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.
Bauhinia (Tribe 15).—The nyctitropic movements of four species were alike, and were highly peculiar. A plant raised from seed sent us from South Brazil by Fritz Müller, was more especially observed. The leaves are large and deeply notched at their ends. At night the two halves rise up and close completely together, like the opposite leaflets of many Leguminosae. With very young plants the petioles rise considerably at the same time; one, which was inclined at noon 45° above the horizon, at night stood at 75°; it thus rose 30°; another rose 34°. Whilst the two halves of the leaf are closing, the midrib at first sinks vertically downwards and afterwards bends backwards, so as to pass close along one side of its own upwardly inclined petiole; the midrib being thus directed towards the stem or axis of the plant. The angle which the midrib formed with the horizon was measured in one case at different hours: at noon it stood horizontally; late in the evening it depended vertically; then rose to the opposite side, and at 10.15 P.M. stood at only 27° beneath the horizon, being directed towards the stem. It had thus travelled through 153°. Owing to this movement—to the leaves being folded—and to the petioles rising, the whole plant is as much more compact at night than during the day, as a fastigiate Lombardy poplar is compared with any other species of poplar. It is remarkable that when our plants had grown a little older, viz., to a height of 2 or 3 feet, the petioles did not rise at night, and the midribs of the folded leaves were no longer bent back along one side of the petiole. We have noticed in some other genera that the petioles of very young plants rise much more at night than do those of older plants.
Tamarindus Indica (Tribe 16).—The leaflets approach or meet each other at night, and are all directed towards the apex of the leaf. They thus become imbricated with their midribs parallel to the petiole. The movement is closely similar to that of Haematoxylon (see Fig. 153), but more striking from the greater number of the leaflets.
Adenanthera, Prosopis, and Neptunia (Tribe 20).—With Adenanthera pavonia the leaflets turn edgeways and sink at night. In Prosopis they turn upwards. With Neptunia oleracea the leaflets on the opposite sides of the same pinna come into contact at night and are directed forwards. The pinnae themselves move downwards, and at the same time backwards or towards the stem of the plant. The main petiole rises.
Mimosa pudica (Tribe 20).—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 (Fig. 157), 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 Fig. 157 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.
Fig. 157 Mimosa pudica: circumnutation and nyctitropic movement of main petiole, traced during 34 h. 30 m.
On two other occasions the movement of the main petiole was observed every two or three minutes, the plants being kept at a rather high temperature, viz., on the first occasion at 77°–81° F., and the filament then described 2½ ellipses in 69 m. On the second occasion, when the temperature was 81°–86° F., it made rather more than 3 ellipses in 67 m. therefore, Fig. 157, though now sufficiently complex, would have been incomparably more so, if dots had been made on the glass every 2 or 3 minutes, instead of every hour or half-hour. Although the main petiole is continually and rapidly describing small ellipses during the day, yet after the great nocturnal rising movement has commenced, if dots are made every 2 or 3 minutes, as was done for an hour between 9.30 and 10.30 P.M. (temp. 84° F.), and the dots are then joined, an almost absolutely straight line is the result.
To show that the movement of the petiole is in all probability due to the varying turgescence of the pulvinus, and not to growth (in accordance with the conclusions of Pfeffer), a very old leaf, with some of its leaflets yellowish and hardly at all sensitive, was selected for observation, and the plant was kept at the highly favourable temp. of 80° F. The petiole fell from 8 A.M. till 10.15 A.M., it then rose a little in a somewhat zigzag line, often remaining stationary, till 5 P.M., when the great evening fall commenced, which was continued till at least 10 P.M. By 7 A.M. on the following morning it had risen to the same level as on the previous morning, and then descended in a zigzag line. But from 10.30 A.M. till 4.15 P.M. it remained almost motionless, all power of movement being now lost. The petiole, therefore, of this very old leaf, which must have long ceased growing, moved periodically; but instead of circumnutating several times during the day, it moved only twice down and twice up in the course of 24 h., with the ascending and descending lines not coincident.
