"Looking," he says, "to the very equal mode in which the characters of the two parents are mingled inhybridoffspring, and to the certainty that thematerialconditions which determine the development of the germ are almost exclusively female, it would seem probable that thedynamicalconditions are, in great part, furnished by the male."[94]
"Looking," he says, "to the very equal mode in which the characters of the two parents are mingled inhybridoffspring, and to the certainty that thematerialconditions which determine the development of the germ are almost exclusively female, it would seem probable that thedynamicalconditions are, in great part, furnished by the male."[94]
§ 12. Could nothing but the foregoing indirect evidence be adduced in proof of the proposition that the spermatozoon is essentially a neural element, and the ovum essentially a hæmal element, we should scarcely claim for it anything more than plausibility. On finding, however, that this indirect evidence is merely introductory to evidence of a quite direct nature, its significance will become apparent. Adding to their weight taken separately the force of their mutual confirmation, these two series of proofs will be seen to give the hypothesis a high degree of probability. The direct evidence now to be considered is of several kinds.
On referring to the description of the process of multiplication in monads, quoted some pages back (§ 5), from Professor Owen, the reader will perceive that it is by the pellucid nucleus that the growth and reproduction of these single-celled creatures are regulated. The nucleus controls the circulation of the plasmatic fluid; the fission of the nucleus is the first step towards the formation of another cell; each half of the divided nucleus establishes round itself an independent current; and, apparently, it is by the repulsion of the nuclei that the separation into twoindividuals is finally effected. All which facts, when generalised, imply that the nucleus is the governing orco-ordinatingpart. Now, Professor Owen subsequently points out that the matter of the sperm-cell performs in the fertilised germ-cell just this same function which the nucleus performs in a single-celled animal. We find the absorption by a germ-cell of the contents of a sperm-cell "followed by the appearance of a pellucid nucleus in the centre of the opaque and altered germ-cell; we further see its successive fissions governed by the preliminary division of the pellucid centre;" and, led by these and other facts, Professor Owen thinks that "one cannot reasonably suppose that the nature and properties of the nucleus of the impregnated germ-cell and that of the monad can be different."[95]And hence he further infers that "the nucleus of the monad is of a nature similar to, if not identical with," the matter of the spermatozoon. But we have seen that in the monad the nucleus is the co-ordinating part; and hence to say that the sperm-cell is, in nature, identical with it, is to say that the sperm-cell consists of co-ordinating matter.
Chemical analysis affords further evidence, though, from the imperfect data at present obtained, less conclusive evidence than could be wished. Partly from the white and gray nervous substances having been analysed together instead of separately, and partly from the difficulty of isolating the efficient contents of the sperm-cells, a satisfactory comparison cannot be made. Nevertheless, possessing in common, as they do, one element, by which they are specially characterised, the analysis, as far as it goes, supports our argument. The following table, which has been made up from data given in theCyclopædia of Anatomy and Physiology, Art.Nervous System, gives the proportion of this element in the brain in different conditions, and shows how important is its presence.
This connection between the quantity of phosphorus present and the degree of mental power exhibited, is sufficientlysignificant; and the fact that in the same individual the varying degrees of cerebral activity are indicated by the varying quantities of alkaline phosphates excreted by the kidneys,[96]still more clearly shows the essentialness of phosphorus as a constituent of nervous matter. Respecting the constitution of sperm-cells chemists do not altogether agree. One thing, however, is certain—that they contain unoxidized phosphorus; and also a fatty acid, that is not improbably similar to the fatty acid contained in neurine.[97]In fact, there would seem to be present the constituents of that oleophosphoric acid which forms so distinctive an element of the brain. That a large quantity of binoxide of protein is also present, may be ascribed to the fact that a great part of the sperm-cell consists merely of the protective membrane and its locomotive appendage; the really efficient portion being but the central contents.[98]
Evidence of a more conclusive nature—evidence, too, which will show in what direction our argument tends—is seen in the marked antagonism of the nervous and generative systems. Thus, the fact that intense mental application, involving great waste of the nervous tissues, and a corresponding consumption of nervous matter for their repair, is accompanied by a cessation in the production of sperm-cells, gives strong support to the hypothesis that the sperm-cells consist essentially of neurine. And this becomes yet clearer on finding that the converse fact is true—that undue production of sperm-cells involves cerebral inactivity. The first result of a morbid excess in this direction is headache, which may be taken to indicate that the brain is out of repair; this is followed by stupidity; should the disorder continue, imbecility supervenes, ending occasionally in insanity.
