Fig. 103. Lupinus speciosus: circumnutation of leaf, traced on vertical glass, from 10.15 A.M. to 5.45 P.M.; i.e., during 6 h. 30 m. [page 237]

(12.) Echeveria stolonifera (Crassulaceae, Fam. 84).—The older leaves of this plant are so thick and fleshy, and the young ones so short and broad, that it seemed very improbable that any circumnutation could be detected. A filament was fixed to a young upwardly inclined leaf, .75 inch in length and .28 in breadth, which stood on the outside of a terminal rosette of leaves, produced by a plant growing very vigorously. Its movement was traced during 3 days, as here shown (Fig. 104). The course was chiefly in an upward direction, and this may be attributed to the elongation of the leaf through growth; but we see that the lines are strongly zigzag, and that occasionally there was distinct circumnutation, though on a very small scale.

Fig. 104. Echeveria stolonifera: circumnutation of leaf, traced from 8.20 A.M. June 25th to 8.45 A.M. 28th. Apex of leaf 12 1/4 inches from the glass, so that the movement was much magnified; temp. 23o - 24 1/2o C. (13.) Bryophyllum (vel Calanchae) calycinum (Crassulaceae).—Duval-Jouve ('Bull. Soc. Bot. de France,' Feb. 14th, 1868) measured the distance between the tips of the upper pair of leaves on this plant, with the result shown in the following Table. It should be noted that the measurements on Dec. 2nd were made on a different pair of leaves: —

8 A.M. 2 P.M. 7 P.M. Nov. 16. . . . . . . . . . . . . . . . . . .15 mm.. . . . . .25 mm. . . .. . . .(?) " 19. . . . . . . . . . . . . . . . . . .48 " . . . . . . . 60 ". . . . . . . 48 mm. Dec. 2. . . . . . . . . . . . . . . . . . .22 ". . . . . . . . 43 ". . . . . . . .28 "

We see from this Table that the leaves stood considerably further apart at 2 P.M. than at either 8 A.M. or 7 P.M.; and this shows that they rise a little in the evening and fall or open in the forenoon.

(14.) Drosera rotundifolia (Droseraceae, Fam. 85).—The movements of a young leaf, having a long petiole but with its tentacles (or gland-bearing hairs) as yet unfolded, were traced during 47 h. 15 m. The figure (Fig. 105) shows that it circumnutated largely, chiefly in a vertical direction, making two ellipses each [page 238] day. On both days the leaf began to descend after 12 or 1 o'clock, and continued to do so all night, though to a very unequal distance on the two occasions. We therefore thought that the movement was periodic; but on observing three other leaves during several successive days and nights, we found this to be an error; and the case is given merely as a caution. On the third morning the above leaf occupied almost exactly the same position as on the first morning; and the tentacles by this time had unfolded sufficiently to project at right angles to the blade or disc.

Fig. 105. Drosera rotundifolia: circumnutation of young leaf, with filament fixed to back of blade, traced from 9.15 A.M. June 7th to 8.30 A.M. June 9th. Figure here reduced to one-half original scale.

The leaves as they grow older generally sink more and more downwards. The movement of an oldish leaf, the glands of which were still secreting freely, was traced for 24 h., during which time it continued to sink a little in a slightly zigzag line. On the following morning, at 7 A.M., a drop of a solution of carbonate of ammonia (2 gr. to 1 oz. of water) was placed on the disc, and this blackened the glands and induced inflection of many of the tentacles. The weight of the drop caused the leaf at first to sink a little; but immediately afterwards it began to rise in a somewhat zigzag course, and continued to do so till 3 P.M. It then circumnutated about the same spot on a very small scale for 21 h.; and during the next 21 h. it sank in a zigzag line to nearly the same level which it had held when the ammonia was first administered. By this time the tentacles had re-expanded, and the glands had recovered their proper colour. We thus learn that an old leaf [page 239] circumnutates on a small scale, at least whilst absorbing carbonate of ammonia; for it is probable that this absorption may stimulate growth and thus re-excite circumnutation. Whether the rising of the glass filament which was attached to the back of the leaf, resulted from its margin becoming slightly inflected (as generally occurs), or from the rising of the petiole, was not ascertained.

In order to learn whether the tentacles or gland-bearing hairs circumnutate, the back of a young leaf, with the innermost tentacles as yet incurved, was firmly cemented with shellac to a flat stick driven into compact damp argillaceous sand. The plant was placed under a microscope with the stage removed and with an eye-piece micrometer, of which each division equalled 1/500 of an inch. It should be stated that as the leaves grow older the tentacles of the exterior rows bend outwards and downwards, so as ultimately to become deflected considerably beneath the horizon. A tentacle in the second row from the margin was selected for observation, and was found to be moving outwards at a rate of 1/500 of an inch in 20 m., or 1/100 of inch in 1 h. 40 m.; but as it likewise moved from side to side to an extent of above 1/500 of inch, the movement was probably one of modified circumnutation. A tentacle on an old leaf was next observed in the same manner. In 15 m. after being placed under the microscope it had moved about 1/1000 of an inch. During the next 7 h. it was looked at repeatedly, and during this whole time it moved only another 1/1000 of an inch; and this small movement may have been due to the settling of the damp sand (on which the plant rested), though the sand had been firmly pressed down. We may therefore conclude that the tentacles when old do not circumnutate; yet this tentacle was so sensitive, that in 23 seconds after its gland had been merely touched with a bit of raw meat, it began to curl inwards. This fact is of some importance, as it apparently shows that the inflection of the tentacles from the stimulus of absorbed animal matter (and no doubt from that of contact with any object) is not due to modified circumnutation.

(15.) Dionoea muscipula (Droseraceae).—It should be premised that the leaves at an early stage of their development have the two lobes pressed closely together. These are at first directed back towards the centre of the plant; but they gradually rise up and soon stand at right angles to the petiole, and ultimately in nearly a straight line with it. A young leaf, which with the [page 240] petiole was only 1.2 inch in length, had a filament fixed externally along the midrib of the still closed lobes, which projected at right angles to the petiole. In the evening this leaf completed an ellipse in the course of 2 h. On the following day (Sept. 25th) its movements were traced during 22 h.; and we see in Fig. 106 that it moved in the same general direction, due to the straightening of the leaf, but in an extremely zigzag line. This line represents several drawn-out or modified ellipses. There can therefore be no doubt that this young leaf circumnutated.

Fig. 106. Dionaea muscipula: circumnutation of a young and expanding leaf, traced on a horizontal glass in darkness, from noon Sept. 24th to 10 A.M. 25th. Apex of leaf 13 inches from the glass, so tracing considerably magnified.

A rather old, horizontally extended leaf, with a filament attached along the under side of the midrib, was next observed during 7 h. It hardly moved, but when one of its sensitive hairs was touched, the blades closed, though not very quickly. A new dot was now made on the glass, but in the course of 14 h. 20 m. there was hardly any change in the position of the filament. We may therefore infer that an old and only moderately sensitive leaf does not circumnutate plainly; but we shall soon see that it by no means follows that such a leaf is absolutely motionless. We may further infer that the stimulus from a touch does not re-excite plain circumnutation.

Another full-grown leaf had a filament attached externally along one side of the midrib and parallel to it, so that the filament would move if the lobes closed. It should be first stated that, although a touch on one of the sensitive hairs of a vigorous leaf causes it to close quickly, often almost instantly, yet when a bit of damp meat or some solution of carbonate of ammonia is placed on the lobes, they close so slowly that generally 24 h. is required for the completion of the act. The above leaf was first observed for 2 h. 30 m., and did not circumnutate, but it ought to have been observed for a [page 241] longer period; although, as we have seen, a young leaf completed a fairly large ellipse in 2 h. A drop of an infusion of raw meat was then placed on the leaf, and within 2 h. the glass filament rose a little; and this implies that the lobes had begun to close, and perhaps the petiole to rise. It continued to rise with extreme slowness for the next 8 h. 30 m. The position of the pot was then (7.15 P.M., Sept. 24th) slightly changed and an additional drop of the infusion given, and a new tracing was begun (Fig. 107). By 10.50 P.M. the filament had risen only a little more, and it fell during the night. On the following morning the lobes were closing more quickly, and by 5 P.M. it was evident to the eye that they had closed considerably; by 8.48. P.M. this was still plainer, and by 10.45 P.M. the marginal spikes were interlocked. The leaf fell a little during the night, and next morning (25th) at 7 A.M. the lobes were completely shut. The course pursued, as may be seen in the figure, was

Fig. 107. Dionoea muscipula: closure of the lobes and circumnutation of a full-grown leaf, whilst absorbing an infusion of raw meat, traced in darkness, from 7.15 P.M. Sept. 24th to 9 A.M. 26th. Apex of leaf 8 inches from the vertical glass. Figure here reduced to two-thirds of original scale.

strongly zigzag, and this indicates that the closing of the lobes was combined with the circumnutation of the whole leaf; and there cannot be much doubt, considering how motionless the leaf was during 2 h. 30 m. before it received the infusion, that the absorption of the animal matter had excited it to circumnutate. The leaf was occasionally observed for the next four days, but was kept in rather too cool a place; nevertheless, it continued to circumnutate to a small extent, and the lobes remained closed.