It has already been stated that the pinnae move independently of the main petiole. The petiole of a leaf was fixed to a cork support, close to the point whence the four pinnae diverge, with a short fine filament cemented longitudinally to one of the two terminal pinnae, and a graduated semicircle was placed close beneath it. By looking vertically down, its angular or lateral movements could be measured with accuracy. Between noon and 4.15 P.M. the pinna changed its position to one side by only 7°; but not continuously in the same direction, as it moved four times to one side, and three times to the opposite side, in one instance to the extent of 16°. This pinna, therefore circumnutated. Later in the evening the four pinnae approach each other, and the one which was observed moved inwards 59° between noon and 6.45 P.M. Ten observations were made in the course of 2 h. 20 m. (at average intervals of 14 m.), between 4.25 and 6.45 P.M.; and there was now, when the leaf was going to sleep, no swaying from side to side, but a steady inward movement. Here therefore there is in the evening the same conversion of a circumnutating into a steady movement in one direction, as in the case of the main petiole.
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 in Fig. 158. 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. Another leaflet was casually observed, and found to be continually circumnutating during the same length of time.
The circumnutation of the leaves is not destroyed by their being subjected to moderately long continued darkness; but the proper periodicity of their movements is lost. Some very young seedlings were kept during two days in the dark (temp. 57°–59° F.) except when the circumnutation of their stems was occasionally observed; and on the evening of the second day the leaflets did not fully and properly go to sleep. The pot was then placed for three days in a dark cupboard, under nearly the same temperature, and at the close of this period the leaflets showed no signs of sleeping, and were only slightly sensitive to a touch. On the following day the stem was cemented to a stick, and the movements of two leaves were traced on a vertical glass during 72 h. The plants were still kept in the dark, excepting that at each observation, which lasted 3 or 4 minutes, they were illuminated by two candles. On the third day the leaflets still exhibited a vestige of sensitiveness when forcibly pressed, but in the evening they showed no signs of sleep. Nevertheless, their petioles continued to circumnutate distinctly, although the proper order of their movements in relation to the day and night was wholly lost. Thus, one leaf descended during the first two nights (i.e. between 10 P.M. and 7 A.M. next morning) instead of ascending, and on the third night it moved chiefly in a lateral direction. The second leaf behaved in an equally abnormal manner, moving laterally during the first night, descending greatly during the second, and ascending to an unusual height during the third night.
Fig 158. Mimosa pudica: circumnutation and nyctitropic movement of a leaflet (with pinna secured), traced on a vertical glass, from 8 A.M. Sept. 14th to 9 A.M. 16th.
With plants kept at a high temperature and exposed to the light, the most rapid circumnutating movement of the apex of a leaf which was observed, amounted to 1/500 of an inch in one second; and this would have equalled 1/8 of an inch in a minute, had not the leaf occasionally stood still. The actual distance travelled by the apex (as ascertained by a measure placed close to the leaf) was on one occasion nearly 3/4 of an inch in a vertical direction in 15 m.; and on another occasion 5/8 of an inch in 60 m.; but there was also some lateral movement.
Mimosa albida.[19]—The leaves of this plant, one of which is here figured (Fig. 159) reduced to 2/3 of the natural size, 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, viz. 7/100 of an inch, whilst the inner one is only 5/100–6/100 long. Now if the basal pair of leaflets of the existing leaves were to become rudimentary, we should expect that the rudiments would still exhibit some trace of their present great inequality of size. The conclusion that the pinnae of the parent-form of M. albida possessed at least three pairs of leaflets, instead of, as at present, only two, is supported by the structure of the first true leaf; for this consists of a simple petiole, often bearing three pairs of leaflets. This latter fact, as well as the presence of the rudiments, both lead to the conclusion that M. albida is descended from a form the leaves of which bore more than two pairs of leaflets. The second leaf above the cotyledons resembles in all respects the leaves on fully developed plants.
[19] Mr. Thiselton Dyer informs us that this Peruvian plant (which was sent to us from Kew) is considered by Mr. Bentham (‘Trans. Linn. Soc.,’ vol. xxx. p. 390) to be “the species or variety which most commonly represents the M. sensitiva of our gardens.”
Fig. 159. Mimosa albida: leaf seen from vertically above.
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. The movement of the main petiole seems to be variable; we have seen it in the evening 27° lower than during the day; but sometimes in nearly the same position. Nevertheless, a sinking movement in the evening and a rising one during the night is probably the normal course, for this was well-marked in the petiole of the first-formed true leaf.
