PLANT MOVEMENT

Mimosa was named by Carl Linnaeus from the Spanish mimoso, meaning “sensitive.” It is a large genus native to the tropical regions of the world, most abundant in the American tropics. Mimosa sensitiva, from Brazil, was introduced to Europe in the seventeenth century as an object of wonder for its touch-sensitive leaves. Darwin’s grandfather Erasmus Darwin, the noted physician and poet, romanticized (and anthropomorphized) the sensitive plant in verse as a shy damsel in The Loves of the Plants: “Weak with nice sense, this chaste Mimosa stands / From each rude touch withdraws her timid hands;”95

Some forty years later, his grandson Charles saw it while on the Beagle voyage, as mentioned in a letter to Joseph Hooker: “By the way I well remember in Brazil walking through a great bed of Mimosa sensitiva and leaving a track as if an elephant had passed that way. The plant has interested me ever since.”96

M. pudica, easier to grow, became much more popular as a curiosity for its immediate shrinking response to shock or touch. Both species and many others have turgid pulvini that enable the leaves to retract and fold on themselves not only by touch, but at nightfall. “The whole appearance of many plants is wonderfully changed at night, as may be seen with Oxalis and still more plainly with Mimosa,” Darwin wrote in the concluding section of Movement.97 With the help of his son William, he tested M. pudica and M. albida for reactions to water and chemicals, though he did not publish those results. It was the circular (circumnutation) and nocturnal (nyctitropic) movement that most fascinated him, leading him to experiment on both cotyledons and mature plants, tracing the slow movement of stems and leaves, including the petioles, pinnae, and leaflets, on glass plates over many hours to illustrate their long, looping movements.

Mimosa pudica—This plant has been the subject of innumerable observations; but there are some points in relation to our subject which have not been sufficiently attended to. At night, as is well known, the opposite leaflets come into contact and point towards the apex of the leaf; they thus become neatly imbricated with their upper surfaces protected. The four pinnae also approach each other closely, and the whole leaf is thus rendered very compact. The main petiole sinks downwards during the day till late in the evening and rises until very early in the morning. The stem is continually circumnutating at a rapid rate, though not to a wide extent. Some very young plants, kept in darkness, were observed during two days, and although subjected to a rather low temperature of 57°–59° F., the stem of one described four small ellipses in the course of 12 h. We shall immediately see that the main petiole is likewise continually circumnutating, as is each separate pinna and each separate leaflet. Therefore, if the movement of the apex of any one leaflet were to be traced, the course described would be compounded of the movements of four separate parts.

A filament had been fixed on the previous evening, longitudinally to the main petiole of a nearly full-grown, highly-sensitive leaf (four inches in length), the stem having been secured to a stick at its base; and a tracing was made on a vertical glass in the hot-house under a high temperature. In the figure given, the first dot was made at 8.30 A.M. August 2nd, and the last at 7 P.M. on the 3rd. During 12 h. on the first day, the petiole moved thrice downwards and twice upwards. Within the same length of time on the second day, it moved five times downwards and four times upwards. As the ascending and descending lines do not coincide, the petiole manifestly circumnutates; the great evening fall and nocturnal rise being an exaggeration of one of the circumnutations. It should, however, be observed that the petiole fell much lower down in the evenings than could be seen on the vertical glass or is represented in the diagram. After 7 P.M. on the 3rd (when the last dot in [the figure] was made) the pot was carried into a bed-room, and the petiole was found at 12.50 A.M. (i.e. after midnight) standing almost upright, and much more highly inclined than it was at 10.40 P.M. When observed again at 4 A.M. it had begun to fall, and continued falling till 6.15 A.M., after which hour it zigzagged and again circumnutated. Similar observations were made on another petiole, with nearly the same result.

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Mimosa pudica: circumnutation and nyctitropic movement of main petiole [left] and circumnutation and nyctitropic movement of a leaflet (with pinna secured) {right}, traced on a vertical glass.

