GROUP IV.
The birds of this group may be characterised by their resemblance in all important points of structure, especially in the beak, to the rock-pigeon. The Trumpeter forms the only well-marked race. Of the numerous other sub-races and varieties I shall specify only a few of the most distinct, which I have myself seen and kept alive.
Race X.—Trumpeter.
(Trommeltaube; pigeon tambour, glouglou.)
A tuft of feathers at the base of the beak curling forward; feet much feathered; voice very peculiar; size exceeding that of the rock-pigeon.
This is a well-marked breed, with a peculiar voice, wholly unlike that of any other pigeon. The coo is rapidly repeated, and is continued for several minutes; hence their name of Trumpeters. They are also characterised by a tuft of elongated feathers, which curls forward over the base of the beak, and which is possessed by no other breed. Their feet are so heavily feathered, that they almost appear like little wings. They are larger birds than the rock-pigeon, but their beak is of very nearly the same proportional size. Their feet are rather small. This breed was perfectly characterised in Moore’s time, in 1735. Mr. Brent says that two varieties exist, which differ in size.
Race XI.—Scarcely differing in structure from the wild Columba livia.
Sub-race I. Laughers.—Size less than the Rock-pigeon; voice very peculiar.—As this bird agrees in nearly all its proportions with the rock-pigeon, though of smaller size, I should not have thought it worthy of mention, had it not been for its peculiar voice—a character supposed seldom to vary with birds. Although the voice of the Laugher is very different from that of the Trumpeter, yet one of my Trumpeters used to utter a single note like that of the Laugher. I have kept two varieties of Laughers, which differed only in one variety being turn-crowned; the smooth-headed kind, for which I am indebted to the kindness of Mr. Brent, besides its peculiar note, used to coo in a singular and pleasing manner, which, independently, struck both Mr. Brent and myself as resembling that of the turtle-dove. Both varieties come from Arabia. This breed was known by Moore in 1735. A pigeon which seems to say Yak-roo is mentioned in 1600 in the ‘Ayeen Akbery’ and is probably the same breed. Sir W. Elliot has also sent me from Madras a pigeon called Yahui, said to have come from Mecca, which does not differ in appearance from the Laugher; it has “a deep melancholy voice, like Yahu, often repeated.” Yahu, yahu, means Oh God, oh God; and Sayzid Mohammed Musari, in the treatise written about 100 years ago, says that these birds “are not flown, because they repeat the name of the most high God.” Mr. Keith Abbott, however, informs me that the common pigeon is called Yahoo in Persia.
Sub-race II. Common Frill-back (die Strupptaube).—Beak rather longer than in the rock-pigeon; feathers reversed.—This is a considerably larger bird than the rock-pigeon, and with the beak, proportionally with the size of body, a little (viz. by ·04 of an inch) longer. The feathers, especially on the wing-coverts, have their points curled upwards or back-wards.
Sub-race III. Nuns (Pigeons coquilles).—These elegant birds are smaller than the rock-pigeon. The beak is actually 1·7, and proportionally with the size of the body ·1 of an inch shorter than in the rock-pigeons, although of the same thickness. In young birds the scutellæ on the tarsi and toes are generally of a leaden-black colour; and this is a remarkable character (though observed in a lesser degree in some other breeds), as the colour of the legs in the adult state is subject to very little variation in any breed. I have on two or three occasions counted thirteen or fourteen feathers in the tail; this likewise occurs in the barely distinct breed called Helmets. Nuns are symmetrically coloured, with the head, primary wing-feathers, tail, and tail-coverts of the same colour, namely, black or red, and with the rest of the body white. This breed has retained the same character since Aldrovandi wrote in 1600. I have received from Madras almost similarly coloured birds.
Sub-race IV. Spots (die Blasstauben; pigeons heurtés).—These birds are a very little larger than the rock-pigeon, with the beak a trace smaller in all its dimensions, and with the feet decidedly smaller. They are symmetrically coloured, with a spot on the forehead, with the tail and tail-coverts of the same colour, the rest of the body being white. This breed existed in 1676;[[22]] and in 1735 Moore remarks that they breed truly, as is the case at the present day.
Sub-race V. Swallows.—These birds, as measured from tip to tip of wing, or from the end of the beak to the end of the tail, exceed in size the rock-pigeon; but their bodies are much less bulky; their feet and legs are likewise smaller. The beak is of about the same length, but rather slighter. Altogether their general appearance is considerably different from that of the rock-pigeon. Their heads and wings are of the same colour, the rest of the body being white. Their flight is said to be peculiar. This seems to be a modern breed, which, however, originated before the year 1795 in Germany, for it is described by Bechstein.
Besides the several breeds now described, three or four other very distinct kinds existed lately, or perhaps still exist, in Germany and France. Firstly, the Karmeliten, or carme pigeon, which I have not seen; it is described as of small size, with very short legs, and with an extremely short beak. Secondly, the Finnikin, which is now extinct in England. It had, according to Moore’s[[23]] treatise, published in 1735, a tuft of feathers on the hinder part of the head, which ran down its back not unlike a horse’s mane. “When it is salacious it rises over the hen and turns round three or four times, flapping its wings, then reverses and turns as many times the other way.” The Turner, on the other hand, when it “plays to the female, turns only one way.” Whether these extraordinary statements may be trusted I know not; but the inheritance of any habit may be believed, after what we have seen with respect to the Ground-tumbler of India. MM. Boitard and Corbié describe a pigeon[[24]] which has the singular habit of sailing for a considerable time through the air, without flapping its wings, like a bird of prey. The confusion is inextricable, from the time of Aldrovandi in 1600 to the present day, in the accounts published of the Draijers, Smiters, Finnikins, Turners, Claquers, etc., which are all remarkable from their manner of flight. Mr. Brent informs me that he has seen one of these breeds in Germany with its wing-feathers injured from having been so often struck together but he did not see it flying. An old stuffed specimen of a Finnikin in the British Museum presents no well-marked character. Thirdly, a singular pigeon with a forked tail is mentioned in some treatises; and as Bechstein[[25]] briefly describes and figures this bird, with a tail “having completely the structure of that of the house-swallow,” it must once have existed, for Bechstein was far too good a naturalist to have confounded any distinct species with the domestic pigeon. Lastly, an extraordinary pigeon imported from Belgium has lately been exhibited at the Philoperisteron Society in London,[[26]] which “conjoins the colour of an archangel with the head of an owl or barb, its most striking peculiarity being the extraordinary length of the tail and wing-feathers, the latter crossing beyond the tail, and giving to the bird the appearance of a gigantic swift (Cypselus), or long-winged hawk.” Mr. Tegetmeier informs me that this bird weighed only 10 ounces, but in length was 15½ inches from tip to beak to end of tail, and 32½ inches from tip to tip of wing; now the wild rock-pigeon weighs 14½ ounces, and measures from tip to beak to end of tail 15 inches, and from tip to tip of wing only 26¾ inches.