That the sperm-cell is co-ordinating matter, and the germ-cell matter to be co-ordinated, is, therefore, an hypothesis not only having muchà prioriprobability, but one supported by numerous facts.
§ 13. This hypothesis alike explains, and is confirmed by, the truth, that throughout the vertebrate tribes the degree of fertility varies inversely as the development of the nervous system.
The necessary antagonism of Individuation and Reproduction does indeed show itself amongst the higher animals, in some degree in the manner hitherto traced; namely, as determining the total bulk. Though the parts now thrown off, being no longer segments or gemmæ, are not obvious diminutions of the parent, yet they must be really such. Under the form of internal fission, the separative tendency is as much opposed to the aggregative tendency as ever; and,other things equal, the greater or less development of the individual depends upon the less or greater production of new individuals or germs of new individuals. As in groups of cells, and series of groups of cells, we saw that there was in each species a limit, passing which, the germ product would not remain united; so in each species of higher animal there is a limit, passing which, the process of cell-multiplication results in the throwing off of cells, instead of resulting in the formation of more tissue. Hence, taking an average view, we see why the smaller animals so soon arrive at a reproductive age, and produce large and frequent broods; and why, conversely, increased size is accompanied by retarded and diminished fertility.
But, as above implied, it is not so much to the bulk of the body as a whole, as to the bulk of the nervous system, that fertility stands related amongst the higher animals. Probably, indeed, it stands thus related in all cases; the difference simply arising from the fact, that whereas in the lower organisms, where the nervous system is not concentrated, its bulk varies as the bulk of the body, in the higher organisms it does not do so. Be this as it may, however, we see clearly that, amongst the vertebrata, the bodily development is not the determining circumstance. In a fish, a reptile, a bird, and a mammal of the same weight, there is nothing like equality of fecundity. Cattle and horses, arriving as they do so soon at a reproductive age, are much more prolific than the human race, at the same time that they are much larger. And whilst, again, the difference in size between the elephant and man is far greater, their respective powers of multiplication are less unlike. Looking in these cases at the nervous systems, however, we find no such discrepancy. On learning that the average ratio of the brain to the body is—in fishes, 1 to 5668; in reptiles, 1 to 1321; in birds, 1 to 212; and in mammals, 1 to 186;[99]their different degrees of fecundity are accounted for. Though an ox will outweigh half-a-dozen men, yet its brain and spinal cord are far less than those of one man; and though in bodily development the elephant so immensely exceeds the human being, yet the elephant's cerebro-spinal system is only thrice the size attained by that of civilizedmen.[100]Unfortunately, it is impossible to trace throughout the animal kingdom this inverse relationship between the nervous and reproductive systems with any accuracy. Partly from the fact that, in each case, the degree of fertility depends on three variable elements—the age at which reproduction begins, the number produced at a birth, and the frequency of the births; partly from the fact that, in respect to most animals, these data are not satisfactorily attainable, and that, when they are attainable, they are vitiated by the influence of domesticity; and partly from the fact that no precise measurement of the respective nervous systems has been made, we are unable to draw any but general and somewhat vague comparisons. These, however, as far as they go, are in our favour. Ascending from beings of the acrite nerveless type, which are the most prolific of all, through the various invertebrate sub-kingdoms, amongst which spontaneous fission disappears as the nervous system becomes developed; passing again to the least nervous and most fertile of the vertebrate series—Fishes, of which, too, the comparatively large-brained cartilaginous kinds multiply much less rapidly than the others; progressing through the more highly endowed and less prolific Reptiles to the Mammalia, amongst which the Rodents, with their unconvoluted brains, are noted for their fecundity; and ending with man and the elephant, the least fertile and largest-brained of all—there seems to be throughout a constant relationship between these attributes.
