A QUEER LITTLE FAMILY ON THE BITTERSWEET

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Initial I. Branch of the Bittersweet
Initial I. Branch of 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 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.

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 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.

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, 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"?

A Bittersweet Covey A Bittersweet Covey

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.

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 beneath 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.

Flushing the Game Flushing the Game

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.

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 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 disclose the little hopper or colony of them headed for its tip.

Specimen Twig Specimen Twig

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 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, I was soon enabled to witness a solution of at least a part of 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."

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"—

"Happy the cicadas' lives,
Since they all have noiseless wives."

I have alluded to the egg of the cicada "inserted in the bark of a twig." This act is accomplished 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 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 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.

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 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.

Building Froth-tent Building Froth-tent

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 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 round to the orthodox 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.


The Studio Door
The Studio Door

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 considered 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.

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 remarkable 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.

Fig 1. A Row of Stamens Fig 1. A Row of Stamens

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 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.

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.

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.

Most of my readers are familiar with the general construction of a flower, but in order to insure 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.

Fig. 2. The Parts of a Flower Fig. 2. The Parts of a Flower

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.

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.

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.

Fig. 3. Historical Series, Showing the Progress of Discovery of Flower Fertilization Fig. 3. Historical Series, Showing the Progress of Discovery of Flower Fertilization

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 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.

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.

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 following 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:

1. "Flowers are fertilized by insects."

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.

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.

"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 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 fact which, singularly enough, the latter's own pages proved without his suspicion.

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.

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.

Many years ago the grangers of Australia determined 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.

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 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 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!

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.

The Garden Sage The Garden Sage

Fig. 4. Cross-fertilization of the Sage Fig. 4. Cross-fertilization of the Sage

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 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 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.

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. 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.

While each family of plants is apt to favor some particular general plan, the modifications in the various species seem almost without limit.

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).

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 cordial spirit by a mimic display of pyrotechnics as the anthers hurl aloft their tiny showers of pollen!

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.

But the twilight cluster in the woods may tell us a pretty story.

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 visitor, at the same time decorating him with their compliments of webby 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).

Fig. 5. Elastic Stamens of Mountain-laurel Fig. 5. Elastic Stamens of Mountain-laurel

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 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).

Andromeda Ligustrina Andromeda 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 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 protrudes beneath the blossom's throat, and the expectant seed-pod above welcomes the good tidings with visions of fruition.

Fig. 6. Fertilisation of Andromeda Fig. 6. Fertilisation of Andromeda

The Laurel The Laurel

Fig. 7. Cross-fertilization of the Blue-flag Fig. 7. Cross-fertilization of the Blue-flag

Blue-flag Blue-flag

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 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.

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 overarching 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 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 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 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 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.

Fig. 8. Devil's-bit Fig. 8. Devil's-bit

The presence of fragrance and honey in a dioecious 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.

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.

Horse-balm. Collinsonia Horse-balm. Collinsonia

Only a few days since, while out on a drive, I passed a luxuriant clump of the plant known as "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.

Fig. 9. Cross-fertilization of the Horse-balm Flowers in Various Stages, and in the Order of their Visitation by the Bee Fig. 9. Cross-fertilization of the Horse-balm Flowers in Various Stages,
and in the Order of their Visitation by the Bee
The Cone-flower The Cone-flower

What I observed is pictured severally at Fig. 9, 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 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]

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?

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 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.

Cone-flower, Showing Numerous Florets, Some in Pollen, Others in Stigmatic Stage Fig. 10. Cone-flower, Showing Numerous Florets,
Some in Pollen, Others in 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.

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 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.)

Fig. 11. Cross-fertilization of Cone-flower Fig. 11. Cross-fertilization of Cone-flower
Fig. 12. The Fertilization of the English Arum, 1st Stage Fig. 12. The Fertilization of the English Arum, 1st Stage

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.

Perhaps even more remarkable than any of the 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.

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 Hermann 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.

Fig. 13. The Fertilization of the English Arum. 2d, 3d, 4th, and 5th Stages Fig. 13. The Fertilization of the English Arum. 2d, 3d, 4th, and 5th Stages

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 stigmas, 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 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.

Fig. 14. Pogonia Fig. 14. Pogonia

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.

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 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 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 remains close within its pocket, and the pollen is thus retained.

Fig. 15. Cross-fertilization Fig. 15. Cross-fertilization

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.

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 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.


                                                                                                                                                                                                                                                                                                           

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