Some characters not proper to the parent-species have certainly been inherited from an extremely remote epoch, and may therefore be considered as firmly fixed. But it is doubtful whether length of inheritance in itself gives fixedness of character; though the chances are obviously in favour of any character which has long been transmitted true or unaltered still being transmitted true as long as the conditions of life remain the same. We know that many species, after having retained the same character for countless ages, whilst living under their natural conditions, when domesticated have varied in the most diversified manner, that is, have failed to transmit their original form; so that no character appears to be absolutely fixed. We can sometimes account for the failure of inheritance by the conditions of life being opposed to the development of certain characters; and still oftener, as with plants cultivated by grafts and buds, by the conditions causing new and slight modifications incessantly to appear. In this latter case it is not that inheritance wholly fails, but that new characters are continually superadded. In some few cases, in which both parents are similarly characterised, inheritance seems to gain so much force by the combined action of the two parents, that it counteracts its own power, and a new modification is the result.
In many cases the failure of the parents to transmit their likeness is due to the breed having been at some former period crossed; and the child takes after his grandparent or more remote ancestor of foreign blood. In other cases, in which the breed has not been crossed, but some ancient character has been lost through variation, it occasionally reappears through reversion, so that the parents apparently fail to transmit their own likeness. In all cases, however, we may safely conclude that the child inherits all its characters from its parents, in whom certain characters are latent, like the secondary sexual characters of one sex in the other. When, after a long succession of bud- generations, a flower or fruit becomes separated into distinct segments, having the colours or other attributes of both parent-forms, we cannot doubt that these characters were latent in the earlier buds, though they could not then be detected, or could be detected only in an intimately commingled state. So it is with animals of crossed parentage, which with advancing years occasionally exhibit characters derived from one of their two parents, of which not a trace could at first be perceived. Certain monstrosities, which resemble what naturalists call the typical form of the group in question, apparently come under the same law of reversion. It is assuredly an astonishing fact that the male and female sexual elements, that buds, and even full-grown animals, should retain characters, during several generations in the case of crossed breeds, and during thousands of generations in the case of pure breeds, written as it were in invisible ink, yet ready at any time to be evolved under certain conditions.
What these conditions precisely are, we do not know. But any cause which disturbs the organisation or constitution seems to be sufficient. A cross certainly gives a strong tendency to the reappearance of long-lost characters, both corporeal and mental. In the case of plants, this tendency is much stronger with those species which have been crossed after long cultivation and which therefore have had their constitutions disturbed by this cause as well as by crossing, than with species which have always lived under their natural conditions and have then been crossed. A return, also, of domesticated animals and cultivated plants to a wild state favours reversion; but the tendency under these circumstances has been much exaggerated.
When individuals of the same family which differ somewhat, and when races or species are crossed, the one is often prepotent over the other in transmitting its character. A race may possess a strong power of inheritance, and yet when crossed, as we have seen with trumpeter-pigeons, yield to the prepotency of every other race. Prepotency of transmission may be equal in the two sexes of the same species, but often runs more strongly in one sex. It plays an important part in determining the rate at which one race can be modified or wholly absorbed by repeated crosses with another. We can seldom tell what makes one race or species prepotent over another; but it sometimes depends on the same character being present and visible in one parent, and latent or potentially present in the other.
Characters may first appear in either sex, but oftener in the male than in the female, and afterwards be transmitted to the offspring of the same sex. In this case we may feel confident that the peculiarity in question is really present though latent in the opposite sex! hence the father may transmit through his daughter any character to his grandson; and the mother conversely to her granddaughter. We thus learn, and the fact is an important one, that transmission and development are distinct powers. Occasionally these two powers seem to be antagonistic, or incapable of combination in the same individual; for several cases have been recorded in which the son has not directly inherited a character from his father, or directly transmitted it to his son, but has received it by transmission through his non-affected mother, and transmitted it through his non-affected daughter. Owing to inheritance being limited by sex, we see how secondary sexual characters may have arisen under nature; their preservation and accumulation being dependent on their service to either sex.
At whatever period of life a new character first appears, it generally remains latent in the offspring until a corresponding age is attained, and then is developed. When this rule fails, the child generally exhibits the character at an earlier period than the parent. On this principle of inheritance at corresponding periods, we can understand how it is that most animals display from the germ to maturity such a marvellous succession of characters.
Finally, though much remains obscure with respect to Inheritance, we may look at the following laws as fairly well established.
FIRSTLY, a tendency in every character, new and old, to be transmitted by seminal and bud generation, though often counteracted by various known and unknown causes.
SECONDLY, reversion or atavism, which depends on transmission and development being distinct powers: it acts in various degrees and manners through both seminal and bud generation.
THIRDLY, prepotency of transmission, which may be confined to one sex, or be common to both sexes.
FOURTHLY, transmission, as limited by sex, generally to the same sex in which the inherited character first appeared; and this in many, probably most cases, depends on the new character having first appeared at a rather late period of life.
FIFTHLY, inheritance at corresponding periods of life, with some tendency to the earlier development of the inherited character.
In these laws of Inheritance, as displayed under domestication, we see an ample provision for the production, through variability and natural selection, of new specific forms.
CHAPTER 2.XV.
ON CROSSING.
