This is a modern-English version of My Studio Neighbors, originally written by Gibson, W. Hamilton (William Hamilton).
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and grammar—to ensure clarity for contemporary readers, while preserving the original spirit and nuance. If
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MY STUDIO NEIGHBORS
BY
WILLIAM HAMILTON GIBSON
ILLUSTRATED BY THE AUTHOR
NEW YORK AND LONDON
HARPER & BROTHERS PUBLISHERS
1898
Copyright, 1897, by Harper & Brothers.
All rights reserved.
NEW YORK AND LONDON
HARPER & BROTHERS PUBLISHERS
1898
Copyright, 1897, by HarperCollins.
All rights reserved.
Transcriber note: Page 132 has wide margins to accommodate the illustration.
Transcriber note: Page 132 has wide margins to fit the illustration.

Page | |
A Familiar Guest | 3 |
The Cuckoos and the Outwitted Cow-bird | 23 |
Door-step Neighbors | 57 |
A Queer Little Family on the Bittersweet | 87 |
The Welcomes of the Flowers | 105 |
A Honey-dew Picnic | 151 |
A Few Native Orchids and Their Insect Sponsors | 171 |
The Milkweed | 227 |
Index | 239 |

Page | |
William Hamilton Gibson | Frontispiece |
Initial. The Studio Door | 3 |
The Rose-bush Episode | 9 |
A Corner of My Table | 12 |
An Animated Brush | 14 |
A Specimen in Three Stages | 16 |
The Studio Table | 18 |
Initial | 23 |
The European Cuckoo | 24 |
The Yellow-billed Cuckoo | 26 |
Browsing Kine | 29 |
A Greedy Foster-child | 34 |
The Yellow Warbler | 44 |
A Blighted Home | 46 |
The Normal Nest of the Yellow Warbler | 47 |
The Yellow Warbler at Home | 49 |
A Suspicious Nest of the Yellow Warbler | 50 |
The Nest Separated | 52 |
Initial | 57 |
The Door-step Arena, with its Pitfalls | 60 |
Fishing for Tigers | 65 |
Tiger-beetle | 68 |
The Spider Victim | 70 |
Filling the Spider's Grave | 71 |
Black Digger-wasp | 73 |
Black Digger-wasp and His Victim, Showing the Egg of the Wasp Attached | 75 |
Protecting the Burrow while Searching for Prey | 79 |
The "Cow-spit" Mystery Disclosed | 81 |
The Tiger's Head, from the Victim's Stand-point | 84 |
Initial. Branch of the Bittersweet | 87 |
A Bittersweet Covey | 90 |
Flushing the Game | 92 |
Specimen Twig | 94 |
Building Froth-tent | 100 |
Butterflies and Flowers | 105 |
A Row of Stamens | 106 |
The Parts of a Flower | 109 |
Historical Series, Showing the Progress of Discovery of Flower Fertilization | 110 |
The Garden Sage | 120 |
Cross-fertilization of the Sage | 121 |
Elastic Stamens. Anthers Inserted in their Pockets | 124 |
Elastic Stamens of Mountain-laurel | 125 |
Andromeda Ligustrina | 127 |
Fertilisation of Andromeda | 128 |
The Laurel | 130 |
Cross-fertilization of the Blue-flag | 131 |
Blue-flag | 132 |
Pogonia and Devil's-bit | 133 |
Devil's-bit | 134 |
Horse-balm. Collinsonia | 135 |
Cross-fertilization of the Horse-balm—Flowers in Various Stages, and in the Order of their Visitation by the Bee | 136 |
The Cone-flower | 137 |
Cone-flower, Showing Numerous Florets, Some in Pollen, Others in Stigmatic Stage | 139 |
Cross-fertilization of Cone-flower | 140 |
The Fertilization of the English Arum, 1st Stage | 141 |
The Fertilization of the English Arum. 2d, 3d, 4th, and 5th Stages | 142 |
Pogonia | 145 |
Cross-fertilization | 146 |
A Pine Branch | 151 |
Initial | 151 |
The Picnic | 159 |
Tail-piece | 167 |
Habenaria Orbiculata | 171 |
Arethusa Bulbosa | 177 |
The Botanical Distribution of an Ordinary Flower and of the Orchid | 182 |
The "Column" in Various Orchids | 183 |
The Result of the Bee's Visit | 184 |
Cross-fertilization of Arethusa | 188 |
Habenaria Orbiculata. A Single Flower Enlarged | 190 |
Orchis Spectabilis | 191 |
Cross-fertilization of H. Orbiculata (Sphinx-moth) | 193 |
The Flower and Column of Orchis Spectabilis, Enlarged | 195 |
Orchis Spectabilis | 195 |
Position of Pollen of Orchis Spectabilis Withdrawn on Pencil | 197 |
The Cross-fertilization of Orchis Spectabilis | 197 |
The Purple-fringed Orchid | 199 |
The Ragged Orchid (Front Section) | 200 |
The Ragged Orchid (Profile Section) | 202 |
The Ragged Orchid (H. Lacera) and the Butterfly's Tongue. Cross-fertilization | 203 |
The Yellow Orchid (H. Flava) | 204 |
The Ragged Orchid (H. Lacera) | 205 |
Cypripedium Acaule | 207 |
Moccasin-flower (C. Acaule) | 208 |
The Bee Imprisoned in the Lips of Cypripedium | 210 |
Moccasin-flower. Bee Sipping Nectar | 211 |
The Bee Passing Beneath the Stigma | 213 |
A Bee Receiving Pollen-plaster on His Thorax | 214 |
Rattlesnake-Plantain—the Young and the Old | 215 |
Cross-fertilization of the Rattlesnake-Plantain. Side Sections | 216 |
Cross-fertilisation of the Rattlesnake-Plantain. Front View | 217 |
The Tongue of a Bumblebee | 218 |
Goodyera, or Periamium Pubescens | 221 |
Milkweed Captives | 231 |
The Pollen Masses and the Fissure | 232 |
The Tragedy of the Bees | 235 |
A Moth Caught by the Tongue in Dogbane | 237 |
A FAMILIAR GUEST


olitude! Where under trees and sky shall you find it? The more solitary the recluse and the more confirmed and grounded his seclusion, the wider and more familiar becomes the circle of his social environment, until at length, like a very dryad of old,[Pg 4] the birds build and sing in his branches and the "wee wild beasties" nest in his pockets. If he fails to be aware of the fact, more's the pity. His desolation is within, not without, in spite of, not because of, his surroundings.
Feeling lonely! Where under trees and sky can you truly find it? The more isolated the recluse and the more established and rooted his solitude, the broader and more familiar his social circle becomes, until eventually, like an ancient dryad,[Pg 4] the birds build their nests and sing in his branches, and the "little wild creatures" settle in his pockets. If he's unaware of this, that's unfortunate. His loneliness comes from within, not from outside, despite his surroundings, not because of them.
Here in my country studio—not a hermitage, 'tis true, but secluded among trees, some distance isolated from my own home and out of sight of any other—what company! What occasional "tumultuous privacy" is mine! I have frequently been obliged to step out upon the porch and request a modulation of hilarity and a more courteous respect for my hospitality. But this is evidently entirely a matter of point of view, and, judging from the effects of my protests at such times, my assumed superior air of condescension is apparently construed as a huge joke. If the resultant rejoinder of wild volapük and expressive pantomime has any significance, it is plain that I am desired to understand that my exact status is that of a squatter on contested territory.
Here in my country studio—not a hermitage, it’s true, but tucked away among trees, a good distance from my home and out of sight of anyone else—what company! What occasional "wild privacy" I have! I’ve often had to step out onto the porch and ask for a little less laughter and a bit more respect for my hospitality. But this is obviously all about perspective, and judging from the reactions during those times, my feigned air of superiority is seen as a big joke. If the resulting outbursts of gibberish and dramatic gestures mean anything, it’s clear that I’m expected to understand that my actual status is that of a squatter on disputed land.
There are those snickering squirrels, for instance! At this moment two of them are having a rollicking game of tag on the shingled roof—a pandemonium of scrambling, scratching, squealing, and growling—ever and anon clambering[Pg 5] down at the eaves to the top of a blind and peeping in at the window to see how I like it.
There are those giggling squirrels, for example! Right now, two of them are having a fun game of tag on the shingled roof—a wild mix of scrambling, scratching, squealing, and growling—occasionally climbing down to the eaves to peek in at the window to see how I’m doing.
A woodchuck is perambulating my porch—he was a moment ago—presumably in renewed quest of that favorite pabulum more delectable than rowen clover, the splintered cribbings from the legs of a certain pine bench, which, up to date, he has lowered about three inches—a process in which he has considered average rather than symmetry, or the comfort of the too trusting visitor who happens to be unaware of his carpentry.
A woodchuck was just wandering around my porch, probably looking for his favorite snack that's even better than clover—some chewed-up bits from the legs of a certain pine bench. So far, he's taken it down by about three inches, focusing more on the result than on how it looks or the comfort of any unsuspecting guests who don’t realize he's been doing some woodwork.
The drone of bees and the carol of birds are naturally an incessant accompaniment to my toil—at least, in these spring and summer months. The tall, straight flue of the chimney, like the deep diapason of an organ, is softly murmurous with the flurry of the swifts in their afternoon or vesper flight. There is a robin's nest close by one window, a vireo's nest on a forked dogwood within touch of the porch, and continual reminders of similar snuggeries of indigo-bird, chat, and oriole within close limits, to say nothing of an ants' nest not far off, whose proximity is soon manifest as you sit in the grass—and immediately get up again.
The buzzing of bees and the songs of birds are naturally an endless background to my work—at least during the spring and summer months. The tall, straight chimney resembles the deep sound of an organ, softly humming with the flurry of the swifts during their afternoon or evening flights. There's a robin's nest right by one window, a vireo's nest on a forked dogwood tree near the porch, and constant reminders of similar cozy nests belonging to indigo birds, chats, and orioles nearby, not to mention an ants' nest not far away, whose presence becomes clear as you sit in the grass—and quickly find yourself standing up again.
Fancy a wild fox for a daily entertainment! For several days in succession last year I spent a[Pg 6] half-hour observing his frisky gambols on the hillside across the dingle below my porch, as he jumped apparently for mice in the sloping rowen-field. How quickly he responded to my slightest interruption of voice or footfall, running to the cover of the alders!
Fancy a wild fox as your daily entertainment! For several days in a row last year, I spent a[Pg 6] half-hour watching his playful antics on the hillside across the valley below my porch, as he jumped around seemingly searching for mice in the sloping field. He reacted so quickly to the slightest sound of my voice or footsteps, darting into the cover of the alders!
The little red-headed chippy, the most familiar and sociable of our birds, of course pays me his frequent visit, hopping in at the door and picking up I don't know what upon the floor. A barn-swallow occasionally darts in through the open window and out again at the door, as though for very sport, only a few days since skimming beneath my nose, while its wings fairly tipped the pen with which I was writing. The chipmonk has long made himself at home, and his scratching footsteps on my door-sill, or even in my closet, is a not uncommon episode. Now and then through the day I hear a soft pat-pat on the hard-wood floor, at intervals of a few seconds, and realize that my pet toad, which has voluntarily taken up its abode in an old bowl on the closet floor, is taking his afternoon outing, and with his always seemingly inconsistent lightning tongue is picking up his casual flies at three inches sight around the base-board.
The little red-headed chipmunk, the friendliest and most social of our birds, often pays me a visit, hopping through the door and picking up who knows what off the floor. A barn swallow sometimes darts in through the open window and out again at the door, almost for fun, just the other day skimming right past my nose, while its wings nearly brushed the pen I was writing with. The chipmunk has made himself quite at home, and it’s not unusual to hear his scratching footsteps on my door sill or even in my closet. Occasionally throughout the day, I hear a soft pat-pat on the hardwood floor, spaced out every few seconds, and I realize that my pet toad, which has chosen to live in an old bowl on the closet floor, is taking his afternoon stroll, and with his seemingly inconsistent lightning-fast tongue, is catching flies that come within three inches of the baseboard.
A mouse, I see, has heaped a neat little pile of[Pg 7] seeds upon the top of the wainscot near by—cherry pits, polygonum, and ragweed seeds, and others, including some small oak-galls, which I find have been abstracted from a box of specimens which I had stored in the closet for safe-keeping. I wonder if it is the same little fellow that built its nest in an old shoe in the same closet last year, and, among other mischief, removed the white grub in a similar lot of specimen galls which I also missed, and subsequently found in the shoe and scattered on the closet floor?
A mouse, I see, has made a neat little pile of [Pg 7] seeds on top of the wainscot nearby—cherry pits, polygonum, ragweed seeds, and others, including some small oak-galls that I’ve noticed were taken from a box of specimens I had kept in the closet for safekeeping. I wonder if it’s the same little guy that built its nest in an old shoe in the same closet last year, and, among other trouble, took the white grub from a similar batch of specimen galls that I also noticed missing and later found in the shoe and scattered on the closet floor?
I have mentioned the murmur of the bees, but the incessant buzzing of flies and wasps is an equally prominent sound. Then there is the occasional sortie of the dragon-fly, making his gauzy, skimming circuit about the room, or suggestively bobbing around against wall or ceiling; and that occasional audible episode of the stifled, expiring buzz of a fly, which is too plainly in the toils of Arachne up yonder! For in one corner of my room I boast of a prize dusty "cobweb," as yet spared from the household broom, a gossamer arena of two years' standing, which makes a dense span of a length of about two feet from a clump of dried hydrangea blossoms to the sill of a transom-window, and which, of course, some[Pg 8]where in its dusty spread, tapers off into a dark tunnel, where lurks the eight-eyed schemer, "o'erlooking all his waving snares around."
I’ve talked about the buzz of the bees, but the constant hum of flies and wasps is just as noticeable. Then there’s the occasional flight of a dragonfly, gliding gracefully around the room or playfully darting against the walls and ceiling; plus, there’s the rare sound of a fly’s muffled, fading buzz, clearly caught in Arachne's trap up there! In one corner of my room, I take pride in a dusty "cobweb," still untouched by the household broom, a delicate web that’s been there for two years, stretching nearly two feet from a bunch of dried hydrangea blossoms to the transom window sill, and, of course, somewhere within its dusty web, it narrows into a dark tunnel, where the eight-eyed hunter waits, “overlooking all his waving snares around.”
Sooner or later, it would seem, every too constant buzzing visitor encroaches on its domain, and is drawn to its silken vortex, and is eventually shed below as a clean dried specimen; for this is an agalena spider, which dispenses with the winding-sheet of the field species—epeira and argiope. Last week a big bumble-bee-like fly paid me a visit and suddenly disappeared. To-day I find him dried and ready for the insect-pin and the cabinet on the window-sill beneath the web, which affords at all times its liberal entomological assortment—Coleoptera, Hymenoptera, Diptera, and Lepidoptera. Many are the rare specimens which I have picked from these charnel remnants of my spider net.
Sooner or later, it seems that every persistent buzzing visitor invades its space, gets drawn into its silky trap, and eventually ends up discarded below as a clean, dried specimen; this is an agalena spider, which does without the wrapping of field species like epeira and argiope. Last week, a large fly that resembled a bumblebee came to visit and suddenly vanished. Today, I find it dried out and ready for pinning and displaying in the cabinet on the windowsill beneath the web, which always offers a generous variety of insects—Coleoptera, Hymenoptera, Diptera, and Lepidoptera. Many rare specimens have been collected from these macabre remnants of my spider's web.
Ah, hark! The talking "robber-fly" (Asilus), with his nasal, twangy buzz! "Waiow! Wha-a-ar are ye?" he seems to say, and with a suggestive onslaught against the window-pane, which betokens his satisfied quest, is out again at the window with a bluebottle-fly in the clutch of his powerful legs, or perhaps impaled on his horny beak.
Ah, listen! The talking "robber-fly" (Asilus), with his sharp, buzzing sound! "Waiow! Where are you?" he seems to say, and with a determined attack against the window, which shows he’s accomplished his mission, he's back at the window with a bluebottle-fly caught in his strong legs, or maybe pinned on his tough beak.
Solitude! Not here. Amid such continual distraction and entertainment concentration on[Pg 9] the immediate task in hand is not always of easy accomplishment.
Solitude! Not here. With constant distractions and entertainment, focusing on the[Pg 9] task at hand isn't always easy.

Last week, after a somewhat distracted morning with some queer beguiling little harlequins on the bittersweet-vine about my porch, of which I have previously written, I had finally settled down to my work, and was engaged in putting the finishing touches upon a long-delayed drawing, when a new visitor claimed my attention—a small hornet, which alights upon the window-sill within half a yard from my face. To be sure, she was no stranger here at my studio—even now there are two of her yonder beneath the spider-nest—and was, moreover, an old friend, whose ways were perfectly familiar to me; but this time the insect engaged my particular attention be[Pg 10]cause it was not alone, being accompanied by a green caterpillar bigger than herself, which she held beneath her body as she travelled along on the window-sill so near my face. "So, so! my little wren-wasp, you have found a satisfactory cranny at last, and have made yourself at home. I have seen you prying about here for a week and wondered where you would take up your abode."
Last week, after a somewhat distracted morning with some charming little harlequins on the bittersweet vine on my porch, which I’ve mentioned before, I finally settled down to work and was putting the finishing touches on a long-overdue drawing when a new visitor caught my eye—a small hornet, landing on the window sill just half a yard from my face. She was no stranger to my studio; even now there are two of her over there beneath the spider’s nest—and she was, in fact, an old friend whose behavior I knew well. But this time, the insect grabbed my attention because she wasn’t alone; she had a green caterpillar, larger than herself, which she was carrying underneath her body as she moved along the window sill so close to my face. “So, so! My little wren-wasp, you’ve finally found a cozy spot and made yourself at home. I’ve seen you exploring around here for a week and wondered where you would settle down.”
The insect now reaches the edge of the sill, and, taking a fresh grip on her burden, starts off in a bee-line across my drawing-board and towards the open door, and disappears. Wondering what her whimsical destination might be, my eye involuntarily began to wander about the room in quest of nail-holes or other available similar crannies, but without reward, and I had fairly settled back to my work and forgotten the incident, when the same visitor, or another just like her, again appeared, this time clearing the window-sill in her flight, and landing directly upon my drawing-board, across which she sped, half creeping, half in flight, and tugging her green caterpillar as before—longer than herself—which she held beneath her body.
The insect reaches the edge of the sill, then grabs her load and heads straight across my drawing board toward the open door before disappearing. Curious about where she was going, I started scanning the room for nail holes or other tiny openings, but found nothing. I settled back into my work and had almost forgotten about the incident when the same visitor, or another one just like her, showed up again. This time, she flew off the window sill and landed right on my drawing board, speeding across it by half crawling and half flying while dragging her green caterpillar, which was longer than herself, beneath her body.
"This time I shall learn your secret," I thought. "Two such challenges as this are not to be ig[Pg 11]nored." So I concluded this time to observe her progress carefully. In a moment she had reached the right-hand edge of my easel-board, from which she made a short flight, and settled upon a large table in the centre of the room, littered with its characteristic chaos of professional paraphernalia—brushes, paints, dishes, bottles, color-boxes, and cloths—among which she disappeared. It was a hopeless task to disclose her, so I waited patiently to observe the spot from which she would emerge, assuming that this, like the window-sill and my easel, was a mere way-station on her homeward travels. But she failed to appear, while I busied my wits in trying to recall which particular item in the collection had a hole in it. Yes, there was a spool among other odds and ends in a Japanese boat-basket. That must be it! But on examination the paper still covered both ends, and I was again at a loss. What, then, can be the attraction on my table? My wondering curiosity was immediately satisfied, for as I turned back to the board and resumed my work I soon discovered another wasp, with its caterpillar freight, on the drawing-board. After a moment's pause she made a quiet short flight towards the table, and what was my astonishment to observe her alight directly upon the tip of the[Pg 12] very brush which I held in my hand, which, I now noted for the first time, had a hole in its end! In another moment she disappeared within the cavity, tugging the caterpillar after her!
"This time I'm going to figure out your secret," I thought. "I can't ignore two challenges like this." So, I decided to carefully watch her progress. In no time, she reached the right edge of my easel, made a quick flight, and landed on a large table in the middle of the room, cluttered with a typical mess of professional supplies—brushes, paints, dishes, bottles, palettes, and rags—among which she vanished. It was a hopeless task to reveal her, so I patiently waited to see where she would come out, assuming that this, like the window sill and my easel, was just another stop on her way home. But she didn’t show up, while I tried to recall which item in the mess had a hole in it. Yes, there was a spool among other odds and ends in a Japanese boat-basket. That had to be it! But when I checked, the paper still covered both ends, and I was stumped again. What could be so interesting on my table? My curiosity was quickly satisfied because when I turned back to the board and got back to work, I soon spotted another wasp with its caterpillar on the drawing board. After a brief pause, it quietly flew toward the table, and I was shocked to see it land directly on the tip of the[Pg 12] very brush I was holding, which, for the first time, I noticed had a hole in its end! In an instant, she disappeared into the opening, pulling the caterpillar along with her!

My bamboo brushes! I had not thought of[Pg 13] them! By mere chance a few years since I happened upon some of these bamboo brushes in a Japanese shop—large, long-handled brushes, with pure white hair nicely stiffened to a tapering point, which was neatly protected with a sheathing cover of bamboo. A number of them were at my elbow, a few inches distant, in a glass of water, and on the table by the vase beyond were a dozen or so in a scattered bundle.
My bamboo brushes! I hadn’t thought about[Pg 13] them! A few years ago, I randomly came across some bamboo brushes in a Japanese store—big, long-handled brushes with pure white bristles that were nicely stiffened to a pointed tip, which was neatly covered with a sheath of bamboo. Several were next to me, just a few inches away, in a glass of water, and on the table by the vase beyond were about a dozen more in a messy bundle.
Normally each of these brushes is closed at the end by the natural pith of the bamboo. I now find them all either open or otherwise tampered with, and the surrounding surface of the table littered with tiny balls, apparently of sawdust. I picked up one of the nearest brushes, and upon inverting it and giving it a slight tap, a tiny green worm fell out of the opening. From the next one I managed to shake out seven of the caterpillars, while the third had passed beyond this stage, the aperture having been carefully plugged with a mud cork, which was even now moist. Two or three others were in the same plugged condition, and investigation showed that no single brush had escaped similar tampering to a greater or less extent. One brush had apparently not given entire satisfaction, for the plug had been removed, and the caterpillars, eight or ten in number, were[Pg 14] scattered about the opening. But the dissatisfaction probably lay with one of these caterpillars rather than with the maternal wasp, who had apparently failed in the full dose of anæsthetic, for one of her victims which I observed was quite lively, and had probably forced out the soft plug, and in his squirming had ousted his luckless companions.
Normally, each of these brushes is closed at the end by the natural pith of the bamboo. I now find them all either open or otherwise messed with, and the surrounding surface of the table littered with tiny balls that look like sawdust. I picked up one of the nearest brushes, and after inverting it and giving it a slight tap, a tiny green worm fell out of the opening. From the next one, I managed to shake out seven caterpillars, while the third had moved beyond this stage, the opening carefully sealed with a mud cork that was still moist. Two or three others were in the same sealed condition, and investigation showed that no single brush had escaped some form of tampering to a greater or lesser degree. One brush clearly hadn’t done the job right, as the plug had been removed, and the caterpillars, eight or ten in number, were scattered about the opening. But the issue probably lay with one of these caterpillars rather than with the mother wasp, who had apparently not done a thorough job with the anesthetic, because one of her victims that I observed was quite lively, and had likely forced out the soft plug, displacing his unfortunate companions in the process.

The caterpillars were all of the same kind, though varying in size, their length being from one-half to three-quarters of an inch. To all appearances they were dead, but more careful observation revealed signs of slight vitality. Recognizing the species as one which I had long known, from its larva to its moth, it was not difficult to understand how my brushes might thus have been expeditiously packed with them. Not far from my studio door is a small thicket of[Pg 15] wild rose, which should alone be sufficient to account for all those victimized caterpillars. This species is a regular dependent on the rose, dwelling within its cocoon-like canopy of leaves, which are drawn together with a few silken webs, and in which it is commonly concealed by day. A little persuasion upon either end of its leafy case, however, soon brings the little tenant to view as he wriggles out, backward or forward, as the case may be, and in a twinkling, spider-like, hangs suspended by a web, which never fails him even in the most sudden emergency.
The caterpillars were all the same type, though they varied in size, measuring between half an inch to three-quarters of an inch long. At first glance, they seemed dead, but a closer look showed they were still slightly alive. Since I recognized the species as one I had known for a long time, from its larva to its moth, it was easy to see how my brushes could have been quickly packed with them. Not far from my studio door, there's a small thicket of[Pg 15] wild rose, which alone could explain the many caterpillars I found. This species regularly relies on the rose, living in its cocoon-like canopy of leaves, which are pulled together with a few strands of silk, and where it usually hides during the day. With a little encouragement from either end of its leafy home, the little creature quickly reveals itself, wriggling out, either backward or forward, depending on the situation, and in an instant, like a spider, it hangs by a web, which always holds strong even in emergencies.
I can readily fancy the tiny hornet making a commotion at one end of this leafy domicile and the next instant catching the evicted caterpillar "on a fly" at the other. Grasping her prey with her legs and jaws, in another moment the wriggling body is passive in her grasp, subdued by the potent anæsthetic of her sting—a hypodermic injection which instantly produces the semblance of death in its insect victim, reducing all the vital functions to the point of dissolution, and then holds them suspended—literally prolongs life, it would sometimes seem, even beyond its normal duration—by a process which I might call ductile equation. This chemical resource is common to all the hornets, whether their victims be grass[Pg 16]hoppers, spiders, cicadæ, or caterpillars. In a condition of helpless stupor they are lugged off to the respective dens provided for them, and then, hermetically sealed on storage, are preserved as fresh living food for the young hornet larva, which is left in charge of them, and has a place waiting for them all. The developments within my brush-handles may serve as a commentary on the ways and transformations of the average hornet.
I can easily imagine the small hornet causing a stir at one end of this leafy home and the next moment catching the evicted caterpillar "on the fly" at the other. Grabbing her prey with her legs and jaws, in an instant the wriggling body goes limp in her hold, subdued by the powerful anesthetic of her sting—a hypodermic injection that quickly gives the illusion of death to its insect victim, slowing all vital functions to the brink of collapse, then keeping them suspended—literally seeming to extend life even beyond its normal duration—through a process I might call ductile equation. This chemical tactic is shared by all hornets, whether their victims are grasshoppers, spiders, cicadas, or caterpillars. In a state of helpless stupor, they are taken to their designated dens, and then, sealed up tightly for storage, they are preserved as fresh living food for the young hornet larvae waiting for them. The things happening within my brush handles may serve as an illustration of the ways and changes of the average hornet.

One after another of the little green caterpillars is packed into the bamboo cell, which is about an inch deep, and plugged with mud at the base. From seven to ten of the victims are thus stored, after which the little wasp deposits an egg among them, and seals the doorway with a pellet of mud. The young larva, which soon hatches from this egg, finds itself in a land of plenty, surrounded[Pg 17] with living food, and, being born hungry, he loses no time in making a meal from the nearest victim. One after another of the caterpillars is devoured, until his larder, nicely calculated to carry him to his full growth, is exhausted. Thus the first stage is passed. The second stage is entered into within a few hours, and is passed within a silken cocoon, with which the white grub now surrounds itself, and with which, transformed to a pupa, it bides its time for about three weeks, as I now recall, when—third stage—out pops the mud cork, and the perfect wasp appears at the opening of the cell. I have shown sections of one of my brushes in the three stages.
One after another, the little green caterpillars are packed into the bamboo cell, which is about an inch deep and sealed with mud at the bottom. Seven to ten of the caterpillars are stored this way, after which the little wasp lays an egg among them and seals the entrance with a pellet of mud. The young larva, which soon hatches from this egg, finds itself in a land of plenty, surrounded[Pg 17] by living food. Being born hungry, it quickly starts feasting on the nearest caterpillar. One by one, the caterpillars are consumed until its carefully calculated stash runs out. This completes the first stage. The second stage begins a few hours later and is spent inside a silken cocoon that the white grub creates around itself. During this time, transformed into a pupa, it waits for about three weeks, as I now recall, when—third stage—the mud cork pops off, and the fully formed wasp appears at the entrance of the cell. I have shown sections of one of my brushes in the three stages.
This interesting little hornet is a common summer species, known as the solitary hornet—one of them—Odynerus flavipes. The insect is about a half-inch in length, and to the careless observer might suggest a yellow-jacket, though the yellow is here confined to two triangular spots on the front of the thorax and three bands upon the abdomen.
This fascinating little hornet is a common summer species, known as the solitary hornet—specifically, Odynerus flavipes. The insect is about half an inch long and might look like a yellow-jacket to someone who isn’t paying close attention, although the yellow is limited to two triangular spots on the front of the thorax and three bands on the abdomen.
Like the wren among birds, it is fond of building in holes, and will generally obtain them ready-made if possible. Burroughs has said of the wren that it "will build in anything that has a hole in it, from an old boot to a bombshell." In[Pg 18] similar whim our little solitary hornet has been known to favor nail-holes, hollow reeds, straws, the barrels of a pistol, holes in kegs, worm-holes in wood, and spools, to which we may now add bamboo brushes.
Like the wren among birds, it enjoys building in holes and usually prefers to use ones that are already available. Burroughs noted that the wren "will build in anything that has a hole in it, from an old boot to a bombshell." In[Pg 18] a similar fashion, our little solitary hornet has been known to choose nail-holes, hollow reeds, straws, the barrels of a pistol, holes in kegs, worm-holes in wood, and spools, to which we can now add bamboo brushes.

Ovid declared and the ancient Greeks believed that hornets were the direct progeny of the snorting war-horse. The phrase "mad as a hornet"[Pg 19] has become a proverb. Think, then, of a brush loaded and tipped with this martial spirit of Vespa, this cavorting afflatus, this testy animus! There is more than one pessimistic "goose-quill," of course, "mightier than the sword," which, it occurs to me in my now charitable mood, might have been thus surreptitiously voudooed by the war-like hornet, and the plug never removed.[Pg 20]
Ovid stated, and the ancient Greeks believed, that hornets were directly descended from snorting war horses. The expression "mad as a hornet"[Pg 19] has become a proverb. So, think of a brush fully loaded and ready with this combative spirit of Vespa, this lively inspiration, this irritable energy! There’s more than one pessimistic "goose-quill," of course, "mightier than the sword," which I realize in my now generous mood might have been secretly influenced by the war-like hornet, and the plug was never taken out.[Pg 20]
THE CUCKOOS AND THE OUTWITTED COW-BIRD


how has that "blessed bird" and "sweet messenger of spring," the "cuckoo," imposed upon the poetic sensibilities of its native land!
how has that "blessed bird" and "sweet messenger of spring," the "cuckoo," impacted the poetic feelings of its homeland!
And what is this cuckoo which has thus bewitched all the poets? What is the personality behind that "wandering voice?" What the distinguishing trait which has made this wily attendant on the spring notorious from the times of Aristotle and Pliny? Think of "following the cuckoo," as Logan longed to do, in its "annual visit around the globe," a voluntary witness and accessory to the blighting curse of its vagrant, almost unnatural life! No, my indiscriminate bards; on this occasion we must part company. I cannot "follow" your cuckoo—except with a[Pg 24] gun, forsooth—nor welcome your "darling of the spring," even though he were never so captivating as a songster.
And what is this cuckoo that has enchanted all the poets? What’s the personality behind that "wandering voice?" What’s the feature that has made this clever herald of spring infamous since the times of Aristotle and Pliny? Think of "following the cuckoo," as Logan wished to do, in its "annual journey around the globe," a willing witness and accomplice to the bitter curse of its wandering, almost unnatural life! No, my indiscriminate poets; this time we must go our separate ways. I cannot "follow" your cuckoo—except with a[Pg 24] gun, really—nor can I embrace your "darling of the spring," even if he were the most captivating singer.

The song and the singer are here identical and inseparable, to my prosaic and rational senses; for does not that "blithe new-comer," as Tennyson says, "tell his name to all the hills"—"Cuckoo! Cuckoo!"
The song and the singer are the same and can't be separated, to my straightforward and logical mind; because doesn't that "cheerful newcomer," as Tennyson puts it, "announce his name to all the hills"—"Cuckoo! Cuckoo!"
The poet of romance is prompted to draw on his imagination for his facts, but the poet of nature must first of all be true, and incidentally as beautiful and good as may be; and a half-truth or a truth with a reservation may be as dangerous[Pg 25] as falsehood. The poet who should so paint the velvety beauty of a rattlesnake as to make you long to coddle it would hardly be considered a safe character to be at large. Likewise an ode to the nettle, or to the autumn splendor of the poison-sumac, which ignored its venom would scarcely be a wise botanical guide for indiscriminate circulation among the innocents. Think, then, of a poetic eulogium on a bird of which the observant Gilbert could have written:
The poet of romance is inspired to use their imagination for their stories, but the poet of nature must always be truthful and, if possible, as beautiful and good as they can be; and a half-truth or a truth with a twist can be just as harmful as a lie[Pg 25]. A poet who describes the smooth beauty of a rattlesnake in a way that makes you want to cuddle it wouldn’t be seen as a trustworthy person. Similarly, a poem about nettles or the autumn beauty of poison-sumac that overlooks its toxicity wouldn’t be a smart guide for people who don’t know better. Now, imagine a poetic tribute to a bird that the keen observer Gilbert could have written:
"This proceeding of the cuckoo, of dropping its eggs as it were by chance, is such a monstrous outrage on maternal affection, one of the first great dictates of nature, and such a violence on instinct, that had it only been related of a bird in the Brazils or Peru, it would never have merited our belief.... She is hardened against her young ones as though they were not hers.... 'Because God hath deprived her of wisdom, neither hath He imparted to her understanding.'"
"This behavior of the cuckoo, casually dropping its eggs as if by accident, is such a shocking violation of maternal care, one of nature's most fundamental principles, and such a distortion of instinct that if it were only reported about a bird in Brazil or Peru, it would seem unbelievable to us.... She shows no warmth towards her chicks as if they don’t belong to her.... 'Because God has taken away her wisdom, He hasn’t given her understanding either.'"
America is spared the infliction of this notorious "cuckoo." Its nearest congeners, our yellow-billed and black-billed cuckoos, while suggesting their foreign ally in shape and somewhat in song, have mended their ways, and though it is true they make a bad mess of it, they at least try to build their own nest, and rear their own young[Pg 26] with tender solicitude. The nest is usually so sparse and flimsy an affair that you can see through its coarse mesh of sticks from below, the fledglings lying as on a grid-iron or toaster; and it is, moreover, occasionally so much higher in the centre than at the sides that the chicks tumble out of bed and perish. Still, it is a beginning in the right direction.
America is lucky enough to avoid the issue of this infamous "cuckoo." Our closest relatives, the yellow-billed and black-billed cuckoos, while similar to their foreign counterpart in shape and somewhat in song, have improved their behavior. Even though they can make a messy attempt, at least they try to build their own nests and raise their own young[Pg 26] with care. The nests are usually so sparse and flimsy that you can see through the rough mesh of sticks from underneath, with the fledglings lying almost like they're on a grid or toaster; sometimes, the nest is higher in the center than at the edges, causing the chicks to fall out and die. Still, it is a step in the right direction.

Yes, it would appear that our American cuckoo is endeavoring to make amends for the sins of its ancestors; but,[Pg 27] what is less to its credit, it has apparently found a scapegoat, to which it would ever appear anxious to call our attention, as it stammers forth, in accents of warning, "c, c, cow, cow, cow! cowow, cowow!" It never gets any further than this; but doubtless in due process of vocal evolution we shall yet hear the "bunting," or "black-bird," which is evidently what he is trying to say.
Yes, it seems like our American cuckoo is trying to make up for its ancestors' mistakes; but, [Pg 27] what's less impressive is that it seems to have found a scapegoat, which it eagerly points out to us, as it nervously calls out, "c, c, cow, cow, cow! cowow, cowow!" It never gets past that; but surely, in time, we will hear the "bunting" or "blackbird," which is clearly what it’s attempting to communicate.
Owing to the onomatopoetic quality of the "kow, kow, kow!" of the bird, it is known in some sections as the "kow-bird," and is thus confounded with the real cow-bird, and gets the credit of her mischief, even as in other parts of the country, under the correct name of "cuckoo," it bears the odium of its foreign relative.
Due to the sound "kow, kow, kow!" made by the bird, it’s referred to as the "kow-bird" in some areas, causing it to be mistaken for the real cow-bird and getting blamed for its mischief. In other parts of the country, it’s properly called "cuckoo," but still carries the blame for its foreign relative.
For though we have no disreputable cuckoo, ornithologically speaking, let us not congratulate ourselves too hastily. We have his counterpart in a black sheep of featherdom which vies with his European rival in deeds of cunning and cruelty, and which has not even a song to recommend him—no vocal accomplishment which by the greatest of license could prompt a poet to exclaim,
For even though we don't have a disreputable cuckoo, in terms of birds, let's not pat ourselves on the back too quickly. We have a counterpart in a shady character of the bird world that competes with its European counterpart in acts of cleverness and cruelty, and it doesn't even have a song to its name—no vocal talent that even with a stretch could inspire a poet to say,
"I hear thee and rejoice,"
"I hear you and rejoice,"
without having his sanity called in question.
without his sanity being questioned.
The cow-blackbird, it is true, executes a certain[Pg 28] guttural performance with its throat—though apparently emanating from a gastric source—which some ornithologists dignify by the name of "song." But it is safe to affirm that with this vocal resource alone to recommend him he or his kind would scarcely have been known to fame. The bird has yet another lay, however, which has made it notorious. Where is the nest of song-sparrow, or Maryland yellow-throat, or yellow warbler, or chippy, that is safe from the curse of the cow-bird's blighting visit?
The cow-blackbird does indeed make a guttural sound with its throat—seemingly coming from its stomach—which some bird watchers call a "song." However, it's fair to say that if this vocal ability were its only claim to fame, neither it nor its species would be well known. The bird has one more trick up its sleeve, though, that has made it infamous. Where is the nest of a song sparrow, Maryland yellow-throat, yellow warbler, or chipping sparrow that is safe from the damaging visit of the cowbird?
And yet how few of us have ever seen the bird to recognize it, unless perchance in the occasional flock clustering about the noses and feet of browsing kine and sheep, or perhaps perched upon their backs, the glossy black plumage of the males glistening with iridescent sheen in the sunshine.
And yet how few of us have ever seen the bird to recognize it, unless maybe in the rare flocks gathering around the noses and feet of grazing cows and sheep, or perhaps sitting on their backs, the shiny black feathers of the males sparkling with iridescent shine in the sunlight.
"Haow them blackbirds doos love the smell o' thet caow's breath!" said an old dame to me once in my boyhood. "I don't blame um: I like it myself." Whether it was this same authority who was responsible for my own similar early impression I do not know, but I do recall the surprise at my ultimate discovery that it was alone the quest of insects that attracted the birds.[Pg 29]
"How those blackbirds do love the smell of that cow's breath!" an old woman said to me once when I was a kid. "I don't blame them; I like it myself." I don't know if it was this same person who influenced my own early impression, but I do remember being surprised when I finally discovered that it was the search for insects that really attracted the birds.[Pg 29]

Upon the first arrival of the bird in the spring an attentive ear might detect its discordant voice, or the chuckling note of his mischievous spouse and accomplice, in the great bird medley; but later her crafty instinct would seem to warn her that silence is more to her interest in the pursuit of her wily mission. In June, when so many an ecstatic love-song among the birds has modulated from accents of ardent love to those of glad fruition, when the sonnet to his "mistress's eyebrow" is shortly to give place to the lullaby, then, like the "worm i' the bud," the cow-bird begins her parasitical career. How many thousands are the bird homes which are blasted in her "annual visit?"
Upon the first arrival of the bird in the spring, a keen ear might catch its jarring call or the playful chirp of its mischievous partner in the great bird chorus. But later, her clever instincts seem to remind her that staying quiet is better for her sly plan. In June, when so many ecstatic love songs among the birds shift from passionate notes to those of joyful fulfillment, and the serenade to his “mistress’s eyebrow” is soon replaced by a lullaby, the cowbird, like the “worm in the bud,” begins her parasitic journey. How many thousands of bird homes are destroyed during her “annual visit?”
Stealthily and silently she pries among the thickets, following up the trail of warbler, sparrow, or thrush like a sleuth-hound. Yonder a tiny yellow-bird with a jet-black cheek flits hither with a wisp of dry grass in her beak, and disappears in the branches of a small tree close to my studio door. Like the shadow of fate the cow-bird suddenly appears, and has doubtless soon ferreted out her cradle.
Stealthily and quietly, she sneaks through the bushes, tracking the sounds of warblers, sparrows, or thrushes like a detective. Over there, a small yellow bird with a black cheek flits over with a piece of dry grass in her beak and disappears into the branches of a small tree near my studio door. Like a shadow, the cowbird suddenly shows up, and she’ll probably soon find the nest.
In a certain grassy bank not far from where I am writing, at the foot of an unsuspecting fern, a song-sparrow has built her nest. It lies in a hol[Pg 31]low among the dried leaves and grass, and is so artfully merged with its immediate surroundings that even though you know its precise location it still eludes you. Only yesterday the last finishing-touches were made upon the nest, and this morning, as I might have anticipated from the excess of lisp and twitter of the mother bird, I find the first pretty brown-spotted egg.
In a grassy area not far from where I’m writing, at the base of an unsuspecting fern, a song sparrow has built her nest. It sits in a hollow among the dried leaves and grass, blending so well with its surroundings that even though you know exactly where it is, it’s still hard to spot. Just yesterday, the final touches were added to the nest, and this morning, as I expected from the chirpy sounds of the mother bird, I found the first pretty brown-spotted egg.
Surely our cow-bird has missed this secret haunt on her rounds. Be not deceived! Within a half-hour after this egg was laid the sparrow and its mate, returning from a brief absence to view their prize, discover two eggs where they had been responsible for but one. The prowling foe had already discovered their secret; for she, too, is "an attendant on the spring," and had been simply biding her time. The parent birds once out of sight, she had stolen slyly upon the nest, and after a very brief interval as slyly retreated, leaving her questionable compliments, presumably with a self-satisfied chuckle. The intruded egg is so like its fellow as to be hardly distinguishable except in its slightly larger size. It is doubtful whether the sparrow, in particular, owing to this similarity, ever realizes the deception. Indeed, the event is possibly considered a cause for self-congratulation rather than otherwise—at least,[Pg 32] until her eyes are opened by the fateful dénouement of a few weeks later. And thus the American cow-bird outcuckoos the cuckoo as an "attendant on the spring," taking her pick among the nurseries of featherdom, now victimizing the oriole by a brief sojourn in the swinging hammock in the elm, here stopping a moment to leave her charge to the care of an indigo-bird, to-morrow creeping through the grass to the secreted nest of the Maryland yellow-throat, or Wilson's thrush, or chewink. And, unaccountable as it would appear, here we find the same deadly token safely lodged in the dainty cobweb nest of the vireo, a fragile pendent fabric hung in the fork of a slender branch which in itself would barely appear sufficiently strong to sustain the weight of a cow-bird without emptying the nest.
Surely our cowbird has missed this hidden spot during her rounds. Don’t be fooled! Within half an hour after this egg was laid, the sparrow and its mate, returning from a short absence to check on their treasure, find two eggs instead of the one they expected. The lurking enemy has already discovered their secret; she, too, is "an attendant of spring" and had simply been waiting for her moment. Once the parent birds were out of sight, she stealthily approached the nest and quickly retreated, leaving her dubious gift, presumably with a self-satisfied chuckle. The intruding egg looks so much like the others that it’s almost impossible to tell them apart, except for its slightly larger size. It’s doubtful whether the sparrow, in particular, ever realizes the trick due to this similarity. In fact, the event might even be seen as a reason to feel proud rather than disappointed—at least, [Pg 32] until reality hits her weeks later. And so the American cowbird out-cuckoos the cuckoo as an "attendant of spring," picking from the nests of various birds, now targeting the oriole by briefly visiting the swinging hammock in the elm, stopping for a moment to leave her egg with an indigo bunting, and tomorrow sneaking through the grass to the hidden nest of the Maryland yellow-throat, Wilson's thrush, or chewink. Amazingly, we find the same deadly gift securely placed in the delicate cobweb nest of the vireo, a fragile hanging structure nestled in the fork of a slender branch that barely seems strong enough to support the weight of a cowbird without causing the nest to collapse.
Indeed, the presence of this intruded egg, like that of the European cuckoo in similar fragile nests, has given rise to the popular belief that the bird must resort to exceptional means in these instances. Sir William Jardine, for instance, in an editorial foot-note in one of Gilbert White's pages, remarks:
Indeed, the presence of this intruded egg, like that of the European cuckoo in similar fragile nests, has led to the common belief that the bird must use extraordinary methods in these cases. Sir William Jardine, for example, in a footnote in one of Gilbert White's pages, notes:
"It is a curious fact, and one, I believe, not hitherto noticed by naturalists, that the cuckoo[Pg 33] deposits its egg in the nests of the titlark, robin, and wagtail by means of its foot. If the bird sat on the nest while the egg was laid, the weight of its body would crush the nest and cause it to be forsaken, and thus one of the ends of Providence would be defeated. I have found the eggs of the cuckoo in the nest of a white-throat, built in so small a hole in a garden wall that it was absolutely impossible for the cuckoo to have got into it."
"It’s an interesting fact, and one I think hasn’t been noticed by naturalists before, that the cuckoo[Pg 33] lays its egg in the nests of the titlark, robin, and wagtail using its foot. If the bird sat on the nest while laying the egg, its weight would crush the nest and cause it to be abandoned, thus defeating one of the purposes of Providence. I’ve found cuckoo eggs in a white-throat’s nest, which was built in such a small hole in a garden wall that it was completely impossible for the cuckoo to have gotten into it."
In the absence of substantiation, this, at best, presumptive evidence is discounted by the well-attested fact that the cuckoo has frequently been shot in the act of carrying a cuckoo's egg in its mouth, and there is on record an authentic account of a cuckoo which was observed through a telescope to lay her egg on a bank, and then take it in her bill and deposit it in the nest of a wagtail.
In the absence of proof, this is, at best, just assumption and is undermined by the well-known fact that cuckoos have often been seen with a cuckoo's egg in their mouth. There's a verified account of a cuckoo being observed through a telescope laying her egg on a bank, then picking it up in her bill and placing it in a wagtail's nest.
There is no evidence to warrant a similar resource in our cow-bird, though the inference would often appear irresistible, did we not know that Wilson actually saw the cow-bird in the act of laying in the diminutive nest of a red-eyed vireo, and also in that of the bluebird.
There is no evidence to support a similar resource in our cowbird, although the conclusion often seems unavoidable if we didn’t know that Wilson actually observed the cowbird laying in the tiny nest of a red-eyed vireo and also in that of the bluebird.
And what is the almost certain doom of the bird-home thus contaminated by the cow-bird?[Pg 34]
And what is the almost certain doom of the bird's nest that has been contaminated by the cowbird?[Pg 34]

