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.
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 compensating in interest what they may lack in other attractive attributes.
[Illustration: Fig. 18 C]
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 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as shown at Fig. 20, D. The sticky gland is brought into immediate contact, and clasps the pin, which, now being withdrawn, brings away the pollen, as in E and F. Thus it is naturally removed on the tongue of its sipping bee.
[Illustration: Fig. 19]
[Illustration: Fig. 21]
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 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 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.
[Illustration: Fig. 20]
[Illustration: A. Extended. B. Folded beneath the head.]
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.
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 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.
