Insectivorous Plants

Experiment 3. – Fragments of a large fly were placed close to the apex of a vigorous leaf, as well as along half one margin. After 4 hrs. 20 m. there was decided incurvation, which increased a little during the afternoon, but was in the same state on the following morning. Near the apex both margins were inwardly curved. I have never seen a case of the apex itself being in the least curved towards the base of the leaf. After 48 hrs. (always reckoning from the time when the flies were placed on the leaf) the margin had everywhere begun to unfold.

Experiment 4. – A large fragment of a fly was placed on a leaf, in a medial line, a little beneath the apex. Both lateral margins were perceptibly incurved in 3 hrs., and after 4 hrs. 20 m. to such a degree that the fragment was clasped by both margins. After 24 hrs. the two infolded edges near the apex (for the lower part of the leaf was not at all affected) were measured and found to be .11 of an inch (2.795 mm.) apart. The fly was now removed, and a stream of water poured over the leaf so as to wash the surface; and after 24 hrs. the margins were .25 of an inch (6.349 mm.) apart, so that they were largely unfolded. After an additional 24 hrs. they were completely unfolded. Another fly was now put on the same spot to see whether this leaf, on which the first fly had been left 24 hrs., would move again; after 10 hrs. there was a trace of incurvation, but this did not increase during the next 24 hrs. A bit of meat was also placed on the margin of a leaf, which four days previously had become strongly incurved over a fragment of a fly and had afterwards re-expanded; but the meat did not cause even a trace of incurvation. On the contrary, the margin became somewhat reflexed, as if injured, and so remained for the three following days, as long as it was observed.

Experiment 5. – A large fragment of a fly was placed halfway between the apex and base of a leaf and halfway between the midrib and one margin. A short space of this margin, opposite the fly, showed a trace of incurvation after 3 hrs., and this became strongly pronounced in 7 hrs. After 24 hrs. the infolded edge was only .16 of an inch (4.064 mm.) from the midrib. The margin now began to unfold, though the fly was left on the leaf; so that by the next morning (i.e. 48 hrs. from the time when the fly was first put on) the infolded edge had almost completely recovered its original position, being now .3 of an inch (7.62 mm.), instead of .16 of an inch, from the midrib. A trace of flexure was, however, still visible.

Experiment 6. – A young and concave leaf was selected with its margins slightly and naturally incurved. Two rather large, oblong, rectangular pieces of roast meat were placed with their ends touching the infolded edge, and .46 of an inch (11.68 mm.) apart from one another. After 24 hrs. the margin was greatly and equally incurved (see fig. 16) throughout this space, and for a length of .12 or .13 of an inch (3.048 or 3.302 mm.) above and below each bit; so that the margin had been affected over a greater length between the two bits, owing to their conjoint action, than beyond them. The bits of meat were too large to be clasped by the margin, but they were tilted up, one of them so as to stand almost vertically. After 48 hrs. the margin was almost unfolded, and the bits had sunk down. When again examined after two days, the margin was quite unfolded, with the exception of the naturally inflected edge; and one of the bits of meat, the end of which had at first touched the edge, was now .067 of an inch (1.70 mm.) distant from it; so that this bit had been pushed thus far across the blade of the leaf.

Experiment 7. – A bit of meat was placed close to the incurved edge of a rather young leaf, and after it had re-expanded, the bit was left lying .11 of an inch (2.795 mm.) from the edge. The distance from the edge to the midrib of the fully expanded leaf was .35 of an inch (8.89 mm.); so that the bit had been pushed inwards and across nearly one-third of its semi-diameter.

Experiment 8. – Cubes of sponge, soaked in a strong infusion of raw meat, were placed in close contact with the incurved edges of two leaves, – an older and younger one. The distance from the edges to the midribs was carefully measured. After 1 hr. 17 m. there appeared to be a trace of incurvation. After 2 hrs. 17 m. both leaves were plainly inflected; the distance between the edges and midribs being now only half what it was at first. The incurvation increased slightly during the next 4 1/2 hrs., but remained nearly the same for the next 17 hrs. 30 m. In 35 hrs. from the time when the sponges were placed on the leaves, the margins were a little unfolded – to a greater degree in the younger than in the older leaf. The latter was not quite unfolded until the third day, and now both bits of sponge were left at the distance of .1 of an inch (2.54 mm.) from the edges; or about a quarter of the distance between the edge and midrib. A third bit of sponge adhered to the edge, and, as the margin unfolded, was dragged backwards, into its original position.

