The Variation of Animals and Plants under Domestication — Volume 2

I am aware that such cases as the foregoing have been ascribed by various authors, not to one species, race, or individual being prepotent over the other in impressing its character on its crossed offspring, but to such rules as that the father influences the external characters and the mother the internal or vital organs. But the great diversity of the rules given by various authors almost proves their falseness. Dr. Prosper Lucas has fully discussed this point, and has shown (14/18. 'L'Hered. Nat.' tome 2 book 2 chapter 1.) that none of the rules (and I could add others to those quoted by him) apply to all animals. Similar rules have been announced for plants, and have been proved by Gartner (14/19. 'Bastarderzeugung' s. 264-266. Naudin 'Nouvelles Archives du Museum' tome 1 page 148 has arrived at a similar conclusion.) to be all erroneous. If we confine our view to the domesticated races of a single species, or perhaps even to the species of the same genus, some such rules may hold good; for instance, it seems that in reciprocally crossing various breeds of fowls the male generally gives colour (14/20. 'Cottage Gardener' 1856 pages 101, 137.); but conspicuous exceptions have passed under my own eyes. It seems that the ram usually gives its peculiar horns and fleece to its crossed offspring, and the bull the presence or absence of horns.

In the following chapter on Crossing I shall have occasion to show that certain characters are rarely or never blended by crossing, but are transmitted in an unmodified state from either parent-form; I refer to this fact here because it is sometimes accompanied on the one side by prepotency, which thus acquires the false appearance of unusual strength. In the same chapter I shall show that the rate at which a species or breed absorbs and obliterates another by repeated crosses, depends in chief part on prepotency in transmission.]

In conclusion, some of the cases above given, — for instance, that of the trumpeter pigeon, — prove that there is a wide difference between mere inheritance and prepotency. This latter power seems to us, in our ignorance, to act in most cases quite capriciously. The very same character, even though it be an abnormal or monstrous one, such as silky feathers, may be transmitted by different species, when crossed, either with prepotent force or singular feebleness. It is obvious, that a purely-bred form of either sex, in all cases in which prepotency does not run more strongly in one sex than the other, will transmit its character with prepotent force over a mongrelised and already variable form. (14/21. See some remarks on this head with respect to sheep by Mr. Wilson in 'Gardener's Chronicle' 1863 page 15. Many striking instances of this result are given by M. Malingie-Nouel 'Journ. R. Agricult. Soc.' volume 14 1853 page 220 with respect to crosses between English and French sheep. He found that he obtained the desired influence of the English breeds by crossing intentionally mongrelised French breeds with pure English breeds.) From several of the above-given cases we may conclude that mere antiquity of character does not by any means necessarily make it prepotent. In some cases prepotency apparently depends on the same character being present and visible in one of the two breeds which are crossed, and latent or invisible in the other breed; and in this case it is natural that the character which is potentially present in both breeds should be prepotent. Thus, we have reason to believe that there is a latent tendency in all horses to be dun-coloured and striped; and when a horse of this kind is crossed with one of any other colour, it is said that the offspring are almost sure to be striped. Sheep have a similar latent tendency to become dark-coloured, and we have seen with what prepotent force a ram with a few black spots, when crossed with white sheep of various breeds, coloured its offspring. All pigeons have a latent tendency to become slaty-blue, with certain characteristic marks, and it is known that, when a bird thus coloured is crossed with one of any other colour, it is most difficult afterwards to eradicate the blue tint. A nearly parallel case is offered by those black bantams which, as they grow old, develop a latent tendency to acquire red feathers. But there are exceptions to the rule: hornless breeds of cattle possess a latent capacity to reproduce horns, yet when crossed with horned breeds they do not invariably produce offspring bearing horns.

