external conditions—Innate causes—Climbing plants; similarity of their
points of difference—Epinastic growth of young leaves—Hyponastic growth
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 seedling4 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 penetrating5 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 modification6 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 acting7 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 ellipses8 directed successively to all points of the compass—in their courses being often interrupted by zigzag9 lines, triangles, loops, or small [page 265] ellipses—in the rate of movement, and in different species revolving10 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 upwards11. In both sets of cases the movement may be modified in a closely analogous12 manner by geotropism and by heliotropism; though few climbing plants are heliotropic. Other points of similarity might be pointed13 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 vigour14, is obvious. No one doubts that this power has been gained for the sake of enabling climbing plants to ascend15 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, secondly16, 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 vertical17 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 catching19 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 twine20 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 remarkable21 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 stiffen22 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 possessed23 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 vertically24, 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 previously25 inclined position so quickly, that the apex26 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 apparently27 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 conspicuously28 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 Würzburg,' 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 downwards30; 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 lateral31 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 lessened32.
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 diverge33 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 diverged34. 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 Petunia35 violacea were traced during four days, and offers a better instance (Fig18. 111, p. 248) as it diverged during the whole of this time in a curiously36 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 affected37 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 Carnation38 (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 oblique39 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 obliquely40 descending42 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 divergence43 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 ascertained45 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 descended46 at first in a nearly straight line, but afterwards zigzagged47, making one or two little loops. The diverging48 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 bent49 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 ascending50 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 zigzags51 (one of them forming an angle of 112o), and this indicates circumnutation.
The still closed lobes52 of a young leaf of Dionaea projected at right angles to the petiole, and were in the act of slowly rising. A glass filament53 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 laterally54 upwards, and thus occupied an unnatural55 position, obliquely to the plane of the foliaceous petiole.
As the hypocotyls and epicotyls of some plants protrude56 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 remains57 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 fully58 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 adhesive59 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 ascertain44, 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 illuminated60 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 perpendicular61, 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 axis62 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 opposition63 to hyponasty. The loop was then fastened upside down, so that its basal half would be simultaneously64 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 filaments65 were fixed66 to the crowns of four hooked tips standing67 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 perfectly68 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 descend41 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 considerably69 curved, circumnutated in a conspicuous29 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 deflected70 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 abruptly71 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 wither72, 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 Würzburg,' 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 relatively73 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 exclusion74 of bees; they consequently withered75 very slowly, and the movements of the sub-peduncles were in like manner much retarded76.
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 diversified77 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]
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innate
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| adj.天生的，固有的，天赋的 | |
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amplitude
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| n.广大；充足；振幅 | |
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seedlings
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seedling
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penetrating
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modification
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acting
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ellipses
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zigzag
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revolving
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upwards
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analogous
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pointed
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vigour
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ascend
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| vi.渐渐上升，升高；vt.攀登，登上 | |
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secondly
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| adv.第二，其次 | |
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vertical
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| adj.垂直的，顶点的，纵向的；n.垂直物，垂直的位置 | |
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fig
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| n.无花果(树) | |
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catching
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| adj.易传染的，有魅力的，迷人的，接住 | |
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twine
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| v.搓，织，编饰；（使）缠绕 | |
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remarkable
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| adj.显著的，异常的，非凡的，值得注意的 | |
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stiffen
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| v.(使)硬，(使)变挺，(使)变僵硬 | |
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possessed
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| adj.疯狂的；拥有的，占有的 | |
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vertically
