The Power of Movement in Plants, Charles Darwin [the reading list book TXT] 📗

curled quite away from the glass; but ultimately both surmounted the glass and pursued their original course. The apex of a third thick stolon swept up the glass in a curved line, recoiled and again came into contact with it; it then moved to the right, and after ascending, descended vertically; ultimately it passed round one end of the glass instead of over it.

 

Many long pins were next driven rather close together into the sand, so as to form a crowd in front of the same two thin lateral branches; but these easily wound their way through the crowd. A thick stolon was much delayed in its passage; at one place it was forced to turn at right angles to its former course; at another place it could not pass through the pins, and the hinder part became bowed; it then curved upwards and passed through an opening between the upper part of some pins which happened to diverge; it then descended and finally emerged through the crowd. This stolon was rendered permanently sinuous to a slight degree, and was thicker where sinuous than elsewhere, apparently from its longitudinal growth having been checked.

 

Cotyledon umbilicus (Crassulaceae).—A plant growing in a pan [page 220]

of damp moss had emitted 2 stolons, 22 and 20 inches in length. One of these was supported, so that a length of 4 � inches projected in a straight and horizontal line, and the movement of the apex was traced. The first dot was made at 9.10 A.M.;

 

Fig. 89. Cotyledon umbilicus: circumnutation of stolon, traced from 11.15

A.M. Aug. 25th to 11 A.M. 27th. Plant illuminated from above. The terminal internode was .25 inch in length, the penultimate 2.25 and the third 3.0

inches in length. Apex of stolon stood at a distance of 5.75 inches from the vertical glass; but it was not possible to ascertain how much the tracing was magnified, as it was not known how great a length of the internode circumnutated.

 

the terminal portion soon began to bend downwards and continued to do so until noon. Therefore a straight line, very nearly as long as the whole figure here given (Fig. 89), was first traced on the glass; but the upper part of this line has not been copied in the diagram. The curvature occurred in the middle

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of the penultimate internode; and its chief seat was at the distance of 1

1/4 inch from the apex; it appeared due to the weight of the terminal portion, acting on the more flexible part of the internode, and not to geotropism. The apex after thus sinking down from 9.10 A.M. to noon, moved a little to the left; it then rose up and circumnutated in a nearly vertical plane until 10.35 P.M. On the following day (26th) it was ob-Fig. 90. Cotyledon umbilicus: circumnutation and downward movement of another stolon, traced on vertical glass, from 9.11 A.M. Aug. 25th to 11

A.M. 27th. Apex close to glass, so that figure but little magnified, and here reduced to two-thirds of original size.

 

served from 6.40 A.M. to 5.20 P.M., and within this time it moved twice up and twice down. On the morning of the 27th the apex stood as high as it did at 11.30 A.M. on the 25th. Nor did it sink down during the 28th, but continued to circumnutate about the same place.

 

Another stolon, which resembled the last in almost every [page 222]

respect, was observed during the same two days, but only two inches of the terminal portion was allowed to project freely and horizontally. On the 25th it continued from 9.10 A.M. to 1.30 P.M. to bend straight downwards, apparently owing to its weight (Fig. 90); but after this hour until 10.35

P.M. it zigzagged. This fact deserves notice, for we here probably see the combined effects of the bending down from weight and of circumnutation. The stolon, however, did not circumnutate when it first began to bend down, as may be observed in the present diagram, and as was still more evident in the last case, when a longer portion of the stolon was left unsupported. On the following day (26th) the stolon moved twice up and twice down, but still continued to fall; in the evening and during the night it travelled from some unknown cause in an oblique direction.]

 

We see from these three cases that stolons or runners circumnutate in a very complex manner. The lines generally extend in a vertical plane, and this may probably be attributed to the effect of the weight of the unsupported end of the stolon; but there is always some, and occasionally a considerable, amount of lateral movement. The circumnutation is so great in amplitude that it may almost be compared with that of climbing plants. That the stolons are thus aided in passing over obstacles and in winding between the stems of the surrounding plants, the observations above given render almost certain. If they had not circumnutated, their tips would have been liable to have been doubled up, as often as they met with obstacles in their path; but as it is, they easily avoid them. This must be a considerable advantage to the plant in spreading from its parent-stock; but we are far from supposing that the power has been gained by the stolons for this purpose, for circumnutation seems to be of universal occurrence with all growing parts; but it is not improbable that the amplitude of the movement may have been specially increased for this purpose.

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CIRCUMNUTATION OF FLOWER-STEMS.

 

We did not think it necessary to make any special observations on the circumnutation of flower-stems, these being axial in their nature, like stems or stolons; but some were incidentally made whilst attending to other subjects, and these we will here briefly give. A few observations have also been made by other botanists. These taken together suffice to render it probable that all peduncles and sub-peduncles circumnutate whilst growing.

 

[Oxalis carnosa.—The peduncle which springs from the thick and woody stem of this plant bears three or four sub-peduncles.