I have now described all the domestic pigeons known to me, and have added a few others on reliable authority. I have classed them under four Groups, in order to mark their affinities and degrees of difference; but the third group is artificial. The kinds examined by me form eleven races, which include several sub-races; and even these latter present differences that would certainly have been thought of specific value if observed in a state of nature. The sub-races likewise include many strictly inherited varieties; so that altogether there must exist, as previously remarked, above 150 kinds which can be distinguished, though generally by characters of extremely slight importance. Many of the genera of the Columbidæ, admitted by ornithologists, do not differ in any great degree from each other; taking this into consideration, there can be no doubt that several of the most strongly characterised domestic forms, if found wild, would have been placed in at least five new genera. Thus a new genus would have been formed for the reception of the improved English Pouter: a second genus for Carriers and Runts; and this would have been a wide or comprehensive genus, for it would have admitted common Spanish Runts without any wattle, short-beaked Runts like the Tronfo, and the improved English Carrier: a third genus would have been formed for the Barb: a fourth for the Fantail: and lastly, a fifth for the short beaked, not-wattled pigeons, such as Turbits and short-faced Tumblers. The remaining domestic forms might have been included, in the same genus with the wild rock-pigeon.
Individual Variability; variations of a remarkable nature.
The differences which we have as yet considered are characteristic of distinct breeds; but there are other differences, either confined to individual birds, or often observed in certain breeds but not characteristic of them. These individual differences are of importance, as they might in most cases be secured and accumulated by man’s power of selection and thus an existing breed might be greatly modified or a new one formed. Fanciers notice and select only those slight differences which are externally visible; but the whole organisation is so tied together by correlation of growth, that a change in one part is frequently accompanied by other changes. For our purpose, modifications of all kinds are equally important, and if affecting a part which does not commonly vary, are of more importance than a modification in some conspicuous part. At the present day any visible deviation of character in a well-established breed is rejected as a blemish; but it by no means follows that at an early period, before well-marked breeds had been formed, such deviations would have been rejected; on the contrary, they would have been eagerly preserved as presenting a novelty, and would then have been slowly augmented, as we shall hereafter more clearly see, by the process of unconscious selection.
I have made numerous measurements of the various parts of the body in the several breeds, and have hardly ever found them quite the same in birds of the same breed,—the differences being greater than we commonly meet with in wild species within the same district. To begin with the primary feathers of the wing and tail; but I must first mention, as some readers may not be aware of the fact, that the number of the primary wing and tail-feathers in wild birds is generally constant, and characterises, not only whole genera, but even whole families. When the tail-feathers are unusually numerous, as for instance in the swan, they are apt to be variable in number; but this does not apply to the several species and genera of the Columbidæ, which never (as far as I can hear) have less than twelve or more than sixteen tail-feathers; and these numbers characterise, with rare exception, whole sub-families.[[27]] The wild rock-pigeon has twelve tail-feathers. With Fantails, as we have seen, the number varies from fourteen to forty-two. In two young birds in the same nest I counted twenty-two and twenty-seven feathers. Pouters are very liable to have additional tail-feathers, and I have seen on several occasions fourteen or fifteen in my own birds. Mr. Bult had a specimen, examined by Mr. Yarrell, with seventeen tail-feathers. I had a Nun with thirteen, and another with fourteen tail-feathers; and in a Helmet, a breed barely distinguishable from the Nun, I have counted fifteen, and have heard of other such instances. On the other hand, Mr. Brent possessed a Dragon, which during its whole life never had more than ten tail-feathers; and one of my Dragons, descended from Mr. Brent’s, had only eleven. I have seen a Bald-head Tumbler with only ten; and Mr. Brent had an Air-Tumbler with the same number, but another with fourteen tail-feathers. Two of these latter Tumblers, bred by Mr. Brent, were remarkable,—one from having the two central tail-feathers a little divergent, and the other from having the two outer feathers longer by three-eighths of an inch than the others; so that in both cases the tail exhibited a tendency, but in different ways, to become forked. And this shows us how a swallow-tailed breed, like that described by Bechstein, might have been formed by careful selection.
With respect to the primary wing-feathers, the number in the Columbidæ, as far as I can find out, is always nine or ten. In the rock-pigeon it is ten; but I have seen no less than eight short-faced Tumblers with only nine primaries, and the occurrence of this number has been noticed by fanciers, owing to ten primaries of a white colour being one of the points in Short-faced Bald-head-Tumblers. Mr. Brent, however, had an Air-Tumbler (not short-faced) which had in both wings eleven primaries. Mr. Corker, the eminent breeder of prize Carriers, assures me that some of his birds had eleven primaries in both wings. I have seen eleven in one wing in two Pouters. I have been assured by three fanciers that they have seen twelve in Scanderoons; but as Neumeister asserts that in the allied Florence Runt the middle flight-feather is often double, the number twelve may have been caused by two of the ten primaries having each two shafts to a single feather. The secondary wing-feathers are difficult to count, but the number seems to vary from twelve to fifteen. The length of the wing and tail relatively to the body, and of the wings to the tail, certainly varies; I have especially noticed this in Jacobins. In Mr. Bult’s magnificent collection of Pouters, the wings and tail varied greatly in length; and were sometimes so much elongated that the birds could hardly play upright. In the relative length of the few first primaries I have observed only a slight degree of variability. Mr. Brent informs me that he has observed the shape of the first feather to vary very slightly. But the variation in these latter points is extremely slight compared with the differences which may be observed in the natural species of the Columbidæ.