The egg is always laid betimes, and is usually the first to hatch, the period of incubation being a day or two less than that of the eggs of the foster-parent. And woe be to the fledglings whom fate has associated with a young cow-bird! He is the "early bird that gets the worm." His is the clamoring red mouth which takes the provender of the entire family. It is all "grist into his mill," and everything he eats seems to go to appetite—his bedfellows, if not thus starved to death, being at length crushed by his comparatively ponderous bulk, or ejected[Pg 35] from the nest to die. It is a pretty well established fact that the cuckoo of Europe deliberately ousts its companion fledglings—a fact first noted by the famous Dr. Jenner. And Darwin has even asserted that the process of anatomical evolution has especially equipped the young cuckoo for such an accomplishment—a practice in which some accommodating philosophic minds detect the act of "divine beneficence," in that "the young cuckoo is thus insured sufficient food, and that its foster-brothers thus perish before they have acquired much feeling."
The egg is always laid early, and it’s usually the first to hatch, with an incubation period that’s a day or two shorter than that of the foster parent's eggs. And woe to the chicks that fate has paired with a young cowbird! He is the "early bird that gets the worm." His is the loud, hungry mouth that demands food from the whole family. Everything he eats seems to go straight to his appetite—his nestmates, if not starved to death this way, eventually get crushed by his relatively heavy weight or are pushed out of the nest to die. It’s pretty well established that the cuckoo in Europe deliberately ousts its nestmates—a fact first pointed out by the famous Dr. Jenner. And Darwin even claimed that the process of anatomical evolution has specially adapted the young cuckoo for this behavior—a practice that some accommodating philosophical thinkers see as an act of "divine beneficence," because "the young cuckoo is thus guaranteed enough food, and its foster-siblings die before they develop much feeling."
The following account, written by an eye-witness, bears the stamp of authenticity, and is furthermore re-enforced by a careful and most graphic drawing made on the spot, which I here reproduce, and fully substantiates the previous statement by Dr. Jenner. The scene of the tragedy was the nest of a pipit, or titlark, on the ground beneath a heather-bush. When first discovered it contained two pipit's eggs and the egg of a cuckoo.
The following account, written by a witness, is authentic and is further supported by a detailed and vivid drawing made right there, which I am including here, and it fully backs up Dr. Jenner's earlier statement. The tragedy took place at a pipit (or titlark) nest on the ground under a heather bush. When first found, it contained two pipit eggs and one cuckoo egg.
"At the next visit, after an interval of forty-eight hours," writes Mrs. Blackburn, "we found the young cuckoo alone in the nest, and both the young pipits lying down the bank, about ten[Pg 36] inches from the margin of the nest, but quite lively after being warmed in the hand. They were replaced in the nest beside the cuckoo, which struggled about till it got its back under one of them, when it climbed backward directly up the open side of the nest and pitched the pipit from its back on to the edge. It then stood quite upright on its legs, which were straddled wide apart, with the claws firmly fixed half-way down the inside of the nest, and, stretching its wings apart and backward, it elbowed the pipit fairly over the margin so far that its struggles took it down the bank instead of back into the nest. After this the cuckoo stood a minute or two feeling back with its wings, as if to make sure that the pipit was fairly overboard, and then subsided into the bottom of the nest.
"During our next visit, two days later," Mrs. Blackburn writes, "we found the young cuckoo alone in the nest, while both young pipits were lying down the bank, about ten[Pg 36] inches from the edge of the nest, but they were quite lively after being warmed in our hands. We placed them back in the nest next to the cuckoo, which struggled until it got its back under one of them. Then it climbed backward up the open side of the nest and tossed the pipit off its back onto the edge. It stood upright on its legs, which were straddled wide apart, with its claws firmly anchored halfway down the inside of the nest. Stretching its wings out and back, it pushed the pipit over the edge so far that its struggles sent it down the bank instead of back into the nest. After that, the cuckoo stood for a minute or two, feeling back with its wings, as if to ensure that the pipit was completely out, and then settled into the bottom of the nest."
"I replaced the ejected one and went home. On returning the next day, both nestlings were found dead and cold out of the nest.... But what struck me most was this: the cuckoo was perfectly naked, without a vestige of a feather, or even a hint of future feathers; its eyes were not yet opened, and its neck seemed too weak to support the weight of the head. The pipit had well-developed quills on the wings and back, and had bright eyes, partially open, yet they seemed quite[Pg 37] helpless under the manipulations of the cuckoo, which looked a much less developed creature. The cuckoo's legs, however, seemed very muscular; and it appeared to feel about with its wings, which were absolutely featherless, as with hands, the spurious wing (unusually large in proportion) looking like a spread-out thumb."
"I replaced the one that was ejected and went home. When I returned the next day, both nestlings were found dead and cold out of the nest.... But what struck me most was this: the cuckoo was completely naked, without a trace of feathers or even a sign of future feathers; its eyes weren’t open yet, and its neck seemed too weak to hold up its head. The pipit had well-developed quills on its wings and back, and bright eyes that were partially open, yet they looked quite[Pg 37] helpless under the influence of the cuckoo, which seemed like a far less developed creature. However, the cuckoo's legs looked very muscular, and it appeared to be feeling around with its wings, which were completely featherless, like hands, with the oddly large wing looking like a spread-out thumb."
Considering how rarely we see the cow-bird in our walks, her merciless ubiquity is astonishing. It occasionally happens that almost every nest I meet in a day's walk will show the ominous speckled egg. In a single stroll in the country I have removed eight of these foreboding tokens of misery. Only last summer I discovered the nest of a wood-sparrow in a hazel-bush, my attention being attracted thither by the parent bird bearing food in her beak. I found the nest occupied, appropriated, monopolized, by a cow-bird fledgling—a great, fat, clamoring lubber, completely filling the cavity of the nest, the one diminutive, puny remnant of the sparrow's offspring being jammed against the side of the nest, and a skeleton of a previous victim hanging among the branches below, with doubtless others lost in the grass somewhere in the near neighborhood, where they had been removed by the bereaved mother. The ravenous young parasite, though not half grown,[Pg 38] was yet bigger by nearly double than the foster-mother. What a monster this! The "Black Douglass" of the bird home; a blot on Nature's page!
Considering how rarely we see the cowbird on our walks, it's surprising how often they show up. It sometimes feels like almost every nest I encounter on a day's walk has that ominous speckled egg. In just one outing in the countryside, I removed eight of these unsettling signs of distress. Just last summer, I found a wood sparrow's nest in a hazel bush, my attention caught by the parent bird bringing food in its beak. When I arrived at the nest, I found it taken over by a cowbird chick—a big, fat, noisy thing that completely filled the nest, while the tiny remains of the sparrow's chick were crammed against the side. There was also the skeleton of a previous victim hanging among the branches below, and likely more lost in the grass nearby, taken away by the grieving mother. The greedy young parasite, though not fully grown, was nearly twice the size of the foster mother. What a monster this is! The "Black Douglass" of the bird world; a stain on Nature's canvas!
As in previous instances, observing that the interloper had a voice fully capable of making his wants known, I gave the comfortable little beast ample room to spread himself on the ground, and let the lone little starveling survivor of the rightful brood have his cot all to himself.
As in previous times, noticing that the intruder had a voice perfectly capable of expressing his needs, I provided the cozy little creature plenty of space to stretch out on the ground, and allowed the solitary little survivor of the rightful group to have his bed all to himself.
And yet, as I left the spot, I confess to a certain misgiving, as the pleading chirrup of the ousted fledgling followed me faintly and more faintly up the hill, recalling, too, the many previous similar acts of mine—and one in particular, when I had slaughtered in cold blood two of these irresponsibles found in a single nest. But sober second thought evoked a more philosophic and conscientious mood, the outcome of which leading, as always, to a semi-conviction that the complex question of reconciliation of duty and humanity in the premises was not thus easily disposed of, considering, as I was bound to do, the equal innocence of the chicks, both of which had been placed in the nest in obedience to a natural law, which in the case of the cow-bird was none the less a divine institution because I failed to un[Pg 39]derstand it. Such is the inevitable, somewhat penitent conclusion which I always arrive at on the cow-bird question; and yet my next cow-bird fledgling will doubtless follow the fate of all its predecessors, the reminiscent qualms of conscience finding a ready philosophy equal to the emergency; for if, indeed, this parasite of the bird home be a factor in the divine plan of Nature's equilibrium, looking towards the survival of the fittest and the regulation of the sparrow and small-bird population, which we must admit, how am I to know but that this righteous impulse of the human animal is not equally a divine, as it is certainly a natural institution looking to the limitations of the cow-bird? One June morning, a year or two ago, I heard a loud squeaking, as of a young bird in the grass near my door, and, on approaching, discovered the spectacle of a cow-bird, almost full-fledged, being fed by its foster-mother, a chippy not more than half its size, and which was obliged to stand on tiptoe to cram the gullet of the parasite.
And yet, as I left the spot, I have to admit I felt a bit uneasy, as the desperate chirping of the ousted baby bird followed me, gradually fading away as I walked up the hill. It reminded me of many similar times I had acted before—especially one instance where I had coldly killed two of these innocent creatures I found in a single nest. But after some serious reflection, I found myself in a more thoughtful and conscientious mood. This usually leads me to a sort of belief that the complicated issue of balancing duty and compassion isn't something that can be easily resolved, especially considering the equal innocence of the chicks, both of which were placed in the nest due to a natural law. In the case of the cowbird, this law is no less a divine institution just because I don’t understand it. This is the inevitable, somewhat guilty conclusion I always arrive at regarding the cowbird; and yet my next cowbird chick will likely meet the same fate as its predecessors, with my lingering guilt easily rationalized. If this bird home parasite is indeed part of Nature’s divine plan for balance, aiming at the survival of the fittest and regulating the sparrow and small bird population—which we have to acknowledge—how can I know if this noble instinct of humans isn’t also a divine, truly natural response to the cowbird's limitations? One June morning, a year or two ago, I heard loud squeaking like a young bird in the grass near my door, and when I went over to check, I saw a nearly fully grown cowbird being fed by its foster mother, a little chipmunk not more than half its size, who had to stand on tiptoes to stuff food down the throat of the parasite.
The victims of the cow-bird are usually, as in this instance, birds of much smaller size, the fly-catchers, the sparrows, warblers, and vireos, though she occasionally imposes on larger species, such as the orioles and the thrushes. The following[Pg 40] are among its most frequent dupes, given somewhat in the order of the bird's apparent choice: song-sparrow, field-sparrow, yellow warbler, chipping-sparrow, other sparrows, Maryland yellow-throat, yellow-breasted chat, vireos, worm-eating warbler, indigo-bird, least-flycatcher, bluebird, Acadian flycatcher, Canada flycatcher, oven-bird, king-bird, cat-bird, phœbe, Wilson's thrush, chewink, and wood-thrush.
The victims of the cowbird are usually, like in this case, much smaller birds, such as flycatchers, sparrows, warblers, and vireos, although she occasionally targets larger species like orioles and thrushes. The following[Pg 40] are among its most frequent victims, listed roughly in order of the bird’s preference: song sparrow, field sparrow, yellow warbler, chipping sparrow, other sparrows, Maryland yellow-throat, yellow-breasted chat, vireos, worm-eating warbler, indigo bunting, least flycatcher, bluebird, Acadian flycatcher, Canada flycatcher, ovenbird, kingbird, catbird, phoebe, Wilson's thrush, chewink, and wood thrush.
But one egg is usually deposited in a single nest; the presence of two eggs probably indicates, as in the case of the European cuckoo, the visits of two cow-birds rather than a second visit from the same individual—the presence of two cow-bird chicks of equal size being rather a proof of this than otherwise, in that kind Nature would seem to have accommodated the bird with an exceptional physiological resource, which matures its eggs at intervals of three or more days, as against the daily oviposition of its dupes, thus giving it plenty of time to make its search and take its pick among the bird-homes. Whether the process of evolution has similarly equipped our cow-bird I am not aware; but the vicious habits of the two birds are so identical that the same accommodating functional conditions might reasonably be expected. It is, indeed, an interesting[Pg 41] fact well known to ornithologists that our own American cuckoos, both the yellow-billed and black-billed, although rudimentary nest-builders, still retain the same exceptional interval in their egg-laying as do their foreign namesake. The eggs are laid from four days to a week apart, instead of daily, as with most birds, their period of perilous nidification on that haphazard apology of a nest being thus possibly prolonged to six weeks. Thus we find, in consequence, the anomalous spectacle of the egg and full-grown chick, and perhaps one or two fledglings of intermediate stages of growth, scattered about at once, helter-skelter, in the same nest. Only two years ago I discovered such a nest not a hundred feet from my house, containing one chick about two days old, another almost full-fledged, while a fresh-broken egg lay upon the ground beneath. Such a household condition would seem rather demoralizing to the cares of incubation, and doubtless the addled or ousted egg is a frequent episode in our cuckoo's experience.
But typically, one egg is laid in a single nest; the presence of two eggs probably indicates, like with the European cuckoo, visits from two cowbirds rather than a second visit from the same individual. The existence of two cowbird chicks of equal size supports this idea, suggesting that nature has given the bird an unusual physiological ability to mature its eggs every three days or more, compared to the daily egg-laying of its hosts. This gives the cowbird plenty of time to search for nests and choose where to lay its eggs. I'm not sure if evolution has done the same for our cowbirds, but the similar behaviors of the two birds lead us to reasonably expect comparable conditions. Interestingly, ornithologists note that our own American cuckoos, both yellow-billed and black-billed, are not great nest builders but still have the same unique interval in egg-laying as their foreign counterparts. They lay their eggs four days to a week apart, instead of daily like most birds, which could extend their risky nesting period to six weeks. As a result, we see the unusual situation where an egg and a fully grown chick, along with one or two fledglings at different growth stages, can all be found together in the same nest. Just two years ago, I found such a nest less than a hundred feet from my house, containing one chick about two days old, another nearly fully feathered, while a freshly broken egg was lying on the ground below. Such a chaotic household environment could be quite stressful for the incubation process, and it's likely that the abandoned or removed egg is a common occurrence in our cuckoo's life.
It is an interesting question which the contrast of the American and European cuckoo thus presents. Is the American species a degenerate or a progressive nest-builder? Has she advanced in process of evolution from a parasitical progenitor[Pg 42] building no nest, or is the bird gradually retrograding to the evil ways of her notorious namesake?
It raises an interesting question when we compare the American and European cuckoo. Is the American species a less evolved or more advanced nest-builder? Has it evolved from a parasitic ancestor[Pg 42] that built no nest, or is the bird slowly reverting to the negative traits of its infamous counterpart?
The evidence of this generic physiological peculiarity in the intervals of oviposition, taken in consideration with the fact of the rudimentary nest, would seem to indicate the retention of a now useless physiological function, and that the bird is thus a reformer who has repudiated the example of her ancestors, and has henceforth determined to look after her own babes.
The proof of this general physical characteristic during the laying of eggs, combined with the existence of the underdeveloped nest, suggests that an outdated physiological function is still being maintained. This means that the bird is a pioneer, rejecting the practices of her ancestors and has now chosen to care for her own young.
With the original presumed object of this remarkable prolonged interval in egg-laying now removed, the period will doubtless be reduced through gradual evolution to accommodate itself to the newly adopted conditions. The week's interval, taken in connection with the makeshift nest or platform of sticks, is now a disastrous element in the life of the bird. Such of the cuckoos, therefore, as build the more perfect nests, or lay at shortest intervals, will have a distinct advantage over their less provident fellows, and the law of heredity will thus insure the continual survival of the fittest.
With the original assumed purpose of this significant extended period of egg-laying now gone, the duration will likely shorten over time to adapt to the new conditions. The week's gap, along with the makeshift nest or platform of sticks, is now a negative factor in the bird's life. Therefore, cuckoos that build better nests or lay eggs at shorter intervals will have a clear advantage over their less prepared counterparts, and the principle of heredity will ensure the continuous survival of the fittest.
The cuckoo is not alone among British birds in its intrusion on other nests. Many other species are occasionally addicted to the same prac[Pg 43]tice, though such acts are apparently accidental rather than deliberate, so far as parasitical intent is concerned. The lapse is especially noticeable among such birds as build in hollow trees and boxes, as the woodpeckers and wagtails. Thus the English starling will occasionally impose upon and dispossess the green woodpecker. In the process of nature in such cases the stronger of the two birds would retain the nest, and thus assume the duties of foster-parent. Starting from this reasonable premise concerning the prehistoric cuckoo, it is not difficult to see how natural selection, working through ages of evolution by heredity, might have developed the habitual resignation of the evicted bird, perhaps to the ultimate entire abandonment of the function of incubation. Inasmuch as "we have no experience in the creation of worlds," we can only presume.
The cuckoo isn't the only British bird that intrudes on other nests. Many other species sometimes engage in this behavior, although these actions seem to be accidental rather than intentional, at least when it comes to parasitic motivation. This tendency is particularly noticeable in birds that nest in hollow trees and boxes, like woodpeckers and wagtails. For example, the English starling may sometimes take over the nest of a green woodpecker. In nature, the stronger bird usually ends up keeping the nest and takes on the role of a foster parent. Starting from this reasonable assumption about the prehistoric cuckoo, it's easy to see how natural selection, acting over countless generations, might have led to the evicted bird developing a habit of resignation, possibly even leading to a complete abandonment of the role of incubator. Since "we have no experience in the creation of worlds," we can only speculate.
Indeed, the similarities and contrasts afforded by a comparison of the habits of all these birds—European cuckoo, American cuckoo, and cow-bird—afford an interesting theme for the student of evolution. What is to be the ultimate outcome of it all? for the murderous cuckoo must be considered merely as an innocent factor in the great scheme of Nature's equilibrium, in which the devourer and the parasite would seem to play the[Pg 44] all-important parts, the present example being especially emphasized because of its conspicuousness and its violence to purely human sentiment. The parasite would often seem to hold the balance of power.
Indeed, the similarities and differences highlighted by comparing the behaviors of these birds—the European cuckoo, American cuckoo, and cowbird—provide an intriguing topic for those studying evolution. What will be the ultimate outcome of all this? The murderous cuckoo should be seen as just one innocent part of the larger scheme of Nature's balance, where the predator and the parasite seem to play equally crucial roles, especially in this case due to its obviousness and its clash with purely human feelings. The parasite often appears to hold the balance of power.

Jonathan Swift's epitome of the subject, if not specifically true, is at least correct in its general application:
Jonathan Swift's summary of the topic, while not universally accurate, is at least generally valid:
"A flea
Has smaller fleas that on him prey;
And these have smaller still to bite 'em;
And so proceed ad infinitum."
[Pg 45]
A flea
Has smaller fleas that feed on him;
And there are even smaller ones that bite them;
"It just goes on forever."
[Pg 45]
Even the tiny egg of a butterfly has its ichneumon parasite, a microscopic wasp, which lays its own egg within the larger one, which ultimately hatches a wasp instead of the baby caterpillar.
Even the small egg of a butterfly has its ichneumon parasite, a tiny wasp that lays its egg inside the larger one, which eventually hatches a wasp instead of a baby caterpillar.
But who ever heard of anything but good luck falling to the lot of cow-bird or cuckoo, except as its blighting course is occasionally arrested by the outraged human? They always find a feathered nest.
But who has ever heard of anything other than good luck coming to the cowbird or cuckoo, unless their harmful actions are sometimes stopped by an angry human? They always manage to find a bird's nest.
In this connection it is interesting to note certain developments in bird life upon the lines of which evolution might work with revolutionary effect. Most of our birds are helpless and generally resigned victims to the cow-bird, but there are indications of occasional effective protest among them. Thus the little Maryland yellow-throat, according to various authorities, often ousts the intruded egg, and its broken remains are also occasionally seen on the ground beneath the nests of the cat-bird and the oriole. The red-eyed vireo, on the other hand, though having apparently an easier task than the latter, in the lesser depth of her pensile nest, commonly abandons it altogether to the unwelcome speckled ovum—always, I believe, if the cow-bird has anticipated her own first egg.[Pg 46]
In this regard, it's interesting to observe certain changes in bird behavior that could significantly impact evolution. Most of our birds seem powerless and typically accept being victims of the cowbird, but there are signs of occasional strong resistance among them. For example, the small Maryland yellow-throat, according to various experts, often removes the cowbird's egg, and its broken pieces are sometimes found on the ground beneath the nests of the catbird and the oriole. The red-eyed vireo, on the other hand, while having what appears to be an easier situation with her shallower hanging nest, often completely abandons it to the unwanted speckled egg—always, as far as I know, if the cowbird lays her egg before she does.[Pg 46]

But we have a more remarkable example of opposition in the resource of the little yellow warbler, which I have noted as one of the favorite dupes of the cow-bird—a deliberate, intelligent, courageous defiance and frequent victory which are unique in bird history, and which, if through evolutionary process they became the fashion in featherdom, would put the cow-bird's mischief greatly at a discount. The[Pg 47] identity of this pretty little warbler is certainly familiar to most observant country dwellers, even if unknown by name, though its golden-yellow plumage faintly streaked with dusky brown upon the breast would naturally suggest its popular title of "summer yellow-bird." It is one of the commonest of the mnio-tiltidæ, or wood-warblers, though more properly a bird of the copse and shrubbery than of the woods.
But we have an even more impressive example of resistance in the little yellow warbler, which I’ve noted as one of the favorite targets of the cowbird—a deliberate, smart, brave defiance and frequent success that are unique in bird history, and which, if they became the norm through evolution, would significantly reduce the cowbird's troublemaking. The[Pg 47] identity of this lovely little warbler is certainly familiar to most observant country folks, even if they don't know its name; its golden-yellow feathers, lightly streaked with dark brown on the chest, would naturally suggest its common nickname of "summer yellow-bird." It is one of the most common of the mnio-tiltidæ, or wood-warblers, though it’s more accurately a bird of thickets and shrubs than of the forest.

the Yellow Warbler
This nest is a beautiful piece of bird architecture. In a walk in search of one only a day or two ago I procured one, which is now before me. It was built in the fork of an elder-bush, to which it was moored by strips of fine bark and cobweb, its downy bulk being composed by a fitted mass of fine grass, willow cotton, fern wood, and other similar ingredients. It is about three inches in depth, outside measurement. But this depth greatly varies in different specimens. Our next specimen may afford quite a contrast, for the yellow[Pg 48] warbler occasionally finds it to her interest to extend the elevation of her dwelling to a remarkable height. On page 50 is shown one of these nests, snugly moored in the fork of a scrub apple-tree. Its depth from the rim to the base, viewed from the outside, is about five inches, at least two inches longer than necessity would seem to require, and apparently with a great waste of material in the lower portion, as the hollow with the pretty spotted eggs is of only the ordinary depth of about two inches, thus hardly reaching half-way to[Pg 49] the base. Let us examine it closely. There certainly is a suspicious line or division across its upper portion, about an inch below the rim, and extending more or less distinctly completely around the nest. By a very little persuasion with our finger-tip the division readily yields, and we discover the summit of the nest to be a mere rim—a top story, as it were—with a full-sized nest beneath it as a foundation. Has our warbler, then, come back to his last year's home and fitted it up anew for this summer's brood? Such would be a natural supposition, did we not see that the foundation is as fresh in material as the summit. Perhaps, then, the bird has already raised her first spring brood, and has simply extended her May domicile, and provided a new[Pg 50] nursery for a second family. But either supposition is quickly dispelled as we further examine the nest; for in separating the upper compartment we have just caught a glimpse of what was, perhaps only yesterday, the hollow of a perfect nest; and, what is more to the point of my story, the hollow contains an egg—perhaps two, in which case they will be very dissimilar, one of delicate white with faint spots of brown on its larger end, the putting of the warbler, the other much larger, with its greenish surface entirely speckled with brown, and which, if we have had any experience in bird-nesting, we immediately recognize as the mischievous token of the cow-bird. We have discovered a most interesting curiosity for our natural-history cabinet—the embodiment of a presumably new form of intelligence in the divine plan looking to the survival of the fittest. It is not known how many years or centuries it has taken the little warbler to develop this clever resource to outwit the cow-bird. It is certain, however, that the little mother has got tired of being thus imposed upon, and is the first of her kind on record which has taken these peculiar measures for rising above her besetting[Pg 51] trouble.
This nest is a stunning example of bird architecture. Just a day or two ago, I went out searching for one and found this one, which is now in front of me. It was built in the fork of an elder bush, secured with strips of fine bark and cobwebs, and its soft structure is made from a mix of fine grass, willow fluff, fern wood, and similar materials. It's about three inches deep from the outside. However, this depth varies significantly among different nests. Our next example may provide quite a contrast, as the yellow[Pg 48] warbler sometimes makes her home much taller than usual. On page 50, there's a picture of one of these nests, cozily positioned in the fork of a scrub apple tree. Its depth from the rim to the base, looking from the outside, is about five inches—at least two inches deeper than what seems necessary—and it appears to have a lot of extra material in the lower part. The hollow that holds the lovely spotted eggs is only about two inches deep, barely reaching halfway to[Pg 49] the base. Let’s take a closer look. There seems to be a noticeable line or division near the top, about an inch below the rim, running all the way around the nest. With a little push from our fingertip, this division gives way, revealing that the top of the nest is just a rim—a sort of second story—with a fully formed nest underneath it serving as the base. Has our warbler returned to last year's home and refurbished it for this summer's brood? That would be a reasonable assumption, except we can see that the foundation is just as new in material as the top. Perhaps the bird has already raised her early spring brood and simply extended her May home, creating a new[Pg 50] nursery for another family. But either idea quickly fades as we continue to examine the nest; for when we separate the upper part, we catch sight of what was likely just yesterday a perfect nest, and more importantly for my story, the hollow holds an egg—maybe two. If there are two, they’ll likely be quite different: one is delicate white with faint brown spots at its larger end, the work of the warbler; the other much larger, with a greenish surface entirely speckled with brown, which, if we've had any experience with bird nesting, we instantly recognize as the sneaky sign of the cowbird. We've stumbled upon a fascinating curiosity for our natural history collection—the embodiment of a potentially new form of intelligence in the divine design focused on survival of the fittest. It's unclear how many years or centuries it has taken the tiny warbler to develop this clever strategy to outsmart the cowbird. What is certain, though, is that this little mother has grown tired of being taken advantage of and is the first of her kind on record to take these unique steps to overcome her persistent[Pg 51] challenges.


the Yellow Warbler
Who can tell what the future may develop in the nests of other birds whose homes are similarly invaded? I doubt not that this crying cow-bird and cuckoo evil comes up as a matter of consideration in bird councils. The two-storied nest may yet become the fashion in featherdom, in which case the cow-bird and European cuckoo would be forced to build nests of their own or perish.
Who can say what the future holds for the nests of other birds whose homes are similarly invaded? I have no doubt that this troublesome cowbird and cuckoo issue comes up in bird discussions. The idea of two-story nests might become popular in the bird world, which would mean that cowbirds and European cuckoos would have to build their own nests or face extinction.
But have we fully examined this nest of our yellow warbler? Even now the lower section seems more bulky than the normal nest should be. Can we not trace still another faint outline of a transverse division in the fabric, about an inch below the one already separated? Yes; it parts easily with a little disentangling of the fibres, and another spotted egg is seen within. A three-storied nest! A nest full of stories—certainly. I recently read of a specimen containing four stories, upon the top of which downy pile the little warbler sat like Patience on a monument,[Pg 52] presumably smiling at the discomfiture of the outwitted cow-bird parasite, who had thus exhausted her powers of mischief for the season, and doubtless convinced herself of the folly of "putting all her eggs in one basket."
But have we really looked closely at this nest of our yellow warbler? Even now, the bottom part looks bulkier than a normal nest should be. Can we spot another faint outline of a division in the structure, about an inch below the one that's already there? Yes; it comes apart easily with a little untangling of the fibers, revealing another spotted egg inside. A three-layered nest! A nest full of stories—definitely. I recently read about one that had four layers, on top of which the little warbler perched like Patience on a monument,[Pg 52] seemingly smiling at the confusion of the cowbird parasite, who had exhausted her mischief for the season and probably convinced herself it was silly to "put all her eggs in one basket."

When we consider the life of the cow-bird, how suggestive is this spectacle which we may see every year in September in the chuckling flocks massing for their migration, occasionally fairly blackening the trees as with a mildew, each one the visible witness of a double or quadruple cold-blooded murder, each the grim substitute for a whole annihilated singing family of song-sparrow, warbler, or thrush! What a blessing, at least humanly speaking, could the epicurean population en route in the annual Southern passage of this dark throng only learn what a surpassing substi[Pg 53]tute they would prove—on toast—for the bobolinks which as "reed-birds" are sacrificed by the thousands to the delectable satisfaction of those "fine-mouthed and daintie wantons who set such store by their tooth"!
When we think about the life of the cowbird, how striking is the scene we witness every year in September, when the noisy flocks gather for their migration, sometimes making the trees look blackened like mildew. Each one is a visible reminder of multiple cold-blooded killings, each one a grim replacement for an entire vanished family of song sparrows, warblers, or thrushes! What a blessing, at least from a human perspective, could the food-loving crowd en route in the annual southern migration of this dark swarm learn about how they could serve as a fantastic substitute—on toast—for the bobolinks, which are sacrificed by the thousands for the delicious pleasure of those "fine-mouthed and dainty wantons who value their taste buds so highly"!
And what the cow-bird is, so is the Continental "cuckoo." Shall we not discriminate in our employment of the superlative? What of the throstle and the lark? Shall we still sing—all together:
And what the cowbird is, so is the Continental "cuckoo." Shouldn’t we be careful with how we use the superlative? What about the thrush and the lark? Should we still sing—all together:
"O cuckoo! I hear thee and rejoice!
Thrice welcome darling of the spring."
"Oh cuckoo! I hear you and feel so happy!"
"Triple welcome, beloved of spring."
DOOR-STEP NEIGHBOURS


ow little do we appreciate our opportunities for natural observation![Pg 57] Even under the most apparently discouraging and commonplace environment, what a neglected harvest! A back-yard city grass-plot, forsooth, what an invitation! Yet there is one interrogation to which the local naturalist is continually called to respond. If perchance he dwells in Connecticut, how repeatedly is he asked, "Don't you find your particular locality in Connecticut a specially rich field for natural observation?" The botanist of New Jersey or the ornithologist of Esopus-on-Hudson is expected to give an affirmative reply to similar questions concerning his chosen hunting-grounds, if, indeed, he does not[Pg 58] avail himself of that happy aphorism with which Gilbert White was wont to instruct his questioners concerning the natural-history harvest of his beloved Selborne: "That locality is always richest which is most observed."
How little do we appreciate our chances for observing nature![Pg 57] Even in the most seemingly discouraging and ordinary environment, what a missed opportunity! A small patch of grass in the backyard of a city, truly, what an invitation! Yet there is one question that local naturalists are always asked to answer. If by chance they live in Connecticut, how often are they asked, "Don't you think your area in Connecticut is a particularly rich place for natural observation?" The botanist from New Jersey or the ornithologist from Esopus-on-Hudson is expected to give a positive answer to similar questions about his favorite spots, unless, of course, he takes advantage of that wise saying that Gilbert White used to share with his questioners about the natural history wealth of his beloved Selborne: "The place that is observed the most is always the richest." [Pg 58]
The arena of the events which I am about to describe and picture comprised a spot of almost bare earth less than one yard square, which lay at the base of the stone step to my studio door in the country.
The area of the events I'm about to describe was a nearly bare patch of dirt less than one yard square, located at the bottom of the stone step leading to my studio door in the countryside.
The path leading to the studio lay through a tangle of tall grass and weeds, with occasional worn patches showing the bare earth. As it approached the door-step the surface of the ground was quite clean and baked in the sun, and barely supported a few scattered, struggling survivors of the sheep's-sorrel, silvery cinquefoil, ragweed, various grasses, and tiny rushes which rimmed the border. Sitting upon this threshold stone one morning in early summer, I permitted my eyes to scan the tiny patch of bare ground at my feet, and what I observed during a very few moments suggested the present article as a good piece of missionary work in the cause of nature, and a suggestive tribute to the glory of the commonplace. The episodes which I shall describe represent the chronicle of a single day—in truth, of but a[Pg 59] few hours in that day—though the same events were seen in frequent repetition at intervals for months. Perhaps the most conspicuous objects—if, indeed, a hole can be considered an "object"—were those two ever-present features of every trodden path and bare spot of earth anywhere, ant-tunnels and that other circular burrow, about the size of a quill, usually associated, and which is also commonly attributed to the ants.
The path to the studio wound through a tangle of tall grass and weeds, with some worn patches revealing the bare ground. As it got closer to the doorstep, the ground was clean and baked by the sun, barely holding a few scattered, struggling plants like sheep's-sorrel, silvery cinquefoil, ragweed, different grasses, and tiny rushes along the edge. One morning in early summer, I sat on this threshold stone, letting my eyes wander over the small patch of bare ground at my feet. What I saw in just a few moments made me think that this would be a great piece of work for nature and a meaningful tribute to the beauty of the ordinary. The events I'll describe happened over the span of a single day—in reality, just a [Pg 59] few hours within that day—though these same events were witnessed repeatedly for months. Perhaps the most noticeable features—if you can even call a hole an "object"—were those two constant elements of every worn path and bare spot of earth: ant tunnels and the other circular burrow, about the size of a quill, which is usually associated with the ants.
As I sat upon my stone step that morning, I counted seven of these smooth clean holes within close range, three of them hardly more than an inch apart. They penetrated beyond the vision, and were evidently very deep. Knowing from past experience the wary tenant which dwelt within them, I adjusted myself to a comfortable attitude, and remaining perfectly motionless, awaited developments. After a lapse of possibly five minutes, I suddenly discovered that I could count but five holes; and while recounting to make sure, moving my eyes as slowly as possible, my numeration was cut short at four. In another moment two more had disappeared, and the remaining two immediately followed in obscurity, until no vestige of a hole of any kind was to be seen. The ground appeared absolutely level and unbroken. Were it not for the circular depression, or "door-[Pg 60]yard," around each hole, their location would, indeed, have been almost impossible. A slight motion of one of my feet at this juncture, however, and, presto! what a change! Seven[Pg 61] black holes in an instant! And now another wait of five minutes, followed by the same hocus-pocus, and the black spots, one by one, vanishing from sight even as I looked upon them. But let us keep perfectly quiet this time and examine the suspected spots more carefully. Locating the position of the hole by the little circular "door-yard," we can now certainly distinguish a new feature, not before noted, at the centre of each—two sharp curved prongs, rising an eighth of an inch or more above the surface and widely extended.
As I sat on my stone step that morning, I counted seven smooth, clean holes nearby, three of them barely an inch apart. They went deeper than I could see and were clearly very deep. From past experience with the cautious creature that lived in them, I got comfortable and stayed perfectly still, waiting for something to happen. After about five minutes, I suddenly noticed I could only count five holes; as I counted again, moving my eyes as slowly as I could, I found only four. In another moment, two more had vanished, and the last two quickly followed into obscurity until there was no sign of any hole left. The ground looked completely flat and unbroken. If it weren't for the circular depression, or "door-yard," around each hole, finding their locations would have been nearly impossible. A slight movement of my foot at that moment, though, and, boom! Seven black holes appeared in an instant! After another wait of five minutes, the same trick happened, and the black spots vanished one by one, even as I watched them. But let's stay perfectly still this time and take a closer look at those spots. By identifying the hole's location with the little circular "door-yard," we can now clearly see a new feature that we hadn't noticed before—two sharp, curved prongs sticking up about an eighth of an inch or more above the surface and splayed out wide.

What a danger signal to the creeping insect innocent in its neighborhood! How many a tragedy in the bug world has been enacted in these inviting, clean-swept little door-yards—these pitfalls, so artfully closed in order that their design may be the more surely effective. As I have said, these tunnels are commonly called "ant-holes," perhaps with some show of reason. It is true that ants occasionally are seen to go into them, but not by their own choice, while the most careful observer will wait in vain to see the ant come out again. Here at the edge of the grass we see one approaching now—a big red ant from yonder ant-hill. He creeps this way and that, and anon is seen trespassing in the precincts of the unhealthy court. He crosses its centre,[Pg 62] when, click! and in an instant his place knows him no more, and a black hole marks the spot where he met his fate, which is now being duly celebrated in a supplementary fête several inches belowground.
What a warning sign for the unsuspecting insect in its neighborhood! How many tragedies in the insect world have played out in these inviting, well-kept little yards—these traps, cleverly hidden to ensure their effectiveness. As I've mentioned, these tunnels are often called "ant holes," perhaps with some justification. It’s true that ants are sometimes seen going into them, but not by their own choice, while even the most observant watcher will wait in vain to see the ant come out again. Here at the edge of the grass, we see one approaching now—a big red ant from that ant hill. He moves around this way and that, and soon is spotted wandering into the dangerous territory. He crosses the middle of it,[Pg 62] when, click! In an instant, he disappears, and a black hole marks the place where he met his end, which is now being celebrated in a little gathering several inches underground.
A poor unfortunate green caterpillar, which, with a very little forcible persuasion in the interest of science, was induced to take a short-cut across this nice clean space of earth to the clover beyond, was the next martyr to my passion for original observation. He might have pursued his even course across the arena unharmed, but he too persisted in trespassing, and suddenly was seen to transform from a slow creeping laggard into the liveliest acrobat, as he stood on his head and apparently dived precipitately into the hole which suddenly appeared beneath him. A certain busy fly made itself promiscuous in the neighborhood, more than once to the demoralization of my necessary composure, as it crept persistently upon my nose. What was my delight when I observed the fickle insect in curious contemplation of a pair of calipers at the centre of one of the little courts! But, whether from past experience or innate philosophy in the insect I know not, the pronged hooks, though coming together with a click once or twice at the near[Pg 63] proximity of the tempter, failed in their opportunity, and the trap was soon seen carefully set again, flush with the ground at the mouth of the burrow.
A poor, unfortunate green caterpillar, which was coaxed with just a bit of force for the sake of science to take a shortcut across this nice clean patch of dirt to the clover beyond, became the next victim of my passion for original observation. He could have made his way across the area without trouble, but he too kept getting in the way, and suddenly transformed from a slow-moving laggard into the liveliest acrobat as he stood on his head and seemingly dove right into the hole that suddenly appeared beneath him. A certain busy fly moved around the area, more than once disrupting my necessary composure as it persistently crawled on my nose. I was thrilled when I saw the fickle insect curiously contemplating a pair of calipers at the center of one of the little courts! But, whether due to past experience or some instinctual wisdom in the insect, the pronged hooks, despite coming together with a click once or twice close to the tempter, missed their chance, and the trap was soon carefully reset, level with the ground at the entrance of the burrow.
The contrast of these clean-swept door-yards with the mound of débris of the ants suggested an investigation of the comparative methods of burrowing and the disposal of the excavated material. Here is a hole evidently some inches in depth; what, then, has become of the earth removed? Suiting action to the thought, I swept into the openings of two or three of the holes quite a quantity of loose earth scraped from the close vicinity, and thus completely obliterated the opening of burrow, door-yard and all.
The difference between these tidy yards and the pile of debris from the ants made me want to investigate how they dig and manage the dirt they remove. Here's a hole that is obviously several inches deep; so what happened to the dirt that was taken out? Acting on this thought, I filled the openings of two or three holes with a good amount of loose dirt that I scraped from nearby, completely covering the entrance of the burrow and the yard.
I awaited in vain any sign of returning activity at the surface, and, my patience being somewhat taxed, I entered my studio, where I remained for a quarter of an hour, perhaps. Upon stealing cautiously to the doorway, I observed all the obliterated holes had reappeared, and upon taking once more my original position I was soon rewarded with a demonstration of the method of excavation. After a moment or two a pellet of earth seemed suddenly to rise from within the cavity, and when arrived at the level of the ground was suddenly shot forth a distance of five[Pg 64] or six inches, as though thrown from a tiny round flat shovel, which suddenly flashed from the opening, and as quickly retired to its depths, though not without a momentary display of two curved prongs and a formidable show of spider-like legs.
I waited in vain for any sign of activity at the surface, and feeling my patience wear thin, I went into my studio, where I stayed for about fifteen minutes. When I cautiously peeked out the doorway, I noticed that all the holes that had been filled in had reappeared. Taking my original position again, I was soon rewarded with a demonstration of how they excavate. After a moment, a clump of earth suddenly rose from the hole, and when it reached ground level, it was shot out a distance of five[Pg 64] or six inches, as if it had been tossed by a small round flat shovel that quickly flashed out from the opening and just as quickly retreated, showing a brief display of two curved prongs and a striking array of spider-like legs.
After a short lapse of time the act was repeated, this time a tiny stone being brought to the surface, and, after a brief pause at the doorway, was jerked to a distance as from a catapult. I now concluded to try the power of this propelling force, and taking a small stone, about three-quarters of an inch in length and a quarter-inch in thickness, laid it over the mouth of the tunnel. A few minutes passed, when I noticed a slight motion in the stone, immediately followed by a forcible ejectment, which threw it nearly an inch, the propelling instrument retiring so quickly into the burrow beneath as to scarce afford a glimpse. The stone appeared almost to have jumped voluntarily.
After a short while, the action was repeated, this time a small stone being lifted to the surface, and, after a brief pause at the entrance, was launched away like from a catapult. I decided to test the strength of this force, so I took a small stone, about three-quarters of an inch long and a quarter-inch thick, and placed it over the tunnel opening. A few minutes went by, and I noticed a slight movement in the stone, quickly followed by a strong push that sent it nearly an inch away, the propelling force retreating so fast into the hole below that it barely gave a glimpse. It almost seemed like the stone jumped on its own.
For an hour or more the bombardment of pellets and small stones continued from the mouth of the pit, until a small pile of the spent ammunition had accumulated at several inches distance, and at length the hole entirely disappeared, the earth in its vicinity presenting an apparently level surface—an armed peace, in truth, with the[Pg 65] two touchy curved calipers on duty, as already described.
For an hour or more, the barrage of pellets and small stones kept coming from the pit, until a small pile of spent ammunition built up several inches away. Eventually, the hole completely vanished, with the ground around it appearing flat—an uneasy peace, really, with the[Pg 65] two sensitive curved calipers on guard, as previously mentioned.

Following the hint of past experience, I concluded to explore the depths of one of these tunnels, especially as I desired a specimen of the wily tenant for portraiture; and it is, indeed, an odd fish that one may land on the surface if he be sufficiently alert in his angling. No hook or bait is required in this sort of fishing. Taking a long culm of timothy-grass, I inserted the tip into the burrow. It progressed without impediment two, three, six, eight inches, and when at the depth of about ten inches appeared to touch bottom, which in this kind of angling is the signal for a "strike" and the landing of the game. Instantly withdrawing the grass culm, I[Pg 66] found my fish at its tip, from which he quickly dropped to the ground. His singular identity is shown in my illustration—an uncouth nondescript among grubs. His body is whitish and soft, with a huge hump on the lower back armed with two small hooks. His enormous head is now seen to be apparently circular in outline, and we readily see how perfectly it would fill the opening of the burrow like an operculum. But a close examination shows us that this operculum is really composed of two halves, on two separate segments of the body, the segment at the extremity only being the true head, armed with its powerful, sharp, curved jaws. As he lies there sprawling on his six spider-like legs, we may now easily test the skill of his trap, and gain some idea of his voracious personality.
Following the lessons of past experiences, I decided to explore the depths of one of these tunnels, especially since I wanted to catch a specimen of the clever inhabitant for a portrait; and it's definitely an unusual catch you might land if you're quick enough in your fishing. No hook or bait is needed for this type of fishing. I took a long blade of timothy grass and inserted the tip into the burrow. It moved smoothly for two, three, six, eight inches, and when it reached about ten inches deep, it seemed to touch bottom, which in this style of fishing means it's time to "strike" and reel in the catch. Quickly pulling out the grass, I[Pg 66] found my catch at the tip, which promptly fell to the ground. Its unique appearance is illustrated in my drawing—an awkward, undefined creature among grubs. Its body is pale and soft, with a large hump on its lower back armed with two small hooks. Its huge head appears almost circular in shape, and it's easy to see how perfectly it would fill the entrance of the burrow like a lid. However, a closer look reveals that this 'lid' is actually made up of two halves, belonging to two separate segments of its body, with only the segment at the end being the true head, equipped with its strong, sharp, curved jaws. As it lies there sprawled on its six spider-like legs, we can now easily evaluate the effectiveness of its trap and get a sense of its insatiable nature.
If with the point of our knife-blade, holding it in the direction of the insect's body, we now touch its tail, what a display of vehement acrobatics! Instantly the agile body is bent backward in a loop, while the teeth fasten to the knife-blade with an audible click. If our finger-tip is substituted for the steel, the force of the stroke and the prick and grip of the jaws are unpleasantly perceptible.
If we use the tip of our knife to touch the insect's tail while pointing it toward its body, what a show of intense acrobatics! Immediately, the agile body bends backward in a loop, while the jaws clamp onto the knife with a noticeable click. If we replace the knife with our fingertip, the force of the impact and the sting and grip of the jaws are uncomfortably noticeable.
In order to fully comprehend the make-up of this curious cave-dweller we must turn biologists for the moment. He must be considered from[Pg 67] the evolutionary stand-point, or at least from the stand-point of comparative anatomy.
In order to fully understand the nature of this interesting cave-dweller, we need to consult biologists for a moment. He should be viewed from[Pg 67] the perspective of evolution, or at least from the perspective of comparative anatomy.
The first discovery that we make is that as we now see him he is crawling on his back—a fact which seems to have escaped his biographers heretofore. It is, in truth, the underside of his head which is uppermost at the mouth of the burrow, and his six zigzag legs are distorted backward to enable him to keep this contrary position. And what a hideous monster is this, whose flat, metallic, dirt-begrimed face stares skyward from this circular burrow! Well might it strike terror to the heart of the helpless insect which should suddenly find himself confronted by the motionless stare of these four cruel, glistening black eyes! But he is now a "fish out of water," and is about as helpless, nature never having intended him to be seen outside of his burrow—at least, in this present form. There he dwells, setting his circular trap at the mouth of his pitfall, and waiting for the voluntary sacrifice of his insect neighbors to fill his maw.
The first thing we notice is that, as we see him now, he is crawling on his back—a detail that seems to have escaped his biographers until now. In reality, it's the underside of his head that's facing up at the entrance of the burrow, and his six zigzag legs are twisted backward to maintain this awkward position. And what a terrifying creature this is, with its flat, metallic, dirt-covered face staring up from this circular hole! It's enough to strike fear into the heart of any helpless insect that suddenly finds itself facing the still gaze of those four cruel, shiny black eyes! But he is now a "fish out of water," utterly helpless, as nature never meant for him to be seen outside of his burrow—at least, not in this form. He resides there, setting his circular trap at the entrance of his pitfall, waiting for his insect neighbors to voluntarily sacrifice themselves to fill his stomach.

