The Power of Movement in Plants · Charles Darwin
CHAPTER I. THE CIRCUMNUTATING MOVEMENTS OF SEEDLING PLANTS.
The movements of three rather old seedlings, about 1½ inch in height, shortly before the protrusion of the leaves, were first traced. They were illuminated exclusively from above; for, as will hereafter be shown, they are excessively sensitive to the action of light; and if any enters even temporarily on one side, they merely bend to this side in slightly zigzag lines. Of the three tracings one alone (Fig. 49) is here given. Had the observations been more frequent during the 12 h. two oval figures would have been described with their longer axes at right angles to one another. The actual amount of movement of the apex from side to side was about .3 of an inch. The figures described by the other two seedlings resembled to a certain extent the one here given. Fig. 49. Phalaris Canariensis: circumnutation of a cotyledon, with a mark placed below the apex, traced on a horizontal glass, from 8.35 A.M. Nov. 26th to 8.45 A.M. 27th. Movement of apex magnified 7 times, here reduced to one-half scale. A seedling which had just broken through the ground and projected only 1/20th of an inch above the surface, was next observed in the same manner as before. It was necessary to clear away the earth all round the seedling to a little depth in order to place a mark beneath the apex. The figure (Fig. 50) shows that the apex moved to one side, but changed its course ten times in the course of the ten hours of observation; so that there can be no doubt about its circumnutation. The cause of the general movement in one direction could hardly be attributed to the entrance of lateral light, as this was carefully guarded against; and we suppose it was in some manner connected with the removal of the earth round the little seedling.
Fig. 50. Phalaris Canariensis: circumnutation of a very young cotyledon, with a mark placed below the apex, traced on a horizontal glass, from 11.37 A.M. to 9.30 P.M. Dec. 13th. Movement of apex greatly magnified, here reduced to one-fourth of original scale. Lastly, the soil in the same pot was searched with the aid of a lens, and the white knife-like apex of a seedling was found on an exact level with that of the surrounding surface. The soil was removed all round the apex to the depth of a quarter of an inch, the seed itself remaining covered. The pot, protected from lateral light, was placed under the microscope with a micrometer eye-piece, so arranged that each division equalled 1/500th of an inch. After an interval of 30 m. the apex was observed, and it was seen to cross a little obliquely two divisions of the micrometer in 9 m. 15 s.; and after a few minutes it crossed the same space in 8 m. 50s. The seedling was again observed after an interval of three-quarters of an hour, and now the apex crossed rather obliquely two divisions in 10 m. We may therefore conclude that it was travelling at about the rate of 1/50th of an inch in 45 minutes. We may also conclude from these and the previous observations, that the seedlings of Phalaris in breaking through the surface of the soil circumnutate as much as the surrounding pressure will permit. This fact accounts (as in the case before given of the asparagus) for a circular, narrow, open space or crack being distinctly visible round several seedlings which had risen through very fine argillaceous sand, kept uniformly damp.
Fig. 51. Zea mays: circumnutation of cotyledon, traced on horizontal glass, from 8.30 A.M. Feb. 4th to 8 A.M. 6th. Movement of bead magnified on an average about 25 times. Zea mays (Gramineæ).—A glass filament was fixed obliquely to the summit of a cotyledon, rising .2 of an inch above the ground; but by the third morning it had grown to exactly thrice this height, so that the distance of the bead from the mark below was greatly increased, consequently the tracing (Fig. 51) was much more magnified on the first than on the second day. The upper part of the cotyledon changed its course by at least as much as a rectangle six times on each of the two days. The plant was illuminated by an obscure light from vertically above. This was a necessary precaution, as on the previous day we had traced the movements of cotyledons placed in a deep box, the inner side of which was feebly illuminated on one side from a distant north-east window, and at each observation by a wax taper held for a minute or two on the same side; and the result was that the cotyledons travelled all day long to this side, though making in their course some conspicuous flexures, from which fact alone we might have concluded that they were circumnutating; but we thought it advisable to make the tracing above given.