And indeed, on turning back to ourà prioriprinciple, no other relationship appears possible. We found it to be the necessary law of maintenance of races, that the ability to maintain individual life and the ability to multiply vary inversely. But the ability to maintain individual lifeis in all cases measured by the development of the nervous system. If it be in good visceral organization that the power of self-preservation is shown, this implies some corresponding nervous apparatus to secure sufficient food. If it be in strength, there must be a provision of nerves and nervous centres answering to the number and size of the muscles. If it be in swiftness and agility, a proportionate development of the cerebellum is presupposed. If it be in intelligence, this varieswith the size of the cerebrum. As in all cases co-ordination of actions constitutes the life, or, what is the same thing, the ability to maintain life; and as throughout the animal kingdom this co-ordination, under all its forms, is effected by nervous agents of some kind or other; and as each of these nervous agents performs but one function; it follows that in proportion to the number of the actions co-ordinated must be the number of nervous agents. Hence the nervous system becomes the universal measure of the degree of co-ordination of actions; that is, of the life, or ability to maintain life. And if the nervous system varies directly as the ability to maintain life, itmustvary inversely as the ability to multiply.[101]
And here, assuming the constitution of the sperm-cell above inferred to be the true one, we see how the obverseà prioriprinciple is fulfilled. Where, as amongst the lowest organisms, bulk is expressive of life, the antagonism of individuation and reproduction was broadly exhibited in the fact that the making of two or more new individuals was theunmaking of the original individual. And now, amongst the higher organisms, where bulk is no longer the measure of life, we see that this antagonism is between the neural elements thrown off, and that internal neural mass whose bulkisthe measure of life. The production of co-ordinating cells must be at the expense of the co-ordinating apparatus; and the aggregation of the co-ordinating apparatus must be at the expense of co-ordinating cells. How the antagonism affects the female economy is not so clear. Possibly the provision required to be made for supplying nervous as well as other nutriment to the embryo, involves an arrest in the development of the nervous system; and if so, probably this arrest takes place early in proportion as the number of the coming offspring makes the required provision great: or rather, to put the facts in their right sequence, an early arrest renders the production of a numerous offspring possible.
§ 14. The law which we have thus traced throughout theanimal kingdom, and which must alike determine the different fertilities of different species, and the variations of fertility in the same species, we have now to consider in its application to mankind.
[The remainder of the essay, which as implied, deals with the application of this general principle to the multiplication of the human race, need not be here reproduced. The subject is treated in full in Part VI.]
[The remainder of the essay, which as implied, deals with the application of this general principle to the multiplication of the human race, need not be here reproduced. The subject is treated in full in Part VI.]
THE INADEQUACY OF NATURAL SELECTION, ETC., ETC.
[In this Appendix are included four essays originally published in theContemporary Reviewand subsequently republished as pamphlets. The first appeared under the above title in February and March, 1893; the second in May of that year under the title "Prof. Weismann's Theories;" the third in December of that year under the title "A Rejoinder to Prof. Weismann;" and the fourth in October, 1894, under the title "Weismannism Once More." As these successive essays practically form parts of one whole, I have thought it needless to keep them separate by repeating their titles, and have simply marked them off from one another by the numbers I, II, III, IV. Of course, as they are components of a controversy, some incompleteness arises from the absence of the essays to which portions of them were replies; but in each the course of the argument sufficiently indicates the counter-arguments which were met.]
I.
Students of psychology are familiar with the experiments of Weber on the sense of touch. He found that different parts of the surface differ widely in their ability to give information concerning the things touched. Some parts, which yielded vivid sensations, yielded little or no knowledge of the sizes or forms of the things exciting them; whereas other parts, from which there came sensations much less acute, furnished clear impressions respecting the tangible characters, even of relatively small objects. These unlikenesses of tactual discriminativeness he ingeniously expressed by actual measurements. Taking a pair of compasses, he found that if they were closed so nearly that the points were less than one-twelfth of an inch apart, the end of the forefinger could not perceive that there were two points: the two points seemed one. But when the compasses were opened so that the points were one-twelfth of an inch apart, then the end of the forefinger distinguished the two points. At the same time, he found that the compasses must be opened to the extent of two and a half inches, before the middle of the back could distinguish between two points and one. That is to say, as thusmeasured, the end of the forefinger has thirty times the tactual discriminativeness which the middle of the back has.
Between these extremes he found gradations. The inner surfaces of the second joints of the fingers can distinguish separateness of positions only half as well as the tip of the forefinger. The innermost joints are still less discriminating, but have powers of discrimination equal to that of the tip of the nose. The end of the great toe, the palm of the hand, and the cheek, have alike one-fifth of the perceptiveness which the tip of the forefinger has; and the lower part of the forehead has but one-half that possessed by the cheek. The back of the hand and the crown of the head are nearly alike in having but a fourteenth or a fifteenth of the ability to perceive positions as distinct, which is possessed by the finger-end. The thigh, near the knee, has rather less, and the breast less still; so that the compasses must be opened more than an inch and a half before the breast distinguishes the two points from one another.
