The Variation of Animals and Plants under Domestication — Volume 2

How many generations are necessary for one species or race to absorb another by repeated crosses has often been discussed (15/9. Sturm 'Ueber Racen, etc.' 1825 s. 107. Bronn 'Geschichte der Natur' b. 2 s. 170 gives a table of the proportions of blood after successive crosses. Dr. P. Lucas 'L'Heredite Nat.' tome 2 page 308.); and the requisite number has probably been much exaggerated. Some writers have maintained that a dozen or score, or even more generations, are necessary; but this in itself is improbable, for in the tenth generation there would be only 1-1024th part of foreign blood in the offspring. Gartner found (15/10. 'Bastarderzeugung' s. 463, 470.), that with plants, one species could be made to absorb another in from three to five generations, and he believes that this could always be effected in from six to seven generations. In one instance, however, Kolreuter (15/11. 'Nova Acta Petrop.' 1794 page 393: see also previous volume.) speaks of the offspring of Mirabilis vulgaris, crossed during eight successive generations by M. longiflora, as resembling this latter species so closely, that the most scrupulous observer could detect "vix aliquam notabilem differentiam" or, as he says, he succeeded, "ad plenariam fere transmutationem." But this expression shows that the act of absorption was not even then absolutely complete, though these crossed plants contained only the 1-256th part of M. vulgaris. The conclusions of such accurate observers as Gartner and Kolreuter are of far higher worth than those made without scientific aim by breeders. The most precise account which I have met with is given by Stonehenge (15/12. 'The Dog' 1867 pages 179-184.) and is illustrated by photographs. Mr. Hanley crossed a greyhound bitch with a bulldog; the offspring in each succeeding generation being recrossed with first-rate greyhounds. As Stonehenge remarks, it might naturally be supposed that it would take several crosses to get rid of the heavy form of the bulldog; but Hysterics, the gr-gr-granddaughter of a bulldog, showed no trace whatever of this breed in external form. She and all of the same litter, however, were "remarkably deficient in stoutness, though fast as well as clever." I believe clever refers to skill in turning. Hysterics was put to a son of Bedlamite, "but the result of the fifth cross is not as yet, I believe, more satisfactory than that of the fourth." On the other hand, with sheep, Fleischmann (15/13. As quoted in the 'True Principles of Breeding' by C.H. Macknight and Dr. H. Madden 1865 page 11.) shows how persistent the effects of a single cross may be: he says "that the original coarse sheep (of Germany) have 5500 fibres of wool on a square inch; grades of the third or fourth Merino cross produced about 8000, the twentieth cross 27,000, the perfect pure Merino blood 40,000 to 48,000." So that common German sheep crossed twenty times successively with Merino did not by any means acquire wool as fine as that of the pure breed. But in all cases, the rate of absorption will depend largely on the conditions of life being favourable to any particular character; and we may suspect that there would be a constant tendency to degeneration in the wool of Merinos under the climate of Germany, unless prevented by careful selection; and thus perhaps the foregoing remarkable case may be explained. The rate of absorption must also depend on the amount of distinguishable difference between the two forms which are crossed, and especially, as Gartner insists, on prepotency of transmission in the one form over the other. We have seen in the last chapter that one of two French breeds of sheep yielded up its character, when crossed with Merinos, very much more slowly than the other; and the common German sheep referred to by Fleischmann may be in this respect analogous. In all cases there will be more or less liability to reversion during many subsequent generations, and it is this fact which has probably led authors to maintain that a score or more of generations are requisite for one race to absorb another. In considering the final result of the commingling of two or more breeds, we must not forget that the act of crossing in itself tends to bring back long-lost characters not proper to the immediate parent-forms.

With respect to the influence of the conditions of life on any two breeds which are allowed to cross freely, unless both are indigenous and have long been accustomed to the country where they live, they will, in all probability, be unequally affected by the conditions, and this will modify the result. Even with indigenous breeds, it will rarely or never occur that both are equally well adapted to the surrounding circumstances; more especially when permitted to roam freely, and not carefully tended, as is generally the case with breeds allowed to cross. As a consequence of this, natural selection will to a certain extent come into action, and the best fitted will survive, and this will aid in determining the ultimate character of the commingled body.