We meet with analogous cases with plants. Striped flowers, though they can be propagated truly by seed, have a latent tendency to become uniformly coloured, but when once crossed by a uniformly coloured variety, they ever afterwards fail to produce striped seedlings. (14/22. Verlot 'Des Varietes' 1865 page 66.) Another case is in some respects more curious: plants bearing peloric flowers have so strong a latent tendency to reproduce their normally irregular flowers, that this often occurs by buds when a plant is transplanted into poorer or richer soil. (14/23. Moquin-Tandon 'Teratologie' page 191.) Now I crossed the peloric snapdragon (Antirrhinum majus), described in the last chapter, with pollen of the common form; and the latter, reciprocally, with peloric pollen. I thus raised two great beds of seedlings, and not one was peloric. Naudin (14/24. 'Nouvelles Archives du Museum' tome 1 page 137.) obtained the same result from crossing a peloric Linaria with the common form. I carefully examined the flowers of ninety plants of the crossed Antirrhinum in the two beds, and their structure had not been in the least affected by the cross, except that in a few instances the minute rudiment of the fifth stamen, which is always present, was more fully or even completely developed. It must not be supposed that this entire obliteration of the peloric structure in the crossed plants can be accounted for by any incapacity of transmission; for I raised a large bed of plants from the peloric Antirrhinum, artificially fertilised by its own pollen, and sixteen plants, which alone survived the winter, were all as perfectly peloric as the parent-plant. Here we have a good instance of the wide difference between the inheritance of a character and the power of transmitting it to crossed offspring. The crossed plants, which perfectly resembled the common snapdragon, were allowed to sow themselves, and out of a hundred and twenty-seven seedlings, eighty-eight proved to be common snapdragons, two were in an intermediate condition between the peloric and normal state, and thirty-seven were perfectly peloric, having reverted to the structure of their one grand-parent. This case seems at first sight to offer an exception to the rule just given, namely, that a character which is present in one form and latent in the other is generally transmitted with prepotent force when the two forms are crossed. For in all the Scrophulariaceae, and especially in the genera Antirrhinum and Linaria, there is, as was shown in the last chapter, a strong latent tendency to become peloric; but there is also, as we have seen, a still stronger tendency in all peloric plants to reacquire their normal irregular structure. So that we have two opposed latent tendencies in the same plants. Now, with the crossed Antirrhinums the tendency to produce normal or irregular flowers, like those of the common Snapdragon, prevailed in the first generation; whilst the tendency to pelorism, appearing to gain strength by the intermission of a generation, prevailed to a large extent in the second set of seedlings. How it is possible for a character to gain strength by the intermission of a generation, will be considered in the chapter on pangenesis.

On the whole, the subject of prepotency is extremely intricate, — from its varying so much in strength, even in regard to the same character, in different animals, — from its running either equally in both sexes, or, as frequently is the case with animals, but not with plants, much stronger in one sex than the other, — from the existence of secondary sexual characters, — from the transmission of certain characters being limited, as we shall immediately see, by sex, — from certain characters not blending together, — and, perhaps, occasionally from the effects of a previous fertilisation on the mother. It is therefore not surprising that no one has hitherto succeeded in drawing up general rules on the subject of prepotency.

INHERITANCE AS LIMITED BY SEX.

New characters often appear in one sex, and are afterwards transmitted to the same sex, either exclusively or in a much greater degree than to the other. This subject is important, because with animals of many kinds in a state of nature, both high and low in the scale, secondary sexual characters, not directly connected with the organs of reproduction, are conspicuously present. With our domesticated animals, characters of this kind often differ widely from those distinguishing the two sexes of the parent species; and the principle of inheritance, as limited by sex, explains how this is possible.