The circumnutation of the main petiole of a young leaf was traced during 2 3/4 days, and was considerable in extent, but less complex than that of M. pudica. The movement was much more lateral than is usual with circumnutating leaves, and this was the sole peculiarity which it presented. The apex of one of the terminal leaflets was seen under the microscope to travel 1/50 of an inch in 3 minutes.
Mimosa marginata.—The opposite leaflets rise up and approach each other at night, but do not come into close contact, except in the case of very young leaflets on vigorous shoots. Full-grown leaflets circumnutate during the day slowly and on a small scale.
Schrankia uncinata (Tribe 20).—A leaf consists of two or three pairs of pinnae, each bearing many small leaflets. These, when the plant is asleep, are directed forwards and become imbricated. The angle between the two terminal pinnae was diminished at night, in one case by 15°; and they sank almost vertically downwards. The hinder pairs of pinnae likewise sink downwards, but do not converge, that is, move towards the apex of the leaf. The main petiole does not become depressed, at least during the evening. In this latter respect, as well as in the sinking of the pinnae, there is a marked difference between the nyctitropic movements of the present plant and of Mimosa pudica. It should, however, be added that our specimen was not in a very vigorous condition. The pinnae of Schrankia aculeata also sink at night.
Acacia Farnesiana (Tribe 22).—The different appearance presented by a bush of this plant when asleep and awake is wonderful. The same leaf in the two states is shown in the following figure (Fig. 160). The leaflets move towards the apex of the pinna and become imbricated, and the pinnae then look like bits of dangling string. The following remarks and measurements do not fully apply to the small leaf here figured. The pinnae move forwards and at the same time sink downwards, whilst the main petiole rises considerably. With respect to the degree of movement: the two terminal pinnae of one specimen formed together an angle of 100° during the day, and at night of only 38°, so each had moved 31° forwards. The penultimate pinnae during the day formed together an angle of 180°, that is, they stood in a straight line opposite one another, and at night each had moved 65° forwards. The basal pair of pinnae were directed during the day, each about 21° backwards, and at night 38° forwards, so each had moved 59° forwards. But the pinnae at the same time sink greatly, and sometimes hang almost perpendicularly downwards. The main petiole, on the other hand, rises much: by 8.30 P.M. one stood 34° higher than at noon, and by 6.40 A.M. on the following morning it was still higher by 10°; shortly after this hour the diurnal sinking movement commenced. The course of a nearly full-grown leaf was traced during 14 h.; it was strongly zigzag, and apparently represented five ellipses, with their longer axes differently directed.
Fig. 160. Acacia Farnesiana: A, leaf during the day; B, the same leaf at night.
Albizzia lophantha (Tribe 23).—The leaflets at night come into contact with one another, and are directed towards the apex of the pinna. The pinnae approach one another, but remain in the same plane as during the day; and in this respect they differ much from those of the above Schrankia and Acacia. The main petiole rises but little. The first-formed leaf above the cotyledons bore 11 leaflets on each side, and these slept like those on the subsequently formed leaves; but the petiole of this first leaf was curved downwards during the day and at night straightened itself, so that the chord of its arc then stood 16° higher than in the day-time.
Melaleuca ericaefolia (Myrtaceae).—According to Bouché (‘Bot. Zeit.,’ 1874, p. 359) the leaves sleep at night, in nearly the same manner as those of certain species of Pimelia.
Œnothera mollissima (Onagrarieae).—According to Linnæus (‘Somnus Plantarum’), the leaves rise up vertically at night.