In the beak I have seen very considerable differences in birds of the same breed, as in carefully bred Jacobins and Trumpeters. In Carriers there is often a conspicuous difference in the degree of attenuation and curvature of the beak. So it is indeed in many breeds: thus I had two strains of black Barbs, which evidently differed in the curvature of the upper mandible. In width of mouth I have found a great difference in two Swallows. In Fantails of first-rate merit I have seen some birds with much longer and thinner necks than in others. Other analogous facts could be given. We have seen that the oil-gland is aborted in all Fantails (with the exception of the sub-race from Java), and, I may add, so hereditary is this tendency to abortion, that some, although not all, of the mongrels which I reared from the Fantail and Pouter had no oil-gland; in one Swallow out of many which I have examined, and in two Nuns, there was no oil-gland.
The number of the scutellæ on the toes often varies in the same breed, and sometimes even differs on the two feet of the same individual; the Shetland rock-pigeon has fifteen on the middle, and six on the hinder toe; whereas I have seen a Runt with sixteen on the middle and eight on the hind toe; and a short-faced Tumbler with only twelve and five on these same toes. The rock-pigeon has no sensible amount of skin between its toes; but I possessed a Spot and a Nun with the skin extending for a space of a quarter of an inch from the fork, between the two inner toes. On the other hand, as will hereafter be more fully shown, pigeons with feathered feet very generally have the bases of their outer toes connected by skin. I had a red Tumbler, which had a coo unlike that of its fellows, approaching in tone to that of the Laugher: this bird had the habit, to a degree which I never saw equalled in any other pigeon, of often walking with its wings raised and arched in an elegant-manner. I need say nothing on the great variability, in almost every breed, in size of body, in colour, in the feathering of the feet, and in the feathers on the back of the head being reversed. But I may mention a remarkable Tumbler[[28]] exhibited at the Crystal Palace, which had an irregular crest of feathers on its head, somewhat like the tuft on the head of the Polish fowl. Mr. Bult reared a hen Jacobin with the feathers on the thigh so long as to reach the ground, and a cock having, but in a lesser degree, the same peculiarity: from these two birds he bred others similarly characterised, which were exhibited at the Philoperisteron Soc. I bred a mongrel pigeon which had fibrous feathers, and the wing and tail-feathers so short and imperfect that the bird could not fly even a foot in height.
There are many singular and inherited peculiarities in the plumage of pigeons: thus Almond-Tumblers do not acquire their perfect mottled feathers until they have moulted three or four times: the Kite Tumbler is at first brindled black and red with a barred appearance, but when “it throws its nest feathers it becomes almost black, generally with a bluish tail, and a reddish colour on the inner webs of the primary wing-feathers.”[[29]] Neumeister describes a breed of a black colour with white bars on the wing and a white crescent-shaped mark on the breast; these marks are generally rusty-red before the first moult, but after the third or fourth moult they undergo a change; the wing-feathers and the crown of the head likewise then become white or grey.[[30]]
It is an important fact, and I believe there is hardly an exception to the rule, that the especial characters for which each breed is valued are eminently variable: thus, in the Fantail, the number and direction of the tail-feathers, the carriage of the body, and the degree of trembling are all highly variable points; in Pouters, the degree to which they pout, and the shape of their inflated crops; in the Carrier, the length, narrowness, and curvature of the beak, and the amount of wattle; in Short-faced Tumblers, the shortness of the beak, the prominence of the forehead, and general carriage,[[31]] and in the Almond-Tumbler the colour of the plumage; in common Tumblers, the manner of tumbling; in the Barb, the breadth and shortness of the beak and the amount of eye-wattle; in Runts, the size of body; in Turbits the frill; and lastly in Trumpeters, the cooing, as well as the size of the tuft of feathers over the nostrils. These, which are the distinctive and selected characters of the several breeds, are all eminently variable.
There is another interesting fact with respect to the characters of the several breeds, namely, that they are often most strongly displayed in the male bird. In Carriers, when the males and females are exhibited in separate pens, the wattle is plainly seen to be much more developed in the males, though I have seen a hen Carrier belonging to Mr. Haynes heavily wattled. Mr. Tegetmeier informs me that, in twenty Barbs in Mr. P. H. Jones’s possession, the males had generally the largest eye-wattles; Mr. Esquilant also believes in this rule, but Mr. H. Weir, a first-rate judge, entertains some doubt on the subject. Male Pouters distend their crops to a much greater size than do the females; I have, however, seen a hen in the possession of Mr. Evans which pouted excellently; but this is an unusual circumstance. Mr. Harrison Weir, a successful breeder of prize Fantails, informs me that his male birds often have a greater number of tail-feathers than the females. Mr. Eaton asserts[[32]] that if a cock and hen Tumbler were of equal merit, the hen would be worth double the money; and as pigeons always pair, so that an equal number of both sexes is necessary for reproduction, this seems to show that high merit is rarer in the female than in the male. In the development of the frill in Turbits, of the hood in Jacobins, of the tuft in Trumpeters, of tumbling in Tumblers, there is no difference between the males and females. I may here add a rather different case, namely, the existence in France[[33]] of a wine-coloured variety of the Pouter, in which the male is generally chequered with black, whilst the female is never so chequered. Dr. Chapuis also remarks[[34]] that in certain light-coloured pigeons the males have their feathers striated with black, and these striæ increase in size at each moult, so that the male ultimately becomes spotted with black. With Carriers, the wattle, both on the beak and round the eyes, and with Barbs that round the eyes, goes on increasing with age. This augmentation of character with advancing age, and more especially the difference between the males and females in the above-mentioned several respects, are remarkable facts, for there is no sensible difference at any age between the two sexes in the aboriginal rock-pigeon; and not often any strongly marked difference throughout the family of the Columbidæ.[[35]]
Osteological Characters.
