CHAPTER XII

INTERMEDIATES

So far as we have gone we have found it possible to express the various characters of animals and plants in terms of definite factors which are carried by the gametes, and are distributed according to a definite scheme. Whatever may be the nature of these factors it is possible for purposes of analysis to treat them as indivisible entities which may or may not be present in any given gamete. When the factor is present it is present as a whole. The visible properties developed by a zygote in the course of its growth depend upon the nature and variety of the factors carried in by the two gametes which went to its making, and to a less degree upon whether each factor was brought in by both gametes or by one only. If the given factor is brought in by one gamete only, the resulting heterozygote may be more or less intermediate between the homozygous form with a double dose of the factor and the homozygous form which is entirely destitute of the factor. Cases in point are those of the primula flowers and the Andalusian fowls. Nevertheless these intermediates produce only pure gametes, as is

shown by the fact that the pure parental types appear in a certain proportion of their offspring. In such cases as these there is but a single type of intermediate, and the simple ratio in which this and the two homozygous forms appear renders the interpretation obvious. But the nature of the F2 generation may be much more complex, and, where we are dealing with factors which interact upon one another, may even present the appearance of a series of intermediate forms grading from the condition found in one of the original parents to that which occurred in the other. As an illustration we may consider the cross between the Brown Leghorn and Silky fowls which we have already dealt with in connection with the inheritance of sex. The offspring of a Silky hen mated with a Brown Leghorn are in both sexes birds with but a trace of the Silky pigmentation. But when such birds are bred together they produce a generation consisting of chicks as deeply pigmented as the original Silky parent, chicks devoid of pigment like the Brown Leghorn, and chicks in which the pigmentation shows itself in a variety of intermediate stages. Indeed from a hundred chicks bred in this way it would be possible to pick out a number of individuals and arrange them in an apparently continuous series of gradually increasing pigmentation, with the completely unpigmented at one end and the most deeply pigmented at the other. Nevertheless, the case is one in which complete segregation of the different factors takes

In connection with intermediates a more cogent objection to the Mendelian view is the case of the first cross between two definite varieties thenceforward breeding true. The case that will naturally occur to the reader is that of the mulatto, which results from the cross between the negro and the white. According to general opinion, these mulattos, of intermediate pigmentation, continue to produce mulattos. Unfortunately this interesting case has never been critically investigated, and the statement that the mulatto breeds true rests almost entirely upon

information that is general and often vague. It may be that the inheritance of skin pigmentation in this instance is a genuine exception to the normal rule, but at the same time it must not be forgotten that it may be one in which several interacting factors are concerned, and that the pure white and the pure black are the result of combinations which from their rarity are apt to be overlooked. But until we are in possession of accurate information it is impossible to pronounce definitely upon the nature of the inheritance in this case.

Pedigree of a family which originated from a cross between a Hindu and a European. Black signs denote individuals as dark as average Hindus. Plain signs denote quite-fair members, while those with a dot in the centre are intermediate.

On the other hand, from the cross between the darkly pigmented Eastern races and the white segregation seems to occur in subsequent generations. Families are to be found in which one parent is a pure white, while the other has arisen from the cross between the dark and light in the first or some subsequent generation. Such families may contain children indistinguishable from pure blonds as well as children of very dark and of intermediate shades. As an example, I may give the following pedigree, which was kindly communicated to me by an Anglo-Indian friend (Fig. 29). The family had resided in England for several generations, so that in this case there was no question of a further admixture of black. Most noticeable is the family produced by a very dark lady who had married a white man. Some of the children were intermediate in colour, but two were fair whites and two were dark as dark Hindus. This sharp segregation or splitting out of blacks and whites in addition to intermediates strongly suggests that the nature of the inheritance is Mendelian, though it may be complicated by the existence of several factors which may also react upon one another. Nor must it be forgotten that in so far as these different factors are concerned the whites themselves may differ in constitution without showing any trace of it in their appearance. Before the case can be regarded as settled all these different possibilities will have to be definitely tested. With the dark Eastern races as with the negro we cannot

hope to come to any conclusion until we have evidence collected by critical and competent observers.

Though for the present we must regard the case of the negro as not proven, there are nevertheless two others in which the heredity would appear not to follow the Mendelian rule. Castle in America crossed the lop-eared rabbit with the normal form, and found that the F1 animals were intermediate with respect to their ears. And subsequent experiment showed that, on the whole, they bred true to this intermediate condition. The other case relates to Lepidoptera. The speckled wood butterfly (Pararge egeria) has a southern form which differs from the northern one in the greater brightness and depth of its yellow-brown markings. The northern form is generally distinguished as var. egeriades. Bateson crossed the southern form from the south of France with the paler British form, and found that the offspring were more or less intermediate in colour, and that in subsequent generations the parental types did not recur. These cases at present stand alone. It is possible that further research may reveal complications which mask or interfere with an underlying process of segregation. Or it may be that segregation does not occur owing to some definite physiological reason which at present we do not understand.

And here it is impossible not to recall Mendel's own experiences with the Hawkweeds (Hieracium). This

genus of plants exhibits an extraordinary profusion of forms differing from one another sometimes in a single feature, sometimes in several. The question as to how far these numerous forms were to be classified as distinct species, how far as varieties, and how far as products of chance hybridisation, was even at that time a source of keen controversy among botanists. There is little doubt that Mendel undertook his experiments on the Hawkweeds in the hope that the conception of unit-characters so brilliantly demonstrated for the pea would serve to explain the great profusion of forms among the Hieraciums. Owing to the minute size of their florets, these plants offer very considerable technical difficulties in the way of cross fertilisation. By dint of great perseverance and labour, however, Mendel succeeded in obtaining a few crosses between different forms. These hybrids were reared and a further generation produced from them, and, no doubt somewhat to Mendel's chagrin, every one of them proved to breed true. There was a complete absence of that segregation of characters which he had shown to exist in peas and beans, and had probably looked forward with some confidence to finding in Hieracium. More than thirty years passed before the matter was cleared up. To-day we know that the peculiar behaviour of the hybrid Hieraciums is due to the fact that they normally produce seed by a peculiar process of parthenogenesis. It is possible to take an unopened flower and to shear off with a

razor all the male organs together with the stigmata through which the pollen reaches the ovules. The flower, nevertheless, sets perfectly good seed. But the cells from which the seeds develop are not of the same nature as the normal ovules of a plant. They are not gametes but retain the double structure of the maternal cells. They are rather to be regarded as of the nature of buds which early become detached from the parent stock to lead an independent existence, and, like buds, they reproduce exactly the maternal characteristics. The discovery of the true nature of this case was only rendered possible by the development of the study of cytology, and it was not given to Mendel to live long enough to learn why his hybrid Hieraciums all bred true.