Passiflora gracilis (Passifloracae).—The young leaves sleep by their blades hanging vertically downwards, and the whole length of the petiole then becomes somewhat curved downwards. Externally no trace of a pulvinus can be seen. The petiole of the uppermost leaf on a young shoot stood at 10.45 A.M. at 33° above the horizon; and at 10.30 P.M., when the blade was vertically dependent, at only 15°, so the petiole had fallen 18°. That of the next older leaf fell only 7°. From some unknown cause the leaves do not always sleep properly. The stem of a plant, which had stood for some time before a north-east window, was secured to a stick at the base of a young leaf, the blade of which was inclined at 40° below the horizon. From its position the leaf had to be viewed obliquely, consequently the vertically ascending and descending movements appeared when traced oblique. On the first day (Oct. 12th) the leaf descended in a zigzag line until late in the evening; and by 8.15 A.M. on the 13th had risen to nearly the same level as on the previous morning. A new tracing was now begun (Fig. 161). The leaf continued to rise until 8.50 A.M., then moved a little to the right, and afterwards descended. Between 11 A.M. and 5 P.M. it circumnutated, and after the latter hour the great nocturnal fall commenced. At 7.15 P.M. it depended vertically. The dotted line ought to have been prolonged much lower down in the figure. By 6.50 A.M. on the following morning (14th) the leaf had risen greatly, and continued to rise till 7.50 A.M., after which hour it redescended. It should be observed that the lines traced on this second morning would have coincided with and confused those previously traced, had not the pot been slided a very little to the left. In the evening (14th) a mark was placed behind the filament attached to the apex of the leaf, and its movement was carefully traced from 5 P.M. to 10.15 P.M. Between 5 and 7.15 P.M. the leaf descended in a straight line, and at the latter hour it appeared vertically dependent. But between 7.15 and 10.15 P.M. the line consisted of a succession of steps, the cause of which we could not understand; it was, however, manifest that the movement was no longer a simple descending one.
Fig. 161. Passiflora gracilis: circumnutation and nyctitropic movement of leaf, traced on vertical glass, from 8.20 A.M. Oct. 13th to 10 A.M. 14th. Figure reduced to two-thirds of original scale.
Siegesbeckia orientalis (Compositæ).—Some seedlings were raised in the middle of winter and kept in the hot-house; they flowered, but did not grow well, and their leaves never showed any signs of sleep. The leaves on other seedlings raised in May were horizontal at noon (June 22nd), and depended at a considerable angle beneath the horizon at 10 P.M. In the case of four youngish leaves which were from 2 to 2½ inches in length, these angles were found to be 50°, 56°, 60°, and 65°. At the end of August when the plants had grown to a height of 10 to 11 inches, the younger leaves were so much curved downwards at night that they might truly be said to be asleep. This is one of the species which must be well illuminated during the day in order to sleep, for on two occasions when plants were kept all day in a room with north-east windows, the leaves did not sleep at night. The same cause probably accounts for the leaves on our seedlings raised in the dead of the winter not sleeping. Professor Pfeffer informs us that the leaves of another species (S. Jorullensis ?) hang vertically down at night.
Fig. 162. Nicotiana glauca: shoots with leaves expanded during the day, and asleep at night. Figures copied from photographs, and reduced.
Ipomœa caerulea and purpurea (Convolvulaceae).—The leaves on very young plants, a foot or two in height, are depressed at night to between 68° and 80° beneath the horizon; and some hang quite vertically downwards. On the following morning they again rise into a horizontal position. The petioles become at night downwardly curved, either through their entire length or in the upper part alone; and this apparently causes the depression of the blade. It seems necessary that the leaves should be well illuminated during the day in order to sleep, for those which stood on the back of a plant before a north-east window did not sleep.
Nicotiana tabacum (var. Virginian) and glauca (Solaneae).—The young leaves of both these species sleep by bending vertically upwards. Figures of two shoots of N. glauca, awake and asleep (Fig. 162), are given on p. 385: one of the shoots, from which the photographs were taken, was accidentally bent to one side.
Fig. 163. Nicotiana tabacum: circumnutation and nyctitropic movement of a leaf (5 inches in length), traced on a vertical glass, from 3 P.M. July 10th to 8.10 A.M. 13th. Apex of leaf 4 inches from glass. Temp. 17½°–18½° C. Figure reduced to one-half original scale.
