt once covered with hair, both sexes having beards; their ears were pointed and capable of movement; and their bodies were provided with a tail, having the proper muscles. Their limbs and bodies were also acted on by many muscles which now only occasionally reappear, but are normally present in the Quadrumana. The great artery and nerve of the humerus ran through a supra-condyloid foramen. At this or some earlier period, the intestine gave forth a much larger diverticulum or cæcum than that now existing. The foot, judging from the condition of the great toe in the fœtus, was then prehensile; and our progenitors, no doubt, were arboreal in their habits, frequenting some warm, forest-clad land. The males207 were provided with great canine teeth, which served them as formidable weapons.
We have so far tried to roughly outline the family tree of Vertebrates by looking at their similarities. Now let's focus on humans as they are today; I believe we can partially reconstruct the features of our early ancestors during different time periods, though not in chronological order. We can achieve this by examining the remnants humans still have, the traits that sometimes appear through reversion, and the principles of morphology and embryology. The various facts I’ll mention here have already been discussed in previous chapters. Early humans were likely once covered in hair, with both males and females having beards; their ears were pointed and able to move; and their bodies had tails with the necessary muscles. Their limbs and bodies were influenced by many muscles that now only occasionally show up but are usually found in Quadrumana. The main artery and nerve of the humerus passed through a supra-condyloid foramen. At this time, or perhaps even earlier, the intestine had a much larger cæcum than what we have today. Judging by the state of the big toe in fetuses, the foot was likely prehensile; our ancestors probably lived in trees, inhabiting warm, forested areas. The males207 had large canine teeth that served as effective weapons.
At a much earlier period the uterus was double; the excreta were voided through a cloaca; and the eye was protected by a third eyelid or nictitating membrane. At a still earlier period the progenitors of man must have been aquatic in their habits; for morphology plainly tells us that our lungs consist of a modified swim-bladder, which once served as a float. The clefts on the neck in the embryo of man show where the branchiæ once existed. At about this period the true kidneys were replaced by the corpora Wolffiana. The heart existed as a simple pulsating vessel; and the chorda dorsalis took the place of a vertebral column. These early predecessors of man, thus seen in the dim recesses of time, must have been as lowly organised as the lancelet or amphioxus, or even still more lowly organised.
At a much earlier time, the uterus was double; waste was expelled through a cloaca; and the eye had a third eyelid or nictitating membrane for protection. Even earlier, our ancestors must have lived in water, as anatomy clearly shows that our lungs are modified swim-bladders that once acted as floats. The slits on the neck of a human embryo indicate where gills used to be. Around this time, the true kidneys were replaced by the Wolffian bodies. The heart was just a simple pulsating tube, and the notochord served as a primitive backbone. These early ancestors of humans, seen through the mists of time, were likely as simply structured as the lancelet or amphioxus, or possibly even more primitive.
There is one other point deserving a fuller notice. It has long been known that in the vertebrate kingdom one sex bears rudiments of various accessory parts, appertaining to the reproductive system, which properly belong to the opposite sex; and it has now been ascertained that at a very early embryonic period both sexes possess true male and female glands. Hence some extremely remote progenitor of the whole vertebrate kingdom appears to have been hermaphrodite or androgynous.277 But here we encounter a singular 208difficulty. In the mammalian class the males possess in their vesiculæ prostraticæ rudiments of a uterus with the adjacent passage; they bear also rudiments of mammæ, and some male marsupials have rudiments of a marsupial sack.278 Other analogous facts could be added. Are we, then, to suppose that some extremely ancient mammal possessed organs proper to both sexes, that is, continued androgynous after it had acquired the chief distinctions of its proper class, and therefore after it had diverged from the lower classes of the vertebrate kingdom? This seems improbable in the highest degree; for had this been the case, we might have expected that some few members of the two lower classes, namely fishes279 and amphibians, would still have remained androgynous. We must, on the contrary, believe that when the five vertebrate classes diverged from their common progenitor the sexes had already become separated. To account, however, for male mammals possessing rudiments of the accessory female organs, and for female mammals possessing rudiments of the masculine organs, we need not suppose that their early progenitors were still androgynous after they had assumed their chief mammalian characters. It is quite possible that as the one sex gradually acquired the accessory organs proper to it, some of the successive steps or modifications were transmitted to the opposite sex. When we treat of sexual selection, we shall meet with innumerable instances of this form of transmission,—as in the case of the spurs, plumes, 209and brilliant colours, acquired by male birds for battle or ornament, and transferred to the females in an imperfect or rudimentary condition.
There’s another point that deserves more attention. It has long been known that in the vertebrate kingdom, one sex has remnants of various accessory parts related to the reproductive system, which actually belong to the opposite sex. It has now been determined that at a very early embryonic stage, both sexes have true male and female glands. Therefore, some very distant ancestor of all vertebrates seems to have been hermaphroditic or androgynous.277 However, we run into an interesting problem. In mammals, males have remnants of a uterus with the nearby passage in their vesiculæ prostraticæ; they also have remnants of mammary glands, and some male marsupials have rudiments of a marsupial pouch.278 Other similar examples could be added. Are we supposed to think that some very ancient mammal had organs typical of both sexes, that is, remained androgynous after it developed the primary characteristics of its class, and thus diverged from the lower classes of the vertebrate kingdom? This seems very unlikely; if it were true, we would expect that a few members of the two lower classes, namely fish279 and amphibians, would still be androgynous. Instead, we must believe that when the five vertebrate classes split from their common ancestor, the sexes were already distinct. However, to explain why male mammals possess remnants of female accessory organs, and female mammals have remnants of male organs, we don’t need to assume that their early ancestors were still androgynous after they developed their main mammalian traits. It’s quite possible that as one sex gradually gained the accessory organs typical of it, some of the changes or adaptations were passed on to the opposite sex. When we discuss sexual selection, we will encounter countless examples of this kind of transmission—such as the spurs, feathers, and bright colors that male birds have developed for competition or display, which get passed on to the females in an incomplete or rudimentary form.
The possession by male mammals of functionally imperfect mammary organs is, in some respects, especially curious. The Monotremata have the proper milk-secreting glands with orifices, but no nipples; and as these animals stand at the very base of the mammalian series, it is probable that the progenitors of the class possessed, in like manner, the milk-secreting glands, but no nipples. This conclusion is supported by what is known of their manner of development; for Professor Turner informs me, on the authority of Kölliker and Lauger, that in the embryo the mammary glands can be distinctly traced before the nipples are in the least visible; and it should be borne in mind that the development of successive parts in the individual generally seems to represent and accord with the development of successive beings in the same line of descent. The Marsupials differ from the Monotremata by possessing nipples; so that these organs were probably first acquired by the Marsupials after they had diverged from, and risen above, the Monotremata, and were then transmitted to the placental mammals. No one will suppose that after the Marsupials had approximately acquired their present structure, and therefore at a rather late period in the development of the mammalian series, any of its members still remained androgynous. We seem, therefore, compelled to recur to the foregoing view, and to conclude that the nipples were first developed in the females of some very early marsupial form, and were then, in accordance with a common law of inheritance, transferred in a functionally imperfect condition to the males.
The fact that male mammals have functionally imperfect mammary organs is, in some ways, quite intriguing. The Monotremata have proper milk-secreting glands with openings, but no nipples; and since these animals are at the very beginning of the mammalian lineage, it's likely that the ancestors of the class also had milk-secreting glands but no nipples. This idea is supported by what we know about their development; Professor Turner tells me, based on the work of Kölliker and Lauger, that in embryos, the mammary glands can be distinctly identified before nipples are even slightly visible. It's worth noting that the development of different parts in an individual generally reflects the evolution of different species along the same lineage. The Marsupials differ from the Monotremata by having nipples; thus, these organs were probably first developed by the Marsupials after they had split off from and advanced beyond the Monotremata, and then passed on to the placental mammals. No one would suggest that after Marsupials had nearly completed their current structure, and therefore at a rather late point in the evolutionary history of mammals, any of its members remained androgynous. Therefore, we are led to revisit the previous idea and conclude that the nipples were first developed in the females of some very early marsupial ancestor and were then passed down in a functionally imperfect form to the males.
Nevertheless a suspicion has sometimes crossed my210 mind that long after the progenitors of the whole mammalian class had ceased to be androgynous, both sexes might have yielded milk and thus nourished their young; and in the case of the Marsupials, that both sexes might have carried their young in marsupial sacks. This will not appear utterly incredible, if we reflect that the males of syngnathous fishes receive the eggs of the females in their abdominal pouches, hatch them, and afterwards, as some believe, nourish the young;280—that certain other male fishes hatch the eggs within their mouths or branchial cavities;—that certain male toads take the chaplets of eggs from the females and wind them round their own thighs, keeping them there until the tadpoles are born;—that certain male birds undertake the whole duty of incubation, and that male pigeons, as well as the females, feed their nestlings with a secretion from their crops. But the above suspicion first occurred to me from the mammary glands in male mammals being developed so much more perfectly than the rudiments of those other accessory reproductive parts, which are found in the one sex though proper to the other. The mammary glands and nipples, as they exist in male mammals, can indeed hardly be called rudimentary; they are simply not fully developed and not functionally active. They are sympathetically affected under the influence of certain diseases, like the same organs in the female. At birth they often secrete a few drops of milk; and they have 211been known occasionally in man and other mammals to become well developed, and to yield a fair supply of milk. Now if we suppose that during a former prolonged period male mammals aided the females in nursing their offspring, and that afterwards from some cause, as from a smaller number of young being produced, the males ceased giving this aid, disuse of the organs during maturity would lead to their becoming inactive; and from two well-known principles of inheritance this state of inactivity would probably be transmitted to the males at the corresponding age of maturity. But at all earlier ages these organs would be left unaffected, so that they would be equally well developed in the young of both sexes.
Nevertheless, I sometimes have a suspicion that long after the ancestors of all mammals stopped being androgynous, both sexes might have produced milk and nourished their young; and in the case of marsupials, that both sexes might have carried their young in pouches. This seems less unbelievable if we consider that male seahorses carry the eggs from females in their abdominal pouches, hatch them, and later, as some believe, feed the young; that some other male fish hatch eggs in their mouths or gills; that some male toads take the eggs from females and wrap them around their thighs until the tadpoles are born; that some male birds take on all the responsibilities of incubation; and that male pigeons, just like females, feed their chicks with a secretion from their crops. However, my suspicion primarily arose from the fact that male mammals have mammary glands that are developed much more fully than the rudimentary accessory reproductive parts that belong to the other sex. The mammary glands and nipples in male mammals can hardly be called rudimentary; they are simply not fully developed and aren't functionally active. They can respond to certain diseases like in females. At birth, they often release a few drops of milk; and there are instances in humans and other mammals where they become well-developed and can yield a decent amount of milk. Now, if we assume that in the past, male mammals helped females in nursing their offspring, and that later, due to a decrease in the number of offspring produced, males stopped providing this aid, then the disuse of these organs during adulthood would cause them to become inactive; and following two well-known principles of inheritance, this inactivity would likely be passed down to males starting from a corresponding age of maturity. However, at all earlier ages, these organs would remain unaffected, so they would be equally well-developed in the young of both sexes.
Conclusion.—The best definition of advancement or progress in the organic scale ever given, is that by Von Baer; and this rests on the amount of differentiation and specialisation of the several parts of the same being, when arrived, as I should be inclined to add, at maturity. Now as organisms have become slowly adapted by means of natural selection for diversified lines of life, their parts will have become, from the advantage gained by the division of physiological labour, more and more differentiated and specialised for various functions. The same part appears often to have been modified first for one purpose, and then long afterwards for some other and quite distinct purpose; and thus all the parts are rendered more and more complex. But each organism will still retain the general type of structure of the progenitor from which it was aboriginally derived. In accordance with this view it seems, if we turn to geological evidence, that organisation on the whole has advanced throughout the world by slow and interrupted steps. In the great212 kingdom of the Vertebrata it has culminated in man. It must not, however, be supposed that groups of organic beings are always supplanted and disappear as soon as they have given birth to other and more perfect groups. The latter, though victorious over their predecessors, may not have become better adapted for all places in the economy of nature. Some old forms appear to have survived from inhabiting protected sites, where they have not been exposed to very severe competition; and these often aid us in constructing our genealogies, by giving us a fair idea of former and lost populations. But we must not fall into the error of looking at the existing members of any lowly-organised group as perfect representatives of their ancient predecessors.
Conclusion.—The best definition of advancement or progress in the organic scale is that given by Von Baer; it focuses on how much differentiation and specialization there is among the different parts of a being, which I would suggest should be considered at maturity. As organisms have gradually adapted through natural selection for diverse ways of life, their parts have become increasingly differentiated and specialized for various functions due to the advantages gained through the division of physiological labor. Often, the same part seems to have been modified first for one purpose and then, much later, for another completely different purpose, making every part more complex. Still, each organism will retain the general structure of the ancestor from which it originally came. Looking at geological evidence, it appears that organization, overall, has progressed slowly and unevenly across the world. In the vast212 kingdom of Vertebrates, this progress culminates in humans. However, we shouldn't assume that groups of organisms are always replaced and disappear right after they give rise to new and more advanced groups. The newer groups, while more successful than their predecessors, may not necessarily be better suited for every role in the natural world. Some older forms seem to have survived by living in protected environments where they weren't subject to intense competition, and these often help us in developing our genealogies by providing a glimpse into past and extinct populations. But we should avoid the mistake of viewing the current members of any lowly-organized group as perfect examples of their ancient ancestors.
The most ancient progenitors in the kingdom of the Vertebrata, at which we are able to obtain an obscure glance, apparently consisted of a group of marine animals,281 resembling the larvæ of existing Ascidians. These animals probably gave rise to a group of fishes, as lowly organised as the lancelet; and from these the Ganoids, and other fishes like the Lepidosiren, must have been developed. From such fish a very small advance would 213carry us on to the amphibians. We have seen that birds and reptiles were once intimately connected together; and the Monotremata now, in a slight degree, connect mammals with reptiles. But no one can at present say by what line of descent the three higher and related classes, namely, mammals, birds, and reptiles, were derived from either of the two lower vertebrate classes, namely amphibians and fishes. In the class of mammals the steps are not difficult to conceive which led from the ancient Monotremata to the ancient Marsupials; and from these to the early progenitors of the placental mammals. We may thus ascend to the Lemuridæ; and the interval is not wide from these to the Simiadæ. The Simiadæ then branched off into two great stems, the New World and Old World monkeys; and from the latter, at a remote period, Man, the wonder and glory of the Universe, proceeded.
The oldest ancestors in the Vertebrate kingdom, which we can only glimpse slightly, seem to have been a group of marine animals,281 that looked like the larvae of modern Ascidians. These creatures likely led to a group of fish as simple as the lancelet; from there, the Ganoids and other fish, such as the Lepidosiren, must have evolved. A small step from those fish would bring us to amphibians. We know that birds and reptiles were once closely related; today, the Monotremata connect mammals and reptiles to a small extent. However, no one can currently determine the exact lineage through which the three higher related classes—mammals, birds, and reptiles—emerged from either of the two lower vertebrate classes—amphibians and fish. In mammals, the evolutionary path from ancient Monotremata to ancient Marsupials, and then to the early ancestors of placental mammals, is relatively easy to imagine. From there, we can trace a line to the Lemuridæ, and the gap to the Simiadæ is not wide. The Simiadæ then split into two major branches: New World and Old World monkeys; and from the latter, at a distant time, Man, the wonder and glory of the Universe, emerged.
Thus we have given to man a pedigree of prodigious length, but not, it may be said, of noble quality. The world, it has often been remarked, appears as if it had long been preparing for the advent of man; and this, in one sense is strictly true, for he owes his birth to a long line of progenitors. If any single link in this chain had never existed, man would not have been exactly what he now is. Unless we wilfully close our eyes, we may, with our present knowledge, approximately recognise our parentage; nor need we feel ashamed of it. The most humble organism is something much higher than the inorganic dust under our feet; and no one with an unbiassed mind can study any living creature, however humble, without being struck with enthusiasm at its marvellous structure and properties.
So, we've given humans a family tree that's incredibly long, but not necessarily impressive. It's often said that the world seems to have been getting ready for the arrival of humans, and in a way, that's true because our existence is the result of a long line of ancestors. If any single link in that chain had never existed, we wouldn't be exactly who we are today. Unless we choose to ignore it, we can now roughly trace our lineage without feeling embarrassed about it. The simplest living organism is still far more complex than the inorganic matter beneath our feet, and anyone who studies any living creature, no matter how basic, can't help but feel amazed by its incredible structure and characteristics.
CHAPTER VII.
On Human Races.
The nature and value of specific characters—Application to the races of man—Arguments in favour of, and opposed to, ranking the so-called races of man as distinct species—Sub-species—Monogenists and polygenists—Convergence of character—Numerous points of resemblance in body and mind between the most distinct races of man—The state of man when he first spread over the earth—Each race not descended from a single pair—The extinction of races—The formation of races—The effects of crossing—Slight influence of the direct action of the conditions of life—Slight or no influence of natural selection—Sexual selection.
The nature and value of specific characters—Application to human races—Arguments for and against classifying so-called human races as separate species—Sub-species—Monogenists and polygenists—Convergence of characteristics—Many similarities in body and mind among the most distinct human races—The condition of humans when they first spread across the planet—Not every race descended from a single pair—The extinction of races—The formation of races—The effects of cross-breeding—Minimal influence of the direct impact of life conditions—Little to no impact of natural selection—Sexual selection.
It is not my intention here to describe the several so-called races of men; but to inquire what is the value of the differences between them under a classificatory point of view, and how they have originated. In determining whether two or more allied forms ought to be ranked as species or varieties, naturalists are practically guided by the following considerations; namely, the amount of difference between them, and whether such differences relate to few or many points of structure, and whether they are of physiological importance; but more especially whether they are constant. Constancy of character is what is chiefly valued and sought for by naturalists. Whenever it can be shewn, or rendered probable, that the forms in question have remained distinct for a long period, this becomes an argument of much weight in favour of treating them as species. Even a slight degree of sterility between any two forms when first crossed, or in their offspring, is generally considered as a decisive215 test of their specific distinctness; and their continued persistence without blending within the same area, is usually accepted as sufficient evidence, either of some degree of mutual sterility, or in the case of animals of some repugnance to mutual pairing.
I’m not here to describe the various so-called races of people; instead, I want to explore the significance of their differences from a classification standpoint and how those differences originated. When deciding whether two or more related forms should be classified as species or varieties, naturalists are guided by a few key considerations: the degree of difference between them, whether those differences involve just a few or many structural features, and whether they're physiologically important; but most importantly, whether they are consistent. The consistency of characteristics is what naturalists primarily value and search for. Whenever it's shown, or can be reasonably suggested, that the forms in question have remained distinct for a long time, it becomes a strong argument for classifying them as species. Even a small amount of sterility between two forms when they are first crossed, or in their offspring, is typically seen as a definitive test of their distinctness as species; and their continued existence without mixing in the same area is generally accepted as sufficient evidence of some degree of mutual sterility, or in the case of animals, some reluctance to mate with each other.215
Independently of blending from intercrossing, the complete absence, in a well-investigated region, of varieties linking together any two closely-allied forms, is probably the most important of all the criterions of their specific distinctness; and this is a somewhat different consideration from mere constancy of character, for two forms may be highly variable and yet not yield intermediate varieties. Geographical distribution is often unconsciously and sometimes consciously brought into play; so that forms living in two widely separated areas, in which most of the other inhabitants are specifically distinct, are themselves usually looked at as distinct; but in truth this affords no aid in distinguishing geographical races from so-called good or true species.
Regardless of blending from intercrossing, the complete absence, in a well-studied area, of varieties that connect any two closely related forms is probably the most significant criterion for their specific distinctness. This is a somewhat different idea from just the consistency of traits, as two forms can be highly variable and still not produce intermediate varieties. Geographical distribution often plays a role, whether consciously or unconsciously; thus, forms found in two widely separated areas, where most of the other inhabitants are specifically distinct, are usually considered distinct themselves. However, this doesn't actually help in distinguishing geographical races from what are called good or true species.
Now let us apply these generally-admitted principles to the races of man, viewing him in the same spirit as a naturalist would any other animal. In regard to the amount of difference between the races, we must make some allowance for our nice powers of discrimination gained by the long habit of observing ourselves. In India, as Elphinstone remarks,282 although a newly-arrived European cannot at first distinguish the various native races, yet they soon appear to him extremely dissimilar; and the Hindoo cannot at first perceive any difference between the several European nations. Even the most distinct races of man, with the exception of certain negro tribes, are much more like each other in form 216than would at first be supposed. This is well shewn by the French photographs in the Collection Anthropologique du Muséum of the men belonging to various races, the greater number of which, as many persons to whom I have shown them have remarked, might pass for Europeans. Nevertheless, these men if seen alive would undoubtedly appear very distinct, so that we are clearly much influenced in our judgment by the mere colour of the skin and hair, by slight differences in the features, and by expression.
Now let's apply these generally accepted principles to human races, looking at them the same way a naturalist would view any other animal. When it comes to the differences between races, we need to consider our keen ability to distinguish nuances developed through observing ourselves over time. In India, as Elphinstone points out,282 a newly arrived European might not initially recognize the various native races, but soon they seem very different; meanwhile, a Hindu might not notice any differences between the various European nations at first. Even the most distinct human races, except for certain African tribes, resemble each other in shape much more than one might think. This is well illustrated by the French photographs in the Collection Anthropologique du Muséum showcasing men from different races, most of whom, as many people I've shown them to have noted, could easily be mistaken for Europeans. However, these men, if seen in person, would undoubtedly appear quite different, indicating that our judgments are greatly influenced by skin and hair color, slight variations in features, and expressions.
There is, however, no doubt that the various races, when carefully compared and measured, differ much from each other,—as in the texture of the hair, the relative proportions of all parts of the body,283 the capacity of the lungs, the form and capacity of the skull, and even in the convolutions of the brain.284 But it would be an endless task to specify the numerous points of structural difference. The races differ also in constitution, in acclimatisation, and in liability to certain diseases. Their mental characteristics are likewise very distinct; chiefly as it would appear in their emotional, but partly in their intellectual, faculties. Every one who has had the opportunity of comparison, must have been struck with the contrast between the taciturn, even morose, aborigines of S. America and the light-hearted, talkative negroes. There is a nearly similar contrast between the Malays and the Papuans,285 who live 217under the same physical conditions, and are separated from each other only by a narrow space of sea.
There is no doubt that different races, when closely compared and measured, vary significantly from one another—like in hair texture, the relative proportions of body parts,283 lung capacity, skull shape and size, and even the patterns of the brain.284 However, it would be a never-ending task to list all the structural differences. The races also differ in their constitution, how they adapt to different environments, and their susceptibility to certain diseases. Their mental traits are distinctly different as well, especially in emotional aspects, but also in intellectual abilities. Anyone who has had the chance to compare them must have noticed the contrast between the reserved, often gloomy, indigenous people of South America and the cheerful, talkative Africans. There is a similar contrast between the Malays and Papuans,285 who live217under the same physical conditions but are separated by a narrow body of water.
We will first consider the arguments which may be advanced in favour of classing the races of man as distinct species, and then those on the other side. If a naturalist, who had never before seen such beings, were to compare a Negro, Hottentot, Australian, or Mongolian, he would at once perceive that they differed in a multitude of characters, some of slight and some of considerable importance. On inquiry he would find that they were adapted to live under widely different climates, and that they differed somewhat in bodily constitution and mental disposition. If he were then told that hundreds of similar specimens could be brought from the same countries, he would assuredly declare that they were as good species as many to which he had been in the habit of affixing specific names. This conclusion would be greatly strengthened as soon as he had ascertained that these forms had all retained the same character for many centuries; and that negroes, apparently identical with existing negroes, had lived at least 4000 years ago.286 He would also hear from an excellent observer, 218 Dr. Lund,287 that the human skulls found in the caves of Brazil, entombed with many extinct mammals, belonged to the same type as that now prevailing throughout the American Continent.
We will first look at the arguments for classifying human races as distinct species, and then we’ll examine the counterarguments. If a naturalist, who had never encountered such people before, were to compare a Black person, a Hottentot, an Australian, or a Mongolian, he would immediately notice that they varied in many ways, some minor and some significant. Upon further investigation, he would discover that they were suited to live in very different climates and that they also had different physical builds and mental traits. If he were then told that hundreds of similar examples could be found from the same regions, he would certainly conclude that they were as distinct a species as many others he had previously named. This conclusion would be reinforced upon discovering that these forms have maintained their characteristics for many centuries, and that Black individuals, seemingly identical to those today, lived at least 4,000 years ago.286 He would also hear from a reliable observer, 218 Dr. Lund,287 that the human skulls found in Brazilian caves, buried with many extinct mammals, belonged to the same type as those currently found across the American continent.
Our naturalist would then perhaps turn to geographical distribution, and he would probably declare that forms differing not only in appearance, but fitted for the hottest and dampest or driest countries, as well as for the arctic regions, must be distinct species. He might appeal to the fact that no one species in the group next to man, namely the Quadrumana, can resist a low temperature or any considerable change of climate; and that those species which come nearest to man have never been reared to maturity, even under the temperate climate of Europe. He would be deeply impressed with the fact, first noticed by Agassiz,288 that the different races of man are distributed over the world in the same zoological provinces, as those inhabited by undoubtedly distinct species and genera of mammals. This is manifestly the case with the Australian, Mongolian, and Negro races of man; in a less well-marked manner with the Hottentots; but plainly with the Papuans and Malays, who are separated, as Mr. Wallace has shewn, by nearly the same line which divides the great Malayan and Australian zoological provinces. The aborigines of America range throughout the Continent; and this at first appears opposed to the above rule, for most of the productions of the Southern and Northern halves differ widely; yet some few living forms, as the 219opossum, range from the one into the other, as did formerly some of the gigantic Edentata. The Esquimaux, like other Arctic animals, extend round the whole polar regions. It should be observed that the mammalian forms which inhabit the several zoological provinces, do not differ from each other in the same degree; so that it can hardly be considered as an anomaly that the Negro differs more, and the American much less, from the other races of man than do the mammals of the same continents from those of the other provinces. Man, it may be added, does not appear to have aboriginally inhabited any oceanic island; and in this respect he resembles the other members of his class.
Our naturalist might then look at geographical distribution and probably conclude that forms that not only look different but are suited for the hottest, dampest, or driest places, as well as the arctic regions, must be distinct species. He might point out that no species in the group closest to humans, namely the primates, can tolerate low temperatures or significant climate changes; and that those species that are closest to humans have never been raised to maturity, even in the temperate climate of Europe. He would be quite struck by the fact, first noted by Agassiz,288 that the various races of humans are spread across the world in the same zoological provinces as those inhabited by clearly distinct species and genera of mammals. This is clearly seen with the Australian, Mongolian, and African races; to a lesser degree with the Hottentots; but distinctly with the Papuans and Malays, who are separated, as Mr. Wallace has shown, by nearly the same line that divides the main Malayan and Australian zoological provinces. The indigenous peoples of the Americas spread across the continent, which at first seems contrary to the above rule since most of the species in the Southern and Northern halves differ greatly; yet a few living forms, like the opossum, cross from one to the other, as did some of the giant Edentata in the past. The Eskimos, like other Arctic animals, spread all around the polar regions. It's worth noting that the mammal forms in different zoological provinces do not differ from each other to the same extent; so it is hardly surprising that the African differs more, and the American much less, from other human races than the mammals on the same continents differ from those in other provinces. Additionally, humans do not seem to have originally lived on any oceanic island, resembling other members of their class in that respect.
In determining whether the varieties of the same kind of domestic animal should be ranked as specifically distinct, that is, whether any of them are descended from distinct wild species, every naturalist would lay much stress on the fact, if established, of their external parasites being specifically distinct. All the more stress would be laid on this fact, as it would be an exceptional one, for I am informed by Mr. Denny that the most different kinds of dogs, fowls, and pigeons, in England, are infested by the same species of Pediculi or lice. Now Mr. A. Murray has carefully examined the Pediculi collected in different countries from the different races of man;289 and he finds that they differ, not only in colour, but in the structure of their claws and limbs. In every case in which numerous specimens were obtained the differences were constant. The surgeon of a whaling ship in the Pacific assured me that when the Pediculi, with which some Sandwich Islanders on board swarmed, strayed on to the bodies of the English sailors, they died in the course of three or four days. These Pediculi 220were darker coloured and appeared different from those proper to the natives of Chiloe in South America, of which he gave me specimens. These, again, appeared larger and much softer than European lice. Mr. Murray procured four kinds from Africa, namely from the Negroes of the Eastern and Western coasts, from the Hottentots and Caffres; two kinds from the natives of Australia; two from North, and two from South America. In these latter cases it may be presumed that the Pediculi came from natives inhabiting different districts. With insects slight structural differences, if constant, are generally esteemed of specific value: and the fact of the races of man being infested by parasites, which appear to be specifically distinct, might fairly be urged as an argument that the races themselves ought to be classed as distinct species.
When deciding if different types of the same domestic animal should be considered distinct species—specifically, whether any of them descend from different wild species—every naturalist would emphasize the importance of their external parasites being distinctly different. This point would be even more significant, as it would be an unusual finding. Mr. Denny has informed me that the most varied breeds of dogs, chickens, and pigeons in England all share the same species of lice. Mr. A. Murray has carefully examined the lice collected from various countries and different human races; 289 he found that they vary not only in color but also in the structure of their claws and limbs. In every case where numerous specimens were collected, the differences were consistent. A surgeon from a whaling ship in the Pacific told me that when the lice from some Sandwich Islanders onboard came into contact with the English sailors, they died within three or four days. These lice were darker and appeared different from those found among the natives of Chiloe in South America, whose specimens he provided to me. These, in turn, seemed larger and much softer than European lice. Mr. Murray collected four types from Africa, specifically from the Negroes of both the Eastern and Western coasts, and from the Hottentots and Caffres; he also found two types from Australia and two from North and South America. In these latter cases, it can be assumed that the lice originated from natives living in different regions. With insects, slight differences in structure, if consistent, are usually considered significant enough to denote a distinct species; thus, the fact that humans from different races are infested by parasites that seem to be distinctly different could reasonably support the argument that these races themselves should be classified as separate species.
Our supposed naturalist having proceeded thus far in his investigation, would next inquire whether the races of men, when crossed, were in any degree sterile. He might consult the work290 of a cautious and philosophical observer, Professor Broca; and in this he would find good, evidence that some races were quite fertile together; but evidence of an opposite nature in regard to other races. Thus it has been asserted that the native women of Australia and Tasmania rarely produce children to European men; the evidence, however, on this head has now been shewn to be almost valueless. The half-castes are killed by the pure blacks; and an account has lately been published of eleven half-caste youths murdered and burnt at the same time, whose remains were found by the police.291 Again, it has often 221been said that when mulattoes intermarry they produce few children; on the other hand, Dr. Bachman of Charlestown292 positively asserts that he has known mulatto families which have intermarried for several generations, and have continued on an average as fertile as either pure whites or pure blacks. Inquiries formerly made by Sir C. Lyell on this subject led him, as he informs me, to the same conclusion. In the United States the census for the year 1854 included, according to Dr. Bachman, 405,751 mulattoes; and this number, considering all the circumstances of the case, seems small; but it may partly be accounted for by the degraded and anomalous position of the class, and by the profligacy of the women. A certain amount of absorption of mulattoes into negroes must always be in progress; and this would lead to an apparent diminution of the former. The inferior vitality of mulattoes is spoken of in a trustworthy work293 as a well-known phenomenon; but this is a different consideration from their lessened fertility; and can hardly be advanced as a proof of the specific distinctness of the parent races. No doubt both animal and vegetable hybrids, when produced from extremely distinct species, are liable to premature death; but the parents of mulattoes cannot be put under the category of extremely distinct species. The common Mule, so notorious for long life and vigour, and yet so sterile, shews how little necessary connection 222there is in hybrids between lessened fertility and vitality: other analogous cases could be added.
Our so-called naturalist, having gone this far in his investigation, would next ask whether the different races of humans, when mixed, are at all sterile. He might look at the work290 of a careful and thoughtful observer, Professor Broca, where he would find solid evidence that some races can successfully reproduce together, but contradictory evidence regarding other races. It has been claimed that the native women of Australia and Tasmania rarely have children with European men; however, recent findings have shown this evidence to be almost worthless. The mixed-race children are often killed by pure blacks, and there’s been a recent report of eleven mixed-race young men who were murdered and burned at the same time, with their remains discovered by the police.291 Furthermore, it has often been said that when mulattoes marry each other, they tend to have few children; however, Dr. Bachman from Charlestown292 confidently claims to have known mulatto families that have intermarried for several generations and remain as fertile on average as either pure whites or pure blacks. Past inquiries by Sir C. Lyell on this topic led him, as he told me, to the same conclusion. In the United States, the census for 1854 recorded, according to Dr. Bachman, 405,751 mulattoes; this figure, considering all relevant circumstances, seems low. Yet, it can partly be explained by the marginalized status of this group and the behavior of the women. Some degree of assimilation of mulattoes into the black population must always be occurring, which would contribute to the apparent decline in the former. Reliable sources293 mention the lower vitality of mulattoes as a well-known phenomenon, but this is a separate issue from their reduced fertility and does not serve as proof of the distinctiveness of the parent races. It’s true that both animal and plant hybrids, when produced from very distinct species, are more likely to die prematurely; however, the parents of mulattoes do not fit into the category of extremely distinct species. The common mule, notorious for its long lifespan and strength but remaining sterile, demonstrates how little connection there is between reduced fertility and vitality in hybrids: there are other similar cases that could be mentioned.
Even if it should hereafter be proved that all the races of men were perfectly fertile together, he who was inclined from other reasons to rank them as distinct species, might with justice argue that fertility and sterility are not safe criterions of specific distinctness. We know that these qualities are easily affected by changed conditions of life or by close inter-breeding, and that they are governed by highly complex laws, for instance that of the unequal fertility of reciprocal crosses between the same two species. With forms which must be ranked as undoubted species, a perfect series exists from those which are absolutely sterile when crossed, to those which are almost or quite fertile. The degrees of sterility do not coincide strictly with the degrees of difference in external structure or habits of life. Man in many respects may be compared with those animals which have long been domesticated, and a large body of evidence can be advanced in favour of the Pallasian doctrine294 that domestication tends to eliminate the 223sterility which is so general a result of the crossing of species in a state of nature. From these several considerations, it may be justly urged that the perfect fertility of the intercrossed races of man, if established, would not absolutely preclude us from ranking them as distinct species.
Even if it is proven later that all human races can interbreed successfully, someone who believes they are different species for other reasons could reasonably argue that fertility and infertility are not reliable indicators of distinct species. We know these traits can be easily influenced by changes in living conditions or by close breeding, and they follow complex rules, such as the varying fertility of hybrid offspring between the same two species. In cases considered clear species, there's a complete range from those that are totally infertile when crossed to those that are nearly or completely fertile. The levels of infertility don’t exactly match the differences in physical structure or lifestyles. Humans can be compared in many ways to domesticated animals, and there is plenty of evidence supporting the idea that domestication tends to reduce the infertility often seen when different species mate in the wild. Given these points, it can be justifiably argued that the complete fertility of interbred human races, if proven, wouldn’t completely rule out classifying them as distinct species.
Independently of fertility, the character of the offspring from a cross has sometimes been thought to afford evidence whether the parent-forms ought to be ranked as species or varieties; but after carefully studying the evidence, I have come to the conclusion that no general rules of this kind can be trusted. Thus with mankind the offspring of distinct races resemble in all respects the offspring of true species and of varieties. This is shewn, for instance, by the manner in which the characters of both parents are blended, and by one form absorbing another through repeated crosses. In this latter case the progeny both of crossed species and varieties retain for a long period a tendency to revert to their ancestors, especially to that one which is prepotent in transmission. When any character has suddenly appeared in a race or species as the result of a 224single act of variation, as is general with monstrosities,295 and this race is crossed with another not thus characterised, the characters in question do not commonly appear in a blended condition in the young, but are transmitted to them either perfectly developed or not at all. As with the crossed races of man cases of this kind rarely or never occur, this may be used as an argument against the view suggested by some ethnologists, namely that certain characters, for instance the blackness of the negro, first appeared as a sudden variation or sport. Had this occurred, it is probable that mulattoes would often have been born, either completely black or completely white.
Regardless of fertility, the traits of the offspring from a cross have sometimes been considered evidence for whether the parent forms should be classified as species or varieties. However, after examining the evidence closely, I have concluded that no general rules of this kind can be relied upon. For example, when it comes to humans, the offspring of distinct races closely resemble the offspring of true species and varieties in every aspect. This is demonstrated by how the traits of both parents blend together and how one form can dominate another through repeated crossings. In this latter situation, the progeny of both crossed species and varieties tend to revert to their ancestors for a long time, especially to the one that is stronger in passing on traits. When a trait suddenly appears in a race or species as a result of a single variation, as is often the case with monstrosities, and this race is crossed with another that does not have that characteristic, the traits in question usually do not appear blended in the young; instead, they are passed on either fully developed or not at all. Since such cases rarely or never occur among crossed human races, this can be used as an argument against the idea suggested by some ethnologists that certain characteristics, like the blackness of the negro, first appeared as a sudden variation or sport. If that had happened, it is likely that mulattoes would frequently have been born, either completely black or completely white.
We have now seen that a naturalist might feel himself fully justified in ranking the races of man as distinct species; for he has found that they are distinguished by many differences in structure and constitution, some being of importance. These differences have, also, remained nearly constant for very long periods of time. He will have been in some degree influenced by the enormous range of man, which is a great anomaly in the class of mammals, if mankind be viewed as a single species. He will have been struck with the distribution of the several so-called races, in accordance with that of other undoubtedly distinct species of mammals. Finally he might urge that the mutual fertility of all the races has not as yet been fully proved; and even if proved would not be an absolute proof of their specific identity.
We can see that a naturalist might feel completely justified in classifying human races as distinct species; he has found that they are marked by many differences in structure and constitution, some of which are significant. These differences have also remained pretty consistent over very long periods. He may have been influenced by the vast range of humans, which is quite unusual among mammals if we consider humanity as a single species. He would likely notice the distribution of the various so-called races, which aligns with that of other clearly distinct species of mammals. Lastly, he might argue that the mutual fertility of all races hasn't been fully proven; and even if it were, that wouldn’t definitively prove their species identity.
On the other side of the question, if our supposed naturalist were to enquire whether the forms of man kept distinct like ordinary species, when mingled to225gether in large numbers in the same country, he would immediately discover that this was by no means the case. In Brazil he would behold an immense mongrel population of Negroes and Portuguese; in Chiloe and other parts of South America, he would behold the whole population consisting of Indians and Spaniards blended in various degrees.296 In many parts of the same continent he would meet with the most complex crosses between Negroes, Indians, and Europeans; and such triple crosses afford the severest test, judging from the vegetable kingdom, of the mutual fertility of the parent-forms. In one island of the Pacific he would find a small population of mingled Polynesian and English blood; and in the Viti Archipelago a population of Polynesians and Negritos crossed in all degrees. Many analogous cases could be added, for instance, in South Africa. Hence the races of man are not sufficiently distinct to co-exist without fusion; and this it is, which in all ordinary cases affords the usual test of specific distinctness.
On the other hand, if our so-called naturalist were to ask whether humans remain distinct like typical species when they mix in large numbers within the same country, he would quickly find out that this is definitely not true. In Brazil, he would see a huge mixed population of Black people and Portuguese; in Chiloé and other areas of South America, he would find the entire population made up of Indians and Spaniards mixed together in various ways. In many other parts of the same continent, he would encounter the most complex mixes of Black people, Indians, and Europeans; and these triple combinations serve as a strong test, based on the plant kingdom, for the mutual fertility of the parent forms. On one island in the Pacific, he would come across a small population of mixed Polynesian and English ancestry; and in the Viti Archipelago, a population of Polynesians and Negritos mixed in various degrees. Many similar examples could be added, for instance, in South Africa. Therefore, human races are not distinct enough to exist together without blending; and this blending is what usually serves as the test for specific distinctness.
Our naturalist would likewise be much disturbed as soon as he perceived that the distinctive characters of every race of man were highly variable. This strikes every one when he first beholds the negro-slaves in Brazil, who have been imported from all parts of Africa. The same remark holds good with the Polynesians, and with many other races. It may be doubted whether any character can be named which is distinctive of a race and is constant. Savages, even within the limits of the same tribe, are not nearly so uniform in character, as has often been said. Hottentot women offer certain 226peculiarities, more strongly marked than those occurring in any other race, but these are known not to be of constant occurrence. In the several American tribes, colour and hairyness differ considerably; as does colour to a certain degree, and the shape of the features greatly, in the Negroes of Africa. The shape of the skull varies much in some races;297 and so it is with every other character. Now all naturalists have learnt by dearly-bought experience, how rash it is to attempt to define species by the aid of inconstant characters.
Our naturalist would also be quite disturbed as soon as he noticed that the unique traits of every race of humans were highly variable. This is evident to anyone who first sees the African slaves in Brazil, who have come from various parts of Africa. The same observation applies to Polynesians and many other races. It's questionable whether any trait can be identified as characteristic of a race and remain constant. Even within the same tribe, Indigenous people are not nearly as uniform in traits as has often been claimed. Hottentot women display certain features that are more pronounced than those found in any other race, but these features are known not to be consistently present. In various American tribes, skin color and hairiness vary significantly; color to some extent, and facial feature shapes vary greatly among Africans of Black descent. The shape of the skull varies significantly in some races; and the same goes for every other characteristic. Now, all naturalists have learned through costly experience how foolish it is to try to define species based on inconsistent traits.
But the most weighty of all the arguments against treating the races of man as distinct species, is that they graduate into each other, independently in many cases, as far as we can judge, of their having intercrossed. Man has been studied more carefully than any other organic being, and yet there is the greatest possible diversity amongst capable judges whether he should be classed as a single species or race, or as two (Virey), as three (Jacquinot), as four (Kant), five (Blumenbach), six (Buffon), seven (Hunter), eight (Agassiz), eleven (Pickering), fifteen (Bory St. Vincent), sixteen (Desmoulins), twenty-two (Morton), sixty (Crawfurd), or as sixty-three, according to Burke.298 This diversity of judgment does not prove that the races ought not to be ranked as species, but it shews that they graduate into each other, and that it is hardly possible to discover clear distinctive characters between them.
But the strongest argument against treating human races as different species is that they blend into each other, often independently, based on our observations, regardless of whether they have interbred. Humans have been studied more closely than any other living beings, yet there's a wide range of opinions among knowledgeable experts about whether they should be categorized as a single species or race, or as two (Virey), three (Jacquinot), four (Kant), five (Blumenbach), six (Buffon), seven (Hunter), eight (Agassiz), eleven (Pickering), fifteen (Bory St. Vincent), sixteen (Desmoulins), twenty-two (Morton), sixty (Crawfurd), or sixty-three, according to Burke.298 This variety of opinions doesn't necessarily mean that races shouldn't be classified as species, but it does indicate that they merge into each other, making it nearly impossible to find clear distinguishing traits between them.
Every naturalist who has had the misfortune to under227take the description of a group of highly varying organisms, has encountered cases (I speak after experience) precisely like that of man; and if of a cautious disposition, he will end by uniting all the forms which graduate into each other as a single species; for he will say to himself that he has no right to give names to objects which he cannot define. Cases of this kind occur in the Order which includes man, namely in certain genera of monkeys; whilst in other genera, as in Cercopithecus, most of the species can be determined with certainty. In the American genus Cebus, the various forms are ranked by some naturalists as species, by others as mere geographical races. Now if numerous specimens of Cebus were collected from all parts of South America, and those forms which at present appear to be specifically distinct, were found to graduate into each other by close steps, they would be ranked by most naturalists as mere varieties or races; and thus the greater number of naturalists have acted with respect to the races of man. Nevertheless it must be confessed that there are forms, at least in the vegetable kingdom,299 which we cannot avoid naming as species, but which are connected together, independently of intercrossing, by numberless gradations.
Every naturalist who has had the unfortunate task of describing a group of highly variable organisms has faced situations (I speak from experience) just like that of humans; and if they are cautious, they will ultimately combine all the forms that transition into one another as a single species because they will think to themselves that they have no right to name things they can't clearly define. These situations occur in the order that includes humans, specifically in certain genera of monkeys; in contrast, in other genera, like Cercopithecus, most species can be identified with certainty. In the American genus Cebus, the various forms are classified by some naturalists as species, while others consider them merely geographical races. If many specimens of Cebus were collected from all parts of South America, and those forms that currently seem to be specifically distinct were found to gradually transition into one another, most naturalists would classify them as simply varieties or races; and this is how most naturalists have approached the races of humans. However, it must be acknowledged that there are forms, at least in the plant kingdom, that we can't avoid naming as species, yet which are connected to each other, regardless of interbreeding, by numerous gradations.
Some naturalists have lately employed the term “sub-species” to designate forms which possess many of the characteristics of true species, but which hardly deserve so high a rank. Now if we reflect on the weighty arguments, above given, for raising the races of man to the dignity of species, and the insuperable difficulties on the other side in defining them, the term “sub-species”228 might here be used with much propriety. But from long habit the term “race” will perhaps always be employed. The choice of terms is only so far important as it is highly desirable to use, as far as that may be possible, the same terms for the same degrees of difference. Unfortunately this is rarely possible; for within the same family the larger genera generally include closely-allied forms, which can be distinguished only with much difficulty, whilst the smaller genera include forms that are perfectly distinct; yet all must equally be ranked as species. So again the species within the same large genus by no means resemble each other to the same degree: on the contrary, in most cases some of them can be arranged in little groups round other species, like satellites round planets.300
Some naturalists have recently started using the term “sub-species” to refer to forms that share many characteristics with true species but don’t quite deserve that high status. If we consider the strong arguments mentioned earlier for elevating human races to the level of species, along with the significant challenges in defining them, the term “sub-species” might fit well here. However, due to habit, the term “race” will likely continue to be used. The choice of terms is important because it’s desirable to use consistent terminology for similar levels of difference. Unfortunately, this is often not possible; within the same family, larger genera usually contain closely related forms that are difficult to distinguish, while smaller genera consist of forms that are quite distinct, yet all must still be classified as species. Likewise, species within the same large genus do not all resemble each other to the same extent: in many cases, some can be grouped around other species, much like satellites orbiting planets.228300
The question whether mankind consists of one or several species has of late years been much agitated by anthropologists, who are divided into two schools of monogenists and polygenists. Those who do not admit the principle of evolution, must look at species either as separate creations or as in some manner distinct entities; and they must decide what forms to rank as species by the analogy of other organic beings which are commonly thus received. But it is a hopeless endeavour to decide this point on sound grounds, until some definition of the term “species” is generally accepted; and the definition must not include an element which cannot possibly be ascertained, such as an act of creation. We might as well attempt without any definition to decide whether a certain number of houses should be called a village, or town, or city. We have a practical illustration of the difficulty in the never-229ending doubts whether many closely-allied mammals, birds, insects, and plants, which represent each other in North America and Europe, should be ranked species or geographical races; and so it is with the productions of many islands situated at some little distance from the nearest continent.
The debate over whether humanity is one species or multiple has recently stirred up a lot of discussion among anthropologists, who are split into two groups: monogenists and polygenists. Those who reject the idea of evolution must view species either as separate creations or as distinct entities in some way; they have to determine which forms to classify as species based on how other living beings are usually categorized. However, trying to resolve this issue on solid grounds is pointless until there’s a commonly accepted definition of "species," and that definition can't include something that can't be determined, like an act of creation. It’s similar to trying to figure out if a certain number of houses should be labeled a village, town, or city without any clear definition. A practical example of the difficulty lies in the ongoing uncertainty about whether many closely related mammals, birds, insects, and plants found in North America and Europe should be classified as species or geographical races; the same applies to the organisms from many islands located a short distance from the nearest continent.
Those naturalists, on the other hand, who admit the principle of evolution, and this is now admitted by the greater number of rising men, will feel no doubt that all the races of man are descended from a single primitive stock; whether or not they think fit to designate them as distinct species, for the sake of expressing their amount of difference.301 With our domestic animals the question whether the various races have arisen from one or more species is different. Although all such races, as well as all the natural species within the same genus, have undoubtedly sprung from the same primitive stock, yet it is a fit subject for discussion, whether, for instance, all the domestic races of the dog have acquired their present differences since some one species was first domesticated and bred by man; or whether they owe some of their characters to inheritance from distinct species, which had already been modified in a state of nature. With mankind no such question can arise, for he cannot be said to have been domesticated at any particular period.
Those naturalists, on the other hand, who accept the principle of evolution—now recognized by most emerging thinkers—will have no doubt that all human races are descended from a single primitive lineage; whether or not they choose to label them as distinct species to indicate their differences.301 With our domestic animals, the question of whether various breeds originated from one or multiple species is different. Even though all these breeds, as well as all natural species within the same genus, have clearly come from the same primitive stock, it's worth discussing whether, for example, all domestic dog breeds have developed their current differences since one species was first domesticated and bred by humans; or whether they have inherited some traits from distinct species that had already undergone changes in nature. For humans, no such question arises, as we can't say that they were domesticated at any specific time.
When the races of man diverged at an extremely remote epoch from their common progenitor, they will have differed but little from each other, and been few in number; consequently they will then, as far as their distinguishing characters are concerned, have had less claim to rank as distinct species, than the existing so230-called races. Nevertheless such early races would perhaps have been ranked by some naturalists as distinct species, so arbitrary is the term, if their differences, although extremely slight, had been more constant than at present, and had not graduated into each other.
When human races split off from their common ancestor a very long time ago, they probably didn't differ much from one another and were few in number. Because of this, in terms of their distinguishing traits, they would have had less justification to be classified as separate species compared to the so-called races we have today. Still, some early naturalists might have considered these early races to be distinct species, since the term is quite arbitrary, if their differences, even though minimal, had been more consistent than they are now and hadn't blended into one another.
It is, however, possible, though far from probable, that the early progenitors of man might at first have diverged much in character, until they became more unlike each other than are any existing races; but that subsequently, as suggested by Vogt,302 they converged in character. When man selects for the same object the offspring of two distinct species, he sometimes induces, as far as general appearance is concerned, a considerable amount of convergence. This is the case, as shewn by Von Nathusius,303 with the improved breeds of pigs, which are descended from two distinct species; and in a less well-marked manner with the improved breeds of cattle. A great anatomist, Gratiolet, maintains that the anthropomorphous apes do not form a natural sub-group; but that the orang is a highly developed gibbon or semnopithecus; the chimpanzee a highly developed macacus; and the gorilla a highly developed mandrill. If this conclusion, which rests almost exclusively on brain-characters, be admitted, we should have a case of convergence at least in external characters, for the anthropomorphous apes are certainly more like each other in many points than they are to other apes. All analogical resemblances, as of a whale to a fish, may indeed be said to be cases of convergence; but this term has never been applied to superficial and adaptive resemblances. It 231would be extremely rash in most cases to attribute to convergence close similarity in many points of structure in beings which had once been widely different. The form of a crystal is determined solely by the molecular forces, and it is not surprising that dissimilar substances should sometimes assume the same form; but with organic beings we should bear in mind that the form of each depends on an infinitude of complex relations, namely on the variations which have arisen, these being due to causes far too intricate to be followed out,—on the nature of the variations which have been preserved, and this depends on the surrounding physical conditions, and in a still higher degree on the surrounding organisms with which each has come into competition,—and lastly, on inheritance (in itself a fluctuating element) from innumerable progenitors, all of which have had their forms determined through equally complex relations. It appears utterly incredible that two organisms, if differing in a marked manner, should ever afterwards converge so closely as to lead to a near approach to identity throughout their whole organisation. In the case of the convergent pigs above referred to, evidence of their descent from two primitive stocks is still plainly retained, according to Von Nathusius, in certain bones of their skulls. If the races of man were descended, as supposed by some naturalists, from two or more distinct species, which had differed as much, or nearly as much, from each other, as the orang differs from the gorilla, it can hardly be doubted that marked differences in the structure of certain bones would still have been discoverable in man as he now exists.
It is possible, though unlikely, that the early ancestors of humans may have started off quite different from each other, becoming more unlike any existing races over time. However, as Vogt suggests,302 they may have come to resemble each other more. When a person breeds two distinct species for the same trait, it can sometimes result in a notable convergence in general appearance. This is evident in the improved breeds of pigs, which come from two different species, as shown by Von Nathusius,303 and to a lesser extent in the improved breeds of cattle. A renowned anatomist, Gratiolet, argues that the anthropoid apes don't form a natural subgroup; instead, the orangutan is a highly developed gibbon or semnopithecus, the chimpanzee is a highly developed macaque, and the gorilla is a highly developed mandrill. If we accept this conclusion, which is based mainly on brain characteristics, it suggests that there might be convergence in external traits, as the anthropoid apes are indeed more similar to each other in several ways than they are to other apes. All analogical similarities, like a whale resembling a fish, can be considered examples of convergence; however, this term has never been used for superficial and adaptive similarities. It would be very reckless to attribute close similarities in many structural features of beings that were once very different to convergence. The shape of a crystal is determined solely by molecular forces, so it's not surprising that different substances can sometimes have the same shape; but with living organisms, we should remember that each form results from an incredibly complex set of relationships, including the variations that have emerged from causes that are too complex to trace—on the nature of the variations that have been preserved, which depends on physical conditions and even more on the organisms with which each has competed—and finally, on heredity (which is itself a variable factor) from countless ancestors, all of which were shaped by equally complex relationships. It seems almost unbelievable that two organisms that are significantly different could later converge so closely that they become nearly identical in their entire structure. In the case of the converging pigs mentioned earlier, evidence of their descent from two basic stocks is still clearly evident, according to Von Nathusius, in certain bones of their skulls. If human races descended, as some naturalists suggest, from two or more distinct species that differed as much, or nearly as much, as the orangutan differs from the gorilla, it’s hard to believe that there wouldn’t still be noticeable differences in the structure of certain bones in modern humans.
Although the existing races of man differ in many respects, as in colour, hair, shape of skull, proportions of the body, &c., yet if their whole organisation be taken232 into consideration they are found to resemble each other closely in a multitude of points. Many of these points are of so unimportant or of so singular a nature, that it is extremely improbable that they should have been independently acquired by aboriginally distinct species or races. The same remark holds good with equal or greater force with respect to the numerous points of mental similarity between the most distinct races of man. The American aborigines, Negroes and Europeans differ as much from each other in mind as any three races that can be named; yet I was incessantly struck, whilst living with the Fuegians on board the “Beagle,” with the many little traits of character, shewing how similar their minds were to ours; and so it was with a full-blooded negro with whom I happened once to be intimate.
Although the different races of humans vary in many ways, like skin color, hair type, skull shape, and body proportions, when you consider their overall structure, they closely resemble each other in many aspects. Many of these similarities are so trivial or unique that it’s unlikely they developed independently in originally distinct species or races. The same observation applies just as strongly or even more so to the numerous intellectual similarities found among the most different human races. The indigenous peoples of the Americas, Africans, and Europeans differ significantly in their thinking, as much as any three races you could name; yet, while I was living with the Fuegians on board the “Beagle,” I was often struck by the many small character traits that showed how similar their minds were to ours. The same was true for a full-blooded African man I once became close with.
He who will carefully read Mr. Tylor’s and Sir J. Lubbock’s interesting works304 can hardly fail to be deeply impressed with the close similarity between the men of all races in tastes, dispositions and habits. This is shewn by the pleasure which they all take in dancing, rude music, acting, painting, tattooing, and otherwise decorating themselves,—in their mutual comprehension of gesture-language—and, as I shall be able to shew in a future essay, by the same expression in their features, and by the same inarticulate cries, when they are excited by various emotions. This similarity, or rather identity, is striking, when contrasted with the different expressions which may be observed in distinct species of monkeys. There is good evidence that the art of shooting with bows and arrows has not been handed down from any common progenitor of 233mankind, yet the stone arrow-heads, brought from the most distant parts of the world and manufactured at the most remote periods, are, as Nilsson has shewn,305 almost identical; and this fact can only be accounted for by the various races having similar inventive or mental powers. The same observation has been made by archæologists306 with respect to certain widely-prevalent ornaments, such as zigzags, &c.; and with respect to various simple beliefs and customs, such as the burying of the dead under megalithic structures. I remember observing in South America,307 that there, as in so many other parts of the world, man has generally chosen the summits of lofty hills, on which to throw up piles of stones, either for the sake of recording some remarkable event, or for burying his dead.
Anyone who takes the time to read Mr. Tylor’s and Sir J. Lubbock’s fascinating works304 will likely be struck by how similar people from all races are in their tastes, personalities, and habits. This is evident in their enjoyment of dancing, basic music, acting, painting, tattooing, and decorating themselves, as well as in how they understand gesture-based communication. As I’ll demonstrate in a future essay, you can also see similar expressions in their faces and the same inarticulate sounds they make when experiencing different emotions. This similarity, or rather identity, is particularly noticeable when compared to the varying expressions seen in different species of monkeys. There’s strong evidence that the skill of using bows and arrows wasn’t passed down from a common ancestor of humanity; however, as Nilsson has shown,305 stone arrowheads found around the world, made at different times, are almost identical. This can only be explained by the fact that various races have similar inventive or mental capabilities. Archaeologists306 have noticed the same thing regarding certain widely used ornaments, like zigzags, and with various simple beliefs and practices, such as burying the dead under megalithic structures. I remember seeing in South America,307 as in many other places, that people typically chose the tops of high hills to build piles of stones, either to commemorate significant events or to bury their dead.
Now when naturalists observe a close agreement in numerous small details of habits, tastes and dispositions between two or more domestic races, or between nearly-allied natural forms, they use this fact as an argument that all are descended from a common progenitor who was thus endowed; and consequently that all should be classed under the same species. The same argument may be applied with much force to the races of man.
Now, when naturalists notice a strong similarity in many small details of habits, tastes, and behaviors among two or more domestic breeds, or between closely related natural forms, they use this observation to argue that they all share a common ancestor who had these traits; therefore, they should all be classified as the same species. The same argument can be applied strongly to the different races of humanity.
As it is improbable that the numerous and unimportant points of resemblance between the several races of man in bodily structure and mental faculties (I do not here refer to similar customs) should all have been independently acquired, they must have been inherited from progenitors who were thus characterised. We thus gain some insight into the early state of man, 234before he had spread step by step over the face of the earth. The spreading of man to regions widely separated by the sea, no doubt, preceded any considerable amount of divergence of character in the several races; for otherwise we should sometimes meet with the same race in distinct continents; and this is never the case. Sir J. Lubbock, after comparing the arts now practised by savages in all parts of the world, specifies those which man could not have known, when he first wandered from his original birthplace; for if once learnt they would never have been forgotten.308 He thus shews that “the spear, which is but a development of the knife-point, and the club, which is but a long hammer, are the only things left.” He admits, however, that the art of making fire probably had already been discovered, for it is common to all the races now existing, and was known to the ancient cave-inhabitants of Europe. Perhaps the art of making rude canoes or rafts was likewise known; but as man existed at a remote epoch, when the land in many places stood at a very different level, he would have been able, without the aid of canoes, to have spread widely. Sir J. Lubbock further remarks how improbable it is that our earliest ancestors could have “counted as high as ten, considering that so many races now in existence cannot get beyond four.” Nevertheless, at this early period, the intellectual and social faculties of man could hardly have been inferior in any extreme degree to those now possessed by the lowest savages; otherwise primeval man could not have been so eminently successful in the struggle for life, as proved by his early and wide diffusion.
As it’s unlikely that all the many minor similarities in body structure and mental abilities among the different races of humans (not referring to similar customs here) were developed independently, they must have been passed down from ancestors who had these traits. This gives us some understanding of the early state of humanity, 234 before people gradually spread across the earth. The movement of humans to regions that are far apart by the sea likely happened before there was a significant divergence in the characteristics of different races; otherwise, we would sometimes find the same race on different continents, which never happens. Sir J. Lubbock, after examining the skills currently used by people labeled as savages around the world, points out the skills that humans could not have known when they first left their original homeland, because if they had been learned, they would never have been forgotten.308 He demonstrates that “the spear, which is just an evolution of the knife-point, and the club, which is just a longer hammer, are the only tools left.” However, he acknowledges that the skill of making fire was probably already discovered, as it is common to all existing races and was known to the ancient people of Europe who lived in caves. It’s possible that the ability to make simple canoes or rafts was also known; but since humans existed a long time ago when the land was at very different levels in many places, they could have spread out widely without needing canoes. Sir J. Lubbock further points out how unlikely it is that our earliest ancestors could have “counted to ten, considering that so many existing races can’t count beyond four.” Nevertheless, at this early stage, the intellectual and social abilities of humans could hardly have been significantly inferior to those of the most primitive groups today; otherwise, early humans could not have been so successful in the fight for survival, as shown by their early and widespread presence.
From the fundamental differences between certain 235languages, some philologists have inferred that when man first became widely diffused he was not a speaking animal; but it may be suspected that languages, far less perfect than any now spoken, aided by gestures, might have been used, and yet have left no traces on subsequent and more highly-developed tongues. Without the use of some language, however imperfect, it appears doubtful whether man’s intellect could have risen to the standard implied by his dominant position at an early period.
From the basic differences between certain 235 languages, some linguists have concluded that when humans first spread out, they might not have been speaking creatures; but it’s possible that languages, much less advanced than any we use today, supported by gestures, could have been in use and yet left no evidence in later, more developed languages. However, without some form of language, no matter how imperfect, it seems unlikely that human intelligence could have reached the level suggested by their leading role in early times.
Whether primeval man, when he possessed very few arts of the rudest kind, and when his power of language was extremely imperfect, would have deserved to be called man, must depend on the definition which we employ. In a series of forms graduating insensibly from some ape-like creature to man as he now exists, it would be impossible to fix on any definite point when the term “man” ought to be used. But this is a matter of very little importance. So again it is almost a matter of indifference whether the so-called races of man are thus designated, or are ranked as species or sub-species; but the latter term appears the most appropriate. Finally, we may conclude that when the principles of evolution are generally accepted, as they surely will be before long, the dispute between the monogenists and the polygenists will die a silent and unobserved death.
Whether early humans, when they had very few basic skills and their ability to communicate was quite limited, should truly be called "human" depends on the definition we use. In a gradual progression from some ape-like ancestor to modern humans, it's impossible to pinpoint a specific moment when the term "human" should apply. However, this is not very significant. Similarly, it hardly matters whether we refer to the so-called races of humanity as such, or classify them as species or subspecies; the latter term seems more fitting. Ultimately, we can conclude that once the principles of evolution are widely accepted, as they certainly will be soon, the debate between monogenists and polygenists will quietly fade away.
One other question ought not to be passed over without notice, namely, whether, as is sometimes assumed, each sub-species or race of man has sprung from a single pair of progenitors. With our domestic animals a new race can readily be formed from a single pair possessing some new character, or even from a single individual thus characterised, by carefully match236ing the varying offspring; but most of our races have been formed, not intentionally from a selected pair, but unconsciously by the preservation of many individuals which have varied, however slightly, in some useful or desired manner. If in one country stronger and heavier horses, and in another country lighter and fleeter horses, were habitually preferred, we may feel sure that two distinct sub-breeds would, in the course of time, be produced, without any particular pairs or individuals having been separated and bred from in either country. Many races have been thus formed, and their manner of formation is closely analogous with that of natural species. We know, also, that the horses which have been brought to the Falkland Islands have become, during successive generations, smaller and weaker, whilst those which have run wild on the Pampas have acquired larger and coarser heads; and such changes are manifestly due, not to any one pair, but to all the individuals having been subjected to the same conditions, aided, perhaps, by the principle of reversion. The new sub-breeds in none of these cases are descended from any single pair, but from many individuals which have varied in different degrees, but in the same general manner; and we may conclude that the races of man have been similarly produced, the modifications being either the direct result of exposure to different conditions, or the indirect result of some form of selection. But to this latter subject we shall presently return.
One other question shouldn't be overlooked, which is whether, as is sometimes assumed, each sub-species or race of humans has come from a single pair of ancestors. With our domestic animals, a new breed can easily be created from a single pair that has some new trait, or even from one individual with that trait, by carefully breeding their varied offspring. However, most of our races have developed, not intentionally from a selected pair, but unconsciously from the preservation of many individuals that have varied, even slightly, in some useful or desirable way. If in one country stronger and heavier horses are preferred, and in another, lighter and faster horses are favored, we can be sure that over time, two distinct sub-breeds would emerge, even without specific pairs or individuals being isolated and bred in either location. Many races have formed this way, and their formation process is quite similar to that of natural species. We also know that the horses brought to the Falkland Islands have become, over generations, smaller and weaker, while those that have gone wild in the Pampas have developed larger and coarser heads. Such changes are clearly due not to any one pair, but to all individuals being subjected to the same conditions, possibly aided by the principle of reversion. In none of these cases do the new sub-breeds descend from a single pair; instead, they come from many individuals that have varied to different extents, but in a similar manner. We can conclude that human races have been produced in a similar way, with modifications being either a direct result of different conditions or an indirect result of some form of selection. But we'll come back to this latter topic shortly.
On the Extinction of the Races of Man.—The partial and complete extinction of many races and sub-races of man are historically known events. Humboldt saw in South America a parrot which was the sole living creature that could speak the language of a lost tribe.237 Ancient monuments and stone implements found in all parts of the world, of which no tradition is preserved by the present inhabitants, indicate much extinction. Some small and broken tribes, remnants of former races, still survive in isolated and generally mountainous districts. In Europe the ancient races were all, according to Schaaffhausen,309 “lower in the scale than the rudest living savages;” they must therefore have differed, to a certain extent, from any existing race. The remains described by Professor Broca310 from Les Eyzies, though they unfortunately appear to have belonged to a single family, indicate a race with a most singular combination of low or simious and high characteristics, and is “entirely different from any other race, ancient or modern, that we have ever heard of.” It differed, therefore, from the quaternary race of the caverns of Belgium.
On the Extinction of the Races of Man.—The partial and complete extinction of many races and sub-races of humans are well-documented historical events. Humboldt observed a parrot in South America that was the only living creature able to speak the language of a lost tribe.237 Ancient monuments and stone tools found around the world, with no traditions preserved by current inhabitants, suggest significant extinction. Some small and fragmented tribes, remnants of past races, still exist in isolated and typically mountainous areas. In Europe, the ancient races were all, according to Schaaffhausen,309 “lower on the scale than the rudest living savages;” thus, they must have been somewhat different from any existing race. The remains described by Professor Broca310 from Les Eyzies, although they unfortunately seem to belong to a single family, indicate a race with a unique mix of primitive and advanced features, and is “entirely different from any other race, ancient or modern, that we have ever known.” It was therefore distinct from the quaternary race of the caves in Belgium.
Unfavourable physical conditions appear to have had but little effect in the extinction of races.311 Man has long lived in the extreme regions of the North, with no wood wherewith to make his canoes or other implements, and with blubber alone for burning and giving him warmth, but more especially for melting the snow. In the Southern extremity of America the Fuegians survive without the protection of clothes, or of any building worthy to be called a hovel. In South Africa the aborigines wander over the most arid plains, where dangerous beasts abound. Man can withstand the deadly influence of the Terai at the foot of the Himalaya, and the pestilential shores of tropical Africa.
Unfavorable physical conditions seem to have had little impact on the extinction of races.311 Humans have long lived in the harsh regions of the North, without wood to make canoes or other tools, relying solely on blubber for warmth and for melting snow. In the southern tip of America, the Fuegians survive without clothing or any structure that could be called a shelter. In South Africa, the indigenous people roam the driest plains, where dangerous animals are abundant. Humans can endure the deadly conditions of the Terai at the base of the Himalayas and the unhealthy shores of tropical Africa.
Extinction follows chiefly from the competition of tribe with tribe, and race with race. Various checks are always in action, as specified in a former chapter, which serve to keep down the numbers of each savage tribe,—such as periodical famines, the wandering of the parents and the consequent deaths of infants, prolonged suckling, the stealing of women, wars, accidents, sickness, licentiousness, especially infanticide, and, perhaps, lessened fertility from less nutritious food, and many hardships. If from any cause any one of these checks is lessened, even in a slight degree, the tribe thus favoured will tend to increase; and when one of two adjoining tribes becomes more numerous and powerful than the other, the contest is soon settled by war, slaughter, cannibalism, slavery, and absorption. Even when a weaker tribe is not thus abruptly swept away, if it once begins to decrease, it generally goes on decreasing until it is extinct.312
Extinction mainly happens due to competition between tribes and races. Various factors are always at play, as mentioned in a previous chapter, that help keep the population of each savage tribe in check—like periodic famines, the wandering of parents leading to the deaths of infants, extended breastfeeding, the kidnapping of women, wars, accidents, illness, promiscuity, especially infanticide, and possibly reduced fertility from less nutritious food, along with many hardships. If any of these factors is reduced even slightly, the favored tribe will likely start to grow; and when one of two neighboring tribes becomes larger and stronger than the other, the situation typically resolves through war, massacre, cannibalism, enslavement, and absorption. Even when a weaker tribe isn't immediately wiped out, if it starts to decline, it usually keeps decreasing until it disappears.312
When civilised nations come into contact with barbarians the struggle is short, except where a deadly climate gives its aid to the native race. Of the causes which lead to the victory of civilised nations, some are plain and some very obscure. We can see that the cultivation of the land will be fatal in many ways to savages, for they cannot, or will not, change their habits. New diseases and vices are highly destructive; and it appears that in every nation a new disease causes much death, until those who are most susceptible to its destructive influence are gradually weeded out;313 and so it may be with the evil effects from spirituous liquors, as well as with the unconquerably strong taste for them shewn by so many savages. It further appears, mysterious as is 239the fact, that the first meeting of distinct and separated people generates disease.314 Mr. Sproat, who in Vancouver Island closely attended to the subject of extinction, believes that changed habits of life, which always follow from the advent of Europeans, induces much ill-health. He lays, also, great stress on so trifling a cause as that the natives become “bewildered and dull by the new life around them; they lose the motives for exertion, and get no new ones in their place.”315
When civilized nations interact with uncivilized ones, the conflict is usually quick, unless a harsh climate supports the local population. Some factors that lead to the triumph of civilized nations are clear, while others are quite hidden. It's obvious that farming can be detrimental to indigenous people because they often cannot or won't adapt their ways. New diseases and harmful behaviors can be incredibly damaging; it seems that in every society, a new illness causes significant fatalities until those most vulnerable to its impacts are gradually eliminated; and the same may apply to the negative effects of alcohol and the strong craving for it seen in many indigenous groups. Additionally, it seems, although it's a puzzling fact, that the first encounters between very different populations lead to disease. Mr. Sproat, who closely studied the issue of extinction on Vancouver Island, believes that the changes in lifestyle that come with European contact lead to significant health issues. He also emphasizes that something as seemingly minor as the natives becoming "confused and lethargic due to the new environment; they lose their motivation to strive and find no new incentives in return."
The grade of civilisation seems a most important element in the success of nations which come in competition. A few centuries ago Europe feared the inroads of Eastern barbarians; now, any such fear would be ridiculous. It is a more curious fact, that savages did not formerly waste away, as Mr. Bagehot has remarked, before the classical nations, as they now do before modern civilised nations; had they done so, the old moralists would have mused over the event; but there is no lament in any writer of that period over the perishing barbarians.316
The level of civilization seems to be a crucial factor in the success of competing nations. A few centuries ago, Europe was worried about the invasions from Eastern barbarians; now, that fear would be laughable. Interestingly, savages didn't decline in front of the classical nations, as Mr. Bagehot pointed out, in the same way they seem to now before modern civilized countries; if they had, the moralists of that time would have reflected on it, but there's no sorrow expressed by any writer from that era over the disappearing barbarians.316
Although the gradual decrease and final extinction of the races of man is an obscure problem, we can see that it depends on many causes, differing in different places and at different times. It is the same difficult problem as that presented by the extinction of one of the higher animals—of the fossil horse, for instance, which disappeared from South America, soon afterwards to be replaced, within the same districts, by countless troops of the Spanish horse. The New Zealander seems 240conscious of this parallelism, for he compares his future fate with that of the native rat almost exterminated by the European rat. The difficulty, though great to our imagination, and really great if we wish to ascertain the precise causes, ought not to be so to our reason, as long as we keep steadily in mind that the increase of each species and each race is constantly hindered by various checks; so that if any new check, or cause of destruction, even a slight one, be superadded, the race will surely decrease in number; and as it has everywhere been observed that savages are much opposed to any change of habits, by which means injurious checks could be counterbalanced, decreasing numbers will sooner or later lead to extinction; the end, in most cases, being promptly determined by the inroads of increasing and conquering tribes.
Although the gradual decline and eventual extinction of human races is a complex issue, it's clear that it results from various causes that differ across locations and time periods. This issue is similar to the extinction of one of the higher animals—like the fossil horse, which vanished from South America only to be replaced by large groups of Spanish horses in the same areas shortly after. The New Zealander seems aware of this parallel, as he likens his future to that of the native rat, which was almost wiped out by the European rat. While it poses a significant challenge to our imagination and is indeed complex if we aim to identify the exact causes, it shouldn't be too difficult for our reasoning, as long as we remember that the growth of each species and race is consistently hindered by various factors. Thus, if any new challenge or destructive cause, no matter how minor, is introduced, the population will likely decline. Additionally, it has been observed that indigenous people often resist changing their habits, which could counterbalance harmful factors, so diminishing numbers will eventually lead to extinction. The end, in many cases, is often quickly determined by the advances of growing and conquering tribes.
On the Formation of the Races of Man.—It may be premised that when we find the same race, though broken up into distinct tribes, ranging over a great area, as over America, we may attribute their general resemblance to descent from a common stock. In some cases the crossing of races already, distinct has led to the formation of new races. The singular fact that Europeans and Hindoos, who belong to the same Aryan stock and speak a language fundamentally the same, differ widely in appearance, whilst Europeans differ but little from Jews, who belong to the Semitic stock and speak quite another language, has been accounted for by Broca317 through the Aryan branches having been largely crossed during their wide diffusion by various indigenous tribes. When two races in close contact 241cross, the first result is a heterogeneous mixture: thus Mr. Hunter, in describing the Santali or hill-tribes of India, says that hundreds of imperceptible gradations may be traced “from the black, squat tribes of the mountains to the tall olive-coloured Brahman, with his intellectual brow, calm eyes, and high but narrow head;” so that it is necessary in courts of justice to ask the witnesses whether they are Santalis or Hindoos.318 Whether a heterogeneous people, such as the inhabitants of some of the Polynesian islands, formed by the crossing of two distinct races, with few or no pure members left, would ever become homogeneous, is not known from direct evidence. But as with our domesticated animals, a crossed breed can certainly, in the course of a few generations, be fixed and made uniform by careful selection,319 we may infer that the free and prolonged intercrossing during many generations of a heterogeneous mixture would supply the place of selection, and overcome any tendency to reversion, so that a crossed race would ultimately become homogeneous, though it might not partake in an equal degree of the characters of the two parent-races.
On the Formation of the Races of Man.—It can be assumed that when we see the same race, even though divided into different tribes, spread across a large area, like in America, we can trace their overall similarity back to a common ancestry. In some instances, the mixing of already distinct races has led to the emergence of new races. The interesting fact that Europeans and Hindoos, who are from the same Aryan ancestry and speak a fundamentally similar language, look very different, while Europeans look quite similar to Jews, who come from the Semitic ancestry and speak a completely different language, has been explained by Broca317 through the notion that the Aryan groups have frequently mixed with various local tribes during their widespread movement. When two races are in close contact and mix, the first result is a diverse blend: for instance, Mr. Hunter, while describing the Santali or hill tribes of India, states that you can trace hundreds of subtle gradations “from the black, squat tribes of the mountains to the tall olive-skinned Brahman, with his thoughtful brow, calm eyes, and high yet narrow head;” thus, in court, it's necessary to ask witnesses if they are Santalis or Hindoos.318 Whether a mixed population, like the people on some Polynesian islands formed by the blending of two distinct races with few or no pure individuals remaining, could ever become uniform is not known from direct evidence. However, just like our domesticated animals, a mixed breed can definitely be stabilized and made uniform through careful selection over a few generations,319 we can deduce that the ongoing and extensive intermixing over many generations of a diverse mixture would serve as a substitute for selection, and counteract any tendency to revert, meaning that a mixed race would ultimately become homogeneous, although it might not exhibit the traits of both parent races equally.
Of all the differences between the races of man, the colour of the skin is the most conspicuous and one of the best marked. Differences of this kind, it was formerly thought, could be accounted for by long exposure under different climates; but Pallas first shewed that this view is not tenable, and he has been followed by almost all anthropologists.320 The view has been 242rejected chiefly because the distribution of the variously coloured races, most of whom must have long inhabited their present homes, does not coincide with corresponding differences of climate. Weight must also be given to such cases as that of the Dutch families, who, as we hear on excellent authority,321 have not undergone the least change of colour, after residing for three centuries in South Africa. The uniform appearance in various parts of the world of gypsies and Jews, though the uniformity of the latter has been somewhat exaggerated,322 is likewise an argument on the same side. A very damp or a very dry atmosphere has been supposed to be more influential in modifying the colour of the skin than mere heat; but as D’Orbigny in South America, and Livingstone in Africa, arrived at diametrically opposite conclusions with respect to dampness and dryness, any conclusion on this head must be considered as very doubtful.323
Of all the differences between human races, skin color is the most noticeable and one of the most distinct. It was once believed that these differences could be explained by long exposure to different climates; however, Pallas was the first to demonstrate that this idea isn't valid, and nearly all anthropologists have since agreed.320 This perspective has been 242discredited primarily because the distribution of the various skin-colored races, most of whom must have lived in their current areas for a long time, does not align with the corresponding climate variations. Consideration should also be given to cases like that of the Dutch families, who, as reported from reliable sources,321 have remained unchanged in skin color after living in South Africa for three centuries. The consistent appearance of gypsies and Jews in different parts of the world, although the uniformity of the latter has been somewhat exaggerated,322 also supports this argument. It has been suggested that a very humid or very dry environment affects skin color more than just heat; however, since D’Orbigny in South America and Livingstone in Africa reached completely opposite conclusions about moisture and dryness, any conclusion on this matter must be considered very uncertain.323
Various facts, which I have elsewhere given, prove that the colour of the skin and hair is sometimes correlated in a surprising manner with a complete immunity from the action of certain vegetable poisons and from the attacks of certain parasites. Hence it occurred to me, that negroes and other dark races might have acquired their dark tints by the darker individuals escaping during a long series of generations from the deadly influence of the miasmas of their native countries.
Various facts, which I have mentioned elsewhere, show that the color of someone's skin and hair can sometimes be surprisingly linked to complete immunity from certain plant poisons and attacks from specific parasites. This led me to think that Black people and other darker-skinned groups may have developed their dark features because individuals with darker skin were able to survive over many generations from the harmful effects of the miasmas in their native lands.
I afterwards found that the same idea had long ago 243occurred to Dr. Wells.324 That negroes, and even mulattoes, are almost completely exempt from the yellow-fever, which is so destructive in tropical America, has long been known.325 They likewise escape to a large extent the fatal intermittent fevers that prevail along, at least, 2600 miles of the shores of Africa, and which annually cause one-fifth of the white settlers to die, and another fifth to return home invalided.326 This immunity in the negro seems to be partly inherent, depending on some unknown peculiarity of constitution, and partly the result of acclimatisation. Pouchet327 states that the negro regiments, borrowed from the Viceroy of Egypt for the Mexican war, which had been recruited near the Soudan, escaped the yellow-fever almost equally well with the negroes originally brought from various parts of Africa, and accustomed to the climate of the West Indies. That acclimatisation plays a part is shewn by the many cases in which negroes, after having resided for some time in a colder climate, have become to a certain extent liable to tropical fevers.328 The nature of the climate under which the white races have long resided, likewise has some influence on them; for during the fearful epidemic of yellow-fever in Demerara during 1837, Dr. Blair found that the death-rate of the immigrants was proportional 244to the latitude of the country whence they had come. With the negro the immunity, as far as it is the result of acclimatisation, implies exposure during a prodigious length of time; for the aborigines of tropical America, who have resided there from time immemorial, are not exempt from yellow-fever; and the Rev. B. Tristram states, that there are districts in Northern Africa which the native inhabitants are compelled annually to leave, though the negroes can remain with safety.
I later discovered that Dr. Wells had already considered the same idea a long time ago. It has long been known that Black people, as well as mixed-race individuals, are almost completely immune to yellow fever, which is so deadly in tropical America. They also largely avoid the fatal intermittent fevers that occur along, at least, 2600 miles of the African coast, which annually cause one in every five white settlers to die and another fifth to return home sick. This immunity in Black people seems to be partly inherent, due to some unknown trait of their biology, and partly the outcome of acclimatization. Pouchet states that the Black regiments borrowed from the Viceroy of Egypt for the Mexican War, which were recruited near Sudan, avoided yellow fever almost as well as the Black individuals originally brought from various parts of Africa, who were used to the climate of the West Indies. The role of acclimatization is shown by numerous cases where Black people, after living for some time in a colder climate, have become somewhat susceptible to tropical fevers. The climate where the white races have lived for a long time also influences them; during the terrible yellow fever epidemic in Demerara in 1837, Dr. Blair found that the death rate among immigrants was proportional to the latitude of the country they came from. For Black people, immunity, as far as it results from acclimatization, requires exposure over an incredibly long time; the native people of tropical America, who have lived there for ages, are not exempt from yellow fever. Additionally, Rev. B. Tristram mentions that there are areas in Northern Africa that native inhabitants must leave every year, whereas Black people can stay safely.
That the immunity of the negro is in any degree correlated with the colour of his skin is a mere conjecture: it may be correlated with some difference in his blood, nervous system, or other tissues. Nevertheless, from the facts above alluded to, and from some connection apparently existing between complexion and a tendency to consumption, the conjecture seemed to me not improbable. Consequently I endeavoured, with but little success,329 to ascertain how far it held good. The 245late Dr. Daniell, who had long lived on the West Coast of Africa, told me that he did not believe in any such relation. He was himself unusually fair, and had withstood the climate in a wonderful manner. When he first arrived as a boy on the coast, an old and experienced negro chief predicted from his appearance that this would prove the case. Dr. Nicholson, of Antigua, after having attended to this subject, wrote to me that he did not think that dark-coloured Europeans escaped the yellow-fever better than those that were light-coloured. Mr. J. M. Harris altogether denies330 that Europeans with dark hair withstand a hot climate better than other men; on the contrary, experience has taught him in making a selection of men for service on the coast of Africa, to choose those with red hair. As far, therefore, as these slight indications serve, there seems no foundation for the hypothesis, which has been accepted by several writers, that the colour of the black races may have resulted from darker and darker individuals having survived in greater numbers, during their exposure to the fever-generating miasmas of their native countries.