FREE INTERCROSSING OBLITERATES THE DIFFERENCES BETWEEN ALLIED BREEDS. WHEN THE NUMBERS OF TWO COMMINGLING BREEDS ARE UNEQUAL, ONE ABSORBS THE OTHER. THE RATE OF ABSORPTION DETERMINED BY PREPOTENCY OF TRANSMISSION, BY THE CONDITIONS OF LIFE, AND BY NATURAL SELECTION. ALL ORGANIC BEINGS OCCASIONALLY INTERCROSS; APPARENT EXCEPTIONS. ON CERTAIN CHARACTERS INCAPABLE OF FUSION; CHIEFLY OR EXCLUSIVELY THOSE WHICH HAVE SUDDENLY APPEARED IN THE INDIVIDUAL. ON THE MODIFICATION OF OLD RACES, AND THE FORMATION OF NEW RACES BY CROSSING. SOME CROSSED RACES HAVE BRED TRUE FROM THEIR FIRST PRODUCTION. ON THE CROSSING OF DISTINCT SPECIES IN RELATION TO THE FORMATION OF DOMESTIC RACES.
In the two previous chapters, when discussing reversion and prepotency, I was necessarily led to give many facts on crossing. In the present chapter I shall consider the part which crossing plays in two opposed directions,—firstly, in obliterating characters, and consequently in preventing the formation of new races; and secondly, in the modification of old races, or in the formation of new and intermediate races, by a combination of characters. I shall also show that certain characters are incapable of fusion.
The effects of free or uncontrolled breeding between the members of the same variety or of closely allied varieties are important; but are so obvious that they need not be discussed at much length. It is free intercrossing which chiefly gives uniformity, both under nature and under domestication, to the individuals of the same species or variety, when they live mingled together and are not exposed to any cause inducing excessive variability. The prevention of free crossing, and the intentional matching of individual animals, are the corner-stones of the breeder's art. No man in his senses would expect to improve or modify a breed in any particular manner, or keep an old breed true and distinct, unless he separated his animals. The killing of inferior animals in each generation comes to the same thing as their separation. In savage and semi-civilised countries, where the inhabitants have not the means of separating their animals, more than a single breed of the same species rarely or never exists. In former times, even in the United States, there were no distinct races of sheep, for all had been mingled together. (15/1. 'Communications to the Board of Agriculture' volume 1 page 367.) The celebrated agriculturist Marshall (15/2. 'Review of Reports, North of England' 1808 page 200.) remarks that "sheep that are kept within fences, as well as shepherded flocks in open countries, have generally a similarity, if not a uniformity, of character in the individuals of each flock;" for they breed freely together, and are prevented from crossing with other kinds; whereas in the unenclosed parts of England the unshepherded sheep, even of the same flock, are far from true or uniform, owing to various breeds having mingled and crossed. We have seen that the half-wild cattle in each of the several British parks are nearly uniform in character; but in the different parks, from not having mingled and crossed during many generations, they differ to a certain small extent.
We cannot doubt that the extraordinary number of varieties and sub-varieties of the pigeon, amounting to at least one hundred and fifty, is partly due to their remaining, differently from other domesticated birds, paired for life once matched. On the other hand, breeds of cats imported into this country soon disappear, for their nocturnal and rambling habits render it hardly possible to prevent free crossing. Rengger (15/3. 'Saugethiere von Paraguay' 1830 s. 212.) gives an interesting case with respect to the cat in Paraguay: in all the distant parts of the kingdom it has assumed, apparently from the effects of the climate, a peculiar character, but near the capital this change has been prevented, owing, as he asserts, to the native animal frequently crossing with cats imported from Europe. In all cases like the foregoing, the effects of an occasional cross will be augmented by the increased vigour and fertility of the crossed offspring, of which fact evidence will hereafter be given; for this will lead to the mongrels increasing more rapidly than the pure parent-breeds.
When distinct breeds are allowed to cross freely, the result will be a heterogeneous body; for instance, the dogs in Paraguay are far from uniform, and can no longer be affiliated to their parent-races. (15/4. Rengger 'Saugethiere' etc. s. 154.) The character which a crossed body of animals will ultimately assume must depend on several contingencies,—namely, on the relative members of the individuals belonging to the two or more races which are allowed to mingle; on the prepotency of one race over the other in the transmission of character; and on the conditions of life to which they are exposed. When two commingled breeds exist at first in nearly equal numbers, the whole will sooner or later become intimately blended, but not so soon, both breeds being equally favoured in all respects, as might have been expected. The following calculation (15/5. White 'Regular Gradation in Man' page 146.) shows that this is the case: if a colony with an equal number of black and white men were founded, and we assume that they marry indiscriminately, are equally prolific, and that one in thirty annually dies and is born; then "in 65 years the number of blacks, whites, and mulattoes would be equal. In 91 years the whites would be 1-10th, the blacks 1-10th, and the mulattoes, or people of intermediate degrees of colour, 8-10ths of the whole number. In three centuries not 1-100th part of the whites would exist."
When one of two mingled races exceed the other greatly in number, the latter will soon be wholly, or almost wholly, absorbed and lost. (15/6. Dr. W.F. Edwards in his 'Caracteres Physiolog. des Races Humaines' page 24 first called attention to this subject, and ably discussed it.) Thus European pigs and dogs have been largely introduced in the islands of the Pacific Ocean, and the native races have been absorbed and lost in the course of about fifty or sixty years (15/7. Rev. D. Tyerman and Bennett 'Journal of Voyages' 1821-1829 volume 1 page 300.); but the imported races no doubt were favoured. Rats may be considered as semi-domesticated animals. Some snake-rats (Mus alexandrinus) escaped in the Zoological Gardens of London "and for a long time afterwards the keepers frequently caught cross-bred rats, at first half-breds, afterwards with less of the character of the snake-rat, till at length all traces of it disappeared." (15/8. Mr. S.J. Salter 'Journal Linn. Soc.' volume 6 1862 page 71.) On the other hand, in some parts of London, especially near the docks, where fresh rats are frequently imported, an endless variety of intermediate forms may be found between the brown, black, and snake rat, which are all three usually ranked as distinct species.