At the base of the petiole of N. tabacum, on the outside, there is a mass of cells, which are rather smaller than elsewhere, and have their longer axes differently directed from the cells of the parenchyma, and may therefore be considered as forming a sort of pulvinus. A young plant of N. tabacum was selected, and the circumnutation of the fifth leaf above the cotyledons was observed during three days. On the first morning (July 10th) the leaf fell from 9 to 10 A.M., which is its normal course, but rose during the remainder of the day; and this no doubt was due to its being illuminated exclusively from above; for properly the evening rise does not commence until 3 or 4 P.M. In the figure as given on p. 386 (Fig. 163) the first dot was made at 3 P.M.; and the tracing was continued for the following 65 h. When the leaf pointed to the dot next above that marked 3 P.M. it stood horizontally. The tracing is remarkable only from its simplicity and the straightness of the lines. The leaf each day described a single great ellipse; for it should be observed that the ascending and descending lines do not coincide. On the evening of the 11th the leaf did not descend quite so low as usual, and it now zigzagged a little. The diurnal sinking movement had already commenced each morning by 7 A.M. The broken lines at the top of the figure, representing the nocturnal vertical position of the leaf, ought to be prolonged much higher up.
Mirabilis longiflora and jalapa (Nyctagineae).—The first pair of leaves above the cotyledons, produced by seedlings of both these species, were considerably divergent during the day, and at night stood up vertically in close contact with one another. The two upper leaves on an older seedling were almost horizontal by day, and at night stood up vertically, but were not in close contact, owing to the resistance offered by the central bud.
Polygonum aviculare (Polygoneae).—Professor Batalin informs us that the young leaves rise up vertically at night. This is likewise the case, according to Linnæus, with several species of Amaranthus (Amaranthaceae); and we observed a sleep movement of this kind in one member of the genus. Again, with Chenopodium album (Chenopodieae), the upper young leaves of some seedlings, about 4 inches in height, were horizontal or sub-horizontal during the day, and at 10 P.M. on March 7th were quite, or almost quite, vertical. Other seedlings raised in the greenhouse during the winter (Jan. 28th) were observed day and night, and no difference could be perceived in the position of their leaves. According to Bouché (‘Bot. Zeitung,’ 1874, p. 359) the leaves of Pimelia linoides and spectabilis (Thymeleae) sleep at night.
Euphorbia jacquiniaeflora (Euphorbiaceae).—Mr. Lynch called our attention to the fact that the young leaves of this plant sleep by depending vertically. The third leaf from the summit (March 11th) was inclined during the day 30° beneath the horizon, and at night hung vertically down, as did some of the still younger leaves. It rose up to its former level on the following morning. The fourth and fifth leaves from the summit stood horizontally during the day, and sank down at night only 38°. The sixth leaf did not sensibly alter its position. The sinking movement is due to the downward curvature of the petiole, no part of which exhibits any structure like that of a pulvinus. Early on the morning of June 7th a filament was fixed longitudinally to a young leaf (the third from the summit, and 2 5/8 inches in length), and its movements were traced on a vertical glass during 72 h., the plant being illuminated from above through a skylight. Each day the leaf fell in a nearly straight line from 7 A.M. to 5 P.M., after which hour it was so much inclined downwards that the movement could no longer be traced; and during the latter part of each night, or early in the morning, the leaf rose. It therefore circumnutated in a very simple manner, making a single large ellipse every 24 h., for the ascending and descending lines did not coincide. On each successive morning it stood at a less height than on the previous one, and this was probably due partly to the increasing age of the leaf, and partly to the illumination being insufficient; for although the leaves are very slightly heliotropic, yet, according to Mr. Lynch’s and our own observations, their inclination during the day is determined by the intensity of the light. On the third day, by which time the extent of the descending movement had much decreased, the line traced was plainly much more zigzag than on any previous day, and it appeared as if some of its powers of movement were thus expended. At 10 P.M. on June 7th, when the leaf depended vertically, its movements were observed by a mark being placed behind it, and the end of the attached filament was seen to oscillate slowly and slightly from side to side, as well as upwards and downwards.
Phyllanthus Niruri (Euphorbiaceae).—The leaflets of this plant sleep, as described by Pfeffer,[20] in a remarkable manner, apparently like those of Cassia, for they sink downwards at night and twist round, so that their lower surfaces are turned outwards. They are furnished as might have been expected from this complex kind of movement, with a pulvinus.
[20] ‘Die Period. Beweg.,’ p. 159.
GYMNOSPERMS.
