Chapter VII (2)

Melilotus (Tribe 3).—The species in this genus sleep in a remarkable manner. The three leaflets of each leaf twist through an angle of 90°, so that their blades stand vertically at night with one lateral edge presented to the zenith (Fig. 140). We shall best understand the other and more complicated movements, if we imagine ourselves always to hold the leaf with the tip of the terminal leaflet pointed to the north. The leaflets in becoming vertical at night could of course twist so that their upper surfaces should face to either side; but the two lateral leaflets always twist so that this surface tends to face the north, but as they move at the same time towards the terminal leaflet, the upper surface of the one faces about N.N.W., and that of the other N.N.E. The terminal leaflet behaves differently, for it twists to either side, the upper surface facing sometimes east and sometimes west, but rather more commonly west than east. The terminal leaflet also moves in another and more remarkable manner, for whilst its blade is twisting and becoming vertical, the whole leaflet bends to one side, and invariably to the side towards which the upper surface is directed; so that if this surface faces the west the whole leaflet bends to the west, until it comes into contact with the upper and vertical surface of the western lateral leaflet. Thus the upper surface of the terminal and of one of the two lateral leaflets is well protected.

The fact of the terminal leaflet twisting indifferently to either side and afterwards bending to the same side, seemed to us so remarkable, that we endeavoured to discover the cause. We imagined that at the commencement of the movement it might be determined by one of the two halves of the leaflet being a little heavier than the other. Therefore bits of wood were gummed on one side of several leaflets, but this produced no effect; and they continued to twist in the same direction as they had previously done. In order to discover whether the same leaflet twisted permanently in the same direction, black threads were tied to 20 leaves, the terminal leaflets of which twisted so that their upper surfaces faced west, and 14 white threads to leaflets which twisted to the east. These were observed occasionally during 14 days, and they all continued, with a single exception, to twist and bend in the same direction; for one leaflet, which had originally faced east, was observed after 9 days to face west. The seat of both the twisting and bending movement is in the pulvinus of the sub-petioles.

Fig. 140. Melilotus officinalis: A, leaf during the daytime. B, another leaf asleep. C, a leaf asleep as viewed from vertically above; but in this case the terminal leaflet did not happen to be in such close contact with the lateral one, as is usual.

We believe that the leaflets, especially the two lateral ones, in performing the above described complicated movements generally bend a little downwards; but we are not sure of this, for, as far as the main petiole is concerned, its nocturnal movement is largely determined by the position which the leaf happens to occupy during the day. Thus one main petiole was observed to rise at night 59°, whilst three others rose only 7° and 9°. The petioles and sub-petioles are continually circumnutating during the whole 24 h., as we shall presently see.

The leaves of the following 15 species, M. officinalis, suaveolens, parviflora, alba, infesta, dentata, gracilis, sulcata, elegans, coerulea, petitpierreana, macrorrhiza, Italica, secundiflora, and Taurica, sleep in nearly the same manner as just described; but the bending to one side of the terminal leaflet is apt to fail unless the plants are growing vigorously. With M. petitpierreana and secundiflora the terminal leaflet was rarely seen to bend to one side. In young plants of M. Italica it bent in the usual manner, but with old plants in full flower, growing in the same pot and observed at the same hour, viz., 8.30 P.M., none of the terminal leaflets on several scores of leaves had bent to one side, though they stood vertically; nor had the two lateral leaflets, though standing vertically, moved towards the terminal one. At 10.30 P.M., and again one hour after midnight, the terminal leaflets had become very slightly bent to one side, and the lateral leaflets had moved a very little towards the terminal one, so that the position of the leaflets even at this late hour was far from the ordinary one. Again, with M. Taurica the terminal leaflets were never seen to bend towards either of the two lateral leaflets, though these, whilst becoming vertical, had bent towards the terminal one. The sub-petiole of the terminal leaflet in this species is of unusual length, and if the leaflet had bent to one side, its upper surface could have come into contact only with the apex of either lateral leaflet; and this, perhaps, is the meaning of the loss of the lateral movement.

The cotyledons do not sleep at night. the first leaf consists of a single orbicular leaflet, which twists at night so that the blade stands vertically. It is a remarkable fact that with M. Taurica, and in a somewhat less degree with M. macrorrhiza and petitpierreana, all the many small and young leaves produced during the early spring from shoots on some cut-down plants in the greenhouse, slept in a totally different manner from the normal one; for the three leaflets, instead of twisting on their own axes so as to present their lateral edges to the zenith, turned upwards and stood vertically with their apices pointing to the zenith. They thus assumed nearly the same position as in the allied genus Trifolium; and on the same principle that embryological characters reveal the lines of descent in the animal kingdom, so the movements of the small leaves in the above three species of Melilotus, perhaps indicate that this genus is descended from a form which was closely allied to and slept like a Trifolium. Moreover, there is one species, M. messanensis, the leaves of which, on full-grown plants between 2 and 3 feet in height, sleep like the foregoing small leaves and like those of a Trifolium. We were so much surprised at this latter case that, until the flowers and fruit were examined, we thought that the seeds of some Trifolium had been sown by mistake instead of those of a Melilotus. It appears therefore probable that M. messanensis has either retained or recovered a primordial habit.