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.)
Although the grandchildren and succeeding generations of cross-bred animals are generally variable in an extreme degree, some curious exceptions to the rule have been observed both with crossed races and species. Thus Boitard and Corbie (15/31. 'Les Pigeons' page 37.) assert that from a Pouter and a Runt "a Cavalier will appear, which we have classed amongst pigeons of pure race, because it transmits all its qualities to its posterity." The editor of the 'Poultry Chronicle' (15/32. Volume 1 1854 page 101.) bred some bluish fowls from a black Spanish cock and a Malay hen; and these remained true to colour "generation after generation." The Himalayan breed of rabbits was certainly formed by crossing two sub-varieties of the silver-grey rabbit; although it suddenly assumed its present character, which differs much from that of either parent-breed, yet it has ever since been easily and truly propagated. I crossed some Labrador and Penguin ducks, and recrossed the mongrels with Penguins; afterwards most of the ducks reared during three generations were nearly uniform in character, being brown with a white crescentic mark on the lower part of the breast, and with some white spots at the base of the beak; so that by the aid of a little selection a new breed might easily have been formed. With regard to crossed varieties of plants, Mr. Beaton (15/33. 'Cottage Gardener' 1856 page 110.) remarks that "Melville's extraordinary cross between the Scotch kale and an early cabbage is as true and genuine as any on record;" but in this case no doubt selection was practised. Gartner (15/34. 'Bastarderzeugung' s. 553.) has given five cases of hybrids, in which the progeny kept constant; and hybrids between Dianthus armeria and deltoides remained true and uniform to the tenth generation. Dr. Herbert likewise showed me a hybrid from two species of Loasa which from its first production had kept constant during several generations.
We have seen in the first chapter, that the several kinds of dogs are almost certainly descended from more than one species, and so it is with cattle, pigs and some other domesticated animals. Hence the crossing of aboriginally distinct species probably came into play at an early period in the formation of our present races. From Rutimeyer's observations there can be little doubt that this occurred with cattle; but in most cases one form will probably have absorbed and obliterated the other, for it is not likely that semi-civilised men would have taken the necessary pains to modify by selection their commingled, crossed, and fluctuating stock. Nevertheless, those animals which were best adapted to their conditions of life would have survived through natural selection; and by this means crossing will often have indirectly aided in the formation of primeval domesticated breeds. Within recent times, as far as animals are concerned, the crossing of distinct species has done little or nothing towards the formation or modification of our races. It is not yet known whether the several species of silk-moth which have been recently crossed in France will yield permanent races. With plants which can be multiplied by buds and cuttings, hybridisation has done wonders, as with many kinds of Roses, Rhododendrons, Pelargoniums, Calceolarias, and Petunias. Nearly all these plants can be propagated by seed, most of them freely; but extremely few or none come true by seed.
Some authors believe that crossing is the chief cause of variability,—that is, of the appearance of absolutely new characters. Some have gone so far as to look at it as the sole cause; but this conclusion is disproved by the facts given in the chapter on Bud-variation. The belief that characters not present in either parent or in their ancestors frequently originate from crossing is doubtful; that they occasionally do so is probable; but this subject will be more conveniently discussed in a future chapter on the causes of Variability.
A condensed summary of this and of the three following chapters, together with some remarks on Hybridism, will be given in the nineteenth chapter.
CHAPTER 2.XVI.
CAUSES WHICH INTERFERE WITH THE FREE CROSSING OF VARIETIES—INFLUENCE OF DOMESTICATION ON FERTILITY.
DIFFICULTIES IN JUDGING OF THE FERTILITY OF VARIETIES WHEN CROSSED. VARIOUS CAUSES WHICH KEEP VARIETIES DISTINCT, AS THE PERIOD OF BREEDING AND SEXUAL PREFERENCE. VARIETIES OF WHEAT SAID TO BE STERILE WHEN CROSSED. VARIETIES OF MAIZE, VERBASCUM, HOLLYHOCK, GOURDS, MELONS, AND TOBACCO, RENDERED IN SOME DEGREE MUTUALLY STERILE. DOMESTICATION ELIMINATES THE TENDENCY TO STERILITY NATURAL TO SPECIES WHEN CROSSED. ON THE INCREASED FERTILITY OF UNCROSSED ANIMALS AND PLANTS FROM DOMESTICATION AND CULTIVATION.
The domesticated races of both animals and plants, when crossed, are, with extremely few exceptions, quite prolific,—in some cases even more so than the purely-bred parent-races. The offspring, also, raised from such crosses are likewise, as we shall see in the following chapter, generally more vigorous and fertile than their parents. On the other hand, species when crossed, and their hybrid offspring, are almost invariably in some degree sterile; and here there seems to exist a broad and insuperable distinction between races and species. The importance of this subject as bearing on the origin of species is obvious; and we shall hereafter recur to it.