Pinus Nordmanniana (Coniferæ).—M. Chatin states[21] that the leaves, which are horizontal during the day, rise up at night, so as to assume a position almost perpendicular to the branch from which they arise; we presume that he here refers to a horizontal branch. He adds: “En même temps, ce mouvement d’érection est accompangé d’un mouvement de torsion imprimé à la partie basilaire de la feuille, et pouvant souvent parcourir un arc de 90 degrés.” As the lower surfaces of the leaves are white, whilst the upper are dark green, the tree presents a widely different appearance by day and night. The leaves on a small tree in a pot did not exhibit with us any nyctitropic movements. We have seen in a former chapter that the leaves of Pinus pinaster and Austriaca are continually circumnutating.
[21] ‘Comptes Rendus,’ Jan. 1876, p. 171.
MONOCOTYLEDONS.
Thalia dealbata (Cannaceae).—the leaves of this plant sleep by turning vertically upwards; they are furnished with a well-developed pulvinus. It is the only instance known to us of a very large leaf sleeping. The blade of a young leaf, which was as yet only 13 1/4 inches in length and 6½ in breadth, formed at noon an angle with its tall petiole of 121°, and at night stood vertically in a line with it, and so had risen 59°. The actual distance travelled by the apex (as measured by an orthogonic tracing) of another large leaf, between 7.30 A.M. and 10 P.M., was 10½ inches. The circumnutation of two young and dwarfed leaves, arising amongst the taller leaves at the base of the plant, was traced on a vertical glass during two days. On the first day the apex of one, and on the second day the apex of the other leaf, described between 6.40 A.M. and 4 P.M. two ellipses, the longer axes of which were extended in very different directions from the lines representing the great diurnal sinking and nocturnal rising movement.
Maranta arundinacea (Cannaceae).—The blades of the leaves, which are furnished with a pulvinus, stand horizontally during the day or between 10° and 20° above the horizon, and at night vertically upwards. They therefore rise between 70° and 90° at night. The plant was placed at noon in the dark in the hot-house, and on the following day the movements of the leaves were traced. Between 8.40 and 10.30 A.M. they rose, and then fell greatly till 1.37 P.M. But by 3 P.M. they had again risen a little, and continued to rise during the rest of the afternoon and night; on the following morning they stood at the same level as on the previous day. Darkness, therefore, during a day and a half does not interfere with the periodicity of their movements. On a warm but stormy evening, the plant whilst being brought into the house, had its leaves violently shaken, and at night not one went to sleep. On the next morning the plant was taken back to the hot-house, and again at night the leaves did not sleep; but on the ensuing night they rose in the usual manner between 70° and 80°. This fact is analogous with what we have observed with climbing plants, namely, that much agitation checks for a time their power of circumnutation; but the effect in this instance was much more strongly marked and prolonged.
Colocasia antiquorum (Caladium esculentum, Hort.) (Aroideae).—The leaves of this plant sleep by their blades sinking in the evening, so as to stand highly inclined, or even quite vertically with their tips pointing to the ground. They are not provided with a pulvinus. The blade of one stood at noon 1 degree beneath the horizon; at 4.20 P.M., 20°; at 6 P.M. 43°; at 7.20 P.M., 69°; and at 8.30 P.M., 68°; so it had now begun to rise; at 10.15 P.M. it stood at 65°, and on the following early morning at 11° beneath the horizon. The circumnutation of another young leaf (with its petiole only 3 1/4 inches, and the blade 4 inches in length), was traced on a vertical glass during 48 h.; it was dimly illuminated through a skylight, and this seemed to disturb the proper periodicity of its movements. Nevertheless, the leaf fell greatly during both afternoons, till either 7.10 P.M. or 9 P.M., when it rose a little and moved laterally. By an early hour on both mornings, it had assumed its diurnal position. The well-marked lateral movement for a short time in the early part of the night, was the only interesting fact which it presented, as this caused the ascending and descending lines not to coincide, in accordance with the general rule with circumnutating organs. The movements of the leaves of this plant are thus of the most simple kind; and the tracing is not worth giving. We have seen that in another genus of the Aroideae, namely, Pistia, the leaves rise so much at night that they may almost be said to sleep.
