The Movements and Habits of Climbing Plants Part 7

Pa.s.siflora quadrangularis.--This is a very distinct species. The tendrils are thick, long, and stiff; they are sensitive to a touch only on the concave surface towards the extremity. When a stick was placed so that the middle of the tendril came into contact with it, no curvature ensued. In the hothouse a tendril made two revolutions, each in 2 hrs. 22 m.; in a cool room one was completed in 3 hrs., and a second in 4 hrs. The internodes do not revolve; nor do those of the hybrid P. floribunda.

Tacsonia manicata.--Here again the internodes do not revolve. The tendrils are moderately thin and long; one made a narrow ellipse in 5 hrs. 20 m., and the next day a broad ellipse in 5 hrs. 7 m. The extremity being lightly rubbed on the concave surface, became just perceptibly curved in 7 m., distinctly in 10 m., and hooked in 20 m.

We have seen that the tendrils in the last three families, namely, the Vitaceae, Sapindaceae and Pa.s.sifloraceae, are modified flower- peduncles. This is likewise the case, according to De Candolle (as quoted by Mohl), with the tendrils of Brunnichia, one of the Polygonaceae. In two or three species of Modecca, one of the Papayaceae, the tendrils, as I hear from Prof. Oliver, occasionally bear flowers and fruit; so that they are axial in their nature.

The Spiral Contraction of Tendrils.

This movement, which shortens the tendrils and renders them elastic, commences in half a day, or in a day or two after their extremities have caught some object. There is no such movement in any leaf- climber, with the exception of an occasional trace of it in the petioles of Tropaeolum tricolorum. On the other hand, the tendrils of all tendril-bearing plants, contract spirally after they have caught an object with the following exceptions. Firstly, Corydalis claviculata, but then this plant might be called a leaf-climber.

Secondly and thirdly, Bignonia unguis with its close allies, and Cardiospermum; but their tendrils are so short that their contraction could hardly occur, and would be quite superfluous. Fourthly, Smilax aspera offers a more marked exception, as its tendrils are moderately long. The tendrils of Dicentra, whilst the plant is young, are short and after attachment only become slightly flexuous; in older plants they are longer and then they contract spirally. I have seen no other exceptions to the rule that tendrils, after clasping with their extremities a support, undergo spiral contraction. When, however, the tendril of a plant of which the stem is immovably fixed, catches some fixed object, it does not contract, simply because it cannot; this, however, rarely occurs. In the common Pea the lateral branches alone contract, and not the central stem; and with most plants, such as the Vine, Pa.s.siflora, Bryony, the basal portion never forms a spire.

I have said that in Corydalis claviculata the end of the leaf or tendril (for this part may be indifferently so called) does not contract into a spire. The branchlets, however, after they have wound round thin twigs, become deeply sinuous or zigzag. Moreover the whole end of the petiole or tendril, if it seizes nothing, bends after a time abruptly downwards and inwards, showing that its outer surface has gone on growing after the inner surface has ceased to grow. That growth is the chief cause of the spiral contraction of tendrils may be safely admitted, as shown by the recent researches of H. de Vries. I will, however, add one little fact in support of this conclusion.

If the short, nearly straight portion of an attached tendril of Pa.s.siflora gracilis, (and, as I believe, of other tendrils,) between the opposed spires, be examined, it will be found to be transversely wrinkled in a conspicuous manner on the outside; and this would naturally follow if the outer side had grown more than the inner side, this part being at the same time forcibly prevented from becoming curved. So again the whole outer surface of a spirally wound tendril becomes wrinkled if it be pulled straight.

Nevertheless, as the contraction travels from the extremity of a tendril, after it has been stimulated by contact with a support, down to the base, I cannot avoid doubting, from reasons presently to be given, whether the whole effect ought to be attributed to growth. An unattached tendril rolls itself up into a flat helix, as in the case of Cardiospermum, if the contraction commences at the extremity and is quite regular; but if the continued growth of the outer surface is a little lateral, or if the process begins near the base, the terminal portion cannot be rolled up within the basal portion, and the tendril then forms a more or less open spire. A similar result follows if the extremity has caught some object, and is thus held fast.

The tendrils of many kinds of plants, if they catch nothing, contract after an interval of several days or weeks into a spire; but in these cases the movement takes place after the tendril has lost its revolving power and hangs down; it has also then partly or wholly lost its sensibility; so that this movement can be of no use. The spiral contraction of unattached tendrils is a much slower process than that of attached ones. Young tendrils which have caught a support and are spirally contracted, may constantly be seen on the same stem with the much older unattached and uncontracted tendrils.

