This is natural enough, for Mr. Wallace has entitled his book Darwinism, and a work denying that use and disuse produced any effect could not conceivably be called Darwinism. Mr. Herbert Spencer has recently collected many passages from The Origin of Species and from Animals and Plants under Domestication,” [{263}] which show how largely, after all, use and disuse entered into Mr. Darwin’s system, and we know that in his later years he attached still more importance to them. It was out of the question, therefore, that Mr. Wallace should categorically deny that their effects were inheritable. On the other hand, the temptation to adopt Professor Weismann’s view must have been overwhelming to one who had been already inclined to minimize the effects of use and disuse. On the whole, one does not see what Mr. Wallace could do, other than what he has done—unless, of course, he changed his title, or had been no longer Mr. Wallace.

Besides, thanks to the works of Mr. Spencer, Professor Mivart, Professor Semper, and very many others, there has for some time been a growing perception that the Darwinism of Charles Darwin was doomed. Use and disuse must either do even more than is officially recognized in Mr. Darwin’s later concessions, or they must do a great deal less. If they can do as much as Mr. Darwin himself said they did, why should they not do more? Why stop where Mr. Darwin did? And again, where in the name of all that is reasonable did he really stop? He drew no line, and on what principle can we say that so much is possible as effect of use and disuse, but so much more impossible? If, as Mr. Darwin contended, disuse can so far reduce an organ as to render it rudimentary, and in many cases get rid of it altogether, why cannot use create as much as disuse can destroy, provided it has anything, no matter how low in structure, to begin with? Let us know where we stand. If it is admitted that use and disuse can do a good deal, what does a good deal mean? And what is the proportion between the shares attributable to use and disuse and to natural selection respectively? If we cannot be told with absolute precision, let us at any rate have something more definite than the statement that natural selection is “the most important means of modification.”

Mr. Darwin gave us no help in this respect; and worse than this, he contradicted himself so flatly as to show that he had very little definite idea upon the subject at all. Thus in respect to the winglessness of the Madeira beetles he wrote:—

“In some cases we might easily put down to disuse modifications of structure, which are wholly or mainly due to natural selection. Mr. Wollaston has discovered the remarkable fact that 200 beetles, out of the 550 species (but more are now known) inhabiting Madeira, are so far deficient in wings that they cannot fly; and that of the 29 endemic genera no less than 23 have all their species in this condition! Several facts—namely, that beetles in many parts of the world are frequently blown out to sea and perish; that the beetles in Madeira, as observed by Mr. Wollaston, lie much concealed until the wind lulls and the sun shines; that the proportion of wingless beetles is larger on the exposed Desertas than in Madeira itself; and especially the extraordinary fact, so strongly insisted on by Mr. Wollaston, that certain large groups of beetles, elsewhere excessively numerous, which absolutely require the use of their wings are here almost entirely absent;—these several considerations make me believe that the wingless condition of so many Madeira beetles is mainly due to the action of natural selection, combined probably with disuse [italics mine]. For during many successive generations each individual beetle which flew least, either from its wings having been ever so little less perfectly developed or from indolent habit, will have had the best chance of surviving, from not being blown out to sea; and, on the other hand, those beetles which most readily took to flight would oftenest have been blown to sea, and thus destroyed.” [{265}]

We should like to know, first, somewhere about how much disuse was able to do after all, and moreover why, if it can do anything at all, it should not be able to do all. Mr. Darwin says: “Any change in structure and function which can be effected by small stages is within the power of natural selection.” “And why not,” we ask, “within the power of use and disuse?” Moreover, on a later page we find Mr. Darwin saying:—

It appears probable that disuse has been the main agent in rendering organs rudimentary [italics mine]. It would at first lead by slow steps to the more and more complete reduction of a part, until at last it has become rudimentary—as in the case of the eyes of animals inhabiting dark caverns, and of the wings of birds inhabiting oceanic islands, which have seldom been forced by beasts of prey to take flight, and have ultimately lost the power of flying. Again, an organ, useful under certain conditions, might become injurious under others, as with the wings of beetles living on small and exposed islands; and in this case natural selection will have aided in reducing the organ, until it was rendered harmless and rudimentary [italics mine].” [{266}]

So that just as an undefined amount of use and disuse was introduced on the earlier page to supplement the effects of natural selection in respect of the wings of beetles on small and exposed islands, we have here an undefined amount of natural selection introduced to supplement the effects of use and disuse in respect of the identical phenomena. In the one passage we find that natural selection has been the main agent in reducing the wings, though use and disuse have had an appreciable share in the result; in the other, it is use and disuse that have been the main agents, though an appreciable share in the result must be ascribed to natural selection.

Besides, who has seen the uncles and aunts going away with the uniformity that is necessary for Mr. Darwin’s contention? We know that birds and insects do often get blown out to sea and perish, but in order to establish Mr. Darwin’s position we want the evidence of those who watched the reduction of the wings during the many generations in the course of which it was being effected, and who can testify that all, or the overwhelming majority, of the beetles born with fairly well-developed wings got blown out to sea, while those alone survived whose wings were congenitally degenerate. Who saw them go, or can point to analogous cases so conclusive as to compel assent from any equitable thinker?

Darwinians of the stamp of Mr. Thiselton Dyer, Professor Ray Lankester, or Mr. Romanes, insist on their pound of flesh in the matter of irrefragable demonstration. They complain of us for not bringing forward someone who has been able to detect the movement of the hour-hand of a watch during a second of time, and when we fail to do so, declare triumphantly that we have no evidence that there is any connection between the beating of a second and the movement of the hour-hand. When we say that rain comes from the condensation of moisture in the atmosphere, they demand of us a rain-drop from moisture not yet condensed. If they stickle for proof and cavil on the ninth part of a hair, as they do when we bring forward what we deem excellent instances of the transmission of an acquired characteristic, why may not we, too, demand at any rate some evidence that the unmodified beetles actually did always, or nearly always, get blown out to sea, during the reduction above referred to, and that it is to this fact, and not to the masterly inactivity of their fathers and mothers, that the Madeira beetles owe their winglessness? If we begin stickling for proof in this way, our opponents would not be long in letting us know that absolute proof is unattainable on any subject, that reasonable presumption is our highest certainty, and that crying out for too much evidence is as bad as accepting too little. Truth is like a photographic sensitized plate, which is equally ruined by over and by under exposure, and the just exposure for which can never be absolutely determined.

Surely if disuse can be credited with the vast powers involved in Mr. Darwin’s statement that it has probably “been the main agent in rendering organs rudimentary,” no limits are assignable to the accumulated effects of habit, provided the effects of habit, or use and disuse, are supposed, as Mr. Darwin supposed them, to be inheritable at all. Darwinians have at length woke up to the dilemma in which they are placed by the manner in which Mr. Darwin tried to sit on the two stools of use and disuse, and natural selection of accidental variations, at the same time. The knell of Charles-Darwinism is rung in Mr. Wallace’s present book, and in the general perception on the part of biologists that we must either assign to use and disuse such a predominant share in modification as to make it the feature most proper to be insisted on, or deny that the modifications, whether of mind or body, acquired during a single lifetime, are ever transmitted at all. If they can be inherited at all, they can be accumulated. If they can be accumulated at all, they can be so, for anything that appears to the contrary, to the extent of the specific and generic differences with which we are surrounded. The only thing to do is to pluck them out root and branch: they are as a cancer which, if the smallest fibre be left unexcised, will grow again, and kill any system on to which it is allowed to fasten. Mr. Wallace, therefore, may well be excused if he casts longing eyes towards Weismannism.