It is unfortunate how few precise observations have been made on the fertility of mongrel animals and plants during several successive generations. Dr. Broca (16/1. 'Journal de Physiolog.' tome 2 1859 page 385.) has remarked that no one has observed whether, for instance, mongrel dogs, bred inter se, are indefinitely fertile; yet, if a shade of infertility be detected by careful observation in the offspring of natural forms when crossed, it is thought that their specific distinction is proved. But so many breeds of sheep, cattle, pigs, dogs, and poultry, have been crossed and recrossed in various ways, that any sterility, if it had existed, would from being injurious almost certainly have been observed. In investigating the fertility of crossed varieties many sources of doubt occur. Whenever the least trace of sterility between two plants, however closely allied, was observed by Kolreuter, and more especially by Gartner, who counted the exact number of seed in each capsule, the two forms were at once ranked as distinct species; and if this rule be followed, assuredly it will never be proved that varieties when crossed are in any degree sterile. We have formerly seen that certain breeds of dogs do not readily pair together; but no observations have been made whether, when paired, they produce the full number of young, and whether the latter are perfectly fertile inter se; but, supposing that some degree of sterility were found to exist, naturalists would simply infer that these breeds were descended from aboriginally distinct species; and it would be scarcely possible to ascertain whether or not this explanation was the true one.
The Sebright Bantam is much less prolific than any other breed of fowls, and is descended from a cross between two very distinct breeds, recrossed by a third sub-variety. But it would be extremely rash to infer that the loss of fertility was in any manner connected with its crossed origin, for it may with more probability be attributed either to long-continued close interbreeding, or to an innate tendency to sterility correlated with the absence of hackles and sickle tail-feathers.
Before giving the few recorded cases of forms, which must be ranked as varieties, being in some degree sterile when crossed, I may remark that other causes sometimes interfere with varieties freely intercrossing. Thus they may differ too greatly in size, as with some kinds of dogs and fowls: for instance, the editor of the 'Journal of Horticulture, etc.' (16/2. December 1863 page 484.) says that he can keep Bantams with the larger breeds without much danger of their crossing, but not with the smaller breeds, such as Games, Hamburghs, etc. With plants a difference in the period of flowering serves to keep varieties distinct, as with the various kinds of maize and wheat: thus Colonel Le Couteur (16/3. On 'The Varieties of Wheat' page 66.) remarks, "the Talavera wheat, from flowering much earlier than any other kind, is sure to continue pure." In different parts of the Falkland Islands the cattle are breaking up into herds of different colours; and those on the higher ground, which are generally white, usually breed, as I am informed by Sir J. Sulivan, three months earlier than those on the lowland; and this would manifestly tend to keep the herds from blending.
Certain domestic races seem to prefer breeding with their own kind; and this is a fact of some importance, for it is a step towards that instinctive feeling which helps to keep closely allied species in a state of nature distinct. We have now abundant evidence that, if it were not for this feeling, many more hybrids would be naturally produced than in this case. We have seen in the first chapter that the alco dog of Mexico dislikes dogs of other breeds; and the hairless dog of Paraguay mixes less readily with the European races, than the latter do with each other. In Germany the female Spitz-dog is said to receive the fox more readily than will other dogs; a female Australian Dingo in England attracted the wild male foxes. But these differences in the sexual instinct and attractive power of the various breeds may be wholly due to their descent from distinct species. In Paraguay the horses have much freedom, and an excellent observer (16/4. Rengger 'Saugethiere von Paraguay' s. 336.) believes that the native horses of the same colour and size prefer associating with each other, and that the horses which have been imported from Entre Rios and Banda Oriental into Paraguay likewise prefer associating together. In Circassia six sub-races of the horse have received distinct names; and a native proprietor of rank (16/5. See a memoir by MM. Lherbette and De Quatrefages in 'Bull. Soc. d'Acclimat.' tome 8 July 1861 page 312.) asserts that horses of three of these races, whilst living a free life, almost always refuse to mingle and cross, and will even attack one another.
It has been observed, in a district stocked with heavy Lincolnshire and light Norfolk sheep, that both kinds; though bred together, when turned out, "in a short time separate to a sheep;" the Lincolnshires drawing off to the rich soil, and the Norfolks to their own dry light soil; and as long as there is plenty of grass, "the two breeds keep themselves as distinct as rooks and pigeons." In this case different habits of life tend to keep the races distinct. On one of the Faroe islands, not more than half a mile in diameter, the half-wild native black sheep are said not to have readily mixed with the imported white sheep. It is a more curious fact that the semi-monstrous ancon sheep of modern origin "have been observed to keep together, separating themselves from the rest of the flock, when put into enclosures with other sheep." (16/6. For the Norfolk sheep see Marshall 'Rural Economy of Norfolk' volume 2 page 136. See Rev. L. Landt 'Description of Faroe' page 66. For the ancon sheep see 'Phil. Transact.' 1813 page 90.) With respect to fallow-deer, which live in a semi-domesticated condition, Mr. Bennett (16/7. White 'Nat. Hist. of Selbourne' edited by Bennett page 39. With respect to the origin of the dark-coloured deer see 'Some Account of English Deer Parks' by E.P. Shirley, Esq.) states that the dark and pale coloured herds, which have long been kept together in the Forest of Dean, in High Meadow Woods, and in the New Forest, have never been known to mingle: the dark-coloured deer, it may be added, are believed to have been first brought by James I. from Norway, on account of their greater hardiness. I imported from the island of Porto Santo two of the feral rabbits, which differ, as described in the fourth chapter, from common rabbits; both proved to be males, and, though they lived during some years in the Zoological Gardens, the superintendent, Mr. Bartlett, in vain endeavoured to make them breed with various tame kinds; but whether this refusal to breed was due to any change in the instinct, or simply to their extreme wildness, or whether confinement had rendered them sterile, as often occurs, cannot be determined.