In the Echinocystis I have seen a tendril with the two lateral branches encircling twigs and contracted into beautiful spires, whilst the main branch which had caught nothing remained for many days straight. In this plant I once observed a main branch after it had caught a stick become spirally flexuous in 7 hrs., and spirally contracted in 18 hrs. Generally the tendrils of the Echinocystis begin to contract in from 12 hrs. to 24 hrs. after catching some object; whilst unattached tendrils do not begin to contract until two or three or even more days after all revolving movement has ceased.

A full-grown tendril of Pa.s.siflora quadrangularis which had caught a stick began in 8 hrs. to contract, and in 24 hrs. formed several spires; a younger tendril, only two-thirds grown, showed the first trace of contraction in two days after clasping a stick, and in two more days formed several spires. It appears, therefore, that the contraction does not begin until the tendril is grown to nearly its full length. Another young tendril of about the same age and length as the last did not catch any object; it acquired its full length in four days; in six additional days it first became flexuous, and in two more days formed one complete spire. This first spire was formed towards the basal end, and the contraction steadily but slowly progressed towards the apex; but the whole was not closely wound up into a spire until 21 days had elapsed from the first observation, that is, until 17 days after the tendril had grown to its full length.

The spiral contraction of tendrils is quite independent of their power of spontaneously revolving, for it occurs in tendrils, such as those of Lathyrus grandiflorus and Ampelopsis hederacea, which do not revolve. It is not necessarily related to the curling of the tips round a support, as we see with the Ampelopsis and Bignonia capreolata, in which the development of adherent discs suffices to cause spiral contraction. Yet in some cases this contraction seems connected with the curling or clasping movement, due to contact with a support; for not only does it soon follow this act, but the contraction generally begins close to the curled extremity, and travels downwards to the base. If, however, a tendril be very slack, the whole length almost simultaneously becomes at first flexuous and then spiral. Again, the tendrils of some few plants never contract spirally unless they have first seized hold of some object; if they catch nothing they hang down, remaining straight, until they wither and drop off: this is the case with the tendrils of Bignonia, which consist of modified leaves, and with those of three genera of the Vitaceae, which are modified flower-peduncles. But in the great majority of cases, tendrils which have never come in contact with any object, after a time contract spirally. All these facts taken together, show that the act of clasping a support and the spiral contraction of the whole length of the tendril, are phenomena not necessarily connected.

The spiral contraction which ensues after a tendril has caught a support is of high service to the plant; hence its almost universal occurrence with species belonging to widely different orders. When a shoot is inclined and its tendril has caught an object above, the spiral contraction drags up the shoot. When the shoot is upright, the growth of the stem, after the tendrils have seized some object above, would leave it slack, were it not for the spiral contraction which draws up the stem as it increases in length. Thus there is no waste of growth, and the stretched stem ascends by the shortest course. When a terminal branchlet of the tendril of Cobaea catches a stick, we have seen how well the spiral contraction successively brings the other branchlets, one after the other, into contact with the stick, until the whole tendril grasps it in an inextricable knot.

When a tendril has caught a yielding object, this is sometimes enveloped and still further secured by the spiral folds, as I have seen with Pa.s.siflora quadrangularis; but this action is of little importance.

A far more important service rendered by the spiral contraction of the tendrils is that they are thus made highly elastic. As before remarked under Ampelopsis, the strain is thus distributed equally between the several attached branches; and this renders the whole far stronger than it otherwise would be, as the branches cannot break separately. It is this elasticity which protects both branched and simple tendrils from being torn away from their supports during stormy weather. I have more than once gone on purpose during a gale to watch a Bryony growing in an exposed hedge, with its tendrils attached to the surrounding bushes; and as the thick and thin branches were tossed to and fro by the wind, the tendrils, had they not been excessively elastic, would instantly have been torn off and the plant thrown prostrate. But as it was, the Bryony safely rode out the gale, like a s.h.i.+p with two anchors down, and with a long range of cable ahead to serve as a spring as she surges to the storm.