That the immunity of Black people is somehow linked to their skin color is just a guess: it might relate to differences in their blood, nervous system, or other tissues. Still, considering the facts mentioned earlier, along with some apparent connection between complexion and a tendency to tuberculosis, this guess didn't seem too unlikely to me. So, I tried, with little success,329 to find out how accurate it is. The late Dr. Daniell, who had lived on the West Coast of Africa for a long time, told me he didn't believe in any such relationship. He was unusually fair himself and had managed to handle the climate exceptionally well. When he first arrived as a boy on the coast, an old and experienced Black chief predicted his resilience based on his appearance. Dr. Nicholson from Antigua, after looking into this topic, wrote to me saying he didn’t think that dark-skinned Europeans were any better at avoiding yellow fever than lighter-skinned ones. Mr. J. M. Harris completely denies330 that Europeans with dark hair cope with hot climates better than others; in fact, his experience in selecting men for service on the coast of Africa leads him to prefer those with red hair. Therefore, based on these minor observations, there seems to be no solid basis for the idea, which several writers have accepted, that the skin color of Black races may have originated from darker individuals surviving more often when exposed to the fever-causing miasmas of their home countries.
Although with our present knowledge we cannot account for the strongly-marked differences in colour between the races of man, either through correlation with constitutional peculiarities, or through the direct action of climate; yet we must not quite ignore the 246latter agency, for there is good reason to believe that some inherited effect is thus produced.331
Although our current understanding doesn't fully explain the significant differences in skin color among human races—neither through links to specific physical traits nor through the direct influence of climate—we shouldn't completely dismiss the impact of climate. There's reason to believe that some inherited effects result from it.246331
We have seen in our third chapter that the conditions of life, such as abundant food and general comfort, affect in a direct manner the development of the bodily frame, the effects being transmitted. Through the combined influences of climate and changed habits of life, European settlers, in the United States undergo, as is generally admitted, a slight but extraordinarily rapid change of appearance. There is, also, a considerable body of evidence shewing that in the Southern States the house-slaves of the third generation present a markedly different appearance from the field-slaves.332
We’ve seen in our third chapter that factors like plenty of food and overall comfort directly influence physical development, and these effects are passed on. Due to the combined influences of climate and lifestyle changes, European settlers in the United States experience a noticeable yet incredibly rapid change in appearance, as is generally acknowledged. Additionally, there is a substantial amount of evidence showing that in the Southern States, house slaves from the third generation look significantly different from field slaves.332
If, however, we look to the races of man, as distributed over the world, we must infer that their characteristic differences cannot be accounted for by the direct action of different conditions of life, even after exposure to them for an enormous period of time. The Esquimaux live exclusively on animal food; they are clothed in thick fur, and are exposed to intense cold and to prolonged darkness; yet they do not differ in any extreme degree from the inhabitants of Southern China, who live entirely on vegetable food and are exposed almost naked to a hot, glaring climate. The unclothed Fuegians live on the marine productions of their inhospitable shores; the Botocudos of Brazil wander 247about the hot forests of the interior and live chiefly on vegetable productions; yet these tribes resemble each other so closely that the Fuegians on board the “Beagle” were mistaken by some Brazilians for Botocudos. The Botocudos again, as well as the other inhabitants of tropical America, are wholly different from the Negroes who inhabit the opposite shores of the Atlantic, are exposed to a nearly similar climate, and follow nearly the same habits of life.
If we look at the different races of humans around the world, it's clear that their unique differences can't be explained just by the various living conditions they've faced, even after a very long time. The Eskimos eat only animal products, wear thick fur, and endure extreme cold and long periods of darkness; yet they don't differ much at all from the people in Southern China, who eat mostly plants and live almost naked in a hot, bright climate. The naked Fuegians depend on the marine life along their harsh shores, while the Botocudos in Brazil roam the hot forests and mainly eat plants; still, these groups are so similar that some Brazilians mistook the Fuegians on board the “Beagle” for Botocudos. The Botocudos, along with other people from tropical America, are completely different from the Africans living on the opposite side of the Atlantic, who are exposed to nearly the same climate and have similar lifestyles.
Nor can the differences between the races of man be accounted for, except to a quite insignificant degree, by the inherited effects of the increased or decreased use of parts. Men who habitually live in canoes, may have their legs somewhat stunted; those who inhabit lofty regions have their chests enlarged; and those who constantly use certain sense-organs have the cavities in which they are lodged somewhat increased in size, and their features consequently a little modified. With civilised nations, the reduced size of the jaws from lessened use, the habitual play of different muscles serving to express different emotions, and the increased size of the brain from greater intellectual activity, have together produced a considerable effect on their general appearance in comparison with savages.333 It is also possible that increased bodily stature, with no corresponding increase in the size of the brain, may have given to some races (judging from the previously adduced cases of the rabbits) an elongated skull of the dolichocephalic type.
The differences between human races can’t really be explained, except in a very minor way, by the inherited effects of how much certain body parts are used. People who regularly live in canoes might have slightly stunted legs; those who live in high-altitude areas may have larger chests; and those who frequently use certain senses might have slightly larger cavities where those senses are located, leading to minor changes in their features. In civilized societies, the smaller jaw size from less usage, the consistent movement of different muscles to express various emotions, and the larger brain size from increased intellectual activity have all significantly impacted their overall appearance compared to less developed societies.333 Additionally, it's possible that a taller body, without a corresponding increase in brain size, may have led some races (based on the previously mentioned rabbit examples) to develop a longer skull typical of the dolichocephalic type.
Lastly, the little-understood principle of correlation will almost certainly have come into action, as in the case of great muscular development and strongly pro248jecting supra-orbital ridges. It is not improbable that the texture of the hair, which differs much in the different races, may stand in some kind of correlation with the structure of the skin; for the colour of the hair and skin are certainly correlated, as is its colour and texture with the Mandans.334 The colour of the skin and the odour emitted by it are likewise in some manner connected. With the breeds of sheep the number of hairs within a given space and the number of the excretory pores stand in some relation to each other.335 If we may judge from the analogy of our domesticated animals, many modifications of structure in man probably come under this principle of correlated growth.
Lastly, the often misunderstood principle of correlation is likely at play, similar to how significant muscle development corresponds with prominent supra-orbital ridges. It's possible that hair texture, which varies greatly among different races, might have some connection to skin structure; for example, hair and skin color are definitely related, as are their coloration and texture with the Mandans.334 Skin color and the odor it emits are also connected in some way. In sheep breeds, the number of hairs in a given area and the quantity of excretory pores are related in some manner.335 If we consider our domesticated animals, many structural changes in humans likely follow this principle of correlated growth.
We have now seen that the characteristic differences between the races of man cannot be accounted for in a satisfactory manner by the direct action of the conditions of life, nor by the effects of the continued use of parts, nor through the principle of correlation. We are therefore led to inquire whether slight individual differences, to which man is eminently liable, may not have been preserved and augmented during a long series of generations through natural selection. But here we are at once met by the objection that beneficial variations alone can be thus preserved; and as far as we are enabled to judge (although always liable to error on this head) not one of the external differences between the races of man are of any direct or 249special service to him. The intellectual and moral or social faculties must of course be excepted from this remark; but differences in these faculties can have had little or no influence on external characters. The variability of all the characteristic differences between the races, before referred to, likewise indicates that these differences cannot be of much importance; for, had they been important, they would long ago have been either fixed and preserved, or eliminated. In this respect man resembles those forms, called by naturalists protean or polymorphic, which have remained extremely variable, owing, as it seems, to their variations being of an indifferent nature, and consequently to their having escaped the action of natural selection.
We’ve now established that the key differences between human races can’t be clearly explained by the direct influence of living conditions, the effects of the regular use of certain traits, or through the principle of correlation. This leads us to explore whether small individual differences, to which humans are particularly prone, might have been maintained and amplified over many generations through natural selection. However, we immediately encounter the issue that only beneficial variations can be preserved this way; and as far as we can tell (though we may be mistaken), none of the external differences between human races serve any direct or special purpose. The intellectual, moral, or social abilities are exceptions to this point, but variations in these skills likely had little to no effect on physical traits. The variability of all these notable differences among the races also suggests that they must not be very significant; otherwise, they would have either been fixed and preserved or eliminated long ago. In this regard, humans are similar to certain forms that naturalists describe as protean or polymorphic, which remain highly variable seemingly because their variations are of an indifferent nature, allowing them to evade the influence of natural selection.
We have thus far been baffled in all our attempts to account for the differences between the races of man; but there remains one important agency, namely Sexual Selection, which appears to have acted as powerfully on man, as on many other animals. I do not intend to assert that sexual selection will account for all the differences between the races. An unexplained residuum is left, about which we can in our ignorance only say, that as individuals are continually born with, for instance, heads a little rounder or narrower, and with noses a little longer or shorter, such slight differences might become fixed and uniform, if the unknown agencies which induced them were to act in a more constant manner, aided by long-continued intercrossing. Such modifications come under the provisional class, alluded to in our fourth chapter, which for the want of a better term have been called spontaneous variations. Nor do I pretend that the effects of sexual selection can be indicated with scientific precision; but it can be shewn that it would be an inexplicable fact if man had not been modified by this agency, which has250 acted so powerfully on innumerable animals, both high and low in the scale. It can further be shewn that the differences between the races of man, as in colour, hairyness, form of features, &c., are of the nature which it might have been expected would have been acted on by sexual selection. But in order to treat this subject in a fitting manner, I have found it necessary to pass the whole animal kingdom in review; I have therefore devoted to it the Second Part of this work. At the close I shall return to man, and, after attempting to shew how far he has been modified through sexual selection, will give a brief summary of the chapters in this First Part.
We have been puzzled in all our efforts to explain the differences between human races; however, there's one significant factor to consider, which is Sexual Selection, that seems to have influenced humans just as it has many other animals. I don’t mean to claim that sexual selection accounts for all the differences among races. There’s a leftover mystery, about which we can only say in our uncertainty, that since individuals are constantly being born with, for example, slightly rounder or narrower heads, and noses that are a bit longer or shorter, these small differences might become fixed and uniform if the unknown factors causing them were to act consistently, supported by prolonged interbreeding. These modifications fall under the temporary category mentioned in our fourth chapter, which, due to the lack of a better term, have been called spontaneous variations. I also don’t claim that the effects of sexual selection can be measured scientifically with exact precision; however, it would be an inexplicable situation if humans had not been influenced by this force, which has250 had such a powerful impact on countless animals, both higher and lower on the evolutionary scale. Additionally, it can be demonstrated that the differences between human races, such as skin color, body hair, and facial features, are the kinds of traits one might expect to be shaped by sexual selection. To address this topic properly, I've found it necessary to review the entire animal kingdom; therefore, I've dedicated the Second Part of this work to it. At the end, I’ll return to humans and, after trying to show the extent to which they have been changed by sexual selection, I will provide a brief summary of the chapters in this First Part.
Part II.—MATE SELECTION.
CHAPTER VIII.
Principles of Sexual Selection.
Secondary sexual characters—Sexual selection—Manner of action—Excess of males—Polygamy—The male alone generally modified through sexual selection—Eagerness of the male—Variability of the male—Choice exerted by the female—Sexual compared with natural selection—Inheritance, at corresponding periods of life, at corresponding seasons of the year, and as limited by sex—Relations between the several forms of inheritance—Causes why one sex and the young are not modified through sexual selection—Supplement on the proportional numbers of the two sexes throughout the animal kingdom—On the limitation of the numbers of the two sexes through natural selection.
Secondary sexual traits—Sexual selection—How it works—Surplus of males—Polygamy—Typically, only the male is affected by sexual selection—The male's eagerness—Variation in males—Female choice—Comparison of sexual and natural selection—Inheritance, at specific life stages, during certain times of the year, and as influenced by sex—Relationships among different inheritance forms—Reasons why one sex and the young don't undergo changes due to sexual selection—Supplement on the ratio of the two sexes across the animal kingdom—Regarding the regulation of the two sexes through natural selection.
With animals which have their sexes separated, the males necessarily differ from the females in their organs of reproduction; and these afford the primary sexual characters. But the sexes often differ in what Hunter has called secondary sexual characters, which are not directly connected with the act of reproduction; for instance, in the male possessing certain organs of sense or locomotion, of which the female is quite destitute, or in having them more highly-developed, in order that he may readily find or reach her; or again, in the male having special organs of prehension so as to hold her securely. These latter organs of infinitely diversified kinds graduate into, and in some cases can hardly be distinguished from, those which are commonly ranked as primary, such as the complex appendages at the apex of the abdomen in male insects. Unless indeed254 we confine the term “primary” to the reproductive glands, it is scarcely possible to decide, as far as the organs of prehension are concerned, which ought to be called primary and which secondary.
With animals that have separate sexes, males obviously have different reproductive organs than females, and these differences represent the primary sexual characteristics. However, the sexes often also differ in what Hunter referred to as secondary sexual characteristics, which are not directly related to reproduction. For example, males may have certain sensory or locomotion organs that females lack, or their organs may be more developed to help them find or reach females more easily. Additionally, males might have specialized grasping organs to hold the female securely. These latter organs come in many variations and can sometimes be difficult to distinguish from primary characteristics, like the complex appendages at the end of the abdomen in male insects. Unless we limit the term “primary” to just the reproductive glands, it’s hard to determine which organs of prehension should be classified as primary and which as secondary.
The female often differs from the male in having organs for the nourishment or protection of her young, as the mammary glands of mammals, and the abdominal sacks of the marsupials. The male, also, in some few cases differs from the female in possessing analogous organs, as the receptacles for the ova possessed by the males of certain fishes, and those temporarily developed in certain male frogs. Female bees have a special apparatus for collecting and carrying pollen, and their ovipositor is modified into a sting for the defence of their larvæ and the community. In the females of many insects the ovipositor is modified in the most complex manner for the safe placing of the eggs. Numerous similar cases could be given, but they do not here concern us. There are, however, other sexual differences quite disconnected with the primary organs with which we are more especially concerned—such as the greater size, strength, and pugnacity of the male, his weapons of offence or means of defence against rivals, his gaudy colouring and various ornaments, his power of song, and other such characters.
The female often differs from the male by having organs for feeding or protecting her young, like the mammary glands in mammals and the pouches in marsupials. In some cases, the male also differs from the female by having similar organs, such as the receptacles for eggs in certain male fish and those that temporarily develop in some male frogs. Female bees have a special system for collecting and carrying pollen, and their ovipositor has evolved into a sting for defending their larvae and the colony. In many female insects, the ovipositor is highly specialized for safely laying eggs. There are many similar examples, but they aren't what we're focusing on here. However, there are other sexual differences that aren't related to the primary organs we're primarily interested in, such as the larger size, strength, and aggressiveness of males, their weapons for fighting or defending against rivals, their bright colors and various decorations, their singing abilities, and other characteristics.
Besides the foregoing primary and secondary sexual differences, the male and female sometimes differ in structures connected with different habits of life, and not at all, or only indirectly, related to the reproductive functions. Thus the females of certain flies (Culicidæ and Tabanidæ) are blood-suckers, whilst the males live on flowers and have their mouths destitute of mandibles.336 The males alone of certain moths and of some 255crustaceans (e.g. Tanais) have imperfect, closed mouths, and cannot feed. The Complemental males of certain cirripedes live like epiphytic plants either on the female or hermaphrodite form, and are destitute of a mouth and prehensile limbs. In these cases it is the male which has been modified and has lost certain important organs, which the other members of the same group possess. In other cases it is the female which has lost such parts; for instance, the female glow-worm is destitute of wings, as are many female moths, some of which never leave their cocoons. Many female parasitic crustaceans have lost their natatory legs. In some weevil-beetles (Curculionidæ) there is a great difference between the male and female in the length of the rostrum or snout;337 but the meaning of this and of many analogous differences, is not at all understood. Differences of structure between the two sexes in relation to different habits of life are generally confined to the lower animals; but with some few birds the beak of the male differs from that of the female. No doubt in most, but apparently not in all these cases, the differences are indirectly connected with the propagation of the species: thus a female which has to nourish a multitude of ova will require more food than the male, and consequently will require special means for procuring it. A male animal which lived for a very short time might without detriment lose through disuse its organs for procuring food; but he would retain his locomotive organs in a perfect state, so that he might reach the female. The female, on the other hand, might safely lose her organs for flying, swimming, 256or walking, if she gradually acquired habits which rendered such powers useless.
Besides the primary and secondary sexual differences mentioned earlier, males and females sometimes have different structures related to their lifestyles that aren't directly tied to reproduction. For example, female flies (like mosquitoes and horseflies) suck blood, while males feed on flowers and lack mandibles. The males of certain moths and some crustaceans (like Tanais) have underdeveloped, closed mouths and cannot eat. The complemental males of some barnacles live similarly to epiphytic plants, either on the female or hermaphrodite form, and lack mouths and grasping limbs. In these instances, it's the male that has changed and lost significant body parts found in other members of the same group. In other situations, it's the female that has lost certain features. For instance, the female glow-worm, along with many female moths, lacks wings, and some of these females never leave their cocoons. Many female parasitic crustaceans have lost their swimming legs. In some weevil beetles, there is a noticeable difference in the length of the rostrum or snout between males and females; however, the significance of this and many other similar differences is not well understood. Structural differences between the sexes regarding lifestyle habits are mostly seen in lower animals, but a few bird species also show differences in beak shape between males and females. It’s likely that, in most but not all cases, these differences are indirectly linked to species reproduction: for instance, a female that has to nourish many eggs will need more food than the male and thus develop specific ways to acquire it. A male that lives only a short time could lose its feeding organs through disuse without negative effects, but it would keep its movement organs in good condition to reach the female. On the flip side, the female could safely lose her capability to fly, swim, or walk if she gradually developed habits that made those abilities unnecessary.
We are, however, here concerned only with that kind of selection, which I have called sexual selection. This depends on the advantage which certain individuals have over other individuals of the same sex and species, in exclusive relation to reproduction. When the two sexes differ in structure in relation to different habits of life, as in the cases above mentioned, they have no doubt been modified through natural selection, accompanied by inheritance limited to one and the same sex. So again the primary sexual organs, and those for nourishing or protecting the young, come under this same head; for those individuals which generated or nourished their offspring best, would leave, cæteris paribus, the greatest number to inherit their superiority; whilst those which generated or nourished their offspring badly, would leave but few to inherit their weaker powers. As the male has to search for the female, he requires for this purpose organs of sense and locomotion, but if these organs are necessary for the other purposes of life, as is generally the case, they will have been developed through natural selection. When the male has found the female he sometimes absolutely requires prehensile organs to hold her; thus Dr. Wallace informs me that the males of certain moths cannot unite with the females if their tarsi or feet are broken. The males of many oceanic crustaceans have their legs and antennæ modified in an extraordinary manner for the prehension of the female; hence we may suspect that owing to these animals being washed about by the waves of the open sea, they absolutely require these organs in order to propagate their kind, and if so their development will have been the result of ordinary or natural selection.
We are, however, only focusing on that type of selection, which I refer to as sexual selection. This is based on the advantages that some individuals have over others of the same sex and species, specifically in relation to reproduction. When the two sexes differ in structure due to different lifestyles, as mentioned earlier, they have likely been shaped by natural selection, along with traits passed down only within one sex. Similarly, the main reproductive organs, and those for nurturing or protecting the young, fall under this same category; because individuals that successfully reproduce or nurture their offspring well will likely leave behind, cæteris paribus, the most offspring to inherit their advantages, while those that do this poorly will leave few to inherit their weaker traits. Since the male needs to find the female, he requires sensory and movement organs for this purpose, but if these organs are also vital for other life functions, as is usually the case, they will have developed through natural selection. Once the male finds the female, he may also need grasping organs to hold onto her; Dr. Wallace informs me that the males of certain moths cannot mate with the females if their feet are damaged. The males of many oceanic crustaceans have their legs and antennae modified in remarkable ways to grasp the female; therefore, we might suspect that since these animals are tossed around by the waves of the open sea, they absolutely need these organs to reproduce, and if so, their development would be due to regular or natural selection.
When the two sexes follow exactly the same habits257 of life, and the male has more highly developed sense or locomotive organs than the female, it may be that these in their perfected state are indispensable to the male for finding the female; but in the vast majority of cases, they serve only to give one male an advantage over another, for the less well-endowed males, if time were allowed them, would succeed in pairing with the females; and they would in all other respects, judging from the structure of the female, be equally well adapted for their ordinary habits of life. In such cases sexual selection must have come into action, for the males have acquired their present structure, not from being better fitted to survive in the struggle for existence, but from having gained an advantage over other males, and from having transmitted this advantage to their male offspring alone. It was the importance of this distinction which led me to designate this form of selection as sexual selection. So again, if the chief service rendered to the male by his prehensile organs is to prevent the escape of the female before the arrival of other males, or when assaulted by them, these organs will have been perfected through sexual selection, that is by the advantage acquired by certain males over their rivals. But in most cases it is scarcely possible to distinguish between the effects of natural and sexual selection. Whole chapters could easily be filled with details on the differences between the sexes in their sensory, locomotive, and prehensile organs. As, however, these structures are not more interesting than others adapted for the ordinary purposes of life, I shall almost pass them over, giving only a few instances under each class.
When both males and females lead the same lifestyle257 and the male has more advanced sensory or movement abilities than the female, it might be that these traits are essential for the male to find the female. However, in most cases, they primarily give one male an edge over another. The less endowed males could succeed in mating with the females if given enough time, and based on the structure of the female, they would be just as well-suited for their daily life. In these situations, sexual selection must play a role because the males have developed their current features not due to being better adapted for survival but because they gained an advantage over other males and passed this advantage only to their male offspring. This distinction is what led me to call this type of selection sexual selection. Similarly, if the main purpose of the male's grasping organs is to stop the female from escaping before other males arrive or when attacked by them, these traits would have been enhanced through sexual selection, meaning through the advantages certain males gained over their competitors. But in many instances, it's nearly impossible to tell the difference between natural and sexual selection. Entire chapters could easily be filled with details about the differences between the sexes in their sensory, movement, and grasping organs. However, since these structures aren't more interesting than others that serve everyday purposes, I will mostly skip over them, providing only a few examples in each category.
There are many other structures and instincts which must have been developed through sexual selection—such as the weapons of offence and the means of defence258 possessed by the males for fighting with and driving away their rivals—their courage and pugnacity—their ornaments of many kinds—their organs for producing vocal or instrumental music—and their glands for emitting odours; most of these latter structures serving only to allure or excite the female. That these characters are the result of sexual and not of ordinary selection is clear, as unarmed, unornamented, or unattractive males would succeed equally well in the battle for life and in leaving a numerous progeny, if better endowed males were not present. We may infer that this would be the case, for the females, which are unarmed and unornamented, are able to survive and procreate their kind. Secondary sexual characters of the kind just referred to, will be fully discussed in the following chapters, as they are in many respects interesting, but more especially as they depend on the will, choice, and rivalry of the individuals of either sex. When we behold two males fighting for the possession of the female, or several male birds displaying their gorgeous plumage, and performing the strangest antics before an assembled body of females, we cannot doubt that, though led by instinct, they know what they are about, and consciously exert their mental and bodily powers.
There are many other traits and instincts that must have developed through sexual selection—like the offensive weapons and defensive mechanisms that males have for fighting off and chasing away their rivals—their courage and aggressiveness—their various ornaments—their ability to produce vocal or instrumental music—and their glands for releasing scents; most of these structures mainly serve to attract or excite females. It’s clear that these traits are the result of sexual rather than ordinary selection, as unarmed, plain, or unattractive males would thrive equally in the struggle for survival and in leaving behind many offspring, if better-equipped males weren't around. We can assume this is true, because females, who are also unarmed and plain, can survive and reproduce their species. The secondary sexual traits mentioned will be discussed in detail in the following chapters, as they are quite interesting, particularly because they depend on the preferences, choices, and competition of individuals from both sexes. When we see two males fighting for the attention of a female, or several male birds flaunting their vibrant feathers and performing unusual displays in front of a group of females, we can't help but believe that, although driven by instinct, they understand what they are doing and actively utilize their mental and physical abilities.
In the same manner as man can improve the breed of his game-cocks by the selection of those birds which are victorious in the cockpit, so it appears that the strongest and most vigorous males, or those provided with the best weapons, have prevailed under nature, and have led to the improvement of the natural breed or species. Through repeated deadly contests, a slight degree of variability, if it led to some advantage, however slight, would suffice for the work of sexual selection; and it is certain that secondary sexual characters259 are eminently variable. In the same manner as man can give beauty, according to his standard of taste, to his male poultry—can give to the Sebright bantam a new and elegant plumage, an erect and peculiar carriage—so it appears that in a state of nature female birds, by having long selected the more attractive males, have added to their beauty. No doubt this implies powers of discrimination and taste on the part of the female which will at first appear extremely improbable; but I hope hereafter to shew that this is not the case.
Just like how people can enhance the breed of their gamecocks by choosing the birds that win in the ring, it seems that the strongest and most vigorous males, or those with the best features, have thrived in nature and contributed to the enhancement of their species. Through repeated intense competition, even a small degree of variability that offers some advantage, no matter how minor, would be enough for sexual selection to take place; and it’s clear that secondary sexual traits259 are quite variable. In the same way that people can make male poultry more beautiful according to their taste—giving the Sebright bantam a new and stylish plumage and a distinctive posture—it appears that in the wild, female birds, having consistently chosen the more appealing males, have enhanced their beauty. This certainly suggests that females have a capacity for judgment and preference that might initially seem very unlikely, but I plan to demonstrate later that this is not the case.
From our ignorance on several points, the precise manner in which sexual selection acts is to a certain extent uncertain. Nevertheless if those naturalists who already believe in the mutability of species, will read the following chapters, they will, I think, agree with me that sexual selection has played an important part in the history of the organic world. It is certain that with almost all animals there is a struggle between the males for the possession of the female. This fact is so notorious that it would be superfluous to give instances. Hence the females, supposing that their mental capacity sufficed for the exertion of a choice, could select one out of several males. But in numerous cases it appears as if it had been specially arranged that there should be a struggle between many males. Thus with migratory birds, the males generally arrive before the females at their place of breeding, so that many males are ready to contend for each female. The bird-catchers assert that this is invariably the case with the nightingale and blackcap, as I am informed by Mr. Jenner Weir, who confirms the statement with respect to the latter species.
Due to our lack of knowledge on several points, the exact way sexual selection functions is somewhat unclear. However, I believe that naturalists who already accept the idea of species changing will find that sexual selection has played a significant role in the history of life on Earth if they read the following chapters. It's clear that most animals experience competition among males for access to females. This fact is so well-known that providing examples would be unnecessary. As a result, females, assuming they have the mental capacity to make choices, could choose one male from several. In many situations, it seems to have been intentionally arranged for multiple males to compete. For instance, with migratory birds, males usually arrive at their breeding grounds before females, leading to many males ready to compete for each female. Bird catchers assert that this is always true for the nightingale and blackcap, as confirmed by Mr. Jenner Weir, who supports this statement regarding the latter species.
Mr. Swaysland of Brighton, who has been in the habit, during the last forty years, of catching our migratory birds on their first arrival, writes to me that he has260 never known the females of any species to arrive before their males. During one spring he shot thirty-nine males of Ray’s wagtail (Budytes Raii) before he saw a single female. Mr. Gould has ascertained by dissection, as he informs me, that male snipes arrive in this country before the females. In the case of fish, at the period when the salmon ascend our rivers, the males in large numbers are ready to breed before the females. So it apparently is with frogs and toads. Throughout the great class of insects the males almost always emerge from the pupal state before the other sex, so that they generally swarm for a time before any females can be seen.338 The cause of this difference between the males and females in their periods of arrival and maturity is sufficiently obvious. Those males which annually first migrated into any country, or which in the spring were first ready to breed, or were the most eager, would leave the largest number of offspring; and these would tend to inherit similar instincts and constitutions. On the whole there can be no doubt that with almost all animals, in which the sexes are separate, there is a constantly recurrent struggle between the males for the possession of the females.
Mr. Swaysland from Brighton, who has spent the last forty years catching our migratory birds on their first arrival, tells me he has260 never seen the females of any species arrive before the males. One spring, he shot thirty-nine male Ray’s wagtails (Budytes Raii) before he spotted a single female. Mr. Gould has found out through dissection, as he mentioned to me, that male snipes arrive in this country before the females. In the case of fish, when salmon swim upstream, the males are usually ready to breed in large numbers before the females. The same seems to happen with frogs and toads. In the vast class of insects, the males almost always emerge from the pupal stage before the females, so they often gather for a while before any females are seen.338 The reason for this difference in the timing of arrival and maturity between males and females is pretty clear. The males that migrate first into any country each year, or those that are ready to breed earlier in the spring, or are the most eager, would leave the largest number of offspring; and these offspring would likely inherit similar instincts and traits. Overall, there’s no doubt that in almost all animals with separate sexes, there’s a constant struggle among the males for the possession of the females.
Our difficulty in regard to sexual selection lies in understanding how it is that the males which conquer other males, or those which prove the most attractive to the females, leave a greater number of offspring to inherit their superiority than the beaten and less 261attractive males. Unless this result followed, the characters which gave to certain males an advantage over others, could not be perfected and augmented through sexual selection. When the sexes exist in exactly equal numbers, the worst-endowed males will ultimately find females (excepting where polygamy prevails), and leave as many offspring, equally well fitted for their general habits of life, as the best-endowed males. From various facts and considerations, I formerly inferred that with most animals, in which secondary sexual characters were well developed, the males considerably exceeded the females in number; and this does hold good in some few cases. If the males were to the females as two to one, or as three to two, or even in a somewhat lower ratio, the whole affair would be simple; for the better-armed or more attractive males would leave the largest number of offspring. But after investigating, as far as possible, the numerical proportions of the sexes, I do not believe that any great inequality in number commonly exists. In most cases sexual selection appears to have been effective in the following manner.
Our challenge with sexual selection is understanding how the males that defeat other males, or those that are the most appealing to females, have more offspring to pass on their traits than the defeated and less attractive males. If this didn’t happen, the traits that give certain males an advantage couldn’t be developed and enhanced through sexual selection. When males and females are equal in number, the least endowed males will eventually find females (unless polygamy is involved) and have as many offspring, equally well adapted to their way of life, as the best endowed males. Based on various facts and observations, I previously concluded that in most animals with distinct secondary sexual traits, males significantly outnumber females; this does apply in a few instances. If males were to females in a ratio of two to one, or three to two, or even a slightly lower ratio, things would be straightforward; the better-equipped or more attractive males would leave more offspring. However, after investigating the numerical ratios of the sexes as thoroughly as possible, I don’t believe there is usually a significant imbalance in numbers. In most cases, sexual selection seems to have worked in the following way.
Let us take any species, a bird for instance, and divide the females inhabiting a district into two equal bodies: the one consisting of the more vigorous and better-nourished individuals, and the other of the less vigorous and healthy. The former, there can be little doubt, would be ready to breed in the spring before the others; and this is the opinion of Mr. Jenner Weir, who has during many years carefully attended to the habits of birds. There can also be no doubt that the most vigorous, healthy, and best-nourished females would on an average succeed in rearing the largest number of offspring. The males, as we have seen, are generally ready to breed before the females; of the males the262 strongest, and with some species the best armed, drive away the weaker males; and the former would then unite with the more vigorous and best-nourished females, as these are the first to breed. Such vigorous pairs would surely rear a larger number of offspring than the retarded females, which would be compelled, supposing the sexes to be numerically equal, to unite with the conquered and less powerful males; and this is all that is wanted to add, in the course of successive generations, to the size, strength and courage of the males, or to improve their weapons.
Let’s take any species, like a bird for example, and split the females in a certain area into two equal groups: one made up of the stronger and better-nourished individuals, and the other of the weaker and less healthy ones. It’s clear that the first group would be ready to breed in the spring before the second; this aligns with the views of Mr. Jenner Weir, who has closely observed birds for many years. There’s also no doubt that the healthiest and best-fed females would, on average, manage to raise the most offspring. As we’ve noted, males are usually ready to breed before females; among the males, the strongest ones and, for some species, those with the best features, will chase away the weaker males. These stronger males would likely mate with the healthiest and best-nourished females, as they are the first to breed. Such strong pairs would obviously produce more offspring than the delayed females, who would have no choice but to breed with the weaker and dominated males, assuming the sexes are roughly equal in number. This dynamic would contribute, over many generations, to the size, strength, and bravery of the males, as well as enhance their physical attributes.
But in a multitude of cases the males which conquer other males, do not obtain possession of the females, independently of choice on the part of the latter. The courtship of animals is by no means so simple and short an affair as might be thought. The females are most excited by, or prefer pairing with, the more ornamented males, or those which are the best songsters, or play the best antics; but it is obviously probable, as has been actually observed in some cases, that they would at the same time prefer the more vigorous and lively males.339 Thus the more vigorous females, which are the first to breed, will have the choice of many males; and though they may not always select the strongest or best armed, they will select those which are vigorous and well armed, and in other respects the most attractive. Such early pairs would have the same advantage in rearing offspring on the female side as above explained, and nearly the same advantage on the male side. And this apparently has sufficed during a long course of generations to add not only to the strength and fighting-powers of 263the males, but likewise to their various ornaments or other attractions.
But in many cases, the males that defeat other males don’t necessarily get access to the females, regardless of the females' choice. Animal courtship isn’t as simple and quick as it might seem. Females are often more attracted to, or prefer mating with, males that are more colorful, have better songs, or perform more entertaining displays; however, it seems likely, as has been observed in some cases, that they would also prefer males that are more vigorous and energetic. 339 So, the more energetic females, who breed first, will have the option to choose from many males, and although they might not always choose the strongest or most well-armed ones, they will go for those that are vigorous, well-armed, and appealing in other ways. These early mating pairs would have the same advantages in raising offspring on the female side as previously mentioned, and nearly the same advantages on the male side. This seems to have been sufficient over many generations to enhance not only the strength and fighting abilities of the males but also their various adornments and other attractions.
In the converse and much rarer case of the males selecting particular females, it is plain that those which were the most vigorous and had conquered others, would have the freest choice; and it is almost certain that they would select vigorous as well as attractive females. Such pairs would have an advantage in rearing offspring, more especially if the male had the power to defend the female during the pairing-season, as occurs with some of the higher animals, or aided in providing for the young. The same principles would apply if both sexes mutually preferred and selected certain individuals of the opposite sex; supposing that they selected not only the more attractive, but likewise the more vigorous individuals.
In the opposite and much rarer situation where males choose specific females, it's obvious that the strongest ones who have defeated others would have the greatest options; and it's almost certain that they would pick both strong and attractive females. Such pairs would have an advantage in raising offspring, especially if the male could protect the female during the mating season, as seen in some higher animals, or helped provide for the young. The same principles would apply if both males and females mutually preferred and selected certain individuals of the opposite sex, assuming they chose not only the more attractive ones but also the stronger individuals.
Numerical Proportion of the Two Sexes.—I have remarked that sexual selection would be a simple affair if the males considerably exceeded in number the females. Hence I was led to investigate, as far as I could, the proportions between the two sexes of as many animals as possible; but the materials are scanty. I will here give only a brief abstract of the results, retaining the details for a supplementary discussion, so as not to interfere with the course of my argument. Domesticated animals alone afford the opportunity of ascertaining the proportional numbers at birth; but no records have been specially kept for this purpose. By indirect means, however, I have collected a considerable body of statistical data, from which it appears that with most of our domestic animals the sexes are nearly equal at birth. Thus with race-horses, 25,560 births have been recorded during twenty-one years, and the male births have been to the female births as 99·7 to 100. With greyhounds the264 inequality is greater than with any other animal, for during twelve years, out of 6878 births, the male births have been as 110·1 to 100 female births. It is, however, in some degree doubtful whether it is safe to infer that the same proportional numbers would hold good under natural conditions as under domestication; for slight and unknown differences in the conditions affect to a certain extent the proportion of the sexes. Thus with mankind, the male births in England are as 104·5, in Russia as 108·9, and with the Jews of Livornia as 120 to 100 females. The proportion is also mysteriously affected by the circumstance of the births being legitimate or illegitimate.
Numerical Proportion of the Two Sexes.—I’ve noticed that sexual selection would be straightforward if there were significantly more males than females. This led me to explore, as much as possible, the ratios between the two sexes in various animals; however, the information available is limited. I will provide a brief summary of the findings here and save the details for a later discussion to keep my argument on track. Only domesticated animals give us the chance to determine the proportional numbers at birth, but no specific records have been maintained for this. Through indirect methods, however, I've gathered quite a bit of statistical data, which suggests that in most of our domestic animals, the sexes are almost equal at birth. For instance, with racehorses, 25,560 births have been recorded over twenty-one years, with male births compared to female births at a ratio of 99.7 to 100. In greyhounds, the discrepancy is greater than with any other animal, as over twelve years, out of 6,878 births, the male births stood at a ratio of 110.1 to 100 female births. However, it's somewhat uncertain whether the same proportional numbers would apply in natural conditions as they do in domestication, since slight and unknown differences in conditions can influence the sex ratio to some degree. For example, among humans, the male births in England are at a ratio of 104.5, in Russia at 108.9, and among the Jewish community of Livornia at 120 to 100 females. The ratio is also intriguingly affected by whether the births are legitimate or illegitimate.
For our present purpose we are concerned with the proportion of the sexes, not at birth, but at maturity, and this adds another element of doubt; for it is a well ascertained fact that with man a considerably larger proportion of males than of females die before or during birth, and during the first few years of infancy. So it almost certainly is with male lambs, and so it may be with the males of other animals. The males of some animals kill each other by fighting; or they drive each other about until they become greatly emaciated. They must, also, whilst wandering about in eager search for the females, be often exposed to various dangers. With many kinds of fish the males are much smaller than the females, and they are believed often to be devoured by the latter or by other fishes. With some birds the females appear to die in larger proportion than the males: they are also liable to be destroyed on their nests, or whilst in charge of their young. With insects the female larvæ are often larger than those of the males, and would consequently be more likely to be devoured: in some cases the mature females are less active and less rapid in their movements than the males,265 and would not be so well able to escape from danger. Hence, with animals in a state of nature, in order to judge of the proportions of the sexes at maturity, we must rely on mere estimation; and this, except perhaps when the inequality is strongly marked, is but little trustworthy. Nevertheless, as far as a judgment can be formed, we may conclude from the facts given in the supplement, that the males of some few mammals, of many birds, of some fish and insects, considerably exceed in number the females.
For our current purpose, we are focused on the ratio of the sexes, not at birth, but at maturity, which adds another layer of uncertainty. It's a well-established fact that in humans, a significantly larger proportion of males than females die before or during birth, and in the first few years of life. The same likely holds true for male lambs and possibly for male animals in general. Male animals of some species fight each other, or they pressure one another until they become severely weakened. While searching aggressively for females, they are also often exposed to various dangers. In many types of fish, the males are much smaller than the females, and they are often believed to be eaten by the females or other fish. In some bird species, females seem to die at a higher rate than males; they are also vulnerable to being harmed while nesting or caring for their young. Insects often have female larvae that are larger than the males, making them more likely to be eaten; in some cases, mature females are less active and slower than males,265 which makes escaping danger more difficult for them. Therefore, when assessing the proportions of the sexes at maturity in wild animals, we can only rely on rough estimates; and this, unless the disparity is very pronounced, is not very reliable. Nevertheless, based on the information provided in the supplement, we can conclude that the males of a few mammals, many birds, and some fish and insects significantly outnumber the females.
The proportion between the sexes fluctuates slightly during successive years: thus with race-horses, for every 100 females born, the males varied from 1O7.1 in one year to 92.6 in another year, and with greyhounds from 116.3 to 95.3. But had larger numbers been tabulated throughout a more extensive area than England, these fluctuations would probably have disappeared; and such as they are, they would hardly suffice to lead under a state of nature to the effective action of sexual selection. Nevertheless with some few wild animals, the proportions seem, as shewn in the supplement, to fluctuate either during different seasons or in different localities in a sufficient degree to lead to such action. For it should be observed that any advantage gained during certain years or in certain localities by those males which were able to conquer other males, or were the most attractive to the females, would probably be transmitted to the offspring and would not subsequently be eliminated. During the succeeding seasons, when from the equality of the sexes every male was everywhere able to procure a female, the stronger or more attractive males previously produced would still have at least as good a chance of leaving offspring as the less strong or less attractive.
The ratio of males to females changes slightly from year to year: for example, with racehorses, for every 100 females born, the number of males ranged from 107.1 one year to 92.6 another year, and for greyhounds, from 116.3 to 95.3. However, if a larger sample had been analyzed over a broader area than just England, these fluctuations might have leveled out; and even as they are, they probably wouldn't be enough to result in meaningful sexual selection in the wild. Still, for a few wild animals, the ratios seem to vary, as shown in the supplement, either during different seasons or in different places to a degree that could trigger such selection. It's important to note that any advantages gained in certain years or locations by males that outcompeted others, or that were more appealing to females, would likely be passed down to their offspring and wouldn't be eliminated later on. In subsequent seasons, when the sex ratio was equal, any male would have the chance to find a mate, but the stronger or more appealing males from previous years would still have at least as good a chance of producing offspring as the less strong or less appealing males.
Polygamy.—The practice of polygamy leads to the266 same results as would follow from an actual inequality in the number of the sexes; for if each male secures two or more females, many males will not be able to pair; and the latter assuredly will be the weaker or less attractive individuals. Many mammals and some few birds are polygamous, but with animals belonging to the lower classes I have found no evidence of this habit. The intellectual powers of such animals are, perhaps, not sufficient to lead them to collect and guard a harem of females. That some relation exists between polygamy and the development of secondary sexual characters, appears nearly certain; and this supports the view that a numerical preponderance of males would be eminently favourable to the action of sexual selection. Nevertheless many animals, especially birds, which are strictly monogamous, display strongly-marked secondary sexual characters; whilst some few animals, which are polygamous, are not thus characterised.
Polygamy.—The practice of polygamy leads to the266 same results as would come from an actual imbalance in the number of males and females; because if each male secures two or more females, many males won't be able to find a partner; and those males will likely be the weaker or less attractive ones. Many mammals and a few birds are polygamous, but I haven’t found evidence of this behavior in lower-class animals. The intellectual abilities of such animals may not be enough for them to gather and protect a group of females. It seems almost certain that there’s a connection between polygamy and the development of secondary sexual traits, and this supports the idea that having more males would greatly favor sexual selection. However, many animals, especially birds that are strictly monogamous, show pronounced secondary sexual traits, while some polygamous animals do not.
We will first briefly run through the class of mammals, and then turn to birds. The gorilla seems to be a polygamist, and the male differs considerably from the female; so it is with some baboons which live in herds containing twice as many adult females as males. In South America the Mycetes caraya presents well-marked sexual differences in colour, beard, and vocal organs, and the male generally lives with two or three wives: the male of the Cebus capucinus differs somewhat from the female, and appears to be polygamous.340 Little is known on this head with respect to most other monkeys, but some species are strictly monogamous. The ruminants are eminently polygamous, and they 267more frequently present sexual differences than almost any other group of mammals, especially in their weapons, but likewise in other characters. Most deer, cattle, and sheep are polygamous; as are most antelopes, though some of the latter are monogamous. Sir Andrew Smith, in speaking of the antelopes of South Africa, says that in herds of about a dozen there was rarely more than one mature male. The Asiatic Antilope saiga appears to be the most inordinate polygamist in the world; for Pallas341 states that the male drives away all rivals, and collects a herd of about a hundred, consisting of females and kids: the female is hornless and has softer hair, but does not otherwise differ much from the male. The horse is polygamous, but, except in his greater size and in the proportions of his body, differs but little from the mare. The wild boar, in his great tusks and some other characters, presents well-marked sexual characters; in Europe and in India he leads a solitary life, except during the breeding-season; but at this season he consorts in India with several females, as Sir W. Elliot, who has had large experience in observing this animal, believes: whether this holds good in Europe is doubtful, but is supported by some statements. The adult male Indian elephant, like the boar, passes much of his time in solitude; but when associating with others, “it is rare to find,” as Dr. Campbell states, “more than one male with a whole herd of females.” The larger males expel or kill the smaller and weaker ones. The male differs from the female by his immense tusks and greater size, strength, and endurance; so great is the difference in these latter 268respects, that the males when caught are valued at twenty per cent. above the females.342 With other pachydermatous animals the sexes differ very little or not at all, and they are not, as far as known, polygamists. Hardly a single species amongst the Cheiroptera and Edentata, or in the great Orders of the Rodents and Insectivora, presents well-developed secondary sexual differences; and I can find no account of any species being polygamous, excepting, perhaps, the common rat, the males of which, as some rat-catchers affirm, live with several females.
We will first quickly cover the class of mammals and then move on to birds. The gorilla appears to be polygamous, with the male looking quite different from the female; the same goes for some baboons that live in groups often consisting of twice as many adult females as males. In South America, the Mycetes caraya shows distinct sexual differences in color, beard, and vocal organs, with the male usually living with two or three partners. The male of the Cebus capucinus is somewhat different from the female and seems to be polygamous.340 Little is known about this regarding most other monkeys, but some species are strictly monogamous. Ruminants are primarily polygamous, and they display sexual differences more frequently than almost any other group of mammals, especially in their weapons but also in other traits. Most deer, cattle, and sheep are polygamous, as are most antelopes, although some of the latter are monogamous. Sir Andrew Smith mentions that in herds of around a dozen antelopes in South Africa, there is rarely more than one mature male. The Asiatic Antilope saiga appears to be the most extreme polygamist in the world; Pallas341 notes that the male drives away all rivals and gathers a herd of about a hundred, consisting of females and young ones: the female is hornless and has softer hair but does not differ much otherwise from the male. The horse is polygamous, but aside from its larger size and body proportions, it does not differ much from the mare. The wild boar shows clear sexual traits in its large tusks and some other characteristics; in Europe and India, it mostly lives alone, except during the breeding season, when it associates with several females in India, according to Sir W. Elliot, who has extensively observed this animal. Whether this is true for Europe is uncertain, though some reports support it. The adult male Indian elephant, like the boar, spends much of his time alone; however, when interacting with others, "it is rare to find," as Dr. Campbell states, "more than one male with a whole herd of females." The larger males drive away or kill the smaller and weaker ones. The male is distinguished from the female by its enormous tusks and greater size, strength, and endurance; the difference is so significant that when caught, males are valued at twenty percent more than females.342 In most other thick-skinned animals, the sexes show very little difference or none at all, and they are not known to be polygamous. Hardly any species among the Cheiroptera and Edentata, or in the larger Orders of Rodents and Insectivora, exhibits well-defined secondary sexual differences; and I can find no records of any species being polygamous, except perhaps for the common rat, whose males, as some rat-catchers claim, live with several females.
The lion in South Africa, as I hear from Sir Andrew Smith, sometimes lives with a single female, but generally with more than one, and, in one case, was found with as many as five females, so that he is polygamous. He is, as far as I can discover, the sole polygamist in the whole group of the terrestrial Carnivora, and he alone presents well-marked sexual characters. If, however, we turn to the marine Carnivora, the case is widely different; for many species of seals offer, as we shall hereafter see, extraordinary sexual differences, and they are eminently polygamous. Thus the male sea-elephant of the Southern Ocean, always possesses, according to Péron, several females, and the sea-lion of Forster is said to be surrounded by from twenty to thirty females. In the North, the male sea-bear of Steller is accompanied by even a greater number of females.
The lion in South Africa, according to Sir Andrew Smith, sometimes lives with one female, but usually with several, and in one instance, he was found with as many as five females, indicating that he is polygamous. As far as I can tell, he is the only polygamist in the entire group of land Carnivora, and he is the only one showing distinct sexual traits. However, when we look at marine Carnivora, the situation is quite different; many species of seals, as we will see later, exhibit remarkable sexual differences and are highly polygamous. For example, the male sea elephant in the Southern Ocean typically has several females, according to Péron, and the sea lion described by Forster is said to be surrounded by twenty to thirty females. In the North, the male sea bear identified by Steller is accompanied by an even greater number of females.
With respect to birds, many species, the sexes of which differ greatly from each other, are certainly monogamous. In Great Britain we see well-marked sexual differences in, for instance, the wild-duck which pairs with a single female, with the common blackbird, 269and with the bullfinch which is said to pair for life. So it is, as I am informed by Mr. Wallace, with the Chatterers or Cotingidæ of South America, and numerous other birds. In several groups I have not been able to discover whether the species are polygamous or monogamous. Lesson says that birds of paradise, so remarkable for their sexual differences, are polygamous, but Mr. Wallace doubts whether he had sufficient evidence. Mr. Salvin informs me that he has been led to believe that humming-birds are polygamous. The male widow-bird; remarkable for his caudal plumes, certainly seems to be a polygamist.343 I have been assured by Mr. Jenner Weir and by others, that three starlings not rarely frequent the same nest; but whether this is a case of polygamy or polyandry has not been ascertained.
Regarding birds, many species in which the males and females look quite different from each other are definitely monogamous. In Great Britain, we can see clear sexual differences in, for example, the wild duck, which pairs with one female, the common blackbird, and the bullfinch, which is said to pair for life. The same is true, as I’ve learned from Mr. Wallace, for the Chatterers or Cotingidæ of South America, along with many other birds. In several groups, I haven’t been able to determine if the species are polygamous or monogamous. Lesson claims that birds of paradise, known for their striking sexual differences, are polygamous, but Mr. Wallace doubts he had enough evidence to support that. Mr. Salvin has informed me that he believes hummingbirds are polygamous. The male widow-bird, noted for its long tail feathers, certainly appears to be a polygamist.343 I have been told by Mr. Jenner Weir and others that three starlings often share the same nest; however, it hasn’t been confirmed whether this is an example of polygamy or polyandry.
The Gallinaceæ present almost as strongly marked sexual differences as birds of paradise or humming-birds, and many of the species are, as is well known, polygamous; others being strictly monogamous. What a contrast is presented between the sexes by the polygamous peacock or pheasant, and the monogamous guinea-fowl or partridge! Many similar cases could be given, as in the grouse tribe, in which the males of the polygamous capercailzie and black-cock differ greatly from the females; whilst the sexes of the monogamous red grouse and ptarmigan differ very little. Amongst the Cursores, no great number of species offer strongly-marked sexual differences, except the bustards, and the great bustard (Otis tarda), is said to 270be polygamous. With the Grallatores, extremely few species differ sexually, but the ruff (Machetes pugnax) affords a strong exception, and this species is believed by Montagu to be a polygamist. Hence it appears that with birds there often exists a close relation between polygamy and the development of strongly-marked sexual differences. On asking Mr. Bartlett, at the Zoological Gardens, who has had such large experience with birds, whether the male tragopan (one of the Gallinaceæ) was polygamous, I was struck by his answering, “I do not know, but should think so from his splendid colours.”
The Gallinaceæ show distinct sexual differences similar to those found in birds of paradise or hummingbirds, and many species are known to be polygamous, while others are strictly monogamous. There’s a clear contrast between the sexes in polygamous species like the peacock or pheasant and monogamous birds like the guinea-fowl or partridge. Numerous similar examples exist, such as in the grouse family, where the males of the polygamous capercailzie and black-cock look very different from the females, while the males and females of the monogamous red grouse and ptarmigan look quite alike. Among the Cursores, few species exhibit significant sexual differences, except for the bustards; the great bustard (Otis tarda) is reported to be polygamous. In the Grallatores, very few species show sexual differences, but the ruff (Machetes pugnax) is a notable exception, and Montagu believes this species is also polygamous. Thus, it seems that there is often a strong link between polygamy and the presence of significant sexual differences in birds. When I asked Mr. Bartlett at the Zoological Gardens, who has extensive experience with birds, whether the male tragopan (a member of the Gallinaceæ) was polygamous, I was surprised by his reply: “I don’t know, but I would think so from his stunning colors.”
It deserves notice that the instinct of pairing with a single female is easily lost under domestication. The wild-duck is strictly monogamous, the domestic-duck highly polygamous. The Rev. W. D. Fox informs me that with some half-tamed wild-ducks, kept on a large pond in his neighbourhood, so many mallards were shot by the gamekeeper that only one was left for every seven or eight females; yet unusually large broods were reared. The guinea-fowl is strictly monogamous; but Mr. Fox finds that his birds succeed best when he keeps one cock to two or three hens.344 Canary-birds pair in a state of nature, but the breeders in England successfully put one male to four or five females; nevertheless the first female, as Mr. Fox has been assured, is alone treated as the wife, she and her young ones being fed by him; the others are treated as concubines. I have noticed these cases, as it renders it in some degree probable that monogamous species, in a state of nature, might readily become either temporarily or permanently polygamous.
It’s worth noting that the instinct to pair with one female easily diminishes under domestication. Wild ducks are strictly monogamous, while domestic ducks are highly polygamous. The Rev. W. D. Fox tells me that with some semi-tamed wild ducks kept in a large pond near him, so many male mallards were shot by the gamekeeper that only one was left for every seven or eight females; yet unusually large broods were raised. The guinea fowl is strictly monogamous; however, Mr. Fox finds that his birds do best when he keeps one male for two or three females. Canary birds pair in the wild, but breeders in England successfully match one male with four or five females; however, the first female, as Mr. Fox has been informed, is treated solely as the wife, with her and her young ones being fed by him, while the others are regarded as concubines. I have noted these examples because they suggest that monogamous species in nature might easily become either temporarily or permanently polygamous.
With respect to reptiles and fishes, too little is known of their habits to enable us to speak of their marriage arrangements. The stickle-back Gasterosteus, however, is said to be a polygamist;345 and the male during the breeding-season differs conspicuously from the female.
With reptiles and fish, we don’t know enough about their behaviors to discuss their mating practices. However, the stickleback fish, Gasterosteus, is said to be a polygamist;345 and the male looks very different from the female during the breeding season.
To sum up on the means through which, as far as we can judge, sexual selection has led to the development of secondary sexual characters. It has been shewn that the largest number of vigorous offspring will be reared from the pairing of the strongest and best-armed males, which have conquered other males, with the most vigorous and best-nourished females, which are the first to breed in the spring. Such females, if they select the more attractive, and at the same time vigorous, males, will rear a larger number of offspring than the retarded females, which must pair with the less vigorous and less attractive males. So it will be if the more vigorous males select the more attractive and at the same time healthy and vigorous females; and this will especially hold good if the male defends the female, and aids in providing food for the young. The advantage thus gained by the more vigorous pairs in rearing a larger number of offspring has apparently sufficed to render sexual selection efficient. But a large preponderance in number of the males over the females would be still more efficient; whether the preponderance was only occasional and local, or permanent; whether it occurred at birth, or subsequently from the greater destruction of the females; or whether it indirectly followed from the practice of polygamy.
To sum up how, based on what we can tell, sexual selection has led to the development of secondary sexual traits. It's been shown that the highest number of healthy offspring comes from pairing the strongest and best-equipped males, who have defeated other males, with the healthiest and best-nourished females, who are the first to breed in spring. Such females, if they choose the more attractive and also strong males, will have a larger number of offspring than the slower females, who must mate with the less strong and less attractive males. The same will apply if the stronger males choose the more attractive and healthy females; this especially holds true if the male protects the female and helps provide food for the young. The advantage gained by these stronger pairs in raising a larger number of offspring seems to make sexual selection effective. However, having a much larger number of males compared to females would be even more effective, whether that imbalance is only occasional and local, or permanent; whether it happens at birth, or later due to a higher mortality rate among females; or whether it indirectly results from the practice of polygamy.
The Male generally more modified than the Female.—Throughout the animal kingdom, when the sexes differ 272from each other in external appearance, it is the male which, with rare exceptions, has been chiefly modified; for the female still remains more like the young of her own species, and more like the other members of the same group. The cause of this seems to lie in the males of almost all animals having stronger passions than the females. Hence it is the males that fight together and sedulously display their charms before the females; and those which are victorious transmit their superiority to their male offspring. Why the males do not transmit their characters to both sexes will hereafter be considered. That the males of all mammals eagerly pursue the females is notorious to every one. So it is with birds; but many male birds do not so much pursue the female, as display their plumage, perform strange antics, and pour forth their song, in her presence. With the few fish which have been observed, the male seems much more eager than the female; and so it is with alligators, and apparently with Batrachians. Throughout the enormous class of insects, as Kirby remarks,346 “the law is, that the male shall seek the female.” With spiders and crustaceans, as I hear from two great authorities, Mr. Blackwall and Mr. C. Spence Bate, the males are more active and more erratic in their habits than the females. With insects and crustaceans, when the organs of sense or locomotion are present in the one sex and absent in the other, or when, as is frequently the case, they are more highly developed in the one than the other, it is almost invariably the male, as far as I can discover, which retains such organs, or has them most developed; and this shews that the male is the more active member in the courtship of the sexes.347
The Male is generally more modified than the Female.—Throughout the animal kingdom, when the sexes look different from one another, it's usually the male that has changed the most; the female tends to resemble the young of her species more closely and looks more like the other members of her group. This seems to be because male animals generally have stronger instincts than females. As a result, it's the males that fight against each other and show off their traits to attract females; those that win pass on their advantages to their male offspring. The reason males don’t pass their traits on to both sexes will be discussed later. Everyone knows that male mammals actively seek out females. The same goes for birds; however, many male birds focus more on flaunting their feathers, performing unusual dances, and singing in front of the female rather than chasing her. In the few observed fish species, the male appears more eager than the female; this is also true for alligators and seemingly for amphibians. Across the vast class of insects, as Kirby notes,346 “the rule is that the male will pursue the female.” As I’ve heard from two respected experts, Mr. Blackwall and Mr. C. Spence Bate, male spiders and crustaceans are more active and unpredictable than females. In insects and crustaceans, when sensory or movement organs are present in one sex but not in the other, or when they are more developed in one sex, it's typically the male who has those organs or has them more developed; this indicates that the male plays a more active role in courtship.347
The female, on the other hand, with the rarest exception, is less eager than the male. As the illustrious Hunter348 long ago observed, she generally “requires to be courted;” she is coy, and may often be seen endeavouring for a long time to escape from the male. Every one who has attended to the habits of animals will be able to call to mind instances of this kind. Judging from various facts, hereafter to be given, and from the results which may fairly be attributed to sexual selection, the female, though comparatively passive, generally exerts some choice and accepts one male in preference to others. Or she may accept, as appearances would sometimes lead us to believe, not the male which is the most attractive to her, but the one which is the least distasteful. The exertion of some choice on the part of the female seems almost as general a law as the eagerness of the male.
The female, in most cases, is less enthusiastic than the male. As the famous Hunter348 noted long ago, she typically “needs to be courted;” she can be shy and is often seen trying to get away from the male. Anyone who has observed animal behavior will recall instances like this. Based on various facts that will be presented later and the results that can be attributed to sexual selection, the female, although relatively passive, usually shows some preference and chooses one male over others. Or, as appearances might sometimes suggest, she might not choose the male she finds most attractive but rather the one she finds least unappealing. The idea that the female exerts some choice appears to be nearly as universal as the male's eagerness.
We are naturally led to enquire why the male in so many and such widely distinct classes has been rendered more eager than the female, so that he searches for her and plays the more active part in courtship. It would be no advantage and some loss of power if both sexes were mutually to search for each other; but why should the male almost always be the seeker? With plants, the ovules after fertilisation have to be nourished for a time; hence the pollen is necessarily brought to the female organs—being placed on the stigma, through the agency of insects or of the wind, 274or by the spontaneous movements of the stamens; and with the Algæ, &c., by the locomotive power of the antherozooids. With lowly-organised animals permanently affixed to the same spot and having their sexes separate, the male element is invariably brought to the female; and we can see the reason; for the ova, even if detached before being fertilised and not requiring subsequent nourishment or protection, would be, from their larger relative size, less easily transported than the male element. Hence plants349 and many of the lower animals are, in this respect, analogous. In the case of animals not affixed to the same spot, but enclosed within a shell with no power of protruding any part of their bodies, and in the case of animals having little power of locomotion, the males must trust the fertilising element to the risk of at least a short transit through the waters of the sea. It would, therefore, be a great advantage to such animals, as their organisation became perfected, if the males when ready to emit the fertilising element, were to acquire the habit of approaching the female as closely as possible. The males of various lowly-organised animals having thus aboriginally acquired the habit of approaching and seeking the females, the same habit would naturally be transmitted to their more highly developed male descendants; and in order that they should become efficient seekers, they would have to be endowed with strong passions. The acquirement of such passions would naturally follow from the more eager males leaving a larger number of offspring than the less eager.
We naturally wonder why males in so many different species are generally more eager than females, leading them to search for their partners and take a more active role in courting. It wouldn’t be beneficial, and could even weaken their position, if both sexes actively sought each other; so why is it that males are almost always the ones doing the seeking? In plants, after fertilization, the ovules need nourishment for a while; that's why pollen is brought to the female organs—either placed on the stigma by insects, wind, or even the natural movements of the stamens, and in some cases, by the swimming antherozooids. For simpler organisms that are fixed to one spot and have separate sexes, the male gametes are consistently brought to the female; and the reason is clear: the eggs, being relatively larger, would be harder to move than the male gametes, even if they were detached before fertilization and didn’t need further care. Thus, in this aspect, plants and many lower animals are similar. In cases where animals are not fixed in one place but are enclosed in shells and cannot extend any part of their bodies, or where animals have limited movement, males must risk transporting their gametes through the sea. So, it would greatly benefit these animals, as they evolved, if males developed the tendency to be as close as possible to females when they were ready to release their gametes. As males of various simpler species originally adopted the behavior of seeking out females, this trait would naturally be passed down to their more advanced male offspring; and for them to be effective seekers, they would need to be driven by strong desires. Such passionate tendencies would arise naturally since the more eager males would produce more offspring than the less motivated ones.
The great eagerness of the male has thus indirectly 275led to the much more frequent development of secondary sexual characters in the male than in the female. But the development of such characters will have been much aided, if the conclusion at which I arrived after studying domesticated animals, can be trusted, namely, that the male is more liable to vary than the female. I am aware how difficult it is to verify a conclusion of this kind. Some slight evidence, however, can be gained by comparing the two sexes in mankind, as man has been more carefully observed than any other animal. During the Novara Expedition350 a vast number of measurements of various parts of the body in different races were made, and the men were found in almost every case to present a greater range of variation than the women; but I shall have to recur to this subject in a future chapter. Mr. J. Wood,351 who has carefully attended to the variation of the muscles in man, puts in italics the conclusion that “the greatest number of abnormalities in each subject is found in the males.” He had previously remarked that “altogether in 102 subjects the varieties of redundancy were found to be half as many again as in females, contrasting widely with the greater frequency of deficiency in females before described.” Professor Macalister like wise remarks352 that variations in the muscles “are probably more common in males than females.” Certain muscles which are not normally present in mankind are also more frequently developed in the male than in the female sex, although exceptions to this rule 276are said to occur. Dr. Burt Wilder353 has tabulated the cases of 152 individuals with supernumerary digits, of which 86 were males, and 39, or less than half, females; the remaining 27 being of unknown sex. It should not, however, be overlooked that women would more frequently endeavour to conceal a deformity of this kind than men. Whether the large proportional number of deaths of the male offspring of man and apparently of sheep, compared with the female offspring, before, during, and shortly after birth (see supplement), has any relation to a stronger tendency in the organs of the male to vary and thus to become abnormal in structure or function, I will not pretend to conjecture.
The strong desire of males has thus indirectly 275led to a much more common development of secondary sexual traits in males than in females. However, the development of these traits is likely enhanced by my conclusion based on the study of domesticated animals, which suggests that males are more prone to variation than females. I understand that it's challenging to confirm such a conclusion. Nonetheless, some evidence can be gathered by comparing the two sexes in humans, as men have been more closely observed than any other animals. During the Novara Expedition350 numerous measurements of various body parts in different races were taken, showing that men typically display a greater range of variation than women; I will revisit this topic in a later chapter. Mr. J. Wood,351 who has closely studied muscle variation in humans, emphasizes that “the greatest number of abnormalities in each subject is found in males.” He previously noted that “overall, in 102 subjects, the varieties of redundancy were found to be about 50% more than in females, contrasting sharply with the higher frequency of deficiencies in females previously described.” Professor Macalister also points out352 that muscle variations “are probably more common in males than in females.” Certain muscles that are usually not present in humans are also more often developed in males than in females, though there are noted exceptions. Dr. Burt Wilder353 has compiled cases of 152 individuals with supernumerary digits, of which 86 were males and 39, or less than half, were females; the remaining 27 had an unknown sex. It should also be noted that women are more likely to hide a deformity of this type than men. Whether the notably higher number of male offspring deaths in humans and apparently in sheep, compared to female offspring, before, during, and shortly after birth (see supplement) is related to a greater tendency for male organs to vary and thus become abnormal in structure or function is something I will not speculate on.
In various classes of animals a few exceptional cases occur, in which the female instead of the male has acquired well pronounced secondary sexual characters, such as brighter colours, greater size, strength, or pugnacity. With birds, as we shall hereafter see, there has sometimes been a complete transposition of the ordinary characters proper to each sex; the females having become the more eager in courtship, the males remaining comparatively passive, but apparently selecting, as we may infer from the results, the more attractive females. Certain female birds have thus been rendered more highly coloured or otherwise ornamented, as well as more powerful and pugnacious than the males, these characters being transmitted to the female offspring alone.
In various groups of animals, there are a few unique cases where the female, instead of the male, has developed distinct secondary sexual traits, like brighter colors, larger size, more strength, or a more aggressive nature. In birds, as we will discuss later, there have been instances where the typical traits of each sex are completely reversed; females have become the more enthusiastic ones in courtship while males remain relatively passive. However, it seems that males tend to choose the most attractive females, as suggested by the outcomes. Some female birds have thus become more brightly colored or decorated, as well as stronger and more aggressive than the males, and these traits are passed down only to female offspring.
It may be suggested that in some cases a double process of selection has been carried on; the males having selected the more attractive females, and the latter the more attractive males. This process however, though it might lead to the modification of both sexes, 277would not make the one sex different from the other, unless indeed their taste for the beautiful differed; but this is a supposition too improbable in the case of any animal, excepting man, to be worth considering. There are, however, many animals, in which the sexes resemble each other, both being furnished with the same ornaments, which analogy would lead us to attribute to the agency of sexual selection. In such cases it may be suggested with more plausibility, that there has been a double or mutual process of sexual selection; the more vigorous and precocious females having selected the more attractive and vigorous males, the latter having rejected all except the more attractive females. But from what we know of the habits of animals, this view is hardly probable, the male being generally eager to pair with any female. It is more probable that the ornaments common to both sexes were acquired by one sex, generally the male, and then transmitted to the offspring of both sexes. If, indeed, during a lengthened period the males of any species were greatly to exceed the females in number, and then during another lengthened period under different conditions the reverse were to occur, a double, but not simultaneous, process of sexual selection might easily be carried on, by which the two sexes might be rendered widely different.
It could be suggested that sometimes a double process of selection has taken place: males have chosen the more attractive females, and those females have chosen the more attractive males. However, while this might lead to changes in both sexes, it wouldn’t make one sex vastly different from the other unless their standards of beauty differed. But this idea is too unlikely for any animal, except humans, to be worth discussing. Many animals, however, show that the sexes look alike, with both having the same traits, which suggests that sexual selection is at play. In these cases, it seems more reasonable to think that there has been a mutual process of sexual selection: the stronger and earlier-maturing females have picked the more attractive and vigorous males, who in turn have rejected all but the most appealing females. However, considering animal behavior, this idea seems unlikely since males usually want to mate with any female they can. It’s more plausible that the traits shared by both sexes were developed by one sex, generally the male, and then passed on to the offspring of both sexes. If, over a long period, the males of a species greatly outnumbered the females, and then during another long period, the opposite occurred under different conditions, a double but not simultaneous process of sexual selection might indeed lead to significant differences between the two sexes.
We shall hereafter see that many animals exist, of which neither sex is brilliantly coloured or provided with special ornaments, and yet the members of both sexes or of one alone have probably been modified through sexual selection. The absence of bright tints or other ornaments may be the result of variations of the right kind never having occurred, or of the animals themselves preferring simple colours, such as plain black or white. Obscure colours have often been acquired through natural selection for the sake of protection, and278 the acquirement through sexual selection of conspicuous colours, may have been checked from the danger thus incurred. But in other cases the males have probably struggled together during long ages, through brute force, or by the display of their charms, or by both means combined, and yet no effect will have been produced unless a larger number of offspring were left by the more successful males to inherit their superiority, than by the less successful males; and this, as previously shewn, depends on various complex contingencies.
We will soon see that many animals exist where neither sex is brightly colored or has special features, yet the members of both sexes or just one may have been changed through sexual selection. The lack of bright colors or ornaments could be due to the right variations never occurring, or the animals themselves might simply prefer basic colors like plain black or white. Dull colors often develop through natural selection for protection, and the acquisition of bright colors through sexual selection may have been hindered due to the risks involved. In other cases, males might have competed for ages through brute force, the display of their traits, or a combination of both, but no change will occur unless the more successful males leave behind more offspring to inherit their advantages than the less successful ones; and this, as previously shown, relies on various complex factors.
Sexual selection acts in a less rigorous manner than natural selection. The latter produces its effects by the life or death at all ages of the more or less successful individuals. Death, indeed, not rarely ensues from the conflicts of rival males. But generally the less successful male merely fails to obtain a female, or obtains later in the season a retarded and less vigorous female, or, if polygamous, obtains fewer females; so that they leave fewer, or less vigorous, or no offspring. In regard to structures acquired through ordinary or natural selection, there is in most cases, as long as the conditions of life remain the same, a limit to the amount of advantageous modification in relation to certain special ends; but in regard to structures adapted to make one male victorious over another, either in fighting or in charming the female, there is no definite limit to the amount of advantageous modification; so that as long as the proper variations arise the work of sexual selection will go on. This circumstance may partly account for the frequent and extraordinary amount of variability presented by secondary sexual characters. Nevertheless, natural selection will determine that characters of this kind shall not be acquired by the victorious males, which would be injurious to them in any high degree, either by expending too much of their vital powers, or279 by exposing them to any great danger. The development, however, of certain structures—of the horns, for instance, in certain stags—has been carried to a wonderful extreme; and in some instances to an extreme which, as far as the general conditions of life are concerned, must be slightly injurious to the male. From this fact we learn that the advantages which favoured males have derived from conquering other males in battle or courtship, and thus leaving a numerous progeny, have been in the long run greater than those derived from rather more perfect adaptation to the external conditions of life. We shall further see, and this could never have been anticipated, that the power to charm the female has been in some few instances more important than the power to conquer other males in battle.
Sexual selection operates in a less strict way than natural selection. The latter has effects through the survival or death of individuals at all ages based on their success. Indeed, death often results from conflicts among rival males. Generally, though, the less successful male simply fails to attract a female, or he gets a female later in the season who is less healthy and vigorous, or, if he practices polygamy, he attracts fewer females. As a result, he leaves behind fewer, weaker, or no offspring. For traits gained through ordinary or natural selection, there is usually a limit to how much advantageous change can happen when conditions of life stay the same; however, for traits that help one male win over another, whether in battle or by attracting females, there’s no clear limit to how much advantageous modification can occur. So, as long as suitable variations come about, the process of sexual selection continues. This might explain the frequent and remarkable amount of variability seen in secondary sexual traits. Still, natural selection ensures that traits acquired by winning males won’t be detrimental to them in any significant way, either by draining their energy or putting them in excessive danger. The growth of certain traits—like horns in some male deer—has reached an astonishing level; in some cases, these traits may actually be slightly harmful to the male considering the overall conditions of life. This shows us that the benefits victorious males gain from defeating other males in either competition or courtship, and thus producing many offspring, have, over time, outweighed the advantages of being better adapted to their environment. We will also see, which is unexpected, that in a few cases, the ability to charm females has proven to be more important than the ability to defeat other males in combat.
LAWS OF INHERITANCE.
In order to understand how sexual selection has acted, and in the course of ages has produced conspicuous results with many animals of many classes, it is necessary to bear in mind the laws of inheritance, as far as they are known. Two distinct elements are included under the term “inheritance,” namely the transmission and the development of characters; but as these generally go together, the distinction is often overlooked. We see this distinction in those characters which are transmitted through the early years of life, but are developed only at maturity or during old age. We see the same distinction more clearly with secondary sexual characters, for these are transmitted through both sexes, though developed in one alone. That they are present in both sexes, is manifest when two species, having strongly-marked sexual characters, are crossed, for each transmits the characters proper to280 its own male and female sex to the hybrid offspring of both sexes. The same fact is likewise manifest, when characters proper to the male are occasionally developed in the female when she grows old or becomes diseased; and so conversely with the male. Again, characters occasionally appear, as if transferred from the male to the female, as when, in certain breeds of the fowl, spurs regularly appear in the young and healthy females; but in truth they are simply developed in the female; for in every breed each detail in the structure of the spur is transmitted through the female to her male offspring. In all cases of reversion, characters are transmitted through two, three, or many generations, and are then under certain unknown favourable conditions developed. This important distinction between transmission and development will be easiest kept in mind by the aid of the hypothesis of pangenesis, whether or not it be accepted as true. According to this hypothesis, every unit or cell of the body throws off gemmules or undeveloped atoms, which are transmitted to the offspring of both sexes, and are multiplied by self-division. They may remain undeveloped during the early years of life or during successive generations; their development into units or cells, like those from which they were derived, depending on their affinity for, and union with, other units or cells previously developed in the due order of growth.
To understand how sexual selection has worked and how, over time, it has led to noticeable changes in many animal species, it's important to consider the known laws of inheritance. The term "inheritance" includes two distinct aspects: the passing down of traits and the development of those traits, though these usually happen together, so the difference is often overlooked. This distinction can be seen in traits that are passed down during early life but only develop fully in adulthood or old age. It's even clearer with secondary sexual traits, which are inherited by both sexes but are developed only in one. Both sexes carry these traits, especially evident when two species with strong sexual traits are crossed; each species passes its unique male and female traits to the hybrid offspring. We also see this when male traits occasionally show up in females as they age or if they get sick, and the same goes for male traits appearing in females. Furthermore, traits like spurs can appear in young, healthy female chickens in some breeds; however, they are just developing in the female, as the structure of the spur is inherited through the female to her male offspring in every breed. In cases of reversion, traits can be passed down through two, three, or several generations before being developed under certain unknown favorable conditions. This crucial difference between transmission and development is easiest to remember through the idea of pangenesis, whether or not one believes it to be true. According to this idea, every cell in the body releases gemmules or undeveloped particles, which are passed to offspring of both sexes and multiplied by self-division. They can remain undeveloped during early life or for several generations; their development into cells similar to their origin depends on their compatibility and fusion with other already developed cells in the proper growth order.
Inheritance at Corresponding Periods of Life.—This tendency is well established. If a new character appears in an animal whilst young, whether it endures throughout life or lasts only for a time, it will reappear, as a general rule, at the same age and in the same manner in the offspring. If, on the other hand, a new character appears at maturity, or even during old age, it tends281 to reappear in the offspring at the same advanced age. When deviations from this rule occur, the transmitted characters much oftener appear before than after the corresponding age. As I have discussed this subject at sufficient length in another work,354 I will here merely give two or three instances, for the sake of recalling the subject to the reader’s mind. In several breeds of the Fowl, the chickens whilst covered with down, in their first true plumage, and in their adult plumage, differ greatly from each other, as well as from their common parent-form, the Gallus bankiva; and these characters are faithfully transmitted by each breed to their offspring at the corresponding period of life. For instance, the chickens of spangled Hamburghs, whilst covered with down, have a few dark spots on the head and rump, but are not longitudinally striped, as in many other breeds; in their first true plumage, “they are beautifully pencilled,” that is each feather is transversely marked by numerous dark bars; but in their second plumage the feathers all become spangled or tipped with a dark round spot.355 Hence in this breed variations have occurred and have been transmitted at three distinct periods of life. The Pigeon offers a more remarkable case, because the aboriginal parent-species does not undergo with advancing age any change of plumage, excepting that at maturity the breast becomes more iridescent; yet there are breeds which do not acquire their characteristic colours until they 282have moulted two, three, or four times; and these modifications of plumage are regularly transmitted.
Inheritance at Corresponding Periods of Life.—This tendency is well established. If a new trait appears in an animal while it’s young, whether it lasts for life or only for a while, it generally reappears in the offspring at the same age and in the same way. Conversely, if a new trait appears during adulthood or even in old age, it tends to show up in the offspring at the same later age. When there are exceptions to this rule, the inherited traits are more likely to appear before the corresponding age rather than after. As I’ve covered this topic in detail in another work,354 I’ll just provide a few examples to remind the reader of the topic. In several breeds of chickens, the chicks differ significantly from each other, as well as from their common ancestor, the Gallus bankiva, in their down-covered stage, their first true feathers, and their adult plumage; these traits are reliably passed on to the offspring at the corresponding life stages. For example, the chicks of spangled Hamburghs have a few dark spots on their heads and rumps while they’re still downy, but they’re not striped like in many other breeds; in their first true plumage, “they are beautifully pencilled,” meaning each feather has numerous dark bars across it; however, in their second plumage, the feathers become spangled or tipped with a dark round spot.355 Thus, in this breed, variations have occurred and have been passed down at three different stages of life. The Pigeon presents an even more remarkable case, as the original parent species does not change its plumage with age, except that the breast becomes more iridescent when mature; yet there are breeds that don’t attain their distinctive colors until they have molted two, three, or four times, and these changes in plumage are consistently passed down.
Inheritance at Corresponding Seasons of the Year.—With animals in a state of nature innumerable instances occur of characters periodically appearing at different seasons. We see this with the horns of the stag, and with the fur of arctic animals which becomes thick and white during the winter. Numerous birds acquire bright colours and other decorations during the breeding-season alone. I can throw but little light on this form of inheritance from facts observed under domestication. Pallas states,356 that in Siberia domestic cattle and horses periodically become lighter-coloured during the winter; and I have observed a similar marked change of colour in certain ponies in England. Although I do not know that this tendency to assume a differently coloured coat during different seasons of the year is transmitted, yet it probably is so, as all shades of colour are strongly inherited by the horse. Nor is this form of inheritance, as limited by season, more remarkable than inheritance as limited by age or sex.
Inheritance at Different Seasons of the Year.—In wild animals, there are countless examples of traits that show up at various times of the year. For instance, we notice this with the antlers of stags and the thick, white fur of Arctic animals in winter. Many birds display vibrant colors and unique features only during their breeding season. I can shed very little light on this type of inheritance based on observations from domesticated animals. Pallas states,356 that in Siberia, domestic cattle and horses periodically turn lighter in color during winter; I have noticed a similar significant color change in certain ponies in England. While I'm not sure if this tendency to change coat color with the seasons is passed down, it likely is, since horses strongly inherit all color variations. This seasonal pattern of inheritance is no more surprising than the inheritance related to age or sex.
Inheritance as Limited by Sex.—The equal transmission of characters to both, sexes is the commonest form of inheritance, at least with those animals which do not present strongly-marked sexual differences, and indeed with many of these. But characters are not rarely transferred exclusively to that sex, in which they first appeared. Ample evidence on this head has been advanced in my work on Variation under Domestica283tion; but a few instances may here be given. There are breeds of the sheep and goat, in which the horns of the male differ greatly in shape from those of the female; and these differences, acquired under domestication, are regularly transmitted to the same sex. With tortoise-shell cats the females alone, as a general rule, are thus coloured, the males being rusty-red. With most breeds of the fowl, the characters proper to each sex are transmitted to the same sex alone. So general is this form of transmission that it is an anomaly when we see in certain breeds variations transmitted equally to both sexes. There are also certain sub-breeds of the fowl in which the males can hardly be distinguished from each other, whilst the females differ considerably in colour. With the pigeon the sexes of the parent-species do not differ in any external character; nevertheless in certain domesticated breeds the male is differently coloured from the female.357 The wattle in the English Carrier pigeon and the crop in the Pouter are more highly developed in the male than in the female; and although these characters have been gained through long-continued selection by man, the difference between the two sexes is wholly due to the form of inheritance which has prevailed; for it has arisen, not from, but rather in opposition to, the wishes of the breeder.
Inheritance as Limited by Sex.—The equal passing down of traits to both sexes is the most common form of inheritance, especially in animals that don’t show strong sexual differences, and even in many that do. However, traits are often passed down exclusively to the sex in which they first appeared. I’ve provided plenty of evidence for this in my work on Variation under Domestication283, but here are a few examples. There are breeds of sheep and goats where the horns of males look very different from those of females, and these differences, developed through domestication, are regularly passed down to the same sex. With tortoiseshell cats, females typically have this coloration, while males are usually rusty-red. In most breeds of chickens, the characteristics specific to each sex are only passed on to that sex. This form of inheritance is so common that it’s unusual to see variations passed down equally to both sexes in certain breeds. There are also some sub-breeds of chickens where the males are hard to tell apart, while the females vary significantly in color. In pigeons, the sexes of the parent species don’t show any external differences; however, in some domesticated breeds, the male has a different color than the female.357 The wattle in the English Carrier pigeon and the crop in the Pouter are more developed in males than in females; and although these traits have been enhanced through long-term selective breeding by humans, the difference between the sexes arises entirely from the form of inheritance that has been at work, as it has emerged not from, but rather against, the breeder's intentions.
Most of our domestic races have been formed by the accumulation of many slight variations; and as some of the successive steps have been transmitted to one sex alone, and some to both sexes, we find in the different breeds of the same species all gradations between great sexual dissimilarity and complete similarity. In284stances have already been given with the breeds of the fowl and pigeon; and under nature analogous cases are of frequent occurrence. With animals under domestication, but whether under nature I will not venture to say, one sex may lose characters proper to it, and may thus come to resemble to a certain extent the opposite sex; for instance, the males of some breeds of the fowl have lost their masculine plumes and hackles. On the other hand the differences between the sexes may be increased under domestication, as with merino sheep, in which the ewes have lost their horns. Again, characters proper to one sex may suddenly appear in the other sex; as with those sub-breeds of the fowl in which the hens whilst young acquire spurs; or, as in certain Polish sub-breeds, in which the females, as there is reason to believe, originally acquired a crest, and subsequently transferred it to the males. All these cases are intelligible on the hypothesis of pangenesis; for they depend on the gemmules of certain units of the body, although present in both sexes, becoming through the influence of domestication dormant in the one sex; or if naturally dormant, becoming developed.