How long a time it would require before such a crossed body of animals would assume a uniform character within a limited area, no one can say; that they would ultimately become uniform from free intercrossing, and from the survival of the fittest, we may feel assured; but the characters thus acquired would rarely or never, as may be inferred from the previous considerations, be exactly intermediate between those of the two parent-breeds. With respect to the very slight differences by which the individuals of the same sub-variety, or even of allied varieties, are characterised, it is obvious that free crossing would soon obliterate such small distinctions. The formation of new varieties, independently of selection, would also thus be prevented; except when the same variation continually recurred from the action of some strongly predisposing cause. We may therefore conclude that free crossing has in all cases played an important part in giving uniformity of character to all the members of the same domestic race and of the same natural species, though largely governed by natural selection and by the direct action of the surrounding conditions.

ON THE POSSIBILITY OF ALL ORGANIC BEINGS OCCASIONALLY INTERCROSSING.

But it may be asked, can free crossing occur with hermaphrodite animals and plants? All the higher animals, and the few insects which have been domesticated, have separate sexes, and must inevitably unite for each birth. With respect to the crossing of hermaphrodites, the subject is too large for the present volume, but in the 'Origin of Species' I have given a short abstract of the reasons which induce me to believe that all organic beings occasionally cross, though perhaps in some cases only at long intervals of time. (15/14. With respect to plants, an admirable essay on this subject (Die Geschlechter-Vertheilung bei den Pflanzen: 1867) has been published by Dr. Hildebrand who arrives at the same general conclusions as I have done. Various other treatises have since appeared on the same subject, more especially by Hermann Muller and Delpino.) I will merely recall the fact that many plants, though hermaphrodite in structure, are unisexual in function; — such as those called by C.K. Sprengel DICHOGAMOUS, in which the pollen and stigma of the same flower are matured at different periods; or those called by me RECIPROCALLY DIMORPHIC, in which the flower's own pollen is not fitted to fertilise its own stigma; or again, the many kinds in which curious mechanical contrivances exist, effectually preventing self-fertilisation. There are, however, many hermaphrodite plants which are not in any way specially constructed to favour intercrossing, but which nevertheless commingle almost as freely as animals with separated sexes. This is the case with cabbages, radishes, and onions, as I know from having experimented on them: even the peasants of Liguria say that cabbages must be prevented "from falling in love" with each other. In the orange tribe, Gallesio (15/15. 'Teoria della Riproduzione Vegetal' 1816 page 12.) remarks that the amelioration of the various kinds is checked by their continual and almost regular crossing. So it is with numerous other plants.

On the other hand, some cultivated plants rarely or never intercross, for instance, the common pea and sweet-pea (Lathyrus odoratus); yet their flowers are certainly adapted for cross fertilisation. The varieties of the tomato and aubergine (Solanum) and the pimenta (Pimenta vulgaris?) are said (15/16. Verlot 'Des Varietes' 1865 page 72.) never to cross, even when growing alongside one another. But it should be observed that these are all exotic plants, and we do not know how they would behave in their native country when visited by the proper insects. With respect to the common pea, I have ascertained that it is rarely crossed in this country owing to premature fertilisation. There exist, however, some plants which under their natural conditions appear to be always self-fertilised, such as the Bee Ophrys (Ophrys apifera) and a few other Orchids; yet these plants exhibit the plainest adaptations for cross-fertilisation. Again, some few plants are believed to produce only closed flowers, called cleistogene, which cannot possibly be crossed. This was long thought to be the case with the Leersia oryzoides (15/17. Duval Jouve 'Bull. Soc. Bot. de France' tome 10 1863 page 194. With respect to the perfect flowers setting seed see Dr. Ascherson in 'Bot. Zeitung' 1864 page 350.), but this grass is now known occasionally to produce perfect flowers, which set seed.

Although some plants, both indigenous and naturalised, rarely or never produce flowers, or if they flower never produce seeds, yet no one doubts that phanerogamic plants are adapted to produce flowers, and the flowers to produce seed. When they fail, we believe that such plants under different conditions would perform their proper function, or that they formerly did so, and will do so again. On analogous grounds, I believe that the flowers in the above specified anomalous cases which do not now intercross, either would do so occasionally under different conditions, or that they formerly did so — the means for affecting this being generally still retained — and will again intercross at some future period, unless indeed they become extinct. On this view alone, many points in the structure and action of the reproductive organs in hermaphrodite plants and animals are intelligible, — for instance, the fact of the male and female organs never being so completely enclosed as to render access from without impossible. Hence we may conclude that the most important of all the means for giving uniformity to the individuals of the same species, namely, the capacity of occasionally intercrossing, is present, or has been formerly present, with all organic beings, except, perhaps, some of the lowest.