When an unattached tendril contracts spirally, the spire always runs in the same direction from tip to base. A tendril, on the other hand, which has caught a support by its extremity, although the same side is concave from end to end, invariably becomes twisted in one part in one direction, and in another part in the opposite direction; the oppositely turned spires being separated by a short straight portion. This curious and symmetrical structure has been noticed by several botanists, but has not been sufficiently explained. {35} It occurs without exception with all tendrils which after catching an object contract spirally, but is of course most conspicuous in the longer tendrils. It never occurs with uncaught tendrils; and when this appears to have occurred, it will be found that the tendril had originally seized some object and had afterwards been torn free.

Commonly, all the spires at one end of an attached tendril run in one direction, and all those at the other end in the opposite direction, with a single short straight portion in the middle; but I have seen a tendril with the spires alternately turning five times in opposite directions, with straight pieces between them; and M. Leon has seen seven or eight such alternations. Whether the spires turn once or more than once in opposite directions, there are as many turns in the one direction as in the other. For instance, I gathered ten attached tendrils of the Bryony, the longest with 33, and the shortest with only 8 spiral turns; and the number of turns in the one direction was in every case the same (within one) as in the opposite direction.

The explanation of this curious little fact is not difficult. I will not attempt any geometrical reasoning, but will give only a practical ill.u.s.tration. In doing this, I shall first have to allude to a point which was almost pa.s.sed over when treating of Twining-plants. If we hold in our left hand a bundle of parallel strings, we can with our right hand turn these round and round, thus imitating the revolving movement of a twining plant, and the strings do not become twisted.

But if we hold at the same time a stick in our left hand, in such a position that the strings become spirally turned round it, they will inevitably become twisted. Hence a straight coloured line, painted along the internodes of a twining plant before it has wound round a support, becomes twisted or spiral after it has wound round. I painted a red line on the straight internodes of a Humulus, Mikania, Ceropegia, Convolvulus, and Phaseolus, and saw it become twisted as the plant wound round a stick. It is possible that the stems of some plants by spontaneously turning on their own axes, at the proper rate and in the proper direction, might avoid becoming twisted; but I have seen no such case.

In the above ill.u.s.tration, the parallel strings were wound round a stick; but this is by no means necessary, for if wound into a hollow coil (as can be done with a narrow slip of elastic paper) there is the same inevitable twisting of the axis. When, therefore, a free tendril coils itself into a spire, it must either become twisted along its whole length (and this never occurs), or the free extremity must turn round as many times as there are spires formed. It was hardly necessary to observe this fact; but I did so by affixing little paper vanes to the extreme points of the tendrils of Echinocystis and Pa.s.siflora quadrangularis; and as the tendril contracted itself into successive spires, the vane slowly revolved.

We can now understand the meaning of the spires being invariably turned in opposite directions, in tendrils which from having caught some object are fixed at both ends. Let us suppose a caught tendril to make thirty spiral turns all in the same direction; the inevitable result would be that it would become twisted thirty times on its own axis. This twisting would not only require considerable force, but, as I know by trial, would burst the tendril before the thirty turns were completed. Such cases never really occur; for, as already stated, when a tendril has caught a support and is spirally contracted, there are always as many turns in one direction as in the other; so that the twisting of the axis in the one direction is exactly compensated by the twisting in the opposite direction. We can further see how the tendency is given to make the later formed coils opposite to those, whether turned to the right or to the left, which are first made. Take a piece of string, and let it hang down with the lower end fixed to the floor; then wind the upper end (holding the string quite loosely) spirally round a perpendicular pencil, and this will twist the lower part of the string; and after it has been sufficiently twisted, it will be seen to curve itself into an open spire, with the curves running in an opposite direction to those round the pencil, and consequently with a straight piece of string between the opposed spires. In short, we have given to the string the regular spiral arrangement of a tendril caught at both ends. The spiral contraction generally begins at the extremity which has clasped a support; and these first-formed spires give a twist to the axis of the tendril, which necessarily inclines the basal part into an opposite spiral curvature. I cannot resist giving one other ill.u.s.tration, though superfluous: when a haberdasher winds up ribbon for a customer, he does not wind it into a single coil; for, if he did, the ribbon would twist itself as many times as there were coils; but he winds it into a figure of eight on his thumb and little finger, so that he alternately takes turns in opposite directions, and thus the ribbon is not twisted. So it is with tendrils, with this sole difference, that they take several consecutive turns in one direction and then the same number in an opposite direction; but in both cases the self-twisting is avoided.

Summary on the Nature and Action of Tendrils.