What is the meaning of these differences? How, in the course of evolution, have they been established? If "natural selection," or survival of the fittest, is the assigned cause, then it is required to show in what way each of these degrees of endowment has advantaged the possessor to such extent that not infrequently life has been directly or indirectly preserved by it. We might reasonably assume that in the absence of some differentiating process, all parts of the surface would have like powers of perceiving relative positions. They cannot have become widely unlike in perceptiveness without some cause. And if the cause alleged is natural selection, then it is necessary to show that the greater degree of the power possessed by this part than by that, has not only conduced to the maintenance of life, but has conduced so much that an individual in whom a variation has produced better adjustment to needs, thereby maintained life when some others lost it; and that among the descendants inheriting this variation, there was a derived advantage such as enabled them to multiply more than the descendants of individuals not possessing it. Can this, or anything like this, be shown?
That the superior perceptiveness of the forefinger-tip has thus arisen, might be contended with some apparent reason. Such perceptiveness is an important aid to manipulation, and may have sometimes given a life-saving advantage. In making arrows or fish-hooks, a savage possessing some extra amount of it may have been thereby enabled to get food where another failed. In civilized life, too, a sempstress with well-endowed finger-ends might be expected to gain a better livelihood than one with finger-ends which were obtuse; though this advantage would not be so great as appears. I have found that two ladies whosefinger-ends were covered with glove-tips, reducing their sensitiveness from one-twelfth of an inch between compass-points to one-seventh, lost nothing appreciable of their quickness and goodness in sewing. An experience of my own here comes in evidence. Towards the close of my salmon-fishing days I used to observe what a bungler I had become in putting on and taking off artificial flies. As the tactual discriminativeness of my finger-ends, recently tested, comes up to the standard specified by Weber, it is clear that this decrease of manipulative power, accompanying increase of age, was due to decrease in the delicacy of muscular co-ordination and sense of pressure—not to decrease of tactual discriminativeness. But not making much of these criticisms, let us admit the conclusion that this high perceptive power possessed by the forefinger-end may have arisen by survival of the fittest; and let us limit the argument to the other differences.
How about the back of the trunk and its face? Is any advantage derived from possession of greater tactual discriminativeness by the last than the first? The tip of the nose has more than three times the power of distinguishing relative positions which the lower part of the forehead has. Can this greater power be shown to have any advantage? The back of the hand has scarcely more discriminative ability than the crown of the head, and has only one-fourteenth of that which the finger-tip has. Why is this? Advantage might occasionally be derived if the back of the hand could tell us more than it does about the shapes of the surfaces touched. Why should the thigh near the knee be twice as perceptive as the middle of the thigh? And, last of all, why should the middle of the forearm, middle of the thigh, middle of the back of the neck, and middle of the back, all stand on the lowest level, as having but one-thirtieth of the perceptive power which the tip of the forefinger has? To prove that these differences have arisen by natural selection, it has to be shown that such small variation in one of the parts as might occur in a generation—say one-tenth extra amount—has yielded an appreciably greater power of self-preservation; and that those inheriting it have continued to be so far advantaged as to multiply more than those who, in other respects equal, were less endowed with this trait. Does any one think he can show this?
But if this distribution of tactual perceptiveness cannot be explained by survival of the fittest, how can it be explained? The reply is that, if there has been in operation a cause which it is now the fashion among biologists to ignore or deny, these various differences are at once accounted for. This cause is the inheritance of acquired characters. As a preliminary to setting forth the argument showing this, I have made some experiments.