It is sometimes stated in botanical works that the lobes close or sleep at night; but this is an error. To test the statement, very long glass filaments were fixed inside the two lobes of three leaves, and the distances between their tips were measured in the middle of the day and at night; but no difference could be detected.

The previous observations relate to the movements of the whole leaf, but the lobes move independently of the petiole, and [page 242] seem to be continually opening and shutting to a very small extent. A nearly full-grown leaf (afterwards proved to be highly sensitive to contact) stood almost horizontally, so that by driving a long thin pin through the foliaceous petiole close to the blade, it was rendered motionless. The plant, with a little triangle of paper attached to one of the marginal spikes, was placed under a microscope with an eye-piece micrometer, each division of which equalled 1/500 of an inch. The apex of the paper-triangle was now seen to be in constant slight movement; for in 4 h. it crossed nine divisions, or 9/500 of an inch, and after ten additional hours it moved back and had crossed 5/500 in an opposite direction. The plant was kept in rather too cool a place, and on the following day it moved rather less, namely, 1/500 in 3 h., and 2/500 in an opposite direction during the next 6 h. The two lobes, therefore, seem to be constantly closing or opening, though to a very small distance; for we must remember that the little triangle of paper affixed to the marginal spike increased its length, and thus exaggerated somewhat the movement. Similar observations, with the important difference that the petiole was left free and the plant kept under a high temperature, were made on a leaf, which was healthy, but so old that it did not close when its sensitive hairs were repeatedly touched, though judging from other cases it would have slowly closed if it had been stimulated by animal matter. The apex of the triangle was in almost, though not quite, constant movement, sometimes in one direction and sometimes in an opposite one; and it thrice crossed five divisions of the micrometer (i.e. 1/100 of an inch) in 30 m. This movement on so small a scale is hardly comparable with ordinary circumnutation; but it may perhaps be compared with the zigzag lines and little loops, by which the larger ellipses made by other plants are often interrupted.

In the first chapter of this volume, the remarkable oscillatory movements of the circumnutating hypocotyl of the cabbage have been described. The leaves of Dionaea present the same phenomenon, which is a wonderful one, as viewed under a low power (2-inch object-glass), with an eye-piece micrometer of which each division (1/500 of an inch) appeared as a rather wide space. The young unexpanded leaf, of which the circumnutating movements were traced (Fig. 106), had a glass filament fixed perpendicularly to it; and the movement of the apex was observed in the hot-house (temp. 84o to 86o F.), with light admitted only from above, and with any lateral currents of air [page 243] excluded. The apex sometimes crossed one or two divisions of the micrometer at an imperceptibly slow rate, but generally it moved onwards by rapid starts or jerks of 2/1000 or 3/1000, and in one instance of 4/1000 of an inch. After each jerk forwards, the apex drew itself backwards with comparative slowness for part of the distance which had just been gained; and then after a very short time made another jerk forwards. Four conspicuous jerks forwards, with slower retreats, were seen on one occasion to occur in exactly one minute, besides some minor oscillations. As far as we could judge, the advancing and retreating lines did not coincide, and if so, extremely minute ellipses were each time described. Sometimes the apex remained quite motionless for a short period. Its general course during the several hours of observation was in two opposite directions, so that the leaf was probably circumnutating.

An older leaf with the lobes fully expanded, and which was afterwards proved to be highly sensitive to contact, was next observed in a similar manner, except that the plant was exposed to a lower temperature in a room. The apex oscillated forwards and backwards in the same manner as before; but the jerks forward were less in extent, viz. about 1/1000 inch; and there were longer motionless periods. As it appeared possible that the movements might be due to currents of air, a wax taper was held close to the leaf during one of the motionless periods, but no oscillations were thus caused. After 10 m., however, vigorous oscillations commenced, perhaps owing to the plant having been warmed and thus stimulated. The candle was then removed and before long the oscillations ceased; nevertheless, when looked at again after an interval of 1 h. 30 m., it was again oscillating. The plant was taken back into the hot-house, and on the following morning was seen to be oscillating, though not very vigorously. Another old but healthy leaf, which was not in the least sensitive to a touch, was likewise observed during two days in the hot-house, and the attached filament made many little jerks forwards of about 2/1000 or only 1/1000 of an inch.

Finally, to ascertain whether the lobes independently of the petiole oscillated, the petiole of an old leaf was cemented close to the blade with shellac to the top of a little stick driven into the soil. But before this was done the leaf was observed, and found to be vigorously oscillating or jerking; and after it had been cemented to the stick, the oscillations of about 2/1000 of an inch still continued. On the following day a little infusion [page 244] of raw meat was placed on the leaf, which caused the lobes to close together very slowly in the course of two days; and the oscillations continued during this whole time and for the next two days. After nine additional days the leaf began to open and the margins were a little everted, and now the apex of the glass filament remained for long periods motionless, and then moved backwards and forwards for a distance of about 1/1000 of an inch slowly, without any jerks. Nevertheless, after warming the leaf with a taper held close to it, the jerking movement recommenced.

This same leaf had been observed 2 months previously, and was then found to be oscillating or jerking. We may therefore infer that this kind of movement goes on night and day for a very long period; and it is common to young unexpanded leaves and to leaves so old as to have lost their sensitiveness to a touch, but which were still capable of absorbing nitrogenous matter. The phenomenon when well displayed, as in the young leaf just described, is a very interesting one. It often brought before our minds the idea of effort, or of a small animal struggling to escape from some constraint.

(16.) Eucalyptus resinifera (Myrtaceae, Fam. 94).—A young leaf, two inches in length together with the petiole, produced by a lateral shoot from a cut-down tree, was observed in the usual manner. The blade had not as yet assumed its vertical position. On June 7th only a few observations were made, and the tracing merely showed that the leaf had moved three times upwards and three downwards. On the following day it was observed more frequently; and two tracings were made (see A and B, Fig. 108), as a single one would have been too complicated. The apex changed its course 13 times in the course of 16 h., chiefly up and down, but with some lateral movement. The actual amount of movement in any one direction was small.

Fig. 108. Eucalyptus resinifera: circumnutation of a leaf, traced, A, from 6.40 A.M. to 1 P.M. June 8th; B, from 1 P.M. 8th to 8.30 A.M. 9th. Apex of leaf 14 inches from the horizontal glass, so figures considerably magnified.

(17.) Dahlia (garden var.) (Compositae, Fam. 122).—A fine young [page 245] leaf 5 3/4 inches in length, produced by a young plant 2 feet high, growing vigorously in a large pot, was directed at an angle of about 45o beneath the horizon. On June 18th the leaf descended from 10 A.M. till 11.35 A.M. (see Fig. 109); it then ascended greatly till 6 P.M., this ascent being probably due to the light

Fig. 109. Dahlia: circumnutation of leaf, traced from 10 A.M. June 18th to 8.10 A.M. 20th, but with a break of 1 h. 40 m. on the morning of the 19th, as, owing to the glass filament pointing too much to one side, the pot had to be slightly moved; therefore the relative position of the two tracings is somewhat arbitrary. The figure here given is reduced to one-fifth of the original scale. Apex of leaf 9 inches from the glass in the line of its inclination, and 4 3/4 in a horizontal line. coming only from above. It zigzagged between 6 P.M. and 10.35 P.M., and ascended a little during the night. It should be remarked that the vertical distances in the lower part of the diagram are much exaggerated, as the leaf was at first deflected beneath the horizon, and after it had sunk downwards, the filament pointed in a very oblique line towards the glass. Next [page 246] day the leaf descended from 8.20 A.M. till 7.15 P.M., then zigzagged and ascended greatly during the night. On the morning of the 20th the leaf was probably beginning to descend, though the short line in the diagram is horizontal. The actual distances travelled by the apex of the leaf were considerable, but could not be calculated with safety. From the course pursued on the second day, when the plant had accommodated itself to the light from above, there cannot be much doubt that the leaves undergo a daily periodic movement, sinking during the day and rising at night.

(18.) Mutisia clematis (Compositae).—The leaves terminate in tendrils and circumnutate like those of other tendril-bearers; but this plant is here mentioned, on account of an erroneous statement* which has been published, namely, that the leaves sink at night and rise during the day. The leaves which behaved in this manner had been kept for some days in a northern room and had not been sufficiently illuminated. A plant therefore was left undisturbed in the hot-house, and three leaves had their angles measured at noon and at 10 P.M. All three were inclined a little beneath the horizon at noon, but one stood at night 2o, the second 21o, and the third 10o higher than in the middle of the day; so that instead of sinking they rise a little at night.