Most of our domestic animal breeds have come about through the accumulation of many slight variations. Since some of these changes have been passed down to just one sex and others to both, we can observe a range of differences in sexual characteristics within the same species, from significant differences to complete similarity. Instances have already been provided using chickens and pigeons; similar cases occur frequently in nature. In domesticated animals, it’s possible for one sex to lose traits typical to it, thus resembling the opposite sex to some extent. For example, the males of some chicken breeds have lost their male feathers and crests. Conversely, the differences between the sexes can become more pronounced through domestication, as seen in merino sheep, where the females have lost their horns. Additionally, traits typical of one sex may suddenly emerge in the other, such as in certain chicken breeds where young hens develop spurs, or in specific Polish breeds where females, believed to have originally developed a crest, later passed it on to the males. All these examples can be explained by the hypothesis of pangenesis, as they rely on the gemmules of specific body units, which may be present in both sexes but become dormant in one sex due to domestication; or if they are naturally dormant, they may become active.
There is one difficult question which it will be convenient to defer to a future chapter; namely, whether a character at first developed in both sexes, can be rendered through selection limited in its development to one sex alone. If, for instance, a breeder observed that some of his pigeons (in which species characters are usually transferred in an equal degree to both sexes) varied into pale blue; could he by long-continued selection make a breed, in which the males alone should be of this tint, whilst the females remained unchanged? I will here only say, that this, though perhaps not impossible, would be extremely difficult; for the natural result of breeding from the pale-blue males would be285 to change his whole stock, including both sexes, into this tint. If, however, variations of the desired tint appeared, which were from the first limited in their development to the male sex, there would not be the least difficulty in making a breed characterised by the two sexes being of a different colour, as indeed has been effected with a Belgian breed, in which the males alone are streaked with black. In a similar manner, if any variation appeared in a female pigeon, which was from the first sexually limited in its development, it would be easy to make a breed with the females alone thus characterised; but if the variation was not thus originally limited, the process would be extremely difficult, perhaps impossible.
There’s one tough question that I’ll put off for a future chapter: can a trait that initially develops in both sexes be developed through selective breeding that's restricted to just one sex? For example, if a breeder noticed that some of his pigeons (where traits usually transfer equally to both sexes) had a pale blue color, could he, through long-term selective breeding, create a strain where only the males were this color while the females stayed the same? I'll just say that while it might not be impossible, it would be really challenging; breeding from the pale-blue males would likely result in changing the entire flock, both males and females, to that color. However, if variations of the desired color appeared and were initially limited to just males, it would be straightforward to develop a breed where the two sexes are different colors, as seen in a Belgian breed where only the males have black streaks. Similarly, if a female pigeon showed any variation from the start that was limited to her sex, it would be easy to establish a breed with only females showing that trait; but if the variation wasn't initially confined like that, the process would be extremely difficult, maybe even impossible.
On the Relation between the period of Development of a Character and its transmission to one sex or to both sexes.—Why certain characters should be inherited by both sexes, and other characters by one sex alone, namely by that sex in which the character first appeared, is in most cases quite unknown. We cannot even conjecture why with certain sub-breeds of the pigeon, black striæ, though transmitted through the female, should be developed in the male alone, whilst every other character is equally transferred to both sexes. Why, again, with cats, the tortoise-shell colour should, with rare exceptions, be developed in the female alone. The very same characters, such as deficient or supernumerary digits, colour-blindness, &c., may with mankind be inherited by the males alone of one family, and in another family by the females alone, though in both cases transmitted through the opposite as well as the same sex.358 Although we are thus ignorant, two rules often hold good, namely 286that variations which, first appear in either sex at a late period of life, tend to be developed in the same sex alone; whilst variations which first appear early in life in either sex tend to be developed in both sexes. I am, however, far from supposing that this is the sole determining cause. As I have not elsewhere discussed this subject, and as it has an important bearing on sexual selection, I must here enter into lengthy and somewhat intricate details.
On the Relation between the Development Period of a Character and its Transmission to One Sex or Both Sexes.—The reason some traits are inherited by both sexes while others are passed down to just one sex, specifically the sex in which the trait first appeared, is largely unknown. We can’t even guess why, in certain pigeon sub-breeds, black striations, though passed through the female, develop only in the male, while every other trait is transferred to both sexes. Similarly, with cats, the tortoiseshell color is typically developed in females only, with rare exceptions. The same traits, like missing or extra digits and color blindness, may be inherited by male members of one family and female members of another, even though they are transmitted through both the same and the opposite sex. Although we don’t fully understand this, two general rules often apply: variations that first emerge in either sex later in life usually develop in just that sex; while variations that arise early in life in either sex tend to develop in both. However, I don’t believe that this is the only factor at play. Since I haven’t discussed this topic elsewhere and it significantly impacts sexual selection, I need to go into detailed and somewhat complex explanations here.
It is in itself probable that any character appearing at an early age would tend to be inherited equally by both sexes, for the sexes do not differ much in constitution, before the power of reproduction is gained. On the other hand, after this power has been gained and the sexes have come to differ in constitution, the gemmules (if I may again use the language of pangenesis) which are cast off from each varying part in the one sex would be much more likely to possess the proper affinities for uniting with the tissues of the same sex, and thus becoming developed, than with those of the opposite sex.
It’s likely that any traits that show up early on would be inherited equally by both genders since they don’t differ much in makeup before they can reproduce. However, once they gain that ability and the sexes start to differ constitutionally, the gemmules (if I can refer to pangenesis again) that are produced from each changing part in one gender would be much more likely to bond with the tissues of the same gender, leading to development, than with those of the opposite gender.
I was first led to infer that a relation of this kind exists, from the fact that whenever and in whatever manner the adult male has come to differ from the adult female, he differs in the same manner from the young of both sexes. The generality of this fact is quite remarkable: it holds good with almost all mammals, birds, amphibians, and fishes; also with many crustaceans, spiders and some few insects, namely certain orthoptera and libellulæ. In all these cases the variations, through the accumulation of which the male acquired his proper masculine characters, must have occurred at a somewhat late period of life; otherwise the young males would have been similarly characterised; and conformably with our rule, they are transmitted to287 and developed in the adult males alone. When, on the other hand, the adult male closely resembles the young of both sexes (these, with rare exceptions, being alike), he generally resembles the adult female; and in most of these cases the variations through which the young and old acquired their present characters, probably occurred in conformity with our rule during youth. But there is here room for doubt, as characters are sometimes transferred to the offspring at an earlier age than that at which they first appeared in the parents, so that the parents may have varied when adult, and have transferred their characters to their offspring whilst young. There are, moreover, many animals, in which the two sexes closely resemble each other, and yet both differ from their young; and here the characters of the adults must have been acquired late in life; nevertheless, these characters in apparent contradiction to our rule, are transferred to both sexes. We must not, however, overlook the possibility or even probability of successive variations of the same nature sometimes occurring, under exposure to similar conditions, simultaneously in both sexes at a rather late period of life; and in this case the variations would be transferred to the offspring of both sexes at a corresponding late age; and there would be no real contradiction to our rule of the variations which occur late in life being transferred exclusively to the sex in which they first appeared. This latter rule seems to hold true more generally than the second rule, namely, that variations which occur in either sex early in life tend to be transferred to both sexes. As it was obviously impossible even to estimate in how large a number of cases throughout the animal kingdom these two propositions hold good, it occurred to me to investigate some striking or crucial instances, and to rely on the result.
I was initially led to believe that this type of relationship exists because whenever and however the adult male differs from the adult female, he also differs in the same way from the young of both sexes. This fact is quite remarkable; it applies to almost all mammals, birds, amphibians, and fish, as well as many crustaceans, spiders, and a few insects, specifically certain orthoptera and dragonflies. In all these cases, the variations that allowed the male to develop his distinct masculine traits must have occurred at a relatively late stage of life; otherwise, young males would have shown similar characteristics. According to our rule, these traits are passed on to and developed in adult males alone. Conversely, when the adult male closely resembles the young of both sexes (which are usually similar, with rare exceptions), he typically resembles the adult female; and in most of these cases, the variations that shaped both the young and old likely occurred during youth. However, there's some uncertainty here, as traits can sometimes be passed to offspring at an earlier age than when they first appeared in the parents, meaning that the parents may have varied when they were adults and passed their traits to their young while still immature. Additionally, many animals exist where the two sexes closely resemble each other, yet both differ from their young; in such cases, the traits of the adults must have been acquired later in life. Still, these traits, seemingly contradicting our rule, are passed on to both sexes. We shouldn't overlook the possibility—and even probability—that similar variations occur simultaneously in both sexes under similar conditions at a relatively late stage of life; in this case, the variations would also be passed to the offspring of both sexes at a similar later age, leading to no real contradiction to our rule that late-life variations are passed exclusively to the sex in which they first arose. This latter rule appears to be more broadly applicable than the second rule, which states that variations occurring in either sex early in life tend to be passed on to both sexes. Since it was clearly impossible to gauge how many cases this holds true for across the animal kingdom, I decided to investigate some notable or critical instances and rely on the results.
288An excellent case for investigation is afforded by the Deer Family. In all the species, excepting one, the horns are developed in the male alone, though certainly transmitted through the female, and capable of occasional abnormal development in her. In the reindeer, on the other hand, the female is provided with horns; so that in this species, the horns ought, according to our rule, to appear early in life, long before the two sexes had arrived at maturity and had come to differ much in constitution. In all the other species of deer the horns ought to appear later in life, leading to their development in that sex alone, in which they first appeared in the progenitor of the whole Family. Now in seven species, belonging to distinct sections of the family and inhabiting different regions, in which the stags alone bear horns, I find that the horns first appear at periods varying from nine months after birth in the roebuck to ten or twelve or even more months in the stags of the six other larger species.359 But with the reindeer the case is widely different, for as I hear from Prof. Nilsson, who kindly made special enquiries for me in Lapland, the horns appear in the young animals within four or five weeks after birth, and at the same time in both sexes. So that here we have a structure, developed at a most unusually early age in one species of the family, and common to both sexes in this one species.
288A great example to examine is the Deer Family. In all species, except for one, the horns are only developed in males, although they are inherited from females and can occasionally develop abnormally in them. In the case of reindeer, however, females also have horns; hence, in this species, horns should appear early in life, well before both sexes mature and show significant differences. In all the other deer species, horns appear later in life, leading to their development only in the sex in which they first appeared in the ancestor of the entire family. Now, in seven species from different sections of the family, living in various regions, where only the stags have horns, I find that the horns first appear at ages ranging from nine months after birth in the roebuck to ten, twelve, or even more months in the stags of the other larger species.359 But with reindeer, the situation is quite different. According to Prof. Nilsson, who was kind enough to make special inquiries for me in Lapland, the horns show up in young reindeer within four to five weeks after birth, and at the same time in both sexes. This means we have a characteristic that develops unusually early in just one species of the family and is shared by both sexes in that species.
In several kinds of antelopes the males alone are 289provided with horns, whilst in the greater number both sexes have horns. With respect to the period of development, Mr. Blyth informs me that there lived at one time in the Zoological Gardens a young koodoo (Ant. strepsiceros), in which species the males alone are horned, and the young of a closely-allied species, viz. the eland (Ant. oreas), in which both sexes are horned. Now in strict conformity with our rule, in the young male koodoo, although arrived at the age of ten months, the horns were remarkably small considering the size ultimately attained by them: whilst in the young male eland, although only three months old, the horns were already very much larger than in the koodoo. It is also worth notice that in the prong-horned antelope,360 in which species the horns, though present in both sexes, are almost rudimentary in the female, they do not appear until about five or six months after birth. With sheep, goats, and cattle, in which the horns are well developed in both sexes, though not quite equal in size, they can be felt, or even seen, at birth or soon afterwards.361 Our rule, however, fails in regard to some breeds of sheep, for instance merinos, in which the rams alone are horned; for I cannot find on enquiry,362 that 290the horns are developed later in life in this breed than in ordinary sheep in which both sexes are horned. But with domesticated sheep the presence or absence of horns is not a firmly fixed character; a certain proportion of the merino ewes bearing small horns, and some of the rams being hornless; whilst with ordinary sheep hornless ewes are occasionally produced.
In several types of antelopes, only the males have horns, while in most species, both males and females have them. Regarding their development, Mr. Blyth told me that there was once a young koodoo (Ant. strepsiceros) at the Zoological Gardens, where only males have horns, and also a young male eland (Ant. oreas) of a closely related species, where both sexes have horns. According to our observations, the young male koodoo, despite being ten months old, had surprisingly small horns compared to their potential size, while the young male eland, only three months old, already had much larger horns than the koodoo. It's also interesting to note that in the pronghorn antelope,360 where both sexes have horns but they are almost absent in females, horns do not appear until about five or six months after birth. In sheep, goats, and cattle, where horns are well-developed in both sexes, they can be felt or even seen at birth or shortly thereafter.361 However, our rule doesn’t apply to some sheep breeds, like merinos, where only the rams have horns. I couldn't find evidence to suggest that the horns in this breed develop later in life compared to common sheep where both sexes have horns. With domesticated sheep, the presence or absence of horns isn't a consistent trait; some merino ewes have small horns, and some rams are hornless, while in regular sheep, it's not uncommon for hornless ewes to be born.
In most of the species of the splendid family of the Pheasants, the males differ conspicuously from the females, and they acquire their ornaments at a rather late period of life. The eared pheasant (Crossoptilon auritum), however, offers a remarkable exception, for both sexes possess the fine caudal plumes, the large ear-tufts and the crimson velvet about the head; and I find on enquiry in the Zoological Gardens that all these characters, in accordance with our rule, appear very early in life. The adult male can, however, be distinguished from the adult female by one character, namely by the presence of spurs; and conformably with our rule, these do not begin to be developed, as I am assured by Mr. Bartlett, before the age of six months, and even at this age, can hardly be distinguished in the two sexes.363 The male and female Peacock differ con291spicuously from each other in almost every part of their plumage, except in the elegant head-crest, which is common to both sexes; and this is developed very early in life, long before the other ornaments which are confined to the male. The wild-duck offers an analogous case, for the beautiful green speculum on the wings is common to both sexes, though duller and somewhat smaller in the female, and it is developed early in life, whilst the curled tail-feathers and other ornaments peculiar to the male are developed later.364 Between such extreme cases of close sexual resemblance and wide dissimilarity, as those of the Crossoptilon and peacock, many intermediate ones could be given, in which the characters follow in their order of development our two rules.
In most species of the beautiful Pheasant family, males are clearly different from females, and they develop their ornamental features later in life. However, the eared pheasant (Crossoptilon auritum) is a notable exception: both males and females have stunning tail feathers, large ear tufts, and crimson velvet around the head. I learned from the Zoological Gardens that these traits appear very early in life, as per our observation. The adult male can be identified from the adult female by one distinct feature—the presence of spurs. According to Mr. Bartlett, these spurs don’t start to develop until around six months old, and even then, they are hard to differentiate between the sexes.363 The male and female Peacock are vastly different in almost every aspect of their plumage, except for the stylish head crest, which they both have, and this develops early in life, long before the other male-specific ornaments. The wild duck is a similar case, as both sexes share the beautiful green wing speculum, which is somewhat duller and smaller in females, and this feature also develops early, while the curled tail feathers and other male-specific decorations develop later.364 Between extreme examples of strong sexual resemblance and wide differences, such as those of the Crossoptilon and the peacock, there are many intermediate cases where the traits develop following our two rules.
As most insects emerge from their pupal state in a mature condition, it is doubtful whether the period of development determines the transference of their characters to one or both sexes. But we do not know that the coloured scales, for instance, in two species of butterflies, in one of which the sexes differ in colour, whilst in the other they are alike, are developed at the same relative age in the cocoon. Nor do we know whether all the scales are simultaneously developed on the wings 292of the same species of butterfly, in which certain coloured marks are confined to one sex, whilst other marks are common to both sexes. A difference of this kind in the period of development is not so improbable as it may at first appear; for with the Orthoptera, which assume their adult state, not by a single metamorphosis, but by a succession of moults, the young males of some species at first resemble the females, and acquire their distinctive masculine characters only during a later moult. Strictly analogous cases occur during the successive moults of certain male crustaceans.
As most insects come out of their pupal stage fully developed, it's unclear if the time spent developing affects how their traits are passed on to one or both sexes. However, we don't know if the colored scales in two butterfly species, where one shows color differences between the sexes while the other does not, develop at the same stage in the cocoon. We also can't say if all the scales on the wings of a butterfly species, where certain colored markings are exclusive to one sex while others are present in both, develop all at once. Differences like this in development time aren't as unlikely as they might seem; for example, in the Orthoptera, which reach adulthood not through one metamorphosis but through multiple molts, young males of some species initially look like females and only develop their distinct male traits during a later molt. Similar situations happen with certain male crustaceans during their molts. 292
We have as yet only considered the transference of characters, relatively to their period of development, with species in a natural state; we will now turn to domesticated animals; first touching on monstrosities and diseases. The presence of supernumerary digits, and the absence of certain phalanges, must be determined at an early embryonic period—the tendency to profuse bleeding is at least congenital, as is probably colour-blindness—yet these peculiarities, and other similar ones, are often limited in their transmission to one sex; so that the rule that characters which are developed at an early period tend to be transmitted to both sexes, here wholly fails. But this rule, as before remarked, does not appear to be nearly so generally true as the converse proposition, namely, that characters which appear late in life in one sex are transmitted exclusively to the same sex. From the fact of the above abnormal peculiarities becoming attached to one sex. long before the sexual functions are active, we may infer that there must be a difference of some kind between the sexes at an extremely early age. With respect to sexually-limited diseases, we know too little of the period at which they originate, to draw any fair conclusion. Gout, however, seems to fall under293 our rule; for it is generally caused by intemperance after early youth, and is transmitted from the father to his sons in a much more marked manner than to his daughters.
We have only looked at how traits transfer regarding their stage of development in animals that are naturally found in the wild. Now, let's focus on domesticated animals, starting with abnormalities and diseases. The presence of extra fingers and the absence of certain bones need to be identified early in embryonic development. The tendency to bleed excessively is at least something you're born with, as is likely color blindness. Yet, these traits and others like them are often only passed down through one sex; thus, the idea that traits developed early on are typically passed to both sexes doesn’t hold up here. However, as mentioned before, this rule does not seem as universally applicable as the opposite idea—that traits that emerge later in life in one sex are passed on only to that same sex. The fact that these unusual traits are associated with one sex long before reproductive functions begin suggests there must be some kind of difference between the sexes at a very early stage. Regarding diseases that are limited to one sex, we don’t know enough about when they arise to make any solid conclusions. Gout, however, seems to align with our rule, as it is usually caused by poor habits after early youth and is passed from fathers to their sons in a much clearer way than to their daughters.
In the various domestic breeds of sheep, goats, and cattle, the males differ from their respective females in the shape or development of their horns, forehead, mane, dewlap, tail, and hump on the shoulders; and these peculiarities, in accordance with our rule, are not fully developed until rather late in life. With dogs, the sexes do not differ, except that in certain breeds, especially in the Scotch deer-hound, the male is much larger and heavier than the female; and as we shall see in a future chapter, the male goes on increasing in size to an unusually late period of life, which will account, according to our rule, for his increased size being transmitted to his male offspring alone. On the other hand, the tortoise-shell colour of the hair, which is confined to female cats, is quite distinct at birth, and this case violates our rule. There is a breed of pigeons in which the males alone are streaked with black, and the streaks can be detected even in the nestlings; but they become more conspicuous at each successive moult, so that this case partly opposes and partly supports the rule. With the English Carrier and Pouter pigeon the full development of the wattle and the crop occurs rather late in life, and these characters, conformably with our rule, are transmitted in full perfection to the males alone. The following cases perhaps come within the class previously alluded to, in which the two sexes have varied in the same manner at a rather late period of life, and have consequently transferred their new characters to both sexes at a corresponding late period; and if so, such cases are not opposed to our rule. Thus there are sub-breeds of the pigeon, described by Neumeis294ter,365 both sexes of which change colour after moulting twice or thrice, as does likewise the Almond Tumbler; nevertheless these changes, though occurring rather late in life, are common to both sexes. One variety of the Canary-bird, namely the London Prize, offers a nearly analogous case.
In different breeds of domestic sheep, goats, and cattle, males differ from females in the shape or development of their horns, foreheads, manes, dewlaps, tails, and shoulder humps; these differences, as our rule states, aren't fully developed until later in life. With dogs, the sexes are mostly similar, except in certain breeds, like the Scotch deer-hound, where males are significantly larger and heavier than females. As we will discuss in a future chapter, males continue to grow in size for an unusually long time, which explains why their increased size is only passed on to male offspring. However, the tortoise-shell fur color in female cats is noticeable at birth, which contradicts our rule. There’s a breed of pigeons where only males have black streaks, and you can see the streaks even in hatchlings, but they become more pronounced with each molt, making this case partly against and partly in support of the rule. For the English Carrier and Pouter pigeons, the full development of the wattle and crop happens later in life, and, in line with our rule, these traits are passed on perfectly to males only. The following instances might align with the previously mentioned category, where both sexes change similarly at a later age and subsequently pass those changes on to both sexes at that same later time; if that’s the case, these instances don’t contradict our rule. For example, there are sub-breeds of pigeons, noted by Neumeister, where both sexes change color after molting two or three times, similar to the Almond Tumbler; however, these changes, while occurring fairly late in life, are found in both sexes. One variety of Canary-bird, specifically the London Prize, presents a nearly comparable situation.
With the breeds of the Fowl the inheritance of various characters by one sex or by both sexes, seems generally determined by the period at which such characters are developed. Thus in all the many breeds in which the adult male differs greatly in colour from the female and from the adult male parent-species, he differs from the young male, so that the newly acquired characters must have appeared at a rather late period of life. On the other hand with most of the breeds in which the two sexes resemble each other, the young are coloured in nearly the same manner as their parents, and this renders it probable that their colours first appeared early in life. We have instances of this fact in all black and white breeds, in which the young and old of both sexes are alike; nor can it be maintained that there is something peculiar in a black or white plumage, leading to its transference to both sexes; for the males alone of many natural species are either black or white, the females being very differently coloured. With the so-called Cuckoo sub-breeds of the fowl, in which the feathers are transversely pencilled with dark stripes, both sexes and the chickens are coloured in nearly the same manner. The laced plumage of the Sebright bantam is the same in both sexes, and in the chickens the feathers are tipped with black, which makes a near approach to lacing. Spangled Hamburghs, however, offer a partial exception, 295for the two sexes, though not quite alike, resemble each other more closely than do the sexes of the aboriginal parent-species, yet they acquire their characteristic plumage late in life, for the chickens are distinctly pencilled. Turning to other characters besides colour: the males alone of the wild parent-species and of most domestic breeds possess a fairly well developed comb, but in the young of the Spanish fowl it is largely developed at a very early age, and apparently in consequence of this it is of unusual size in the adult females. In the Game breeds pugnacity is developed at a wonderfully early age, of which curious proofs could be given; and this character is transmitted to both sexes, so that the hens, from their extreme pugnacity, are now generally exhibited in separate pens. With the Polish breeds the bony protuberance of the skull which supports the crest is partially developed even before the chickens are hatched, and the crest itself soon begins to grow, though at first feebly;366 and in this breed a great bony protuberance and an immense crest characterise the adults of both sexes.
With chicken breeds, the inheritance of different traits by one or both sexes usually depends on when those traits develop. In many breeds where the adult male has a significantly different color from the female and the adult male parent species, he differs from the young male, indicating that these traits likely appear later in life. On the other hand, in most breeds where the two sexes look similar, the young are colored almost the same as their parents, suggesting that their colors appear early in life. We can see this in all-black and white breeds, where both young and old of both sexes look alike. It also can’t be argued that there’s something special about black or white feathers leading to them being passed on to both sexes since in many natural species only the males are either black or white, while the females have different colors. The so-called Cuckoo sub-breeds of chicken, where the feathers have dark stripes, have both sexes and chicks colored very similarly. The laced feathers of the Sebright bantam are the same for both sexes, and in the chicks, the feathers are tipped with black, which is close to lacing. However, Spangled Hamburghs are a partial exception, as the two sexes, while not identical, look more alike than the sexes in the original parent species, yet they develop their unique feathers late in life since the chicks are distinctly penciled. Looking at other traits besides color: the males of the wild parent species and most domestic breeds have a well-developed comb, but in young Spanish fowl, it develops early, resulting in unusually large combs in adult females. In Game breeds, aggressiveness develops at an impressively early age, and interesting evidence can be provided for this; this trait is passed down to both sexes, so the hens, due to their extreme aggression, are usually kept in separate pens. In Polish breeds, the skull bump that supports the crest develops partially before the chicks are hatched, and the crest starts growing soon after, although initially weakly; and in this breed, both sexes are characterized by a significant bony protrusion and a large crest in adults.
Finally, from what we have now seen of the relation which exists in many natural species and domesticated races, between the period of the development of their characters and the manner of their transmission—for example the striking fact of the early growth of the horns in the reindeer, in which both sexes have horns, in comparison with their much later growth in the other species in which the male alone bears horns—we may conclude that one cause, though not the sole 296cause, of characters being exclusively inherited by one sex, is their development at a late age. And secondly, that one, though apparently a less efficient, cause of characters being inherited by both sexes is their development at an early age, whilst the sexes differ but little in constitution. It appears, however, that some difference must exist between the sexes even during an early embryonic period, for characters developed at this age not rarely become attached to one sex.
Finally, from what we have observed about the relationship that exists in many natural species and domesticated breeds, between the period of character development and how they are passed on—for instance, the notable fact of the early growth of horns in reindeer, where both sexes have horns, compared to the much later growth in other species where only the males have horns—we can conclude that one reason, though not the only reason, 296 for certain traits being inherited exclusively by one sex is because they develop at a later age. Additionally, while it seems to be a less significant reason, early development of traits, when the sexes are quite similar in constitution, is a reason why some traits are inherited by both sexes. However, it appears that some differences must exist between the sexes even during the early embryonic phase, as traits that develop during this stage often become associated with one sex.
Summary and concluding remarks.—From the foregoing discussion on the various laws of inheritance, we learn that characters often or even generally tend to become developed in the same sex, at the same age, and periodically at the same season of the year, in which they first appeared in the parents. But these laws, from unknown causes, are very liable to change. Hence the successive steps in the modification of a species might readily be transmitted in different ways; some of the steps being transmitted to one sex, and some to both; some to the offspring at one age, and some at all ages. Not only are the laws of inheritance extremely complex, but so are the causes which induce and govern variability. The variations thus caused are preserved and accumulated by sexual selection, which is in itself an extremely complex affair, depending, as it does, on ardour in love, courage, and the rivalry of the males, and on the powers of perception, taste, and will of the female. Sexual selection will also be dominated by natural selection for the general welfare of the species. Hence the manner in which the individuals of either sex or of both sexes are affected through sexual selection cannot fail to be complex in the highest degree.
Summary and concluding remarks.—From the earlier discussion on the various laws of inheritance, we understand that traits often develop similarly in the same sex, at the same age, and typically during the same season of the year as they first appeared in the parents. However, these laws, for unknown reasons, can easily change. Therefore, the different stages in the evolution of a species can be passed down in various ways; some stages may be passed to one sex, and some to both; some to offspring at one age, and some at all ages. Not only are the laws of inheritance incredibly complex, but so are the factors that cause and govern variability. The variations caused by these factors are maintained and accumulated through sexual selection, which is itself very complicated, relying on passion in love, bravery, and competition among males, as well as the abilities of perception, taste, and will of the female. Sexual selection is also influenced by natural selection for the overall health of the species. As a result, the ways in which individuals of either sex or both are affected by sexual selection are bound to be extremely complex.
When variations occur late in life in one sex, and are297 transmitted to the same sex at the same age, the other sex and the young are necessarily left unmodified. When they occur late in life, but are transmitted to both sexes at the same age, the young alone are left unmodified. Variations, however, may occur at any period of life in one sex or in both, and be transmitted to both sexes at all ages, and then all the individuals of the species will be similarly modified. In the following chapters it will be seen that all these cases frequently occur under nature.
When changes happen later in life for one gender and are297 passed on to the same gender at the same age, the other gender and the young ones remain unchanged. When these changes happen later in life but are passed on to both genders at the same age, only the young ones stay unchanged. However, changes can happen at any point in life for one gender or both and can be passed on to both genders at any age, resulting in all individuals of the species being similarly altered. In the following chapters, you will see that all these scenarios frequently occur in nature.
Sexual selection can never act on any animal whilst young, before the age for reproduction has arrived. From the great eagerness of the male it has generally acted on this sex and not on the females. The males have thus become provided with weapons for fighting with their rivals, or with organs for discovering and securely holding the female, or for exciting and charming her. When the sexes differ in these respects, it is also, as we have seen, an extremely general law that the adult male differs more or less from the young male; and we may conclude from this fact that the successive variations, by which the adult male became modified, cannot have occurred much before the age for reproduction. How then are we to account for this general and remarkable coincidence between the period of variability and that of sexual selection,—principles which are quite independent of each other? I think we can see the cause: it is not that the males have never varied at an early age, but that such variations have commonly been lost, whilst those occurring at a later age have been preserved.
Sexual selection can't act on any animal while it's young, before it reaches reproductive age. Due to the strong drive of males, this process usually affects them more than the females. As a result, males have developed features for fighting rivals, attracting, and securely holding onto females. When there are differences between the sexes, it's a common pattern that adult males differ noticeably from younger males; this suggests that the changes which modified the adult male likely didn't happen until after they reached reproductive age. So, how do we explain this notable coincidence between the period of change and the time of sexual selection—two concepts that are fundamentally independent? I believe the reason is clear: males likely have varied at a younger age, but those early variations usually didn't persist, while later variations were more likely to be kept.
All animals produce more offspring than can survive to maturity; and we have every reason to believe that death falls heavily on the weak and inexperienced young. If then a certain proportion of the offspring298 were to vary at birth or soon afterwards, in some manner which at this age was of no service to them, the chance of the preservation of such variations would be small. We have good evidence under domestication how soon variations of all kinds are lost, if not selected. But variations which occurred at or near maturity, and which were of immediate service to either sex, would probably be preserved; as would similar variations occurring at an earlier period in any individuals which happened to survive. As this principle has an important bearing on sexual selection, it may be advisable to give an imaginary illustration. We will take a pair of animals, neither very fertile nor the reverse, and assume that after arriving at maturity they live on an average for five years, producing each year five young. They would thus produce 25 offspring; and it would not, I think, be an unfair estimate to assume that 18 or 20 out of the 25 would perish before maturity, whilst still young and inexperienced; the remaining seven or five sufficing to keep up the stock of mature individuals. If so, we can see that variations which occurred during youth, for instance in brightness, and which were not of the least service to the young, would run a good chance of being utterly lost. Whilst similar variations, which occurring at or near maturity in the comparatively few individuals surviving to this age, and which immediately gave an advantage to certain males, by rendering them more attractive to the females, would be likely to be preserved. No doubt some of the variations in brightness which occurred at an earlier age would by chance be preserved, and eventually give to the male the same advantage as those which appeared later; and this will account for the young males commonly partaking to a certain extent (as may be observed with many birds) of the bright colours of their299 adult male parents. If only a few of the successive variations in brightness were to occur at a late age, the adult male would be only a little brighter than the young male; and such cases are common.
All animals produce more offspring than can survive to adulthood, and it's clear that death often impacts the weaker and less experienced young more heavily. If a certain percentage of the offspring298 were to have variations at birth or shortly after, which weren’t helpful to them at that age, the likelihood of those variations being preserved would be low. We see clear evidence under domestication that variations of all types can quickly disappear if they aren’t selected. However, variations that happen around or after maturity, and that are beneficial to either sex, are likely to be preserved; similarly, variations occurring earlier in individuals that manage to survive would also be retained. Since this principle is significant to sexual selection, it’s useful to illustrate it with a hypothetical example. Let’s consider a pair of animals that are neither highly fertile nor completely infertile and assume they live an average of five years after reaching maturity, producing five young each year. That means they would have 25 offspring, and it’s reasonable to estimate that 18 or 20 out of those 25 would not survive to adulthood, dying while still young and inexperienced; the remaining seven or five would be enough to maintain the population of adults. From this, we can see that variations occurring during youth, for example in brightness, that were not beneficial to the young would likely be lost entirely. In contrast, variations that appear around or after maturity in the relatively few individuals that survive to this stage, and that provide an immediate advantage to certain males—by making them more appealing to females—would likely be preserved. It’s certain some of the variations in brightness that happened earlier would, by chance, also be preserved and eventually give males the same advantage as those that emerged later; this explains why young males often share some of the bright colors of their299 adult male parents. If only a few of the successive brightness variations occur late in life, the adult male will be only slightly brighter than the young male, and such cases are quite common.
In this illustration I have assumed that the young varied in a manner which was of no service to them; but many characters proper to the adult male would be actually injurious to the young,—as bright colours from making them conspicuous, or horns of large size from expending much vital force. Such variations in the young would promptly be eliminated through natural selection. With the adult and experienced males, on the other hand, the advantage thus derived in their rivalry with other males would often more than counterbalance exposure to some degree of danger. Thus we can understand how it is that variations which must originally have appeared rather late in life have alone or in chief part been preserved for the development of secondary sexual characters; and the remarkable coincidence between the periods of variability and of sexual selection is intelligible.
In this example, I’ve assumed that the young were varied in a way that didn’t benefit them; however, many traits typical of adult males could actually harm the young—like bright colors that make them stand out or large horns that require a lot of energy. These variations in the young would quickly be eliminated through natural selection. On the other hand, for adult and experienced males, the advantage gained in competing with other males often outweighs the exposure to some danger. This helps us understand why variations that likely appeared later in life have mainly been preserved for the development of secondary sexual traits; the striking alignment between the times of variability and sexual selection makes sense.
As variations which give to the male an advantage in lighting with other males, or in finding, securing, or charming the female, would be of no use to the female, they will not have been preserved in this sex either during youth or maturity. Consequently such variations would be extremely liable to be lost; and the female, as far as these characters are concerned, would be left unmodified, excepting in so far as she may have received them by transference from the male. No doubt if the female varied and transferred serviceable characters to her male offspring, these would be favoured through sexual selection; and then both sexes would thus far be modified in the same manner. But I shall hereafter have to recur to these more intricate contingencies.
As variations that give males an edge in competing with other males, or in attracting, securing, or charming females, wouldn't benefit the females, they wouldn't be maintained in females during their youth or adulthood. As a result, these variations would likely be lost, and females, regarding these traits, would remain unchanged, unless they happen to inherit them from males. If females did have variations and passed on useful traits to their male offspring, those traits would be favored through sexual selection; thus, both sexes would be modified in a similar way. However, I will need to revisit these more complex situations later.
300In the following chapters, I shall treat of the secondary sexual characters in animals of all classes, and shall endeavour in each case to apply the principles explained in the present chapter. The lowest classes will detain us for a very short time, but the higher animals, especially birds, must be treated at considerable length. It should be borne in mind that for reasons already assigned, I intend to give only a few illustrative instances of the innumerable structures by the aid of which the male finds the female, or, when found, holds her. On the other hand, all structures and instincts by which the male conquers other males, and by which he allures or excites the female, will be fully discussed, as these are in many ways the most interesting.
300In the upcoming chapters, I will discuss the secondary sexual traits in animals across all classes and will strive to apply the principles outlined in this chapter to each case. We will spend only a brief time on the lower classes, but we will explore the higher animals, particularly birds, in much greater detail. It's important to remember that, for reasons previously stated, I will provide only a few examples of the countless structures that help males find females or, once found, maintain their hold on them. Conversely, I will cover in depth all the structures and behaviors through which males compete with other males and attract or excite females, as these aspects are often the most fascinating.
Supplement on the proportional numbers of the two sexes in animals belonging to various classes.
As no one, as far as I can discover, has paid attention to the relative numbers of the two sexes throughout the animal kingdom, I will here give such materials as I have been able to collect, although they are extremely imperfect. They consist in only a few instances of actual enumeration, and the numbers are not very large. As the proportions are known with certainty on a large scale in the case of man alone, I will first give them, as a standard of comparison.
As far as I can tell, no one has really looked into the relative numbers of the two sexes across the animal kingdom, so I’ll share the information I've been able to gather, even though it’s not very complete. It includes only a few actual counts, and the numbers aren't very large. Since we know the proportions with certainty on a large scale only in the case of humans, I’ll start with that as a standard for comparison.
Man.—In England during ten years (from 1857 to 1866) 707,120 children on an annual average have been born alive, in the proportion of 104.5 males to 100 females. But in 1857 the male births throughout England were as 105.2, and in 1865 as 104.0 to 100. Looking to separate districts, in Buckinghamshire (where on an average 5000 children are annually born)301 the mean proportion of male to female births, during the whole period of the above ten years, was as 102.8 to 100; whilst in N. Wales (where the average annual births are 12,873) it was as high as 106.2 to 100. Taking a still smaller district, viz., Rutlandshire (where the annual births average only 739), in 1864 the male births were as 114.6, and in 1862 as 97.0 to 100; but even in this small district the average of the 7385 births during the whole ten years was as 104.5 to 100; that is in the same ratio as throughout England.367 The proportions are sometimes slightly disturbed by unknown causes; thus Prof. Faye states “that in some districts of Norway there has been during a decennial period a steady deficiency of boys, whilst in others the opposite condition has existed.” In France during forty-four years the male to the female births have been as 106.2 to 100; but during this period it has occurred five times in one department, and six times in another, that the female births have exceeded the males. In Russia the average proportion is as high as 108.9 to 100.368 It is a singular fact that with Jews the proportion of male births is decidedly larger than with Christians: thus in Prussia the proportion is as 113, in Breslau as 114, and in Livonia as 120 to 100; the Christian births in these countries being the same as usual, for instance, in Livonia as 104 to 100.369 It is a still more singular fact that in different nations, under different conditions and climates, in Naples, Prussia, Westphalia, France and England, the 302excess of male over female births is less when they are illegitimate than when legitimate.370
Man.—In England over a ten-year period (from 1857 to 1866), an average of 707,120 children were born alive each year, with a ratio of 104.5 males for every 100 females. In 1857, the male births across England were at 105.2, and in 1865 they dropped to 104.0 per 100 females. Looking at specific areas, in Buckinghamshire (where about 5,000 children are born each year)301, the average male to female birth ratio over those ten years was 102.8 to 100; meanwhile, in North Wales (with average annual births of 12,873), it was as high as 106.2 to 100. In an even smaller area, Rutlandshire (where the annual average is only 739 births), the male birth ratio in 1864 was 114.6 and in 1862 it was 97.0 to 100; yet even in this small area, the average for all 7,385 births over the ten years was 104.5 to 100, consistent with the national ratio in England.367 The ratios can sometimes be slightly affected by unknown factors; for instance, Prof. Faye notes that “in some areas of Norway, there has been a consistent shortage of boys over a ten-year period, while in other places the opposite has been true.” In France, over a span of forty-four years, the male to female birth ratio has been 106.2 to 100; however, during this time, there were five instances in one region and six in another where female births outnumbered male births. In Russia, the average ratio is as high as 108.9 to 100.368 Interestingly, among Jews, the male birth ratio is noticeably higher than among Christians: for instance, in Prussia, the ratio is 113, in Breslau it’s 114, and in Livonia, it reaches 120 to 100; the Christian birth ratios in these regions remain standard, such as 104 to 100 in Livonia.369 Even more intriguingly, in different countries, under varying conditions and climates—including Naples, Prussia, Westphalia, France, and England—the excess of male to female births is lower for illegitimate births compared to legitimate ones.370
In various parts of Europe, according to Prof. Faye and other authors, “a still greater preponderance of males would be met with, if death struck both sexes in equal proportion in the womb and during birth. But the fact is, that for every 100 still-born females, we have in several countries from 134.6 to 144.9 still-born males.” Moreover during the first four or five years of life more male children die than females; “for example in England, during the first year, 126 boys die for every 100 girls,—a proportion which in France is still more unfavourable.”371 As a consequence of this excess in the death-rate of male children, and of the exposure of men when adult to various dangers, and of their tendency to emigrate, the females in all old-settled countries, where statistical records have been kept,372 are found to preponderate considerably over the males.
In different parts of Europe, according to Prof. Faye and other authors, “there would be an even greater imbalance of males if death affected both sexes equally in the womb and during birth. The reality is that for every 100 stillborn females, several countries report between 134.6 and 144.9 stillborn males.” Additionally, during the first four or five years of life, more boys die than girls; “for instance, in England, during the first year, 126 boys die for every 100 girls—a ratio that is even more unfavorable in France.”371 As a result of this higher death rate among male children, along with adult men facing various dangers and their tendency to emigrate, in all long-established countries with recorded statistics,372 females are found to significantly outnumber males.
It has often been supposed that the relative ages of the parents determine the sex of the offspring; and Prof. Leuckart373 has advanced what he considers 303sufficient evidence, with respect to man and certain domesticated animals, to shew that this is one important factor in the result. So again the period of impregnation has been thought to be the efficient cause; but recent observations discountenance this belief. Again, with mankind polygamy has been supposed to lead to the birth of a greater proportion of female infants; but Dr. J. Campbell374 carefully attended to this subject in the harems of Siam, and he concludes that the proportion of male to female births is the same as from monogamous unions. Hardly any animal has been rendered so highly polygamous as our English race-horses, and we shall immediately see that their male and female offspring are almost exactly equal in number.
It has often been believed that the ages of parents affect the sex of their children; and Prof. Leuckart373 has provided what he thinks is 303enough evidence, regarding humans and some domesticated animals, to show that this is an important factor in the outcome. Additionally, the timing of conception has been considered a key cause; however, recent studies contradict this idea. Furthermore, it's been suggested that polygamy leads to more female births; but Dr. J. Campbell374 closely examined this issue in the harems of Siam, and found that the ratio of male to female births is the same as in monogamous relationships. Very few animals are as polygamous as our English racehorses, and we will soon see that their male and female offspring are nearly equal in number.
Horses.—Mr. Tegetmeier has been so kind as to tabulate for me from the ‘Racing Calendar’ the births of race-horses during a period of twenty-one years, viz. from 1846 to 1867; 1849 being omitted, as no returns were that year published. The total births have been 25,560,375 consisting of 12,763 males and 12,797 females, or in the proportion of 99.7 males to 100 females. As these numbers are tolerably large, and as they are drawn from all parts of England, during several years, we may with much confidence conclude that with the domestic horse, or at least with the race-horse, the two sexes are produced in almost equal numbers. The fluctuations in the proportions during successive years are closely like those which occur with mankind, when a small and thinly-populated area is considered: thus in 1856 the male horses were as 107.1, and in 1867 as only 92.6 to 100 females. In the tabulated returns the proportions vary in cycles, for the males exceeded the females during six successive years; and the females exceeded the males during two 304periods each of four years: this, however, may be accidental; at least I can detect nothing of the kind with man in the decennial table in the Registrar’s Report for 1866. I may add that certain, mares, and this holds good with certain cows and with women, tend to produce more of one sex than of the other; Mr. Wright of Yeldersley House, informs me that one of his Arab mares, though put seven times to different horses, produced seven fillies.
Horses.—Mr. Tegetmeier has kindly compiled for me a list from the ‘Racing Calendar’ detailing the births of racehorses over a period of twenty-one years, from 1846 to 1867; the year 1849 is excluded because no returns were published that year. The total number of births is 25,560,375 made up of 12,763 males and 12,797 females, which gives a ratio of 99.7 males to 100 females. Since these figures are quite significant and collected from all over England over several years, we can confidently conclude that, at least with domestic and racehorses, the two sexes are produced in nearly equal numbers. The fluctuations in the ratios from year to year are similar to those observed in human populations in small, sparsely populated areas: for example, in 1856, the ratio of male horses was 107.1, while in 1867 it dropped to only 92.6 males for every 100 females. The tabulated data shows cyclic variations in the proportions, with males outnumbering females for six consecutive years, and females exceeding males during two four-year periods. This might be coincidental; in fact, I don’t see anything similar in the decennial table in the Registrar’s Report for 1866. I should also mention that certain mares, much like some cows and women, tend to produce more of one sex than the other; Mr. Wright of Yeldersley House tells me that one of his Arab mares, despite being bred seven times to different stallions, produced seven fillies.
Dogs.—During a period of twelve years, from 1857 to 1868, the births of a large number of greyhounds, throughout England, have been sent to the ‘Field’ newspaper; and I am again indebted to Mr. Tegetmeier for carefully tabulating the results. The recorded, births have been 6878, consisting of 3605 males and 3273 females, that is, in the proportion of 110.1 males to 100 females. The greatest fluctuations occurred in 1864, when the proportion was as 95.3 males, and in 1867, as 116.3 males to 100 females. The above average proportion of 110.1 to 100 is probably nearly correct in the case of the greyhound, but whether it would hold with other domesticated breeds is in some degree doubtful. Mr. Cupples has enquired from several great breeders of dogs, and finds that all without exception believe that females are produced in excess; he suggests that this belief may have arisen from females being less valued and the consequent disappointment producing a stronger impression on the mind.
Dogs.—Over a span of twelve years, from 1857 to 1868, a significant number of greyhound births across England were reported to the ‘Field’ newspaper. I am once again grateful to Mr. Tegetmeier for meticulously compiling the results. The recorded births totaled 6,878, which includes 3,605 males and 3,273 females, representing a ratio of 110.1 males to 100 females. The most notable fluctuations were in 1864, with a ratio of 95.3 males, and in 1867, which saw a ratio of 116.3 males to 100 females. While the average ratio of 110.1 to 100 likely holds true for greyhounds, it's uncertain whether this would apply to other domesticated breeds. Mr. Cupples has asked several prominent dog breeders and found that all of them agree females are produced more frequently; he suggests this perception may stem from females being less valued, leading to greater disappointment that leaves a stronger impression.
Sheep.—The sexes of sheep are not ascertained by agriculturists until several months after birth, at the period when the males are castrated; so that the following returns do not give the proportions at birth. Moreover, I find that several great breeders in Scotland, who annually raise some thousand sheep, are firmly convinced that a larger proportion of males than of females die during the first one or two years; therefore the proportion of males would be somewhat greater at birth than at the age of castration. This is a remarkable coincidence with what occurs, as we have seen, with mankind, and both cases probably depend on some common cause. I have received returns from four gentlemen in England who have bred lowland sheep, chiefly Leicesters, during the last ten or sixteen years; they amount altogether to 8965 births, consisting of 4407 males and 4558 females; that is in the proportion of 96.7 males to 100 females. With respect to Cheviot and black-faced sheep bred in Scotland, I have received returns from six breeders, two of them on a large scale, chiefly for the years 1867-1869, but some of the returns extending back to 1862. The total number recorded amounts to 50,685, consisting of 25,071 males and 25,614 females, or in the proportion of 97.9 males to 100 females. If we take the English and Scotch returns together, the total number amounts 305to 59,650, consisting of 29,478 males and 30,172 females, or as 97·7 to 100. So that with sheep at the age of castration the females are certainly in excess of the males; but whether this would hold good at birth is doubtful, owing to the greater liability in the males to early death.376
Sheep.—Farmers can't determine the sex of sheep until a few months after they're born, when the males are castrated; therefore, the stats provided don't reflect the proportions at birth. Additionally, I have found that several major breeders in Scotland, who raise thousands of sheep each year, strongly believe that more males than females die in the first one or two years; so the ratio of males at birth is likely somewhat higher than at the time of castration. This is an interesting parallel to what happens with humans, and both situations probably arise from some common factor. I have received data from four men in England who have been breeding lowland sheep, mainly Leicesters, over the last ten to sixteen years; overall, they report 8,965 births, with 4,407 males and 4,558 females, giving a ratio of 96.7 males to every 100 females. Regarding Cheviot and black-faced sheep bred in Scotland, I've received reports from six breeders, two of whom operate on a large scale, mostly covering the years 1867-1869, with some data dating back to 1862. The total recorded number is 50,685, comprised of 25,071 males and 25,614 females, or a ratio of 97.9 males to 100 females. Combining the English and Scottish data, the overall total amounts to 59,650, consisting of 29,478 males and 30,172 females, or about 97.7 males for every 100 females. So at the time of castration, there are certainly more females than males; however, it's uncertain if this holds true at birth, due to the higher mortality rate among males.376
Of Cattle I have received returns from nine gentlemen of 982 births, too few to be trusted; these consisted of 477 bull-calves and 505 cow-calves; i.e. in the proportion of 94·4 males to 100 females. The Rev. W. D. Fox informs me that in 1867 out of 34 calves born on a farm in Derbyshire only one was a bull. Mr. Harrison Weir writes to me that he has enquired from several breeders of Pigs, and most of them estimate the male to the female births as about 7 to 6. This same gentleman has bred Rabbits for many years, and has noticed that a far greater number of bucks are produced than does.
Of Cattle, I've received data from nine gentlemen showing 982 births, which is too few to be reliable; this included 477 bull calves and 505 cow calves; i.e. a ratio of 94.4 males to 100 females. Rev. W. D. Fox tells me that in 1867, out of 34 calves born on a farm in Derbyshire, only one was a bull. Mr. Harrison Weir informs me that he has asked several pig breeders, and most estimate the male to female births as about 7 to 6. This same gentleman has been breeding Rabbits for many years and has observed that a significantly higher number of bucks are produced than does.
Of mammalia in a state of nature I have been able to learn very little. In regard to the common rat, I have received conflicting statements. Mr. R. Elliot of Laighwood, informs me that a rat-catcher assured him that he had always found the males in great excess, even with the young in the nest. In consequence of this, Mr. Elliot himself subsequently examined some hundred old ones, and found the statement true. Mr. F. Buckland has bred a large number of white rats, and he also believes that the males greatly exceed the females. In regard to Moles, it is said that “the males are much more numerous than the females;”377 and as the catching of these animals is a special occupation, the statement may perhaps be trusted. Sir A. Smith, in describing an antelope of S. Africa378 (Kobus ellipsiprymnus), remarks, that in the herds of this and other species, the males are few in number compared with the females: the natives believe that they are born in this proportion; others believe that the younger males are expelled from the herds, and Sir A. Smith says, that though he has himself never seen herds consisting of young males alone, others affirm that this does occur. It appears probable that the young males when expelled from the herd, would be likely to fell a prey to the many beasts of prey of the country.
I've learned very little about wild mammals. When it comes to the common rat, I've heard conflicting reports. Mr. R. Elliot from Laighwood told me that a rat-catcher claimed he consistently found more males than females, even with young ones in the nest. As a result, Mr. Elliot examined a few hundred adult rats himself and found this to be true. Mr. F. Buckland has bred a large number of white rats and also believes that there are many more males than females. Regarding moles, it is said that “the males are much more numerous than the females;” and since catching these animals is a specialized job, this claim may be reliable. Sir A. Smith, while describing an antelope from South Africa (Kobus ellipsiprymnus), notes that in herds of this and other species, males are much fewer than females. The locals think they are born in this ratio, while others believe that younger males are expelled from the herds. Sir A. Smith mentions that while he has never seen herds made up solely of young males, others claim that this does happen. It seems likely that the young males expelled from the herd would fall prey to the many predators in the area.
BIRDS.
With respect to the Fowl, I have received only one account, namely, that out of 1001 chickens of a highly-bred stock of Cochins, reared during eight years by Mr. Stretch, 487 proved males and 514 females: i.e. as 94.7 to 100. In regard to domestic pigeons there is good evidence that the males are produced in excess, or that their lives are longer; for these birds invariably pair, and single males, as Mr. Tegetmeier informs me, can always be purchased cheaper than females. Usually the two birds reared from the two eggs laid in the same nest consist of a male and female; but Mr. Harrison Weir, who has been so large a breeder, says that he has often bred two cocks from the same nest, and seldom two hens; moreover the hen is generally the weaker of the two, and more liable to perish.
Regarding the Fowl, I've only received one report, which states that out of 1001 chickens from a high-quality stock of Cochins raised over eight years by Mr. Stretch, there were 487 males and 514 females: i.e. a ratio of 94.7 to 100. Concerning domestic pigeons, there is strong evidence that males are produced more frequently or that they live longer; these birds always pair up, and single males, as Mr. Tegetmeier informs me, are usually cheaper to buy than females. Typically, the two birds raised from the two eggs laid in the same nest consist of one male and one female; however, Mr. Harrison Weir, a prolific breeder, reports that he has often produced two cocks from the same nest and rarely two hens; furthermore, the hen is usually the weaker of the two and more likely to die.
With respect to birds in a state of nature, Mr. Gould and others379 are convinced that the males are generally the more numerous; and as the young males of many species resemble the females, the latter would naturally appear to be the most numerous. Large numbers of pheasants are reared by Mr. Baker of Leadenhall from eggs laid by wild birds, and he informs Mr. Jenner Weir that four or five males to one female are generally produced. An experienced observer remarks380 that in Scandinavia the broods of the capercailzie and black-cock contain more males than females; and that with the Dal-ripa (a kind of ptarmigan) more males than females attend the leks or places of courtship; but this latter circumstance is accounted for by some observers by a greater number of hen birds being killed by vermin. From various facts given by White of Selbourne,381 it seems clear that the males of the partridge must be in considerable excess in the south of England; and I have been assured that this is the case in Scotland. Mr. Weir on enquiring from the dealers who receive at certain seasons large numbers of ruffs (Machetes pugnax) was told that the males are much the most numerous. This same naturalist has also enquired for me from the bird-catchers, who annually catch an astonishing number of various small species alive for the London market, and he was unhesitatingly answered by an old and trustworthy man, that with the chaffinch the males are in large excess; he thought as high as 2 males to 3071 female, or at least as high as 5 to 3.382 The males of the blackbird, he likewise maintained, were by far the most numerous, whether caught by traps or by netting at night. These statements may apparently be trusted, because the same man said that the sexes are about equal with the lark, the twite (Linaria montana), and goldfinch. On the other hand he is certain that with the common linnet, the females preponderate greatly, but unequally during different years; during some years he has found the females to the males as four to one. It should, however, be borne in mind, that the chief season for catching birds does not begin till September, so that with some species partial migrations may have begun, and the flocks at this period often consist of hens alone. Mr. Salvin paid particular attention to the sexes of the humming-birds in Central America, and he is convinced that with most of the species the males are in excess; thus one year he procured 204 specimens belonging to ten species, and these consisted of 166 males and of 38 females. With two other species the females were in excess: but the proportions apparently vary either during different seasons or in different localities; for on one occasion the males of Campylopterus hemileucurus were to the females as five to two, and on another occasion383 in exactly the reversed ratio. As bearing on this latter point, I may add, that Mr. Powys found in Corfu and Epirus the sexes of the chaffinch keeping apart, and “the females by far the most numerous;” whilst in Palestine Mr. Tristram found “the male flocks appearing greatly to exceed the female in number.”384 So again with the Quiscalus major, Mr. G. Taylor385 says, that in Florida there were “very few females in proportion to the males,” whilst in Honduras the proportion was the other way, the species there having the character of a polygamist.
With regard to birds in the wild, Mr. Gould and others379 believe that males are usually more numerous; and since young males of many species look like females, the females might naturally seem to be the majority. Many pheasants are raised by Mr. Baker of Leadenhall from eggs laid by wild birds, and he tells Mr. Jenner Weir that generally four or five males are produced for every female. An experienced observer notes380 that in Scandinavia the broods of the capercaillie and black grouse have more males than females; and that with the Dal-ripa (a type of ptarmigan), more males than females gather at the leks or courtship areas; however, some researchers believe this is because more female birds are killed by predators. According to various observations by White of Selbourne,381 it appears that male partridges are significantly more common in southern England, and I've been told this is also true in Scotland. Mr. Weir asked dealers who receive large numbers of ruffs (Machetes pugnax) at certain times of the year, and they indicated that males are much more plentiful. This same naturalist also asked bird-catchers, who catch a remarkable number of various small species alive for the London market each year, and he received a confident response from an experienced and reliable man, stating that with chaffinches, males are significantly more abundant, estimating it might be as much as 2 males to 3071 female, or at least as much as 5 to 3.382 He also claimed that blackbird males are far more numerous, whether caught using traps or netting at night. These claims can seemingly be trusted because the same man mentioned that the sexes are about equal with larks, twites (Linaria montana), and goldfinches. However, he is sure that with common linnets, females greatly outnumber males, but this varies yearly; in some years he has seen a ratio of four females to one male. It should be noted, though, that the primary season for catching birds doesn't start until September, so some species may have begun partial migrations, and flocks at that time often consist solely of hens. Mr. Salvin paid close attention to the sexes of hummingbirds in Central America and believes that in most species, males are in excess; for instance, one year he collected 204 specimens from ten species, including 166 males and 38 females. For two other species, females were in excess: but the proportions seem to change either during different seasons or in different regions; for one species, the males of Campylopterus hemileucurus were five times greater than females, and at another time383 the ratio was reversed. To add to this point, Mr. Powys observed in Corfu and Epirus that the sexes of the chaffinch were separated, with “the females clearly the most numerous;” while in Palestine, Mr. Tristram observed “the male flocks greatly outnumbering the females.”384 Likewise, concerning Quiscalus major, Mr. G. Taylor385 stated that in Florida there were “very few females compared to males,” whereas in Honduras the ratio was reversed, with the species exhibiting polygamous behavior.
FISH.
With Fish the proportional numbers of the sexes can be ascertained only by catching them in the adult or nearly adult state; and there 308are many difficulties in arriving at any just conclusion.386 Infertile females might readily be mistaken for males, as Dr. Günther has remarked to me in regard to trout. With some species the males are believed to die soon after fertilising the ova. With many species the males are of much smaller size than the females, so that a large number of males would escape from the same net by which the females were caught. M. Carbonnier,387 who has especially attended to the natural history of the pike (Esox lucius) states that many males, owing to their small size, are devoured by the larger females; and he believes that the males of almost all fish are exposed from the same cause to greater danger than the females. Nevertheless in the few cases in which the proportional numbers have been actually observed, the males appear to be largely in excess. Thus Mr. R. Buist, the superintendent of the Stormontfield experiments, says that in 1865, out of 70 salmon first landed for the purpose of obtaining the ova, upwards of 60 were males. In 1867 he again “calls attention to the vast disproportion of the males to the females. We had at the outset at least ten males to one female.” Afterwards sufficient females for obtaining ova were procured. He adds, “from the great proportion of the males, they are constantly fighting and tearing each other on the spawning-beds.”388 This disproportion, no doubt, can be accounted for in part, but whether wholly is very doubtful, by the males ascending the rivers before the females. Mr. F. Buckland remarks in regard to trout, that “it is a curious fact that the males preponderate very largely in number over the females. It invariably happens that when the first rush of fish is made to the net, there will be at least seven or eight males to one female found captive. I cannot quite account for this; either the males are more numerous than the females, or the latter seek safety by concealment rather than flight.” He then adds, that by carefully searching the banks, sufficient females for obtaining ova can be found.389 Mr. H. Lee informs me that out of 212 trout, taken for this purpose in Lord Portsmouth’s park, 150 were males and 62 females.
With fish, the proportions of males and females can only be determined by catching them when they are adults or nearly adults; however, there are many challenges in reaching any accurate conclusions. Infertile females might easily be mistaken for males, as Dr. Günther noted to me about trout. For some species, males are believed to die shortly after they fertilize the eggs. In many species, males are significantly smaller than females, which means a lot of males could escape the same net that catches the females. M. Carbonnier, who has specifically studied the natural history of the pike (Esox lucius), states that many males are eaten by the larger females due to their smaller size, and he believes that nearly all male fish face greater danger than females because of this. Nevertheless, in the few situations where the actual ratios have been observed, it seems that there are significantly more males. For example, Mr. R. Buist, the supervisor of the Stormontfield experiments, notes that in 1865, out of 70 salmon caught to obtain eggs, over 60 were males. In 1867, he again "points out the vast imbalance of males to females. At the start, we had at least ten males for every female." Later, enough females were collected for obtaining eggs. He adds, "due to the high number of males, they are constantly fighting and tearing each other apart in the spawning areas." This imbalance can certainly be explained in part, but it is very questionable whether it is the whole reason, by males moving upstream before females. Mr. F. Buckland comments regarding trout that "it's a strange fact that males greatly outnumber females. It always happens that when the first rush of fish is caught in the net, there will be at least seven or eight males for every female captured. I can't quite figure this out; either males are more numerous than females, or females prefer to hide rather than flee." He then adds that by searching carefully along the banks, enough females can be found for obtaining eggs. Mr. H. Lee tells me that out of 212 trout caught for this purpose in Lord Portsmouth’s park, 150 were males and 62 were females.
With the Cyprinidæ the males likewise seem to be in excess; but several members of this Family, viz., the carp, tench, bream and minnow, appear regularly to follow the practice, rare in the 309animal kingdom, of polyandry; for the female whilst spawning is always attended by two males, one on each side, and in the case of the bream by three or four males. This fact is so well known, that it is always recommended to stock a pond with two male tenches to one female, or at least with three males to two females. With the minnow, an excellent observer states, that on the spawning-beds the males are ten times as numerous as the females; when a female comes amongst the males, “she is immediately pressed closely by a male on each side; and when they have been in that situation for a time, are superseded by other two males.”390
With the Cyprinidae, the males also seem to outnumber the females; however, several members of this family, like carp, tench, bream, and minnows, regularly practice polyandry—a behavior that’s rare in the animal kingdom. When spawning, a female is always accompanied by two males, one on each side, and in the case of bream, she may have three or four males with her. This is so well recognized that it’s recommended to stock a pond with two male tenches for every female, or at least with three males for every two females. An expert on minnows notes that during spawning seasons, males are ten times more numerous than females. When a female swims into a group of males, “she is immediately closely followed by a male on each side; and after a while, they are replaced by other two males."390
INSECTS.
In this class, the Lepidoptera alone afford the means of judging of the proportional numbers of the sexes; for they have been collected with special care by many good observers, and have been largely bred from the egg or caterpillar state. I had hoped that some breeders of silk-moths might have kept an exact record, but after writing to France and Italy, and consulting various treatises, I cannot find that this has ever been done. The general opinion appears to be that the sexes are nearly equal, but in Italy as I hear from Professor Canestrini, many breeders are convinced that the females are produced in excess. The same naturalist, however, informs me, that in the two yearly broods of the Ailanthus silk-moth (Bombyx cynthia), the males greatly preponderate in the first, whilst in the second the two sexes are nearly equal, or the females rather in excess.
In this class, only the Lepidoptera provide a way to judge the relative numbers of the sexes; they have been carefully collected by many good observers and have also been largely bred from the egg or caterpillar stage. I had hoped that some silk-moth breeders might have kept detailed records, but after reaching out to France and Italy and consulting various sources, I can’t find any evidence that this has ever been done. The general consensus seems to be that the sexes are almost equal, but in Italy, as I heard from Professor Canestrini, many breeders believe that females are produced more frequently. However, the same naturalist tells me that in the two annual broods of the Ailanthus silk-moth (Bombyx cynthia), males are much more common in the first brood, while in the second, the two sexes are almost equal, or the females are somewhat in excess.
In regard to Butterflies in a state of nature, several observers have been much struck by the apparently enormous preponderance of the males.391 Thus Mr. Bates,392 in speaking of the species, no less than about a hundred in number, which inhabit the Upper Amazons, says that the males are much more numerous than the females, even in the proportion of a hundred to one. In North America, Edwards, who had great experience, estimates in the genus Papilio the males to the females as four to one; and Mr. 310Walsh, who informed me of this statement, says that with P. turnus this is certainly the case. In South Africa, Mr. R. Trimen found the males in excess in 19 species;393 and in one of these, which swarms in open places, he estimated the number of males as fifty to one female. With another species, in which the males are numerous in certain localities, he collected during seven years only five females. In the island of Bourbon, M. Maillard states that the males of one species of Papilio are twenty times as numerous as the females.394 Mr. Trimen informs me that as far as he has himself seen, or heard from others, it is rare for the females of any butterfly to exceed in number the males; but this is perhaps the case with three South African species. Mr. Wallace395 states that the females of Ornithoptera crœsus, in the Malay archipelago, are more common and more easily caught than the males; but this is a rare butterfly. I may here add, that in Hyperythra, a genus of moths, Guenée says, that from four to five females are sent in collections from India for one male.
In terms of butterflies in the wild, many observers have been really surprised by the huge number of males.391 For instance, Mr. Bates,392 discussing the species, which number around a hundred in the Upper Amazonas, notes that males greatly outnumber females, with a ratio of even a hundred to one. In North America, Edwards, who has a lot of experience, estimates that in the Papilio genus, the ratio of males to females is four to one; and Mr. 310Walsh, who shared this with me, confirms that this is definitely the case with P. turnus. In South Africa, Mr. R. Trimen found that males outnumbered females in 19 species;393 and in one species, which is abundant in open areas, he estimated there were fifty males for every female. In another species, where males are plentiful in certain spots, he collected only five females over seven years. On the island of Bourbon, M. Maillard states that males of one Papilio species are twenty times more numerous than females.394 Mr. Trimen also tells me that, as far as he has seen or heard from others, it's rare for females of any butterfly to outnumber males; although this might be true for three South African species. Mr. Wallace395 mentions that females of Ornithoptera crœsus in the Malay archipelago are more common and easier to catch than males, but this butterfly is quite rare. I can also add that in Hyperythra, a moth genus, Guenée says that about four to five females are sent in collections from India for every male.
When this subject of the proportional numbers of the sexes of insects was brought before the Entomological Society,396 it was generally admitted that the males of most Lepidoptera, in the adult or imago state, are caught in greater numbers than the females; but this fact was attributed by various observers to the more retiring habits of the females, and to the males emerging earlier from the cocoon. This latter circumstance is well known to occur with most Lepidoptera, as well as with other insects. So that, as M. Personnat remarks, the males of the domesticated Bombyx yamamai, are lost at the beginning of the season, and the females at the end, from the want of mates.397 I cannot however persuade myself that these causes suffice to explain the great excess of males in the cases, above given, of butterflies which are extremely common in their native countries. Mr. Stainton, who has paid such close attention during many years to the smaller moths, informs me that when he collected them in the imago state, he thought that the males were ten times as numerous as the females, but that since he has reared them on a large scale from the caterpillar state, he is convinced that the females are the most 311numerous. Several entomologists concur in this view. Mr. Doubleday, however, and some others, take an opposite view, and are convinced that they have reared from the egg and caterpillar states a larger proportion of males than of females.
When the topic of the proportional numbers of male and female insects was presented to the Entomological Society,396 it was generally accepted that male Lepidoptera, in their adult or imago stage, are caught in larger numbers than females. However, various observers attributed this to the more reserved behavior of females and the fact that males emerge from their cocoons earlier. This is well known to happen with most Lepidoptera, as well as other insects. Thus, as M. Personnat points out, the males of the domesticated Bombyx yamamai are lost at the beginning of the season, while females are lost at the end due to the lack of mates.397 However, I can’t convince myself that these reasons fully explain the significant excess of males in the cases of butterflies that are very common in their native regions. Mr. Stainton, who has closely studied smaller moths for many years, tells me that when he collected them in the imago state, he believed that males were ten times more numerous than females. But since he has raised them in large numbers from the caterpillar stage, he is convinced that females are actually the more numerous ones. Several entomologists agree with this perspective. Mr. Doubleday and some others, however, hold a different opinion and believe they have raised a larger proportion of males than females from the egg and caterpillar stages.
Besides the more active habits of the males, their earlier emergence from the cocoon, and their frequenting in some cases more open stations, other causes may be assigned for an apparent or real difference in the proportional numbers of the sexes of Lepidoptera, when captured in the imago state, and when reared from the egg or caterpillar state. It is believed by many breeders in Italy, as I hear from Professor Canestrini, that the female caterpillar of the silk-moth suffers more from the recent disease than the male; and Dr. Staudinger informs me that in rearing Lepidoptera more females die in the cocoon than males. With many species the female caterpillar is larger than the male, and a collector would naturally choose the finest specimens, and thus unintentionally collect a larger number of females. Three collectors have told me that this was their practice; but Dr. Wallace is sure that most collectors take all the specimens which they can find of the rarer kinds, which alone are worth the trouble of rearing. Birds when surrounded by caterpillars would probably devour the largest; and Professor Canestrini informs me that in Italy some breeders believe, though on insufficient evidence, that in the first brood of the Ailanthus silk-moth, the wasps destroy a larger number of the female than of the male caterpillars. Dr. Wallace further remarks that female caterpillars, from being larger than the males, require more time for their development and consume more food and moisture; and thus they would be exposed during a longer time to danger from ichneumons, birds, &c., and in times of scarcity would perish in greater numbers. Hence it appears quite possible that, in a state of nature, fewer female Lepidoptera may reach maturity than males; and for our special object we are concerned with the numbers at maturity, when the sexes are ready to propagate their kind.
In addition to the more active behaviors of males, their earlier emergence from the cocoon, and their tendency to inhabit more open areas in some cases, there are other factors that might explain the noticeable or actual difference in the ratio of male to female Lepidoptera when they are captured in their adult form versus when they are raised from the egg or caterpillar stage. Many breeders in Italy believe, as I learned from Professor Canestrini, that female silk-moth caterpillars are more affected by a recent disease than the males; Dr. Staudinger has informed me that more female Lepidoptera die in the cocoon than males when reared. With many species, female caterpillars are larger than males, and a collector would naturally select the best specimens, potentially resulting in a higher number of females being collected. Three collectors have mentioned this practice; however, Dr. Wallace is confident that most collectors take all the rare specimens they can find, which are the ones worth the effort of raising. Birds, when surrounded by caterpillars, would likely eat the largest ones; and Professor Canestrini has told me that in Italy, some breeders suspect—though without strong evidence—that in the first brood of Ailanthus silk-moths, wasps eliminate a higher number of female caterpillars compared to males. Dr. Wallace also points out that female caterpillars, being larger than the males, require more time to develop and consume more food and moisture; thus, they would be exposed to danger from ichneumons, birds, etc., for a longer period of time, and during times of scarcity, they would likely perish in greater numbers. Therefore, it seems quite possible that, in the wild, fewer female Lepidoptera reach maturity compared to males; and for our specific purpose, we are interested in the numbers that reach maturity when the sexes are ready to reproduce.
The manner in which the males of certain moths congregate in extraordinary numbers round a single female, apparently indicates a great excess of males, though this fact may perhaps be accounted for by the earlier emergence of the males from their cocoons. Mr. Stainton informs me that from twelve to twenty males may often be seen congregated round a female Elachista rufocinerea. It is well known that if a virgin Lasiocampa quercus or Saturnia carpini be exposed in a cage, vast numbers of males collect round her, and if confined in a room will even come down the chimney to her. 312Mr. Doubleday believes that he has seen from fifty to a hundred males of both these species attracted in the course of a single day by a female under confinement. Mr. Trimen exposed in the Isle of Wight a box in which a female of the Lasiocampa had been confined on the previous day, and five males soon endeavoured to gain admittance. M. Verreaux, in Australia, having placed the female of a small Bombyx in a box in his pocket, was followed by a crowd of males, so that about 200 entered the house with him.398
The way male moths gather in huge numbers around a single female suggests that there are way more males than females, though this might be explained by the males emerging from their cocoons earlier. Mr. Stainton tells me that you can often see between twelve to twenty males clustered around a female Elachista rufocinerea. It's well-known that if a virgin Lasiocampa quercus or Saturnia carpini is put in a cage, lots of males will swarm around her, and if they're kept in a room, they'll even come down the chimney to reach her. 312 Mr. Doubleday believes he has seen between fifty to a hundred males of both species attracted to a confined female in just one day. Mr. Trimen set up a box on the Isle of Wight that had housed a female Lasiocampa the day before, and five males quickly tried to get in. M. Verreaux, in Australia, placed a female small Bombyx in a box in his pocket and was followed by a swarm of males, so about 200 came into the house with him.398
Mr. Doubleday has called my attention to Dr. Staudinger’s399 list of Lepidoptera, which gives the prices of the males and females of 300 species or well-marked varieties of (Rhopalocera) butterflies. The prices for both sexes of the very common species are of course the same; but with 114 of the rarer species they differ; the males being in all cases, excepting one, the cheapest. On an average of the prices of the 113 species, the price of the male to that of the female is as 100 to 149; and this apparently indicates that inversely the males exceed the females in number in the same proportion. About 2000 species or varieties of moths (Heterocera) are catalogued, those with wingless females being here excluded on account of the difference in habits of the two sexes: of these 2000 species, 141 differ in price according to sex, the males of 130 being cheaper, and the males of only 11 being dearer than the females. The average price of the males of the 130 species, to that of the females, is as 100 to 143. With respect to the butterflies in this priced list, Mr. Doubleday thinks (and no man in England has had more experience), that there is nothing in the habits of the species which can account for the difference in the prices of the two sexes, and that it can be accounted for only by an excess in the numbers of the males. But I am bound to add that Dr. Staudinger himself, as he informs me, is of a different opinion. He thinks that the less active habits of the females and the earlier emergence of the males will account for his collectors securing a larger number of males than of females, and consequently for the lower prices of the former With respect to specimens reared from the caterpillar-state, Dr. Staudinger believes, as previously stated, that a greater number of females than of males die under confinement in the cocoons. He adds that with certain species one sex seems to preponderate over the other during certain years.
Mr. Doubleday pointed out Dr. Staudinger’s399 list of butterflies, which shows the prices of male and female specimens for 300 species or well-marked varieties of (Rhopalocera) butterflies. The prices for both sexes of the very common species are the same, but for 114 of the rarer species, they differ, with males being cheaper in all cases except one. On average, the prices of the 113 species show that the price of males compared to females is as 100 to 149, which seemingly indicates that males outnumber females in the same proportion. About 2000 species or varieties of moths (Heterocera) are cataloged, excluding those with wingless females due to the differences in the behaviors of the two sexes. Of these 2000 species, 141 have price differences based on sex, with the males of 130 being cheaper and the males of only 11 being more expensive than the females. On average, the price of males for the 130 species is as 100 to 143 when compared to the females. Regarding the butterflies in this priced list, Mr. Doubleday believes (and no one in England has more experience) that there’s nothing about the species’ habits that can explain the price difference between the sexes, and it can only be attributed to a greater number of males. However, I must add that Dr. Staudinger, as he has told me, holds a different view. He believes that the less active habits of females and the earlier emergence of males account for collectors obtaining more males than females, which leads to the lower prices for males. Concerning specimens raised from caterpillars, Dr. Staudinger believes, as stated earlier, that more females than males die in confinement within the cocoons. He also notes that for certain species, one sex seems to outnumber the other in some years.
Of direct observations on the sexes of Lepidoptera, reared either 313from eggs or caterpillars, I have received only the few following cases:—
Of the direct observations on the sexes of butterflies and moths, raised either 313from eggs or caterpillars, I have only received the following few cases:—
Males. | Females. | |
The Rev. J. Hellins400 of Exeter reared, during 1868, imagos of 73 species, which consisted of | 153 | 137 |
Mr. Albert Jones of Eltham reared, during 1868, imagos of 9 species, which, consisted of | 159 | 126 |
During 1869 he reared imagos from 4 species, consisting of | 114 | 112 |
Mr. Buckler of Emsworth, Hants, during 1869, reared imagos from 74 species, consisting of | 180 | 169 |
Dr. Wallace of Colchester reared from one brood of Bombyx cynthia | 52 | 48 |
Dr. Wallace raised, from cocoons of Bombyx Pernyi sent from China, during 1869 | 224 | 123 |
Dr. Wallace raised, during 1868 and 1869, from two lots of cocoons of Bombyx Yamamai | 52 | 46 |
—— | —— | |
Total | 934 | 761 |
So that in these eight lots of cocoons and eggs, males were produced in excess. Taken together the proportion of males is as 122.7 to 100 females. But the numbers are hardly large enough to be trustworthy.
So, in these eight batches of cocoons and eggs, there were more males than females. Overall, the ratio of males is 122.7 to 100 females. However, the numbers aren't really large enough to be reliable.
On the whole, from the above various sources of evidence, all pointing to the same direction, I infer that with most species of Lepidoptera, the males in the imago state generally exceed the females in number, whatever the proportions may be at their first emergence from the egg.
On the whole, based on the various sources of evidence mentioned above, which all point in the same direction, I conclude that in most species of Lepidoptera, the adult males usually outnumber the females, regardless of the ratios at their initial emergence from the egg.
With reference to the other Orders of insects, I have been able to collect very little reliable information. With the stag-beetle (Lucanus cervus) “the males appear to be much more numerous than the females;” but when, as Cornelius remarked during 1867, an unusual number of these beetles appeared in one part of Germany, the females appeared to exceed the males as six so one. With one of the Elateridæ, the males are said to be much more numerous than the females, and “two or three are often found united with one female;”401 so that here polyandry seems to prevail. 314 With Siagonium (Staphylinidæ), in which the males are furnished with horns, “the females are far more numerous than the opposite sex.” Mr. Janson stated at the Entomological Society that the females of the bark-feeding Tomicus villosus are so common as to be a plague, whilst the males are so rare as to be hardly known. In other Orders, from unknown causes, but apparently in some instances owing to parthenogenesis, the males of certain species have never been discovered or are excessively rare, as with several of the Cynipidæ.402 In all the gall-making Cynipidæ known to Mr. Walsh, the females are four or five times as numerous as the males; and so it is, as he informs me, with the gall-making Cecidomyiiæ (Diptera). With some common species of Saw-flies (Tenthredinæ) Mr. F. Smith has reared hundreds of specimens from larvæ of all sizes, but has never reared a single male: on the other hand Curtis says,403 that with certain species (Athalia), bred by him, the males to the females were as six to one; whilst exactly the reverse occurred with the mature insects of the same species caught in the fields. With the Neuroptera, Mr. Walsh states that in many, but by no means in all, the species of the Odonatous groups (Ephemerina), there is a great overplus of males: in the genus Hetærina, also, the males are generally at least four times as numerous as the females. In certain species in the genus Gomphus the males are equally numerous, whilst in two other species, the females are twice or thrice as numerous as the males. In some European species of Psocus thousands of females may be collected without a single male, whilst with other species of the same genus both sexes are common.404 In England, Mr. MacLachlan has captured hundreds of the female Apatania muliebris, but has never seen the male; and of Boreus hyemalis only four or five males have been here seen.405 With most of these species (excepting, as I have heard, with the Tenthredinæ) there is no reason to suppose that the females are subject to parthenogenesis; and thus we see how ignorant we are on the causes of the apparent discrepancy in the proportional numbers of the two sexes.
With regard to other groups of insects, I've been able to gather very little reliable information. In the case of the stag beetle (Lucanus cervus), “the males seem to be much more numerous than the females;” however, as Cornelius noted in 1867, when an unusual number of these beetles appeared in one area of Germany, the females outnumbered the males at a ratio of six to one. For one of the Elateridae, it’s said that the males are significantly more common than the females, and “two or three are often found together with one female;”401 suggesting that polyandry is common in this instance. 314 In Siagonium (Staphylinidae), where males have horns, “the females greatly outnumber the males.” Mr. Janson mentioned at the Entomological Society that the females of the bark-feeding Tomicus villosus are so plentiful that they have become a nuisance, while the males are so rare that they're hardly ever seen. In other orders, for unknown reasons — but seemingly in some cases due to parthenogenesis — the males of certain species have never been found or are extremely rare, such as with several of the Cynipidae.402 Among all the gall-making Cynipidae known to Mr. Walsh, the females are four or five times more numerous than the males; and the same applies, as he informs me, to the gall-making Cecidomyiiæ (Diptera). With some common species of sawflies (Tenthredinæ), Mr. F. Smith has raised hundreds of specimens from larvae of all sizes, yet he has never reared a single male: on the other hand, Curtis states,403 that for certain species (Athalia) he bred, the ratio of males to females was six to one; whereas the opposite occurred with the mature insects of the same species captured in the fields. Regarding the Neuroptera, Mr. Walsh notes that in many, but not all, species of the Odonatous groups (Ephemerina), there is a significant excess of males: in the genus Hetærina, for example, males are generally at least four times more numerous than females. In some species of the genus Gomphus, the males are equally common, while in two other species, the females outnumber the males by two or three times. For some European species of Psocus, thousands of females can be collected without encountering a single male, although in other species of the same genus, both sexes are readily found.404 In England, Mr. MacLachlan has captured hundreds of the female Apatania muliebris, but has never seen a male; and only four or five males of Boreus hyemalis have been observed here.405 For most of these species (except, as I’ve heard, with the Tenthredinæ), there’s no reason to believe that the females are undergoing parthenogenesis; thus, we see how little we understand the reasons behind the apparent imbalance in the proportions of the two sexes.
In the other Classes of the Articulata I have been able to collect still less information. With Spiders, Mr. Blackwall, who has carefully attended to this class during many years, writes to me that the males from their more erratic habits are more commonly seen, 315and therefore appear to be the more numerous. This is actually the case with a few species; but he mentions several species in six genera, in which the females appear to be much more numerous than the males.406 The small size of the males in comparison with the females, which is sometimes carried to an extreme degree, and their widely different appearance, may account in some instances for their rarity in collections.407
In the other groups of the Articulata, I’ve been able to gather even less information. Regarding spiders, Mr. Blackwall, who has studied this class meticulously for many years, tells me that the males, due to their more erratic behavior, are seen more often, which makes them seem more numerous. This is true for a few species; however, he points out several species in six genera where the females actually outnumber the males significantly. The small size of the males compared to the females, which can be extreme in some cases, along with their very different appearance, might explain why they are less common in collections.
Some of the lower Crustaceans are able to propagate their kind asexually, and this will account for the extreme rarity of the males. With some other forms (as with Tanais and Cypris) there is reason to believe, as Fritz Müller informs me, that the male is much shorter-lived than the female, which, supposing the two sexes to be at first equal in number, would explain the scarcity of the males. On the other hand this same naturalist has invariably taken, on the shores of Brazil, far more males than females of the Diastylidæ and of Cypridina; thus with a species in the latter genus, 63 specimens caught the same day, included 57 males; but he suggests that this preponderance may be due to some unknown difference in the habits of the two sexes. With one of the higher Brazilian crabs, namely a Gelasimus, Fritz Müller found the males to be more numerous than the females. The reverse seems to be the case, according to the large experience of Mr. C. Spence Bate, with six common British crabs, the names of which he has given me.
Some lower Crustaceans can reproduce without mating, which explains why males are so rare. In other species (like Tanais and Cypris), as Fritz Müller told me, the males seem to have a much shorter lifespan than the females. If both sexes start out equal in number, this would account for the lack of males. However, this same naturalist consistently found many more males than females along the shores of Brazil, particularly among the Diastylidæ and Cypridina. In one species of the latter genus, for example, he caught 63 specimens in one day, of which 57 were males. He speculates that this imbalance could be due to some unknown difference in behavior between the sexes. In the case of a higher Brazilian crab, specifically a Gelasimus, Fritz Müller observed that males were more numerous than females. Conversely, according to Mr. C. Spence Bate's extensive experience with six common British crabs, the situation appears to be the opposite.