It is a current belief that the fingers of the blind, morepractised in tactual exploration than the fingers of those who can see, acquire greater discriminativeness: especially the fingers of those blind who have been taught to read from raised letters. Not wishing to trust to this current belief, I recently tested two youths, one of fifteen and the other younger, at the School for the Blind in Upper Avenue Road, and found the belief to be correct. I found that instead of being unable to distinguish between points of the compasses until they were opened to one-twelfth of an inch apart, both of them could distinguish between points when only one-fourteenth of an inch apart. They had thick and coarse skins; and doubtless, had the intervening obstacle, so produced, been less, the discriminative power would have been greater. It afterwards occurred to me that a better test would be furnished by those whose finger-ends are exercised in tactual perceptions, not occasionally, as by the blind in reading, but all day long in pursuit of their occupations. The facts answered expectation. Two skilled compositors, on whom I experimented, were both able to distinguish between points when they were only one-seventeenth of an inch apart. Thus we have clear proof that constant exercise of the tactual nervous structure leads to further development.[102]
Now if acquired structural traits are inheritable, the various contrasts above set down are obvious consequences; for the gradations in tactual perceptiveness correspond with the gradations in the tactual exercises of the parts. Save by contact with clothes, which present only broad surfaces having but slight and indefinite contrast, the trunk has scarcely any converse withexternal bodies, and it has but small discriminative power; but what discriminative power it has is greater on its face than on its back, corresponding to the fact that the chest and abdomen are much more frequently explored by the hands: this difference being probably in part inherited from inferior creatures; for, as we may see in dogs and cats, the belly is far more accessible to feet and tongue than the back. No less obtuse than the back are the middle of the back of the neck, the middle of the forearm, and the middle of the thigh; and these parts have but rare experiences of irregular foreign bodies. The crown of the head is occasionally felt by the fingers, as also the back of one hand by the fingers of the other; but neither of these surfaces, which are only twice as perceptive as the back, is used with any frequency for touching objects, much less for examining them. The lower part of the forehead, though more perceptive than the crown of the head, in correspondence with a somewhat greater converse with the hands, is less than one-third as perceptive as the tip of the nose; and manifestly, both in virtue of its relative prominence, in virtue of its contacts with things smelt at, and in virtue of its frequent acquaintance with the handkerchief, the tip of the nose has far greater tactual experience. Passing to the inner surfaces of the hands, which, taken as wholes, are more constantly occupied in touching than are the back, breast, thigh, forearm, forehead, or back of the hand, Weber's scale shows that they are much more perceptive, and that the degrees of perceptiveness of different parts correspond with their tactual activities. The palms have but one-fifth the perceptiveness possessed by the forefinger-ends; the inner surfaces of the finger-joints next the palms have but one-third; while the inner surfaces of the second joints have but one-half. These abilities correspond with the facts that whereas the inner parts of the hand are used only in grasping things, the tips of the fingers come into play not only when things are grasped, but when such things, as well as smaller things, are felt at or manipulated. It needs but to observe the relative actions of these parts in writing, in sewing, in judging textures, &c., to see that above all other parts the finger-ends, and especially the forefinger-ends, have the most multiplied experiences. If, then, it be that the extra perceptiveness acquired from actual tactual activities, as in a compositor, is inheritable, these gradations of tactual perceptiveness are explained.
Doubtless some of those who remember Weber's results, have had on the tip of the tongue the argument derived from the tip of the tongue. This part exceeds all other parts in power of tactual discrimination: doubling, in that respect, the power of the forefinger-tip. It can distinguish points that are only one-twenty-fourth of an inch apart. Why this unparalleledperceptiveness? If survival of the fittest be the ascribed cause, then it has to be shown what the advantages achieved have been; and, further, that those advantages have been sufficiently great to have had effects on the maintenance of life.
Besides tasting, there are two functions conducive to life, which the tongue performs. It enables us to move about food during mastication, and it enables us to make many of the articulations constituting speech. But how does the extreme discriminativeness of the tongue-tip aid these functions? The food is moved about, not by the tongue-tip, but by the body of the tongue; and even were the tip largely employed in this process, it would still have to be shown that its ability to distinguish between points one-twenty-fourth of an inch apart, is of service to that end, which cannot be shown. It may, indeed, be said that the tactual perceptiveness of the tongue-tip serves for detection of foreign bodies in the food, as plum-stones or as fish-bones. But such extreme perceptiveness is needless for the purpose. A perceptiveness equal to that of the finger-ends would suffice. And further, even were such extreme perceptiveness useful, it could not have caused survival of individuals who possessed it in slightly higher degrees than others. It needs but to observe a dog crunching small bones, and swallowing with impunity the sharp-angled pieces, to see that but a very small amount of mortality would be prevented.