Radicles.—Glass filaments were fixed to two short radicles, placed so as to stand almost upright, and whilst bending downwards through geotropism their courses were strongly zigzag; from this latter circumstance circumnutation might have been inferred, had not their tips become slightly withered after the first 24 h., though they were watered and the air kept very damp. Nine radicles were next arranged in the manner formerly described, so that in growing downwards they left tracks on smoked glass-plates, inclined at various angles between 45° and 80° beneath the horizon. Almost every one of these tracks offered evidence in their greater or less breadth in different parts, or in little bridges of soot being left, that the apex had come alternately into more and less close contact with the glass. In the accompanying figure (Fig. 52) we have an accurate copy of one such track. In two instances alone (and in these the plates were highly inclined) there was some evidence of slight lateral movement. We presume therefore that the friction of the apex on the smoked surface, little as this could have been, sufficed to check the movement from side to side of these delicate radicles. Fig. 52. Zea mays: track left on inclined smoked glass-plate by tip of radicle in growing downwards.
Avena sativa (Gramineæ).—A cotyledon, 1½ inch in height, was placed in front of a north-east window, and the movement of the apex was traced on a horizontal glass during two days. It moved towards the light in a slightly zigzag line from 9 to 11.30 A.M. on October 15th; it then moved a little backwards and zigzagged much until 5 P.M., after which hour, and curing the night, it continued to move towards the window. On the following morning the same movement was continued in a nearly straight line until 12.40 P.M., when the sky remained until 2.35 extraordinarily dark from thunder-clouds. During this interval of 1 h. 55 m., whilst the light was obscure, it was interesting to observe how circumnutation overcame heliotropism, for the apex, instead of continuing to move towards the window in a slightly zigzag line, reversed its course four times, making two small narrow ellipses. A diagram of this case will be given in the chapter on Heliotropism. A filament was next fixed to a cotyledon only 1/4 of an inch in height, which was illuminated exclusively from above, and as it was kept in a warm greenhouse, it grew rapidly; and now there could be no doubt about its circumnutation, for it described a figure of 8 as well as two small ellipses in 5½ hours.
Nephrodium molle (Filices).—A seedling fern of this species came up by chance in a flowerpot near its parent. The frond, as yet only slightly lobed, was only .16 of an inch in length and .2 in breadth, and was supported on a rachis as fine as a hair and .23 of an inch in height. A very thin glass filament, which projected for a length of .36 of an inch, was fixed to the end of the frond. The movement was so highly magnified that the figure (Fig. 53) cannot be fully trusted; but the frond was constantly moving in a complex manner, and the bead greatly changed its course eighteen times in the 12 hours of observation. Within half an hour it often returned in a line almost parallel to its former course. The greatest amount of movement occurred between 4 and 6 P.M. The circumnutation of this plant is interesting, because the species in the genus Lygodium are well known to circumnutate conspicuously and to twine round any neighbouring object. Fig. 53. Nephrodium molle: circumnutation of very young frond, traced in darkness on horizontal glass, from 9 A.M. to 9 P.M. Oct. 30th. Movement of bead magnified 48 times. Selaginella Kraussii (?) (Lycopodiaceæ).—A very young plant, only .4 of an inch in height, had sprung up in a pot in the hot-house. An extremely fine glass filament was fixed to the end of the frond-like stem, and the movement of the bead traced on a horizontal glass. It changed its course several times, as shown in Fig. 54, whilst observed during 13 h. 15 m., and returned at night to a point not far distant from that whence it had started in the morning. There can be no doubt that this little plant circumnutated.