Whilst matching for the sake of experiment many of the most distinct breeds of pigeons, it frequently appeared to me that the birds, though faithful to their marriage vow, retained some desire after their own kind. Accordingly I asked Mr. Wicking, who has kept a larger stock of various breeds together than any man in England, whether he thought that they would prefer pairing with their own kind, supposing that there were males and females enough of each; and he without hesitation answered that he was convinced that this was the case. It has often been noticed that the dovecote pigeon seems to have an actual aversion towards the several fancy breeds (16/8. 'The Dovecote' by the Rev. E.S. Dixon page 155; Bechstein 'Naturgesch. Deutschlands' b. 4 1795 page 17.) yet all have certainly sprung from a common progenitor. The Rev. W.D. Fox informs me that his flocks of white and common Chinese geese kept distinct.
These facts and statements, though some of them are incapable of proof, resting only on the opinion of experienced observers, show that some domestic races are led by different habits of life to keep to a certain extent separate, and that others prefer coupling with their own kind, in the same manner as species in a state of nature, though in a much less degree.
[With respect to sterility from the crossing of domestic races, I know of no well-ascertained case with animals. This fact, seeing the great difference in structure between some breeds of pigeons, fowls, pigs, dogs, etc., is extraordinary, in contrast with the sterility of many closely allied natural species when crossed; but we shall hereafter attempt to show that it is not so extraordinary as it at first appears. And it may be well here to recall to mind that the amount of external difference between two species is not a safe guide for predicting whether or not they will breed together,—some closely allied species when crossed being utterly sterile, and others which are extremely unlike being moderately fertile. I have said that no case of sterility in crossed races rests on satisfactory evidence; but here is one which at first seems trustworthy. Mr. Youatt (16/9. 'Cattle' page 202.) and a better authority cannot be quoted, states, that formerly in Lancashire crosses were frequently made between longhorn and shorthorn cattle; the first cross was excellent, but the produce was uncertain; in the third or fourth generation the cows were bad milkers; "in addition to which, there was much uncertainty whether the cows would conceive; and full one-third of the cows among some of these half-breds failed to be in calf." This at first seems a good case: but Mr. Wilkinson states (16/10. Mr. J. Wilkinson in 'Remarks addressed to Sir J. Sebright' 1820 page 38.), that a breed derived from this same cross was actually established in another part of England; and if it had failed in fertility, the fact would surely have been noticed. Moreover, supposing that Mr. Youatt had proved his case, it might be argued that the sterility was wholly due to the two parent-breeds being descended from primordially distinct species.
In the case of plants Gartner states that he fertilised thirteen heads (and subsequently nine others) on a dwarf maize bearing yellow seed (16/11. 'Bastarderzeugung' s. 87, 169. See also the Table at the end of volume.) with pollen of a tall maize having red seed; and one head alone produced good seed, but only five in number. Though these plants are monoecious, and therefore do not require castration, yet I should have suspected some accident in the manipulation, had not Gartner expressly stated that he had during many years grown these two varieties together, and they did not spontaneously cross; and this, considering that the plants are monoecious and abound with pollen, and are well known generally to cross freely, seems explicable only on the belief that these two varieties are in some degree mutually infertile. The hybrid plants raised from the above five seeds were intermediate in structure, extremely variable, and perfectly fertile. (16/12. 'Bastarderzeugung' s. 87, 577.) In like manner Prof. Hildebrand (16/13. 'Bot. Zeitung' 1868 page 327.) could not succeed in fertilising the female flowers of a plant bearing brown grains with pollen from a certain kind bearing yellow grains; although other flowers on the same plant, which were fertilised with their own pollen, yielded good seed. No one, I believe, even suspects that these varieties of maize are distinct species; but had the hybrids been in the least sterile, no doubt Gartner would at once have so classed them. I may here remark, that with undoubted species there is not necessarily any close relation between the sterility of a first cross and that of the hybrid offspring. Some species can be crossed with facility, but produce utterly sterile hybrids; others can be crossed with extreme difficulty, but the hybrids when produced are moderately fertile. I am not aware, however, of any instance quite like this of the maize, namely, of a first cross made with difficulty, but yielding perfectly fertile hybrids. (16/14. Mr. Shirreff formerly thought ('Gardener's Chronicle' 1858 page 771) that the offspring from a cross between certain varieties of wheat became sterile in the fourth generation; but he now admits ('Improvement of the Cereals' 1873) that this was an error.)