Experiment 9. – A chain of fibres of roast meat, as thin as bristles and moistened with saliva, were placed down one whole side, close to the narrow, naturally incurved edge of a leaf. In 3 hrs. this side was greatly incurved along its whole length, and after 8 hrs. formed a cylinder, about 1/20 of an inch (1.27 mm) in diameter, quite concealing the meat. This cylinder remained closed for 32 hrs., but after 48 hrs. was half unfolded, and in 72 hrs. was as open as the opposite margin where no meat had been placed. As the thin fibres of meat were completely overlapped by the margin, they were not pushed at all inwards, across the blade.

Experiment 10. – Six cabbage seeds, soaked for a night in water, were placed in a row close to the narrow incurved edge of a leaf. We shall hereafter see that these seeds yield soluble matter to the glands. In 2 hrs. 25 m. the margin was decidedly inflected; in 4 hrs. it extended over the seeds for about half their breadth, and in 7 hrs. over three-fourths of their breadth, forming a cylinder not quite closed along the inner side, and about .7 of an inch (1.778 mm.) in diameter. After 24 hrs. the inflection had not increased, perhaps had decreased. The glands which had been brought into contact with the upper surfaces of the seeds were now secreting freely. In 36 hrs. from the time when the seeds were put on the leaf the margin had greatly, and after 48 hrs. had completely, re-expanded. As the seeds were no longer held by the inflected margin, and as the secretion was beginning to fail, they rolled some way down the marginal channel.

Experiment 11. – Fragments of glass were placed on the margins of two fine young leaves. After 2 hrs. 30 m. the margin of one certainly became slightly incurved; but the inflection never increased, and disappeared in 16 hrs. 30 m. from the time when the fragments were first applied. With the second leaf there was a trace of incurvation in 2 hrs. 15 m., which became decided in 4 hrs. 30 m., and still more strongly pronounced in 7 hrs., but after 19 hrs. 30 m. had plainly decreased. The fragments excited at most a slight and doubtful increase of the secretion; and in two other trials, no increase could be perceived. Bits of coal-cinders, placed on a leaf, produced no effect, either owing to their lightness or to the leaf being torpid.

Experiment 12. – We now turn to fluids. A row of drops of a strong infusion of raw meat were placed along the margins of two leaves; squares of sponge soaked in the same infusion being placed on the opposite margins. My object was to ascer- tain whether a fluid would act as energetically as a substance yielding the same soluble matter to the glands. No distinct difference was perceptible; certainly none in the degree of incurvation; but the incurvation round the bits of sponge lasted rather longer, as might perhaps have been expected from the sponge remaining damp and supplying nitrogenous matter for a longer time. The margins, with the drops, became plainly incurved in 2 hrs. 17 m. The incurvation subsequently increased somewhat, but after 24 hrs. had greatly decreased.

Experiment 13. – Drops of the same strong infusion of raw meat were placed along the midrib of a young and rather deeply concave leaf. The distance across the broadest part of the leaf, between the naturally incurved edges, was .55 of an inch (13.97 mm.). In 3 hrs. 27 m. this distance was a trace less; in 6 hrs. 27 m. it was exactly .45 of an inch (11.43 mm.), and had therefore decreased by .1 of an inch (2.54 mm.). After only 10 hrs. 37 m. the margin began to re-expand, for the distance from edge to edge was now a trace wider, and after 24 hrs. 20 m. was as great, within a hair's breadth, as when the drops were first placed on the leaf. From this experiment we learn that the motor impulse can be transmitted to a distance of .22 of an inch (5.590 mm.) in a transverse direction from the midrib to both margins; but it would be safer to say .2 of an inch (5.08 mm.) as the drops spread a little beyond the midrib. The incurvation thus caused lasted for an unusually short time.

Experiment 14. – Three drops of a solution of one part of carbonate of ammonia to 218 of water (2 grs. to 1 oz.) were placed on the margin of a leaf. These excited so much secretion that in 1 h. 22 m. all three drops ran together; but although the leaf was observed for 24 hrs., there was no trace of inflection. We know that a rather strong solution of this salt, though it does not injure the leaves of Drosera, paralyses their power of movement, and I have no doubt, from the following case, that this holds good with Pinguicula.

