Life Movements in Plants Part 1

Life Movements in Plants.

Volume II.

1919.

by Sir Jagadis Chunder Bose.

PREFACE.

I have in the present volume dealt with the intricate phenomena of different tropisms. The movements in plants under the stimuli of the environment--the twining of tendrils, the effect of temperature, the action of light inducing movements sometimes towards and at other times away from the stimulus, the diametrically opposite responses of the shoot and the root to the same stimulus of gravity, the day and night positions of organs of plants--these, and many others present such diversities that it must have appeared a hopeless endeavour to discover any fundamental reaction applicable in all cases. It has therefore been customary to a.s.sume different sensibilities especially evolved for the advantage of the plant. But teleological argument and the use of descriptive phrases, like positive and negative tropism, offer no real explanation of the phenomena. Thus to quote Pfeffer "When we say that an organ curves towards a source of illumination, because of its heliotropic irritability we are simply expressing an ascertained fact in a conveniently abbreviated form, without explaining why such curvature is possible or how it is produced.... Many observers have unfortunately devoted their attention to artificially cla.s.sifying the phenomenon observed, and have entirely neglected the explanation of causes underlying them." He also adds that in regard to the phenomenon of growth and its variations, an empirical treatment is all that is possible in the present state of our knowledge; but deduction from results of experimental investigation "still remains the ideal of physiology, and only when this ideal has been attained, shall we be able to obtain a comprehensive view of the interacting factors at work in the living organism."

In my previous work on "Plant Response" (1906) I described detailed investigations on irritability of plants which I carried out with highly sensitive recorders. The plant was thus made to tell its own story by means of its self-made records. The results showed that there is no specific difference in physiological reaction of different organs to justify the a.s.sumption of positive and negative irritabilities. A generalisation was obtained which gave a complete explanation of diverse movements in plants. The results were fully confirmed by an independent method of inquiry, namely that of electric response, which I have been able to elaborate so as to become a very important means of research.

The investigations described in the present volume not only support the conclusions reached in my earlier works, but have led to important additions. It is evident that the range of our investigation is limited only by our power of recording the rate of plant-movement, that is to say, in the measurement of length and time. In these respects the instruments that I have been able to devise have surpa.s.sed my sanguine expectations. The Resonant Recorder traces time-intervals as short as a thousandth part of a second, while my Balanced Crescograph enables us to measure variation of rate of growth as minute as 1/1000 millionth of an inch per second, the sensitiveness of this apparatus thus rivals that of the spectroscope. The increasing refinement in our experimental methods cannot but lead to important advances towards a deeper understanding of underlying reactions in the living organism.

I shall here draw attention to only a few of the important results given in the present volume. The tropic effect of light has been shown to have a definite relation to the quant.i.ty of incident light. A complete tropic curve has been obtained from sub-minimal to maximal stimulation which shows the inadequacy of Weber's law, for the sub-minimal stimulus induces a _qualitative_ difference in physiological reaction. It has further been shown that the prevalent idea that perception and heliotropic excitation are two distinct phenomena is without any foundation.

With reference to the effect of ether waves on plants, I have given an account of my discovery of the response of all plants to wireless stimulation, the results being similar to that induced by visible light.

The perceptive range of the plant is thus infinitely greater than ours; for it not only perceives, but also responds to different rays of the vast ethereal spectrum.

The results obtained by the method of geo-electric response show that the responsive reaction of the root is in no way different from that of the shoot, the opposite movements being due to the fact that in the shoot the stimulation is direct, and in the root it is indirect.

Full description is given of the new method of physiological exploration by means of the electric probe, by which the particular layer which perceives the stimulus of gravity is definitely localised. The method of electric probe is also found to be of extended application in the detection of physiological changes in the interior of an organ.

An important factor of nyct.i.tropic movements, hitherto unsuspected, is the effect of variation of temperature on geotropic curvature. This and other co-operative factors have been fully a.n.a.lysed, and a satisfactory explanation has been offered of various types of diurnal movement.

