Darwin and Modern Science Part 22

The writer has advanced the following theory of these instinctive reactions. Animals of the type of those mentioned are automatically orientated by the light in such a way that symmetrical elements of their retina (or skin) are struck by the rays of light at the same angle.

In this case the intensity of light is the same for both retinae or symmetrical parts of the skin.

This automatic orientation is determined by two factors, first a peculiar photo-sensitiveness of the retina (or skin), and second a peculiar nervous connection between the retina and the muscular apparatus. In symmetrically built heliotropic animals in which the symmetrical muscles partic.i.p.ate equally in locomotion, the symmetrical muscles work with equal energy as long as the photo-chemical processes in both eyes are identical. If, however, one eye is struck by stronger light than the other, the symmetrical muscles will work unequally and in positively heliotropic animals those muscles will work with greater energy which bring the plane of symmetry back into the direction of the rays of light and the head towards the source of light. As soon as both eyes are struck by the rays of light at the same angle, there is no more reason for the animal to deviate from this direction and it will move in a straight line. All this holds good on the supposition that the animals are exposed to only one source of light and are very sensitive to light.

Additional proof for the correctness of this theory was furnished through the experiments of G.H. Parker and S.J. Holmes. The former worked on a b.u.t.terfly, Vanessa antiope, the latter on other arthropods.

All the animals were in a marked degree positively heliotropic. These authors found that if one cornea is blackened in such an animal, it moves continually in a circle when it is exposed to a source of light, and in these motions the eye which is not covered with paint is directed towards the centre of the circle. The animal behaves, therefore, as if the darkened eye were in the shade.

(b) THE PRODUCTION OF POSITIVE HELIOTROPISM BY ACIDS AND OTHER MEANS AND THE PERIODIC DEPTH-MIGRATIONS OF PELAGIC ANIMALS.

When we observe a dense ma.s.s of copepods collected from a freshwater pond, we notice that some have a tendency to go to the light while others go in the opposite direction and many, if not the majority, are indifferent to light. It is an easy matter to make the negatively heliotropic or the indifferent copepods almost instantly positively heliotropic by adding a small but definite amount of carbon-dioxide in the form of carbonated water to the water in which the animals are contained. If the animals are contained in 50 cubic centimetres of water it suffices to add from three to six cubic centimetres of carbonated water to make all the copepods energetically positively heliotropic.

This heliotropism lasts about half an hour (probably until all the carbon-dioxide has again diffused into the air.) Similar results may be obtained with any other acid.

The same experiments may be made with another freshwater crustacean, namely Daphnia, with this difference, however, that it is as a rule necessary to lower the temperature of the water also. If the water containing the Daphniae is cooled and at the same time carbon-dioxide added, the animals which were before indifferent to light now become most strikingly positively heliotropic. Marine copepods can be made positively heliotropic by the lowering of the temperature alone, or by a sudden increase in the concentration of the sea-water.

These data have a bearing upon the depth-migrations of pelagic animals, as was pointed out years ago by Theo. T. Groom and the writer. It is well known that many animals living near the surface of the ocean or freshwater lakes, have a tendency to migrate upwards towards evening and downwards in the morning and during the day. These periodic motions are determined to a large extent, if not exclusively, by the heliotropism of these animals. Since the consumption of carbon-dioxide by the green plants ceases towards evening, the tension of this gas in the water must rise and this must have the effect of inducing positive heliotropism or increasing its intensity. At the same time the temperature of the water near the surface is lowered and this also increases the positive heliotropism in the organisms.

The faint light from the sky is sufficient to cause animals which are in a high degree positively heliotropic to move vertically upwards towards the light, as experiments with such pelagic animals, e.g. copepods, have shown. When, in the morning, the absorption of carbon-dioxide by the green algae begins again and the temperature of the water rises, the animals lose their positive heliotropism, and slowly sink down or become negatively heliotropic and migrate actively downwards.

These experiments have also a bearing upon the problem of the inheritance of instincts. The character which is transmitted in this case is not the tendency to migrate periodically upwards and downwards, but the positive heliotropism. The tendency to migrate is the outcome of the fact that periodically varying external conditions induce a periodic change in the sense and intensity of the heliotropism of these animals.

It is of course immaterial for the result, whether the carbon-dioxide or any other acid diffuse into the animal from the outside or whether they are produced inside in the tissue cells of the animals. Davenport and Cannon found that Daphniae, which at the beginning of the experiment, react sluggishly to light react much more quickly after they have been made to go to the light a few times. The writer is inclined to attribute this result to the effect of acids, e.g. carbon-dioxide, produced in the animals themselves in consequence of their motion. A similar effect of the acids was shown by A.D. Waller in the case of the response of nerve to stimuli.

