The last family is the Hydrocharideæ. They are submersed aquatics, or a few of them with long-stalked, floating leaves. Two forms, the ditch-moss (Elodea) ([Fig. 91], G, I) and eel-grass (Vallisneria) are very common in stagnant or slow-running water. In both of these the plants are completely submersed, but there is a special arrangement for bringing the flowers to the surface of the water. Like the arrowhead, the flowers are unisexual, but borne on different plants. The female flowers (H, L) are comparatively large, especially in Vallisneria, and are borne on long stalks, by means of which they reach the surface of the water, where they expand and are ready for pollination. The male flowers ([Fig. 91], J, K) are extremely small and borne, many together, surrounded by a membranous envelope, the whole inflorescence attached by a short stalk. When the flowers are ready to open, they break away from their attachment, and the envelope opens, allowing them to escape, and they immediately rise to the surface where they expand and collect in great numbers about the open female flowers. Sometimes these are so abundant during the flowering period (late in summer) that the surface of the water looks as if flour had been scattered over it. After pollination is effected, the stem of the female flower coils up like a spring, drawing the flower beneath the water where the fruit ripens.
The cells of these plants show very beautifully the circulation of the protoplasm, the movement being very marked and continuing for a long time under the microscope. To see this the whole leaf of Elodea, or a section of that of Vallisneria, may be used.
CHAPTER XVII.
DICOTYLEDONS.
Fig. 92.—End of a branch of a horsechestnut in winter, showing the buds covered by the thick, brown scale leaves, × 1.
The second sub-class of the angiosperms, the dicotyledons, receive their name from the two opposite seed leaves or cotyledons with which the young plant is furnished. These leaves are usually quite different in shape from the other leaves, and not infrequently are very thick and fleshy, filling nearly the whole seed, as may be seen in a bean or pea. The number of the dicotyledons is very large, and very much the greater number of living spermaphytes belong to this group. They exhibit much greater variety in the structure of the flowers than the monocotyledons, and the leaves, which in the latter are with few exceptions quite uniform in structure, show here almost infinite variety. Thus the leaves may be simple (undivided); e.g. oak, apple; or compound, as in clover, locust, rose, columbine, etc. The leaves may be stalked or sessile (attached directly to the stem), or even grown around the stem, as in some honeysuckles. The edges of the leaves may be perfectly smooth (“entire”), or they may be variously lobed, notched, or wavy in many ways. As many of the dicotyledons are trees or shrubs that lose their leaves annually, special leaves are developed for the protection of the young leaves during the winter. These have the form of thick scales, and often are provided with glands secreting a gummy substance which helps render them water-proof. These scales are best studied in trees with large, winter buds, such as the horsechestnut ([Fig. 92]), hickory, lilac, etc. On removing the hard, scale leaves, the delicate, young leaves, and often the flowers, may be found within the bud. If we examine a young shoot of lilac or buckeye, just as the leaves are expanding in the spring, a complete series of forms may be seen from the simple, external scales, through immediate forms, to the complete foliage leaf. The veins of the leaves are almost always much-branched, the veins either being given off from one main vein or midrib (feather-veined or pinnate-veined), as in an apple leaf, or there may be a number of large veins radiating from the base of the leaf, as in the scarlet geranium or mallow. Such leaves are said to be palmately veined.
Some of them are small herbaceous plants, either upright or prostrate upon the ground, over which they may creep extensively, becoming rooted at intervals, as in the white clover, or sending out special runners, as is seen in the strawberry. Others are woody stemmed plants, persisting from year to year, and often becoming great trees that live for hundreds of years. Still others are climbing plants, either twining their stems about the support, like the morning-glory, hop, honeysuckle, and many others, or having special organs (tendrils) by which they fasten themselves to the support. These tendrils originate in different ways. Sometimes, as in the grape and Virginia creeper, they are reduced branches, either coiling about the support, or producing little suckers at their tips by which they cling to walls or the trunks of trees. Other tendrils, as in the poison ivy and the true ivy, are short roots that fasten themselves firmly in the crevices of bark or stones. Still other tendrils, as those of the sweet-pea and clematis, are parts of the leaf.
The stems may be modified into thorns for protection, as we see in many trees and shrubs, and parts of leaves may be similarly changed, as in the thistle. The underground stems often become much changed, forming bulbs, tubers, root stocks, etc. much as in the monocotyledons. These structures are especially found in plants which die down to the ground each year, and contain supplies of nourishment for the rapid growth of the annual shoots.