But this uncouth shape, which so courts obscurity, is not always thus so reasonably retiring. A few glass tumblers inverted above as many of these larger holes during the summer will intercept the winged sprite into which he is shortly to[Pg 68] be transfigured—a brilliant metallic-hued beetle, perhaps flashing with bronzy gold or glittering like an emerald—the beautiful cicindela, or tiger-beetle, known to the entomologist as the most agile winged among the coleopterous tribe; known to the populace, perhaps, simply as a bright glittering fly that revels in the hot summer sands of the sea-shore or dusty country road, making its short spans of glittering flight from the very feet of the observer.
But this awkward shape, which seems to shy away from attention, isn't always so discreet. A few glass tumblers turned upside down over these larger holes during the summer will catch the flying creature, into which it will soon transform—a brilliant metallic-colored beetle, possibly shining with bronzy gold or sparkling like an emerald—the beautiful cicindela, or tiger beetle, known to entomologists as the swiftest flyer among the beetle family; and known to the general public, perhaps, simply as a bright, shining bug that thrives in the hot summer sand at the beach or on dusty country roads, making its short, dazzling flights just in front of the observer's feet.
If we capture one of them with our butterfly-net he will be found to bear a general resemblance to the portrait here indicated—a slender-legged, proportionably large-headed beetle, with formidable jaws capable of wide extension, and re-enforced by an insatiate carnivorous hunger inherited from his former estate.
If we catch one of them with our butterfly net, it will look quite similar to the picture shown here—a slender-legged beetle with a relatively large head, strong jaws that can open wide, and a relentless carnivorous appetite passed down from its previous life.
It will thus be seen that all the holes which we observe in the ground are not ant-holes; nor, indeed, are they monopolized by the tiger-beetles. There were other tunnels which I saw dug in my square yard of earth on that morning, which, while not of quite such depth, represented equally deep-laid plans.
It can be seen that not all the holes we see in the ground are ant holes; nor are they solely made by tiger beetles. There were other tunnels I noticed dug in my little patch of dirt that morning, which, although not as deep, indicated equally serious intentions.
While observing my cicindelas on that morn[Pg 69]ing, my attention was at length diverted by an old friend of mine, who gave promise of much entertainment—a tiny black wasp, whose restless, rapid, zigzag, apparently aimless wanderings over the ground brought him into continual danger of contact with the snatching jaws of the cave-dwelling tiger, from which, however, he somehow escaped, though I distinctly heard the occasional clicking of the eager jaws.
While I was watching my cicindelas that morning[Pg 69], I was eventually distracted by an old friend of mine who promised to be quite entertaining—a small black wasp. Its restless, fast, zigzag, seemingly aimless movements on the ground constantly put it in danger of getting caught by the cave-dwelling tiger. Somehow, it managed to escape, although I could definitely hear the occasional clicking of the tiger's eager jaws.

With short abrupt flights or agile runs of a few inches, accompanied by nervous periodic flirts of the folded wings, the insect had covered pretty much of the ground in a short time, until she at length appeared to have discovered the object of her search, as she withdrew from beneath a sorrel leaf a big fat spider several times as large as herself. Its legs were folded beneath its body, and it was perfectly plain that this was not the first time that it had been in the toils of the wasp, which had evidently stung it into submission and stupor some minutes previous. Tugging bravely at her charge, the little black Amazon dragged her burden nimbly over the ground, pulling it after her in entire disregard of obstacles, now this way, now that, with the same exasperating disregard of eternity which she at first displayed, and at length deposited it on the top of a little flat weed, where it[Pg 70] was left, while for five minutes more she pursued the same zigzag, apparently senseless meandering over the entire field of earth. Now she seems again to stumble upon her neglected prey, and taking it once more in her formidable jaws, she lugs it again for a long helter-skelter jaunt, this time depositing it in the neighborhood of a hole, which at first sight might have been considered an "ant-hole," from the débris which lay scattered about in its vicinity. After considerable needless delay, she is seen for once motionless, so far as her legs are concerned, but with her head over the tunnel, while, with flipping wings and rapidly waving antennæ, she investigates its depths. Satisfied that all is well, she again reaches her drowsy spider, by a tangled circuit of about a quarter of a mile—wasp measurement—and taking the victim in her teeth for the third time, finally succeeds in reaching the burrow, into which, without a parti[Pg 71]cle of ceremony, she instantly retreats, dragging her helpless burden after her. Both wasp and spider are soon out of sight, and so remain perhaps for a space of two minutes, when the tips of the nervous antennæ appear at the doorway and the wasp emerges. What now follows is most curious and interesting. With an energy and directness in striking contrast to her previous proceedings, she proceeds to fill the cavity, biting the earth with her mandibles, and with her spiked legs kicking and shoving in the loose soil thus collected, ever and anon backing up to the hole and inserting the tip of her tail to force down the mass. As the filling is nearly completed, with the fore feet and jaws the surrounding earth is scraped for material, which she immediately proceeds to pack by a rhythmic tamping motion of the tail, until, at the end of five minutes, perhaps, the ground-level is finally reached, the surface smoothed, and no sign remains to mark the grave of the stupefied spider victim.
With quick, sudden flights or agile scurries of just a few inches, paired with nervous flicks of her folded wings, the insect managed to cover a lot of ground in no time. Eventually, it seemed she found what she was looking for, pulling a big, fat spider several times her size from under a sorrel leaf. Its legs were tucked beneath its body, making it clear that this was not the first time it had fallen prey to the wasp, which had clearly stung it into submission and dazed it a few minutes earlier. Bravely tugging at her catch, the little black wasp skillfully dragged her burden over the ground, pulling it behind her without a care for any obstacles, sometimes this way, then that, showing the same frustrating disregard for eternity that she had at first, and eventually dropped it on top of a small flat weed, where it[Pg 70] remained as she spent another five minutes zigzagging around the entire area aimlessly. She then seemed to accidentally rediscover her neglected prey, and once again grabbing it firmly in her strong jaws, she lugged it off on another chaotic journey, this time dropping it near a hole that at first glance could have been mistaken for an "ant-hole" due to the debris scattered around it. After some unnecessary delay, she was seen motionless—well, her legs were still—but with her head over the tunnel, flipping her wings and waving her antennae as she checked the depths. Satisfied everything was okay, she took a roundabout route of about a quarter of a mile—wasp measurement—to grab her drowsy spider for a third time, finally making it to the burrow, where, without any hesitation, she quickly retreated, dragging her helpless prize along with her. Soon, both wasp and spider were out of sight, remaining that way for perhaps two minutes, until the tips of her nervous antennae appeared at the doorway and she emerged. What happens next is truly curious and fascinating. With energy and directness that sharply contrasted her previous actions, she began to fill the cavity, biting the earth with her jaws, and using her spiked legs to kick and shove the loose dirt she collected while occasionally backing up to the hole to insert the tip of her tail to pack it down. As she neared the end of the filling, she scraped at the surrounding earth with her forelegs and jaws for more material, which she then rhythmically tamped down with her tail, until, in about five minutes, the ground level was finally restored, the surface smoothed over, leaving no trace to indicate the grave of the dazed spider victim.

Not an hour after this episode I was treated to[Pg 72] another of even more interest. As I took my seat upon the door-step I started into flight a big black wasp, upon whose doings I had evidently been intruding.
Not an hour after this event, I witnessed[Pg 72] something even more interesting. As I sat down on the doorstep, a large black wasp took off, clearly disturbed by my presence.
This wasp was much larger than the one just described, being about an inch in length. Its wings were pale brown and its body jet-black, with sundry small yellowish spots about the thorax. But its most conspicuous feature, and one which would ever fix the identity of the creature, was the long, slender, wire-like waist, occupying a quarter of the length of its entire body.
This wasp was much larger than the one just described, about an inch long. Its wings were light brown and its body was jet black, with several small yellowish spots around the thorax. But its most noticeable feature, which would always make it easy to identify, was the long, thin, wire-like waist that took up a quarter of its total body length.
In a moment or two the wasp had returned, and stood at the mouth of the shallow pit. Eying me intently for a space, and satisfied that there was nothing to fear, she dived into the hollow and began to excavate, turning round and round as she gnawed the earth at the bottom, and shovelling it out with her spiked legs. Now and then she would back out of the burrow to reconnoitre, and her alert attitude at such times was very amusing—her antennæ drooping towards the burrow and in incessant motion; the abdomen on its long wire stem bobbing up and down at regular intervals, accompanied by a flipping motion of the wings; the short fore legs, one or both, upraised with comical effect.[Pg 73]
In a moment, the wasp had returned and was at the entrance of the shallow pit. After watching me closely for a bit and realizing there was no danger, she dove into the hole and started digging, turning around and around as she chewed at the earth at the bottom and shoveling it out with her spiked legs. Every so often, she would back out of the burrow to check her surroundings, and her alert stance during these moments was really amusing—her antennae drooping toward the burrow and constantly moving; her abdomen bouncing up and down on its long, thin stalk at regular intervals, along with a flicking motion of her wings; and her short front legs, one or both, raised in a comical manner.[Pg 73]

As the tunnel was deepened a new method of excavation was employed. It has now reached a depth of an[Pg 74] inch, only the extremity of the insect's body appearing, and the two hindermost legs clinging to surrounding earth for purchase. The deep digging is now accompanied by a continual buzzing noise, resembling that produced by a bluebottle fly held captive between one's fingers. At intervals of about ten or fifteen seconds the wasp would quickly back out of the burrow, bringing a load of sand, which it held between the back of the jaws and its thorax, sustained at the sides by the two upraised fore legs. After a moment's pause with this burden, the insect would make a sudden short darting flight of a foot or more in a quick circuit, hurling the sand a yard or more distant from the burrow. At the end of about fifteen minutes the burrow was sunk to the depth of an inch and a half, the wasp entirely disappearing, and indicated only by the continuous buzzing.
As the tunnel got deeper, a new digging method was used. It has now reached a depth of an[Pg 74] inch, with only the tip of the insect's body showing, and its two back legs gripping the surrounding soil for stability. The deep digging comes with a constant buzzing sound, similar to that of a bluebottle fly trapped between someone's fingers. Every ten to fifteen seconds, the wasp would quickly back out of the burrow, carrying a load of sand, which it held between its jaws and thorax, stabilized on the sides by its two raised front legs. After pausing briefly with this load, the insect would suddenly dart off about a foot in a quick circle, tossing the sand a yard or more away from the burrow. After about fifteen minutes, the burrow reached a depth of an inch and a half, with the wasp completely disappearing, indicated only by the continuous buzzing.
At this time, the luncheon hour having arrived, I was obliged to pause in my investigations, and in order to be able to locate the burrow in the event of its obliteration by the wasp before my return, I scratched a circle in the hard dirt, the hole being at its exact centre.[Pg 75]
At that moment, lunchtime arrived, so I had to stop my investigations. To ensure I could find the burrow again in case the wasp covered it up before I got back, I scratched a circle in the hard ground, with the hole at its exact center.[Pg 75]

Upon my return, an hour later, I was met with a surprise. The ways of the digger-wasps of various species were familiar, but I now noted a feature of wasp-engineering which indeed seems to await its chron[Pg 76]icler, as I find no mention of it by the wasp-historians.
Upon my return, an hour later, I was met with a surprise. The behavior of the digger wasps from different species was familiar to me, but I began to notice a detail in wasp engineering that really seems to need a chron[Pg 76]icler, as I haven't seen any mention of it by the wasp historians.
At the exact centre of my circle, in place of a cavity, I now found a tiny pile of stones, supported upon a small stick and fragment of leaf, which had been first drawn across the opening.
At the exact center of my circle, instead of a hole, I now saw a small pile of stones, balanced on a tiny stick and a piece of leaf, which had been placed across the opening.
This was evidently a mere temporary protection of the burrow, I reasoned, while the digger had departed in search of prey, and my surmise was soon proved to be correct, as I observed the wasp, with bobbing abdomen and flipping wings, zigzagging about the vicinity. Presently disappearing beneath a small plantain leaf, she quickly emerged, drawing behind her not a spider, as in the case of her smaller predecessor, but a big green caterpillar, nearly double her own length, and as large around as a slate-pencil—a peculiar, pungent, waspy-scented species of "puss-moth" larva, which is found on the elm, and with which I chanced to be familiar.
This was obviously just a temporary cover for the burrow, I thought, while the digger went off to look for food, and my guess was soon confirmed when I saw the wasp, with its bobbing abdomen and fluttering wings, zigzagging around the area. After a moment, it disappeared under a small plantain leaf, then quickly came back out, pulling behind it not a spider like her smaller relative, but a big green caterpillar, almost twice her length and as thick as a pencil—a strange, strong-smelling, wasp-scented type of "puss-moth" larva that I happened to know about, which is found on the elm.
The victim being now ready for burial, the wasp sexton proceeded to open the tomb. Seizing one stone after another in her widely opened jaws, they were scattered right and left, when, with apparent ease and prompt despatch, the listless larva was drawn towards the burrow, into whose depths he soon disappeared. Then, after a short[Pg 77] and suggestive interval, followed the emergence of the wasp, and the prompt filling in of the requisite earth to level the cavity, much as already described, after which the wasp took wing and disappeared, presumably bent upon a repetition of the performance elsewhere. But she had not simply buried this caterpillar victim, nor was the caterpillar dead, for these wasp cemeteries are, in truth, living tombs, whose apparently dead inmates are simply sleeping, narcotized by the venom of the wasp sting, and thus designed to afford fresh living food for the young wasp grub, into whose voracious care they are committed.
The victim was now ready for burial, so the wasp sexton started to open the tomb. Grabbing one stone after another in her wide-open jaws, she scattered them left and right. Then, with apparent ease and quickness, the sluggish larva was pulled toward the burrow, and soon it disappeared into the depths. After a brief[Pg 77] and suggestive pause, the wasp emerged and quickly filled in the necessary earth to level the cavity, just as described before. After that, the wasp took off and flew away, presumably to repeat the process somewhere else. But she hadn't just buried this caterpillar victim, nor was the caterpillar dead. These wasp cemeteries are, in reality, living tombs, where the seemingly dead occupants are just sleeping, numbed by the venom of the wasp's sting, and are meant to provide fresh living food for the young wasp grub they are entrusted to.
By inserting my knife-blade deep into the soil in the neighborhood of this burrow I readily unearthed the buried caterpillar, and disclosed the ominous egg of the wasp firmly imbedded in its body. The hungry larva which hatches from this egg soon reaches maturity upon the all-sufficient food thus stored, and before many weeks is transformed to the full-fledged, long-waisted wasp like its parent.
By pushing my knife deep into the ground near this burrow, I quickly dug up the buried caterpillar and revealed the spooky egg of the wasp firmly embedded in its body. The hungry larva that hatches from this egg soon grows up on the ample food stored inside, and in just a few weeks, it transforms into a fully grown, long-waisted wasp like its parent.
The disproportion in the sizes of the predatory wasps and their insect prey is indeed astonishing. The great sand-hornet selects for its most frequent victim the buzzing cicada, or harvest-fly, an insect much larger than itself, and which it carries[Pg 78] off to its long sand tunnels by short flights from successive elevated points, such as the limbs of trees and summits of rocks, to which it repeatedly lugs its clumsy prey. In the present instance the contrast between the slight body of the wasp and the plump dimensions of the caterpillar was even more marked, and I determined to ascertain the proportionate weight of victor and victim. Constructing a tiny pair of balances with a dead grass stalk, thread, and two disks of paper, I weighed the wasp, using small square pieces of paper of equal size as my weights. I found that the wasp exactly balanced four of the pieces. Removing the wasp and substituting the caterpillar, I proceeded to add piece after piece of the paper squares until I had reached a total of twenty-eight, or seven times the number required by the wasp, before the scales balanced. Similar experiments with the tiny black wasp and its spider victim showed precisely the same proportion, and the ratio was once increased eight to one in the instance of another species of slender orange-and-black-bodied digger which I subsequently found tugging its caterpillar prey upon my door-step patch.[Pg 79]
The difference in size between predatory wasps and their insect prey is truly remarkable. The large sand-hornet often targets the buzzing cicada, or harvest-fly, an insect much bigger than itself, which it drags[Pg 78] into its long sand tunnels by making short flights from high points like tree branches and rock tops, where it awkwardly hauls its unwieldy catch. In this case, the contrast between the slim body of the wasp and the fat size of the caterpillar was even more noticeable, so I decided to measure the weight difference between the victor and the victim. I made a small balance using a dried grass stalk, thread, and two paper disks, then weighed the wasp with equal-sized paper squares as weights. I found that the wasp balanced exactly with four of these squares. After removing the wasp and replacing it with the caterpillar, I kept adding paper squares until I reached a total of twenty-eight, which is seven times what the wasp required, before the scales finally balanced. I conducted similar tests with a small black wasp and its spider prey, which showed the same ratio, and in another case, I found a different slender orange-and-black digger wasp pulling its caterpillar prey on my doorstep, and the ratio was even increased to eight to one.[Pg 79]

The peculiar feature of the piling of stones above the completed burrow was not a mere individual accomplishment of my wire-waisted wasp. On several occasions since I have observed the same manœuvre, which is doubtless the regular procedure with this and other species. The smaller orange-spotted wasp just alluded to indicated to me the location of her den by pausing suggestively in front of a tiny cairn. In this instance a small flat stone, considerably larger than the tunnel, had been laid over the opening, and the others piled upon it. On two[Pg 80] occasions I have surprised this same species of wasp industriously engaged in the selection of a suitable flat foundation-stone with which to cover her burrow: her widely extended slender jaws enable her to grasp a pebble nearly a third of an inch in width.
The unusual practice of stacking stones above the finished burrow wasn't just a unique achievement of my slender wasp. On several occasions, I've seen the same behavior, which is probably standard procedure for this and other wasp species. The smaller orange-spotted wasp mentioned earlier pointed out her nest to me by pausing meaningfully in front of a small pile of stones. In this case, a flat stone, much larger than the tunnel, had been placed over the entrance, with other stones stacked on top of it. I've caught this same type of wasp hard at work on two[Pg 80] occasions, carefully choosing a suitable flat stone to cover her burrow: her long, slender jaws allow her to grip a pebble nearly a third of an inch wide.
In my opening vignette I have indicated two other door-step neighbors which bore my industrious wasps company in their arena of one square yard. To the left, surrounding a grass stem, will be seen an object which is unpleasantly familiar to most country folks—that salivary mass variously known by the libellous names of "snake-spit," "cow-spit," "cuckoo-spit," "toad-spit," and "sheep-spit," or the inelegant though expressive substitute of "gobs." The foam-bath pavilion of the "spume-bearer," with his glittering, bubbly domicile of suds, is certainly familiar to most of my readers; but comparatively few, I find, have cared to investigate the mysterious mass, or to learn the identity of the proprietor of the foamy lavatory.
In my opening vignette, I've mentioned two other door-step neighbors sharing their small space with my busy wasps. To the left, surrounding a grass stem, you can see something that’s all too familiar to most country folks—that foamy substance known by less-than-flattering names like "snake spit," "cow spit," "cuckoo spit," "toad spit," and "sheep spit," or the more straightforward term "gobs." The frothy home of the "spume-bearer," complete with his sparkling, bubbly place of suds, is definitely something most of my readers will recognize; however, I’ve found that relatively few have taken the time to investigate this mysterious substance or to learn who the owner of the bubbly bath is.
The common name of "cow-spit," with the implied indignity to our "rural divinity," becomes singularly ludicrous when we observe not only the frequent generous display of the suds samples, thousands upon thousands in a single small[Pg 81] meadow, but the further fact that each mass is so exactly landed upon the central stalk of grass or other plant—"spitted" through its centre, as it were. The true expectorator is within, laved in his own home-made suds. If we care to blow or scrape off the bubbles, we readily disclose him—- a green speckled bug, about a third of an inch in length in larger specimens, with prominent black eyes, and blunt, wedge-shaped body.
The common name "cow-spit," which seems to insult our "rural divinity," is comically ironic when we notice not just the countless suds samples—thousands in a small [Pg 81] meadow—but also the fact that each mass lands perfectly on the central stalk of grass or other plants, "spitting" right through the middle, so to speak. The real creator of this phenomenon is hidden inside, surrounded by its own homemade suds. If we decide to blow or scrape off the bubbles, we can easily reveal it—a green speckled bug, roughly a third of an inch long in larger individuals, with noticeable black eyes and a blunt, wedge-shaped body.

In the appended sketch I have indicated two views of him, back and profile, creeping upon a grass stalk. A glance at the insect tells the entomologist just where to place him, as he is plainly allied to the cicadæ, and thus belongs to the order Hemiptera, or family of "bugs," which implies, among other things, that the insect possesses a "beak for sucking." To what extent this tiny soaker is possessed of such a beak may be inferred from the amount of moisture with which[Pg 82] he manages to inundate himself, which has all been withdrawn from the stem upon which he has fastened himself, and finally exuded from the pores of his body.
In the attached sketch, I've shown two views of him—back and side—crawling on a blade of grass. A quick look at the insect tells the entomologist exactly where to categorize him, as he's clearly related to the cicadas, which means he's part of the order Hemiptera, or the "bugs" family. This indicates, among other things, that the insect has a "beak for sucking." The extent to which this tiny sipper has such a beak can be inferred from the amount of moisture that[Pg 82] he manages to soak up, all of which comes from the stem he's attached to and is eventually exuded through the pores of his body.
This is the spume-bearer, Aprophora, in his first or larval estate, which continues for a few weeks only. Erelong he will graduate from these ignominious surroundings, and we shall see quite another sort of creature—an agile, pretty atom, one of which I have indicated in flight, its upper wings being often brilliantly colored, and re-enforced by a pair of hind feet which emulate those of the flea in their powers of jumping, which agility has won the insect the popular name of "froghopper." They abound in the late summer meadow, and hundreds of them may be captured by a few sweeps of a butterfly-net among the grass.
This is the spume-bearer, Aprophora, in its early, larval stage, which only lasts for a few weeks. Soon, it will emerge from this humble state, and we will see a completely different creature—an agile, charming little thing, one of which I have shown in flight, with its upper wings often brightly colored, reinforced by a pair of hind legs that jump like a flea, earning the insect the common name "froghopper." They are plentiful in the late summer meadow, and you can catch hundreds of them with a few swipes of a butterfly net through the grass.
My other remaining claimant for notice, shown upon the plant at the right margin of page 60, is a modest and inconspicuous individual, and might readily escape attention, save that a more intent observer might possibly wonder at the queer little tubular pinkish blossoms upon the plant—a rush—while a keen-eyed botanist would instantly challenge the right of a juncus to such a tubular blossom at all, especially at seed-time, and thus[Pg 83] investigate. But the entomologist will probably classify this peculiar blossom at a glance, from its family resemblance to other specimens with which he is familiar. He will know, for instance, that this is a sort of peripatetic or nomadic blossom that will travel about on the plant, with which its open end will always remain in close contact. Many of the individuals are seen apparently growing upright out of the rounded seed-pod of the rush; and when the pink or speckled tube finally concludes to take up its travels, a clean round hole marks the spot of its tarrying, and an empty globular shell tells the secret of this brief attachment.
My other remaining plant to note, shown in the margin on page 60, is a simple and unassuming individual that might easily go unnoticed. However, a more attentive observer might be intrigued by the strange little tubular pinkish blossoms on the plant—a rush. A sharp-eyed botanist would quickly question the right of a juncus to have such a tubular blossom, especially during seed time, and would investigate. But an entomologist will likely identify this unusual blossom right away, based on its resemblance to other specimens he's familiar with. He will recognize that this is a sort of wandering or nomadic blossom that moves around on the plant while keeping its open end in close contact. Many of the blossoms appear to grow upright from the rounded seed pod of the rush, and when the pink or speckled tube eventually decides to move on, a clean round hole remains where it was attached, and an empty globular shell reveals the story of this brief connection.
For this petal-like tube, so commonly to be seen upon the little rush of our paths, is, in truth, a tiny silken case enclosing the body of a small larva—a diminutive psychid, or sack-bearer, which I have not chanced to see described. Only the head and six prolegs of the occupant ever emerge from its case. Dragging its house along upon the plant, it attaches the open mouth of the sack close to the green seed-pod, after which the shell is gnawed through at the point of contact, and the young seeds devoured at pleasure, when a new journey is made to the next capsule, and thus until the maturity of the larva. At this time the[Pg 84] case is about half an inch in length. It is now firmly attached to the plant. The opening is completely spun over with silk, and the case becomes a cocoon for the winter; and a few of these September cocoons are well worth gathering, if only to see the queer little moth which will emerge from them the following spring.
For this petal-like tube, often seen on the little rush of our paths, is actually a tiny silk case that holds a small larva—a little psychid, or sack-bearer, which I haven’t seen described anywhere. Only the head and six prolegs of the occupant ever stick out from the case. Dragging its home along the plant, it attaches the open mouth of the sack close to the green seed-pod, and then it gnaws through the shell at the point where they touch, devouring the young seeds at will. After that, it moves on to the next capsule, and this continues until the larva matures. At this point, the[Pg 84] case is about half an inch long. It is now securely attached to the plant. The opening is completely covered with silk, turning the case into a cocoon for the winter. A few of these September cocoons are definitely worth collecting, if only to see the strange little moth that will emerge from them the following spring.

A QUEER LITTLE FAMILY ON THE BITTERSWEET


n a recent half-hour's relaxation, while comfortably stretched in my hammock upon the porch of my country studio, I was surprised with a singular entertainment. I soon found myself most studiously engaged. Entwining the corner post of the piazza, and extending for some distance along the eaves, a luxuriant vine of bittersweet had made itself at home. The currant-like clusters of green fruits, hanging in pendent clusters here and there, were now nearly mature, and were taking on their golden hue, and the long, free shoots of tender growth were reaching out for conquest on right and left in all manner of graceful curves and spirals. Through[Pg 88] an opening in this shadowy foliage came a glimpse of the hill-side slope across the valley upon whose verge my studio is perched, and as my eye penetrated this pretty vista it was intercepted by what appeared to be a shadowed portion of a rose branch crossing the opening and mingling with the bittersweet stems. In my idle mood I had for some moments so accepted it without a thought, and would doubtless have left the spot with this impression had I not chanced to notice that this stem, so beset with conspicuous thorns, was not consistent in its foliage. My suspicions aroused, I suddenly realized that my thorny stem was in truth merely a bittersweet branch in masquerade, and that I had been "fooled" by a sly midget who had been an old-time acquaintance of my boyhood, but whom I had long neglected.
n a recent half-hour of relaxation, while comfortably stretched in my hammock on the porch of my country studio, I was surprised by a unique distraction. I soon found myself deeply engaged. A lush bittersweet vine had made itself at home, wrapping around the corner post of the piazza and extending along the eaves. The clusters of green fruits, resembling currants, were now nearly ripe, starting to take on their golden color, and the long, free shoots of new growth were reaching out in all sorts of graceful curves and spirals. Through[Pg 88] an opening in this shadowy foliage, I caught a glimpse of the hillside slope across the valley on which my studio sits. As I admired this pretty scene, my view was interrupted by what seemed to be a shadowed part of a rose branch crossing the opening and mixing with the bittersweet stems. In my relaxed state, I accepted this without thinking for a moment and would have left the spot with that impression if I hadn’t noticed that this thorny stem didn’t match its foliage. My suspicions aroused, I suddenly realized that my thorny stem was actually just a bittersweet branch in disguise, and that I had been "fooled" by a clever little plant that had once been an old friend from my childhood, but whom I had long forgotten.
Every one knows the climbing-bittersweet, or "waxwork" (Celastrus scandens), with its bright berries hanging in clusters in the autumn copses, each yellow berry having now burst open in thin sections and exposed the scarlet-coated seeds. Almost any good-sized vine, if examined early in the months of July and August, will show us the thorns, and more sparingly until October, and queer thorns they are, indeed! Here an isolated one, there two or three together, or perhaps a[Pg 89] dozen in a quaint family circle around the stem, their curved points all, no matter how far separated, inclined in the same direction, as thorns properly should be. Let us gently invade the little colony with our finger-tip. Touch one never so gently and it instantly disappears. Was ever thorn so deciduous? And now observe its fellows. Here one slowly glides up the stem; another in the opposite direction; another sideways. In a moment more the whole family have entirely disappeared, as if by hocus-pocus, until we discover, by a change of our point of view, that they have all congregated on the opposite side of the stem, with an agility which would have done credit to the proverbial gray squirrel.
Everyone knows the climbing bittersweet, or "waxwork" (Celastrus scandens), with its bright berries hanging in clusters in the autumn woods. Each yellow berry has now burst open in thin sections, exposing the scarlet-coated seeds. Almost any decent-sized vine, if checked early in July and August, will show us the thorns, and more sparingly until October. And what strange thorns they are! Here’s an isolated one, there are two or three together, or maybe a dozen in a quirky little family circle around the stem, all their curved points, no matter how far apart, leaning in the same direction, just like thorns should. Let’s gently poke at this little colony with our fingertip. Touch one ever so lightly and it vanishes instantly. Has there ever been a thorn so fickle? Now, watch its companions. One slowly climbs up the stem; another goes in the opposite direction; another moves sideways. In just a moment, the whole group has completely vanished, as if by magic, until we realize, by changing our perspective, that they've all gathered on the other side of the stem, moving with a speed that would impress even the legendary gray squirrel.
This animated thorn is about a quarter of an inch long, and dark brown in color, with two yellowish spots on the edge of its back.
This animated thorn is about a quarter of an inch long and dark brown in color, with two yellowish spots on the edge of its back.
Nor is this all the witchery of this bittersweet thorn. It is well worth our further careful study. Seen collectively, the thorny rose branch is instantly suggested, but occasionally, when we observe a single isolated specimen, especially in the month of July, he will certainly masquerade in an entirely new guise. Look! quick. Turn your magnifier hither on this green shoot. No thorn this. Is it not rather a whole covey of quail,[Pg 90] mother and young creeping along the vine? Who would ever have thought of a thorn! Turning now to our original group, how perfectly do they take the hint, for are they not a family of tiny birds with long necks and swelling breasts and drooping tails, verily like an autumn brood of "Bob Whites"?
Nor is this all the charm of this bittersweet thorn. It's definitely worth further careful study. When you look at it as a whole, the thorny rose branch is immediately recognizable, but sometimes, when you focus on a single isolated piece, especially in July, it takes on an entirely new appearance. Look! Quick. Bring your magnifier over to this green shoot. No thorn here. Doesn’t it look more like a whole group of quail, mother and young, moving along the vine? Who would have guessed it was a thorn! Now, back to our original group, how perfectly they fit the description, for aren’t they like a family of tiny birds with long necks, puffed-out chests, and drooping tails, just like a fall brood of "Bob Whites"?

But the little harlequin is as wary a bird as he was a thorn! No sooner do we touch his head with our finger than with an audible "click" he is off on a most agile jump, which he extends with buzzing wings, and is even now perhaps aping a thorn among a little group of his fellows somewhere among the larger bittersweet branches.
But the little harlequin is just as cautious as he was sharp! No sooner do we touch his head with our finger than with a noticeable "click" he hops away in a quick jump, flapping his buzzing wings, and maybe even pretending to be a thorn among a small group of his friends somewhere among the larger bittersweet branches.
It is only as we capture one of the little protean acrobats between our finger-tips and examine him with a magnifier that we can really make "head or tail" of his queer anatomy. Even thus enlarged it is difficult to get entirely rid of the idea of a bird. I have shown a group of the insects in various attitudes, the position of the eyes alone serving as a starting-point for our comprehension of his singular make-up. The tall neck-like or thorn-like prominence is then seen to be a mere elongated helmet, which is prolonged into a steep angle behind, so as to cover the back of the creature like a peaked roof, a feature from which the scientific name of this particular group of insects is derived, Membracis, meaning sharp-edged, the sides of the slope being covered by the close-fitting wings, which, though apparently compact with the body of the insect, are nevertheless always available for instant and most agile flight. We now discover two pairs of stout legs just be[Pg 92]neath the edge of the wings, a third more slender pair being concealed behind, ready for immediate use in association with these buzzing wings when the whim of the midget prompts it to leap.
It’s only when we catch one of those little flexible acrobats between our fingertips and look at it through a magnifier that we can really make sense of its strange anatomy. Even when enlarged, it's hard to completely shake the idea of it being a bird. I've displayed a group of these insects in different positions, with the placement of the eyes serving as a starting point for understanding their unique structure. The tall neck-like or thorn-like feature is actually just an elongated helmet that extends sharply behind, covering the back of the creature like a peaked roof. This is where the scientific name for this group of insects comes from, Membracis, which means sharp-edged. The sides of the slope are covered by tightly fitting wings, which, although they seem merged with the insect's body, are always ready for quick and agile flight. We can now see two pairs of sturdy legs just beneath the edge of the wings, with a third, more slender pair hidden behind, ready to spring into action along with those buzzing wings whenever this little creature feels like jumping.

This insect is the tree-hopper, and is but one of many equally curious and mimetic species to be found among the smaller branches of various trees and shrubs.
This insect is the tree-hopper, and it's just one of many equally fascinating and mimicking species found among the smaller branches of different trees and shrubs.
Our largest membracis is to be seen—with difficulty—on the terminal twigs of the locust-tree, its outlines so exactly imitating the thorny growths of the branch as to escape detection even by the closest scrutiny. Another remarkable species is a protégé of the oak, so closely simulating the warty bark of the smaller branches upon which it is[Pg 93] found that our eyes may rest upon it repeatedly without recognizing it. The life history of these singular insects is quite similar, and is soon told. The membracis belongs to the tribe of "Bugs," Hemiptera, which implies that it possesses a beak instead of jaws, by which it sucks the sap of plants, precisely like the aphis, or plant-louse. This tiny beak we can readily distinguish bent beneath the body of our bittersweet hopper. Inserting it deep into the succulent bark, the parasite remains for hours as motionless as the thorn it imitates, the lower outline of its body hugging close against the bark. The curious suggestion of the thorn is produced not only by the outline, but by the curious fact that the hopper never sits across the twig, but always in the direction of its length; and, what is more, the projecting point of the thorax is always directed towards the end of the branch, or direction of growth. It is no easy thing even for the casual botanist to determine this nice point in a given segment of a bittersweet branch placed in his hand, the position of the chance leaf or leaf scar being his only guide. But the Membracis binotata rarely—indeed never, so far as I have examined—makes a mistake. Thus the wandering spray of bittersweet, recurve and twist upon itself as it may, will always dis[Pg 94]close the little hopper or colony of them headed for its tip.
Our largest membracis can be spotted—with some effort—on the ends of locust tree twigs, its shape so closely resembling the thorny growths of the branch that it can go unnoticed even under close examination. Another interesting species is found on the oak, mimicking the bumpy bark of the smaller branches so well that we can look at it repeatedly without realizing it's there. The life cycle of these unique insects is quite similar and can be quickly summed up. Membracis belongs to the "Bugs" tribe, Hemiptera, which means it has a beak instead of jaws, allowing it to suck the sap from plants, just like an aphis or plant louse. We can easily spot this tiny beak tucked under the body of our bittersweet hopper. By inserting it deep into the juicy bark, the insect remains as still as the thorn it resembles for hours, with the bottom outline of its body pressed closely against the bark. The suggestion of a thorn comes not only from its shape but also from the fact that the hopper never sits across the twig but always along its length; additionally, the protruding part of the thorax always points towards the tip of the branch or the direction of growth. Even a casual botanist might find it challenging to determine this subtle detail on a bittersweet branch placed in their hand, relying only on the position of a random leaf or leaf scar as a guide. However, the Membracis binotata rarely—if ever, based on my observations—makes a mistake. Therefore, the wandering spray of bittersweet, even as it curves and twists, will always reveal the little hopper or colony of them heading towards its end.

But I have omitted to mention one singular feature which is the usual accompaniment of my group of hoppers, and is, indeed, the most conspicuous sign of their presence on any given shrub. In the cut below I have indicated a short section of a bittersweet branch as it commonly appears, the twig apparently beset with tiny tufts of cotton, occasionally so numerous as to present a continuous white mass, usually on the lower side of the branch, where its direction is horizontal. They are thus easily seen from below, and a closer examination will always reveal one or more of the black animated thorns in their immediate vicinity, suggesting the responsible[Pg 95] source. These tufts are pure white, a little over an eighth of an inch in length, and semicircular in vertical outline. The natural presumption is the idea of maternity, the mother hopper guarding her bundles of white eggs, or her infant hoppers, perhaps, snugly tucked up in their downy swaddling-clothes. But a closer examination completely dispels this illusion. Instead of the supposed fluffy cotton, we now discover the white substance to be of firm though somewhat sticky consistency, its surface, moreover, beautifully ridged from base to summit in parallel rounded flutings, which meet and interfold like a braid along the summit. If with a sharp knife we now cut downward through and across the mass, we find our tuft to be a mere frothy shell containing two hollow compartments, with a thin central partition extending through the whole length of the cavity. But there is no sign of an egg or other life to be disclosed anywhere, either in its substance or its concealment. What, then, is the office of this tiny fragile house of congealed foam, with its snowy aerated structure, its double arched chambers, its corrugated walls and ceilings, and missing tenant or host? Such was the riddle which it propounded to me, and guided by some previous knowledge of the habits of allied insects,[Pg 96] I was soon enabled to witness a solution of at least a part of its mystery.
But I forgot to mention one unique feature that usually accompanies my group of hoppers, and is, in fact, the most noticeable sign of their presence on any shrub. In the image below, I've highlighted a short section of a bittersweet branch as it typically looks, the twig seemingly covered in tiny tufts of cotton, sometimes so numerous that they form a continuous white mass, usually on the underside of the branch where it grows horizontally. They’re easily spotted from below, and a closer look will always reveal one or more of the black, lively thorns nearby, suggesting the source of the tufts.[Pg 95] These tufts are pure white, a little over an eighth of an inch long, and semicircular in shape when viewed from the side. The natural assumption is that it represents motherhood, with the mother hopper protecting her bundles of white eggs or her young hoppers, maybe snugly wrapped in their soft clothing. But a closer look completely shatters this illusion. Instead of the expected fluffy cotton, we discover that the white material is firm yet somewhat sticky, with a surface beautifully ridged from bottom to top in smooth, rounded grooves that intertwine and form a braid along the top. If we use a sharp knife to cut through the mass, we find that our tuft is just a frothy shell containing two hollow compartments, with a thin central partition running the entire length of the cavity. However, there are no signs of an egg or any life to be found anywhere, either within its substance or hidden away. So, what is the purpose of this delicate little house of solid foam, with its airy snowy structure, its double-arched chambers, its ridged walls and ceilings, and lack of any occupant? This was the puzzle it presented to me, and drawing on some prior knowledge of the habits of related insects,[Pg 96] I was soon able to observe a partial solution to its mystery.
This little thorn-like tree-hopper and all of its queer harlequin tribe are near relatives to the buzzing cicada, or harvest-fly, whose whizzing din in the dog-days has won it the popular misnomer of "locust."
This tiny thorny treehopper and all of its strange harlequin relatives are closely related to the buzzing cicada, or harvest fly, whose noisy racket during the hot summer days has earned it the common nickname "locust."
To the average listener this insect is a mere "wandering voice and a mystery," and its singular form, wide prominent eyes, glassy wings, and double drums are always a surprise to the tyro who first identifies the grotesque as his well-known "locust." Its musical accomplishments during this brief period of its life are known to all, but few have cared to interest themselves in the early history of the singer, ere it perfected its musical resources "for the delight of man." But the naturalist, and especially the arboriculturist and fruit-grower, know to their cost of other tricks of the cicada, or rather of Mrs. Cicada, immortalized by Zenarchus the Rhodian as his "noiseless wife"—
To the average listener, this insect is just a "wandering voice and a mystery," and its unique shape, large, prominent eyes, shiny wings, and dual drums always surprise the beginner who first recognizes this odd creature as the familiar "locust." Everyone knows about its musical talents during this short phase of its life, but few have taken the time to learn about the early life of the singer before it developed its musical abilities "for the delight of man." However, naturalists, especially arborists and fruit growers, are well aware of the cicada's other habits, or rather those of Mrs. Cicada, famously referred to by Zenarchus the Rhodian as his "noiseless wife"—
"Happy the cicadas' lives,
Since they all have noiseless wives."
"Cicadas are lucky,"
"Because they all have silent partners."
I have alluded to the egg of the cicada "inserted in the bark of a twig." This act is accom[Pg 97]plished by a knife-like ovipositor, which literally gouges a deep gash into the tender wood of various twigs, a number of the eggs being implanted in its depths, often causing the death of the branch. Shortly after hatching, the young cicadas leap for the ground, and burrowing beneath the surface, remain for a period varying from three to seventeen years, according to the species, to complete their transformations. Now the habits of my little tree-hopper are somewhat modelled after its big cousin. Knowing that the little insect was provided with a keen-edged ovipositor, and was in the habit of thrusting its tiny eggs beneath the bark, and realizing, too, that these strange tufts were of course in some way connected with the maternal instinct, I was led to investigate. Selecting a branch where the tufts and hoppers seemed most prolific, I brought my magnifying-glass to bear upon them at a respectful distance. Was ever actual thorn more motionless or non-committal than most of these?—their under surfaces hugging close against the bark, their telltale feet closely withdrawn, and all their pointed helmets inclined in the same parallel direction. One after another of the sly little family was examined without a revelation. Not until I had reached the upper limit of the group[Pg 98] did I get any encouragement. Here I discovered one of the midgets in a new position, its pointed helmet inclined farther downward, and its other extremity correspondingly raised, so that I could see beneath its body. I now observed what at first appeared to be the hind leg of the farther side of the body protruding beneath, but in another moment noted my error, and saw that its sharp point had penetrated the bark, into which it soon sank quite deeply, and I realized that the ovipositor was now conducting its tiny eggs into the cambium layer of the bark. Without waiting for this particular individual to finish her labors, which might be extended for hours for aught I knew, I turned my glass upon its nearest neighbor, and a most accommodating specimen she proved, disclosing all the mysteries of the little froth house, its strange material, and unique method of construction. What I saw reminded me irresistibly of the technique of the cake-frosting art of the fancy baker, with its flowing tube of white condiment, and its following tracery of questionable design in high relief. This accommodating specimen had apparently just completed her egg-laying, or had perhaps just filled one nest; and while her attitude was precisely similar to that of her neighbor, I noticed a tiny[Pg 99] ball of glistening froth at the tip of the ovipositor. This was attached to the bark by a touch, and from this starting-point the construction of the glistening house was continued, the apex of the ovipositor pouring out its endless puffy roll of aerated cement, which seemed to set as soon as laid.
I have mentioned the cicada's egg "inserted in the bark of a twig." This is done using a knife-like ovipositor, which literally carves a deep gash into the soft wood of various twigs, implanting several eggs in its depths, often leading to the branch's death. Shortly after hatching, the young cicadas jump to the ground and burrow beneath the surface, remaining there for a period ranging from three to seventeen years, depending on the species, to complete their transformations. Now, the habits of my little tree-hopper are somewhat similar to those of its larger relative. Knowing that the tiny insect has a sharp ovipositor and typically thrusts its tiny eggs beneath the bark, and realizing that these strange tufts are somehow linked to maternal instinct, I felt compelled to investigate. I chose a branch where the tufts and hoppers seemed most abundant and brought my magnifying glass to observe them from a respectful distance. Was there ever a thorn more motionless or indifferent than most of these?—their undersides pressed close against the bark, their telltale feet pulled in tight, and all their pointed helmets leaning in the same parallel direction. I examined one after another of these sly little creatures without gaining any insights. Not until I reached the upper limit of the group did I find any encouragement. Here, I discovered one of the little insects in a new position, its pointed helmet tilted further downward and the other end raised, allowing me to see beneath its body. At first, I thought I was looking at the hind leg of the opposite side of the body sticking out, but soon I realized my mistake; its sharp point had pierced the bark, sinking in quite deeply, and I recognized that the ovipositor was now depositing its tiny eggs into the cambium layer of the bark. Without waiting for this particular individual to finish her work, which could take hours, I turned my glass on its nearest neighbor, who turned out to be very accommodating, revealing all the mysteries of the little froth house, its strange material, and unique method of construction. What I saw reminded me irresistibly of the cake-frosting technique used by fancy bakers, with its flowing tube of white frosting, leaving a design in high relief. This accommodating specimen had apparently just finished laying her eggs or had just filled one nest; and while her posture was exactly like that of her neighbor, I noticed a tiny ball of glistening froth at the tip of the ovipositor. This was attached to the bark with a touch, and from this starting point, the construction of the shiny house continued, with the apex of the ovipositor pouring out its endless puffy roll of aerated cement, which seemed to set as soon as it was laid.
And what a convenient implement this for a froth-house builder who is compelled to work behind her back—mortar-feeder, trowel, darby, compass, and level all in one! Beginning with the first touch of the cement, the flowing point describes a very small half-circle to the right, again meeting the bark. It is now carried inward and upward, describing a very close circle with scarcely any space intervening, a similar circle being repeated on the left side. A new tier is then begun in the same manner, only this time a little larger in the sweep, and leaving a perceptible opening at the right as the central wall is carried upward with slightly decreased material. Returning down the central wall again, the white coil is carried to the left along the bark, and up again on the other outer edge, until it once more meets its fellow at the ridge-pole, where the two coils appear to interlock as in a braid. And thus the little builder continues, enlarging the cavity[Pg 100] with each circuit, until the full height is reached, and then decreasing proportionately until the glistening braided dome is tapered off again against the bark.
And what a handy tool this is for a builder working on a frothy structure who needs to operate discreetly—mortar feeder, trowel, darby, compass, and level all rolled into one! Starting with the first dab of the cement, the flowing point creates a tiny half-circle to the right, meeting the bark again. It's then moved inward and upward, forming a very close circle with barely any space in between, with a similar circle made on the left side. A new layer is started the same way, but this time a bit larger in sweep, leaving a noticeable opening on the right as the central wall is built up with slightly less material. Coming back down the central wall, the white coil is drawn to the left along the bark, and then up again on the other outer edge until it meets its counterpart at the ridge-pole, where the two coils seem to interlock like a braid. And so, the little builder goes on, expanding the cavity[Pg 100] with each round until it reaches full height, then decreasing in size gradually until the shiny braided dome tapers off against the bark.