On the Power of Natural Selection to regulate the proportional Numbers of the Sexes, and General Fertility.—In some peculiar cases, an excess in the number of one sex over the other might be a great advantage to a species, as with the sterile females of social insects, or with those animals in which more than one male is requisite to fertilise the female, as with certain cirripedes and perhaps certain fishes. An inequality between the sexes in these cases might have been acquired through natural selection, but from their rarity they need not here be further considered. In all ordinary 316cases an inequality would be no advantage or disadvantage to certain individuals more than to others; and therefore it could hardly have resulted from natural selection. We must attribute the inequality to the direct action of those unknown conditions, which with mankind lead to the males being born in a somewhat larger excess in certain countries than in others, or which cause the proportion between the sexes to differ slightly in legitimate and illegitimate births.
On the Power of Natural Selection to regulate the proportional Numbers of the Sexes, and General Fertility.—In some specific cases, having more of one sex than the other could be beneficial for a species, like with the sterile females of social insects, or with animals where multiple males are needed to fertilize a female, such as certain barnacles and possibly some fish. This imbalance between the sexes might have evolved through natural selection, but because it’s uncommon, we won’t explore it further here. In most typical 316 cases, having an unequal number wouldn’t advantage or disadvantage certain individuals over others; therefore, it’s unlikely to have come from natural selection. We should attribute this imbalance to the direct influence of those unknown factors, which, among humans, lead to a slightly higher number of males being born in some countries than in others, or which cause the ratio of sexes to vary slightly between legitimate and illegitimate births.
Let us now take the case of a species producing from the unknown causes just alluded to, an excess of one sex—we will say of males—these being superfluous and useless, or nearly useless. Could the sexes be equalised through natural selection? We may feel sure, from all characters being variable, that certain pairs would produce a somewhat less excess of males over females than other pairs. The former, supposing the actual number of the offspring to remain constant, would necessarily produce more females, and would therefore be more productive. On the doctrine of chances a greater number of the offspring of the more productive pairs would survive; and these would inherit a tendency to procreate fewer males and more females. Thus a tendency towards the equalisation of the sexes would be brought about. But our supposed species would by this process be rendered, as just remarked, more productive; and this would in many cases be far from an advantage; for whenever the limit to the numbers which exist, depends, not on destruction by enemies, but on the amount of food, increased fertility will lead to severer competition and to most of the survivors being badly fed. In this case, if the sexes were equalised by an increase in the number of the females, a simultaneous decrease in the total number of the offspring would be beneficial, or even necessary, for the existence of the species; and317 this, I believe, could be effected through natural selection in the manner hereafter to be described. The same train of reasoning is applicable in the above, as well as in the following case, if we assume that females instead of males are produced in excess, for such females from not uniting with males would be superfluous and useless. So it would be with polygamous species, if we assume the excess of females to be inordinately great.
Let’s look at a case where a species produces an excess of one sex—let’s say males—due to the unknown causes mentioned earlier. These excess males would be superfluous and mostly useless. Could natural selection balance the sexes? We can be confident, since all traits are variable, that certain pairs would produce slightly fewer males compared to females than other pairs. Those pairs, assuming the overall number of offspring remains constant, would naturally produce more females and be more productive. According to chance, more offspring from these productive pairs would survive, and they would pass on a tendency to have fewer males and more females. This would lead to a shift towards equalizing the sexes. However, this hypothetical species would become, as mentioned, more productive through this process, which might not always be an advantage. When the limit to the population size is not determined by predators, but by the availability of food, increased fertility leads to greater competition, resulting in most survivors being poorly nourished. In this case, if the sexes were balanced by an increase in females, a simultaneous reduction in the total number of offspring would actually be beneficial or even necessary for the species’ survival; and317 this, I believe, could be achieved through natural selection as described later. The same logic applies if we assume an excess of females is produced instead of males, as these females would also be superfluous and useless if they don’t mate with males. This would also hold true for polygamous species, assuming the excess of females is excessively high.
An excess of either sex, we will again say of the males, could, however, apparently be eliminated through natural selection in another and indirect manner, namely by an actual diminution of the males, without any increase of the females, and consequently without any increase in the productiveness of the species. From the variability of all characters, we may feel assured that some pairs, inhabiting any locality, would produce a rather smaller excess of superfluous males, but an equal number of productive females. When the offspring from the more and the less male-productive parents were all mingled together, none would have any direct advantage over the others; but those that produced few superfluous males would have one great indirect advantage, namely that their ova or embryos would probably be larger and finer, or their young better nurtured in the womb and afterwards. We see this principle illustrated with plants; as those which bear a vast number of seed produce small ones; whilst those which bear comparatively few seeds, often produce large ones well-stocked with nutriment for the use of the seedlings.408 Hence the offspring of the parents which 318had wasted least force in producing superfluous males would be the most likely to survive, and would inherit the same tendency not to produce superfluous males, whilst retaining their full fertility in the production of females. So it would be with the converse case of the female sex. Any slight excess, however, of either sex could hardly be checked in so indirect a manner. Nor indeed has a considerable inequality between the sexes been always prevented, as we have seen in some of the cases given in the previous discussion. In these cases the unknown causes which determine the sex of the embryo, and which under certain conditions lead to the production of one sex in excess over the other, have not been mastered by the survival of those varieties which were subjected to the least waste of organised matter and force by the production of superfluous individuals of either sex. Nevertheless we may conclude that natural selection will always tend, though sometimes inefficiently, to equalise the relative numbers of the two sexes.
An excess of either sex, particularly males, could, it seems, be reduced through natural selection in a different, indirect way—specifically, by actually decreasing the number of males without increasing the number of females, and therefore without boosting the overall productivity of the species. Given the variability of all traits, we can be confident that some pairs living in any area would produce a somewhat smaller surplus of unnecessary males, while still having an equal number of productive females. When offspring from both more and less male-producing parents were mixed together, none would have any direct advantage over the others; however, those that produced fewer unnecessary males would have a major indirect advantage—their eggs or embryos would likely be larger and healthier, or their young better cared for in the womb and afterward. We can see this principle in plants; those that produce a large number of seeds tend to have smaller ones, while those that produce fewer seeds often create larger ones that are well-supplied with nutrients for the seedlings.408 Thus, the offspring of parents who expended the least energy producing excess males would be the most likely to survive and would inherit the same tendency not to create unnecessary males, while maintaining their full fertility for producing females. The same goes for the opposite scenario with females. Any slight excess of either sex, however, would be difficult to address in such an indirect way. Additionally, we have seen that significant inequality between the sexes has not always been avoided, as shown in some cases discussed earlier. In these situations, the unknown factors determining the sex of the embryo—which under certain conditions can lead to one sex being produced in excess—have not been overcome by the survival of those varieties that wasted the least organized matter and energy on creating excess individuals of either sex. Nevertheless, we can conclude that natural selection will always strive, though sometimes ineffectively, to balance the relative numbers of the two sexes.
Having said this much on the equalisation of the sexes, it may be well to add a few remarks on the regulation through natural selection of the ordinary fertility of species. Mr. Herbert Spencer has shewn in an able discussion409 that with all organisms a ratio exists between what he calls individuation and genesis; whence it follows that beings which consume much matter or force in their growth, complicated structure or activity, or which produce ova and embryos of large size, or which expend much energy in nurturing their young, cannot be so productive as beings of an opposite nature. Mr. Spencer further shews that minor differences in fertility will be regulated through natural selection. Thus 319the fertility of each species will tend to increase, from the more fertile pairs producing a larger number of offspring, and these from their mere number will have the best chance of surviving, and will transmit their tendency to greater fertility. The only check to a continued augmentation of fertility in each organism seems to be either the expenditure of more power and the greater risks run by the parents that produce a more numerous progeny, or the contingency of very numerous eggs and young being produced of smaller size, or less vigorous, or subsequently not so well nurtured. To strike a balance in any case between the disadvantages which follow from the production of a numerous progeny, and the advantages (such as the escape of at least some individuals from various dangers) is quite beyond our power of judgment.
Having discussed the equality of the sexes, it’s useful to add a few thoughts on how natural selection regulates the typical fertility of species. Mr. Herbert Spencer has shown in a detailed discussion409 that all organisms have a ratio between what he calls individuation and genesis; this means that beings that use a lot of resources or energy for growth, complex structures, or activity, or that produce large eggs and embryos, or that spend significant energy raising their young, cannot be as productive as beings that are the opposite. Mr. Spencer further explains that small differences in fertility will be managed through natural selection. Thus, 319the fertility of each species will likely increase, because the more fertile pairs will have more offspring, and these numerous offspring will have a better chance of surviving and will pass on their tendency for greater fertility. The only limit to the ongoing increase in fertility for each organism seems to be either the requirement of more energy and the greater risks faced by parents who produce more offspring, or the chance that a very high number of eggs and young will be smaller, less vigorous, or not well cared for later on. Balancing the disadvantages of producing many offspring against the advantages (such as the survival of at least some individuals from various dangers) is beyond our ability to assess.
When an organism has once been rendered extremely fertile, how its fertility can be reduced through natural selection is not so clear as how this capacity was first acquired. Yet it is obvious that if individuals of a species, from a decrease of their natural enemies, were habitually reared in larger numbers than could be supported, all the members would suffer. Nevertheless the offspring from the less fertile parents would have no direct advantage over the offspring from the more fertile parents, when all were mingled together in the same district. All the individuals would mutually tend to starve each other. The offspring indeed of the less fertile parents would lie under one great disadvantage, for from the simple fact of being produced in smaller numbers, they would be the most liable to extermination. Indirectly, however, they would partake of one great advantage; for under the supposed condition of severe competition, when all were pressed for food, it is extremely probable that those individuals which from320 some variation in their constitution produced fewer eggs or young, would produce them of greater size or vigour; and the adults reared from such eggs or young would manifestly have the best chance of surviving, and would inherit a tendency towards lessened fertility. The parents, moreover, which had to nourish or provide for fewer offspring would themselves be exposed to a less severe strain in the struggle for existence, and would have a better chance of surviving. By these steps, and by no others as far as I can see, natural selection under the above conditions of severe competition for food, would lead to the formation of a new race less fertile, but better adapted for survival, than the parent-race.
When an organism becomes highly fertile, it's not as clear how that fertility can be reduced through natural selection as it is how this ability was initially gained. However, it's obvious that if individuals of a species are consistently raised in larger numbers than their environment can support, all members would suffer. Still, the offspring of less fertile parents wouldn't have any direct advantage over the offspring of more fertile parents when mixed in the same area. All individuals would end up competing for resources and starving each other. In fact, the offspring of less fertile parents would face a significant disadvantage because they are produced in smaller numbers, making them more vulnerable to extinction. Indirectly, though, they would gain one major advantage; in a situation of intense competition for food, it's very likely that those individuals which, due to some variation, produced fewer eggs or young would create larger or healthier offspring. The adults coming from such larger or healthier eggs or young would clearly have a better chance of surviving and would also carry a tendency toward reduced fertility. Additionally, the parents that have to care for fewer offspring would face less of a strain in the struggle for survival and would be better positioned to survive. Through these processes, and likely no others, natural selection, under the described conditions of fierce competition for food, would lead to the emergence of a new, less fertile but better-adapted race than the original parent race.
CHAPTER IX.
Secondary Sexual Characteristics in the Lower Classes of the Animal Kingdom.
These characters absent in the lowest classes—Brilliant colours—Mollusca—Annelids—Crustacea, secondary sexual characters strongly developed; dimorphism; colour; characters not acquired before maturity—Spiders, sexual colours of; stridulation by the males—Myriapoda.
These characters missing in the lowest classes—Bright colors—Mollusks—Segmented worms—Crustaceans, secondary sexual characteristics strongly developed; dimorphism; color; traits not acquired before maturity—Spiders, sexual colors of; stridulation by the males—Millipedes.
In the lowest classes the two sexes are not rarely united in the same individual, and therefore secondary sexual characters cannot be developed. In many cases in which the two sexes are separate, both are permanently attached to some support, and the one cannot search or struggle for the other. Moreover it is almost certain that these animals have too imperfect senses and much too low mental powers to feel mutual rivalry, or to appreciate each other’s beauty or other attractions.
In the lower classes, both sexes are often found in the same individual, which prevents the development of secondary sexual characteristics. In many instances where the two sexes are separate, both are permanently attached to some support, and one cannot seek or fight for the other. Furthermore, it's very likely that these animals have insufficient senses and low mental abilities to experience mutual rivalry or to recognize each other’s beauty or other attractions.
Hence in these classes, such as the Protozoa, Cœlenterata, Echinodermata, Scolecida, true secondary sexual characters do not occur; and this fact agrees with the belief that such characters in the higher classes have been acquired through sexual selection, which depends on the will, desires, and choice of either sex. Nevertheless some few apparent exceptions occur; thus, as I hear from Dr. Baird, the males of certain Entozoa, or internal parasitic worms, differ slightly in colour from the females; but we have no reason to suppose that such differences have been augmented through sexual selection.
Hence in these groups, like Protozoa, Cœlenterata, Echinodermata, and Scolecida, true secondary sexual traits don’t appear; and this aligns with the idea that such traits in the more advanced groups have developed through sexual selection, which relies on the preferences, wants, and choices of either sex. However, there are a few apparent exceptions; for instance, as I learned from Dr. Baird, the males of certain Entozoa, or internal parasitic worms, show slight differences in color compared to the females; but we have no reason to think that these differences have been enhanced through sexual selection.
322Many of the lower animals, whether hermaphrodites or with the sexes separate, are ornamented with the most brilliant tints, or are shaded and striped in an elegant manner. This is the case with many corals and sea-anemonies (Actineæ), with some jelly-fish (Medusæ, Porpita, &c.), with some Planariæ, Ascidians, numerous Star-fishes, Echini, &c.; but we may conclude from the reasons already indicated, namely the union of the two sexes in some of these animals, the permanently affixed condition of others, and the low mental powers of all, that such colours do not serve as a sexual attraction, and have not been acquired through sexual selection. With the higher animals the case is very different; for with them when one sex is much more brilliantly or conspicuously coloured than the other, and there is no difference in the habits of the two sexes which will account for this difference, we have reason to believe in the influence of sexual selection; and this belief is strongly confirmed when the more ornamented individuals, which are almost always the males, display their attractions before the other sex. We may also extend this conclusion to both sexes, when coloured alike, if their colours are plainly analogous to those of one sex alone in certain other species of the same group.
322Many lower animals, whether they are hermaphrodites or have separate sexes, display bright colors or are elegantly shaded and striped. This is true for many corals and sea anemones (Actineæ), some jellyfish (Medusæ, Porpita, etc.), certain planarians, ascidians, and various starfish and sea urchins. However, we can conclude from the reasons already mentioned—such as the merging of the two sexes in some of these animals, the permanent attachment of others, and the lower cognitive abilities across all of them—that these colors do not function as a sexual attraction and were not developed through sexual selection. The situation is quite different for higher animals; when one sex is much more vividly or noticeably colored than the other, and there's no difference in behavior to explain this, we can assume sexual selection is at play. This assumption is strongly supported when the more colorful individuals, usually the males, display their traits to attract the opposite sex. We can also apply this conclusion to both sexes when they are similarly colored, as long as their colors clearly resemble those of one sex in other related species.
How, then, are we to account for the beautiful or even gorgeous colours of many animals in the lowest classes? It appears very doubtful whether such colours usually serve as a protection; but we are extremely liable to err in regard to characters of all kinds in relation to protection, as will be admitted by every one who has read Mr. Wallace’s excellent essay on this subject. It would not, for instance, at first occur to any one that the perfect transparency of the Medusæ, or jelly-fishes, was of the highest service to them as a323 protection; but when we are reminded by Häckel that not only the medusæ but many floating mollusca, crustaceans, and even small oceanic fishes partake of this same glass-like structure, we can hardly doubt that they thus escape the notice of pelagic birds and other enemies.
How, then, can we explain the beautiful or even stunning colors of many animals in the lower classes? It seems quite uncertain whether these colors usually provide protection; however, we are very prone to make mistakes regarding the characteristics of all kinds in relation to protection, as anyone who has read Mr. Wallace’s excellent essay on this topic would agree. For example, it wouldn’t initially occur to anyone that the perfect transparency of jellyfish, or Medusae, is incredibly beneficial for their protection; but when we’re reminded by Häckel that not only jellyfish but also many floating mollusks, crustaceans, and even small oceanic fish share this same glass-like appearance, we can hardly doubt that this helps them avoid detection by pelagic birds and other predators.
Notwithstanding our ignorance how far colour in many cases serves as a protection, the most probable view in regard to the splendid tints of many of the lowest animals seems to be that their colours are the direct result either of the chemical nature or the minute structure of their tissues, independently of any benefit thus derived. Hardly any colour is finer than that of arterial blood; but there is no reason to suppose that the colour of the blood is in itself any advantage; and though it adds to the beauty of the maiden’s cheek, no one will pretend that it has been acquired for this purpose. So again with many animals, especially the lower ones, the bile is richly coloured; thus the extreme beauty of the Eolidæ (naked sea-slugs) is chiefly due, as I am informed by Mr. Hancock, to the biliary glands seen through the translucent integuments; this beauty being probably of no service to these animals. The tints of the decaying leaves in an American forest are described by every one as gorgeous; yet no one supposes that these tints are of the least advantage to the trees. Bearing in mind how many substances closely analogous to natural organic compounds have been recently formed by chemists, and which exhibit the most splendid colours, it would have been a strange fact if substances similarly coloured had not often originated, independently of any useful end being thus gained, in the complex laboratory of living organisms.
Despite our lack of understanding about how color often serves as protection, the most likely explanation for the vibrant colors of many low-level animals is that their hues come from the chemical makeup or the minute structure of their tissues, without any benefit derived from them. Few colors can rival that of arterial blood, but there's no reason to believe that the blood's color provides any advantage; while it enhances the beauty of a woman's blush, no one would suggest it evolved for that reason. The same goes for many animals, particularly the lower ones, where bile is richly colored; for example, the stunning colors of Eolidæ (naked sea slugs) are mainly due, as Mr. Hancock informs me, to the biliary glands visible through their translucent skin, and this beauty likely serves no purpose for these creatures. The vibrant colors of decaying leaves in an American forest are widely acknowledged as beautiful, yet no one thinks these colors offer any advantage to the trees. Considering how many substances similar to natural organic compounds have recently been created by chemists that display striking colors, it would be peculiar if substances of similar hues didn't often arise, independently of any useful purpose, in the intricate laboratory of living organisms.
324The sub-kingdom of the Mollusca.—Throughout this great division (taken in its largest acceptation) of the animal kingdom, secondary sexual characters, such as we are here considering, never, as far as I can discover, occur. Nor could they be expected in the three lowest classes, namely in the Ascidians, Polyzoa, and Brachiopods (constituting the Molluscoida of Huxley), for most of these animals are permanently affixed to a support or have their sexes united in the same individual. In the Lamellibranchiata, or bivalve shells, hermaphroditism is not rare. In the next higher class of the Gasteropoda, or marine univalve shells, the sexes are either united or separate. But in this latter case the males never possess special organs for finding, securing, or charming the females, or for fighting with other males. The sole external difference between the sexes consists, as I am informed by Mr. Gwyn Jeffreys, in the shell sometimes differing a little in form; for instance, the shell of the male periwinkle (Littorina littorea) is narrower and has a more elongated spire than that of the female. But differences of this nature, it may be presumed, are directly connected with the act of reproduction or with the development of the ova.
324The sub-kingdom of the Mollusca.—In this vast division of the animal kingdom, secondary sexual characteristics, like those we are discussing, don't seem to appear. They wouldn’t be expected in the three lowest classes: the Ascidians, Polyzoa, and Brachiopods (which make up the Molluscoida as classified by Huxley), since most of these creatures are either permanently attached to a surface or have both sexes combined in one individual. In the Lamellibranchiata, or bivalve shells, hermaphroditism is not uncommon. In the next higher class, the Gasteropoda, or marine univalve shells, the sexes are either combined or separate. However, in the latter case, males do not have special organs for locating, attracting, or winning over females, nor for fighting other males. The only noticeable difference between the sexes, as noted by Mr. Gwyn Jeffreys, is that the shell may differ slightly in shape; for example, the male periwinkle (Littorina littorea) has a narrower shell with a more elongated spire compared to the female. But these kinds of differences likely relate directly to reproduction or the development of eggs.
The Gasteropoda, though capable of locomotion and furnished with imperfect eyes, do not appear to be endowed with sufficient mental powers for the members of the same sex to struggle together in rivalry, and thus to acquire secondary sexual characters. Nevertheless with the pulmoniferous gasteropods, or land-shells, the pairing is preceded by courtship; for these animals, though hermaphrodites, are compelled by their structure to pair together. Agassiz remarks,410 “Quiconque a eu l’occasion d’observer les amours des lima325çons, ne saurait mettre en doute la séduction déployée dans les mouvements et les allures qui préparent et accomplissent le double embrassement de ces hermaphrodites.” These animals appear also susceptible of some degree of permanent attachment: an accurate observer, Mr. Lonsdale, informs me that he placed a pair of land-shells (Helix pomatia), one of which was weakly, into a small and ill-provided garden. After a short time the strong and healthy individual disappeared, and was traced by its track of slime over a wall into an adjoining well-stocked garden. Mr. Lonsdale concluded that it had deserted its sickly mate; but after an absence of twenty-four hours it returned, and apparently communicated the result of its successful exploration, for both then started along the same track and disappeared over the wall.
The Gasteropoda, while able to move and equipped with rudimentary eyes, don’t seem to have enough mental capacity for individuals of the same sex to compete against each other, so they don’t develop secondary sexual traits. However, with the pulmoniferous gasteropods, or land snails, courtship occurs before mating; these creatures, although hermaphrodites, must pair up because of their anatomy. Agassiz notes,410 “Anyone who has had the chance to observe the courtship of the land snails cannot doubt the allure displayed in the movements and behaviors that prepare for and accomplish the mutual embrace of these hermaphrodites.” These animals also seem capable of some level of lasting attachment: a keen observer, Mr. Lonsdale, told me that he placed a pair of land snails (Helix pomatia), one of which was weak, into a small, poorly maintained garden. After a little while, the strong and healthy one vanished and was traced by its slime trail over a wall into a neighboring well-kept garden. Mr. Lonsdale thought it had abandoned its sickly partner; but after twenty-four hours, it came back and seemingly shared what it had discovered, because they both then took the same path and disappeared over the wall.
Even in the highest class of the Mollusca, namely the Cephalopoda or cuttle-fishes, in which the sexes are separate, secondary sexual characters of the kind which we are here considering, do not, as far as I can discover, occur. This is a surprising circumstance, as these animals possess highly-developed sense-organs and have considerable mental powers, as will be admitted by every one who has watched their artful endeavours to escape from an enemy.411 Certain Cephalopoda, however, are characterised by one extraordinary sexual character, namely, that the male element collects within one of the arms or tentacles, which is then cast off, and, clinging by its sucking-discs to the female, lives for a time an independent life. So completely does the cast-off arm resemble a separate animal, that it was described by Cuvier as a parasitic worm under the name 326of Hectocotyle. But this marvellous structure may be classed as a primary rather than as a secondary sexual character.
Even in the highest class of Mollusca, known as Cephalopoda or cuttle-fishes, where the sexes are separate, the secondary sexual traits we're discussing don't seem to appear. This is surprising since these creatures have well-developed sense organs and significant mental abilities, as anyone who has observed their clever attempts to escape from predators would agree.411 However, certain Cephalopoda are distinguished by one remarkable sexual feature: the male's sperm is collected within one of its arms or tentacles, which is then discarded. This arm clings to the female with its suckers and lives independently for a while. It resembles a separate creature so closely that Cuvier described it as a parasitic worm, naming it Hectocotyle. However, this remarkable structure is better categorized as a primary rather than a secondary sexual characteristic.
Although with the Mollusca sexual selection does not seem to have come into play; yet many univalve and bivalve shells, such as volutes, cones, scallops, &c., are beautifully coloured and shaped. The colours do not appear in most cases to be of any use as a protection; they are probably the direct result, as in the lowest classes, of the nature of the tissues; the patterns and the sculpture of the shell depending on its manner of growth. The amount of light seems to a certain extent to be influential; for although, as repeatedly stated by Mr. Gwyn Jeffreys, the shells of some species living at a profound depth are brightly coloured, yet we generally see the lower surfaces and the parts covered by the mantle less highly coloured than the upper and exposed surfaces.412 In some cases, as with shells living amongst corals or brightly-tinted sea-weeds, the bright colours may serve as a protection. But many of the nudibranch mollusca, or sea-slugs, are as beautifully coloured as any shells, as may be seen in Messrs. Alder and Hancock’s magnificent work; and from information kindly given me by Mr. Hancock, it is extremely doubtful whether these colours usually serve as a protection. With some species this may be the case, as with one which lives on the green leaves of algæ, and is itself bright-green. But many brightly-coloured, white or otherwise conspicuous species, do not seek concealment; whilst again some equally conspicuous species, as well as other dull-coloured kinds, live under stones and in 327dark recesses. So that with these nudibranch molluscs, colour apparently does not stand in any close relation to the nature of the places which they inhabit.
Although sexual selection doesn’t seem to apply to Mollusca, many univalve and bivalve shells, like volutes, cones, scallops, etc., are beautifully colored and shaped. In most cases, these colors don’t seem to provide any protection; they are probably just a result of the tissue structure, with patterns and textures of the shell depending on how it grows. The amount of light appears to influence this to some extent; for even though, as Mr. Gwyn Jeffreys has noted, some species' shells found at great depths are brightly colored, we generally see that the lower surfaces and parts covered by the mantle are less vividly colored than the upper and exposed surfaces.412 In some cases, like shells living among corals or brightly colored seaweeds, bright colors may serve as protection. However, many nudibranch mollusks, or sea slugs, are just as beautifully colored as any shells, as shown in Messrs. Alder and Hancock’s magnificent work. According to Mr. Hancock, it’s very doubtful that these colors usually provide protection. For some species, like one that lives on the green leaves of algae and is bright green itself, this might be true. But many brightly colored species, whether white or otherwise conspicuous, don’t seek concealment; while some equally noticeable species, along with dull-colored ones, live under stones and in 327dark recesses. Thus, with these nudibranch mollusks, color doesn’t seem closely related to the types of environments they inhabit.
These naked sea-slugs are hermaphrodites, yet they pair together, as do land-snails, many of which have extremely pretty shells. It is conceivable that two hermaphrodites, attracted by each others’ greater beauty, might unite and leave offspring which would inherit their parents’ greater beauty. But with such lowly-organised creatures this is extremely improbable. Nor is it at all obvious how the offspring from the more beautiful pairs of hermaphrodites would have any advantage, so as to increase in numbers, over the offspring of the less beautiful, unless indeed vigour and beauty generally coincided. We have not here a number of males becoming mature before the females, and the more beautiful ones selected by the more vigorous females. If, indeed, brilliant colours were beneficial to an hermaphrodite animal in relation to its general habits of life, the more brightly-tinted individuals would succeed best and would increase in number; but this would be a case of natural and not of sexual selection.
These naked sea slugs are hermaphrodites, but they still pair up, similar to land snails, many of which have really beautiful shells. It's possible that two hermaphrodites, drawn to each other's beauty, could come together and produce offspring that would inherit their enhanced looks. However, with such basic organisms, this is highly unlikely. It's also not clear how the offspring of the more attractive hermaphrodite pairs would have any advantage or increase in numbers compared to the offspring of less attractive ones, unless strength and beauty just happened to go hand in hand. We're not seeing a situation where males mature before the females, with the more attractive ones being chosen by the stronger females. If bright colors were advantageous for a hermaphrodite in terms of its overall lifestyle, then the more vividly colored individuals would thrive and reproduce more; however, that would be an example of natural selection, not sexual selection.
Sub-kingdom of the Vermes or Annulosa: Class, Annelida (or Sea-worms).—In this class, although the sexes (when separate) sometimes differ from each other in characters of such importance that they have been placed under distinct genera or even families, yet the differences do not seem of the kind which can be safely attributed to sexual selection. These animals, like those in the preceding classes, apparently stand too low in the scale, for the individuals of either sex to exert any choice in selecting a partner, or for the individuals of the same sex to struggle together in rivalry.
Sub-kingdom of the Vermes or Annulosa: Class, Annelida (or Sea-worms).—In this class, even though the sexes (when separate) sometimes show differences so significant that they have been classified into distinct genera or even families, these differences don't seem to be the kind that can clearly be linked to sexual selection. These animals, similar to those in the previous classes, appear to be too low on the evolutionary scale for individuals of either sex to have any real choice in selecting a partner, or for individuals of the same sex to compete with each other.
328Sub-kingdom of the Arthropoda: Class, Crustacea.—In
this great class we first meet with undoubted secondary
sexual characters, often developed in a remarkable
manner. Unfortunately the habits of crustaceans
are very imperfectly known, and we cannot explain the
uses of many structures peculiar to one sex. With
the lower parasitic species the males are of small size,
and they alone are furnished with perfect swimming-legs,
antennæ and sense-organs; the females being
destitute of these organs, with their bodies often consisting
of a mere distorted mass. But these extraordinary
Fig. 3. Labidocera Darwinii,
(from Lubbock).
a. Part of right-hand anterior antenna
of male, forming a prehensile organ.
b. Posterior pair of thoracic legs of male.
c. Ditto of female.
differences between the two sexes are no doubt related
to their widely different habits of life, and consequently
do not concern us. In various crustaceans, belonging
to distinct families, the anterior antennæ are furnished
with peculiar thread-like bodies, which are believed to
act as smelling-organs, and these are much more numerous
in the males than in the females. As the males,
without any unusual development of their olfactory
organs, would almost certainly be able sooner or later
to find the females, the increased number of the smelling-threads
has probably been acquired through sexual
selection, by the better provided males having been the
most successful in finding partners and in leaving offspring.
Fritz Müller has described a remarkable dimorphic
species of Tanais, in which the male is represented
by two distinct forms, never graduating into each other.
In the one form the male is furnished with more
numerous smelling-threads, and in the other form with
more powerful and more elongated chelæ or pincers
which serve to hold the female. Fritz Müller suggests
that these differences between the two male forms of the
same species must have originated in certain individuals
having varied in the number of the smelling-threads,
whilst other individuals varied in the shape and size of329
their chelæ; so that of the former, those which were best
able to find the female, and of the latter, those which were
best able to hold her when found,
have left the greater number of
progeny to inherit their respective
advantages.413
328Sub-kingdom of the Arthropoda: Class, Crustacea.—In this large class, we first encounter clear secondary sexual characteristics, often developed in a striking way. Unfortunately, the behaviors of crustaceans are not well understood, and we can't explain the functions of many structures that are unique to one sex. In the lower parasitic species, the males are quite small and are the only ones that have fully developed swimming legs, antennae, and sensory organs. The females lack these features and often have bodies that consist of nothing more than a distorted mass. However, these remarkable differences between the sexes are likely related to their vastly different lifestyles, so they aren't our primary focus. In various crustaceans from different families, the front antennae are equipped with specific thread-like structures believed to function as smell receptors, and these are much more abundant in males than in females. Since males, without any unusual development of their smell organs, would almost certainly eventually find the females, the greater number of these smell threads has likely evolved through sexual selection, as better-equipped males were more successful at locating partners and producing offspring. Fritz Müller described a fascinating dimorphic species of Tanais, where the male exists in two distinct forms that do not transition into each other. In one form, the male has more smell threads, while in the other, he has more robust and elongated pincers that help him hold onto the female. Fritz Müller suggests that these differences between the two male forms of the same species must have arisen from certain individuals varying in the number of smell threads, while others changed in the shape and size of their pincers; thus, those males that were better at finding females, and those that were better at holding onto them, would have left behind more offspring to inherit these advantageous traits. 329
In some of the lower crustaceans, the right-hand anterior antenna of the male differs greatly in structure from the left-hand one, the latter resembling in its simple tapering joints the antennæ of the female. In the male the modified antenna is either swollen in the middle or angularly bent, or converted (fig. 3) into an elegant, and sometimes wonderfully complex, prehensile organ.414 It serves, as I hear from Sir J. Lubbock, to hold the female, and for this same purpose one of the two posterior legs (b) on the same side of the body is converted into a forceps. In another family the inferior or posterior antennæ are “curiously zigzagged” in the males alone.
In some lower crustaceans, the right front antenna of the male is very different in structure from the left one, which looks like the female's simple, tapering joints. In the male, the modified antenna is either thick in the middle, bent at an angle, or transformed (fig. 3) into a sleek, sometimes incredibly intricate, grasping organ.414 According to Sir J. Lubbock, it's used to hold the female, and for this same purpose, one of the two back legs (b) on the same side of the body becomes a pincer. In another family, the lower or back antennas are “curiously zigzagged” in males only.

Fig. 4. Anterior part of body of Callianassa (from Milne-Edwards), showing the unequal and differently-constructed right and left-hand chelæ of the male.
Fig. 4. Front part of the body of Callianassa (from Milne-Edwards), showing the uneven and differently-structured right and left claws of the male.
N.B.—The artist by mistake has reversed the drawing, and made the left-hand chela the largest.
N.B.—The artist accidentally flipped the drawing, making the left claw the biggest.
Fig. 5. | Fig. 6. |
Fig. 5. Second leg of male Orchestia Tucuratinga (from Fritz Müller).
Fig. 5. Second leg of male Orchestia Tucuratinga (from Fritz Müller).
Fig. 6. Ditto of female.
Fig. 6. Same for female.
In the higher crustaceans the anterior legs form a pair of chelæ or pincers, and these are generally larger in the male than in the female. In many species the chelæ on the opposite sides of the body are of unequal size, the right-hand one being, as I am informed by Mr. C. Spence Bate, generally, though not invariably, the largest. This inequality is often much greater in the male than in the female. The two chelæ also often differ in structure (figs. 4 and 5), the smaller one resembling those of the female. What advantage331 is gained by their inequality in size on the opposite sides of the body, and by the inequality being much greater in the male than in the female; and why, when they are of equal size, both are often much larger in the male than in the female, is not known. The chelæ are sometimes of such length and size that they cannot possibly be used, as I hear from Mr. Spence Bate, for carrying food to the mouth. In the males of certain freshwater prawns (Palæmon) the right leg is actually longer than the whole body.415 It is probable that the great size of one leg with its chelæ may aid the male in fighting with his rivals; but this use will not account for their inequality in the female on the opposite sides of the body. In Gelasimus, according to a statement quoted by Milne-Edwards,416 the male and female live in the same burrow, which is worth notice, as shewing that they pair, and the male closes the mouth of the burrow with one of its chelæ, which is enormously developed; so that here it indirectly serves as a means of defence. Their main use, however, probably is to seize and to secure the female, and this in some instances, as with Gammarus, is known to be the case. The sexes, however, of the common shore-crab (Carcinus mænas), as Mr. Spence Bate informs me, unite directly after the female has moulted her hard shell, and when she is so soft that she would be injured if seized by the strong pincers of the male; but as she is caught and carried about by the male previously to the act of moulting, she could then be seized with impunity.
In higher crustaceans, the front legs form a pair of pincers, which are usually larger in males than in females. In many species, the pincers on opposite sides of the body are of different sizes, with the right one, as informed by Mr. C. Spence Bate, typically being the largest, although not always. This size difference is often more pronounced in males than in females. The two pincers often have different structures (figs. 4 and 5), with the smaller one resembling those of the female. The reason behind the size discrepancy on opposite sides of the body, and why it is more significant in males than in females, remains unknown. Sometimes the pincers are so large that, according to Mr. Spence Bate, they can't be used to bring food to the mouth. In males of certain freshwater prawns (Palæmon), the right leg can actually be longer than the entire body.415 It’s likely that the large size of one leg with its pincers helps the male fight other males, but this doesn’t explain the size difference in the female's pincers on opposite sides of the body. In Gelasimus, as noted by Milne-Edwards,416 males and females share the same burrow, showing that they mate, and the male closes the burrow’s entrance with one of its greatly enlarged pincers, serving as a means of defense. However, their main purpose is probably to grab and hold onto the female, which is known to happen in some cases, like with Gammarus. However, in the common shore crab (Carcinus mænas), as Mr. Spence Bate tells me, the two unite right after the female has shed her hard shell, when she is soft enough to be hurt by the male’s strong pincers; but since she is caught and carried around by the male before the molting happens, she can be seized without risk then.
Fritz Müller states that certain species of Melita are 332distinguished from all other amphipods by the females having “the coxal lamellæ of the penultimate pair of feet produced into hook-like processes, of which the males lay hold with the hands of the first pair.” The development of these hook-like processes probably resulted from those females which were the most securely held during the act of reproduction, having left the largest number of offspring. Another Brazilian amphipod (Orchestia Darwinii, fig. 7) is described by Fritz Müller, as presenting a case of dimorphism, like that of Tanais; for there are two male forms, which differ in the structure of their chelæ.417 As chelæ of either shape would certainly have sufficed to hold the female, for both are now used for this purpose, the two male forms probably originated, by some having varied in one manner and some in another; both forms having derived certain special, but nearly equal advantages, from their differently shaped organs.
Fritz Müller points out that certain species of Melita are 332distinct from all other amphipods because the females have “the coxal lamellae of the second-to-last pair of legs developed into hook-like structures, which the males grasp using their first pair of limbs.” The development of these hook-like structures likely resulted from those females that were held most securely during reproduction, leaving behind the highest number of offspring. Another Brazilian amphipod (Orchestia Darwinii, fig. 7) is described by Fritz Müller as an example of dimorphism, similar to that of Tanais; there are two male forms that differ in the structure of their claws. 417 Since either type of claw would be effective for holding the female, as both are now used for this purpose, the two male forms probably emerged because some varied in one way and some in another; both forms have gained certain distinct, yet nearly equal advantages from their differently shaped claws.
It is not known that male crustaceans fight together for the possession of the females, but this is probable; for with most animals when the male is larger than the female, he seems to have acquired his greater size by having conquered during many generations other males. Now Mr. Spence Bate informs me that in most of the crustacean orders, especially in the highest or the Brachyura, the male is larger than the female; the parasitic genera, however, in which the sexes follow different habits of life, and most of the Entomostraca must be excepted. The chelæ of many crustaceans are weapons well adapted for fighting. Thus a Devil-crab (Portunus puber) was seen by a son of Mr. Bate fighting with a Carcinus mænas, and the latter was soon thrown on its back, and had every limb torn from its body. 333 When several males of a Brazilian Gelasimus, a species furnished with immense pincers, were placed together by Fritz Müller in a glass vessel, they mutilated and killed each other. Mr. Bate put a large male Carcinus mænas into a pan of water, inhabited by a female paired with a smaller male; the latter was soon dispossessed, but, as Mr. Bate adds, “if they fought, the victory334 was a bloodless one, for I saw no wounds.” This same naturalist separated a male sand-skipper (so common on our sea-shores), Gammarus marinus, from its female, both of which were imprisoned in the same vessel with many individuals of the same species. The female being thus divorced joined her comrades. After an interval the male was again put into the same vessel and he then, after swimming about for a time, dashed into the crowd, and without any fighting at once took away his wife. This fact shews that in the Amphipoda, an order low in the scale, the males and females recognise each other, and are mutually attached.
It’s not confirmed that male crustaceans fight for the females, but it’s likely; in most animals, when the male is larger than the female, it seems his size is a result of beating other males over many generations. Mr. Spence Bate informs me that in most crustacean groups, especially in the highest category, the Brachyura, males are bigger than females; however, the parasitic types, where the sexes lead different lifestyles, and most of the Entomostraca are exceptions. The claws of many crustaceans are designed well for fighting. For instance, a Devil-crab (Portunus puber) was observed by Mr. Bate’s son fighting a Carcinus mænas, and the latter was quickly flipped onto its back and had every limb torn off. 333 When several male Brazilian Gelasimus, a species with huge pincers, were placed together in a glass container by Fritz Müller, they injured and killed each other. Mr. Bate put a large male Carcinus mænas into a pan of water that a female was sharing with a smaller male; the smaller male was quickly ousted, but as Mr. Bate noted, “if they fought, the victory was a bloodless one, for I saw no wounds.” The same naturalist separated a male sand-skipper (common on our shores), Gammarus marinus, from its female, both of which were kept in the same container with many others of their kind. After the female was separated, she rejoined her peers. Later, when the male was placed back in the same container, he swam around for a bit before charging into the group and, without any fighting, took his mate away. This shows that in the Amphipoda, a lower order, males and females recognize each other and are attached to one another.

The mental powers of the Crustacea are probably higher than might have been expected. Any one who has tried to catch one of the shore-crabs, so numerous on many tropical coasts, will have perceived how wary and alert they are. There is a large crab (Birgos latro), found on coral islands, which makes at the bottom of a deep burrow a thick bed of the picked fibres of the cocoa-nut. It feeds on the fallen fruit of this tree by tearing off the husk, fibre by fibre; and it always begins at that end where the three eye-like depressions are situated. It then breaks through one of these eyes by hammering with its heavy front pincers, and turning round, extracts the albuminous core with its narrow posterior pincers. But these actions are probably instinctive, so that they would be performed as well by a young as by an old animal. The following case, however, can hardly be so considered: a trustworthy naturalist, Mr. Gardner,418 whilst watching a shore-crab (Gelasimus) making its burrow, 335threw some shells towards the hole. One rolled in, and three other shells remained within a few inches of the mouth. In about five minutes the crab brought out the shell which had fallen in, and carried it away to the distance of a foot; it then saw the three other shells lying near, and evidently thinking that they might likewise roll in, carried them to the spot where it had laid the first. It would, I think, be difficult to distinguish this act from one performed by man by the aid of reason.
The mental abilities of crustaceans are likely greater than we might expect. Anyone who has tried to catch one of the many shore crabs found along tropical coasts will notice how cautious and alert they are. There is a large crab (Birgos latro) that lives on coral islands and creates a thick bed of picked coconut fibers at the bottom of its deep burrow. It feeds on the fallen fruit of this tree by tearing off the husk, fiber by fiber, starting from the end with the three eye-like indentations. It then breaks through one of these eyes by pounding with its strong front pincers, and after turning around, it uses its narrow back pincers to pull out the soft core. However, these actions are likely instinctive, so they would be done just as well by a young crab as by an older one. But consider this next example, which can't be dismissed in the same way: a reliable naturalist, Mr. Gardner,418 while observing a shore crab (Gelasimus) digging its burrow, tossed some shells towards the hole. One rolled in, while three others stayed a few inches from the entrance. In about five minutes, the crab retrieved the shell that had fallen in and carried it away about a foot. It then noticed the three shells nearby and, clearly thinking that they might also roll in, took them to the same spot where it had placed the first shell. I think it would be hard to differentiate this action from something a human would do using reason.
With respect to colour which so often differs in the two sexes of animals belonging to the higher classes, Mr. Spence Bate does not know of any well-marked instances with our British crustaceans. In some cases, however, the male and female differ slightly in tint, but Mr. Bate thinks not more than may be accounted for by their different habits of life, such as by the male wandering more about and being thus more exposed to the light. In a curious Bornean crab, which inhabits sponges, Mr. Bate could always distinguish the sexes by the male not having the epidermis so much rubbed off. Dr. Power tried to distinguish by colour the sexes of the species which inhabit the Mauritius, but always failed, except with one species of Squilla, probably the S. stylifera, the male of which is described as being “of a beautiful blueish-green,” with some of the appendages cherry-red, whilst the female is clouded with brown and grey, “with the red about her much less vivid than in the male.”419 In this case, we may suspect the agency of sexual selection. With Saphirina (an oceanic genus of Entomostraca, and therefore low in the scale) the males are furnished with 336minute shields or cell-like bodies, which exhibit beautiful changing colours; these being absent in the females, and in the case of one species in both sexes.420 It would, however, be extremely rash to conclude that these curious organs serve merely to attract the females. In the female of a Brazilian species of Gelasimus, the whole body, as I am informed by Fritz Müller, is of a nearly uniform greyish-brown. In the male the posterior part of the cephalo-thorax is pure white, with the anterior part of a rich green, shading into dark brown; and it is remarkable that these colours are liable to change in the course of a few minutes—the white becoming dirty grey or even black, the green “losing much of its brilliancy.” The males apparently are much more numerous than the females. It deserves especial notice that they do not acquire their bright colours until they become mature. They differ also from the females in the larger size of their chelæ. In some species of the genus, probably in all, the sexes pair and inhabit the same burrow. They are also, as we have seen, highly intelligent animals. From these various considerations it seems highly probable that the male in this species has become gaily ornamented in order to attract or excite the female.
Regarding color, which often differs between male and female animals in higher classes, Mr. Spence Bate isn't aware of any prominent examples among British crustaceans. However, in some cases, the male and female show slight differences in shade, but Mr. Bate believes this is likely due to their different lifestyles, like the male being more active and thus more exposed to light. In a unique crab from Borneo that lives in sponges, Mr. Bate could always tell the sexes apart because the male's skin wasn't as worn away. Dr. Power attempted to distinguish the sexes of species found in Mauritius by color but only succeeded with one species of Squilla, probably the S. stylifera, where the male is described as “a beautiful bluish-green,” with some appendages cherry-red, while the female is speckled with brown and gray, “with the red much less vibrant than in the male.”419 In this case, we might suspect the role of sexual selection. In Saphirina (an oceanic genus of Entomostraca, and thus lower on the evolutionary scale), males have tiny shields or cell-like structures that show stunning shifting colors, which are absent in females and in one species present in both sexes.420 However, it would be very unwise to conclude that these intriguing features exist solely to attract females. In the female of a Brazilian species of Gelasimus, the body is almost uniformly greyish-brown, according to Fritz Müller. In the male, the rear part of the cephalo-thorax is pure white, while the front is a rich green that fades into dark brown; notably, these colors can change within minutes—the white turning dirty grey or even black, and the green “losing much of its brightness.” Males are apparently much more numerous than females. It’s important to point out that they don’t develop their bright colors until they reach maturity, and they also differ from females in having larger claws. In some species of this genus, probably all, the sexes pair and share the same burrow. They are also, as noted, highly intelligent animals. Considering all these factors, it seems quite likely that the male of this species has become brightly colored to attract or stimulate the female.
It has just been stated that the male Gelasimus does not acquire his conspicuous colours until mature and nearly ready to breed. This seems the general rule in the whole class with the many remarkable differences in structure between the two sexes. We shall hereafter find the same law prevailing throughout the great sub-kingdom of the Vertebrata, and in all cases it is eminently distinctive of characters which have been 337acquired through sexual selection. Fritz Müller421 gives some striking instances of this law; thus the male sand-hopper (Orchestia) does not acquire his large claspers, which are very differently constructed from those of the female, until nearly full-grown; whilst young his claspers resemble those of the female. Thus, again, the male Brachyscelus possesses, like all other amphipods, a pair of posterior antennæ; the female, and this is a most extraordinary circumstance, is destitute of them, and so is the male as long as he remains immature.
It has just been noted that the male Gelasimus doesn't develop his distinctive colors until he reaches maturity and is almost ready to breed. This seems to be a general rule across the entire class, with many notable structural differences between the two sexes. We will later see the same rule in the broader sub-kingdom of Vertebrates, and in all instances, it highlights characteristics shaped by sexual selection. Fritz Müller421 provides some striking examples of this rule; for instance, the male sand-hopper (Orchestia) only develops his large claspers, which are quite differently shaped from those of the female, when he is nearly fully grown; when young, his claspers resemble those of the female. Similarly, the male Brachyscelus, like all other amphipods, has a pair of posterior antennae; however, the female, quite surprisingly, lacks them, and so does the male while he remains immature.
Class, Arachnida (Spiders).—The males are often darker, but sometimes lighter than the females, as may be seen in Mr. Blackwall’s magnificent work.422 In some species the sexes differ conspicuously from each other in colour; thus the female of Sparassus smaragdulus is dullish-green; whilst the adult male has the abdomen of a fine yellow, with three longitudinal stripes of rich red. In some species of Thomisus the two sexes closely resemble each other; in others they differ much; thus in T. citreus the legs and body of the female are pale-yellow or green, whilst the front legs of the male are reddish-brown: in T. floricolens, the legs of the female are pale-green, those of the male being ringed in a conspicuous manner with various tints. Numerous analogous cases could be given in the genera Epeira, Nephila, Philodromus, Theridion, Linyphia, &c. It is often difficult to say which of the two sexes departs most from the ordinary coloration of the genus to which the species belong; but Mr. Blackwall 338thinks that, as a general rule, it is the male. Both sexes whilst young, as I am informed by the same author, usually resemble each other; and both often undergo great changes in colour during their successive moults before arriving at maturity. In other cases the male alone appears to change colour. Thus the male of the above-mentioned brightly-coloured Sparassus at first resembles the female and acquires his peculiar tints only when nearly adult. Spiders are possessed of acute senses, and exhibit much intelligence. The females often shew, as is well known, the strongest affection for their eggs, which they carry about enveloped in a silken web. On the whole it appears probable that well-marked differences in colour between the sexes have generally resulted from sexual selection, either on the male or female side. But doubts may be entertained on this head from the extreme variability in colour of some species, for instance of Theridion lineatum, the sexes of which differ when adult; this great variability indicates that their colours have not been subjected to any form of selection.
Class, Arachnida (Spiders).—Males are often darker, but sometimes lighter than females, as shown in Mr. Blackwall’s impressive work.422 In some species, the sexes have noticeable differences in color; for example, the female of Sparassus smaragdulus is a dull green, while the adult male has a bright yellow abdomen with three long red stripes. In some Thomisus species, the two sexes look quite similar; in other cases, they differ significantly. For instance, in T. citreus, the female's legs and body are pale yellow or green, while the male's front legs are reddish-brown. In T. floricolens, the female's legs are pale green, and the male's are distinctly ringed with various colors. Many similar examples can be found in the genera Epeira, Nephila, Philodromus, Theridion, Linyphia, etc. It's often hard to determine which sex strays most from the typical colors of their genus; however, Mr. Blackwall believes that, generally, it is the male. Both sexes, when young, usually look alike, and both often undergo significant color changes during their molts before reaching maturity. In some cases, only the male changes color. For instance, the male of the previously mentioned brightly colored Sparassus initially resembles the female and only develops his distinct colors as he nears adulthood. Spiders have sharp senses and show considerable intelligence. Females, as is well-known, often show the strongest affection for their eggs, which they carry wrapped in silk. Overall, it seems likely that marked color differences between the sexes usually stem from sexual selection, either from the male or female perspective. However, there are questions about this due to the extreme variability in color observed in some species, such as Theridion lineatum, which show differences between the sexes when adult; this significant variability suggests that their colors have not undergone any form of selection.
Mr. Blackwall does not remember to have seen the males of any species fighting together for the possession of the female. Nor, judging from analogy, is this probable; for the males are generally much smaller than the females, sometimes to an extraordinary degree.423 Had the males been in the habit of fighting together, they would, it is probable, have gradually 339acquired greater size and strength. Mr. Blackwall has sometimes seen two or more males on the same web with a single female; but their courtship is too tedious and prolonged an affair to be easily observed. The male is extremely cautious in making his advances, as the female carries her coyness to a dangerous pitch. De Geer saw a male that “in the midst of his preparatory caresses was seized by the object of his attractions, enveloped by her in a web and then devoured, a sight which, as he adds, filled him with horror and indignation.”424
Mr. Blackwall doesn't recall seeing males of any species fighting for the chance to mate with a female. And, based on what we know, that seems unlikely; males are usually much smaller than females, sometimes to an extreme extent. If males had a habit of battling for females, they likely would have developed greater size and strength over time. Mr. Blackwall has occasionally seen two or more males on the same web with one female, but their courtship is such a lengthy and complicated process that it’s hard to observe. The male is very careful in his approach because the female can be extremely evasive. De Geer once witnessed a male that, while trying to woo a female, was caught by her, wrapped up in her web, and then eaten—a sight that he described as horrifying and infuriating.
Westring has made the interesting discovery that the males of several species of Theridion425 have the power of making a stridulating sound (like that made by many beetles and other insects, but feebler), whilst the females are quite mute. The apparatus consists of a serrated ridge at the base of the abdomen, against which the hard hinder part of the thorax is rubbed; and of this structure not a trace could be detected in the females. From the analogy of the Orthoptera and Homoptera, to be described in the next chapter, we may feel almost sure that the stridulation serves, as Westring remarks, either to call or to excite the female; and this is the first case in the ascending scale of the animal kingdom, known to me, of sounds emitted for this purpose.
Westring has made an interesting discovery that the males of several species of Theridion425 can produce a stridulating sound (similar to the sounds made by many beetles and other insects, but quieter), while the females are completely silent. The mechanism consists of a serrated ridge at the base of the abdomen, which rubs against the hard back part of the thorax; and this structure was not found in the females. Based on the similarities with Orthoptera and Homoptera, which will be discussed in the next chapter, we can almost confidently say that the stridulation serves, as Westring notes, either to attract or excite the female. This is the first known case in the progression of the animal kingdom where sounds are used for this purpose.
Class, Myriapoda.—In neither of the two orders in this class, including the millipedes and centipedes, 340can I find any well-marked instances of sexual differences such as more particularly concern us. In Glomeris limbata, however, and perhaps in some few other species, the males differ slightly in colour from the females; but this Glomeris is a highly variable species. In the males of the Diplopoda, the legs belonging to one of the anterior segments of the body, or to the posterior segment, are modified into prehensile hooks which serve to secure the female. In some species of Iulus the tarsi of the male are furnished with membranous suckers for the same purpose. It is a much more unusual circumstance, as we shall see when we treat of Insects, that it is the female in Lithobius which is furnished with prehensile appendages at the extremity of the body for holding the male.426
Class, Myriapoda.—In neither of the two orders in this class, which include millipedes and centipedes, 340 can I find any clear examples of sexual differences that particularly concern us. In Glomeris limbata, however, and perhaps in a few other species, the males are slightly different in color from the females; but this Glomeris is a highly variable species. In male Diplopoda, the legs from one of the front body segments or from the back segment are modified into prehensile hooks that help secure the female. In some species of Iulus, the male's tarsi are equipped with membranous suckers for the same reason. It is much rarer, as we will see when we discuss Insects, that the female in Lithobius has prehensile appendages at the end of her body for holding onto the male.426
CHAPTER X.
Insect Secondary Sexual Characteristics.
Diversified structures possessed by the males for seizing the females—Differences between the sexes, of which the meaning is not understood—Difference in size between the sexes—Thysanura—Diptera—Hemiptera—Homoptera, musical powers possessed by the males alone—Orthoptera, musical instruments of the males, much diversified in structure; pugnacity; colours—Neuroptera, sexual differences in colour—Hymenoptera, pugnacity and colours—Coleoptera, colours; furnished with great horns, apparently as an ornament; battles; stridulating organs generally common to both sexes.
Diversified structures that males have for capturing females—Differences between the sexes that aren't fully understood—Size differences between males and females—Thysanura—Diptera—Hemiptera—Homoptera, where only males have musical abilities—Orthoptera, where male musical instruments have a lot of structural variety; aggression; colors—Neuroptera, sexual color differences—Hymenoptera, aggression and colors—Coleoptera, colors; equipped with large horns that seem to serve as ornaments; fights; stridulating organs usually found in both sexes.
In the immense class of insects the sexes sometimes differ in their organs for locomotion, and often in their sense-organs, as in the pectinated and beautifully plumose antennæ of the males of many species. In one of the Ephemeræ, namely Chloëon, the male has great pillared eyes, of which the female is entirely destitute.427 The ocelli are absent in the females of certain other insects, as in the Mutillidæ, which are likewise destitute of wings. But we are chiefly concerned with structures by which one male is enabled to conquer another, either in battle or courtship, through his strength, pugnacity, ornaments, or music. The innumerable contrivances, therefore, by which the male is able to seize the female, may be briefly passed over. Besides the complex structures at the apex of the abdomen, which ought perhaps to be ranked as primary 342organs,428 “it is astonishing,” as Mr. B. D. Walsh429 has remarked, “how many different organs are worked in by nature, for the seemingly insignificant object of enabling the male to grasp the female firmly.” The mandibles or jaws are sometimes used for this purpose; thus the male Corydalis cornutus (a neuropterous insect in some degree allied to the Dragon-flies, &c.) has immense curved jaws, many times longer than those of the female; and they are smooth instead of being toothed, by which means he is enabled to seize her without injury.430 One of the stag-beetles of North America (Lucanus elaphus) uses his jaws, which are much larger than those of the female, for the same purpose, but probably likewise for fighting. In one of the sand-wasps (Ammophila) the jaws in the two sexes are closely alike, but are used for widely different purposes; the males, as Professor Westwood observes, “are exceedingly ardent, seizing their partners round the neck with their sickle-shaped jaws;”431 whilst the females use 343these organs for burrowing in sand-banks and making their nests.
In the vast category of insects, males and females can differ significantly in their movement organs and often in their sensory organs, like the finely designed, feathery antennae found in the males of many species. In the case of one type of mayfly, Chloëon, the male has large, columnar eyes, which the female completely lacks.427 Some other insects, such as certain Mutillidae, also lack ocelli and have no wings. However, we are mainly interested in the features that allow one male to overpower another, whether in combat or during courtship, based on his strength, aggression, physical attractiveness, or sound. Therefore, we can briefly overlook the many adaptations that enable a male to grasp a female. Besides the complex structures at the end of the abdomen, which might be considered primary organs, 342 as Mr. B. D. Walsh428 noted, "it's remarkable how many various organs are developed by nature, for the seemingly trivial purpose of allowing the male to hold onto the female securely." Sometimes, the mandibles or jaws serve this function; for example, the male Corydalis cornutus (a neuropteran insect somewhat related to dragonflies, etc.) has huge curved jaws, significantly longer than the female's. These jaws are smooth rather than serrated, allowing him to grip her without causing harm.430 Similarly, one of North America's stag beetles (Lucanus elaphus) uses his much larger jaws for the same purpose, likely also for fighting. In one sand wasp species (Ammophila), the jaws of both sexes are quite similar but used for very different functions; as Professor Westwood points out, "the males are incredibly enthusiastic, gripping their partners around the neck with their sickle-shaped jaws;"431 while females use these jaws for digging in sandbanks and constructing their nests.
The tarsi of the front-legs are dilated in many male
beetles, or are furnished with broad cushions of hairs;
and in many genera of water-beetles they are armed
with a round flat sucker, so that the male may adhere
to the slippery body of the female. It is a much more
unusual circumstance that the females of some water-beetles
Fig. 8. Crabro cribrarius. Upper figure,
male: lower figure, female.
(Dytiscus) have their
elytra deeply grooved, and
in Acilius sulcatus thickly set
with hairs, as an aid to the
male. The females of some
other water-beetles (Hydroporus)
have their elytra
punctured for the same object.432
In the male of Crabro
cribrarius (fig. 8.), it is the
tibia which is dilated into a
broad horny plate, with minute
membraneous dots, giving
to it a singular appearance
like that of a riddle.433
In the male of Penthe (a
genus of beetles) a few of
the middle joints of the antennæ
are dilated and furnished on the inferior surface
344with cushions of hair, exactly like those on the tarsi of
the Carabidæ, “and obviously for the same end.” In
male dragon-flys, “the appendages at the tip of the tail
are modified in an almost infinite variety of curious
patterns to enable them to embrace
the neck of the female.” Lastly in
the males of many insects, the legs
are furnished with peculiar spines,
knobs or spurs; or the whole leg is
bowed or thickened, but this is by
no means invariably a sexual character;
Fig. 9. Taphroderes distortus
(much enlarged). Upper
figure, male; lower figure,
female.
or one pair, or all three
pairs are elongated, sometimes to
an extravagant length.434
The front leg tarsi of many male beetles are widened or have broad patches of hair, and in various types of water beetles, they possess a round flat suction cup, allowing the male to cling to the slippery body of the female. It’s much rarer that the females of some water beetles (Dytiscus) have their elytra deeply grooved, or, in the case of *Acilius sulcatus*, densely covered with hair to assist the male. The females of some other water beetles (Hydroporus) also have their elytra punctured for the same purpose.432 In the male of *Crabro cribrarius* (fig. 8.), the tibia is expanded into a broad, horny plate with tiny, membranous dots that make it look like a riddle.433 In the male of Penthe (a genus of beetles), a few of the middle segments of the antennae are widened and have patches of hair on the underside, similar to those on the tarsi of Carabidæ, “and obviously for the same purpose.” In male dragonflies, “the appendages at the tip of the tail are shaped in an almost endless variety of unique patterns to help them grasp the female's neck.” Finally, many male insects have legs equipped with unusual spines, knobs, or spurs; or the entire leg may be bent or thickened, but this is not consistently a sexual trait;
Fig. 9. Taphroderes distortus
(greatly enlarged). Top
image, male; bottom image,
female.
or one pair, or all three pairs of legs may be elongated, sometimes to a striking length.434
In all the orders, the sexes of many species present differences, of which the meaning is not understood. One curious case is that of a beetle (fig. 9), the male of which has the left mandible much enlarged; so that the mouth is greatly distorted. In another Carabidous beetle, the Eurygnathus,435 we have the unique case, as far as known to Mr. Wollaston, of the head of the female being much broader and larger, though in a variable degree, than that of the male. Any number of such cases could be given. They abound in the Lepidoptera: one of the most extraordinary is that certain male butterflies have their fore-legs more or 345less atrophied, with the tibiæ and tarsi reduced to mere rudimentary knobs. The wings, also, in the two sexes often differ in neuration,436 and sometimes considerably in outline, as in the Aricoris epitus, which was shown to me in the British Museum by Mr. A. Butler. The males of certain South American butterflies have tufts of hair on the margins of the wings, and horny excrescences on the discs of the posterior pair.437 In several British butterflies, the males alone, as shewn by Mr. Wonfor, are in parts clothed with peculiar scales.
In all groups, the sexes of many species show differences that we don’t fully understand. One interesting example is a beetle (fig. 9) where the male has a significantly enlarged left mandible, which distorts its mouth. In another kind of ground beetle, the Eurygnathus,435 there’s a unique situation, as noted by Mr. Wollaston, where the female’s head is much broader and larger, though to varying degrees, than that of the male. Many such examples could be cited. They are common in butterflies: one of the most remarkable is that some male butterflies have their front legs mostly atrophied, with their tibiae and tarsi reduced to tiny knobs. The wings also often differ between the sexes in structure,436 and sometimes quite a bit in shape, as seen in the Aricoris epitus, which Mr. A. Butler showed me at the British Museum. The males of certain South American butterflies have tufts of hair along the edges of their wings and hard growths on the discs of the hind wings.437 In several British butterflies, only the males, as shown by Mr. Wonfor, have special scales in certain areas.
The purpose of the luminosity in the female glow-worm is likewise not understood; for it is very doubtful whether the primary use of the light is to guide the male to the female. It is no serious objection to this latter belief that the males emit a feeble light; for secondary sexual characters proper to one sex are often developed in a slight degree in the other sex. It is a more valid objection that the larvæ shine, and in some species brilliantly: Fritz Müller informs me that the most luminous insect which he ever beheld in Brazil, was the larva of some beetle. Both sexes of certain luminous species of Elater emit light. Kirby and Spence suspect that the phosphorescence serves to frighten and drive away enemies.
The purpose of the glow in female glow-worms isn't fully understood; it's uncertain if the light primarily helps guide males to females. The fact that males also emit a faint light doesn’t strongly oppose this idea, as secondary sexual traits can sometimes appear to a small extent in the other sex. A more compelling counterpoint is that the larvae also glow, and in some cases, quite brightly: Fritz Müller told me that the most luminous insect he saw in Brazil was the larva of a beetle. Both males and females of certain luminous species of Elater emit light. Kirby and Spence believe that the glow may help scare off predators.
Difference in Size between the Sexes.—With insects of all kinds the males are commonly smaller than the females;438 and this difference can often be detected even in the larval state. So considerable is the difference 346between the male and female cocoons of the silk-moth (Bombyx mori), that in France they are separated by a particular mode of weighing.439 In the lower classes of the animal kingdom, the greater size of the females seems generally to depend on their developing an enormous number of ova; and this may to a certain extent hold good with insects. But Dr. Wallace has suggested a much more probable explanation. He finds, after carefully attending to the development of the caterpillars of Bombyx cynthia and Yamamai, and especially of some dwarfed caterpillars reared from a second brood on unnatural food, “that in proportion as the individual moth is finer, so is the time required for its metamorphosis longer; and for this reason the female, which is the larger and heavier insect, from having to carry her numerous eggs, will be preceded by the male, which is smaller and has less to mature.”440 Now as most insects are short-lived, and as they are exposed to many dangers, it would manifestly be advantageous to the female to be impregnated as soon as possible. This end would be gained by the males being first matured in large numbers ready for the advent of the females; and this again would naturally follow, as Mr. A. E. Wallace has remarked,441 through natural selection; for the smaller males would be first matured, and thus would procreate a large number of offspring which would inherit the reduced size of their male parents, whilst the larger males from being matured later would leave fewer offspring.
Difference in Size between the Sexes.—In insects of all types, males are usually smaller than females;438 and this difference can often be seen even in the larval stage. The difference is so notable between the male and female cocoons of the silk moth (Bombyx mori) that in France, they are distinguished by a specific weighing method.439 In the lower levels of the animal kingdom, the larger size of the females generally appears to result from their producing a vast number of eggs; and this might also be somewhat true for insects. However, Dr. Wallace has proposed a more likely explanation. He notes that after closely observing the development of the caterpillars of Bombyx cynthia and Yamamai, especially some stunted caterpillars grown from a second brood on unnatural food, “the finer the individual moth, the longer the time it takes to undergo metamorphosis; and for this reason, the female, being the larger and heavier insect, needs to carry her many eggs, so she will be preceded by the smaller male, which has less to develop.”440 Since most insects have short lifespans and face numerous dangers, it would clearly benefit the female to be fertilized as quickly as possible. This could be achieved by having the males mature first and in large numbers to be ready for the females; and this would naturally happen, as Mr. A. E. Wallace pointed out,441 through natural selection; the smaller males would mature first, thus producing a large number of offspring that would inherit the smaller size of their male parents, while the larger males, maturing later, would have fewer offspring.
There are, however, exceptions to the rule of male insects being smaller than the females; and some of 347these exceptions are intelligible. Size and strength would be an advantage to the males, which fight for the possession of the female; and in these cases the males, as with the stag-beetle (Lucanus), are larger than the females. There are, however, other beetles which are not known to fight together, of which the males exceed the females in size; and the meaning of this fact is not known; but in some of these cases, as with the huge Dynastes and Megasoma, we can at least see that there would be no necessity for the males to be smaller than the females, in order to be matured before them, for these beetles are not short-lived, and there would be ample time for the pairing of the sexes. So, again, male dragon-flies (Libellulidæ) are sometimes sensibly larger, and never smaller, than the females;442 and they do not, as Mr. MacLachlan believes, generally pair with the females, until a week or fortnight has elapsed, and until they have assumed their proper masculine colours. But the most curious case, shewing on what complex and easily-overlooked relations, so trifling a character as a difference in size between the sexes may depend, is that of the aculeate Hymenoptera; for Mr. F. Smith informs me that throughout nearly the whole of this large group the males, in accordance with the general rule, are smaller than the females and emerge about a week before them; but amongst the Bees, the males of Apis mellifica, Anthidium manicatum and Anthophora acervorum, and amongst the Fossores, the males of the Methoca ichneumonides, are larger than the females. The explanation of this anomaly is that a marriage-flight is absolutely necessary 348with these species, and the males require great strength and size in order to carry the females through the air. Increased size has here been acquired in opposition to the usual relation between size and the period of development, for the males, though larger, emerge before the smaller females.
There are, however, exceptions to the rule that male insects are smaller than females, and some of these exceptions make sense. Larger size and strength would benefit males, particularly when they fight for the attention of females. In such cases, like with the stag beetle (Lucanus), males are bigger than females. There are also other beetles that don't fight each other, where males are larger than females, and the reason for this is unclear. However, in some cases, such as with the massive Dynastes and Megasoma, it’s evident that males don’t need to be smaller than females to mature before them, because these beetles aren’t short-lived, allowing plenty of time for mating. Similarly, male dragonflies (Libellulidae) are sometimes noticeably larger, and they are never smaller than females; according to Mr. MacLachlan, they usually don’t pair with females until a week or two has passed, and until they display their full male coloration. The most interesting case showing how seemingly trivial size differences between sexes can depend on complex and often overlooked relationships is with the aculeate Hymenoptera. Mr. F. Smith tells me that almost throughout this entire large group, males, following the usual rule, are smaller than females and emerge about a week before them. However, among bees, the males of Apis mellifica, Anthidium manicatum, and Anthophora acervorum, as well as among the Fossores, the males of Methoca ichneumonides, are larger than the females. This anomaly arises because a mating flight is crucial for these species, and the males need to be strong and big enough to carry the females through the air. In these cases, increased size has developed contrary to the typical relationship between size and developmental timing, as the males, though larger, emerge before the smaller females.
We will now review the several Orders, selecting such facts as more particularly concern us. The Lepidoptera (Butterflies and Moths) will be retained for a separate chapter.
We will now review the various Orders, picking out the facts that are most relevant to us. The Lepidoptera (Butterflies and Moths) will be covered in a separate chapter.
Order, Thysanura.—The members of this Order are lowly organised for their class. They are wingless, dull-coloured, minute insects, with ugly, almost misshapen heads and bodies. The sexes do not differ; but they offer one interesting fact, by showing that the males pay sedulous court to their females even low down in the animal scale. Sir J. Lubbock443 in describing the Smynthurus luteus, says: “it is very amusing to see these little creatures coquetting together. The male, which is much smaller than the female, runs round her, and they butt one another, standing face to face, and moving backward and forward like two playful lambs. Then the female pretends to run away and the male runs after her with a queer appearance of anger, gets in front and stands facing her again; then she turns coyly round, but he, quicker and more active, scuttles round too, and seems to whip her with his antennæ; then for a bit they stand face to face, play with their antennæ, and seem to be all in all to one another.”
Order, Thysanura.—The members of this Order are less complex for their class. They are small, wingless, dull-colored insects with awkward, almost misshapen heads and bodies. There’s no difference between the sexes, but one interesting fact is that the males are very attentive in courting their females, even at such a basic level in the animal kingdom. Sir J. Lubbock443 describes the Smynthurus luteus by saying: “it’s quite amusing to watch these little creatures flirting with each other. The male, which is much smaller than the female, runs around her, and they butt heads while standing face to face, moving back and forth like two playful lambs. Then the female pretends to run away, and the male chases her with a funny look of anger, gets in front, and faces her again; then she shyly turns away, but he, quicker and more agile, scuttles around too, seeming to flick her with his antennae; then for a moment, they stand face to face, play with their antennae, and appear to be everything to one another.”
Order, Diptera (Flies).—The sexes differ little in colour. The greatest difference, known to Mr. F. Walker, 349is in the genus Bibio, in which the males are blackish or quite black, and the females obscure brownish-orange. The genus Elaphomyia, discovered by Mr. Wallace444 in New Guinea, is highly remarkable, as the males are furnished with horns, of which the females are quite destitute. The horns spring from beneath the eyes, and curiously resemble those of stags, being either branched or palmated. They equal in length the whole of the body in one of the species. They might be thought to serve for fighting, but as in one species they are of a beautiful pink colour, edged with black, with a pale central stripe, and as these insects have altogether a very elegant appearance, it is perhaps more probable that the horns serve as ornaments. That the males of some Diptera fight together is certain; for Prof. Westwood445 has several times seen this with some species of Tipula or Harry-long-legs. Many observers believe that when gnats (Culicidæ) dance in the air in a body, alternately rising and falling, the males are courting the females. The mental faculties of the Diptera are probably fairly well developed, for their nervous system is more highly developed than in most other Orders of insects.446
Order, Diptera (Flies).—The males and females are pretty similar in color. The biggest difference, noted by Mr. F. Walker, is in the genus Bibio, where the males are blackish or fully black, while the females are a dull brownish-orange. The genus Elaphomyia, discovered by Mr. Wallace in New Guinea, is particularly interesting because the males have horns that the females completely lack. These horns emerge from just below the eyes and oddly resemble stag horns, being either branched or palm-shaped. In one species, the horns are as long as the entire body. They might seem to be used for fighting, but since in one species they are a beautiful pink with black edges and a pale central stripe, and since these insects are very elegantly shaped overall, it's more likely that the horns are ornamental. It's certain that males of some Diptera engage in fights, as Prof. Westwood has repeatedly observed this in certain species of Tipula, or crane flies. Many observers believe that when gnats (Culicidæ) swarm and dance in the air, rising and falling, the males are trying to attract females. The mental abilities of Diptera are likely quite developed, as their nervous system is more advanced than in most other insect Orders.
Order, Hemiptera (Field-Bugs).—Mr. J. W. Douglas, who has particularly attended to the British species, has kindly given me an account of their sexual differences. The males of some species are furnished with wings, whilst the females are wingless; the sexes differ in the form of the body and elytra; in the second joints of their antennæ and in their tarsi; but as the signification 350of these differences is quite unknown, they may be here passed over. The females are generally larger and more robust than the males. With British, and, as far as Mr. Douglas knows, with exotic species, the sexes do not commonly differ much in colour; but in about six British species the male is considerably darker than the female, and in about four other species the female is darker than the male. Both sexes of some species are beautifully marked with vermilion and black. It is doubtful whether these colours serve as a protection. If in any species the males had differed from the females in an analogous manner, we might have been justified in attributing such conspicuous colours to sexual selection with transference to both sexes.
Order, Hemiptera (Field-Bugs).—Mr. J. W. Douglas, who has specifically focused on the British species, has kindly provided me with details about their sexual differences. Males of some species have wings, while females do not; the sexes vary in body shape and elytra; in the second segments of their antennae and in their tarsi; but since the meaning of these differences is completely unknown, we can skip over them here. Females are generally larger and more robust than males. With British species, and as far as Mr. Douglas knows, with exotic species as well, the sexes usually don't differ much in color. However, in about six British species, the male is significantly darker than the female, and in about four other species, the female is darker than the male. Both sexes of some species are beautifully marked with red and black. It's unclear whether these colors provide any protection. If in any species the males had differed from the females in a similar way, we could have reasonably attributed such striking colors to sexual selection applied to both sexes.
Some species of Reduvidæ make a stridulating noise; and, in the case of Pirates stridulus, this is said447 to be effected by the movement of the neck within the pro-thoracic cavity. According to Westring, Reduvius personatus also stridulates. But I have not been able to learn any particulars about these insects; nor have I any reason to suppose that they differ sexually in this respect.
Some species of Reduvidæ make a chirping noise; and for Pirates stridulus, it's said447 that this is caused by the movement of the neck within the pro-thoracic cavity. According to Westring, Reduvius personatus also makes a chirping sound. However, I haven't been able to find any specific information about these insects, nor do I have any reason to believe that they differ by sex in this regard.
Order, Homoptera.—Every one who has wandered in a tropical forest must have been astonished at the din made by the male Cicadæ. The females are mute; as the Grecian poet Xenarchus says, “Happy the Cicadas live, since they all have voiceless wives.” The noise thus made could be plainly heard on board the “Beagle,” when anchored at a quarter of a mile from the shore of Brazil; and Captain Hancock says it can be heard at the distance of a mile. The Greeks formerly kept, and the Chinese now keep, these insects 351in cages for the sake of their song, so that it must be pleasing to the ears of some men.448 The Cicadidæ usually sing during the day; whilst the Fulgoridæ appear to be night-songsters. The sound, according to Landois,449 who has recently studied the subject, is produced by the vibration of the lips of the spiracles, which are set into motion by a current of air emitted from the tracheæ. It is increased by a wonderfully complex resounding apparatus, consisting of two cavities covered by scales. Hence the sound may truly be called a voice. In the female the musical apparatus is present, but very much less developed than in the male, and is never used for producing sound.
Order, Homoptera.—Anyone who has explored a tropical forest must have been amazed by the noise made by male cicadas. The females are silent; as the Greek poet Xenarchus said, “Blessed are the cicadas, since they all have silent wives.” The noise could clearly be heard on board the “Beagle,” even when anchored a quarter of a mile from the shore of Brazil; Captain Hancock states it can be heard from a mile away. The Greeks once kept these insects, and the Chinese still do, in cages for their song, showing that it must be pleasing to some people's ears.351 The Cicadidae typically sing during the day, while the Fulgoridae seem to be night singers. According to Landois, who recently studied this, the sound is created by the vibration of the lips of the spiracles, set into motion by an airflow from the tracheae. This sound is amplified by a remarkably complex resonating system made up of two cavities covered by scales. Therefore, the sound can truly be called a voice. In females, the musical system is present, but it is much less developed than in males and is never used to produce sound.
With respect to the object of the music, Dr. Hartman in speaking of the Cicada septemdecim of the United States, says,450 “the drums are now (June 6th and 7th, 1851) heard in all directions. This I believe to be the marital summons from the males. Standing in thick chestnut sprouts about as high as my head, where hundreds were around me, I observed the females coming around the drumming males.” He adds, “this season (Aug. 1868) a dwarf pear-tree in my garden produced about fifty larvæ of Cic. pruinosa; and I several times noticed the females to alight near a male while he was uttering his clanging notes.” Fritz Müller writes to me from S. Brazil that he has often listened to a musical contest between two or three males of a Cicada, having a particularly loud voice, and seated at a considerable distance from each other. As 352soon as the first had finished his song, a second immediately began; and after he had concluded, another began, and so on. As there is so much rivalry between the males, it is probable that the females not only discover them by the sounds emitted, but that, like female birds, they are excited or allured by the male with the most attractive voice.
Regarding the purpose of the music, Dr. Hartman talks about the Cicada septemdecim of the United States, saying,450 “the drums can now be heard in all directions (June 6th and 7th, 1851). I believe this is a mating call from the males. Standing among thick chestnut sprouts that were about as high as my head, with hundreds around me, I noticed the females approaching the drumming males.” He also mentions, “this season (Aug. 1868) a dwarf pear-tree in my garden produced about fifty larvae of Cic. pruinosa; and I saw several times that the females landed near a male while he was making his loud calls.” Fritz Müller writes to me from South Brazil that he has often listened to a musical competition between two or three male Cicadas with particularly loud voices, situated at a considerable distance from one another. As soon as the first finished its song, the second immediately started; and after he finished, another began, and so on. Since there is significant competition among the males, it’s likely that the females not only hear them through the sounds they make, but that, similar to female birds, they are attracted or drawn to the male with the most appealing voice.
I have not found any well-marked cases of ornamental differences between the sexes of the Homoptera. Mr. Douglas informs me that there are three British species, in which the male is black or marked with black bands, whilst the females are pale-coloured or obscure.
I haven't come across any clear cases of noticeable differences in appearance between male and female Homoptera. Mr. Douglas tells me that there are three British species where the males are black or have black bands, while the females are lighter or less distinct.
Order, Orthoptera.—The males in the three saltatorial
families belonging to this Order are remarkable
for their musical powers, namely the Achetidæ or
crickets, the Locustidæ for which there is no exact
equivalent name in English, and the Acridiidæ or grasshoppers.
The stridulation produced by some of the
Locustidæ is so loud that it can be heard during the
night at the distance of a mile;451 and that made by
certain species is not unmusical even to the human
ear, so that the Indians on the Amazons keep them
in wicker cages. All observers agree that the sounds
serve either to call or excite the mute females. But it
has been noticed452 that the male migratory locust of
Russia (one of the Acridiidæ) whilst coupled with the
female, stridulates from anger or jealousy when approached
by another male. The house-cricket when
surprised at night uses its voice to warn its fellows.453 In
North America the Katy-did (Platyphyllum concavum,
353one of the Locustidæ) is described454 as mounting on the
upper branches of a tree, and in the evening beginning
“his noisy babble, while rival notes issue from the neighbouring
trees, and the groves resound with the call of
Katy-did-she-did, the live-long night.” Mr. Bates, in
speaking of the European field-cricket (one of the Achetidæ),
says, “the male has been observed to place itself
in the evening at the entrance of its burrow, and
stridulate until a female approaches, when the louder
notes are succeeded by a more subdued tone, whilst
the successful musician caresses with his antennæ
Fig. 10. Gryllus campestris (from Landois).
Right-hand figure, under side of part of the
wing-nervure, much magnified, showing
the teeth, st.
Left-hand figure, upper surface of wing-cover,
with the projecting, smooth nervure, r.,
across which the teeth (st) are scraped.
the mate he has won.”455
Dr. Scudder was able to
excite one of these insects
to answer him, by rubbing
on a file with a quill.456
In both sexes a remarkable
auditory apparatus
has been discovered by
Von Siebold, situated in
the front legs.457
Order, Orthoptera.—The males in the three jumping families in this Order are notable for their musical abilities: the Achetidæ or crickets, the Locustidæ which doesn’t have a direct equivalent in English, and the Acridiidæ or grasshoppers. The stridulation made by some of the Locustidæ is so loud that it can be heard at night up to a mile away; 451 and some species produce sounds that are actually pleasant to human ears, which is why indigenous people in the Amazon keep them in wicker cages. Observers agree that these sounds either attract or stimulate the silent females. However, it's been noted 452 that the male migratory locust of Russia (one of the Acridiidæ) will stridulate out of anger or jealousy when another male approaches while he's with a female. The house-cricket warns its fellow crickets with its voice when startled at night. 453 In North America, the Katy-did (Platyphyllum concavum, 353one of the Locustidæ) is noted 454 for climbing to the top branches of a tree and starting “his noisy chatter in the evening, while competing sounds come from the nearby trees, filling the groves with the call of Katy-did-she-did all night long.” Mr. Bates mentions the European field-cricket (one of the Achetidæ), stating, “the male has been seen at night at the entrance of its burrow, stridulating until a female comes close, at which point the louder notes turn into a softer tone, while the successful musician gently touches his mate with his antennae.
Fig. 10. Gryllus campestris (from Landois).
The right figure shows the underside of part of the wing nerve, highly magnified, revealing the teeth, st.
The left figure displays the upper surface of the wing cover, featuring the smooth, raised nerve, r, where the teeth (st) are scraped.
Dr. Scudder managed to get one of these insects to respond by rubbing on a file with a quill. 456 Both male and female crickets have a unique auditory system located in their front legs discovered by Von Siebold. 457
In the three Families
the sounds are differently
produced. In the males Of
the Achetidæ both wing-covers
have the same
structure; and this in the
field-cricket (Gryllus campestris, fig. 10) consists, as de354scribed
by Landois,458 of from 131 to 138 sharp, transverse
ridges or teeth (st) on the under side of one of the
nervures of the wing-cover. This toothed nervure is
rapidly scraped across a projecting, smooth, hard nervure
(r) on the upper surface of the opposite wing. First
Fig. 11. Teeth of Nervure
of Gryllus domesticus
(from Landois).
one wing is rubbed over the other,
and then the movement is reversed.