[ON CERTAIN CHARACTERS NOT BLENDING.

When two breeds are crossed their characters usually become intimately fused together; but some characters refuse to blend, and are transmitted in an unmodified state either from both parents or from one. When grey and white mice are paired, the young are piebald, or pure white or grey, but not of an intermediate tint; so it is when white and common collared turtle-doves are paired. In breeding Game fowls, a great authority, Mr. J. Douglas, remarks, "I may here state a strange fact: if you cross a black with a white game, you get birds of both breeds of the clearest colour." Sir R. Heron crossed during many years white, black, brown, and fawn-coloured Angora rabbits, and never once got these colours mingled in the same animal, but often all four colours in the same litter. (15/18. Extract of a letter from Sir R. Heron 1838 given me by Mr. Yarrell. With respect to mice see 'Annal. des Sc. Nat.' tome 1 page 180; and I have heard of other similar cases. For turtle-doves Boitard and Corbie 'Les Pigeons' etc. page 238. For the Game fowl 'The Poultry Book' 1866 page 128. For crosses of tailless fowls see Bechstein 'Naturges. Deutsch.' b. 3 s. 403. Bronn 'Geschichte der Natur' b. 2 s. 170 gives analogous facts with horses. On the hairless condition of crossed South American dogs see Rengger 'Saugethiere von Paraguay' s. 152; but I saw in the Zoological Gardens mongrels, from a similar cross, which were hairless, quite hairy, or hairy in patches, that is, piebald with hair. For crosses of Dorking and other fowls see 'Poultry Chronicle' volume 2 page 355. About the crossed pigs, extract of letter from Sir R. Heron to Mr. Yarrell. For other cases see P. Lucas 'L'Hered. Nat.' tome 1 page 212.) From cases like these, in which the colours of the two parents are transmitted quite separately to the offspring, we have all sorts of gradations, leading to complete fusion. I will give an instance: a gentleman with a fair complexion, light hair but dark eyes, married a lady with dark hair and complexion: their three children have very light hair, but on careful search about a dozen black hairs were found scattered in the midst of the light hair on the heads of all three.

When turnspit dogs and ancon sheep, both of which have dwarfed limbs, are crossed with common breeds, the offspring are not intermediate in structure, but take after either parent. When tailless or hornless animals are crossed with perfect animals, it frequently, but by no means invariably, happens that the offspring are either furnished with these organs in a perfect state, or are quite destitute of them. According to Rengger, the hairless condition of the Paraguay dog is either perfectly or not at all transmitted to its mongrel offspring; but I have seen one partial exception in a dog of this parentage which had part of its skin hairy, and part naked, the parts being distinctly separated as in a piebald animal. When Dorking fowls with five toes are crossed with other breeds, the chickens often have five toes on one foot and four on the other. Some crossed pigs raised by Sir R. Heron between the solid- hoofed and common pig had not all four feet in an intermediate condition, but two feet were furnished with properly divided, and two with united hoofs.