Now what is the object of this frothy pavilion? The life history of the insect, in contrast to that of the cicada, will perhaps throw a little light on that question. In the cicada, as I have shown, the eggs are inserted in the bark, but the young, hatching about six weeks later, immediately forsake the parent tree and enter the ground. But the young of our bittersweet membracis are not thus fickle, the entire life of the insect being spent on the plant. Moreover, its eggs are laid in late summer, and do not hatch until the following[Pg 101] spring. What, then, is this canopy of the tree-hopper but the provision of a thoughtful mother, a pavilion about her offspring as a shelter through the winter storms? In early July the tiny hoppers emerge from their egg-cases, and presumably creep out from their luminous domicile, and later on in the season these broods of varying numbers and all sizes are to be seen among the young stems of the plant, their beaks inserted, their pointed heads invariably in the same direction—towards the top of the branch. Even though in flight one of the midgets is seen to alight in violence to the rule, he instantly recognizes his mistake, and quickly glides[Pg 102] round to the orthodox position.
Now, what’s the purpose of this frothy pavilion? The life cycle of the insect, compared to that of the cicada, might shed some light on that question. In the cicada, as I've explained, the eggs are laid in the bark, but the young ones, hatching about six weeks later, immediately leave the parent tree and burrow into the ground. However, the young of our bittersweet membracis are not so fickle; they spend their entire lives on the plant. Additionally, the eggs are laid in late summer and don’t hatch until the following[Pg 101] spring. So, what is this canopy of the tree-hopper if not a thoughtful mother's provision, a shelter for her offspring against winter storms? In early July, the tiny hoppers emerge from their egg-cases, and presumably make their way out from their bright home. Later in the season, you can see these broods in varying numbers and sizes among the young stems of the plant, their beaks inserted, their pointed heads always facing the same direction—toward the top of the branch. Even though one of the little ones might momentarily break this rule by landing differently, he quickly realizes his mistake and smoothly adjusts[Pg 102] back to the proper position.
This curious insect is chiefly confined to the bittersweet, though he is occasionally found in the company of a much bigger cousin of his on the branches of the locust, where these same telltale corrugated frothy pavilions are often seen to clothe the young twigs in their white tufts, the similar product of the larger species, which thus also presumably spends its entire life upon the locust-tree.[Pg 103]
This interesting insect mainly stays on the bittersweet, but it can sometimes be found with a much larger relative on the locust branches, where those distinctive corrugated frothy pavilions are often seen covering the young twigs in their white tufts. This similar feature also comes from the larger species, which presumably spends its whole life on the locust tree.[Pg 103]


It is now some thirty years since the scientific world was startled by the publication of that wonderful volume, "The Fertilization of Orchids," by Charles Darwin; for though slightly anticipated by his previous work, "Origin of Species," this volume was the first important presentation of the theory of cross-fertilization in the vegetable kingdom, and is the one that is primarily associated with the subject in the popular mind. The interpretation and elucidation of the mysteries which had so long lain hidden within those strange flowers, whose eccentric forms had always excited the curiosity and awe alike of the botanical fraternity and the casual observer, came almost like a divine revelation to every thoughtful reader of his remarkable pages. Blossoms heretofore con[Pg 106]sidered as mere caprices and grotesques were now shown to be eloquent of deep divine intention, their curious shapes a demonstrated expression of welcome and hospitality to certain insect counterparts upon whom their very perpetuation depended.
It has been about thirty years since the scientific community was amazed by the release of the remarkable book, "The Fertilization of Orchids," by Charles Darwin. Although it was somewhat foreshadowed by his earlier work, "Origin of Species," this book was the first significant introduction of the theory of cross-fertilization among plants, and it's the one that most people associate with the topic. The explanation and insight into the mysteries that had long been hidden in those unusual flowers—whose odd shapes had always fascinated both botanists and casual observers—felt almost like a divine revelation to every thoughtful reader of his extraordinary pages. Flowers that were previously seen as mere oddities and curiosities were now understood to express profound divine purpose, their strange forms serving as a clear invitation and welcome to specific insects upon which their very survival depended.
Thus primarily identified with the orchid, it was perhaps natural and excusable that popular prejudice should have associated the subject of cross-fertilization with the orchid alone; for it is even to-day apparently a surprise to the average mind that almost any casual wild flower will reveal a floral mechanism often quite as astonishing as those of the orchids described in Darwin's volume. Let us glance, for instance, at the row of stamens below (Fig. 1), selected at random from different flowers, with one exception wild flowers. Almost everybody knows that the function of the stamen is the secretion of pollen. This function, however, has really no reference whatever to the external form of the stamen. Why, then, this re[Pg 107]markable divergence? Here is an anther with its two cells connected lengthwise, and opening at the sides, perhaps balanced at the centre upon the top of its stalk or filament, or laterally attached and continuous with it; here is another opening by pores at the tip, and armed with two or four long horns; here is one with a feathery tail. In another the twin cells are globular and closely associated, while in its neighbor they are widely divergent. Another is club-shaped, and opens on either side by one or more upraised lids; and here is an example with its two very unequal cells separated by a long curved arm or connective, which is hinged at the tip of its filament; and the procession might be continued across two pages with equal variation.
Thus primarily associated with the orchid, it was probably natural and understandable that popular belief would link the topic of cross-fertilization exclusively with orchids; even today, it seems to surprise most people that almost any random wildflower has a floral mechanism that's often just as remarkable as those of the orchids described in Darwin's book. Let's take a look, for example, at the row of stamens below (Fig. 1), chosen at random from different flowers, with the one exception being wildflowers. Almost everyone knows that the stamen's job is to produce pollen. However, this function has no real connection to the external shape of the stamen. So why this significant difference? Here is an anther with its two cells linked lengthwise, opening at the sides, perhaps balanced at the center atop its stalk or filament, or attached laterally and continuous with it; here’s another that opens by pores at the tip and has two or four long horns; here’s one with a feathery tail. In another instance, the twin cells are round and closely grouped, while in a neighboring one, they are widely spaced. Another is club-shaped and opens on either side with one or more raised lids; and here’s an example with two very uneven cells separated by a long curved arm or connective, which is hinged at the tip of its filament; and this variety could be illustrated across two pages with equal differences.

As far back as botanical history avails us these forms have been the same, each true to its particular species of flower, each with an underlying purpose which has a distinct and often simple reference to its form; and yet, incredible as it now seems to us, the botanist of the past has been content with the simple technical description of the feature, without the slightest conception of its meaning, dismissing it, perhaps, with passing comment upon its "eccentricity" or "curious shape." Indeed, prior to Darwin's time it might be said[Pg 108] that the flower was as a voice in the wilderness. In 1735, it is true, faint premonitions of its present message began to be heard through their first though faltering interpreter, Christian Conrad Sprengel, a German botanist and school-master, who upon one occasion, while looking into the chalice of the wild geranium, received an inspiration which led him to consecrate his life thence-forth to the solution of the floral hieroglyphics. Sprengel, it may be said, was the first to exalt the flower from the mere status of a botanical specimen.
As far back as botanical history allows, these forms have remained unchanged, each true to its specific type of flower, each serving a purpose that has a clear and often simple connection to its shape. Yet, astonishing as it seems now, botanists in the past settled for straightforward technical descriptions of these features, without any understanding of their significance, maybe remarking on their "eccentricity" or "curious shape." Indeed, before Darwin's time, one might say[Pg 108] that the flower was like a voice in the wilderness. In 1735, however, faint hints of its current message began to emerge through its first, albeit hesitant, interpreter, Christian Conrad Sprengel, a German botanist and schoolmaster. One day, while examining the chalice of the wild geranium, he had an inspiration that led him to dedicate his life to unraveling the floral hieroglyphics. It could be said that Sprengel was the first to elevate the flower beyond just a botanical specimen.
This philosophic observer was far in advance of his age, and to his long and arduous researches—a basis built upon successively by Andrew Knight, Köhlreuter, Herbert, Darwin, Lubbock, Müller, and others—we owe our present divination of the flowers.
This thoughtful observer was well ahead of his time, and thanks to his extensive and challenging research—a foundation that was built upon by Andrew Knight, Köhlreuter, Herbert, Darwin, Lubbock, Müller, and others—we have our current understanding of flowers.
In order to fully appreciate this present contrast, it is well to briefly trace the progress, step by step, from the consideration of the mere anatomical and physiological specimen of the earlier botanists to the conscious blossom of to-day, with its embodied hopes, aspirations, and welcome companionships.
To fully appreciate this contrast, it’s helpful to briefly trace the journey, step by step, from the focus on just the anatomical and physiological specimens of earlier botanists to the conscious flower of today, with its hopes, aspirations, and cherished connections.
Most of my readers are familiar with the general construction of a flower, but in order to in[Pg 109]sure such comprehension it is well, perhaps, to freshen our memory by reference to the accompanying diagram (Fig. 2) of an abstract flower, the various parts being indexed.
Most of my readers know the basic structure of a flower, but to make sure everyone understands it, it might be helpful to look at the diagram (Fig. 2) of a simplified flower, with its different parts labeled.

The calyx usually encloses the bud, and may be tubular, or composed of separate leaves or sepals, as in a rose. The corolla, or colored portion, may consist of several petals, as in the rose, or of a single one, as in the morning-glory. At the centre is the pistil, one or more, which forms the ultimate fruit. The pistil is divided into three parts, ovary, style, and stigma. Surrounding the pistil are the stamens, few or many, the anther at the extremity containing the powdery pollen.
The calyx typically surrounds the bud and can be tubular or made up of separate leaves or sepals, like in a rose. The corolla, or the colorful part, can have several petals, as seen in roses, or just one, like in the morning glory. In the center is the pistil, which may be one or more, and it produces the final fruit. The pistil has three parts: the ovary, style, and stigma. Surrounding the pistil are the stamens, which can be few or many, with the anther at the tip containing the powdery pollen.
Although these physiological features have been familiar to observers for thousands of years, the several functions involved were scarcely dreamed of until within a comparatively recent period.
Although these physiological features have been known to observers for thousands of years, the various functions involved were hardly imagined until fairly recently.
In the writings of ancient Greeks and Romans we find suggestive references to sexes in flowers, but it was not until the close of the seventeenth century that the existence of sex was generally recognized.[Pg 110]
In the writings of ancient Greeks and Romans, there are hints about the sexes in flowers, but it wasn't until the end of the seventeenth century that the existence of sex was widely acknowledged.[Pg 110]

In 1682 Nehemias Grew announced to the scientific world that it was necessary for the pollen of a flower to reach the stigma or summit of the pistil in order to insure the fruit. I have indicated his claim pictorially at A (Fig. 3), in the series of historical progression. So radical was this "theory" considered that it precipitated a lively discussion among the wiseheads, which was prolonged for fifty years, and only finally settled by Linnæus, who reaffirmed the[Pg 111] facts declared by Grew, and verified them by such absolute proof that no further doubts could be entertained. The inference of these early authorities regarding this process of pollination is perfectly clear from their statements. The stamens in most flowers were seen to surround the pistil, "and of course the presumption was that they naturally shed the pollen upon the stigma," as illustrated at B in my series. The construction of most flowers certainly seemed designed to fulfil this end. But there were other considerations which had been ignored, and the existence of color, fragrance, honey, and insect association still continued to challenge the wisdom of the more philosophic seekers. How remarkable were some of those early speculations in regard to "honey," or, more properly, nectar! Patrick Blair, for instance, claimed that "honey absorbed the pollen," and thus fertilized the ovary. Pontidera thought that its office was to keep the ovary in a moist condition. Another botanist argued that it was "useless material thrown off in process of growth." Krunitz noted that "bee-visited meadows were most healthy," and his inference was that "honey was injurious to the flowers, and that bees were useful in carrying it off"! The great Linnæus confessed himself puzzled as to its function.[Pg 112]
In 1682, Nehemias Grew informed the scientific community that for a flower to produce fruit, its pollen needed to reach the stigma, or the top of the pistil. I've illustrated his claim at A (Fig. 3) in the historical progression series. This "theory" was considered so groundbreaking that it sparked a lively debate among experts that lasted for fifty years, only to be resolved by Linnæus, who reaffirmed the[Pg 111] facts established by Grew and provided such conclusive evidence that there were no further doubts. The thoughts of these early authorities on the pollination process are quite clear from their comments. The stamens of most flowers were observed to encircle the pistil, "and naturally, it was assumed that they shed the pollen onto the stigma," as shown at B in my series. The structure of most flowers certainly appeared to be designed for this purpose. However, other factors that had been overlooked persisted, such as color, fragrance, nectar, and the role of insects, raising questions for the more philosophical researchers. Some of those early theories about "honey," or more accurately, nectar, were quite remarkable! For instance, Patrick Blair suggested that "honey absorbed the pollen," thereby fertilizing the ovary. Pontidera believed its purpose was to keep the ovary moist. Another botanist argued that it was simply "useless material discarded during growth." Krunitz observed that "meadows visited by bees were the healthiest," concluding that "honey was harmful to the flowers and that bees were beneficial by removing it"! Even the great Linnæus admitted he was perplexed about its role.[Pg 112]
For a period of fifty years the progress of interpretation was completely arrested. The flowers remained without a champion until 1787, when Sprengel began his investigations, based upon the unsolved mysteries of color and markings of petals, fragrance, nectar, and visiting insects. The prevalent idea of the insect being a mere idle accessory to the flower found no favor with him. He chose to believe that some deep plan must lie beneath this universal association. At the inception of this conviction he chanced to observe in the flower of the wild geranium (G. sylvaticum) a fact which only an inspired vision could have detected—that the minute hairs at the base of the petal, while disclosing the nectar to insects, completely protected it from rain. Investigation showed the same conditions in many other flowers, and the inference he drew was further strengthened by the remarkable discovery of his "honey-guides" in a long list of blossoms, by which the various decorations of spots, rings, and converging veins upon the petals indicated the location of the nectar.
For fifty years, the advancement of interpretation was completely stalled. The flowers were left without a supporter until 1787, when Sprengel started his research, focusing on the unanswered questions surrounding the colors and patterns of petals, fragrance, nectar, and the insects that visit them. He rejected the common belief that insects were merely passive accessories to the flower. Instead, he believed that there must be a deeper purpose behind this widespread relationship. At the start of this belief, he happened to notice in the flower of the wild geranium (G. sylvaticum) a fact that only a visionary could have seen—that the tiny hairs at the base of the petal, while revealing the nectar to insects, entirely protected it from rain. Further investigation revealed the same conditions in many other flowers, and his conclusion was bolstered by his remarkable discovery of "honey-guides" in a wide variety of blossoms, where the various patterns of spots, rings, and converging veins on the petals indicated the position of the nectar.
His labors were now concentrated on the work of interpretation, until at length his researches, covering a period of two or three years, were given to the world. In a volume bearing the fol[Pg 113]lowing victorious title, "The Secrets of Nature in Forms and Fertilization of Flowers Discovered," he presented a vast chronicle of astonishing facts. The previous discoveries of Grew and Linnæus were right so far as they went—viz., "the pollen must reach the stigma"—but those learned authorities had missed the true secret of the process. In proof of which Sprengel showed that in a great many flowers, as I have shown at C (Fig. 3), this deposit of pollen is naturally impossible, owing to the relative position of the floral parts, and that the pollen could not reach the stigma except by artificial aid. He then announced his startling theory:
His work was now focused on interpretation, and after two or three years of research, he shared his findings with the world. In a book titled "The Secrets of Nature in Forms and Fertilization of Flowers Discovered," he presented a comprehensive account of incredible facts. The earlier discoveries by Grew and Linnæus were correct in part—specifically, "the pollen must reach the stigma"—but those scholars missed the real secret of the process. To demonstrate this, Sprengel showed that in many flowers, as I have indicated at C (Fig. 3), this pollen transfer is naturally impossible due to the arrangement of the flower parts, and that the pollen could only reach the stigma with artificial assistance. He then revealed his groundbreaking theory:
1. "Flowers are fertilized by insects."
1. "Insects pollinate flowers."
2. Insects in approaching the nectar brush the pollen from the anthers with various hairy parts of their bodies, and in their motions convey it to the stigma.
2. Insects, while collecting nectar, pick up pollen from the anthers with the hairy parts of their bodies, and as they move, they transfer it to the stigma.
But Sprengel's seeming victory was doomed to be turned to defeat. The true "secret" was yet unrevealed in his pages. He had given a poser to Linnæus (C), yet his own work abounded with similar strange inconsistencies, which, while being scarcely admitted by himself, or ingeniously explained, were nevertheless fatal to the full recognition of his wonderful researches. For seventy years his book lay almost unnoticed.[Pg 114]
But Sprengel's apparent victory was destined to become a defeat. The real "secret" had not yet been disclosed in his writing. He had presented a challenge to Linnæus (C), but his own work was filled with similar odd inconsistencies that he barely acknowledged, or tried to explain away, yet these were crucial to the complete appreciation of his remarkable research. For seventy years, his book remained largely ignored.[Pg 114]
"Let us not underrate the value of a fact; it will one day flower in a truth." The defects in Sprengel's work were, after all, not actual defects. The error lay simply in his interpretation of his carefully noted facts. As Hermann Müller has said, "Sprengel's investigations afford an example of how even work that is rich in acute observation and happy interpretation may remain inoperative if the idea at its foundation is defective." What, then, was the flaw in Sprengel's work? Simply that he had seen but half the "secret" which he claimed to have "discovered." Starting to prove that insects fertilize the flowers, his carefully observed facts only served to demonstrate in many cases the reverse—that insects could not fertilize flowers in the manner he had declared. He was met at every hand, for instance, by floral problems such as are shown at E and F, where the pollen and the stigma in the same flower matured at different periods; and even though he recognized and admitted that the pollen must in many cases be transferred from one flower to another, he failed to divine that such was actually the common vital plan involved. It may readily be imagined that his great work precipitated an intense and prolonged controversy, and incited emulous investigation by the botanists of his[Pg 115] time. Though a few of the more advanced of his followers, among them Andrew Knight (1799), Köhlreuter (1811), Herbert (1837), Gärtner (1844), clearly recognized the principle and foreshadowed the later theory of cross-fertilization, it was not until the inspired insight of Darwin, as voiced in his "Origin of Species," contemplated these strange facts and inconsistencies of Sprengel that their full significance and actual value were discovered and demonstrated, and his remarkable book, forgotten for seventy years, at last appreciated for its true worth. Alas for the irony of fate! Under Darwin's interpretation the very "defects" which had rendered Sprengel's work a failure now became the absolute witness of a deeper truth which Sprengel had failed to discern. One more short step and he had reached the goal. But this last step was reserved for the later seer. He took the fatal double problem of Sprengel—as shown at E and F, to express the consummation pictorially—and by the simple drawing of a line, as it were, as indicated between G and H, instantly reconciled all the previous perplexities and inconsistencies, thus demonstrating the fundamental plan involved in floral construction to be not merely "insect fertilization," the fatal postulate assumed by Sprengel, but cross-fertilization—a[Pg 116] fact which, singularly enough, the latter's own pages proved without his suspicion.
"Let’s not underestimate the importance of a fact; it will one day blossom into a truth." The flaws in Sprengel's work were not truly flaws. The mistake was simply in how he interpreted his carefully documented facts. As Hermann Müller stated, "Sprengel's investigations show how even work rich in keen observation and insightful interpretation can remain ineffective if the foundational idea is flawed." So, what was the flaw in Sprengel's work? Simply that he had only seen half of the "secret" he claimed to have "discovered." In trying to prove that insects fertilize flowers, his well-observed facts often demonstrated the opposite—that insects could not fertilize flowers in the way he suggested. He encountered floral issues everywhere, like those shown at E and F, where the pollen and stigma in the same flower matured at different times; even though he acknowledged that pollen often needed to be transferred from one flower to another, he failed to grasp that this was the common biological plan at play. It’s easy to imagine that his significant work sparked a passionate and prolonged debate and inspired competitive research among the botanists of his[Pg 115] time. Although a few of his more advanced followers, including Andrew Knight (1799), Köhlreuter (1811), Herbert (1837), and Gärtner (1844), clearly recognized the principle and hinted at the later theory of cross-fertilization, it wasn’t until Darwin's inspired insights in his "Origin of Species" that the strange facts and inconsistencies in Sprengel’s work were fully understood and demonstrated, finally appreciating his remarkable book, which had been forgotten for seventy years, for its true value. Alas for the irony of fate! Under Darwin's interpretation, the very "flaws" that had made Sprengel's work a failure became strong evidence of a deeper truth that Sprengel had failed to see. If only he had taken one more short step, he would have reached the conclusion, but that last step was left for the later visionary. He tackled the complex double problem of Sprengel—as shown at E and F, to illustrate the outcome—and by simply drawing a line, as suggested between G and H, he instantly resolved all previous confusions and inconsistencies, demonstrating that the fundamental design in floral construction was not simply "insect fertilization," the fatal assumption made by Sprengel, but cross-fertilization—a[Pg 116] fact which, interestingly enough, Sprengel's own pages proved without him realizing it.
Thus we see the four successive steps in progressive knowledge, from Grew in 1682, Linnæus, 1735, Sprengel, 1787, to Darwin, 1857-1858, and realize with astonishment that it has taken over one hundred and seventy-five years for humanity to learn this apparently simple lesson, which for untold centuries has been noised abroad on the murmuring wings of every bee in the meadow, and demonstrated in almost every flower.
Thus we see the four consecutive steps in the advancement of knowledge, from Grew in 1682, Linnæus in 1735, Sprengel in 1787, to Darwin in 1857-1858, and we realize with amazement that it has taken more than one hundred and seventy-five years for humanity to grasp this seemingly simple lesson, which has been shared for countless centuries by the gentle hum of every bee in the meadow and shown in nearly every flower.
This infinite field now open before him, Darwin began his investigations, and the whole world knows his triumphs. He has been followed by a host of disciples, to whom his books have come as an inspiration and ennobling impulse. Hildebrand, Delpino, Axell, Lubbock, and, latest and perhaps most conspicuous, Hermann Müller, to whom the American reader is especially referred. "The Fertilization of Flowers," by this most scholarly and indefatigable chronicler, presents the most complete compendium and bibliography of the literature on the subject that have yet appeared. Even to the unscientific reader it will prove full of revelations of this awe-inspiring interassociation and interdependence of the flower and the insect.
This vast field now laid out before him, Darwin began his research, and the entire world recognizes his achievements. He has been followed by many followers, who find inspiration and motivation in his books. Hildebrand, Delpino, Axell, Lubbock, and, most recently and notably, Hermann Müller, to whom American readers are particularly directed. "The Fertilization of Flowers," by this highly knowledgeable and tireless scholar, offers the most comprehensive collection and bibliography on the subject that has been published so far. Even for those without a scientific background, it will reveal the incredible connections and dependencies between flowers and insects.
Many years ago the grangers of Australia de[Pg 117]termined to introduce our red clover into that country, the plant not being native there. They imported American seed, and sowed it, with the result of a crop luxuriant in foliage and bloom, but not a seed for future sowing! Why? Because the American bumblebee had not been consulted in the transaction. The clover and the bee are inseparable counterparts, and the plant refuses to become reconciled to the separation. Upon the introduction and naturalization of the American bumblebee, however, the transported clover became reconciled to its new habitat, and now flourishes in fruition as well as bloom.
Many years ago, the farmers of Australia decided to bring our red clover to their country, as the plant wasn’t native there. They imported American seeds and planted them, resulting in a crop rich in leaves and flowers, but not a single seed for future planting! Why? Because the American bumblebee wasn’t involved in the process. The clover and the bee are two sides of the same coin, and the plant refuses to adapt without it. However, once the American bumblebee was introduced and adapted to its new environment, the imported clover adjusted to its surroundings and now thrives in both growth and bloom.
Botany and entomology must henceforth go hand-in-hand. The flower must be considered as an embodied welcome to an insect affinity, and all sorts of courtesies prevail among them in the reception of their invited guests. The banquet awaits, but various singular ceremonies are enjoined between the cup and the lip, the stamens doing the hospitalities in time-honored forms of etiquette. Flora exacts no arbitrary customs. Each flower is a law unto itself. And how expressive, novel, and eccentric are these social customs! The garden salvia, for instance, slaps the burly bumblebee upon the back and marks him for her own as he is ushered in to the feast. The[Pg 118] mountain-laurel welcomes the twilight moth with an impulsive multiple embrace. The desmodium and genesta celebrate their hospitality with a joke, as it were, letting their threshold fall beneath the feet of the caller, and startling him with an explosion and a cloud of yellow powder, suggesting the day pyrotechnics of the Chinese. The prickly-pear cactus encloses its buzzing visitor in a golden bower, from which he must emerge at the roof as dusty as a miller. The barberry, in similar vein, lays mischievous hold of the tongue of its sipping bee, and I fancy, in his early acquaintance, before he has learned its ways, gives him more of a welcome than he had bargained for. The evening primrose, with outstretched filaments, hangs a golden necklace about the welcome murmuring noctuid, while the various orchids excel in the ingenuity of their salutations. Here is one which presents a pair of tiny clubs to the sphinx-moth at its threshold, gluing them to its bulging eyes. Another attaches similar tokens to the tongues of butterflies, while the cypripedium speeds its parting guest with a sticking-plaster smeared all over its back. And so we might continue almost indefinitely. From the stand-point of frivolous human etiquette we smile, perhaps, at customs apparently so whimsical and[Pg 119] unusual, forgetting that such a smile may partake somewhat of irreverence. For what are they all but the divinely imposed conditions of interassociation? say, rather, interdependence, between the flower and the insect, which is its ordained companion, its faithful messenger, often its sole sponsor—the meadows murmuring with an intricate and eloquent system of intercommunings beside which the most inextricable tangle of metropolitan electrical currents is not a circumstance. What a storied fabric were this murmurous tangle woven day by day, could each one of these insect messengers, like the spider, leave its visible trail behind it!
Botany and entomology now need to work together. Flowers should be seen as a warm invitation to insects, and various courtesies are exchanged as they welcome their guests. The feast is ready, but there are unique rituals that take place, with the stamens playing host in traditional manners. Flowers have no strict rules of conduct; each one is its own authority. And how expressive, unique, and quirky are these social practices! For example, the garden salvia gives the big bumblebee a friendly pat on the back and claims him as he arrives at the party. The mountain-laurel greets the twilight moth with a spontaneous hug. The desmodium and genesta celebrate their hospitality with a playful twist, letting their entrance drop beneath the visitor’s feet, surprising him with a blast and a cloud of yellow pollen, reminiscent of Chinese firecracker displays. The prickly-pear cactus wraps its buzzing guest in a golden shelter, from which he has to exit all dust-covered like a flour mill operator. The barberry, in a similar fashion, playfully grabs the tongue of the bee sipping from it, and I imagine that during his first encounter, before he learns the rules, he receives a more boisterous welcome than expected. The evening primrose, with its stretched filaments, drapes a golden necklace around the welcome whispering moth, while various orchids showcase their creative greetings. One flower offers little clubs to the sphinx-moth at its entrance, sticking them to its bulging eyes. Another attaches similar tokens to the butterflies' tongues, while the cypripedium sends its departing guest off with a sticky bandage all over its back. And we could go on almost forever. From a lighthearted human perspective, we might chuckle at these seemingly odd customs, forgetting that such laughter might hint at irreverence. For what are they if not the divinely established rules of interaction—rather, interdependence—between the flower and the insect, which is its destined companion, its loyal messenger, often its sole ally—the meadows buzzing with a complex and eloquent network of communications that surpasses even the most tangled web of city electrical systems. What an incredible story this buzzing network would weave day by day if each of these insect messengers could leave a visible trail like a spider!
As a rule, these blossom ceremonies are of the briefest description. Occasionally, however, as in the cypripedium and in certain of the arums, or "jack-in-the-pulpit," and aristolochias, the welcome becomes somewhat aggressive, the guest being forcibly detained awhile after tea, or, as in the case of our milkweed, occasionally entrapped for life.
As a rule, these blossom ceremonies are very brief. However, sometimes, like with cypripediums and certain arums or "jack-in-the-pulpit" and aristolochias, the welcome can get a bit intense, with the guest being held back for a while after tea, or, in the case of our milkweed, occasionally trapped for life.


From this companionable point of view let us now look again at the strange curved stamen of the sage. Why this peculiar formation of the long curved arm pivoted on its stalk? Considered in the abstract, it can have no possible meaning; but taken in association with the insect to[Pg 120] which it is shaped, how perfect is its adaptation, how instantly intelligible it becomes! Every one is familiar with the sage of the country garden, its lavender flowers arranged in whorls in a long cluster at the tips of the stems. One of these flowers, a young one from the top of the cluster, is shown at A (Fig. 4), in section, the long thread-like pistil starting from[Pg 121] the ovary, and curving upward beneath the arch of the flower, with its forked stigma barely protruding (B). There are two of the queer stamens, one on each side of the opening of the blossom, and situated as shown, their anthers concealed in the hood above, and only their lower extremity appears below, the minute growth near it being one of the rudiments of two former stamens which have become aborted. If we take a flower from the lower portion of the cluster (D), we find that the thread-like pistil has been elongated nearly a third of an inch, its forked stigma now hanging directly at the threshold of the flower. The object of this will be clearly demonstrated if we closely observe this bee upon the blossoms. He has now reached the top of the cluster among the younger blossoms. He creeps up the outstretched platform of the flower, and has barely thrust his head within its tube when down comes the pair of clappers on his back (C). Presently he backs out, bearing a generous dab of yellow pollen, which is further increased from each subsequent flower. He has now finished this cluster, and flies to the next, alighting as usual on the lowermost tier of bloom. In them the elongated stigma now hangs directly in his path, and comes in contact with the pollen on his back as the insect sips the nectar. Cross-fertilization is thus insured; and, moreover, cross-fertilization not only from a distinct flower, but from a separate cluster, or even a separate plant. For in these older stigmatic flowers the anther as it comes down upon his back is seen to be withered, having shed its pollen several days since, the supply of pollen on the bee's body being sufficient to fertilize all the stigmas in the cluster, until a new supply is obtained from the pollen-bearing blossoms above. And thus he continues his rounds.[Pg 122]
From this friendly perspective, let’s take another look at the strange curved stamen of the sage. Why does it have this unusual shape with a long curved arm attached to its stalk? In theory, it doesn’t seem to have any significance, but when considered alongside the insect it's designed for, its adaptation is perfect and instantly clear! Everyone knows the sage in the country garden, with its lavender flowers arranged in whorls at the tips of the stems. One of these young flowers, taken from the top of the cluster, is shown at A (Fig. 4) in section, with the long thread-like pistil emerging from the ovary and curving upward beneath the arch of the flower, its forked stigma barely sticking out (B). There are two odd stamens, one on each side of the flower's opening, positioned as shown, their anthers hidden in the hood above, and only their lower parts visible below, with a tiny growth nearby being remnants of two former stamens that didn’t develop. If we take a flower from the lower part of the cluster (D), we see that the thread-like pistil has grown nearly a third of an inch longer, with its forked stigma now hanging directly at the flower's entrance. This will be clearly illustrated if we closely observe a bee on the blossoms. He has now reached the top of the cluster among the younger flowers. He climbs up the extended platform of the flower and, just as his head enters its tube, down comes the pair of clappers on his back (C). Soon he backs out, carrying a generous amount of yellow pollen that increases with each subsequent flower. He finishes this cluster and flies to the next, landing as usual on the lowest level of blooms. In these, the elongated stigma now hangs directly in his way, touching the pollen on his back as the insect drinks the nectar. This ensures cross-fertilization; additionally, it’s cross-fertilization not just from a different flower, but from an entire separate cluster or even a different plant. In these older stigmatic flowers, the anther that comes down upon his back is shriveled, having released its pollen several days ago, with the pollen on the bee's body being enough to fertilize all the stigmas in the cluster until he acquires a new supply from the pollen-rich flowers above. And so he continues his rounds.[Pg 122]
The sage is a representative of the large botanical order known as the Mint family, the labiates, or gaping two-lipped flowers, the arched hood here answering to the upper lip, the spreading base forming the lower lip, which is usually designed as a convenient threshold for the insects while sipping the nectar deep within the tube.[Pg 123] This mechanism of the sage is but one of many curious and various contrivances in the Mint family, all designed for the same end, the intercrossing of the flowers.
The sage is part of a large plant group known as the Mint family, characterized by their two-lipped flowers. The arched top acts like the upper lip, while the open base serves as the lower lip, often designed to help insects access the nectar deep inside the flower's tube.[Pg 123] This feature of the sage is just one of many interesting adaptations found in the Mint family, all aimed at promoting the cross-pollination of the flowers.
While each family of plants is apt to favor some particular general plan, the modifications in the various species seem almost without limit.
While each family of plants tends to prefer a specific overall design, the variations among the different species appear to be almost limitless.
Let us now look at the Heath family. The family of the heath, cranberry, pyrola, Andromeda, and mountain-laurel—how do these blossoms welcome their insect friends? This group is particularly distinguished by the unusual exception in the form of its anthers, which open by pores at their tips, instead of the ordinary side fissures. Two or three forms of these anthers are shown in my row of stamens (Fig. 1).
Let’s take a look at the Heath family. The family that includes heaths, cranberries, pyrolas, Andromedas, and mountain laurels—how do these flowers greet their insect friends? This group stands out notably due to the unique structure of its anthers, which open through pores at the tips instead of the usual side slits. You can see two or three types of these anthers in my row of stamens (Fig. 1).
Seen thus in their detached condition, how incomprehensible and grotesque do they appear! And yet, when viewed at home, in their bell-shaped corollas, their hospitable expression and greeting are seen to be quite as expressive and rational as those of the sage. Take the mountain-laurel, for instance; what a singular exhibition is this which we may observe on any twilight evening in the laurel copse, the dense clusters of pink-white bloom waited upon by soft-winged fluttering moths, and ever and anon celebrating its[Pg 124] cordial spirit by a mimic display of pyrotechnics as the anthers hurl aloft their tiny showers of pollen!
Seen this way, how confusing and strange do they look! Yet, when you see them in their natural setting, with their bell-shaped flowers, their welcoming vibe and greetings seem just as meaningful and sensible as those of a wise person. Take the mountain-laurel, for example; what a unique sight we can witness on any twilight evening in the laurel thicket, the dense clusters of pink-white flowers surrounded by soft-winged, fluttering moths, occasionally showcasing their friendly spirit with a mock fireworks display as the anthers shoot tiny showers of pollen into the air!

Anthers Placed in their Pockets
Every one is familiar with the curious construction of this flower, with its ten radiating stamens, each with its anther snugly tucked away in a pouch at the rim of its saucer-shaped corolla. Thus they appear in the freshly opened flower, and thus will they remain and wither if the flower is brought indoors and placed in a vase upon our mantel. Why? Because the hope of the blossom's life is not fulfilled in these artificial conditions; its natural counterpart, the insect, has failed to respond to its summons.
Everyone is familiar with the unique structure of this flower, which has ten radiating stamens, each with its anther neatly tucked away in a pouch at the edge of its saucer-shaped petals. This is how they look when the flower first opens, and that’s how they will stay and eventually fade if the flower is taken indoors and placed in a vase on our mantel. Why? Because the flower’s chance for life isn’t fulfilled in these artificial conditions; its natural counterpart, the insect, hasn’t responded to its call.
But the twilight cluster in the woods may tell us a pretty story.
But the group of trees at dusk might share a lovely story with us.
Here a tiny moth hovers above the tempting chalice, and now settles upon it with eager tongue extended for the nectar at its centre. What an immediate and expressive welcome! No sooner has this little feathery body touched the filaments than the eager anthers are released from their pockets, and, springing inwards, clasp their little[Pg 125] visitor, at the same time decorating him with their compliments of webby pollen (A, Fig. 5).
Here, a tiny moth flits above the enticing cup and then lands on it, eagerly extending its tongue for the nectar at the center. What an instant and expressive welcome! The moment this little feathery body touches the filaments, the eager anthers pop out of their pockets and spring inward to embrace their little[Pg 125] visitor, while also showering him with their fine pollen (A, Fig. 5).
The nectary now drained of its sweets, the moth creeps or flutters to a second blossom, and its pollen-dusted body thus coming in contact with its stigma, cross-fertilization is accomplished. The pollen of the laurel differs from that of most of the Heath blooms, its grains being more or less adherent by a cobwebby connective which permeates the mass as indicated in my magnified representation (B, Fig. 5).
The nectar is now gone, so the moth crawls or flutters to another flower. By coming into contact with its stigma, cross-fertilization happens. The pollen from the laurel is different from that of most Heath flowers; its grains stick together with a web-like substance that runs through the mass, as shown in my magnified representation (B, Fig. 5).

It is probable that an accessory cross-fertilization frequently results from a mass of the pollen falling directly upon the stigma of a neighboring blossom, or even upon its own stigma, but even in[Pg 126] the latter case, as has been absolutely demonstrated as a general law by the experiments of Darwin, the pollen from a separate flower is almost invariably prepotent, and leads to the most perfect fruition, and thus to the survival of the fittest—the cross-fertilized. And, in any event, the insect is to be credited for the release of the tiny catapults by which the pollen is discharged. But the laurel may be considered as an exceptional example of the Heath family. Let us look at a more perfect type of the order to which it belongs, the globular blossom of the Andromeda (A. ligustrina).
It's likely that accessory cross-fertilization often happens when a mass of pollen lands directly on the stigma of a nearby flower, or even on its own stigma. However, even in[Pg 126] this case, as shown by Darwin's experiments which establish it as a general rule, pollen from a different flower is almost always dominant and results in the most successful fruit development, leading to the survival of the fittest—those that are cross-fertilized. Additionally, we owe the release of the tiny catapults that discharge the pollen to insects. However, the laurel can be seen as an exceptional case within the Heath family. Let’s consider a more typical example from its group, the round blossom of the Andromeda (A. ligustrina).

Only a short walk from my studio door in the country I recently observed
its singular reception to the tiny black-and-white banded bee, which
seems to be its especial companion, none the less constant and forgiving
in spite of a hospitality which, from the human stand-point, would
certainly seem rather discouraging. Fancy a morning call upon your
particular friend. You knock at the door, and are immediately greeted at
the threshold with a quart of sulphur thrown into your face. Yet this is
precisely the experience of this patient little insect, which manifests
no disposition to retaliate with the concealed weapon which on much less
provocation he is quick to[Pg 127] employ. Here he comes, eager for the fray.
He alights upon one of the tiny bells scarce half the size of his body.
Creeping down beneath it, he inserts his tongue into the narrowed
opening. Instantly a copious shower of dust is poured down upon his face
and body. But he has been used to it all his life, and by heredity he
knows that this is Andromeda's peculiar whim, and is content to humor it
for the sweet recompense which she bestows. The nectar drained, the
insect, as dusty as a miller, visits another flower, but before he
enters must of necessity first pay his toll of pollen to the drooping
stigma which barely[Pg 128] protrudes beneath the blossom's throat, and the
expectant seed-pod above welcomes the good tidings with visions of
fruition.
Only a short walk from my studio door in the country, I recently noticed the unique relationship with the tiny black-and-white striped bee, which seems to be its special friend—always there and forgiving, even with a hospitality that, from a human perspective, would definitely seem quite discouraging. Imagine visiting your friend in the morning. You knock on the door, and are immediately met with a quart of sulfur thrown in your face. Yet this is exactly the experience of this patient little insect, which shows no desire to retaliate with the hidden stinger he uses on much less provocation. Here he comes, ready for action. He lands on one of the tiny flowers, barely half his size. Crawling underneath it, he sticks his tongue into the narrow opening. Instantly, a shower of dust pours down onto his face and body. But he’s been dealing with this his whole life, and through instinct, he knows this is just Andromeda’s quirky preference, and he’s happy to go along with it for the sweet reward she gives. After drinking the nectar, the insect, as dusty as a miller, visits another flower, but before he gets in, he must first pay his pollen fee to the drooping stigma that barely pokes out from under the blossom's throat, and the eager seed pod above welcomes the good news with visions of growth.




And how beautiful is the minute mechanical adaptation by which this end is accomplished! This species of Andromeda is a shrub of about four feet in height, its blossoms being borne in close panicled clusters at the summit of the branches. The individual flower is hardly more than an eighth of an inch in diameter. From one of three blossoms I made the accompanying series of three sectional drawings (Fig. 6). The first shows the remarkable interior arrangement of the ten stamens surrounding the pistil. The[Pg 129] second presents a sectional view of these stamens, showing their peculiar S-shaped filaments and ring of anthers—one of the latter being shown separate at the right, with its two pores and exposed pollen. The freshly opened blossom discloses the entire ring of anthers in perfect equilibrium, each with its two orifices closed by close contact with the style, thus retaining the pollen. It will readily be seen that an insect's tongue, as indicated by the needle, in probing between them in search for nectar, must needs dislocate one or more of the anthers, and thus release their dusty contents, while the position of the stigma below is such as to escape all contact.
And how beautiful is the precise mechanical adjustment that makes this possible! This type of Andromeda is a shrub about four feet tall, with its flowers blooming in tight clusters at the tops of the branches. Each individual flower is barely more than an eighth of an inch wide. From one of three flowers, I created the following series of three sectional drawings (Fig. 6). The first shows the impressive internal structure of the ten stamens surrounding the pistil. The[Pg 129] second provides a sectional view of these stamens, highlighting their unique S-shaped filaments and a ring of anthers—one of which is shown separately on the right, featuring its two pores and exposed pollen. The newly opened flower reveals the complete ring of anthers perfectly balanced, each with its two openings sealed by close contact with the style, thus holding the pollen. It's clear that an insect's tongue, as suggested by the needle, must dislocate one or more of the anthers while probing between them for nectar, which would release their dusty contents, while the stigma's position below avoids any contact.
In most flowers, with the exception of the orchids, the stamens and pollen are plainly visible; but who ever sees the anthers of the blue-flag? Surely none but the analytical botanist and the companion insect to whom it is so artfully adjusted and so demonstrative. This insect is likely to be either a bumblebee or a species of large fly. In apt illustration of Sprengel's theory of the "path-finder" or honey-guide, the insect does not alight at the centre of the flower, but upon one of the three large drooping sepals, whose veins, converging to the narrow trough above, indicate the path to the nectar. Closely overarch[Pg 130]ing this portion is a long and narrow curved roof—one of three divisions to the style, each surmounting its veined sepals. Beneath this our visiting bee disappears, and a glance at my sectional drawing shows what happens. Concealed within, against the ridge-pole, as it were, the anther awaits his coming, and in his passage to and from the nectar below spreads its pollen over his head and[Pg 131] back. Having backed out of this segment of the blossom (A, Fig. 7), he proceeds to the next; but the shelf-like stigma awaits him at the door, and scrapes off or rubs off a few grains of the pollen from his back (B). Thus he continues until the third segment is reached, from which he carries away a fresh load of pollen to another flower. It will be seen that only the outer side of this appendage is stigmatic, and that it is thus naturally impossible for the blue-flag to self-fertilize—only[Pg 132] one instance of thousands in which the anther and stigma, though placed in the closest proximity, and apparently even in contact—seemingly with the design of self-fertilization—are actually more perfectly separated functionally than if in separate flowers, the insect alone consummating their affinity.
In most flowers, except for orchids, the stamens and pollen are easy to see; but who ever notices the anthers of the blue-flag? Probably only the detailed botanist and the insect that works so well with it. This insect is likely a bumblebee or a large fly. To illustrate Sprengel's theory of the "path-finder" or honey-guide, the insect doesn’t land at the center of the flower, but on one of the three large drooping sepals, whose veins lead the way to the nectar. Above this area is a long and narrow curved roof—one of three sections of the style, each above its veined sepals. Below this, our visiting bee disappears, and a look at my sectional drawing shows what occurs. Hidden away against a ridge, the anther waits for its arrival, and as the bee moves to and from the nectar below, it spreads pollen over its head and back. After backing out of this part of the flower (A, Fig. 7), it goes to the next; but the shelf-like stigma is waiting at the entrance and scrapes off a few grains of pollen from its back (B). It keeps going until it reaches the third section, where it carries away fresh pollen to another flower. You'll see that only the outer side of this part is stigmatic, making it impossible for the blue-flag to self-fertilize—just one example among thousands where the anther and stigma, despite being very close together and seemingly meant for self-fertilization, are actually more effectively separated functionally than if they were in different flowers, with the insect being the key to their connection.
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In some flowers this separation is effected, as I have shown, by their
maturing at different periods; in others, as in the iris, by mere
mechanical means; while in a long list of plants, as in the willow,
poplar, hemp, oak, and nettle, the cross-fertilization is absolutely
necessitated by the fact of the staminate and stigmatic flowers being
either separated on the same stalk or on different plants, the pollen
being carried by insects or the wind. We may see a pretty illustration
of this in the little wild flower known as the devil's-bit (Chamælirium
luteum,), whose long, white, tapering spire of feathery bloom may often
be seen rising above the sedges in the swamp. Two years ago I chanced
upon a little colony of four or five plants at the edge of a bog. The
flowers, all of them, were mere petals and stamens (B, Fig. 8). I looked
in vain for a single stigmatic plant or flower; but far across the
swamp, a thousand feet distant, I at length discovered a single spire,
composed entirely of pistillate flowers, as shown in A (Fig. 8), and my
magnifying-glass clearly revealed the pollen upon their
stigmas—doubtless a welcome message brought from the isolated affinity
afar by some winged sponsor, to whom the peculiar fragrance of the
flower offers a special attraction, and thus to whom the fortunes of the
devil's-bit have been committed.
In some flowers, this separation happens because they mature at different times; in others, like the iris, it's due to simple mechanical means. For many plants, such as willows, poplars, hemp, oaks, and nettles, cross-fertilization is necessary because the male and female flowers are either on the same stalk or on different plants, with pollen being carried by insects or the wind. A nice example of this is the little wildflower known as the devil's-bit (Chamælirium luteum,) which often grows with its long, white, feathery bloom above the sedges in the swamp. Two years ago, I came across a small group of four or five plants at the edge of a bog. All the flowers were just petals and stamens (B, Fig. 8). I searched in vain for a single female plant or flower; but far across the swamp, a thousand feet away, I finally found a single spire made entirely of female flowers, as shown in A (Fig. 8). My magnifying glass clearly showed the pollen on their stigmas—most likely a welcome gift brought from the distant plants by some insect attracted to the flower's unique scent, thus binding the fate of the devil's-bit to this winged messenger.