Both wings are raised a little at the
same time, so as to increase the resonance.
In some species the wing-covers
of the males are furnished at
the base with a talc-like plate.459 I
have here given a drawing (fig. 11)
of the teeth on the under side of the
nervure of another species of Gryllus,
viz. G. domesticus.
In the three families, the sounds are produced in different ways. In male Achetidæ, both wing covers have the same structure, and for the field cricket (Gryllus campestris, fig. 10), this consists of 131 to 138 sharp, transverse ridges or teeth (st) on the underside of one of the wing cover's nervures, as described by Landois. This toothed nervure is quickly scraped against a smooth, hard nervure (r) on the upper surface of the opposite wing. First, one wing is rubbed over the other, and then the movement is reversed. Both wings are slightly raised at the same time to enhance the resonance. In some species, the wing covers of the males have a talc-like plate at the base. Here is a drawing (fig. 11) of the teeth on the underside of the nervure of another species of Gryllus, namely G. domesticus.
In the Locustidæ the opposite wing-covers differ in structure (fig. 12), and cannot, as in the last family, be indifferently used in a reversed manner. The left wing, which acts as the bow of the fiddle, lies over the right wing which serves as the fiddle itself. One of the nervures (a) on the under surface of the former is finely serrated, and is scraped across the prominent nervures on the upper surface of the opposite or right wing. In our British Phasgonura viridissima it appeared to me that the serrated nervure is rubbed against the rounded hind corner of the opposite wing, the edge of which is thickened, coloured brown, and very sharp. In the right wing, but not in the left, there is a little plate, as transparent as talc, surrounded by nervures, and called the speculum. In Ephippiger vitium, a member of this same family, we have a curious 355subordinate modification; for the wing-covers are greatly reduced in size, but “the posterior part of the pro-thorax is elevated into a kind of dome over the wing-covers, and which has probably the effect of increasing the sound.”460
In the Locustidae, the two wing covers have different structures (fig. 12) and can't be used interchangeably like in the last family. The left wing, which works like the bow of a fiddle, sits over the right wing, which acts as the fiddle itself. One of the veins (a) on the underside of the left wing is finely serrated and scrapes against the prominent veins on the upper side of the right wing. In our British Phasgonura viridissima, it seemed to me that the serrated vein rubs against the rounded back corner of the right wing, the edge of which is thickened, brown, and very sharp. The right wing has a small, transparent plate, as clear as talc, surrounded by veins, called the speculum. In Ephippiger vitium, a member of this same family, there's an interesting subordinate modification; the wing covers are significantly reduced in size, but "the back part of the prothorax is raised into a sort of dome over the wing covers, which probably enhances the sound."460

Fig. 12. Chlorocœlus Tanana (from Bates), a, b. Lobes of opposite wing-covers.
Fig. 12. Chlorocœlus Tanana (from Bates), a, b. Lobes of opposite wing covers.
We thus see that the musical apparatus is more differentiated or specialised in the Locustidæ, which includes I believe the most powerful performers in the Order, than in the Achetidæ, in which both wing-covers have the same structure and the same function.461 Landois, however, detected in one of the Locustidæ, namely in Decticus, a short and narrow row of small 356teeth, mere rudiments, on the inferior surface of the right wing-cover, which underlies the other and is never used as the bow. I observed the same rudimentary structure on the under side of the right wing-cover in Phasgonura viridissima. Hence we may with confidence infer that the Locustidæ are descended from a form, in which, as in the existing Achetidæ, both wing-covers had serrated nervures on the under surface, and could be indifferently used as the bow; but that in the Locustidæ the two wing-covers gradually became differentiated and perfected, on the principle of the division of labour, the one to act exclusively as the bow and the other as the fiddle. By what steps the more simple apparatus in the Achetidæ originated, we do not know, but it is probable that the basal portions of the wing-covers overlapped each other formerly as at present, and that the friction of the nervures produced a grating sound, as I find is now the case with the wing-covers of the females.462 A grating sound thus occasionally and accidentally made by the males, if it served them ever so little as a love-call to the females, might readily have been intensified through sexual selection by fitting variations in the roughness of the nervures having been continually preserved.
We can see that the sound-making mechanism is more specialized in the Locustidae, which I believe includes the most powerful performers in this group, than in the Achetidæ, where both wing covers have the same structure and function.461 However, Landois discovered a short and narrow row of small356 teeth, just remnants, on the underside of the right wing cover of one of the Locustidae, specifically in Decticus, which is beneath the other and is never used as the bow. I noticed the same rudimentary structure on the underside of the right wing cover in Phasgonura viridissima. Therefore, we can confidently infer that the Locustidae evolved from a form where, like the current Achetidæ, both wing covers had serrated veins on the underside and could be used interchangeably as the bow; but in the Locustidae, the two wing covers gradually became specialized and perfected, based on the principle of division of labor, with one acting exclusively as the bow and the other as the fiddle. We don't know the exact process by which the simpler mechanism in the Achetidæ originated, but it's likely that the base parts of the wing covers used to overlap each other as they do now, and that the friction of the veins produced a grating sound, similar to what I observe with the wing covers of the females.462 A grating sound occasionally made by the males, if it served even a little as a love call to the females, might have been enhanced through sexual selection, with variations in the roughness of the veins being continually retained.
In the last and third Family, namely the Acridiidæ
or grasshoppers, the stridulation is produced in a very
different manner, and is not so shrill, according to Dr.
Scudder, as in the preceding Families. The inner surface
of the femur (fig. 13, r) is furnished with a longitudinal
row of minute, elegant, lancet-shaped, elastic
teeth, from 85 to 93 in number;463 and these are scraped
357across the sharp, projecting nervures on the wing-covers,
which, are thus made to vibrate and resound. Harris464
Fig. 13, Hind-leg of Stenobothrus pratorum:
r, the stridulating ridge; lower figure, the
teeth, forming the ridge, much magnified
(from Landois).
says that when one of
the males begins to play,
he first “bends the shank
of the hind-leg beneath,
the thigh, where it is
lodged in a furrow designed
to receive it,
and then draws the leg
briskly up and down.
He does not play both
fiddles together, but alternately
first upon one
and then on the other.”
In many species, the base
of the abdomen is hollowed out into a great cavity
which is believed to act as a resounding board. In
Pneumora (fig. 14), a S. African genus belonging to
this same family, we meet with a new and remarkable
modification: in the males a small notched ridge projects
obliquely from each side of the abdomen, against
which the hind femora are rubbed.465 As the male is
furnished with wings, the female being wingless, it is
remarkable that the thighs are not rubbed in the usual
manner against the wing-covers; but this may perhaps
be accounted for by the unusually small size of the hind-legs.
I have not been able to examine the inner
surface of the thighs, which, judging from analogy,
would be finely serrated. The species of Pneumora
have been more profoundly modified for the sake of
stridulation than any other orthopterous insect; for
358in the male the whole body has been converted into a
musical instrument, being distended with air, like a
great pellucid bladder, so as to increase the resonance.
Mr. Trimen informs me that at the Cape of Good Hope
these insects make a wonderful noise during the night
There is one exception to the rule that the females
in these three Families are destitute of an efficient
musical apparatus; for both sexes of Ephippiger (Locustidæ)
are said466 to be thus provided. This case may
359be compared with that of the reindeer, in which species
alone both sexes possess horns. Although the female
orthoptera are thus almost invariably mute, yet Landois467
found rudiments of the stridulating organs on the femora
of the female Acridiidæ, and similar rudiments on the
under surface of the wing-covers of the female Achetidæ;
but he failed to find any rudiments in the females
of Decticus, one of the Locustidæ. In the Homoptera
the mute females of Cicada, have the proper musical
apparatus in an undeveloped state; and we shall hereafter
meet in other divisions of the animal kingdom with
innumerable instances of structures proper to the male
being present in a rudimentary condition in the female.
Such cases appear at first sight to indicate that both
sexes were primordially constructed in the same manner,
but that certain organs were subsequently lost by the
females. It is, however, a more probable view, as previously
explained, that the organs in question were
acquired by the males and partially transferred to the
females.
In the last and third family, the Acridiidæ or grasshoppers, the way they produce sound is quite different and isn’t as high-pitched, according to Dr. Scudder, as in the previous families. The inner surface of the femur (fig. 13, r) has a longitudinal row of small, elegant, lancet-shaped, elastic teeth, numbering between 85 to 93;463 and these teeth are scraped against the sharp, projecting veins on the wing covers, causing them to vibrate and make sound. Harris464 says that when a male starts to play, he first “bends the shank of the hind leg beneath the thigh, where it fits into a groove designed for it, and then quickly moves the leg up and down. He doesn’t play both legs at once, but alternates between one and then the other.” In many species, the base of the abdomen is hollowed out into a large cavity, which is thought to serve as a resonating chamber. In Pneumora (fig. 14), a South African genus in this family, there’s an interesting modification: in males, a small notched ridge sticks out diagonally from each side of the abdomen, which the hind femora rub against.465 Since the males have wings and the females do not, it’s surprising that the thighs aren’t rubbed against the wing covers in the usual way; this might be due to the hind legs being unusually small. I haven't been able to examine the inside of the thighs, which, based on similar species, would probably have fine serrations. Pneumora species have undergone more modifications for sound production than any other orthopteran insect; in the males, the entire body has been transformed into a musical instrument, inflated with air like a large clear bladder, to enhance the resonance. Mr. Trimen tells me that at the Cape of Good Hope, these insects make an amazing noise at night. There is one exception to the rule that females in these three families lack an effective sound-producing mechanism; both sexes of Ephippiger (Locustidæ) are reported466 to be equipped this way. This case can be compared to reindeer, where only this species has both sexes with horns. Although female orthopterans are generally silent, Landois467 found remnants of sound-producing organs on the femora of female Acridiidæ, and similar remnants on the undersides of the wing covers of female Achetidæ; however, he did not find any remnants in the females of Decticus, one of the Locustidæ. In the Homoptera, the silent females of Cicada have the appropriate sound-producing organs in an undeveloped form; and we will encounter numerous instances in other parts of the animal kingdom where male-specific structures exist in a rudimentary form in females. At first glance, such cases seem to indicate that both sexes were initially designed in the same way but that certain organs were later lost in females. However, it is more likely, as previously noted, that the organs in question were developed in males and partially transferred to females.

Fig. 14. Pneumora (from specimens in the British Museum). Upper figure, male; lower figure, female.
Fig. 14. Pneumora (from specimens in the British Museum). Upper figure, male; lower figure, female.
Landois has observed another interesting fact, namely that in the females of the Acridiidæ, the stridulating teeth on the femora remain throughout life in the same condition in which they first appear in both sexes during the larval state. In the males, on the other hand, they become fully developed and acquire their perfect structure at the last moult, when the insect is mature and ready to breed.
Landois noticed another interesting fact: in female Acridiidæ, the stridulating teeth on the femora stay in the same condition throughout their lives as they appear during the larval stage in both sexes. In males, however, these teeth fully develop and reach their final structure at the last molt, when the insect is mature and ready to reproduce.
From the facts now given, we see that the means by which the males produce their sounds are extremely diversified in the Orthoptera, and are altogether different from those employed by the Homoptera. But throughout the animal kingdom we incessantly find the 360same object gained by the most diversified means; this being due to the whole organisation undergoing in the course of ages multifarious changes; and as part after part varies, different variations are taken advantage of for the same general purpose. The diversification of the means for producing sound in the three families of the Orthoptera and in the Homoptera, impresses the mind with the high importance of these structures to the males, for the sake of calling or alluring the females. We need feel no surprise at the amount of modification which the Orthoptera have undergone in this respect, as we now know, from Dr. Scudder’s remarkable discovery,468 that there has been more than ample time. This naturalist has lately found a fossil insect in the Devonian formation of New Brunswick, which is furnished with “the well-known tympanum or stridulating apparatus of the male Locustidæ.” This insect, though in most respects related to the Neuroptera, appears to connect, as is so often the case with very ancient forms, the two Orders of the Neuroptera and Orthoptera which are now generally ranked as quite distinct.
From the information now provided, we can see that the ways in which males produce their sounds are highly varied in the Orthoptera and are completely different from those used by the Homoptera. However, throughout the animal kingdom, we consistently find the same goal achieved through a variety of methods; this is due to the entire structure of organisms undergoing many changes over ages. As parts change, different variations are utilized for the same general purpose. The diversity in sound production methods in the three families of Orthoptera and in the Homoptera highlights the significant importance of these structures to males for attracting or calling females. We shouldn't be surprised by the extent of modification that Orthoptera have undergone in this regard, as we now know, thanks to Dr. Scudder’s remarkable discovery, that there has been plenty of time for these changes. This naturalist has recently discovered a fossil insect in the Devonian formation of New Brunswick that has “the well-known tympanum or stridulating apparatus of the male Locustidae.” This insect, although related to the Neuroptera in many ways, seems to connect, as often happens with very old forms, the two orders of Neuroptera and Orthoptera which are now typically considered quite distinct.
I have but little more to say on the Orthoptera. Some of the species are very pugnacious: when two male field-crickets (Gryllus campestris) are confined together, they fight till one kills the other; and the species of Mantis are described as manœuvring with their sword-like front-limbs, like hussars with their sabres. The Chinese keep these insects in little bamboo cages and match them like game-cocks.469 With respect to colour, some exotic locusts are beautifully ornamented; the posterior wings being marked with red, 361blue, and black; but as throughout the Order the two sexes rarely differ much in colour, it is doubtful whether they owe these bright tints to sexual selection. Conspicuous colours may be of use to these insects as a protection, on the principle to be explained in the next chapter, by giving notice to their enemies that they are unpalatable. Thus it has been observed470 that an Indian brightly-coloured locust was invariably rejected when offered to birds and lizards. Some cases, however, of sexual differences in colour in this Order are known. The male of an American cricket471 is described as being as white as ivory, whilst the female varies from almost white to greenish-yellow or dusky. Mr. Walsh informs me that the adult male of Spectrum femoratum (one of the Phasmidæ) “is of a shining brownish-yellow colour; the adult female being of a dull, opaque, cinereous-brown; the young of both sexes being green.” Lastly, I may mention that the male of one curious kind of cricket472 is furnished with “a long membranous appendage, which falls over the face like a veil;” but whether this serves as an ornament is not known.
I have a little more to say about Orthoptera. Some species are quite aggressive: when two male field crickets (Gryllus campestris) are placed together, they fight until one kills the other; and Mantis species are described as maneuvering with their sword-like front limbs, like hussars wielding their sabers. The Chinese keep these insects in small bamboo cages and match them like fighting cocks.469 Regarding color, some exotic locusts are beautifully adorned; their hind wings feature red, blue, and black markings; however, since the two sexes in this order rarely differ much in color, it’s uncertain if these bright hues are a result of sexual selection. Bright colors may serve as protection for these insects by signaling to their predators that they are unpalatable, a principle that will be discussed in the next chapter. For instance, it has been noted470 that a brightly colored locust in India is consistently rejected by birds and lizards. There are some known cases of sexual color differences within this order. The male of an American cricket471 is said to be as white as ivory, while the female ranges from nearly white to greenish-yellow or dusky. Mr. Walsh informs me that the adult male of Spectrum femoratum (one of the Phasmidæ) “is a shiny brownish-yellow, while the adult female is a dull, opaque, ash-brown; the young of both sexes are green.” Lastly, I should mention that the male of one interesting type of cricket472 has “a long membranous appendage that falls over its face like a veil;” whether this serves as decoration is unknown.
Order, Neuroptera.—Little need here be said, except in regard to colour. In the Ephemeridæ the sexes often differ slightly in their obscure tints;473 but it is not probable that the males are thus rendered attractive to the females. The Libellulidæ or dragon-flies are ornamented with splendid green, blue, yellow, and 362vermilion metallic tints; and the sexes often differ. Thus, the males of some of the Agrionidæ, as Prof. Westwood remarks474 “are of a rich blue with black wings, whilst the females are fine green with colourless wings.” But in Agrion Ramburii these colours are exactly reversed in the two sexes.475 In the extensive N. American genus of Hetærina, the males alone have a beautiful carmine spot at the base of each wing. In Anax junius the basal part of the abdomen in the male is a vivid ultra-marine blue, and in the female grass-green. In the allied genus Gomphus, on the other hand, and in some other genera, the sexes differ but little in colour. Throughout the animal kingdom, similar cases of the sexes of closely-allied forms either differing greatly, or very little, or not at all, are of frequent occurrence. Although with many Libellulidæ there is so wide a difference in colour between the sexes, it is often difficult to say which is the most brilliant; and the ordinary coloration of the two sexes is exactly reversed, as we have just seen, in one species of Agrion. It is not probable that their colours in any case have been gained as a protection. As Mr. MacLachlan, who has closely attended to this family, writes to me, dragon-flies—the tyrants of the insect-world—are the least liable of any insect to be attacked by birds or other enemies. He believes that their bright colours serve as a sexual attraction. It deserves notice, as bearing on this subject, that certain dragon-flies appear to be attracted by particular colours: Mr. Patterson observed476 that the species of Agrionidæ, of which the males are blue, settled in numbers on the blue float of a fishing 363line; whilst two other species were attracted by shining white colours.
Order, Neuroptera.—There’s not much to say here except about color. In the Ephemeridæ, the two sexes often slightly differ in their subtle shades;473 but it's unlikely that the males are more attractive to the females because of this. The Libellulidæ, or dragonflies, are decorated with stunning metallic shades of green, blue, yellow, and vermilion; and the sexes often look different. For instance, males of some Agrionidæ, as noted by Prof. Westwood474, “are a rich blue with black wings, while females are a striking green with clear wings.” However, in Agrion Ramburii, these colors are completely reversed between the sexes.475 In the large North American genus Hetærina, only the males have a beautiful carmine spot at the base of each wing. In Anax junius, the male's abdomen is a bright ultra-marine blue, while the female's is grass-green. In the related genus Gomphus and some other genera, the color differences between the sexes are minimal. Throughout the animal kingdom, there are many instances where closely related species have sexes that either differ greatly, differ slightly, or not at all. Although many Libellulidæ show significant color differences between the sexes, it's often hard to determine which one is more brilliant; as we have just seen, the typical colors of the two sexes can be exactly reversed in one species of Agrion. It's unlikely that their colors have evolved for protection. As Mr. MacLachlan, who has studied this family closely, writes to me, dragonflies—the rulers of the insect world—are the least likely insects to be attacked by birds or other predators. He believes that their bright colors are used as sexual attraction. It’s interesting to note that certain dragonflies seem to be drawn to specific colors: Mr. Patterson observed476 that species of Agrionidæ, whose males are blue, gathered in large numbers on the blue float of a fishing line; meanwhile, two other species were attracted to shiny white colors.
It is an interesting fact, first observed by Schelver, that the males, in several genera belonging to two sub-families, when they first emerge from the pupal state are coloured exactly like the females; but that their bodies in a short time assume a conspicuous milky-blue tint, owing to the exudation of a kind of oil, soluble in ether and alcohol. Mr. MacLachlan believes that in the male of Libellula depressa this change of colour does not occur until nearly a fortnight after the metamorphosis, when the sexes are ready to pair.
It’s an interesting fact, first noted by Schelver, that the males in several genera from two sub-families, when they first come out of the pupal stage, are colored exactly like the females. But soon after, their bodies take on a noticeable milky-blue hue due to the release of a type of oil that dissolves in ether and alcohol. Mr. MacLachlan thinks that in the male of Libellula depressa, this color change doesn’t happen until almost two weeks after the metamorphosis, when the sexes are ready to mate.
Certain species of Neurothemis present, according to Brauer477 a curious case of dimorphism, some of the females having their wings netted in the usual manner; whilst other females have them “very richly netted as in the males of the same species.” Brauer “explains the phenomenon on Darwinian principles by the supposition that the close netting of the veins is a secondary sexual character in the males.” This latter character is generally developed in the males alone, but being, like every other masculine character, latent in the female, is occasionally developed in them. We have here an illustration of the manner in which the two sexes of many animals have probably come to resemble each other, namely by variations first appearing in the males, being preserved in them, and then transmitted to and developed in the females; but in this particular genus a complete transference is occasionally and abruptly effected. Mr. MacLachlan informs me of another case of dimorphism occurring in several species of Agrion in which a certain number of individuals are found of an orange colour, and these are 364invariably females. This is probably a case of reversion, for in the true Libellulæ, when the sexes differ in colour, the females are always orange or yellow, so that supposing Agrion to be descended from some primordial form having the characteristic sexual colours of the typical Libellulæ, it would not be surprising that a tendency to vary in this manner should occur in the females alone.
Certain species of Neurothemis show an interesting case of dimorphism, where some females have their wings patterned in the usual way, while other females have them "very richly patterned like the males of the same species." Brauer explains this phenomenon through Darwinian principles, suggesting that the intricate patterning of the veins is a secondary sexual trait in the males. This trait typically develops only in males, but, like many male traits, it can occasionally appear in females. This illustrates how the two sexes of many animals have likely come to resemble each other, with variations appearing first in males, being preserved in them, and then transmitted to and developed in females; however, in this particular genus, a complete transfer can sometimes happen suddenly. Mr. MacLachlan informs me of another case of dimorphism in several species of Agrion, where a certain number of individuals are orange, and these are always females. This is likely a case of reversion, because in the true Libellulæ, when the sexes differ in color, the females are always orange or yellow. Therefore, if Agrion is descended from some primitive form that had the typical sexual colors of the Libellulæ, it wouldn't be surprising for a tendency to vary in this way to occur solely in the females.
Although many dragon-flies are such large, powerful, and fierce insects, the males have not been observed by Mr. MacLachlan to fight together, except, as he believes, in the case of some of the smaller species of Agrion. In another very distinct group in this Order, namely in the Termites or white ants, both sexes at the time of swarming may be seen running about, “the male after the female, sometimes two chasing one female, and contending with great eagerness who shall win the prize.”478
Although many dragonflies are large, powerful, and fierce insects, Mr. MacLachlan has not observed the males fighting each other, except, as he believes, in some of the smaller species of Agrion. In another very distinct group within this Order, specifically the termites or white ants, both males and females can be seen running around during swarming time, "the male following the female, sometimes two chasing one female, eagerly competing to see who will win the prize."478
Order, Hymenoptera.—That inimitable observer, M. Fabre,479 in describing the habits of Cerceris, a wasp-like insect, remarks that “fights frequently ensue between the males for the possession of some particular female, who sits an apparently unconcerned beholder of the struggle for supremacy, and when the victory is decided, quietly flies away in company with the conqueror.” Westwood480 says that the males of one of the saw-flies (Tenthredinæ) “have been found fighting together, with their mandibles locked.” As M. Fabre speaks of the males of Cerceris striving to obtain a particular female, it may be well to bear in 365mind that insects belonging to this Order have the power of recognising each other after long intervals of time, and are deeply attached. For instance, Pierre Huber, whose accuracy no one doubts, separated some ants, and when after an interval of four months they met others which had formerly belonged to the same community, they mutually recognised and caressed each other with their antennæ. Had they been strangers they would have fought together. Again, when two communities engage in a battle, the ants on the same side in the general confusion sometimes attack each other, but they soon perceive their mistake, and the one ant soothes the other.481
Order, Hymenoptera.—The keen observer, M. Fabre,479 noted that in describing the habits of Cerceris, a wasp-like insect, “fights often break out between the males for the chance to mate with a specific female, who watches the struggle for dominance without concern, and once the victor is determined, she calmly flies off with the winning male.” Westwood480 mentions that the males of one of the saw-flies (Tenthredinæ) “have been seen fighting with their mandibles locked.” When M. Fabre discusses the males of Cerceris competing for a particular female, it's worth noting that insects in this Order can recognize each other after long periods apart and form strong bonds. For example, Pierre Huber, whose reliability is unquestionable, separated some ants, and after an interval of four months, when they met others from the same colony, they recognized and fondly greeted each other with their antennæ. If they had been strangers, they would have fought instead. Furthermore, during battles between two colonies, ants on the same side sometimes accidentally attack each other amidst the chaos, but they quickly realize their mistake, and one ant will comfort the other.481
In this Order slight differences in colour, according to sex, are common, but conspicuous differences are rare except in the family of Bees; yet both sexes of certain groups are so brilliantly coloured—for instance in Chrysis, in which vermilion and metallic greens prevail—that we are tempted to attribute the result to sexual selection. In the Ichneumonidæ, according to Mr. Walsh,482 the males are almost universally lighter coloured than the females. On the other hand, in the Tenthredinidæ the males are generally darker than the females. In the Siricidæ the sexes frequently differ; thus the male of Sirex juvencus is banded with orange, whilst the female is dark purple; but it is difficult to say which sex is the most ornamented. In Tremex columbæ the female is much brighter coloured than the male. With ants, as I am informed by Mr. F. Smith, the males of several species are black, the females being testaceous. In the family of Bees, especially in 366the solitary species, as I hear from the same distinguished entomologist, the sexes often differ in colour. The males are generally the brightest, and in Bombus as well as in Apathus, much more variable in colour than the females. In Anthophora retusa the male is of a rich fulvous-brown, whilst the female is quite black: so are the females of several species of Xylocopa, the males being bright yellow. In an Australian bee (Lestis bombylans), the female is of an extremely brilliant steel-blue, sometimes tinted with vivid green; the male being of a bright brassy colour clothed with rich fulvous pubescence. As in this group the females are provided with excellent defensive weapons in their stings, it is not probable that they have come to differ in colour from the males for the sake of protection.
In this order, slight differences in color based on sex are common, but noticeable differences are rare except in the bee family. However, both sexes of certain groups are so vividly colored—like in Chrysis, where vermilion and metallic greens dominate—that it's tempting to think these colors are due to sexual selection. In the Ichneumonidae, according to Mr. Walsh,482 the males are generally lighter in color than the females. In contrast, in the Tenthredinidae, the males are usually darker than the females. In the Siricidae, the sexes often look different; for instance, the male of Sirex juvencus has orange bands, while the female is dark purple. It's hard to determine which sex is more decorated. In Tremex columbæ, the female is much brighter than the male. With ants, as Mr. F. Smith informs me, the males of several species are black, while the females are more reddish-tan. In the bee family, especially among solitary species, as noted by the same distinguished entomologist, the sexes often differ in color. Males are usually the brightest and, in Bombus and Apathus, much more variable in color than females. In Anthophora retusa, the male is a rich fulvous-brown, while the female is entirely black; this is also true for females of several Xylocopa species, where males are bright yellow. In an Australian bee (Lestis bombylans), the female is an incredibly brilliant steel-blue, sometimes with vivid green hues, while the male has a bright brassy color covered in rich fulvous hair. Since the females in this group have great defensive abilities with their stings, it's unlikely that their color differences from the males are for protection.
Mutilla Europæa emits a stridulating noise; and according to Goureau483 both sexes have this power. He attributes the sound to the friction of the third and preceding abdominal segments; and I find that these surfaces are marked with very fine concentric ridges, but so is the projecting thoracic collar, on which the head articulates; and this collar, when scratched with the point of a needle, emits the proper sound. It is rather surprising that both sexes should have the power of stridulating, as the male is winged and the female wingless. It is notorious that Bees express certain emotions, as of anger, by the tone of their humming, as do some dipterous insects; but I have not referred to these sounds, as they are not known to be in any way connected with the act of courtship.
Mutilla Europæa makes a stridulating noise, and according to Goureau483, both males and females can produce this sound. He attributes it to the friction between the third and previous abdominal segments, and I’ve noticed that these surfaces have very fine concentric ridges. However, the projecting thoracic collar, where the head connects, has similar markings; when scratched with a needle, it also makes the same sound. It’s quite surprising that both males and females can stridulate, especially since the male has wings while the female does not. It is well-known that bees express certain emotions, like anger, through the tone of their humming, similar to some flies; however, I haven’t mentioned these sounds because they are not thought to be related to courtship.
Order, Coleoptera (Beetles).—Many beetles are coloured so as to resemble the surfaces which they 367habitually frequent. Other species are ornamented with gorgeous metallic tints,—for instance, many Carabidæ, which live on the ground and have the power of defending themselves by an intensely acrid secretion,—the splendid diamond-beetles which are protected by an extremely hard covering,—many species of Chrysomela, such as C. cerealis, a large species beautifully striped with various colours, and in Britain confined to the bare summit of Snowdon,—and a host of other species. These splendid colours, which are often arranged in stripes, spots, crosses and other elegant patterns, can hardly be beneficial, as a protection, except in the case of some flower-feeding species; and we cannot believe that they are purposeless. Hence the suspicion arises, that they serve as a sexual attraction; but we have no evidence on this head, for the sexes rarely differ in colour. Blind beetles, which cannot of course behold each other’s beauty, never exhibit, as I hear from Mr. Waterhouse, jun., bright colours, though they often have polished coats: but the explanation of their obscurity may be that blind insects inhabit caves and other obscure stations.
Order, Coleoptera (Beetles).—Many beetles are colored to blend in with the surfaces they typically inhabit. Other species are adorned with stunning metallic shades—like many Carabidæ, which dwell on the ground and can protect themselves with a highly irritating secretion—the beautiful diamond-beetles that have an extremely tough shell—many species of Chrysomela, such as C. cerealis, a large species with vibrant stripes of various colors, found only at the bare summit of Snowdon in Britain—and many more. These striking colors, often arranged in stripes, spots, crosses, and other elegant patterns, seem unlikely to provide protection unless for certain flower-feeding species; we can't believe they're without purpose. This raises the question of whether they serve as a form of sexual attraction, but we have no evidence to support this claim, as the sexes usually don't differ in color. Blind beetles, which can't see each other’s beauty, don’t display bright colors, as I hear from Mr. Waterhouse, Jr., although they often have shiny exteriors. However, their lack of color may be because blind insects live in caves and other dark places.
Some Longicorns, however, especially certain Prionidæ, offer an exception to the common rule that the sexes of beetles do not differ in colour. Most of these insects are large and splendidly coloured. The males in the genus Pyrodes,484 as I saw in Mr. Bates’ collection, are 368generally redder but rather duller than the females, the latter being coloured of a more or less splendid golden green. On the other hand, in one species the male is golden-green, the female being richly tinted with red and purple. In the genus Esmeralda the sexes differ so greatly in colour that they have been ranked as distinct species: in one species both are of a beautiful shining green, but the male has a red thorax. On the whole, as far as I could judge, the females of those Prionidæ, in which the sexes differ, are coloured more richly than the males; and this does not accord with the common rule in regard to colour when acquired through sexual selection.
Some Longicorns, particularly certain Prionidæ, break the usual pattern where male and female beetles look the same in color. Most of these insects are large and vibrantly colored. The males in the genus Pyrodes, as I observed in Mr. Bates’ collection, are generally redder but quite a bit duller than the females, who are more stunningly colored in a golden green. Conversely, in one species, the male is golden-green while the female flaunts rich red and purple hues. In the genus Esmeralda, the color difference between the sexes is so pronounced that they've been classified as different species: in one species, both are beautifully shiny green, but the male has a red thorax. Overall, based on my observations, the females of those Prionidæ where the sexes differ tend to be more richly colored than the males, which doesn't align with the usual rule regarding color variation driven by sexual selection.

Fig. 15. Chalcosoma atlas. Upper figure, male (reduced); lower figure, female (nat. size).
Fig. 15. Chalcosoma atlas. Upper figure, male (reduced); lower figure, female (actual size).

Fig. 16. Copris isidis. (Left-hand figures, males.)
Fig. 16. Copris isidis. (Left-hand figures, males.)
A most remarkable distinction between the sexes of many beetles is presented by the great horns which rise from the head, thorax, or clypeus of the males; and in some few cases from the under surface of the body. These horns, in the great family of the Lamellicorns, resemble those of various quadrupeds, such as stags, rhinoceroses, &c., and are wonderful both from their size and diversified shapes. Instead of describing them, I have given figures of the males and females of some of the more remarkable forms. (Figs. 15 to 19.) The females generally exhibit rudiments of the horns in the form of small knobs or ridges; but some are destitute of even a rudiment. On the other hand, the horns are nearly as well developed in the female as in the male of Phanæus lancifer; and only a little less well developed in the females of some other species of the same genus and of Copris. In the several subdivisions of the family, the differences in structure of the horns do not run parallel, as I am informed by Mr. Bates, with their more important and characteristic differences; thus within the same natural section of the genus Onthophagus, there are species which have either a single cephalic horn, or two distinct horns.
A striking difference between male and female beetles is the large horns that extend from the head, thorax, or clypeus of the males; in some cases, they even emerge from the underside of the body. These horns, found in the large family of Lamellicorns, resemble those of certain four-legged animals, like stags and rhinoceroses, and are impressive both in size and diverse shapes. Instead of describing them in detail, I've provided images of the males and females of some of the more notable forms. (Figs. 15 to 19.) Females usually show small bumps or ridges as remnants of horns, but some have no traces at all. However, in the case of Phanæus lancifer, the horns are nearly as well-formed in females as in males, and some other species in the same genus and Copris also have females with well-developed horns. In the various subdivisions of the family, the differences in horn structure don't align with their more significant and characteristic differences; for example, within the same natural section of the genus Onthophagus, there are species with either a single head horn or two distinct horns.
In almost all cases, the horns are remarkable from their excessive variability; so that a graduated series can be formed, from the most highly developed males to others so degenerate that they can barely be distinguished from the females. Mr. Walsh485 found that in Phanæus carnifex the horns were thrice as long in some males as in others. Mr. Bates, after examining above a hundred males of Onthophagus rangifer (fig. 19), thought that he had at last discovered a species in 371which the horns did not vary; but further research proved the contrary.
In almost all cases, the horns are notable for their extreme variability, allowing for a graduated range from the most highly developed males to those so underdeveloped that they can barely be told apart from the females. Mr. Walsh485 found that in Phanæus carnifex, the horns were three times longer in some males compared to others. Mr. Bates, after examining over a hundred males of Onthophagus rangifer (fig. 19), believed he had finally found a species on page 371 where the horns did not vary; but further research proved otherwise.
The extraordinary size of the horns, and their widely different structure in closely-allied forms, indicate that they have been formed for some important purpose; but their excessive variability in the males of the same species leads to the inference that this purpose cannot be of a definite nature. The horns do not show marks of friction, as if used for any ordinary work. Some authors suppose486 that as the males wander much more than the females, they require horns as a defence against their enemies; but in many cases the horns do not seem well adapted for defence, as they are not sharp. The most obvious conjecture is that they are used by the males for fighting together; but they have never been observed to fight; nor could Mr. Bates, after a careful examination of numerous species, find any sufficient evidence in their mutilated or broken condition of their having been thus used. If the males had been habitual fighters, their size would probably have been increased through sexual selection, so as to have exceeded that of the female; but Mr. Bates, after comparing the two sexes in above a hundred species of the Copridæ, does not find in well-developed individuals any marked difference in this respect. There is, moreover, one beetle, belonging to the same great division of the Lamellicorns, namely Lethrus, the males of which are known to fight, but they are not provided with horns, though their mandibles are much larger than those of the female.
The unusual size of the horns and their vastly different structure in closely related forms suggest they were developed for some significant purpose; however, the extreme variability among males of the same species implies that this purpose may not be specific. The horns don’t show signs of wear, as if used for any typical function. Some authors believe that since males roam much more than females, they need horns for protection against predators; however, in many instances, the horns don't seem suitable for defense, as they aren't sharp. The most straightforward theory is that they are used by males for fighting each other; yet, they have never been observed doing so, and Mr. Bates, after examining numerous species, found no solid evidence in their damaged or broken states that they have been used in this way. If males had been regular fighters, their size would likely have increased through sexual selection to surpass that of females; however, Mr. Bates, after comparing over a hundred species of the Copridæ, found no significant difference in size between the sexes in well-developed individuals. Additionally, there is one beetle, from the same major group of Lamellicorns, called Lethrus, whose males are known to fight, but they don’t have horns, even though their mandibles are much larger than those of the female.
The conclusion, which best agrees with the fact of the horns having been so immensely yet not fixedly developed,—as shewn by their extreme variability in 372the same species and by their extreme diversity in closely-allied species—is that they have been acquired as ornaments. This view will at first appear extremely improbable; but we shall hereafter find with many animals, standing much higher in the scale, namely fishes, amphibians, reptiles and birds, that various kinds of crests, knobs, horns and combs have been developed apparently for this sole purpose.
The conclusion that best fits the fact that the horns have developed significantly but not permanently—shown by their extreme variability in 372 the same species and their wide range in closely-related species—is that they have been obtained as decorative features. This idea may seem really unlikely at first, but we'll later see that many animals higher up the evolutionary ladder, like fish, amphibians, reptiles, and birds, have developed various types of crests, knobs, horns, and combs seemingly just for this reason.
The males of Onitis furcifer (fig. 20) are furnished
with singular projections on their anterior femora, and
Fig. 20. Onitis furcifer, male,
viewed from beneath.
with a great fork or pair of horns on
the lower surface of the thorax. This
situation seems extremely ill adapted
for the display of these projections,
and they may be of some real service;
but no use can at present be
assigned to them. It is a highly
remarkable fact, that although the
males do not exhibit even a trace of
horns on the upper surface of the
body, yet in the females a rudiment of a single horn on
the head (fig. 21, a), and of a crest (b) on the thorax,
are plainly visible. That the slight thoracic crest in the
female is a rudiment of a projection proper to the male,
though entirely absent in the male of this particular
species, is clear: for the female of Bubas bison (a form373
which comes next to Onitis) has a similar slight crest
on the thorax, and the male has in the same situation a
great projection. So again there can be no doubt that
the little point (a) on the head of the female Onitis
furcifer, as well of the females of two or three allied
species, is a rudimentary representative of the cephalic
horn, which is common to the males of so many lamellicorn
beetles, as in Phanæus, fig. 17. The males indeed
of some unnamed beetles in the British Museum, which
are believed actually to belong to the genus Onitis, are
furnished with a similar horn. The remarkable nature
of this case will be best perceived by an illustration:
the Ruminant quadrupeds run parallel with the lamellicorn
beetles, in some females possessing horns as large
as those of the male, in others having them much
smaller, or existing as mere rudiments (though this is
as rare with ruminants as it is common with Lamellicorns),
or in having none at all. Now if a new species
of deer or sheep were discovered with the female
bearing distinct rudiments of horns, whilst the head
of the male was absolutely smooth, we should have a
case like that of Onitis furcifer.
The males of Onitis furcifer (fig. 20) have unique projections on their front femurs, and
Fig. 20. Onitis furcifer, male, viewed from below.
a large fork or pair of horns on the underside of the thorax. This arrangement seems poorly suited for displaying these projections, but they might serve some purpose; however, we currently can't identify what that use might be. It's quite remarkable that, while the males show no signs of horns on the upper body, the females have a small horn rudiment on the head (fig. 21, a) and a crest (b) on the thorax, which is clearly visible. The slight thoracic crest in the female is a remnant of a feature that typically belongs to the male, even though it's completely absent in the male of this specific species: the female of Bubas bison (which is closely related to Onitis) has a similar slight crest on the thorax, whereas the male has a prominent projection in the same area. Additionally, it’s evident that the small point (a) on the head of the female Onitis furcifer, as well as in the females of a few related species, is a rudimentary version of the cephalic horn found in many male lamellicorn beetles, as seen in Phanæus, fig. 17. In fact, some unnamed beetles in the British Museum, believed to belong to the genus Onitis, also have similar horns. The uniqueness of this situation can be better understood through an analogy: ruminant quadrupeds parallel lamellicorn beetles, with some females displaying horns as large as those of the males, others having significantly smaller horns or just rudiments (though this is rarer among ruminants than it is common among lamellicorns), or not having any horns at all. If we were to discover a new species of deer or sheep in which the female had clear horn rudiments while the male's head was completely smooth, we would have a situation similar to that of Onitis furcifer.
Fig. 21. Left-hand figure, male of Onitis furcifer, viewed laterally. Right-hand figure, female. a. Rudiment of cephalic horn. b. Trace of thoracic horn or crest.
Fig. 21. Left figure, male Onitis furcifer, seen from the side. Right figure, female. a. Small remnant of the head horn. b. Indication of the thoracic horn or crest.
In this case the old belief of rudiments having been created to complete the scheme of nature is so far from holding good, that all ordinary rules are completely broken through. The view which seems the most probable is that some early progenitor of Onitis acquired, like other Lamellicorns, horns on the head and thorax, and then transferred them, in a rudimentary condition, as with so many existing species, to the female, by whom they have ever since been retained. The subsequent loss of the horns by the male may have resulted through the principle of compensation from the development of the projections on the lower surface, whilst the female has not been thus affected, as she is not furnished with374 these projections, and consequently has retained the rudiments of the horns on the upper surface. Although this view is supported by the case of Bledius immediately to be given, yet the projections on the lower surface differ greatly in structure and development in the males of the several species of Onitis, and are even rudimentary in some; nevertheless the upper surface in all these species is quite destitute of horns. As secondary sexual characters are so eminently variable, it is possible that the projections on the lower surface may have been first acquired by some progenitor of Onitis and produced their effect through compensation, and then have been in certain cases almost completely lost.
In this case, the old belief that rudiments were created to complete the natural scheme is far from accurate, as all ordinary rules are completely disregarded. The most likely explanation is that an early ancestor of Onitis developed horns on the head and thorax, similar to other Lamellicorns, and then passed them on, in a rudimentary state, to the female, who has kept them ever since. The male may have lost its horns due to the principle of compensation, as the projections on the lower surface developed, while the female was not affected, as she lacks these projections and has therefore retained the rudiments of the horns on the upper surface. While this perspective is supported by the case of Bledius, the projections on the lower surface vary significantly in structure and development among the males of different Onitis species, and are even rudimentary in some; however, all these species lack horns on the upper surface. Since secondary sexual traits are highly variable, it's possible that the projections on the lower surface were first acquired by some ancestor of Onitis and resulted in changes through compensation, eventually leading to their near-total loss in certain cases.
Fig. 22. Bledius taurus, magnified. Left-hand figure, male; right-hand figure, female.
Fig. 22. Bledius taurus, enlarged. Left figure, male; right figure, female.
All the cases hitherto given refer to the Lamellicorns, but the males of some few other beetles, belonging to two widely distinct groups, namely, the Curculionidæ and Staphylinidæ, are furnished with horns,—in the former on the lower surface of the body,487 in the latter on the upper surface of the head and thorax. In the Staphylinidæ the horns of the males in the same species are extraordinarily variable, just as we have seen with the Lamellicorns. In Siagonium we have a case of dimorphism, for the males can be divided into two sets, differing greatly in the size of their bodies, and in the development of their horns, without any intermediate gradations. In a species of Bledius (fig. 22), also belonging to the Staphylinidæ, male specimens can be found in the same locality, as 375 Professor Westwood states, “in which the central horn of the thorax is very large, but the horns of the head quite rudimental; and others, in which the thoracic horn is much shorter, whilst the protuberances on the head are long.”488 Here, then, we apparently have an instance of compensation of growth, which throws light on the curious case just given of the loss of the upper horns by the males of Onitis furcifer.
All the cases mentioned so far relate to the Lamellicorns, but the males of a few other beetle species from two very different groups, the Curculionidae and Staphylinidae, also have horns—on the underside of the body in the former and on the top of the head and thorax in the latter. In the Staphylinidae, the male horns within the same species vary greatly, similar to what we’ve observed with the Lamellicorns. In Siagonium, we see a case of dimorphism, where the males can be divided into two groups that differ significantly in body size and horn development, with no gradual transitions between them. In a species of Bledius (fig. 22), also part of the Staphylinidae, male specimens found in the same area, as Professor Westwood notes, “have a very large central horn on the thorax, but rudimentary horns on the head; and others, where the thoracic horn is much shorter, while the head protrusions are long.” Here, we seemingly have an example of growth compensation, which provides insight into the interesting case of the males of Onitis furcifer losing their upper horns.
Law of Battle.—Some male beetles, which seem ill fitted for fighting, nevertheless engage in conflicts for the possession of the females. Mr. Wallace489 saw two males of Leptorhynchus angustatus, a linear beetle with a much elongated rostrum, “fighting for a female, who stood close by busy at her boring. They pushed at each other with their rostra, and clawed and thumped, apparently in the greatest rage.” The smaller male, however, “soon ran away, acknowledging himself vanquished.” In some few cases the males are well adapted for fighting, by possessing great toothed mandibles, much larger than those of the females. This is the case with the common stag-beetle (Lucanus cervus), the males of which emerge from the pupal state about a week before the other sex, so that several may often be seen pursuing the same female. At this period they engage in fierce conflicts. When Mr. A. H. Davis490 enclosed two males with one female in a box, the larger male severely pinched the smaller one, until he resigned his pretensions. A friend informs me 376that when a boy he often put the males together to see them fight, and he noticed that they were much bolder and fiercer than the females, as is well known to be the case with the higher animals. The males would seize hold of his finger, if held in front, but not so the females. With many of the Lucanidæ, as well as with the above-mentioned Leptorhynchus, the males are larger and more powerful insects than the females. The two sexes of Lethrus cephalotes (one of the Lamellicorns) inhabit the same burrow; and the male has larger mandibles than the female. If, during the breeding-season, a strange male attempts to enter the burrow, he is attacked; the female does not remain passive, but closes the mouth of the burrow, and encourages her mate by continually pushing him on from behind. The action does not cease until the aggressor is killed or runs away.491 The two sexes of another lamellicorn beetle, the Ateuchus cicatricosus live in pairs, and seem much attached to each other; the male excites the female to roll the balls of dung in which the ova are deposited; and if she is removed, he becomes much agitated. If the male is removed, the female ceases all work, and as M. Brulerie492 believes, would remain on the spot until she died.
Law of Battle.—Some male beetles, which may not look like they’re made for fighting, still compete for females. Mr. Wallace489 observed two males of Leptorhynchus angustatus, a long beetle with an elongated snout, “fighting for a female who was nearby, busy with her boring. They pushed each other with their snouts, clawed, and thumped, seeming really angry.” The smaller male, however, “quickly ran away, admitting defeat.” In a few instances, males are well-equipped for fighting, having large, toothed jaws that are much bigger than the females’. This is true for the common stag-beetle (Lucanus cervus), where the males emerge from their pupal stage about a week before the females, resulting in several males often chasing the same female. During this time, they engage in fierce battles. When Mr. A. H. Davis490 put two males with one female in a box, the larger male aggressively pinched the smaller one until he gave up his claims. A friend told me 376 that when he was a boy, he often put the males together to see them fight, and he noticed they were much bolder and fiercer than the females, which is well known to be true among higher animals. The males would grab his finger if he held it out, but the females wouldn’t do the same. With many Lucanidæ, as well as the previously mentioned Leptorhynchus, the males are larger and stronger insects than the females. The two sexes of Lethrus cephalotes (one of the Lamellicorns) live in the same burrow, and the male has larger jaws than the female. If a strange male tries to enter the burrow during breeding season, he is attacked; the female doesn't just sit there but closes off the entrance and encourages her mate by constantly pushing him from behind. The action doesn't stop until either the intruder is killed or runs away.491 The two sexes of another lamellicorn beetle, Ateuchus cicatricosus, live in pairs and seem very bonded to each other; the male prompts the female to roll the dung balls where the eggs are laid, and if she is taken away, he becomes very agitated. If the male is removed, the female stops all work and, according to M. Brulerie492, would stay in place until she dies.
The great mandibles of the male Lucanidæ are extremely
variable both in size and structure, and in this
respect resemble the horns on the head and thorax
of many male Lamellicorns and Staphylinidæ. A perfect
series can be formed from the best-provided to the
worst-provided or degenerate males. Although the
mandibles of the common stag-beetle, and probably of
377many other species, are used as efficient weapons for
fighting, it is doubtful whether their great size can
Fig. 23. Chiasognathus grantii,
reduced. Upper figure, male;
lower figure, female.
thus be accounted for. We have
seen that with the Lucanus elaphus
of N. America they are used
for seizing the female. As they
are so conspicuous and so elegantly
branched, the suspicion
has sometimes crossed my mind
that they may be serviceable to
the males as an ornament, in the
same manner as the horns on the
head and thorax of the various
above described species. The
male Chiasognathus grantii of S.
Chile—a splendid beetle belonging
to the same family—has enormously-developed
mandibles (fig.
23); he is bold and pugnacious;
when threatened on any side he
faces round, opening his great
jaws, and at the same time stridulating
loudly; but the mandibles
were not strong enough to pinch
my finger so as to cause actual
pain.
The large jaws of male Lucanidae are highly variable in both size and shape, similar to the horns found on the heads and thoraxes of many male Lamellicorns and Staphylinidae. A complete range can be created from the best-equipped males to those that are poorly equipped or degenerate. While the jaws of the common stag beetle, and likely many other species, serve as effective weapons for fighting, it's uncertain whether their large size can be fully justified.
Fig. 23. Chiasognathus grantii, reduced. Top figure, male; bottom figure, female.
We've observed that in the Lucanus elaphus of North America, their jaws are used for grabbing the female. Because these jaws are so noticeable and intricately branched, I've sometimes wondered if they might also serve as ornaments for the males, similar to the horns seen in the various species described earlier. The male Chiasognathus grantii from southern Chile—a stunning beetle in the same family—has greatly developed jaws (fig. 23); he is fearless and aggressive; when threatened from any angle, he turns around, opens his large jaws, and simultaneously stridulates loudly; however, his jaws were not strong enough to pinch my finger with enough force to cause real pain.
Sexual selection, which implies the possession of considerable perceptive powers and of strong passions, seems to have been more effective with the Lamellicorns than with any other family of the Coleoptera or beetles. With some species the males are provided with weapons for fighting; some live in pairs and show mutual affection;378 many have the power of stridulating when excited; many are furnished with the most extraordinary horns, apparently for the sake of ornament; some which are diurnal in their habits are gorgeously coloured; and, lastly, several of the largest beetles in the world belong to this family, which was placed by Linnæus and Fabricius at the head of the Order of the Coleoptera.493
Sexual selection, which suggests a high level of awareness and intense desires, appears to have been more impactful in the Lamellicorns than in any other group of beetles within the Coleoptera family. In some species, males have fighting features; some live in pairs and demonstrate mutual affection;378 many can produce sounds when excited; many have striking horns, seemingly for decoration; some are brightly colored and active during the day; and finally, several of the largest beetles in the world are part of this group, which was ranked by Linnæus and Fabricius at the top of the Coleoptera Order.493
Stridulating organs.—Beetles belonging to many and widely distinct families possess these organs. The sound can sometimes be heard at the distance of several feet or even yards,494 but is not comparable with that produced by the Orthoptera. The part which may be called the rasp generally consists of a narrow slightly-raised surface, crossed by very fine, parallel ribs, sometimes so fine as to cause iridescent colours, and having a very elegant appearance under the microscope. In some cases, for instance, with Typhæus, it could be plainly seen that extremely minute, bristly, scale-like prominences, which cover the whole surrounding surface in approximately parallel lines, give rise to the ribs of the rasp by becoming confluent and straight, and at the same time more prominent and smooth. A hard ridge on any adjoining part of the body, which in some cases is specially modified for the purpose, serves as the scraper for the rasp. The scraper is rapidly moved across the rasp, or conversely the rasp across the scraper.
Stridulating organs.—Many different families of beetles have these organs. The sound can sometimes be heard from several feet or even yards away,494 but it doesn't compare to the sounds made by Orthoptera. The part that can be called the rasp usually has a narrow, slightly raised surface crossed by very fine, parallel ribs, which can be so delicate that they create iridescent colors and look quite elegant under a microscope. In some cases, such as with Typhæus, it's clearly visible that tiny, bristly, scale-like projections cover the surrounding surface in roughly parallel lines, forming the ribs of the rasp by coming together, straightening out, and becoming more prominent and smooth. A hard ridge on an adjacent part of the body, which is sometimes specially modified for this purpose, acts as the scraper for the rasp. The scraper moves quickly across the rasp, or the rasp moves across the scraper.
Fig. 24. Necrophorus (from Landois). r. The two rasps. Left-hand figure, part of the rasp highly magnified.
Fig. 24. Necrophorus (from Landois). r. The two rasps. The figure on the left shows a highly magnified part of the rasp.
These organs are situated in widely different positions. In the carrion-beetles (Necrophorus) two parallel rasps (r, fig. 24) stand on the dorsal surface of the fifth abdominal segment, each rasp being crossed, as described by Landois,495 by from 126 to 140 fine ribs. These 379ribs are scraped by the posterior margins of the elytra, a small portion of which projects beyond the general outline. In many Crioceridæ, and in Clythra 4-punctata (one of the Chrysomelidæ), and in some Tenebrionidæ, &c.,496 the rasp is seated on the dorsal apex of the abdomen, on the pygidium or pro-pygidium, and is scraped as above by the elytra. In Heterocerus, which belongs to another family, the rasps are placed on the sides of the first abdominal segment, and are scraped by ridges on the femora.497 In certain Curculionidæ and Carabidæ,498 the parts are completely reversed in position, 380for the rasps are seated on the inferior surface of the elytra, near their apices, or along their outer margins, and the edges of the abdominal segments serve as the scrapers. In Pelobius hermanni (one of Dytiscidæ or water-beetles) a strong ridge runs parallel and near to the sutural margin of the elytra, and is crossed by ribs, coarse in the middle part, but becoming gradually finer at both ends, especially at the upper end; when this insect is held under water or in the air, a stridulating noise is produced by scraping the extreme horny margin of the abdomen against the rasp. In a great number of long-horned beetles (Longicornia) the organs are altogether differently situated, the rasp being on the meso-thorax, which is rubbed against the pro-thorax; Landois counted 238 very fine ribs on the rasp of Cerambyx heros.
These organs are found in very different places. In carrion beetles (Necrophorus), two parallel rasps (r, fig. 24) are located on the upper side of the fifth abdominal segment, each rasp having between 126 and 140 fine ribs, as described by Landois,495 These ribs are scraped by the back edges of the elytra, which slightly extends beyond the overall shape. In many Crioceridæ, in Clythra 4-punctata (a member of the Chrysomelidæ), and in some Tenebrionidæ, &c.,496 the rasp is located on the upper apex of the abdomen, on the pygidium or pro-pygidium, and is scraped in the same manner by the elytra. In Heterocerus, which is part of a different family, the rasps are positioned on the sides of the first abdominal segment and are scraped by ridges on the femora.497 In certain Curculionidæ and Carabidæ,498 the positions are completely reversed, as the rasps are found on the underside of the elytra, near their tips or along their outer edges, while the edges of the abdominal segments act as scrapers. In Pelobius hermanni (a type of Dytiscidæ or water beetle), a strong ridge runs parallel and close to the seam of the elytra, crossed by ribs that are coarse in the middle but gradually finer at both ends, especially at the upper end; when this insect is held underwater or in the air, a stridulating sound is made by scraping the very hard edge of the abdomen against the rasp. In many long-horned beetles (Longicornia), the organs are situated quite differently, with the rasp located on the mesothorax, which is rubbed against the prothorax; Landois counted 238 very fine ribs on the rasp of Cerambyx heros.
Many Lamellicorns have the power of stridulating,
and the organs differ greatly in position. Some species
Fig. 25. Hind-leg of Geotrupes
stercorarius (from Landois).
r. Rasp. c. Coxa. f. Femur.
t. Tibia. tr. Tarsi.
stridulate very loudly, so that when
Mr. F. Smith caught a Trox sabulosus,
a gamekeeper who stood by
thought that he had caught a
mouse; but I failed to discover the
proper organs in this beetle. In
Geotrupes and Typhæus a narrow
ridge runs obliquely across (r, fig.
25) the coxa of each hind-leg,
having in G. stercorarius 84 ribs,
which are scraped by a specially-projecting
part of one of the abdominal
segments. In the nearly
allied Copris lunaris, an excessively
narrow fine rasp runs along the
sutural margin of the elytra, with another short rasp
near the basal outer margin; but in some other Coprini381
the rasp is seated, according to Leconte,499 on the dorsal
surface of the abdomen. In Oryctes it is seated on the
pro-pygidium, and in some other Dynastini, according to
the same entomologist, on the under surface of the
elytra. Lastly, Westring states that in Omaloplia brunnea
the rasp is placed on the pro-sternum, and the scraper
on the meta-sternum, the parts thus occupying the under
surface of the body, instead of the upper surface as in
the Longicorns.
Many Lamellicorns can stridulate, and their organs vary significantly in position. Some species
Fig. 25. Hind leg of Geotrupes stercorarius (from Landois).
r. Rasp. c. Coxa. f. Femur. t. Tibia. tr. Tarsi.
stridulate very loudly, so much so that when Mr. F. Smith caught a Trox sabulosus, a gamekeeper nearby thought he had caught a mouse; however, I couldn't find the specific organs in this beetle. In Geotrupes and Typhæus, a narrow ridge runs diagonally across (r, fig. 25) the coxa of each hind leg, with G. stercorarius having 84 ribs that are scraped by a specially projecting part of one of the abdominal segments. In the closely related Copris lunaris, a very narrow fine rasp runs along the sutural margin of the elytra, with another short rasp near the outer margin at the base; but in some other Coprini381, the rasp is located, according to Leconte,499 on the dorsal surface of the abdomen. In Oryctes, it is located on the pro-pygidium, and in some other Dynastini, as noted by the same entomologist, on the underside of the elytra. Finally, Westring states that in Omaloplia brunnea, the rasp is found on the pro-sternum, and the scraper on the meta-sternum, with both parts occupying the underside of the body, unlike the upper surface as in the Longicorns.
We thus see that the stridulating organs in the different coleopterous families are wonderfully diversified in position, but not much in structure. Within the same family some species are provided with these organs, and some are quite destitute of them. This diversity is intelligible, if we suppose that originally various species made a shuffling or hissing noise by the rubbing together of the hard and rough parts of their bodies which were in contact; and that from the noise thus produced being in some way useful, the rough surfaces were gradually developed into regular stridulating organs. Some beetles as they move, now produce, either intentionally or unintentionally, a shuffling noise, without possessing any proper organs for the purpose. Mr. Wallace informs me that the Euchirus longimanus (a Lamellicorn, with the anterior legs wonderfully elongated in the male) “makes, whilst moving, a low hissing sound by the protrusion and contraction of the abdomen; and when seized it produces a grating sound by rubbing its hind-legs against the edges of the elytra.” The hissing sound is clearly due to a narrow rasp running along the sutural margin of each elytron; and I could likewise make the grating 382sound by rubbing the shagreened surface of the femur against the granulated margin of the corresponding elytron; but I could not here detect any proper rasp; nor is it likely that I could have overlooked it in so large an insect. After examining Cychrus and reading what Westring has written in his two papers about this beetle, it seems very doubtful whether it possesses any true rasp, though it has the power of emitting a sound.
We can see that the stridulating organs in different beetle families are incredibly varied in location, but not so much in structure. Within the same family, some species have these organs, while others completely lack them. This variation makes sense if we consider that initially various species created a shuffling or hissing noise by rubbing together the hard and rough parts of their bodies that were in contact; and that the noise produced turned out to be beneficial, leading to the rough surfaces gradually evolving into proper stridulating organs. Some beetles, as they move, produce a shuffling noise, either on purpose or by accident, without having any specialized organs for it. Mr. Wallace tells me that the Euchirus longimanus (a Lamellicorn with the males having impressively elongated front legs) “makes a low hissing sound while moving by extending and contracting its abdomen; and when captured, it creates a grating sound by rubbing its hind legs against the edges of its wing covers.” The hissing sound clearly comes from a narrow rasp along the sutural margin of each wing cover; I could also create the grating sound by rubbing the rough surface of the femur against the granulated edge of the matching wing cover, but I couldn’t find any proper rasp here; nor could it be likely that I would have missed it in such a large insect. After looking into Cychrus and reading what Westring has written in his two papers about this beetle, it seems quite uncertain whether it actually has any true rasp, although it is capable of producing a sound.
From the analogy of the Orthoptera and Homoptera, I expected to find that the stridulating organs in the Coleoptera differed according to sex; but Landois, who has carefully examined several species, observed no such difference; nor did Westring; nor did Mr. G. R. Crotch in preparing the numerous specimens which he had the kindness to send me for examination. Any slight sexual difference, however, would be difficult to detect, on account of the great variability of these organs. Thus in the first pair of the Necrophorus humator and of the Pelobius which I examined, the rasp was considerably larger in the male than in the female; but not so with succeeding specimens. In Geotrupes stercorarius the rasp appeared to me thicker, opaquer, and more prominent in three males than in the same number of females; consequently my son, Mr. F. Darwin, in order to discover whether the sexes differed in their power of stridulating, collected 57 living specimens, which he separated into two lots, according as they made, when held in the same manner, a greater or lesser noise. He then examined their sexes, but found that the males were very nearly in the same proportion to the females in both lots. Mr. F. Smith has kept alive numerous specimens of Mononychus pseudacori (Curculionidæ), and is satisfied that both sexes stridulate, and apparently in an equal degree.
From the comparison of Orthoptera and Homoptera, I thought the stridulating organs in Coleoptera would differ between the sexes. However, Landois, who has thoroughly examined several species, found no such difference; neither did Westring, nor did Mr. G. R. Crotch when preparing the many specimens he kindly sent me for analysis. Any slight sexual difference would be hard to spot due to the significant variability of these organs. In the first pair of Necrophorus humator and Pelobius I examined, the rasp was noticeably larger in the male than the female, but this was not the case in later specimens. In Geotrupes stercorarius, I noticed the rasp seemed thicker, less transparent, and more prominent in three males compared to the same number of females. Consequently, my son, Mr. F. Darwin, collected 57 living specimens to see if there were differences in their stridulation ability, separating them into two groups based on the loudness of the noise they made when held the same way. He then checked their sexes and found the males were nearly in the same proportion to the females in both groups. Mr. F. Smith has kept many specimens of Mononychus pseudacori (Curculionidæ) alive and is confident that both sexes stridulate, apparently to an equal extent.
Nevertheless the power of stridulating is certainly a383 sexual character in some few Coleoptera. Mr. Crotch has discovered that the males alone of two species of Heliopathes (Tenebrionidæ) possess stridulating organs. I examined five males of H. gibbus, and in all these there was a well-developed rasp, partially divided into two, on the dorsal surface of the terminal abdominal segment; whilst in the same number of females there was not even a rudiment of the rasp, the membrane of this segment being transparent and much thinner than in the male. In H. cribratostriatus the male has a similar rasp, excepting that it is not partially divided into two portions, and the female is completely destitute of this organ; but in addition the male has on the apical margins of the elytra, on each side of the suture, three or four short longitudinal ridges, which are crossed by extremely fine ribs, parallel to and resembling those on the abdominal rasp; whether these ridges serve as an independent rasp, or as a scraper for the abdominal rasp, I could not decide: the female exhibits no trace of this latter structure.
However, the ability to stridulate definitely has a383 sexual aspect in a few Coleoptera. Mr. Crotch found that only the males of two species of Heliopathes (Tenebrionidae) have stridulating organs. I checked five males of H. gibbus, and all of them had a well-developed rasp, which is partially split into two on the top surface of their last abdominal segment; meanwhile, in the same number of females, there was no sign of the rasp, and the membrane of this segment was transparent and much thinner than in the males. In H. cribratostriatus, the male features a similar rasp, but it isn’t partially divided into two parts, and the female completely lacks this organ; additionally, the male has three or four short longitudinal ridges on the edge of the elytra on each side of the suture, which are crossed by very fine ribs that run parallel to and resemble those on the abdominal rasp. I couldn’t determine whether these ridges act as an independent rasp or as a scraper for the abdominal rasp; the female shows no sign of this structure at all.
Again, in three species of the Lamellicorn genus Oryctes, we have a nearly parallel case. In the females of O. gryphus and nasicornis the ribs on the rasp of the pro-pygidium are less continuous and less distinct than in the males; but the chief difference is that the whole upper surface of this segment, when held in the proper light, is seen to be clothed with hairs, which are absent or are represented by excessively fine down in the males. It should be noticed that in all Coleoptera the effective part of the rasp is destitute of hairs. In O. senegalensis the difference between the sexes is more strongly marked, and this is best seen when the proper segment is cleaned and viewed as a transparent object. In the female the whole surface is covered with little separate crests, bearing spines; whilst in the male these crests384 become, in proceeding towards the apex, more and more confluent, regular, and naked; so that three-fourths of the segment is covered with extremely fine parallel ribs, which are quite absent in the female. In the females, however, of all three species of Oryctes, when the abdomen of a softened specimen is pushed backwards and forwards, a slight grating or stridulating sound can be produced.
Again, in three species of the Lamellicorn genus Oryctes, we have a nearly parallel case. In the females of O. gryphus and nasicornis, the ribs on the rasp of the pro-pygidium are less continuous and less distinct than in the males; but the main difference is that the entire upper surface of this segment, when viewed in the right light, appears to be covered with hairs, which are missing or represented by very fine down in the males. It's worth noting that in all Coleoptera, the effective part of the rasp lacks hairs. In O. senegalensis, the difference between the sexes is more pronounced, and this is best observed when the segment is cleaned and viewed as a transparent object. In the female, the entire surface is covered with small separate crests that have spines, whereas in the male, these crests384 become increasingly merged, regular, and bare towards the apex, resulting in three-fourths of the segment being covered with extremely fine parallel ribs, which are completely absent in the female. However, in the females of all three species of Oryctes, when the abdomen of a softened specimen is moved back and forth, a slight grating or stridulating sound can be produced.
In the case of the Heliopathes and Oryctes there can hardly be a doubt that the males stridulate in order to call or to excite the females; but with most beetles the stridulation apparently serves both sexes as a mutual call. This view is not rendered improbable from beetles stridulating under various emotions; we know that birds use their voices for many purposes besides singing to their mates. The great Chiasognathus stridulates in anger or defiance; many species do the same from distress or fear, when held so that they cannot escape; Messrs. Wollaston and Crotch were able, by striking the hollow stems of trees in the Canary Islands, to discover the presence of beetles belonging to the genus Acalles by their stridulation. Lastly the male Ateuchus stridulates to encourage the female in her work, and from distress when she is removed.500 Some naturalists believe that beetles make this noise to frighten away their enemies; but I cannot think that the quadrupeds and birds which are able to devour the larger beetles with their extremely hard coats, would be frightened by so slight a grating sound. The belief that the stridulation serves as a sexual call is supported by the fact that death-ticks (Anobium tesselatum) are well known to answer each other’s ticking, or, as I have 385myself observed, a tapping noise artificially made; and Mr. Doubleday informs me that he has twice or thrice observed a female ticking,501 and in the course of an hour or two has found her united with a male, and on one occasion surrounded by several males. Finally, it seems probable that the two sexes of many kinds of beetles were at first enabled to find each other by the slight shuffling noise produced by the rubbing together of the adjoining parts of their hard bodies; and that as the males or females which made the greatest noise succeeded best in finding partners, the rugosities on various parts of their bodies were gradually developed by means of sexual selection into true stridulating organs.
In the case of the Heliopathes and Oryctes, there’s no doubt that the males stridulate to attract or excite the females; however, with most beetles, stridulation seems to serve as a mutual call for both sexes. This idea is not unlikely since beetles stridulate in various emotional states; we know that birds use their voices for many reasons apart from singing to their partners. The large Chiasognathus stridulates when it's angry or defiant; many species do the same out of distress or fear when they are held in a way that prevents escape. Messrs. Wollaston and Crotch were able to identify the presence of beetles from the genus Acalles by striking the hollow stems of trees in the Canary Islands based on their stridulation. Lastly, the male Ateuchus stridulates to encourage the female while she works, and out of distress when she is removed.500 Some naturalists believe that beetles make this noise to scare away predators, but I don't think that the larger quadrupeds and birds capable of preying on beetles with their tough exoskeletons would be intimidated by such a faint grating sound. The belief that stridulation acts as a sexual call is backed by the fact that death-ticks (Anobium tesselatum) are known to respond to each other's ticking, or, as I have personally observed, to an artificially created tapping noise; and Mr. Doubleday has told me that he has seen a female ticking a few times and, over the course of an hour or two, found her paired with a male, and on one occasion, surrounded by several males. Ultimately, it seems likely that the two sexes of many beetle species were initially able to locate each other by the faint shuffling sound created from the rubbing of the adjoining parts of their hard bodies; and that as the males or females that made the loudest sounds were more successful in finding partners, the rough areas on different parts of their bodies gradually evolved into true stridulating organs via sexual selection.
CHAPTER XI.
Bugs, continued.—Order Lepidoptera.
Courtship of butterflies—Battles—Ticking noise—Colours common to both sexes, or more brilliant in the males—Examples—Not due to the direct action of the conditions of life—Colours adapted for protection—Colours of moths—Display—Perceptive powers of the Lepidoptera—Variability—Causes of the difference in colour between the males and females—Mimickry, female butterflies more brilliantly coloured than the males—Bright colours of caterpillars—Summary and concluding remarks on the secondary sexual characters of insects—Birds and insects compared.
Courtship of butterflies—Battles—Ticking noise—Colors common to both sexes, or more vibrant in the males—Examples—Not due to the direct influence of life conditions—Colors adapted for protection—Colors of moths—Display—Perception abilities of Lepidoptera—Variability—Causes of color differences between males and females—Mimicry, female butterflies more vividly colored than the males—Bright colors of caterpillars—Summary and concluding remarks on the secondary sexual traits of insects—Birds and insects compared.
In this great Order the most interesting point for us is the difference in colour between the sexes of the same species, and between the distinct species of the same genus. Nearly the whole of the following chapter will be devoted to this subject; but I will first make a few remarks on one or two other points. Several males may often be seen pursuing and crowding round the same female. Their courtship appears to be a prolonged affair, for I have frequently watched one or more males pirouetting round a female until I became tired, without seeing the end of the courtship. Although butterflies are such weak and fragile creatures, they are pugnacious, and an Emperor butterfly502 has been captured with the tips of its wings broken from a conflict with another male. Mr. Collingwood in speaking of the frequent battles 387between the butterflies of Borneo says, “They whirl round each other with the greatest rapidity, and appear to be incited by the greatest ferocity.” One case is known of a butterfly, namely the Ageronia feronia, which makes a noise like that produced by a toothed wheel passing under a spring catch, and which could be heard at the distance of several yards. At Rio de Janeiro this sound was noticed by me, only when two were chasing each other in an irregular course, so that it is probably made during the courtship of the sexes; but I neglected to attend to this point.503
In this fascinating Order, the most interesting aspect for us is the color differences between the sexes of the same species and among different species within the same genus. The majority of the upcoming chapter will focus on this topic, but first, I’ll share a few comments on a couple of other points. It’s common to see several males chasing and surrounding the same female. Their courtship seems to be a lengthy process, as I’ve often observed one or more males swirling around a female for so long that I grew tired of watching, without ever seeing the courtship come to an end. Despite being such weak and delicate creatures, butterflies can be quite aggressive, and an Emperor butterfly502 has been found with the tips of its wings damaged from fighting another male. Mr. Collingwood, when discussing the frequent battles among the butterflies of Borneo, notes, “They spin around each other with great speed and seem driven by intense ferocity.” There is one recorded case of a butterfly, the Ageronia feronia, that produces a sound similar to a toothed wheel moving under a spring catch, which can be heard from several yards away. In Rio de Janeiro, I only noticed this sound when two butterflies were chasing each other in a chaotic manner, suggesting it likely occurs during their courtship, although I didn’t pay enough attention to this detail.503
Every one has admired the extreme beauty of many butterflies and of some moths; and we are led to ask, how has this beauty been acquired? Have their colours and diversified patterns simply resulted from the direct action of the physical conditions to which these insects have been exposed, without any benefit being thus derived? Or have successive variations been accumulated and determined either as a protection or for some unknown purpose, or that one sex might be rendered attractive to the other? And, again, what is the meaning of the colours being widely different in the males and females of certain species, and alike in the two sexes of other species? Before attempting to answer these questions a body of facts must be given.
Everyone has admired the striking beauty of many butterflies and some moths; and we are led to ask, how has this beauty come about? Have their colors and varied patterns simply resulted from the direct influence of the physical conditions these insects have experienced, without any benefits arising? Or have successive variations been accumulated and shaped either for protection or some unknown purpose, or to make one sex more attractive to the other? Additionally, what does it mean that the colors are vastly different in the males and females of certain species, yet the same in both sexes of others? Before trying to answer these questions, a collection of facts must be presented.
With most of our English butterflies, both those which are beautiful, such as the admiral, peacock, and painted lady (Vanessæ), and those which are plain-coloured, such as the meadow-browns (Hipparchiæ), the sexes are alike. This is also the case with the magnificent Heliconidæ and Danaidæ of the tropics. But in certain 388other tropical groups, and with some of our English butterflies, as the purple emperor, orange-tip, &c. (Apatura Iris and Anthocharis cardamines), the sexes differ either greatly or slightly in colour. No language suffices to describe the splendour of the males of some tropical species. Even within the same genus we often find species presenting an extraordinary difference between the sexes, whilst others have their sexes closely alike. Thus in the South American genus Epicalia, Mr. Bates, to whom I am much indebted for most of the following facts and for looking over this whole discussion, informs me that he knows twelve species, the two sexes of which haunt the same stations (and this is not always the case with butterflies), and therefore cannot have been differently affected by external conditions504. In nine of these species the males rank amongst the most brilliant of all butterflies, and differ so greatly from the comparatively plain females that they were formerly placed in distinct genera. The females of these nine species resemble each other in their general type of coloration, and likewise resemble both sexes in several allied genera, found in various parts of the world. Hence in accordance with the descent-theory we may infer that these nine species, and probably all the others of the genus, are descended from an ancestral form which was coloured in nearly the same manner. In the tenth species the female still retains the same general colouring, but the male resembles her, so that he is coloured in a much less gaudy and contrasted manner than the males of the previous species. In the eleventh and twelfth species, the females depart from the type of colouring which 389is usual with their sex in this genus, for they are gaily decorated in nearly the same manner as the males, but in a somewhat less degree. Hence in these two species the bright colours of the males seem to have been transferred to the females; whilst the male of the tenth species has either retained or recovered the plain colours of the female as well as of the parent-form of the genus; the two sexes being thus rendered in both cases, though in an opposite manner, nearly alike. In the allied genus Eubagis, both sexes of some of the species are plain-coloured and nearly alike; whilst with the greater number the males are decorated with beautiful metallic tints, in a diversified manner, and differ much from their females. The females throughout the genus retain the same general style of colouring, so that they commonly resemble each other much more closely than they resemble their own proper males.
With most of our British butterflies, both the beautiful ones like the admiral, peacock, and painted lady (Vanessæ), and the plainer ones like the meadow-browns (Hipparchiæ), the sexes look pretty similar. This is also true for the stunning Heliconidæ and Danaidæ found in the tropics. However, in some other tropical groups, and with certain British butterflies like the purple emperor and orange-tip (Apatura Iris and Anthocharis cardamines), the sexes differ significantly or slightly in color. No words can adequately describe the brilliance of the males of some tropical species. Even within the same genus, we often see species that display remarkable differences between the sexes, while others appear very alike. For example, in the South American genus Epicalia, Mr. Bates, who has been very helpful in providing most of the following information and reviewing this discussion, tells me he knows twelve species where both sexes frequent the same locations (and this is not always the case with butterflies), so they couldn’t have been affected differently by external conditions504. In nine of these species, the males are among the most vibrant of all butterflies and differ so much from the relatively plain females that they used to be classified in different genera. The females of these nine species share a common type of coloration and also resemble both sexes in several related genera found around the world. Thus, according to the theory of descent, we may infer that these nine species, and likely all the others in the genus, descended from an ancestral form that had a similar coloring. In the tenth species, the female still has a similar general coloration, but the male resembles her, appearing much less flashy and contrasting than the males of the previous species. In the eleventh and twelfth species, the females deviate from the typical coloration seen in their sex in this genus; they are brightly decorated in a way similar to the males, though to a lesser extent. Therefore, in these two species, the males' bright colors seem to have been transferred to the females, while the male of the tenth species has either retained or regained the plain colors of the female as well as the ancestral form of the genus; thus, the two sexes are rendered quite similar in both cases, albeit in opposite ways. In the related genus Eubagis, both sexes of some species are plain-colored and nearly identical; however, in most cases, the males are adorned with beautiful metallic shades that differ significantly from their females. Throughout the genus, females generally maintain the same broad color scheme, resulting in them often resembling each other much more closely than they do their own males.
In the genus Papilio, all the species of the Æneas group are remarkable for their conspicuous and strongly contrasted colours, and they illustrate the frequent tendency to gradation in the amount of difference between the sexes. In a few species, for instance in P. ascanius, the males and females are alike; in others the males are a little or very much more superbly coloured than the females. The genus Junonia allied to our Vanessæ offers a nearly parallel case, for although the sexes of most of the species resemble each other and are destitute of rich colours, yet in certain species, as in J. œnone, the male is rather more brightly coloured than the female, and in a few (for instance J. andremiaja) the male is so different from the female that he might be mistaken for an entirely distinct species.
In the genus Papilio, all the species in the Æneas group are known for their striking and contrasting colors, showcasing the common trend of differences between the sexes. In a few species, like P. ascanius, the males and females look alike; in others, the males are somewhat or significantly more colorful than the females. The genus Junonia, which is related to our Vanessæ, presents a similar situation. Most species have sexes that look alike and lack vibrant colors, but in certain cases, like J. œnone, the male is a bit more vividly colored than the female. In a few species, like J. andremiaja, the male is so different from the female that he could easily be mistaken for a completely different species.
Another striking case was pointed out to me in the British museum by Mr. A. Butler, namely one of the Tropical American Theclæ, in which both sexes390 are nearly alike and wonderfully splendid; in another, the male is coloured in a similarly gorgeous manner, whilst the whole upper surface of the female is of a dull uniform brown. Our common little English blue butterflies of the genus Lycæna, illustrate the various differences in colour between the sexes, almost as well, though not in so striking a manner, as the above exotic genera. In Lycæna agestis both sexes have wings of a brown colour, bordered with small ocellated orange spots, and are consequently alike. In L. œgon the wings of the male are of a fine blue, bordered with black; whilst the wings of the female are brown, with a similar border, and closely resemble those of L. agestis. Lastly, in L. arion both sexes are of a blue colour and nearly alike, though in the female the edges of the wings are rather duskier, with the black spots plainer; and in a bright blue Indian species both sexes are still more closely alike.
Another striking example was pointed out to me at the British Museum by Mr. A. Butler, specifically one of the Tropical American Theclæ, where both sexes390 are nearly identical and incredibly vibrant; in another, the male is colored in a similarly stunning way, while the entire upper surface of the female is a dull, uniform brown. Our common little English blue butterflies of the genus Lycæna showcase the various differences in color between the sexes, almost as effectively, though not as dramatically, as the exotic species mentioned earlier. In Lycæna agestis, both sexes have brown wings that are edged with small, eye-catching orange spots, making them quite similar. In L. œgon, the male's wings are a brilliant blue with a black border; meanwhile, the female's wings are brown with a similar border, closely resembling those of L. agestis. Finally, in L. arion, both sexes have blue wings and are nearly identical, although the female’s wing edges are slightly darker, with the black spots more pronounced; in a bright blue Indian species, both sexes look even more alike.
I have given the foregoing cases in some detail in order to shew, in the first place, that when the sexes of butterflies differ, the male as a general rule is the most beautiful, and departs most from the usual type of colouring of the group to which the species belongs. Hence in most groups the females of the several species resemble each other much more closely than do the males. In some exceptional cases, however, to which I shall hereafter allude, the females are coloured more splendidly than the males. In the second place these cases have been given to bring clearly before the mind that within the same genus, the two sexes frequently present every gradation from no difference in colour to so great a difference that it was long before the two were placed by entomologists in the same genus. In the third place, we have seen that when the sexes nearly resemble each other, this apparently may be due either to the391 male having transferred his colours to the female, or to the male having retained, or perhaps recovered, the primordial colours of the genus to which the species belongs. It also deserves notice that in those groups in which the sexes present any difference of colour, the females usually resemble the males to a certain extent, so that when the males are beautiful to an extraordinary degree, the females almost invariably exhibit some degree of beauty. From the numerous cases of gradation in the amount of difference between the sexes, and from the prevalence of the same general type of coloration throughout the whole of the same group, we may conclude that the causes, whatever they may be, which have determined the brilliant colouring of the males alone of some species, and of both sexes in a more or less equal degree of other species, have generally been the same.
I have provided the previous cases in some detail to show, first, that when butterfly sexes differ, the male is usually the more beautiful and strays further from the typical coloring of its species group. Therefore, in most groups, females of different species resemble each other much more than the males do. However, in some exceptional cases that I will mention later, females are more vibrantly colored than males. Secondly, these cases highlight that within the same genus, the two sexes often display every possible gradient from no color difference to such a significant difference that it took entomologists a long time to classify them in the same genus. Thirdly, we have observed that when the sexes closely resemble each other, this may either be because the male has passed his colors onto the female or because the male has retained, or possibly regained, the original colors of the genus. It’s also worth noting that in groups where the sexes show any color difference, females usually resemble males to some degree, so that when males are exceptionally beautiful, females almost always show some beauty as well. From the many examples of varying degrees of difference between the sexes and from the consistent general type of coloration across the whole group, we can conclude that the factors, whatever they may be, that have led to the brilliant coloring of the males alone in some species and to both sexes having a more or less equal degree of beauty in others have generally been the same.
As so many gorgeous butterflies inhabit the tropics, it has often been supposed that they owe their colours to the great heat and moisture of these zones; but Mr. Bates505 has shewn by the comparison of various closely-allied groups of insects from the temperate and tropical regions, that this view cannot be maintained; and the evidence becomes conclusive when brilliantly-coloured males and plain-coloured females of the same species inhabit the same district, feed on the same food, and follow exactly the same habits of life. Even when the sexes resemble each other, we can hardly believe that their brilliant and beautifully-arranged colours are the purposeless result of the nature of the tissues, and the action of the surrounding conditions.
As many beautiful butterflies live in tropical areas, it’s often thought that their colors come from the intense heat and humidity of these regions. However, Mr. Bates505 has shown through comparisons of various closely related groups of insects from temperate and tropical areas that this idea doesn't hold up. The evidence becomes clear when you see that brightly colored males and plain-colored females of the same species live in the same area, eat the same food, and share identical lifestyles. Even when the sexes look alike, it’s hard to believe that their vivid, beautifully arranged colors are just random outcomes of tissue properties and environmental influences.