With the majority of tendril-bearing plants the young internodes revolve in more or less broad ellipses, like those made by twining plants; but the figures described, when carefully traced, generally form irregular ellipsoidal spires. The rate of revolution varies from one to five hours in different species, and consequently is in some cases more rapid than with any twining plant, and is never so slow as with those many twiners which take more than five hours for each revolution. The direction is variable even in the same individual plant. In Pa.s.siflora, the internodes of only one species have the power of revolving. The Vine is the weakest revolver observed by me, apparently exhibiting only a trace of a former power.

In the Eccremocarpus the movement is interrupted by many long pauses.

Very few tendril-bearing plants can spirally twine up an upright stick. Although the power of twining has generally been lost, either from the stiffness or shortness of the internodes, from the size of the leaves, or from some other unknown cause, the revolving movement of the stem serves to bring the tendrils into contact with surrounding objects.

The tendrils themselves also spontaneously revolve. The movement begins whilst the tendril is young, and is at first slow. The mature tendrils of Bignonia littoralis move much slower than the internodes.

Generally, the internodes and tendrils revolve together at the same rate; in Cissus, Cobaea, and most Pa.s.siflorae, the tendrils alone revolve; in other cases, as with Lathyrus aphaca, only the internodes move, carrying with them the motionless tendrils; and, lastly (and this is the fourth possible case), neither internodes nor tendrils spontaneously revolve, as with Lathyrus grandiflorus and Ampelopsis.

In most Bignonias, Eccremocarpus Mutisia, and the Fumariaceae, the internodes, petioles and tendrils all move harmoniously together. In every case the conditions of life must be favourable in order that the different parts should act in a perfect manner.

Tendrils revolve by the curvature of their whole length, excepting the sensitive extremity and the base, which parts do not move, or move but little. The movement is of the same nature as that of the revolving internodes, and, from the observations of Sachs and H. de Vries, no doubt is due to the same cause, namely, the rapid growth of a longitudinal band, which travels round the tendril and successively bows each part to the opposite side. Hence, if a line be painted along that surface which happens at the time to be convex, the line becomes first lateral, then concave, then lateral, and ultimately again convex. This experiment can be tried only on the thicker tendrils, which are not affected by a thin crust of dried paint. The extremities are often slightly curved or hooked, and the curvature of this part is never reversed; in this respect they differ from the extremities of twining shoots, which not only reverse their curvature, or at least become periodically straight, but curve themselves in a greater degree than the lower part. In most other respects a tendril acts as if it were one of several revolving internodes, which all move together by successively bending to each point of the compa.s.s. There is, however, in many cases this unimportant difference, that the curving tendril is separated from the curving internode by a rigid petiole. With most tendril-bearers the summit of the stem or shoot projects above the point from which the tendril arises; and it is generally bent to one side, so as to be out of the way of the revolutions swept by the tendril. In those plants in which the terminal shoot is not sufficiently out of the way, as we have seen with the Echinocystis, as soon as the tendril comes in its revolving course to this point, it stiffens and straightens itself, and thus rising vertically up pa.s.ses over the obstacle in an admirable manner.

All tendrils are sensitive, but in various degrees, to contact with an object, and curve towards the touched side. With several plants a single touch, so slight as only just to move the highly flexible tendril, is enough to induce curvature. Pa.s.siflora gracilis possesses the most sensitive tendrils which I have observed: a bit of platina wire 0.02 of a grain (1.23 mg.) in weight, gently placed on the concave point, caused a tendril to become hooked, as did a loop of soft, thin cotton thread weighing one thirty-second of a grain (2.02 mg.) With the tendrils of several other plants, loops weighing one sixteenth of a grain (4.05 mg.) sufficed. The point of a tendril of Pa.s.siflora gracilis began to move distinctly in 25 seconds after a touch, and in many cases after 30 seconds. Asa Gray also saw movement in the tendrils of the Cucurbitaceous genus, Sicyos, in 30 seconds. The tendrils of some other plants, when lightly rubbed, moved in a few minutes; with Dicentra in half-an- hour; with Smilax in an hour and a quarter or half; and with Ampelopsis still more slowly. The curling movement consequent on a single touch continues to increase for a considerable time, then ceases; after a few hours the tendril uncurls itself, and is again ready to act. When the tendrils of several kinds of plants were caused to bend by extremely light weights suspended on them, they seemed to grow accustomed to so slight a stimulus, and straightened themselves, as if the loops had been removed. It makes no difference what sort of object a tendril touches, with the remarkable exception of other tendrils and drops of water, as was observed with the extremely sensitive-tendrils of Pa.s.siflora gracilis and of the Echinocystis. I have, however, seen tendrils of the Bryony which had temporarily caught other tendrils, and often in the case of the vine.