The presence of fragrance and honey in a diœcious flower may be accepted in the abstract as almost conclusive of an insect affinity, as in most flowers of this class, notably the beech, pine, dock, grasses, etc., the wind is the fertilizing agent, and there is absence alike of conspicuous color, fragrance, and nectar—attributes which refer alone to insects, or possibly humming-birds in certain species.[Pg 135]
The presence of fragrance and honey in a dioecious flower can generally be understood as a strong indication of a connection to insects, since in most flowers of this type, like beech, pine, dock, grasses, and others, the wind serves as the pollinator, and there is a lack of noticeable color, fragrance, and nectar—features that are typically associated with insects, or possibly hummingbirds in some cases.[Pg 135]
Look where we will among the blossoms, we find the same beautiful plan of intercommunion and reciprocity everywhere demonstrated. The means appear without limit in their evolved—rather, I should say, involved—ingenuity. Pluck the first flower that you meet in your stroll to-morrow, and it will tell you a new story.
Look where we will among the flowers, we see the same beautiful pattern of connection and mutual exchange everywhere shown. The possibilities seem endless in their developed—rather, I should say, complex—ingenuity. Pick the first flower you come across during your walk tomorrow, and it will share a new story with you.

Only a few days since, while out on a drive, I passed a luxuriant clump of the plant known as[Pg 136] "horse-balm." I had known it all my life, and twenty years previously had made a careful analytical drawing of the mere botanical specimen. What could it say to me now in my more questioning mood? Its queer little yellow-fringed flowers hung in profusion from their spreading terminal racemes. I recalled their singular shape, and the two outstretched stamens protruding from their gaping corolla, and could distinctly see them as I sat in the carriage. I had never chanced to read of this flower in the literature of cross-fertilization, and murmuring, half aloud, "What pretty mystery is yours, my Collinsonia?" prepared to investigate.
Just a few days ago, while I was out for a drive, I came across a lush cluster of the plant known as[Pg 136] "horse-balm." I had recognized it all my life, and twenty years earlier, I had created a detailed analytical drawing of this botanical specimen. What could it reveal to me now in my more curious state of mind? Its strange little yellow-fringed flowers hung abundantly from their spreading terminal clusters. I remembered their unique shape and the two extended stamens sticking out from their open corolla, and I could clearly picture them as I sat in the carriage. I had never come across this flower in any literature about cross-fertilization, and murmuring, half to myself, "What pretty mystery do you hold, my Collinsonia?" I got ready to investigate.

and in the Sequence of their Visits by the Bee

What I observed is pictured severally at Fig. 9,[Pg 137] the flowers being shown from above, showing the two spreading stamens and the decidedly exceptional unsymmetrical position of the long style extending to the side. A small nectar-seeking bumblebee had approached, and in alighting upon the fringed platform grasped the filaments for support, and thus clapped the pollen against his sides. Reasoning from analogy, it would of course be absolutely clear that this pollen has thus been deposited where it will come in contact with the stigma of another flower. So, of course, it proved. In the bee's continual visits to the several flowers he came at length to the younger blooms, where the forked stigmas were turned directly to the front, while the immature stamens were still curled up in the flower tubes. Even the unopened buds showed a number of species where the early matured stigma actually protruded[Pg 138] through a tiny orifice in precisely the right position to strike the pollen-dusted body of the bee, as he forced his tongue through the tiny aperture.[A]
What I saw is illustrated multiple times in Fig. 9,[Pg 137] showing the flowers from above, highlighting the two spreading stamens and the clearly unique asymmetrical position of the long style extending to the side. A small bumblebee searching for nectar approached, and when it landed on the fringed platform, it held onto the filaments for support, effectively transferring pollen onto its sides. By drawing an analogy, it clearly shows that this pollen has been deposited where it can meet the stigma of another flower. And indeed, that was the case. As the bee continued to visit different flowers, it eventually arrived at the younger blooms, where the forked stigmas were facing directly forward, while the immature stamens were still curled up inside the flower tubes. Even the unopened buds displayed several species where the early-developed stigma actually protruded[Pg 138] through a tiny opening positioned perfectly to come into contact with the pollen-dusted body of the bee as it pushed its tongue through the small aperture.[A]
If their dainty mechanism excite our wonder, what shall be said of the revelations in the great order of the Compositæ, where each so-called flower, as in the dandelion, daisy, cone-flower, marigold, is really a dense cluster of minute flowers, each as perfect in its construction as in the examples already mentioned, each with its own peculiar plan designed to insure the transfer of its own pollen to the stigma of its neighbor, while excluding it from its own?
If their delicate design amazes us, what can we say about the revelations in the amazing order of the Compositæ, where each so-called flower, like in the dandelion, daisy, cone-flower, and marigold, is actually a tight group of tiny flowers, each as perfectly constructed as the examples already mentioned, each with its own unique plan to ensure the transfer of its pollen to the stigma of its neighbor while keeping it away from its own?
All summer long the cone-flower, Fig. 10 (Rudbeckia hirta), blooms in our fields, but how few of us imagine the strange processes which are being enacted in that purple cone! Let us examine it closely. If we pluck one of the blossom's heads and keep it in a vase over-night, we shall probably see on the following morning a tiny yellow ring of pollen encircling the outer edge of the cone. In this way only[Pg 139] are we likely to see the ring in its perfection, as in a state of nature the wind and insects rarely permit it to remain.
All summer long, the cone flower, Fig. 10 (Rudbeckia hirta), blooms in our fields, but how few of us think about the unusual processes happening in that purple cone! Let’s take a closer look. If we pick one of the flower heads and keep it in a vase overnight, we’ll probably notice a tiny yellow ring of pollen around the outer edge of the cone the next morning. This is the only way[Pg 139] we’re likely to see the ring in its full glory, as in nature, the wind and insects rarely allow it to stay.

some with pollen, others in the stigmatic stage.
If we now with a sharp knife make a vertical section, as shown at A (Fig. 3), we may observe the conical receptacle studded with its embryo seeds, each bearing a tiny tubular blossom. Three distinct forms of these flowers are to be seen. The lower and older ones are conspicuous by their double feathery tails, the next by their extended anthers bearing the pollen at their extremity, and above these again the buds in all stages of growth. These various states are indicated in Fig. 11.
If we now make a vertical cut with a sharp knife, as shown at A (Fig. 3), we can see the conical container filled with its embryo seeds, each with a tiny tubular flower. There are three distinct types of these flowers. The lower and older ones are noticeable because of their double feathery tails, the next have extended anthers that hold the pollen at their tips, and above these are the buds in various stages of growth. These different states are shown in Fig. 11.
As in all the Compositæ, the anthers are here united in a tube, the pollen being discharged within. At the base of this anther-tube rises the pistil, which gradually elongates, and like a piston forces out the pollen at the top. Small insects in[Pg 140] creeping over the cone quickly dislodge it. In the next stage the anthers have withered, the flower-tube elongated, and the top of the two-parted pistil begins to protrude, and at length expands its tips, disclosing at the centre the stigmatic surface, which has until now been protected by close contact. (See section.)
As with all Compositæ, the anthers are fused into a tube, and the pollen is released inside. At the base of this anther tube, the pistil rises, gradually getting longer, and like a piston, pushes out the pollen at the top. Small insects in[Pg 140] crawling over the cone quickly dislodge it. In the next stage, the anthers have shriveled, the flower tube has lengthened, and the top of the two-part pistil starts to stick out, eventually opening its tips to reveal the stigmatic surface, which has been protected by close contact until now. (See section.)


A glance at Fig. 11 will reveal the plan involved. The ring of pollen is
inevitably scattered to the stigmas of the neighboring flowers, and
cross-fertilization continually insured. Similar contrivances are to be
found in most of the Compositæ, through the same method being variously
applied.
A look at Fig. 11 will show the plan in action. The ring of pollen is naturally spread to the stigmas of nearby flowers, ensuring continuous cross-fertilization. Similar mechanisms are found in most of the Compositæ, although the method is applied in various ways.
Perhaps even more remarkable than any of the[Pg 141] foregoing, which are more or less automatic in their movements, is the truly astonishing and seemingly conscious mechanism displayed in the wild arum of Great Britain—the "lords and ladies" of the village lanes, the foreign counterpart of our well-known jack-in-the-pulpit, or Indian-turnip, with its purple-streaked canopy, and sleek "preacher" standing erect beneath it. A representation of this arum is shown in Fig. 12, and a cross section at A, properly indexed.
Perhaps even more impressive than any of the[Pg 141] above, which move in a mostly automatic way, is the truly amazing and seemingly aware mechanism seen in the wild arum of Great Britain—the "lords and ladies" found along village paths. It's similar to our familiar jack-in-the-pulpit, or Indian turnip, with its purple-streaked canopy and upright "preacher" underneath it. A representation of this arum is shown in Fig. 12, with a cross-section at A, properly indexed.
How confidently would the superficial—nay, even careful—examination of one of the old-time botanists have interpreted its structure: "How simple and perfect the structure! Observe how the anthers are placed so that pollen shall naturally fall directly on the stigmas and fertilize them!" Such would indeed appear to be intended, until it is actually discovered that the stigmas have withered when the pollen is shed—a device which, acting in association with the little ring of hairs, tells a strange story. It is not my fortune to have seen one of these singular blossoms, but from the description of the process of fertilization given in Her[Pg 142]mann Müller's wonderful work, aided by a botanical illustration of the structure of the flower, I am readily enabled to picture the progressive stages of the mechanism.
How confidently would a casual—no, even careful—look from an old-fashioned botanist have interpreted its structure: "How simple and perfect the structure! Look at how the anthers are positioned so that pollen falls directly onto the stigmas to fertilize them!" That would really seem to be the intention, until you actually find out that the stigmas have withered when the pollen is released—a feature that, along with the little ring of hairs, tells a strange story. I haven't had the chance to see one of these unique flowers, but from the description of the fertilization process found in Her[Pg 142]mann Müller's fantastic work, along with a botanical illustration of the flower's structure, I can easily imagine the stages of the mechanism.

In the first stage (B, Fig. 13) small flies with bodies dusted with pollen from a previous arum blossom (for insects, as a rule, remain faithful or partial to one species of flowers while it is in bloom) are entering the narrowed tube, easily passing through the drooping fringe of hairs. Nectar is secreted by the stigmas, and here the flies assemble, thus dusting them with pollen. Their appetite temporarily satisfied, the insects seek escape, but find their exit effectually barred by the intruding fringe of hairs (C). In this second stage the stig[Pg 143]mas, having now been fertilized, have withered, at the same time exuding a fresh supply of nectar, which again attracts the flies, whereupon, as shown at D, the anthers open and discharge their pollen upon the insects. In the fourth stage (E), all the functions of the flower having now been fulfilled, the fringe of hairs withers, and the imprisoned pollen-laden flies are permitted to escape to another flower, where the beautiful scheme is again enacted.
In the first stage (B, Fig. 13), small flies covered in pollen from a previous arum blossom (since insects generally stick to one type of flower while it’s blooming) are entering the narrow tube, easily making their way through the drooping fringe of hairs. Nectar is produced by the stigmas, and this is where the flies gather, dusting them with pollen. Once their hunger is momentarily satisfied, the insects try to leave but find their exit effectively blocked by the encroaching fringe of hairs (C). In this second stage, the stigmas, now fertilized, have dried up, but they release a new supply of nectar, attracting the flies again. As shown at D, the anthers open and release their pollen onto the insects. In the fourth stage (E), after all the functions of the flower have been completed, the fringe of hairs withers, allowing the pollen-covered flies to escape to another flower, where the beautiful process happens all over again.
In a paper of this kind it is of course possible only to hint at a few representative examples of floral mechanisms, but these would be indeed incomplete without a closing reference to that wonderful tribe of flowers with which the theory of cross-fertilization will ever be memorably associated. I have previously alluded to the absolute dependence of the red clover upon the bumblebee. This instance may be considered somewhat exceptional, though numerous parallel cases are known. Among ordinary flowers this intervention of the insect is largely a preferable intention, and though almost invariably fulfilled, a large proportion of flowers still retain, as a dernier ressort, the power of at least partial self-fertilization and perpetuity in the absence or neglect of their insect counterpart.[Pg 144]
In a paper like this, we can only touch on a few representative examples of floral mechanisms, but it wouldn't be complete without mentioning that amazing group of flowers associated with the theory of cross-fertilization. I’ve already mentioned how the red clover relies entirely on the bumblebee. This example might be somewhat unique, although there are many similar cases. In general flowers, the involvement of insects is often a preferable choice, and while it usually happens, many flowers still have, as a dernier ressort, the ability to at least partially self-fertilize and continue to thrive even without their insect partners.[Pg 144]

The numerous and conclusive demonstrations of Darwin, however, have proved that in the competition for existence such self-fertilized offspring quickly yield before the progeny of cross-fertilization.
The many convincing demonstrations by Darwin, however, have shown that in the struggle for survival, self-fertilized offspring quickly fall behind the offspring of cross-fertilization.
But the distinctive feature of the orchids lies in the fact that this dependence on the insect is wellnigh universally absolute. Here are a great host of plants which are doomed to extinction if for any reason their insect sponsors should permanently neglect them. The principal botanical feature which differentiates the orchid from other plants lies in the construction of the floral organs, the pistil, stigma, and anthers here being united into a distinct part known as the column. The pollen is, moreover, peculiar, being collected into more or less compact masses, and variously concealed in the flower. Some of these are club-shaped, with a viscid extremity, others of the consistency of a sticking-plaster, and all are hidden from external view in pouches and pockets, from which they never emerge unless withdrawn on the body of an insect. The various devices by which this removal is insured are most astonishing and awe-inspiring. Nor is it necessary to go to the conservatory for a tropical specimen, as is commonly supposed. An orchid is an orchid[Pg 145] wherever it grows, and our native list of some fifty species will afford examples of as strange mechanical adaptations as are to be found among Darwin's pages. Indeed, a few of our American species are there described. One example will suffice for present illustration—the sweet-pogonia or grass-pink of our sedgy swamps (Pogonia ophioglossoides). Its solitary rosy blossom, nodding on its slender stem above the sedges, is always a welcome episode to the sauntering botanist, and its perfume, suggesting ripe red raspberries, is unique in the wild bouquet. One of these flowers is shown in profile at Fig. 14, its various parts indexed. Concealed behind the petals is the column, elsewhere indicated from various points of view. Attracted by its color and fragrance, the insect seeks the flower; its outstretched fringy lip offers a cordial invitation at its threshold, and conducts its visitor directly to the sweets above. In his entrance, as seen at D (Fig. 15), the narrowed passage compresses his back against the underside of the[Pg 146] column, forcing his head and back against the stigma. The effect of this inward pressure, as will be seen, only serves to force the anther more firmly within its pocket; but as the insect, having drained the nectar, now backs out, note the result. The lip of the anther catches upon the back, swings outward on its hinge, and deposits its sticky pollen all over the insect's back, returning to its original position after his departure. In another moment he is seen upon another blossom, as at D again, his pollen-laden back now coming in contact with the stigma, and the intention of the blossom is accomplished; for without this assistance from the insect the little lid[Pg 147] remains close within its pocket, and the pollen is thus retained.
But the unique characteristic of orchids is that their reliance on insects is nearly total. There are many plants that face extinction if their insect partners ever stop visiting them. The main botanical trait that sets orchids apart from other plants is the structure of their floral organs; the pistil, stigma, and anthers are fused into a distinct part called the column. The pollen is also unusual, collected into compact masses and hidden in the flower. Some are club-shaped with a sticky end, while others have a consistency similar to adhesive bandages, and all are concealed in pouches and pockets that only release when an insect pulls them out. The various mechanisms that ensure this transfer are truly astonishing and fascinating. It's also a common misconception that you need to visit a conservatory to see a tropical specimen. An orchid is an orchid[Pg 145] no matter where it grows, and even our native species list of around fifty includes examples of remarkable mechanical adaptations just like those found in Darwin's work. In fact, a few of our American species are described there. One example that illustrates this well is the sweet-pogonia, or grass-pink, found in our marshy areas (Pogonia ophioglossoides). Its solitary pink flower, nodding on its delicate stem above the grasses, is always a delightful sight for a wandering botanist, and its fragrance, reminiscent of ripe red raspberries, is unique in the wildflower bouquet. A profile of this flower is shown in Fig. 14, with its parts labeled. Hidden behind the petals is the column, shown from various perspectives elsewhere. Attracted by its color and scent, the insect approaches the flower; its extended fringed lip offers a warm welcome at the entrance and guides the visitor directly to the nectar above. Inside, as seen at D (Fig. 15), the narrow passage presses the insect's back against the underside of the[Pg 146] column, forcing its head and back into contact with the stigma. This inward pressure simply helps to push the anther deeper into its pocket; but as the insect sucks up the nectar and begins to back out, notice what happens. The lip of the anther catches on the insect’s back, swings outward on its hinge, and deposits its sticky pollen all over the insect. After the insect leaves, the anther returns to its original position. In a moment, you can see the insect on another flower, as at D again, with its pollen-covered back now touching the stigma. The flower's goal is achieved; without the insect's help, the little lid[Pg 147] remains closed in its pocket, and the pollen stays locked away.

What startling disclosures are revealed to the inward eye within the hearts of all these strange orchidaceous flowers! Blossoms whose functions, through long eras of adaptation, have gradually shaped themselves to the forms of certain chosen insect sponsors; blossoms whose chalices are literally fashioned to bees or butterflies; blossoms whose slender, prolonged nectaries invite and reward the murmuring sphinx-moth alone, the floral throat closely embracing his head while it attaches its pollen masses to the bulging eyes, or perchance to the capillary tongue! And thus in endless modifications, evidences all of the same deep vital purpose.
What surprising insights are revealed to the inner mind in the hearts of these strange orchid-like flowers! Flowers whose roles, over long periods of adaptation, have gradually formed to attract specific insect partners; flowers whose structures are literally designed for bees or butterflies; flowers whose long, narrow nectar tubes entice and reward only the humming sphinx moth, with the flower's throat tightly wrapping around its head while it gathers pollen from its bulging eyes, or maybe from its delicate tongue! And so, through countless variations, all show the same deep vital intention.
Let us then content ourselves no longer with being mere "botanists"—historians of structural facts. The flowers are not mere comely or curious vegetable creations, with colors, odors, petals, stamens, and innumerable technical attributes. The wonted insight alike of scientist, philosopher, theologian, and dreamer is now repudiated in the new revelation. Beauty is not "its own excuse for being," nor was fragrance ever "wasted on the desert air." The seer has at last heard and interpreted the voice in the wilderness. The flower is[Pg 148] no longer a simple passive victim in the busy bee's sweet pillage, but rather a conscious being, with hopes, aspirations, and companionships. The insect is its counterpart. Its fragrance is but a perfumed whisper of welcome, its color is as the wooing blush and rosy lip, its portals are decked for his coming, and its sweet hospitalities humored to his tarrying; and as it finally speeds its parting affinity rests content that its life's consummation has been fulfilled.[Pg 149]
Let’s no longer settle for being just "botanists"—historians of structural facts. Flowers aren't just pretty or interesting plant creations, with their colors, scents, petals, stamens, and countless technical details. The usual perspectives of scientists, philosophers, theologians, and dreamers are now challenged by this new understanding. Beauty isn't just "its own reason for being," nor was fragrance ever "wasted on the desert air." The seer has finally listened to and interpreted the message in the wilderness. The flower is[Pg 148] no longer just a passive victim in the busy bee's sweet foraging; it’s a conscious being, full of hopes, dreams, and relationships. The insect is its partner. Its fragrance is a scented whisper of welcome, its color is like a flirtatious blush and rosy lips, its openings are adorned for his arrival, and its warm hospitality encourages him to stay; and as it eventually bids farewell, it finds peace knowing its purpose in life has been achieved.[Pg 149]
A HONEY-DEW PICNIC


everal of our notable as well as notorious human, social, and civic customs find their prehistoric prototypes in the insect kingdom. The monarchical institution sees its singular prophecy in the domestic economy of the bees. War and slavery have always been carried on systematically and effectually by ants, and, according to Huber and other authorities, agriculture, gardening, and an industry very like dairy farming have been time-honored customs among this same wise and[Pg 152] thrifty insect tribe, whose claims to thoughtful consideration were so long ago voiced by Solomon of proverbial fame. Thévenot mentions "Solomon's ant" as among the "beasts which shall enter paradise." Indeed, the human saint as well as sluggard may "go to the ant" for many suggestive hints and commentaries.
Several of our famous and infamous human, social, and civic customs have their roots in the insect world. The idea of monarchy finds its unique representation in the organization of bees. Ants have always engaged in war and slavery in a systematic and effective way, and according to Huber and other experts, agriculture, gardening, and practices similar to dairy farming have been longstanding traditions among these wise and [Pg 152] resourceful insects, whose value for thoughtful consideration was noted long ago by the famously wise Solomon. Thévenot lists "Solomon's ant" among the "beasts that shall enter paradise." Indeed, both the diligent and the lazy human can take many insightful lessons and reflections from the ant.
These are only a few of the more notable parallelisms which suggest themselves. But others are not wanting if we care to follow the subject. In addition to the many models of thrift and virtuous industry, embodying types of many of the trade employments known to humanity, have we not also among these "meadow tribes" our luxurious "idlers" and "exquisites," the butterflies and flower-haunting flies and "dandy" beetles; and, opposed to all these, the suggestive antithesis of the promiscuous marauders, thieves, and brigands everywhere interspersed?
These are just a few of the more notable similarities that come to mind. But there are more if we choose to explore the topic further. Besides the many examples of thrift and hard work, representing various types of jobs known to people, don't we also have among these "meadow tribes" our lavish "idlers" and "exquisites," the butterflies and flower-loving flies and "dandy" beetles? And in contrast to all of these, we see the striking opposite of the random marauders, thieves, and bandits scattered everywhere?
Thus we have our individual insect assassin and assassination organized in war; so, on the other hand, have we our insect merrymakers; why not, then, our picnic or carnival?
Thus we have our individual insect assassin and assassination organized in war; so, on the other hand, we also have our insect merrymakers; why not, then, our picnic or carnival?
Such I am moved to call the singular episode which I observed last summer, and which I have endeavored to picture as true to the life as possible in the accompanying presentment The scep[Pg 153]tic will perhaps remark on examination that the scene is characterized by somewhat too free a license to warrant the ideal of a "picnic." But he is hypercritical. There are picnics and picnics—picnics of high and of low degree. Do I not recall more than one notorious festive outing of the "next lower than the angels" in which the personnel seemed about similarly proportioned, and the fun and attraction comparatively related to the license?
I feel compelled to describe the unique event I witnessed last summer, and I've tried to capture it as accurately as possible in the following portrayal. Some skeptics might point out that the scene might have a bit too much creative freedom to truly represent a "picnic." But that's being overly critical. There are all kinds of picnics—some fancy and some more casual. Don’t I remember several infamous gatherings involving people who were "one step below angels," where the mix of guests was similar and the enjoyment and allure were tied to how relaxed things were?
One July afternoon a year ago I was returning home from one of my botanizing strolls. I had just emerged from a deep wood, and was skirting its border, when my attention was caught by a small fluttering swarm of butterflies, which started up at my approach and hovered about a blossoming blackberry bush a few yards in advance of me at the side of my path. The diversity of the butterfly species in the swarm struck me as singular, and the mere allurement of the blackberry blossoms—not usually of especial attraction to butterflies—could hardly explain so extensive a gathering. Here was the great yellow swallow-tail (Turnus), red admiral (Atlanta), small yellow butterfly (Philodice), white cabbage-butterfly, comma and semicolon, and numerous small fry, fluttering about me in evident protest against my intrusion. They showed no inclination to vacate the[Pg 154] premises, so, in pursuance of one of the first articles of my saunterer's creed, I concluded to retreat softly a few paces and watch for developments. One by one the swarm sought their original haunt, settling on the bramble, and I now noticed that only in occasional instances did the insects seek the flowers, the attraction seeming to be confined to the leaves. I stole up softly for a nearer point of observation, and could now distinctly see the beautiful yellow and black open wings of the swallow-tail softly gliding or gently fluttering as it hung from the edge of a leaf, while it explored its surface with its uncoiled capillary tongue. Just beyond my Turnus, on another leaf, I now noted a new presence, the orange Aphrodite butterfly, silvery spotted, its nether wings being folded over its back, too much absorbed to have been startled by my first approach. Occasionally, without any cause which I could detect from my present position—certainly in no way connected with my presence—a small swarm of the butterflies would rise in a flutter above the bush, as though actuated by a common whim—a brief winged tangle in which a beautiful sprite of velvety black hovering in a globular halo, shot through with two white semicircular arcs, was always a momentary feature.[Pg 155]
One July afternoon a year ago, I was heading home from one of my plant research walks. I had just come out of a dense forest and was walking along its edge when I noticed a small group of butterflies. They flew up as I got closer and hovered around a blooming blackberry bush a few yards ahead of me on the side of my path. The variety of butterfly species in the group caught my attention, and the appeal of the blackberry blossoms, which usually aren’t particularly attractive to butterflies, couldn’t explain such a large gathering. Among them were the great yellow swallow-tail (Turnus), red admiral (Atlanta), small yellow butterfly (Philodice), white cabbage-butterfly, comma, semicolon, and many smaller ones, all flitting around me as if protesting my intrusion. They showed no signs of wanting to leave the[Pg 154] area, so, following one of the main principles of my leisurely walks, I decided to quietly step back a few paces and watch what happened. One by one, the butterflies returned to their original spot, landing on the bramble, and I now noticed that they only occasionally visited the flowers; their interest seemed to be mainly in the leaves. I quietly moved in for a closer look and could see the beautiful yellow and black wings of the swallow-tail gliding lightly or gently flapping as it hung from the edge of a leaf, exploring the surface with its long, coiled tongue. Just beyond my Turnus, on another leaf, I noticed a new butterfly, the orange Aphrodite, with silvery spots, its lower wings folded over its back, completely absorbed and unfazed by my earlier arrival. Occasionally, without any apparent reason from my viewpoint—definitely not related to my presence—a small group of butterflies would suddenly rise up in a flutter above the bush, as if compelled by a shared impulse—a brief swirling display that often featured a beautiful black sprite surrounded by a circular halo, accented with two white semicircular arcs.[Pg 155]
Carefully stealing through the tall grass, I now approached to within touching distance of the haunt, and was soon lost in mingled wonder, amusement, and surprise at the picnic now disclosed, the occasional butterfly swarm being now easily explained. From my first point of view only the top of the bramble spray was visible above the grass, and by far the most interesting portion of the exercises had been concealed from view. The butterflies, while naturally the most conspicuous element, were now seen to be in a small minority among the insect gathering, the bramble leaves being peopled with a most motley and democratic assemblage of insects. Class distinctions were apparently forgotten in the common enthusiasm; the plebeian bluebottle and blowfly now consorted with Aphrodite and sipped at the same drop. Many a leaf was begemmed with the blue bodies closely set side by side or in a close cluster. The meat-fly, house-fly, and horse-fly made themselves promiscuous in every portion of the spray, and what with the rainbow-eyed and ruby-eyed flies, black and silver-banded flower-flies, and other tiny, restless, iridescent atoms of the fly fraternity, the family of Musca was well represented at the feast.
Carefully sneaking through the tall grass, I got close enough to touch the spot and was soon lost in a mix of wonder, amusement, and surprise at the picnic laid out before me, which explained the occasional swarms of butterflies. From my initial viewpoint, I could only see the top of the bramble above the grass, and the most interesting parts of the gathering had been hidden from sight. While the butterflies were obviously the most noticeable, I now saw they made up a small part of the insect crowd, as the bramble leaves were filled with a wildly diverse and equal mix of insects. Class differences seemed to have disappeared in the shared excitement; the ordinary bluebottle and blowfly mingled with Aphrodite and drank from the same drop. Numerous leaves were adorned with blue bodies tightly packed together or in clusters. The meat-fly, house-fly, and horse-fly were scattered throughout the bramble, and with the rainbow-eyed and ruby-eyed flies, as well as the black and silver-banded flower-flies and other tiny, restless, shimmering members of the fly community, the family of Musca was well represented at the gathering.
Nor were these all the guests at the banquet[Pg 156]—for banquet there certainly was, judging from the eager sipping and crowding everywhere upon the leaves, the flowers even yet, as I first noticed, seeming to have little attraction.
Nor were these all the guests at the banquet[Pg 156]—because there was definitely a banquet happening, judging by the eager sipping and the crowding everywhere on the leaves; the flowers, as I first noticed, seemed to have little appeal.
I have no direct means of knowing as to the social discrimination of the host as shown in the entertainment, for that invitations were issued the subsequent facts would show. But I have good reasons for believing, from the course of events, that the gathering included a number of questionable personages that were not counted upon.
I have no way of knowing for sure about the host's social discrimination as reflected in the entertainment, but the given invitations would later reveal the facts. However, I have strong reasons to believe, based on what happened, that the gathering included some questionable individuals that weren't expected.
Here, for instance, was an overwhelming contingent of the whole tough gang of wasps and hornets—brown wasps from under the eaves and fences; black hornets from the big paper nests; yellow-jackets from where you please; deep steel-blue wire-waisted wasps from the mud cells in the garret, to say nothing of an occasional longer-waisted digger-wasp, and a host of their allied lesser associates scattered around generously among the assemblage.
Here, for example, was a huge group of the entire tough crew of wasps and hornets—brown wasps nesting under the eaves and fences; black hornets from the big paper nests; yellow-jackets from wherever you look; and deep steel-blue, wire-waisted wasps from the mud cells in the attic, not to mention the occasional longer-waisted digger wasp, along with numerous smaller relatives scattered generously among the gathering.
Every now and then a big darning-needle took a shimmering circuit about the bush, and doubtless knew what he was about; as did also what at first glimpse appeared to be a big bumblebee, which seemed to find attraction in the neighborhood, although he seldom alighted upon the[Pg 157] leaves, preferring to sit upon a neighboring weed and watch his opportunities.
Every now and then, a large darning needle flew around the bush, clearly knowing what it was doing; the same went for what at first looked like a big bumblebee, which seemed drawn to the area, even though it rarely landed on the[Pg 157] leaves, choosing instead to rest on a nearby weed and observe its surroundings.
I have thus described a few of the more prominent guests or personages present at the feast. But I have reported little of their "goings on." Doubtless there were appropriate toasts and responses, or what in bug etiquette answered to this seemingly indispensable human fad, while as to that other festive social essential of after-dinner speeches, coupled in this case with most vigorous discussion, I am certain the air was blue with something of this sort, if the eloquent pantomime bore any significance. Here, for instance, is one isolated, but frequent, episode. A peaceable little group of plain bluebottle-flies, with but a single thought, are all sipping at the same drop in contentment. A brief respite, for now the tips of a pair of inquisitive antennæ appear from the under edge of the leaf upon which they are sipping, and gingerly explore the upper surface. They are quickly followed by the covetous almond-eyed gaze of a brown wasp, that now steals cautiously around to the upper surface, and appears wholly engrossed in licking the leaf. Nearer and nearer he sidles up to the group of flies, and now with deliberate purpose and open jaws makes a dash among them. But they are too quick for him,[Pg 158] and are away in a glittering blue tangle, which finally concentrates itself upon a neighboring leaf, where the eager tippling is immediately resumed. The wasp now holds the fort, and seems in no mood to be trifled with. With head and fore feet upraised and open jaws he seems "spoiling for a fight," and ready to make war upon the first comer. But no, he is evidently expecting a friend that, I now observe, approaches him determinedly down the stem of the leaf. The new-comer, a brown wasp like himself, is now at close range, and in an instant more, without any visible courteous preliminaries, the two set upon each other with a common enthusiasm, and with jaws working and stings fencing the interlocked combatants fall to the ground for a finish. I presume the affair was carried to the fourteenth round without any undue interference.
I’ve described some of the prominent guests at the feast, but I haven’t shared much about what they did. There were probably the usual toasts and responses, or whatever etiquette dictates for this seemingly essential human tradition. As for the other must-have part of any festive gathering—after-dinner speeches—combined with lively discussions, I’m sure the atmosphere was charged with that energy, if the expressive gestures meant anything at all. Here’s one example of what happened repeatedly. A calm little group of plain bluebottle flies, focused on a single drop, is happily sipping together. Just for a moment, then the tips of some curious antennae peek out from the edge of the leaf they’re on, carefully exploring the surface above. They’re quickly followed by the greedy gaze of a brown wasp that stealthily approaches the top of the leaf and seems totally absorbed in licking it. He inches closer to the group of flies, and now with clear intent and open jaws, he lunges at them. But they’re too fast for him, and they escape in a sparkling blue swirl, eventually settling on a nearby leaf to resume their drinking. The wasp now stands guard, looking like he’s ready for a fight, with his head and front feet raised and his jaws open, prepared to take on anyone who comes near. But no, he’s clearly waiting for a friend, which I now see is making its way determinedly down the stem of the leaf. The new brown wasp arrives close by, and in an instant, without any polite preliminaries, the two attack each other with enthusiasm. With their jaws moving and their stingers fencing, they tumble to the ground, fully engaged in their battle. I assume their scuffle went on for quite a while without any significant interruptions.
Another and another of these friendly meetings between them and other wasps took place in the half-hour in which I watched the sport. There were lulls in hostilities, during which an atmosphere of perfect peace and harmony seemed to reign around my bramble-bush. The flies were motionless in their ecstasy, and the hornet element seemed by common consent to keep temporarily shady, and even the butterflies seemed to[Pg 159] forget that they had wings. But not for long, for now with a shimmering glitter our darning-needle invades the scene, and retires to a convenient perch with a ruby-eyed fly in his teeth, while a swarm of very startled butterflies tells conspicuously of the demoralization which he has left in his path. Among the butterfly representatives I at length observed one individual which at first had escaped me, an exclusive white cabbage-butterfly which sipped quietly at his leaf in the shade, and seemed to take little interest in the disreputable actions of his associates. Nothing could move him or entice him away from his convivial employment. But, alas! his folly soon found him out, for, on happening to look again, I observed he had found a new acquaintance—a hornet that had evidently been long desirous of meeting him. One by one I saw my butterfly's dismembered wings fall to the grassy jungle below, while a big black wasp proceeded to enjoy the collected sweets which he had doubtless observed were being so carefully stored away there in the shady retreat.
Another and another of these friendly meetings between them and other wasps happened during the half-hour I watched the scene. There were pauses in the fighting, creating an atmosphere of perfect peace and harmony around my bramble-bush. The flies were frozen in their joy, and the hornets seemed to agree to keep a low profile, even the butterflies seemed to forget they had wings. But not for long, as our darning-needle suddenly appeared, sparkling in the sunlight, and retreated to a convenient spot with a ruby-eyed fly in its grip, while a startled swarm of butterflies revealed the chaos it had caused. Among the butterfly crowd, I eventually noticed one individual I had missed at first, a solitary white cabbage-butterfly quietly sipping from its leaf in the shade, showing little interest in the questionable behavior of its companions. Nothing could move him or tempt him away from his delightful task. But, alas! his naivety soon caught up with him, for when I looked again, I saw he had made a new acquaintance—a hornet that had clearly been eager to meet him. One by one, I watched as my butterfly's torn wings fell to the grassy ground below, while a large black wasp enjoyed the collected sweets that it had doubtless noticed being carefully stored away in that shady spot.

And now my pretty black butterfly—no, it proved to be the little day-flying grape-vine-moth, the eight-spotted black Alypia—appeared from some unseen source, and spun his crapy white-[Pg 161]streaked halo among the leaves, at length settling among a little company of flies. Softly behind him creeps a brown wasp (Polistes), with his mouth watering, while from the opposite quarter a steel-blue mud-wasp approaches, with apparently similar designs. Neither invader sees the other. Simultaneously, as though answering to a signal, the two make a dash at the moth; but he is too quick for them. In a twinkling he is off in his pretty halo again, while the two disappointed contestants have clinched, and with stings and jaws vigorously plying fall to the jungle below, and seek satisfaction in mortal combat.
And now my beautiful black butterfly—no, it turned out to be the small, day-flying grape-vine moth, the eight-spotted black Alypia—emerged from some hidden place and spun its crinkly white-[Pg 161]streaked halo among the leaves, eventually landing among a small group of flies. Softly trailing behind it is a brown wasp (Polistes), its mouth watering, while from the other side a steel-blue mud-wasp approaches, seemingly with the same goals. Neither invader notices the other. Simultaneously, as if responding to a cue, the two rush at the moth; but he's too fast for them. In an instant, he’s off in his beautiful halo again, while the two frustrated competitors have locked onto each other, and with stings and jaws working hard, they tumble to the jungle below, seeking satisfaction in a deadly fight.
Here is a pretty little yellow and black banded flower-fly, which is having a quiet little picnic all by himself on a bed of yarrow bloom close by. But a big black paper-hornet has suddenly seen an attraction hither also, and is soon creeping stealthily among the blossoms with a wild and hungry look. But the hornets seemed to waste their time on the flies. Seemingly confident in their less complicated wing machinery, the two-winged fly rarely sought escape until within very close range of his enemy, and his resources never seemed to disappoint him at the critical moment.
Here is a pretty little yellow and black striped flower fly, enjoying a quiet picnic all by itself on a bed of yarrow flowers nearby. But a big black paper wasp has suddenly noticed the spot too, and is soon creeping stealthily among the blooms with a wild and hungry look. However, the wasps seem to waste their time on the flies. Seemingly confident in their simpler wing design, the two-winged fly rarely tries to escape until it’s very close to its enemy, and its abilities never seem to let it down at the crucial moment.
Among the insect assemblage was a large number of ants of all kinds and sizes, the common[Pg 162] large black species being conspicuous. Here is one creeping and sipping along a grass stem. A small digger-wasp likes this grass stem too, but instead of exchanging courtesies on the subject, the wasp proceeds to bite the ant's head off without ceremony, and continues sipping at the stem as though decapitation were a mere casual incident in its daily walk.
Among the group of insects was a large number of ants of all kinds and sizes, with the common[Pg 162] large black species standing out. Here’s one crawling and sipping along a grass stem. A small digger wasp likes this grass stem too, but instead of being polite about it, the wasp casually bites the ant's head off and keeps sipping at the stem as if decapitating the ant were just a regular part of its day.
On the same stem a big blowfly has alighted. Judging from appearances, he has had his fill of good things, and is now making his leisurely toilet in the peculiar fashion of his kind, rubbing down his back and wings with his hind legs, twisting his front feet into spirals, and ever and anon testing the strength of his elastic neck attachment as he threatens to pull his head from his body.
On the same branch, a large blowfly has landed. From the looks of it, he’s had his share of indulgence and is now taking his time grooming in the unique way of his species, using his hind legs to clean his back and wings, twisting his front feet into spirals, and occasionally testing the flexibility of his neck as if he's about to pull his head off.
This worldly act has been progressing for some moments under the gaze of a big black digger-wasp, who now concludes to cut it short. When at close range with his prey, the fly suddenly discovers the unhealthy location which he occupies, and actually protruding his tongue by way of parting salute, he is off with a buzz. He has barely taken wing, however, when a still louder buzz is heard, while a great black bumblebee follows closely in his wake, until the sounds of both[Pg 163] are lost in the distance. The hum of this bumblebee is a frequent musical feature of the entertainment, and many is the dance that is set to its minstrelsy, as the burly insect darts in among the merrymakers and is off to his perch near by. It is only as we steal away and observe him closely that we learn the secret of his occasional sorties. There on a clover blossom he sits—sipping honey? Oh no. It is honey-dew that he is enjoying, and second-hand at that, as he devours the satiated bluebottle-fly which is empaled on his black horny beak. For this is only a bumblebee in masquerade—a carnivorous fly, in truth, which, safe in its disguise of respectability, hovers in the flowery haunts of the innocents and, of course, reaps his reward.
This worldly act has been going on for a while under the watchful eye of a large black digger wasp, who now decides to put an end to it. When the fly gets close to its prey, it suddenly realizes the dangerous spot it's in, and after an awkward farewell, it zooms off with a buzz. But just as it takes flight, a louder buzz is heard, and a big black bumblebee closely follows behind, until the sounds of both[Pg 163] fade away into the distance. The hum of this bumblebee is a familiar tune in the scenery, and many a dance is set to its music as the hefty insect darts among the fun-seekers and heads to its nearby resting spot. It’s only when we quietly move in for a closer look that we uncover the truth behind its occasional visits. There, on a clover blossom, it sits—sipping honey? Oh no. It's enjoying honeydew, and second-hand at that, as it devours the well-fed bluebottle fly speared on its black, hard beak. For this is just a bumblebee in disguise—a carnivorous fly, in reality, cleverly disguised as respectable while it mingles in the flowery domains of the innocent and, of course, reaps the rewards.
And what is this? A yellow-jacket has found an ambrosial attraction here upon the bramble leaf. Meanwhile a great black and white paper-hornet has seen his opportunity, and is soon slyly approaching behind the sipper. That he has designs on that jacket and its contents is apparent. In a moment the onslaught is consummated, and in the struggle which ensues the black assailant relieves his victim—of his watch presumably, for he has captured the entire garment, which he soon rifles and discards with some show of satisfaction.[Pg 164]
And what do we have here? A yellow jacket has discovered a sweet spot on the bramble leaf. Meanwhile, a large black and white paper hornet has spotted an opportunity and is quietly sneaking up behind the sipper. It's obvious he has his sights set on that jacket and what’s inside. In a moment, the attack happens, and during the struggle that follows, the black attacker takes everything from his victim—presumably its watch—because he grabs the whole jacket, quickly searches through it, and tosses it aside, looking quite satisfied.[Pg 164]
And so my carnival proceeds. So it began with the dawn; so it will continue till dusk; and through the night, with new revels, for aught I know, and will be prolonged for days or weeks.
And so my carnival goes on. It started with dawn; it will continue until dusk; and through the night, with new celebrations, for all I know, and might last for days or weeks.
Reflective reader, how often, as you have strolled through some nook in the suburban wood, have you paused in philosophic mood at the motley relics of good cheer which sophisticated the retreat, so pathetically eloquent of pristine joys to which you had been a stranger? Here in my present picnic is the suggestive parallel, for even though no such actual episodes as those I have described had been witnessed by me, an examination of the premises beneath my bramble were a sufficient commentary. These were the unimpeachable witnesses of the pleasures which I have pictured. Dismembered butterfly wings strewed the grassy jungle, among which were a fair sprinkling from that black and white halo already noted. Occasional dead wasps and detached members of wasp and hornet anatomy were frequent, while the blue glitter of the bodies of flies lit up a shadowy recess here and there, showing that Musca had not always so correctly gauged his comparative wing resources as my observation had indicated.[Pg 165]
Reflective reader, how often, as you’ve wandered through a corner of the suburban woods, have you stopped in a thoughtful mood at the colorful remnants of joy that adorned the retreat, so sadly reminiscent of the simple pleasures that you’ve never experienced? Here at my current picnic is a telling example, for even though I hadn’t witnessed any of the actual events I’ve described, looking at the surroundings under my bramble was enough to tell the story. These were undeniable witnesses to the joys I’ve imagined. Broken butterfly wings scattered across the grassy thicket, among which were a fair mix from that black and white halo I mentioned earlier. Occasionally, dead wasps and dismembered parts of wasps and hornets were common sights, while the blue shimmer of fly bodies lit up a shadowy corner here and there, proving that Musca hadn’t always accurately judged his wing capabilities as my observations suggested.[Pg 165]
It was interesting to discover, too, down deep among the herbage, another suggestive fact in the presence of a shrewd spider that showed a keen eye to the main chance, and had spread his gossamer catch-all beneath the bramble. It was all grist into his mill, and no doubt his charnel-house at the base of his silken tunnel could have borne eloquent testimony alike to his wise sagacity and his epicurean luxury.
It was interesting to find, hidden among the plants, another telling sign in the form of a clever spider that was quick to seize opportunities, having spread its delicate web beneath the bramble. Everything that came into its web was useful, and no doubt its lair at the base of its silk tunnel could have told stories about both its smart strategy and its lavish lifestyle.
I have pictured my picnic, and the question naturally arises, what was it all about—what the occasion for this celebration? There was certainly no distinct visible cause for the social gathering upon this particular bramble-bush. There were a number of other bramble-bushes in the near neighborhood which, it would seem, should possess equal attractions, but which were ignored. In what respect did the one selected differ from the others?
I have imagined my picnic, and the question comes to mind, what was it really about—what was the reason for this celebration? There was definitely no obvious reason for this social gathering at this particular bramble bush. There were several other bramble bushes nearby that should have been just as appealing, but they were overlooked. In what way did the chosen one stand out from the rest?
This bramble had become the scene of my carnival simply because it chanced to be directly beneath an overhanging branch of pine some twenty feet above. Here dwelt mine host who had issued the invitations and spread the feast, the limb for about a foot space being surrounded by a colony of aphides, or plant-lice, from whose distilling pipes the rain of sweet honey-dew had[Pg 166] fallen ceaselessly upon the leaves below. The flies, butterflies, and ants had been attracted, as always, by its sweets; the preoccupied convivial flies, in turn, were a tempting bait for the wasps and hornets, and my dragon-fly and mock bumblebee found a similar attraction in the neighborhood.
This thicket had turned into the setting for my celebration simply because it happened to be right under an overhanging pine branch about twenty feet above. Here lived my host who sent out the invitations and laid out the feast, with the branch for about a foot being surrounded by a colony of aphids, or plant lice, from whose dripping pipes the sweet honeydew had[Pg 166] continuously rained down on the leaves below. The flies, butterflies, and ants had been drawn in, as usual, by its sweetness; the distracted, partying flies were, in turn, tempting bait for the wasps and hornets, and my dragonfly and faux bumblebee found similar allure in the area.
An examination of the trunk of the pine showed the inevitable double procession of ants, both up and down the tree, with the habitual interchange of comment; and could we but have obtained a closer glimpse of the pine branch above, we might certainly have observed the queer spectacle of the small army of ants interspersed everywhere among the swarm of aphides. Not in antagonism; indeed, quite the reverse; herders, in truth, jealously guarding their feeding flock, creeping among them with careful tread, caressing them with their antennæ while they sipped at the honeyed pipes everywhere upraised in most expressive and harmonious welcome.
An examination of the trunk of the pine tree revealed the usual flow of ants moving both up and down the tree, constantly exchanging observations. If we could have gotten a closer look at the pine branch above, we would have definitely seen the curious sight of a small army of ants scattered among a swarm of aphids. Not as enemies; in fact, quite the opposite; they were herders, carefully protecting their feeding flock, moving among them with gentle steps, touching them with their antennae as they drank from the sweet droplets offered everywhere in a warm and welcoming way.
This intimate and friendly association of the ants and aphides has been the subject of much interesting scientific investigation and surprising discovery. Huber and Lubbock have given to the world many startling facts, the significance of which may be gathered from the one statement[Pg 167] that certain species of ants carry their devotion so far as literally to cultivate the aphides, carrying them bodily into their tunnels, where they are placed in underground pens, reared and fed and utilized in a manner which might well serve as a pattern for the modern dairy farm. Indeed, after all that we have already seen upon a single bramble-bush, would it be taking too much license with fact to add one more pictorial chronicle—an exhilarated and promiscuous group of butterflies, ants, hornets, wasps, and flies uniting in "a health to the jolly aphis"?
This close and friendly relationship between ants and aphids has been the focus of many fascinating scientific studies and surprising findings. Huber and Lubbock have revealed numerous astonishing facts, the importance of which can be highlighted by the simple observation[Pg 167] that some species of ants go so far as to literally farm aphids, carrying them into their tunnels, where they are placed in underground pens, raised, fed, and used in a way that could easily serve as a model for a modern dairy farm. In fact, considering everything we've already observed on a single bramble bush, would it be too much to add one more vivid scene—an excited and mixed group of butterflies, ants, hornets, wasps, and flies coming together to toast "the cheerful aphis"?

