The facts that have now been adduced, though not very numerous, are sufficiently conclusive to prove that the old belief, of the universal sterility of hybrids and fertility of mongrels, is incorrect. The doctrine that such a universal law existed was never more than a plausible generalisation, founded on a few inconclusive facts derived from domesticated animals and cultivated plants. The facts were, and still are, inconclusive for several reasons. They are founded, primarily, on what occurs among animals in domestication; and it has been shown that domestication both tends to increase fertility, and was itself rendered possible by the fertility of those particular species being little affected by changed conditions. The exceptional fertility of all the varieties of domesticated animals does not prove that a similar fertility exists among natural varieties. In the next place, the generalisation is founded on too remote crosses, as in the case of the horse and the ass, the two most distinct and widely separated species of the genus Equus, so distinct indeed that they have been held by some naturalists to form distinct genera. Crosses between the two species of zebra, or even between the zebra and the quagga, or the quagga and the ass, might have led to a very different result. Again, in pre-Darwinian times it was so universally the practice to argue in a circle, and declare that the fertility of the offspring of a cross proved the identity of species of the parents, that experiments in hybridity were usually made between very remote species and even between species of different genera, to avoid the possibility of the reply: "They are both really the same species;" and the sterility of the hybrid offspring of such remote crosses of course served to strengthen the popular belief.
Now that we have arrived at a different standpoint, and look upon a species, not as a distinct entity due to special creation, but as an assemblage of individuals which have become somewhat modified in structure, form, and constitution so as to adapt them to slightly different conditions of life; which can be differentiated from other allied assemblages; which reproduce their like, and which usually breed together—we require a fresh set of experiments calculated to determine the matter of fact,—whether such species crossed with their near allies do always produce offspring which are more or less sterile inter se. Ample materials for such experiments exist, in the numerous "representative species" inhabiting distinct areas on a continent or different islands of a group; or even in those found in the same area but frequenting somewhat different stations.
To carry out these experiments with any satisfactory result, it will be necessary to avoid the evil effects of confinement and of too close interbreeding. If birds are experimented with, they should be allowed as much liberty as possible, a plot of ground with trees and bushes being enclosed with wire netting overhead so as to form a large open aviary. The species experimented with should be obtained in considerable numbers, and by two separate persons, each making the opposite reciprocal cross, as explained at p. 155. In the second generation these two stocks might be themselves crossed to prevent the evil effects of too close interbreeding. By such experiments, carefully carried out with different groups of animals and plants, we should obtain a body of facts of a character now sadly wanting, and without which it is hopeless to expect to arrive at a complete solution of this difficult problem. There are, however, some other aspects of the question that need to be considered, and some theoretical views which require to be carefully examined, having done which we shall be in a condition to state the general conclusions to which the facts and reasonings at our command seem to point.
Sterility due to changed Conditions and usually correlated with other Characters, especially with Colour.
The evidence already adduced as to the extreme susceptibility of the reproductive system, and the curious irregularity with which infertility or sterility appears in the crosses between some varieties or species while quite absent in those between others, seem to indicate that sterility is a characteristic which has a constant tendency to appear, either by itself or in correlation with other characters. It is known to be especially liable to occur under changed conditions of life; and, as such change is usually the starting-point and cause of the development of new species, we have already found a reason why it should so often appear when species become fully differentiated.
In almost all the cases of infertility or sterility between varieties or species, we have some external differences with which it is correlated; and though these differences are sometimes slight, and the amount of the infertility is not always, or even usually, proportionate to the external difference between the two forms crossed, we must believe that there is some connection between the two classes of facts. This is especially the case as regards colour; and Mr. Darwin has collected a body of facts which go far to prove that colour, instead of being an altogether trifling and unimportant character, as was supposed by the older naturalists, is really one of great significance, since it is undoubtedly often correlated with important constitutional differences. Now colour is one of the characters that most usually distinguishes closely allied species; and when we hear that the most closely allied species of plants are infertile together, while those more remote are fertile, the meaning usually is that the former differ chiefly in the colour of their flowers, while the latter differ in the form of the flowers or foliage, in habit, or in other structural characters.
It is therefore a most curious and suggestive fact, that in all the recorded cases, in which a decided infertility occurs between varieties of the same species, those varieties are distinguished by a difference of colour. The infertile varieties of Verbascum were white and yellow flowered respectively; the infertile varieties of maize were red and yellow seeded; while the infertile pimpernels were the red and the blue flowered varieties. So, the differently coloured varieties of hollyhocks, though grown close together, each reproduce their own colour from seed, showing that they are not capable of freely intercrossing. Yet Mr. Darwin assures us that the agency of bees is necessary to carry the pollen from one plant to another, because in each flower the pollen is shed before the stigma is ready to receive it. We have here, therefore, either almost complete sterility between varieties of different colours, or a prepotent effect of pollen from a flower of the same colour, bringing about the same result.
Similar phenomena have not been recorded among animals; but this is not to be wondered at when we consider that most of our pure and valued domestic breeds are characterised by definite colours which constitute one of their distinctive marks, and they are, therefore, seldom crossed with these of another colour; and even when they are so crossed, no notice would be taken of any slight diminution of fertility, since this is liable to occur from many causes. We have also reason to believe that fertility has been increased by long domestication, in addition to the fact of the original stocks being exceptionally fertile; and no experiments have been made on the differently coloured varieties of wild animals. There are, however, a number of very curious facts showing that colour in animals, as in plants, is often correlated with constitutional differences of a remarkable kind, and as these have a close relation to the subject we are discussing, a brief summary of them will be here given.
Correlation of Colour with Constitutional Peculiarities.
The correlation of a white colour and blue eyes in male cats with deafness, and of the tortoise-shell marking with the female sex of the same animal, are two well-known but most extraordinary cases. Equally remarkable is the fact, communicated to Darwin by Mr. Tegetmeier, that white, yellow, pale blue, or dun pigeons, of all breeds, have the young birds born naked, while in all other colours they are well covered with down. Here we have a case in which colour seems of more physiological importance than all the varied structural differences between the varieties and breeds of pigeons. In Virginia there is a plant called the paint-root (Lachnanthes tinctoria), which, when eaten by pigs, colours their bones pink, and causes the hoofs of all but the black varieties to drop off; so that black pigs only can be kept in the district.[58] Buckwheat in flower is also said to be injurious to white pigs but not to black. In the Tarentino, black sheep are not injured by eating the Hypericum crispum—a species of St. John's-wort—which kills white sheep. White terriers suffer most from distemper; white chickens from the gapes. White-haired horses or cattle are subject to cutaneous diseases from which the dark coloured are free; while, both in Thuringia and the West Indies, it has been noticed that white or pale coloured cattle are much more troubled by flies than are those which are brown or black. The same law even extends to insects, for it is found that silkworms which produce white cocoons resist the fungus disease much better than do those which produce yellow cocoons.[59] Among plants, we have in North America green and yellow-fruited plums not affected by a disease that attacked the purple-fruited varieties. Yellow-fleshed peaches suffer more from disease than white-fleshed kinds. In Mauritius, white sugar-canes were attacked by a disease from which the red canes were free. White onions and verbenas are most liable to mildew; and red-flowered hyacinths were more injured by the cold during a severe winter in Holland than any other kinds.[60]