Strephium floribundum[22] (Gramineæ).—The oval leaves are provided with a pulvinus, and are extended horizontally or declined a little beneath the horizon during the day. Those on the upright culms simply rise up vertically at night, so that their tips are directed towards the zenith. (Fig. 164.) Horizontally extended leaves arising from much inclined or almost horizontal culms, move at night so that their tips point towards the apex of the culm, with one lateral margin directed towards the zenith; and in order to assume this position the leaves have to twist on their own axes through an angle of nearly 90°. Thus the surface of the blade always stands vertically, whatever may be the position of the midrib or of the leaf as a whole.
[22] A. Brongniart first observed that the leaves of this plant and of Marsilea sleep: see ‘Bull. de la Soc. Bot. de France,’ tom. vii. 1860, p. 470.
Fig. 164. Strephium floribundum: culms with leaves during the day, and when asleep at night. Figures reduced.
The circumnutation of a young leaf (2.3 inches in length) was traced during 48 h. (Fig. 165). The movement was remarkably simple; the leaf descended from before 6.40 A.M. until 2 or 2.50 P.M., and then rose so as to stand vertically at about 6 P.M., descending again late in the night or in the very early morning. On the second day the descending line zigzagged slightly. As usual, the ascending and descending lines did not coincide. On another occasion, when the temperature was a little higher, viz., 24°–26½° C., a leaf was observed 17 times between 8.50 A.M. and 12.16 P.M.; it changed its course by as much as a rectangle six times in this interval of 3 h. 26 m., and described two irregular triangles and a half. The leaf, therefore, on this occasion circumnutated rapidly and in a complex manner.
Fig. 165. Strephium floribundum: circumnutation and nyctitropic movement of a leaf, traced from 9 A.M. June 26th to 8.45 A.M. 27th; filament fixed along the midrib. Apex of leaf 8 1/4 inches from the vertical glass; plant illuminated from above. Temp. 23½°–24½° C.
ACOTYLEDONS.
Marsilea quadrifoliata (Marsileaceae).—The shape of a leaf, expanded horizontally during the day, is shown at A (Fig. 166). Each leaflet is provided with a well-developed pulvinus. When the leaves sleep, the two terminal leaflets rise up, twist half round and come into contact with one another (B), and are afterwards embraced by the two lower leaflets (C); so that the four leaflets with their lower surfaces turned outwards form a vertical packet. The curvature of the summit of the petiole of the leaf figured asleep, is merely accidental. The plant was brought into a room, where the temperature was only a little above 60° F., and the movement of one of the leaflets (the petiole having been secured) was traced during 24 h. (Fig. 167). The leaf fell from the early morning till 1.50 P.M., and then rose till 6 P.M., when it was asleep. A vertically dependent glass filament was now fixed to one of the terminal and inner leaflets; and part of the tracing in Fig. 167, after 6 P.M., shows that it continued to sink, making one zigzag, until 10.40 P.M. At 6.45 A.M. on the following morning, the leaf was awaking, and the filament pointed above the vertical glass, but by 8.25 A.M. it occupied the position shown in the figure. The diagram differs greatly in appearance from most of those previously given; and this is due to the leaflet twisting and moving laterally as it approaches and comes into contact with its fellow. The movement of another leaflet, when asleep, was traced between 6 P.M. and 10.35 P.M., and it clearly circumnutated, for it continued for two hours to sink, then rose, and then sank still lower than it was at 6 P.M. It may be seen in the preceding figure (167) that the leaflet, when the plant was subjected to a rather low temperature in the house, descended and ascended during the middle of the day in a somewhat zigzag line; but when kept in the hot-house from 9 A.M. to 3 P.M. at a high but varying temperature (viz., between 72° and 83° F.) a leaflet (with the petiole secured) circumnutated rapidly, for it made three large vertical ellipses in the course of the six hours. According to Brongniart, Marsilea pubescens sleeps like the present species. These plants are the sole cryptogamic ones known to sleep.
Fig. 166. Marsilea quadrifoliata: A, leaf during the day, seen from vertically above; B, leaf beginning to go to sleep, seen laterally; C, the same asleep. Figures reduced to one-half of natural scale.
Fig. 167. Marsilea quadrifoliata: circumnutation and nyctitropic movement of leaflet traced on vertical glass, during nearly 24 h. Figure reduced to two-thirds of original scale. Plant kept at rather too low a temperature.