The circumnutation of a leaf of M. officinalis was traced, the stem being left free; and the apex of the terminal leaflet described three laterally extended ellipses, between 8 A.M. and 4 P.M.; after the latter hour the nocturnal twisting movement commenced. It was afterwards ascertained that the above movement was compounded of the circumnutation of the stem on a small scale, of the main petiole which moved most, and of the sub-petiole of the terminal leaflet. The main petiole of a leaf having been secured to a stick, close to the base of the sub-petiole of the terminal leaflet, the latter described two small ellipses between 10.30 A.M., and 2 P.M. At 7.15 P.M., after this same leaflet (as well as another) had twisted themselves into their vertical nocturnal position, they began to rise slowly, and continued to do so until 10.35 P.M., after which hour they were no longer observed.

As M. messanensis sleeps in an anomalous manner, unlike that of any other species in the genus, the circumnutation of a terminal leaflet, with the stem secured, was traced during two days. On each morning the leaflet fell, until about noon, and then began to rise very slowly; but on the first day the rising movement was interrupted between 1 and 3 P.M. by the formation of a laterally extended ellipse, and on the second day, at the same time, by two smaller ellipses. The rising movement then recommenced, and became rapid late in the evening, when the leaflet was beginning to go to sleep. The awaking or sinking movement had already commenced by 6.45 A.M. on both mornings.

Trifolium (Tribe 3).—The nyctitropic movements of 11 species were observed, and were found to be closely similar. If we select a leaf of T. repens having an upright petiole, and with the three leaflets expanded horizontally, the two lateral leaflets will be seen in the evening to twist and approach each other, until their upper surfaces come into contact. At the same time they bend downwards in a plane at right angles to that of their former position, until their midribs form an angle of about 45° with the upper part of the petiole. This peculiar change of position requires a considerable amount of torsion in the pulvinus. The terminal leaflet merely rises up without any twisting and bends over until it rests on and forms a roof over the edges of the now vertical and united lateral leaflets. Thus the terminal leaflet always passes through an angle of at least 90°, generally of 130° or 140°, and not rarely—as was often observed with T. subterraneum—of 180°. In this latter case the terminal leaflet stands at night horizontally (as in Fig. 141), with its lower surface fully exposed to the zenith. Besides the difference in the angles, at which the terminal leaflets stand at night in the individuals of the same species, the degree to which the lateral leaflets approach each other often likewise differs.

Fig. 141. Trifolium repens: A, leaf during the day; B, leaf asleep at night.

We have seen that the cotyledons of some species and not of others rise up vertically at night. The first true leaf is generally unifoliate and orbicular; it always rises, and either stands vertically at night or more commonly bends a little over so as to expose the lower surface obliquely to the zenith, in the same manner as does the terminal leaflet of the mature leaf. But it does not twist itself like the corresponding first simple leaf of Melilotus. With T. Pannonicum the first true leaf was generally unifoliate, but sometimes trifoliate, or again partially lobed and in an intermediate condition.

Circumnutation.—Sachs described in 1863[10] the spontaneous up and down movements of the leaflets of T. incarnatum, when kept in darkness. Pfeffer made many observations on the similar movements in T. pratense.[11] He states that the terminal leaflet of this species, observed at different times, passed through angles of from 30° to 120° in the course of from 1½ to 4 h. We observed the movements of T. subterraneum, resupinatum, and repens.

[10] ‘Flora,’ 1863, p. 497.

[11] ‘Die Period. Bewegungen,’ 1875, pp. 35, 52.

Trifolium subterraneum.—A petiole was secured close to the base of the three leaflets, and the movement of the terminal leaflet was traced during 26½ h., as shown in the figure on the next page.

Between 6.45 A.M. and 6 P.M. the apex moved 3 times up and 3 times down, completing 3 ellipses in 11 h. 15 m. The ascending and descending lines stand nearer to one another than is usual with most plants, yet there was some lateral motion. At 6 P.M. the great nocturnal rise commenced, and on the next morning the sinking of the leaflet was continued until 8.30 A.M., after which hour it circumnutated in the manner just described. In the figure the great nocturnal rise and the morning fall are greatly abbreviated, from the want of space, and are merely represented by a short curved line. The leaflet stood horizontally when at a point a little beneath the middle of the diagram; so that during the daytime it oscillated almost equally above and beneath a horizontal position. At 8.30 A.M. it stood 48° beneath the horizon, and by 11.30 A.M. it had risen 50° above the horizon; so that it passed through 98° in 3 h. By the aid of the tracing we ascertained that the distance travelled in the 3 h. by the apex of this leaflet was 1.03 inch. If we look at the figure, and prolong upwards in our mind’s eye the short curved broken line, which represents the nocturnal course, we see that the latter movement is merely an exaggeration or prolongation of one of the diurnal ellipses. The same leaflet had been observed on the previous day, and the course then pursued was almost identically the same as that here described.

Fig. 142. Trifolium subterraneum: circumnutation and nyctitropic movement of terminal leaflet (.68 inch in length), traced from 6.45 A.M. July 4th to 9.15 A.M. 5th. Apex of leaf 3 7/8 inches from the vertical glass, and movement, as here shown, magnified 5 1/4 times, reduced to one-half of original scale. Plant illuminated from above; temp. 16°–17° C.