The writer observed many years ago that winged male and female ants are positively helioptropic and that their heliotropic sensitiveness increases and reaches its maximum towards the period of nuptial flight.

Since the workers show no heliotropism it looks as if an internal secretion from the s.e.xual glands were the cause of their heliotropic sensitiveness. V. Kellogg has observed that bees also become intensely positively heliotropic at the period of their wedding flight, in fact so much so that by letting light fall into the observation hive from above, the bees are prevented from leaving the hive through the exit at the lower end.

We notice also the reverse phenomenon, namely, that chemical changes produced in the animal destroy its heliotropism. The caterpillars of Porthesia chrysorrhoea are very strongly positively heliotropic when they are first aroused from their winter sleep. This heliotropic sensitiveness lasts only as long as they are not fed. If they are kept permanently without food they remain permanently positively heliotropic until they die from starvation. It is to be inferred that as soon as these animals take up food, a substance or substances are formed in their bodies which diminish or annihilate their heliotropic sensitiveness.

The heliotropism of animals is identical with the heliotropism of plants. The writer has shown that the experiments on the effect of acids on the heliotropism of copepods can be repeated with the same result in Volvox. It is therefore erroneous to try to explain these heliotropic reactions of animals on the basis of peculiarities (e.g. vision) which are not found in plants.

We may briefly discuss the question of the transmission through the s.e.x cells of such instincts as are based upon heliotropism. This problem reduces itself simply to that of the method whereby the gametes transmit heliotropism to the larvae or to the adult. The writer has expressed the idea that all that is necessary for this transmission is the presence in the eyes (or in the skin) of the animal of a photo-sensitive substance.

For the transmission of this the gametes need not contain anything more than a catalyser or ferment for the synthesis of the photo-sensitive substance in the body of the animal. What has been said in regard to animal heliotropism might, if s.p.a.ce permitted, be extended, mutatis mutandis, to geotropism and stereotropism.

(c) THE TROPIC REACTIONS OF CERTAIN TISSUE-CELLS AND THE MORPHOGENETIC EFFECTS OF THESE REACTIONS.

Since plant-cells show heliotropic reactions identical with those of animals, it is not surprising that certain tissue-cells also show reactions which belong to the cla.s.s of tropisms. These reactions of tissue-cells are of special interest by reason of their bearing upon the inheritance of morphological characters. An example of this is found in the tiger-like marking of the yolk-sac of the embryo of Fundulus and in the marking of the young fish itself. The writer found that the former is entirely, and the latter at least in part, due to the creeping of the chromatoph.o.r.es upon the blood-vessels. The chromatoph.o.r.es are at first scattered irregularly over the yolk-sac and show their characteristic ramifications. There is at that time no definite relation between blood-vessels and chromatoph.o.r.es. As soon as a ramification of a chromatoph.o.r.e comes in contact with a blood-vessel the whole ma.s.s of the chromatoph.o.r.e creeps gradually on the blood-vessel and forms a complete sheath around the vessel, until finally all the chromatoph.o.r.es form a sheath around the vessels and no more pigment cells are found in the meshes between the vessels. n.o.body who has not actually watched the process of the creeping of the chromatoph.o.r.es upon the blood-vessels would antic.i.p.ate that the tiger-like colouration of the yolk-sac in the later stages of the development was brought about in this way. Similar facts can be observed in regard to the first marking of the embryo itself. The writer is inclined to believe that we are here dealing with a case of chemotropism, and that the oxygen of the blood may be the cause of the spreading of the chromatoph.o.r.es around the blood-vessels.

Certain observations seem to indicate the possibility that in the adult the chromatoph.o.r.es have, in some forms at least, a more rigid structure and are prevented from acting in the way indicated. It seems to the writer that such observations as those made on Fundulus might simplify the problem of the hereditary transmission of certain markings.

Driesch has found that a tropism underlies the arrangement of the skeleton in the pluteus larvae of the sea-urchin. The position of this skeleton is predetermined by the arrangement of the mesenchyme cells, and Driesch has shown that these cells migrate actively to the place of their destination, possibly led there under the influence of certain chemical substances. When Driesch scattered these cells mechanically before their migration, they nevertheless reached their destination.