A generalisation has been obtained which explains all the diverse movements of plants, under all modes of stimulation: _it has been shown that direct stimulation induces contraction and r.e.t.a.r.dation of growth, and that indirect stimulation induces an expansion and acceleration of growth._

Another generalisation of still greater importance is the establishment of identical nature of physiological reaction in the plant and the animal, leading to advances in general physiology. Thus the discovery of a method for immediate enhancement or inhibition of nervous impulse in the plant led to my success in the control of nervous impulse in the animal. Another important discovery was the dual nervous impulses in plants, and I have very recently been able to establish, that the nervous impulse generated in the animal nerve by stimulus is not single, but double.

The study of the responsive phenomena in plants must thus form an integral part of physiological investigation into various problems relating to the irritability of all living tissues, and without such study the investigation must in future remain incomplete.

_October 1919._

J. C. BOSE.

PART III.

TROPISM IN PLANTS.

XXII.--THE BALANCED CRESCOGRAPH

_By_

SIR J. C. BOSE.

We shall in the succeeding series of papers deal with the subject of tropism in general. Different plant organs undergo curvature or bending, sometimes towards and at other times away from the stimulus which induces it. The problem is very intricate; the possibility of its solution will depend greatly on the accurate determination of the immediate and after-effects of various stimuli on the responding organ.

The curvature induced in the growing organ is brought about by variation, often extremely slight, of the rate of growth; the result, moreover, is liable to be modified by the duration and point of application of stimulus. The difficulties connected with the problem can only be removed by the detection and measurement of the minutest variation in growth, and by securing a continuous and automatic record of the entire history of the change.

In the chapter on High Magnification Crescograph an account is given of the apparatus which I have devised by which the rate of growth may be magnified from ten thousand to ten millions times. It is thus possible to measure the imperceptible growth of plants for a period shorter than a single second. The variation of normal rate of growth is also found by measuring successive growth records on a stationary plate at regular intervals, say of ten seconds, or from the flexure in the growth-curve taken on a moving plate (p. 163).

I was next desirous of exalting the sensitiveness to a still higher degree by an independent method, which would not only reveal very slight variation induced in the rate of growth, but also the latent period and time-relations of the change. For this purpose I at first devised the Optical Method of Balance[1] which was considered at the time to be extremely sensitive. The spot of light from the Optical Lever (which magnified the rate of growth) was made to fall upon a mirror to which a compensating movement was imparted so that the light-spot after double reflection remained stationary. Any change of rate of growth--acceleration or r.e.t.a.r.dation--was at once detected by the movement of the hitherto stationary spot of light in one direction or the other.

[1] "Plant Response"--p. 413.

A very careful manipulation was required for the adjustment of the Optical Balance; the record moreover was not automatic. For these reasons I have been engaged for several years past in perfecting a new apparatus by which, (1) the balance could be directly obtained with the utmost exact.i.tude, (2) where an attached scale would indicate the exact rate of growth, and (3) in which the upsetting of the balance by external stimulus would be automatically recorded, the curve giving the time relations of the change.

PRINCIPLE OF THE METHOD OF BALANCE.

I shall take a concrete example in explanation of the method of balance.

Taking the rate of growth per second of a plant to be 1/50,000 inch or 05 , per second (equal to the wave length of sodium light), the tip of the plant will be maintained at the same point in s.p.a.ce if we succeeded in making the plant-holder subside exactly at the same rate. The growth-elongation of the plant will then be exactly balanced by a compensating movement downwards. The state of exact balance is indicated when the recording lever of the Crescograph traces a horizontal line on the moving plate. Overbalance or underbalance will deflect the record below or above the horizontal line.

[Ill.u.s.tration: FIG. 93.--Arrangement for compensation of growth-movement by equal subsidence of plant-holder; S, adjusting screw for regulation of speed of rotation; G, governor; W, heavy weight; P, plant-holder.]

COMPENSATING MOVEMENT.

For securing exact balance the holder of the plant P, in the given example, will have to subside at a rate of 1/50,000 inch per second.