Trifolium resupinatum.—A plant left entirely free was placed before a north-east window, in such a position that a terminal leaflet projected at right angles to the source of the light, the sky being uniformly clouded all day. The movements of this leaflet were traced during two days, and on both were closely similar. Those executed on the second day are shown in Fig. 143. The obliquity of the several lines is due partly to the manner in which the leaflet was viewed, and partly to its having moved a little towards the light. From 7.50 A.M. to 8.40 A.M. the leaflet fell, that is, the awakening movement was continued. It then rose and moved a little laterally towards the light. At 12.30 it retrograded, and at 2.30 resumed its original course, having thus completed a small ellipse during the middle of the day. In the evening it rose rapidly, and by 8 A.M. on the following morning had returned to exactly the same spot as on the previous morning. The line representing the nocturnal course ought to be extended much higher up, and is here abbreviated into a short, curved, broken line. The terminal leaflet, therefore, of this species described during the daytime only a single additional ellipse, instead of two additional ones, as in the case of T. subterraneum. But we should remember that it was shown in the fourth chapter that the stem circumnutates, as no doubt does the main petiole and the sub-petioles; so that the movement represented in Fig. 143 is a compounded one. We tried to observe the movements of a leaf kept during the day in darkness, but it began to go to sleep after 2 h. 15 m., and this was well pronounced after 4 h. 30 m.

Fig 143. Trifolium resupinatum: circumnutation and nyctitropic movements of the terminal leaflet during 24 hours.

Trifolium repens.—A stem was secured close to the base of a moderately old leaf, and the movement of the terminal leaflet was observed during two days. This case is interesting solely from the simplicity of the movements, in contrast with those of the two preceding species. On the first day the leaflet fell between 8 A.M. and 3 P.M., and on the second between 7 A.M. and 1 P.M. On both days the descending course was somewhat zigzag, and this evidently represents the circumnutating movement of the two previous species during the middle of the day. After 1 P.M., Oct. 1st (Fig. 144), the leaflet began to rise, but the movement was slow on both days, both before and after this hour, until 4 P.M. The rapid evening and nocturnal rise then commenced. Thus in this species the course during 24 h. consists of a single great ellipse; in T. resupinatum of two ellipses, one of which includes the nocturnal movement and is much elongated; and in T. subterraneum of three ellipses, of which the nocturnal one is likewise of great length.

Securigera coronilla (Tribe 4).—The leaflets, which stand opposite one another and are numerous, rise up at night, come into close contact, and bend backwards at a moderate angle towards the base of the petiole.

Fig. 144. Trifolium repens: circumnutation and nyctitropic movements of a nearly full-grown terminal leaflet, traced on a vertical glass from 7 A.M. Sept. 30th to 8 A.M. Oct. 1st. Nocturnal course, represented by curved broken line, much abbreviated.

Lotus (Tribe 4).—The nyctitropic movements of 10 species in this genus were observed, and found to be the same. The main petiole rises a little at night, and the three leaflets rise till they become vertical, and at the same time approach each other. This was conspicuous with L. Jacoboeus, in which the leaflets are almost linear. In most of the species the leaflets rise so much as to press against the stem, and not rarely they become inclined a little inwards with their lower surfaces exposed obliquely to the zenith. This was clearly the case with L. major, as its petioles are unusually long, and the leaflets are thus enabled to bend further inwards. The young leaves on the summits of the stems close up at night so much, as often to resemble large buds. The stipule-like leaflets, which are often of large size, rise up like the other leaflets, and press against the stem (Fig. 145). All the leaflets of L. Gebelii, and probably of the other species, are provided at their bases with distinct pulvini, of a yellowish colour, and formed of very small cells. The circumnutation of a terminal leaflet of L. peregrinus (with the stem secured) was traced during two days, but the movement was so simple that it is not worth while to give the diagram. The leaflet fell slowly from the early morning till about 1 P.M. It then rose gradually at first, but rapidly late in the evening. It occasionally stood still for about 20 m. during the day, and sometimes zigzagged a little. The movement of one of the basal, stipule-like leaflets was likewise traced in the same manner and at the same time, and its course was closely similar to that of the terminal leaflet.

Fig. 145. Lotus Creticus: A, stem with leaves awake during the day; B, with leaves asleep at night. SS, stipule-like leaflets.

In Tribe 5 of Bentham and Hooker, the sleep-movements of species in 12 genera have been observed by ourselves and others, but only in Robinia with any care. Psoralea acaulis raises its three leaflets at night; whilst Amorpha fruticosa,[12] Dalea alopecuroides, and Indigofera tinctoria depress them. Ducharte[13] states that Tephrosia caribaea is the sole example of “folioles couchées le long du pétiole et vers la base;” but a similar movement occurs, as we have already seen, and shall again see in other cases. Wistaria Sinensis, according to Royer,[14] “abaisse les folioles qui par une disposition bizarre sont inclinées dans la même feuille, les supérieures vers le sommet, les inférieures vers la base du petiole commun;” but the leaflets on a young plant observed by us in the greenhouse merely sank vertically downwards at night. The leaflets are raised in Sphaerophysa salsola, Colutea arborea, and Astragalus uliginosus, but are depressed, according to Linnæus, in Glycyrrhiza. The leaflets of Robinia pseudo-acacia likewise sink vertically down at night, but the petioles rise a little, viz., in one case 3°, and in another 4°. The circumnutating movements of a terminal leaflet on a rather old leaf were traced during two days, and were simple. The leaflet fell slowly, in a slightly zigzag line, from 8 A.M. to 5 P.M., and then more rapidly; by 7 A.M. on the following morning it had risen to its diurnal position. There was only one peculiarity in the movement, namely, that on both days there was a distinct though small oscillation up and down between 8.30 and 10 A.M., and this would probably have been more strongly pronounced if the leaf had been younger.

[12] Ducharte, ‘Eléments de Botanique’, 1867, p. 349.

[13] Ibid., p. 347.

[14] ‘Ann. des Sciences Nats. Bot.’ (5th series), ix. 1868.