[Dr. P. Lucas has shown (14/25. 'L'Hered. Nat.' tome 2 pages 137-165. See also Mr. Sedgwick's four memoirs, immediately to be referred to.) that when a peculiarity, in no manner connected with the reproductive organs, appears in either parent, it is often transmitted exclusively to the offspring of the same sex, or to a much greater number of them than of the opposite sex. Thus, in the family of Lambert, the horn-like projections on the skin were transmitted from the father to his sons and grandsons alone; so it has been with other cases of ichthyosis, with supernumerary digits, with a deficiency of digits and phalanges, and in a lesser degree with various diseases, especially with colour-blindness and the haemorrhagic diathesis, that is, an extreme liability to profuse and uncontrollable bleeding from trifling wounds. On the other hand, mothers have transmitted, during several generations, to their daughters alone, supernumerary and deficient digits, colour-blindness and other peculiarities. So that the very same peculiarity may become attached to either sex, and be long inherited by that sex alone; but the attachment in certain cases is much more frequent to one than the other sex. The same peculiarities also may be promiscuously transmitted to either sex. Dr. Lucas gives other cases, showing that the male occasionally transmits his peculiarities to his daughters alone, and the mother to her sons alone; but even in this case we see that inheritance is to a certain extent, though inversely, regulated by sex. Dr. Lucas, after weighing the whole evidence, comes to the conclusion that every peculiarity tends to be transmitted in a greater or lesser degree to that sex in which it first appears. But a more definite rule, as I have elsewhere shown (14/26. 'Descent of Man' 2nd edition page 32.) generally holds good, namely, that variations which first appear in either sex at a late period of life, when the reproductive functions are active, tend to be developed in that sex alone; whilst variations which first appear early in life in either sex are commonly transmitted to both sexes. I am, however, far from supposing that this is the sole determining cause.

A few details from the many cases collected by Mr. Sedgwick (14/27. On Sexual Limitation in Hereditary Diseases 'Brit. and For. Med. — Chirurg. Review' April 1861 page 477; July page 198; April 1863 page 445; and July page 159. Also in 1867 'On the influence of Age in Hereditary Disease.'), may be here given. Colour-blindness, from some unknown cause, shows itself much oftener in males than in females; in upwards of two hundred cases collected by Mr. Sedgwick, nine-tenths related to men; but it is eminently liable to be transmitted through women. In the case given by Dr. Earle, members of eight related families were affected during five generations: these families consisted of sixty-one individuals, namely, of thirty-two males, of whom nine-sixteenths were incapable of distinguishing colour, and of twenty-nine females, of whom only one-fifteenth were thus affected. Although colour-blindness thus generally clings to the male sex, nevertheless, in one instance in which it first appeared in a female, it was transmitted during five generations to thirteen individuals, all of whom were females. The haemorrhagic diathesis, often accompanied by rheumatism, has been known to affect the males alone during five generations, being transmitted, however, through the females. It is said that deficient phalanges in the fingers have been inherited by the females alone during ten generations. In another case, a man thus deficient in both hands and feet, transmitted the peculiarity to his two sons and one daughter; but in the third generation, — out of nineteen grandchildren, twelve sons had the family defect, whilst the seven daughters were free. In ordinary cases of sexual limitation, the sons or daughters inherit the peculiarity, whatever it may be, from their father or mother, and transmit it to their children of the same sex; but generally with the haemorrhagic diathesis, and often with colour-blindness, and in some other cases, the sons never inherit the peculiarity directly from their fathers, but the daughters alone transmit the latent tendency, so that the sons of the daughters alone exhibit it. Thus the father, grandson, and great-great-grandson will exhibit a peculiarity, — the grandmother, daughter, and great-grand-daughter having transmitted it in a latent state. Hence we have, as Mr. Sedgwick remarks, a double kind of atavism or reversion; each grandson apparently receiving and developing the peculiarity from his grandfather, and each daughter apparently receiving the latent tendency from her grandmother.

From the various facts recorded by Dr. Prosper Lucas, Mr. Sedgwick, and others, there can be no doubt that peculiarities first appearing in either sex, though not in any way necessarily or invariably connected with that sex, strongly tend to be inherited by the offspring of the same sex, but are often transmitted in a latent state through the opposite sex.