Fig. 54. Selaginella Kraussii (?): circumnutation of young plant, kept in darkness, traced from 8.45 A.M. to 10 P.M. Oct. 31st. CHAPTER II. GENERAL CONSIDERATIONS ON THE MOVEMENTS AND GROWTH OF SEEDLING PLANTS. Generality of the circumnutating movement—Radicles, their circumnutation of service—Manner in which they penetrate the ground—Manner in which hypocotyls and other organs break through the ground by being arched—Singular manner of germination in Megarrhiza, etc.—Abortion of cotyledons—Circumnutation of hypocotyls and epicotyls whilst still buried and arched—Their power of straightening themselves—Bursting of the seed-coats—Inherited effect of the arching process in hypogean hypocotyls—Circumnutation of hypocotyls and epicotyls when erect—Circumnutation of cotyledons—Pulvini or joints of cotyledons, duration of their activity, rudimentary in Oxalis corniculata, their development—Sensitiveness of cotyledons to light and consequent disturbance of their periodic movements—Sensitiveness of cotyledons to contact. The circumnutating movements of the several parts or organs of a considerable number of seedling plants have been described in the last chapter. A list is here appended of the Families, Cohorts, Sub-classes, etc., to which they belong, arranged and numbered according to the classification adopted by Hooker.[1] Any one who will consider this list will see that the young plants selected for observation, fairly represent the whole vegetable series excepting the lowest cryptogams, and the movements of some of the latter when mature will hereafter be described. As all the seedlings which were observed, including Conifers, Cycads and Ferns, which belong to the most ancient types amongst plants, were continually circumnutating, we may infer that this kind of movement is common to every seedling species.
Radicles.—In all the germinating seeds observed by us, the first change is the protrusion of the radicle, which immediately bends downwards and endeavours to penetrate the ground. In order to effect this, it is almost necessary that the seed should be pressed down so as to offer some resistance, unless indeed the soil is extremely loose; for otherwise the seed is lifted up, instead of the radicle penetrating the surface. But seeds often get covered by earth thrown up by burrowing quadrupeds or scratching birds, by the castings of earth-worms, by heaps of excrement, the decaying branches of trees, etc., and will thus be pressed down; and they must often fall into cracks when the ground is dry, or into holes. Even with seeds lying on the bare surface, the first developed root-hairs, by becoming attached to stones or other objects on the surface, are able to hold down the upper part of the radicle, whilst the tip penetrates the ground. Sachs has shown[2] how well and closely root-hairs adapt themselves by growth to the most irregular particles in the soil, and become firmly attached to them. This attachment seems to be effected by the softening or liquefaction of the outer surface of the wall of the hair and its subsequent consolidation, as will be on some future occasion more fully described. This intimate union plays an important part, according to Sachs, in the absorption of water and of the inorganic matter dissolved in it. The mechanical aid afforded by the root-hairs in penetrating the ground is probably only a secondary service.
Nevertheless, when young radicles of _Phaseolus multiflorus_ were fixed vertically close over damp sand, in the expectation that as soon as they reached it they would form circular furrows, this did not occur,—a fact which may be accounted for, as we believe, by the furrow being filled up as soon as formed by the rapid increase of thickness in the apex of the radicle. Whether or not a radicle, when surrounded by softened earth, is aided in forming a passage for itself by circumnutating, this movement can hardly fail to be of high importance, by guiding the radicle along a line of least resistance, as will be seen in the next chapter when we treat of the sensibility of the tip to contact. If, however, a radicle in its downward growth breaks obliquely into any crevice, or a hole left by a decayed root, or one made by the larva of an insect, and more especially by worms, the circumnutating movement of the tip will materially aid it in following such open passage; and we have observed that roots commonly run down the old burrows of worms.[4] [4] See, also, Prof. Hensen’s statements (‘Zeitschrift für Wissen, Zool.,’ B. xxviii. p. 354, 1877) to the same effect. He goes so far as to believe that roots are able to penetrate the ground to a great depth only by means of the burrows made by worms.
