be admitted that all leguminous plants with hypogean cotyledons are descended from forms which once raised their cotyledons above the ground in the ordinary manner; and in doing so, it is certain that their hypocotyls would have been abruptly arched, as in the case of every other dicotyledonous plant. This is especially clear in the case of Phaseolus, for out of five species, the seedlings of which we observed, namely, P. multiflorus, caracalla, vulgaris, Hernandesii and Roxburghii (inhabitants of the Old and New Worlds), the three last-named species have well-developed hypocotyls which break through the ground as arches. Now, if we imagine a seedling of the common bean or of P. multiflorus, to behave as its progenitors once did, the hypocotyl (h, Fig. 59), in whatever position the seed may have been buried, would become so much arched that the upper part would be doubled down parallel to the lower part; and
* An instrument devised by Sachs, consisting essentially of a slowly revolving horizontal axis, on which the plant under observation is supported: see 'Würzburg Arbeiten,' 1879, p. 209. [page 94]
this is exactly the kind of curvature which actually occurs in these two plants, though to a much less degree. Therefore we can hardly doubt that their short hypocotyls have retained by inheritance a tendency to curve themselves in the same manner as they did at a former period, when this movement was highly important to them for breaking through the ground, though now rendered useless by the cotyledons being hypogean. Rudimentary structures are in most cases highly variable, and we might expect that rudimentary or obsolete actions would be equally so; and Sachs' curvature varies extremely in amount, and sometimes altogether fails. This is the sole instance known to us of the inheritance, though in a feeble degree, of movements which have become superfluous from changes which the species has undergone.
Rudimentary Cotyledons.—A few remarks on this subject may be here interpolated. It is well known that some dicotyledonous plants produce only a single cotyledon; for instance, certain species of Ranunculus, Corydalis, Chaerophyllum; and we will here endeavour to show that the loss of one or both cotyledons is apparently due to a store of nutriment being laid up in some other part, as in the hypocotyl or one of the two cotyledons, or one of the secondary radicles.
Fig. 60. Citrus aurantium: two young seedlings: c, larger cotyledon; c', smaller cotyledon; h, thickened hypocotyl; r, radicle. In A the epicotyl is still arched, in B it has become erect. [page 95]
With the orange (Citrus aurantium) the cotyledons are hypogean, and one is larger than the other, as may be seen in A (Fig. 60). In B the inequality is rather greater, and the stem has grown between the points of insertion of the two petioles, so that they do not stand opposite to one another; in another case the separation amounted to one-fifth of an inch. The smaller cotyledon of one seedling was extremely thin, and not half the length of the larger one, so that it was clearly becoming rudimentary,* In all these seedlings the hypocotyl was enlarged or swollen.
Fig. 61. Abronia umbellata: seedling twice natural size: c cotyledon; c', rudimentary cotyledon; h, enlarged hypocotyl, with a heel or projection (h') at the lower end; r, radicle.
With Abronia umbellata one of the cotyledons is quite rudimentary, as may be seen (c') in Fig. 61. In this specimen it consisted of a little green flap,⅛4th inch in length, destitute of a petiole and covered with glands like those on the fully developed cotyledon (c). At first it stood opposite to the larger cotyledon; but as the petiole of the latter increased in length and grew in the same line with the hypocotyl (h), the rudiment appeared in older seedlings as if seated some way down the hypocotyl. With Abronia arenaria there is a similar rudiment, which in one
* In Pachira aquatica, as described by Mr. R. I. Lynch ('Journal Linn. Soc. Bot.' vol. xvii. 1878, p. 147), one of the hypogean cotyledons is of immense size; the other is small and soon falls off; the pair do not always stand opposite. In another and very different water-plant, 'Trapa natans', one of the cotyledons, filled with farinaceous matter, is much larger than the other, which is scarcely visible, as is stated by Aug. de Candolle, 'Physiologie Veg.' tom. ii. p. 834, 1832. [page 96]
specimen was only 1/100th and in another ⅙0th inch in length; it
ultimately appeared as if seated halfway down the hypocotyl. In both these
species the hypocotyl is so much enlarged, especially at a very early age,
that it might almost be called a corm. The lower end forms a heel or
projection, the use of which will hereafter be described.
In Cyclamen Persicum the hypocotyl, even whilst still within the seed, is
enlarged into a regular corm,* and only a single cotyledon is at first
developed (see former Fig. 57). With Ranunculus ficaria two cotyledons are
never produced, and here one of the secondary radicles is developed at an
early age into a so-called bulb.** Again, certain species of Chaerophyllum
and Corydalis produce only a single cotyledon;*** in the former the
hypocotyl, and in the latter the radicle is enlarged, according to Irmisch,
into a bulb.
In the several foregoing cases one of the cotyledons is delayed in its development, or reduced in size, or rendered rudimentary, or quite aborted; but in other cases both cotyledons are represented by mere rudiments. With Opuntia basilaris this is not the case, for both cotyledons are thick and large, and the hypocotyl shows at first no signs of enlargement; but afterwards, when the cotyledons have withered and disarticulated themselves, it becomes thickened, and from its tapering form, together with its smooth, tough, brown skin, appears, when ultimately drawn down to some depth into the soil, like a root. On the other
* Dr. H. Gressner, 'Bot. Zeitung,' 1874, p. 824.
** Irmisch, 'Beiträge zur Morphologie der Pflanzen,' 1854, pp. 11, 12; 'Bot. Zeitung,' 1874, p. 805.
*** Delpino, 'Rivista Botanica,' 1877, p. 21. It is evident from Vaucher's account ('Hist. Phys. des Plantes d'Europe,' tom. i. 1841, p. 149) of the germination of the seeds of several species of Corydalis, that the bulb or tubercule begins to be formed at an extremely early age. [page 97]
hand, with several other Cacteae, the hypocotyl is from the first much enlarged, and both cotyledons are almost or quite rudimentary. Thus with Cereus Landbeckii two little triangular projections, representing the cotyledons, are narrower than the hypocotyl, which is pear-shaped, with the point downwards. In Rhipsalis cassytha the cotyledons are represented by mere points on the enlarged hypocotyl. In Echinocactus viridescens the hypocotyl is globular, with two little prominences on its summit. In Pilocereus Houlletii the hypocotyl, much swollen in the upper part, is merely notched on the summit; and each side of the notch evidently represents a cotyledon. Stapelia sarpedon, a member of the very distinct family of the Asclepiadeae, is fleshy like a cactus; and here again the upper part of the flattened hypocotyl is much thickened and bears two minute cotyledons, which, measured internally, were only .15 inch in length, and in breadth not equal to one-fourth of the diameter of the hypocotyl in its narrow axis; yet these minute cotyledons are probably not quite useless, for when the hypocotyl breaks through the ground in the form of an arch, they are closed or pressed against one another, and thus protect the plumule. They afterwards open.
From the several cases now given, which refer to widely distinct plants, we may infer that there is some close connection between the reduced size of one or both cotyledons and the formation, by the enlargement of the hypocotyl or of the radicle, of a so-called bulb. But it may be asked, did the cotyledons first tend to abort, or did a bulb first begin to be formed? As all dicotyledons naturally produce two well-developed cotyledons, whilst the thickness of the