With animals of all kinds, whenever colour has been modified for some special purpose, this has been, as far 392as we can judge, either for protection or as an attraction between the sexes. With many species of butterflies the upper surfaces of the wings are obscurely coloured, and this in all probability leads to their escaping observation and danger. But butterflies when at rest would be particularly liable to be attacked by their enemies; and almost all the kinds when resting raise their wings vertically over their backs, so that the lower sides alone are exposed to view. Hence it is this side which in many cases is obviously coloured so as to imitate the surfaces on which these insects commonly rest. Dr. Rössler, I believe, first noticed the similarity of the closed wings of certain Vanessæ and other butterflies to the bark of trees. Many analogous and striking facts could be given. The most interesting one is that recorded by Mr. Wallace506 of a common Indian and Sumatran butterfly (Kallima), which disappears like magic when it settles in a bush; for it hides its head and antennæ between its closed wings, and these in form, colour, and veining cannot be distinguished from a withered leaf together with the footstalk. In some other cases the lower surfaces of the wings are brilliantly coloured, and yet are protective; thus in Thecla rubi the wings when closed are of an emerald green and resemble the young leaves of the bramble, on which this butterfly in the spring may often be seen seated.
With all kinds of animals, whenever color has been changed for a specific reason, it seems to be either for protection or to attract mates. Many species of butterflies have dark-colored upper wings, which likely helps them avoid being seen and staying safe from danger. However, when butterflies rest, they are particularly vulnerable to predators; almost all species raise their wings vertically over their backs, exposing only the underside. Because of this, the underside is often colored to blend in with the surfaces where these insects usually rest. Dr. Rössler was the first to notice that the closed wings of certain Vanessæ and other butterflies resemble tree bark. Many similar and remarkable examples exist. The most fascinating one is noted by Mr. Wallace about a common Indian and Sumatran butterfly (Kallima), which appears to vanish like magic when it lands on a bush. It hides its head and antennae between its closed wings, which, in shape, color, and veining, perfectly mimic a withered leaf along with its stalk. In other cases, the underside of the wings is brightly colored yet still offers protection; for example, in Thecla rubi, the wings, when closed, are bright emerald green and look like young bramble leaves, where this butterfly can often be seen resting in the spring.
Although the obscure tints of the upper or under surface of many butterflies no doubt serve to conceal them, yet we cannot possibly extend this view to the brilliant and conspicuous colours of many kinds, such as our admiral and peacock Vanessæ, our white 393cabbage-butterflies (Pieris), or the great swallow-tail Papilio which haunts the open fens—for these butterflies are thus rendered visible to every living creature. With these species both sexes are alike; but in the common brimstone butterfly (Gonepteryx rhamni), the male is of an intense yellow, whilst the female is much paler; and in the orange-tip (Anthocharis cardamines) the males alone have the bright orange tips to their wings. In these cases the males and females are equally conspicuous, and it is not credible that their difference in colour stands in any relation to ordinary protection. Nevertheless it is possible that the conspicuous colours of many species may be in an indirect manner beneficial, as will hereafter be explained, by leading their enemies at once to recognise them as unpalatable. Even in this case it does not certainly follow that their bright colours and beautiful patterns were acquired for this special purpose. In some other remarkable cases, beauty has been gained for the sake of protection, through the imitation of other beautiful species, which inhabit the same district and enjoy an immunity from attack by being in some way offensive to their enemies.
Although the subtle colors on the upper or lower surfaces of many butterflies help to camouflage them, we can’t really say the same about the bright and eye-catching colors of various species, like our admiral and peacock butterflies, our white cabbage butterflies (Pieris), or the large swallowtail Papilio that frequents open marshes—these butterflies are clearly visible to all living creatures. In these species, both males and females look the same; however, in the common brimstone butterfly (Gonepteryx rhamni), the male is a vibrant yellow, while the female is much lighter; and in the orange-tip (Anthocharis cardamines), only the males have the bright orange tips on their wings. In these instances, both males and females stand out, and it’s hard to believe that their color differences relate to regular protection. Still, it may be that the bright colors of many species have an indirect advantage by helping predators recognize them as unappetizing. Even then, it doesn’t necessarily mean their vivid colors and striking patterns evolved specifically for this reason. In some other interesting cases, beauty has been developed for the sake of protection, by mimicking other attractive species that live in the same area and manage to avoid being attacked because they are somehow distasteful to their enemies.
The female of our orange-tip butterfly, above referred to, and of an American species (Anth. genutia) probably shew us, as Mr. Walsh has remarked to me, the primordial colours of the parent-species of the genus; for both sexes of four or five widely-distributed species are coloured in nearly the same manner. We may infer here, as in several previous cases, that it is the males of Anth. cardamines and genutia which have departed from the usual type of colouring of their genus. In the Anth. sara from California, the orange-tips have become partially developed in the female; for her wings are tipped with reddish-orange, but paler than in the394 male, and slightly different in some other respects. In an allied Indian form, the Iphias glaucippe, the orange-tips are fully developed in both sexes. In this Iphias the under surface of the wings marvellously resembles, as pointed out to me by Mr. A. Butler, a pale-coloured leaf; and in our English orange-tip, the under surface resembles the flower-head of the wild parsley, on which it may be seen going to rest at night.507 The same reasoning power which compels us to believe that the lower surfaces have here been coloured for the sake of protection, leads us to deny that the wings have been tipped, especially when this character is confined to the males, with bright orange for the same purpose.
The female orange-tip butterfly mentioned earlier, as well as an American species (Anth. genutia), likely represent the original colors of the parent species of the genus, as Mr. Walsh pointed out to me. Both males and females of four or five widely distributed species have similar coloring. We can conclude, as in several earlier cases, that it’s the males of Anth. cardamines and genutia that have strayed from the usual color pattern of their genus. In the Anth. sara from California, the female's orange tips are somewhat developed; her wings have a reddish-orange tip, though it’s lighter than in the male, and somewhat different in other ways. In a related Indian species, the Iphias glaucippe, the orange tips are fully developed in both sexes. In this Iphias, the underside of the wings strikingly resembles, as Mr. A. Butler pointed out to me, a light-colored leaf; while in our English orange-tip, the underside resembles the flower head of wild parsley, where it may be seen resting at night.394 The same reasoning that leads us to believe the undersides are colored for protection also makes us reject the idea that the wings are tipped, especially since this feature is limited to the males, with bright orange for the same reason.
Turning now to Moths: most of these rest motionless with their wings depressed during the whole or greater part of the day; and the upper surfaces of their wings are often shaded and coloured in an admirable manner, as Mr. Wallace has remarked, for escaping detection. With most of the Bombycidæ and Noctuidæ,508 when at rest, the front-wings overlap and conceal the hind-wings; so that the latter might be brightly coloured without much risk; and they are thus coloured in many species of both families. During the act of flight, moths would often be able to escape from their enemies; nevertheless, as the hind-wings are then fully exposed to view, their bright colours must generally have been acquired at the cost of some little risk. But the following fact shews us how cautious we ought to be in drawing conclusions on this head. The common yellow under-wings 395(Triphaena) often fly about during the day or early evening, and are then conspicuous from the colour of their hind-wings. It would naturally be thought that this would be a source of danger; but Mr. J. Jenner Weir believes that it actually serves them as a means of escape, for birds strike at these brightly coloured and fragile surfaces, instead of at the body. For instance, Mr. Weir turned into his aviary a vigorous specimen of Triphaena pronuba, which was instantly pursued by a robin; but the bird’s attention being caught by the coloured wings, the moth was not captured until after about fifty attempts, and small portions of the wings were repeatedly broken off. He tried the same experiment, in the open air, with a T. fimbria and swallow; but the large size of this moth probably interfered with its capture.509 We are thus reminded of a statement made by Mr. Wallace,510 namely, that in the Brazilian forests and Malayan islands, many common and highly-decorated butterflies are weak flyers, though furnished with a broad expanse of wings; and they “are often captured with pierced and broken wings, as if they had been seized by birds, from which they had escaped: if the wings had been much smaller in proportion to the body, it seems probable that the insect would more frequently have been struck or pierced in a vital part, and thus the increased expanse of the wings may have been indirectly beneficial.”
Turning now to moths: most of them stay still with their wings down for most of the day. The upper surfaces of their wings are often beautifully shaded and colored, as Mr. Wallace noted, to help them avoid being seen. In most of the Bombycidae and Noctuidae families,508 when at rest, the front wings overlap and hide the hind wings, so the hind wings can be brightly colored without much risk. Many species in both families are indeed brightly colored. While moths can often escape from predators when flying, their hind wings are fully visible then, so their bright colors must come with some risk. However, one fact shows us to be careful when making conclusions on this topic. The common yellow under-wings 395(Triphaena) often fly during the day or early evening and are noticeable because of their colorful hind wings. You would think this poses a danger, but Mr. J. Jenner Weir believes it actually helps them escape. Birds tend to strike at these bright, delicate wings instead of the moth's body. For example, Mr. Weir put a strong specimen of Triphaena pronuba into his aviary, and it was immediately chased by a robin. However, the bird was distracted by the colored wings, and the moth wasn't caught until after around fifty attempts, during which small parts of its wings were repeatedly broken off. He performed the same test outdoors with a T. fimbria and a swallow, but the large size of this moth likely made it harder to catch.509 This reminds us of a statement made by Mr. Wallace,510 who said that in the Brazilian forests and Malayan islands, many common and beautifully decorated butterflies are weak flyers, even though they have large wings. They “often end up with pierced and broken wings, as if they had been grabbed by birds but managed to escape. If their wings were much smaller in proportion to their bodies, it seems likely they would more often be hit or pierced in a vital area, and thus their larger wings may have been indirectly beneficial.”
Display.—The bright colours of butterflies and of some moths are specially arranged for display, whether or not they serve in addition as a protection. Bright 396colours would not be visible during the night; and there can be no doubt that moths, taken as a body, are much less gaily decorated than butterflies, all of which are diurnal in their habits. But the moths in certain families, such as the Zygænidæ, various Sphingidæ, Uraniidæ, some Arctiidæ and Saturniidæ, fly about during the day or early evening, and many of these are extremely beautiful, being far more brightly coloured than the strictly nocturnal kinds. A few exceptional cases, however, of brightly-coloured nocturnal species have been recorded.511
Display.—The vibrant colors of butterflies and some moths are specifically arranged for show, whether or not they also provide protection. Bright colors wouldn’t be seen at night; and it’s clear that moths, as a group, are generally less brightly patterned than butterflies, which are all active during the day. However, some moth families, like the Zygænidæ, various Sphingidæ, Uraniidæ, certain Arctiidæ, and Saturniidæ, fly during the day or early evening, and many of these are exceptionally beautiful, being much more vividly colored than the strictly nocturnal types. There have been a few rare instances of brightly colored nocturnal species being documented.511
There is evidence of another kind in regard to display. Butterflies, as before remarked, elevate their wings when at rest, and whilst basking in the sunshine often alternately raise and depress them, thus exposing to full view both surfaces; and although the lower surface is often coloured in an obscure manner as a protection, yet in many species it is as highly coloured as the upper surface, and sometimes in a very different manner. In some tropical species the lower surface is even more brilliantly coloured than the upper.512 In one English fritillary, the Argynnis aglaia, the lower surface alone is ornamented with shining silver discs. Nevertheless, as a general rule, the upper surface, which is probably the most fully exposed, is coloured more brightly and in a more diversified manner than the lower. Hence the lower surface generally affords 397to entomologists the most useful character for detecting the affinities of the various species.
There’s another kind of evidence when it comes to display. Butterflies, as mentioned before, raise their wings when they’re at rest, and while basking in the sun, they often lift and lower them alternately, showing both surfaces fully. Although the underside is often colored in a way that makes it less noticeable for protection, in many species, it is just as colorful as the top side, and sometimes in a very different way. In some tropical species, the underside is even more vibrantly colored than the top. In one English fritillary, the Argynnis aglaia, only the underside is decorated with shiny silver discs. However, as a general rule, the upper surface, which is likely the most exposed, is colored more brightly and in a more varied manner than the lower. Therefore, the underside usually provides 397entomologists with the most useful characteristics for identifying the relationships between different species.
Now if we turn to the enormous group of moths, which do not habitually expose to full view the under surface of their wings, this side is very rarely, as I hear from Mr. Stainton, coloured more brightly than the upper side, or even with equal brightness. Some exceptions to the rule, either real or apparent, must be noticed, as that of Hypopira, specified by Mr. Wormald.513 Mr. R. Trimen informs me that in Guenée’s great work, three moths are figured, in which the under surface is much the most brilliant. For instance, in the Australian Gastrophora the upper surface of the fore-wing is pale greyish-ochreous, while the lower surface is magnificently ornamented by an ocellus of cobalt-blue, placed in the midst of a black mark, surrounded by orange-yellow, and this by bluish-white. But the habits of these three moths are unknown; so that no explanation can be given of their unusual style of colouring. Mr. Trimen also informs me that the lower surface of the wings in certain other Geometræ514 and quadrifid Noctuæ are either more variegated or more brightly-coloured than the upper surface; but some of these species have the habit of “holding their wings quite erect over their backs, retaining them in this position for a considerable time,” and thus exposing to view the under surface. Other species when settled on the ground or herbage have the habit of now and then suddenly and slightly lifting up their wings. Hence the lower surface of the wings being more brightly-coloured than the upper sur398face in certain moths is not so anomalous a circumstance as it at first appears. The Saturniidæ include some of the most beautiful of all moths, their wings being decorated, as in our British Emperor moth, with fine ocelli; and Mr. T. W. Wood515 observes that they resemble butterflies in some of their movements; “for instance, in the gentle waving up and down of the wings, as if for display, which is more characteristic of diurnal than of nocturnal Lepidoptera.”
Now, if we look at the large group of moths that usually don’t show the underside of their wings, this side is rarely, according to Mr. Stainton, colored more brightly than the top side, or even equally bright. There are a few exceptions to this rule, either actual or seeming, like that of Hypopira, mentioned by Mr. Wormald.513 Mr. R. Trimen tells me that in Guenée’s major work, three moths are illustrated where the underside is much more vibrant. For example, in the Australian Gastrophora, the top side of the forewing is a pale greyish-yellow, while the underside is beautifully decorated with a cobalt-blue ocellus set in a black mark, surrounded by orange-yellow, and then by bluish-white. However, the behaviors of these three moths are unknown, so we can’t explain their unusual color patterns. Mr. Trimen also notes that the undersides of the wings in certain other Geometræ514 and quadrifid Noctuæ are either more colorful or brighter than the upper side; but some of these species have the behavior of “holding their wings straight up over their backs, keeping them in this position for a long time,” which shows the underside. Other species, when resting on the ground or plants, sometimes suddenly and slightly lift their wings. Thus, the fact that the underside of the wings is more brightly colored than the upper side in certain moths isn’t as unusual as it may first seem. The Saturniidæ includes some of the most beautiful moths, their wings adorned, as seen in our British Emperor moth, with fine ocelli; and Mr. T. W. Wood515 points out that they move similarly to butterflies; “for instance, in the gentle up-and-down waving of their wings, as if to display, which is more typical of daytime than nighttime Lepidoptera.”
It is a singular fact that no British moths, nor as far as I can discover hardly any foreign species, which are brilliantly coloured, differ much in colour according to sex; though this is the case with many brilliant butterflies. The male, however, of one American moth, the Saturnia Io, is described as having its fore-wings deep yellow, curiously marked with purplish-red spots; whilst the wings of the female are purple-brown, marked with grey lines.516 The British moths which differ sexually in colour are all brown, or various tints of dull yellow, or nearly white. In several species the males are much darker than the females,517 and these belong to groups which generally fly about during the afternoon. On the other hand, in many genera, as Mr. Stainton informs me, 399the males have the hind-wings whiter than those of the female—of which, fact Agrotis exclamationis offers a good instance. The males are thus rendered more conspicuous than the females, whilst flying about in the dusk. In the Ghost Moth (Hepialus humuli) the difference is more strongly marked; the males being white and the females yellow with darker markings. It is difficult to conjecture what the meaning can be of these differences between the sexes in the shades of darkness or lightness; but we can hardly suppose that they are the result of mere variability with sexually-limited inheritance, independently of any benefit thus derived.
It’s a unique fact that British moths, and as far as I can tell, nearly all foreign species that are brightly colored, don’t show much difference in color between males and females; this is not the case with many bright butterflies. However, the male of one American moth, the Saturnia Io, is said to have deep yellow fore-wings marked with purplish-red spots, while the female’s wings are purple-brown with grey lines.516 The British moths that do show sexual color differences are all brown or various shades of dull yellow or nearly white. In several species, the males are much darker than the females,517 and these belong to groups that typically fly around in the afternoon. On the other hand, many genera, as Mr. Stainton informs me, 399have males with hind-wings that are whiter than those of the female—this is well illustrated by Agrotis exclamationis. This makes the males stand out more than the females while they’re flying in the dusk. In the Ghost Moth (Hepialus humuli), the difference is even more pronounced; the males are white and the females are yellow with darker markings. It’s hard to guess what these differences in lightness or darkness between the sexes mean, but we can hardly think they’re just the result of variability with sexually-limited inheritance without any benefits involved.
From the foregoing statements it is impossible to admit that the brilliant colours of butterflies and of some few moths, have commonly been acquired for the sake of protection. We have seen that their colours and elegant patterns are arranged and exhibited as if for display. Hence I am led to suppose that the females generally prefer, or are most excited by the more brilliant males; for on any other supposition the males would be ornamented, as far as we can see, for no purpose. We know that ants and certain lamellicorn beetles are capable of feeling an attachment for each other, and that ants recognise their fellows after an interval of several months. Hence there is no abstract improbability in the Lepidoptera, which probably stand nearly or quite as high in the scale as these insects, having sufficient mental capacity to admire bright colours. They certainly discover flowers by colour, and, as I have elsewhere shewn, the plants which are fertilised exclusively by the wind never have a conspicuously-coloured corolla. The Humming-bird Sphinx may often be seen to swoop down from a distance on a bunch of flowers in the midst of green foliage;400 and I have been assured by a friend, that these moths repeatedly visited flowers painted on the walls of a room in the South of France. The common white butterfly, as I hear from Mr. Doubleday, often flies down to a bit of paper on the ground, no doubt mistaking it for one of its own species. Mr. Collingwood518 in speaking of the difficulty of collecting certain butterflies in the Malay Archipelago, states that “a dead specimen pinned upon a conspicuous twig will often arrest an insect of the same species in its headlong flight, and bring it down within easy reach of the net, especially if it be of the opposite sex.”
From the earlier statements, it's clear that the bright colors of butterflies and some moths are not typically developed just for protection. Their colors and striking patterns seem to be designed for display. This leads me to believe that females generally prefer or are more attracted to the more colorful males; otherwise, the males would be adorned without any real reason. We know that ants and some beetles can form bonds with each other, and ants can recognize their companions after several months apart. Therefore, there's no reason to doubt that Lepidoptera, which likely rank similarly to these insects in intelligence, have enough mental capacity to appreciate bright colors. They definitely locate flowers by color, and as I've shown elsewhere, plants that are solely wind-pollinated never have notably colored petals. The Hummingbird Sphinx can often be seen diving down from afar toward a cluster of flowers amidst green leaves; a friend of mine has told me that these moths frequently visit flowers painted on walls in southern France. The common white butterfly, as Mr. Doubleday mentions, often flies down to a piece of paper on the ground, likely mistaking it for one of its kind. Mr. Collingwood, discussing the challenges of collecting certain butterflies in the Malay Archipelago, notes that “a dead specimen pinned to a noticeable twig will often catch an insect of the same species in its fast flight, bringing it down within easy reach of the net, especially if it's the opposite sex.”
The courtship of butterflies is a prolonged affair. The males sometimes fight together in rivalry; and many may be seen pursuing or crowding round the same female. If, then, the females do not prefer one male to another, the pairing must be left to mere chance, and this does not appear to me a probable event. If, on the other hand, the females habitually, or even occasionally, prefer the more beautiful males, the colours of the latter will have been rendered brighter by degrees, and will have been transmitted to both sexes or to one sex, according to which law of inheritance prevailed. The process of sexual selection will have been much facilitated, if the conclusions arrived at from various kinds of evidence in the supplement to the ninth chapter can be trusted; namely that the males of many Lepidoptera, at least in the imago state, greatly exceed in number the females.
The courtship of butterflies takes a long time. The males sometimes compete with each other, and many can be seen chasing or surrounding the same female. If the females don’t prefer one male over another, then pairing must be left to chance, which seems unlikely. On the other hand, if females often or even sometimes prefer the more beautiful males, the colors of those males will likely have become brighter over time and will be passed on to both sexes or just one, depending on which inheritance rule is in play. The process of sexual selection would be much easier, if the conclusions drawn from various types of evidence in the supplement to the ninth chapter are reliable; namely that the males of many Lepidoptera, at least in the adult stage, significantly outnumber the females.
Some facts, however, are opposed to the belief that female butterflies prefer the more beautiful males; thus, as I have been assured by several observers, fresh females may frequently be seen paired with battered, faded or 401dingy males; but this is a circumstance which could hardly fail often to follow from the males emerging from their cocoons earlier than the females. With moths of the family of the Bombycidæ, the sexes pair immediately after assuming the imago state; for they cannot feed, owing to the rudimentary condition of their mouths. The females, as several entomologists have remarked to me, lie in an almost torpid state, and appear not to evince the least choice in regard to their partners, This is the case with the common silk-moth (B. mori), as I have been told by some continental and English breeders. Dr. Wallace, who has had such immense experience in breeding Bombyx cynthia, is convinced that the females evince no choice or preference. He has kept above 300 of these moths living together, and has often found the most vigorous females mated with stunted males. The reverse apparently seldom occurs; for, as he believes, the more vigorous males pass over the weakly females, being attracted by those endowed with most vitality. Although we have been indirectly induced to believe that the females of many species prefer the more beautiful males, I have no reason to suspect, either with moths or butterflies, that the males are attracted by the beauty of the females. If the more beautiful females had been continually preferred, it is almost certain, from the colours of butterflies being so frequently transmitted to one sex alone, that the females would often have been rendered more beautiful than their male partners. But this does not occur except in a few instances; and these can be explained, as we shall presently see, on the principle of mimickry and protection.
Some facts, however, challenge the idea that female butterflies prefer the more attractive males. As I've been told by several observers, fresh females are often seen paired with worn out, faded, or dingy males. This situation likely happens because the males emerge from their cocoons before the females. In the case of moths from the Bombycidae family, the males and females pair up right after they become adults since they can't feed due to their underdeveloped mouths. The females, as several entomologists have pointed out to me, lie in a nearly motionless state and don't seem to show any real preference for their partners. This is true for the common silk moth (B. mori), according to some breeders from Europe and England. Dr. Wallace, who has extensive experience breeding Bombyx cynthia, believes that females show no choice or preference. He has kept over 300 of these moths together, and he often finds the strongest females paired with stunted males. The opposite rarely happens; he thinks the more robust males skip over weaker females, attracted instead to those with greater vitality. While we've been led to believe that females of many species prefer the more beautiful males, I have no reason to think that, with either moths or butterflies, males are drawn to the beauty of females. If the more attractive females had always been favored, it’s almost certain that, since butterfly colors are frequently passed on to one sex only, females would often be more beautiful than their male counterparts. However, this only occurs in a few cases, which can be explained, as we will soon discuss, through the principles of mimicry and protection.
As sexual selection primarily depends on variability, a few words must be added on this subject. In respect402 to colour there is no difficulty, as any number of highly variable Lepidoptera could be named. One good instance will suffice. Mr. Bates shewed me a whole series of specimens of Papilio sesostris and childrenæ; in the latter the males varied much in the extent of the beautifully enamelled green patch on the fore-wings, and in the size of the white mark, as well as of the splendid crimson stripe on the hind-wings; so that there was a great contrast between the most and least gaudy males. The male of Papilio sesostris, though a beautiful insect, is much less so than P. childrenæ. It likewise varies a little in the size of the green patch on the fore-wings, and in the occasional appearance of a small crimson stripe on the hind-wings, borrowed, as it would seem, from its own female; for the females of this and of many other species in the Æneas group possess this crimson stripe. Hence between the brightest specimens of P. sesostris and the least bright of P. childrenæ, there was but a small interval; and it was evident that as far as mere variability is concerned, there would be no difficulty in permanently increasing by means of selection the beauty of either species. The variability is here almost confined to the male sex; but Mr. Wallace and Mr. Bates have shewn519 that the females of some other species are extremely variable, the males being nearly constant. As I have before mentioned the Ghost Moth (Hepialus humuli) as one of the best instances in Britain of a difference in colour between the sexes of moths, it may be worth adding520 that in the Shetland 403Islands, males are frequently found which closely resemble the females. In a future chapter I shall have occasion to shew that the beautiful eye-like spots or ocelli, so common on the wings of many Lepidoptera, are eminently variable.
As sexual selection mainly relies on variability, a few words need to be said about it. When it comes to color, there’s no issue, as many highly variable butterflies can be named. One good example is enough. Mr. Bates showed me a whole collection of specimens of Papilio sesostris and P. childrenæ; in the latter, the males varied greatly in the size of the beautifully colored green patch on their fore-wings and in the size of the white mark, as well as the striking crimson stripe on their hind-wings, resulting in a significant contrast between the most and least vivid males. The male of P. sesostris, while a stunning insect, is much less impressive than P. childrenæ. It also varies somewhat in the size of the green patch on the fore-wings and occasionally features a small crimson stripe on the hind-wings, seemingly borrowed from its own female; the females of this species and many others in the Æneas group possess this crimson stripe. Thus, between the brightest examples of P. sesostris and the dullest of P. childrenæ, there is only a small gap; it’s clear that, just in terms of variability, increasing the beauty of either species through selection would be possible. The variability is mostly limited to the males; however, Mr. Wallace and Mr. Bates have shown that the females of some other species are extremely variable while the males stay nearly constant. As I previously mentioned, the Ghost Moth (Hepialus humuli) is one of the best examples in Britain of a difference in color between the sexes of moths, and it’s worth noting that in the Shetland Islands, males are often found that closely resemble the females. In a future chapter, I will explain that the beautiful eye-like spots or ocelli, which are common on the wings of many butterflies, are highly variable.
On the whole, although many serious objections may be urged, it seems probable that most of the species of Lepidoptera which are brilliantly coloured, owe their colours to sexual selection, excepting in certain cases, presently to be mentioned, in which conspicuous colours are beneficial as a protection. From the ardour of the male throughout the animal kingdom, he is generally willing to accept any female; and it is the female which usually exerts a choice. Hence if sexual selection has here acted, the male, when the sexes differ, ought to be the most brilliantly coloured; and this undoubtedly is the ordinary rule. When the sexes are brilliantly coloured and resemble each other, the characters acquired by the males appear to have been transmitted to both sexes. But will this explanation of the similarity and dissimilarity in colour between the sexes suffice?
Overall, even though there are several serious objections that can be raised, it's likely that most of the brightly colored species of Lepidoptera owe their colors to sexual selection, except for certain cases, which will be mentioned soon, where noticeable colors are advantageous for protection. In the animal kingdom, males are generally eager to mate with any female, while it's usually the female who makes the choice. Therefore, if sexual selection plays a role here, the male, when the sexes are different, should be the one that is most vividly colored, which is typically the case. When both sexes are brightly colored and look alike, the traits developed by the males seem to have been passed down to both genders. But does this explanation regarding the similarities and differences in color between the sexes hold up?
The males and females of the same species of butterfly are known521 in several cases to inhabit different stations, the former commonly basking in the sunshine, the latter haunting gloomy forests. It is therefore possible that different conditions of life may have acted directly on the two sexes; but this is not probable,522 as in the adult state they are exposed during a very short period to different conditions; and the larvæ of both are exposed to the same conditions. Mr. Wallace believes 404that the less brilliant colours of the female have been specially gained in all or almost all cases for the sake of protection. On the contrary it seems to me more probable that the males alone, in the large majority of cases, have acquired their bright colours through sexual selection, the females having been but little modified. Consequently the females of distinct but allied species ought to resemble each other much more closely than do the males of the same species; and this is the general rule. The females thus approximately show us the primordial colouring of the parent-species of the group to which they belong. They have, however, almost always been modified to a certain extent by some of the successive steps of variation, through the accumulation of which the males were rendered beautiful, having been transferred to them. The males and females of allied though distinct species will also generally have been exposed during their prolonged larval state to different conditions, and may have been thus indirectly affected; though with the males any slight change of colour thus caused will often have been completely masked by the brilliant tints gained through sexual selection. When we treat of Birds, I shall have to discuss the whole question whether the differences in colour between the males and females have been in part specially gained by the latter as a protection; so that I will here only give unavoidable details.
The males and females of the same butterfly species are known521 to live in different environments in some cases: the males usually bask in the sun, while the females prefer dark, shady forests. It's possible that different living conditions could have directly affected both sexes, but that's unlikely,522 since as adults, they are only exposed to different conditions for a short time, and both larvae experience the same environment. Mr. Wallace believes404 that the less vibrant colors of the female have developed mainly for protection. However, I think it's more likely that the males, in most cases, have developed their bright colors through sexual selection, while the females have not changed much. Therefore, females of different but related species are expected to look much more alike than the males of the same species, which is generally true. The females often reflect the original coloring of the ancestral species of their group. Nevertheless, they have usually been slightly altered by various stages of variation, which have contributed to the males' beauty. The males and females of related but distinct species will also typically have experienced different conditions during their extended larval stage, potentially affecting them indirectly; however, any subtle color changes in males from this could be entirely overshadowed by the vivid colors achieved through sexual selection. When we discuss birds, I will need to address whether the color differences between males and females were partially developed in females for protective reasons, so for now, I'll only mention the essential details.
In all cases when the more common form of equal inheritance by both sexes has prevailed, the selection of bright-coloured males would tend to make the females bright-coloured; and the selection of dull-coloured females would tend to make the males dull. If both processes were carried on simultaneously, they would tend to neutralise each other. As far as I can see, it would be extremely difficult to change through selection the405 one form of inheritance into the other. But by the selection of successive variations, which were from the first sexually limited in their transmission, there would not be the slightest difficulty in giving bright colours to the males alone, and at the same time or subsequently, dull colours to the females alone. In this latter manner female butterflies and moths may, as I fully admit, have been rendered inconspicuous for the sake of protection, and widely different from their males.
In instances where equal inheritance is commonly shared between both sexes, choosing brightly colored males would likely lead to females becoming bright-colored as well, while selecting dull-colored females would likely result in dull males. If both processes occur at the same time, they would tend to balance each other out. From what I can see, it would be very challenging to change one type of inheritance into another through selection. However, by selecting successive variations that are initially limited in their sexual transmission, it would be easy to give bright colors to males alone, and at the same time or later, dull colors to females alone. In this way, it's possible that female butterflies and moths have become less noticeable for protection purposes and have diverged significantly from their male counterparts.
Mr. Wallace523 has argued with much force in favour of his view that when the sexes differ, the female has been specially modified for the sake of protection; and that this has been effected by one form of inheritance, namely, the transmission of characters to both sexes, having been changed through the agency of natural selection into the other form, namely, transmission to one sex. I was at first strongly inclined to accept this view; but the more I have studied the various classes throughout the animal kingdom, the less probable it has appeared. Mr. Wallace urges that both sexes of the Heliconidæ, Danaidæ, Acroeidæ are equally brilliant because both are protected from the attacks of birds and other enemies, by their offensive odour; but that in other groups, which do not possess this immunity, the females have been rendered inconspicuous, from having more need of protection than the males. This supposed difference in the “need of protection by the two sexes” is rather deceptive, and requires some discussion. It is obvious that brightly-coloured individuals, whether males or females, would equally attract, and obscurely-coloured individuals equally escape, the 406attention of their enemies. But we are concerned with the effects of the destruction or preservation of certain individuals of either sex, on the character of the race. With insects, after the male has fertilised the female, and after the latter has laid her eggs, the greater or less immunity from danger of either sex could not possibly have any effect on the offspring. Before the sexes have performed their proper functions, if they existed in equal numbers and if they strictly paired (all other circumstances being the same), the preservation of the males and females would be equally important for the existence of the species and for the character of the offspring. But with most animals, as is known to be the case with the domestic silk-moth, the male can fertilise two or three females; so that the destruction of the males would not be so injurious to the species as that of the females. On the other hand, Dr. Wallace believes that with moths the progeny from a second or third fertilisation is apt to be weakly, and therefore would not have so good chance of surviving. When the males exist in much greater numbers than the females, no doubt many males might be destroyed with impunity to the species; but I cannot see that the results of ordinary selection for the sake of protection would be influenced by the sexes existing in unequal numbers; for the same proportion of the more conspicuous individuals, whether males or females, would probably be destroyed. If indeed the males presented a greater range of variation in colour, the result would be different; but we need not here follow out such complex details. On the whole I cannot perceive that an inequality in the numbers of the two sexes would influence in any marked manner the effects of ordinary selection on the character of the offspring.
Mr. Wallace523 has strongly argued that when the sexes differ, the female has been specifically adapted for protection; and that this has happened through one form of inheritance, specifically the passing down of traits to both sexes, which has been altered by natural selection to become the other form, where traits are passed to one sex. Initially, I was quite inclined to accept this view; however, as I have studied various classes throughout the animal kingdom, it has seemed less and less likely. Mr. Wallace contends that both sexes of the Heliconidæ, Danaidæ, and Acroeidæ are equally vibrant because both are shielded from birds and other predators by their unpleasant smell; but in other groups that lack this protection, females have become less noticeable due to needing more protection than males. This assumed difference in the “need for protection between the two sexes” is somewhat misleading and needs further discussion. It’s clear that brightly colored individuals, whether male or female, would attract attention equally, while dull-colored individuals would escape notice just as easily. However, we are focused on how the loss or survival of certain individuals of either sex impacts the species' characteristics. With insects, after the male fertilizes the female, and she lays her eggs, the level of danger faced by either sex would not affect the offspring. Before the sexes perform their respective roles, if they exist in equal numbers and pair up strictly (under the same circumstances), the survival of the males and females would be equally important for the species' existence and the traits of the offspring. But with most animals, as is known with the domestic silk-moth, a single male can fertilize multiple females; thus, losing males wouldn’t harm the species as much as losing females would. On the flip side, Dr. Wallace argues that offspring from a second or third fertilization tend to be weaker and thus have a poorer chance of surviving. When males outnumber females significantly, it's true that many males could be eliminated without harming the species; however, I don’t see how the outcomes of typical selection for protection would be influenced by unequal sex ratios; the same percentage of the more noticeable individuals, whether male or female, would likely be eliminated. If males showed more variation in color, the outcome could be different; but we don’t need to delve into such intricate details here. Overall, I don’t think that a significant difference in the numbers of the two sexes would notably affect the results of standard selection on the offspring's characteristics.
Female Lepidoptera require, as Mr. Wallace insists,407 some days to deposit their fertilised ova and to search for a proper place; during this period (whilst the life of the male was of no importance) the brighter-coloured females would be exposed to danger and would be liable to be destroyed. The duller-coloured females on the other hand would survive, and thus would influence, it might be thought, in a marked manner the character of the species,—either of both sexes or of one sex, according to which form of inheritance prevailed. But it must not be forgotten that the males emerge from the cocoon-state some days before the females, and during this period, whilst the unborn females were safe, the brighter-coloured males would be exposed to danger; so that ultimately both sexes would probably be exposed during a nearly equal length of time to danger, and the elimination of conspicuous colours would not be much more effective in the one than the other sex.
Female butterflies need, as Mr. Wallace points out,407 a few days to lay their fertilized eggs and find a suitable spot. During this time (while the life of the male is not at risk), the more colorful females would be vulnerable and likely to be killed. In contrast, the dull-colored females would survive, which could significantly influence the species' traits—either for both sexes or just one, depending on dominant inheritance patterns. However, it’s important to remember that males emerge from their cocoons a few days before females, and during this time, while the yet-to-be-born females are safe, the brightly colored males would be at risk. Therefore, both sexes would likely face danger for about the same amount of time, and the elimination of conspicuous colors wouldn’t be any more effective for one sex than the other.
It is a more important consideration that female Lepidoptera, as Mr. Wallace remarks, and as is known to every collector, are generally slower flyers than the males. Consequently the latter, if exposed to greater danger from being conspicuously coloured, might be able to escape from their enemies, whilst the similarly-coloured females would be destroyed; and thus the females would have the most influence in modifying the colour of their progeny.
It’s more important to note that female moths and butterflies, as Mr. Wallace points out and every collector knows, generally fly more slowly than the males. As a result, the males, who are often brighter in color and face greater risks from predators, might be able to escape, while the similarly colored females would be more vulnerable and might be caught. This means that the females would have the greatest impact on changing the color of their offspring.
There is one other consideration: bright colours, as far as sexual selection is concerned, are commonly of no service to the females; so that if the latter varied in brightness, and the variations were sexually limited in their transmission, it would depend on mere chance whether the females had their bright colours increased; and this would tend throughout the Order to diminish the number of species with brightly-coloured females408 in comparison with the species having brightly-coloured males. On the other hand, as bright colours are supposed to be highly serviceable to the males in their love-struggles, the brighter males (as we shall see in the chapter on Birds) although exposed to rather greater danger, would on an average procreate a greater number of offspring than the duller males. In this case, if the variations were limited in their transmission to the male sex, the males alone would be rendered more brilliantly coloured; but if the variations were not thus limited, the preservation and augmentation of such variations would depend on whether more evil was caused to the species by the females being rendered conspicuous, than good to the males by certain individuals being successful over their rivals.
There's one more thing to think about: bright colors, in terms of sexual selection, usually don't benefit the females. If females varied in brightness and these variations were only passed on sexually, it would be a matter of chance whether the females became brighter. This would likely lead to fewer species of brightly-colored females compared to those with brightly-colored males. On the flip side, since bright colors are thought to really help males during courtship battles, the brighter males (as we’ll discuss in the chapter on Birds) would generally have more offspring, even though they face slightly more danger. In this scenario, if the variations were only passed down to the males, only the males would end up being more brightly colored. But if the variations weren't limited like that, the survival and increase of such variations would depend on whether the disadvantages of having conspicuous females outweighed the advantages for males when certain individuals beat their rivals.408
As there can hardly be a doubt that both sexes of many butterflies and moths have been rendered dull-coloured for the sake of protection, so it may have been with the females alone of some species in which successive variations towards dullness first appeared in the female sex and were from the first limited in their transmission to the same sex. If not thus limited, both sexes would become dull-coloured. We shall immediately see, when we treat of mimickry, that the females alone of certain butterflies have been rendered extremely beautiful for the sake of protection, without any of the successive protective variations having been transferred to the male, to whom they could not possibly have been in the least degree injurious, and therefore could not have been eliminated through natural selection. Whether in each particular species, in which the sexes differ in colour, it is the female which has been specially modified for the sake of protection; or whether it is the male which has been specially modified for the sake of sexual attraction, the409 female having retained her primordial colouring only slightly changed through the agencies before alluded to; or whether again both sexes have been modified, the female for protection and the male for sexual attraction, can only be definitely decided when we know the life-history of each species.
As there's little doubt that both male and female butterflies and moths have become dull-colored for protection, it’s possible that in some species, the females alone experienced a shift toward dullness first, which was then limited to passing on that trait only to other females. If this change wasn't limited, we would see both sexes becoming dull-colored. We'll soon see, when discussing mimicry, that in certain butterflies, only the females have become exceptionally beautiful for protection, with none of the protective changes passed to the males, who would not have been negatively affected and thus wouldn't have been eliminated through natural selection. It's still unclear in each specific species, where males and females differ in color, whether the female specifically adapted for protection, or if the male was modified for sexual attraction, while the female kept her original coloration with only minor changes due to previous influences. Alternatively, it's possible that both sexes adapted, with the female for protection and the male for attraction, but we can only provide a definite answer once we understand the life history of each species.
Without distinct evidence, I am unwilling to admit that a double process of selection has long been going on with a multitude of species,—the males having been rendered more brilliant by beating their rivals; and the females more dull-coloured by having escaped from their enemies. We may take as an instance the common brimstone butterfly (Gonepteryx), which appears early in the spring before any other kind. The male of this species is of a far more intense yellow than the female, though she is almost equally conspicuous; and in this case it does not seem probable that she specially acquired her pale tints as a protection, though it is probable that the male acquired his bright colours as a sexual attraction. The female of Anthocharis cardamines does not possess the beautiful orange tips to her wings with which the male is ornamented; consequently she closely resembles the white butterflies (Pieris) so common in our gardens; but we have no evidence that this resemblance is beneficial. On the contrary, as she resembles both sexes of several species of the same genus inhabiting various quarters of the world, it is more probable that she has simply retained to a large extent her primordial colours.
Without clear evidence, I’m not ready to accept that a dual process of selection has been happening with many species—males becoming more vibrant by competing with each other, and females becoming more muted by evading their predators. A good example is the common brimstone butterfly (Gonepteryx), which appears early in the spring before any other type. The male of this species is a much brighter yellow than the female, though she is still quite noticeable; in this case, it doesn’t seem likely that she specifically developed her lighter colors for protection, though it’s possible the male developed his bright colors for attraction. The female of Anthocharis cardamines lacks the beautiful orange tips on her wings that the male has; as a result, she closely resembles the white butterflies (Pieris) that are common in our gardens. However, we have no evidence that this similarity is advantageous. In fact, since she resembles both sexes of several species in the same genus found in different parts of the world, it seems more likely that she has largely retained her original colors.
Various facts support the conclusion that with the greater number of brilliantly-coloured Lepidoptera, it is the male which has been modified; the two sexes having come to differ from each other, or to resemble each other, according to which form of inheritance has prevailed. Inheritance is governed by so many un410known laws or conditions, that they seem to us to be most capricious in their action;524 and we can so far understand how it is that with closely-allied species the sexes of some differ to an astonishing degree, whilst the sexes of others are identical in colour. As the successive steps in the process of variation are necessarily all transmitted through the female, a greater or less number of such steps might readily become developed in her; and thus we can understand the frequent gradations from an extreme difference to no difference at all between the sexes of the species within the same group. These cases of gradation are much too common to favour the supposition that we here see females actually undergoing the process of transition and losing their brightness for the sake of protection; for we have every reason to conclude that at any one time the greater number of species are in a fixed condition. With respect to the differences between the females of the species in the same genus or family, we can perceive that they depend, at least in part, on the females partaking of the colours of their respective males. This is well illustrated in those groups in which the males are ornamented to an extraordinary degree; for the females in these groups generally partake to a certain extent of the splendour of their male partners. Lastly, we continually find, as already remarked, that the females of almost all the species in the same genus, or even family, resemble each other much more closely in colour than do the males; and this indicates that the males have undergone a greater amount of modification than the females.
Various facts support the conclusion that among the brilliantly colored butterflies, it is the male that has undergone more changes; the two sexes have come to differ from or resemble each other depending on which form of inheritance has dominated. Inheritance is governed by so many unknown laws or conditions that it seems quite unpredictable in its effects; and we can understand why, among closely related species, some sexes differ greatly in appearance while others look identical. Since the steps in the process of variation are necessarily passed down through the female, a greater or lesser number of these steps could easily develop in her; thus, we can understand the frequent gradations ranging from extreme differences to no differences at all between the sexes of species within the same group. These cases of gradation are too common to support the idea that we are witnessing females actually transitioning and losing their brightness for protection; we have every reason to believe that the majority of species are in a stable condition at any given time. Regarding the differences between females of species within the same genus or family, we can see that they partly depend on the females sharing the colors of their respective males. This is well illustrated in groups where males are exceptionally ornamented; the females in these groups generally share some of the male's splendor. Finally, as already noted, we often find that the females of almost all species within the same genus, or even family, are much more similar in color than the males; this suggests that the males have undergone more significant changes than the females.
411Mimickry.—This principle was first made clear in an admirable paper by Mr. Bates,525 who thus threw a flood of light on many obscure problems. It had previously been observed that certain butterflies in S. America belonging to quite distinct families, resembled the Heliconidæ so closely in every stripe and shade of colour that they could not be distinguished except by an experienced entomologist. As the Heliconidæ are coloured in their usual manner, whilst the others depart from the usual colouring of the groups to which they belong, it is clear that the latter are the imitators, and the Heliconidæ the imitated. Mr. Bates further observed that the imitating species are comparatively rare, whilst the imitated swarm in large numbers; the two sets living mingled together. From the fact of the Heliconidæ being conspicuous and beautiful insects, yet so numerous in individuals and species, he concluded that they must be protected from the attacks of birds by some secretion or odour; and this hypothesis has now been confirmed by a considerable body of curious evidence.526 From these considerations Mr. Bates inferred that the butterflies which imitate the protected species had acquired their present marvellously deceptive appearance, through variation and natural selection, in order to be mistaken for the protected kinds and thus to escape being devoured. No explanation is here attempted of the brilliant colours of the imitated, but only of the imitating butterflies. We must account for the colours of the former in the same general manner, as in the cases previously discussed in this chapter. Since the publication of Mr. Bates’ paper, similar and equally striking facts have been observed 412by Mr. Wallace527 in the Malayan region, and by Mr. Trimen in South Africa.
411Mimicry.—This principle was first clearly outlined in an impressive paper by Mr. Bates,525 who shed light on many unclear issues. It had been noted before that certain butterflies in South America, belonging to completely different families, closely resembled the Heliconidæ in every stripe and shade of color, to the point that only an experienced entomologist could tell them apart. Since the Heliconidæ are colored in their usual way, while the others differ from the typical colors of their respective groups, it's evident that the latter are the imitators and the Heliconidæ are the ones being copied. Mr. Bates further noticed that the imitating species are relatively rare, while the imitated ones are quite numerous; the two groups coexist. Given that the Heliconidæ are striking and beautiful insects, yet very common in both numbers and species, he concluded they must be protected from bird predation by some sort of secretion or scent; this hypothesis has now been supported by a substantial amount of intriguing evidence.526 Based on these observations, Mr. Bates inferred that the butterflies mimicking the protected species developed their remarkably deceptive appearance through variation and natural selection, in order to be mistaken for the protected types and thus avoid being eaten. No attempt is made to explain the brilliant colors of the imitated butterflies here, but only those of the mimicking ones. We should account for the colors of the former similarly to the cases discussed earlier in this chapter. Since the publication of Mr. Bates’ paper, similar and equally notable findings have been made412by Mr. Wallace527 in the Malayan region, and by Mr. Trimen in South Africa.
As some writers528 have felt much difficulty in understanding how the first steps in the process of mimickry could have been effected through natural selection, it may be well to remark that the process probably has never commenced with forms widely dissimilar in colour. But with two species moderately like each other, the closest resemblance if beneficial to either form could readily be thus gained; and if the imitated form was subsequently and gradually modified through sexual selection or any other means, the imitating form would be led along the same track, and thus be modified to almost any extent, so that it might ultimately assume an appearance or colouring wholly unlike that of the other members of the group to which it belonged. As extremely slight variations in colour would not in many cases suffice to render a species so like another protected species as to lead to its preservation, it should be remembered that many species of Lepidoptera are liable to considerable and abrupt variations in colour. A few instances have been given in this chapter; but under this point of view Mr. Bates’ original paper on mimickry, as well as Mr. Wallace’s papers, should be consulted.
As some writers528 have found it very hard to understand how the first steps in the process of mimicry could have happened through natural selection, it’s worth noting that the process probably never started with forms that were very different in color. Instead, it would begin with two species that are somewhat similar to each other; the closest resemblance, if beneficial to either species, could easily be achieved this way. If the imitated form was then gradually changed through sexual selection or other means, the imitating form would follow the same path and could be altered to a significant extent, eventually looking completely different from other members of its group. Since tiny color variations often aren’t enough to make a species look similar enough to another protected species to ensure its survival, it’s important to remember that many species of butterflies and moths can experience considerable and sudden changes in color. A few examples have been provided in this chapter, but for more detail, Mr. Bates’ original paper on mimicry and Mr. Wallace’s papers should be referred to.
In the foregoing cases both sexes of the imitating species resemble the imitated; but occasionally the 413female alone mocks a brilliantly-coloured and protected species inhabiting the same district. Consequently the female differs in colour from her own male, and, which is a rare and anomalous circumstance, is the more brightly-coloured of the two. In all the few species of Pieridæ, in which the female is more conspicuously coloured than the male, she imitates, as I am informed by Mr. Wallace, some protected species inhabiting the same region. The female of Diadema anomala is rich purple-brown with almost the whole surface glossed with satiny blue, and she closely imitates the Euplœa midamus, “one of the commonest butterflies of the East;” whilst the male is bronzy or olive-brown, with only a slight blue gloss on the outer parts of the wings.529 Both sexes of this Diadema and of D. bolina follow the same habits of life, so that the differences in colour between the sexes cannot be accounted for by exposure to different conditions;530 even if this explanation were admissible in other instances.531
In the cases mentioned above, both male and female of the mimicking species look like the species they imitate; however, sometimes only the female mimics a brightly colored, protected species that lives in the same area. As a result, the female has a different color from her male counterpart and, in an unusual twist, is more brightly colored than he is. In the few species of Pieridae where the female is more brightly colored than the male, she mimics, as Mr. Wallace informs me, some protected species in the same region. The female of Diadema anomala is a deep purple-brown with a glossy, satiny blue covering almost its entire surface, closely resembling Euplœa midamus, "one of the most common butterflies in the East," while the male is bronzy or olive-brown with only a slight blue sheen on the outer parts of the wings.529 Both sexes of this Diadema and D. bolina live the same lifestyle, so the color differences between them can't be explained by exposure to different conditions;530 even if that explanation could be valid in other cases.531
The above cases of female butterflies which are more brightly-coloured than the males, shew us, firstly, that variations have arisen in a state of nature in the female sex, and have been transmitted exclusively, or almost exclusively, to the same sex; and, secondly, that this form of inheritance has not been determined through natural selection. For if we assume that the females, before they became brightly coloured in imitation of some protected kind, were exposed during each season for a longer period to danger than the males; or if we assume that 414they could not escape so swiftly from their enemies, we can understand how they alone might originally have acquired through natural selection and sexually-limited inheritance their present protective colours. But except on the principle of these variations having been transmitted exclusively to the female offspring, we cannot understand why the males should have remained dull-coloured; for it would surely not have been in any way injurious to each individual male to have partaken by inheritance of the protective colours of the female, and thus to have had a better chance of escaping destruction. In a group in which brilliant colours are so common as with butterflies, it cannot be supposed that the males have been kept dull-coloured through sexual selection by the females rejecting the individuals which were rendered as beautiful as themselves. We may, therefore, conclude that in these cases inheritance by one sex is not due to the modification through natural selection of a tendency to equal inheritance by both sexes.
The examples of female butterflies that are more brightly colored than the males show us, first, that variations have occurred in nature within the female sex and have been passed down almost exclusively to females; and second, that this type of inheritance hasn’t been shaped by natural selection. If we consider that the females, before they became brightly colored in imitation of some protected species, faced more dangers than the males each season; or if we think that they couldn’t escape from their predators as quickly, we can see how they might have originally developed their protective colors through natural selection and sexually-limited inheritance. However, without the idea that these variations have been passed down exclusively to female offspring, it’s hard to understand why the males would remain dull-colored. After all, it wouldn’t have been harmful for individual males to inherit the protective colors of the females, giving them a better chance of survival. In a group where bright colors are so prevalent, such as among butterflies, it doesn’t make sense to think that males remained dull-colored because females chose to mate with only less colorful individuals. Therefore, we can conclude that in these situations, inheritance by one sex isn’t a result of natural selection modifying a tendency for equal inheritance in both sexes.
It may be well here to give an analogous case in another Order, of characters acquired only by the female, though not in the least injurious, as far as we can judge, to the male. Amongst the Phasmidæ, or spectre-insects, Mr. Wallace states that “it is often the females alone that so strikingly resemble leaves, while the males show only a rude approximation.” Now, whatever may be the habits of these insects, it is highly improbable that it could be disadvantageous to the males to escape detection by resembling leaves.532 Hence we may conclude 415that the females alone in this latter as in the previous cases originally varied in certain characters; these characters having been preserved and augmented through ordinary selection for the sake of protection and from the first transmitted to the female offspring alone.
It might be useful to provide a similar example in another group, where traits have been developed only in females, which, as far as we can tell, don't negatively impact the males. According to Mr. Wallace, among the Phasmidæ, or stick insects, “it is often the females alone that so strikingly resemble leaves, while the males show only a rough approximation.” Regardless of the behaviors of these insects, it seems very unlikely that it would be harmful for the males to blend in by looking like leaves.532 Therefore, we can conclude that, just like in the previous examples, it was primarily the females that initially developed these specific traits; these traits were retained and enhanced through natural selection for protection and were passed down only to female offspring.
Bright Colours of Caterpillars.—Whilst reflecting on the beauty of many butterflies, it occurred to me that some caterpillars were splendidly coloured, and as sexual selection could not possibly have here acted, it appeared rash to attribute the beauty of the mature insect to this agency, unless the bright colours of their larvæ could be in some manner explained. In the first place it may be observed that the colours of caterpillars do not stand in any close correlation with those of the mature insect. Secondly, their bright colours do not 416serve in any ordinary manner as a protection. As an instance of this, Mr. Bates informs me that the most conspicuous caterpillar which he ever beheld (that of a Sphinx) lived on the large green leaves of a tree on the open llanos of South America; it was about four inches in length, transversely banded with black and yellow, and with its head, legs, and tail of a bright red. Hence it caught the eye of any man who passed by at the distance of many yards, and no doubt of every passing bird.
Bright Colors of Caterpillars.—While thinking about the beauty of many butterflies, I realized that some caterpillars are brilliantly colored, and since sexual selection couldn’t possibly account for this, it seemed unwise to attribute the beauty of the adult insect to that influence unless the bright colors of their larvae could be explained in some way. First, it should be noted that the colors of caterpillars don’t closely match those of the adult insect. Second, their bright colors don’t typically serve as a form of protection. For example, Mr. Bates tells me that the most noticeable caterpillar he ever saw (that of a Sphinx) lived on the large green leaves of a tree in the open plains of South America; it was about four inches long, with black and yellow bands, and had a bright red head, legs, and tail. As a result, it caught the attention of anyone passing by from many yards away, and undoubtedly every bird that flew by as well.
I then applied to Mr. Wallace, who has an innate genius for solving difficulties. After some consideration he replied: “Most caterpillars require protection, as may be inferred from some kinds being furnished with spines or irritating hairs, and from many being coloured green like the leaves on which they feed, or curiously like the twigs of the trees on which they live.” I may add as another instance of protection, that there is a caterpillar of a moth, as I am informed by Mr. J. Mansel Weale, which lives on the mimosas in South Africa, and fabricates for itself a case, quite undistinguishable from the surrounding thorns. From such considerations Mr. Wallace thought it probable that conspicuously-coloured caterpillars were protected by having a nauseous taste; but as their skin is extremely tender, and as their intestines readily protrude from a wound, a slight peck from the beak of a bird would be as fatal to them as if they had been devoured. Hence, as Mr. Wallace remarks, “distastefulness alone would be insufficient to protect a caterpillar unless some outward sign indicated to its would-be destroyer that its prey was a disgusting morsel.” Under these circumstances it would be highly advantageous to a caterpillar to be instantaneously and certainly recognised as unpalatable by all birds and other animals.417 Thus the most gaudy colours would be serviceable, and might have been gained by variation and the survival of the most easily-recognised individuals.
I then went to Mr. Wallace, who has a natural talent for solving problems. After thinking it over, he said, “Most caterpillars need protection, as we can see from some species having spines or irritating hairs, and from many being green like the leaves they eat, or oddly similar to the twigs of the trees where they live.” I can add another example of protection: there’s a caterpillar of a moth, as I was told by Mr. J. Mansel Weale, that lives on the mimosas in South Africa and makes a case for itself that looks just like the surrounding thorns. From these observations, Mr. Wallace believed it was likely that brightly colored caterpillars are protected by having a bad taste; however, since their skin is very delicate, and their intestines can easily stick out from a wound, a single peck from a bird could be fatal for them, just as if they had been eaten. Therefore, as Mr. Wallace points out, “just being distasteful wouldn’t be enough to protect a caterpillar unless there was some outward sign that indicated to potential predators that it was a disgusting meal.” Given these conditions, it would be very beneficial for a caterpillar to be instantly and unmistakably identified as unappetizing by all birds and other animals.417 So, the brightest colors would be useful and could have developed through variation and the survival of those that are most easily recognized.
This hypothesis appears at first sight very bold; but when it was brought before the Entomological Society533 it was supported by various statements; and Mr. J. Jenner Weir, who keeps a large number of birds in an aviary, has made, as he informs me, numerous trials, and finds no exception to the rule, that all caterpillars of nocturnal and retiring habits with smooth skins, all of a green colour, and all which imitate twigs, are greedily devoured by his birds. The hairy and spinose kinds are invariably rejected, as were four conspicuously-coloured species. When the birds rejected a caterpillar, they plainly shewed, by shaking their heads and cleansing their beaks, that they were disgusted by the taste.534 Three conspicuous kinds of caterpillars and moths were also given by Mr. A. Butler to some lizards and frogs, and were rejected; though other kinds were eagerly eaten. Thus the probable truth of Mr. Wallace’s view is confirmed, namely, that certain caterpillars have been made conspicuous for their own good, so as to be easily recognised by their enemies, on nearly the same principle that certain poisons are coloured by druggists for the good of man. This view will, it is probable, be hereafter extended to many animals, which are coloured in a conspicuous manner.
This idea seems really bold at first glance; however, when it was presented to the Entomological Society533, it was backed by various observations. Mr. J. Jenner Weir, who has a large aviary with many birds, told me that he has conducted numerous experiments and has found no exceptions to the rule that all caterpillars with smooth skins, nocturnal habits, and green coloration that mimic twigs are eagerly eaten by his birds. In contrast, hairy and spiny types are consistently rejected, as were four brightly colored species. When the birds turned away from a caterpillar, they clearly showed their disgust by shaking their heads and cleaning their beaks.534 Mr. A. Butler also offered three notable types of caterpillars and moths to some lizards and frogs, and those were rejected as well, while other types were happily consumed. This supports Mr. Wallace’s idea that some caterpillars have bright colors for their benefit, making it easier for predators to recognize them—similar to how certain poisons are colored by pharmacists for humans' safety. This perspective will likely be applied to many animals that are brightly colored in the future.
Summary and Concluding Remarks on Insects.—Looking back to the several Orders, we have seen that the sexes often differ in various characters, the meaning 418of which is not understood. The sexes, also, often differ in their organs of sense or locomotion, so that the males may quickly discover or reach the females, and still oftener in the males possessing diversified contrivances for retaining the females when found. But we are not here much concerned with sexual differences of these kinds.
Summary and Concluding Remarks on Insects.—Looking back at the different Orders, we've seen that males and females often differ in various traits, the significance of which isn't clear. The sexes also frequently vary in their sensory or movement organs, allowing males to quickly locate or reach females, and even more often, males have various adaptations to keep the females close once they do find them. However, we won't focus much on these kinds of sexual differences.
In almost all the Orders, the males of some species, even of weak and delicate kinds, are known to be highly pugnacious; and some few are furnished with special weapons for fighting with their rivals. But the law of battle does not prevail nearly so widely with insects as with the higher animals. Hence probably it is that the males have not often been rendered larger and stronger than the females. On the contrary they are usually smaller, in order that they may be developed within a shorter time, so as to be ready in large numbers for the emergence of the females.
In almost all the Orders, male members of some species, even the weaker and more delicate ones, are known to be quite aggressive; and a few of them have specialized weapons to fight their rivals. However, the concept of battle isn’t nearly as prevalent among insects as it is among higher animals. This is probably why males are rarely larger and stronger than females. In fact, they are usually smaller so they can develop more quickly and be ready in large numbers when the females emerge.
In two families of the Homoptera the males alone possess, in an efficient state, organs which may be called vocal; and in three families of the Orthoptera the males alone possess stridulating organs. In both cases these organs are incessantly used during the breeding-season, not only for calling the females, but for charming or exciting them in rivalry with other males. No one who admits the agency of natural selection, will dispute that these musical instruments have been acquired through sexual selection. In four other Orders the members of one sex, or more commonly of both sexes, are provided with organs for producing various sounds, which apparently serve merely as call-notes. Even when both sexes are thus provided, the individuals which were able to make the loudest or most continuous noise would gain partners before those which were less noisy, so that their organs have probably been gained419 through sexual selection. It is instructive to reflect on the wonderful diversity of the means for producing sound, possessed by the males alone or by both sexes in no less than six Orders, and which were possessed by at least one insect at an extremely remote geological epoch. We thus learn how effectual sexual selection has been in leading to modifications of structure, which sometimes, as with the Homoptera, are of an important nature.
In two families of Homoptera, only the males have fully developed organs that can be called vocal; and in three families of Orthoptera, only the males have stridulating organs. During the breeding season, these organs are constantly used not just to call females but also to attract or stimulate them in competition with other males. Anyone who accepts natural selection will agree that these musical instruments have been developed through sexual selection. In four other orders, members of one sex, or more often both sexes, have organs that create various sounds, which seem to function mainly as call notes. Even when both sexes have these organs, individuals that can produce the loudest or most continuous sounds are more likely to attract partners compared to those that are quieter, indicating that their organs have likely evolved through sexual selection. It's intriguing to consider the incredible variety of sound-producing mechanisms found in males or both sexes across at least six orders, which can also be traced back to at least one insect from a very distant geological period. This demonstrates how effective sexual selection has been in leading to structural modifications, which can be significantly important, especially in Homoptera.
From the reasons assigned in the last chapter, it is probable that the great horns of the males of many lamellicorn, and some other beetles, have been acquired as ornaments. So perhaps it may be with certain other peculiarities confined to the male sex. From the small size of insects, we are apt to undervalue their appearance. If we could imagine a male Chalcosoma (fig. 15) with its polished, bronzed coat of mail, and vast complex horns, magnified to the size of a horse or even of a dog, it would be one of the most imposing animals in the world.
From the reasons given in the last chapter, it's likely that the large horns of male lamellicorn beetles and some other beetles have developed as decorative features. It might also be true for certain other traits that are specific to males. Because insects are so small, we often underestimate their appearance. If we could picture a male Chalcosoma (fig. 15) with its shiny, bronzed exoskeleton and enormous, intricate horns blown up to the size of a horse or even a dog, it would be one of the most impressive animals on the planet.
The colouring of insects is a complex and obscure subject. When the male differs slightly from the female, and neither are brilliantly coloured, it is probable that the two sexes have varied in a slightly different manner, with the variations transmitted to the same sex, without any benefit having been thus derived or evil suffered. When the male is brilliantly coloured and differs conspicuously from the female, as with some dragon-flies and many butterflies, it is probable that he alone has been modified, and that he owes his colours to sexual selection; whilst the female has retained a primordial or very ancient type of colouring, slightly modified by the agencies before explained, and has therefore not been rendered obscure, at least in most cases, for the sake of protection. But the female alone has some420times been coloured brilliantly so as to imitate other protected species inhabiting the same district. When the sexes resemble each other and both are obscurely coloured, there is no doubt that they have been in a multitude of cases coloured for the sake of protection. So it is in some instances when both are brightly coloured, causing them to resemble surrounding objects such as flowers, or other protected species, or indirectly by giving notice to their enemies that they are of an unpalatable nature. In many other cases in which the sexes resemble each other and are brilliantly coloured, especially when the colours are arranged for display, we may conclude that they have been gained by the male sex as an attraction, and have been transferred to both sexes. We are more especially led to this conclusion whenever the same type of coloration prevails throughout a group, and we find that the males of some species differ widely in colour from the females, whilst both sexes of other species are quite alike, with intermediate gradations connecting these extreme states.
The coloring of insects is a complex and unclear topic. When the male is slightly different from the female, and neither is vibrantly colored, it’s likely that the two sexes have varied in slightly different ways, with the differences passed down to the same sex, without any resulting advantage or disadvantage. When the male is brightly colored and strikingly different from the female, like some dragonflies and many butterflies, it’s likely that he alone has changed, receiving his colors through sexual selection; meanwhile, the female has kept a more primitive or ancient type of coloring, slightly altered by the processes previously mentioned, and is therefore not rendered inconspicuous, at least in most cases, for the sake of protection. However, sometimes the female is brightly colored to mimic other protected species in the same area. When the sexes look alike and both are dull-colored, it’s clear that in many cases, they have adopted that coloration for protection. The same applies in some cases where both are brightly colored, making them resemble surrounding objects like flowers or other protected species, or indirectly signaling to their predators that they are unpalatable. In many other cases where the sexes look alike and are brightly colored, especially when the colors are arranged to attract attention, we can infer that the male has developed these traits to attract the female, and they have spread to both sexes. This conclusion is particularly supported when the same color patterns are common throughout a group, where we find that males of some species differ greatly in color from females, while both sexes of other species are quite similar, with intermediate gradations connecting these extreme states.
In the same manner as bright colours have often been partially transferred from the males to the females, so it has been with the extraordinary horns of many lamellicorn and some other beetles. So, again, the vocal or instrumental organs proper to the males of the Homoptera and Orthoptera have generally been transferred in a rudimentary, or even in a nearly perfect condition to the females; yet not sufficiently perfect to be used for producing sound. It is also an interesting fact, as bearing on sexual selection, that the stridulating organs of certain male Orthoptera are not fully developed until the last moult; and that the colours of certain male dragon-flies are not fully developed until some little time after their emergence from the pupal state, and when they are ready to breed.
In the same way that bright colors have often been passed from males to females, the same goes for the impressive horns of many lamellicorn beetles and some others. Similarly, the vocal or instrumental organs found in male Homoptera and Orthoptera have mostly been transferred to females in a rudimentary, or even nearly complete, form; however, they aren't quite developed enough to produce sound. It’s also interesting in terms of sexual selection that the stridulating organs of certain male Orthoptera don’t fully develop until after their last molt, and that the colors of some male dragonflies aren’t fully realized until some time after they emerge from the pupal stage, just as they're about to breed.
421Sexual selection implies that the more attractive individuals are preferred by the opposite sex; and as with insects, when the sexes differ, it is the male which, with rare exceptions, is the most ornamented and departs most from the type to which the species belongs;—and as it is the male which searches eagerly for the female, we must suppose that the females habitually or occasionally prefer the more beautiful males, and that these have thus acquired their beauty. That in most or all the orders the females have the power of rejecting any particular male, we may safely infer from the many singular contrivances possessed by the males, such as great jaws, adhesive cushions, spines, elongated legs, &c., for seizing the female; for these contrivances shew that there is some difficulty in the act. In the case of unions between distinct species, of which many instances have been recorded, the female must have been a consenting party. Judging from what we know of the perceptive powers and affections of various insects, there is no antecedent improbability in sexual selection having come largely into action; but we have as yet no direct evidence on this head, and some facts are opposed to the belief. Nevertheless, when we see many males pursuing the same female, we can hardly believe that the pairing is left to blind chance—that the female exerts no choice, and is not influenced by the gorgeous colours or other ornaments, with which the male alone is decorated.
421Sexual selection means that the more attractive individuals are favored by the opposite sex; and just like with insects, when there are differences between the sexes, it is typically the male that is more adorned and deviates more from the standard for that species. Since it is the male that actively seeks out the female, we can assume that the females regularly or occasionally prefer the more attractive males, and that’s how those males have developed their beauty. We can confidently conclude that in most or all species, females have the ability to reject any specific male, as evidenced by the various unique features that males possess, such as large jaws, sticky pads, spines, long legs, etc., which are used to grab hold of the female; these features indicate that there is some challenge in this process. In cases of mating between different species, of which many examples have been documented, the female must have agreed to the union. Based on what we understand about the sensory abilities and preferences of various insects, it seems quite plausible that sexual selection has played a significant role; however, we still lack direct evidence for this, and some facts contradict the idea. Still, when we observe multiple males chasing after the same female, it’s hard to believe that the pairing is left entirely to chance—that the female has no say and isn’t swayed by the striking colors and other decorations that only the male flaunts.
If we admit that the females of the Homoptera and Orthoptera appreciate the musical tones emitted by their male partners, and that the various instruments for this purpose have been perfected through sexual selection, there is little improbability in the females of other insects appreciating beauty in form or colour, and consequently in such characters having been thus gained422 by the males. But from the circumstance of colour being so variable, and from its having been so often modified for the sake of protection, it is extremely difficult to decide in how large a proportion of cases sexual selection has come into play. This is more especially difficult in those Orders, such as the Orthoptera, Hymenoptera, and Coleoptera, in which the two sexes rarely differ much in colour; for we are thus cut off from our best evidence of some relation between the reproduction of the species and colour. With the Coleoptera, however, as before remarked, it is in the great lamellicorn group, placed by some authors at the head of the Order, and in which we sometimes see a mutual attachment between the sexes, that we find the males of some species possessing weapons for sexual strife, others furnished with wonderful horns, many with stridulating organs, and others ornamented with splendid metallic tints. Hence it seems probable that all these characters have been gained through the same means, namely sexual selection.
If we accept that female Homoptera and Orthoptera enjoy the musical sounds made by their male partners, and that the different instruments used for this purpose have been refined through sexual selection, then it's not unlikely that females of other insects also appreciate beauty in form or color. As a result, these traits may have been developed by the males. However, because color is so variable and often altered for protection, it's really hard to determine how frequently sexual selection has played a role. This challenge is particularly evident in groups like Orthoptera, Hymenoptera, and Coleoptera, where the two sexes usually don’t differ much in color. This lack of difference makes it hard to find evidence linking color to species reproduction. Nevertheless, in the Coleoptera, particularly within the large lamellicorn group, which some authors place at the top of the Order and where we sometimes observe a bond between the sexes, we find that the males of certain species possess weapons for fighting, others feature impressive horns, many have stridulating organs, and others display beautiful metallic colors. Therefore, it seems likely that all of these traits have developed through the same process, namely sexual selection.
When we treat of Birds, we shall see that they present in their secondary sexual characters the closest analogy with insects. Thus, many male birds are highly pugnacious, and some are furnished with special weapons for fighting with their rivals. They possess organs which are used during the breeding-season for producing vocal and instrumental music. They are frequently ornamented with combs, horns, wattles and plumes of the most diversified kinds, and are decorated with beautiful colours, all evidently for the sake of display. We shall find that, as with insects, both sexes, in certain groups, are equally beautiful, and are equally provided with ornaments which are usually confined to the male sex. In other groups both sexes are equally plain-coloured and unornamented. Lastly, in some few423 anomalous cases, the females are more beautiful than the males. We shall often find, in the same group of birds, every gradation from no difference between the sexes, to an extreme difference. In the latter case we shall see that the females, like female insects, often possess more or less plain traces of the characters which properly belong to the males. The analogy, indeed, in all these respects between birds and insects, is curiously close. Whatever explanation applies to the one class probably applies to the other; and this explanation, as we shall hereafter attempt to shew, is almost certainly sexual selection.
When we talk about birds, we’ll find that their secondary sexual traits closely resemble those of insects. Many male birds are quite aggressive, and some have special features for battling their rivals. They have organs used during the breeding season to create vocal and musical sounds. They're often adorned with combs, horns, wattles, and a variety of feathers, showcasing stunning colors, all clearly meant for display. As with insects, in some groups, both males and females are equally attractive and sport decorations typically found only on males. In other groups, both sexes might be plain and unadorned. Finally, in a few unusual cases, females are more striking than males. In a single group of birds, we can see a whole range of differences, from no distinction between the sexes to significant variation. In the latter case, females, like female insects, often show faint traces of features that are typically associated with males. The similarities between birds and insects in these respects are remarkably close. Any explanation that fits one group likely applies to the other, and this explanation, as we will discuss later, is almost certainly sexual selection.
FOOTNOTES:
1 As the works of the first-named authors are so well known, I need not give the titles; but as those of the latter are less well known in England, I will give them:—‘Sechs Vorlesungen über die Darwin’sche Theorie:’ zweite Auflage, 1868, von Dr. L. Büchner; translated into French under the title ‘Conférences sur la Théorie Darwinienne,’ 1869. ‘Der Mensch, im Lichte der Darwin’sche Lehre,’ 1865, von Dr. F. Rolle. I will not attempt to give references to all the authors who have taken the same side of the question. Thus G. Canestrini has published (‘Annuario della Soc. d. Nat.,’ Modena, 1867, p. 81) a very curious paper on rudimentary characters, as bearing on the origin of man. Another work has (1869) been published by Dr. Barrago Francesco, bearing in Italian the title of “Man, made in the image of God, was also made in the image of the ape.”
1 Since the works of the first authors are well known, I won't list the titles; however, the latter authors are less familiar in England, so I’ll share their titles:—‘Sechs Vorlesungen über die Darwin’sche Theorie’: second edition, 1868, by Dr. L. Büchner; translated into French as ‘Conférences sur la Théorie Darwinienne,’ 1869. ‘Der Mensch, im Lichte der Darwin’sche Lehre,’ 1865, by Dr. F. Rolle. I won't try to reference all the authors who support the same viewpoint. For example, G. Canestrini published a fascinating paper on rudimentary traits related to the origin of man in the ‘Annuario della Soc. d. Nat.,’ Modena, 1867, p. 81. Additionally, another work published in 1869 by Dr. Barrago Francesco is titled in Italian “Man, made in the image of God, was also made in the image of the ape.”
2 Prof. Häckel is the sole author who, since the publication of the ‘Origin,’ has discussed, in his various works, in a very able manner, the subject of sexual selection, and has seen its full importance.
2 Prof. Häckel is the only author who, since the release of the 'Origin,' has skillfully addressed the topic of sexual selection in his various works and has recognized its significance.
7 With respect to insects see Dr. Laycock ‘On a General Law of Vital Periodicity,’ British Association, 1842. Dr. Macculloch, ‘Silliman’s North American Journal of Science,’ vol. xvii. p. 305, has seen a dog suffering from tertian ague.
7 Regarding insects, see Dr. Laycock “On a General Law of Vital Periodicity,” British Association, 1842. Dr. Macculloch, in “Silliman’s North American Journal of Science,” vol. xvii, p. 305, has observed a dog suffering from tertian ague.
9 “Mares e diversis generibus Quadrumanorum sine dubio dignoscunt feminas humanas a maribus. Primum, credo, odoratu, postea aspectu. Mr. Youatt, qui diu in Hortis Zoologicis (Bestiariis) medicus animalium erat, vir in rebus observandis cautus et sagax, hoc mihi certissime probavit, et curatores ejusdem loci et alii e ministris confirmaverunt. Sir Andrew Smith et Brehm notabant idem in Cynocephalo. Illustrissimus Cuvier etiam narrat multa de hac re quâ ut opinor nihil turpius potest indicari inter omnia hominibus et Quadrumanis communia. Narrat enim Cynocephalum quendam in furorem incidere aspectu feminarum aliquarum, sed nequaquam accendi tanto furore ab omnibus. Semper eligebat juniores, et dignoscebat in turba, et advocabat voce gestuque.”
9 “Without a doubt, female primates can distinguish human females from males. First, I believe, by smell, then by sight. Mr. Youatt, who was a veterinarian at the Zoological Gardens for a long time, and who was careful and insightful in his observations, confirmed this with certainty, and his colleagues and other staff agreed. Sir Andrew Smith and Brehm noted the same about the baboon. The renowned Cuvier also mentioned much about this, stating that nothing could be more shameful among all that humans and primates share. He recounts a particular baboon that would go into a frenzy at the sight of certain females, but was not ignited by passion for all of them. It always favored younger ones, recognized them in a crowd, and called to them with voice and gesture.”
10 This remark is made with respect to Cynocephalus and the anthropomorphous apes by Geoffroy Saint-Hilaire and F. Cuvier, ‘Hist. Nat. des Mammifères,’ tom. i. 1824.
10 This comment refers to Cynocephalus and the human-like apes by Geoffroy Saint-Hilaire and F. Cuvier, ‘Hist. Nat. des Mammifères,’ vol. i. 1824.
13 The human embryo (upper fig.) is from Ecker, ‘Icones Phys.,’ 1851-1859, tab. xxx. fig. 2. This embryo was ten lines in length, so that the drawing is much magnified. The embryo of the dog is from Bischoff, ‘Entwicklungsgeschichte des Hunde-Eies,’ 1845, tab. xi. fig. 42 B. This drawing is five times magnified, the embryo being 25 days old. The internal viscera have been omitted, and the uterine appendages in both drawings removed. I was directed to these figures by Prof. Huxley, from whose work, ‘Man’s Place in Nature.’ the idea of giving them was taken. Häckel has also given analogous drawings in his ‘Schöpfungsgeschichte.’
13 The human embryo (top figure) is from Ecker, ‘Icones Phys.,’ 1851-1859, tab. xxx. fig. 2. This embryo measured ten lines in length, so the drawing is highly magnified. The embryo of the dog is from Bischoff, ‘Entwicklungsgeschichte des Hunde-Eies,’ 1845, tab. xi. fig. 42 B. This drawing is five times enlarged, with the embryo being 25 days old. The internal organs have been left out, and the uterine attachments in both drawings have been removed. I was pointed to these figures by Prof. Huxley, from whose work, ‘Man’s Place in Nature,’ the idea to include them was taken. Häckel has also provided similar drawings in his ‘Schöpfungsgeschichte.’
20 I had written a rough copy of this chapter before reading a valuable paper, “Caratteri rudimentali in ordine all’origine del uomo” (‘Annuario della Soc. d. Nat.,’ Modena, 1867, p. 81), by G. Canestrini, to which paper I am considerably indebted. Häckel has given admirable discussions on this whole subject, under the title of Dysteleology, in his ‘Generelle Morphologie’ and ‘Schöpfungsgeschichte.’
20 I had written a rough draft of this chapter before reading a helpful paper, “Caratteri rudimentali in ordine all’origine del uomo” (‘Annuario della Soc. d. Nat.,’ Modena, 1867, p. 81), by G. Canestrini, which I owe a lot to. Häckel has provided excellent discussions on this entire topic, under the title of Dysteleology, in his ‘Generelle Morphologie’ and ‘Schöpfungsgeschichte.’
23 For instance M. Richard (‘Annales des Sciences Nat.’ 3rd series, Zoolog. 1852, tom. xviii. p. 13) describes and figures rudiments of what he calls the “muscle pédieux de la main,” which he says is sometimes “infiniment petit.” Another muscle, called “le tibial postérieur,” is generally quite absent in the hand, but appears from time to time in a more or less rudimentary condition.
23 For example, M. Richard ('Annales des Sciences Nat.' 3rd series, Zoolog. 1852, tom. xviii. p. 13) describes and illustrates the remnants of what he calls the "peddie muscle of the hand," which he notes can sometimes be "infinitely small." Another muscle, known as "the posterior tibial," is usually missing in the hand but occasionally shows up in a more or less basic form.
27 See also some remarks, and the drawings of the ears of the Lemuroidea, in Messrs. Murie and Mivart’s excellent paper in ‘Transact. Zoolog. Soc.’ vol. vii. 1869, pp. 6 and 90.
27 Check out some comments and the illustrations of the ears of the Lemuroidea in the outstanding paper by Messrs. Murie and Mivart in ‘Transact. Zoolog. Soc.’ vol. vii. 1869, pp. 6 and 90.
28 Müller’s ‘Elements of Physiology,’ Eng. translat., 1842, vol. ii. p. 1117. Owen, ‘Anatomy of Vertebrates,’ vol. iii. p. 260; ibid. on the Walrus, ‘Proc. Zoolog. Soc.’ November 8th, 1854. See also R. Knox, 'Great Artists and Anatomists,’ p. 106. This rudiment apparently is somewhat larger in Negroes and Australians than in Europeans, see Carl Vogt, ‘Lectures on Man,’ Eng. translat. p. 129.
28 Müller’s ‘Elements of Physiology,’ English translation, 1842, vol. ii. p. 1117. Owen, ‘Anatomy of Vertebrates,’ vol. iii. p. 260; ibid. on the Walrus, ‘Proc. Zoolog. Soc.’ November 8th, 1854. See also R. Knox, 'Great Artists and Anatomists,’ p. 106. This rudiment seems to be a bit larger in Black individuals and Australians than in Europeans, see Carl Vogt, ‘Lectures on Man,’ English translation, p. 129.
30 Eschricht, Ueber die Richtung der Haare am menschlichen Körper 'Müllers Archiv für Anat. und Phys.’ 1837, s. 47. I shall often have to refer to this very curious paper.
30 Eschricht, On the Direction of Hair on the Human Body 'Müller's Archives for Anatomy and Physiology’ 1837, p. 47. I will frequently reference this very interesting paper.
38 M. C. Martins (“De l’Unité Organique,” in ‘Revue des Deux Mondes,’ June 15, 1862, p. 16), and Häckel (‘Generelle Morphologie,’ B. ii. s. 278), have both remarked on the singular fact of this rudiment sometimes causing death.
38 M. C. Martins (“De l’Unité Organique,” in ‘Revue des Deux Mondes,’ June 15, 1862, p. 16), and Häckel (‘Generelle Morphologie,’ B. ii. s. 278), have both noted the unusual fact that this rudiment can sometimes lead to death.
39 ‘The Lancet,’ Jan. 24, 1863, p. 83. Dr. Knox, ‘Great Artists and Anatomists,’ p. 63. See also an important memoir on this process by Dr. Grube, in the ‘Bulletin de l’Acad. Imp. de St. Pétersbourg,’ tom. xii. 1867, p. 448.
39 ‘The Lancet,’ Jan. 24, 1863, p. 83. Dr. Knox, ‘Great Artists and Anatomists,’ p. 63. Check out an important paper on this process by Dr. Grube, in the ‘Bulletin de l’Acad. Imp. de St. Pétersbourg,’ vol. xii. 1867, p. 448.
43 Leuckart, in Todd’s ‘Cyclop. of Anat.’ 1849-52, vol. iv. p. 1415. In man this organ is only from three to six lines in length, but, like so many other rudimentary parts, it is variable in development as well as in other characters.
43 Leuckart, in Todd’s ‘Cyclop. of Anat.’ 1849-52, vol. iv. p. 1415. In humans, this organ is only about three to six lines long, but, like many other undeveloped parts, it varies in size and other characteristics.
51 All the following statements, given on the authority of these two naturalists, are taken from Rengger’s ‘Naturges. der Säugethiere von Paraguay,’ 1830, s. 41-57, and from Brehm’s ‘Thierleben,’ B. i. s. 10-87.
51 All the following statements, based on the authority of these two naturalists, are taken from Rengger’s ‘Naturges. der Säugethiere von Paraguay,’ 1830, pp. 41-57, and from Brehm’s ‘Thierleben,’ Vol. I, pp. 10-87.
52 ‘Bridgewater Treatise,’ p. 263.