Experiment 15. – A row of drops of a solution of one part of carbonate of ammonia to 875 of water (1 gr. to 2 oz.) was placed on the margin of a leaf. In 1 hr. there was apparently some slight incurvation, and this was well-marked in 3 hrs. 30 m. After 24 hrs. the margin was almost completely re-expanded.

Experiment 16. – A row of large drops of a solution of one part of phosphate of ammonia to 4375 of water (1 gr. to 10 oz.) was placed along the margin of a leaf. No effect was produced, and after 8 hrs. fresh drops were added along the same margin without the least effect. We know that a solution of this strength acts powerfully on Drosera, and it is just possible that the solution was too strong. I regret that I did not try a weaker solution.

Experiment 17. – As the pressure from bits of glass causes incurvation, I scratched the margins of two leaves for some minutes with a blunt needle, but no effect was produced. The surface of a leaf beneath a drop of a strong infusion of raw meat was also rubbed for 10. m. with the end of a bristle, so as to imitate the struggles of a captured insect; but this part of the margin did not bend sooner than the other parts with undisturbed drops of the infusion.]

We learn from the foregoing experiments that the margins of the leaves curl inwards when excited by the mere pressure of objects not yielding any soluble matter, by objects yielding such matter, and by some fluids – namely an infusion of raw meat and a week solution of carbonate of ammonia. A stronger solution of two grains of this salt to an ounce of water, though exciting copious secretion, paralyses the leaf. Drops of water and of a solution of sugar or gum did not cause any movement. Scratching the surface of the leaf for some minutes produced no effect. Therefore, as far as we at present know, only two causes – namely slight continued pressure and the absorption of nitrogenous matter – excite movement. It is only the margins of the leaf which bend, for the apex never curves towards the base. The pedicels of the glandular hairs have no power of movement. I observed on several occasions that the surface of the leaf became slightly concave where bits of meat or large flies had long lain, but this may have been due to injury from over-stimulation.

The shortest time in which plainly marked movement was observed was 2 hrs. 17 m., and this occurred when either nitrogenous substances or fluids were placed on the leaves; but I believe that in some cases there was a trace of movement in 1 hr. or 1 hr. 30 m. The pressure from fragments of glass excites movement almost as quickly as the absorption of nitrogenous matter, but the degree of incurvation thus caused is much less. After a leaf has become well incurved and has again expanded, it will not soon answer to a fresh stimulus. The margin was affected longitudinally, upwards or downwards, for a distance of .13 of an inch (3.302 mm.) from an excited point, but for a distance of .46 of an inch between two excited points, and transversely for a distance of .2 of an inch (5.08 mm.). The motor impulse is not accompanied, as in the case of Drosera, by any influence causing increased secretion; for when a single gland was strongly stimulated and secreted copiously, the surrounding glands were not in the least affected. The incurvation of the margin is independent of increased secretion, for fragments of glass cause little or no secretion, and yet excite movement; whereas a strong solution of carbonate of ammonia quickly excites copious secretion, but no movement.

One of the most curious facts with respect to the movement of the leaves is the short time during which they remain incurved, although the exciting object is left on them. In the majority of cases there was well-marked re-expansion within 24 hrs. from the time when even large pieces of meat, &c., were placed on the leaves, and in all cases within 48 hrs. In one instance the margin of a leaf remained for 32 hrs. closely inflected round thin fibres of meat; in another instance, when a bit of sponge, soaked in a strong infusion of raw meat, had been applied to a leaf, the margin began to unfold in 35 hrs. Fragments of glass keep the margin incurved for a shorter time than do nitrogenous bodies; for in the former case there was complete re-expansion in 16 hrs. 30 m. Nitrogenous fluids act for a shorter time than nitrogenous substances; thus, when drops of an infusion of raw meat were placed on the midrib of a leaf, the incurved margins began to unfold in only 10 hrs. 37 m., and this was the quickest act of re-expansion observed by me; but it may have been partly due to the distance of the margins from the midrib where the drops lay.