Tendrils of which the extremities are permanently and slightly curved, are sensitive only on the concave surface; other tendrils, such as those of the Cobaea (though furnished with h.o.r.n.y hooks directed to one side) and those of Cissus discolor, are sensitive on all sides. Hence the tendrils of this latter plant, when stimulated by a touch of equal force on opposite sides, did not bend. The inferior and lateral surfaces of the tendrils of Mutisia are sensitive, but not the upper surface. With branched tendrils, the several branches act alike; but in the Hanburya the lateral spur-like branch does not acquire (for excellent reasons which have been explained) its sensitiveness nearly so soon as the main branch. With most tendrils the lower or basal part is either not at all sensitive, or sensitive only to prolonged contact. We thus see that the sensitiveness of tendrils is a special and localized capacity. It is quite independent of the power of spontaneously revolving; for the curling of the terminal portion from touch does not in the least interrupt the former movement. In Bignonia unguis and its close allies, the petioles of the leaves, as well as the tendrils, are sensitive to a touch.

Twining plants when they come into contact with a stick, curl round it invariably in the direction of their revolving movement; but tendrils curl indifferently to either side, in accordance with the position of the stick and the side which is first touched. The clasping movement of the extremity is apparently not steady, but undulatory or vermicular in its nature, as may be inferred from the curious manner in which the tendrils of the Echinocystis slowly crawled round a smooth stick.

As with a few exceptions tendrils spontaneously revolve, it may be asked,--why have they been endowed with sensitiveness?--why, when they come into contact with a stick, do they not, like twining plants, spirally wind round it? One reason may be that they are in most cases so flexible and thin, that when brought into contact with any object, they would almost certainly yield and be dragged onwards by the revolving movement. Moreover, the sensitive extremities have no revolving power as far as I have observed, and could not by this means curl round a support. With twining plants, on the other hand, the extremity spontaneously bends more than any other part; and this is of high importance for the ascent of the plant, as may be seen on a windy day. It is, however, possible that the slow movement of the basal and stiffer parts of certain tendrils, which wind round sticks placed in their path, may be a.n.a.logous to that of twining plants.

But I hardly attended sufficiently to this point, and it would have been difficult to distinguish between a movement due to extremely dull irritability, from the arrestment of the lower part, whilst the upper part continued to move onwards.

Tendrils which are only three-fourths grown, and perhaps even at an earlier age, but not whilst extremely young, have the power of revolving and of grasping any object which they touch. These two capacities are generally acquired at about the same period, and both fail when the tendril is full grown. But in Cobaea and Pa.s.siflora punctata the tendrils begin to revolve in a useless manner, before they have become sensitive. In the Echinocystis they retain their sensitiveness for some time after they have ceased to revolve and after they have sunk downwards; in this position, even if they were able to seize an object, such power would be of no service in supporting the stem. It is a rare circ.u.mstance thus to detect any superfluity or imperfection in the action of tendrils--organs which are so excellently adapted for the functions which they have to perform; but we see that they are not always perfect, and it would be rash to a.s.sume that any existing tendril has reached the utmost limit of perfection.

Some tendrils have their revolving motion accelerated or r.e.t.a.r.ded, in moving to or from the light; others, as with the Pea, seem indifferent to its action; others move steadily from the light to the dark, and this aids them in an important manner in finding a support.

For instance, the tendrils of Bignonia capreolata bend from the light to the dark as truly as a wind-vane from the wind. In the Eccremocarpus the extremities alone twist and turn about so as to bring their finer branches and hooks into close contact with any dark surface, or into crevices and holes.

A short time after a tendril has caught a support, it contracts with some rare exceptions into a spire; but the manner of contraction and the several important advantages thus gained have been discussed so lately, that nothing need here be repeated on the subject. Tendrils soon after catching a support grow much stronger and thicker, and sometimes more durable to a wonderful degree; and this shows how much their internal tissues must be changed. Occasionally it is the part which is wound round a support which chiefly becomes thicker and stronger; I have seen, for instance, this part of a tendril of Bignonia aequinoctialis twice as thick and rigid as the free basal part. Tendrils which have caught nothing soon shrink and wither; but in some species of Bignonia they disarticulate and fall off like leaves in autumn.