Coronilla rosea (Tribe 6).—the leaves bear 9 or 10 pairs of opposite leaflets, which during the day stand horizontally, with their midribs at right angles to the petiole. At night they rise up so that the opposite leaflets come nearly into contact, and those on the younger leaves into close contact. At the same time they bend back towards the base of the petiole, until their midribs form with it angles of from 40° to 50° in a vertical plane, as here figured (Fig. 146). The leaflets, however, sometimes bend so much back that their midribs become parallel to and lie on the petiole. They thus occupy a reversed position to what they do in several Leguminosae, for instance, in Mimosa pudica; but, from standing further apart, they do not overlap one another nearly so much as in this latter plant. The main petiole is curved slightly downwards during the day, but straightens itself at night. In three cases it rose from 3° above the horizon at noon, to 9° at 10 P.M.; from 11° to 33°; and from 5° to 33°—the amount of angular movement in this latter case amounting to 28°. In several other species of Coronilla the leaflets showed only feeble movements of a similar kind.

Fig. 146. Coronilla rosea: leaf asleep.

Hedysarum coronarium (Tribe 6).—The small lateral leaflets on plants growing out of doors rose up vertically at night, but the large terminal one became only moderately inclined. The petioles apparently did not rise at all.

Smithia Pfundii (Tribe 6).—The leaflets rise up vertically, and the main petiole also rises considerably.

Arachis hypogoea (Tribe 6).—The shape of a leaf, with its two pairs of leaflets, is shown at A (Fig. 147); and a leaf asleep, traced from a photograph (made by the aid of aluminium light), is given at B. The two terminal leaflets twist round at night until their blades stand vertically, and approach each other until they meet, at the same time moving a little upwards and backwards. The two lateral leaflets meet each other in this same manner, but move to a greater extent forwards, that is, in a contrary direction to the two terminal leaflets, which they partially embrace. Thus all four leaflets form together a single packet, with their edges directed to the zenith, and with their lower surfaces turned outwards. On a plant which was not growing vigorously the closed leaflets seemed too heavy for the petioles to support them in a vertical position, so that each night the main petiole became twisted, and all the packets were extended horizontally, with the lower surfaces of the leaflets on one side directed to the zenith in a most anomalous manner. This fact is mentioned solely as a caution, as it surprised us greatly, until we discovered that it was an anomaly. The petioles are inclined upwards during the day, but sink at night, so as to stand at about right angles with the stem. The amount of sinking was measured only on one occasion, and found to be 39°. A petiole was secured to a stick at the base of the two terminal leaflets, and the circumnutating movement of one of these leaflets was traced from 6.40 A.M. to 10.40 P.M., the plant being illuminated from above. The temperature was 17°–17½° C., and therefore rather too low. During the 16 h. the leaflet moved thrice up and thrice down, and as the ascending and descending lines did not coincide, three ellipses were formed.

Fig. 147. Arachis hypogoea: A, leaf during the day, seen from vertically above; B, leaf asleep, seen laterally, copied from a photograph. Figures much reduced.

Fig. 148. Desmodium gyrans: leaf seen from above, reduced to one-half natural size. The minute stipules unusually large.

Desmodium gyrans (Tribe 6).—A large and full-grown leaf of this plant, so famous for the spontaneous movements of the two little lateral leaflets, is here represented (Fig. 148). The large terminal leaflet sleeps by sinking vertically down, whilst the petiole rises up. The cotyledons do not sleep, but the first-formed leaf sleeps equally well as the older ones. The appearance presented by a sleeping branch and one in the day-time, copied from two photographs, are shown at A and B (Fig. 149), and we see how at night the leaves are crowded together, as if for mutual protection, by the rising of the petioles. The petioles of the younger leaves near the summits of the shoots rise up at night, so as to stand vertical and parallel to the stem; whilst those on the sides were found in four cases to have risen respectively 46½°, 36°, 20°, and 19.5° above the inclined positions which they had occupied during the day. For instance, in the first of these four cases the petiole stood in the day at 23°, and at night at 69½° above the horizon. In the evening the rising of the petioles is almost completed before the leaflets sink perpendicularly downwards.

Circumnutation.—The circumnutating movements of four young shoots were observed during 5 h. 15 m.; and in this time each completed an oval figure of small size. The main petiole also circumnutates rapidly, for in the course of 31 m. (temp. 91° F.) it changed its course by as much as a rectangle six times, describing a figure which apparently represented two ellipses. The movement of the terminal leaflet by means of its sub-petiole or pulvinus is quite as rapid, or even more so, than that of the main petiole, and has much greater amplitude. Pfeffer has seen[15] these leaflets move through an angle of 8° in the course of from 10 to 30 seconds.

[15] ‘Die Period. Beweg.,’ p. 35.

Fig. 149. Desmodium gyrans: A, stem during the day; B, stem with leaves asleep. Figures reduced.

A fine, nearly full-grown leaf on a young plant, 8 inches in height, with the stem secured to a stick at the base of the leaf, was observed from 8.30 A.M. June 22nd to 8 A.M. June 24th. In the diagram given on the next page (Fig. 150), the two curved broken lines at the base, which represent the nocturnal courses, ought to be prolonged far downwards. On the first day the leaflet moved thrice down and thrice up, and to a considerable distance laterally; the course was also remarkably crooked. The dots were generally made every hour; if they had been made every few minutes all the lines would have been zigzag to an extraordinary degree, with here and there a loop formed. We may infer that this would have been the case, because five dots were made in the course of 31 m. (between 12.34 and 1.5 P.M.), and we see in the upper part of the diagram how crooked the course here is; if only the first and last dots had been joined we should have had a straight line. Exactly the same fact may be seen in the lines representing the course between 2.24 P.M. and 3 P.M., when six intermediate dots were made; and again at 4.46 and 4.50. But the result was widely different after 6 P.M.,—that is, after the great nocturnal descent had commenced; for though nine dots were then made in the course of 32 m., when these were joined (see Figure) the line thus formed was almost straight. The leaflets, therefore, begin to descend in the afternoon by zigzag lines, but as soon as the descent becomes rapid their whole energy is expended in thus moving, and their course becomes rectilinear. After the leaflets are completely asleep they move very little or not at all.

