Andrœcium.—The main points of morphological interest relating to the andrœcium, referred to in this volume, are those concerning the structure of the anther ([see p. 292]), the compound nature of the stamens in some orders ([see pp. 294], [345]), and the nature of the andrœcium in orchids ([see p. 380]).
Inferior ovary.—Is the pistil always foliar in its morphological nature, or is it, in some cases, as Schleiden taught, formed from the axis alone? To a great extent the reply to this question is dependent on the conclusions that may be arrived at as to the true nature of the calyx-tube. Considered from a teratological point of view, there is no reason for considering the inferior ovary to be purely axial. On the contrary, the evidence derived from this source supports the ordinary opinion that the carpels are invaginated within the expanded top of the flower-stalk and more or less adherent to it. Some of the gourds afford good illustrations of this, the upper part of the carpels in these fruits projecting beyond the axial portion. But this matter loses much of its importance if the morphological identity of axis and leaf-organ be conceded. The carpels in inferior ovaries seldom or never correspond to the lamina of the leaf, and between the vaginal portion of the carpellary leaf, and the axis who shall draw the distinction?
Placentation.—Some botanists have considered the placentas to be portions of the carpel, and have compared the production of ovules on them to the formation of buds on the leaf of Bryophyllum. Others have been led to see in each placenta, even when it is, to all outward appearance, a portion of the carpellary leaf, a direct prolongation from the axis, adherent to the leaf. Teratology shows that ovules may be formed indifferently on leaf-organs or on stem-organs. Sutural, parietal, axile, free-central placentation, and, if there be more forms, all may be met with even in the same ovary ([see pp. 96], [508]). Now, if there were such special tendencies in the axis, as contrasted with the leaf, to produce ovules, it is hardly likely that such anomalous arrangements as those just mentioned would be as frequent as they are. But as leaves produce other leaves, from their edges or their surfaces, and as they form buds in the same situations, just as axial organs do,[561] there is surely little ground for considering the placentas, or ovuliferous portions of the plant, to be of necessity axial. Here again, much of the difficulty vanishes if the morphological identity of the leaf-form and of the stem-form be admitted.
Structure of the ovule.—The nature of the ovule and of its coverings has been a fertile source of controversy. The teratological data bearing on this subject have been given at pp. 262–272. These data strongly support the notion of the foliar nature of the coatings, and of the axial nature of the nucleus, taking leaf and axis either in the ordinary sense, or as modifications one of the other. It has been shown that the ovular coats may themselves become carpels, and that ovules may be developed upon ovules, p. 268. Whether the intra-carpellary siliques of Cheiranthus, not uncommonly met with (p. 182), are instances of ovular transmutation may be open to doubt.
The axial nature of the nucleus has been inferred from its position, mode of growth, and from its occasionally lengthening into a leafy or even a floriferous shoot. Probably it may occasionally be invested by sheathing coats, more analogous to tubular processes from the receptacle, than to foliar organs, as is the case in Welwitschia. The discussion of this matter, however, pertains rather to normal morphology than to teratology.
Morphology of conifers.—The nature of the pseudo-leaves of Sciadopitys, and probably of other Conifers, is illustrated by teratology, as also is the true constitution of the scale of the cone ([see pp. 192], [24]5, [352]), though it must be admitted that little or no light is thrown on that much-contested point—the true nature of the ovule of Gymnosperms.
Relative position of organs.—When organs are considered, not separately, but in their relations to each other, the appearances presented are referable to similar causes. Thus, the separation of parts usually united has been shown to depend on an excess of development, the persistent union of parts, usually separate in the adult state, has been traced to an arrest of the process of development, by no means necessarily coexistent with diminished growth. The diminished or increased number of parts is, in like manner, attributable to analogous causes, as also are the variations in arrangement and form, spoken of under the heads of Displacement, Peloria, Substitution, &c.
In the instance of displacements, it has been shown how slight a change is required to transform the so-called inferior ovary into a superior one. A defective development of the top of the flower-stalk in some cases, in others a lack of union between the tube of the receptacle or of the calyx (comprising in those terms not only the apex of the receptacle, but the base of the sepals) and the carpels, suffice to bring about this change in a character which for systematic purposes is of great value.
Law of alternation.—The circumstances that interfere with the law of alternation may be briefly alluded to. The deviations from the customary arrangement have been very generally attributed to suppression, or to chorisis. It is unquestionable that either of these affords an efficient explanation of the arrangement in question, as also does that modification of chorisis, as it may be considered, which has been treated of under the head of Enation. Spiral torsion of the axis would likewise bring about analogous results. Still, it is quite conceivable that opposition or superposition of organs may occur without the intervention of any such operations. This will be the more readily conceded when it is remembered that the phyllotaxis of leaves not unfrequently varies on different branches of the same individual tree, and that a similar variation in the flower would at once disturb the customary alternate arrangement. Coalescence of the vascular bundles in an unusual manner, and an irregular disposition of these cords have also been considered to bring about deviations from the rule of alternation, but in general the formation of the cords is subsequent to that of the growing points or mamelons.
Adhesions, accompanied by displacements, occasionally produce similar deviations, the nature of which is usually easily detected.