(19.) Cyclamen Persicum (Primulaceae, Fam. 135).—A young leaf, 1.8 of an inch in length, petiole included, produced by an old root-stock, was observed during three days in the usual manner (Fig. 110). On the first day the leaf fell more than afterwards, apparently from adjusting itself to the light from above. On all three days it fell from the early morning to about 7 P.M., and from that hour rose during the night, the course being slightly zigzag. The movement therefore is strictly periodic. It should be noted that the leaf would have sunk each evening a little lower down than it did, had not the glass filament rested between 5 and 6 P.M. on the rim of the pot. The amount of movement was considerable; for if we assume that the whole leaf to the base of the petiole became bent, the tracing would be magnified rather less than five times, and this would give to the apex a rise and fall of half an inch, with some lateral movement. This amount, however, would not attract attention without the aid of a tracing or measurement of some kind.

* 'The Movements and Habits of Climbing Plants,' 1875, p. 118. [page 247]

(20.) Allamanda Schottii (Apocyneae, Fam. 144).—The young leaves of this shrub are elongated, with the blade bowed so much

Fig. 110. Cyclamen Persicum: circumnutation of leaf, traced from 6.45 A.M. June 2nd to 6.40 A.M. 5th. Apex of leaf 7 inches from the vertical glass.

downwards as almost to form a semicircle. The chord—that is, a line drawn from the apex of the blade to the base of the petiole—of a young leaf, 4 3/4 inches in length, stood at 2.50 P.M. on [page 248] Dec. 5th at an angle of 13o beneath the horizon, but by 9.30 P.M. the blade had straightened itself so much, which implies the raising of the apex, that the chord now stood at 37o above the horizon, and had therefore risen 50o. On the next day similar angular measurements of the same leaf were made; and at noon the chord stood 36o beneath the horizon, and 9.30 P.M. 3 1/2o above it, so had risen 39 1/2o. The chief cause of the rising movement lies in the straightening of the blade, but the short petiole rises between 4o and 5o. On the third night the chord stood at 35o above the horizon, and if the leaf occupied the same position at noon, as on the previous day, it had risen 71o. With older leaves no such change of curvature could be detected. The plant was then brought into the house and kept in a north-east room, but at night there was no change in the curvature of the young leaves; so that previous exposure to a strong light is apparently requisite for the periodical change of curvature in the blade, and for the slight rising of the petiole.

(21.) Wigandia (Hydroleaceae, Fam. 149).—Professor Pfeffer informs us that the leaves of this plant rise in the evening; but as we do not know whether or not the rising is great, this species ought perhaps to be classed amongst sleeping plants.

Fig. 111. Petunia violacea: downward movement and circumnutation of a very young leaf, traced from 10 A.M. June 2nd to 9.20 A.M. June 6th. N.B.—At 6.40 A.M. on the 5th it was necessary to move the pot a little, and a new tracing was begun at the point where two dots are not joined in the diagram. Apex of leaf 7 inches from the vertical glass. Temp. generally 17 1/2o C. [page 249]

(22.) Petunia violacea (Solaneae, Fam. 157).—A very young leaf, only 3/4 inch in length, highly inclined upwards, was observed for four days. During the whole of this time it bent outwards and downwards, so as to become more and more nearly horizontal. The strongly marked zigzag line in the figure on p. 248 (Fig. 111), shows that this was effected by modified circumnutation; and during the latter part of the time there was much ordinary circumnutation on a small scale. The movement in the diagram is magnified between 10 and 11 times. It exhibits a clear trace of periodicity, as the leaf rose a little each evening; but this upward tendency appeared to be almost conquered by the leaf striving to become more and more horizontal as it grew older. The angles which two older leaves formed together, were measured in the evening and about noon on 3 successive days, and each night the angle decreased a little, though irregularly.

Fig. 112. Acanthus mollis: circumnutation of young leaf, traced from 9.20 A.M. June 14th to 8.30 A.M. 16th. Apex of leaf 11 inches from the vertical glass, so movement considerably magnified. Figure here reduced to one-half of original scale. Temp. 15o - 16 1/2o C.

(23.) Acanthus mollis (Acanthaceae, Fam. 168).—The younger of two leaves, 2 1/4 inches in length, petiole included, produced by a seedling plant, was observed during 47 h. Early on each of the three mornings, the apex of the leaf fell; and it continued to fall till 3 P.M., on the two afternoons when observed. After 3 P.M. it rose considerably, and continued to rise on the second night until the early morning. But on the first night it fell instead of rising, and we have little doubt that this was owing to the leaf being very young and becoming through epinastic growth more and more horizontal; for it may be seen in the diagram (Fig. 112), that the leaf stood on a higher level on the first than on the second day. The leaves of an allied species ('A. spinosus') certainly rose every night; and the rise between noon and 10.15 P.M., when measured on one occasion, was 10o. This rise was chiefly [page 250] or exclusively due to the straightening of the blade, and not to the movement of the petiole. We may therefore conclude that the leaves of Acanthus circumnutate periodically, falling in the morning and rising in the afternoon and night.

(24.) Cannabis sativa (Cannabineae, Fam. 195).—We have here the rare case of leaves moving downwards in the evening, but not to a sufficient degree to be called sleep.* In the early morning, or in the latter part of the night, they move upwards. For instance, all the young leaves near the summits of several stems stood almost horizontally at 8 A.M. May 29th and at 10.30 P.M. were considerably declined. On a subsequent day two leaves stood at 2 P.M. at 21o and 12o beneath the horizon, and at 10 P.M. at 38o beneath it. Two other leaves on a younger plant were horizontal at 2 P.M., and at 10 P.M. had sunk to 36o beneath the horizon. With respect to this downward movement of the leaves, Kraus believes that it is due to their epinastic growth. He adds, that the leaves are relaxed during the day, and tense at night, both in sunny and rainy weather.

(25.) Pinus pinaster (Coniferae, Fam. 223).—The leaves on the summits of the terminal shoots stand at first in a bundle almost upright, but they soon diverge and ultimately become almost horizontal. The movements of a young leaf, nearly one inch in length, on the summit of a seedling plant only 3 inches high, were traced from the early morning of June 2nd to the evening of the 7th. During these five days the leaf diverged, and its apex descended at first in an almost straight line; but during the two latter days it zigzagged so much that it was evidently circumnutating. The same little plant, when grown to a height of 5 inches, was again observed during four days. A filament was fixed transversely to the apex of a leaf, one inch in length, and which had already diverged considerably from its originally upright position. It continued to diverge (see A, Fig. 113), and to descend from 11.45 A.M. July 31st to 6.40 A.M. Aug. 1st. On August 1st it circumnutated about the same small space, and again descended at night. Next morning the pot was moved nearly one inch to the right, and a new tracing was begun (B). From this time, viz., 7 A.M. August 2nd to 8.20 A.M. on the 4th,

* We were led to observe this plant by Dr. Carl Kraus' paper, 'Beitrge zur Kentniss der Bewegungen Wachsender Laubbltter,' Flora, 1879, p. 66. We regret that we cannot fully understand parts of this paper. [page 251]

the leaf manifestly circumnutated. It does not appear from the diagram that the leaves move periodically, for the descending course during the first two nights, was clearly due to epinastic

Fig. 113. Pinus pinaster: circumnutation of young leaf, traced from 11.45 A.M. July 31st to 8.20 A.M. Aug. 4th. At 7 A.M. Aug. 2nd the pot was moved an inch to one side, so that the tracing consists of two figures. Apex of leaf 14 inches from the vertical glass, so movements much magnified.

growth, and at the close of our observations the leaf was not nearly so horizontal as it would ultimately become.

Pinus austriaca.—Two leaves, 3 inches in length, but not [page 252] quite fully grown, produced by a lateral shoot, on a young tree 3 feet in height, were observed during 29 h. (July 31st), in the same manner as the leaves of the previous species. Both these leaves certainly circumnutated, making within the above period two, or two and a half, small, irregular ellipses.

(26.) Cycas pectinata (Cycadeae, Fam. 224).—A young leaf, 11 inches in length, of which the leaflets had only recently become uncurled, was observed during 47 h. 30 m. The main petiole was secured to a stick at the base of the two terminal leaflets. To one of the latter, 3 3/4 inches in length, a filament was fixed; the leaflet was much bowed downward, but as the terminal part was upturned, the filament projected almost horizontally. The leaflet moved (see Fig. 114) largely and periodically, for it fell until about 7 P.M. and rose during the night, falling again next morning after 6.40 A.M. The descending lines are in a marked manner zigzag, and so probably would have been the ascending lines, if they had been traced throughout the night.

Fig. 114. Cycas pectinata: circumnutation of one of the terminal leaflets, traced from 8.30 A.M. June 22nd to 8 A.M. June 24th. Apex of leaflet 7 3/4 inches from the vertical glass, so tracing not greatly magnified, and here reduced to one-third of original scale; temp. 19o - 21o C.