We are naturally led to inquire what is the use of this movement which lasts for so short a time? If very small objects, such as fibres of meat, or moderately small objects, such as little flies or cabbage-seeds, are placed close to the margin, they are either completely or partially embraced by it. The glands of the overlapping margin are thus brought into contact with such objects and pour forth their secretion, afterwards absorbing the digested matter. But as the incurvation lasts for so short a time, any such benefit can be of only slight importance, yet perhaps greater than at first appears. The plant lives in humid districts, and the insects which adhere to all parts of the leaf are washed by every heavy shower of rain into the narrow channel formed by the naturally incurved edges. For instance, my friend in North Wales placed several insects on some leaves, and two days afterwards (there having been heavy rain in the interval) found some of them quite washed away, and many others safely tucked under the now closely inflected margins, the glands of which all round the insects were no doubt secreting. We can thus, also, understand how it is that so many insects, and fragments of insects, are generally found lying within the incurved margins of the leaves.

The incurvation of the margin, due to the presence of an exciting object, must be serviceable in another and probably more important way. We have seen that when large bits of meat, or of sponge soaked in the juice of meat, were placed on a leaf, the margin was not able to embrace them, but, as it became incurved, pushed them very slowly towards the middle of the leaf, to a distance from the outside of fully .1 of an inch (2.54 mm.), that is, across between one-third and one-fourth of the space between the edge and midrib. Any object, such as a moderately sized insect, would thus be brought slowly into contact with a far larger number of glands, inducing much more secretion and absorption, than would otherwise have been the case. That this would be highly serviceable to the plant, we may infer from the fact that Drosera has acquired highly developed powers of movement, merely for the sake of bringing all its glands into contact with captured insects. So again, after a leaf of Dionaea has caught an insect, the slow pressing together of the two lobes serves merely to bring the glands on both sides into contact with it, causing also the secretion charged with animal matter to spread by capillary attraction over the whole surface. In the case of Pinguicula, as soon as an insect has been pushed for some little distance towards the midrib, immediate re-expansion would be beneficial, as the margins could not capture fresh prey until they were unfolded. The service rendered by this pushing action, as well as that from the marginal glands being brought into contact for a short time with the upper surfaces of minute captured insects, may perhaps account for the peculiar movements of the leaves; otherwise, we must look at these movements as a remnant of a more highly developed power formerly possessed by the progenitors of the genus.

In the four British species, and, as I hear from Prof. Dyer, in most or all the species of the genus, the edges of the leaves are in some degree naturally and permanently incurved. This incurvation serves, as already shown, to prevent insects from being washed away by the rain; but it likewise serves for another end. When a number of glands have been powerfully excited by bits of meat, insects, or any other stimulus, the secretion often trickles down the leaf, and is caught by the incurved edges, instead of rolling off and being lost. As it runs down the channel, fresh glands are able to absorb the animal matter held in solution. Moreover, the secretion often collects in little pools within the channel, or in the spoon-like tips of the leaves; and I ascertained that bits of albumen, fibrin, and gluten, are here dissolved more quickly and completely than on the surface of the leaf, where the secretion cannot accumulate; and so it would be with naturally caught insects. The secretion was repeatedly seen thus to collect on the leaves of plants protected from the rain; and with exposed plants there would be still greater need of some provision to prevent, as far as possible, the secretion, with its dissolved animal matter, being wholly lost.

It has already been remarked that plants growing in a state of nature have the margins of their leaves much more strongly incurved than those grown in pots and prevented from catching many insects. We have seen that insects washed down by the rain from all parts of the leaf often lodge within the margins, which are thus excited to curl farther inwards; and we may suspect that this action, many times repeated during the life of the plant, leads to their permanent and well-marked incurvation. I regret that this view did not occur to me in time to test its truth.

It may here be added, though not immediately bearing on our subject, that when a plant is pulled up, the leaves immediately curl downwards so as almost to conceal the roots, – a fact which has been noticed by many persons. I suppose that this is due to the same tendency which causes the outer and older leaves to lie flat on the ground. It further appears that the flower-stalks are to a certain extent irritable, for Dr. Johnson states that they "bend backwards if rudely handled."77

Secretion, Absorption, and Digestion. – I will first give my observations and experiments, and then a summary of the results.

[The Effects of Objects containing Soluble Nitrogenous Matter.