In the developing eggs of insects the nuclei, together with some cytoplasm, migrate to the periphery of the egg. Herbst pointed out that this might be a case of chemotropism, caused by the oxygen surrounding the egg. The writer has expressed the opinion that the formation of the blastula may be caused generally by a tropic reaction of the blastomeres, the latter being forced by an outside influence to creep to the surface of the egg.

These examples may suffice to indicate that the arrangement of definite groups of cells and the morphological effects resulting therefrom may be determined by forces lying outside the cells. Since these forces are ubiquitous and constant it appears as if we were dealing exclusively with the influence of a gamete; while in reality all that it is necessary for the gamete to transmit is a certain form of irritability.

(d) FACTORS WHICH DETERMINE PLACE AND TIME FOR THE DEPOSITION OF EGGS.

For the preservation of species the instinct of animals to lay their eggs in places in which the young larvae find their food and can develop is of paramount importance. A simple example of this instinct is the fact that the common fly lays its eggs on putrid material which serves as food for the young larvae. When a piece of meat and of fat of the same animal are placed side by side, the fly will deposit its eggs upon the meat on which the larvae can grow, and not upon the fat, on which they would starve. Here we are dealing with the effect of a volatile nitrogenous substance which reflexly causes the peristaltic motions for the laying of the egg in the female fly.

Kammerer has investigated the conditions for the laying of eggs in two forms of salamanders, e.g. Salamandra atra and S. maculosa. In both forms the eggs are fertilised in the body and begin to develop in the uterus. Since there is room only for a few larvae in the uterus, a large number of eggs perish and this number is the greater the longer the period of gestation. It thus happens that when the animals retain their eggs a long time, very few young ones are born; and these are in a rather advanced stage of development, owing to the long time which elapsed since they were fertilised. When the animal lays its eggs comparatively soon after copulation, many eggs (from 12 to 72) are produced and the larvae are of course in an early stage of development.

In the early stage the larvae possess gills and can therefore live in water, while in later stages they have no gills and breathe through their lungs. Kammerer showed that both forms of Salamandra can be induced to lay their eggs early or late, according to the physical conditions surrounding them. If they are kept in water or in proximity to water and in a moist atmosphere they have a tendency to lay their eggs earlier and a comparatively high temperature enhances the tendency to shorten the period of gestation. If the salamanders are kept in comparative dryness they show a tendency to lay their eggs rather late and a low temperature enhances this tendency.

Since Salamandra atra is found in rather dry alpine regions with a relatively low temperature and Salamandra maculosa in lower regions with plenty of water and a higher temperature, the fact that S. atra bears young which are already developed and beyond the stage of aquatic life, while S. maculosa bears young ones in an earlier stage, has been termed adaptation. Kammerer's experiments, however, show that we are dealing with the direct effects of definite outside forces. While we may speak of adaptation when all or some of the variables which determine a reaction are unknown, it is obviously in the interest of further scientific progress to connect cause and effect directly whenever our knowledge allows us to do so.

VII. CONCLUDING REMARKS.

The discovery of De Vries, that new species may arise by mutation and the wide if not universal applicability of Mendel's Law to phenomena of heredity, as shown especially by Bateson and his pupils, must, for the time being, if not permanently, serve as a basis for theories of evolution. These discoveries place before the experimental biologist the definite task of producing mutations by physico-chemical means. It is true that certain authors claim to have succeeded in this, but the writer wishes to apologise to these authors for his inability to convince himself of the validity of their claims at the present moment.

He thinks that only continued breeding of these apparent mutants through several generations can afford convincing evidence that we are here dealing with mutants rather than with merely pathological variations.

What was said in regard to the production of new species by physico-chemical means may be repeated with still more justification in regard to the second problem of transformation, namely the making of living from inanimate matter. The purely morphological imitations of bacteria or cells which physicists have now and then proclaimed as artificially produced living beings; or the plays on words by which, e.g. the regeneration of broken crystals and the regeneration of lost limbs by a crustacean were declared identical, will not appeal to the biologist. We know that growth and development in animals and plants are determined by definite although complicated series of catenary chemical reactions, which result in the synthesis of a DEFINITE compound or group of compounds, namely, NUCLEINS.

The nucleins have the peculiarity of acting as ferments or enzymes for their own synthesis. Thus a given type of nucleus will continue to synthesise other nuclein of its own kind. This determines the continuity of a species; since each species has, probably, its own specific nuclein or nuclear material. But it also shows us that whoever claims to have succeeded in making living matter from inanimate will have to prove that he has succeeded in producing nuclein material which acts as a ferment for its own synthesis and thus reproduces itself. n.o.body has thus far succeeded in this, although nothing warrants us in taking it for granted that this task is beyond the power of science.

