Part 10

Thus, by adaptation and variation the organism acquires new functions, organs, features, and it gives up and eventually loses others. Its offspring is like it. Like produces like. This is the principle of heredity. Adaptation, when going on generation after generation on the same lines in the same direction, becomes continuous, and has an intensifying, cumulative effect. By always weeding out from a flock of pigeons those birds which possess more dark feathers than the rest, we ultimately produce an entirely white race. We hurry on what Nature does slowly.

The inheritance of acquired characters becomes very obvious in the following example: The Monera are the lowest living organisms known; they consist of a mass of protoplasm, and are still devoid of even a nucleus. They multiply simply by division; each half is like the other, and like the parent (which by this process has ceased to exist), except that each is smaller and has to grow. A certain Moneron, Protomyxa aurantiaca, is orange-coloured, and its offspring is from the beginning of the same colour, and this colour has been acquired by that kind of Monera-like protoplasm which thereby has become the species called Aurantiaca. We have no reason for assuming that there existed from the beginning of life not only colourless, but also red, orange, and other kinds of protoplasm. In these simplest of organisms the whole process of heredity seems very obvious; but in the higher ones, in those which propagate by eggs, the problem is infinitely more complicated. It is true that the egg is, strictly, nothing but a small part of the parental organism, and we know from everyday experience that this single egg-cell has in it all the attributes and characteristics of the parent; but these attributes and characteristics make their appearance successively, just as the egg cell of a chick has neither wings nor feathers, not even a backbone, but develops these organs because its parents have them.

The theory that acquired characters are hereditary has often been vigorously attacked; but the champions of the negative position have not given us anything satisfactory instead. They question, also, the principle of adaptation as a factor in Evolution, and substitute 'variation,' coupled with 'natural selection.'

They point to Darwin's argument: (1) It is a fact that animals and plants produce a much greater number of young than in their turn grow up to propagate the race; (2) no two of the frequently many individuals of the same breed are exactly alike, although the differences may be hidden to our perception (this is quite true, because no two entities can live in absolutely the same place and conditions); (3) through heredity the offspring takes over the faculties and features of the parents; (4) what decides which of the many individuals (each one possessing some aberration or variation) are to live and to propagate the race?--obviously those individual variations which happen to make the lucky possessors most fit for the struggle for life.

So far, well; but the 'Neo-Darwinians' imagine that 'adaptation' is not the cause, but the result, the effect, of the formation of species. According to them, the species are neither adapted by, nor do they adapt themselves to, their surroundings. Adaptation is to them an accomplished fact, a condition which a species happens to be in because its particular variation is the one which, to the exclusion of others, suits or fits into its surroundings. Such a view simply takes variation for granted, and stipulates it as a something a priori, without raising the further necessary question, why there should be any variations at all. Why, indeed, unless they are caused by external influences? Haeckel elucidated this by the conception of adaptation as explained in the foregoing pages.

These and kindred speculations have produced some rather curious discussions, which not infrequently end in conundrums. If we speak of a case of adaptation as a condition, a fact, we easily run the risk of getting into confusion about cause and effect. For example: Is the stag swift because he has long and slender legs, or are his legs long because he is swift? In reality, swiftness and length of legs are cause and effect in one. His legs have been so modified as to make him swift, because he has put them continuously to whatever was his full speed, which in his thick-footed ancestors was probably a very slow one. The above question reads, therefore, more sensibly as follows: Has the stag become swift because his legs have become long and slender, or have his legs become long and slender because he has attained swiftness? Now, we see that both halves of the double question are practically the same and instantly suggest the answer.

A fundamental difference between artificial machines and living organisms is that the former are worn out by use, while the latter not only repair the loss caused by use, but are also stimulated to further increase. On the other hand, organs which are not put into function, or are not used, degenerate. The various cells of the organ react upon external stimuli by increased activity. Why this should be so is another question--perhaps because those which do not would soon be not fit to survive. Each cell has a function; the more specialized the more intense it is. Every external stimulus, every contact with the outer surroundings, is an insult, necessarily of detrimental effect, as it disturbs the equilibrium of the cell body. It must, therefore, be of advantage to the cells' well-being to return as soon as possible to the status quo ante, and this can only be done by increased activity.