This is accomplished by a system of reducing worm and pinion, also of clock wheels (Fig. 93). The clock at first used for this purpose was worked by the usual balance wheel. Though this secured an _average_ balance yet as each tick of the clock consisted of sudden movement and stoppage, it caused minute variation in the rate of subsidence; this became magnified by the Crescograph and appeared as a series of oscillations about a mean position of equilibrium. This particular defect was obviated by the subst.i.tution of a fan governor for the balance wheel. But the speed of rotation slows down with the unwinding of the main spring, and the balance obtained at the beginning was found to be insufficient later on. The difficulty was finally overcome by the use of a heavy weight W, in the place of coiled spring. The complete apparatus is seen in figure 94.

[Ill.u.s.tration: FIG. 94.--Photographic reproduction of the Balanced Crescograph. L, L', magnifying compound lever. R, recording plate.

P, plant. C, clock work for oscillation of the plate and lateral movement. G, governor. M, circular growth-scale. V, plant-chamber.]

For purpose of simplicity of explanation, I a.s.sumed the growth rate to have a definite value of 1/50,000 inch per second. But the rate varies widely in different plants and even in the same plant at different days and seasons. In practice the rate of growth for which compensation has to be made varies from 1/150,000 to 1/25,000 inch, or from 017 to 10 per second. We have thus to secure some means of _continuous_ adjustment for growth, the rate of which could be continuously varied from one to six times. This range of adjustment I have been able to secure by the compound method of frictional resistance and of centrifugal governor. As regards frictional resistance the two pointed ends of a hinged fork rub against a horizontal circular plate not shown in the figure. By means of the screw head S, the free ends of the fork spread out and the circ.u.mference of the frictional circle continuously increased. The centrifugal governor is also spread out by the action of the adjusting screw. By the joint actions of the frictional control and the centrifugal governor, the speed of rotation can be continuously adjusted from 1 to 6 times. When the adjusting screw is set in a particular position, the speed of rotation, and therefore the rate of subsidence of plant-holder, remains absolutely constant for several hours. The attainment of this constancy is a matter of fundamental importance, and it was only by the employment or the compound system of regulation that I was able to secure it.

The method of obtaining balance now becomes extremely simple. Before starting the balancing movement by clock regulation, the plant is made to record its magnified growth by the Crescograph. The compensation is effected as follows: the speed of the clockwork is at the beginning adjusted at its lowest value, and the pressure of a b.u.t.ton starts the balancing movement of the plant downwards. On account of partial balance the record will be found to be less steep than before; the speed of the clock is gradually increased till the record becomes perfectly horizontal under exact balance. Overbalance makes the record slope downwards. In figure 95 is seen records of underbalance (_a_) and overbalance (_b_), to the extent of about 3 per cent.

[Ill.u.s.tration: FIG. 95.--Balanced Crescographic record: (_a_) showing effect of underbalance and (_b_) overbalance of about 3 per cent.

(Magnification 2,000 times.)]

It will thus be seen that the effect of an external agent may be detected by the upsetting of the balance; an up-movement indicates (unless stated to the contrary) an enhancement of the rate of growth above the normal; and a down-movement, on the other hand, a depression of the normal rate.

_Calibration._--The calibration of the instrument is obtained in two different ways. The rate of subsidence of the plant-holder, by which the balance is obtained, is strictly proportional to the rate of rotation of the vertical spindle and the attached train of clock-wheels. A striker is attached to one of the wheels, and a bell is struck at each complete revolution. The clockwork is adjusted at a medium speed, the bell striking 35 times in a minute. A microscope micrometer is focussed on a mark made on the plant-holder, and the amount of subsidence of the mark determined after one minute; this was found to be 00525 mm. As this fall occurred after 35 strokes of the bell the subsidence per stroke was 00015 mm.

_Determination of the absolute rate of growth._--If growth be found balanced at N strokes of bell per minute, the rate of subsidence per second

= N 0015/60 mm. per second = N 000025 mm. per second = N 025 per second = N 10^{-5} inch per second.