A FEW NATIVE ORCHIDS AND THEIR INSECT PARTNERS. |
In a previous article I discussed the general subject of the fertilization of flowers, briefly outlining the several historical and chronological steps which ultimately led to Darwin's triumphant revelation of the divine plan of "cross-fertilization" as the mystery which had so long been hidden beneath the forms and faces of the flowers.
In a previous article, I talked about the overall topic of how flowers are fertilized, giving a quick overview of the historical and chronological developments that eventually led to Darwin's groundbreaking discovery of the divine purpose of "cross-fertilization," the mystery that had been concealed for so long beneath the shapes and appearances of the flowers.
In the same paper I presented many illustra[Pg 172]tive examples among our common wild flowers possessing marvellous evolved devices, mechanisms, and peculiarities of form by which this necessary cross-fertilization was assured.
In the same paper, I shared many illustrative examples from our common wildflowers that have amazing evolved features, mechanisms, and shapes that make sure this important cross-fertilization happens.
Prior to Darwin's time the flower was a voice in the wilderness, heard only in faintest whispers, and by the few. But since his day they have bloomed with fresher color and more convincing perfume. Science brought us their message. Demoralizing as it certainly was to humanity's past ideals, philosophic, theologic, and poetic, it bore the spirit of absolute conviction, and must be heard.
Before Darwin's time, the flower was like a voice in the wilderness, heard only in faint whispers by a select few. But since then, they have bloomed with brighter colors and stronger scents. Science has delivered their message. Although it was disheartening for humanity's previous ideals—philosophical, theological, and poetic—it carried an undeniable spirit of conviction that we must acknowledge.
What a contrast this winged botany of to-day to that of a hundred years ago! The flower now no longer the mere non-committal, structural, botanical specimen. No longer the example of mere arbitrary, independent creation, reverently and solely referred to the orthodox "delight of man." The blossom whose unhappy fate was bemoaned by the poet because, forsooth, it must needs "blush unseen," or "waste its sweetness on the desert air," is found alone in that musty hortus siccus of a blind and deluded past. From the status of mere arbitrary creation, however "beautiful," "curious," "eccentric," hitherto accepted alone on faith—"it is thus because it is created[Pg 173] thus: what need to ask the reason why?"—it has become a part of our inspiring heritage, a reasonable, logical, comprehensible result, a manifestation of a beautiful divine scheme, and is thus an ever-present witness and prophet of divine care and supervision.
What a contrast this winged botany of today is to that of a hundred years ago! The flower is no longer just a neutral, structural, botanical specimen. It’s no longer just an arbitrary, independent creation, reverently and only referred to as the orthodox "delight of man." The blossom, which the poet lamented because it must "blush unseen" or "waste its sweetness on the desert air," now exists only in that outdated hortus siccus of a blind and misguided past. From being merely an arbitrary creation, however "beautiful," "curious," or "eccentric," previously accepted on faith—"it is what it is simply because it was created this way: why ask the reason?"—it has become part of our inspiring heritage, a reasonable, logical, and comprehensible result, a manifestation of a beautiful divine scheme, and thus stands as a constant witness and prophet of divine care and watchfulness.
The flower of to-day! What an inspiration to our reverential study! What a new revelation is borne upon its perfume! Its forms and hues, what invitations to our devotion! This spot upon the petal; this peculiar quality of perfume or odor; this fringe within the throat; this curving stamen; this slender tube! What a catechism to one who knows that each and all represent an affinity to some insect, towards whose vital companionship the flower has been adapting itself through the ages, looking to its own more certain perpetuation!
The flower of today! What an inspiration for our respectful study! What a new revelation comes with its scent! Its shapes and colors, what invitations to our devotion! This mark on the petal; this unique quality of scent; this fringe in the throat; this bending stamen; this narrow tube! What a lesson for someone who understands that each detail represents a connection to some insect, to whose vital companionship the flower has been adjusting over the ages, aiming for its own more certain survival!
The great Linnæus would doubtless have claimed to "know" the "orchid," which perhaps he named. Indeed, did he not "know" it to the core of its physical, if not of its physiological, being? But could he have solved the riddle of the orchid's persistent refusal to set a pod in the conservatory? Could he have divined why the orchid blossom continues in bloom for weeks and weeks in this artificial glazed tropic—perhaps[Pg 174] weeks longer than its more fortunate fellows left behind in their native haunts—and then only to wither and perish without requital? Know the orchid?—without the faintest idea of the veritable divorce which its kidnapping had involved!
The great Linnæus would likely have claimed he "knew" the "orchid," possibly naming it himself. Did he truly "know" it to the core of its physical, if not physiological, makeup? But could he have figured out why the orchid stubbornly refuses to produce a pod in the conservatory? Could he have sensed why the orchid blossom stays in bloom for weeks and weeks in this artificial tropical environment—maybe[Pg 174] weeks longer than its luckier counterparts left in their natural habitats—and then just fades away without any reward? Know the orchid?—without the slightest clue about the real separation that its abduction had caused!
Thanks to the new dispensation, we may indeed claim a deeper sympathy with the flower than is implied in a mere recognition of its pretty face. We know that this orchid is but the half of itself, as it were; that its color, its form, however eccentric and incomprehensible, its twisted inverted position on its individual stalk-like ovary, its slender nectary, its carefully concealed pollen—all are anticipations of an insect complement, a long-tongued night-moth perhaps, with whose life its own is mysteriously linked through the sweet bond of perfume and nectar, and in the sole hope of posterity.
Thanks to the new understanding, we can definitely say we feel a deeper connection to the flower than just appreciating its beauty. We realize that this orchid is only half of what it is; its color, its shape—no matter how strange or hard to understand, its unique position on its stalk-like ovary, its thin nectar tube, its carefully hidden pollen—all are designed to attract an insect partner, maybe a long-tongued moth, whose life is mysteriously intertwined with the flower's through the sweet connection of scent and nectar, all for the sake of future generations.
And the flower had been stolen from its haunt while its consort slept, and had awakened in a glazed prison—doubtless sufficiently comfortable, save for the absence of that one indispensable counterpart, towards whom we behold in the blossom's very being the embodied expression of welcome.
And the flower had been taken from its home while its partner slept, and had woken up in a shiny prison—probably quite comfortable, except for the lack of that one essential counterpart, toward which we see in the flower's very existence the clear expression of welcome.
Blooming day after day in anticipation of his coming, and week after week still hoping against[Pg 175] hope, we see the flower fade upon its stalk, and with what one might verily believe to be evidences of disconsolation, were it not that the ultra-scientist objects to such a sentimental assumption with regard to a flower, which is unfortunate enough to show no sign of nerves or gray matter in its composition. Who shall claim to know his orchid who knows not its insect sponsor?
Blooming day after day waiting for his arrival, and week after week still hoping against hope, we watch the flower fade on its stem, along with what one might genuinely believe to be signs of sadness, if not for the ultra-scientist who argues against such a sentimental view of a flower, which is unfortunate enough to show no signs of nerves or brain in its makeup. Who can claim to know his orchid if they don't know its insect partner?
To take one of our own wild species. Here is the Arethusa bulbosa of Linnæus, for instance. Its pollen must reach its stigma—so he supposed—in order for the flower to become fruitful. But this is clearly impossible, as the pollen never leaves its tightly closed box unless removed by outside aid, which aid must also be required to place it upon the stigma. This problem, which confronted him in practically every orchid he met, Linnæus, nor none of his contemporaries, nor indeed his followers for many years, ever solved.
To consider one of our own wild species, take the Arethusa bulbosa described by Linnæus, for example. He believed that its pollen had to reach its stigma for the flower to produce seeds. However, this is clearly impossible since the pollen never leaves its tightly closed capsule unless it is removed by an external source, which is also needed to place it on the stigma. This challenge, which Linnæus faced with nearly every orchid he encountered, was never solved by him, his contemporaries, or indeed his followers for many years.
Not until the time of Christian Conrad Sprengel (1735) did this and other similar riddles begin to be cleared up, that distinguished observer having been the first to discover in the honey-sipping insect the key to the omnipresent mystery. Many flowers, he discovered, were so constructed or so planned that their pollen could not reach[Pg 176] their own stigmas, as previously believed. The insect, according to Sprengel, enjoyed the anomalous distinction of having been called in, in the emergency, to fulfil this apparent default in the plain intentions of nature, as shown in the flower. Attracted by the color and fragrance of the blossom, with their implied invitation to the assured feast of nectar, the insect visited the flower, and thus became dusted with the pollen, and in creeping or flying out from it conveyed the fecundating grains to the receptive stigma, which they could not otherwise reach. Such was Sprengel's belief, which he endeavored to substantiate in an exhaustive volume containing the result of his observations pursuant to this theory.
Not until the time of Christian Conrad Sprengel (1735) did this and other similar puzzles start to be solved, as this keen observer was the first to find the answer to the widespread mystery in the honey-sipping insect. He discovered that many flowers were structured in such a way that their pollen could not reach[Pg 176] their own stigmas, contrary to previous beliefs. According to Sprengel, the insect played a unique role in addressing this apparent flaw in nature's design, as seen in the flower. Attracted by the flower's color and fragrance, which hinted at a plentiful nectar feast, the insect visited the flower and got covered in pollen. As it crawled or flew away, it transferred the fertilizing grains to the receptive stigma that could not be reached otherwise. This was Sprengel's belief, which he aimed to support in a detailed book that included the results of his observations related to this theory.
But Sprengel had divined but half the truth. The insect was necessary, it was true, but the Sprengel idea was concerned only with the individual flower, and the great botanist was soon perplexed and confounded by an opposing array of facts which completely destroyed the authority of his work—facts which showed conclusively that the insect could not thus convey the pollen as described, because the stigma in the flower was either not yet ready to receive it—perhaps tightly closed against it—or was past its receptive period, even decidedly withered.[Pg 177]
But Sprengel had figured out only part of the truth. The insect was necessary, that much is true, but Sprengel's idea focused solely on the individual flower. The great botanist soon found himself puzzled and overwhelmed by a set of conflicting facts that completely undermined his work—facts that clearly demonstrated that the insect could not transfer the pollen as he described, because the stigma in the flower was either not yet ready to receive it—perhaps tightly closed against it—or was already past its receptive stage, possibly even quite withered.[Pg 177]

This radical assumption of fertilization in the individual flower, which lay at the base of Sprengel's theory, thus so completely exposed as false, discredited his entire work. The good was condemned with the bad, and the noble volume was lost in comparative oblivion—only to be finally resurrected and its full value and significance revealed by the keen scientific insight of Darwin (1859). From the new stand-point of evolution through natural selection the facts in Sprengel's work took on a most important significance. Darwin now reaffirmed the Sprengel theory so far as the necessity of the insect was concerned, but showed that all those perplexing floral conditions which had disproved Sprengel's assumption, instead of having for their object the conveying of pollen to the stigma of the same flower, implied its transfer to the stigma of another, cross-fertilization being the evident design, or evolved and perpetuated advantage.
This radical assumption about fertilization happening within individual flowers, which was the foundation of Sprengel's theory, was completely proven false and discredited his entire work. The good was judged alongside the bad, and the valuable volume faded into relative obscurity—only to be eventually revived and its full worth and significance uncovered by Darwin's sharp scientific perspective in 1859. From the new viewpoint of evolution through natural selection, the facts in Sprengel's work gained significant importance. Darwin reaffirmed Sprengel's theory regarding the necessity of insects but demonstrated that all those confusing floral traits that had disproved Sprengel's assumption were instead aimed at transferring pollen to the stigma of another flower, with cross-fertilization being the clear intent, or an evolved and sustained benefit.
This solution was made logical and tenable only on the assumption that such evolved conditions, insuring cross-fertilization, were of distinct advantage to the flower in the competitive struggle for existence, and that all cross-fertilized flowers were thus the final result of natural selection.[Pg 179]
This solution only makes sense if we assume that these evolved conditions, which ensure cross-fertilization, give the flower an advantage in the struggle for survival, and that all cross-fertilized flowers are the ultimate result of natural selection.[Pg 179]
The early ancestors of this flower were self-fertilized; a chance seedling at length, among other continual variations, showed the singular variation of ripening its stigma in advance of its pollen—or other condition insuring cross-fertilization—thus acquiring a strain of fresh vigor. The seedlings of this flower, coming now into competition with the existing weaker self-fertilized forms, by the increased vigor won in the struggle of their immediate surroundings, and inheriting the peculiarity of their parent, showed flowers possessing the same cross-fertilizing device. The seeds from these, again scattering, continued the unequal struggle in a larger and larger field and in increasing numbers, continually crowding out all their less vigorous competitors of the same species, at length to become entire masters of the field and the only representatives left to perpetuate the line of descent.
The early ancestors of this flower were self-pollinating; eventually, a random seedling among many variations displayed the unique trait of maturing its stigma before its pollen, or another way of ensuring cross-pollination, thereby gaining a new strain of vitality. The seedlings of this flower, now competing with the existing weaker self-pollinating varieties, gained strength through the challenges of their environment and inherited the unusual trait from their parent, resulting in flowers with the same cross-pollination mechanism. The seeds from these flowers dispersed further, continuing the unequal competition over a larger area and in increasing numbers, constantly pushing out their less vigorous relatives of the same species, until they ultimately dominated the area and became the sole survivors to carry on the lineage.
Thus we find in almost every flower we meet some astonishing development by which this cross-fertilization is effected, by which the transferrence of the pollen from one flower to the stigma of another is assured, largely through the agency of insects, frequently by the wind and water, occasionally by birds. In many cases this is assured by the pollen-bearing flowers and stig[Pg 180]matic flowers being entirely distinct, as in cucumbers and Indian-corn; perhaps on different plants, as in the palms and willows; again by the pollen maturing and disseminating before the stigma is mature, as already mentioned, and vice versa.
We find that almost every flower we encounter has some incredible development that allows for cross-fertilization, ensuring the transfer of pollen from one flower to the stigma of another. This process is largely facilitated by insects, often by the wind and water, and sometimes by birds. In many cases, this is guaranteed by the male and female flowers being entirely different, like in cucumbers and corn; sometimes they are on different plants, as with palms and willows; and at other times, the pollen matures and spreads before the stigma is ready, and vice versa.
From these, the simplest forms, we pass on to more and more complicated conditions, anomalies of form and structure—devices, mechanisms, that are past belief did we not observe them in actuality with our own eyes, as well as the absolutely convincing demonstration of the intention embodied: exploding flowers, shooting flowers, flower-traps, stamen embraces, pollen showers, pollen plasters, pollen necklaces, and floral pyrotechnics—all demonstrations in the floral etiquette of welcome and au revoir to insects.
From these simplest forms, we move on to increasingly complex conditions, oddities of form and structure—devices and mechanisms that would be hard to believe if we didn't see them for ourselves, along with the completely convincing evidence of the intention behind them: exploding flowers, shooting flowers, flower traps, stamen embraces, pollen showers, pollen plasters, pollen necklaces, and floral pyrotechnics—all displays in the floral etiquette of greeting and saying goodbye to insects.
From the simplest and regular types of flowers, as in the buttercup, we pass on to more and more involved and unsymmetrical forms, as the columbine, monk's-hood, larkspur, aristolochia, and thus finally to the most highly specialized or involved forms of all, as seen in the orchid—the multifarious, multiversant orchid; the beautiful orchid; the ugly orchid; the fragrant orchid; the fetid orchid; the graceful, homely, grotesque, uncanny, mimetic, and, until the year 1859, the absolutely non-committal and inexplicable flower; the blossom which[Pg 181] had waited through the ages for Darwin, its chosen interpreter, ere she yielded her secret to humanity.
From the simplest and most regular types of flowers, like the buttercup, we move on to more complex and asymmetrical forms, such as the columbine, monk's-hood, larkspur, aristolochia, and eventually to the most specialized and intricate forms of all, seen in the orchid—the diverse, numerous orchid; the beautiful orchid; the unattractive orchid; the fragrant orchid; the foul-smelling orchid; the elegant, plain, grotesque, eerie, mimicking, and, until the year 1859, the completely ambiguous and puzzling flower; the blossom which[Pg 181] had waited throughout the ages for Darwin, its chosen interpreter, before it revealed its secret to humanity.
And what is an orchid? How are we to know that this blossom which we plucked is an orchid? The average reader will exclaim, "Because it is an air-plant"—the essential requisite, it would seem, in the popular mind. Of over 3000 known species of orchids, it is true a great majority are air-plants, or epiphytes—growing upon trees and other plants, obtaining their sustenance from the air, and not truly parasitic; but of the fifty-odd native species of the northeastern United States, not one is of this character, all growing in the ground, like other plants. It is only by the botanical structure of the flowers that the orchid may be readily distinguished, the epiphytic character being of little significance botanically.
And what is an orchid? How can we tell that this flower we just picked is an orchid? The average reader might say, "Because it’s an air-plant"—which seems to be the key requirement in most people's minds. Out of over 3000 known species of orchids, it’s true that a large majority are air-plants, or epiphytes—growing on trees and other plants, getting their nutrients from the air, and not truly parasitic; however, of the fifty-odd native species in the northeastern United States, none fit that description, as they all grow in the ground like other plants. The orchid can be easily identified only by the botanical structure of its flowers, since its epiphytic nature is not very significant in botanical terms.
A brief glance at this structural peculiarity may properly precede our more elaborate consideration of a few species of these remarkable flowers.
A quick look at this unique structure should come before we take a deeper look at a few types of these amazing flowers.
The orchids are usually very irregular, and six-parted. The ovary is one-celled, and becomes a pod containing an enormous yield of minute, almost spore-like, seeds (Fig. 3) in some species, as in the vanilla pod, to the number of a million, and[Pg 182] in one species of the maxillaria, as has been carefully computed, 1,750,000.
The orchids are typically very irregular and have six parts. The ovary is one-celled and turns into a pod that holds a huge number of tiny, almost spore-like seeds (Fig. 3) in some species, like the vanilla pod, with as many as a million seeds, and[Pg 182] in one species of maxillaria, which has been carefully calculated to be 1,750,000.

of a Common Flower and
of the Orchid
The pollen, unlike ordinary flowers, is gathered together in waxy masses of varying consistency, variously formed and disposed in the blossom, its grains being connected with elastic cobwebby threads, which occasionally permit the entire mass to be stretched to four or five times its length, and recover its original shape when released. This is noticeable specially in the O. spectabilis, later described. The grains thus united are readily disentangled from their mass when brought into contact with a viscid object, as, for instance, the stigma.
The pollen, unlike regular flowers, comes together in waxy clumps that have different textures, shaped and arranged in the blossom. Its grains are linked by stretchy, cobweb-like threads that sometimes allow the whole mass to stretch four or five times its original length and return to its shape when released. This is especially noticeable in the O. spectabilis, which will be described later. The grains that are stuck together can easily be separated from the mass when they touch a sticky surface, like the stigma.
But the most significant botanical contrast and distinction is found in the union of the style and stamens in one organ, called the column (Fig. 2), the stigma and the pollen being thus disposed upon a single common stalk. The contrast to the ordinary flower will be readily appreciated by comparison of the accompanying diagrams (Fig. 1).
But the most important botanical difference and distinction is found in the combination of the style and stamens into one structure, called the column (Fig. 2), with the stigma and pollen arranged on a single common stalk. You can easily understand the difference compared to a typical flower by looking at the accompanying diagrams (Fig. 1).
When, therefore, we find a blossom with the[Pg 183] anthers or pollen receptacle united to a stalk upon which the stigma is also placed, we have an orchid.
When we find a flower with the[Pg 183] anthers or pollen receptacle joined to a stalk that also has the stigma, we have an orchid.
The order is further remarkable, as Darwin first demonstrated in his wonderful volume "The Fertilization of Orchids," in that the entire group, with very few exceptions, are absolutely dependent upon insects for their perpetuation through seed. They possess no possible resource for self-fertilization in the neglect of these insect sponsors.
The order is even more impressive, as Darwin first showed in his amazing book "The Fertilization of Orchids," because the whole group, with very few exceptions, completely relies on insects for their reproduction through seeds. They have no way to self-fertilize if these insect helpers are not around.

Many of our common wild flowers, as perfectly and effectually planned for cross-fertilization as the orchids, do retain the reserve power of final self-fertilization if unfertilized by foreign pollen.
Many of our common wildflowers, just as well designed for cross-fertilization as orchids, do have the backup ability for final self-fertilization if they aren’t fertilized by outside pollen.
But the orchid has lost such power, and in the progress of evolution has gradually adapted itself to the insect, often to a particular species of insect, its sole sponsor, which natural selec[Pg 184]tion has again gradually modified in relation to the flower.
But the orchid has lost that power, and over time, it has adapted to insects, often to a specific species of insect that supports it, which natural selection has also gradually adjusted in relation to the flower.
The above work by Darwin was mostly concerned with foreign species, generally under artificial cultivation, and so startling were the disclosures concerning these hitherto sphinx-like floral beings that a most extensive bibliography soon attested the widespread inspiration and interest awakened by its pages.
The work by Darwin mentioned above mainly focused on foreign species, usually grown under controlled conditions, and the revelations about these previously mysterious plants were so surprising that a huge bibliography quickly reflected the broad inspiration and interest sparked by its content.
But it is by no means necessary to visit the tropics or the conservatory for examples of these wonders. Our own Asa Gray, one of Darwin's instant proselytes, was prompt to demonstrate that the commonest of our native American species might afford revelations quite as astonishing as those exotic species which Darwin had described.
But it’s not necessary to go to the tropics or the greenhouse to find examples of these wonders. Our own Asa Gray, one of Darwin's early followers, quickly showed that even the most common native American species could reveal insights just as amazing as those exotic species that Darwin described.

During a period of many years the writer has devoted much study to our native species of orchids from this evolutionary stand-point of their cross-fertilization tendencies. Of the following examples, selected from his list, some are elabora[Pg 185]tions of previous descriptions of Gray and others, though pictorially and descriptively the result of direct original study from nature; others are from actual observation of the insects at work on the flowers; and others still, original demonstrations based upon analogy and the obvious intention of the floral construction, the action of the insect—its head or tongue—having been artificially imitated by pins, bristles, or other probe-like bodies.
Over many years, the writer has focused a lot of study on our native orchid species, particularly looking at their cross-fertilization tendencies from an evolutionary perspective. The following examples, taken from his list, include some elaborations on earlier descriptions by Gray, while others are the result of direct, original observations from nature, both pictorially and descriptively. Some are based on actual observations of insects pollinating the flowers, and others are original demonstrations that rely on analogy and the clear purpose of the flower's structure, with the insect's head or tongue being imitated using pins, bristles, or other probe-like objects.
How many an enthusiastic flower-hunter has plucked his fragrant bouquet of the beautiful Arethusa, in its sedgy haunt, without a suspicion of the beautiful secret which lay beneath its singular form! Indeed, how many a learned botanist, long perfectly familiar with its peculiarities of shape and structure, has been entirely content with this simple fact, nor cared to seek further for its interpretation! But
How many excited flower hunters have picked their lovely bunch of the beautiful Arethusa in its grassy home, without a clue about the amazing secret hidden beneath its unique appearance! Truly, how many knowledgeable botanists, who have been completely familiar with its shape and structure for a long time, have been entirely satisfied with this basic fact, without wanting to dig deeper for its meaning! But
"All may have the flower now,
For all have got the seed."
"Now everyone can have the flower,
"Because everyone has the potential."
With Darwin as our guide and the insect as our key—an open sesame—the hidden treasure is revealed. It is now quite possible, as Darwin demonstrated, to look upon a flower for the first time and from its structure foretell the method of its intended cross-fertilization; nay, more, possibly[Pg 186] the kind, or even the species, of insect to which this cross-fertilization is intrusted.
With Darwin as our guide and the insect as our key—an open sesame—the hidden treasure is revealed. It's now quite possible, as Darwin showed, to look at a flower for the first time and, based on its structure, predict how it intends to be cross-fertilized; moreover, perhaps even the type, or maybe the species, of insect responsible for this cross-fertilization.
Let us look at our Arethusa. The writer has never happened to observe an insect at work upon this flower, but the intention of its structure is so plain that by a mere examination we may safely prophesy not only what must happen when the insect seeks its nectar, but with equal assurance the kind of insect thus invited and expected. I have indicated a group of the orchids in their usual marshy haunt, and in Fig. 4, separately, a series of diagrams presents sections of the flower, natural size and duly indexed, which renders detailed description hardly necessary. The column is here quite elongated, forked at the tip, the space between the forks occupied by the anther, which is hinged to the upper division. This anther lid is closed tightly, with the sticky mass of pollen hidden behind it in the cavity. The stigma is on the external inner side of the lower division, and thus distinctly separated from the pollen. The "lip" is extended forward as a hospitable threshold to the insect. And to what insect might we assume this invitation of color, fragrance, nectar, and threshold to be extended?
Let’s take a look at our Arethusa. The writer has never actually seen an insect working on this flower, but the purpose of its design is so obvious that just by looking, we can confidently predict not only what will happen when the insect comes for its nectar, but also what kind of insect is being attracted and expected. I’ve shown a group of orchids in their typical marshy habitat, and in Fig. 4, there are diagrams that show sections of the flower at actual size, clearly labeled, which makes a detailed description unnecessary. The column is quite elongated, forked at the tip, with the space between the forks filled by the anther, which is attached to the upper part. This anther lid is tightly closed, hiding the sticky pollen behind it in the cavity. The stigma is located on the inner side of the lower part, clearly separate from the pollen. The "lip" extends forward as a welcoming threshold for the insect. And which insect might we think this invitation of color, fragrance, nectar, and threshold is meant for?
Let us consider the flower simply as a device to insure its own cross-fertilization. The insect[Pg 187] is welcomed; it must alight and sip the nectar; in departing it must bear away this pollen upon its body, and convey it to the next Arethusa blossom which it visits, and leave it upon its stigma. These are the conditions expressed; and how admirably they are fulfilled we may observe when we examine flower after flower of a group, and find their nectaries drained, their anther cells empty, and pollen upon all their stigmas. The nectar is here secreted in a well—not very deep—and the depth of this nectar from the entrance is of great significance among all the flowers, having distinct reference to the length of the tongue which is expected to sip it. In the Arethusa, it is true, the butterfly or moth might sip at the throat of the flower, but the long tongues of these insects might permit the nectary to be drained without bringing their bodies in contact with the stigma. Smaller insects might creep into the nectary and sip without the intended fulfilment. It is clear that to neither of such visitors is the welcome extended. What, then, are the conditions embodied? The insect must have a tongue of such a length that, when in the act of sipping, its head must pass beyond the anther well into the opening of the flower. Its body must be sufficiently large to come in contact with the an[Pg 188]ther. Such requisites are perfectly fulfilled by the humblebee, and we may well hazard the prophecy that the Bombus is the welcomed affinity of the flower.
Let’s think of the flower as a way to ensure its own cross-pollination. The insect[Pg 187] is invited; it must land and drink the nectar; when it leaves, it carries pollen on its body and takes it to the next Arethusa flower it visits, depositing it on its stigma. These are the conditions laid out; and we can see how well they are met when we look at flower after flower in a group and find their nectar drained, their anther cells empty, and pollen on all their stigmas. The nectar is stored in a not-too-deep well, and the depth of this nectar from the entrance is very important among all the flowers, as it relates to the length of the tongue that’s supposed to sip it. In the Arethusa, while a butterfly or moth might sip from the flower's throat, their long tongues could drain the nectar without getting their bodies near the stigma. Smaller insects might sneak into the nectary and sip without achieving the intended goal. It's clear that neither of these visitors is truly welcomed. So, what are the conditions? The insect must have a tongue long enough that, while sipping, its head goes past the anther into the flower's opening. Its body must be large enough to touch the an[Pg 188]ther. These requirements are perfectly met by the humblebee, and we can confidently predict that Bombus is the flower's desired visitor.

The diagrams (Fig. 4) sufficiently illustrate the efficacy of the beautiful plan involved. At A the bee is seen sipping the nectar. His forward movement thus far to this point has only seemed to press the edge of the anther inward, and thus keep it even more effectually closed. As the bee retires (B), the backward motion opens the lid, and the sticky pollen is thus brought against the insect's back, where it adheres in a solid mass. He now flies to the next Arethusa blossom, enters it as before, and in retiring slides his back against the receptive viscid stigma, which retains a portion of the pollen, and thus effects the cross-fertilization (C). Professor Gray surmised that the[Pg 189] pollen was withdrawn on the insect's head, and it might be so withdrawn, but in other allied orchids of the tribe Arethusæ, however, in which the structure is very similar, the pollen is deposited on the thorax, and such is probably the fact in this species. In either case cross-fertilization would be effected. Nothing else is possible in the flower, and whether it is Bombus or not that effects it, the method is sufficiently evident.
The diagrams (Fig. 4) clearly show how effective the beautiful plan is. At A, you can see the bee sipping the nectar. Its forward movement up to this point has only pressed the edge of the anther inward, keeping it even more securely closed. As the bee pulls back (B), the backward motion opens the lid, and the sticky pollen comes into contact with the insect's back, where it sticks in a solid mass. It then flies to the next Arethusa blossom, enters it as before, and as it exits, its back brushes against the receptive, sticky stigma, which holds onto some of the pollen and achieves cross-fertilization (C). Professor Gray thought that the pollen was collected on the insect's head, and that might be the case, but in other related orchids of the Arethusæ tribe, where the structure is quite similar, the pollen is actually deposited on the thorax, and that is probably what happens in this species as well. In either case, cross-fertilization would occur. There's no other option in the flower, and whether it's Bombus or not that causes it, the method is clear enough.

Habenaria Orbiculata.
An Enlarged Single Flower
Having thus had one initiation into this most enticing realm of riddles, each successive orchid whose structure we examine from this stand-point becomes a most interesting, perhaps a fresh, problem, whose assumed solution may often be verified by studying the insect in its haunts. Darwin thus foretold the precise manner of the cross-fertilization of Habenaria mascula, and also the insect agent, simply by the structural prophecy of the flower itself.
Having had an introduction to this fascinating world of riddles, each new orchid we look at from this perspective presents a really interesting, and maybe even a new, challenge, whose proposed solution can often be confirmed by observing the insect in its natural habitat. Darwin accurately predicted how Habenaria mascula would be cross-fertilized, as well as the insect involved, just by analyzing the flower's structure.
Suppose, for example, an unknown orchid blossom to be placed in our hands. Its nectary tube is five inches in length, and as slender as a knitting-needle. The nectar is secreted far within its lip. The evolution of the long nectary implies an adaptation to an insect's tongue of equal length. What insect has a tongue five inches long, and sufficiently slender to probe this nec[Pg 190]tary? The sphinx-moth only. Hence we infer the sphinx-moth to be the insect complement to the blossom, and we may correctly infer, moreover, that the flower is thus a night-bloomer. Examination of the flower, with the form of this moth in mind, will show other adaptations to the insect's form in the position of pollen and stigma, looking to the flower's cross-fertilization. In some cases this is effected by the aid of the insect's tongue; in others, by its eyes.
Suppose, for instance, we have an unknown orchid blossom in our hands. Its nectary tube measures five inches long and is as thin as a knitting needle. The nectar is produced deep within its lip. The development of the long nectary suggests it has adapted to an insect with a tongue of equal length. What insect has a tongue that's five inches long and thin enough to reach this nectary? Only the sphinx moth. So, we can conclude that the sphinx moth is the insect that complements the blossom, and we can also correctly deduce that this flower blooms at night. Examining the flower with the shape of this moth in mind will reveal other adaptations to the insect's form in the positioning of pollen and stigma, aimed at cross-fertilization of the flower. In some cases, this is achieved with the help of the insect's tongue; in others, it involves its eyes.
In our own native orchids we have a remarkable example of the latter form in the Habenaria orbiculata, whose structure and mechanism have also been admirably described by Asa Gray.
In our native orchids, we have a remarkable example of the latter type in the Habenaria orbiculata, whose structure and mechanism have also been excellently described by Asa Gray.
All orchid-hunters know this most exceptional example of our local flora, and the thrill of delight experienced when one first encounters it in the mountain wilderness, its typical haunt, is an event to date from—its two great, glistening, fluted[Pg 191] leaves, sometimes as large as a dinner-plate, spreading flat upon the mould, and surmounted by the slender leafless stalk, with its terminal loose raceme of greenish-white bloom.
All orchid enthusiasts know this remarkable example of our local plants, and the thrill of joy felt when seeing it for the first time in the mountain wilderness, its usual home, is a moment to remember—its two large, shiny, fluted[Pg 191] leaves, sometimes as big as a dinner plate, lying flat on the ground, topped by the slender, leafless stalk with its cluster of greenish-white flowers at the top.


A single blossom of the species is shown in Fig. 5, the parts indexed. The opening to the nectary is seen just below the stigmatic surface, the nectary itself being nearly two inches in length. The pollen is in two club-like bodies, each hidden within a fissured pouch on either side of the stigma, and coming to the surface at the base in their opposing sticky discs as shown. Many of the group Habenaria or Platanthera, to which this flower belongs, are similarly planned. But mark the peculiarly logical association of the parts here exhibited. The nectary implies a welcome to a tongue two inches long, and will reward none other. This clearly shuts out the bees, butterflies, and smaller moths. What insect, then, is here implied? The sphinx-moth again, one of the lesser of the group. A larger individual might sip the nectar, it is true, but its longer tongue would reach the base of the tube without effecting the slightest contact with the pollen, which is of course the desideratum here embodied, and which has reference to a tongue corresponding to the length of the nectary. There[Pg 193] are many of these smaller sphinxes. Let us suppose one to be hovering at the blossom's throat. Its slender capillary tongue enters the opening. Ere it can reach the sweets the insect's head must be forced well into the throat of the blossom, where we now observe a most remarkable special provision, the space between the two pollen discs being exactly adjusted to the diameter of the insect's head. What follows this entrance of the moth is plainly pictured in the progressive series of illustrations (Fig. 6). A represents the insect sipping; the sticky discs are brought in contact with the moth's eyes, to which they adhere, and by which they are withdrawn from their pouches[Pg 194] as the moth departs (B). At this time they are in the upright position shown at C, but in a few seconds bend determinedly downward and slightly towards each other to the position D. This change takes place as the moth is flitting from flower to flower. At E we see the moth with its tongue entering the nectary of a subsequent blossom. By the new position of the pollen clubs they are now forced directly against the stigma (E). This surface is viscid, and as the insect leaves the blossom retains the grains in contact (F), which in turn withdraw others from the mass by means of the cobwebby threads by which the pollen grains are continuously attached. At G we see the orchid after the moth's visit—the stigma covered with pollen, and the flower thus cross-fertilized.
A single flower of this species is shown in Fig. 5, with the parts labeled. The opening to the nectar chamber is just below the stigmatic surface, and the nectar chamber itself is nearly two inches long. The pollen is found in two club-shaped bodies, each concealed within a split pouch on either side of the stigma, emerging to the surface at the base as sticky discs, as shown. Many flowers in the Habenaria or Platanthera groups, to which this flower belongs, have a similar design. Notice the unique and logical connection between the parts displayed here. The nectar chamber is designed for a two-inch-long tongue, rewarding no other. This clearly excludes bees, butterflies, and smaller moths. So, which insect is hinted at here? It’s the sphinx moth again, one of the smaller members of this group. A larger individual might drink the nectar, but its longer tongue would reach the base of the tube without making any contact with the pollen, which is the goal in this arrangement, relating to a tongue that matches the length of the nectar chamber. There[Pg 193] are many of these smaller sphinx moths. Let’s imagine one hovering at the flower’s entrance. Its slender tongue slips into the opening. Before it can get to the nectar, the insect's head must push well into the flower’s throat, where we can now see a remarkable special adaptation: the space between the two pollen discs fits perfectly with the diameter of the insect’s head. The process that follows this entry of the moth is clearly depicted in the series of illustrations (Fig. 6). A shows the insect sipping; the sticky discs come in contact with the moth's eyes, sticking to them, and are pulled from their pouches[Pg 194] as the moth leaves (B). At this time, they are in an upright position as shown at C, but within a few seconds, they bend downward and slightly towards each other in position D. This change occurs as the moth flits from flower to flower. At E, we see the moth with its tongue entering the nectar chamber of another flower. The new position of the pollen clubs forces them directly against the stigma (E). This surface is sticky, and as the insect departs, it retains the grains in contact (F), which then pull away others from the mass using the cobweb-like threads to which the pollen grains are attached. At G, we see the orchid after the moth's visit—its stigma covered with pollen, thus achieving cross-fertilization.
In effecting the cross-fertilization of one of the younger flowers its eyes are again brought into contact with this second pair of discs, and these, with their pollen clubs, are in turn withdrawn, at length perhaps resulting in such a plastering of the insect's eyes as might seriously impair its vision, were it not fortunately of the compound sort.
In the process of pollinating one of the younger flowers, its eyes come into contact with this second pair of discs, and after a while, these discs, with their bundles of pollen, are pulled away. This might ultimately cover the insect's eyes to the point that it could seriously affect its vision, if not for the fact that its eyes are made up of many small parts.

In another allied example of the orchids—the Showy Orchid—we have, however, what would appear a clear adaptation to the head of a bee,[Pg 195] though one which might also avail of the service of an occasional butterfly. A group of this beautiful species is shown in my illustration. A favored haunt is the dark damp woods, especially beneath hemlocks, and with its deep pink hood and pure white lip is quite showy enough to warrant its specific title, "spectabilis." An enlarged view of the blossom is seen in Fig. 7, and in Fig. 8 a still greater enlargement of the column.
In another related example of orchids—the Showy Orchid—we see what seems like a clear adaptation for attracting bees,[Pg 195] although it might also attract the occasional butterfly. A group of this stunning species is depicted in my illustration. They often thrive in dark, damp woods, especially under hemlocks, and with its deep pink hood and pure white lip, it’s definitely eye-catching enough to earn its name, "spectabilis." An enlarged view of the flower can be seen in Fig. 7, and Fig. 8 shows an even larger view of the column.


Position of Pollen of Orchis Spectabilis
Drawn with Pencil
I have seen many specimens with the pollen masses withdrawn, and others with their stigmas well covered with the grains. Though I have never seen an insect at work upon it in its haunt, the whole form of the opening of the flower would seem to imply a bee, particularly a bumblebee. If we insert the point of a lead-pencil into this opening, thus imitating the entrance of a bee, its bevelled surface comes in contact with the viscid discs by the rupture of a veil of membrane, which has hitherto protected them. The discs adhere to the pencil, and are withdrawn upon it (Fig. 9). At first in upright position, they soon assume the forward inclination, as previously described. The nectary is about the length of a bumblebee's tongue, and is, moreover, so amply expanded at the throat below the stigma as to comfortably admit its wedge-shaped head. The three progressive diagrams (Fig. 10) indicate the result in the event of such a visit.
I’ve seen many flowers with their pollen masses retracted, and others with their stigmas covered in pollen. Even though I’ve never actually seen an insect working on it in its natural setting, the shape of the flower opening suggests that a bee, especially a bumblebee, is involved. If we insert the tip of a pencil into this opening, mimicking a bee's entrance, its angled surface will touch the sticky discs after breaking through a membrane that has been covering them. The discs stick to the pencil and get pulled off (Fig. 9). Initially positioned upright, they soon tilt forward as described earlier. The nectary is about the same length as a bumblebee's tongue and is wide enough at the base below the stigma to easily fit its wedge-shaped head. The three diagrams (Fig. 10) show the outcome of such a visit.
The pollen discs are here very close together, and are protected within a membraneous cup, in which they sit as in a socket. As the insect inserts his head at the opening (A) it is brought against this tender membrane, which ruptures and exposes the viscid glands of the pollen masses, which become instantly attached to the face or[Pg 197] head, perhaps the eyes, of the burly visitor. As the insect retreats from the flower, one or both of the pollinia are withdrawn, as at B. Then immediately follows a downward movement, which exactly anticipates the position of the stigma, and as the bee enters the next flower the pollen clubs are forced against it (C), as in the previous example.
The pollen discs are really close together and are protected by a membranous cup, where they sit like in a socket. As the insect puts its head into the opening (A), it touches this delicate membrane, which breaks and reveals the sticky glands of the pollen masses, which quickly stick to the face or[Pg 197] head, maybe even the eyes, of the robust visitor. When the insect pulls back from the flower, one or both of the pollinia come out, like at B. Then it immediately moves downwards, which perfectly matches the position of the stigma, and as the bee enters the next flower, the pollen clubs press against it (C), just like in the previous example.
In the case of a smaller bee visiting the flower, the insect would find it necessary to creep further into the opening, and thus might bring its thorax against the pollen-glands. In either case the change of position in the pollinia would insure the same result.
In the case of a smaller bee visiting the flower, the insect would need to crawl further into the opening, which could cause its thorax to touch the pollen glands. In either case, the shift in position of the pollinia would guarantee the same result.


We have thus seen adaptation to the thorax, the eyes, and the face in the three examples given. And the entrance of the flower in each instance is so formed as to insure the proper angle of approach for the insect for the accomplishment of the desired result. This direct approach, so necessary in many orchids, is insured by various devices—by the position of the lip upon which the insect must alight; by the narrowed entrance of the throat of the flower in front of the nectary; by a fissure in the centre of the lip, by which the tongue is conducted, etc.
We have seen adaptations in the thorax, eyes, and face in the three examples provided. The entrance of the flower in each case is designed to ensure the right angle for the insect to achieve the desired outcome. This direct approach, which is crucial in many orchids, is guaranteed by various features—such as the placement of the lip where the insect must land; the narrowed entrance of the flower's throat leading to the nectar; and a slit in the middle of the lip that guides the tongue, among others.
Many other species allied to the above possess similar devices, with slight variations; and there is still another group whose structure is distinctly adjusted to the tongues of insects—adaptations not merely of position of pollen masses, but even to the extent of a special modification in the entrance to the flower and the shape of the sticky gland, by which it may more securely adhere to that sipping member.
Many other species related to the ones mentioned above have similar features, with small differences; and there is also another group whose structure is specifically designed for the tongues of insects—adaptations not just in the positioning of pollen masses, but even to the point of a unique adjustment in the entry of the flower and the shape of the sticky gland, which helps it stick more securely to that feeding part.
In the common pretty Purple-fringed Orchid,[Pg 199] whose dense cylindrical spikes of plumy blossoms occasionally empurple whole marshes, we have an arrangement quite similar to the H. orbicularis just described, with the exception that the pollen-pouches are almost parallel, and not noticeably spread at the base (Fig. 11). In this case the eyes of sipping butterflies occasionally get their decoration of a tiny golden club, but more frequently their tongues.
In the common beautiful Purple-fringed Orchid,[Pg 199] which has thick, cylindrical spikes of fluffy blossoms that can sometimes turn entire marshes purple, we see an arrangement quite similar to the H. orbicularis just mentioned, except that the pollen sacs are almost parallel and not noticeably flared at the base (Fig. 11). In this case, the eyes of butterflies sipping nectar sometimes get decorated with a tiny golden club, but more often it’s their tongues that do.

If, however, the butterfly should approach directly in front of the flower, as in a larger blossom he would be most apt to do, he might sip the nectar indefinitely and withdraw his tongue without bringing it in contact with the viscid pollen discs. But in the dense crowding of the flowers, over which the insect flutters indiscriminately, the approach is oftenest made obliquely, and thus the tongue brushes the disc on the side approached, and the pollen mass is withdrawn. But an examination of this orchid affords no pronounced evidence of any specific intention. There is no unmistakable sign to demonstrate which approach is[Pg 200] preferred or designed by the flower, and this dependence on the insect's tongue or eye would seem to be left to chance.
If the butterfly comes directly in front of the flower, like it would with a larger bloom, it might drink the nectar forever and pull back its tongue without touching the sticky pollen discs. But in the crowded field of flowers, where the insect flits around randomly, it usually approaches at an angle, causing its tongue to brush against the disc on that side, resulting in the pollen being picked up. However, looking closely at this orchid reveals no clear evidence of any particular intention. There’s no obvious indication of which approach is[Pg 200] preferred or intended by the flower, and it seems that the interaction with the insect’s tongue or eye is left to chance.
In another closely allied species, however, we have a distinct provision which insures the proper approach of the tongue—one of many similar devices by which the tongue is conducted directly to one or the other of the pollen discs.
In another closely related species, however, we have a specific feature that ensures the tongue approaches correctly—one of many similar mechanisms that guide the tongue directly to one of the pollen discs.

