So far what I have written applies to hybridization—the inter-breeding of distinct species. A similar but by no means identical subject is that of the inter-breeding of distinct races or varieties of one species, and the production of "mongrels." "Mongrels" are to races what "hybrids" are to species. To this branch of the subject belongs the study of the effects of intermarriage between distinct races of men.


CHAPTER XII

THE CROSS-BREEDING OF RACES

WE have seen that there is no simple rule as to the "mating" of individuals of a species with individuals of another closely allied but distinct species. Such mating very rarely comes about in natural conditions, but man by his interference sometimes succeeds in procuring "hybrids" between allied species. Hybrids between species belonging to groups so different as to be distinguished by zoologists as distinct "families" or "orders" are quite unknown under any circumstances. Such remoteness of natural character and structure as is indicated by the two great divisions of hoofed mammals—the even-toed (including sheep, cattle, deer, antelopes, giraffes, pigs and camels), and the odd-toed (including tapirs, rhinoceroses, horses, asses and zebras) is an absolute bar to inter-breeding. So, too, the carnivora (cats, dogs, bears and seals, and smaller kinds) are so remote in their nature from the rabbits, hares and rats—called "the rodents"—that no mating between members of the one and the other of these groups has ever been observed, either in nature or under artificial conditions.

Even when individuals of closely allied species mate with one another it is a very rare occurrence that the hybrids so produced ripen their ova and sperms so as to be capable of carrying on the hybrid race, though sometimes they do ripen them and breed. The great naturalist Alfred Wallace, in his most valuable and readable book called "Darwinism," expressed the opinion that the apparent failure of hybrid races to perpetuate themselves by breeding was to a large extent due to the small number of individuals used in experiments on this matter, and the in-and-in breeding which was the consequence. One of the great generalizations established by Darwin is that in-and-in breeding is, as a rule, resisted in all animals and plants, and leads when it occurs to a dying-out of the inbred race by resulting feebleness and infertility. A large part of Darwin's work consisted in demonstrating the devices existing in the natural structure and qualities of plants and animals for securing cross-fertilization among individuals of the same species but of different stock. Both extremes seem to be barred in nature—namely, the inter-breeding of stocks so diverse in structure and quality as to be what we call "distinct species," and again the inter-breeding of individuals of the same immediate parentage or near cousinship. What seems to be favoured by the natural structure and qualities of the plant or the animal is that it shall only breed within a certain group—the species—and shall within that group avoid constant self-fertilization or fertilization by near cousins. Thus we find numerous cases in which, though the same flower has both pollen and ovules, and might fertilize itself, the visits of insects (specially made use of by mechanisms in the flower) carry the pollen of one flower to the ovules of another and to flowers on separate plants growing at a distance. It is necessary to note that there are, nevertheless, self-fertilizing flowers, and also self-fertilizing lower animals, the special conditions of which require and have received careful examination and consideration, upon which I cannot now enter.

In relation to the question of the possibility of establishing hybrids between various species experimentally, I must (before going on to the cognate question of "mongrels") tell of an interesting suggestion made to me by my friend Professor Alphonse Milne-Edwards not long before he died, and never published by him. He was director of the Jardin des Plantes in Paris, where there is a menagerie of living beasts as well as a botanic garden and great museum collections and laboratories. He held it to be probable, as many physiologists would agree, that the fertilization of the egg of one species by the sperm of another, even a remotely related one, is ultimately prevented by a chemical incompatibility—chemical in the sense that the highly complex molecular constitution of such bodies as the anti-toxins and serums with which physiologists are beginning to deal is "chemical"—and that all the other and secondary obstacles to fertilization can be overcome or evaded in the course of experiment. He proposed to inject one species by "serums" extracted from the other, in such a way as seemed most likely to bring the chemical state of their reproductive elements into harmony, that is to say, into a condition in which they should not be actively antagonistic but admit of fusion and union. He proposed, by the exchange of living or highly organized fluids (by means of injection or transfusion) between a male and female of separate species, to assimilate the chemical constitution of one to that of the other, and thus possibly so to affect their reproductive elements that the one could tolerate and fertilize the other. The suggestion is not unreasonable, but would require a long series of experiments in which the possibility of producing such "assimilation," even to a small extent and in respect of less complex processes than those ultimately aimed at, would have to be, first of all, established. My friend did not live to commence this investigation, but it is possible that some day we may see the obstacle to the union of ovum and sperm of species, which are to some extent allied, removed in this way by transfusion or injection of important fluids from the one into the other.

We must not lose sight of the fact, in the midst of these various and diverging observations about the fertilization of the ova of one species by sperms of another species, that there is such a thing as "parthenogenesis," or virgin-birth. In some of the insects and lower forms of animals the egg-cell habitually and regularly develops and gives rise to a new individual without being fertilized at all. And in other cases by special treatment, such as rubbing with a brush, or in the case of marine animals by addition of certain salts to the water in which the eggs are floating—or, again, in the case of the eggs of the common frog by gently scratching them with a needle—the eggs which usually and regularly require to be penetrated by and fused with a spermatozoon or sperm-filament before they will develop, proceed to develop into complete new individuals without the action upon them of any spermatozoon. In such marine animals as the sea-urchins or sea-eggs it has been found that the eggs deposited in pure sea-water, though they would die and decompose if left there alone, can be made to develop and proceed on their growth by the addition to the sea-water of the sperm filaments of a star-fish (the feather star or comatula). The spermatozoa or sperm-filaments do not, however, in this case fuse with the egg-cells. They mechanically pierce the egg-coat, but contribute no substance to the embryo into which the egg develops. They have merely served, like the scratch of a needle on the frog's egg and the brushing of insects' eggs, to start the egg on its growth, to "stimulate" it and set changes going. It appears thus that the fertilizing sperm-filaments of organisms generally have two separate and very important influences upon the egg-cells with which they fuse. The one is to stimulate the egg and start the changes of embryonic growth; the other is to contribute some living material from the male parent to the new individual arising from the growth and shaping of the egg-cell. The first influence can be exercised without the second, as is seen in the case of the eggs of some sea-urchins stimulated to growth by the spermatozoa of some star-fishes. It happens that these marine animals are convenient for study and experiment because their eggs are small and transparent and that they and the spermatozoa are freely passed into the sea-water at the breeding season, in which the fertilization of the eggs takes place.

When these facts are considered we have to admit that in the mating of two species which will not regularly and naturally breed together, there may be a limited action of the spermatic element which may stimulate the egg to development without contributing by fusion in the regular way to the actual substance of the young so produced, or only contributing an amount insufficient to produce a full and normal development of the hybrid young. Such cases not improbably sometimes occur in higher animals, though they have not been, as yet, shown to exist except in the experiments with sea-urchins' eggs and feather-star's sperm.