Turning now to domesticated animals, we find that certain characters not proper to the parent species are often confined to, and inherited by, one sex alone; but we do not know the history of the first appearance of such characters. In the chapter on Sheep, we have seen that the males of certain races differ greatly from the females in the shape of their horns, these being absent in the ewes of some breeds; they differ also in the development of fat in the tail and in the outline of the forehead. These differences, judging from the character of the allied wild species, cannot be accounted for by supposing that they have been derived from distinct parent forms. There is, also, a great difference between the horns of the two sexes in one Indian breed of goats. The bull zebu is said to have a larger hump than the cow. In the Scotch deer-hound the two sexes differ in size more than in any other variety of the dog (14/28. W. Scrope 'Art of Deer Stalking' page 354.) and, judging from analogy, more than in the aboriginal parent-species. The peculiar colour called tortoise-shell is very rarely seen in a male cat; the males of this variety being of a rusty tint.

In various breeds of the fowl the males and females often differ greatly; and these differences are far from being the same with those which distinguish the two sexes of the parent-species, the Gallus bankiva; and consequently have originated under domestication. In certain sub-varieties of the Game race we have the unusual case of the hens differing from each other more than the cocks. In an Indian breed of a white colour shaded with black, the hens invariably have black skins, and their bones are covered by a black periosteum, whilst the cocks are never or most rarely thus characterised. Pigeons offer a more interesting case; for throughout the whole great family the two sexes do not often differ much; and the males and females of the parent-form, the C. livia, are undistinguishable: yet we have seen that with pouters the male has the characteristic quality of pouting more strongly developed than the female; and in certain sub-varieties the males alone are spotted or striated with black, or otherwise differ in colour. When male and female English carrier-pigeons are exhibited in separate pens, the difference in the development of the wattle over the beak and round the eyes is conspicuous. So that here we have instances of the appearance of secondary sexual characters in the domesticated races of a species in which such differences are naturally quite absent.]

On the other hand, secondary sexual characters which belong to the species in a state of nature are sometimes quite lost, or greatly diminished, under domestication. We see this in the small size of the tusks in our improved breeds of the pig, in comparison with those of the wild boar. There are sub- breeds of fowls, in which the males have lost the fine-flowing tail-feathers and hackles; and others in which there is no difference in colour between the two sexes. In some cases the barred plumage, which in gallinaceous birds is commonly the attribute of the hen, has been transferred to the cock, as in the cuckoo sub-breeds. In other cases masculine characters have been partly transferred to the female, as with the splendid plumage of the golden-spangled Hamburgh hen, the enlarged comb of the Spanish hen, the pugnacious disposition of the Game hen, and as in the well-developed spurs which occasionally appear in the hens of various breeds. In Polish fowls both sexes are ornamented with a topknot, that of the male being formed of hackle-like feathers, and this is a new male character in the genus Gallus. On the whole, as far as I can judge, new characters are more apt to appear in the males of our domesticated animals than in the females (14/29. I have given in my 'Descent of Man' 2nd edition page 223 sufficient evidence that male animals are usually more variable than the females.), and afterwards to be inherited exclusively or more strongly by the males. Finally, in accordance with the principle of inheritance as limited by sex, the preservation and augmentation of secondary sexual characters in natural species offers no especial difficulty, as this would follow through that form of selection which I have called sexual selection.

INHERITANCE AT CORRESPONDING PERIODS OF LIFE.

This is an important subject. Since the publication of my 'Origin of Species' I have seen no reason to doubt the truth of the explanation there given of one of the most remarkable facts in biology, namely, the difference between the embryo and the adult animal. The explanation is, that variations do not necessarily or generally occur at a very early period of embryonic growth, and that such variations are inherited at a corresponding age. As a consequence of this the embryo, even after the parent-form has undergone great modification, is left only slightly modified; and the embryos of widely-different animals which are descended from a common progenitor remain in many important respects like one another and probably like their common progenitor. We can thus understand why embryology throws a flood of light on the natural system of classification, as this ought to be as far as possible genealogical. When the embryo leads an independent life, that is, becomes a larva, it has to be adapted to the surrounding conditions in its structure and instincts, independently of those of its parents; and the principle of inheritance at corresponding periods of life renders this possible.

