The Power of Movement in Plants by Charles Darwin (book club books TXT) 📖

trace is left of their former abrupt curvature, excepting in the case of Allium cepa, in which the cotyledon rarely becomes quite straight, owing to the protuberance developed on the crown of the arch.

 

The increased growth along the inner surface of the arch which renders it straight, apparently begins in the basal leg or that which is united to the radicle; for this leg, as we often observed, is first bowed backwards from the other leg. This movement facilitates the withdrawal of the tip of the epicotyl or of the cotyledons, as the case may be, from within the seed-coats and from the ground. But the cotyledons often emerge from the ground still tightly enclosed within the seed-coats, which apparently serve to protect them. The seed-coats are afterwards ruptured and cast off by the swelling of the closely conjoined cotyledons, and not by any movement or their separation from one another.

 

Nevertheless, in some few cases, especially with the [page 102]

Cucurbitaceae, the seed-coats are ruptured by a curious contrivance, described by M. Flahault.* A heel or peg is developed on one side of the summit of the radicle or base of the hypocotyl; and this holds down the lower half of the seed-coats (the radicle being fixed into the ground) whilst the continued growth of the arched hypocotyl forced upwards the upper half, and tears asunder the seed-coats at one end, and the cotyledons are then easily withdrawn.

 

Fig. 62. Cucurbita ovifera: germinating seed, showing the heel or peg projecting on one side from summit of radicle and holding down lower tip of seed-coats, which have been partially ruptured by the growth of the arched hypocotyl.

 

The accompanying figure (Fig. 62) will render this description intelligible. Forty-one seeds of Cucurbita ovifera were laid on friable peat and were covered by a layer about an inch in thickness, not much pressed down, so that the cotyledons in being dragged up were subjected to very little friction, yet forty of them came up naked, the seed-coats being left buried in the peat. This was certainly due to the action of the peg, for when it was prevented from acting, the cotyledons, as we shall presently see, were lifted up still enclosed in their seed-coats. They were, however, cast off in the course of two or three days by the swelling of the cotyledons. Until this occurs light is excluded, and the cotyledons cannot decompose carbonic acid; but no one probably would have thought that the advantage thus gained by a little earlier cast-

 

* ‘Bull. Soc. Bot. de France,’ tom. xxiv. 1877, p. 201.

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ing off of the seed-coats would be sufficient to account for the development of the peg. Yet according to M. Flahault, seedlings which have been prevented from casting their seed-coats whilst beneath the ground, are inferior to those which have emerged with their cotyledons naked and ready to act.

 

The peg is developed with extraordinary rapidity; for it could only just be distinguished in two seedlings, having radicles .35 inch in length, but after an interval of only 24 hours was well developed in both. It is formed, according to Flahault, by the enlargement of the layers of the cortical parenchyma at the base of the hypocotyl. If, however, we judge by the effects of a solution of permanganate of potassium, it is developed on the exact line of junction between the hypocotyl and radicle; for the flat lower surface, as well as the edges, were coloured brown like the radicle; whilst the upper slightly inclined surface was left uncoloured like the hypocotyl, excepting indeed in one out of 33 immersed seedlings in which a large part of the upper surface was coloured brown. Secondary roots sometimes spring from the lower surface of the peg, which thus seems in all respects to partake of the nature of the radicle. The peg is always developed on the side which becomes concave by the arching of the hypocotyl; and it would be of no service if it were formed on any other side. It is also always developed with the flat lower side, which, as just stated, forms a part of the radicle, at right angles to it, and in a horizontal plane. This fact was clearly shown by burying some of the thin flat seeds in the same position as in Fig. 62, excepting that they were not laid on their flat broad sides, but with one edge downwards. Nine seeds were thus planted, and the peg was developed in the [page 104]

same position, relatively to the radicle, as in the figure; consequently it did not rest on the flat tip of the lower half of the seed-coats, but was inserted like a wedge between the two tips. As the arched hypocotyl grew upwards it tended to draw up the whole seed, and the peg necessarily rubbed against both tips, but did not hold either down. The result was, that the cotyledons of five out of the nine seeds thus placed were raised above the ground still enclosed within their seed-coats. Four seeds were buried with the end from which the radicle protrudes pointing vertically downwards, and owing to the peg being always developed in the same position, its apex alone came into contact with, and rubbed against the tip on one side; the result was, that the cotyledons of all four emerged still within their seed-coats. These cases show us how the peg acts in co-ordination with the position which the flat, thin, broad seeds would almost always occupy when naturally sown. When the tip of the lower half of the seed-coats was cut off, Flahault found (as we did likewise) that the peg could not act, since it had nothing to press on, and the cotyledons were raised above the ground with their seed-coats not cast off. Lastly, nature shows us the use of the peg; for in the one Cucurbitaceous genus known to us, in which the cotyledons are hypogean and do not cast their seed-coats, namely, Megarrhiza, there is no vestige of a peg. This structure seems to be present in most of the other genera in the family, judging from Flahault’s statements’ we found it well-developed and properly acting in Trichosanthes anguina, in which we hardly expected to find it, as the cotyledons are somewhat thick and fleshy. Few cases can be advanced of a structure better adapted for a special purpose than the present one.