In the skeletons of the various breeds there is much variability; and though certain differences occur frequently, and others rarely, in certain breeds, yet none can be said to be absolutely characteristic of any breed. Considering that strongly-marked domestic races have been formed chiefly by man’s selection, we ought not to expect to find great and constant differences in the skeleton; for fanciers neither see, nor do they care for, modifications of structure in the internal framework. Nor ought we to expect changes in the skeletons from changed habits of life; as every facility is given to the most distinct breeds to follow the same habits, and the much modified races are never allowed to wander abroad and procure their own food in various ways. Moreover, I find, on comparing the skeletons of Columba livia, oenas, palumbus, and turtur, which are ranked by all systematists in two or three distinct though allied genera, that the differences are extremely slight, certainly less than between the skeletons of some of the most distinct domestic breeds. How far the skeleton of the wild rock-pigeon is constant I have had no means of judging, as I have examined only two.
Fig. 24—Skulls of Pigeons, viewed laterally.
Skull.—The individual bones, especially those at the base, do not differ in shape. But the whole skull, in its proportions, outline, and relative direction of the bones, differs greatly in some of the breeds, as may be seen by comparing the figures of (A) the wild rock-pigeon, (B) the Short-faced Tumbler, (C) the English Carrier, and (D) the Bagadotten Carrier (of Neumeister), all drawn of the natural size and viewed laterally. In the Carrier, besides the elongation of the bones of the face, the space between the orbits is proportionally a little narrower than in the rock-pigeon. In the Bagadotten the upper mandible is remarkably arched, and the premaxillary bones are proportionally broader. In the Short-faced Tumbler the skull is more globular: all the bones of the face are much shortened, and the front of the skull and descending nasal bones are almost perpendicular: the maxillo-jugal arch and premaxillary bones form an almost straight line; the space between the prominent edges of the eye-orbits is depressed. In the Barb the premaxillary bones are much shortened, and their anterior portion is thicker than in the rock-pigeon, as is the lower part of the nasal bone. In two Nuns the ascending branches of the premaxillaries, near their tips, were somewhat attenuated, and in these birds, as well as in some others, for instance in the Spot, the occipital crest over the foramen was considerably more prominent than in the rock-pigeon.
Fig. 25—Lower jaws, seen from above.
Fig. 26—Skull of Runt.
Fig. 27—Lateral view of jaws.
In the lower jaw, the articular surface is proportionably smaller in many breeds than in the rock-pigeon; and the vertical diameter, more especially of the outer part of the articular surface, is considerably shorter. May not this be accounted for by the lessened use of the jaws, owing to nutritious food having been given during a long period to all highly improved pigeons? In Runts, Carriers, and Barbs (and in a lesser degree in several breeds), the whole side of the jaw near the articular end is bent inwards in a highly remarkable manner; and the superior margin of the ramus, beyond the middle, is reflexed in an equally remarkable manner, as may be seen in fig. 25, in comparison with the jaw of the rock-pigeon. This reflection of the upper margin of the lower jaw is plainly connected with the singularly wide gape of the mouth, as has been described in Runts, Carriers, and Barbs. The reflection is well shown in fig. 26 of the head of a Runt seen from above; here a wide open space may be observed on each side, between the edges of the lower jaw and of the premaxillary bones. In the rock-pigeon, and in several domestic breeds, the edges of the lower jaw on each side come close up to the premaxillary bones, so that no open space is left. The degree of downward curvature of the distal half of the lower jaw also differs to an extraordinary degree in some breeds, as may be seen in the drawings (fig. 27 A) of the rock-pigeon, (B) of the Short-faced Tumbler, and (C) of the Bagadotten Carrier of Neumeister. In some Runts the symphysis of the lower jaw is remarkably solid. No one would readily have believed that jaws differing in the several above-specified points so greatly could have belonged to the same species.
Vertebræ.—All the breeds have twelve cervical vertebræ.[[36]] But in a Bussorah Carrier from India the twelfth vertebra carried a small rib, a quarter of an inch in length, with a perfect double articulation.
The dorsal vertebræ are always eight. In the rock-pigeon all eight bear ribs; the eighth rib being very thin, and the seventh having no process. In Pouters all the ribs are extremely broad, eight bear ribs; the eighth rib being very thin and the seventh having no process. In Pouters all the ribs are extremely broad, and, in three out of four skeletons examined by me, the eighth rib was twice or even thrice as broad as in the rock-pigeon; and the seventh pair had distinct processes. In many breeds there are only seven ribs, as in seven out of eight skeletons of various Tumblers, and in several skeletons of Fantails, Turbits and Nuns.>
In all these breeds the seventh pair was very small, and was destitute of processes, in which respect it differed from the same rib in the rock-pigeon. In one Tumbler, and in the Bussorah Carrier, even the sixth pair had no process. The hypapophysis of the second dorsal vertebra varies much in development; being sometimes (as in several, but not all Tumblers) nearly as prominent as that of the third dorsal vertebra; and the two hypapophyses together tend to form an ossified arch. The development of the arch, formed by the hypapophyses of the third and fourth dorsal vertebræ, also varies considerably, as does the size of the hypapophysis of the fifth vertebra.
The rock-pigeon has twelve sacral vertebræ; but these vary in number, relative size, and distinctness, in the different breeds. In Pouters, with their elongated bodies, there are thirteen or even fourteen, and, as we shall immediately see, an additional number of caudal vertebræ. In Runts and Carriers there is generally the proper number, namely twelve; but in one Runt, and in the Bussorah Carrier, there were only eleven. In Tumblers there are either eleven, or twelve, or thirteen sacral vertebræ.
The caudal vertebræ are seven in number in the rock-pigeon. In Fantails, which have their tails so largely developed, there are eight or nine, and apparently in one case ten, and they are a little longer than in the rock-pigeon, and their shape varies considerably. Pouters, also, have eight or nine caudal vertebræ. I have seen eight in a Nun and Jacobin. Tumblers, though such small birds, always have the normal number seven; as have Carriers, with one exception, in which there were only six.