(1) Flies were placed on many leaves, and excited the glands to secrete copiously; the secretion always becoming acid, though not so before. After a time these insects were rendered so tender that their limbs and bodies could be separated by a mere touch, owing no doubt to the digestion and disintegration of their muscles. The glands in contact with a small fly continued to secrete for four days, and then became almost dry. A narrow strip of this leaf was cut off, and the glands of the longer and shorter hairs, which had lain in contact for the four days with the fly, and those which had not touched it, were compared under the microscope and presented a wonderful contrast. Those which had been in contact were filled with brownish granular matter, the others with homogeneous fluid. There could therefore be no doubt that the former had absorbed matter from the fly.

(2) Small bits of roast meat, placed on a leaf, always caused much acid secretion in the course of a few hours – in one case within 40 m. When thin fibres of meat were laid along the margin of a leaf which stood almost upright, the secretion ran down to the ground. Angular bits of meat, placed in little pools of the secretion near the margin, were in the course of Sowerby; edit. of 1832, tab. 24, 25, 26.

two or three days much reduced in size, rounded, rendered more or less colourless and transparent, and so much softened that they fell to pieces on the slightest touch. In only one instance was a very minute particle completely dissolved, and this occurred within 48 hrs. When only a small amount of secretion was excited, this was generally absorbed in from 24 hrs. to 48 hrs.; the glands being left dry. But when the supply of secretion was copious, round either a single rather large bit of meat, or round several small bits, the glands did not become dry until six or seven days had elapsed. The most rapid case of absorption observed by me was when a small drop of an infusion of raw meat was placed on a leaf, for the glands here became almost dry in 3 hrs. 20 m. Glands excited by small particles of meat, and which have quickly absorbed their own secretion, begin to secrete again in the course of seven or eight days from the time when the meat was given them.

(3) Three minute cubes of tough cartilage from the leg-bone of a sheep were laid on a leaf. After 10 hrs. 30 m. some acid secretion was excited, but the cartilage appeared little or not at all affected. After 24 hrs. the cubes were rounded and much reduced in size; after 32 hrs. they were softened to the centre, and one was quite liquefied; after 35 hrs. mere traces of solid cartilage were left; and after 48 hrs. a trace could still be seen through a lens in only one of the three. After 82 hrs. not only were all three cubes completely liquefied, but all the secretion was absorbed and the glands left dry.

(4) Small cubes of albumen were placed on a leaf; in 8 hrs. feebly acid secretion extended to a distance of nearly 1/10 of an inch round them, and the angles of one cube were rounded. After 24 hrs. the angles of all the cubes were rounded, and they were rendered throughout very tender; after 30 hrs. the secretion began to decrease, and after 48 hrs. the glands were left dry; but very minute bits of albumen were still left undissolved.

(5) Smaller cubes of albumen (about 1/50 or 1/60 of an inch,508 or .423 mm.) were placed on four glands; after 18 hrs. one cube was completely dissolved, the others being much reduced in size, softened, and transparent. After 24 hrs. two of the cubes were completely dissolved, and already the secretion on these glands was almost wholly absorbed. After 42 hrs. the two other cubes were completely dissolved. These four glands began to secrete again after eight or nine days.

(6) Two large cubes of albumen (fully 1/20 of an inch, 1.27 mm.) were placed, one near the midrib and the other near the margin of a leaf; in 6 hrs. there was much secretion, which after 48 hrs. accumulated in a little pool round the cube near the margin. This cube was much more dissolved than that on the blade of the leaf; so that after three days it was greatly reduced in size, with all the angles rounded, but it was too large to be wholly dissolved. The secretion was partially absorbed after four days. The cube on the blade was much less reduced, and the glands on which it rested began to dry after only two days.

(7) Fibrin excites less secretion than does meat or albumen. Several trials were made, but I will give only three of them. Two minute shreds were placed on some glands, and in 3 hrs. 45 m. their secretion was plainly increased. The smaller shred of the two was completely liquefied in 6 hrs. 15 m., and the other in 24 hrs.; but even after 48 hrs. a few granules of fibrin could still be seen through a lens floating in both drops of secretion. After 56 hrs. 30 m. these granules were completely dissolved. A third shred was placed in a little pool of secretion, within the margin of a leaf where a seed had been lying, and this was completely dissolved in the course of 15 hrs. 30 m.