 

Fig. 91. Oxalis carnosa: flower-stem, feebly illuminated from above, its circumnutation traced from 9 A.M. April 13th to 9 A.M. 15th. Summit of flower 8 inches beneath the horizontal glass. Movement probably magnified about 6 times.

 

A filament with little triangles of paper was fixed within the calyx of a flower which stood upright. Its movements were observed for 48 h.; during the first half of this time the flower was fully expanded, and during the second half withered. The figure here given (Fig. 91) represents 8 or 9

ellipses. Although the main peduncle circumnutated, and described one large and

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two smaller ellipses in the course of 24 h., yet the chief seat of movement lies in the sub-peduncles, which ultimately bend vertically downwards, as will be described in a future chapter. The peduncles of Oxalis acetosella likewise bend downwards, and afterwards, when the pods are nearly mature, upwards; and this is effected by a circumnutating movement.

 

It may be seen in the above figure that the flower-stem of O. carnosa circumnutated during two days about the same spot. On the other hand, the flower-stem of O. sensitiva undergoes a strongly marked, daily, periodical change of position, when kept at a proper temperature. In the middle of the day it stands vertically up, or at a high angle; in the afternoon it sinks, and in the evening projects horizontally, or almost horizontally, rising again during the night. This movement continues from the period when the flowers are in bud to when, as we believe, the pods are mature: and it ought perhaps to have been included amongst the so-called sleep-movements of plants. A tracing was not made, but the angles were measured at successive periods during one whole day; and these showed that the movement was not continuous, but that the peduncle oscillated up and down. We may therefore conclude that it circumnutated. At the base of the peduncle there is a mass of small cells, forming a well-developed pulvinus, which is exteriorly coloured purple and hairy. In no other genus, as far as we know, is the peduncle furnished with a pulvinus. The peduncle of O. Ortegesii behaved differently from that of O. sensitiva, for it stood at a less angle above the horizon in the middle of the day, then in the morning or evening.

By 10.20 P.M. it had risen greatly. During the middle of the day it oscillated much up and down.

 

Trifolium subterraneum.—A filament was fixed vertically to the uppermost part of the peduncle of a young and upright flower-head (the stem of the plant having been secured to a stick); and its movements were traced during 36 h. Within this time it described (see Fig. 92) a figure which represents four ellipses; but during the latter part of the time the peduncle began to bend downwards, and after 10.30 P.M. on the 24th it curved so rapidly down, that by 6.45 A.M. on the 25th it stood only 19o above the horizon. It went on circumnutating in nearly the same position for two days. Even after the flower-heads have buried themselves in the ground they continue, as will hereafter be shown, to circumnutate. It will also be seen in the next chapter that the sub-peduncles of the separate flowers of [page 225]

Trifolium repens circumnutate in a complicated course during several days.

I may add that the gynophore of Arachis hypogoea, Fig. 92. Trifolium subterraneum: main flower-peduncle, illuminated from above, circumnutation traced on horizontal glass, from 8.40 A.M. July 23rd to 10.30 P.M. 24th.

 

which looks exactly like a peduncle, circumnutates whilst growing vertically downwards, in order to bury the young pod in the ground.

 

The movements of the flowers of Cyclamen Persicum were not observed; but the peduncle, whilst the pod is forming, increases much in length, and bows itself down by a circumnutating movement. A young peduncle of Maurandia semperflorens, 1 � inch in length, was carefully observed during a whole day, and it made 4 � narrow, vertical, irregular and short ellipses, each at an average rate of about 2 h. 25 m. An adjoining peduncle described during the same time similar, though fewer, ellipses.* According to Sachs**

the flower-stems, whilst growing,

 

* ‘The Movements and Habits of Climbing Plants,’ 2nd edit., 1875, p. 68.

 

** ‘Text-Book of Botany,’ 1875,

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p. 766. Linnaeus and Treviranus (according to Pfeffer, ‘Die Periodischen Bewegungen,’ etc., p. 162) state that the flower-stalks of many plants occupy different positions by night and day, and we shall see in the chapter on the Sleep of Plants that this implies circumnutation.

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of many plants, for instance, those of Brassica napus, revolve or circumnutate; those of Allium porrum bend from side to side, and, if this movement had been traced on a horizontal glass, no doubt ellipses would have been formed. Fritz M�ller has described* the spontaneous revolving movements of the flower-stems of an Alisma, which he compares with those of a climbing plant.

 

We made no observations on the movements of the different parts of flowers.

Morren, however, has observed** in the stamens of Sparmannia and Cereus a “fremissement spontan�,” which, it may be suspected, is a circumnutating movement. The circumnutation of the gynostemium of Stylidium, as described by Gad,*** is highly remarkable, and apparently aids in the fertilisation of the flowers. The gynostemium, whilst spontaneously moving, comes into contact with the viscid labellum, to which it adheres, until freed by the increasing tension of the parts or by being touched.]

 

We have now seen that the flower-stems of plants belonging to such widely different families as the Cruciferae, Oxalidae, Leguminosae, Primulaceae, Scrophularineae, Alismaceae, and Liliaceae, circumnutate; and that there are indications of this movement in many other families. With these