59 Mr. L. H. Morgan’s work on ‘The American Beaver,’ 1868, offers a good illustration of this remark. I cannot, however, avoid thinking that he goes too far in underrating the power of Instinct.
59 Mr. L. H. Morgan’s work on ‘The American Beaver,’ 1868, provides a solid example of this statement. However, I can’t help but feel that he underestimates the strength of Instinct.
74 Rengger, ibid. s. 45.
76 See a discussion on this subject in Mr. E. B. Tylor’s very interesting work, ‘Researches into the Early History of Mankind,’ 1865, chaps. ii. to iv.
76 Check out a discussion on this topic in Mr. E. B. Tylor’s fascinating book, ‘Researches into the Early History of Mankind,’ 1865, chapters ii to iv.
77 Hon. Daines Barrington in ‘Philosoph. Transactions,’ 1773, p. 262. See also Dureau de la Malle, in ‘Ann. des Sc. Nat.’ 3rd series, Zoolog. tom. x. p. 119.
77 Hon. Daines Barrington in ‘Philosoph. Transactions,’ 1773, p. 262. See also Dureau de la Malle, in ‘Ann. des Sc. Nat.’ 3rd series, Zoolog. vol. x. p. 119.
78 ‘On the Origin of Language,’ by H. Wedgwood, 1866. ‘Chapters on Language,’ by the Rev. F. W. Farrar, 1865. These works are most interesting. See also ‘De la Phys. et de Parole,’ par Albert Lemoine, 1865, p. 190. The work on this subject, by the late Prof. Aug. Schleicher, has been translated by Dr. Bikkers into English, under the title of ‘Darwinism tested by the Science of Language,’ 1869.
78 ‘On the Origin of Language,’ by H. Wedgwood, 1866. ‘Chapters on Language,’ by Rev. F. W. Farrar, 1865. These works are really interesting. Check out ‘De la Phys. et de Parole,’ by Albert Lemoine, 1865, p. 190. The late Prof. Aug. Schleicher's work on this topic has been translated into English by Dr. Bikkers, titled ‘Darwinism Tested by the Science of Language,’ 1869.
79 Vogt, ‘Mémoire sur les Microcéphales,’ 1867, p. 169. With respect to savages, I have given some facts in my ‘Journal of Researches,’ &c., 1845, p. 206.
79 Vogt, ‘Memoir on Microcephaly,’ 1867, p. 169. Regarding primitive people, I shared some facts in my ‘Journal of Researches,’ etc., 1845, p. 206.
85 Macgillivray, ‘Hist. of British Birds,’ vol. ii. 1839, p. 29. An excellent observer, Mr. Blackwall, remarks that the magpie learns to pronounce single words, and even short sentences, more readily than almost any other British bird; yet, as he adds, after long and closely investigating its habits, he has never known it, in a state of nature, display any unusual capacity for imitation. ‘Researches in Zoology,’ 1834, p. 158.
85 Macgillivray, ‘Hist. of British Birds,’ vol. ii. 1839, p. 29. An excellent observer, Mr. Blackwall, notes that the magpie learns to say individual words, and even short phrases, more easily than nearly any other British bird; however, as he points out, after thoroughly studying its behavior, he has never seen it, in the wild, show any exceptional ability for imitation. ‘Researches in Zoology,’ 1834, p. 158.
86 See the very interesting parallelism between the development of speech and languages, given by Sir C. Lyell in ‘The Geolog. Evidences of the Antiquity of Man,’ 1863, chap. xxiii.
86 Notice the fascinating similarities between how speech and languages develop, as described by Sir C. Lyell in ‘The Geolog. Evidences of the Antiquity of Man,’ 1863, chap. xxiii.
87 See remarks to this effect by the Rev. F. W. Farrar, in an interesting article, entitled “Philology and Darwinism” in ‘Nature,’ March 24th, 1870, p. 528.
87 See comments on this topic by Rev. F. W. Farrar in a compelling article titled “Philology and Darwinism” in ‘Nature,’ March 24th, 1870, p. 528.
90 Buckland, ‘Bridgewater Treatise,’ p. 411.
95 See an excellent article on this subject by the Rev. F. W. Farrar, in the ‘Anthropological Review,’ Aug. 1864, p. ccxvii. For further facts see Sir J. Lubbock, ‘Prehistoric Times,’ 2nd edit. 1869. p. 564; and especially the chapters on Religion in his ‘Origin of Civilisation,’ 1870.
95 Check out a great article on this topic by Rev. F. W. Farrar in the ‘Anthropological Review,’ August 1864, page ccxvii. For more information, see Sir J. Lubbock's ‘Prehistoric Times,’ 2nd edition, 1869, page 564; and especially the chapters on Religion in his ‘Origin of Civilisation,’ 1870.
97 Tylor, ‘Early History of Mankind,’ 1865, p. 6. See also the three striking chapters on the Development of Religion, in Lubbock’s ‘Origin of Civilisation,’ 1870. In a like manner Mr. Herbert Spencer, in his ingenious essay in the ‘Fortnightly Review’ (May 1st, 1870, p. 535), accounts for the earliest forms of religious belief throughout the world, by man being led through dreams, shadows, and other causes, to look at himself as a double essence, corporeal and spiritual. As the spiritual being is supposed to exist after death and to be powerful, it is propitiated by various gifts and ceremonies, and its aid invoked. He then further shews that names or nicknames given from some animal or other object to the early progenitors or founders of a tribe, are supposed after a long interval to represent the real progenitor of the tribe; and such animal or object is then naturally believed still to exist as a spirit, is held sacred, and worshipped as a god. Nevertheless I cannot but suspect that there is a still earlier and ruder stage, when anything which manifests power or movement is thought to be endowed with some form of life, and with mental faculties analogous to our own.
97 Tylor, ‘Early History of Mankind,’ 1865, p. 6. Also, check out the three compelling chapters on the Development of Religion in Lubbock’s ‘Origin of Civilisation,’ 1870. Similarly, Mr. Herbert Spencer, in his insightful essay in the ‘Fortnightly Review’ (May 1st, 1870, p. 535), explains the earliest forms of religious belief worldwide, suggesting that people were influenced by dreams, shadows, and other factors, leading them to view themselves as having both a physical and spiritual existence. Because the spiritual being is believed to continue after death and hold power, it is honored with various gifts and rituals, with people seeking its assistance. He further demonstrates that names or nicknames based on animals or other objects given to the early ancestors or founders of a tribe are thought, after a significant time, to represent the actual ancestor of the tribe; thus, that animal or object is believed to still exist as a spirit, is considered sacred, and is worshipped as a god. However, I can't help but suspect that there was an even earlier and more primitive stage when anything that shows power or movement was thought to be alive and to possess mental abilities similar to our own.
100 ‘Prehistoric Times,’ 2nd edit. p. 571. In this work (at p. 553) there will be found an excellent account of the many strange and capricious customs of savages.
100 'Prehistoric Times,' 2nd ed. p. 571. In this book (at p. 553) you'll find a great description of the various strange and unpredictable customs of primitive people.
104 Mr. Bain gives a list (‘Mental and Moral Science,’ 1868, p. 543-725) of twenty-six British authors who have written on this subject, and whose names are familiar to every reader; to these, Mr. Bain’s own name, and those of Mr. Lecky, Mr. Shadworth Hodgson, and Sir J. Lubbock, as well as of others, may be added.
104 Mr. Bain provides a list (‘Mental and Moral Science,’ 1868, p. 543-725) of twenty-six British authors who have written on this topic, and whose names are known to every reader. To this list, you can also add Mr. Bain himself, Mr. Lecky, Mr. Shadworth Hodgson, and Sir J. Lubbock, among others.
105 Sir B. Brodie, after observing that man is a social animal (‘Psychological Enquiries,’ 1854, p. 192), asks the pregnant question, “ought not this to settle the disputed question as to the existence of a moral sense?” Similar ideas have probably occurred to many persons, as they did long ago to Marcus Aurelius. Mr. J. S. Mill speaks, in his celebrated work, ‘Utilitarianism,’ (1864, p. 46), of the social feelings as a “powerful natural sentiment,” and as “the natural basis of sentiment for utilitarian morality;” but on the previous page he says, “if, as is my own belief, the moral feelings are not innate, but acquired, they are not for that reason less natural.” It is with hesitation that I venture to differ from so profound a thinker, but it can hardly be disputed that the social feelings are instinctive or innate in the lower animals; and why should they not be so in man? Mr. Bain (see, for instance, ‘The Emotions and the Will,’ 1865, p. 481) and others believe that the moral sense is acquired by each individual during his lifetime. On the general theory of evolution this is at least extremely improbable.
105 Sir B. Brodie, after noting that humans are social beings (‘Psychological Enquiries,’ 1854, p. 192), poses the thought-provoking question, “shouldn’t this resolve the debate over whether a moral sense exists?” Similar thoughts have likely crossed the minds of many, as they did for Marcus Aurelius long ago. Mr. J. S. Mill discusses, in his famous work, ‘Utilitarianism,’ (1864, p. 46), social feelings as a “strong natural sentiment” and as “the natural foundation of sentiment for utilitarian morality;” but on the previous page, he states, “if, as I believe, moral feelings are not inherent but learned, that doesn’t make them any less natural.” I hesitantly disagree with such a profound thinker, but it’s hard to deny that social feelings are instinctive or innate in lower animals; so why wouldn’t they be the same in humans? Mr. Bain (see, for example, ‘The Emotions and the Will,’ 1865, p. 481) and others contend that the moral sense is developed by each individual throughout their lives. Based on the general theory of evolution, this idea seems highly unlikely.
106 ‘Die Darwin’sche Theorie,’ s. 101.
__A_TAG_PLACEHOLDER_0__ 'The Darwinian Theory,' see 101.
108 Brehm, ‘Thierleben,’ B. i. 1864, s. 52, 79. For the case of the monkeys extracting thorns from each other, see s. 54. With respect to the Hamadryas turning over stones, the fact is given (s. 76) on the evidence of Alvarez, whose observations Brehm thinks quite trustworthy. For the cases of the old male baboons attacking the dogs, see s. 79; and with respect to the eagle, s. 56.
108 Brehm, ‘Animal Life,’ Vol. I, 1864, pp. 52, 79. For the monkeys pulling thorns from one another, see p. 54. Concerning the Hamadryas flipping over stones, this fact is mentioned (p. 76) based on Alvarez's evidence, which Brehm considers quite reliable. For instances of the older male baboons attacking dogs, see p. 79; and regarding the eagle, see p. 56.
111 As quoted by Mr. L. H. Morgan, ‘The American Beaver,’ 1868, p. 272. Capt. Stansbury also gives an interesting account of the manner in which a very young pelican, carried away by a strong stream, was guided and encouraged in its attempts to reach the shore by half a dozen old birds.
111 As quoted by Mr. L. H. Morgan, ‘The American Beaver,’ 1868, p. 272. Captain Stansbury also shares an interesting story about how a very young pelican, swept away by a strong current, was guided and supported in its efforts to reach the shore by six older birds.
113 ‘Thierleben,’ B. i. s. 85.
117 See the first and striking chapter in Adam Smith’s ‘Theory of Moral Sentiments.’ Also Mr. Bain’s ‘Mental and Moral Science,’ 1868, p. 244, and 275-282. Mr. Bain states, that “sympathy is, indirectly, a source of pleasure to the sympathiser;” and he accounts for this through reciprocity. He remarks that “the person benefited, or others in his stead, may make up, by sympathy and good offices returned, for all the sacrifice.” But if, as appears to be the case, sympathy is strictly an instinct, its exercise would give direct pleasure, in the same manner as the exercise, as before remarked, of almost every other instinct.
117 Check out the first and compelling chapter in Adam Smith’s ‘Theory of Moral Sentiments.’ Also refer to Mr. Bain’s ‘Mental and Moral Science,’ 1868, p. 244, and 275-282. Mr. Bain says that “sympathy is, indirectly, a source of pleasure to the sympathizer;” and he explains this through reciprocity. He notes that “the person benefited, or others in his place, may make up, by sympathy and returned good deeds, for all the sacrifice.” However, if, as seems to be the case, sympathy is purely an instinct, using it would provide direct pleasure, just like the use of almost every other instinct, as mentioned earlier.
118 This fact, the Rev. L. Jenyns states (see his edition of ‘White’s Nat. Hist. of Selborne,’ 1853, p. 204) was first recorded by the illustrious Jenner, in ‘Phil. Transact.’ 1824, and has since been confirmed by several observers, especially by Mr. Blackwall. This latter careful observer examined, late in the autumn, during two years, thirty-six nests; he found that twelve contained young dead birds, five contained eggs on the point of being hatched, and three eggs not nearly hatched. Many birds not yet old enough for a prolonged flight are likewise deserted and left behind. See Blackwall, ‘Researches in Zoology,’ 1834, pp. 108, 118. For some additional evidence, although this is not wanted, see Leroy, ‘Lettres Phil.’ 1802, p. 217.
118 The Rev. L. Jenyns mentions that this fact was first noted by the renowned Jenner in ‘Phil. Transact.’ 1824, and it has been confirmed by several observers since then, particularly by Mr. Blackwall. This meticulous observer studied thirty-six nests over two years in late autumn; he found that twelve had young dead birds, five had eggs about to hatch, and three had eggs that were not close to hatching. Many birds that are not old enough for a long flight are also abandoned and left behind. See Blackwall, ‘Researches in Zoology,’ 1834, pp. 108, 118. For some additional evidence, though it is not necessary, refer to Leroy, ‘Lettres Phil.’ 1802, p. 217.
119 Hume remarks (‘An Enquiry Concerning the Principles of Morals,’ edit. of 1751, p. 132), “there seems a necessity for confessing that the happiness and misery of others are not spectacles altogether indifferent to us, but that the view of the former ... communicates a secret joy; the appearance of the latter ... throws a melancholy damp over the imagination.”
119 Hume notes (“An Enquiry Concerning the Principles of Morals,” edit. of 1751, p. 132), “we must admit that the happiness and suffering of others matter to us. Seeing others happy brings us a hidden joy, while witnessing their misery casts a gloomy shadow over our thoughts.”
121 I have given one such case, namely of three Patagonian Indians who preferred being shot, one after the other, to betraying the plans of their companions in war (‘Journal of Researches,’ 1845, p. 103).
121 I shared one example, specifically about three Patagonian Indians who chose to be shot, one after the other, rather than revealing their comrades' battle plans (‘Journal of Researches,’ 1845, p. 103).
122 Dr. Prosper Despine, in his ‘Psychologie Naturelle,’ 1868 (tom. i. p. 243; tom ii. p. 169) gives many curious cases of the worst criminals, who apparently have been entirely destitute of conscience.
122 Dr. Prosper Despine, in his ‘Natural Psychology,’ 1868 (vol. i, p. 243; vol. ii, p. 169) presents numerous fascinating cases of the most notorious criminals who seem to have been completely lacking in conscience.
123 See an able article in the ‘North British Review,’ 1867, p. 395. See also Mr. W. Bagehot’s articles on the Importance of Obedience and Coherence to Primitive Man, in the ‘Fortnightly Review,’ 1867, p. 529, and 1868, p. 457, &c.
123 Check out a great article in the ‘North British Review,’ 1867, p. 395. Also, see Mr. W. Bagehot’s articles on the Importance of Obedience and Coherence to Primitive Man, in the ‘Fortnightly Review,’ 1867, p. 529, and 1868, p. 457, etc.
124 The fullest account which I have met with is by Dr. Gerland, in his ‘Ueber das Aussterben der Naturvölker,’ 1868; but I shall have to recur to the subject of infanticide in a future chapter.
124 The most detailed account I've come across is by Dr. Gerland, in his 'On the Extinction of Indigenous Peoples,' 1868; however, I will need to return to the topic of infanticide in a later chapter.
132 This term is used in an able article in the ‘Westminster Review,’ Oct. 1869, p. 498. For the Greatest Happiness principle, see J. S. Mill, ‘Utilitarianism,’ p. 17.
132 This term is used in a capable article in the ‘Westminster Review,’ Oct. 1869, p. 498. For the Greatest Happiness principle, see J. S. Mill, ‘Utilitarianism,’ p. 17.
133 Good instances are given by Mr. Wallace in ‘Scientific Opinion,’ Sept. 15, 1869; and more fully in his ‘Contributions to the Theory of Natural Selection,’ 1870, p. 353.
133 Good examples are provided by Mr. Wallace in ‘Scientific Opinion,’ September 15, 1869; and more extensively in his ‘Contributions to the Theory of Natural Selection,’ 1870, p. 353.
137 A writer in the ‘North British Review’ (July, 1869, p. 531), well capable of forming a sound judgment, expresses himself strongly to this effect. Mr. Lecky (‘Hist. of Morals,’ vol. i. p. 143) seems to a certain extent to coincide.
137 A writer in the ‘North British Review’ (July, 1869, p. 531), clearly able to make a solid judgment, expresses his opinion strongly on this matter. Mr. Lecky (‘Hist. of Morals,’ vol. i. p. 143) appears to agree to some degree.
138 See his remarkable work on ‘Hereditary Genius,’ 1869, p. 349. The Duke of Argyll (‘Primeval Man,’ 1869, p. 188) has some good remarks on the contest in man’s nature between right and wrong.
138 Check out his amazing work on ‘Hereditary Genius,’ 1869, p. 349. The Duke of Argyll (‘Primeval Man,’ 1869, p. 188) has some insightful comments on the struggle between right and wrong in human nature.
141 With respect to the “Cranial forms of the American aborigines,” see Dr. Aitken Meigs in ‘Proc. Acad. Nat. Sci.’ Philadelphia, May, 1866. On the Australians, see Huxley, in Lyell’s ‘Antiquity of Man,’ 1863, p. 87. On the Sandwich Islanders, Prof. J. Wyman, ‘Observations on Crania,’ Boston, 1868, p. 18.
141 For information on the "Cranial forms of the American aborigines," refer to Dr. Aitken Meigs in ‘Proc. Acad. Nat. Sci.’ Philadelphia, May, 1866. For details on Australians, see Huxley in Lyell’s ‘Antiquity of Man,’ 1863, p. 87. Regarding the Sandwich Islanders, check out Prof. J. Wyman’s ‘Observations on Crania,’ Boston, 1868, p. 18.
150 Mr. Bates remarks (‘The Naturalist on the Amazons,’ 1863, vol. ii. p. 159), with respect to the Indians of the same S. American tribe, “no two of them were at all similar in the shape of the head; one man had an oval visage with fine features, and another was quite Mongolian in breadth and prominence of cheek, spread of nostrils, and obliquity of eyes.”
150 Mr. Bates points out (‘The Naturalist on the Amazons,’ 1863, vol. ii. p. 159), regarding the Indians of the same South American tribe, “no two of them were at all alike in the shape of their heads; one man had an oval face with delicate features, while another had a more Mongolian appearance with broad cheeks, wide nostrils, and slanted eyes.”
152 Godron, ‘De l’Espèce,’ 1859, tom. ii. livre 3. Quatrefages, ‘Unité de l’Espèce Humaine,’ 1861. Also Lectures on Anthropology, given in the ‘Revue des Cours Scientifiques,’ 1866-1868.
152 Godron, ‘On Species,’ 1859, vol. ii, book 3. Quatrefages, ‘Unity of the Human Species,’ 1861. Also, Lectures on Anthropology, published in the ‘Review of Scientific Courses,’ 1866-1868.
154 I have fully discussed these laws in my ‘Variation of Animals and Plants under Domestication,’ vol. ii. chap. xxii. and xxiii. M. J. P. Durand has lately 1868; published a valuable essay ‘De l’Influence des Milieux, &c.’ He lays much stress on the nature of the soil.
154 I have thoroughly covered these laws in my ‘Variation of Animals and Plants under Domestication,’ vol. ii, chapters xxii and xxiii. M. J. P. Durand recently published a valuable essay in 1868 titled ‘De l’Influence des Milieux, &c.’ He emphasizes the importance of the soil's nature.
156 For the Polynesians, see Prichard’s ‘Physical Hist. of Mankind,’ vol. v. 1847, p. 145, 283. Also Godron, ‘De l’Espèce,’ tom. ii. p. 289. There is also a remarkable difference in appearance between the closely-allied Hindoos inhabiting the Upper Ganges and Bengal; see Elphinstone’s 'History of India,’ vol. i. p. 324.
156 For the Polynesians, see Prichard’s ‘Physical History of Mankind,’ vol. v. 1847, p. 145, 283. Also Godron, ‘On the Species,’ vol. ii, p. 289. There’s also a noticeable difference in appearance between the closely related Hindoos living in the Upper Ganges and Bengal; see Elphinstone’s 'History of India,’ vol. i, p. 324.
159 I have given authorities for these several statements in my ‘Variation of Animals under Domestication,’ vol. ii. p. 297-300. Dr. Jaeger, “Ueber das Längenwachsthum der Knochen,” ‘Jenaischen Zeitschrift,’ B. v. Heft i.
159 I've provided sources for these various statements in my ‘Variation of Animals under Domestication,’ vol. ii. pp. 297-300. Dr. Jaeger, “On the Growth of Bone Length,” ‘Jena Journal,’ vol. v, part i.
168 ‘Säugethiere von Paraguay,’ s. 8, 10. I have had good opportunities for observing the extraordinary power of eyesight in the Fuegians.’ See also Lawrence (‘Lectures on Physiology,’ &c., 1822, p. 404) on this same subject. M. Giraud-Teulon has recently collected (‘Revue des Cours Scientifiques,’ 1870, p. 625) a large and valuable body of evidence proving that the cause of short-sight, “C’est le travail assidu, de près.”
168 ‘Mammals of Paraguay,’ pp. 8, 10. I’ve had great chances to observe the incredible eyesight of the Fuegians.’ Also see Lawrence (‘Lectures on Physiology,’ etc., 1822, p. 404) on this topic. M. Giraud-Teulon recently gathered (‘Revue des Cours Scientifiques,’ 1870, p. 625) a significant and valuable collection of evidence showing that the cause of nearsightedness is, “It's the constant work up close.”
172 Dr. Wilckens (‘Landwirthschaft. Wochenblatt,’ No. 10, 1869) has lately published an interesting essay shewing how domestic animals, which live in mountainous regions, have their frames modified.
172 Dr. Wilckens (‘Landwirthschaft. Wochenblatt,’ No. 10, 1869) has recently published an intriguing essay showing how domesticated animals that live in hilly areas adapt their bodies.
174 See Dr. A. Farre’s well-known article in the ‘Cyclop. of Anat. and Phys.’ vol. v. 1859, p. 642. Owen ‘Anatomy of Vertebrates,’ vol. iii. 1868, p. 687. Prof. Turner in ‘Edinburgh Medical Journal,’ Feb. 1865.
174 See Dr. A. Farre’s famous article in the ‘Cyclopedia of Anatomy and Physiology,’ vol. v. 1859, p. 642. Owen ‘Anatomy of Vertebrates,’ vol. iii. 1868, p. 687. Prof. Turner in ‘Edinburgh Medical Journal,’ Feb. 1865.
175 ‘Annuario della Soc. dei Naturalisti in Modena,’ 1867, p. 83. Prof. Canestrini gives extracts on this subject from various authorities. Laurillard remarks, that as he has found a complete similarity in the form, proportions, and connexion of the two malar bones in several human subjects and in certain apes, he cannot consider this disposition of the parts as simply accidental.
175 ‘Annuario della Soc. dei Naturalisti in Modena,’ 1867, p. 83. Prof. Canestrini shares quotes on this topic from different experts. Laurillard notes that since he has observed a complete similarity in the shape, proportions, and connections of the two cheekbones in several humans and certain apes, he can't view this arrangement of the parts as merely coincidental.
177 In my ‘Variation of Animals under Domestication’ (vol. ii. p. 57) I attributed the not very rare cases of supernumerary mammæ in women to reversion. I was led to this as a probable conclusion, by the additional mammæ being generally placed symmetrically on the breast, and more especially from one case, in which a single efficient mamma occurred in the inguinal region of a woman, the daughter of another woman with supernumerary mammæ. But Prof. Preyer (‘Der Kampf um das Dasein,’ 1869, s. 45) states that mammæ erraticæ have been known to occur in other situations, even on the back; so that the force of my argument is greatly weakened or perhaps quite destroyed.
177 In my ‘Variation of Animals under Domestication’ (vol. ii. p. 57) I suggested that the relatively uncommon occurrences of extra breasts in women might be due to reversion. I reached this conclusion as a likely possibility because these extra breasts are usually found symmetrically on the chest, especially in one instance where a single functional breast appeared in the groin area of a woman, who was the daughter of another woman with extra breasts. However, Professor Preyer (‘Der Kampf um das Dasein,’ 1869, s. 45) mentions that mammæ erraticæ have been reported in other locations, even on the back; therefore, my argument's strength is significantly diminished, if not entirely invalidated.
With much hesitation I, in the same work (vol. ii. p. 12), attributed the frequent cases of polydactylism in men to reversion. I was partly led to this through Prof. Owen’s statement, that some of the Ichthyopterygia possess more than five digits, and therefore, as I supposed, had retained a primordial condition; but after reading Prof. Gegenbaur’s paper (‘Jenaischen Zeitschrift,’ B. v. Heft 3, s. 341), who is the highest authority in Europe on such a point, and who disputes Owen’s conclusion, I see that it is extremely doubtful whether supernumerary digits can thus be accounted for. It was the fact that such digits not only frequently occur and are strongly inherited, but have the power of regrowth after amputation, like the normal digits of the lower vertebrata, that chiefly led me to the above conclusion. This extraordinary fact of their regrowth remains inexplicable, if the belief in reversion to some extremely remote progenitor must be rejected. I cannot, however, follow Prof. Gegenbaur in supposing that additional digits could not reappear through reversion, without at the same time other parts of the skeleton being simultaneously and similarly modified; for single characters often reappear through reversion.
With a lot of hesitation, I, in the same work (vol. ii. p. 12), suggested that the frequent instances of polydactylism in humans are due to reversion. I was partly influenced by Prof. Owen’s statement that some Ichthyopterygia have more than five digits, which I thought indicated they had retained a primitive condition. However, after reading Prof. Gegenbaur’s paper (‘Jenaischen Zeitschrift,’ B. v. Heft 3, s. 341), who is the leading authority in Europe on this issue and challenges Owen’s conclusion, I now see that it's really uncertain whether extra digits can be explained this way. The fact that these extra digits not only occur frequently and are strongly inherited but also have the ability to regrow after being amputated—like the normal digits of lower vertebrates—was primarily what led me to my earlier conclusion. This remarkable ability to regrow remains a mystery if we reject the idea of reversion to some very distant ancestor. However, I can't agree with Prof. Gegenbaur's view that extra digits couldn't reappear through reversion unless other parts of the skeleton were also simultaneously and similarly modified, as individual traits often reappear through reversion.
184 These papers deserve careful study by any one who desires to learn how frequently our muscles vary, and in varying come to resemble those of the Quadrumana. The following references relate to the few points touched on in my text: vol. xiv. 1865, p. 379-384; vol. xv. 1866, p. 241, 242; vol. xv. 1867, p. 544; vol. xvi. 1868, p. 524. I may here add that Dr. Murie and Mr. St. George Mivart have shewn in their Memoir on the Lemuroidea (‘Transact. Zoolog. Soc.’ vol. vii. 1869, p. 96), how extraordinarily variable some of the muscles are in these animals, the lowest members of the Primates. Gradations, also, in the muscles leading to structures found in animals still lower in the scale, are numerous in the Lemuroidea.
184 These papers are worth a close look for anyone interested in understanding how often our muscles change, and how, through these changes, they can start to resemble those of the Quadrumana. The following references pertain to the few points mentioned in my text: vol. xiv. 1865, p. 379-384; vol. xv. 1866, p. 241, 242; vol. xv. 1867, p. 544; vol. xvi. 1868, p. 524. I should also mention that Dr. Murie and Mr. St. George Mivart demonstrated in their Memoir on the Lemuroidea (‘Transact. Zoolog. Soc.’ vol. vii. 1869, p. 96) how remarkably variable some muscles are in these animals, which are among the most primitive members of the Primates. There are also many gradations in the muscles that lead to structures found in even more primitive animals within the Lemuroidea.
186 Prof. Macalister (ibid. p. 121) has tabulated his observations, and finds that muscular abnormalities are most frequent in the fore-arms, secondly in the face, thirdly in the foot, &c.
186 Prof. Macalister (ibid. p. 121) has organized his observations into a table, showing that muscle abnormalities are most commonly found in the forearms, followed by the face, then the foot, etc.
187 The Rev. Dr. Haughton, after giving (‘Proc. R. Irish Academy,’ June 27, 1864, p. 715) a remarkable case of variation in the human flexor pollicis longus, adds, “This remarkable example shews that man may sometimes possess the arrangement of tendons of thumb and fingers characteristic of the macaque; but whether such a case should be regarded as a macaque passing upwards into a man, or a man passing downwards into a macaque, or as a congenital freak of nature, I cannot undertake to say.” It is satisfactory to hear so capable an anatomist, and so embittered an opponent of evolutionism, admitting even the possibility of either of his first propositions. Prof. Macalister has also described (‘Proc. R. Irish Acad.’ vol. x. 1864, p. 138) variations in the flexor pollicis longus, remarkable from their relations to the same muscle in the Quadrumana.
187 The Rev. Dr. Haughton, after presenting a notable case of variation in the human flexor pollicis longus (‘Proc. R. Irish Academy,’ June 27, 1864, p. 715), states, “This remarkable example shows that humans can sometimes have the arrangement of tendons in the thumb and fingers that is typical of the macaque; however, whether this case should be seen as a macaque evolving into a human, a human evolving into a macaque, or just a congenital oddity, I can’t say.” It’s encouraging to hear such a skilled anatomist, who strongly opposes evolutionism, acknowledge even the possibility of either of his first ideas. Prof. Macalister has also documented variations in the flexor pollicis longus (‘Proc. R. Irish Acad.’ vol. x. 1864, p. 138) that are notable due to their connections to the same muscle in the Quadrumana.
194 ‘Primitive Marriage,’ 1865.
‘Primitive Marriage,’ 1865.
197 Messrs. Murie and Mivart in their “Anatomy of the Lemuroidea” (‘Transact. Zoolog. Soc.’ vol. vii. 1869, p. 96-98) say, “some muscles are so irregular in their distribution that they cannot be well classed in any of the above groups.” These muscles differ even on the opposite sides of the same individual.
197 Messrs. Murie and Mivart in their “Anatomy of the Lemuroidea” (‘Transact. Zoolog. Soc.’ vol. vii. 1869, p. 96-98) say, “some muscles are so irregular in their distribution that they can’t be easily categorized into any of the groups listed above.” These muscles vary even on opposite sides of the same individual.
198 ‘Quarterly Review,’ April, 1869, p. 392. This subject is more fully discussed in Mr. Wallace’s ‘Contributions to the Theory of Natural Selection,’ 1870, in which all the essays referred to in this work are republished. The ‘Essay on Man’ has been ably criticised by Prof. Claparède, one of the most distinguished zoologists in Europe, in an article published in the ‘Bibliothèque Universelle,’ June, 1870. The remark quoted in my text will surprise every one who has read Mr. Wallace’s celebrated paper on ‘The Origin of Human Races deduced from the Theory of Natural Selection,’ originally published in the ‘Anthropological Review,’ May, 1864, p. clviii. I cannot here resist quoting a most just remark by Sir J. Lubbock (‘Prehistoric Times,’ 1865, p. 479) in reference to this paper, namely, that Mr. Wallace, “with characteristic unselfishness, ascribes it (i.e. the idea of natural selection) unreservedly to Mr. Darwin, although, as is well known, he struck out the idea independently, and published it, though not with the same elaboration, at the same time.”
198 ‘Quarterly Review,’ April, 1869, p. 392. This topic is discussed in more detail in Mr. Wallace’s ‘Contributions to the Theory of Natural Selection,’ 1870, which includes all the essays mentioned in this work. The ‘Essay on Man’ has been effectively critiqued by Prof. Claparède, one of Europe’s leading zoologists, in an article published in the ‘Bibliothèque Universelle,’ June, 1870. The remark quoted in my text will surprise anyone who has read Mr. Wallace’s famous paper on ‘The Origin of Human Races deduced from the Theory of Natural Selection,’ originally published in the ‘Anthropological Review,’ May, 1864, p. clviii. I cannot resist quoting a very fair point made by Sir J. Lubbock (‘Prehistoric Times,’ 1865, p. 479) regarding this paper, which states that Mr. Wallace, “with characteristic unselfishness, gives full credit for the idea of natural selection to Mr. Darwin, even though he independently came up with the idea and published it, albeit not as thoroughly, at the same time.”
199 Quoted by Mr. Lawson Tait in his “Law of Natural Selection,”—‘Dublin Quarterly Journal of Medical Science,’ Feb. 1869. Dr. Keller is likewise quoted to the same effect.
199 Cited by Mr. Lawson Tait in his “Law of Natural Selection,”—‘Dublin Quarterly Journal of Medical Science,’ Feb. 1869. Dr. Keller is also quoted in a similar way.
202 In Hylobates syndactylus, as the name expresses, two of the digits regularly cohere; and this, as Mr. Blyth informs me, is occasionally the case with the digits of H. agilis, lar, and leuciscus.
202 In Hylobates syndactylus, as the name suggests, two of the fingers are usually fused; and according to Mr. Blyth, this sometimes happens with the fingers of H. agilis, lar, and leuciscus.
205 Häckel has an excellent discussion on the steps by which man became a biped: ‘Natürliche Schöpfungsgeschichte,’ 1868, s. 507. Dr. Büchner (‘Conférences sur la Théorie Darwinienne,’ 1869, p. 135) has given good cases of the use of the foot as a prehensile organ by man; also on the manner of progression of the higher apes to which I allude in the following paragraph: see also Owen (‘Anatomy of Vertebrates,’ vol. iii. p. 71) on this latter subject.
205 Häckel has a great discussion on how humans became bipedal: ‘Natürliche Schöpfungsgeschichte,’ 1868, p. 507. Dr. Büchner (‘Conférences sur la Théorie Darwinienne,’ 1869, p. 135) provides solid examples of how humans use their feet as grasping organs; he also discusses how higher apes move, which I refer to in the next paragraph: see also Owen (‘Anatomy of Vertebrates,’ vol. iii. p. 71) on this topic.
206 “On the Primitive Form of the Skull,” translated in ‘Anthropological Review,’ Oct. 1868, p. 428. Owen (‘Anatomy of Vertebrates,’ vol. ii. 1866, p. 551) on the mastoid processes in the higher apes.
206 “On the Primitive Form of the Skull,” translated in ‘Anthropological Review,’ Oct. 1868, p. 428. Owen (‘Anatomy of Vertebrates,’ vol. ii. 1866, p. 551) discusses the mastoid processes in higher apes.
208 Dujardin, ‘Annales des Sc. Nat.’ 3rd series, Zoolog. tom. xiv. 1850, p. 203. See also Mr. Lowne, ‘Anatomy and Phys. of the Musca vomitoria,’ 1870, p. 14. My son, Mr. F. Darwin, dissected for me the cerebral ganglia of the Formica rufa.
208 Dujardin, ‘Annales des Sc. Nat.’ 3rd series, Zoolog. vol. xiv. 1850, p. 203. Also, see Mr. Lowne, ‘Anatomy and Phys. of the Musca vomitoria,’ 1870, p. 14. My son, Mr. F. Darwin, dissected the brain ganglia of the Formica rufa for me.
209 ‘Philosophical Transactions,’ 1869, p. 513.
213 Schaaffhausen gives from Blumenbach and Busch, the cases of the spasms and cicatrix, in ‘Anthropolog. Review,’ Oct. 1868, p. 420. Dr. Jarrold (‘Anthropologia,’ 1808, p. 115, 116) adduces from Camper and from his own observations, cases of the modification of the skull from the head being fixed in an unnatural position. He believes that certain trades, such as that of a shoemaker, by causing the head to be habitually held forward, makes the forehead more rounded and prominent.
213 Schaaffhausen references Blumenbach and Busch regarding cases of spasms and scars in the ‘Anthropolog. Review,’ Oct. 1868, p. 420. Dr. Jarrold (‘Anthropologia,’ 1808, p. 115, 116) cites Camper and his own observations, presenting cases of skull modification caused by the head being held in an unnatural position. He argues that certain professions, like shoemaking, which require the head to be regularly tilted forward, result in a more rounded and prominent forehead.
217 Isidore Geoffroy St.-Hilaire remarks (‘Hist. Nat. Générale,’ tom. ii. 1859, p. 215-217) on the head of man being covered with long hair; also on the upper surfaces of monkeys and of other mammals being more thickly clothed than the lower surfaces. This has likewise been observed by various authors. Prof. P. Gervais (‘Hist. Nat. des Mammifères,’ tom. i. 1854, p. 28), however, states that in the Gorilla the hair is thinner on the back, where it is partly rubbed off, than on the lower surface.
217 Isidore Geoffroy St.-Hilaire notes (‘Hist. Nat. Générale,’ vol. ii. 1859, pp. 215-217) that humans have long hair on their heads; he also points out that the top surfaces of monkeys and other mammals have denser fur than their lower surfaces. This observation has been confirmed by several authors. However, Prof. P. Gervais (‘Hist. Nat. des Mammifères,’ vol. i. 1854, p. 28) mentions that the hair on the back of the Gorilla is thinner, where it has been partly rubbed off, compared to the lower surface.
218 Mr. St. George Mivart, ‘Proc. Zoolog. Soc.’ 1865, p. 562, 583. Dr. J. E. Gray, ‘Cat. Brit. Mus.: Skeletons.’ Owen, ‘Anatomy of Vertebrates,’ vol. ii. p. 517. Isidore Geoffroy, ‘Hist. Nat. Gén.’ tom. ii. p. 244.
218 Mr. St. George Mivart, ‘Proc. Zoolog. Soc.’ 1865, p. 562, 583. Dr. J. E. Gray, ‘Cat. Brit. Mus.: Skeletons.’ Owen, ‘Anatomy of Vertebrates,’ vol. ii. p. 517. Isidore Geoffroy, ‘Hist. Nat. Gén.’ tom. ii. p. 244.
220 ‘Primeval Man,’ 1869, p. 66.
‘Primeval Man,’ 1869, p. 66.
222 After a time the members or tribes which are absorbed into another tribe assume, as Mr. Maine remarks (‘Ancient Law,’ 1861, p. 131), that they are the co-descendants of the same ancestors.
222 After a while, the groups or tribes that get absorbed into another tribe start to believe, as Mr. Maine points out (‘Ancient Law,’ 1861, p. 131), that they are all descendants of the same ancestors.
230 ‘Fraser’s Magazine,’ Sept. 1868, p. 353. This article seems to have struck many persons, and has given rise to two remarkable essays and a rejoinder in the ‘Spectator,’ Oct. 3rd and 17th 1868. It has also been discussed in the ‘Q. Journal of Science,’ 1869, p. 152, and by Mr. Lawson Tait in the ‘Dublin Q. Journal of Medical Science,’ Feb. 1869, and by Mr. E. Ray Lankester in his ‘Comparative Longevity,’ 1870, p. 128. Similar views appeared previously in the ‘Australasian,’ July 13, 1867. I have borrowed ideas from several of these writers.
230 ‘Fraser’s Magazine,’ Sept. 1868, p. 353. This article seems to have caught the attention of many people, leading to two significant essays and a response in the ‘Spectator,’ Oct. 3rd and 17th 1868. It has also been talked about in the ‘Q. Journal of Science,’ 1869, p. 152, and by Mr. Lawson Tait in the ‘Dublin Q. Journal of Medical Science,’ Feb. 1869, and by Mr. E. Ray Lankester in his ‘Comparative Longevity,’ 1870, p. 128. Similar opinions were expressed earlier in the ‘Australasian,’ July 13, 1867. I have drawn on ideas from several of these authors.
231 For Mr. Wallace, see ‘Anthropolog. Review,’ as before cited. Mr. Galton in ‘Macmillan’s Magazine,’ Aug. 1865, p. 318; also his great work, ‘Hereditary Genius,’ 1870.
231 For Mr. Wallace, see ‘Anthropolog. Review,’ as previously mentioned. Mr. Galton in ‘Macmillan’s Magazine,’ Aug. 1865, p. 318; also his major work, ‘Hereditary Genius,’ 1870.
232 ‘Hereditary Genius,’ 1870, p. 132-140.
233 See the fifth and sixth columns, compiled from good authorities, in the table given in Mr. E. R. Lankester’s ‘Comparative Longevity,’ 1870, p. 115.
233 Check out the fifth and sixth columns, gathered from reliable sources, in the table provided in Mr. E. R. Lankester’s ‘Comparative Longevity,’ 1870, p. 115.
234 ‘Hereditary Genius,’ 1870, p. 330.
236 ‘Hereditary Genius,’ 1870, p. 347.
237 E. Ray Lankester, ‘Comparative Longevity,’ 1870, p. 115. The table of the intemperate is from Nelson’s ‘Vital Statistics.’ In regard to profligacy, see Dr. Farr, “Influence of Marriage on Mortality,” ‘Nat. Assoc. for the Promotion of Social Science,’ 1858.
237 E. Ray Lankester, ‘Comparative Longevity,’ 1870, p. 115. The table of the intemperate is from Nelson’s ‘Vital Statistics.’ For information on profligacy, see Dr. Farr, “Influence of Marriage on Mortality,” ‘Nat. Assoc. for the Promotion of Social Science,’ 1858.
238 ‘Fraser’s Magazine,’ Sept. 1868, p. 353. ‘Macmillan’s Magazine,’ Aug. 1865, p. 318. The Rev. F. W. Farrar (‘Fraser’s Mag.,’ Aug. 1870, p. 264) takes a different view.
238 ‘Fraser’s Magazine,’ Sept. 1868, p. 353. ‘Macmillan’s Magazine,’ Aug. 1865, p. 318. The Rev. F. W. Farrar (‘Fraser’s Mag.,’ Aug. 1870, p. 264) has a different perspective.
239 “On the Laws of the Fertility of Women,” in ‘Transact. Royal Soc.’ Edinburgh, vol. xxiv. p. 287. See, also, Mr. Galton, ‘Hereditary Genius,’ p. 352-357, for observations to the above effect.
239 “On the Laws of Women’s Fertility,” in ‘Transactions of the Royal Society,’ Edinburgh, vol. xxiv. p. 287. Also, refer to Mr. Galton, ‘Hereditary Genius,’ p. 352-357, for comments that support this.
241 These quotations are taken from our highest authority on such questions, namely, Dr. Farr, in his paper “On the Influence of Marriage on the Mortality of the French People,” read before the Nat. Assoc. for the Promotion of Social Science, 1858.
241 These quotes come from our top expert on these issues, Dr. Farr, in his paper “On the Influence of Marriage on the Mortality of the French People,” presented to the National Association for the Promotion of Social Science in 1858.
243 I have taken the mean of the quinquennial means, given in ‘The Tenth Annual Report of Births, Deaths, &c., in Scotland,’ 1867. The quotation from Dr. Stark is copied from an article in the ‘Daily News,’ Oct. 17th, 1868, which Dr. Farr considers very carefully written.
243 I calculated the average of the five-year averages provided in ‘The Tenth Annual Report of Births, Deaths, &c., in Scotland,’ 1867. The quote from Dr. Stark is taken from an article in the ‘Daily News,’ dated October 17, 1868, which Dr. Farr regards as very well written.
246 ‘Hereditary Genius,’ 1870, p. 357-359. The Rev. F. H. Farrar (‘Fraser’s Mag.’, Aug. 1870, p. 257) advances arguments on the other side. Sir C. Lyell had already (‘Principles of Geology,’ vol. ii. 1868, p. 489) called attention, in a striking passage, to the evil influence of the Holy Inquisition in having lowered, through selection, the general standard of intelligence in Europe.
246 ‘Hereditary Genius,’ 1870, p. 357-359. The Rev. F. H. Farrar (‘Fraser’s Mag.,’ Aug. 1870, p. 257) presents arguments on the opposite side. Sir C. Lyell had already pointed out in a compelling section of ‘Principles of Geology,’ vol. ii, 1868, p. 489, the negative impact of the Holy Inquisition in reducing the overall intelligence level in Europe through selective processes.
250 ‘Primeval Man,’ 1869.
‘Primeval Man,’ 1869.
252 ‘Primitive Marriage,’ 1865. See, likewise, an excellent article, evidently by the same author, in the ‘North British Review,’ July, 1869. Also, Mr. L. H. Morgan, “A Conjectural Solution of the Origin of the Class. System of Relationship,” in ‘Proc. American Acad. of Sciences,’ vol. vii. Feb. 1868. Prof. Schaaffhausen (‘Anthropolog. Review,’ Oct. 1869, p. 373) remarks on “the vestiges of human sacrifices found both in Homer and the Old Testament.”
252 ‘Primitive Marriage,’ 1865. Also, check out a great article, clearly by the same author, in the ‘North British Review,’ July, 1869. Additionally, Mr. L. H. Morgan’s “A Conjectural Solution of the Origin of the Class. System of Relationship,” in ‘Proc. American Acad. of Sciences,’ vol. vii. Feb. 1868. Prof. Schaaffhausen (‘Anthropolog. Review,’ Oct. 1869, p. 373) comments on “the traces of human sacrifices found both in Homer and the Old Testament.”
255 Isidore Geoffroy St.-Hilaire gives a detailed account of the position assigned to man by various naturalists in their classifications: ‘Hist. Nat. Gén.’ tom. ii. 1859, p. 170-189.
255 Isidore Geoffroy St.-Hilaire provides a thorough description of the role assigned to humans by different naturalists in their classification systems: ‘Hist. Nat. Gén.’ vol. ii. 1859, pp. 170-189.
262 On the hair in Hylobates, see ‘Nat. Hist. of Mammals,’ by C. L. Martin, 1841, p. 415. Also, Isid. Geoffroy on the American monkeys and other kinds, ‘Hist. Nat. Gén.’ vol. ii. 1859, p. 216, 243. Eschricht, ibid. s. 46, 55, 61. Owen, ‘Anat. of Vertebrates,’ vol. iii. p. 619. Wallace, ‘Contributions to the Theory of Natural Selection,’ 1870. p. 344.
262 For information on the hair of Hylobates, see "Natural History of Mammals" by C. L. Martin, 1841, p. 415. Also, check Isid. Geoffroy on American monkeys and other species in "Historie Naturelle Générale," vol. ii, 1859, pp. 216, 243. Eschricht, ibid. s. 46, 55, 61. Owen, "Anatomy of Vertebrates," vol. iii, p. 619. Wallace, "Contributions to the Theory of Natural Selection," 1870, p. 344.
265 This is nearly the same classification as that provisionally adopted by Mr. St. George Mivart (‘Transact. Philosoph. Soc.’ 1867, p. 300), who, after separating the Lemuridæ, divides the remainder of the Primates into the Hominidæ, the Simiadæ answering to the Catarhines, the Cebidæ, and the Hapalidæ,—these two latter groups answering to the Platyrhines.
265 This is almost the same classification as the one temporarily adopted by Mr. St. George Mivart (‘Transact. Philosoph. Soc.’ 1867, p. 300), who, after separating the Lemurs, divides the rest of the Primates into the Hominids, with the Simians corresponding to the Catarhines, and the Cebids and Hapalids—these last two groups corresponding to the Platyrhines.
269 Häckel has come to this same conclusion. See ‘Ueber die Entstehung des Menschengeschlechts,’ in Virchow’s ‘Sammlung. gemein. wissen. Vorträge,’ 1868, s. 61. Also his ‘Natürliche Schöpfungsgeschichte,’ 1868, in which he gives in detail his views on the genealogy of man.
269 Häckel has reached the same conclusion. See ‘On the Origin of Mankind,’ in Virchow’s ‘Collection of Public Lectures,’ 1868, p. 61. Also his ‘Natural History of Creation,’ 1868, where he elaborates on his views regarding human ancestry.
273 Elaborate tables are given in his ‘Generelle Morphologie’ (B. ii. s. cliii. and s. 425); and with more especial reference to man in his 'Natürliche Schöpfungsgeschichte,’ 1868. Prof. Huxley, in reviewing this latter work (‘The Academy,’ 1869, p. 42) says, that he considers the phylum or lines of descent of the Vertebrata to be admirably discussed by Häckel, although he differs on some points. He expresses, also, his high estimate of the value of the general tenor and spirit of the whole work.
273 Detailed tables are provided in his ‘Generelle Morphologie’ (B. ii. s. cliii. and s. 425); and with a specific focus on humans in his 'Natürliche Schöpfungsgeschichte,’ 1868. Professor Huxley, in a review of this later work (‘The Academy,’ 1869, p. 42), states that he thinks the phylum or lines of descent of the Vertebrates are excellently examined by Häckel, although he disagrees on some points. He also shares his high regard for the overall value and spirit of the entire work.
274 ‘Palæontology,’ 1860, p. 199.
‘Paleontology,’ 1860, p. 199.
275 I had the satisfaction of seeing, at the Falkland Islands, in April, 1833, and therefore some years before any other naturalist, the locomotive larvæ of a compound Ascidian, closely allied to, but apparently generically distinct from, Synoicum. The tail was about five times as long as the oblong head, and terminated in a very fine filament. It was plainly divided, as sketched by me under a simple microscope, by transverse opaque partitions, which I presume represent the great cells figured by Kowalevsky. At an early stage of development the tail was closely coiled round the head of the larva.
275 I had the pleasure of seeing, at the Falkland Islands, in April 1833, and therefore some years before any other naturalist, the free-swimming larvae of a type of compound ascidian, which is closely related to, but seems to be a different genus from, Synoicum. The tail was about five times longer than the oblong head and ended in a very fine filament. It was clearly segmented, as I observed through a simple microscope, by transverse opaque partitions, which I assume represent the large cells depicted by Kowalevsky. At an early stage of development, the tail was tightly coiled around the head of the larva.
277 This is the conclusion of one of the highest authorities in comparative anatomy, namely, Prof. Gegenbaur: ‘Grundzüge der vergleich. Anat.’ 1870, s. 876. The result has been arrived at chiefly from the study of the Amphibia; but it appears from the researches of Waldeyer (as quoted in Humphry’s ‘Journal of Anat. and Phys.’ 1869, p. 161), that the sexual organs of even “the higher vertebrata are, in their early condition, hermaphrodite.” Similar views have long been held by some authors, though until recently not well based.
277 This is the conclusion of one of the top experts in comparative anatomy, Prof. Gegenbaur: ‘Grundzüge der vergleich. Anat.’ 1870, p. 876. This conclusion has mainly come from studying amphibians; however, research by Waldeyer (as cited in Humphry’s ‘Journal of Anat. and Phys.’ 1869, p. 161) shows that the sexual organs of even "higher vertebrates are, in their early stage, hermaphroditic." Similar opinions have been held by various authors for a long time, although they were not well supported until recently.
279 Serranus is well known often to be in an hermaphrodite condition; but Dr. Günther informs me that he is convinced that this is not its normal state. Descent from an ancient androgynous prototype would, however, naturally favour and explain, to a certain extent, the recurrence of this condition in these fishes.
279 The Serranus is commonly known to often be in a hermaphrodite state; however, Dr. Günther has informed me that he believes this is not its usual condition. Descent from an ancient androgynous ancestor would, though, naturally support and partly explain the recurring presence of this condition in these fish.
280 Mr. Lockwood believes (as quoted in ‘Quart. Journal of Science,’ April, 1868, p. 269), from what he has observed of the development of Hippocampus, that the walls of the abdominal pouch of the male in some way afford nourishment. On male fishes hatching the ova in their mouths, see a very interesting paper by Prof. Wyman, in ‘Proc. Boston Soc. of Nat. Hist.’ Sept. 15, 1857; also Prof. Turner, in ‘Journal of Anat. and Phys.’ Nov. 1, 1866, p. 78. Dr. Günther has likewise described similar cases.
280 Mr. Lockwood believes (as quoted in ‘Quart. Journal of Science,’ April 1868, p. 269), based on his observations of the development of Hippocampus, that the walls of the male's abdominal pouch somehow provide nourishment. For male fish incubating the eggs in their mouths, see an interesting paper by Prof. Wyman in ‘Proc. Boston Soc. of Nat. Hist.’ Sept. 15, 1857; also Prof. Turner in ‘Journal of Anat. and Phys.’ Nov. 1, 1866, p. 78. Dr. Günther has also described similar cases.
281 All vital functions tend to run their course in fixed and recurrent periods, and with tidal animals the periods would probably be lunar; for such animals must have been left dry or covered deep with water,—supplied with copious food or stinted,—during endless generations, at regular lunar intervals. If then the Vertebrata are descended from an animal allied to the existing tidal Ascidians, the mysterious fact, that with the higher and now terrestrial Vertebrata, not to mention other classes, many normal and abnormal vital processes run their course according to lunar periods, is rendered intelligible. A recurrent period, if approximately of the right duration, when once gained, would not, as far as we can judge, be liable to be changed; consequently it might be thus transmitted during almost any number of generations. This conclusion, if it could be proved sound, would be curious; for we should then see that the period of gestation in each mammal, and the hatching of each bird’s eggs, and many other vital processes, still betrayed the primordial birthplace of these animals.
281 All essential functions tend to follow fixed and repetitive cycles, and for tidal creatures, these cycles are likely lunar; these animals must have experienced being left out of the water or covered deeply with it—given abundant food or limited amounts—over countless generations, at regular lunar intervals. If the Vertebrates are descended from an animal related to the current tidal Ascidians, the intriguing fact that many normal and abnormal vital processes in higher and now land-dwelling Vertebrates, as well as in other classes, occur according to lunar cycles becomes clear. A recurring cycle, if it's about the right length, once established, seems unlikely to change; thus, it could be passed down through many generations. This conclusion, if proven correct, would be fascinating; it would mean that the gestation period of each mammal, the hatching of each bird’s eggs, and many other vital processes still reveal the ancient origins of these animals.
283 A vast number of measurements of Whites, Blacks, and Indians, are given in the ‘Investigations in the Military and Anthropolog. Statistics of American Soldiers,’ by B. A. Gould, 1869, p. 298-358; on the capacity of the lungs, p. 471. See also the numerous and valuable tables, by Dr. Weisbach, from the observations of Dr. Scherzer and Dr. Schwarz, in the ‘Reise der Novara: Anthropolog. Theil,’ 1867.
283 A large number of measurements of Whites, Blacks, and Indigenous people are found in ‘Investigations in the Military and Anthropological Statistics of American Soldiers,’ by B. A. Gould, 1869, pages 298-358; on lung capacity, page 471. Also, check out the various valuable tables by Dr. Weisbach, based on the observations of Dr. Scherzer and Dr. Schwarz, in ‘Reise der Novara: Anthropolog. Theil,’ 1867.
286 With respect to the figures in the famous Egyptian caves of Abou-Simbel, M. Pouchet says (‘The Plurality of the Human Races,’ Eng. translat. 1864, p. 50), that he was far from finding recognisable representations of the dozen or more nations which some authors believe that they can recognise. Even some of the most strongly-marked races cannot be identified with that degree of unanimity which might have been expected from what has been written on the subject. Thus Messrs. Nott and Gliddon (‘Types of Mankind,’ p. 148) state that Rameses II., or the Great, has features superbly European; whereas Knox, another firm believer in the specific distinction of the races of man (‘Races of Man,’ 1850, p. 201), speaking of young Memnon (the same person with Rameses II., as I am informed by Mr. Birch) insists in the strongest manner that he is identical in character with the Jews of Antwerp. Again, whilst looking in the British Museum with two competent judges, officers of the establishment, at the statue of Amunoph III., we agreed that he had a strongly negro cast of features; but Messrs. Nott and Gliddon (ibid. p. 146, fig. 53) describe him as “a hybrid, but not of negro intermixture.”
286 Regarding the figures in the famous Egyptian caves of Abou-Simbel, M. Pouchet states (‘The Plurality of the Human Races,’ Eng. translat. 1864, p. 50) that he didn’t find recognizable representations of the dozen or more nations that some authors claim to identify. Even some of the most distinct races can't be identified with the level of agreement one might have expected based on what's been written about it. For example, Messrs. Nott and Gliddon (‘Types of Mankind,’ p. 148) claim that Rameses II, or the Great, has distinctly European features; however, Knox, another strong advocate for the specific distinctions of human races (‘Races of Man,’ 1850, p. 201), asserts about young Memnon (who is the same person as Rameses II, as I was informed by Mr. Birch) that he is very similar to the Jews of Antwerp. Additionally, while I was in the British Museum with two credible officials examining the statue of Amunoph III, we all agreed he had distinctly Black features; yet, Messrs. Nott and Gliddon (ibid. p. 146, fig. 53) describe him as “a hybrid, but not of Black ancestry.”
287 As quoted by Nott and Gliddon, ‘Types of Mankind,’ 1854, p. 439. They give also corroborative evidence; but C. Vogt thinks that the subject requires further investigation.
287 As quoted by Nott and Gliddon, ‘Types of Mankind,’ 1854, p. 439. They also provide supporting evidence, but C. Vogt believes the topic needs more research.
291 See the interesting letter by Mr. T. A. Murray, in the ‘Anthropolog. Review,’ April, 1868, p. liii. In this letter Count Strzelecki’s statement, that Australian women who have borne children to a white man are afterwards sterile with their own race, is disproved. M. A. de Quatrefages has also collected (‘Revue des Cours Scientifiques,’ March, 1869, p. 239) much evidence that Australians and Europeans are not sterile when crossed.
291 Check out the intriguing letter from Mr. T. A. Murray in the ‘Anthropolog. Review,’ April 1868, p. liii. This letter refutes Count Strzelecki’s claim that Australian women who have had children with a white man are then sterile with their own race. M. A. de Quatrefages has also gathered a lot of evidence (‘Revue des Cours Scientifiques,’ March 1869, p. 239) showing that Australians and Europeans are not sterile when interbreeding.
294 ‘The Variation of Animals and Plants under Domestication,’ vol. ii. p. 109. I may here remind the reader that the sterility of species when crossed is not a specially-acquired quality; but, like the incapacity of certain trees to be grafted together, is incidental on other acquired differences. The nature of these differences is unknown, but they relate more especially to the reproductive system, and much less to external structure or to ordinary differences in constitution. One important element in the sterility of crossed species apparently lies in one or both having been long habituated to fixed conditions; for we know that changed conditions have a special influence on the reproductive system, and we have good reason to believe (as before remarked) that the fluctuating conditions of domestication tend to eliminate that sterility which is so general with species in a natural state when crossed. It has elsewhere been shewn by me (ibid. vol. ii. p. 185, and ‘Origin of Species,’ 5th edit. p. 317) that the sterility of crossed species has not been acquired through natural selection: we can see that when two forms have already been rendered very sterile, it is scarcely possible that their sterility should be augmented by the preservation or survival of the more and more sterile individuals; for as the sterility increases fewer and fewer offspring will be produced from which to breed, and at last only single individuals will be produced, at the rarest intervals. But there is even a higher grade of sterility than this. Both Gärtner and Kölreuter have proved that in genera of plants including numerous species, a series can be formed from species which when crossed yield fewer and fewer seeds, to species which never produce a single seed, but yet are affected by the pollen of the other species, for the germen swells. It is here manifestly impossible to select the more sterile individuals, which have already ceased to yield seeds; so that the acme of sterility, when the germen alone is affected, cannot be gained through selection. This acme, and no doubt the other grades of sterility, are the incidental results of certain unknown differences in the constitution of the reproductive system of the species which are crossed.
294 ‘The Variation of Animals and Plants under Domestication,’ vol. ii. p. 109. I want to remind readers that the infertility of species when crossed isn’t a specially acquired trait; rather, it’s linked to other differences that have been developed. The specifics of these differences are unclear, but they relate mainly to the reproductive system, rather than to external structure or typical differences in constitution. One key factor in the infertility of crossed species seems to be that one or both have adapted to stable conditions for a long time; we know that changes in conditions significantly affect the reproductive system, and it’s reasonable to think (as noted before) that the variable conditions of domestication tend to reduce the infertility that is so common among species in their natural state when crossed. I have previously shown (ibid. vol. ii. p. 185, and ‘Origin of Species,’ 5th edit. p. 317) that the infertility of crossed species hasn’t come about through natural selection: it’s clear that once two forms have become very sterile, the chances of their sterility increasing are slim since the more sterile they become, the fewer offspring will be produced for breeding, eventually leading to only a few individuals being produced, very rarely. However, there is an even higher level of infertility than this. Both Gärtner and Kölreuter have demonstrated that in plant genera with many species, there’s a range from species that yield fewer and fewer seeds when crossed to species that never produce any seeds at all, yet still respond to the pollen from other species, causing the ovary to swell. It’s evident that selecting the more sterile individuals that no longer produce seeds is impossible; therefore, this peak of sterility, where only the ovary is affected, cannot be achieved through selection. This peak, along with other levels of infertility, are incidental outcomes of some unknown differences in the reproductive system constitution of the species that are crossed.
296 M. de Quatrefages has given (‘Anthropolog. Review,’ Jan. 1869, p. 22) an interesting account of the success and energy of the Paulistas in Brazil, who are a much crossed race of Portuguese and Indians, with a mixture of the blood of other races.
296 M. de Quatrefages has provided an engaging account in the ‘Anthropolog. Review,’ January 1869, p. 22, about the determination and achievements of the Paulistas in Brazil, who are a mixed group of Portuguese and Indigenous people, along with influences from other racial backgrounds.
297 For instance with the aborigines of America and Australia. Prof. Huxley says (‘Transact. Internat. Congress of Prehist. Arch.’ 1868. p. 105) that the skulls of many South Germans and Swiss are “as short and as broad as those of the Tartars,” &c.
297 For example, with the indigenous people of America and Australia. Prof. Huxley states (‘Transact. Internat. Congress of Prehist. Arch.’ 1868. p. 105) that the skulls of many South Germans and Swiss are “as short and as broad as those of the Tartars,” etc.
298 See a good discussion on this subject in Waitz, ‘Introduct. to Anthropology,’ Eng. translat. 1863, p. 198-208, 227. I have taken some of the above statements from H. Tuttle’s ‘Origin and Antiquity of Physical Man,’ Boston, 1866, p. 35.
298 Check out a good discussion on this topic in Waitz, ‘Introduct. to Anthropology,’ English translation, 1863, pp. 198-208, 227. I’ve borrowed some of the statements above from H. Tuttle’s ‘Origin and Antiquity of Physical Man,’ Boston, 1866, p. 35.
299 Prof. Nägeli has carefully described several striking cases in his 'Botanische Mittheilungen,’ B. ii. 1866, s. 294-369. Prof. Asa Gray has made analogous remarks on some intermediate forms in the Compositæ of N. America.
299 Prof. Nägeli has thoroughly detailed several impressive examples in his 'Botanische Mittheilungen,’ Vol. ii, 1866, pp. 294-369. Prof. Asa Gray has made similar observations on some transitional forms in the Compositæ of North America.
303 ‘Die Racen des Schweines,’ 1860, s. 46. ‘Vorstudien für Geschichte, &c., Schweineschädel,’ 1864, s. 104. With respect to cattle, see M. de Quatrefages, ‘Unité de l’Espèce Humaine,’ 1861, p. 119.
303 ‘The Breeds of Pigs,’ 1860, p. 46. ‘Preliminary Studies for History, &c., Pig Skulls,’ 1864, p. 104. Regarding cattle, see M. de Quatrefages, ‘Unity of the Human Species,’ 1861, p. 119.
304 Tylor’s ‘Early History of Mankind,’ 1865; for the evidence with respect to gesture-language, see p. 54. Lubbock’s ‘Prehistoric Times,’ 2nd edit. 1869.
304 Tylor’s ‘Early History of Mankind,’ 1865; for the evidence regarding gesture-language, see p. 54. Lubbock’s ‘Prehistoric Times,’ 2nd ed. 1869.
308 ‘Prehistoric Times,’ 1869, p. 574.
310 ‘Transact. Internat. Congress of Prehistoric Arch.’ 1868, p. 172-175. See also Broca (translation) in ‘Anthropological Review,’ Oct. 1868, p. 410.
310 ‘Transact. Internat. Congress of Prehistoric Arch.’ 1868, p. 172-175. See also Broca (translation) in ‘Anthropological Review,’ Oct. 1868, p. 410.
314 I have collected (‘Journal of Researches, Voyage of the “Beagle,”’ p. 435) a good many cases bearing on this subject: see also Gerland, ibid. s. 8. Poeppig speaks of the “breath of civilisation as poisonous to savages.”
314 I have gathered (’Journal of Researches, Voyage of the “Beagle,” p. 435) several examples related to this topic: also see Gerland, ibid. s. 8. Poeppig refers to the “breath of civilization as toxic to natives.”
320 Pallas, ‘Act. Acad. St. Petersburgh,’ 1780, part ii. p. 69. He was followed by Rudolphi, in his ‘Beyträge zur Anthropologie,’ 1812. An excellent summary of the evidence is given by Godron, ‘De l’Espèce,’ 1859, vol. ii. p. 246, &c.
320 Pallas, ‘Act. Acad. St. Petersburgh,’ 1780, part ii. p. 69. He was followed by Rudolphi, in his ‘Beyträge zur Anthropologie,’ 1812. An excellent summary of the evidence is given by Godron, ‘De l’Espèce,’ 1859, vol. ii. p. 246, &c.
324 See a paper read before the Royal Soc. in 1813, and published in his Essays in 1818. I have given an account of Dr. Wells’ views in the Historical Sketch (p. xvi) to my ‘Origin of Species.’ Various cases of colour correlated with constitutional peculiarities are given in my 'Variation of Animals under Domestication,’ vol. ii. p. 227, 335.
324 Check out a paper presented to the Royal Society in 1813 and published in his Essays in 1818. I’ve summarized Dr. Wells’ ideas in the Historical Sketch (p. xvi) of my ‘Origin of Species.’ Several examples of color linked to specific traits are discussed in my 'Variation of Animals under Domestication,’ vol. ii. p. 227, 335.
328 Quatrefages, ‘Unité de l’Espèce Humaine,’ 1861, p. 205. Waitz, 'Introduct. to Anthropology,’ translat. vol. i. 1863, p. 124. Livingstone gives analogous cases in his ‘Travels.’
328 Quatrefages, ‘Unity of the Human Species,’ 1861, p. 205. Waitz, 'Introduction to Anthropology,’ translated, vol. i. 1863, p. 124. Livingstone provides similar examples in his ‘Travels.’
329 In the spring of 1862 I obtained permission from the Director-General of the Medical department of the Army, to transmit to the surgeons of the various regiments on foreign service a blank table, with the following appended remarks, but I have received no returns. “As several well-marked cases have been recorded with our domestic animals of a relation between the colour of the dermal appendages and the constitution; and it being notorious that there is some limited degree of relation between the colour of the races of man and the climate inhabited by them; the following investigation seems worth consideration. Namely, whether there is any relation in Europeans between the colour of their hair, and their liability to the diseases of tropical countries. If the surgeons of the several regiments, when stationed in unhealthy tropical districts, would be so good as first to count, as a standard of comparison, how many men, in the force whence the sick are drawn, have dark and light-coloured hair, and hair of intermediate or doubtful tints; and if a similar account were kept by the same medical gentlemen, of all the men who suffered from malarious and yellow fevers, or from dysentery, it would soon be apparent, after some thousand cases had been tabulated, whether there exists any relation between the colour of the hair and constitutional liability to tropical diseases. Perhaps no such relation would be discovered, but the investigation is well worth making. In case any positive result were obtained, it might be of some practical use in selecting men for any particular service. Theoretically the result would be of high interest, as indicating one means by which a race of men inhabiting from a remote period an unhealthy tropical climate, might have become dark-coloured by the better preservation of dark-haired or dark-complexioned individuals during a long succession of generations.”
329 In the spring of 1862, I got permission from the Director-General of the Army Medical Department to send a blank table to the surgeons of various regiments serving overseas, along with the following remarks, but I haven't received any responses. “Since several well-documented cases have been noted in our domestic animals showing a relationship between the color of their skin features and their constitution, and it is widely recognized that there is some connection between the skin color of different human races and the climates they live in, this investigation seems worth considering. Specifically, we should look into whether there's any link among Europeans between hair color and vulnerability to diseases common in tropical regions. If the surgeons of the regiments, when assigned to unhealthy tropical areas, could first count, as a baseline for comparison, how many men in the unit from which sick individuals are drawn have dark, light, and hair of intermediate or uncertain shades of color; and if the same medical professionals kept similar records of all men who suffered from malaria, yellow fever, or dysentery, it would soon become clear, after a few thousand cases are compiled, whether there is any relationship between hair color and susceptibility to tropical diseases. It’s possible that no such link would be found, but the investigation is definitely worthwhile. If any conclusive results were reached, it could be practically useful in selecting individuals for specific duties. Theoretically, the findings would be of great interest, as they might indicate a way that a group of people living in an unhealthy tropical climate for a long time could have developed darker skin by the better survival of individuals with dark hair or darker complexions over many generations.”
331 See, for instance, Quatrefages (‘Revue des Cours Scientifiques,’ Oct. 10, 1868, p. 724) on the effects of residence in Abyssinia and Arabia, and other analogous cases. Dr. Rolle (‘Der Mensch, seine Abstammung,’ &c., 1865, s. 99) states, on the authority of Khanikof, that the greater number of German families settled in Georgia, have acquired in the course of two generations dark hair and eyes. Mr. D. Forbes informs me that the Quichuas in the Andes vary greatly in colour, according to the position of the valleys inhabited by them.
331 For example, see Quatrefages (‘Revue des Cours Scientifiques,’ Oct. 10, 1868, p. 724) regarding the impacts of living in Abyssinia and Arabia, along with other similar cases. Dr. Rolle (‘Der Mensch, seine Abstammung,’ etc., 1865, p. 99) reports, citing Khanikof, that most German families who settled in Georgia have developed dark hair and eyes over two generations. Mr. D. Forbes tells me that the Quichuas in the Andes show a wide range of colors depending on the valleys they live in.
334 Mr. Catlin states (‘N. American Indians,’ 3rd edit. 1842, vol. i. p. 49) that in the whole tribe of the Mandans, about one in ten or twelve of the members of all ages and both sexes have bright silvery grey hair, which is hereditary. Now this hair is as coarse and harsh as that of a horse’s mane, whilst the hair of other colours is fine and soft.
334 Mr. Catlin states (‘N. American Indians,’ 3rd edit. 1842, vol. i. p. 49) that in the entire Mandan tribe, about one in ten or twelve members of all ages and both genders have bright silvery grey hair, which is hereditary. This hair is coarse and rough, like a horse’s mane, while hair of other colors is fine and soft.
335 On the odour of the skin, Godron, ‘Sur l’Espèce,’ tom. ii. p. 217. On the pores in the skin, Dr. Wilckens, ‘Die Aufgaben der landwirth. Zootechnik,’ 1869, s. 7.
335 On the scent of the skin, Godron, ‘On the Species,’ vol. ii, p. 217. On the pores in the skin, Dr. Wilckens, ‘The Tasks of Agriculture and Animal Husbandry,’ 1869, p. 7.
336 Westwood, ‘Modern Class. of Insects,’ vol. ii. 1810, p. 541. In regard to the statement about Tanais, mentioned below, I am indebted to Fritz Müller.
336 Westwood, ‘Modern Classification of Insects,’ vol. ii. 1810, p. 541. Regarding the statement about Tanais mentioned below, I am grateful to Fritz Müller.
338 Even with those of plants in which the sexes are separate, the male flowers are generally mature before the female. Many hermaphrodite plants are, as first shewn by C. K. Sprengel, dichogamous; that is, their male and female organs are not ready at the same time, so that they cannot be self-fertilised. Now with such plants the pollen is generally mature in the same flower before the stigma, though there are some exceptional species in which the female organs are mature before the male.
338 Even in plants with separate sexes, the male flowers typically mature before the female ones. Many hermaphrodite plants are, as first shown by C. K. Sprengel, dichogamous; this means their male and female parts don't become ready at the same time, preventing self-fertilization. For these plants, the pollen usually matures in the same flower before the stigma does, although there are some rare species where the female parts mature before the male ones.
339 I have received information, hereafter to be given, to this effect with respect to poultry. Even with birds, such as pigeons, which pair for life, the female, as I hear from Mr. Jenner Weir, will desert her mate if he is injured or grows weak.
339 I have received information, which will be provided shortly, about poultry. Even with birds like pigeons, which mate for life, the female, according to Mr. Jenner Weir, will abandon her partner if he is hurt or becomes weak.
340 On the Gorilla, Savage and Wyman, ‘Boston Journal of Nat. Hist.’ vol. v. 1845-47, p. 423. On Cynocephalus, Brehm, ‘Illust. Thierleben,’ B. i. 1864, s. 77. On Mycetes, Rengger, ‘Naturgesch.: Säugethiere von Paraguay,’ 1830, s. 14, 20. On Cebus, Brehm, ibid. s. 108.
340 On the Gorilla, Savage and Wyman, ‘Boston Journal of Nat. Hist.’ vol. v. 1845-47, p. 423. On Cynocephalus, Brehm, ‘Illust. Thierleben,’ B. i. 1864, s. 77. On Mycetes, Rengger, ‘Naturgesch.: Säugethiere von Paraguay,’ 1830, s. 14, 20. On Cebus, Brehm, ibid. s. 108.
341 Pallas, ‘Spicilegia Zoolog.’ Fasc. xii. 1777, p. 29. Sir Andrew Smith, ‘Illustrations of the Zoology of S. Africa,’ 1849, pl. 29, on the Kobus. Owen, in his ‘Anatomy of Vertebrates’ (vol. iii. 1868, p. 633) gives a table incidentally showing which species of Antelopes pair and which are gregarious.
341 Pallas, ‘Spicilegia Zoolog.’ Fasc. xii. 1777, p. 29. Sir Andrew Smith, ‘Illustrations of the Zoology of S. Africa,’ 1849, pl. 29, on the Kobus. Owen, in his ‘Anatomy of Vertebrates’ (vol. iii. 1868, p. 633) provides a table that incidentally shows which species of antelopes mate and which ones are social.
342 Dr. Campbell, in ‘Proc. Zoolog. Soc.’ 1869, p. 138. See also an interesting paper, by Lieut. Johnstone, in ‘Proc. Asiatic Soc. of Bengal,’ May, 1868.
342 Dr. Campbell, in ‘Proc. Zoolog. Soc.’ 1869, p. 138. Check out an interesting paper by Lieut. Johnstone in ‘Proc. Asiatic Soc. of Bengal,’ May, 1868.
343 ‘The Ibis,’ vol. iii. 1861, p. 133, on the Progne Widow-bird. See also on the Vidua axillaris, ibid. vol. ii. 1860, p. 211. On the polygamy of the Capercailzie and Great Bustard, see L. Lloyd, ‘Game Birds of Sweden,’ 1867, p. 19, and 182. Montagu and Selby speak of the Black Grouse as polygamous and of the Red Grouse as monogamous.
343 ‘The Ibis,’ vol. iii. 1861, p. 133, on the Progne Widow-bird. See also on the Vidua axillaris, ibid. vol. ii. 1860, p. 211. For information on the polygamy of the Capercaillie and Great Bustard, refer to L. Lloyd, ‘Game Birds of Sweden,’ 1867, p. 19, and 182. Montagu and Selby describe the Black Grouse as polygamous and the Red Grouse as monogamous.
344 The Rev. E. S. Dixon, however, speaks positively (‘Ornamental Poultry,’ 1848, p. 76) about the eggs of the guinea-fowl being infertile when more than one female is kept with the same male.
344 The Rev. E. S. Dixon, however, strongly states (‘Ornamental Poultry,’ 1848, p. 76) that the eggs of the guinea-fowl are infertile when multiple females are kept with the same male.
345 Noel Humphreys, ‘River Gardens,’ 1857.
__A_TAG_PLACEHOLDER_0__ Noel Humphreys, ‘River Gardens,’ 1857.
347 One parasitic Hymenopterous insect (Westwood, ‘Modern Class. of Insects,’ vol. ii, p. 160) forms an exception to the rule, as the male has rudimentary wings, and never quits the cell in which it is born, whilst the female has well-developed wings. Audouin believes that the females are impregnated by the males which are born in the same cells with them; but it is much more probable that the females visit other cells, and thus avoid close inter-breeding. We shall hereafter meet with a few exceptional cases, in various classes, in which the female, instead of the male, is the seeker and wooer.
347 One parasitic Hymenopterous insect (Westwood, ‘Modern Class. of Insects,’ vol. ii, p. 160) is an exception to the rule, as the male has underdeveloped wings and never leaves the cell where it was born, while the female has fully developed wings. Audouin believes that the females are fertilized by the males born in the same cells; however, it is more likely that the females visit other cells to avoid inbreeding. We will encounter a few exceptional cases in various classes where the female, rather than the male, is the one who seeks and pursues.
349 Prof. Sachs (‘Lehrbuch der Botanik,’ 1870, s. 633) in speaking of the male and female reproductive cells, remarks, “verhält sich die eine bei der Vereinigung activ, ... die andere erscheint bei der Vereinigung passiv.”
349 Prof. Sachs ('Textbook of Botany,' 1870, p. 633) states about the male and female reproductive cells, "one acts actively during the union, ... while the other appears passive during the union."
350 ‘Reise der Novara: Anthropolog. Theil,’ 1867, s. 216-269. The results were calculated by Dr. Weisbach from measurements made by Drs. K. Scherzer and Schwarz. On the greater variability of the males of domesticated animals, see my ‘Variation of Animals and Plants under Domestication,’ vol. ii. 1868, p. 75.
350 ‘Voyage of the Novara: Anthropological Part,’ 1867, pp. 216-269. The results were calculated by Dr. Weisbach from measurements taken by Drs. K. Scherzer and Schwarz. For more on the greater variability of male domesticated animals, see my ‘Variation of Animals and Plants under Domestication,’ vol. ii. 1868, p. 75.
354 ‘The Variation of Animals and Plants under Domestication,’ vol. ii. 1868, p. 75. In the last chapter but one, the provisional hypothesis of pangenesis, above alluded to, is fully explained.
354 'The Variation of Animals and Plants under Domestication,' vol. ii. 1868, p. 75. In the second to last chapter, the temporary theory of pangenesis, mentioned earlier, is explained in detail.
355 These facts are given on the high authority of a great breeder, Mr. Teebay, in Tegetmeier’s ‘Poultry Book,’ 1868, p. 158. On the characters of chickens of different breeds, and on the breeds of the pigeon, alluded to in the above paragraph, see ‘Variation of Animals,’ &c., vol. i. p. 160, 249; vol. ii. p. 77.
355 These facts come from the reputable breeder, Mr. Teebay, in Tegetmeier’s ‘Poultry Book,’ 1868, p. 158. For details on the traits of chickens from different breeds and the breeds of pigeons mentioned in the previous paragraph, refer to ‘Variation of Animals,’ &c., vol. i. p. 160, 249; vol. ii. p. 77.
356 ‘Novæ species Quadrupedum e Glirium ordine,’ 1778, p. 7. On the transmission of colour by the horse, see ‘Variation of Animals, &c. under Domestication,’ vol. i. p. 21. Also vol. ii. p. 71, for a general discussion on Inheritance as limited by Sex.
356 ‘New Species of Quadrupeds from the Order of Gliridae,’ 1778, p. 7. For information on how horses transmit color, see ‘Variation of Animals, &c. under Domestication,’ vol. i. p. 21. Also check vol. ii. p. 71 for a general discussion on Inheritance as affected by Sex.
359 I am much obliged to Mr. Cupples for having made enquiries for me in regard to the Roebuck and Red Deer of Scotland from Mr. Robertson, the experienced head-forester to the Marquis of Breadalbane. In regard to Fallow-deer, I am obliged to Mr. Eyton and others for information. For the Cervus alces of N. America, see ‘Land and Water,’ 1868, p. 221 and 254; and for the C. Virginianus and strongyloceros of the same continent, see J. D. Caton, in ‘Ottawa Acad. of Nat. Sc.’ 1868, p. 13. For Cervus Eldi of Pegu, see Lieut. Beavan, ‘Proc. Zoolog. Soc.’ 1867, p. 762.
359 I am very grateful to Mr. Cupples for checking on the Roebuck and Red Deer of Scotland with Mr. Robertson, the knowledgeable head forester for the Marquis of Breadalbane. Regarding Fallow-deer, I appreciate the information from Mr. Eyton and others. For the Cervus alces of North America, see ‘Land and Water,’ 1868, p. 221 and 254; and for the C. Virginianus and strongyloceros of the same continent, refer to J. D. Caton, in ‘Ottawa Acad. of Nat. Sc.’ 1868, p. 13. For Cervus Eldi of Pegu, see Lieut. Beavan, ‘Proc. Zoolog. Soc.’ 1867, p. 762.
361 I have been assured that the horns of the sheep in North Wales can always be felt, and are sometimes even an inch in length, at birth. With cattle Youatt says (‘Cattle,’ 1834, p. 277) that the prominence of the frontal bone penetrates the cutis at birth, and that the horny matter is soon formed over it.
361 I've been told that the horns of sheep in North Wales can always be felt and can even be about an inch long at birth. Regarding cattle, Youatt mentions (‘Cattle,’ 1834, p. 277) that the prominence of the frontal bone breaks through the skin at birth, and that the horn material forms quickly over it.
362 I am greatly indebted to Prof. Victor Carus for having made inquiries for me, from the highest authorities, with respect to the merino sheep of Saxony. On the Guinea coast of Africa there is a breed of sheep in which, as with merinos, the rams alone bear horns; and Mr. Winwood Reade informs me that in the one case observed, a young ram born on Feb. 10th first showed horns on March 6th, so that in this instance the development of the horns occurred at a later period of life, conformably with our rule, than in the Welsh sheep, in which both sexes are horned.
362 I am very grateful to Prof. Victor Carus for making inquiries on my behalf from the highest authorities about the merino sheep of Saxony. On the Guinea coast of Africa, there’s a breed of sheep where, like merinos, only the rams have horns. Mr. Winwood Reade tells me that in the one case he observed, a young ram born on February 10th first showed horns on March 6th, which means that in this case, the horns developed later in life than what we see in Welsh sheep, where both males and females have horns.
363 In the common peacock (Pavo cristatus) the male alone possesses spurs, whilst both sexes of the Java peacock (P. muticus) offer the unusual case of being furnished with spurs. Hence I fully expected that in the latter species they would have been developed earlier in life than in the common peacock; but M. Hegt of Amsterdam informs me, that with young birds of the previous year, belonging to both species, compared on April 23rd, 1869, there was no difference in the development of the spurs. The spurs, however, were as yet represented merely by slight knobs or elevations. I presume that I should have been informed if any difference in the rate of development had subsequently been observed.