Any one who had not closely observed tendrils of many kinds would probably infer that their action was uniform. This is the case with the simpler kinds, which simply curl round an object of moderate thickness, whatever its nature may be. {36} But the genus Bignonia shows us what diversity of action there may be between the tendrils of closely allied species. In all the nine species observed by me, the young internodes revolve vigorously; the tendrils also revolve, but in some of the species in a very feeble manner; and lastly the petioles of nearly all revolve, though with unequal power. The petioles of three of the species, and the tendrils of all are sensitive to contact. In the first-described species, the tendrils resemble in shape a bird's foot, and they are of no service to the stem in spirally ascending a thin upright stick, but they can seize firm hold of a twig or branch. When the stem twines round a somewhat thick stick, a slight degree of sensitiveness possessed by the petioles is brought into play, and the whole leaf together with the tendril winds round it. In B. unguis the petioles are more sensitive, and have greater power of movement than those of the last species; they are able, together with the tendrils, to wind inextricably round a thin upright stick; but the stem does not twine so well. B. Tweedyana has similar powers, but in addition, emits aerial roots which adhere to the wood. In B. venusta the tendrils are converted into elongated three-p.r.o.nged grapnels, which move spontaneously in a conspicuous manner; the petioles, however, have lost their sensitiveness. The stem of this species can twine round an upright stick, and is aided in its ascent by the tendrils seizing the stick alternately some way above and then contracting spirally.

In B. littoralis the tendrils, petioles, and internodes, all revolve spontaneously. The stem, however, cannot twine, but ascends an upright stick by seizing it above with both tendrils together, which then contract into a spire. The tips of these tendrils become developed into adhesive discs. B. speciosa possesses similar powers of movement as the last species, but it cannot twine round a stick, though it can ascend by clasping the stick horizontally with one or both of its unbranched tendrils. These tendrils continually insert their pointed ends into minute crevices or holes, but as they are always withdrawn by the subsequent spiral contraction, the habit seems to us in our ignorance useless. Lastly, the stem of B.

capreolata twines imperfectly; the much-branched tendrils revolve in a capricious manner, and bend from the light to the dark; their hooked extremities, even whilst immature, crawl into crevices, and, when mature, seize any thin projecting point; in either case they develop adhesive discs, and these have the power of enveloping the finest fibres.

In the allied Eccremocarpus the internodes, petioles, and much- branched tendrils all spontaneously revolve together. The tendrils do not as a whole turn from the light; but their bluntly-hooked extremities arrange themselves neatly on any surface with which they come into contact, apparently so as to avoid the light. They act best when each branch seizes a few thin stems, like the culms of a gra.s.s, which they afterwards draw together into a solid bundle by the spiral contraction of all the branches. In Cobaea the finely- branched tendrils alone revolve; the branches terminate in sharp, hard, double, little hooks, with both points directed to the same side; and these turn by well-adapted movements to any object with which they come into contact. The tips of the branches also crawl into dark crevices or holes. The tendrils and internodes of Ampelopsis have little or no power of revolving; the tendrils are but little sensitive to contact; their hooked extremities cannot seize thin objects; they will not even clasp a stick, unless in extreme need of a support; but they turn from the light to the dark, and, spreading out their branches in contact with any nearly flat surface, develop discs. These adhere by the secretion of some cement to a wall, or even to a polished surface; and this is more than the discs of the Bignonia capreolata can effect.

The rapid development of these adherent discs is one of the most remarkable peculiarities possessed by any tendrils. We have seen that such discs are formed by two species of Bignonia, by Ampelopsis, and, according to Naudin, {37} by the Cucurbitaceous genus Peponopsis adhaerens. In Anguria the lower surface of the tendril, after it has wound round a stick, forms a coa.r.s.ely cellular layer, which closely fits the wood, but is not adherent; whilst in Hanburya a similar layer is adherent. The growth of these cellular out-growths depends, (except in the case of the Haplolophium and of one species of Ampelopsis,) on the stimulus from contact. It is a singular fact that three families, so widely distinct as the Bignoniaceae, Vitaceae, and Cucurbitaceae, should possess species with tendrils having this remarkable power.