The following table will serve as a summary, and will show the most remarkable deviations in the number of the vertebra and ribs which I have observed:—
| Rock Pigeon. | Pouter, from Mr. Bult. | Tumbler, Dutch Roller. | Bussorah Carrier. | |
| Cervical Vertebræ | 12 | 12 | 12 | 12 The 12th bore a small rib. |
| Dorsal Vertebræ | 8 | 8 | 8 | 8 |
| Dorsal Ribs | 8 The 6th pair with processes, the 7th pair without a process. | 8 The 6th and 7th pair with processes. | 7 The 6th and 7th pair without processes. | 7 The 6th and 7th pair without processes. |
| Sacral Vertebræ | 12 | 14 | 11 | 11 |
| Caudal Vertebræ | 7 | 8 or 9 | 7 | 7 |
| Total Vertebræ | 39 | 42 or 43 | 38 | 38 |
The pelvis differs very little in any breed. The anterior margin of the ilium, however, is sometimes a little more equally rounded on both sides than in the rock-pigeon. The ischium is also frequently rather more elongated. The obturator-notch is sometimes, as in many Tumblers, less developed than in the rock-pigeon. The ridges on the ilium are very prominent in most Runts.
Fig. 28—Scapulæ of Pigeons.
Fig. 29—Furcula of Pigeons.
In the bones of the extremities I could detect no difference, except in their proportional lengths; for instance, the metatarsus in a Pouter was 1·65 inch, and in a Short-faced Tumbler only ·95 in length; and this is a greater difference than would naturally follow from their differently-sized bodies; but long legs in the Pouter, and small feet in the Tumbler, are selected points. In some Pouters the scapula is rather straighter, and in some Tumblers it is straighter, with the apex less elongated, than in the rock-pigeon: in fig. 28, the scapula of the rock-pigeon (A), and of a short-faced Tumbler (B), are given. The processes at the summit of the coracoid, which receive the extremities of the furculum, form a more perfect cavity in some Tumblers than in the rock-pigeon: in Pouters these processes are larger and differently shaped, and the exterior angle of the extremity of the coracoid, which is articulated to the sternum, is squarer.
The two arms of the furculum in Pouters diverge less, proportionally to their length, than in the rock-pigeon; and the symphysis is more solid and pointed. In Fantails the degree of divergence of the two arms varies in a remarkable manner. In fig. 29, B and C represent the furcula of two Fantails; and it will be seen that the divergence in B is rather less even than in the furculum of the short-faced, small-sized Tumbler (A), whereas the divergence in C equals that in a rock-pigeon, or in the Pouter (D), though the latter is a much larger bird. The extremities of the furculum, where articulated to the coracoids, vary considerably in outline.
In the sternum the differences in form are slight, except in the size and outline of the perforations, which, both in the larger and lesser sized breeds, are sometimes small. These perforations, also, are sometimes either nearly circular, or elongated as is often the case with Carriers. The posterior perforations occasionally are not complete, being left open posteriorly. The marginal apophyses forming the anterior perforations vary greatly in development. The degree of convexity of the posterior part of the sternum differs much, being sometimes almost perfectly flat. The manubrium is rather more prominent in some individuals than in others, and the pore immediately under it varies greatly in size.
Correlation of Growth.—By this term I mean that the whole organisation is so connected, that when one part varies, other parts vary; but which of two correlated variations ought to be looked at as the cause and which as the effect, or whether both result from some common cause, we can seldom or never tell. The point of interest for us is that, when fanciers, by the continued selection of slight variations, have largely modified one part, they often unintentionally produce other modifications. For instance, the beak is readily acted on by selection, and, with its increased or diminished length, the tongue increases or diminishes, but not in due proportion; for, in a Barb and Short-faced Tumbler, both of which have very short beaks, the tongue, taking the rock-pigeon as the standard of comparison, was proportionally not shortened enough, whilst in two Carriers and in a Runt the tongue, proportionally with the beak, was not lengthened enough, thus, in a first-rate English Carrier, in which the beak from the tip to the feathered base was exactly thrice as long as in a first-rate Short-faced Tumbler, the tongue was only a little more than twice as long. But the tongue varies in length independently of the beak: thus in a Carrier with a beak 1·2 inch in length, the tongue was ·67 in length: whilst in a Runt which equalled the Carrier in length of body and in stretch of wings from tip to tip, the beak was ·92 whilst the tongue was ·73 of an inch in length, so that the tongue was actually longer than in the carrier with its long beak. The tongue of the Runt was also very broad at the root. Of two Runts, one had its beak longer by ·23 of an inch, whilst its tongue was shorter by ·14 than in the other.
With the increased or diminished length of the beak the length of the slit forming the external orifice of the nostrils varies, but not in due proportion, for, taking the rock-pigeon as the standard, the orifice in a Short-faced Tumbler was not shortened in due proportion with its very short beak. On the other hand (and this could not have been anticipated), the orifice in three English Carriers, in the Bagadotten Carrier, and in a Runt (pigeon cygne), was longer by above the tenth of an inch than would follow from the length of the beak proportionally with that of the rock-pigeon. In one Carrier the orifice of the nostrils was thrice as long as in the rock-pigeon, though in body and length of beak this bird was not nearly double the size of the rock-pigeon. This greatly increased length of the orifice of the nostrils seems to stand partly in correlation with the enlargement of the wattled skin on the upper mandible and over the nostrils; and this is a character which is selected by fanciers. So again, the broad, naked, and wattled skin round the eyes of Carriers and Barbs is a selected character; and in obvious correlation with this, the eyelids, measured longitudinally, are proportionally more than double the length of those of the rock-pigeon.
The great difference (see fig. 27) in the curvature of the lower jaw in the rock-pigeon, the Tumbler, and Bagadotten Carrier, stands in obvious relation to the curvature of the upper jaw, and more especially to the angle formed by the maxillo-jugal arch with the premaxillary bones. But in Carriers, Runts, and Barbs the singular reflexion of the upper margin of the middle part of the lower jaw (see fig. 25) is not strictly correlated with the width or divergence (as may be clearly seen in fig. 26) of the premaxillary bones, but with the breadth of the horny and soft parts of the upper mandible, which are always overlapped by the edges of the lower mandible.
In Pouters, the elongation of the body is a selected character, and the ribs, as we have seen, have generally become very broad, with the seventh pair furnished with processes; the sacral and caudal vertebræ have been augmented in number; the sternum has likewise increased in length (but not in the depth of the crest) by ·4 of an inch more than would follow from the greater bulk of the body in comparison with that of the rock-pigeon. In Fantails, the length and number of the caudal vertebræ have increased. Hence, during the gradual progress of variation and selection, the internal bony framework and the external shape of the body have been, to a certain extent, modified in a correlated manner.
