If the accessory body is really to be regarded as bearing the factor for femaleness, then in Mendelian terms female is DD and male is DR. The eggs are indifferent and the spermatozoa are each male, OR female. But according to the evidence derived from a study of the ***-limited descent of certain features in other animals the conclusion seems equally clear that in them female must be regarded as DR and male as RR. The eggs are thus each either male or female and the spermatozoa are indifferent. How this contradictory evidence is to be reconciled we do not yet know. The breeding work concerns fowls, canaries, and the Currant moth (Abraxas grossulariata). The accessory chromosome has been now observed in most of the great divisions of insects (As Wilson has proved, the unpaired body is not a universal feature even in those orders in which it has been observed.
Nearly allied types may differ. In some it is altogether unpaired. In others it is paired with a body of much smaller size, and by selection of various types all gradations can be demonstrated ranging to the condition in which the members of the pair are indistinguishable from each other.), except, as it happens, Lepidoptera. At first sight it seems difficult to suppose that a feature apparently so fundamental as *** should be differently constituted in different animals, but that seems at present the least improbable inference. I mention these two groups of facts as illustrating the nature and methods of modern genetic work. We must proceed by minute and specific analytical investigation. Wherever we look we find traces of the operation of precise and specific rules.
In the light of present knowledge it is evident that before we can attack the Species-problem with any hope of success there are vast arrears to be made up. He would be a bold man who would now assert that there was no sense in which the term Species might not have a strict and concrete meaning in contradistinction to the term Variety. We have been taught to regard the difference between species and variety as one of degree. Ithink it unlikely that this conclusion will bear the test of further research. To Darwin the question, What is a variation? presented no difficulties. Any difference between parent and offspring was a variation.
Now we have to be more precise. First we must, as de Vries has shown, distinguish real, genetic, variation from FLUCTUATIONAL variations, due to environmental and other accidents, which cannot be transmitted. Having excluded these sources of error the variations observed must be expressed in terms of the factors to which they are due before their significance can be understood. For example, numbers of the variations seen under domestication, and not a few witnessed in nature, are simply the consequence of some ingredient being in an unknown way omitted from the composition of the varying individual. The variation may on the contrary be due to the addition of some new element, but to prove that it is so is by no means an easy matter. Casual observation is useless, for though these latter variations will always be dominants, yet many dominant characteristics may arise from another cause, namely the meeting of complementary factors, and special study of each case in two generations at least is needed before these two phenomena can be distinguished.
When such considerations are fully appreciated it will be realised that medleys of most dissimilar occurrences are all confused together under the term Variation. One of the first objects of genetic analysis is to disentangle this mass of confusion.
To those who have made no study of heredity it sometimes appears that the question of the effect of conditions in causing variation is one which we should immediately investigate, but a little thought will show that before any critical inquiry into such possibilities can be attempted, a knowledge of the working of heredity under conditions as far as possible uniform must be obtained. At the time when Darwin was writing, if a plant brought into cultivation gave off an albino variety, such an event was without hesitation ascribed to the change of life. Now we see that albino GAMETES, germs, that is to say, which are destitute of the pigment-forming factor, may have been originally produced by individuals standing an indefinite number of generations back in the ancestry of the actual albino, and it is indeed almost certain that the variation to which the appearance of the albino is due cannot have taken place in a generation later than that of the grandparents. It is true that when a new DOMINANT appears we should feel greater confidence that we were witnessing the original variation, but such events are of extreme rarity, and no such case has come under the notice of an experimenter in modern times, as far as I am aware. That they must have appeared is clear enough. Nothing corresponding to the Brown-breasted Game fowl is known wild, yet that colour is a most definite dominant, and at some moment since Gallus bankiva was domesticated, the element on which that special colour depends must have at least once been formed in the germ-cell of a fowl; but we need harder evidence than any which has yet been produced before we can declare that this novelty came through over-feeding, or change of climate, or any other disturbance consequent on domestication. When we reflect on the intricacies of genetic problems as we must now conceive them there come moments when we feel almost thankful that the Mendelian principles were unknown to Darwin. The time called for a bold pronouncement, and he made it, to our lasting profit and delight. With fuller knowledge we pass once more into a period of cautious expectation and reserve.