The following case is much more remarkable, and evidently perplexed Gartner, whose strong wish it was to draw a broad line of distinction between species and varieties. In the genus Verbascum, he made, during eighteen years, a vast number of experiments, and crossed no less than 1085 flowers and counted their seeds. Many of these experiments consisted in crossing white and yellow varieties of both V. lychnitis and V. blattaria with nine other species and their hybrids. That the white and yellow flowered plants of these two species are really varieties, no one has doubted; and Gartner actually raised in the case of both species one variety from the seed of the other. Now in two of his works (16/15. 'Kenntniss der Befruchtung' s. 137; 'Bastarderzeugung' s. 92, 181. On raising the two varieties from seed see s. 307.) he distinctly asserts that crosses between similarly-coloured flowers yield more seed than between dissimilarly-coloured; so that the yellow-flowered variety of either species (and conversely with the white-flowered variety), when crossed with pollen of its own kind, yields more seed than when crossed with that of the white variety; and so it is when differently coloured species are crossed. The general results may be seen in the Table at the end of his volume. In one instance he gives (16/16. 'Bastarderzeugung' s. 216.) the following details; but I must premise that Gartner, to avoid exaggerating the degree of sterility in his crosses, always compares the MAXIMUM number obtained from a cross with the AVERAGE number naturally given by the pure mother-plant. The white variety of V. lychnitis, naturally fertilised by its own pollen, gave from an AVERAGE of twelve capsules ninety-six good seeds in each; whilst twenty flowers fertilised with pollen from the yellow variety of this same species, gave as the MAXIMUM only eighty-nine good seeds; so that we have the proportion of 1000 to 908, according to Gartner's usual scale. I should have thought it possible that so small a difference in fertility might have been accounted for by the evil effects of the necessary castration; but Gartner shows that the white variety of V. lychnitis, when fertilised first by the white variety of V. blattaria, and then by the yellow variety of this species, yielded seed in the proportion of 622 to 438; and in both these cases castration was performed. Now the sterility which results from the crossing of the differently coloured varieties of the same species, is fully as great as that which occurs in many cases when distinct species are crossed. Unfortunately Gartner compared the results of the first unions alone, and not the sterility of the two sets of hybrids produced from the white variety of V. lychnitis when fertilised by the white and yellow varieties of V. blattaria, for it is probable that they would have differed in this respect.
Mr. J. Scott has given me the results of a series of experiments on Verbascum, made by him in the Botanic Gardens of Edinburgh. (16/17. The results have since been published in 'Journ. Asiatic Soc. of Bengal' 1867 page 145.) He repeated some of Gartner's experiments on distinct species, but obtained only fluctuating results, some confirmatory, the greater number contradictory; nevertheless these seem hardly sufficient to overthrow the conclusion arrived at by Gartner from experiments tried on a larger scale. Mr. Scott also experimented on the relative fertility of unions between similarly and dissimilarly-coloured varieties of the same species. Thus he fertilised six flowers of the yellow variety of V. lychnitis by its own pollen, and obtained six capsules; and calling, for the sake of comparison, the average number of good seed in each of their capsules one hundred, he found that this same yellow variety, when fertilised by the white variety, yielded from seven capsules an average of ninety-four seed. On the same principle, the white variety of V. lychnitis by its own pollen (from six capsules), and by the pollen of the yellow variety (eight capsules), yielded seed in the proportion of 100 to 82. The yellow variety of V. thapsus by its own pollen (eight capsules), and by that of the white variety (only two capsules), yielded seed in the proportion of 100 to 94. Lastly, the white variety of V. blattaria by its own pollen (eight capsules), and by that of the yellow variety (five capsules), yielded seed in the proportion of 100 to 79. So that in every case the unions of similarly-coloured varieties of the same species were more fertile than the unions of dissimilarly-coloured varieties; when all the cases are grouped together, the difference of fertility is as 100 to 86. Some additional trials were made, and altogether thirty-six similarly-coloured unions yielded thirty-five good capsules; whilst thirty-five dissimilarly- coloured unions yielded only twenty-six good capsules. Besides the foregoing experiments, the purple V. phoeniceum was crossed by a rose-coloured and a white variety of the same species; these two varieties were also crossed together, and these several unions yielded less seed than V. phoeniceum by its own pollen. Hence it follows from Mr. Scott's experiments, that in the genus Verbascum the similarly and dissimilarly-coloured varieties of the same species behave, when crossed, like closely allied but distinct species. (16/18. The following facts, given by Kolreuter in his 'Dritte Fortsetzung' ss. 34, 39, appear at first sight strongly to confirm Mr. Scott's and Gartner's statements; and to a certain limited extent they do so. Kolreuter asserts, from innumerable observations, that insects incessantly carry pollen from one species and variety of Verbascum to another; and I can confirm this assertion; yet he found that the white and yellow varieties of Verbascum lychnitis often grew wild mingled together: moreover, he cultivated these two varieties in considerable numbers during four years in his garden, and they kept true by seed; but when he crossed them, they produced flowers of an intermediate tint. Hence it might have been thought that both varieties must have a stronger elective affinity for the pollen of their own variety than for that of the other; this elective affinity, I may add of each species for its own pollen (Kolreuter 'Dritte Forts.' s. 39 and Gartner 'Bastarderz.' passim) being a perfectly well-ascertained power. But the force of the foregoing facts is much lessened by Gartner's numerous experiments, for, differently from Kolreuter, he never once got ('Bastarderz.' s. 307) an intermediate tint when he crossed the yellow and white flowered varieties of Verbascum. So that the fact of the white and yellow varieties keeping true to their colour by seed does not prove that they were not mutually fertilised by the pollen carried by insects from one to the other.)