Although the wings and tail often vary in length independently of each other, it is scarcely possible to doubt that they generally tend to become elongated or shortened in correlation. This is well seen in Jacobins, and still more plainly in Runts, some varieties of which have their wings and tail of great length, whilst others have both very short. With Jacobins, the remarkable length of the tail and wing-feathers is not a character which is intentionally selected by fanciers; but fanciers have been trying for centuries, at least since the year 1600, to increase the length of the reversed feathers on the neck, so that the hood may more completely enclose the head; and it may be suspected that the increased length of the wing and tail-feathers stand in correlation with the increased length of the neck-feathers. Short-faced Tumblers have short wings in nearly due proportion with the reduced size of their bodies; but it is remarkable, seeing that the number of the primary wing-feathers is a constant character in most birds, that these Tumblers generally have only nine instead of ten primaries. I have myself observed this in eight birds; and the Original Columbarian Society[[37]] reduced the standard for Bald-head Tumblers from ten to nine white flight-feathers, thinking it unfair that a bird which had only nine feathers should be disqualified for a prize because it had not ten white flight-feathers. On the other hand, in Carriers and Runts, which have large bodies and long wings, eleven primary feathers have occasionally been observed.
Mr. Tegetmeier has informed me of a curious and inexplicable case of correlation, namely, that young pigeons of all breeds which when mature become white, yellow, silver (i.e., extremely pale blue), or dun-coloured, are born almost naked; whereas pigeons of other colours are born well-clothed with down. Mr. Esquilant, however, has observed that young dun Carriers are not so bare as young dun Barbs and Tumblers. Mr. Tegetmeier has seen two young birds in the same nest, produced from differently coloured parents, which differed greatly in the degree to which they were at first clothed with down.
I have observed another case of correlation which at first sight appears quite inexplicable, but on which, as we shall see in a future chapter, some light can be thrown by the law of homologous parts varying in the same manner. The case is, that, when the feet are much feathered, the roots of the feathers are connected by a web of skin, and apparently in correlation with this the two outer toes become connected for a considerable space by skin. I have observed this in very many specimens of Pouters, Trumpeters, Swallows, Roller-tumblers (likewise observed in this breed by Mr. Brent), and in a lesser degree in other feather-footed pigeons.
The feet of the smaller and larger breeds are of course much smaller or larger than those of the rock-pigeon; but the scutellæ or scales covering the toes and tarsi have not only decreased or increased in size, but likewise in number. To give a single instance, I have counted eight scutellæ on the hind toe of a Runt, and only five on that of a Short-faced Tumbler. With birds in a state of nature the number of the scutellæ on the feet is usually a constant character. The length of the feet and the length of the beak apparently stand in correlation; but as disuse apparently has affected the size of the feet, this case may come under the following discussion.
On the Effects of Disuse.—In the following discussion on the relative proportions of the feet, sternum, furculum, scapulæ, and wings, I may premise, in order to give some confidence to the reader, that all my measurements were made in the same manner, and that they were made without the least intention of applying them to the following purpose.
Table I.
Pigeons with their beaks generally shorter than that of the Rock-pigeon, proportionally to the size of their bodies.
| Name of Breed. | Actual length of Feet | Difference between actual and calculated length of feet, in proportion to length of feet and size of body in the Rock-pigeon. | |
| Wild rock-pigeon (mean measurement) | 2·02 | Too short by | Too long by |
| Short-faced Tumbler, blad-head | 1·57 | 0·11 | — |
| Short-faced Tumbler, almond | 1·60 | 0·16 | — |
| Tumbler, red magpie | 1·75 | 0·19 | — |
| Tumbler, red common (by standard to end of tail) | 1·85 | 0·07 | — |
| Tumbler, common bald-head | 1·85 | 0·18 | — |
| Tumbler, roller | 1·80 | 0·06 | — |
| Turbit | 1·75 | 0·17 | — |
| Turbit | 1·80 | 0·01 | — |
| Turbit | 1·84 | 0·15 | — |
| Jacobin | 1·90 | 0·02 | — |
| Trumpeter, white | 2·02 | 0·06 | — |
| Trumpeter, mottled | 1·95 | 0·18 | — |
| Fantail (by standard to end of tail) | 1·85 | 0·15 | — |
| Fantail (by standard to end of tail) | 1·95 | 0·15 | — |
| Fantail crested va. (by standard to end of tail) | 1·95 | 0·0 | 0·0 |
| Indian Frill-back (by standard to end of tail) | 1·80 | 0·19 | — |
| English Frill-back | 2·10 | 0·03 | — |
| Nun | 1·82 | 0·02 | — |
| Laugher | 1·65 | 0·16 | — |
| Barb | 2·00 | 0·03 | — |
| Barb | 2·00 | — | 0·03 |
| Spot | 1·90 | 0·02 | — |
| Spot | 1·90 | 0·07 | — |
| Swallow, red | 1·85 | 0·18 | — |
| Swallow, blue | 2·00 | — | 0·03 |
| Pouter | 2·42 | — | 0·11 |
| Pouter, German | 2·30 | — | 0·09 |
| Bussorah Carrier | 2·17 | — | 0·09 |
| Number of specimens | 28 | 22 | 5 |
I measured most of the birds which came into my possession, from the feathered base of the beak (the length of beak itself being so variable) to the end of the tail, and to the oil-gland, but unfortunately (except in a few cases) not to the root of the tail; I measured each bird from the extreme tip to tip of wing; and the length of the terminal folded part of the wing, from the extremity of the primaries to the joint of the radius. I measured the feet without the claws, from the end of the middle toe to the end of the hind toe; and the tarsus and middle toe together. I have taken in every case the mean measurement of two wild rock-pigeons from the Shetland Islands, as the standard of comparison. The following table shows the actual length of the feet in each bird; and the difference between the length which the feet ought to have had according to the size of body of each, in comparison with the size of body and length of feet of the rock-pigeon, calculated (with a few specified exceptions) by the standard of the length of the body from the base of the beak to the oil-gland. I have preferred this standard, owing to the variability of the length of tail. But I have made similar calculations, taking as the standard the length from tip to tip of wing, and likewise in most cases from the base of the beak to the end of the tail; and the result has always been closely similar. To give an example: the first bird in the table, being a Short-faced Tumbler, is much smaller than the rock-pigeon, and would naturally have shorter feet; but it is found on calculation to have feet too short by ·11 of an inch, in comparison with the feet of the rock-pigeon, relatively to the size of the body in these two birds, as measured from the base of beak to the oil-gland. So again, when this same Tumbler and the rock-pigeon were compared by the length of their wings, or by the extreme length of their bodies, the feet of the Tumbler were likewise found to be too short in very nearly the same proportion. I am well aware that the measurements pretend to greater accuracy than is possible, but it was less trouble to write down the actual measurements given by the compasses in each case than an approximation.