Fig. 150. Desmodium gyrans: circumnutation and nyctitropic movement of leaf (3 3/4 inches in length, petiole included) during 48 h. Filament affixed to midrib of terminal leaflet; its apex 6 inches from the vertical glass. Diagram reduced to one-third of original scale. Plant illuminated from above. Temp. 19°–20° C.

Had the above plant been subjected to a higher temperature than 67°–70° F., the movements of the terminal leaflet would probably have been even more rapid and wider in extent than those shown in the diagram; for a plant was kept for some time in the hot-house at from 92°–93° F., and in the course of 35 m. the apex of a leaflet twice descended and once ascended, travelling over a space of 1.2 inch in a vertical direction and of .82 inch in a horizontal direction. Whilst thus moving the leaflet also rotated on its own axis (and this was a point to which no attention had been before paid), for the plane of the blade differed by 41° after an interval of only a few minutes. Occasionally the leaflet stood still for a short time. There was no jerking movement, which is so characteristic of the little lateral leaflets. A sudden and considerable fall of temperature causes the terminal leaflet to sink downwards; thus a cut-off leaf was immersed in water at 95° F., which was slowly raised to 103° F., and afterwards allowed to sink to 70° F., and the sub-petiole of the terminal leaflet then curved downwards. The water was afterwards

raised to 120° F., and the sub-petiole straightened itself. Similar experiments with leaves in water were twice repeated, with nearly the same result. It should be added, that water raised to even 122° F. does not soon kill a leaf. A plant was placed in darkness at 8.37 A.M., and at 2 P.M. (i.e. after 5 h. 23 m.), though the leaflets had sunk considerably, they had by no means acquired their nocturnal vertically dependent position. Pfeffer, on the other hand, says[16] that this occurred with him in from 3/4 h. to 2 h.; perhaps the difference in our results may be due to the plant on which we experimented being a very young and vigorous seedling.

[16] ‘Die Period. Beweg.,’ p. 39.

The Movements of the little Lateral Leaflets .—These have been so often described, that we will endeavour to be as brief as possible in giving a few new facts and conclusions. The leaflets sometimes quickly change their position by as much as nearly 180°; and their sub-petioles can then be seen to become greatly curved. They rotate on their own axes, so that their upper surfaces are directed to all points of the compass. The figure described by the apex is an irregular oval or ellipse. They sometimes remain stationary for a period. In these several respects there is no difference, except in rapidity and extent, between their movements and the lesser ones performed by the large terminal leaflet whilst making its great oscillations. The movements of the little leaflets are much influenced, as is well known, by temperature. This was clearly shown by immersing leaves with motionless leaflets in cold water, which was slowly raised to 103° F., and the leaflets then moved quickly, describing about a dozen little irregular circles in 40 m. By this time the water had become much cooler, and the movements became slower or almost ceased; it was then raised to 100° F., and the leaflets again began to move quickly. On another occasion a tuft of fine leaves was immersed in water at 53° F., and the leaflets were of course motionless. The water was raised to 99°, and the leaflets soon began to move; it was raised to 105°, and the movements became much more rapid; each little circle or oval being completed in from 1 m. 30 s. to 1 m. 45 s. There was, however, no jerking, and this fact may perhaps be attributed to the resistance of the water.

Sachs states that the leaflets do not move until the surrounding air is as high as 71°–72° F., and this agrees with our experience on full-grown, or nearly full-grown, plants. But the leaflets of young seedlings exhibit a jerking movement at much lower temperatures. A seedling was kept (April 16th) in a room for half the day where the temperature was steady at 64° F., and the one leaflet which it bore was continually jerking, but not so rapidly as in the hot-house. The pot was taken in the evening into a bed-room where the temperature remained at 62° during nearly the whole night; at 10 and 11 P.M. and at 1 A.M. the leaflet was still jerking rapidly; at 3.30 A.M. it was not seen to jerk, but was observed during only a short time. It was, however, now inclined at a much lower angle than that occupied at 1 A.M. At 6.30 A.M. (temp. 61° F.) its inclination was still less than before, and again less at 6.45 A.M.; by 7.40 A.M. it had risen, and at 8.30 A.M. was again seen to jerk. This leaflet, therefore, was moving during the whole night, and the movement was by jerks up to 1 A.M. (and possibly later) and again at 8.30 A.M., though the temperature was only 61° to 62° F. We must therefore conclude that the lateral leaflets produced by young plants differ somewhat in constitution from those on older plants.