CIRCUMNUTATION OF LEAVES: MONOCOTYLEDONS.

(27.) Canna Warscewiczii (Cannaceae, Fam. 2).—The movements of a young leaf, 8 inches in length and 3 in breadth, produced by a vigorous young plant, were observed during 45 h. 50 m., as shown in Fig. 115. The pot was slided about an inch to the right on the morning of the 11th, as a single figure would have been too complicated; but the two figures are continuous in time. The movement is periodical, as the leaf descended from the early morning until about 5 P.M., and ascended during the rest of the evening and [page 253] part of the night. On the evening of the 11th it circumnutated on a small scale for some time about the same spot.

Fig. 115. Canna Warscewiczii: circumnutation of leaf, traced (A) from 11.30 A.M. June 10th to 6.40 A.M. 11th; and (B) from 6.40 A.M. 11th to 8.40 A.M. 12th. Apex of leaf 9 inches from the vertical glass.

(28.) Iris pseudo-acorus (Irideae, Fam. 10).—The movements of a young leaf, rising 13 inches above the water in which the plant grew, were traced as shown in the figure (Fig. 116), during 27 h. 30 m. It manifestly circumnutated, though only to a small extent. On the second morning, between 6.40 A.M. and 2 P.M. (at which latter hour the figure here given ends), the apex changed its course five times. During the next 8 h. 40 m. it zigzagged much, and descended as far as the lowest dot in the figure, making in its course two very small ellipses; but if these lines had been added to the diagram it would have been too complex.

Fig. 116. Iris pseudo-acorus: circumnutation of leaf, traced from 10.30 A.M. May 28th to 2 P.M. 29th. Tracing continued to 11 P.M., but not here copied. Apex of leaf 12 inches beneath the horizontal glass, so figure considerably magnified. Temp. 15o - 16o C. (29.) Crinum Capense (Amaryllideae, Fam. 11).—The leaves of this plant are remarkable for their great length and narrowness: one was measured and found to be 53 inches long and only 1.4 broad at the base. Whilst quite young they stand up almost vertically to the height of about a foot; afterwards [page 254] their tips begin to bend over, and subsequently hang vertically down, and thus continue to grow. A rather young leaf was selected, of which the dependent tapering point was as yet only 5 inches in length, the upright basal part being 20 inches high, though this part would ultimately become shorter by being more bent over. A large bell-glass was placed over the plant, with a black dot on one side; and by bringing the dependent apex of the leaf into a line with this dot, the accompanying figure (Fig. 117) was traced on the other side of the bell, during 2 days. During the first day (22nd) the tip travelled laterally far to the left, perhaps in consequence of the plant having been

Fig. 117. Crinum Capense: circumnutation of dependent tip of young leaf, traced on a bell-glass, from 10.30 P.M. May 22nd to 10.15 A.M. 25th. Figure not greatly magnified.

disturbed; and the last dot made at 10.30 P.M. on this day is alone here given. As we see in the figure, there can be no doubt that the apex of this leaf circumnutated.

A glass filament with little triangles of paper was at the same time fixed obliquely across the tip of a still younger leaf, which stood vertically up and was as yet straight. Its movements were traced from 3 P.M. May 22nd to 10.15 A.M. 25th. The leaf was growing rapidly, so that the apex ascended greatly during this period; as it zigzagged much it was clearly circumnutating, and it apparently tended to form one ellipse each day. The lines traced during the night were much more vertical than those traced during the day; and this indicates that the tracing would have exhibited a nocturnal rise and a diurnal fall, if the leaf had not grown so quickly. The movement of this same leaf after an interval of six days (May 31st), by which time the tip had curved outwards into a horizontal position, [page 255] and had thus made the first step towards becoming dependent, was traced orthogonically by the aid of a cube of wood (in the manner before explained); and it was thus ascertained that the actual distance travelled by the apex, and due to circumnutation, was 3 1/8 inches in the course of 20 h. During the next 24 h. it travelled 2 inches. The circumnutating movement, therefore, of this young leaf was strongly marked.

(30.) Pancratium littorale (Amaryllideae).—The movements, much magnified, of a leaf, 9 inches in length and inclined at about 45o above the horizon, were traced during two days. On the first day it changed its course completely, upwards and downwards and laterally, 9 times in 12 h.; and the figure traced apparently represented five ellipses. On the second day it was observed seldomer, and was therefore not seen to change its course so often, viz., only 6 times, but in the same complex manner as before. The movements were small in extent, but there could be no doubt about the circumnutation of the leaf.

(31.) Imatophyllum vel Clivia (sp.?) (Amaryllideae).—A long glass filament was fixed to a leaf, and the angle formed by it with the horizon was measured occasionally during three successive days. It fell each morning until between 3 and 4 P.M., and rose at night. The smallest angle at any time above the horizon was 48o, and the largest 50o; so that it rose only 2o at night; but as this was observed each day, and as similar observations were nightly made on another leaf on a distinct plant, there can be no doubt that the leaves move periodically, though to a very small extent. The position of the apex when it stood highest was .8 of an inch above its lowest point.

(32.) Pistia stratiotes (Aroideae, Fam. 30).—Hofmeister remarks that the leaves of this floating water-plant are more highly inclined at night than by day.* We therefore fastened a fine glass filament to the midrib of a moderately young leaf, and on Sept. 19th measured the angle which it formed with the horizon 14 times between 9 A.M. and 11.50 P.M. The temperature of the hot-house varied during the two days of observation between 18 1/2o and 23 1/2o C. At 9 A.M. the filament stood at 32o above the horizon; at 3.34 P.M. at 10o and at 11.50 P.M. at 55o; these two latter angles being the highest and the lowest observed during the day, showing a difference of 45o. The rising did not become strongly marked until between

* 'Die Lehre von der Pflanzenzelle,' 1867, p. 327. [page 256]

5 and 6 P.M. On the next day the leaf stood at only 10o above the horizon at 8.25 A.M., and it remained at about 15o till past 3 P.M.; at 5.40 P.M. it was 23o, and at 9.30 P.M. 58o; so that the rise was more sudden this evening than on the previous one, and the difference in the angle amounted to 48o. The movement is obviously periodical, and as the leaf stood on the first night at 55o, and on the second night at 58o above the horizon, it appeared very steeply inclined. This case, as we shall see in a future chapter, ought perhaps to have been included under the head of sleeping plants.

(33.) Pontederia (sp.?) (from the highlands of St. Catharina,

Fig. 118. Pontederia (sp.?): circumnutation of leaf, traced from 4.50 P.M. July 2nd to 10.15 A.M. 4th. Apex of leaf 16 inches from the vertical glass, so tracing greatly magnified. Temp. about 17o C., and therefore rather too low.

Brazil) (Pontederiaceae, Fam. 46).—A filament was fixed across the apex of a moderately young leaf, 7 inches in height, and its movements were traced during 42 h. (see Fig. 118). On the first evening, when the tracing was begun, and during the night, the leaf descended considerably. On the next morning it ascended in a strongly marked zigzag line, and descended again in the evening and during the night. The movement, therefore, seems to be periodic, but some doubt is thrown on this conclusion, because another leaf, 8 inches in height, appearing older and standing more highly inclined, behaved differently. During the first 12 h. it circumnutated over a [page 257] small space, but during the night and the whole following day it ascended in the same general direction; the ascent being effected by repeated up and down well-pronounced oscillations.

CRYPTOGAMS.

(34.) Nephrodium molle (Filices, Fam. 1).—A filament was fixed near the apex of a young frond of this Fern, 17 inches in height, which was not as yet fully uncurled; and its movements were traced during 24 h. We see in Fig. 119 that it

Fig. 119. Nephrodium molle: circumnutation of rachis, traced from 9.15 A.M. May 28th to 9 A.M. 29th. Figure here given two-thirds of original scale.

plainly circumnutated. The movement was not greatly magnified as the frond was placed near to the vertical glass, and would probably have been greater and more rapid had the day been warmer. For the plant was brought out of a warm greenhouse and observed under a skylight, where the temperature was between 15o and 16o C. We have seen in Chap. I. that a frond of this Fern, as yet only slightly lobed and with a rachis only .23 inch in height, plainly circumnutated.*

* Mr. Loomis and Prof. Asa Gray have described ('Botanical Gazette,' 1880, pp. 27, 43), an extremely curious case of movement in the fronds, but only in the fruiting fronds, of Asplenium trichomanes. They move almost as rapidly as the little leaflets of Desmodium gyrans, alternately backwards and forwards through from 20 to 40 degrees, in a plane at right angles to that of the frond. The apex of the frond describes "a long and very narrow ellipse," so that it circumnutates. But the movement differs from ordinary [[page 258]] circumnutation as it occurs only when the plant is exposed to the light; even artificial light "is sufficient to excite motion for a few minutes." [page 258]

In the chapter on the Sleep of Plants the conspicuous circumnutation of Marsilea quadrifoliata (Marsileaceae, Fam. 4) will be described.