But what about speech? Well, neither here can there be shown any advantage derived from this extreme perceptiveness. For making thesandz, the tongue has to be partially applied to a portion of the palate next the teeth. Not only, however, must the contact be incomplete, but its place is indefinite—may be half an inch further back. To make theshandzh, the contact has to be made, not with the tip, but with the upper surface of the tongue; and must be an incomplete contact. Though, for making the liquids, the tip of the tongue and the sides of the tongue are used, yet the requisite is not any exact adjustment of the tip, but an imperfect contact with the palate. For theth, the tip is used along with the edges of the tongue; but no perfect adjustment is required, either to the edges of the teeth, or to the junction of the teeth with the palate, where the sound may equally well be made. Though for thetanddcomplete contact of the tip and edges of the tongue with the palate is required, yet the place of contact is not definite, and the tip takes no more important share in the action than the sides. Any one who observes the movements of his tongue in speaking, will find that there occur no cases in which the adjustments must have an exactness corresponding to the extreme power of discrimination which the tip possesses: for speech, this endowment is useless. Even wereit useful, it could not be shown that it has been developed by survival of the fittest; for though perfect articulation is an aid, yet imperfect articulation has rarely such an effect as to impede a man in the maintenance of his life. If he is a good workman, a German's interchanges ofb'sandp'sdo not disadvantage him. A Frenchman who, in place of the sound ofth, always makes the sound ofz, succeeds as a teacher of music or dancing, no less than if he achieved the English pronunciation. Nay, even such an imperfection of speech as that which arises from cleft palate, does not prevent a man from getting on if he is capable. True, it may go against him as a candidate for Parliament, or as an "orator" of the unemployed (mostly not worth employing). But in the struggle for life he is not hindered by the effect to the extent of being less able than others to maintain himself and his offspring. Clearly, then, even if this unparalleled perceptiveness of the tongue-tip is required for perfect speech, such use is not sufficiently important to have been developed by natural selection.
How, then, is this remarkable trait of the tongue-tip to be accounted for? Without difficulty, if there is inheritance of acquired characters. For the tongue-tip has, above all other parts of the body, unceasing experiences of small irregularities of surface. It is in contact with the teeth, and either consciously or unconsciously is continually exploring them. There is hardly a moment in which impressions of adjacent but different positions are not being yielded to it by either the surfaces of the teeth or their edges; and it is continually being moved about from some of them to others. No advantage is gained. It is simply that the tongue's position renders perpetual exploration almost inevitable; and by perpetual exploration is developed this unique power of discrimination. Thus the law holds throughout, from this highest degree of perceptiveness of the tongue-tip to its lowest degree on the back of the trunk; and no other explanation of the facts seems possible.
"Yes, there is another explanation," I hear some one say: "they may be explained bypanmixia." Well, in the first place, as the explanation bypanmixiaimplies that these gradations of perceptiveness have been arrived at by the dwindling of nervous structures, there lies at the basis of the explanation an unproved and improbable assumption; and, in the second place, even were there no such difficulty, it may with certainty be denied thatpanmixiacan furnish an explanation. Let us look at its pretensions.
*****
It was not without good reason that Bentham protested against metaphors. Figures of speech in general, valuable as theyare in poetry and rhetoric, cannot be used without danger in science and philosophy. The title of Mr. Darwin's great work furnishes us with an instance of the misleading effects produced by them. It runs:—The Origin of Species by means of Natural Selection, or the Preservation of favoured Races in the Struggle for Life. Here are two figures of speech which conspire to produce an impression more or less erroneous. The expression "natural selection" was chosen as serving to indicate some parallelism with artificial selection—the selection exercised by breeders. Now selection connotes volition, and thus gives to the thoughts of readers a wrong bias. Some increase of this bias is produced by the words in the second title, "favoured races;" for anything which is favoured implies the existence of some agent conferring a favour. I do not mean that Mr. Darwin himself failed to recognize the misleading connotations of his words, or that he did not avoid being misled by them. In chapter iv of theOrigin of Species, he says that, considered literally, "natural selection is a false term," and that the personification of Nature is objectionable; but he thinks that readers, and those who adopt his views, will soon learn to guard themselves against the wrong implications. Here I venture to think that he was mistaken. For thinking this, there is the reason that even his disciple, Mr. Wallace—no, not his disciple, but his co-discoverer, ever to be honoured—has apparently been influenced by them. When, for example, in combating a view of mine, he says that "the very thing said to be impossible by variation and natural selection has been again and again effected, by variation and artificial selection," he seems clearly to imply that the processes are analogous, and operate in the same way. Now this is untrue. They are analogous only within certain narrow limits; and, in the great majority of cases, natural selection is utterly incapable of doing that which artificial selection does.