This is the Ragged Orchid, a near relative of the foregoing, H. psycodes, but far less fortunate in its attributes of beauty, its long scattered spike of greenish-white flowers being so inconspicuous in its sedgy haunt as often to conceal the fact of its frequency. Its individual flower is shown enlarged at Fig. 12—the lip here cut with a lacerated fringe (H. lacera). The pollen-pouches approach slightly at the base, directly opposite the nectary, where the two viscid pollen-glands stand on guard. Now were the opening of the nectary at this point unimpeded, the same condition[Pg 201] would exist as in the H. psycodes—the tongue might be inserted between the pollen discs and withdrawn without touching them. But here comes the remarkable and very exceptional provision to make this contact a certainty—a suggestive structural feature of this flower of which I am surprised to find no mention either in our botanies or in the literature of cross-fertilization, so far as I am familiar with its bibliography. Even Dr. Gray's description of the fertilization device of this species makes no mention of this singular and very important feature. The nectary here, instead of being freely open, as in other orchids described, is abruptly closed at the central portion by a firm protuberance or palate, which projects downward from the base of the stigma, and closely meets the lip below.
This is the Ragged Orchid, which is a close relative of the previously mentioned H. psycodes, but it lacks the same beauty. Its long spike of greenish-white flowers is often so hidden in its grassy habitat that people might not realize how common it is. An individual flower is shown enlarged in Fig. 12—the lip is edged with a frayed fringe (H. lacera). The pollen pouches come together slightly at the base, directly across from the nectary, where the two sticky pollen glands stand ready. If the opening of the nectary were unobstructed, the same situation[Pg 201] would occur as with the H. psycodes—the tongue could be inserted between the pollen discs and pulled out without touching them. However, there's an interesting and very unusual adaptation that ensures this contact happens—a noteworthy structural characteristic of this flower that I’m surprised isn't noted in our botany texts or in the literature on cross-fertilization, based on what I know of its bibliography. Even Dr. Gray's description of the fertilization mechanism for this species fails to mention this unique and significant trait. Here, the nectary isn’t wide open like in other orchids discussed; instead, it's abruptly closed in the center by a firm bump or palate that extends downward from the base of the stigma and closely aligns with the lip below.
The throat of the nectary, thus centrally divided, presents two small lateral openings, each of which, from the line of approach through the much-narrowed entrance of the flower, is thus brought directly beneath the waiting disc upon the same side. The structure is easily understood from the two diagrams Figs. 12 and 13, both of which are indexed.
The throat of the nectary, now split in the center, has two small openings on the sides. Each opening, from the narrow entrance of the flower, leads directly under the waiting disc on the same side. This structure is easy to understand from the two diagrams, Figs. 12 and 13, which are both labeled.

The viscid pollen-gland is here very peculiarly formed, elongated and pointed at each end, and it[Pg 202] is not until we witness the act of its removal on the tongue of the butterfly that we can fully appreciate its significance.
The sticky pollen gland has a very unique shape, being long and pointed at both ends, and it[Pg 202] is not until we see it being taken off the butterfly's tongue that we can truly understand its importance.
I have often seen butterflies at work upon this orchid, and have observed their tongues generously decorated with the glands and remnants of the pollen masses.
I have often noticed butterflies working on this orchid, and I've seen their tongues adorned with the glands and leftover bits of pollen.
The series of diagrams (Fig. 14) will, I think, fully demonstrate how this blossom utilizes the butterfly. At A we see the insect sipping, its tongue now in contact with the elongated disc, which adheres to and clasps it. The withdrawal of the tongue (B) removes the pollen from its pouch. At C it is seen entirely free and upright, from which position it quickly assumes the new attitude shown at D. As the tongue is now inserted into the subsequent blossom this pollen mass is thrust against the stigma (E), and a few of the pollen grains are thus withheld upon its viscid surface as the insect departs (F).[Pg 203]
The series of diagrams (Fig. 14) will clearly show how this flower benefits from the butterfly. At A, we see the insect sipping, its tongue touching the elongated disc, which holds onto it. When the tongue pulls back (B), it takes off the pollen from its pouch. At C, it is completely free and upright, then quickly shifts to the new position shown at D. As the tongue is inserted into the next flower, this pollen mass presses against the stigma (E), and a few pollen grains stick to its sticky surface as the insect leaves (F).[Pg 203]
In this orchid we thus find a distinct adaptation to the tongue of a moth or butterfly.
In this orchid, we can see a unique adaptation for the tongue of a moth or butterfly.
Another similar device for assuring the necessary side approach is seen in H. flava (Fig. 15), a yellowish spiked species, more or less common in swamps and rich alluvial haunts.
Another similar device for ensuring the necessary side approach is seen in H. flava (Fig. 15), a yellowish spiked species, fairly common in swamps and fertile river habitats.

Professor Wood remarks, botanically, "The tubercle (or palate) of the lip is a remarkable character." But he, too, has failed to note the equally remarkable palate of the ragged orchid, just described, both provisions having the same purpose, the insurance of an oblique approach to the nectary. In H. flava this "tubercle," instead[Pg 204] of depending from the throat, grows upward from the lip, and, as we look at the flower directly from the front, completely hides the opening to the nectary, and an insect is compelled to insert its tongue on one side, which direction causes it to pass directly beneath the pollen disc, as in H. lacera, and with the same result.
Professor Wood notes, from a botanical perspective, "The tubercle (or palate) of the lip is a notable feature." However, he has also overlooked the equally impressive palate of the ragged orchid that was just described; both adaptations serve the same function: ensuring an angled approach to the nectary. In H. flava, this "tubercle," instead[Pg 204] of hanging down from the throat, grows upward from the lip and completely obscures the opening to the nectary when viewed head-on. This forces an insect to insert its tongue from one side, which leads it directly under the pollen disc, just like in H. lacera, resulting in the same outcome.


Of all our native orchids, at least in the northeastern United States,
the Cypripedium, or Moc[Pg 205]casin-Flower, is perhaps the general favorite,
and certainly the most widely known. This is readily accounted for not
only by its frequency, but by its conspicuousness. The term
"moccasin-flower" is applied more or less indiscriminately to all
species. The flower is also known as the ladies'-slipper, more
specifically Venus's-slipper—as warranted by its generic botanical
title—from a fancied resemblance in the form of the inflated lip, which
is characteristic of the genus. We may readily infer that the fair
goddess was not consulted at the christening.
Of all the native orchids in the northeastern United States, the Cypripedium, or Moccasin Flower, is likely the most popular and definitely the most well-known. This is easily explained by how common and noticeable it is. The name "moccasin-flower" is often used for various species. The flower is also called the ladies' slipper, more specifically Venus's slipper, due to its botanical name, which reflects a fancied resemblance to the shape of its distinctive inflated lip. It’s safe to say that the beautiful goddess wasn’t involved in naming it.
There are six native species of the cypripedium in this Eastern region, varying in shape and in color—shades of white, yellow, crimson, and pink.[Pg 206] The mechanism of their cross-fertilization is the same in all, with only slight modifications.
There are six native species of cypripedium in this eastern region, varying in shape and color—shades of white, yellow, crimson, and pink.[Pg 206] The process of their cross-fertilization is the same for all, with just a few minor differences.
The most common of the group, the C. acaule, most widely known as the moccasin-flower, whose large, nodding, pale crimson blooms we so irresistibly associate with the cool hemlock woods, will afford a good illustration.
The most common of the group, the C. acaule, better known as the moccasin-flower, with its large, drooping, pale crimson blooms that we can’t help but associate with the cool hemlock woods, serves as a great example.
The lip in all the cypripediums is more or less sac-like and inflated.
In the present species, C. acaule, however, we see a unique variation,
this portion of the flower being conspicuously bag-like, and cleft by a
fissure down its entire anterior face. In Fig. 16 is shown a front view
of the blossom, showing this fissure. The "column" (B) in the
cypripedium is very distinctive, and from the front view is very
non-committal. It is only as we see it in side section, or from beneath,
that we fully comprehend the disposition of stigma and pollen. Upon the
stalk of this column there appear from the front three lobes—two small
ones at the sides, each of which hides an anther attached to its under
face—the large terminal third lobe being in truth a barren rudiment of
a former stamen, and which now overarches the stigma. The relative
position of these parts may be seen in the under view.
The lip of all cypripediums is somewhat sac-like and swollen. However, in this species, C. acaule, we notice a unique variation where this part of the flower is notably bag-like and has a split running down its entire front side. In Fig. 16, you can see a front view of the blossom that highlights this split. The "column" (B) in the cypripedium is quite distinctive and appears ambiguous from the front view. We only fully understand the arrangement of the stigma and pollen when we look at it from the side or underneath. On the stalk of this column, there are three lobes visible from the front—two small ones on the sides, each hiding an anther attached to its underside, and the large terminal lobe is actually a non-functional remnant of a former stamen that arches over the stigma. The relative positions of these parts can be observed from the underneath view.

The anthers in this genus, then, are two, instead[Pg 207] of the previous single anther with its two pollen-cells. The pollen is also quite different in its character, being here in the form of a pasty mass, whose entire exposed surface, as the anther opens, is coated with a very viscid gluten.
The anthers in this genus are now two instead[Pg 207] of the previous single anther with its two pollen cells. The pollen is also quite different, appearing as a pasty mass, with the entire exposed surface coated in a very sticky gluten when the anther opens.

With the several figures illustrating the cross-fertilization, the reader will readily anticipate any description of the process, and only a brief commentary will be required in my text.
With the various illustrations showing the cross-fertilization, the reader can easily expect a description of the process, and only a short commentary will be needed in my text.
I have repeatedly examined the flowers of C. acaule in their haunts, have observed groups wherein every flower still retained its pollen, others where one or both pollen masses had been withdrawn, and in several instances associated with them I have observed the inflated lip most outrageously bruised, torn, and battered, and occasionally perforated by a large hole. I had ob[Pg 209]served these facts in boyhood. The inference, of course, was that some insect had been guilty of the mutilation; but not until I read Darwin's description of the cross-fertilization of this species did I realize the full significance of these telltale evidences of the escape of the imprisoned insect. Since that time, many years ago, I have often sat long and patiently in the haunt of the cypripedium awaiting a natural demonstration of its cross-fertilization, but as yet no insect has rewarded my devotion.
I have repeatedly looked at the flowers of C. acaule in their natural environments, observed groups where every flower still had its pollen, and others where one or both pollen masses had been removed. In several cases, I noticed the inflated lip incredibly bruised, torn, and battered, and sometimes even pierced by a large hole. I had noticed these things in my childhood. The conclusion, of course, was that some insect was responsible for the damage; but not until I read Darwin's description of the cross-fertilization of this species did I understand the full significance of these obvious signs of the escaped insect. Since then, many years ago, I have often sat patiently in the habitat of the cypripedium, waiting for a natural demonstration of its cross-fertilization, but until now, no insect has rewarded my dedication.

The Bee Trapped in the Lips of Cypripedium
At length, in hopelessness of reward by such means, I determined to see the process by more prosaic methods. Gathering a cluster of the freshly opened flowers, which still retained their pollen, I took them to my studio. I then captured a bumblebee, and forcibly persuaded him to enact the demonstration which I had so long waited for him peaceably to fulfil. Taking him by the wings, I pushed him into the fissure by which he is naturally supposed to enter without persuasion. He was soon within the sac, and the inflexed wings of the margin had closed above him, as shown in section, Fig. 17. He is now enclosed in a luminous prison, and his buzzing protests are audible and his vehemence visible from the outside of the sac. Let us suppose that he[Pg 210] at length has become reconciled to his condition, and has determined to rationally fulfil the ideal of his environment, as he may perhaps have already done voluntarily before. The buzzing ceases, and our bee is now finding sweet solace for his incarceration in the copious nectar which he finds secreted among the fringy hairs in the upper narrowed portion of the flower, as shown at Fig. 18 A. Having satiated his appetite, he concludes to quit his close quarters. After a few moments of more vehement futile struggling and buzzing, he at length espies, through the passage above the nectary fringe, a gleaming light, as from two windows (A). Towards these he now approaches. As he advances the passage becomes narrower and narrower, until at length his back is brought against the overhanging stigma (Fig. 18 B). So narrow is the pass at this point that the efforts of the bee are distinctly manifest from the outside in the distension of the part and the consequent[Pg 211] slight change in the droop of the lip. In another moment he has passed this ordeal, and his head is seen protruding from the window-like opening (A) on one side of the column. But his struggles are not yet ended, for his egress is still slightly checked by the narrow dimensions of the opening, and also by the detention of the anther, which his thorax has now encountered. A strange etiquette this of the cypripedium, which speeds its[Pg 212] parting guest with a sticky plaster smeared all over its back. As the insect works its way beneath the viscid contact, the anther is seen to be drawn outward upon its hinge, and its yellow contents are spread upon the insect's back (Fig. 18 C), verily like a plaster. Catching our bee before he has a chance to escape with his generous floral compliments, we unceremoniously introduce him into another cypripedium blossom, to which, if he were more obliging, he would naturally fly. He loses no time in profiting by his past experience, and is quickly creeping the gantlet, as it were, or braving the needle's eye of this narrow passage. His pollen-smeared thorax is soon crowding beneath the overhanging stigma again, whose forward-pointed papillæ scrape off a portion of it (Fig. 18 B), thus insuring the cross-fertilizing of the flower, the bee receiving a fresh effusion of cypripedium compliments piled upon the first as he says "good-bye." It is doubtful whether in his natural life he ever fully effaces the telltale effects of this demonstrative au revoir.
At last, feeling hopeless about getting results through those means, I decided to observe the process using more straightforward methods. I gathered a bunch of freshly bloomed flowers that still had their pollen and took them to my studio. I then caught a bumblebee and forced him to perform the demonstration I had long waited for him to do willingly. Grabbing him by the wings, I pushed him into the opening where he’s supposed to enter naturally. He quickly made his way inside the sac, and the bent wings of the edge closed above him, as shown in section, Fig. 17. Now he was trapped in a glowing prison, and I could hear his buzzing protests and see his struggles from outside the sac. Let’s imagine that he has finally come to terms with his situation and has decided to logically adapt to his environment, just as he may have done voluntarily before. The buzzing stops, and our bee is now finding comfort in the plentiful nectar secreted among the fringed hairs in the upper narrow part of the flower, as shown in Fig. 18 A. Once he’s satisfied his hunger, he decides to leave his cramped space. After a few moments of more intense struggling and buzzing, he finally spots, through the passage above the nectary fringe, a bright light as if from two windows (A). He moves toward them. As he approaches, the passage gets tighter and tighter until his back hits the overhanging stigma (Fig. 18 B). At this point, the opening is so narrow that his efforts are clearly visible from the outside in the stretching of the area and the slight change in the droop of the lip. In a moment, he has passed this challenge, and his head is seen poking out from the window-like opening (A) on one side of the column. However, his struggles aren’t over yet, as his exit is still slightly obstructed by the narrow size of the opening and also by the anther, which his thorax has now come into contact with. It’s a strange etiquette of the cypripedium, which sends off its departing guest with a sticky plaster spread all over its back. As the insect works its way under the tacky substance, the anther is pulled outward on its hinge, and its yellow contents coat the insect's back (Fig. 18 C), truly like a plaster. Before our bee has a chance to escape with his generous floral gifts, we quickly toss him into another cypripedium flower, which he would naturally fly to if he were more cooperative. He wastes no time using his past experience and quickly navigates this narrow passage. His pollen-covered thorax soon squeezes beneath the overhanging stigma again, whose forward-pointing tips scrape off some of it (Fig. 18 B), ensuring the flower is cross-fertilized, while the bee receives a fresh layer of cypripedium gifts piled on top of the first as he says "goodbye." It’s doubtful he ever completely erases the evidence of this showy farewell in his natural life.

Such, with slight modifications, is the plan evolved by the whole cypripedium tribe. Darwin mentions bees as the implied fertilizers, and doubtless many of the smaller bees do effect cross-fertilization in the smaller species. But the[Pg 213] more ample passage in acaule would suggest the medium-sized Bombus as better adapted—as the experiment herewith pictured from my own experience many times would seem to verify, while a honey-bee introduced into the flower failed to fulfil the demonstration, emerging at the little doorway above without a sign of the cordial parting token.
Such, with a few changes, is the plan developed by the entire cypripedium tribe. Darwin mentions bees as the intended pollinators, and surely many of the smaller bees do contribute to cross-pollination in the smaller species. However, the[Pg 213] larger entrance in acaule seems to indicate that medium-sized Bombus bees are more suited—this is backed up by my own repeated experiences captured in the experiment depicted here, while a honeybee introduced into the flower failed to show the expected outcome, leaving through the small doorway above without any sign of the friendly parting token.

Occasionally I suppose a fool bumblebee is entrapped within the petal bower and fails to find the proper exit, or it may be—much less a fool—having run the gantlet once too often, decides to escape the ordeal; hence the occasional mutilated blossom already described.
Occasionally, I suppose a foolish bumblebee gets trapped in the flower petals and can't find the way out, or maybe—much less foolish—after going through it too many times, it decides to escape the situation; hence the occasional damaged blossom previously mentioned.
One of the most beautiful of our orchids, though its claims to admiration in this instance are chiefly confined to the foliage, is the common "Rattlesnake-Plantain," its prostrate rosettes of exquisitely white reticulated leaves carpeting many a nook in the shadows of the hemlocks, its dense spikes of yellowish-white blossoms signalling their welcome to the bees, and fully compen[Pg 214]sating in interest what they may lack in other attractive attributes.
One of our most beautiful orchids, although its appeal here mainly comes from its leaves, is the common "Rattlesnake-Plantain." Its flat rosettes of stunning white veined leaves cover many corners in the shade of the hemlocks, and its thick spikes of yellowish-white flowers signal a warm welcome to the bees, making up for any lack of other impressive features.

Bee Getting Pollen on Its Thorax
The single flower is shown enlarged in Fig. 19—A, a young blossom, with analyses B and C, the latter indexed; D, an older blossom, with similar analyses (E and F). Both sorts are to be found upon every spike of bloom, as the inflorescence begins at the base and proceeds upward. As we look into the more open flower we observe a dark-colored speck, which, by analysis, proves to be the lid of the anther. This portion is further shown enlarged in Fig. 20, A. If we gently lift it with a pin, we disclose the pollen masses in the cavity (B) thus opened (C, profile section), the two pairs united to a common viscid gland at the base, this gland again secreted behind a veil of moist membrane, as also shown at B. This membrane is, moreover, very sensitive to the touch. Below the flattened tip of the column, and at a sharp inward angle, is the stigma. In the[Pg 215] freshly opened flower (Fig. 19, A) the column inclines forward, bringing the anther low down, and its base directly opposite the V-shaped orifice in the lip, which also is quite firmly closed beneath the equally converging upper hood of the blossom. The entrance is thus much narrowed. If we insert a pin in this V-shaped entrance it comes in contact with the sensitive membrane below the anther, and it is immediately ruptured, as shown at Fig. 20, D. The sticky gland is brought into immediate contact, and clasps the pin, which, now[Pg 216] being withdrawn, brings away the pollen, as in E and F. Thus it is naturally removed on the tongue of its sipping bee.
The single flower is shown enlarged in Fig. 19—A, a young blossom, with analyses B and C, the latter indexed; D, an older blossom, with similar analyses (E and F). Both types are found on every spike of bloom, starting from the base and moving upward. When we look into the more open flower, we notice a dark-colored speck, which analysis shows is the lid of the anther. This part is further enlarged in Fig. 20, A. If we gently lift it with a pin, we reveal the pollen masses in the cavity (B) that’s opened (C, profile section), with two pairs connected to a common sticky gland at the base, this gland being shielded by a veil of moist membrane, as shown at B. This membrane is also very sensitive to touch. Below the flattened tip of the column, at a sharp inward angle, is the stigma. In the[Pg 215] freshly opened flower (Fig. 19, A), the column tilts forward, positioning the anther low down and its base directly opposite the V-shaped opening in the lip, which is also tightly closed beneath the converging upper hood of the blossom. The entrance is thus significantly narrowed. If we insert a pin into this V-shaped opening, it touches the sensitive membrane beneath the anther, causing it to rupture immediately, as shown in Fig. 20, D. The sticky gland then makes contact and grips the pin, which, when[Pg 216] withdrawn, takes the pollen with it, as in E and F. In this way, the pollen is naturally removed on the tongue of the bee sipping it.


The further demonstration will be better shown by profile sections (Fig. 21). Nectar is secreted in the hollow of the lip indicated, somewhat as in the cypripedium. If we now imitate with a probe the habit of the insect and the action of its tongue, we may witness a beautiful contrivance for cross-fertilization. We will suppose the bee to[Pg 217] be working at the top of the spike. He thrusts his tongue into the narrow opening (G). The membrane protecting the pollen-gland, thus surely touched, ruptures as described, and the exposed gland attaches itself to the tongue, being withdrawn as at H, and located on the insect's tongue, as in F, Fig. 20. The bee leaves this flower cluster and flies to another, upon which it will usually begin operation at the bottom. The flower thus first encountered is an old bloom, as in Fig. 19, D. Its sepals are more spreading, the lip slightly lowered, and the column so changed[Pg 218] as to present the plane of the stigma, before out of sight, in such a new position as to invariably receive the pollen. The tongue of a bee entering this flower conveys the pollen directly against the stigmatic surface (I), which retains its disentangled fecundating grains, as at J, and the flower's functional adaptations are fulfilled.
The further demonstration will be better shown by profile sections (Fig. 21). Nectar is secreted in the hollow of the indicated lip, similar to the cypripedium. If we now use a probe to imitate the insect's behavior and tongue action, we can observe a beautiful mechanism for cross-fertilization. Let's assume the bee is working at the top of the spike. It pushes its tongue into the narrow opening (G). The membrane protecting the pollen gland, which is surely touched, breaks as described, and the exposed gland sticks to the tongue, being pulled away as at H, and positioned on the insect's tongue, as in F, Fig. 20. The bee leaves this flower cluster and flies to another, where it usually starts working at the bottom. The first flower it encounters is an older bloom, as shown in Fig. 19, D. Its sepals are more spread out, the lip is slightly lowered, and the column has changed in such a way as to present the plane of the stigma, which was previously out of sight, in a new position that will always receive the pollen. When the bee’s tongue enters this flower, it delivers the pollen directly against the stigmatic surface (I), which retains its separated fertilizing grains, as shown at J, and the flower's functional adaptations are fulfilled.


In the allied Spiranthes, or "Lady's-Tresses," a somewhat similar mechanism prevails, by which fertilization is largely effected by the changed position or angle of the stigma plane.
In the related Spiranthes, or "Lady's-Tresses," a somewhat similar mechanism exists, where fertilization primarily occurs due to the altered position or angle of the stigma plane.
And thus we might proceed through all the orchid genera, each new device, though based upon one of the foregoing plans, affording its new surprise in its special modification in adaptation to its insect sponsor—all these various shapes, folds of petals, positions, colors, the size, length, and thickness of nectary, the relative positions of pollen and stigma, embodying an expression of welcome to the insect with which its life is so marvellously linked. Occasionally this astounding[Pg 219] affinity is faithful to a single species of insect, which thus becomes the sole sponsor of the blossom, without whose association the orchid would become extinct. A remarkable instance of this special adaptation is seen in the great Angræcum orchid of Madagascar, described by Darwin; and inasmuch as this species glorifies Darwin's faith in the truth of his theory, and marks a notable victory in the long battle for its supremacy, it affords an inspiring theme for my closing paragraphs.
And so we could go through all the orchid genera, each new design, while based on one of the previous plans, offering a new surprise in how it's specifically adapted to its insect partner—all these different shapes, petal folds, positions, colors, the size, length, and thickness of the nectary, the placement of pollen and stigma, all reflect a welcoming message to the insect whose life is so remarkably connected to it. Sometimes this incredible[Pg 219]relationship is devoted to a single species of insect, which becomes the only supporter of the flower, and without this connection, the orchid would die out. A striking example of this specific adaptation can be found in the large Angræcum orchid of Madagascar, as described by Darwin; and since this species confirms Darwin's belief in the validity of his theory, and represents a significant triumph in the long struggle for its dominance, it provides a motivating topic for my concluding paragraphs.
Among the host of sceptics—and were they not legion?—who met this evolutionary and revolutionary theory with incredulity, not to say ridicule or worse, was one who thus challenged its author shortly after the appearance of his "Fertilization of Orchids," addressing Darwin from Madagascar substantially as follows: "Upon your theory of evolution through natural selection all the various contrasting structural features of the orchids have direct reference to some insect which shall best cross-fertilize them. If an orchid has a nectary one inch long, an insect's tongue of equivalent length is implied; a nectary six inches in length likewise implies a tongue six inches long. What have you to say in regard to an orchid which flourishes here in Madagascar possessing a[Pg 220] long nectary as slender as a knitting-needle and eleven inches in length? On your hypothesis there must be a moth with a tongue eleven inches long, or this nectary would never have been elaborated."
Among the many skeptics—and weren't there a lot?—who reacted to this evolutionary and revolutionary theory with disbelief, and even mockery, was someone who challenged its author shortly after the release of his "Fertilization of Orchids." Addressing Darwin from Madagascar, he said something like this: "According to your theory of evolution through natural selection, all the different structural features of orchids relate directly to some insect that will best cross-fertilize them. If an orchid has a nectary one inch long, then an insect's tongue of the same length is expected; a six-inch nectary similarly implies a six-inch tongue. What do you say about an orchid that thrives here in Madagascar with a nectary that is as long and slender as a knitting needle and eleven inches in length? Based on your hypothesis, there must be a moth with an eleven-inch tongue, or this nectary could never have developed."
Darwin's reply was magnificent in its proof of the sublime conviction of the truth of his belief: "The existence of an orchid with a slender nectary eleven inches in length, and with nectar secreted at its tip, is a conclusive demonstration of the existence of a moth with a tongue eleven inches in length, even though no such moth is known."
Darwin's response was impressive in its demonstration of his deep conviction in the truth of his belief: "The existence of an orchid with a slender nectary eleven inches long, which has nectar at its tip, is a clear indication of the existence of a moth with a tongue eleven inches long, even if no such moth is known."
Many of us remember the ridicule which was heaped upon him for this apparently blind adherence to an untenable theory. But victory complete and demoralizing to his opponents awaited this oracular utterance when later a disciple of Darwin, led by the same spirit of faith and conviction, visited Madagascar, and was soon able to affirm that he had caught the moth, a huge sphinx-moth, and that its tongue measured eleven inches in length.
Many of us recall the mockery he faced for his seemingly blind loyalty to an unreasonable theory. But a complete and demoralizing victory for him awaited with this prophetic statement when a follower of Darwin, driven by the same spirit of faith and conviction, visited Madagascar and soon confirmed that he had captured a huge sphinx moth, and that its tongue measured eleven inches long.

Here we see the prophecy of the existence of an unknown moth, founded on the form of a blossom. At that time the moth had not been actually seen at work on the orchid, but who shall[Pg 222] question for a moment that had the flower been visited in its twilight or moonlight haunt the murmur of humming wings about the blossom's throat would have attested the presence of the flower's affinity, for without the kiss of this identical moth the Angræcum must become extinct. No other moth can fulfil the conditions necessary to its perpetuation. The floral adaptation is such that the moth must force its large head far into the opening of the blossom in order to reach the sweets in the long nectary. In so doing the pollen becomes attached to the base of the tongue, and is withdrawn as the insect leaves the flower, and is thrust against the stigma in the next blossom visited. This was clearly demonstrated by Darwin in specimens sent to him, by means of a probe of the presumable length and diameter of the moth's tongue. Shorter-tongued moths would fail to remove the pollen, and also to reach the nectar, and would thus soon learn to realize that they were not welcome.
Here we see the prophecy of an unknown moth based on the shape of a flower. At that time, the moth had not actually been seen working on the orchid, but who can[Pg 222] question for a moment that if the flower had been visited in its twilight or moonlight, the sound of humming wings around the flower’s throat would have shown the flower's connection to the moth. Without this specific moth, the Angræcum will become extinct. No other moth can meet the conditions needed for its survival. The flower is adapted so that the moth has to force its large head deep into the opening of the blossom to reach the nectar in the long tube. As it does this, the pollen attaches to the base of its tongue and is carried away when the insect leaves the flower, then is deposited on the stigma of the next flower it visits. This was clearly shown by Darwin using specimens sent to him, with a probe that matched the presumed length and width of the moth's tongue. Moths with shorter tongues would fail to pick up the pollen and reach the nectar, and would quickly learn that they were not welcome.
The Angræcum also affords in this long pendent nectary a most lucid illustration of the present workings of natural selection. The normal length of that nectary should be about eleven inches, but in fact this length varies considerably in the flowers of different plants, this tendency to[Pg 223] variation in all organic life being an essential and amply demonstrated postulate of the entire theory of natural selection. Let us suppose a flower whose nectary chances to be only six inches in length. The moth visits this flower, but the tip of its tongue reaches the nectar long before it can bring its head into the opening of the tube. This being a vital condition, the moth fails to withdraw the pollen; and inasmuch as the pollen is usually deposited close to the head of the moth, this flower would receive no pollen upon its stigma. This particular blossom would thus be both barren and sterile. None of its pollen would be carried to other stigmas, nor would it set a seed to perpetuate by inheritance its shorter nectary.
The Angræcum provides a clear example of how natural selection works through its long hanging nectar tube. The average length of this tube should be about eleven inches, but in reality, this length varies quite a bit among different plants. This tendency for variation in all living organisms is a fundamental and well-supported idea behind the whole theory of natural selection. Let’s consider a flower with a nectar tube that's only six inches long. A moth visits this flower, but the tip of its tongue can access the nectar long before it can fit its head into the opening of the tube. Because of this crucial factor, the moth fails to pick up the pollen; and since the pollen is typically positioned near the moth's head, this flower would not receive any pollen on its stigma. This particular flower would therefore be both barren and sterile. None of its pollen would be transferred to other stigmas, and it wouldn’t produce seeds to pass on its shorter nectar tube to future generations.
Again, let us suppose the variation of an extra long nectary, and the writer recently saw a number of these orchids with nectaries thirteen inches in length. The moth comes, and now must needs insert its head to the utmost into the opening of the flower. This would insure its fertilization by the pollen on the insect's tongue; and even though the sipper failed to reach the nectar, the pollen would be withdrawn upon the tongue, to be carried to other flowers, which might thus be expected to inherit from the paternal side the ten[Pg 224]dency to the longer nectary. The tendency towards the perpetuation of the short nectary is therefore stopped, while that of the longer nectary is insured.[Pg 225]
Again, let’s consider the variation of an extra-long nectary, and the writer recently observed several of these orchids with nectaries that are thirteen inches long. The moth arrives and must insert its head all the way into the flower's opening. This will ensure its fertilization by the pollen on the insect's tongue; and even if the sipper fails to reach the nectar, the pollen will be gathered on the tongue, ready to be taken to other flowers, which might then be expected to inherit from their paternal side the tendency for a longer nectary. Therefore, the trend towards the continuation of the short nectary is halted, while the trend towards the longer nectary is secured.[Pg 225]
THE MILKWEED
The singular hospitality of our milkweed blossom is nowhere matched among Flora's minions, and would seem occasionally in need of supervision.
The unique hospitality of our milkweed blossom is unmatched among Flora's followers, and it sometimes seems to require oversight.
Just outside the door here at my country studio, almost in touch of its threshold, year after year there blooms a large clump of milkweed (Asclepias cornuta), and, what with the fragrance of its purple pompons and the murmurous music of its bees, its fortnight of bloom is not permitted to be forgotten for a moment. Only a moment ago a whiff of more than usual redolence from the open window at which I am sitting reminded me that the flowers were even now in the heyday of their prime, and the loud droning music betokened that the bees were making the most of their opportunities.
Just outside the door of my country studio, almost at its threshold, a large clump of milkweed (Asclepias cornuta) blooms year after year. With the sweet scent of its purple pom-poms and the soft buzz of its bees, its two-week bloom can't be forgotten for a second. Just a moment ago, a strong whiff of fragrance from the open window where I’m sitting reminded me that the flowers are currently at their peak, and the loud buzzing indicated that the bees are taking full advantage of the moment.
Yielding to the temptation, I was soon standing in the midst of the plants. The purple fragrant umbels of bloom hung close about me on all sides, each flower, with its five generous horns[Pg 228] of plenty, drained over and over again by the eager sipping swarm.
Giving in to temptation, I soon found myself surrounded by the plants. The purple, fragrant clusters of blooms hung around me on all sides, each flower, with its five generous petals[Pg 228] of abundance, constantly drained by the eager sipping swarm.
But the July sun is one thing to a bee and quite another thing to me. I have lingered long enough, however, to witness again the beautiful reciprocity, and to realize anew, with awe and reverence, how divinely well the milkweed and the bee understand each other. After a brief search among the blossom clusters I return to my seclusion with a few interesting specimens, which may serve as a text here at my desk by the open window.
But the July sun feels different to a bee than it does to me. I’ve stuck around long enough, though, to see once again the amazing connection between them, and to appreciate with wonder how perfectly the milkweed and the bee communicate. After a short search among the flower clusters, I retreat back to my space with a few fascinating specimens, which might inspire me here at my desk by the open window.
Two months hence an occasional silky messenger will float away from the glistening clouds about the open milkweed pods, but who ever thanks the bees of June for them? The flower is but a bright anticipation—an expression of hope in the being of the parent plant. It has but one mission. All its fragrance, all its nectar, all its beauty of form and hue are but means towards the consummation of the eternal edict of creation—"Increase and multiply." To that end we owe all the infinite forms, designs, tints, decorations, perfumes, mechanisms, and other seemingly inexplicable attributes. Its threshold must bear its own peculiar welcome to its insect, or perhaps to its humming-bird friend, or counterpart; its nec[Pg 229]taries must both tempt and reward his coming, and its petals assist his comfortable tarrying.
Two months from now, a few silky messengers will drift away from the shimmering clouds around the open milkweed pods, but who ever thanks the bees of June for them? The flower is just a bright promise—an expression of hope in the life of the parent plant. It has only one purpose. All its fragrance, nectar, and beauty are just means to fulfill the eternal command of creation—"Increase and multiply." To that end, we owe all the endless forms, designs, colors, decorations, scents, mechanisms, and other seemingly mysterious features. Its entrance must greet its insect, or maybe its hummingbird friend, in its own unique way; its nectaries must both entice and reward its arrival, while its petals help make its stay comfortable.
Next to the floral orchids, the mechanism of our milkweed blossom is perhaps the most complex and remarkable, and illustrates as perfectly as any of the orchid examples given in Darwin's noble work the absolute divine intention of the dependence of a plant species upon the visits of an insect.
Next to the floral orchids, the structure of our milkweed flower is probably the most intricate and impressive, showcasing as clearly as any of the orchid examples in Darwin's great work the clear divine purpose of a plant species relying on the visits of an insect.
Our milkweed flower is a deeply planned contrivance to insure such an end. It fills the air with enticing fragrance. Its nectaries are stored with sweets, and I fancy each opening bud keenly alert with conscious solicitude for its affinity. Though many other flowers manage imperfectly to perpetuate their kind in the default of insect intervention, the milkweed, like most of the orchids, is helpless and incapable of such resource. Inclose this budded umbel in tarlatan gauze and it will bloom days after its fellow-blooms have fallen, anticipating its consummation, but no pods will be seen upon this cluster.
Our milkweed flower is carefully designed to ensure that happens. It fills the air with a captivating fragrance. Its nectaries are filled with sweet nectar, and I can imagine each opening bud eagerly aware of its surroundings. While many other flowers manage to reproduce even without insect help, the milkweed, like most orchids, is unable to do so on its own. If you enclose this budding cluster in a fine mesh, it will bloom long after its neighboring flowers have faded, reaching for its full potential, but no pods will appear on this group.
What a singular decree has Nature declared with reference to the milkweed! She says, in plainest terms, "Your pollen must be removed on the leg of an insect, preferably a bee, or your kind shall perish from the face of the earth." And[Pg 230] what is the deep-laid plan by which this end is assured? My specimens here on the desk will disclose it all.
What a unique decision Nature has made regarding the milkweed! She clearly states, "Your pollen needs to be transferred by an insect, ideally a bee, or your species will disappear from the earth." And[Pg 230] what is the intricate strategy that guarantees this outcome? The specimens I have on my desk will reveal everything.
Here are two bees, a fly, and a beetle, each hanging dead by its legs from a flower, an extreme sacrificial penalty, which is singularly frequent, but which was certainly not exacted nor contemplated in the design of the flower. A careful search among almost any good-sized cluster of milkweeds will show us many such prisoners. As in all flowers, the pollen of the milkweed blossom must come in contact with its stigma before fruition is possible. In this peculiar family of plants, however, the pollen is distinct in character, and closely suggests the orchids in its consistency and disposition. The yellow powdery substance with which we are all familiar in ordinary flowers is here absent, the pollen being collected in two club-shaped or, more properly, spatula-shaped masses, linked in pairs at their slender prolonged tips, each of which terminates in a sticky disc-shaped appendage united in V-shape below. These pollen masses are concealed in pockets (B) around the cylindrical centre of the flower, the discs only being exposed at the surface, at five equidistant points around its rim, where they lie in wait for the first unwary foot[Pg 231] that shall touch them. A glance at the two views of this central portion of the flower, as it appears through my magnifying-glass—the honey-horns and sepals having been removed—will, I think, indicate its peculiar anatomy or mechanism. No stigma is to be seen in the flower, the stigmatic surface which is to receive the pollen being concealed within five compartments, each of which is protected by a raised tent-like covering, cleft along its entire apex by a fine fissure (A). Outside of each of these, and entirely separated from the stigma in the cavity, lie the pollen masses within their pockets, each pair uniting at the rim below in V-shape, the union at the lower limit of the fissure.
Here are two bees, a fly, and a beetle, each hanging dead by their legs from a flower, an extreme sacrificial penalty that happens quite often, but it definitely wasn't intended or planned in the design of the flower. A careful search among almost any decent-sized cluster of milkweeds will reveal many such captives. As with all flowers, the pollen from the milkweed blossom must touch its stigma before it can produce fruit. However, in this unique family of plants, the pollen is distinctive and closely resembles the consistency and arrangement of orchids. The yellow, powdery substance we’re used to seeing in regular flowers is absent here; instead, the pollen is gathered in two club-shaped, or more accurately, spatula-shaped clumps, linked in pairs at their slender extended tips, with each tip ending in a sticky disc-shaped appendage joined in a V-shape below. These pollen masses are hidden in pockets (B) around the cylindrical center of the flower, with only the discs exposed at the surface, positioned at five equal points around its edge, waiting for the first unsuspecting foot[Pg 231] that touches them. A look at the two views of this central part of the flower, as seen through my magnifying glass—the honey-horns and sepals removed—should, I believe, reveal its unique anatomy or function. No stigma is visible in the flower; the stigmatic surface that will receive the pollen is hidden within five compartments, each protected by a raised, tent-like cover that is split along its entire top by a fine crack (A). Outside each of these, completely separate from the stigma in the cavity, lie the pollen masses in their pockets, with each pair joining at the rim below in a V-shape, where they meet at the lower end of the crack.


With this more intimate knowledge of the floral anatomy, let us now visit our milkweed-plant and observe closely.
With this deeper understanding of the flower's structure, let's now check out our milkweed plant and take a closer look.
A bee alights upon the flower—the object of its visit being, of course, the sweets located in the five horn-shaped nectaries. In order to reach[Pg 233] this nectar the insect must hang to the bulky blossom. Instantly, and almost of necessity, it would seem, one or more of the feet are seen to enter the upper opening of the fissure, and during the insect's movements are drawn through to the base. The foot is thus conducted directly between the two viscid discs, which immediately cling closer than a brother, and as the foot is finally withdrawn, the pollen is pulled from its cell. The member now released seeks a fresh hold, and the same result follows, the leg almost inevitably entering the fissure, and this time drawing in the pollen directly against the sticky stigmatic surface within. The five honey-horns have now been drained, and as our bee leaves the flower he is plainly detained by this too hearty "shake" or "grip" of his host, and quite commonly must exert a slight struggle to free himself. As the foot is thus forcibly torn away, the pollen mass is commonly scraped entirely off and retained within the fissure, or perhaps parts at the stalk, leaving the terminal disc clinging on the insect's leg. Occasionally, when more than one leg is entangled, the dangling blossom is tossed and swayed for several seconds by the vigorous pulling and buzzing, and a number of these temporary captives upon a single milkweed-plant are always to be seen.[Pg 234]
A bee lands on the flower, which it visits for the sweet nectar found in the five horn-shaped glands. To get to this nectar, the insect clings to the large blossom. Almost instinctively, one or more of its feet slip into the upper opening of the crack and are pulled through to the bottom as the bee moves. The foot is then guided right between the two sticky discs, which immediately stick tighter than a brother. When the foot is finally pulled out, the pollen is removed from its cell. The freed foot looks for a new grip, and the same thing happens again—the leg inevitably goes into the crack, this time bringing pollen directly against the sticky surface inside. The five honey glands are now empty, and when the bee leaves the flower, it's clearly held back by this strong "shake" or "grip" from its host, often having to struggle a bit to free itself. As the foot is yanked away, the pollen mass is usually scraped off completely and stays in the crack, or maybe some stays behind on the stalk, leaving the end disc stuck to the bee's leg. Sometimes, when more than one leg gets caught, the flower sways back and forth for several seconds from the bee's vigorous pulling and buzzing, and it's common to see several of these temporary captives on one milkweed plant.[Pg 234]
Not unfrequently the mechanism so well adapted exceeds its functions and proves a veritable trap, as indicated in my specimens. I have found three dead bees thus entrapped in a single umbel of blossoms, having been exhausted in their struggles for escape; and a search among the flowers at any time will show the frequency of this fatality, the victims including gnats, flies, crane-flies, bugs, wasps, beetles, and small butterflies. In every instance this prisoner is found dangling by one or more legs, with the feet firmly held in the grip of the fissure.
Not infrequently, the mechanism that is so well designed goes beyond its intended purpose and becomes a real trap, as shown in my specimens. I've found three dead bees caught in a single cluster of flowers, having exhausted themselves trying to escape. A search among the flowers at any time reveals how often this happens, with victims including gnats, flies, crane-flies, bugs, wasps, beetles, and small butterflies. In every case, this trapped insect is found hanging by one or more legs, with its feet firmly stuck in the opening.
Almost any bee which we may catch at random upon a milkweed gives perfect evidence of his surroundings, its toes being decorated with the tiny yellow tags, each successive flower giving and taking, exchanging compliments, as it were, with his fellows. Ordinarily this fringe can hardly prove more than an embarrassment; but we may frequently discern an individual here and there which for some reason has received more than his share of the milkweed's compliments. His legs are conspicuously fringed with the yellow tags. He rests with a discouraged air upon a neighboring leaf, while honey, and even wings, are seemingly forgotten in his efforts to scrape off the cumbersome handicap.[Pg 235]
Almost any bee we randomly catch on a milkweed shows clear evidence of its surroundings, as its toes are covered with tiny yellow tags. Each flower gives and takes, exchanging compliments with the bees. Usually, this fringe is more of a nuisance than anything else; however, we often notice a bee here and there that has collected more than its fair share of the milkweed's tags. Its legs are noticeably adorned with the yellow tags. It sits on a nearby leaf, looking defeated, while it seems to have forgotten about honey and even its wings as it tries to scrape off this heavy burden.[Pg 235]

An interesting incident, apropos of our embarrassed bee, was narrated to me by the late Alphonso Wood, the noted botanist. He had received by mail from California a small box containing a hundred or more dead bees, accompanied by a letter. The writer, an old bee-keeper, had experience, and desired enlightenment and advice. The letter stated that his bees were "dying by thousands from the attacks of a peculiar fungus." The ground around the hive was littered with the victims in all stages of helplessness, and the dead insects were found everywhere at greater distances scattered around his premises. It needed only a casual glance at the encumbered insects to see the nature of the malady. They were laden two or three pairs deep, as it were, with the pollen masses of a milkweed. The botanist wrote immediately to his anxious correspondent, informing him, and suggesting as a remedy the[Pg 236] discovery and destruction of the mischievous plants, which must be thriving somewhere in his neighborhood. A subsequent letter conveyed the thanks of the bee-keeper, stating that the milkweeds—a whole field of them—had been found and destroyed, and the trouble had immediately ceased. I am not aware that Mr. Wood ever ascertained the particular species of milkweed in this case. It is not probable that our Eastern species need ever seriously threaten the apiary, though unquestionably large numbers of bees are annually destroyed by its excessive hospitality. I have repeatedly found honey-bees dead beneath the plants, and my cabinet shows a specimen of a large bumblebee which had succumbed to its pollen burden, its feet, and even the hairs upon its body, being fringed deep with the tiny clubs—one of the many specimens which I have discovered as the "grist in the mill" of that wise spider which usually spreads his catch-all beneath the milkweeds.
An interesting story related to our embarrassed bee was shared with me by the late Alphonso Wood, a well-known botanist. He had received a small box in the mail from California containing over a hundred dead bees, along with a letter. The writer, an experienced bee-keeper, sought insight and advice. The letter mentioned that his bees were "dying by the thousands due to a strange fungus." The ground around the hive was covered in helpless victims, and dead insects were found scattered all over his property. It took just a quick look at the overwhelmed insects to understand the issue. They were piled up with layers of pollen from a milkweed. The botanist quickly wrote back to his concerned correspondent, informing him of the problem and suggesting that he identify and remove the troublesome plants, which were likely flourishing nearby. A follow-up letter expressed the bee-keeper's gratitude, stating that he had found and destroyed an entire field of milkweeds, and the problem stopped immediately. I’m not sure if Mr. Wood ever identified the specific type of milkweed in this instance. It's unlikely that our Eastern species pose a serious threat to beekeeping, although many bees do die each year due to their overwhelming abundance. I have often found honeybees dead underneath these plants, and my collection includes a large bumblebee that fell victim to its pollen overload, with its feet and even the hairs on its body coated with tiny pollen masses—one of many specimens I've discovered as "grist for the mill" of that clever spider that usually sets its web beneath the milkweeds.
Allied to the milkweed is another plant, the dogbane (Apocynum), which has a similar trick of entrapping its insect friends. Its drooping, fragrant, bell-shaped white flowers and long slender pods will help to recall it. But its method of[Pg 237] capture is somewhat similar to the milkweed. The anthers are divided by a V-shaped cavity, into which the insect's tongue is guided as it is withdrawn from the flower, and into which it often becomes so tightly wedged as to render escape impossible. I have found small moths dangling by the tongue, as seen in the illustration below.
Allied with the milkweed is another plant, dogbane (Apocynum), which traps its insect companions in a similar way. Its drooping, fragrant, bell-shaped white flowers and long slender pods will help you recognize it. However, its method of[Pg 237] capture is quite similar to that of the milkweed. The anthers are separated by a V-shaped cavity that guides the insect's tongue as it pulls away from the flower, often getting wedged in so tightly that escape becomes impossible. I've seen small moths hanging by their tongues, as shown in the illustration below.