It has also been shown in Chap. I. that a very young Selaginella (Lycopodiaceae, Fam. 6), only .4 inch in height, plainly circumnutated; we may therefore conclude that older plants, whilst growing, would do the same.

Fig. 120. Lunularia vulgaris: circumnutation of a frond, traced from 9 A.M. Oct 25th to 8 A.M. 27th.

(35.) Lunularia vulgaris (Hepaticae, Fam. 11, Muscales).—The earth in an old flower-pot was coated with this plant, bearing gemmae. A highly inclined frond, which projected .3 inch above the soil and was .4 inch in breadth, was selected for observation. A glass hair of extreme tenuity, .75 inch in length, with its end whitened, was cemented with shellac to the frond at right angles to its breadth; and a white stick with a minute black spot was driven into the soil close behind the end of the hair. The white end could be accurately brought into a line with the black spot, and dots could thus be successively made on the vertical glass-plate in front. Any movement of the frond would of course be exhibited and increased by the long glass hair; and the black spot was placed so close behind the end of the hair, relatively to the distance of the glass-plate in front, that the movement of the end was magnified about 40 times. Nevertheless, we are convinced that our tracing gives a fairly faithful representation of the movements of the frond. In the intervals between each observation, the plant was covered by a small bell-glass. The frond, as already stated, [page 259] was highly inclined, and the pot stood in front of a north-east window. During the five first days the frond moved downwards or became less inclined; and the long line which was traced was strongly zigzag, with loops occasionally formed or nearly formed; and this indicated circumnutation. Whether the sinking was due to epinastic growth, or apheliotropism, we do not know. As the sinking was slight on the fifth day, a new tracing was begun on the sixth day (Oct. 25th), and was continued for 47 h.; it is here given (Fig. 120). Another tracing was made on the next day (27th) and the frond was found to be still circumnutating, for during 14 h. 30 m. it changed its course completely (besides minor changes) 10 times. It was casually observed for two more days, and was seen to be continually moving.

The lowest members of the vegetable series, the Thallogens, apparently circumnutate. If an Oscillaria be watched under the microscope, it may be seen to describe circles about every 40 seconds. After it has bent to one side, the tip first begins to bend back to the opposite side and then the whole filament curves over in the same direction. Hofmeister* has given a minute account of the curious, but less regular though constant, movements of Spirogyra: during 2 h. the filament moved 4 times to the left and 3 times to the right, and he refers to a movement at right angles to the above. The tip moved at the rate of about 0.1 mm. in five minutes. He compares the movement with the nutation of the higher plants.** We shall hereafter see that heliotropic movements result from modified circumnutation, and as unicellular Moulds bend to the light we may infer that they also circumnutate.]

CONCLUDING REMARKS ON THE CIRCUMNUTATION OF LEAVES.

The circumnutating movements of young leaves in 33 genera, belonging to 25 families, widely distributed

* 'Ueber die Bewegungen der Faden der Spirogyra princeps: Jahreshefte des Vereins fr vaterlndische Naturkunde in Wrttemberg,' 1874, p. 211.

** Zukal also remarks (as quoted in 'Journal R. Microscop. Soc.,' 1880, vol. iii. p. 320) that the movements of Spirulina, a member of the Oscillatorieae, are closely analogous "to the well-known rotation of growing shoots and tendrils." [page 260]

amongst ordinary and gymnospermous Dicotyledons and amongst Monocotyledons, together with several Cryptogams, have now been described. It would, therefore, not be rash to assume that the growing leaves of all plants circumnutate, as we have seen reason to conclude is the case with cotyledons. The seat of movement generally lies in the petiole, but sometimes both in the petiole and blade, or in the blade alone. The extent of the movement differed much in different plants; but the distance passed over was never great, except with Pistia, which ought perhaps to have been included amongst sleeping plants. The angular movement of the leaves was only occasionally measured; it commonly varied from only 2o (and probably even less in some instances) to about 10o; but it amounted to 23o in the common bean. The movement is chiefly in a vertical plane, but as the ascending and descending lines never coincided, there was always some lateral movement, and thus irregular ellipses were formed. The movement, therefore, deserves to be called one of circumnutation; for all circumnutating organs tend to describe ellipses,—that is, growth on one side is succeeded by growth on nearly but not quite the opposite side. The ellipses, or the zigzag lines representing drawn-out ellipses, are generally very narrow; yet with the Camellia, their minor axes were half as long, and with the Eucalyptus more than half as long as their major axes. In the case of Cissus, parts of the figure more nearly represented circles than ellipses. The amount of lateral movement is therefore sometimes considerable. Moreover, the longer axes of the successively formed ellipses (as with the Bean, Cissus, and Sea-kale), and in several instances the zigzag lines representing ellipses, were extended in very different directions during the same day or on [page 261] the next day. The course followed was curvilinear or straight, or slightly or strongly zigzag, and little loops or triangles were often formed. A single large irregular ellipse may be described on one day, and two smaller ones by the same plant on the next day. With Drosera two, and with Lupinus, Eucalyptus and Pancratium, several were formed each day.

The oscillatory and jerking movements of the leaves of Dionaea, which resemble those of the hypocotyl of the cabbage, are highly remarkable, as seen under the microscope. They continue night and day for some months, and are displayed by young unexpanded leaves, and by old ones which have lost their sensibility to a touch, but which, after absorbing animal matter, close their lobes. We shall hereafter meet with the same kind of movement in the joints of certain Gramineae, and it is probably common to many plants while circumnutating. It is, therefore, a strange fact that no such movement could be detected in the tentacles of Drosera rotundifolia, though a member of the same family with Dionaea; yet the tentacle which was observed was so sensitive, that it began to curl inwards in 23 seconds after being touched by a bit of raw meat.

One of the most interesting facts with respect to the circumnutation of leaves is the periodicity of their movements; for they often, or even generally, rise a little in the evening and early part of the night, and sink again on the following morning. Exactly the same phenomenon was observed in the case of cotyledons. The leaves in 16 genera out of the 33 which were observed behaved in this manner, as did probably 2 others. Nor must it be supposed that in the remaining 15 genera there was no periodicity in their movements; for 6 of them were observed during too short a period for any judgment to be formed on this head, [page 262] and 3 were so young that their epinastic growth, which serves to bring them down into a horizontal position, overpowered every other kind of movement. In only one genus, Cannabis, did the leaves sink in the evening, and Kraus attributes this movement to the prepotency of their epinastic growth. That the periodicity is determined by the daily alternations of light and darkness there can hardly be a doubt, as will hereafter be shown. Insectivorous plants are very little affected, as far as their movements are concerned, by light; and hence probably it is that their leaves, at least in the cases of Sarracenia, Drosera, and Dionaea, do not move periodically. The upward movement in the evening is at first slow, and with different plants begins at very different hours;—with Glaucium as early as 11 A.M., commonly between 3 and 5 P.M., but sometimes as late as 7 P.M. It should be observed that none of the leaves described in this chapter (except, as we believe, those of Lupinus speciosus) possess a pulvinus; for the periodical movements of leaves thus provided have generally been amplified into so-called sleep-movements, with which we are not here concerned. The fact of leaves and cotyledons frequently, or even generally, rising a little in the evening and sinking in the morning, is of interest as giving the foundation from which the specialised sleep-movements of many leaves and cotyledons, not provided with a pulvinus, have been developed. the above periodicity should be kept in mind, by any one considering the problem of the horizontal position of leaves and cotyledons during the day, whilst illuminated from above. [page 263]

CHAPTER V.

MODIFIED CIRCUMNUTATION: CLIMBING PLANTS; EPINASTIC AND HYPONASTIC MOVEMENTS.

Circumnutation modified through innate causes or through the action of external conditions—Innate causes—Climbing plants; similarity of their movements with those of ordinary plants; increased amplitude; occasional points of difference—Epinastic growth of young leaves—Hyponastic growth of the hypocotyls and epicotyls of seedlings—Hooked tips of climbing and other plants due to modified circumnutation—Ampelopsis tricuspidata— Smithia Pfundii—Straightening of the tip due to hyponasty—Epinastic growth and circumnutation of the flower-peduncles of Trifolium repens and Oxalis carnosa.