In the present state of our knowledge, we can approach only the simplest cases of acquisition of characteristics. Mostly they are so complicated, subject to so many unthought-of conditions, that we do not know from which end to approach the problem. Frequently the supposed use of certain obvious features is the merest guesswork. This applies especially to features to which we are not accustomed (although wrongly so) to assign a function--for example, coloration. A green tree-frog will with predilection rest on green leaves. The advantages of concealment are obvious, and in this case he 'adapts himself' to the surroundings by making for green localities: if he did not he would be eaten up sooner than his more circumspect comrades. But this making for, and sitting in, the green has not necessarily made him of that colour. Extreme advocates of one view would argue as follows: Once upon a time there were among the offspring of ancestral tree-frogs some which, among other colours, exhibited green, not much, perhaps not even perceptible to our eyes. The occurrence of this colour, according to them, was spontaneous, a freak--as if in reality there were anything spontaneous in the sense of being causeless. The descendants of these more greenish creatures, provided they did not pair with frogs of the ordinary set, became still greener (by accumulative inheritance), and so on, until the green was pronounced sufficient to be of advantage when competition could set in.

With this view there is always the difficulty of understanding how the initial very small changes can be useful, unless we have to deal with extremely simple organisms. Is it likely in the case of our frogs that an almost imperceptible variation in colour makes them more fit to live? We have to assume that 'luck' or chance kept them for generations out of harm's reach, until the accumulation of green, hitherto quite ineffective, neither harmful nor useful, became strong enough to be effective. Such cases undoubtedly happen.

But we can also argue out this problem in a somewhat different way, which goes nearer to the root of the whole process. The original slight, imperceptible change in pigmentation is not a spontaneous freak; it was caused by the direct influence of the surroundings in which the particular frogs happened to live, be this factor light or temperature or food. Thus it stands to reason that the offspring, living under similar conditions, will be acted upon in the same way. That factor which has added green to the parents will add green to the children, until by accumulative inheritance a more decidedly green race is produced.

The offspring of green plants do not become green when grown in the dark; the young plants inherit not the green, but the capacity of becoming green when acted upon by sunlight. This as an instance of direct influence of the surroundings on a substance (chlorophyll), which has not yet performed a function. But the kittens of a pair of black cats produce black hair before they are born, and we have no reason to doubt that the black pigment in their tegumentary structures is ultimately referable to the action of the sunlight. In many instances creatures living for generations in darkness become white, pigmentless, and they regain it when exposed to light. For example, the white, colourless Proteus from the caves of Adelsberg becomes clouded grey, and ultimately jet black, when kept in a tank whence light is not strictly excluded.

Blindness is a very general characteristic of creatures which dwell in darkness. There are all stages between total blindness and weak eyes. Now, do these blind creatures live in darkness because they are blind, or have they become first weak-eyed and then blind because of the continuous disuse of their eyes? The former explanation has actually been suggested! Individuals not smitten, but spontaneously, as a freak, born with sore eyes, have crept into the darkness for relief and have produced a blind race! To carry such a notion to the bitter end leads to absurdities. Anyhow, it is not understandable where the benefit of losing the eyesight arises. It can be explained only by continued disuse: witness Spalax typhlus, the blind mole, and, above all, the Endoparasites.

Let us now take an example to explain the influence of a tangible external stimulus. Repeated pressure produces callosities. Although they are not exactly beneficial in the shape of corns on our toes, they are so on our hands. At any rate, the morphologist can trace the development of the footpads, nails, hoofs, and horns, step by step from small beginnings. The cells of the Malpighian stratum, of the inner, active portion of our epidermis, are excited to extra activity, and by continually producing more horn cells than peel off the surface of the skin in the normal process of wear and tear cause the formation of the pad. It need scarcely be mentioned that hypertrophic growths are not necessarily useful; they are often harmful, and in that case pathological.

Lastly, a few words about the very difficult question of teleology. In trying to explain Evolution in a mechanical--sometimes called monistic, but in reality natural--way, we exclude anything like a set purpose, a goal, or ideal, a final condition which the organism strives to attain. Unknown, however, to many morphologists, especially embryologists, their writings are full of this teleological notion. Indeed, there are many cases in which an organism becomes changed, and quickly, too, in a way which cannot but be called reasonable. It starts modifications, be they outgrowths, alterations in shape or colour, or the making good of injuries received, which by 'short-cuts' produce the only advantageous result that can reasonably satisfy the new requirement or altered circumstances.

Trees growing in precarious positions, after part of the supporting rock has slipped away, throw out new roots, and rearrange some of the old ones in the only way which could save the tree. In animals which have lost part of a limb the wound closes up, and what is left is turned into a serviceable stump--for example, in water-tortoises (creatures in which reproduction of lost limbs does not happen). In frogs and newts the lost part is reproduced, not correctly, but in a good semblance. Tortoises which have had their shell smashed can throw off an astonishingly large portion and renew the bone as well as the overlapping scutes; but this mending is not neatly done. It serves the requirement, but it is patchwork; the new shell is such as no tortoise ever possessed before.

Mammals transported into colder countries, or subjected to continued exposure, grow a thicker coat; and the same kind of tree which in a sheltered valley is tall, large-leaved, and soft-wooded, assumes a very different aspect, although perhaps growing into a healthy specimen, when planted on a wind-exposed hill.