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With Mimosa pudica the radicle protrudes from a small hole in the sharp edge of the seed; and on its summit, where united with the hypocotyl, a transverse ridge is developed at an early age, which clearly aids in splitting the tough seed-coats; but it does not aid in casting them off, as this is subsequently effected by the swelling of the cotyledons after they have been raised above the ground. The ridge or heel therefore acts rather differently from that of Cucurbita. Its lower surface and the edges were coloured brown by the permanganate of potassium, but not the upper surface.

It is a singular fact that after the ridge has done its work and has escaped from the seed-coats, it is developed into a frill all round the summit of the radicle.*

 

At the base of the enlarged hypocotyl of Abronia umbellata, where it blends into the radicle, there is a projection or heel which varies in shape, but its outline is too angular in our former figure (Fig. 61). The radicle first protrudes from a small hole at one end of the tough, leathery, winged fruit. At this period the upper part of the radicle is packed within the fruit parallel to the hypocotyl, and the single cotyledon is doubled back parallel to the latter. The swelling of these three parts, and especially the rapid development of the thick heel between the hypocotyl and radicle at the point where they are doubled, ruptures the tough fruit at the upper end and allows the arched hypocotyl to emerge; and this seems to be the function of the heel. A seed was cut out of the fruit and * Our attention was called to this case by a brief statement by Nobbe in his ‘Handbuch der Samenkunde,’ 1876, p. 215, where a figure is also given of a seedling of Martynia with a heel or ridge at the junction of the radicle and hypocotyl. This seed possesses a very hard and tough coat, and would be likely to require aid in bursting and freeing the cotyledons.

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allowed to germinate in damp air, and now a thin flat disc was developed all round the base of the hypocotyl and grew to an extraordinary breadth, like the frill described under Mimosa, but somewhat broader. Flahault says that with Mirabilis, a member of the same family with Abronia, a heel or collar is developed all round the base of the hypocotyl, but more on one side than on the other; and that it frees the cotyledons from their seed-coats. We observed only old seeds, and these were ruptured by the absorption of moisture, independently of any aid from the heel and before the protrusion of the radicle; but it does not follow from our experience that fresh and tough fruits would behave in a like manner.

 

In concluding this section of the present chapter it may be convenient to summarise, under the form of an illustration, the usual movements of the hypocotyls and epicotyls of seedlings, whilst breaking through the ground and immediately afterwards. We may suppose a man to be thrown down on his hands and knees, and at the same time to one side, by a load of hay falling on him. He would first endeavour to get his arched back upright, wriggling at the same time in all directions to free himself a little from the surrounding pressure; and this may represent the combined effects of apogeotropism and circumnutation, when a seed is so buried that the arched hypocotyl or epicotyl protrudes at first in a horizontal or inclined plane.

The man, still wriggling, would then raise his arched back as high as he could; and this may represent the growth and continued circumnutation of an arched hypocotyl or epicotyl, before it has reached the surface of the ground. As soon as the man felt himself at all free, he would raise the upper part of his body, whilst still on

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his knees and still wriggling; and this may represent the bowing backwards of the basal leg of the arch, which in most cases aids in the withdrawal of the cotyledons from the buried and ruptured seed-coats, and the subsequent straightening of the whole hypocotyl or epicotyl—circumnutation still continuing.

 

Circumnutation of Hypocotyls and Epicotyls, when erect.—The hypocotyls, epicotyls, and first shoots of the many seedlings observed by us, after they had become straight and erect, circumnutated continuously. The diversified figures described by them, often during two successive days, have been shown in the woodcuts in the last chapter. It should be recollected that the dots were joined by straight lines, so that the figures are angular; but if the observations had been made every few minutes the lines would have been more or less curvilinear, and irregular ellipses or ovals, or perhaps occasionally circles, would have been formed.

The direction of the longer axes of the ellipses made during the same day or on successive days generally changed completely, so as to stand at right angles to one another. The number of irregular ellipses or circles made within a given time differs much with different species. Thus with Brassica oleracea, Cerinthe major, and Cucurbita ovifera about four such figures were completed in 12 h.; whereas with Solanum palinacanthum and Opuntia basilaris, scarcely more than one. The figures likewise differ greatly in size; thus they were very small and in some degree doubtful in Stapelia,