This principle is, indeed, in one way so obvious that it escapes attention. We possess a number of races of animals and plants, which, when compared with one another and with their parent-forms, present conspicuous differences, both in their immature and mature states. Look at the seeds of the several kinds of peas, beans, maize, which can be propagated truly, and see how they differ in size, colour, and shape, whilst the full-grown plants differ but little. Cabbages, on the other hand, differ greatly in foliage and manner of growth, but hardly at all in their seeds; and generally it will be found that the differences between cultivated plants at different periods of growth are not necessarily closely connected together, for plants may differ much in their seeds and little when full-grown, and conversely may yield seeds hardly distinguishable, yet differ much when full-grown. In the several breeds of poultry, descended from a single species, differences in the eggs and chickens whilst covered with down, in the plumage at the first and subsequent moults, as well as in the comb and wattles, are all inherited. With man peculiarities in the milk and second teeth (of which I have received the details) are inheritable, and longevity is often transmitted. So again with our improved breeds of cattle and sheep, early maturity, including the early development of the teeth, and with certain breeds of fowl the early appearance of secondary sexual characters, all come under the same head of inheritance at corresponding periods.

Numerous analogous facts could be given. The silk-moth, perhaps, offers the best instance; for in the breeds which transmit their characters truly, the eggs differ in size, colour, and shape: the caterpillars differ, in moulting three or four times, in colour, even in having a dark-coloured mark like an eyebrow, and in the loss of certain instincts; — the cocoons differ in size, shape, and in the colour and quality of the silk; these several differences being followed by slight or barely distinguishable differences in the mature moth.

But it may be said that, if in the above cases a new peculiarity is inherited, it must be at the corresponding stage of development; for an egg or seed can resemble only an egg or seed, and the horn in a full-grown ox can resemble only a horn. The following cases show inheritance at corresponding periods more plainly, because they refer to peculiarities which might have supervened, as far as we can see, earlier or later in life, yet are inherited at the same period at which they first appeared.

[In the Lambert family the porcupine-like excrescences appeared in the father and sons at the same age, namely, about nine weeks after birth. (14/30. Prichard 'Phys. Hist. of Mankind' 1851 volume 1 page 349.) In the extraordinary hairy family described by Mr. Crawfurd (14/31. 'Embassy to the Court of Ava' volume 1 page 320. The third generation is described by Capt. Yule in his 'Narrative of the Mission to the Court of Ava' 1855 page 94.), children were produced during three generations with hairy ears; in the father the hair began to grow over his body at six years old; in his daughter somewhat earlier, namely, at one year; and in both generations the milk teeth appeared late in life, the permanent teeth being afterwards singularly deficient. Greyness of hair at an unusually early age has been transmitted in some families. These cases border on diseases inherited at corresponding periods of life, to which I shall immediately refer.

It is a well-known peculiarity with almond-tumbler pigeons, that the full beauty and peculiar character of the plumage does not appear until the bird has moulted two or three times. Neumeister describes and figures a brace of pigeons in which the whole body is white except the breast, neck, and head; but in their first plumage all the white feathers have coloured edges. Another breed is more remarkable: its first plumage is black, with rusty-red wing-bars and a crescent-shaped mark on the breast; these marks then become white, and remain so during three or four moults; but after this period the white spreads over the body, and the bird loses its beauty. (14/32. 'Das Ganze der Taubenzucht' 1837 s. 24 tab. 4 figure 2 s. 21 tab. 1 figure 4.) Prize canary- birds have their wings and tail black: "this colour, however, is only retained until the first moult, so that they must be exhibited ere the change takes place. Once moulted, the peculiarity has ceased. Of course all the birds emanating from this stock have black wings and tails the first year." (14/33. Kidd 'Treatise on the Canary' page 18.) A curious and somewhat analogous account has been given (14/34. Charlesworth 'Mag. of Nat. Hist.' volume 1 1837 page 167.) of a family of wild pied rooks which were first observed in 1798, near Chalfont, and which every year from that date up to the period of the published notice, viz., 1837 "have several of their brood particoloured, black and white. This variegation of the plumage, however, disappears with the first moult; but among the next young families there are always a few pied ones." These changes of plumage, which are inherited at various corresponding periods of life in the pigeon, canary-bird, and rook, are remarkable, because the parent-species passes through no such change.