To see this it needs only to de-personalise Nature, and to remember that, as Mr. Darwin says, Nature is "only the aggregate action and product of many natural laws [forces]." Observe its relative shortcomings. Artificial selection can pick out a particular trait, and, regardless of other traits of the individuals displaying it, can increase it by selective breeding in successive generations. For, to the breeder or fancier, it matters little whether such individuals are otherwise well constituted. They may be in this or that way so unfit for carrying on the struggle for life, that were they without human care, they would disappear forthwith. On the other hand, if we regard Nature as that which it is, an assemblage of various forces, inorganic and organic, some favourable to the maintenance of life and many at variance with its maintenance—forces which operate blindly—we see thatthere is no such selection of this or that trait; but that there is a selection only of individuals which are, by the aggregate of their traits, best fitted for living. And here I may note an advantage possessed by the expression "survival of the fittest;" since this does not tend to raise the thought of any one character which, more than others, is to be maintained or increased; but tends rather to raise the thought of a general adaptation for all purposes. It implies the process which Nature can alone carry on—the leaving alive of those which are best able to utilize surrounding aids to life, and best able to combat or avoid surrounding dangers. And while this phrase covers the great mass of cases in which there are preserved well-constituted individuals, it also covers those special cases which are suggested by the phrase "natural selection," in which individuals succeed beyond others in the struggle for life, by the help of particular characters which conduce in important ways to prosperity and multiplication. For now observe the fact which here chiefly concerns us, that survival of the fittest can increase any serviceable trait, only if that trait conduces to prosperity of the individual, or of posterity, or of both,in an important degree. There can be no increase of any structure by natural selection unless, amid all the slightly varying structures constituting the organism, increase of this particular one is so advantageous as to cause greater multiplication of the family in which it arises than of other families. Variations which, though advantageous, fail to do this, must disappear again. Let us take a case.
Keenness of scent in a deer, by giving early notice of approaching enemies, subserves life so greatly that, other things equal, an individual having it in an unusual degree is more likely than others to survive; and, among descendants, to leave some similarly endowed or more endowed, who again transmit the variation with, in some cases, increase. Clearly this highly useful power may be developed by natural selection. So also, for like reasons, may quickness of vision and delicacy of hearing; though it may be remarked in passing that since this extra sense-endowment, serving to give early alarm, profits the herd as a whole, which takes the alarm from one individual, selection of it is not so easy, unless it occurs in a conquering stag. But now suppose that one member of the herd—perhaps because of more efficient teeth, perhaps by greater muscularity of stomach, perhaps by secretion of more appropriate gastric juices—is enabled to eat and digest a not uncommon plant which the others refuse. This peculiarity may, if food is scarce, conduce to better self-maintenance, and better fostering of young if the individual is a hind. But unless this plant is abundant, and the advantage consequently great, the advantages which other members of the herd gain from otherslight variations may be equivalent. This one has unusual agility, and leaps a chasm which others balk at. That one develops longer hair in winter, and resists the cold better. Another has a skin less irritated by flies, and can graze without so much interruption. Here is one which has an unusual power of detecting food under the snow; and there is one which shows extra sagacity in the choice of a shelter from wind and rain. That the variation giving ability to eat a plant before unutilized, may become a trait of the herd, and eventually of a variety, it is needful that the individual in which it occurs shall have more descendants, or better descendants, or both, than have the various other individuals severally having their small superiorities. If these other individuals severally profit by their small superiorities, and transmit them to equally large numbers of offspring, no increase of the variation in question can take place: it must soon be cancelled. Whether in theOrigin of SpeciesMr. Darwin has recognized this fact, I do not remember, but he has certainly done it by implication in hisAnimals and Plants under Domestication. Speaking of variations in domestic animals, he there says that "any particular variation would generally be lost by crossing, reversion, and the accidental destruction of the varying individuals, unless carefully preserved by man." (Vol. II, p. 292.) That which survival of the fittest does in cases like the one I have instanced, is to keep all faculties up to the mark, by destroying such individuals as have faculties in some respect below the mark; and it can produce development of some one faculty only if that faculty is predominantly important. It seems to me that many naturalists have practically lost sight of this, and assume that natural selection will increaseanyadvantageous trait. Certainly a view now held by some assumes as much.