Table II.
Pigeons with their beaks longer than that of the Rock-pigeon, proportionally to the size of their bodies.
| Name of Breed. | Actual length of Feet | Difference between actual and calculated length of feet, in proportion to length of feet and size of body in the Rock-pigeon. | |
| Wild rock-pigeon (mean measurement) | 2·02 | Too short by | Too long by |
| Short-faced Tumbler, bald-head | 1·57 | 0·11 | — |
| Carrier | 2·60 | — | 0·31 |
| Carrier | 2·60 | — | 0·25 |
| Carrier | 2·40 | — | 0·21 |
| Carrier Dragon | 2·25 | — | 0·06 |
| Bagadotten Carrier | 2·80 | — | 0·56 |
| Scanderoon, white | 2·80 | — | 0·37 |
| Scanderoon, Pigeon cygne | 2·85 | — | 0·29 |
| Runt | 2·75 | — | 0·27 |
| Number of specimens | 8 | — | 8 |
In these two tables (Tables I and II) we see in the first column the actual length of the feet in thirty-six birds belonging to various breeds, and in the two other columns we see by how much the feet are too short or too long, according to the size of bird, in comparison with the rock-pigeon. In the first table twenty-two specimens have their feet too short, on an average by a little above the tenth of an inch (viz. ·107); and five specimens have their feet on an average a very little too long, namely, by ·07 of an inch. But some of these latter cases can be explained; for instance, with Pouters the legs and feet are selected for length, and thus any natural tendency to a diminution in the length of the feet will have been counteracted. In the Swallow and Barb, when the calculation was made on any standard of comparison besides the one used (viz. length of body from base of beak to oil-gland), the feet were found to be too small.
In the second table we have eight birds, with their beaks much longer than in the rock-pigeon, both actually and proportionally with the size of body, and their feet are in an equally marked manner longer, namely, in proportion, on an average by ·29 of an inch. I should here state that in Table I there are a few partial exceptions to the beak being proportionally shorter than in the rock-pigeon: thus the beak of the English Frill-back is just perceptibly longer, and that of the Bussorah Carrier of the same length or slightly longer, than in the rock-pigeon. The beaks of Spots, Swallows, and Laughers are only a very little shorter, or of the same proportional length, but slenderer. Nevertheless, these two tables, taken conjointly, indicate pretty plainly some kind of correlation between the length of the beak and the size of the feet. Breeders of cattle and horses believe that there is an analogous connection between the length of the limbs and head; they assert that a race-horse with the head of a dray-horse, or a grey-hound with the head of a bulldog, would be a monstrous production. As fancy pigeons are generally kept in small aviaries, and are abundantly supplied with food, they must walk about much less than the wild rock-pigeon; and it may be admitted as highly probable that the reduction in the size of the feet in the twenty-two birds in the first table has been caused by disuse,[[38]] and that this reduction has acted by correlation on the beaks of the great majority of the birds in Table I. When, on the other hand, the beak has been much elongated by the continued selection of successive slight increments of length, the feet by correlation have likewise become much elongated in comparison with those of the wild rock-pigeon, notwithstanding their lessened use.
As I had taken measures from the end of the middle toe to the heel of the tarsus in the rock-pigeon and in the above thirty-six birds, I have made calculations analogous with those above given, and the result is the same— namely, that in the short-beaked breeds, with equally few exceptions as in the former case, the middle toe conjointly with the tarsus has decreased in length; whereas in the long-beaked breeds it has increased in length, though not quite so uniformly as in the former case, for the leg, in some varieties of the Runt varies much in length.
As fancy pigeons are generally confined in aviaries of moderate size, and as even when not confined they do not search for their own food, they must during many generations have used their wings incomparably less than the wild rock-pigeon. Hence it seemed to me probable that all the parts of the skeleton subservient to flight would be found to be reduced in size. With respect to the sternum, I have carefully measured its extreme length in twelve birds of different breeds, and in two wild rock-pigeons from the Shetland Islands. For the proportional comparison I have tried three standards of measurement, with all twelve birds namely, the length from the base of the beak to the oil-gland, to the end of the tail, and from the extreme tip to tip of wings. The result has been in each case nearly the same, the sternum being invariably found to be shorter than in the wild rock-pigeon. I will give only a single table, as calculated by the standard from the base of the beak to the oil-gland; for the result in this case is nearly the mean between the results obtained by the two other standards.
Length of Sternum.
| Name of Breed | Actual Length. Inches | Too short by |
| Wild Rock-pigeon | 2·55 | — |
| Wild Rock-pigeon | 2·55 | — |
| Pied Scanderoon | 2·80 | 0·60 |
| Bagadotten Carrier | 2·80 | 0·17 |
| Dragon | 2·45 | 0·41 |
| Carrier | 2·75 | 0·35 |
| Short-faced Tumbler | 2·05 | 0·28 |
| Barb | 2·35 | 0·34 |
| Nun | 2·27 | 0·15 |
| German Pouter | 2·36 | 0·54 |
| Jacobin | 2·33 | 0·22 |
| English Frill-back | 2·40 | 0·43 |
| Swallow | 2·45 | 0·17 |
This table shows that in these twelve breeds the sternum is of an average one-third of an inch (exactly ·332) shorter than in the rock-pigeon, proportionally with the size of their bodies; so that the sternum has been reduced by between one-seventh and one-eighth of its entire length; and this is a considerable reduction.