Sachs attributes all the movements of tendrils to rapid growth on the side opposite to that which becomes concave. These movements consist of revolving nutation, the bending to and from the light, and in opposition to gravity, those caused by a touch, and spiral contraction. It is rash to differ from so great an authority, but I cannot believe that one at least of these movements--curvature from a touch--is thus caused. {38} In the first place it may be remarked that the movement of nutation differs from that due to a touch, in so far that in some cases the two powers are acquired by the same tendril at different periods of growth; and the sensitive part of the tendril does not seem capable of nutation. One of my chief reasons for doubting whether the curvature from a touch is the result of growth, is the extraordinary rapidity of the movement. I have seen the extremity of a tendril of Pa.s.siflora gracilis, after being touched, distinctly bent in 25 seconds, and often in 30 seconds; and so it is with the thicker tendril of Sicyos. It appears hardly credible that their outer surfaces could have actually grown in length, which implies a permanent modification of structure, in so short a time. The growth, moreover, on this view must be considerable, for if the touch has been at all rough the extremity is coiled in two or three minutes into a spire of several turns.

When the extreme tip of the tendril of Echinocystis caught hold of a smooth stick, it coiled itself in a few hours (as described at p.

132) twice or thrice round the stick, apparently by an undulatory movement. At first I attributed this movement to the growth of the outside; black marks were therefore made, and the inters.p.a.ces measured, but I could not thus detect any increase in length. Hence it seems probable in this case and in others, that the curvature of the tendril from a touch depends on the contraction of the cells along the concave side. Sachs himself admits {39} that "if the growth which takes place in the entire tendril at the time of contact with a support is small, a considerable acceleration occurs on the convex surface, but in general there is no elongation on the concave surface, or there may even be a contraction; in the case of a tendril of Cucurbita this contraction amounted to nearly one-third of the original length." In a subsequent pa.s.sage Sachs seems to feel some difficulty in accounting for this kind of contraction. It must not however be supposed from the foregoing remarks that I entertain any doubt, after reading De Vries' observations, about the outer and stretched surfaces of attached tendrils afterwards increasing in length by growth. Such increase seems to me quite compatible with the first movement being independent of growth. Why a delicate touch should cause one side of a tendril to contract we know as little as why, on the view held by Sachs, it should lead to extraordinarily rapid growth of the opposite side. The chief or sole reason for the belief that the curvature of a tendril when touched is due to rapid growth, seems to be that tendrils lose their sensitiveness and power of movement after they have grown to their full length; but this fact is intelligible, if we bear in mind that all the functions of a tendril are adapted to drag up the terminal growing shoot towards the light. Of what use would it be, if an old and full-grown tendril, arising from the lower part of a shoot, were to retain its power of clasping a support? This would be of no use; and we have seen with tendrils so many instances of close adaptation and of the economy of means, that we may feel a.s.sured that they would acquire irritability and the power of clasping a support at the proper age--namely, youth- -and would not uselessly retain such power beyond the proper age.

CHAPTER V.--HOOK AND ROOT-CLIMBERS.--CONCLUDING REMARKS.

Plants climbing by the aid of hooks, or merely scrambling over other plants--Root-climbers, adhesive matter secreted by the rootlets-- General conclusions with respect to climbing plants, and the stages of their development.

Hook-Climbers.--In my introductory remarks, I stated that, besides the two first great cla.s.ses of climbing plants, namely, those which twine round a support, and those endowed with irritability enabling them to seize hold of objects by means of their petioles or tendrils, there are two other cla.s.ses, hook-climbers and root-climbers. Many plants, moreover, as Fritz Muller has remarked, {40} climb or scramble up thickets in a still more simple fas.h.i.+on, without any special aid, excepting that their leading shoots are generally long and flexible. It may, however, be suspected from what follows, that these shoots in some cases tend to avoid the light. The few hook- climbers which I have observed, namely, Galium aparine, Rubus australis, and some climbing Roses, exhibit no spontaneous revolving movement. If they had possessed this power, and had been capable of twining, they would have been placed in the cla.s.s of Twiners; for some twiners are furnished with spines or hooks, which aid them in their ascent. For instance, the Hop, which is a twiner, has reflexed hooks as large as those of the Galium; some other twiners have stiff reflexed hairs; and Dipladenia has a circle of blunt spines at the bases of its leaves. I have seen only one tendril-bearing plant, namely, Smilax aspera, which is furnished with reflexed spines; but this is the case with several branch-climbers in South Brazil and Ceylon; and their branches graduate into true tendrils. Some few plants apparently depend solely on their hooks for climbing, and yet do so efficiently, as certain palms in the New and Old Worlds. Even some climbing Roses will ascend the walls of a tall house, if covered with a trellis. How this is effected I know not; for the young shoots of one such Rose, when placed in a pot in a window, bent irregularly towards the light during the day and from the light during the night, like the shoots of any common plant; so that it is not easy to understand how they could have got under a trellis close to the wall. {41}