INDEX
Agalena, house-spider, 7.
Alypia, grape-vine-moth, 160.
Andromeda (A. ligustrina),
singular greeting to the bee, 126;
interior arrangement of flower, 128;
release of the pollen, 129.
Angræcum, orchid of Madagascar, with nectary eleven inches long, 219.
Ants,
herding the aphides, 166;
a model honey-farm, 167.
"Ant-holes," 61.
Aphides, plant-lice,
founders of the feast, 165;
herded by ants, 167.
Apocynum, dogbane, 236.
Aprophora, spume-bearer, 82.
Arethusa bulbosa, orchid, 175.
Argiope, field spider, 8.
Aristolochias, 119.
Aristotle, 23.
Arum, wild:
—Position of the anthers, 141;
progressive stages of change, 142.
Asclepias cornuta, milkweed, 227.
Asilus, "robber-fly", 8.
Axell, a follower of Darwin, 116.
Bees:
—The drone of, 5;
a counterpart of clover; dependence of clover on, 117;
manner of approach, 121;
black-and-white banded, 126;
approach to the blue-flag, 131;
experiment with the bumblebee, 209;
his escape from the flower, 210;
manner of cross-fertilizing, 212;
manner of conveying the pollen, 218;
his difficulties with the milkweed flower, 233;
the cumbersome handicap, 234;
destroyed by the milkweed, 235.
Beetles (Cicindela), tiger, 68.
Birds:
—Swifts, 5;
robin, 5;
vireo, 5, 45;
indigo, 5;
chat, 5, 40;
oriole, 5, 32;
red-headed chippy; barn-swallow, 6, 28, 39, 40;
cuckoo, 23;
"kow-bird"; cow black-bird; bunting, 27;
song-sparrow, 30, 40;
Maryland yellow-throat, 28, 45;
Wilson's thrush; chewink, 32;
fly-catcher; bluebird; oven-bird; cat-bird; ph[oe]be, 40;
bobolink; "reed-bird," 53;
humming, 227.
Birds' nests:
—Flimsy structure of the cuckoo's, 26;
song-sparrow's, 30;
oriole's swinging hammock; cobweb structure of the vireo's, 32;
size of yellow-bird's; summer yellow-bird's beautiful home, 47;
a four-story house, a possible fashion in featherdom, 51;
pipit's, 35;
wood-sparrow's, 37.
Bittersweet (Celastrus scandens), queer little harlequins on, 9;
its scarlet-coated seeds, 88.
Blackburn, Mrs., quoted, 35.
Blair, Patrick, his claims concerning pollen, 111.
Blossom ceremonies, 119.
Blue-flag,
its hidden anthers reached only by the bumblebee or large fly,129;
manner of the bee's approach, 131.
Burroughs on wren-building, 17.
Butterflies:
—Great yellow swallow-tail (Papilio turnus); red admiral (Pyrameis Atlanta); small yellow (Philodice); semicolon (Grapta interrogationis); comma (Vanessa comma), 153;
orange; white (Aphrodite), 154;
white cabbage (Pontia oleracea) 153.
Cactus, prickly-pear, its golden bower, 118.
Collinsonia, horse-balm, 136.
Caterpillars, 10, 14, 15, 62.
Celastrus scandens, bittersweet, 88.
Chamælirium luteum, devil's-bit, 133.
Chipmonk, 6.
Cicada,
victim of the sand-hornet, 77;
manner of depositing its eggs; period of transformation, 97;
time of hatching, 100.
Cicindela, tiger-beetle, 68.
Clover, cause of failure of crop in Australia, 117.
Cobwebs:
—A dusty prize; a two year's span, 7;
a mixed assortment in, 8.
Cone-flower (Rudbeckia hirta), 138;
embryo seeds; arrangement of the anthers, 139.
Cow black-bird, 27;
his favorite perch; old dame's theory, 28;
an unwelcome intruder, 30;
a prowling foe, 31.
Cow-bird:
—Ravenous young parasite, 31;
a clamoring lubber, 37;
"Black Douglas" of the bird-home, 38;
selected victims, 39;
distribution of its eggs; vicious habits, 40;
egg-laying intervals; demoralizing conditions; American species an improvement, 41;
survival of the fittest, 42;
balance of power, 44;
outwitted, 51;
massing for migration, 52.
"Cow-spit," 80.
Cross-fertilization, 115, 122, 178, 189, 194.
"Cuckoo-spit," 80.
Cuckoos:
—Poetic misnomer, 23;
outrage on maternal affection; yellow-billed; black-billed; imagination versus facts, 25;
bad workmanship of nest, 26;
its stammering cry, 27;
manner of depositing its eggs; handling the egg with her bill, 33;
short period of incubation; voracious appetite of the young; aggressive selfishness, 34;
the tragedy of the nest, 35;
manner of disposing of its nest-mates, 36.
Cypripedium acaule, moccasin-flower; ladies'-slipper; Venus's-slipper, 205.
Darwin:
—Process of anatomical evolution, 35;
theory of cross-fertilization, 105;
inspired insight, 115;
his disciples, 116;
experiments with pollen, 126;
weakness of self-fertilizing flowers, 144;
triumphant revelation, 171;
reaffirming Sprengel's theory, 178;
a chosen interpreter, 181;
dependence on insects, 183;
revealing the hidden treasure, 185;
foretelling the manner of cross-fertilization, 189;
description of the cross-fertilization, 209;
bees as implied fertilizers, 212;
truth of his belief, 220.
Darning-needle, dragon-fly (Libellulidæ), 156;
his dainty morsel, 160.
Delpino, a follower of Darwin, 116.
Desmodium, its hospitable welcome, 118.
Devil's-bit (Chamælirium luteum), 133.
Digger wasp,
its color and wire-like waist, 72;
manner of working, 74;
covering its tracks; opening the tomb, 76;
living food for the young grub, 77;
its remarkable carrying power, 78.
Dogbane (Apocynum),
its fragrant, bell-shaped flowers, 236;
trapping moths, 237.
Dogwood, 5.
Door-Step Neighbors:
—Chronicle of a day, 58;
disappearing holes, 59, 16;
"ant-holes"; a danger signal; an unhealthy court, 61;
a transformation, 62;
an experiment; method of excavation, 63;
a stalwart worker, 64;
an uncouth nondescript; spider-like legs, 66;
crawls on his back, 67;
a tiny black wasp; a spider-catcher, 69;
resting on her wings; inspecting her burrow, 70;
manner of burying her prey; skilful workmanship, 71;
a new-comer; her wire-like waist; digging her tunnel, 72;
manner of working; sound of labor, 74;
covering her tracks; opening the tomb, 76;
fresh living food, 77;
carrying seven times its weight; peculiar features of stone-piling, 78;
color of the wasp, 79;
the spume-bearer, 81;
nomadic blossoms; a sack bearer, 83;
winter quarters, 84.
Epeira, field spider, 8.
Epiphytes, air-plants, 181.
Evening primrose, its golden necklace, 118.
"Fertilization of Flowers," 116;
wrong theory, 114.
Fertilization of orchids, 105, 183.
Flies:
—Robber, 8;
bluebottle, 8;
harvest ichneumon, 45, 77, 96.
Foxes, wild gambols of, 6.
Froghopper. See Spume-bearer (Aprophora), 82.
Gärtner, recognizing the theory of cross-fertilization, 115.
Genesta, its reception of insects, 118.
Geranium, wild (G. sylvaticum), 112.
Gilbert, concerning cuckoo's eggs, 25.
"Gobs," 80.
Gray, Asa:
—Demonstration concerning orchids, 184;
surmise concerning the withdrawal of pollen, 188;
orchid structure, 190.
Grew, Nehemias, discovery concerning pollen, 110;
discoveries about pollen, 113;
first step in progress, 116.
Habenaria flava:
—Yellow-spiked, 203;
H. lacera, ragged, 200;
H. orbicularis, showy, 194, 199;
H. psycodes, purple-fringed, 200;
H. mascula, 189.
Heath, its distinguishing characteristics, 123.
Hemiptera, bugs with sucking beaks, 81.
Herbert:
—A follower of Sprengel, 108;
recognizing the principle of cross-fertilization, 115.
"Honey-dew Picnic":
—Gathering of the clans, 153;
a selected spot, 154;
a motley assemblage, 155;
an outlaw, 157;
a finish fight, 158;
funeral baked meats, 164;
gathering his grist;
the founder of the feast, 158.
Honey-guides, 112, 129.
Hornets:
—Its heavy load, 9;
on the watch, 15;
"solitary," 17;
queer home of, 18;
great sand, 77;
black paper, 161.
Horse-balm (Collinsonia), its singular shape, 136;
manner of bee's approach to, 138.
Huber:
—On insect slavery, 151;
on the cultivation of the aphides, 166.
Insect Fertilization, 115.
Jack-in-the-Pulpit, detaining its guests, 119.
Jardine, Sir William, concerning cuckoo's eggs, 32.
Jenner, Dr., habits of the young cuckoo, 35.
Knight, Andrew:
—On the divination of flowers, 108;
theory of cross-fertilization, 115.
Köhlreuter:
—Recognizing Sprengel's principles, 108;
a botanical pioneer, 115.
Krunitz, on flower honey, 111.
Labiates, flowers with lips, 122.
Ladies'-tresses (Spiranthes), 218.
Larva:
—Hornet, 16;
"puss-moth," 76;
psychid, 83.
Linnæus:
—Settling the theory of fertilization, 110;
puzzled as to the function of honey, 111;
a second step, 116;
imperfect knowledge of the orchid, 173.
Logan, concerning the cuckoo, 23.
Lubbock:
—On the divination of flowers, 108;
follower of Darwin, 116;
on the cultivation of aphides, 166.
Martial Spirit of Vespa, 19.
Membracis binotata, insect with a sharp beak, a tree-hopper, 91.
Milkweed:
—Its matchless hospitality;
purple pompons;
its five horns, 227;
its one mission;
the humming-bird its friend, 228;
complex mechanism;
enticing fragrance;
removal of pollen on insects' legs, 229;
four captives, 230;
its honey trap;
its tenacious grip, 233;
an assortment of victims;
cumbersome handicap, 234;
a wholesale destroyer, 235.
Mint family, 122.
Mnio-tiltidæ, summer yellow-bird, 47.
Moccasin-flower (Cypripedium acaule), 205.
Moths:
—Twilight;
sphinx, 118, 190, 220;
grape-vine, 160.
Mountain laurel:
—Showers of pollen of;
curious construction of flower of;
withers if brought indoors, 124;
character of the pollen, 125.
Mouse, motley collection of food of;
mischief of, 7.
Müller, Hermann:
—On the divination of flowers, 108;
on defective observation, 114;
the relations between the flower and insect, 116;
on fertilization, 142
Nature's Equilibrium, 39.
Natural observation, 57.
Nomadic blossoms, 83.
Orchids:
—Dependence on insects, 144;
strange mechanical adaptation;
sweet-pogonia;
perfume suggesting raspberries, 145;
intention of the blossom, 146;
adaptation for insects, 147;
its fragrance a perfumed whisper of welcome, 148;
a contrast, 172;
form of invitation, 173;
insect complement, 174;
Arethusa bulbosa, 175;
theories concerning the conveyance of the pollen, 176;
the most highly specialized form of flowers, 180;
distinguished by its structure;
American varieties not air-plants;
form of flower, 181;
elasticity of the pollen of the Spectabilis, 182;
self-fertilizing, 183;
American and exotic species, 184;
Arethusa's fragrance, 185;
its structure, 186;
significant depth of nectar wells;
conditions demanded of insects, 187;
Gray's surmise, 188;
sphinx-moth its only complement, 190;
manner of carrying the pollen by sphinx-moth, 193;
extracting the pollen with a pencil;
length of the nectary, 196;
purple-fringed, 198;
ragged, 200;
very exceptional provision, 201;
yellow-spiked, 203;
moccasin-flower;
ladies'-slipper;
Venus's-slipper;
the color of, 205;
distinctive character of, 206;
practical experiment, 209;
imprisonment of the bee;
manner of its release, 210;
rattlesnake-plantain, 213;
Angræcum, its long nectary, 219;
tongue of a sphinx-moth eleven inches long, 220;
nectary thirteen inches long, 223.
"Origin of Species":
—First important presentation of the theory of cross-fertilization, 105;
tardy appreciation of the work, 115.
Odynerus flavipes, wren-wasp, 10.
Ovid, concerning hornets, 18.
Parallels in Nature, 152.
Platanthera, orchid group, 192.
Pliny, 23.
Pogonia ophioglossoides, sweet-pogonia, 145.
Polistes, brown wasp, 161.
Primrose, evening, 118.
Psychid:
—A sack-bearer; drags its house with it; feeds on seed-pods, 83;
winter quarters of silk, 84.
Queer Little Family:
—Tree-hopper (Membracis binotata); a singular entertainment; graceful curves, 87;
a branch in masquerade; queer thorns, 88;
a sudden disappearance; animated thorns; like a covey of quails, 89;
like "Bob White," 90;
singular agility; queer anatomy; always ready for flight, 91;
fondness for locust and oak-trees, simulating the color and character of the branches, 92;
manner of sitting on the branches, 93;
always headed towards the top; tiny tufts of cotton, 94;
color and size of the tufts; a mere frothy shell; a riddle, 95;
its relations, 96;
an investigation, 97;
its technique, 98;
aërated cement; froth-house builder, 99;
period of hatching, 100;
a house for the winter; not a wanderer, 101.
Ragged Orchid (H. lacera), 200.
"Rattlesnake-plantain," 213.
Rudbeckia hirta, cone-flower, 138.
Sage (Salvia officinalis), strange curved stamen, 119;
nature's arrangement, 112.
Salvia, its welcome to the bee, 117.
Self-fertilization, 141.
Sheep-spit, 80.
Showy orchid (H. orbicularis),194.
Snorting war-horse, 18.
Solitude, the pleasures of, 3.
"Solomon's ant," 152.
Spectabilis, orchid, 182;
its favorite haunt, 195.
Spiders, agalena, epeira, argiope, 8;
a two years' span, 7;
a silken vortex;
miscellaneous food, 8.
Spiranthes, "Lady's-tresses," 218.
Sprengel, Christian Conrad:
—Inspiration from the wild geranium, 108;
on the mystery of color, 112;
theory of fertilization;
a poser to Linnæus, 113;
his wrong theory, 114;
divining half the truth, 176;
assumption disproved, 178.
Spume-bearer (Aprophora), its domicile of suds;
wonderful power of jumping, 82.
Starling, dispossessing woodpecker from nest, 43.
Studio Company:
—"Tumultuous privacy"; contested territory; snickering squirrels, 4;
selected food; unsymmetrical carpentry; drone of bees; carol of birds; flurry of swifts; accompaniments to my toil, 5;
wild fox; pet chipmonk; pet toad; his lightning tongue; home in a bowl, 6;
an old friend, 9.
Summer yellow-bird (Mnio-tiltidæ), 47.
Sweet-pogonia (P. ophioglossoides), 145.
Swift, Jonathan, on parasites, 44.
Tennyson, quoted, 24.
"The Secrets of Nature in Forms and Fertilization of Flowers Discovered," Sprengel's work, 113.
Thévenot, concerning the thrift of insects, 152.
Tiger-beetle (Cicindela), 68.
Toads, 6.
Toad-spit, 80.
Tree-hopper, 93.
Venus's-slipper (Cypripedium acaule), 205.
Vireo, abandons its nest, 45.
Wasps:
—Wren, 10;
microscopic, 45;
tiny black, 69;
digger, 72, 162;
orange-spotted, 79;
brown; mud, 161.
"Waxwork" bittersweet (Celastrus scandens), 88.
Welcome of the flowers:
—The function of the stamen, 106;
difference in cells, 107;
condition of the flower, 108;
physiological features; recognition of sex in flowers, 109;
exchange of courtesies; each flower a law unto itself, 117;
action of "jack-in-the-pulpit"; cypripedium and aristolochias; peculiarity of the sage, 119;
queer stamens; nature's arrangement, 121;
cross-fertilization insured, 122;
showers of laurel pollen; curious construction of flower, 124;
singular greeting to the bee, 126;
remarkable interior arrangement of the Andromeda, 128;
hidden anthers of the blue-flag, 129;
intercommunication and reciprocity, 135.
Wild geranium (G. sylvaticum), 112.
Wild volapük, 4.
Wilson, cow-bird's eggs, 33.
Wind as a fertilizing agent, 154.
White, Gilbert, cuckoo's eggs, 32;
rich localities, 58.
Wood, Alphonso:
—On tubercles, 203;
on embarrassed bees, 235.
Woodchucks, 5.
Wren-wasp (Odynerus flavipes):
—A cumbersome prize, 10;
selecting a home; way stations; a second instalment, 11;
very familiar, 12;
a well-stocked home, 13;
impotent anæsthetic, 14;
manner of catching her prey; a hypodermic injection, 15;
food on storage; closing the cell after depositing egg, 16;
living food; preference for ready-made houses; resemblance to the yellow-jacket, 17.
Zenarchus, concerning the cicada, 96.
Agalena, house spider, 7.
Alypia, grape vine moth, 160.
Andromeda (A. ligustrina),
a special greeting to the bee, __A_TAG_PLACEHOLDER_0__;
flower's inner structure, __A_TAG_PLACEHOLDER_0__;
pollen release, __A_TAG_PLACEHOLDER_0__.
Angræcum, orchid from Madagascar, with a nectary that’s eleven inches long, 219.
Ants,
caring for the aphids, __A_TAG_PLACEHOLDER_0__;
a model honey farm, __A_TAG_PLACEHOLDER_0__.
"Ant holes," 61.
Aphids, plant lice,
hosts of the feast, __A_TAG_PLACEHOLDER_0__;
herded by ants, __A_TAG_PLACEHOLDER_0__.
Apocynum, dogbane, 236.
Aprophora, spume bearer, 82.
Arethusa bulbosa, orchid, 175.
Argiope, field spider, 8.
Aristolochias, 119.
Aristotle, 23.
Arum, wild:
—Anther position, __A_TAG_PLACEHOLDER_0__;
stages of change, __A_TAG_PLACEHOLDER_0__.
Asclepias cornuta, milkweed, 227.
Asilus, "robber fly", 8.
Axell, a follower of Darwin, 116.
Bees:
—The buzz of, __A_TAG_PLACEHOLDER_0__;
a version of clover; clover's dependence on, __A_TAG_PLACEHOLDER_0__;
approach, __A_TAG_PLACEHOLDER_0__;
black and white striped, __A_TAG_PLACEHOLDER_0__;
approaching the blue flag, __A_TAG_PLACEHOLDER_0__;
experiment with the bumblebee, __A_TAG_PLACEHOLDER_0__;
his escape from the flower, __A_TAG_PLACEHOLDER_0__;
cross-fertilization method, __A_TAG_PLACEHOLDER_0__;
method of transferring pollen, __A_TAG_PLACEHOLDER_0__;
his issues with the milkweed flower, __A_TAG_PLACEHOLDER_0__;
the awkward obstacle, __A_TAG_PLACEHOLDER_0__;
destroyed by the milkweed, __A_TAG_PLACEHOLDER_0__.
Beetles (Cicindela), tiger, 68.
Birds:
—Swifts, __A_TAG_PLACEHOLDER_0__;
robin, __A_TAG_PLACEHOLDER_0__;
vireo, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__;
indigo, __A_TAG_PLACEHOLDER_0__;
chat, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__;
oriole, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__;
red-headed chick; barn swallow, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__, __A_TAG_PLACEHOLDER_2__, __A_TAG_PLACEHOLDER_3__;
cuckoo, __A_TAG_PLACEHOLDER_0__;
"cowbird"; cow blackbird; bunting, __A_TAG_PLACEHOLDER_0__;
song sparrow, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__;
Maryland yellow throat, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__;
Wilson's thrush; chewink, __A_TAG_PLACEHOLDER_0__;
flycatcher; bluebird; ovenbird; catbird; phoebe, __A_TAG_PLACEHOLDER_0__;
bobolink; "reed bird," __A_TAG_PLACEHOLDER_0__;
humming, __A_TAG_PLACEHOLDER_0__.
Bird nests:
—Weak structure of the cuckoo's, __A_TAG_PLACEHOLDER_0__;
song sparrow's, __A_TAG_PLACEHOLDER_0__;
oriole's swinging hammock; the cobweb structure of the vireo's, __A_TAG_PLACEHOLDER_0__;
size of the yellow bird; the summer yellow bird's beautiful home, __A_TAG_PLACEHOLDER_0__;
a four-story house, a potential design in the bird world, __A_TAG_PLACEHOLDER_0__;
pipit's, __A_TAG_PLACEHOLDER_0__;
wood sparrow's, __A_TAG_PLACEHOLDER_0__.
Bittersweet (Celastrus scandens), quirky little harlequins on, 9;
its bright red seeds, __A_TAG_PLACEHOLDER_0__.
Blackburn, Mrs., quoted, 35.
Blair, Patrick, his claims about pollen, 111.
Blossom ceremonies, 119.
Blue-flag,
its hidden anthers can only be accessed by the bumblebee or a large fly, __A_TAG_PLACEHOLDER_0__;
bee's approach method, __A_TAG_PLACEHOLDER_0__.
Burroughs on wren building, 17.
Butterflies:
—Great yellow swallowtail (Papilio turnus); red admiral (Pyrameis Atlanta); small yellow (Philodice); semicolon (Grapta interrogationis); comma (Vanessa comma), __A_TAG_PLACEHOLDER_0__;
orange; white (Aphrodite), __A_TAG_PLACEHOLDER_0__;
white cabbage (Pontia oleracea) __A_TAG_PLACEHOLDER_0__.
Cactus, prickly pear, its golden bower, 118.
Collinsonia, horse balm, 136.
Caterpillars, 10, 14, 15, 62.
Celastrus scandens, bittersweet, 88.
Chamælirium luteum, devil's bit, 133.
Chipmunk, 6.
Cicada,
victim of the sand hornet, __A_TAG_PLACEHOLDER_0__;
method of laying its eggs; transformation period, __A_TAG_PLACEHOLDER_0__;
hatching time, __A_TAG_PLACEHOLDER_0__.
Cicindela, tiger beetle, 68.
Clover, reason for crop failure in Australia, 117.
Cobwebs:
—A dusty prize; a two-year period, __A_TAG_PLACEHOLDER_0__;
a mixed assortment in, __A_TAG_PLACEHOLDER_0__.
Cone flower (Rudbeckia hirta), 138;
embryo seeds; arrangement of the anthers, __A_TAG_PLACEHOLDER_0__.
Cow blackbird, 27;
his favorite spot; the old woman's theory, __A_TAG_PLACEHOLDER_0__;
an unwanted intruder, __A_TAG_PLACEHOLDER_0__;
a lurking enemy, __A_TAG_PLACEHOLDER_0__.
Cowbird:
—Ravenous young parasite, __A_TAG_PLACEHOLDER_0__;
a noisy person, __A_TAG_PLACEHOLDER_0__;
"Black Douglas" of the bird home, __A_TAG_PLACEHOLDER_0__;
selected victims, __A_TAG_PLACEHOLDER_0__;
distribution of its eggs; aggressive behaviors, __A_TAG_PLACEHOLDER_0__;
egg-laying intervals; discouraging conditions; American species seen as an upgrade, __A_TAG_PLACEHOLDER_0__;
survival of the fittest, __A_TAG_PLACEHOLDER_0__;
balance of power, __A_TAG_PLACEHOLDER_0__;
outsmarted, __A_TAG_PLACEHOLDER_0__;
migrating together, __A_TAG_PLACEHOLDER_0__.
"Cow spit," 80.
Cross-fertilization, 115, 122, 178, 189, 194.
"Cuckoo spit," 80.
Cuckoos:
—Poetic mistake, __A_TAG_PLACEHOLDER_0__;
outrage over maternal instincts; yellow-billed; black-billed; imagination vs. facts, __A_TAG_PLACEHOLDER_0__;
shoddy nest craftsmanship, __A_TAG_PLACEHOLDER_0__;
its stuttering call, __A_TAG_PLACEHOLDER_0__;
method of laying its eggs; using her bill to handle the egg, __A_TAG_PLACEHOLDER_0__;
short incubation period; intense hunger of the young; aggressive selfishness, __A_TAG_PLACEHOLDER_0__;
the tragedy of the nest, __A_TAG_PLACEHOLDER_0__;
way of getting rid of its nest mates, __A_TAG_PLACEHOLDER_0__.
Cypripedium acaule, moccasin flower; lady's sliper; Venus's slipper, 205.
Darwin:
—Anatomical evolution process, __A_TAG_PLACEHOLDER_0__;
cross-fertilization theory, __A_TAG_PLACEHOLDER_0__;
inspired insight, __A_TAG_PLACEHOLDER_0__;
his followers, __A_TAG_PLACEHOLDER_0__;
pollen experiments, __A_TAG_PLACEHOLDER_0__;
self-fertilizing flowers' weakness, __A_TAG_PLACEHOLDER_0__;
epic reveal, __A_TAG_PLACEHOLDER_0__;
reaffirming Sprengel's theory, __A_TAG_PLACEHOLDER_0__;
a selected interpreter, __A_TAG_PLACEHOLDER_0__;
reliance on bugs, __A_TAG_PLACEHOLDER_0__;
uncovering the hidden treasure, __A_TAG_PLACEHOLDER_0__;
predicting cross-fertilization method, __A_TAG_PLACEHOLDER_0__;
description of the cross-fertilization, __A_TAG_PLACEHOLDER_0__;
bees as natural fertilizers, __A_TAG_PLACEHOLDER_0__;
truth of his belief, __A_TAG_PLACEHOLDER_0__.
Darning needle, dragonfly (Libellulidæ), 156;
his delicate snack, __A_TAG_PLACEHOLDER_0__.
Delpino, a follower of Darwin, 116.
Desmodium, its warm welcome, 118.
Devil's bit (Chamælirium luteum), 133.
Digger wasp,
its color and wasp waist, __A_TAG_PLACEHOLDER_0__;
work style, __A_TAG_PLACEHOLDER_0__;
covering its tracks; opening the tomb, __A_TAG_PLACEHOLDER_0__;
food for young grubs, __A_TAG_PLACEHOLDER_0__;
its impressive carrying capacity, __A_TAG_PLACEHOLDER_0__.
Dogbane (Apocynum),
its fragrant, bell-shaped flowers, __A_TAG_PLACEHOLDER_0__;
catching moths, __A_TAG_PLACEHOLDER_0__.
Dogwood, 5.
Doorstep Neighbors:
—Chronicle of a day, __A_TAG_PLACEHOLDER_0__;
disappearing holes, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__;
"ant holes"; a warning sign; an unhealthy environment, __A_TAG_PLACEHOLDER_0__;
a change, __A_TAG_PLACEHOLDER_0__;
an experiment; digging method, __A_TAG_PLACEHOLDER_0__;
a hard worker, __A_TAG_PLACEHOLDER_0__;
an awkward nondescript; spindly legs, __A_TAG_PLACEHOLDER_0__;
crawls on its back, __A_TAG_PLACEHOLDER_0__;
a small black wasp; a spider catcher, __A_TAG_PLACEHOLDER_0__;
resting on its wings; inspecting her burrow, __A_TAG_PLACEHOLDER_0__;
way of burying her prey; skilled craftsmanship, __A_TAG_PLACEHOLDER_0__;
a newcomer; her slender waist; digging her tunnel, __A_TAG_PLACEHOLDER_0__;
way of working; sound of labor, __A_TAG_PLACEHOLDER_0__;
covering her tracks; opening the tomb, __A_TAG_PLACEHOLDER_0__;
fresh whole food, __A_TAG_PLACEHOLDER_0__;
carrying seven times its weight; unusual characteristics of stone stacking, __A_TAG_PLACEHOLDER_0__;
color of the wasp, __A_TAG_PLACEHOLDER_0__;
the foam bearer, __A_TAG_PLACEHOLDER_0__;
nomadic blooms; a bag carrier, __A_TAG_PLACEHOLDER_0__;
winter quarters, __A_TAG_PLACEHOLDER_0__.
Epeira, field spider, 8.
Epiphytes, air plants, 181.
Evening primrose, its golden necklace, 118.
"Fertilization of Flowers," 116;
wrong theory, __A_TAG_PLACEHOLDER_0__.
Fertilization of orchids, 105, 183.
Flies:
—Thief, __A_TAG_PLACEHOLDER_0__;
bluebottle, __A_TAG_PLACEHOLDER_0__;
harvest ichneumon, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__, __A_TAG_PLACEHOLDER_2__.
Foxes, wild antics of, 6.
Froghopper. See Spume bearer (Aprophora), 82.
Gärtner, recognizing the theory of cross-fertilization, 115.
Genesta, its reception of insects, 118.
Geranium, wild (G. sylvaticum), 112.
Gilbert, regarding cuckoo's eggs, 25.
"Gobs," 80.
Gray, Asa:
—Orchid demonstration, __A_TAG_PLACEHOLDER_0__;
speculation about the removal of pollen, __A_TAG_PLACEHOLDER_0__;
orchid anatomy, __A_TAG_PLACEHOLDER_0__.
Grew, Nehemias, discovery about pollen, 110;
discoveries about pollen, __A_TAG_PLACEHOLDER_0__;
first step in progress, __A_TAG_PLACEHOLDER_0__.
Habenaria flava:
—Yellow-spiked, __A_TAG_PLACEHOLDER_0__;
H. lacera, ragged, __A_TAG_PLACEHOLDER_0__;
H. orbicularis, vibrant, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__;
H. psycodes, purple-fringed, __A_TAG_PLACEHOLDER_0__;
H. mascula, __A_TAG_PLACEHOLDER_0__.
Heath, its distinguishing features, 123.
Hemiptera, bugs with sucking beaks, 81.
Herbert:
—A follower of Sprengel, __A_TAG_PLACEHOLDER_0__;
recognizing the idea of collaboration, __A_TAG_PLACEHOLDER_0__.
"Honey-dew Picnic":
—Clans gathering, __A_TAG_PLACEHOLDER_0__;
a selected location, __A_TAG_PLACEHOLDER_0__;
a diverse group, __A_TAG_PLACEHOLDER_0__;
a criminal, __A_TAG_PLACEHOLDER_0__;
a final showdown, __A_TAG_PLACEHOLDER_0__;
funeral treats, __A_TAG_PLACEHOLDER_0__;
claiming his share;
the host of the party, __A_TAG_PLACEHOLDER_0__.
Honey guides, 112, 129.
Hornets:
—Its heavy load, __A_TAG_PLACEHOLDER_0__;
keeping an eye out, __A_TAG_PLACEHOLDER_0__;
"alone," __A_TAG_PLACEHOLDER_0__;
strange home of __A_TAG_PLACEHOLDER_0__;
great sand, __A_TAG_PLACEHOLDER_0__;
black paper, __A_TAG_PLACEHOLDER_0__.
Horse balm (Collinsonia), its unique shape, 136;
method of how the bee approaches __A_TAG_PLACEHOLDER_0__.
Huber:
—On insect slavery, __A_TAG_PLACEHOLDER_0__;
on growing aphids, __A_TAG_PLACEHOLDER_0__.
Insect Fertilization, 115.
Jack-in-the-Pulpit, detaining its guests, 119.
Jardine, Sir William, regarding cuckoo's eggs, 32.
Jenner, Dr., habits of the young cuckoo, 35.
Knight, Andrew:
—On flower divination, __A_TAG_PLACEHOLDER_0__;
cross-fertilization theory, __A_TAG_PLACEHOLDER_0__.
Köhlreuter:
—Recognizing Sprengel's principles, __A_TAG_PLACEHOLDER_0__;
a plant expert, __A_TAG_PLACEHOLDER_0__.
Krunitz, on flower honey, 111.
Labiates, flowers with lips, 122.
Ladies'-tresses (Spiranthes), 218.
Larva:
—Hornet, __A_TAG_PLACEHOLDER_0__;
"puss moth," __A_TAG_PLACEHOLDER_0__;
psychid, __A_TAG_PLACEHOLDER_0__.
Linnæus:
—Finalizing the fertilization theory, __A_TAG_PLACEHOLDER_0__;
uncertain about the role of honey, __A_TAG_PLACEHOLDER_0__;
a second step, __A_TAG_PLACEHOLDER_0__;
limited knowledge of the orchid, __A_TAG_PLACEHOLDER_0__.
Logan, regarding the cuckoo, 23.
Lubbock:
—On flower divination, __A_TAG_PLACEHOLDER_0__;
Darwin supporter, __A_TAG_PLACEHOLDER_0__;
on growing aphids, __A_TAG_PLACEHOLDER_0__.
Martial Spirit of Vespa, 19.
Membracis binotata, insect with a sharp beak, a tree hopper, 91.
Milkweed:
—Its unparalleled hospitality;
purple pom-poms;
its five horns, __A_TAG_PLACEHOLDER_0__;
its only purpose;
the hummingbird as its friend, __A_TAG_PLACEHOLDER_0__;
complicated system
alluring scent;
pollen removal on bugs' legs, __A_TAG_PLACEHOLDER_0__;
four captives, __A_TAG_PLACEHOLDER_0__;
its honey trap;
its strong grip, __A_TAG_PLACEHOLDER_0__;
a range of victims;
awkward barrier, __A_TAG_PLACEHOLDER_0__;
a total destroyer, __A_TAG_PLACEHOLDER_0__.
Mint family, 122.
Mnio-tiltidæ, summer yellow bird, 47.
Moccasin flower (Cypripedium acaule), 205.
Moths:
—Twilight;
sphinx, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__, __A_TAG_PLACEHOLDER_2__;
grapevine, __A_TAG_PLACEHOLDER_0__.
Mountain laurel:
—Pollen showers from;
curious flower building;
dies if taken inside, __A_TAG_PLACEHOLDER_0__;
pollen characteristics, __A_TAG_PLACEHOLDER_0__.
Mouse, mixed collection of food;
mischief of, __A_TAG_PLACEHOLDER_0__.
Müller, Hermann:
—On flower divination, __A_TAG_PLACEHOLDER_0__;
on flawed observation, __A_TAG_PLACEHOLDER_0__;
the connection between flowers and insects, __A_TAG_PLACEHOLDER_0__;
on fertilization, __A_TAG_PLACEHOLDER_0__
Nature's Equilibrium, 39.
Natural observation, 57.
Nomadic blossoms, 83.
Orchids:
—Dependence on insects, __A_TAG_PLACEHOLDER_0__;
weird mechanical adjustment;
sweet pogonia;
raspberry-scented perfume, __A_TAG_PLACEHOLDER_0__;
intent of the bloom, __A_TAG_PLACEHOLDER_0__;
insect adaptation, __A_TAG_PLACEHOLDER_0__;
its scent a fragrant greeting, __A_TAG_PLACEHOLDER_0__;
a contrast, __A_TAG_PLACEHOLDER_0__;
invitation type, __A_TAG_PLACEHOLDER_0__;
insect complement, __A_TAG_PLACEHOLDER_0__;
Arethusa bulbosa, __A_TAG_PLACEHOLDER_0__;
theories about pollen transfer, __A_TAG_PLACEHOLDER_0__;
the most specialized flower types, __A_TAG_PLACEHOLDER_0__;
defined by its structure;
American varieties are not air plants;
flower shape, __A_TAG_PLACEHOLDER_0__;
the elasticity of the pollen from Spectabilis, __A_TAG_PLACEHOLDER_0__;
self-pollinating, __A_TAG_PLACEHOLDER_0__;
American and exotic species, __A_TAG_PLACEHOLDER_0__;
Arethusa's fragrance, __A_TAG_PLACEHOLDER_0__;
its structure, __A_TAG_PLACEHOLDER_0__;
notable depth of nectar sources;
conditions needed from insects, __A_TAG_PLACEHOLDER_0__;
Gray's thoughts, __A_TAG_PLACEHOLDER_0__;
sphinx moth as its only partner, __A_TAG_PLACEHOLDER_0__;
how sphinx moth pollinates, __A_TAG_PLACEHOLDER_0__;
using a pencil to collect pollen
nectary length, __A_TAG_PLACEHOLDER_0__;
purple fringed, __A_TAG_PLACEHOLDER_0__;
ragged, __A_TAG_PLACEHOLDER_0__;
very exceptional provision, __A_TAG_PLACEHOLDER_0__;
yellow spiked, __A_TAG_PLACEHOLDER_0__;
moccasin flower
lady's slipper
Venus flytrap;
the color of __A_TAG_PLACEHOLDER_0__;
distinctive features of __A_TAG_PLACEHOLDER_0__;
hands-on experiment, __A_TAG_PLACEHOLDER_0__;
catching the bee;
method of its release, __A_TAG_PLACEHOLDER_0__;
rattlesnake plantain, __A_TAG_PLACEHOLDER_0__;
Angræcum, its long nectar tube, __A_TAG_PLACEHOLDER_0__;
the sphinx moth's tongue is eleven inches long, __A_TAG_PLACEHOLDER_0__;
nectary 13 inches long, __A_TAG_PLACEHOLDER_0__.
"Origin of Species":
—First major presentation of the theory of cross-fertilization, __A_TAG_PLACEHOLDER_0__;
late acknowledgment of the work, __A_TAG_PLACEHOLDER_0__.
Odynerus flavipes, wren wasp, 10.
Ovid, concerning hornets, 18.
Parallels in Nature, 152.
Platanthera, orchid group, 192.
Pliny, 23.
Pogonia ophioglossoides, sweet pogonia, 145.
Polistes, brown wasp, 161.
Primrose, evening, 118.
Psychid:
—A sack carrier; drags its home with it; feeds on seed pods, __A_TAG_PLACEHOLDER_0__;
silk winter quarters, __A_TAG_PLACEHOLDER_0__.
Queer Little Family:
—Tree hopper (Membracis binotata); a one-of-a-kind spectacle; elegant curves, __A_TAG_PLACEHOLDER_0__;
a hidden branch; unusual thorns, __A_TAG_PLACEHOLDER_0__;
a sudden vanishing; lively thorns; like a group of quails, __A_TAG_PLACEHOLDER_0__;
like "Bob White," __A_TAG_PLACEHOLDER_0__;
unique agility; distinctive body structure; always prepared to take off, __A_TAG_PLACEHOLDER_0__;
a love for locust and oak trees, imitating the color and texture of the branches, __A_TAG_PLACEHOLDER_0__;
way of sitting on the branches, __A_TAG_PLACEHOLDER_0__;
always facing upward; small clumps of cotton, __A_TAG_PLACEHOLDER_0__;
color and size of the tufts; just a frothy shell; a mystery, __A_TAG_PLACEHOLDER_0__;
its connections, __A_TAG_PLACEHOLDER_0__;
an investigation, __A_TAG_PLACEHOLDER_0__;
its method, __A_TAG_PLACEHOLDER_0__;
aerated cement; foam concrete builder, __A_TAG_PLACEHOLDER_0__;
hatching time, __A_TAG_PLACEHOLDER_0__;
a home for the winter; not a traveler, __A_TAG_PLACEHOLDER_0__.
Ragged Orchid (H. lacera), 200.
"Rattlesnake-plantain," 213.
Rudbeckia hirta, cone flower, 138.
Sage (Salvia officinalis), unusual curved stamen, 119;
nature's setup, __A_TAG_PLACEHOLDER_0__.
Salvia, its welcome to the bee, 117.
Self-fertilization, 141.
Sheep spit, 80.
Showy orchid (H. orbicularis), 194.
Snorting war horse, 18.
Solitude, the pleasures of, 3.
"Solomon's ant," 152.
Spectabilis, orchid, 182;
its favorite place, __A_TAG_PLACEHOLDER_0__.
Spiders, agalena, epeira, argiope, 8;
a period of two years, __A_TAG_PLACEHOLDER_0__;
a silky whirlpool;
diverse diet, __A_TAG_PLACEHOLDER_0__.
Spiranthes, "Lady's-tresses," 218.
Sprengel, Christian Conrad:
—Inspired by the wild geranium, __A_TAG_PLACEHOLDER_0__;
on the mystery of color, __A_TAG_PLACEHOLDER_0__;
fertilization theory
a challenge to Linnæus, __A_TAG_PLACEHOLDER_0__;
his wrong theory, __A_TAG_PLACEHOLDER_0__;
divining half the truth, __A_TAG_PLACEHOLDER_0__;
assumptions proven wrong, __A_TAG_PLACEHOLDER_0__.
Spume bearer (Aprophora), its sudsy home;
incredible jumping skills, __A_TAG_PLACEHOLDER_0__.
Starling, evicting woodpecker from nest, 43.
Studio Company:
—"Chaotic privacy"; disputed area; chuckling squirrels, __A_TAG_PLACEHOLDER_0__;
chosen food; uneven carpentry; buzzing of bees; singing of birds; swarm of swifts; additions to my work, __A_TAG_PLACEHOLDER_0__;
wild fox; pet chipmunk; pet toad; his quick tongue; home in a bowl, __A_TAG_PLACEHOLDER_0__;
an old friend, __A_TAG_PLACEHOLDER_0__.
Summer yellow bird (Mnio-tiltidæ), 47.
Sweet pogonia (P. ophioglossoides), 145.
Swift, Jonathan, on parasites, 44.
Tennyson, quoted, 24.
"The Secrets of Nature in Forms and Fertilization of Flowers Discovered," Sprengel's work, 113.
Thévenot, regarding the thrift of insects, 152.
Tiger beetle (Cicindela), 68.
Toads, 6.
Toad spit, 80.
Tree hopper, 93.
Venus's slipper (Cypripedium acaule), 205.
Vireo, abandoning its nest, 45.
Wasps:
—Wren, __A_TAG_PLACEHOLDER_0__;
microscopic, __A_TAG_PLACEHOLDER_0__;
tiny black, __A_TAG_PLACEHOLDER_0__;
digger, __A_TAG_PLACEHOLDER_0__, __A_TAG_PLACEHOLDER_1__;
orange-spotted, __A_TAG_PLACEHOLDER_0__;
brown; mud, __A_TAG_PLACEHOLDER_0__.
"Waxwork" bittersweet (Celastrus scandens), 88.
Welcome of the flowers:
—The stamen's role, __A_TAG_PLACEHOLDER_0__;
difference in cells, __A_TAG_PLACEHOLDER_0__;
condition of the flower, __A_TAG_PLACEHOLDER_0__;
physiological characteristics; understanding gender in flowers, __A_TAG_PLACEHOLDER_0__;
exchange of pleasantries; each flower has its own rules, __A_TAG_PLACEHOLDER_0__;
the action of "jack-in-the-pulpit"; cypripedium and aristolochias; the uniqueness of the sage, __A_TAG_PLACEHOLDER_0__;
uncommon stamens; nature's design, __A_TAG_PLACEHOLDER_0__;
cross-fertilization guaranteed, __A_TAG_PLACEHOLDER_0__;
showers of laurel pollen; unique flower structure, __A_TAG_PLACEHOLDER_0__;
special greeting to the bee, __A_TAG_PLACEHOLDER_0__;
the impressive internal structure of the Andromeda, __A_TAG_PLACEHOLDER_0__;
hidden anthers of the blue flag, __A_TAG_PLACEHOLDER_0__;
interconnectedness and reciprocity, __A_TAG_PLACEHOLDER_0__.
Wild geranium (G. sylvaticum), 112.
Wild volapük, 4.
Wilson, cowbird's eggs, 33.
Wind as a fertilizing agent, 154.
White, Gilbert, cuckoo's eggs, 32;
rich ecosystems, __A_TAG_PLACEHOLDER_0__.
Wood, Alphonso:
—On tubercles, __A_TAG_PLACEHOLDER_0__;
on confused bees, __A_TAG_PLACEHOLDER_0__.
Woodchucks, 5.
Wren-wasp (Odynerus flavipes):
—A burdensome prize, __A_TAG_PLACEHOLDER_0__;
choosing a home; stopovers; a follow-up, __A_TAG_PLACEHOLDER_0__;
very familiar, __A_TAG_PLACEHOLDER_0__;
a fully stocked home, __A_TAG_PLACEHOLDER_0__;
numb anesthetic, __A_TAG_PLACEHOLDER_0__;
method of capturing her prey: a hypodermic injection, __A_TAG_PLACEHOLDER_0__;
food stored; sealing the cell after laying an egg, __A_TAG_PLACEHOLDER_0__;
living food; preference for pre-built houses; similarity to the yellow jacket, __A_TAG_PLACEHOLDER_0__.
Zenarchus, regarding the cicada, 96.
FOOTNOTE
[A] In numerous instances observed since the above was written I have noted the larger bumblebees upon the blossom. These insects have a different method of approach, hanging beneath the flower, the anthers being clapped against their thorax at the juncture of the wings, instead of the abdomen, as in the smaller bee.
[A] Since I wrote the above, I've seen larger bumblebees on the flowers numerous times. These insects approach differently, hanging underneath the flower, with the pollen structures hitting their thorax at the point where their wings meet, instead of their abdomen like the smaller bees do.
THE END
WILLIAM HAMILTON GIBSON'S WORKS.
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