It is obvious that these changes are not such as we should expect as a result of the transmission of the mutilation of the tail which is so commonly practised. If the artificial injury were transmitted we should not expect that a variable number of the mesial vertebrae would be absent, but rather those of the tip. There would be no reason why the existing vertebrae should be degenerate as in the majority of the caudal vertebrae of the dogs examined by Bonnet.
Entirely similar phenomena have been observed by Döderlein in the tailless cats which not infrequently occur in Japan. In these cats the rudimentary vertebrae of the tail were reduced to a short, thin, inflexible spiral, which formed a knot densely covered with hair on the posterior part of the animal.
Such a reduction of the tail occurs quite independently of artificial injury, in individuals of which the parents were not injured: it is even found in races, such as the dachshund, which, as far as we know, have never been habitually mutilated.
But the fact is rendered especially interesting because the reduction of the vertebral column in the region of the tail takes place in very various degrees. Sometimes only four vertebrae are absent, sometimes as many as ten. The degree of abnormality in shape and the degree of coalescence between the vertebrae also differ greatly. Hence Bonnet rightly concludes that a slow and gradual process of reduction is going on in these animals, a process which tends, as it were, to shorten the tail. I intentionally say ‘as it were,’ for of course the statement must not be taken literally, and we must not conclude that the process of reduction is a consequence of some hypothetical developmental force seated in the organism, of which the purpose is to remove the tail. On the contrary, this instance shows very clearly that the appearance of a development guided in a certain direction may be produced without the existence of any motive developmental force.
The disposition of the tail to become rudimentary, in cats and dogs, may be explained in the simplest way, by the process which I have formerly called panmixia. The tail is now of hardly any use to these animals; and neither dog nor cat would perish because they possessed only an incomplete tail. Hence natural selection does not now exercise any influence over these parts, and an occasional reduction is no longer eliminated by the early destruction of its possessor: therefore such reduction may be transmitted to the offspring.
The race of tailless foxes which, according to Settegast, existed during the present century on the hunting-grounds of Prince Wilhelm zu Solms-Braunfels, very soon disappeared; while cats and dogs with rudimentary tails have been preserved in many cases. Such results are to be expected, because in these domesticated animals the absence of the tail did not cause any inferiority in the struggle for existence.
But these facts appear to me to be remarkable in another direction. I previously mentioned the tailless race of Manx cats. Tradition does not tell us how it happened that the descendants of the first tailless cat in the Isle of Man were able to increase and spread in such a manner as to form the dominant race in the island. But we can easily imagine how it happened, when we learn that tailless cats are especially prized[[300]] in Japan, because people think that they are better mousers. Every one in Japan wishes to possess a tailless cat, and people even cut off the tails of normal cats when they cannot obtain those with congenital rudimentary tails, because they believe that cats become better mousers in consequence of taillessness. In Waldkirch the same account of the superiority of tailless cats is curiously enough also found. We thus see how a slight but striking variation may at once cause an energetic process of artificial selection, which helps this variation to predominance: a hint for us to be careful in passing judgment upon sexual selection, for the latter also works upon such functionally indifferent but striking variations. In the case of the cats, man has favoured a particular variation, because the novelty rather than the beauty of the character surprised and attracted him. He has attached an imaginary value to the new character, and by artificial selection has helped it to predominate over the normal form. I see no reason why the same process should not take place in animals by the operation of sexual selection.
But now, after this little digression, let us return to the transmission of mutilations.
We have seen that the rudimentary tails of cats and dogs, as far as they can be submitted to scientific investigation, do not depend upon the transmission of artificial mutilation, but upon the spontaneous appearance of degeneration in the vertebral column of the tail. The opinion may, however, be still held that the customary artificial mutilation of the tail, in many races of dogs and cats, has at least produced a number of rudimentary tails, although, perhaps, not all of them. It might be maintained that the fact of the spontaneous appearance of rudimentary tails does not disprove the supposition that the character may also depend upon the transmission of artificial mutilation.
Obviously, such a question can only be decided by experiment: not, of course, experiments upon dogs and cats, as Bonnet rightly remarks, but experiments upon animals the tails of which are not already in a process of reduction. Bonnet proposes that the question should be investigated in white rats or mice, in which the length of the tail is very uniform, and the occurrence of rudimentary tails is unknown.