THE radicles, hypocotyls and epicotyls of seedling plants, even before they emerge from the ground, and afterwards the cotyledons, are all continually circumnutating. So it is with the stems, stolons, flower-peduncles, and leaves of older plants. We may, therefore, infer with a considerable degree of safety that all the growing parts of all plants circumnutate. Although this movement, in its ordinary or unmodified state, appears in some cases to be of service to plants, either directly or indirectly—for instance, the circumnutation of the radicle in penetrating the ground, or that of the arched hypocotyl and epicotyl in breaking through the surface—yet circumnutation is so general, or rather so universal a phenomenon, that we cannot suppose it to have been gained for any special purpose. We must believe that it follows in some unknown way from the manner in which vegetable tissues grow. [page 264]

We shall now consider the many cases in which circumnutation has been modified for various special purposes; that is, a movement already in progress is temporarily increased in some one direction, and temporarily diminished or quite arrested in other directions. These cases may be divided in two sub-classes; in one of which the modification depends on innate or constitutional causes, and is independent of external conditions, excepting in so far that the proper ones for growth must be present. In the second sub-class the modification depends to a large extent on external agencies, such as the daily alternations of light and darkness, or light alone, temperature, or the attraction of gravity. The first small sub-class will be considered in the present chapter, and the second sub-class in the remainder of this volume.

THE CIRCUMNUTATION OF CLIMBING PLANTS.

The simplest case of modified circumnutation is that offered by climbing plants, with the exception of those which climb by the aid of motionless hooks or of rootlets: for the modification consists chiefly in the greatly increased amplitude of the movement. This would follow either from greatly increased growth over a small length, or more probably from moderately increased growth spread over a considerable length of the moving organ, preceded by turgescence, and acting successively on all sides. The circumnutation of climbers is more regular than that of ordinary plants; but in almost every other respect there is a close similarity between their movements, namely, in their tendency to describe ellipses directed successively to all points of the compass—in their courses being often interrupted by zigzag lines, triangles, loops, or small [page 265] ellipses—in the rate of movement, and in different species revolving once or several times within the same length of time. In the same internode, the movements cease first in the lower part and then slowly upwards. In both sets of cases the movement may be modified in a closely analogous manner by geotropism and by heliotropism; though few climbing plants are heliotropic. Other points of similarity might be pointed out.

That the movements of climbing plants consist of ordinary circumnutation, modified by being increased in amplitude, is well exhibited whilst the plants are very young; for at this early age they move like other seedlings, but as they grow older their movements gradually increase without undergoing any other change. That this power is innate, and is not excited by any external agencies, beyond those necessary for growth and vigour, is obvious. No one doubts that this power has been gained for the sake of enabling climbing plants to ascend to a height, and thus to reach the light. This is effected by two very different methods; first, by twining spirally round a support, but to do so their stems must be long and flexible; and, secondly, in the case of leaf-climbers and tendril-bearers, by bringing these organs into contact with a support, which is then seized by the aid of their sensitiveness. It may be here remarked that these latter movements have no relation, as far as we can judge, with circumnutation. In other cases the tips of tendrils, after having been brought into contact with a support, become developed into little discs which adhere firmly to it.

We have said that the circumnutation of climbing plants differs from that of ordinary plants chiefly by its greater amplitude. But most leaves circumnutate [page 266] in an almost vertical plane, and therefore describe very narrow ellipses, whereas the many kinds of tendrils which consist of metamorphosed leaves, make much broader ellipses or nearly circular figures; and thus they have a far better chance of catching hold of a support on any side. The movements of climbing plants have also been modified in some few other special ways. Thus the circumnutating stems of Solnanum dulcamara can twine round a support only when this is as thin and flexible as a string or thread. The twining stems of several British plants cannot twine round a support when it is more than a few inches in thickness; whilst in tropical forests some can embrace thick trunks;* and this great difference in power depends on some unknown difference in their manner of circumnutation. The most remarkable special modification of this movement which we have observed is in the tendrils of Echinocystis lobata; these are usually inclined at about 45o above the horizon, but they stiffen and straighten themselves so as to stand upright in a part of their circular course, namely, when they approach and have to pass over the summit or the shoot from which they arise. If they had not possessed and exercised this curious power, they would infallibly have struck against the summit of the shoot and been arrested in their course. As soon as one of these tendrils with its three branches begins to stiffen itself and rise up vertically, the revolving motion becomes more rapid; and as soon as it has passed over the point of difficulty, its motion coinciding with that from its own weight, causes it to fall into its previously inclined position so quickly, that the apex can be seen travelling like the hand of a gigantic clock.

* 'The Movements and Habits of Climbing Plants,' p. 36. [page 267]

A large number of ordinary leaves and leaflets and a few flower-peduncles are provided with pulvini; but this is not the case with a single tendril at present known. The cause of this difference probably lies in the fact, that the chief service of a pulvinus is to prolong the movement of the part thus provided after growth has ceased; and as tendrils or other climbing-organs are of use only whilst the plant is increasing in height or growing, a pulvinus which served to prolong their movements would be useless.

It was shown in the last chapter that the stolons or runners of certain plants circumnutate largely, and that this movement apparently aids them in finding a passage between the crowded stems of adjoining plants. If it could be proved that their movements had been modified and increased for this special purpose, they ought to have been included in the present chapter; but as the amplitude of their revolutions is not so conspicuously different from that of ordinary plants, as in the case of climbers, we have no evidence on this head. We encounter the same doubt in the case of some plants which bury their pods in the ground. This burying process is certainly favoured by the circumnutation of the flower-peduncle; but we do not know whether it has been increased for this special purpose.

EPINASTY—HYPONASTY.

The term epinasty is used by De Vries* to express greater longitudinal growth along the upper than

* 'Arbeiten des Bot. Inst., in Wrzburg,' Heft ii. 1872, p. 223. De Vries has slightly modified (p. 252) the meaning of the above two terms as first used by Schimper, and they have been adopted in this sense by Sachs. [page 268]

along the lower side of a part, which is thus caused to bend downwards; and hyponasty is used for the reversed process, by which the part is made to bend upwards. These actions come into play so frequently that the use of the above two terms is highly convenient. The movements thus induced result from a modified form of circumnutation; for, as we shall immediately see, an organ under the influence of epinasty does not generally move in a straight line downwards, or under that of hyponasty upwards, but oscillates up and down with some lateral movement: it moves, however, in a preponderant manner in one direction. This shows that there is some growth on all sides of the part, but more on the upper side in the case of epinasty, and more on the lower side in that of hyponasty, than on the other sides. At the same time there may be in addition, as De Vries insists, increased growth on one side due to geotropism, and on another side due to heliotropism; and thus the effects of epinasty or of hyponasty may be either increased or lessened.

He who likes, may speak of ordinary circumnutation as being combined with epinasty, hyponasty, the effects of gravitation, light, etc.; but it seems to us, from reasons hereafter to be given, to be more correct to say that circumnutation is modified by these several agencies. We will therefore speak of circumnutation, which is always in progress, as modified by epinasty, hyponasty, geotropism, or other agencies, whether internal or external.

[One of the commonest and simplest cases of epinasty is that offered by leaves, which at an early age are crowded together round the buds, and diverge as they grow older. Sachs first remarked that this was due to increased growth along the upper side of the petiole and blade; and De Vries has now shown in more detail that the movement is thus caused, aided slightly by [page 269] the weight of the leaf, and resisted as he believes by apogeotropism, at least after the leaf has somewhat diverged. In our observations on the circumnutation of leaves, some were selected which were rather too young, so that they continued to diverge or sink downwards whilst their movements were being traced. This may be seen in the diagrams (Figs. 98 and 112, pp. 232 and 249) representing the circumnutation of the young leaves of Acanthus mollis and Pelargonium zonale. Similar cases were observed with Drosera. The movements of a young leaf, only 3/4 inch in length, of Petunia violacea were traced during four days, and offers a better instance (Fig. 111, p. 248) as it diverged during the whole of this time in a curiously zigzag line with some of the angles sharply acute, and during the latter days plainly circumnutated. Some young leaves of about the same age on a plant of this Petunia, which had been laid horizontally, and on another plant which was left upright, both being kept in complete darkness, diverged in the same manner for 48 h., and apparently were not affected by apogeotropism; though their stems were in a state of high tension, for when freed from the sticks to which they had been tied, they instantly curled upwards.

The leaves, whilst very young, on the leading shoots of the Carnation (Dianthus caryophyllus) are highly inclined or vertical; and if the plant is growing vigorously they diverge so quickly that they become almost horizontal in a day. But they move downwards in a rather oblique line and continue for some time afterwards to move in the same direction, in connection, we presume, with their spiral arrangement on the stem. The course pursued by a young leaf whilst thus obliquely descending was traced, and the line was distinctly yet not strongly zigzag; the larger angles formed by the successive lines amounting only to 135o, 154o, and 163o. The subsequent lateral movement (shown in Fig. 96, p. 231) was strongly zigzag with occasional circumnutations. The divergence and sinking of the young leaves of this plant seem to be very little affected by geotropism or heliotropism; for a plant, the leaves of which were growing rather slowly (as ascertained by measurement) was laid horizontally, and the opposite young leaves diverged from one another symmetrically in the usual manner, without any upturning in the direction of gravitation or towards the light.