363 In the common peacock (Pavo cristatus), only the males have spurs, while both male and female Java peacocks (P. muticus) have the unusual feature of having spurs. I expected that in the Java peacock, these spurs would develop earlier in life than in the common peacock. However, M. Hegt from Amsterdam told me that when comparing young birds of both species on April 23, 1869, there was no difference in spur development. At that time, the spurs were just small knobs or bumps. I believe I would have been notified if any differences in the rate of development were later observed.
364 In some other species of the Duck Family the speculum in the two sexes differs in a greater degree; but I have not been able to discover whether its full development occurs later in life in the males of such species, than in the male of the common duck, as ought to be the case according to our rule. With the allied Mergus cucullatus we have, however, a case of this kind: the two sexes differ conspicuously in general plumage, and to a considerable degree in the speculum, which is pure white in the male and greyish-white in the female. Now the young males at first resemble, in all respects, the female, and have a greyish-white speculum, but this becomes pure white at an earlier age than that at which the adult male acquires his other more strongly-marked sexual differences in plumage: see Audubon, ‘Ornithological Biography,’ vol. iii. 1835, p. 249-250.
364 In some other species of the Duck Family, the speculum differs more between the two sexes; however, I haven't been able to find out if its full development happens later in life for the males of these species than for the male common duck, as it should according to our rule. In the related Mergus cucullatus, we do see a clear example of this: the two sexes are noticeably different in overall plumage, and to a significant extent in the speculum, which is pure white in the male and greyish-white in the female. Initially, young males resemble females in every way and have a greyish-white speculum, but this changes to pure white at an earlier age than when the adult male develops his other more pronounced sexual differences in plumage: see Audubon, ‘Ornithological Biography,’ vol. iii. 1835, p. 249-250.
365 ‘Das Ganze der Taubenzucht,’ 1837, s. 21, 24. For the case of the streaked pigeons, see Dr. Chapuis, ‘Le Pigeon Voyageur Belge.’ 1865, p. 87.
365 days ‘The Complete Guide to Pigeon Breeding,’ 1837, pp. 21, 24. For the case of the striped pigeons, see Dr. Chapuis, ‘The Belgian Racing Pigeon,’ 1865, p. 87.
366 For full particulars and references on all these points respecting the several breeds of the Fowl, see ‘Variation of Animals and Plants under Domestication,’ vol. i. p. 250, 256. In regard to the higher animals, the sexual differences which have arisen under domestication are described in the same work under the head of each species.
366 For complete details and references on all these topics about the different breeds of chickens, see ‘Variation of Animals and Plants under Domestication,’ vol. i. p. 250, 256. Regarding the higher animals, the sexual differences that have developed through domestication are discussed in the same work under the section for each species.
368 For Norway and Russia, see abstract of Prof. Faye’s researches, in ‘British and Foreign Medico-Chirurg. Review,’ April, 1867, p. 343, 345. For France, the ‘Annuaire pour l’An 1867.’ p. 213.
368 For Norway and Russia, see the summary of Prof. Faye’s research in the ‘British and Foreign Medico-Chirurgical Review,’ April 1867, pp. 343, 345. For France, refer to the ‘Annuaire pour l’An 1867,’ p. 213.
370 Babbage, ‘Edinburgh Journal of Science,’ 1829, vol. i. p. 88; also p. 90, on still-born children. On illegitimate children in England, see ‘Report of Registrar-General for 1866,’ p. xv.
370 Babbage, ‘Edinburgh Journal of Science,’ 1829, vol. i. p. 88; also p. 90, on stillborn children. For information on illegitimate children in England, refer to ‘Report of Registrar-General for 1866,’ p. xv.
371 ‘British and Foreign Medico-Chirurg. Review,’ April, 1867, p. 343. Dr. Stark also remarks (‘Tenth Annual Report of Births, Deaths, &c., in Scotland,’ 1867, p. xxviii) that “These examples may suffice to shew that, at almost every stage of life, the males in Scotland have a greater liability to death and a higher death-rate than the females. The fact, however, of this peculiarity being most strongly developed at that infantile period of life when the dress, food, and general treatment of both sexes are alike, seems to prove that the higher male death-rate is an impressed, natural, and constitutional peculiarity due to sex alone.”
371 ‘British and Foreign Medico-Chirurg. Review,’ April, 1867, p. 343. Dr. Stark also notes (‘Tenth Annual Report of Births, Deaths, &c., in Scotland,’ 1867, p. xxviii) that “These examples may be enough to show that, at almost every stage of life, males in Scotland are more likely to die and have a higher death rate compared to females. However, the fact that this pattern is most pronounced during infancy, when clothing, food, and general treatment of both sexes are similar, suggests that the higher male death rate is an inherent, natural, and constitutional trait solely due to sex.”
372 With the savage Guaranys of Paraguay, according to the accurate Azara (‘Voyages dans l’Amérique mérid.’ tom. ii. 1809, p. 60, 179), the women in proportion to the men are as 14 to 13.
372 According to the reliable Azara ('Voyages dans l’Amérique mérid.' vol. ii. 1809, p. 60, 179), among the fierce Guaranys of Paraguay, there are about 14 women for every 13 men.
375 During the last eleven years a record has been kept of the number of mares which have proved barren or prematurely slipped their foals; and it deserves notice, as shewing how infertile these highly-nurtured and rather closely-interbred animals have become, that not far from one-third of the mares failed to produce living foals. Thus during 1866, 809 male colts and 816 female colts were born, and 743 mares failed to produce offspring. During 1867, 836 males and 902 females were born, and 794 mares failed.
375 Over the last eleven years, there has been a record of the number of mares that have either failed to conceive or lost their foals early; it’s worth noting how infertile these well-bred and somewhat inbred animals have become, as nearly one-third of the mares didn't produce living foals. In 1866, 809 male foals and 816 female foals were born, while 743 mares did not have any offspring. In 1867, 836 males and 902 females were born, with 794 mares failing to produce.
376 I am much indebted to Mr. Cupples for having procured for me the above returns from Scotland, as well as some of the following returns on cattle. Mr. R. Elliot, of Laighwood, first called my attention to the premature deaths of the males,—a statement subsequently confirmed by Mr. Aitchison and others. To this latter gentleman, and to Mr. Payan, I owe my thanks for the larger returns on sheep.
376 I am very grateful to Mr. Cupples for getting me the returns from Scotland mentioned above, as well as some of the upcoming returns on cattle. Mr. R. Elliot from Laighwood was the first to bring my attention to the early deaths of the males—a point later backed up by Mr. Aitchison and others. I also want to thank Mr. Aitchison and Mr. Payan for the additional returns on sheep.
382 Mr. Jenner Weir received similar information, on making enquiries during the following year. To shew the number of chaffinches caught, I may mention that in 1869 there was a match between two experts; and one man caught in a day 62, and another 40, male chaffinches. The greatest number ever caught by one man in a single day was 70.
382 Mr. Jenner Weir received similar information when he asked about it the following year. To illustrate the number of chaffinches caught, I should mention that in 1869 there was a competition between two experts; one person caught 62 male chaffinches in a day, and the other caught 40. The highest number ever caught by one person in a single day was 70.
383 ‘Ibis,’ vol. ii. p. 260, as quoted in Gould’s ‘Trochilidæ,’ 1861, p. 52. For the foregoing proportions, I am indebted to Mr. Salvin for a table of his results.
383 ‘Ibis,’ vol. ii. p. 260, as quoted in Gould’s ‘Trochilidæ,’ 1861, p. 52. For the proportions mentioned above, I thank Mr. Salvin for providing a table of his findings.
385 ‘Ibis,’ 1862, p. 137.
390 Yarrell, ‘Hist. British Fishes,’ vol. i. 1836, p. 307; on the Cyprinus carpio, p. 331; on the Tinca vulgaris, p. 331; on the Abramis brama, p. 336. See, for the minnow (Leuciscus phoxinus), ‘Loudon’s Mag. of Nat. Hist.’ vol. v. 1832, p. 682.
390 Yarrell, ‘Hist. British Fishes,’ vol. i. 1836, p. 307; on the Cyprinus carpio, p. 331; on the Tinca vulgaris, p. 331; on the Abramis brama, p. 336. See, for the minnow (Leuciscus phoxinus), ‘Loudon’s Mag. of Nat. Hist.’ vol. v. 1832, p. 682.
391 Leuckart quotes Meinecke (Wagner, ‘Handwörterbuch der Phys.’ B. iv. 1853, s. 775) that with Butterflies the males are three or four times as numerous as the females.
391 Leuckart cites Meinecke (Wagner, ‘Handwörterbuch der Phys.’ B. iv. 1853, s. 775) stating that with butterflies, the males are three or four times more numerous than the females.
400 This naturalist has been so kind as to send me some results from former years, in which the females seemed to preponderate; but so many of the figures were estimates, that I found it impossible to tabulate them.
400 This naturalist has kindly shared some results from previous years, where it seemed like there were more females; however, since many of the figures were estimates, I found it impossible to organize them into a table.
401 Günther’s ‘Record of Zoological Literature,’ 1867, p. 260. On the excess of female Lucanus, ibid. p. 250. On the males of Lucanus in England, Westwood, ‘Modern Class. of Insects,’ vol. i. p. 187. On the Siagonium, ibid. p. 172.
401 Günther’s ‘Record of Zoological Literature,’ 1867, p. 260. Regarding the abundance of female Lucanus, see ibid. p. 250. For information on the males of Lucanus in England, refer to Westwood, ‘Modern Class. of Insects,’ vol. i. p. 187. On the Siagonium, see ibid. p. 172.
403 ‘Farm Insects,’ p. 45-46.
404 ‘Observations on N. American Neuroptera,’ by H. Hagen and B. D. Walsh, ‘Proc. Ent. Soc. Philadelphia,’ Oct. 1863, p. 168, 223, 239.
404 'Observations on North American Neuroptera,' by H. Hagen and B. D. Walsh, 'Proceedings of the Entomological Society of Philadelphia,' October 1863, p. 168, 223, 239.
406 Another great authority in this class, Prof. Thorell of Upsala (‘On European Spiders,’ 1869-70, part i. p. 205) speaks as if female spiders were generally commoner than the males.
406 Another respected expert in this field, Prof. Thorell from Upsala (‘On European Spiders,’ 1869-70, part i. p. 205) suggests that female spiders are typically more common than males.
408 I have often been struck with the fact, that in several species of Primula the seeds in the capsules which contained only a few were very much larger than the numerous seeds in the more productive capsules.
408 I've often noticed that in several species of Primula, the seeds in the capsules that had only a few were much larger than the numerous seeds in the more productive capsules.
412 I have given (‘Geolog. Observations on Volcanic Islands,’ 1844, p. 53) a curious instance of the influence of light on the colours of a frondescent incrustation, deposited by the surf on the coast-rocks of Ascension, and formed by the solution of triturated sea-shells.
412 I shared an interesting example of how light affects the colors of a leafy crust that the surf deposited on the coastal rocks of Ascension, which was made from the solution of crushed sea shells (Geolog. Observations on Volcanic Islands, 1844, p. 53).
413 ‘Facts and Arguments for Darwin,’ English translat. 1869, p. 20. See the previous discussion on the olfactory threads. Sars has described a somewhat analogous case (as quoted in ‘Nature,’ 1870, p. 455) in a Norwegian crustacean, the Pontoporeia affinis.
413 ‘Facts and Arguments for Darwin,’ English translation, 1869, p. 20. See the earlier discussion on the olfactory threads. Sars described a somewhat similar case (as mentioned in ‘Nature,’ 1870, p. 455) in a Norwegian crustacean, the Pontoporeia affinis.
414 See Sir J. Lubbock in ‘Annals. and Mag. of Nat. Hist.’ vol. xi. 1853, pl. i. and x.; and vol. xii. (1853) pl. vii. See also Lubbock in 'Transact. Ent. Soc.’ vol. iv. new series, 1856-1858, p. 8. With respect to the zigzagged antennæ mentioned below, see Fritz Müller, ‘Facts and Arguments for Darwin’ 1869, p. 40, foot-note.
414 Check out Sir J. Lubbock in ‘Annals. and Mag. of Nat. Hist.’ vol. xi. 1853, pl. i. and x.; and vol. xii. (1853) pl. vii. Also refer to Lubbock in 'Transact. Ent. Soc.’ vol. iv. new series, 1856-1858, p. 8. For the zigzagged antennae mentioned below, see Fritz Müller, ‘Facts and Arguments for Darwin’ 1869, p. 40, foot-note.
415 See a paper by Mr. C. Spence Bate, with figures, in ‘Proc. Zoolog. Soc.’ 1868, p. 363; and on the nomenclature of the genus, ibid. p. 585. I am greatly indebted to Mr. Spence Bate for nearly all the above statements with respect to the chelæ of the higher crustaceans.
415 Check out a paper by Mr. C. Spence Bate, including figures, in ‘Proc. Zoolog. Soc.’ 1868, p. 363; and regarding the naming of the genus, see p. 585 of the same publication. I'm very thankful to Mr. Spence Bate for providing almost all of the information above about the claws of the higher crustaceans.
423 Aug. Vinson (‘Aranéides des Iles de la Réunion,’ pl. vi. figs. 1 and 2) gives a good instance of the small size of the male in Epeira nigra. In this species, as I may add, the male is testaceous and the female black with legs banded with red. Other even more striking cases of inequality in size between the sexes have been recorded (‘Quarterly Journal of Science,’ 1868, July, p. 429); but I have not seen the original accounts.
423 Aug. Vinson (‘Aranéides des Iles de la Réunion,’ pl. vi. figs. 1 and 2) provides a good example of the small size of the male in Epeira nigra. In this species, the male is a reddish color, while the female is black with red-banded legs. There are other even more remarkable instances of size differences between the sexes that have been documented (‘Quarterly Journal of Science,’ 1868, July, p. 429); however, I haven’t seen the original sources.
425 Theridion (Asagena, Sund.) serratipes, 4-punctatum et guttatum; see Westring, in Kroyer, ‘Naturhist. Tidskrift,’ vol. iv. 1842-1843, p. 349; and vol. ii. 1846-1849, p. 342. See, also, for other species, 'Araneæ Svecicæ,’ p. 184.
425 Theridion (Asagena, Sund.) serratipes, 4-punctatum, and guttatum; see Westring, in Kroyer, ‘Naturhist. Tidskrift,’ vol. iv. 1842-1843, p. 349; and vol. ii. 1846-1849, p. 342. See also, for other species, 'Araneæ Svecicæ,’ p. 184.
427 Sir J. Lubbock, ‘Transact. Linnean Soc.’ vol. xxv. 1866, p. 484. With respect to the Mutillidæ see Westwood, ‘Modern Class. of Insects,’ vol. ii. p. 213.
427 Sir J. Lubbock, ‘Transact. Linnean Soc.’ vol. xxv. 1866, p. 484. For information on the Mutillidae, refer to Westwood, ‘Modern Class. of Insects,’ vol. ii. p. 213.
428 These organs in the male often differ in closely-allied species, and afford excellent specific characters. But their importance, under a functional point of view, as Mr. E. MacLachlan has remarked to me, has probably been overrated. It has been suggested, that slight differences in these organs would suffice to prevent the intercrossing of well-marked varieties or incipient species, and would thus aid in their development. That this can hardly be the case, we may infer from the many recorded cases (see for instance, Bronn, ‘Geschichte der Natur,’ B. ii. 1843, s. 164; and Westwood, ‘Transact. Ent. Soc.’ vol. iii. 1842, p. 195) of distinct species having been observed in union. Mr. MacLachlan informs me (vide ‘Stett. Ent. Zeitung,’ 1867, s. 155) that when several species of Phryganidæ, which present strongly-pronounced differences of this kind, were confined together by Dr. Aug. Meyer, they coupled, and one pair produced fertile ova.
428 In males, these organs often vary between closely related species and provide clear specific characteristics. However, as Mr. E. MacLachlan pointed out to me, their functional significance has likely been overstated. It's been suggested that minor differences in these organs could be enough to prevent interbreeding between well-defined varieties or emerging species, promoting their development. However, we can infer that this is unlikely given the numerous documented instances (see, for example, Bronn, ‘Geschichte der Natur,’ B. ii. 1843, s. 164; and Westwood, ‘Transact. Ent. Soc.’ vol. iii. 1842, p. 195) of different species observed in mating. Mr. MacLachlan informed me (see ‘Stett. Ent. Zeitung,’ 1867, s. 155) that when several species of Phryganidæ, which exhibit pronounced differences, were kept together by Dr. Aug. Meyer, they mated, and one pair produced fertile eggs.
431 ‘Modern Classification of Insects,’ vol. ii. 1840, p. 206, 205. Mr. Walsh, who called my attention to this double use of the jaws, says that he has repeatedly observed this fact.
431 ‘Modern Classification of Insects,’ vol. ii. 1840, p. 206, 205. Mr. Walsh, who pointed out this dual use of the jaws to me, says that he has seen this happen multiple times.
432 We have here a curious and inexplicable case of dimorphism, for some of the females of four European species of Dytiscus, and of certain species of Hydroporus, have their elytra smooth; and no intermediate gradations between sulcated or punctured and quite smooth elytra have been observed. See Dr. H. Schaum, as quoted in the ‘Zoologist,’ vol. v.-vi. 1847-48, p. 1896. Also Kirby and Spence, ‘Introduction to Entomology,’ vol. iii. 1826, p. 305.
432 We have an interesting and puzzling case of dimorphism here, as some females of four European species of Dytiscus and certain species of Hydroporus have smooth elytra. No intermediate forms between sulcated or punctured and completely smooth elytra have been found. See Dr. H. Schaum, as referenced in the ‘Zoologist,’ vol. v.-vi. 1847-48, p. 1896. Also Kirby and Spence, ‘Introduction to Entomology,’ vol. iii. 1826, p. 305.
433 Westwood, ‘Modern Class.’ vol. ii. p. 193. The following statement about Penthe, and others in inverted commas, are taken from Mr. Walsh, ‘Practical Entomologist,’ Philadelphia, vol. ii. p. 88.
433 Westwood, ‘Modern Class.’ vol. ii. p. 193. The following statement about Penthe, and others in quotes, is taken from Mr. Walsh, ‘Practical Entomologist,’ Philadelphia, vol. ii. p. 88.
435 ‘Insecta Maderensia,’ 1854, p. 20.
436 E. Doubleday, ‘Annals and Mag. of Nat. Hist.’ vol. i. 1848, p. 379. I may add that the wings in certain Hymenoptera (see Shuckard, 'Fossorial Hymenop.’ 1837, p. 39-43) differ in neuration according to sex.
436 E. Doubleday, ‘Annals and Mag. of Nat. Hist.’ vol. i. 1848, p. 379. I can also mention that the wings in some Hymenoptera (see Shuckard, 'Fossorial Hymenop.’ 1837, p. 39-43) have different vein patterns depending on the sex.
437 H. W. Bates, in ‘Journal of Proc. Linn. Soc.’ vol. vi. 1862, p. 74. Mr. Wonfor’s observations are quoted in ‘Popular Science Review,’ 1868, p. 343.
437 H. W. Bates, in ‘Journal of Proc. Linn. Soc.’ vol. vi. 1862, p. 74. Mr. Wonfor’s observations are mentioned in ‘Popular Science Review,’ 1868, p. 343.
442 For this and other statements on the size of the sexes, see Kirby and Spence, ibid. vol. iii. p. 300; on the duration of life in insects, see p. 344.
442 For this and other comments on the size of males and females, see Kirby and Spence, ibid. vol. iii. p. 300; for information on the lifespan of insects, see p. 344.
448 These particulars are taken from Westwood’s ‘Modern Class. of Insects,’ vol. ii. 1840, p. 422. See, also, on the Fulgoridæ, Kirby and Spence, ‘Introduct.’ vol. ii. p. 401.
448 These details are sourced from Westwood’s ‘Modern Classification of Insects,’ vol. ii. 1840, p. 422. Also, see Kirby and Spence, ‘Introduction,’ vol. ii. p. 401 for information on the Fulgoridae.
455 ‘The Naturalist on the Amazons,’ vol. i. 1863, p. 252. Mr. Bates gives a very interesting discussion on the gradations in the musical apparatus of the three families. See also Westwood, ‘Modern Class.’ vol. ii. p. 445 and 453.
455 ‘The Naturalist on the Amazons,’ vol. i. 1863, p. 252. Mr. Bates discusses the different stages in the musical features of the three families in a very interesting way. Also check out Westwood, ‘Modern Class.’ vol. ii. p. 445 and 453.
462 Mr. Walsh also informs me that he has noticed that the female of the Platyphyllum concavum, “when captured makes a feeble grating noise by shuffling her wing-covers together.”
462 Mr. Walsh also tells me that he has observed that the female of the Platyphyllum concavum "makes a weak grating sound by rubbing her wing covers together when captured."
463 Landois, ibid. s. 113.
484 Pyrodes pulcherrimus, in which the sexes differ conspicuously, has been described by Mr. Bates in ‘Transact. Ent. Soc.’ 1869, p. 50. I will specify the few other cases in which I have heard of a difference in colour between the sexes of beetles. Kirby and Spence (‘Introduct. to Entomology,’ vol. iii. p. 301) mention a Cantharis, Meloe, Rhagium, and the Leptura testacea; the male of the latter being testaceous, with a black thorax, and the female of a dull red all over. These two latter beetles belong to the Order of Longicorns. Messrs. R. Trimen and Waterhouse, junr., inform me of two Lamellicorns, viz., a Peritrichia and Trichius, the male of the latter being more obscurely coloured than the female. In Tillus elongatus the male is black, and the female always, as it is believed, of a dark blue colour with a red thorax. The male, also, of Orsodacna atra, as I hear from Mr. Walsh, is black, the female (the so-called O. ruficollis) having a rufous thorax.
484 Pyrodes pulcherrimus, which has noticeable differences between the sexes, was described by Mr. Bates in 'Transact. Ent. Soc.' 1869, p. 50. I will mention the few other instances where I’ve heard of color differences between male and female beetles. Kirby and Spence ('Introduct. to Entomology,' vol. iii. p. 301) talk about a Cantharis, Meloe, Rhagium, and the Leptura testacea; the male of the latter is testaceous with a black thorax, while the female is a dull red throughout. These two beetles are part of the Longicorns order. Messrs. R. Trimen and Waterhouse, junr., told me about two Lamellicorns, specifically a Peritrichia and Trichius, with the male of the latter being more subtly colored than the female. In Tillus elongatus, the male is black, and the female is believed to always be a dark blue color with a red thorax. Additionally, Mr. Walsh informs me that the male of Orsodacna atra is black, while the female (known as O. ruficollis) has a reddish thorax.
488 ‘Modern Classification of Insects,’ vol. i. p. 172. On the same page there is an account of Siagonium. In the British Museum I noticed one male specimen of Siagonium in an intermediate condition, so that the dimorphism is not strict.
488 ‘Modern Classification of Insects,’ vol. i. p. 172. On the same page, there's a description of Siagonium. At the British Museum, I saw one male specimen of Siagonium in an intermediate state, indicating that the dimorphism isn't absolute.
490 ‘Entomological Magazine,’ vol. i. 1833, p. 82. See also on the conflicts of this species, Kirby and Spence, ibid. vol. iii. p. 314; and Westwood, ibid. vol. i. p. 187.
490 ‘Entomological Magazine,’ vol. i. 1833, p. 82. See also on the conflicts of this species, Kirby and Spence, ibid. vol. iii. p. 314; and Westwood, ibid. vol. i. p. 187.
496 I am greatly indebted to Mr. G. R. Crotch for having sent me numerous prepared specimens of various beetles belonging to these three families and others, as well as for valuable information of all kinds. He believes that the power of stridulation in the Clythra has not been previously observed. I am also much indebted to Mr. E. W. Janson, for information and specimens. I may add that my son, Mr. F. Darwin, finds that Dermestes murinus stridulates, but he searched in vain for the apparatus. Scolytus has lately been described by Mr. Algen as a stridulator, in the ‘Edinburgh Monthly Magazine,’ 1869, Nov., p. 130.
496 I am really grateful to Mr. G. R. Crotch for sending me many prepared specimens of different beetles from these three families and others, as well as for all the valuable information he provided. He thinks that the stridulation ability in the Clythra has not been noticed before. I also owe a lot to Mr. E. W. Janson for his information and specimens. Additionally, my son, Mr. F. Darwin, found that Dermestes murinus makes stridulating sounds, but he couldn’t find the mechanism. Scolytus has recently been described by Mr. Algen as a stridulator in the ‘Edinburgh Monthly Magazine,’ 1869, Nov., p. 130.
498 Westring has described (Kroyer, ‘Naturhist. Tidskrift,’ B. ii. 1848-49, p. 334) the stridulating organs in these two, as well as in other families. In the Carabidæ I have examined Elaphrus uliginosus and Blethisa multipunctata, sent to me by Mr. Crotch. In Blethisa the transverse ridges on the furrowed border of the abdominal segment do not come into play, as far as I could judge, in scraping the rasps on the elytra.
498 Westring has described (Kroyer, ‘Naturhist. Tidskrift,’ B. ii. 1848-49, p. 334) the stridulating organs in these two, as well as in other families. In the Carabidæ, I have examined Elaphrus uliginosus and Blethisa multipunctata, which were sent to me by Mr. Crotch. In Blethisa, the transverse ridges on the furrowed border of the abdominal segment don’t seem to play a role, as far as I could tell, in scraping the rasps on the elytra.
501 Mr. Doubleday informs me that “the noise is produced by the insect raising itself on its legs as high as it can, and then sinking its thorax five or six times, in rapid succession, against the substance upon which it is sitting.” For references on this subject see Landois, 'Zeitschrift für wissen. Zoolog.’ B. xvii. s. 131. Olivier says (as quoted by Kirby and Spence, ‘Introduct.’ vol. ii. p. 395) that the female of Pimelia striata produces a rather loud sound by striking her abdomen against any hard substance, “and that the male, obedient to this call, soon attends her and they pair.”
501 Mr. Doubleday tells me that “the noise is made when the insect raises itself on its legs as high as it can, and then rapidly brings its thorax down five or six times against the surface it’s on.” For more information on this topic, see Landois, 'Zeitschrift für wissen. Zoolog.’ B. xvii. s. 131. Olivier states (as cited by Kirby and Spence, ‘Introduct.’ vol. ii. p. 395) that the female of Pimelia striata creates a rather loud sound by hitting her abdomen against any hard surface, “and that the male, responding to this signal, quickly comes to her and they mate.”
502 Apatura Iris: ‘The Entomologist’s Weekly Intelligencer,’ 1859, p. 139. For the Bornean Butterflies see C. Collingwood, ‘Rambles of a Naturalist,’ 1868, p. 183.
502 Apatura Iris: ‘The Entomologist’s Weekly Intelligencer,’ 1859, p. 139. For the Bornean Butterflies see C. Collingwood, ‘Rambles of a Naturalist,’ 1868, p. 183.
503 See my ‘Journal of Researches,’ 1845, p. 33. Mr. Doubleday has detected (‘Proc. Ent. Soc.’ March 3rd, 1845, p. 123) a peculiar membranous sac at the base of the front wings, which is probably connected with the production of the sound.
503 See my ‘Journal of Researches,’ 1845, p. 33. Mr. Doubleday has discovered ('Proc. Ent. Soc.' March 3rd, 1845, p. 123) a unique membranous sac at the base of the front wings, which is likely related to the production of the sound.
504 See also Mr. Bates’ paper in ‘Proc. Ent. Soc. of Philadelphia,’ 1865, p. 206. Also Mr. Wallace on the same subject, in regard to Diadema, in ‘Transact. Entomolog. Soc. of London,’ 1869, p. 278.
504 See also Mr. Bates’ paper in ‘Proceedings of the Entomological Society of Philadelphia,’ 1865, p. 206. Also Mr. Wallace on the same topic, regarding Diadema, in ‘Transactions of the Entomological Society of London,’ 1869, p. 278.
506 See the interesting article in the ‘Westminster Review,’ July, 1867, p. 10. A woodcut of the Kallima is given by Mr. Wallace in Hardwicke’s 'Science Gossip,’ Sept. 1867, p. 196.
506 Check out the interesting article in the 'Westminster Review,' July 1867, p. 10. Mr. Wallace provides a woodcut of the Kallima in Hardwicke's 'Science Gossip,' Sept. 1867, p. 196.
511 For instance, Lithosia; but Prof. Westwood (‘Modern Class. of Insects,’ vol. ii. p. 390) seems surprised at this case. On the relative colours of diurnal and nocturnal Lepidoptera, see ibid. p. 333 and 392; also Harris, ‘Treatise on the Insects of New England,’ 1842, p. 315.
511 For example, Lithosia; however, Prof. Westwood (‘Modern Class. of Insects,’ vol. ii. p. 390) appears to be surprised by this case. Regarding the relative colors of daytime and nighttime Lepidoptera, see ibid. p. 333 and 392; also Harris, ‘Treatise on the Insects of New England,’ 1842, p. 315.
512 Such differences between the upper and lower surfaces of the wings of several species of Papilio, may be seen in the beautiful plates to Mr. Wallace’s Memoir on the Papilionidæ of the Malayan Region, in ‘Transact. Linn. Soc.’ vol. xxv. part i. 1865.
512 You can see these differences between the upper and lower surfaces of the wings of various species of Papilio in the stunning plates from Mr. Wallace’s Memoir on the Papilionidæ of the Malayan Region, published in ‘Transact. Linn. Soc.’ vol. xxv. part i. 1865.
514 See also an account of the S. American genus Erateina (one of the Geometræ) in ‘Transact. Ent. Soc.’ new series, vol. v. pl. xv. and xvi.
514 Also check out the description of the South American genus Erateina (a member of the Geometræ) in ‘Transact. Ent. Soc.’ new series, vol. v. pl. xv. and xvi.
517 For instance, I observe in my son’s cabinet that the males are darker than the females in the Lasiocampa quercus, Odonestis potatoria, Hypogymna dispar, Dasychira pudibunda, and Cycnia mendica. In this latter species the difference in colour between the two sexes is strongly marked; and Mr. Wallace informs me that we here have, as he believes, an instance of protective mimickry confined to one sex, as will hereafter be more fully explained. The white female of the Cycnia resembles the very common Spilosoma menthrasti, both sexes of which are white; and Mr. Stainton observed that this latter moth was rejected with utter disgust by a whole brood of young turkeys, which were fond of eating other moths; so that if the Cycnia was commonly mistaken by British birds for the Spilosoma, it would escape being devoured, and its white deceptive colour would thus be highly beneficial.
517 For example, I've noticed in my son's cabinet that the males are darker than the females in the Lasiocampa quercus, Odonestis potatoria, Hypogymna dispar, Dasychira pudibunda, and Cycnia mendica. In the case of the latter species, the color difference between the sexes is quite pronounced; and Mr. Wallace tells me that we might have, as he believes, an example of protective mimicry that is specific to one sex, which will be explained further later. The white female of the Cycnia resembles the very common Spilosoma menthrasti, both sexes of which are white; and Mr. Stainton noted that this latter moth was rejected with total disgust by an entire brood of young turkeys, which liked to eat other moths. So, if British birds often confuse the Cycnia with the Spilosoma, it would avoid being eaten, making its white deceptive color very advantageous.
519 Wallace on the Papilionidæ of the Malayan Region, in ‘Transact. Linn. Soc. vol. xxv. 1865, p. 8, 36. A striking case of a rare variety, strictly intermediate between two other well-marked female varieties, is given by Mr. Wallace. See also Mr. Bates, in ‘Proc. Entomolog. Soc.’ Nov. 19th, 1866, p. xl.
519 Wallace on the Papilionidae of the Malayan Region, in ‘Transact. Linn. Soc. vol. xxv. 1865, p. 8, 36. A notable example of a rare variety that lies perfectly between two other distinct female varieties is presented by Mr. Wallace. See also Mr. Bates, in ‘Proc. Entomolog. Soc.’ Nov. 19th, 1866, p. xl.
523 A. R. Wallace, in ‘The Journal of Travel,’ vol. i. 1868, p. 88. 'Westminster Review,’ July, 1857, p. 37. See also Messrs. Wallace and Bates in ‘Proc. Ent. Soc.’ Nov. 19th, 1866, p. xxxix.
523 A. R. Wallace, in ‘The Journal of Travel,’ vol. i. 1868, p. 88. 'Westminster Review,’ July, 1857, p. 37. See also Wallace and Bates in ‘Proc. Ent. Soc.’ Nov. 19th, 1866, p. xxxix.
528 See an ingenious article entitled, “Difficulties of the Theory of Natural Selection,” in the ‘Month,’ 1869. The writer strangely supposes that I attribute the variations in colour of the Lepidoptera, by which certain species belonging to distinct families have come to resemble others, to reversion to a common progenitor; but there is no more reason to attribute these variations to reversion than in the case of any ordinary variation.
528 Check out a clever article called “Difficulties of the Theory of Natural Selection” in the ‘Month,’ 1869. The author oddly assumes that I believe the color variations in Lepidoptera, which have caused certain species from different families to look alike, are due to reverting to a common ancestor. However, there's no more reason to link these variations to reversion than with any typical variation.
532 See Mr. Wallace in ‘Westminster Review,’ July, 1867, p. 11 and 37. The male of no butterfly, as Mr. Wallace informs me, is known to differ in colour, as a protection, from the female; and he asks me how I can explain this fact on the principle that one sex alone has varied and has transmitted its variations exclusively to the same sex, without the aid of selection to check the variations being inherited by the other sex. No doubt if it could be shewn that the females of very many species had been rendered beautiful through protective mimickry, but that this has never occurred with the males, it would be a serious difficulty. But the number of cases as yet known hardly suffices for a fair judgment. We can see that the males, from having the power of flying more swiftly, and thus escaping danger, would not be so likely as the females to have had their colours modified for the sake of protection; but this would not in the least have interfered with their receiving protective colours through inheritance from the females. In the second place, it is probable that sexual selection would actually tend to prevent a beautiful male from becoming obscure, for the less brilliant individuals would be less attractive to the females. Supposing that the beauty of the male of any species had been mainly acquired through sexual selection, yet if this beauty likewise served as a protection, the acquisition would have been aided by natural selection. But it would be quite beyond our power to distinguish between the two processes of sexual and ordinary selection. Hence it is not likely that we should be able to adduce cases of the males having been rendered brilliant exclusively through protective mimickry, though this is comparatively easy with the females, which have rarely or never been rendered beautiful, as far as we can judge, for the sake of sexual attraction, although they have often received beauty through inheritance from their male parents.
532 Check out Mr. Wallace in ‘Westminster Review,’ July, 1867, p. 11 and 37. According to Mr. Wallace, there’s no butterfly species where the male distinctly differs in color from the female for protective purposes. He questions how I can explain this fact based on the idea that only one sex has varied and passed on those variations strictly to the same sex, without selection preventing the other sex from inheriting those variations. It would indeed be a significant issue if we could demonstrate that the females in many species became beautiful through protective mimicry, while this was never the case for the males. However, the number of known cases is still too small for a proper assessment. We can understand that males, being able to fly faster and evade danger, are less likely than females to have their colors changed for protection; still, that doesn’t mean they wouldn’t inherit protective colors from the females. Additionally, sexual selection might actually keep a beautiful male from becoming less noticeable, as less striking individuals would likely attract fewer females. If we assume that a male’s beauty mainly came about through sexual selection, but also served as protection, then natural selection would have facilitated that acquisition. However, it would be challenging for us to distinguish between sexual selection and regular selection. Thus, it’s unlikely that we would find cases where males became bright purely through protective mimicry, even though this is relatively easier to demonstrate with females, who seldom seem to have gained beauty for the purpose of attracting mates, even though they often inherit beauty from their male ancestors.
534 See Mr. J. Jenner Weir’s paper on insects and insectivorous birds, in ‘Transact. Ent. Soc.’ 1869, p. 21; also Mr. Butler’s paper, ibid. p. 27.
534 See Mr. J. Jenner Weir’s article on insects and insect-eating birds in 'Transactions of the Entomological Society' 1869, p. 21; also Mr. Butler’s article, ibid. p. 27.
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HISTORY OF GERMANY, from the Invasion of the Kingdom by the Romans under Marius, continued down to 1867. On the Plan of MRS. MARKHAM. With 50 Woodcuts.
HISTORY OF GERMANY, from the Invasion of the Kingdom by the Romans under Marius, continued up to 1867. Based on the work of MRS. MARKHAM. Featuring 50 illustrations.
SHALL AND WILL; or, the Future Auxiliary Verb. By SIR EDMUND HEAD.
SHALL AND WILL; or, the Future Auxiliary Verb. By SIR EDMUND HEAD.
Four Shillings and Sixpence.
CHILDREN OF THE LAKE. A Poem. By EDWARD SALLESBURY.
CHILDREN OF THE LAKE. A Poem. By EDWARD SALLESBURY.
A LADY’S DIARY OF THE SIEGE OF LUCKNOW.
A LADY’S DIARY OF THE SIEGE OF LUCKNOW.
HOUSEHOLD SURGERY; or, Hints on Emergencies. By JOHN F. SOUTH. With Woodcuts.8
HOUSEHOLD SURGERY; or, Tips on Emergencies. By JOHN F. SOUTH. With Illustrations.8
Five Shillings.
ANCIENT SPANISH BALLADS; Historical and Romantic. Translated with Notes by J. G. LOCKHART. With Portrait and Illustrations.
ANCIENT SPANISH BALLADS; Historical and Romantic. Translated with Notes by J. G. LOCKHART. With Portrait and Illustrations.
MISCELLANIES. By LORD BYRON. 2 vols.
MISCELLANIES. By LORD BYRON. 2 volumes.
INTRODUCTIONS TO THE STUDY OF THE GREEK CLASSIC POETS. By HENRY NELSON COLERIDGE.
INTRODUCTIONS TO THE STUDY OF THE GREEK CLASSIC POETS. By HENRY NELSON COLERIDGE.
HYMNS IN PROSE FOR CHILDREN. By MRS. BARBAULD. With 112 Illustrations.
HYMNS IN PROSE FOR KIDS. By MRS. BARBAULD. With 112 Illustrations.
RECOLLECTIONS OF THE DRUSES, and some Notes on their Religion. By LORD CARNARVON.
RECOLLECTIONS OF THE DRUSES, and some Notes on Their Religion. By LORD CARNARVON.
THE ORIGIN OF LANGUAGE. BASED ON MODERN RESEARCHES. By REV. F. W. FARRAR.
THE ORIGIN OF LANGUAGE. BASED ON MODERN RESEARCH. By REV. F. W. FARRAR.
MODERN DOMESTIC COOKERY. Founded on Principles of Economy and Practical Knowledge, and adapted for Private Families. With Woodcuts.
MODERN DOMESTIC COOKING. Based on Principles of Economy and Practical Knowledge, and tailored for Private Households. With Illustrations.
DRAMAS AND PLAYS. By LORD BYRON. 2 vols.
DRAMAS AND PLAYS. By LORD BYRON. 2 vols.
THE HORSE AND HIS RIDER. By SIR FRANCIS HEAD. With Woodcuts.
THE HORSE AND HIS RIDER. By SIR FRANCIS HEAD. With Illustrations.
HANDBOOK OF FAMILIAR QUOTATIONS, chiefly from English Authors.
HANDBOOK OF FAMILIAR QUOTATIONS, mainly from English Authors.
THE CHACE—THE TURF—AND THE ROAD. A Series of Popular Essays. By C. J. APPERLEY (Nimrod). With Portrait and Illustrations.
THE CHACE—THE TURF—AND THE ROAD. A Series of Popular Essays. By C. J. APPERLEY (Nimrod). With Portrait and Illustrations.
AUNT IDA’S WALKS AND TALKS. A Story Book for Children. By A LADY.
AUNT IDA’S WALKS AND TALKS. A Story Book for Kids. By A LADY.
STORIES FOR DARLINGS. A Book for Boys and Girls. With Illustrations.
STORIES FOR DARLINGS. A Book for Kids. With Illustrations.
THE CHARMED ROE. A Story Book for Young People. Illustrated by OTTO SPECKTER.
THE CHARMED ROE. A Story Book for Young People. Illustrated by OTTO SPECKTER.
DON JUAN AND BEPPO. By LORD BYRON. 2 vols.
DON JUAN AND BEPPO. By LORD BYRON. 2 vols.
LIFE IN THE LIGHT OF GOD’S WORD. By ARCHBISHOP THOMSON, D.D.
LIFE IN THE LIGHT OF GOD’S WORD. By ARCHBISHOP THOMSON, D.D.
ATHENS AND ATTICA; Notes of a Tour. By BISHOP WORDSWORTH, D.D. With Illustrations.
ATHENS AND ATTICA; Notes of a Tour. By BISHOP WORDSWORTH, D.D. With Illustrations.
ANNALS OF THE WARS—XVIIITH CENTURY, 1700-1799. Compiled from the most Authentic Sources. By SIR EDWARD CUST, D.C.L. With Maps. 5 vols. Post 8vo. 5s. each.
ANNALS OF THE WARS—18TH CENTURY, 1700-1799. Compiled from the most Reliable Sources. By SIR EDWARD CUST, D.C.L. With Maps. 5 vols. Post 8vo. £5 each.
ANNALS OF THE WARS—XIXth CENTURY, 1800-15. Compiled from the most Authentic Sources. By SIR EDWARD CUST. 4 vols. Fcap. 8vo. 5s. each.9
ANNALS OF THE WARS—19th CENTURY, 1800-15. Compiled from the most reliable sources. By SIR EDWARD CUST. 4 vols. Fcap. 8vo. 5s. each.9
Six Shillings.
BENEDICITE; or, THE SONG of the THREE CHILDREN. Being Illustrations of the Power, Beneficence, and Design manifested by the Creator in His Works. By DR. CHAPLIN CHILD.
BENEDICITE; or, THE SONG of the THREE CHILDREN. Being Images of the Energy, Kindness, and Design shown by the Content Creator in His Creations. By DR. CHAPLIN CHILD.
OLD DECCAN DAYS; or, HINDOO FAIRY LEGENDS current in Southern India. By M. FRERE. With Introduction by Sir Bartle Frere. With Illustrations.
OLD DECCAN DAYS; or, HINDOO FAIRY LEGENDS current in Southern India. By M. FRERE. With Introduction by Sir Bartle Frere. Featuring Illustrations.
THE WILD GARDEN; or, Our Groves and Shrubberies made beautiful by the Naturalization of Hardy Exotic Plants. By WILLIAM ROBINSON. With Frontispiece.
THE WILD GARDEN; or, Our gardens and shrubs are enhanced by the introduction of hardy exotic plants.. By WILLIAM ROBINSON. With Frontispiece.
MISSIONARY TRAVELS AND RESEARCHES IN SOUTH AFRICA. By DAVID LIVINGSTONE, M.D. With Map and Illustrations.
MISSIONARY TRAVELS AND RESEARCHES IN SOUTH AFRICA. By DAVID LIVINGSTONE, M.D. With Map and Illustrations.
FIVE YEARS OF A HUNTER’S LIFE IN SOUTH AFRICA; By GORDON CUMMING. With Illustrations.
FIVE YEARS OF A HUNTER’S LIFE IN SOUTH AFRICA; By GORDON CUMMING. With Illustrations.
THOUGHTS ON ANIMALCULES; or, The Invisible World, as revealed by the Microscope. By GIDEON A. MANTELL. With Plates.
THOUGHTS ON ANIMALCULES; or, The Invisible World, as revealed by the Microscope. By GIDEON A. MANTELL. With Plates.
LIVES OF BRINDLEY AND THE EARLY ENGINEERS. By SAMUEL SMILES. With Woodcuts.
LIVES OF BRINDLEY AND THE EARLY ENGINEERS. By SAMUEL SMILES. With Illustrations.
LIFE OF TELFORD. With a History of Roads and Travelling in England. By SAMUEL SMILES. With Woodcuts.
LIFE OF TELFORD. With a History of Roads and Travel in England. By SAMUEL SMILES. Featuring Illustrations.
LIVES OF GEORGE AND ROBERT STEPHENSON. By SAMUEL SMILES. With Woodcuts.
LIVES OF GEORGE AND ROBERT STEPHENSON. By SAMUEL SMILES. With Illustrations.
SELF-HELP. With Illustrations of Character and Conduct. By SAMUEL SMILES.
SELF-HELP. With Illustrations of Character and Conduct. By SAMUEL SMILES.
INDUSTRIAL BIOGRAPHY: Iron-workers and Toolmakers. A Sequel to ‘Self-help.’ By SAMUEL SMILES.
INDUSTRIAL BIOGRAPHY: Ironworkers and Toolmakers. A Sequel to ‘Self-help.’ By SAMUEL SMILES.
THE HUGUENOTS IN ENGLAND AND IRELAND: their Settlements, Churches, and Industries. By SAMUEL SMILES.
THE HUGUENOTS IN ENGLAND AND IRELAND: their Settlements, Churches, and Industries. By SAMUEL SMILES.
WILD WALES; its People, Language, and Scenery. With Introductory Remarks. By GEORGE BORROW.
WILD WALES; its People, Language, and Scenery. With Introductory Remarks. By GEORGE BORROW.
A MANUAL OF ETHNOLOGY; or, A Popular History of the Races of the Old World. By CHARLES L. BRACE.
A MANUAL OF ETHNOLOGY; or, A Brief History of the Races of the Old World. By CHARLES L. BRACE.
Seven Shillings.
JOURNALS OF A TOUR IN INDIA. By BISHOP HEBER. 2 vols.
JOURNALS OF A TOUR IN INDIA. By BISHOP HEBER. 2 volumes.
ADVENTURES AMONG THE MARQUESAS AND SOUTH SEA ISLANDERS. By HERMAN MELVILLE. 2 vols.
ADVENTURES AMONG THE MARQUESAS AND SOUTH SEA ISLANDERS. By HERMAN MELVILLE. 2 vols.
CONSTITUTIONAL PROGRESS. By MONTAGU BURROWS, M.A.
CONSTITUTIONAL PROGRESS. By MONTAGU BURROWS, M.A.
LIFE AND POETICAL WORKS OF REV. GEORGE CRABBE. Edited by HIS SON. With Notes, Portrait, and Illustrations.10
LIFE AND POETICAL WORKS OF REV. GEORGE CRABBE. Edited by HIS SON. With Notes, Portrait, and Illustrations.10
Seven Shillings and Sixpence.
THE ART OF TRAVEL; or, Hints on the Shifts and Contrivances available in Wild Countries. By FRANCIS GALTON. With Woodcuts.
THE ART OF TRAVEL; or, Tips on the Strategies and Tricks Available in Untamed Places. By FRANCIS GALTON. With Illustrations.
VISITS TO THE MONASTERIES OF THE LEVANT. By HON. R. CURZON. With Illustrations.
VISITS TO THE MONASTERIES OF THE LEVANT. By HON. R. CURZON. With Illustrations.
LETTERS FROM HIGH LATITUDES; an Account of a Yacht Voyage to Iceland, Jan Mayen, and Spitzbergen, &c. By LORD DUFFERIN. With Illustrations.
LETTERS FROM HIGH LATITUDES; an Account of a Yacht Voyage to Iceland, Jan Mayen, and Spitzbergen, etc. By LORD DUFFERIN. With Illustrations.
BUBBLES FROM THE BRUNNEN OF NASSAU. By an Old Man (SIR FRANCIS HEAD). With Illustrations.
BUBBLES FROM THE BRUNNEN OF NASSAU. By an Old Man (SIR FRANCIS HEAD). With Illustrations.
NINEVEH AND ITS REMAINS; a Narrative of an Expedition to Assyria in 1845-47. By A. H. LAYARD. With Illustrations.
NINEVEH AND ITS REMAINS; a Story of an Expedition to Assyria in 1845-47. By A. H. LAYARD. With Illustrations.
NINEVEH AND BABYLON; a Narrative of a Second Expedition to Assyria in 1849-51. By A. H. LAYARD. With Illustrations.
NINEVEH AND BABYLON; a Story of a Second Trip to Assyria in 1849-51. By A. H. LAYARD. With Illustrations.
THREE YEARS’ RESIDENCE IN ABYSSINIA, with Travels in that Country. By MANSFIELD PARKYNS. With Illustrations.
THREE YEARS LIVING IN ABYSSINIA, with Travels in that Country. By MANSFIELD PARKYNS. With Illustrations.
FIVE YEARS IN DAMASCUS, with Travels in Palmyra, Lebanon, and among the Giant Cities of Bashan and The Hauran. By REV. J. L. PORTER. With Illustrations.
FIVE YEARS IN DAMASCUS, with Travel in Palmyra, Lebanon, and around the Giant Cities of Bashan and The Hauran. By REV. J. L. PORTER. With Illustrations.
THE VOYAGE OF THE ‘FOX’ IN THE ARCTIC SEAS, and the Discovery of the Fate of Sir John Franklin and his Companions. By SIR LEOPOLD McCLINTOCK. With Illustrations.
THE VOYAGE OF THE 'FOX' IN THE ARCTIC SEAS, and the Discovery of What Happened to Sir John Franklin and His Companions. By SIR LEOPOLD McCLINTOCK. With Illustrations.
REMINISCENCES OF ATHENS AND THE MOREA, during Travels in Greece. By LORD CARNARVON. With Map.
REMINISCENCES OF ATHENS AND THE MOREA, during Travels in Greece. By LORD CARNARVON. With Map.
PEN AND PENCIL SKETCHES IN INDIA. By GENERAL MUNDY. With Illustrations.
PEN AND PENCIL SKETCHES IN INDIA. By GENERAL MUNDY. With Illustrations.
PHILOSOPHY IN SPORT, MADE SCIENCE IN EARNEST: or, The First Principles of Natural Philosophy explained by the Toys and Sports of Youth. By DR. PARIS. With Woodcuts.
PHILOSOPHY IN SPORT, MADE SCIENCE IN EARNEST: or, The First Principles of Natural Philosophy explained through the Toys and Sports of Youth. By DR. PARIS. With Illustrations.
BLIND PEOPLE; their Works and Ways. With Lives of some famous Blind Men. By REV. B. G. JOHNS. With Illustrations.
BLIND PEOPLE; their Works and Ways. With Lives of some famous Blind Men. By REV. B. G. JOHNS. With Illustrations.
HORACE: A New Edition of the Text. Edited by DEAN MILMAN. With 100 Woodcuts.
HORACE: A New Edition of the Text. Edited by DEAN MILMAN. Includes 100 Woodcuts.
THE BOOK OF THE CHURCH. By ROBERT SOUTHEY.
THE BOOK OF THE CHURCH. By ROBERT SOUTHEY.
A HANDBOOK FOR YOUNG PAINTERS. By C. R. LESLIE, R.A. With 24 Illustrations.
A HANDBOOK FOR YOUNG PAINTERS. By C. R. LESLIE, R.A. With 24 Illustrations.
A GEOGRAPHICAL HANDBOOK OF FERNS, with Tables to show their Distribution. By K. M. LYELL. With a Frontispiece.
A GEOGRAPHICAL HANDBOOK OF FERNS, with Tables to show their Distribution. By K. M. LYELL. With a Frontispiece.
THE STORY OF THE LIFE OF LORD BACON. By W. HEPWORTH DIXON.11
THE STORY OF THE LIFE OF LORD BACON. By W. HEPWORTH DIXON.11
A SMALLER DICTIONARY OF THE BIBLE; Its Antiquities, Geography, Biography, and Natural History. By DR. WM. SMITH. With Maps and Illustrations.
A SMALLER DICTIONARY OF THE BIBLE; Its Antiquities, Geography, Biography, and Natural History. By DR. WM. SMITH. With Maps and Illustrations.
A SMALLER CLASSICAL DICTIONARY OF MYTHOLOGY, BIOGRAPHY, AND GEOGRAPHY. By DR. WM. SMITH. With 200 Woodcuts.
A SMALLER CLASSICAL DICTIONARY OF MYTHOLOGY, BIOGRAPHY, AND GEOGRAPHY. By DR. WM. SMITH. With 200 illustrations.
A SMALLER DICTIONARY OF GREEK AND ROMAN ANTIQUITIES. By DR. WM. SMITH. With 200 Woodcuts.
A SMALLER DICTIONARY OF GREEK AND ROMAN ANTIQUITIES. By DR. WM. SMITH. With 200 Illustrations.
A SMALLER LATIN-ENGLISH DICTIONARY. With a Dictionary of Proper Names, and Tables of the Roman Calendar, Measures, Weights, and Moneys. By DR. WM. SMITH.
A SMALLER LATIN-ENGLISH DICTIONARY. With a Dictionary of Proper Names, and Tables of the Roman Calendar, Measures, Weights, and Moneys. By DR. WM. SMITH.
A SMALLER ENGLISH-LATIN DICTIONARY, By DR. WM. SMITH.
A SMALLER ENGLISH-LATIN DICTIONARY, By DR. WM. SMITH.
THE STUDENT’S HUME; An Epitome of the History Of England. By DAVID HUME. Corrected and continued to 1868. With Woodcuts.
THE STUDENT’S HUME; Summary of the History of England. By DAVID HUME. Updated and extended to 1868. With Illustrations.
THE STUDENT’S CONSTITUTIONAL HISTORY OF ENGLAND. By HENRY HALLAM. With the Author’s latest Additions. Edited by Dr. Wm. Smith. [In the Press.
THE STUDENT’S CONSTITUTIONAL HISTORY OF ENGLAND. By HENRY HALLAM. With the Author’s latest Additions. Edited by Dr. William Smith. [In the Press.
THE STUDENT’S HISTORY OF THE MIDDLE AGES OF EUROPE. By HENRY HALLAM. With the Author’s Supplemental Notes. Edited by Dr. Wm. Smith. [In the Press.
THE STUDENT’S HISTORY OF THE MIDDLE AGES OF EUROPE. By HENRY HALLAM. With the Author’s Supplemental Notes. Edited by Dr. William Smith. [In the Press.
THE STUDENT’S HISTORY OF FRANCE. From the Earliest Times to the Establishment of the Second Empire, 1852. With Woodcuts.
THE STUDENT’S HISTORY OF FRANCE. From Ancient Times to the Formation of the Second Empire, 1852. With Illustrations.
THE STUDENT’S HISTORY OF ROME. From the Earliest Times to the Establishment of the Empire. With Chapters on the History of Literature and Art. By DEAN LIDDELL. With Woodcuts.
THE STUDENT’S HISTORY OF ROME. From the earliest times to the establishment of the empire. With Chapters on the History of Literature and Art. By DEAN LIDDELL. With Illustrations.
THE STUDENT’S GIBBON; An Epitome of the History of the Decline and Fall of the Roman Empire. By EDWARD GIBBON. With Woodcuts.
THE STUDENT’S GIBBON; A Summary of the History of the Decline and Fall of the Roman Empire. By EDWARD GIBBON. With Illustrations.
THE STUDENT’S HISTORY OF GREECE. From the Earliest Times to the Roman Conquest. With Chapters on the History of Literature and Art. By DR. WM. SMITH. With Woodcuts.
THE STUDENT’S HISTORY OF GREECE. From the Beginning to the Roman Conquest. With Chapters on the History of Literature and Art. By DR. WM. SMITH. With Woodcuts.
THE STUDENT’S ANCIENT HISTORY OF THE EAST. From the Earliest Times to the Conquests of Alexander the Great, including Egypt, Assyria, Babylonia, Media, Persia, Asia Minor, and Phœnicia. By PHILIP SMITH, B.A. With Woodcuts.
THE STUDENT’S ANCIENT HISTORY OF THE EAST. From the Earliest Times to the Conquests of Alexander the Great, including Egypt, Assyria, Babylonia, Media, Persia, Asia Minor, and Phoenicia. By PHILIP SMITH, B.A. With Illustrations.
THE STUDENT’S OLD TESTAMENT HISTORY. From the Creation to the Return of the Jews from Captivity. With Maps and Woodcuts.
THE STUDENT’S OLD TESTAMENT HISTORY. From Creation to the Return of the Jews from Captivity. With Maps and Illustrations.
THE STUDENT’S NEW TESTAMENT HISTORY. With an Introduction, containing the connection of the Old and New Testaments. With Maps and Woodcuts.
THE STUDENT’S NEW TESTAMENT HISTORY. With an Introduction, covering the link between the Old and New Testaments. Featuring Maps and Illustrations.
THE STUDENT’S MANUAL OF THE ENGLISH LANGUAGE. By GEORGE P. MARSH. Edited, with additional Chapters and Notes.12
THE STUDENT’S MANUAL OF THE ENGLISH LANGUAGE. By GEORGE P. MARSH. Edited, with additional Chapters and Notes.12
THE STUDENT’S MANUAL OF ENGLISH LITERATURE. By T. B. SHAW, M.A. Edited, with Notes and Illustrations.
THE STUDENT'S MANUAL OF ENGLISH LITERATURE. By T. B. SHAW, M.A. Edited, with Notes and Illustrations.
THE STUDENT’S SPECIMENS OF ENGLISH LITERATURE. Selected from the Best Writers. By THOS. B. SHAW, M.A. Edited, with Additions.
THE STUDENT’S SPECIMENS OF ENGLISH LITERATURE. Selected from the Top Writers. By THOS. B. SHAW, M.A. Edited, with Additions.
THE STUDENT’S MANUAL OF ANCIENT GEOGRAPHY. By REV. W. L. BEVAN. With Woodcuts.
THE STUDENT’S MANUAL OF ANCIENT GEOGRAPHY. By REV. W. L. BEVAN. With Illustrations.
THE STUDENT’S MANUAL OF MODERN GEOGRAPHY. Mathematical, Physical, and Descriptive. By REV. W. L. BEVAN. With Woodcuts.
THE STUDENT’S MANUAL OF MODERN GEOGRAPHY. Mathematical, Physical, and Descriptive. By REV. W. L. BEVAN. With Woodcuts.
THE STUDENT’S MANUAL OF MORAL PHILOSOPHY. With Quotations and References. By WILLIAM FLEMING, D.D.
THE STUDENT’S MANUAL OF MORAL PHILOSOPHY. With Quotations and References. By WILLIAM FLEMING, D.D.
THE STUDENT’S BLACKSTONE. A Systematic Abridgment of the entire Commentaries. By R. MALCOLM KERR, LL.D.
THE STUDENT’S BLACKSTONE. A Systematic Summary of the complete Commentaries. By R. MALCOLM KERR, LL.D.
A PRACTICAL HEBREW GRAMMAR. With the Hebrew text of Genesis i.-vi. and Psalms i.-vi., Grammatical Analysis and Vocabulary. By REV. STANLEY LEATHES.
A PRACTICAL HEBREW GRAMMAR. With the Hebrew text of Genesis 1-6 and Psalms 1-6, along with Grammatical Analysis and Vocabulary. By Rev. Stanley Leathes.
Nine Shillings.
THE CONNECTION OF THE PHYSICAL SCIENCES. By MARY SOMERVILLE. With Woodcuts.
THE CONNECTION OF THE PHYSICAL SCIENCES. By MARY SOMERVILLE. With illustrations.
PHYSICAL GEOGRAPHY. By MARY SOMERVILLE. Revised by H. W. BATES. With Portrait.
PHYSICAL GEOGRAPHY. By MARY SOMERVILLE. Revised by H. W. BATES. With Portrait.
THE STUDENT’S ELEMENTS OF GEOLOGY. By SIR CHARLES LYELL. With 600 Woodcuts.
THE STUDENT’S ELEMENTS OF GEOLOGY. By SIR CHARLES LYELL. With 600 illustrations.
A MANUAL OF SCIENTIFIC INQUIRY. By Various Writers. Edited by SIR J. F. HERSCHEL and REV. ROBERT MAIN.
A MANUAL OF SCIENTIFIC INQUIRY. By Different Writers. Edited by SIR J. F. HERSCHEL and REV. ROBERT MAIN.
POETICAL WORKS OF LORD BYRON. With Notes, Illustrations, and Portrait.
POETICAL WORKS OF LORD BYRON. With Notes, Illustrations, and Portrait.
LIFE OF LORD BYRON; with his Letters and Journals. By THOMAS MOORE. With Portraits.
LIFE OF LORD BYRON; with his Letters and Journals. By THOMAS MOORE. With Portraits.
ARCHBISHOP BECKET; A BIOGRAPHY. By CANON ROBERTSON, M.A. With Illustrations.
ARCHBISHOP BECKET: A BIOGRAPHY by Canon Robertson, M.A. With Illustrations.
PICTURES OF THE CHINESE, DRAWN BY THEMSELVES. Described by REV. R. H. COBBOLD. With 34 Illustrations.
PICTURES OF THE CHINESE, DRAWN BY THEMSELVES. Described by REV. R. H. COBBOLD. With 34 Illustrations.
THE ENGLISH BATTLES AND SIEGES OF THE PENINSULAR WAR. By SIR WILLIAM NAPIER. With Portrait.
THE ENGLISH BATTLES AND SIEGES OF THE PENINSULAR WAR. By SIR WILLIAM NAPIER. With Portrait.
THE YOUNG OFFICER’S COMPANION; or, Essays on Military Duties and Qualities: with Illustrations from History. By LORD DE ROS.
THE YOUNG OFFICER’S COMPANION; or, Essays on Military Tasks and Traits: with Images from History. By LORD DE ROS.
DOG-BREAKING; the most Expeditious, Certain, and Easy Method, whether great Excellence or only Mediocrity be required. With a Few Hints for those who Love the Dog and the Gun. By GENERAL HUTCHINSON. With Woodcuts.13
DOG-BREAKING; the quickest, most reliable, and easiest method, whether you aim for great skill or just decent performance. With some tips for those who love dogs and hunting. By GENERAL HUTCHINSON. With illustrations.13
LIST OF SCHOOL CLASSICS.
By DR. WILLIAM SMITH.
PRINCIPIA LATINA, Part I. A First Latin Course. A Grammar, Delectus, and Exercise Book with Vocabularies. 13th Edition. 3s. 6d.
PRINCIPIA LATINA, Part I. An Introductory Latin Course. A Grammar, Delectus, and Exercise Book with Vocabularies. 13th Edition. £3.50.
*** This Edition contains the Accidence arranged for the ‘Public School Latin Primer.’
*** This edition includes the Accidence organized for the 'Public School Latin Primer.'
PRINCIPIA LATINA, Part II. Latin Reading Book. An Introduction to Ancient Mythology, Geography, Roman Antiquities, and History. With Notes and a Dictionary. 3s. 6d.
PRINCIPIA LATINA, Part II. Latin Reading Guide. An Introduction to Ancient Mythology, Geography, Roman Antiquities, and History. With Notes and a Dictionary. 3s. 6d.
PRINCIPIA LATINA, Part III. Latin Poetry. 1. Easy Hexameters and Pentameters. 2. Eclogæ Ovidianæ. 3. Prosody and Metre. 4. First Latin Verse Book. 3s. 6d.
PRINCIPIA LATINA, Part III. Latin Poetry. 1. Simple Hexameters and Pentameters. 2. Ovidian Eclogues. 3. Prosody and Meter. 4. Introductory Latin Verse Book. 3s. 6d.
PRINCIPIA LATINA, Part IV. Latin Prose Composition. Rules of Syntax, with Examples, Explanations of Synonyms, and Exercises on the Syntax. 3s. 6d.
PRINCIPIA LATINA, Part IV. Latin Writing Skills. Rules of Syntax, with Examples, Explanations of Synonyms, and Exercises on the Syntax. £3.60
PRINCIPIA LATINA, Part V. Short Tales and Anecdotes from Ancient History, for Translation into Latin Prose. 3s.
PRINCIPIA LATINA, Part V. Short Stories and Anecdotes from Ancient History for Translation into Latin Prose. 3s.
A LATIN-ENGLISH VOCABULARY, with a Latin-English Dictionary to Phædrus, Cornelius Nepos, and Cæsar’s ‘Gallic War.’ 3s. 6d.
A LATIN-ENGLISH VOCABULARY, with a Latin-English Dictionary for Phædrus, Cornelius Nepos, and Cæsar’s ‘Gallic War.’ 3s. 6d.
THE STUDENT’S LATIN GRAMMAR. By WM. SMITH, D.C.L., and THEOPHILUS D. HALL. 6s.
THE STUDENT’S LATIN GRAMMAR. By WM. SMITH, D.C.L., and THEOPHILUS D. HALL. 6s.
A SMALLER LATIN GRAMMAR. Abridged from the above Work. 3s. 6d.
A SMALLER LATIN GRAMMAR. Abridged from the above Work. £3.50
INITIA GRÆCA, Part I. A First Greek Course, containing Grammar, Delectus, Exercise Book, and Vocabularies. By DR. WM. SMITH. 3s. 6d.
INITIA GRÆCA, Part I. An Introductory Greek Course, including Grammar, Delectus, Exercise Book, and Vocabularies. By DR. WM. SMITH. 3s. 6d.
INITIA GRÆCA, Part II. A Reading Book; containing short Tales, Anecdotes, Fables, Mythology, and Grecian History. With a Lexicon. 3s. 6d.
INITIA GRÆCA, Part II. A Reading Book; featuring short stories, anecdotes, fables, mythology, and Greek history. Includes a lexicon. 3s. 6d.
INITIA GRÆCA, Part III. Greek Prose Composition; containing the Rules of Syntax, with copious Examples and Exercises. 3s. 6d.
INITIA GRÆCA, Part III. Greek Prose Writing; including the Rules of Syntax, with plenty of Examples and Exercises. 3s. 6d.
THE STUDENT’S GREEK GRAMMAR. By PROFESSOR CURTIUS, and WM. SMITH, D.C.L. 6s.
THE STUDENT’S GREEK GRAMMAR. By PROFESSOR CURTIUS and WM. SMITH, D.C.L. 6s.
A SMALLER GREEK GRAMMAR. Abridged from the above Work. 3s. 6d.
A SMALLER GREEK GRAMMAR. Abridged from the above Work. £3.50
PRINCIPIA GRÆCA. A First Greek Course. A Grammar, Delectus, and Exercise Book, with Vocabularies. By H. E. BUTTON, M.A. 3s. 6d.
PRINCIPIA GRÆCA. Introductory Greek Course. A Grammar, Delectus, and Exercise Book, with Vocabularies. By H. E. BUTTON, M.A. 3s. 6d.
MATTHIÆ’S GREEK GRAMMAR. Abridged by BLOMFIELD. Revised and enlarged, by E. S. Crooke, B.A. 4s.
MATTHIÆ’S GREEK GRAMMAR. Abridged by BLOMFIELD. Revised and enlarged by E.S. Crooke, B.A. 4s.
KING EDWARD VI.’S FIRST LATIN BOOK; including a Short Syntax and Prosody with an English Translation. 2s. 6d.
KING EDWARD VI.’S FIRST LATIN BOOK; including a Short Syntax and Prosody with an English Translation. 2s. 6d.
KING EDWARD VI.’S LATIN GRAMMAR. 3s. 6d.
King Edward VI Latin Grammar. £3.60
ENGLISH NOTES FOR LATIN ELEGIACS; designed for Early Proficients in the Art of Latin Versification. By REV. W. OXENHAM. 3s. 6d.14
ENGLISH NOTES FOR LATIN ELEGIACS; created for early learners in the art of Latin verse writing. By REV. W. OXENHAM. 3s. 6d.14
LIST OF HANDBOOKS FOR TRAVELLERS.
THE CONTINENT, &c.
THE CONTINENT, etc.
HANDBOOK—TRAVEL TALK,—English, French, German, and Italian. 3s. 6d.
HANDBOOK—TRAVEL TALK,—English, French, German, and Italian. £3.50
HANDBOOK—NORTH GERMANY, Holland, Belgium, Prussia, and the Rhine to Switzerland. With Map and Plans.
HANDBOOK—NORTH GERMANY, Holland, Belgium, Prussia, and the Rhine up to Switzerland. With Map and Plans.
HANDBOOK—SOUTH GERMANY, The Tyrol, Bavaria, Austria, Salzburg, Styria, Hungary, and The Danube, from Ulm to the Black Sea. With Map and Plans. 10s.
HANDBOOK—SOUTH GERMANY, The Tyrol, Bavaria, Austria, Salzburg, Styria, Hungary, and the Danube, from Ulm to the Black Sea. With Map and Plans. £10.
HANDBOOK—SWITZERLAND, The Alps of Savoy and Piedmont. With Maps and Plans. 10s.
HANDBOOK—SWITZERLAND, The Alps of Savoy and Piedmont. With Maps and Plans. 10s.
HANDBOOK—FRANCE, Normandy, Brittany, The French Alps, Dauphine, Provence, and the Pyrenees. With Maps. 12s.
HANDBOOK—FRANCE, Normandy, Brittany, the French Alps, Dauphine, Provence, and the Pyrenees. With Maps. 12s.
HANDBOOK—PARIS AND ITS ENVIRONS. With Map and Plans. 3s. 6d.
HANDBOOK—PARIS AND ITS SURROUNDINGS. With Map and Plans. £3.60
*** Murray’s Plan of Paris. 3s. 6d.
*** Murray’s Plan of Paris. £3.30
HANDBOOK—CORSICA AND SARDINIA. With Map. 4s.
HANDBOOK—CORSICA AND SARDINIA. With Map. £4.
HANDBOOK—SPAIN, Madrid, The Castiles, The Basque Provinces, Leon, The Asturias, Galicia, Estremadura, Andalusia, Ronda, Granada, Murcia, Valencia, Catalonia, Aragon, Navarre, The Balearic Islands, &c., &c. With Maps. 2 vols. 24s.
HANDBOOK—SPAIN, Madrid, the Castiles, the Basque Provinces, León, the Asturias, Galicia, Extremadura, Andalusia, Ronda, Granada, Murcia, Valencia, Catalonia, Aragón, Navarre, the Balearic Islands, etc., etc. With Maps. 2 vols. 24s.
HANDBOOK—PORTUGAL, Lisbon, Porto, Cintra, Mafra, &c. With Map. 9s.
HANDBOOK—PORTUGAL, Lisbon, Porto, Sintra, Mafra, &c. With Map. 9s.
HANDBOOK—NORTH ITALY, Piedmont, Nice, Lombardy, Venice, Parma, Modena, and Romagna. With Map and Plans. 12s.
HANDBOOK—NORTH ITALY, Piedmont, Nice, Lombardy, Venice, Parma, Modena, and Romagna. With Map and Plans. £12.
HANDBOOK—CENTRAL ITALY, Tuscany, Florence, Lucca, Umbria, The Marches, and the Patrimony of St. Peter. With Map. 10s.
HANDBOOK—CENTRAL ITALY, Tuscany, Florence, Lucca, Umbria, The Marches, and the Vatican City. With Map. 10s.
HANDBOOK—ROME AND ITS ENVIRONS. With Map and Plans. 9s.
HANDBOOK—ROME AND ITS SURROUNDINGS. With Map and Plans. 9s.
HANDBOOK—SOUTH ITALY, Two Sicilies, Naples, Pompeii, Herculaneum, Vesuvius, Abruzzi, &c. With Map. 10s.
HANDBOOK—SOUTH ITALY, Two Sicilies, Naples, Pompeii, Herculaneum, Vesuvius, Abruzzi, & etc. With Map. 10s.
HANDBOOK—SICILY, Palermo, Messina, Catania, Syracuse, Etna, and the Ruins of the Greek Temples. With Map. 12s.
HANDBOOK—SICILY, Palermo, Messina, Catania, Syracuse, Mount Etna, and the Ruins of the Greek Temples. With Map. £12.
HANDBOOK—EGYPT, The Nile, Alexandria, Cairo, Thebes, and the Overland Route to India. With Map. 15s.
HANDBOOK—EGYPT, The Nile, Alexandria, Cairo, Thebes, and the Overland Route to India. With Map. £15.
HANDBOOK—GREECE, The Ionian Islands, Athens, Albania, Thessaly, and Macedonia. With Map.
HANDBOOK—GREECE, The Ionian Islands, Athens, Albania, Thessaly, and Macedonia. With Map.
HANDBOOK—Constantinople, The Bosphorus, Dardanelles, Brousa, and Plain of Troy, with General Hints for Travellers in Turkey, &c. With Map.15
HANDBOOK—Istanbul, The Bosphorus Strait, Dardanelles, Bursa and Troad Plain, along with General Tips for Travelers in Turkey, &c. With Map.15
HANDBOOK—DENMARK, Norway, Sweden, and Iceland. With Map and Plans.
HANDBOOK—DENMARK, Norway, Sweden, and Iceland. With map and plans.
HANDBOOK—RUSSIA, St. Petersburg, Moscow, Finland, &c. With Map. 15s.
HANDBOOK—RUSSIA, St. Petersburg, Moscow, Finland, etc. With Map. 15s.
HANDBOOK—INDIA, Bombay and Madras. With Map. 2 vols. 12s. each.
HANDBOOK—INDIA, Mumbai and Chennai. With Map. 2 volumes. £12 each.
HANDBOOK—HOLY LAND, Syria, Palestine, Sinai, Edom, and the Syrian Deserts. With Map. 2 vols. 24s.
HANDBOOK—HOLY LAND, Syria, Palestine, Sinai, Edom, and the Syrian deserts. With Map. 2 vols. £24.
KNAPSACK GUIDES FOR TRAVELLERS.
KNAPSACK GUIDE TO SWITZERLAND. With Plans. 5s.
KNAPSACK GUIDE TO SWITZERLAND. With Maps. 5s.
KNAPSACK GUIDE TO NORWAY. With Map. 6s.
KNAPSACK GUIDE TO NORWAY. With Map. £6.
KNAPSACK GUIDE TO ITALY. With Plans. 6s.
KNAPSACK GUIDE TO ITALY. With Maps. £6.
KNAPSACK GUIDE TO THE TYROL. With Plans. 6s.
KNAPSACK GUIDE TO THE TYROL. With Maps. 6s.
ENGLAND AND WALES.
England and Wales.
HANDBOOK—LONDON AS IT IS. With Map and Plans. 3s. 6d.
HANDBOOK—LONDON AS IT IS. With Map and Plans. £3.60.
HANDBOOK—ESSEX, CAMBRIDGE, SUFFOLK, AND NORFOLK—Chelmsford, Colchester, Maldon, Cambridge, Ely, Newmarket, Bury, Ipswich, Woodbridge, Felixstowe, Lowestoft, Norwich, Yarmouth, Cromer, &c. With Maps and Plans. 12s.
HANDBOOK—ESSEX, CAMBRIDGE, SUFFOLK, AND NORFOLK—Chelmsford, Colchester, Maldon, Cambridge, Ely, Newmarket, Bury, Ipswich, Woodbridge, Felixstowe, Lowestoft, Norwich, Yarmouth, Cromer, etc. With Maps and Plans. £12.
HANDBOOK—KENT AND SUSSEX—Canterbury, Dover, Ramsgate, Rochester, Chatham, Brighton, Chichester, Worthing, Hastings, Lewes, Arundel. With Map. 10s.
HANDBOOK—KENT AND SUSSEX—Canterbury, Dover, Ramsgate, Rochester, Chatham, Brighton, Chichester, Worthing, Hastings, Lewes, Arundel. With Map. £10.
HANDBOOK—SURREY AND HANTS—Kingston, Croydon, Reigate, Guildford, Dorking, Boxhill, Winchester, Southampton, Portsmouth, and The Isle of Wight. With Map. 10s.
HANDBOOK—SURREY AND HANTS—Kingston, Croydon, Reigate, Guildford, Dorking, Boxhill, Winchester, Southampton, Portsmouth, and the Isle of Wight. With Map. 10s.
HANDBOOK—BERKS, BUCKS, AND OXON—Windsor, Eton, Reading, Aylesbury, Henley, Oxford, and the Thames. With Map. 7s. 6d.
HANDBOOK—BERKS, BUCKS, AND OXON—Windsor, Eton, Reading, Aylesbury, Henley, Oxford, and the Thames. Includes Map. 7.50
HANDBOOK—WILTS, DORSET, AND SOMERSET—Salisbury, Chippenham, Weymouth, Sherborne, Wells, Bath, Bristol, Taunton, &c. With Map. 10s.
HANDBOOK—WILTS, DORSET, AND SOMERSET—Salisbury, Chippenham, Weymouth, Sherborne, Wells, Bath, Bristol, Taunton, etc. With Map. £10.
HANDBOOK—DEVON AND CORNWALL—Exeter, Ilfracombe, Linton, Sidmouth, Dawlish, Teignmouth, Plymouth, Devonport, Torquay, Launceston, Penzance, Falmouth, The Lizard, Land‘s End, &c. With Map. 10s.16
HANDBOOK—DEVON AND CORNWALL—Exeter, Ilfracombe, Linton, Sidmouth, Dawlish, Teignmouth, Plymouth, Devonport, Torquay, Launceston, Penzance, Falmouth, The Lizard, Land's End, etc. With Map. £10.16
HANDBOOK—GLOUCESTER, HEREFORD, AND WORCESTER—Cirencester, Cheltenham, Stroud, Tewkesbury, Leominster, Ross, Malvern, Kidderminster, Dudley, Bromsgrove, Evesham. With Map. 6s. 6d.
HANDBOOK—GLOUCESTER, HEREFORD, AND WORCESTER—Cirencester, Cheltenham, Stroud, Tewkesbury, Leominster, Ross, Malvern, Kidderminster, Dudley, Bromsgrove, Evesham. With Map. 6s. 6d.
HANDBOOK—NORTH WALES—Bangor, Carnarvon, Beaumaris, Snowdon, Conway, &c. With Map. 6s. 6d.
HANDBOOK—NORTH WALES—Bangor, Caernarfon, Beaumaris, Snowdon, Conwy, etc. With Map. 6s. 6d.
HANDBOOK—SOUTH WALES—Monmouth, Carmarthen, Tenby, Swansea, and the Wye, &c. With Map. 7s.
HANDBOOK—SOUTH WALES—Monmouth, Carmarthen, Tenby, Swansea, and the Wye, etc. With Map. 7s.
HANDBOOK—DERBY, NOTTS, LEICESTER, AND STAFFORD—Matlock, Bakewell, Chatsworth, The Peak, Buxton, Hardwick, Dove Dale, Ashborne, Southwell, Mansfield, Retford, Burton, Belvoir, Melton Mowbray, Wolverhampton, Litchfield, Walsall, Tamworth. With Map. 7s. 6d.
HANDBOOK—DERBY, NOTTS, LEICESTER, AND STAFFORD—Matlock, Bakewell, Chatsworth, The Peak, Buxton, Hardwick, Dove Dale, Ashbourne, Southwell, Mansfield, Retford, Burton, Belvoir, Melton Mowbray, Wolverhampton, Lichfield, Walsall, Tamworth. With Map. 7s. 6d.
HANDBOOK—SHROPSHIRE, CHESHIRE, AND LANCASHIRE—Shrewsbury, Ludlow, Bridgnorth, Oswestry, Chester, Crewe, Alderley, Stockport, Birkenhead, Warrington, Bury, Manchester, Liverpool, Burnley, Clitheroe, Bolton, Blackburn, Wigan, Preston, Rochdale, Lancaster, Southport, Blackpool, &c. With Map. 10s.
HANDBOOK—SHROPSHIRE, CHESHIRE, AND LANCASHIRE—Shrewsbury, Ludlow, Bridgnorth, Oswestry, Chester, Crewe, Alderley, Stockport, Birkenhead, Warrington, Bury, Manchester, Liverpool, Burnley, Clitheroe, Bolton, Blackburn, Wigan, Preston, Rochdale, Lancaster, Southport, Blackpool, etc. With Map. £10.
HANDBOOK—YORKSHIRE—Doncaster, Hull, Selby, Beverley, Scarborough, Whitby, Harrogate, Ripon, Leeds, Wakefield, Bradford, Halifax, Huddersfield, Sheffield. With Map. 12s.
HANDBOOK—YORKSHIRE—Doncaster, Hull, Selby, Beverley, Scarborough, Whitby, Harrogate, Ripon, Leeds, Wakefield, Bradford, Halifax, Huddersfield, Sheffield. With Map. 12s.
HANDBOOK—DURHAM AND NORTHUMBERLAND—Newcastle, Darlington, Bishop Auckland, Stockton, Hartlepool, Sunderland, Shields, Berwick, Tynemouth, Alnwick. With Map. 9s.
HANDBOOK—DURHAM AND NORTHUMBERLAND—Newcastle, Darlington, Bishop Auckland, Stockton, Hartlepool, Sunderland, Shields, Berwick, Tynemouth, Alnwick. With Map. 9s.
HANDBOOK—WESTMORLAND AND CUMBERLAND—Lancaster, Furness Abbey, Ambleside, Kendal, Windermere, Coniston, Keswick, Grasmere, Carlisle, Cockermouth, Penrith, Appleby. With Map. 6s.
HANDBOOK—WESTMORLAND AND CUMBERLAND—Lancaster, Furness Abbey, Ambleside, Kendal, Windermere, Coniston, Keswick, Grasmere, Carlisle, Cockermouth, Penrith, Appleby. With Map. 6s.
*** Murray‘s Map of the Lake District, 3s. 6d.
*** Murray's Map of the Lake District, £3.60
HANDBOOK—SCOTLAND—Edinburgh, Melrose, Kelso, Glasgow, Dumfries, Ayr, Stirling, Arran, The Clyde, Oban, Inverary, Loch Lomond, Loch Katrine and Trosachs, Caledonian Canal, Inverness, Perth, Dundee, Aberdeen, Braemar, Skye, Caithness, Ross, and Sutherland. With Maps and Plans. 9s.
HANDBOOK—SCOTLAND—Edinburgh, Melrose, Kelso, Glasgow, Dumfries, Ayr, Stirling, Arran, The Clyde, Oban, Inveraray, Loch Lomond, Loch Katrine and Trosachs, Caledonian Canal, Inverness, Perth, Dundee, Aberdeen, Braemar, Skye, Caithness, Ross, and Sutherland. With Maps and Plans. 9s.
HANDBOOK—IRELAND—Dublin, Belfast, Donegal, Galway, Wexford, Cork, Limerick, Waterford, Killarney, Munster. With Map. 12s.
HANDBOOK—IRELAND—Dublin, Belfast, Donegal, Galway, Wexford, Cork, Limerick, Waterford, Killarney, Munster. With Map. 12s.
JOHN MURRAY, 50a, ALBEMARLE STREET.
LONDON: PRINTED BY WILLIAM CLOWES AND SONS, STAMFORD STREET, AND CHARING CROSS.
TRANSCRIBERS' NOTES
Footnote 292 spells the city Charleston but the text has it as Charlestown. This is as in the original book.
Footnote 292 spells the city Charleston, but the text refers to it as Charlestown. This is consistent with the original book.
Inconsistent spelling of St. Petersburg/Petersburgh as in the original text.
Inconsistent spelling of St. Petersburg/Petersburgh as in the original text.
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