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 gametogenesis of a pigmented individual; that is, in Mendelian fashion. Or, to express it otherwise, an albino extracted from yellow parents, bred with an albino extracted from black parents, will give an albino offspring whose gametes in equal numbers are bearers of the black and yellow determinants. And when one of these albinoes is bred with a pure coloured individual, a mixed offspring will appear in the first generation. Some of the individuals will be one or other of the two colours, the determinants of which were borne by the albino, and others the colour of the pigmented parent. But in such albino crosses the colour characters are latent because albinoes do not carry the whole of the complements for colour production. They carry only some determinant or determinants which are capable of developing colour when they interact with some other determinant or determinants carried alone by pigmented individuals. Whether albinoes carry the tyrosinase or other ferment, or whether they carry the chromogen or chromogens, is not yet settled. Miss Durham’s work suggests that they carry the latter. But that they never bear both is proved by the fact that, when albinoes are crossed with each other, none but albinoes ever result in the offspring. One apparent exception to this rule only is known, and this almost certainly was due to error.

It is not only among albino animals that colour factors are carried in a latent condition, but also in white flowers. W. Bateson has shown this to be the case for the sweet-pea (Lathyrus odoratus), var. Emily Henderson, and for certain white and cream stocks (Matthiola). When white Emily Henderson (the race having round pollen grains) is crossed with a blue-flowered pea, purple offspring result. Similarly, when white Emily Henderson (long pollen grains) is crossed with white Emily Henderson (round pollen grains), the offspring wholly consists of the reversionary purple type, and sometimes wholly of a red bicolor form known as “Painted Lady.” These two types never appear in the same family. With the stocks, when a white-flowered and hairless form is crossed with a cream-flowered and hairless one, all the offspring are purple and hairy. Bateson considers that the purple colour is due to the simultaneous existence in the plant of two colour factors which may be designated by C and R. If either one of these two is absent the plant is colourless. Cream-coloured flowers are regarded as white because cream is due to yellow plastids and not to sap colour. Thus the cream plant may carry C and the white one R. When they are crossed the two factors for colour production are brought together. Obviously, we may regard C as a tyrosinase and R as a chromogen, or vice versa; and in the case of the white sweetpea crossed with a blue-flowered one, and producing purple offspring, we may imagine that the white flower brought in an additional tyrosinase or a chromogen not present in the blue flower, which, when combined or mixed with the chromogen or tyrosinase for blue, gave purple. A similar explanation may apply to C. Correns’s experiment, in which he crossed white Mirabilis jalapa with a yellow form, and always obtained red-flowered offspring.

In heredity, complete albinism among animals is always recessive; and partial albinism (piebald) is always recessive to complete pigmentation (self-coloured). When an albino mouse, rat, guinea-pig or rabbit is crossed with either a pure self or pure pied-coloured form, the offspring are similar to, though not always exactly like, the coloured parent; provided, of course, that the albino is pure and is not carrying some colour or pattern determinant which is dominant to that of the coloured parent used. No albinoes, in such a case, will appear among the first generation, but if the individuals of this (F.1) generation are crossed inter se or back crossed with the albino parent, then albino individuals reappear among the offspring. In the former case they would form one-quarter of the individuals of this second (F.2) generation, and in the latter, one-half.

The recessive nature of albinism and its distribution in Mendelian fashion is almost certainly as true for man as for lower forms. This has been shown by W. C. Farabee for negroes in Coahoma county, Mississippi. The facts are as follows. An albino negro married a normal negress. They had three children, all males. All three sons married, and two of them had only normal children, judged of course by somatic characters. But the third son married twice, and by the first wife had five normal and one albino children, and by the second, six normal and three albino children. If we assume that the two negresses which the third son married were themselves carrying albinism recessive—an exceedingly probable condition considering that albino negroes are not uncommon—the result is accurately in accordance, as W. E. Castle has shown, with Mendelian expectation. For there is expected in the offspring of this third son coloured individuals and albinoes in the proportion of 3:1. There is actually 11:4, which is the nearest possible approximation with the number 15.

The operation of Mendelian processes in human heredity is further shown by the close relationship that exists between the appearance of albinoes and cousin marriages. An albino is a homozygote; that is, all its gametes are carrying the character of albinism and none of them bear the alternative character—the allelomorph—of pigmentation. By pigmentation is here meant all those factors which go to its production. Now such a gametic (egg or sperm) constitution can only result when two individuals, all or some of whose gametes are pure with regard to the character albinism, meet in fertilization. Hence it is readily seen that it is among cousin marriages that the greater probabilities exist that two individuals bearing identical characters will meet, than in the population at large. This can be illustrated in the following scheme. Let A stand for a pure albino and (A)N for a normal person, who nevertheless carries the character albinism (A) recessive. Then, in the scheme below, if Ab and (A)Nb are two brothers who both marry normal wives N, their children N(A) in the first case will be all normal in appearance but will be carrying albinism recessive; and in the second case some will be pure normal individuals N, and some will be like the children of the first brother, i.e. N(A). Now, if one of these latter children of the second brother marries a cousin—a child of the first brother,—their offspring, if large enough, will consist of some pure normals N, impure normals N(A), and of albinoes A.

No other rational explanation of the close relationship between albinism and cousin marriages is at present forthcoming. And, when the whole facts are borne in mind, there can be no reasonable doubt that the Mendelian principles offer an intelligible solution of the problem.

A popular conception exists that albinoes are less constitutionally strong than the pigmented individuals of the same species. In support of this belief there is more or less scientifically ascertained evidence. Conversely, there is, however, conclusive evidence that in some instances and in respect of certain qualities the opposite belief is true.

To deal with the former belief first, we have the remarkable case cited by Charles Darwin on the authority of Professor I. J. Wyman. In Virginia the paint-root plant (Lachnanthes tinctoria) occurs abundantly, and Professor Wyman noticed that all the pigs in this district were black. Upon inquiry of the farmers he found that all the white pigs born in a litter were destroyed, because they could not be reared to maturity. The root of this plant, when eaten by white pigs, caused their bones to turn to a pink colour and their hoofs to fall off, but the black pigs could eat the same plant with impunity. Partial albinism in this case was undoubtedly correlated with some inherent constitutional defect, in virtue of which the individuals characterized by it were injuriously affected by the juices of a plant quite innocuous to their pigmented brethren. Heusinger has shown that white sheep and pigs are injured by the ingestion