The pianist, whom I have already used as an illustration, may by practice develope the muscles of his fingers so as to ensure the highest dexterity and power; but such an effect would be entirely transient, for it depends upon a modification in local nutrition which would be unable to cause any change in the molecular structure of the germ-cells, and could not therefore produce any effect upon the offspring. And even if we admit that some change might be caused in the germ-cells, the chances would be infinity to nothing against the production of the appropriate effect, viz. such a change as would lead to the development in the child of the acquired characters of the parent.

In the lowest unicellular organisms, however, the case is entirely different. Here parent and offspring are still, in a certain sense, one and the same thing: the child is a part, and usually half, of the parent. If therefore the individuals of a unicellular species are acted upon by any of the various external influences, it is inevitable that hereditary individual differences will arise in them; and as a matter of fact it is indisputable that changes are thus produced in these organisms, and that the resulting characters are transmitted. It has been directly observed that individual differences do occur in unicellular organisms,—differences in size, colour, form, and the number or arrangement of cilia. It must be admitted that we have not hitherto paid sufficient attention to this point, and moreover our best microscopes are only very rough means of observation when we come to deal with such minute organisms. Nevertheless we cannot doubt that the individuals of the same species are not absolutely identical.

We are thus driven to the conclusion that the ultimate origin of hereditary individual differences lies in the direct action of external influences upon the organism. Hereditary variability cannot however arise in this way at every stage of organic development, as biologists have hitherto been inclined to believe. It can only arise in the lowest unicellular organisms; and when once individual difference had been attained by these, it necessarily passed over into the higher organisms when they first appeared. Sexual reproduction coming into existence at the same time, the hereditary differences were increased and multiplied, and arranged in ever-changing combinations.

Sexual reproduction can also increase the differences between individuals, because constant cross-breeding must necessarily and repeatedly lead to a combination of forces which tend in the same direction, and which may determine the constitution of any part of the body. If, for instance, the same part of the body is strongly developed in both parents, the experience of breeders tells us that the part in question is likely to be even more strongly developed in the offspring; and that weakly developed parts will in the same manner tend to become still weaker. Amphigonic reproduction therefore ensures that every character which is subject to individual fluctuation must appear in many individuals with a strengthened degree of development, in many others with a development which is less than normal, while in a still larger number of individuals the average development will be reached. Such differences afford the material by means of which natural selection is able to increase or weaken each character according to the needs of the species. By the removal of the less well-adapted individuals, natural selection increases the chance of beneficial cross-breeding in the subsequent generations.

Every one must admit that, if a species came into existence having only a small number of individual differences which appeared in the different parts of different individuals, the number of differences would increase with each sexually produced generation, until all the parts in which the variations occurred had received a peculiar character in all individuals.

Moreover sexual reproduction not only adds to the number of existing differences, but it also brings them into new combinations, and this latter consequence is as important as the former.

The former consequence can hardly make itself felt in any existing species, because in them every part already possesses its peculiar character in all individuals. The second consequence is, however, more important, viz. the production of new combinations of individual characters by sexual reproduction; for, as Darwin has already pointed out, we must imagine that not only are single characters changed in the process of breeding, but that probably several, and perhaps very many characters, are simultaneously modified. No two species, however nearly allied, differ from each other in but a single character. Even our eyesight, which has by no means reached the highest pitch of development, can always detect several, and often very many points of difference; and if we possessed the powers necessary for making an absolutely accurate comparison, we should probably find that everything is different in two nearly allied species.

It is true that a great number of these differences depend upon correlation, but others must depend upon simultaneous primary changes.

A large butterfly (Kallima paralecta), found in the East Indian forests, has often been described in its position of rest as almost exactly resembling a withered leaf; the resemblance in colour being aided by the markings which imitate the venation of a leaf. These markings are composed of two parts, the upper of which is on the fore-wings, while the lower one is on the hind wings. The butterfly when at rest must therefore keep the wings in such a position that the two parts of each marking exactly correspond, for otherwise the character would be valueless; and as a matter of fact the wings are held in the appropriate position, although the butterfly is of course unconscious of what it is doing. Hence a mechanism must exist in the insect’s brain which compels it to assume this attitude, and it is clear that the mechanism cannot have been developed before the peculiar manner of holding the wings became advantageous to the butterfly, viz. before the similarity to a leaf had made its first appearance. Conversely, this latter resemblance could not develope before the butterfly had gained the habit of holding its wings in the appropriate position. Both characters must therefore have come into existence simultaneously, and must have undergone increase side by side: the marking progressing from an imperfect to a very close similarity, while the position of the wings gradually approached the attitude which was exactly appropriate. The development of certain minute structural elements of the central nervous system, and the appropriate distribution of colouring matter on the wings, must have taken place simultaneously, and only those individuals have been selected to continue the species which possessed the favourable variations in both these directions.

It is, however, obvious that sexual reproduction will readily afford such combinations of required characters, for by its means the most diverse features are continually united in the same individual, and this seems to me to be one of its most important results.