It has also been stated that each separate leaflet circumnutates. A pinna was cemented with shellac on the summit of a little stick driven firmly into the ground, immediately beneath a pair of leaflets, to the midribs of both of which excessively fine glass filaments were attached. This treatment did not injure the leaflets, for they went to sleep in the usual manner, and long retained their sensitiveness. the movements of one of them were traced during 49 h., as shown. On the first day, the leaflet sank down till 11.30 A.M., and then rose till late in the evening in a zigzag line, indicating circumnutation. On the second day, when more accustomed to its new state, it oscillated twice up and twice down during the 24 h. This plant was subjected to a rather low temperature, viz., 62°–64° F.; had it been kept warmer, no doubt the movements of the leaflet would have been much more rapid and complicated. It may be seen in the diagram that the ascending and descending lines do not coincide; but the large amount of lateral movement in the evening is the result of the leaflets bending towards the apex of the leaf when going to sleep.

Mimosa albida.—The leaves of this plant, one of which is here figured present some interesting peculiarities. It consists of a long petiole bearing only two pinnae (here represented as rather more divergent than is usual), each with two pairs of leaflets. But the inner basal leaflets are greatly reduced in size, owing probably to the want of space for their full development, so that they may be considered as almost rudimentary. They vary somewhat in size, and both occasionally disappear, or only one. Nevertheless, they are not in the least rudimentary in function, for they are sensitive, extremely heliotropic, circumnutate at nearly the same rate as the fully developed leaflets and assume when asleep exactly the same position. With M. pudica the inner leaflets at the base and between the pinnae are likewise much shortened and obliquely truncated; this fact was well seen in some seedlings of M. pudica, in which the third leaf above the cotyledons bore only two pinnae, each with only 3 or 4 pairs of leaflets, of which the inner basal one was less than half as long as its fellow; so that the whole leaf resembled pretty closely that of M. albida. In this latter species, the main petiole terminates in a little point, and on each side of this there is a pair of minute, flattened, lancet-shaped projections, hairy on their margins, which drop off and disappear soon after the leaf is fully developed. There can hardly be a doubt that these little projections are the last and fugacious representatives of an additional pair of leaflets to each pinna; for the outer one is twice as broad as the inner one, and a little longer.

When the leaves go to sleep, each leaflet twists half round, so as to present its edge to the zenith, and comes into close contact with its fellow. The pinnae also approach each other closely, so that the four terminal leaflets come together. The large basal leaflets (with the little rudimentary ones in contact with them) move inwards and forwards, so as to embrace the outside of the united terminal leaflets, and thus all eight leaflets (the rudimentary ones included) form together a single vertical packet. The two pinnae at the same time that they approach each other sink downwards, and thus instead of extending horizontally in the same line with the main petiole, as during the day, they depend at night at about 45°, or even at a greater angle, beneath the horizon.

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Mimosa albida: leaf seen from vertically above.

The torsion or rotation of leaves and leaflets, which occurs in so many cases, apparently always serves to bring their upper surfaces into close approximation with one another, or with other parts of the plant, for their mutual protection. We see this best in such cases as those of Arachis, Mimosa albida, and Marsilea, in which all the leaflets form together at night a single vertical packet. If with Mimosa pudica the opposite leaflets had merely moved upwards, their upper surfaces would have come into contact and been well protected; but as it is, they all successively move towards the apex of the leaf; and thus not only their upper surfaces are protected, but the successive pairs become imbricated and mutually protect one another as well as the petioles. This imbrication of the leaflets of sleeping plants is a common phenomenon.

Any one who had never observed continuously a sleeping plant, would naturally suppose that the leaves moved only in the evening when going to sleep, and in the morning when awaking; but he would be quite mistaken, for we have found no exception to the rule that leaves which sleep continue to move during the whole twenty-four hours; they move, however, more quickly when going to sleep and when awaking than at other times.

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Mitchella repens. Drawing by T. Boys for Conrad Loddiges, The Botanical Cabinet, Consisting of Colored Delineations of Plants.