Analogous facts have been observed with plants: Major Trevor Clarke crossed the little, glabrous-leaved, annual stock (Matthiola), with pollen of a large, red-flowered, rough-leaved, biennial stock, called cocardeau by the French, and the result was that half the seedlings had glabrous and the other half rough leaves, but none had leaves in an intermediate state. That the glabrous seedlings were the product of the rough-leaved variety, and not accidentally of the mother-plant's own pollen, was shown by their tall and strong habit of growth. (15/19. 'Internat. Hort. and Bot. Congress of London' 1866.) in the succeeding generations raised from the rough-leaved crossed seedlings, some glabrous plants appeared, showing that the glabrous character, though incapable of blending with and modifying the rough leaves, was all the time latent in this family of plants. The numerous plants formerly referred to, which I raised from reciprocal crosses between the peloric and common Antirrhinum, offer a nearly parallel case; for in the first generation all the plants resembled the common form, and in the next generation, out of one hundred and thirty-seven plants, two alone were in an intermediate condition, the others perfectly resembling either the peloric or common form. Major Trevor Clarke also fertilised the above-mentioned red-flowered stock with pollen from the purple Queen stock, and about half the seedlings scarcely differed in habit, and not at all in the red colour of the flower, from the mother-plant, the other half bearing blossoms of a rich purple, closely like those of the paternal plant. Gartner crossed many white and yellow-flowered species and varieties of Verbascum; and these colours were never blended, but the offspring bore either pure white or pure yellow blossoms; the former in the larger proportion. (15/20. 'Bastarderzeugung' s. 307. Kolreuter 'Dritte Fortsetszung' s. 34, 39 however, obtained intermediate tints from similar crosses in the genus Verbascum. With respect to the turnips see Herbert 'Amaryllidaceae' 1837 page 370.) Dr. Herbert raised many seedlings, as he informed me, from Swedish turnips crossed by two other varieties, and these never produced flowers of an intermediate tint, but always like one of their parents. I fertilised the purple sweet-pea (Lathyrus odoratus), which has a dark reddish-purple standard-petal and violet-coloured wings and keel, with pollen of the painted lady sweet-pea, which has a pale cherry-coloured standard, and almost white wings and keel; and from the same pod I twice raised plants perfectly resembling both sorts; the greater number resembling the father. So perfect was the resemblance, that I should have thought there had been some mistake, if the plants which were at first identical with the paternal variety, namely, the painted-lady, had not later in the season produced, as mentioned in a former chapter, flowers blotched and streaked with dark purple. I raised grandchildren and great-grandchildren from these crossed plants, and they continued to resemble the painted-lady, but during later generations became rather more blotched with purple, yet none reverted completely to the original mother-plant, the purple sweet-pea. The following case is slightly different, but still shows the same principle: Naudin (15/21. 'Nouvelles Archives du Museum' tome 1 page 100.) raised numerous hybrids between the yellow Linaria vulgaris and the purple L. purpurea, and during three successive generations the colours kept distinct in different parts of the same flower.

From cases such as the foregoing, in which the offspring of the first generation perfectly resemble either parent, we come by a small step to those cases in which differently coloured flowers borne on the same root resemble both parents, and by another step to those in which the same flower or fruit is striped or blotched with the two parental colours, or bears a single stripe of the colour or other characteristic quality of one of the parent-forms. With hybrids and mongrels it frequently or even generally happens that one part of the body resembles more or less closely one parent and another part the other parent; and here again some resistence to fusion, or, what comes to the same thing, some mutual affinity between the organic atoms of the same nature, apparently comes into play, for otherwise all parts of the body would be equally intermediate in character. So again, when the offspring of hybrids or mongrels, which are themselves nearly intermediate in character, revert either wholly or by segments to their ancestors, the principle of the affinity of similar, or the repulsion of dissimilar atoms, must come into action. To this principle, which seems to be extremely general, we shall recur in the chapter on pangenesis.

It is remarkable, as has been strongly insisted upon by Isidore Geoffroy St. Hilaire in regard to animals, that the transmission of characters without fusion occurs very rarely when species are crossed; I know of one exception alone, namely, with the hybrids naturally produced between the common and hooded crow (Corvus corone and cornix), which, however, are closely allied species, differing in nothing except colour. Nor have I met with any well- ascertained cases of transmission of this kind, even when one form is strongly prepotent over another, when two races are crossed which have been slowly formed by man's selection, and therefore resemble to a certain extent natural species. Such cases as puppies in the same litter closely resembling two distinct breeds, are probably due to superfoetation, — that is, to the influence of two fathers. All the characters above enumerated, which are transmitted in a perfect state to some of the offspring and not to others, — such as distinct colours, nakedness of skin, smoothness of leaves, absence of horns or tail, additional toes, pelorism, dwarfed structure, etc., — have all been known to appear suddenly in individual animals and plants. From this fact, and from the several slight, aggregated differences which distinguish domestic races and species from one another, not being liable to this peculiar form of transmission, we may conclude that it is in some way connected with the sudden appearance of the characters in question.]

ON THE MODIFICATION OF OLD RACES AND THE FORMATION OF NEW RACES BY CROSSING.

We have hitherto chiefly considered the effects of crossing in giving uniformity of character; we must now look to an opposite result. There can be no doubt that crossing, with the aid of rigorous selection during several generations, has been a potent means in modifying old races, and in forming new ones. Lord Orford crossed his famous stud of greyhounds once with the bulldog, in order to give them courage and perseverance. Certain pointers have been crossed, as I hear from the Rev. W.D. Fox, with the foxhound, to give them dash and speed. Certain strains of Dorking fowls have had a slight infusion of Game blood; and I have known a great fancier who on a single occasion crossed his turbit-pigeons with barbs, for the sake of gaining greater breadth of beak.

