The USES are few, mostly as ornamental plants in conservatories. The tubers of several Orchis-species are OFFICINAL; they contain starch and mucilage and are used us “salep.” The fruits of Vanilla planifolia are used as condiments and differ from other Orchid-fruits in being rather fleshy and in dehiscing irregularly; the seeds are very small, shining and black.
Class II. Dicotyledones.
In this class THE EMBRYO has 2 seed-leaves, a rule from which there are few exceptions (e.g. Ficaria, Cyclamen, Pinguicula, certain species of Corydalis, with only 1; and a few, mostly parasitic forms, e.g. Monotropa, Orobanche, Pyrola, entirely without cotyledons). On germination the cotyledons nearly always raise themselves above the ground as green, assimilating leaves and are then termed aerial or epigean, in contradistinction to the underground or hypogean which are always buried. The structure of the seed varies (endospermous or exendospermous); the embryo may be straight or curved. In many instances the primary root grows as a vigorous tap-root, with weaker branches arising acropetally (in annuals, biennials, many perennials, especially woody plants); but in a large number of herbaceous perennials, which have rhizomes, the root behaves very much as in the Monocotyledons. The roots generally increase in thickness by means of a cambium.
The stem, when seen in transverse section, has its vascular bundles arranged in a ring; in reality, however, they form a kind of cylindrical network in the stem; the bundles are open, and thickening takes place by means of a cambium; annual rings are formed in the perennial stems. There is a rich and very varied form of branching. The two first leaves of a shoot (fore-leaves) are placed nearly always to the right and to the left; the same arrangement is found in the two first leaves developed on the flower-stalk, and these are, as a rule, the only two; they are found below the calyx and are usually termed the “bracteoles.” It has become customary to indicate the bracteoles by the letters α and β, according to their sequence of growth, and in that sense these letters will be employed in the following diagrams.
The arrangement of the leaves varies very much; there is also a great variety of shapes in the leaves and their venation, but the linear leaves, with parallel venation, so frequent in the Monocotyledons, are seldom met with, as also the large sheaths (though the sheath is well developed in the Umbelliferous plants); stipules occur much more frequently.
The flower is most commonly cyclic, but acyclic or hemicyclic forms also occur. The type which may be taken as a basis consists in the majority of instances, as in the Monocotyledons, of 5 whorls, of which the 4 outer ones (calyx, corolla, and the 2 whorls of stamens) are most frequently 4 or 5 in number and placed in regular alternation, whilst the innermost one (the carpels) has generally fewer members, probably on account of space (Figs. [360], [361], [421], [429], [487], etc.). Trimerous (Figs. [384], [387], etc.) flowers, or those in which the members of the flower are in threes or a multiple of three, also occur, as well as dimerous flowers; other numbers are rare. It is of the greatest importance in connection with the relative position of the members of the flower to the axis and bract (orientation), whether the bracteoles are typically present (even though they may not be developed), or are typically absent. If there are 2 bracteoles present, then their position in a pentamerous flower is often as follows: the first sepal turns obliquely forward, the second is posterior and median, the third obliquely forward, the fourth and fifth obliquely backward; quincuncial æstivation is often found in these buds (Figs. [360], [429], [471], [475], [584]). The first and third leaves, in the following chapters, are most frequently alluded to as the “anterior,” the fourth and fifth as the “lateral” leaves. The reversed arrangement, with the median sepal in the front, occurs for instance in Papilionaceæ (Fig. [511]), Lobeliaceæ (Fig. [594]), Rhodoracecæ. If any bracteoles are present below a tetramerous flower, the relation is generally that 2 sepals (the first ones) stand in the median plane, the two next ones transversely (Fig. [393]), and the corolla then adopts a diagonal position (Fig. [397]); but a diagonal position of the calyx generally shows that the flower is not, strictly speaking, tetramerous, as in Plantago (Fig. [567]), Veronica (Fig. [559] C) and others.
If the bracteoles are not typically present, then the position of the sepals is changed accordingly, and the two outer sepals endeavour to assume the position which the bracteoles would otherwise have occupied, e.g. in Primula (Fig. [547]). Other positions are also found when the number of bracteoles is more or less than two.
The leaves which follow the sepals occupy definite positions with regard to them, which we may consider later. An arrangement must, however, be mentioned here; when the flower is “diplostemonous” that is, has two whorls of stamens (thus, Sn, Pn, An + n), these may be arranged in two ways. Either the first-formed whorl of stamens, which are termed the “calyx-stamens,” stands directly in front of the sepals (that is “episepalous”), and is the outermost whorl, and in this case a regular alternation takes place between sepals, petals and the two whorls of stamens, which is also continued into the carpels if their number is the same as that of the other whorls: the carpels are then placed opposite the sepals (Fig. [278]) and the flower is isomerous and Gn should be added to the formula above. Or, the calyx-stamens form the innermost whorl, and the corolla-stamens, which are subsequently formed (“epipetalous” stamens), stand outside these (Figs. [360], [429]); if the number of carpels is the same as that of the preceding whorls, they are often placed right in front of the petals and the corolla-stamens. The first-mentioned arrangement is termed Diplostemonous, and the second Obdiplostemonous. Both arrangements may be found in one and the same order, e.g. Caryophyllaceæ. The size and relation of the members of the flowers, and also the contact with other members in the early stages of their development, play an important part in determining the arrangement.
The great number of structural arrangements found in this enormously large class, may, as is the case in the Monocotyledons, be further varied by suppression and division of certain leaves (especially the stamens). Instances of this will occur in the following (Figs. [559], [568].—[426], [441], [445], etc.).
The Dicotyledons were formerly divided into 3 sub-classes: Apetalæ (those without corolla), Sympetalæ or Gamopetalæ (those with the petals united), and Choripetalæ or Polypetalæ (the petals not united). This division has now been abandoned because it has been proved that the Apetalæ were merely reduced or incomplete forms of the Choripetalæ, and they have therefore been distributed among the various families of the latter sub-class.