The needle-like leaves of Pinus pinaster form a bundle whilst young; afterwards they slowly diverge, so that those on the upright shoots become horizontal. The movements of one such [page 270] young leaf was traced during 4 days, and the tracing here given (Fig. 121) shows that it descended at first in a nearly straight line, but afterwards zigzagged, making one or two little loops. The diverging and descending movements of a rather older leaf were also traced (see former Fig. 113, p. 251): it descended during the first day and night in a somewhat zigzag line; it then circumnutated round a small space and again descended. By this time the leaf had nearly assumed its final position, and now plainly circumnutated. As in the case of the Carnation, the leaves, whilst very young, do not seem to be much affected by geotropism or heliotropism, for those on a young plant laid horizontally, and those on another plant left upright, both kept in the dark, continued to diverge in the usual manner without bending to either side.

Fig. 121. Pinus pinaster: epinastic downward movement of a young leaf, produced by a young plant in a pot, traced on a vertical glass under a skylight, from 6.45 A.M. June 2nd to 10.40 P.M. 6th.

With Coboea scandens, the young leaves, as they successively diverge from the leading shoot which is bent to one side, rise up so as to project vertically, and they retain this position for some time whilst the tendril is revolving. The diverging and ascending movements of the petiole of one such a leaf, were traced on a vertical glass under a skylight; and the course pursued was in most parts nearly straight, but there were two [page 271] well-marked zigzags (one of them forming an angle of 112o), and this indicates circumnutation.

The still closed lobes of a young leaf of Dionaea projected at right angles to the petiole, and were in the act of slowly rising. A glass filament was attached to the under side of the midrib, and its movements were traced on a vertical glass. It circumnutated once in the evening, and on the next day rose, as already described (see Fig. 106, p. 240), by a number of acutely zigzag lines, closely approaching in character to ellipses. This movement no doubt was due to epinasty, aided by apogeotropism, for the closed lobes of a very young leaf on a plant which had been placed horizontally, moved into nearly the same line with the petiole, as if the plant had stood upright; but at the same time the lobes curved laterally upwards, and thus occupied an unnatural position, obliquely to the plane of the foliaceous petiole.

As the hypocotyls and epicotyls of some plants protrude from the seed-coats in an arched form, it is doubtful whether the arching of these parts, which is invariably present when they break through the ground, ought always to be attributed to epinasty; but when they are at first straight and afterwards become arched, as often happens, the arching is certainly due to epinasty. As long as the arch is surrounded by compact earth it must retain its form; but as soon as it rises above the surface, or even before this period if artificially freed from the surrounding pressure, it begins to straighten itself, and this no doubt is mainly due to hyponasty. The movement of the upper and lower half of the arch, and of the crown, was occasionally traced; and the course was more or less zigzag, showing modified circumnutation.

With not a few plants, especially climbers, the summit of the shoot is hooked, so that the apex points vertically downwards. In seven genera of twining plants* the hooking, or as it has been called by Sachs, the nutation of the tip, is mainly due to an exaggerated form of circumnutation. That is, the growth is so great along one side that it bends the shoot completely over to the opposite side, thus forming a hook; the longitudinal line or zone of growth then travels a little laterally round the shoot, and the hook points in a slightly different direction, and so onwards until the hook is completely reversed. Ultimately it

* 'The Movements and Habits of Climbing Plants,' 2nd edit. p. 13. [page 272]

comes back to the point whence it started. This was ascertained by painting narrow lines with Indian ink along the convex surface of several hooks, and the line was found slowly to become at first lateral, then to appear along the concave surface, and ultimately back again on the convex surface. In the case of Lonicera brachypoda the hooked terminal part of the revolving shoot straightens itself periodically, but is never reversed; that is, the periodically increased growth of the concave side of the hook is sufficient only to straighten it, and not to bend it over to the opposite side. The hooking of the tip is of service to twining plants by aiding them to catch hold of a support, and afterwards by enabling this part to embrace the support much more closely than it could otherwise have done at first, thus preventing it, as we often observed, from being blown away by a strong wind. Whether the advantage thus gained by twining plants accounts for their summits being so frequently hooked, we do not know, as this structure is not very rare with plants which do not climb, and with some climbers (for instance, Vitis, Ampelopsis, Cissus, etc.) to whom it does not afford any assistance in climbing.

With respect to those cases in which the tip remains always bent or hooked towards the same side, as in the genera just named, the most obvious explanation is that the bending is due to continued growth in excess along the convex side. Wiesner, however, maintains* that in all cases the hooking of the tip is the result of its plasticity and weight,—a conclusion which from what we have already seen with several climbing plants is certainly erroneous. Nevertheless, we fully admit that the weight of the part, as well as geotropism, etc., sometimes come into play.

Ampelopsis tricuspidata.—This plant climbs by the aid of adhesive tendrils, and the hooked tips of the shoots do not appear to be of any service to it. The hooking depends chiefly, as far as we could ascertain, on the tip being affected by epinasty and geotropism; the lower and older parts continually straightening themselves through hyponasty and apogeotropism. We believe that the weight of the apex is an unimportant element, because on horizontal or inclined shoots the hook is often extended horizontally or even faces upwards. Moreover shoots frequently form loops instead of hooks; and in this case the

* 'Sitzb. der k. Akad. der Wissensch.,' Vienna, Jan. 1880, p. 16. [page 273]

Fig. 122. Ampelopsis tricuspidata: hyponastic movement of hooked tip of leading shoot, traced from 8.10 A.M. July 13th to 8 A.M. 15th. Apex of shoot 5 inches from the vertical glass. Plant illuminated through a skylight. Temp. 17 1/2o - 19o C. Diagram reduced to one-third of original scale.

extreme part, instead of hanging vertically down as would follow if weight was the efficient cause, extends horizontally or even points upwards. A shoot, which terminated in a rather open hook, was fastened in a highly inclined downward position, so that the concave side faced upwards, and the result was that the apex at first curved upwards. This apparently was due to epinasty and not to apogeotropism, for the apex, soon after passing the perpendicular, curved so rapidly downwards that we could not doubt that the movement was at least aided by geotropism. In the course of a few hours the hook was thus converted into a loop with the apex of the shoot pointing straight downwards. The longer axis of the loop was at first horizontal, but afterwards became vertical. During this same time the basal part of the hook (and subsequently of the loop) curved itself slowly upwards; and this must have been wholly due to apogeotropism in opposition to hyponasty. The loop was then fastened upside down, so that its basal half would be simultaneously acted on by hyponasty (if present) and by apogeotropism; and now it curved itself so greatly upwards in the course of only 4 h. that there could hardly be a doubt that both forces were acting [page 274] together. At the same time the loop became open and was thus reconverted into a hook, and this apparently was effected by the geotropic movement of the apex in opposition to epinasty. In the case of Ampelopsis hederacea, weight plays, as far as we could judge, a more important part in the hooking of the tip.

In order to ascertain whether the shoots of A. tricuspidata in straightening themselves under the combined action of hyponasty and apogeotropism moved in a simple straight course, or whether they circumnutated, glass filaments were fixed to the crowns of four hooked tips standing in their natural position; and the movements of the filaments were traced on a vertical glass. All four tracings resembled each other in a general manner; but we will give only one (see Fig. 122, p. 273). The filament rose at first, which shows that the hook was straightening itself; it then zigzagged, moving a little to the left between 9.25 A.M. and 9 P.M. From this latter hour on the 13th to 10.50 A.M. on the following morning (14th) the hook continued to straighten itself, and then zigzagged a short distance to the right. But from 1 P.M. to 10.40 P.M. on the 14th the movement

Fig. 123. Smithia Pfundii: hyponastic movement of the curved summit of a stem, whilst straightening itself, traced from 9 A.M. July 10th to 3 P.M. 13th. Apex 9 inches from the vertical glass. Diagram reduced to one-fifth of original scale. Plant illuminated through skylight; temp. 17 1/2o - 19o C. [page 275]

was reversed and the shoot became more hooked. During the night, after 10.40 P.M. to 8.15 A.M. on the 15th, the hook again opened or straightened itself. By this time the glass filament had become so highly inclined that its movements could no longer be traced with accuracy; and by 1.30 P.M. on this same day, the crown of the former arch or hook had become perfectly straight and vertical. There can therefore be no doubt that the straightening of the hooked shoot of this plant is effected by the circumnutation of the arched portion—that is, by growth alternating between the upper and lower surface, but preponderant on the lower surface, with some little lateral movement.

We were enabled to trace the movement of another straightening shoot for a longer period (owing to its slower growth and to its having been placed further from the vertical glass), namely, from the early morning on July 13th to late in the evening of the 16th. During the whole daytime of the 14th, the hook straightened itself very little, but zigzagged and plainly circumnutated about nearly the same spot. By the 16th it had become nearly straight, and the tracing was no longer accurate, yet it was manifest that there was still a considerable amount of movement both up and down and laterally; for the crown whilst continuing to straighten itself occasionally became for a short time more curved, causing the filament to descend twice during the day.