Root-climbers.--A good many plants come under this cla.s.s, and are excellent climbers. One of the most remarkable is the Marcgravia umbellata, the stem of which in the tropical forests of South America, as I hear from Mr. Spruce, grows in a curiously flattened manner against the trunks of trees; here and there it puts forth claspers (roots), which adhere to the trunk, and, if the latter be slender, completely embrace it. When this plant has climbed to the light, it produces free branches with rounded stems, clad with sharp- pointed leaves, wonderfully different in appearance from those borne by the stem as long as it remains adherent. This surprising difference in the leaves, I have also observed in a plant of Marcgravia dubia in my hothouse. Root-climbers, as far as I have seen, namely, the Ivy (Hedera helix), Ficus repens, and F. barbatus, have no power of movement, not even from the light to the dark. As previously stated, the Hoya carnosa (Asclepiadaceae) is a spiral twiner, and likewise adheres by rootlets even to a flat wall. The tendril-bearing Bignonia Tweedyana emits roots, which curve half round and adhere to thin sticks. The Tecoma radicans (Bignoniaceae), which is closely allied to many spontaneously revolving species, climbs by rootlets; nevertheless, its young shoots apparently move about more than can be accounted for by the varying action of the light.

I have not closely observed many root-climbers, but can give one curious fact. Ficus repens climbs up a wall just like Ivy; and when the young rootlets are made to press lightly on slips of gla.s.s, they emit after about a week's interval, as I observed several times, minute drops of clear fluid, not in the least milky like that exuded from a wound. This fluid is slightly viscid, but cannot be drawn out into threads. It has the remarkable property of not soon drying; a drop, about the size of half a pin's head, was slightly spread out on gla.s.s, and I scattered on it some minute grains of sand. The gla.s.s was left exposed in a drawer during hot and dry weather, and if the fluid had been water, it would certainly have dried in a few minutes; but it remained fluid, closely surrounding each grain of sand, during 128 days: how much longer it would have remained I cannot say. Some other rootlets were left in contact with the gla.s.s for about ten days or a fortnight, and the drops of secreted fluid were now rather larger, and so viscid that they could be drawn out into threads.

Some other rootlets were left in contact during twenty-three days, and these were firmly cemented to the gla.s.s. Hence we may conclude that the rootlets first secrete a slightly viscid fluid, subsequently absorb the watery parts, (for we have seen that the fluid will not dry by itself,) and ultimately leave a cement. When the rootlets were torn from the gla.s.s, atoms of yellowish matter were left on it, which were partly dissolved by a drop of bisulphide of carbon; and this extremely volatile fluid was rendered very much less volatile by what it had dissolved.

As the bisulphide of carbon has a strong power of softening indurated caoutchouc, I soaked in it during a short time several rootlets of a plant which had grown up a plaistered wall; and I then found many extremely thin threads of transparent, not viscid, excessively elastic matter, precisely like caoutchouc, attached to two sets of rootlets on the same branch. These threads proceeded from the bark of the rootlet at one end, and at the other end were firmly attached to particles of silex or mortar from the wall. There could be no mistake in this observation, as I played with the threads for a long time under the microscope, drawing them out with my dissecting- needles and letting them spring back again. Yet I looked repeatedly at other rootlets similarly treated, and could never again discover these elastic threads. I therefore infer that the branch in question must have been slightly moved from the wall at some critical period, whilst the secretion was in the act of drying, through the absorption of its watery parts. The genus Ficus abounds with caoutchouc, and we may conclude from the facts just given that this substance, at first in solution and ultimately modified into an unelastic cement, {42} is used by the Ficus repens to cement its rootlets to any surface which it ascends. Whether other plants, which climb by their rootlets, emit any cement I do not know; but the rootlets of the Ivy, placed against gla.s.s, barely adhered to it, yet secreted a little yellowish matter. I may add, that the rootlets of the Marcgravia dubia can adhere firmly to smooth painted wood.