XV. THE VALUE OF COLOUR IN THE STRUGGLE FOR LIFE. By E.B. Poulton.

Hope Professor of Zoology in the University of Oxford.

INTRODUCTION.

The following pages have been written almost entirely from the historical stand-point. Their princ.i.p.al object has been to give some account of the impressions produced on the mind of Darwin and his great compeer Wallace by various difficult problems suggested by the colours of living nature. In order to render the brief summary of Darwin's thoughts and opinions on the subject in any way complete, it was found necessary to say again much that has often been said before. No attempt has been made to display as a whole the vast contribution of Wallace; but certain of its features are incidentally revealed in pa.s.sages quoted from Darwin's letters. It is a.s.sumed that the reader is familiar with the well-known theories of Protective Resemblance, Warning Colours, and Mimicry both Batesian and Mullerian. It would have been superfluous to explain these on the present occasion; for a far more detailed account than could have been attempted in these pages has recently appeared.

(Poulton, "Essays on Evolution" Oxford, 1908, pages 293-382.) Among the older records I have made a point of bringing together the princ.i.p.al observations scattered through the note-books and collections of W.J.

Burch.e.l.l. These have never hitherto found a place in any memoir dealing with the significance of the colours of animals.

INCIDENTAL COLOURS.

Darwin fully recognised that the colours of living beings are not necessarily of value as colours, but that they may be an incidental result of chemical or physical structure. Thus he wrote to T. Meehan, Oct. 9, 1874: "I am glad that you are attending to the colours of dioecious flowers; but it is well to remember that their colours may be as unimportant to them as those of a gall, or, indeed, as the colour of an amethyst or ruby is to these gems." ("More Letters of Charles Darwin", Vol. I. pages 354, 355. See also the admirable account of incidental colours in "Descent of Man" (2nd edition), 1874, pages 261, 262.)

Incidental colours remain as available a.s.sets of the organism ready to be turned to account by natural selection. It is a probable speculation that all pigmentary colours were originally incidental; but now and for immense periods of time the visible tints of animals have been modified and arranged so as to a.s.sist in the struggle with other organisms or in courts.h.i.+p. The dominant colouring of plants, on the other hand, is an essential element in the paramount physiological activity of chlorophyll. In exceptional instances, however, the shapes and visible colours of plants may be modified in order to promote concealment.

TELEOLOGY AND ADAPTATION.

In the department of Biology which forms the subject of this essay, the adaptation of means to an end is probably more evident than in any other; and it is therefore of interest to compare, in a brief introductory section, the older with the newer teleological views.

The distinctive feature of Natural Selection as contrasted with other attempts to explain the process of Evolution is the part played by the struggle for existence. All naturalists in all ages must have known something of the operations of "Nature red in tooth and claw"; but it was left for this great theory to suggest that vast extermination is a necessary condition of progress, and even of maintaining the ground already gained.

Realising that fitness is the outcome of this fierce struggle, thus turned to account for the first time, we are sometimes led to a.s.sociate the recognition of adaptation itself too exclusively with Natural Selection. Adaptation had been studied with the warmest enthusiasm nearly forty years before this great theory was given to the scientific world, and it is difficult now to realise the impetus which the works of Paley gave to the study of Natural History. That they did inspire the naturalists of the early part of the last century is clearly shown in the following pa.s.sages.

In the year 1824 the Ashmolean Museum at Oxford was intrusted to the care of J.S. Duncan of New College. He was succeeded in this office by his brother, P.B. Duncan, of the same College, author of a History of the Museum, which shows very clearly the influence of Paley upon the study of nature, and the dominant position given to his teachings: "Happily at this time (1824) a taste for the study of natural history had been excited in the University by Dr Paley's very interesting work on Natural Theology, and the very popular lectures of Dr Kidd on Comparative Anatomy, and Dr Buckland on Geology." In the arrangement of the contents of the Museum the ill.u.s.tration of Paley's work was given the foremost place by J.S. Duncan: "The first division proposes to familiarize the eye to those relations of all natural objects which form the basis of argument in Dr Paley's Natural Theology; to induce a mental habit of a.s.sociating the view of natural phenomena with the conviction that they are the media of Divine manifestation; and by such a.s.sociation to give proper dignity to every branch of natural science." (From "History and Arrangement of the Ashmolean Museum" by P.B. Duncan: see pages vi, vii of "A Catalogue of the Ashmolean Museum", Oxford, 1836.)