Smithia Pfundii.—The stiff terminal shoots of this Leguminous water-plant from Africa project so as to make a rectangle with the stem below; but this occurs only when the plants are growing vigorously, for when kept in a cool place, the summits of the stems become straight, as they likewise did at the close of the growing season. The direction of the rectangularly bent part is independent of the chief source of light. But from observing the effects of placing plants in the dark, in which case several shoots became in two or three days upright or nearly upright, and when brought back into the light again became rectangularly curved, we believe that the bending is in part due to apheliotropism, apparently somewhat opposed by apogeotropism. On the other hand, from observing the effects of tying a shoot downwards, so that the rectangle faced upwards, we are led to believe that the curvature is partly due to epinasty. As the rectangularly bent portion of an upright stem grows older, the lower part straightens itself; and this is effected through hyponasty. He who has read Sachs' recent Essay on the vertical [page 276] and inclined positions of the parts of plants* will see how difficult a subject this is, and will feel no surprise at our expressing ourselves doubtfully in this and other such cases.

A plant, 20 inches in height, was secured to a stick close beneath the curved summit, which formed rather less than a rectangle with the stem below. The shoot pointed away from the observer; and a glass filament pointing towards the vertical glass on which the tracing was made, was fixed to the convex surface of the curved portion. Therefore the descending lines in the figure represent the straightening of the curved portion as it grew older. The tracing (Fig. 123, p. 274) was begun at 9 A.M. on July 10th; the filament at first moved but little in a zigzag line, but at 2 P.M. it began rising and continued to do so till 9 P.M.; and this proves that the terminal portion was being more bent downwards. After 9 P.M. on the 10th an opposite movement commenced, and the curved portion began to straighten itself, and this continued till 11.10 A.M. on the 12th, but was interrupted by some small oscillations and zigzags, showing movement in different directions. After 11.10 A.M. on the 12th this part of the stem, still considerably curved, circumnutated in a conspicuous manner until nearly 3 P.M. on the 13th; but during all this time a downward movement of the filament prevailed, caused by the continued straightening of the stem. By the afternoon of the 13th, the summit, which had originally been deflected more than a right angle from the perpendicular, had grown so nearly straight that the tracing could no longer be continued on the vertical glass. There can therefore be no doubt that the straightening of the abruptly curved portion of the growing stem of this plant, which appears to be wholly due to hyponasty, is the result of modified circumnutation. We will only add that a filament was fixed in a different manner across the curved summit of another plant, and the same general kind of movement was observed.

Trifolium repens.—In many, but not in all the species of Trifolium, as the separate little flowers wither, the sub-peduncles bend downwards, so as to depend parallel to the upper part of the main peduncle. In Tr. subterraneum the main peduncle curves downwards for the sake of burying its capsules, and in this species the sub-peduncles of the separate flowers bend

* 'Ueber Orthotrope und Plagiotrope Pflanzentheile;' 'Arbeiten des Bot. Inst., in Wrzburg,' Heft ii. 1879, p. 226. [page 277]

Fig. 124. Trifolium repens: circumnutating and epinastic movements of the sub-peduncle of a single flower, traced on a vertical glass under a skylight, in A from 11.30 A.M. Aug. 27th to 7 A.M. 30th; in B from 7 A.M. Aug. 30th to a little after 6 P.M. Sept. 8th. [page 278]

upwards, so as to occupy the same position relatively to the upper part of the main peduncle as in Tr. repens. This fact alone would render it probable that the movements of the sub-peduncles in Tr. repens were independent of geotropism. Nevertheless, to make sure, some flower-heads were tied to little sticks upside down and others in a horizontal position; their sub-peduncles, however, all quickly curved upwards through the action of heliotropism. We therefore protected some flower-heads, similarly secured to sticks, from the light, and although some of them rotted, many of their sub-peduncles turned very slowly from their reversed or from their horizontal positions, so as to stand in the normal manner parallel to the upper part of the main peduncle. These facts show that the movement is independent of geotropism or apheliotropism; it must there[fore] be attributed to epinasty, which however is checked, at least as long as the flowers are young, by heliotropism. Most of the above flowers were never fertilised owing to the exclusion of bees; they consequently withered very slowly, and the movements of the sub-peduncles were in like manner much retarded.

To ascertain the nature of the movement of the sub-peduncle, whilst bending downwards, a filament was fixed across the summit of the calyx of a not fully expanded and almost upright flower, nearly in the centre of the head. The main peduncle was secured to a stick close beneath the head. In order to see the marks on the glass filament, a few flowers had to be cut away on the lower side of the head. The flower under observation at first diverged a little from its upright position, so as to occupy the open space caused by the removal of the adjoining flowers. This required two days, after which time a new tracing was begun (Fig. 124). In A we see the complex circumnutating course pursued from 11.30 A.M. Aug. 26th to 7 A.M. on the 30th. The pot was then moved a very little to the right, and the tracing (B) was continued without interruption from 7 A.M. Aug. 30th to after 6 P.M. Sept. 8th. It should be observed that on most of these days, only a single dot was made each morning at the same hour. Whenever the flower was observed carefully, as on Aug. 30th and Sept. 5th and 6th, it was found to be circumnutating over a small space. At last, on Sept. 7th, it began to bend downwards, and continued to do so until after 6 P.M. on the 8th, and indeed until the morning of the 9th, when its movements could no longer be traced on the vertical glass. It was carefully observed during the whole of the 8th, and by [page 279] 10.30 P.M. it had descended to a point lower down by two-thirds of the length of the figure as here given; but from want of space the tracing has been copied in B, only to a little after 6 P.M. On the morning of the 9th the flower was withered, and the sub-peduncle now stood at an angle of 57o beneath the horizon. If the flower had been fertilised it would have withered much sooner, and have moved much more quickly. We thus see that the sub-peduncle oscillated up and down, or circumnutated, during its whole downward epinastic course.

The sub-peduncles of the fertilised and withered flowers of Oxalis carnosa likewise bend downwards through epinasty, as will be shown in a future chapter; and their downward course is strongly zigzag, indicating circumnutation.]

The number of instances in which various organs move through epinasty or hyponasty, often in combination with other forces, for the most diversified purposes, seems to be inexhaustibly great; and from the several cases which have been here given, we may safely infer that such movements are due to modified circumnutation. [page 280]

CHAPTER VI.

MODIFIED CIRCUMNUTATION: SLEEP OR NYCTITROPIC MOVEMENTS, THEIR USE: SLEEP OF COTYLEDONS.

Preliminary sketch of the sleep or nyctitropic movements of leaves— Presence of pulvini—The lessening of radiation the final cause of nyctitropic movements—Manner of trying experiments on leaves of Oxalis, Arachis, Cassia, Melilotus, Lotus and Marsilea and on the cotyledons of Mimosa—Concluding remarks on radiation from leaves—Small differences in the conditions make a great difference in the result - Description of the nyctitropic position and movements of the cotyledons of various plants— List of species—Concluding remarks—Independence of the nyctitropic movements of the leaves and cotyledons of the same species—Reasons for believing that the movements have been acquired for a special purpose.

The so-called sleep of leaves is so conspicuous a phenomenon that it was observed as early as the time of Pliny;* and since Linnaeus published his famous Essay, 'Somnus Plantarum,' it has been the subject of several memoirs. Many flowers close at night, and these are likewise said to sleep; but we are not here concerned with their movements, for although effected by the same mechanism as in the case of young leaves, namely, unequal growth on the opposite sides (as first proved by Pfeffer), yet they differ essentially in being excited chiefly by changes of temperature instead of light; and in being effected, as far as we can judge, for a different purpose. Hardly any one supposes that there is any real analogy

* Pfeffer has given a clear and interesting sketch of the history of this subject in his 'Die Periodischen Bewegungen der Blattorgane,' 1875, P. 163. [page 281]

between the sleep of animals and that of plants,* whether of leaves or flowers. It seems therefore, advisable to give a distinct name to the so-called sleep-movements of plants. These have also generally been confounded, under the term "periodic," with the slight daily rise and fall of leaves, as described in the fourth chapter; and this makes it all the more desirable to give some distinct name to sleep-movements. Nyctitropism and nyctitropic, i.e. night-turning, may be applied both to leaves and flowers, and will be occasionally used by us; but it would be best to confine the term to leaves. The leaves of some few plants move either upwards or downwards when the sun shines intensely on them, and this movement has sometimes been called diurnal sleep; but we believe it to be of an essentially different nature from the nocturnal movement, and it will be briefly considered in a future chapter.

The sleep or nyctitropism of leaves is a large subject, and we think that the most convenient plan will be first to give a brief account of the position which leaves assume at night, and of the advantages apparently thus gained. Afterwards the more remarkable cases will be described in detail, with respect to cotyledons in the present chapter, and to leaves in the next chapter. Finally, it will be shown that these movements result from circumnutation, much modified and regulated by the alternations of day and night, or light and darkness; but that they are also to a certain extent inherited.