In the large genus Desmodium by far the greater number of the species are trifoliate; but some are unifoliate, and even the same plant may bear uni- and trifoliate leaves. In most of the species the lateral leaflets are only a little smaller than the terminal one. Therefore the lateral leaflets of D. gyrans (see Fig. 148) must be considered as almost rudimentary. They are also rudimentary in function, if this expression may be used; for they certainly do not sleep like the full-sized terminal leaflets. It is, however, possible that the sinking down of the leaflets between 1 A.M. and 6.45 A.M., as above described, may represent sleep. It is well known that the leaflets go on jerking during the early part of the night; but my gardener observed (Oct. 13th) a plant in the hot-house between 5 and 5.30 A.M., the temperature having been kept up to 82° F., and found that all the leaflets were inclined, but he saw no jerking movement until 6.55 A.M., by which time the terminal leaflet had risen and was awake. Two days afterwards (Oct. 15th) the same plant was observed by him at 4.47 A.M. (temp. 77° F.), and he found that the large terminal leaflets were awake, though not quite horizontal; and the only cause which we could assign for this anomalous wakefulness was that the plant had been kept for experimental purposes during the previous day at an unusually high temperature; the little lateral leaflets were also jerking at this hour, but whether there was any connection between this latter fact and the sub-horizontal position of the terminal leaflets we do not know. Anyhow, it is certain that the lateral leaflets do not sleep like the terminal leaflets; and in so far they may be said to be in a functionally rudimentary condition. They are in a similar condition in relation to irritability; for if a plant be shaken or syringed, the terminal leaflets sink down to about 45° beneath the horizon; but we could never detect any effect thus produced on the lateral leaflets; yet we are not prepared to assert positively that rubbing or pricking the pulvinus produces no effect.

As in the case of most rudimentary organs, the leaflets are variable in size; they often depart from their normal position and do not stand opposite one another; and one of the two is frequently absent. This absence appeared in some, but not in all the cases, to be due to the leaflet having become completely confluent with the main petiole, as might be inferred from the presence of a slight ridge along its upper margin, and from the course of the vessels. In one instance there was a vestige of the leaflet, in the shape of a minute point, at the further end of the ridge. The frequent, sudden and complete disappearance of one or both of the rudimentary leaflets is a rather singular fact; but it is a much more surprising one that the leaves which are first developed on seedling plants are not provided with them. Thus, on one seedling the seventh leaf above the cotyledons was the first which bore any lateral leaflets, and then only a single one. On another seedling, the eleventh leaf first bore a leaflet; of the nine succeeding leaves five bore a single lateral leaflet, and four bore none at all; at last a leaf, the twenty-first above the cotyledons, was provided with two rudimentary lateral leaflets. From a widespread analogy in the animal kingdom, it might have been expected that these rudimentary leaflets would have been better developed and more regularly present on very young than on older plants. But bearing in mind, firstly, that long-lost characters sometimes reappear late in life, and secondly, that the species of Desmodium are generally trifoliate, but that some are unifoliate, the suspicion arises that D. gyrans is descended from a unifoliate species, and that this was descended from a trifoliate one; for in this case both the absence of the little lateral leaflets on very young seedlings, and their subsequent appearance, may be attributed to reversion to more or less distant progenitors.[17]

[17] Desmodium vespertilionis is closely allied to D. gyrans, and it seems only occasionally to bear rudimentary lateral leaflets. Duchartre, ‘Eléments de Botanique,’ 1867, p. 353.

No one supposes that the rapid movements of the lateral leaflets of ‘D. gyrans’ are of any use to the plant; and why they should behave in this manner is quite unknown. We imagined that their power of movement might stand in some relation with their rudimentary condition, and therefore observed the almost rudimentary leaflets of Mimosa albida vel sensitiva (of which a drawing will hereafter be given, Fig. 159); but they exhibited no extraordinary movements, and at night they went to sleep like the full-sized leaflets. There is, however, this remarkable difference in the two cases; in Desmodium the pulvinus of the rudimentary leaflets has not been reduced in length, in correspondence with the reduction of the blade, to the same extent as has occurred in the Mimosa; and it is on the length and degree of curvature of the pulvinus that the amount of movement of the blade depends. Thus the average length of the pulvinus in the large terminal leaflets of Desmodium is 3 mm., whilst that of the rudimentary leaflets is 2.86 mm.; so that they differ only a little in length. But in diameter they differ much, that of the pulvinus of the little leaflets being only 0.3 mm. to 0.4 mm.; whilst that of the terminal leaflets is 1.33 mm. If we now turn to the Mimosa, we find that the average length of the pulvinus of the almost rudimentary leaflets is only 0.466 mm., or rather more than a quarter of the length of the pulvinus of the full-sized leaflets, namely, 1.66 mm. In this small reduction in length of the pulvinus of the rudimentary leaflets of Desmodium, we apparently have the proximate cause of their great and rapid circumnutating movement, in contrast with that of the almost rudimentary leaflets of the Mimosa. The small size and weight of the blade, and the little resistance opposed by the air to its movement, no doubt also come into play; for we have seen that these leaflets if immersed in water, when the resistance would be much greater, were prevented from jerking forwards. Why, during the reduction of the lateral leaflets of Desmodium, or during their reappearance—if they owe their origin to reversion—the pulvinus should have been so much less affected than the blade, whilst with the Mimosa the pulvinus has been greatly reduced, we do not know. Nevertheless, it deserves notice that the reduction of the leaflets in these two genera has apparently been effected by a different process and for a different end; for with the Mimosa the reduction of the inner and basal leaflets was necessary from the want of space; but no such necessity exists with Desmodium, and the reduction of its lateral leaflets seems to have been due to the principle of compensation, in consequence of the great size of the terminal leaflet. Uraria (Tribe 6) and Centrosema (Tribe 8).—The leaflets of Uraria lagopus and the leaves of a Centrosema from Brazil both sink vertically down at night. In the latter plant the petiole at the same time rose 16½°.