Summary and Concluding Remarks on the Nyctitropic or Sleep-movements of Leaves.—That these movements are in some manner of high importance to the plants which exhibit them, few will dispute who have observed how complex they sometimes are. Thus with Cassia, the leaflets which are horizontal during the day not only bend at night vertically downwards with the terminal pair directed considerably backwards, but they also rotate on their own axes, so that their lower surfaces are turned outwards. The terminal leaflet of Melilotus likewise rotates, by which movement one of its lateral edges is directed upwards, and at the same time it moves either to the left or to the right, until its upper surface comes into contact with that of the lateral leaflet on the same side, which has likewise rotated on its own axis. With Arachis, all four leaflets form together during the night a single vertical packet; and to the effect this the two anterior leaflets have to move upwards and the two posterior ones forwards, besides all twisting on their own axes. In the genus Sida the leaves of some species move at night through an angle of 90° upwards, and of others through the same angle downwards. We have seen a similar difference in the nyctitropic movements of the cotyledons in the genus Oxalis. In Lupinus, again, the leaflets move either upwards or downwards; and in some species, for instance L. luteus, those on one side of the star-shaped leaf move up, and those on the opposite side move down; the intermediate ones rotating on their axes; and by these varied movements, the whole leaf forms at night a vertical star instead of a horizontal one, as during the day. Some leaves and leaflets, besides moving either upwards or downwards, become more or less folded at night, as in Bauhinia and in some species of Oxalis. The positions, indeed, which leaves occupy when asleep are almost infinitely diversified; they may point either vertically upwards or downwards, or, in the case of leaflets, towards the apex or towards the base of the leaf, or in any intermediate position. They often rotate at least as much as 90° on their own axes. The leaves which arise from upright and from horizontal or much inclined branches on the same plant, move in some few cases in a different manner, as with Porlieria and Strephium. The whole appearance of many plants is wonderfully changed at night, as may be seen with Oxalis, and still more plainly with Mimosa. A bush of Acacia Farnesiana appears at night as if covered with little dangling bits of string instead of leaves. Excluding a few genera not seen by ourselves, about which we are in doubt, and excluding a few others the leaflets of which rotate at night, and do not rise or sink much, there are 37 genera in which the leaves or leaflets rise, often moving at the same time towards the apex or towards the base of the leaf, and 32 genera in which they sink at night.
The nyctitropic movements of leaves, leaflets, and petioles are effected in two different ways; firstly, by alternately increased growth on their opposite sides, preceded by increased turgescence of the cells; and secondly by means of a pulvinus or aggregate of small cells, generally destitute of chlorophyll, which become alternately more turgescent on nearly opposite sides; and this turgescence is not followed by growth except during the early age of the plant. A pulvinus seems to be formed (as formerly shown) by a group of cells ceasing to grow at a very early age, and therefore does not differ essentially from the surrounding tissues. The cotyledons of some species of Trifolium are provided with a pulvinus, and others are destitute of one, and so it is with the leaves in the genus Sida. We see also in this same genus gradations in the state of the development of the pulvinus; and in Nicotiana we have what may probably be considered as the commencing development of one. The nature of the movement is closely similar, whether a pulvinus is absent or present, as is evident from many of the diagrams given in this chapter. It deserves notice that when a pulvinus is present, the ascending and descending lines hardly ever coincide, so that ellipses are habitually described by the leaves thus provided, whether they are young or so old as to have quite ceased growing. This fact of ellipses being described, shows that the alternately increased turgescence of the cells does not occur on exactly opposite sides of the pulvinus, any more than the increased growth which causes the movements of leaves not furnished with pulvini. When a pulvinus is present, the nyctitropic movements are continued for a very much longer period than when such do not exist. This has been amply proved in the case of cotyledons, and Pfeffer has given observations to the same effect with respect to leaves. We have seen that a leaf of Mimosa pudica continued to move in the ordinary manner, though somewhat more simply, until it withered and died. It may be added that some leaflets of Trifolium pratense were pinned open during 10 days, and on the first evening after being released they rose up and slept in the usual manner. Besides the long continuance of the movements when effected by the aid of a pulvinus (and this appears to be the final cause of its development), a twisting movement at night, as Pfeffer has remarked, is almost confined to leaves thus provided.