The great naturalist, W.J. Burch.e.l.l, in his cla.s.sical work shows the same recognition of adaptation in nature at a still earlier date.

Upon the subject of collections he wrote ("Travels in the Interior of Southern Africa", London, Vol. I. 1822, page 505. The references to Burch.e.l.l's observations in the present essay are adapted from the author's article in "Report of the British and South African a.s.sociations", 1905, Vol. III. pages 57-110.): "It must not be supposed that these charms (the pleasures of Nature) are produced by the mere discovery of new objects: it is the harmony with which they have been adapted by the Creator to each other, and to the situations in which they are found, which delights the observer in countries where Art has not yet introduced her discords." The remainder of the pa.s.sage is so admirable that I venture to quote it: "To him who is satisfied with ama.s.sing collections of curious objects, simply for the pleasure of possessing them, such objects can afford, at best, but a childish gratification, faint and fleeting; while he who extends his view beyond the narrow field of nomenclature, beholds a boundless expanse, the exploring of which is worthy of the philosopher, and of the best talents of a reasonable being."

On September 14, 1811, Burch.e.l.l was at Zand Valley (Vlei), or Sand Pool, a few miles south-west of the site of Prieska, on the Orange River. Here he found a Mesembryanthemum (M. turbiniforme, now M. truncatum) and also a "Gryllus" (Acridian), closely resembling the pebbles with which their locality was strewn. He says of both of these, "The intention of Nature, in these instances, seems to have been the same as when she gave to the Chameleon the power of accommodating its color, in a certain degree, to that of the object nearest to it, in order to compensate for the deficiency of its locomotive powers. By their form and colour, this insect may pa.s.s un.o.bserved by those birds, which otherwise would soon extirpate a species so little able to elude its pursuers, and this juicy little Mesembryanthemum may generally escape the notice of cattle and wild animals." (Loc. cit. pages 310, 311. See Sir William Thiselton-Dyer "Morphological Notes", XI.; "Protective Adaptations", I.; "Annals of Botany", Vol. XX. page 124. In plates VII., VIII. and IX. accompanying this article the author represents the species observed by Burch.e.l.l, together with others in which a.n.a.logous adaptations exist. He writes: "Burch.e.l.l was clearly on the track on which Darwin reached the goal.

But the time had not come for emanc.i.p.ation from the old teleology. This, however, in no respect detracts from the merit or value of his work.

For, as Huxley has pointed out ("Life and Letters of Thomas Henry Huxley", London, 1900, I. page 457), the facts of the old teleology are immediately transferable to Darwinism, which simply supplies them with a natural in place of a supernatural explanation.") Burch.e.l.l here seems to miss, at least in part, the meaning of the relations.h.i.+p between the quiescence of the Acridian and its cryptic colouring. Quiescence is an essential element in the protective resemblance to a stone--probably even more indispensable than the details of the form and colouring.

Although Burch.e.l.l appears to overlook this point he fully recognised the community between protection by concealment and more aggressive modes of defence; for, in the pa.s.sage of which a part is quoted above, he specially refers to some earlier remarks on page 226 of his Vol. I. We here find that even when the oxen were resting by the Juk rivier (Yoke river), on July 19, 1811, Burch.e.l.l observed "Geranium spinosum, with a fleshy stem and large white flowers...; and a succulent species of Pelargonium... so defended by the old panicles, grown to hard woody thorns, that no cattle could browze upon it." He goes on to say, "In this arid country, where every juicy vegetable would soon be eaten up by the wild animals, the Great Creating Power, with all-provident wisdom, has given to such plants either an acrid or poisonous juice, or sharp thorns, to preserve the species from annihilation... " All these modes of defence, especially adapted to a desert environment, have since been generally recognised, and it is very interesting to place beside Burch.e.l.l's statement the following pa.s.sage from a letter written by Darwin, Aug. 7, 1868, to G.H. Lewes; "That Natural Selection would tend to produce the most formidable thorns will be admitted by every one who has observed the distribution in South America and Africa (vide Livingstone) of thorn-bearing plants, for they always appear where the bushes grow isolated and are exposed to the attacks of mammals. Even in England it has been noticed that all spine-bearing and sting-bearing plants are palatable to quadrupeds, when the thorns are crushed." ("More Letters", I. page 308.)

ADAPTATION AND NATURAL SELECTION.