Amphicarpoea monoica (Tribe 8).—The leaflets sink down vertically at night, and the petioles likewise fall considerably. A petiole, which was carefully observed, stood during the day 25° above the horizon and at night 32° below it; it therefore fell 57°. A filament was fixed transversely across the terminal leaflet of a fine young leaf (2 1/4 inches in length including the petiole), and the movement of the whole leaf was traced on a vertical glass. This was a bad plan in some respects, because the rotation of the leaflet, independently of its rising or falling, raised and depressed the filament; but it was the best plan for our special purpose of observing whether the leaf moved much after it had gone to sleep. The plant had twined closely round a thin stick, so that the circumnutation of the stem was prevented. The movement of the leaf was traced during 48 h., from 9 A.M. July 10th to 9 A.M. July 12th. In the figure given (Fig. 151) we see how complicated its course was on both days: during the second day it changed its course greatly 13 times. The leaflets began to go to sleep a little after 6 P.M., and by 7.15 P.M. hung vertically down and were completely asleep; but on both nights they continued to move from 7.15 P.M. to 10.40 and 10.50 P.M., quite as much as during the day; and this was the point which we wished to ascertain. We see in the figure that the great sinking movement late in the evening does not differ essentially from the circumnutation during the day.

Fig. 151. Amphicarpoea monoica: circumnutation and nyctitropic movement of leaf during 48 h.; its apex 9 inches from the vertical glass. Figure reduced to one-third of original scale. Plant illuminated from above; temp 17½°–18½° C.

Glycine hispida (Tribe 8).—The three leaflets sink vertically down at night.

Erythrina (Tribe 8).—Five species were observed, and the leaflets of all sank vertically down at night; with E. caffra and with a second unnamed species, the petioles at the same time rose slightly. The movements of the terminal leaflet of E. crista-galli (with the main petiole secured to a stick) were traced from 6.40 A.M. June 8th, to 8 A.M. on the 10th. In order to observe the nyctitropic movements of this plant, it is necessary that it should have grown in a warm greenhouse, for out of doors in our climate it does not sleep. We see in the tracing (Fig. 152) that the leaflet oscillated twice up and down between early morning and noon; it then fell greatly, afterwards rising till 3 P.M. At this latter hour the great nocturnal fall commenced. On the second day (of which the tracing is not given) there was exactly the same double oscillation before noon, but only a very small one in the afternoon. On the third morning the leaflet moved laterally, which was due to its beginning to assume an oblique position, as seems invariably to occur with the leaflets of this species as they grow old. On both nights after the leaflets were asleep and hung vertically down, they continued to move a little both up and down, and from side to side.

Erythrina caffra.—A filament was fixed transversely across a terminal leaflet, as we wished to observe its movements when asleep. The plant was placed in the morning of June 10th under a skylight, where the light was not bright; and we do not know whether it was owing to this cause or to the plant having been disturbed, but the leaflet hung vertically down all day; nevertheless it circumnutated in this position, describing a figure which represented two irregular ellipses. On the next day it circumnutated in a greater degree, describing four irregular ellipses, and by 3 P.M. had risen into a horizontal position. By 7.15 P.M. it was asleep and vertically dependent, but continued to circumnutate as long as observed, until 11 P.M.

Fig. 152. Erythrina crista-galli: circumnutation and nyctitropic movement of terminal leaflet, 3 3/4 inches in length, traced during 25 h.; apex of leaf 3½ inches from the vertical glass. Figure reduced to one-half of original scale. Plant illuminated from above; temp. 17½°–18½° C.

Erythrina corallodendron.—The movements of a terminal leaflet were traced. During the second day it oscillated four times up and four times down between 8 A.M. and 4 P.M., after which hour the great nocturnal fall commenced. On the third day the movement was equally great in amplitude, but was remarkably simple, for the leaflet rose in an almost perfectly straight line from 6.50 A.M. to 3 P.M., and then sank down in an equally straight line until vertically dependent and asleep.

Apios tuberosa (Tribe 8).—The leaflets sink vertically down at night.

Phaseolus vulgaris (Tribe 8).—The leaflets likewise sink vertically down at night. In the greenhouse the petiole of a young leaf rose 16°, and that of an older leaf 10° at night. With plants growing out of doors the leaflets apparently do not sleep until somewhat late in the season, for on the nights of July 11th and 12th none of them were asleep; whereas on the night of August 15th the same plants had most of their leaflets vertically dependent and asleep. With Ph. caracalla and Hernandesii, the primary unifoliate leaves and the leaflets of the secondary trifoliate leaves sink vertically down at night. This holds good with the secondary trifoliate leaves of Ph. Roxburghii, but it is remarkable that the primary unifoliate leaves which are much elongated, rise at night from about 20° to about 60° above the horizon. With older seedlings, however, having the secondary leaves just developed, the primary leaves stand in the middle of the day horizontally, or are deflected a little beneath the horizon. In one such case the primary leaves rose from 26° beneath the horizon at noon, to 20° above it at 10 P.M.; whilst at this same hour the leaflets of the secondary leaves were vertically dependent. Here, then, we have the extraordinary case of the primary and secondary leaves on the same plant moving at the same time in opposite directions.

We have now seen that the leaflets in the six genera of Phaseoleae observed by us (with the exception of the primary leaves of Phaseolus Roxburghii) all sleep in the same manner, namely, by sinking vertically down. The movements of the petioles were observed in only three of these genera. They rose in Centrosema and Phaseolus, and sunk in Amphicarpæa.

Sophora chrysophylla (Tribe 10).—The leaflets rise at night, and are at the same time directed towards the apex of the leaf, as in Mimosa pudica.