The consideration of this view, to which the foregoing paragraph is introductory, may now be entered upon. This view concerns, not direct selection, but what has been called, in questionable logic, "reversed selection"—the selection which effects, not increase of an organ, but decrease of it. For as, under some conditions, it is of advantage to an individual and its descendants to have some structure of larger size, it may be, under other conditions—namely, when the organ becomes useless—of advantage to have it of smaller size; since, even if it is not in the way, its weight and the cost of its nutrition are injurious taxes on the organism. But now comes the truth to be emphasized. Just as direct selection can increase an organ only in certain cases, so can reversed selection decrease it only in certain cases. Like the increase produced by a variation, the decrease produced by one must be such as will sensibly conduce to preservation and multiplication. It is, for instance, conceivable that were the long andmassive tail of the kangaroo to become useless (say by the forcing of the species into a mountainous and rocky habitat filled with brushwood), a variation which considerably reduced the tail might sensibly profit the individual in which it occurred; and, in seasons when food was scarce, might cause survival when individuals with large tails died. But the economy of nutrition must be considerable before any such result could occur. Suppose that in this new habitat the kangaroo had no enemies; and suppose that, consequently, quickness of hearing not being called for, large ears gave no greater advantage than small ones. Would an individual with smaller ears than usual, survive and propagate better than other individuals, in consequence of the economy of nutrition achieved? To suppose this is to suppose that the saving of a grain or two of protein per day would determine the kangaroo's fate.
Long ago I discussed this matter in thePrinciples of Biology(§ 166), taking as an instance the decrease of the jaw implied by the crowding of the teeth, and now proved by measurement to have taken place. Here is the passage:—
"No functional superiority possessed by a small jaw over a large jaw, in civilized life, can be named as having caused the more frequent survival of small-jawed individuals. The only advantage which smallness of jaw might be supposed to give, is the advantage of economized nutrition; and this could not be great enough to further the preservation of men possessing it. The decrease of weight in the jaw and co-operative parts that has arisen in the course of many thousands of years, does not amount to more than a few ounces. This decrease has to be divided among the many generations that have lived and died in the interval. Let us admit that the weight of these parts diminished to the extent of an ounce in a single generation (which is a large admission); it still cannot be contended that the having to carry an ounce less in weight, or having to keep in repair an ounce less of tissue, could sensibly affect any man's fate. And if it never did this—nay, if it did not cause afrequentsurvival of small-jawed individuals where large-jawed individuals died, natural selection could neither cause nor aid diminution of the jaw and its appendages."
"No functional superiority possessed by a small jaw over a large jaw, in civilized life, can be named as having caused the more frequent survival of small-jawed individuals. The only advantage which smallness of jaw might be supposed to give, is the advantage of economized nutrition; and this could not be great enough to further the preservation of men possessing it. The decrease of weight in the jaw and co-operative parts that has arisen in the course of many thousands of years, does not amount to more than a few ounces. This decrease has to be divided among the many generations that have lived and died in the interval. Let us admit that the weight of these parts diminished to the extent of an ounce in a single generation (which is a large admission); it still cannot be contended that the having to carry an ounce less in weight, or having to keep in repair an ounce less of tissue, could sensibly affect any man's fate. And if it never did this—nay, if it did not cause afrequentsurvival of small-jawed individuals where large-jawed individuals died, natural selection could neither cause nor aid diminution of the jaw and its appendages."
When writing this passage in 1864, I never dreamt that a quarter of a century later, the supposable cause of degeneration here examined and excluded as impossible, would be enunciated as an actual cause and named "reversed selection."
One of the arguments used to show the adequacy of natural selection under its direct or indirect form consists of a counter-argument to the effect that inheritance of functionally-wrought changes, supposing it to be operative, does not explain certain of the facts. This is alleged by Prof. Weismann as a part justification for his doctrine of Panmixia. Concerning the "blind fish and amphibia" found in dark places, which have but rudimentary eyes "hidden under the skin," he argues that "it is difficult to reconcile the facts of the case with the ordinary theory that the eyes of theseanimals have simply degenerated through disuse." After giving instances of rapid degeneration of disused organs, he argues that if "the effects of disuse are so striking in a single life, we should certainly expect, if such effects can be transmitted, that all traces of an eye would soon disappear from a species which lives in the dark." Doubtless this is a reasonable conclusion. To explain the facts on the hypothesis that acquired characters are inheritable, seems very difficult. One possible explanation may, indeed, be named. It appears to be a general law of organization that structures are stable in proportion to their antiquity—that while organs of relatively modern origin have but a comparatively superficial root in the constitution, and readily disappear if the conditions do not favour their maintenance, organs of ancient origin have deep-seated roots in the constitution, and do not readily disappear. Having been early elements in the type, and having continued to be reproduced as parts of it during a period extending throughout many geological epochs, they are comparatively persistent. Now the eye answers to this description as being a very early organ. But waiving possible explanations, let us take the particular instance cited by Prof. Weismann and see what is to be made of it. He writes:—