There is no room, or, rather, no time, to apply to these cases the principle of many variations or the long-continued accumulation of infinitely small changes. The thing is to be done quickly, or not at all. Nor can we explain the mending of a wound, which implies an activity of countless cells, simply as a case of, or similar to, the reproduction of a lost part; against such an explanation militates the almost absolute unlikelihood of that precise injury having happened before to any of the creature's ancestors.

Still, I think we are brought near the solution of the mystery by such considerations. We see no difficulty in the regeneration of a few cells, or in the making good of the disturbance suffered by one of the most simple organisms; but we become suspicious when we see that countless cells, not of one kind, but of the most varied tissues and parts of the body, make common cause in remedying a defect in a serviceable way.

We must assume that since the beginning of life organisms have been subjected to countless insults. We can scarcely speak of a wound in an Amæba; but these insults have always been made good, and whenever this was not the case, that particular organism came to an end. As these organisms developed into more complicated ones, the possible insults became more serious, more complicated; and the organisms took adaptive measures so as to be superior to them. This action, I have no hesitation in declaring, became by heredity a habit. The whole creature became so thoroughly 'imbued' (for want of a better word) with the finding of ways and means for meeting sudden, serious conditions, that it now acts directly, and produces by a short-cut, with the least amount of time and with the smallest possible waste of material, that which meets the occasion, thereby saving the life of the individual and that of the race. This we cannot but call reasonable and to the purpose, although it is all carried out by causæ efficientes without there being any causæ finales.

GEOLOGICAL TIME AND EVOLUTION.

One million years is a stretch of time beyond our conception. We can arrive at a more or less adequate understanding of what a million individuals or concrete things means. Several Continental nations can put more than a million men into the field. We can gaze at a building which contains as many bricks; and we know that our own body is composed of millions of millions of cells. No such help applies to time, because that itself is an entirely relative, abstract conception. We can imagine what one hundred years are like--a span of time seemingly short to the hale and hearty octogenarian, enormous to the child, totally inapplicable to certain animals whose whole life is crowded into one single day.

Astronomers have long ceased to reckon distances by miles or any other understandable unit. They express the distances between us and the stars and nebulæ by 'years of light.' Try to imagine a unit of length equal to that which is passed through by light (186,000 miles per second) in one year. Not so very long ago the enormous distances resulting from astronomical calculations were looked upon as the most serious objection to the correctness of the astronomers' views as to the distances which separate our globe from the nearest fixed stars. We have not yet accustomed ourselves to reckoning time by some similar broadly-conceived standard--say æons of so many thousand years each.

Unfortunately, we possess no data whatever for calculating the age of the successive geological strata. Thanks to Lyell, the theory of violent universal cataclysms has been done away with. It is more probable that the same agencies have acted which are now changing the aspect of the globe; and these changes are slow, as far as we know them--at least, as far as the formation of sedimentary strata is concerned, and these alone we have to deal with. Various calculations have been made, based upon the denudation of the mountains, the filling up of the valleys by the débris, the formation of deltas, etc. The results give enormous stretches of time, but all of them unsatisfactory, because the methods are so very local in their application.

The least objectionable attempt is that which, based upon astronomical calculations, tried to fix the height of the last Glacial epoch at about 200,000 years ago, and asserted that since its beginning in the Pliocene epoch as many as 270,000 years have elapsed. The duration of the whole Tertiary period has by the same authorities been fixed approximately at 3,000,000 to 4,000,000 years. Beyond this we cannot venture without the wildest speculation; but we know to a certain extent the thickness of the various sedimentary strata, which amount in all to from 100,000 to 175,000 feet--on the average perhaps 130,000 feet, or about twenty miles.

James Croll: 'On Geological Time, and the Probable Date of the Glacial and Upper Miocene Period,' Philos. Magazine, xxxv., 1868, pp. 363-384; xxxvi., pp. 141-154; 362-386.

Unless we prefer giving up all attempt at calculation as absolutely hopeless, and thus resign the whole problem, we must at least try to arrive at some results, and then see if these cannot reasonably be made use of.

Neither geologist nor physicist, and no zoologist, would accept the suggestion that these 130,000 feet of stratified rocks have been deposited within only as many years, although the average rate of deposit would in that case be not more than 1 foot per year. On the other hand, an indignant protest is raised against the assumption of 1,000,000,000 years.

Lord Kelvin has come to the conclusion (from data which various other authorities regard as very unsatisfactory) that not much more than 100,000,000 years can have elapsed since the molten globe acquired a consolidated crust. Further time must have passed before the surface had become stable and cool enough to allow the temperature of the collecting oceans to fall below boiling-point, and it is obvious that life cannot possibly have begun until after this had happened.