When a radicle is placed in a horizontal or inclined position, the terminal growing part, as is well known, bends down towards the centre of the earth; and Sachs[5] has shown that whilst thus bending, the growth of the lower surface is greatly retarded, whilst that of the upper surface continues at the normal rate, or may be even somewhat increased. He has further shown by attaching a thread, running over a pulley, to a horizontal radicle of large size, namely that of the common bean, that it was able to pull up a weight of only one gramme, or 15.4 grains. We may therefore conclude that geotropism does not give a radicle force sufficient to penetrate the ground, but merely tells it (if such an expression may be used) which course to pursue. Before we knew of Sachs’ more precise observations we covered a flat surface of damp sand with the thinnest tin-foil which we could procure (.02 to .03 mm., or .00012 to .00079 of an inch in thickness), and placed a radicle close above, in such a position that it grew almost perpendicularly downwards. When the apex came into contact with the polished level surface it turned at right angles and glided over it without leaving any impression; yet the tin-foil was so flexible, that a little stick of soft wood, pointed to the same degree as the end of the radicle and gently loaded with a weight of only a quarter of an ounce (120 grains) plainly indented the tin-foil.
Fig. 55. Outline of piece of stick (reduced to one-half natural size) with a hole through which the radicle of a bean grew. Thickness of stick at narrow end .08 inch, at broad end .16; depth of hole .1 inch. We succeeded better in ascertaining the force exerted transversely by these radicles. Two were so placed as to penetrate small holes made in little sticks, one of which was cut into the shape here exactly copied (Fig. 55). The short end of the stick beyond the hole was purposely split, but not the opposite end. As the wood was highly elastic, the split or fissure closed immediately after being made. After six days the stick and bean were dug out of the damp sand, and the radicle was found to be much enlarged above and beneath the hole. The fissure which was at first quite closed, was now open to a width of 4 mm.; as soon as the radicle was extracted, it immediately closed to a width of 2 mm. The stick was then suspended horizontally by a fine wire passing through the hole lately filled by the radicle, and a little saucer was suspended beneath to receive the weights; and it required 8 lbs. 8 ozs. to open the fissure to the width of 4 mm.—that is, the width before the root was extracted. But the part of the radicle (only .1 of an inch in length) which was embedded in the hole, probably exerted a greater transverse strain even than 8 lbs. 8 ozs., for it had split the solid wood for a length of rather more than a quarter of an inch (exactly .275 inch), and this fissure is shown in Fig. 55. A second stick was tried in the same manner with almost exactly the same result.
Fig. 56. Wooden pincers, kept closed by a spiral brass spring, with a hole (.14 inch in diameter and .6 inch in depth) bored through the narrow closed part, through which a radicle of a bean was allowed to grow. Temp. 50°–60° F. We then followed a better plan. Holes were bored near the narrow end of two wooden clips or pincers (Fig. 56), kept closed by brass spiral springs. Two radicles in damp sand were allowed to grow through these holes. The pincers rested on glass-plates to lessen the friction from the sand. The holes were a little larger (viz..14 inch) and considerably deeper (viz..6 inch) than in the trials with the sticks; so that a greater length of a rather thicker radicle exerted a transverse strain. After 13 days they were taken up. The distance of two dots (see the figure) on the longer ends of the pincers was now carefully measured; the radicles were then extracted from the holes, and the pincers of course closed. They were then suspended horizontally in the same manner as were the bits of sticks, and a weight of 1500 grams (or 3 pounds 4 ounces) was necessary with one of the pincers to open them to the same extent as had been effected by the transverse growth of the radicle. As soon as this radicle had slightly opened the pincers, it had grown into a flattened form and had escaped a little beyond the hole; its diameter in one direction being 4.2 mm., and at rightangles 3.5 mm. If this escape and flattening could have been prevented, the radicle would probably have exerted a greater strain than the 3 pounds 4 ounces. With the other pincers the radicle escaped still further out of the hole; and the weight required to open them to the same extent as had been effected by the radicle, was only 600 grams.
With these facts before us, there seems little difficulty in understanding how a radicle penetrates the ground. The apex is pointed and is protected by the root-cap; the terminal growing part is rigid, and increases in length with a force equal, as far as our observations can be trusted, to the pressure of at least a quarter of a pound, probably with a much greater force when prevented from bending to any side by the surrounding earth. Whilst thus increasing in length it increases in thickness, pushing away the damp earth on all sides, with a force of above 8 pounds in one case, of 3 pounds in another case. It was impossible to decide whether the actual apex exerts, relatively to its diameter, the same transverse strain as the parts a little higher up; but there seems no reason to doubt that this would be the case. The growing part therefore does not act like a nail when hammered into a board, but more like a wedge of wood, which whilst slowly driven into a crevice continually expands at the same time by the absorption of water; and a wedge thus acting will split even a mass of rock.