Caesalpinia, Hoematoxylon, Gleditschia, Poinciana.—The leaflets of two species of Caesalpinia (Tribe 13) rose at night. With Haematoxylon Campechianum (Tribe 13) the leaflets move forwards at night, so that their midribs stand parallel to the petiole, and their now vertical lower surfaces are turned outwards (Fig. 153). The petiole sinks a little. In Gleditschia, if we understand correctly Duchartre’s description, and in Poinciana Gilliesii (both belonging to Tribe 13), the leaves behave in the same manner.

Fig. 153. Haematoxylon Campechianum: A, branch during daytime; B, branch with leaves asleep, reduced to two-thirds of natural scale.

Cassia (Tribe 14).—The nyctitropic movements of the leaves in many species in this genus are closely alike, and are highly complex. They were first briefly described by Linnæus, and since by Duchartre. Our observations were made chiefly on C. floribunda[18] and corymbosa, but several other species were casually observed. The horizontally extended leaflets sink down vertically at night; but not simply, as in so many other genera, for each leaflet rotates on its own axis, so that its lower surface faces outwards. The upper surfaces of the opposite leaflets are thus brought into contact with one another beneath the petiole, and are well protected (Fig. 154). The rotation and other movements are effected by means of a well-developed pulvinus at the base of each leaflet, as could be plainly seen when a straight narrow black line had been painted along it during the day. The two terminal leaflets in the daytime include rather less than a right angle; but their divergence increases greatly whilst they sink downwards and rotate, so that they stand laterally at night, as may be seen in the figure. Moreover, they move somewhat backwards, so as to point towards the base of the petiole. In one instance we found that the midrib of a terminal leaflet formed at night an angle of 36°, with a line dropped perpendicularly from the end of the petiole. The second pair of leaflets likewise moves a little backwards, but less than the terminal pair; and the third pair moves vertically downwards, or even a little forwards. Thus all the leaflets, in those species which bear only 3 or 4 pairs, tend to form a single packet, with their upper surfaces in contact, and their lower surfaces turned outwards. Lastly, the main petiole rises at night, but with leaves of different ages to very different degrees, namely some rose through an angle of only 12°, and others as much as 41°.

[18] I am informed by Mr. Dyer that Mr. Bentham believes that C. floribunda (a common greenhouse bush) is a hybrid raised in France, and that it comes very near to C. laevigata. It is no doubt the same as the form described by Lindley (‘Bot. Reg.,’ Tab. 1422) as C. Herbertiana.

Fig. 154. Cassia corymbosa: A, plant during day; B, same plant at night. Both figures copied from photographs.

Cassia calliantha.—The leaves bear a large number of leaflets, which move at night in nearly the same manner as just described; but the petioles apparently do not rise, and one which was carefully observed certainly fell 3°. Cassia pubescens.—The chief difference in the nyctitropic movements of this species, compared with those of the former species, consists in the leaflets not rotating nearly so much; therefore their lower surfaces face but little outwards at night. The petioles, which during the day are inclined only a little above the horizon, rise at night in a remarkable manner, and stand nearly or quite vertically. This, together with the dependent position of the leaflets, makes the whole plant wonderfully compact at night. In the two foregoing figures, copied from photographs, the same plant is represented awake and asleep (Fig. 155), and we see how different is its appearance.

Fig. 155. Cassia pubescens: A, upper part of plant during the day; B, same plant at night. Figures reduced from photographs.

Cassia mimosoides.—At night the numerous leaflets on each leaf rotate on their axes, and their tips move towards the apex of the leaf; they thus become imbricated with their lower surfaces directed upwards, and with their midribs almost parallel to the petiole. Consequently, this species differs from all the others seen by us, with the exception of the following one, in the leaflets not sinking down at night. A petiole, the movement of which was measured, rose 8° at night.

Cassia Barclayana.—The leaflets of this Australian species are numerous, very narrow, and almost linear. At night they rise up a little, and also move towards the apex of the leaf. For instance, two opposite leaflets which diverged from one another during the day at an angle of 104°, diverted at night only 72°; so that each had risen 16° above its diurnal position. The petiole of a young leaf rose at night 34°, and that of an older leaf 19°. Owing to the slight movement of the leaflets and the considerable movement of the petiole, the bush presents a different appearance at night to what it does by day; yet the leaves can hardly be said to sleep.

The circumnutating movements of the leaves of C. floribunda, calliantha, and pubescens were observed, each during three or four days; they were essentially alike, those of the last-named species being the simplest. The petiole of C. floribunda was secured to a stick at the base of the two terminal leaflets, and a filament was fixed along the midrib of one of them. Its movements were traced from 1 P.M. on August 13th to 8.30 A.M. 17th; but those during the last 2 h. are alone given in Fig. 156. From 8 A.M. on each day (by which hour the leaf had assumed its diurnal position) to 2 or 3 P.M., it either zigzagged or circumnutated over nearly the same small space; at between 2 and 3 P.M. the great evening fall commenced. The lines representing this fall and the early morning rise are oblique, owing to the peculiar manner in which the leaflets sleep, as already described. After the leaflet was asleep at 6 P.M., and whilst the glass filament hung perpendicularly down, the movement of its apex was traced until 10.30 P.M.; and during this whole time it swayed from side to side, completing more than one ellipse.

Fig 156. Cassia floribunda: circumnutation and nyctitropic movement of a terminal leaflet (1 5/6 inch in length) traced from 8.30 A.M. to same hour on following morning. Apex of leaflet 5½ inches from the vertical glass. Main petiole 3 3/4 inches long. Temp. 16°–17½° C. Figure reduced to one-half of the original scale.