In the foregoing cases breeds have been crossed once, for the sake of modifying some particular character; but with most of the improved races of the pig, which now breed true, there have been repeated crosses, — for instance, the improved Essex owes its excellence to repeated crosses with the Neapolitan, together probably with some infusion of Chinese blood. (15/22. Richardson 'Pigs' 1847 pages 37, 42; S. Sidney's edition of 'Youatt on the Pig' 1860 page 3.) So with our British sheep: almost all the races, except the Southdown, have been largely crossed; "this, in fact, has been the history of our principal breeds." (15/23. See Mr. W.C. Spooner's excellent paper on Cross-Breeding 'Journal Royal Agricult. Soc.' volume 20 part 2: see also an equally good article by Mr. Ch. Howard in 'Gardener's Chronicle' 1860 page 320.) To give an example, the "Oxfordshire Downs" now rank as an established breed. (15/24. 'Gardener's Chronicle' 1857 pages 649, 652.) They were produced about the year 1830 by crossing "Hampshire and in some instances Southdown ewes with Cotswold rams: " now the Hampshire ram was itself produced by repeated crosses between the native Hampshire sheep and Southdowns; and the long-woolled Cotswold were improved by crosses with the Leicester, which latter again is believed to have been a cross between several long-woolled sheep. Mr. Spooner, after considering the various cases which have been carefully recorded, concludes, "that from a judicious pairing of cross-bred animals it is practicable to establish a new breed." On the continent the history of several crossed races of cattle and of other animals has been well ascertained. To give one instance: the King of Wurtemburg, after twenty-five years' careful breeding, that is, after six or seven generations, made a new breed of cattle from a cross between a Dutch and a Swiss breed, combined with other breeds. (15/25. 'Bulletin de La Soc. d'Acclimat.' 1862 tome 9 page 463. See also for other cases MM. Moll and Gayot 'Du Boeuf' 1860 page 32.) The Sebright bantam, which breeds as true as any other kind of fowl, was formed about sixty years ago by a complicated cross. (15/26. 'Poultry Chronicle' volume 2 1854 page 36.) Dark Brahmas, which are believed by some fanciers to constitute a distinct species, were undoubtedly formed (15/27. 'The Poultry Book' by W.B. Tegetmeier 1866 page 58.) in the United States, within a recent period, by a cross between Chittagongs and Cochins. With plants there is little doubt that the Swede-turnip originated from a cross; and the history of a variety of wheat, raised from two very distinct varieties, and which after six years' culture presented an even sample, has been recorded on good authority. (15/28. 'Gardener's Chronicle' 1852 page 765.)

Until lately, cautious and experienced breeders, though not averse to a single infusion of foreign blood, were almost universally convinced that the attempt to establish a new race, intermediate between two widely distinct races, was hopeless "they clung with superstitious tenacity to the doctrine of purity of blood, believing it to be the ark in which alone true safety could be found." (15/29. Spooner in 'Journal Royal Agricult. Soc.' volume 20 part 2) Nor was this conviction unreasonable: when two distinct races are crossed, the offspring of the first generation are generally nearly uniform in character; but even this sometimes fails to be the case, especially with crossed dogs and fowls, the young of which from the first are sometimes much diversified. As cross-bred animals are generally of large size and vigorous, they have been raised in great numbers for immediate consumption. But for breeding they are found utterly useless; for though they may themselves be uniform in character, they yield during many generations astonishingly diversified offspring. The breeder is driven to despair, and concludes that he will never form an intermediate race. But from the cases already given, and from others which have been recorded, it appears that patience alone is necessary; as Mr. Spooner remarks, "nature opposes no barrier to successful admixture; in the course of time, by the aid of selection and careful weeding, it is practicable to establish a new breed." After six or seven generations the hoped-for result will in most cases be obtained; but even then an occasional reversion, or failure to keep true, may be expected. The attempt, however, will assuredly fail if the conditions of life be decidedly unfavourable to the characters of either parent-breed. (15/30. See Colin 'Traite de Phys. Comp. des Animaux Domestiques' tome 2 page 536, where this subject is well treated.)