Manner in which Hypocotyls, Epicotyls, etc., rise up and break through the ground.—After the radicle has penetrated the ground and fixed the seed, the hypocotyls of all the dicotyledonous seedlings observed by us, which lift their cotyledons above the surface, break through the ground in the form of an arch. When the cotyledons are hypogean, that is, remain buried in the soil, the hypocotyl is hardly developed, and the epicotyl or plumule rises in like manner as an arch through the ground. In all, or at least in most of such cases, the downwardly bent apex remains for a time enclosed within the seed-coats. With Corylus avellena the cotyledons are hypogean, and the epicotyl is arched; but in the particular case described in the last chapter its apex had been injured, and it grew laterally through the soil like a root; and in consequence of this it had emitted two secondary shoots, which likewise broke through the ground as arches. Cyclamen does not produce any distinct stem, and only a single cotyledon appears at first;[6] its petiole breaks through the ground as an arch (Fig. 57). Abronia has only a single fully developed cotyledon, but in this case it is the hypocotyl which first emerges and is arched. Abronia umbellata, however, presents this peculiarity, that the enfolded blade of the one developed cotyledon (with the enclosed endosperm) whilst still beneath the surface has its apex upturned and parallel to the descending leg of the arched hypocotyl; but it is dragged out of the ground by the continued growth of the hypocotyl, with the apex pointing downward. With Cycas pectinata the cotyledons are hypogean, and a true leaf first breaks through the ground with its petiole forming an arch.
We can see how this inequality of development and the arching of the petiole could have been gradually acquired, if they were beneficial to the seedlings by favouring their emergence; for with A. candelabrum, spinosus, and latifolius there was a great variability in the inequality between the two first leaves and in the arching of their petioles. In one seedling of A. candelabrum the first leaf was arched and nine times as long as the second, which latter consisted of a mere little, yellowish-white, straight, hairy style. In other seedlings the difference in length between the two leaves was as 3 to 2, or as 4 to 3, or as only .76 to .62 inch. In these latter cases the first and taller leaf was not properly arched. Lastly, in another seedling there was not the least difference in size between the two first leaves, and both of them had their petioles straight; their laminae were enfolded and pressed against each other, forming a lance or wedge, by which means they had broken through the ground. Therefore in different individuals of this same species of Acanthus the first pair of leaves breaks through the ground by two widely different methods; and if either had proved decidedly advantageous or disadvantageous, one of them no doubt would soon have prevailed. Asa Gray has described[7] the peculiar manner of germination of three widely different plants, in which the hypocotyl is hardly at all developed. These were therefore observed by us in relation to our present subject.
Megarrhiza Californica.—The cotyledons of this Gourd never free themselves from the seed-coats and are hypogean. Their petioles are completely confluent, forming a tube which terminates downwards in a little solid point, consisting of a minute radicle and hypocotyl, with the likewise minute plumule enclosed within the base of the tube. This structure was well exhibited in an abnormal specimen, in which one of the two cotyledons failed to produce a petiole, whilst the other produced one consisting of an open semicylinder ending in a sharp point, formed of the parts just described. As soon as the confluent petioles protrude from the seed they bend down, as they are strongly geotropic, and penetrate the ground. The seed itself retains its original position, either on the surface or buried at some depth, as the case may be. If, however, the point of the confluent petioles meets with some obstacle in the soil, as appears to have occurred with the seedlings described and figured by Asa Gray,[8] the cotyledons are lifted up above the ground. The petioles are clothed with root-hairs like those on a true radicle, and they likewise resemble radicles in becoming brown when immersed in a solution of permanganate of potassium.
Text from Project Gutenberg, public domain in the United States.