This remarkable fact of the sexual affinity of similarly-coloured varieties, as observed by Gartner and Mr. Scott, may not be of very rare occurrence; for the subject has not been attended to by others. The following case is worth giving, partly to show how difficult it is to avoid error. Dr. Herbert (16/19. 'Amaryllidaceae' 1837 page 366. Gartner has made a similar observation.) has remarked that variously-coloured double varieties of the Hollyhock (Althea rosea) may be raised with certainty by seed from plants growing close together. I have been informed that nurserymen who raise seed for sale do not separate their plants; accordingly I procured seed of eighteen named varieties; of these, eleven varieties produced sixty-two plants all perfectly true to their kind; and seven produced forty-nine plants, half of which were true and half false. Mr. Masters of Canterbury has given me a more striking case; he saved seed from a great bed of twenty-four named varieties planted in closely adjoining rows, and each variety reproduced itself truly with only sometimes a shade of difference in tint. Now in the hollyhock the pollen, which is abundant, is matured and nearly all shed before the stigma of the same flower is ready to receive it (16/20. Kolreuter first observed this fact, 'Mem. de l'Acad. de St. Petersburg' volume 3 page 127. See also C.K. Sprengel 'Das Entdeckte Geheimniss' s. 345.); and as bees covered with pollen incessantly fly from plant to plant, it would appear that adjoining varieties could not escape being crossed. As, however, this does not occur, it appeared to me probable that the pollen of each variety was prepotent on its own stigma over that of all other varieties, but I have no evidence on this point. Mr. C. Turner of Slough, well known for his success in the cultivation of this plant, informs me that it is the doubleness of the flowers which prevents the bees gaining access to the pollen and stigma; and he finds that it is difficult even to cross them artificially. Whether this explanation will fully account for varieties in close proximity propagating themselves so truly by seed, I do not know.
The following cases are worth giving, as they relate to monoecious forms, which do not require, and consequently cannot have been injured by, castration. Girou de Buzareingues crossed what he designates three varieties of gourd (16/21. Namely Barbarines, Pastissons, Giraumous: 'Annal. des Sc. Nat.' tome 30 1833 pages 398 and 405.), and asserts that their mutual fertilisation is less easy in proportion to the difference which they present. I am aware how imperfectly the forms in this group were until recently known; but Sageret (16/22. 'Memoire sur les Cucurbitaceae' 1826 pages 46, 55.), who ranked them according to their mutual fertility, considers the three forms above alluded to as varieties, as does a far higher authority, namely, M. Naudin. (16/23. 'Annales des Sc. Nat.' 4th series tome 6. M. Naudin considers these forms as undoubtedly varieties of Cucurbita pepo.) Sageret (16/24. 'Mem. Cucurb.' page 8.) has observed that certain melons have a greater tendency, whatever the cause may be, to keep true than others; and M. Naudin, who has had such immense experience in this group, informs me that he believes that certain varieties intercross more readily than others of the same species; but he has not proved the truth of this conclusion; the frequent abortion of the pollen near Paris being one great difficulty. Nevertheless, he has grown close together, during seven years, certain forms of Citrullus, which, as they could be artificially crossed with perfect facility and produced fertile offspring, are ranked as varieties; but these forms when not artificially crossed kept true. Many other varieties, on the other hand, in the same group cross with such facility, as M. Naudin repeatedly insists, that without being grown far apart they cannot be kept in the least true.
Another case, though somewhat different, may be here given, as it is highly remarkable, and is established on excellent evidence. Kolreuter minutely describes five varieties of the common tobacco (16/25. 'Zweite Forts.' s. 53 namely Nicotiana major vulgaris; (2) perennis; (3) transylvanica; (4) a sub- var. of the last; (5) major latifol. fl. alb.) which were reciprocally crossed, and the offspring were intermediate in character and as fertile as their parents: from this fact Kolreuter inferred that they are really varieties; and no one, as far as I can discover, seems to have doubted that such is the case. He also crossed reciprocally these five varieties with N. glutinosa, and they yielded very sterile hybrids; but those raised from the var. perennis, whether used as the father or mother plant, were not so sterile as the hybrids from the four other varieties. (16/26. Kolreuter was so much struck with this fact that he suspected that a little pollen of N. glutinosa in one of his experiments might have accidentally got mingled with that of var. perennis, and thus aided its fertilising power. But we now know conclusively from Gartner ('Bastarderz.' s. 34, 43) that the pollen of two species never acts CONJOINTLY on a third species; still less will the pollen of a distinct species, mingled with a plant's own pollen, if the latter be present in sufficient quantity, have any effect. The sole effect of mingling two kinds of pollen is to produce in the same capsule seeds which yield plants, some taking after the one and some after the other parent.) So that the sexual capacity of this one variety has certainly been in some degree modified, so as to approach in nature that of N. glutinosa. (16/27. Mr. Scott has made some observations on the absolute sterility of a purple and white primrose (Primula vulgaris) when fertilised by pollen from the common primrose ('Journal of Proc. of Linn. Soc.' volume 8 1864 page 98); but these observations require confirmation. I raised a number of purple-flowered long- styled seedlings from seed kindly sent me by Mr. Scott, and, though they were all in some degree sterile, they were much more fertile with pollen taken from the common primrose than with their own pollen. Mr. Scott has likewise described a red equal-styled cowslip (P. veris ibid page 106), which was found by him to be highly sterile when crossed with the common cowslip; but this was not the case with several equal-styled red seedlings raised by me from his plant. This variety of the cowslip presents the remarkable peculiarity of combining male organs in every respect like those of the short-styled form, with female organs resembling in function and partly in structure those of the long-styled form; so that we have the singular anomaly of the two forms combined in the same flower. Hence it is not surprising that these flowers should be spontaneously self-fertile in a high degree.)
These facts with respect to plants show that in some few cases certain varieties have had their sexual powers so far modified, that they cross together less readily and yield less seed than other varieties of the same species. We shall presently see that the sexual functions of most animals and plants are eminently liable to be affected by the conditions of life to which they are exposed; and hereafter we shall briefly discuss the conjoint bearing of this fact, and others, on the difference in fertility between crossed varieties and crossed species.