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| adv.垂直地 | |
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previously
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| adv.以前，先前（地） | |
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apex
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| n.顶点，最高点 | |
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apparently
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| adv.显然地；表面上，似乎 | |
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conspicuously
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| ad.明显地，惹人注目地 | |
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conspicuous
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| adj.明眼的，惹人注目的；炫耀的，摆阔气的 | |
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downwards
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| adj./adv.向下的（地），下行的（地） | |
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lateral
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| adj.侧面的，旁边的 | |
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lessened
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| 减少的，减弱的 | |
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diverge
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| v.分叉，分歧，离题，使...岔开，使转向 | |
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diverged
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| 分开( diverge的过去式和过去分词 )； 偏离； 分歧； 分道扬镳 | |
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petunia
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| n.矮牵牛花 | |
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curiously
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| adv.有求知欲地；好问地；奇特地 | |
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affected
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| adj.不自然的，假装的 | |
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carnation
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| n.康乃馨（一种花） | |
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oblique
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| adj.斜的，倾斜的，无诚意的，不坦率的 | |
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obliquely
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| adv.斜； 倾斜； 间接； 不光明正大 | |
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descend
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| vt./vi.传下来，下来，下降 | |
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descending
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| n. 下行 adj. 下降的 | |
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divergence
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| n.分歧，岔开 | |
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ascertain
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| vt.发现，确定，查明，弄清 | |
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ascertained
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| v.弄清，确定，查明( ascertain的过去式和过去分词 ) | |
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descended
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| a.为...后裔的，出身于...的 | |
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zigzagged
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| adj.呈之字形移动的v.弯弯曲曲地走路，曲折地前进( zigzag的过去式和过去分词 ) | |
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diverging
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| 分开( diverge的现在分词 )； 偏离； 分歧； 分道扬镳 | |
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bent
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| n.爱好，癖好；adj.弯的；决心的，一心的 | |
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ascending
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| adj.上升的，向上的 | |
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zigzags
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| n.锯齿形的线条、小径等( zigzag的名词复数 )v.弯弯曲曲地走路，曲折地前进( zigzag的第三人称单数 ) | |
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lobes
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| n.耳垂( lobe的名词复数 )；（器官的）叶；肺叶；脑叶 | |
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filament
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| n.细丝；长丝；灯丝 | |
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laterally
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| ad.横向地；侧面地；旁边地 | |
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unnatural
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| adj.不自然的；反常的 | |
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protrude
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| v.使突出，伸出，突出 | |
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remains
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| n.剩余物，残留物；遗体，遗迹 | |
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fully
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| adv.完全地，全部地，彻底地；充分地 | |
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adhesive
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| n.粘合剂；adj.可粘着的，粘性的 | |
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illuminated
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| adj.被照明的；受启迪的 | |
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perpendicular
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| adj.垂直的，直立的；n.垂直线，垂直的位置 | |
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axis
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| n.轴，轴线，中心线；坐标轴，基准线 | |
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opposition
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| n.反对，敌对 | |
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simultaneously
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| adv.同时发生地，同时进行地 | |
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filaments
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| n.（电灯泡的）灯丝( filament的名词复数 )；丝极；细丝；丝状物 | |
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fixed
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| adj.固定的，不变的，准备好的；(计算机)固定的 | |
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standing
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| n.持续，地位；adj.永久的，不动的，直立的，不流动的 | |
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perfectly
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| adv.完美地，无可非议地，彻底地 | |
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considerably
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| adv.极大地；相当大地；在很大程度上 | |
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deflected
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| 偏离的 | |
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abruptly
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| adv.突然地，出其不意地 | |
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wither
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| vt.使凋谢，使衰退，(用眼神气势等)使畏缩；vi.枯萎，衰退，消亡 | |
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relatively
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| adv.比较...地，相对地 | |
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exclusion
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| n.拒绝，排除，排斥，远足，远途旅行 | |
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withered
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| adj. 枯萎的，干瘪的，（人身体的部分器官）因病萎缩的或未发育良好的 动词wither的过去式和过去分词形式 | |
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retarded
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| a.智力迟钝的，智力发育迟缓的 | |
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diversified
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| adj.多样化的，多种经营的v.使多样化，多样化( diversify的过去式和过去分词 )；进入新的商业领域 | |
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