DOMESTICATION ELIMINATES THE TENDENCY TO STERILITY WHICH IS GENERAL WITH SPECIES WHEN CROSSED.
This hypothesis was first propounded by Pallas (16/28. 'Act. Acad. St. Petersburg' 1780 part 2 pages 84, 100.), and has been adopted by several authors. I can find hardly any direct facts in its support; but unfortunately no one has compared, in the case of either animals or plants, the fertility of anciently domesticated varieties, when crossed with a distinct species, with that of the wild parent-species when similarly crossed. No one has compared, for instance, the fertility of Gallus bankiva and of the domesticated fowl, when crossed with a distinct species of Gallus or Phasianus; and the experiment would in all cases be surrounded by many difficulties. Dureau de la Malle, who has so closely studied classical literature, states (16/29. 'Annales des Sc. Nat.' tome 21 1st series page 61.) that in the time of the Romans the common mule was produced with more difficulty than at the present day; but whether this statement may be trusted I know not. A much more important, though somewhat different, case is given by M. Groenland (16/30. 'Bull. Bot. Soc. de France' December 27, 1861 tome 8 page 612.), namely, that plants, known from their intermediate character and sterility to be hybrids between Aegilops and wheat, have perpetuated themselves under culture since 1857, WITH A RAPID BUT VARYING INCREASE OF FERTILITY IN EACH GENERATION. In the fourth generation the plants, still retaining their intermediate character, had become as fertile as common cultivated wheat.
The indirect evidence in favour of the Pallasian doctrine appears to me to be extremely strong. In the earlier chapters I have shown that our various breeds of the dog are descended from several wild species; and this probably is the case with sheep. There can be no doubt that the Zebu or humped Indian ox belongs to a distinct species from European cattle: the latter, moreover, are descended from two forms, which may be called either species or races. We have good evidence that our domesticated pigs belong to at least two specific types, S. scrofa and indicus. Now a widely extended analogy leads to the belief that if these several allied species, when first reclaimed, had been crossed, they would have exhibited, both in their first unions and in their hybrid offspring, some degree of sterility. Nevertheless, the several domesticated races descended from them are now all, as far as can be ascertained, perfectly fertile together. If this reasoning be trustworthy, and it is apparently sound, we must admit the Pallasian doctrine that long- continued domestication tends to eliminate that sterility which is natural to species when crossed in their aboriginal state.
ON INCREASED FERTILITY FROM DOMESTICATION AND CULTIVATION.
Increased fertility from domestication, without any reference to crossing, may be here briefly considered. This subject bears indirectly on two or three points connected with the modification of organic beings. As Buffon long ago remarked (16/31. Quoted by Isid. Geoffroy St. Hilaire 'Hist. Naturelle Generale' tome 3 page 476. Since this MS. has been sent to press a full discussion on the present subject has appeared in Mr. Herbert Spencer's 'Principles of Biology' volume 2 1867 page 457 et seq.), domestic animals breed oftener in the year and produce more young at a birth than wild animals of the same species; they, also, sometimes breed at an earlier age. The case would hardly have deserved further notice, had not some authors lately attempted to show that fertility increases and decreases in an inverse ratio with the amount of food. This strange doctrine has apparently arisen from individual animals when supplied with an inordinate quantity of food, and from plants of many kinds when grown on excessively rich soil, as on a dunghill, becoming sterile: but to this latter point I shall have occasion presently to return. With hardly an exception, our domesticated animals, which have been long habituated to a regular and copious supply of food, without the labour of searching for it, are more fertile than the corresponding wild animals. It is notorious how frequently cats and dogs breed, and how many young they produce at a birth. The wild rabbit is said generally to breed four times yearly, and to produce each time at most six young; the tame rabbit breeds six or seven times yearly, producing each time from four to eleven young; and Mr. Harrison Weir tells me of a case of eighteen young having been produced at a birth, all of which survived. The ferret, though generally so closely confined, is more prolific than its supposed wild prototype. The wild sow is remarkably prolific; she often breeds twice in the year, and bears from four to eight and sometimes even twelve young; but the domestic sow regularly breeds twice a year, and would breed oftener if permitted; and a sow that produces less than eight at a birth "is worth little, and the sooner she is fattened for the butcher the better." The amount of food affects the fertility of the same individual: thus sheep, which on mountains never produce more than one lamb at a birth, when brought down to lowland pastures frequently bear twins. This difference apparently is not due to the cold of the higher land, for sheep and other domestic animals are said to be extremely prolific in Lapland. Hard living, also, retards the period at which animals conceive; for it has been found disadvantageous in the northern islands of Scotland to allow cows to bear calves before they are four years old. (16/32. For cats and dogs etc. see Bellingeri in 'Annal. des Sc. Nat.' 2nd series, Zoolog. tome 12 page 155. For ferrets Bechstein 'Naturgeschichte Deutschlands' b. 1 1801 s. 786, 795. For rabbits ditto s. 1123, 1131; and Bronn 'Geschichte der Natur.' b. 2 s. 99. For mountain sheep ditto s. 102. For the fertility of the wild sow, see Bechstein 'Naturgesch. Deutschlands' b. 1 1801 s. 534; for the domestic pig Sidney's edition of 'Youatt on the Pig' 1860 page 62. With respect to Lapland see Acerbi 'Travels to the North Cape' English translation volume 2 page 222. About the Highland cows see 'Hogg on Sheep' page 263.)