I have also measured in twenty-one birds, including the above dozen, the prominence of the crest of the sternum relatively to its length, independently of the size of the body. In two of the twenty-one birds the crest was prominent in the same relative degree as in the rock-pigeon; in seven it was more prominent; but in five out of these seven, namely, in a Fantail, two Scanderoons, and two English Carriers, this greater prominence may to a certain extent be explained, as a prominent breast is admired and selected by fanciers; in the remaining twelve birds the prominence was less. Hence it follows that the crest exhibits a slight, though uncertain, tendency to be reduced in prominence in a greater degree than does the length of the sternum relatively to the size of body, in comparison with the rock-pigeon.
I have measured the length of the scapula in nine different large and small-sized breeds, and in all the scapula is proportionally shorter (taking the same standard as before) than in the wild rock-pigeon. The reduction in length on an average is very nearly one-fifth of an inch, or about one-ninth of the length of the scapula in the rock-pigeon.
The arms of the furcula in all the specimens which I compared, diverged less, proportionally with the size of body, than in the rock-pigeon; and the whole furculum was proportionally shorter. Thus in a Runt, which measured from tip to tip of wings 38½ inches, the furculum was only a very little longer (with the arms hardly more divergent) than in a rock-pigeon which measured from tip to tip 26½ inches. In a Barb, which in all its measurements was a little larger than the same rock-pigeon, the furculum was a quarter of an inch shorter. In a Pouter, the furculum had not been lengthened proportionally with the increased length of the body. In a Short-faced Tumbler, which measured from tip to tip of wings 24 inches, therefore only 2½ inches less than the rock-pigeon, the furculum was barely two-thirds of the length of that of the rock-pigeon.
We thus clearly see that the sternum, scapula, and furculum are all reduced in proportional length; but when we turn to the wings we find what at first appears a wholly different and unexpected result. I may here remark that I have not picked out specimens, but have used every measurement made by me. Taking the length from the base of beak to the end of the tail as the standard of comparison, I find that, out of thirty-five birds of various breeds, twenty-five have wings of greater, and ten have them of less proportional length, than in the rock-pigeon. But from the frequently correlated length of the tail and wing-feathers, it is better to take as the standard of comparison the length from the base of the beak to the oil-gland; and by this standard, out of twenty-six of the same birds which had been thus measured, twenty-one had wings too long, and only five had them too short. In the twenty-one birds the wings exceeded in length those of the rock-pigeon, on an average, by 1-1/3 inch; whilst in the five birds they were less in length by only ·8 of an inch. As I was much surprised that the wings of closely confined birds should thus so frequently have been increased in length, it occurred to me that it might be solely due to the greater length of the wing-feathers; for this certainly is the case with the Jacobin, which has wings of unusual length. As in almost every case I had measured the folded wings, I subtracted the length of this terminal part from that of the expanded wings, and thus I obtained, with a moderate degree of accuracy, the length of the wings from the ends of the two radii, answering from wrist to wrist in our arms. The wings, thus measured in the same twenty-five birds, now gave a widely different result; for they were proportionally with those of the rock-pigeon too short in seventeen birds, and in only eight too long. Of these eight birds, five were long-beaked,[[39]] and this fact perhaps indicates that there is some correlation of the length of the beak with the length of the bones of the wings, in the same manner as with that of the feet and tarsi. The shortening of the humerus and radius in the seventeen birds may probably be attributed to disuse, as in the case of the scapula and furculum to which the wing-bones are attached;—the lengthening of the wing-feathers, and consequently the expansion of the wings from tip to tip, being, on the other hand, as completely independent of use and disuse as is the growth of the hair or wool on our long-haired dogs or long-woolled sheep.
To sum up: we may confidently admit that the length of the sternum, and frequently the prominence of its crest, the length of the scapula and furculum, have all been reduced in size in comparison with the same parts in the rock-pigeon. And I presume that this may be attributed to disuse or lessened exercise. The wings, as measured from the ends of the radii, have likewise been generally reduced in length; but, owing to the increased growth of the wing-feathers, the wings, from tip to tip, are commonly longer than in the rock-pigeon. The feet, as well as the tarsi conjointly with the middle toe, have likewise in most cases become reduced; and this it is probable has been caused by their lessened use; but the existence of some sort of correlation between the feet and beak is shown more plainly than the effects of disuse. We have also some faint indication of a similar correlation between the main bones of the wing and the beak.
Summary on the Points of Difference between the several Domestic Races, and between the individual Birds.—The beak, together with the bones of the face, differ remarkably in length, breadth, shape, and curvature. The skull differs in shape, and greatly in the angle formed by the union of the pre-maxillary, nasal, and maxillo-jugal bones. The curvature of the lower jaw and the reflection of its upper margin, as well as the gape of the mouth, differ in a highly remarkable manner. The tongue varies much in length, both independently and in correlation with the length of the beak. The development of the naked, wattled skin over the nostrils and round the eyes varies in an extreme degree. The eyelids and the external orifices of the nostrils vary in length, and are to a certain extent correlated with the degree of development of the wattle. The size and form of the œsophagus and crop, and their capacity for inflation, differ immensely. The length of the neck varies. With the varying shape of the body, the breadth and number of the ribs, the presence of processes, the number of the sacral vertebræ, and the length of the sternum, all vary. The number and size of the coccygeal vertebræ vary, apparently in correlation with the increased size of the tail. The size and shape of the perforations in the sternum, and the size and divergence of the arms of the furculum, differ. The oil-gland varies in development, and is sometimes quite aborted. The direction and length of certain feathers have been much modified, as in the hood of the Jacobin and the frill of the Turbit. The wing and tail-feathers generally vary in length together, but sometimes independently of each other and of the size of the body. The number and position of the tail-feather vary to an unparalleled degree. The primary and secondary wing-feathers occasionally vary in number, apparently in correlation with the length of the wing. The length of the leg and the size of the feet, and, in connection with the latter, the number of the scutellæ, all vary. A web of skin sometimes connects the bases of the two inner toes, and almost invariably the two outer toes when the feet are feathered.
The size of the body differs greatly: a Runt has been known to weigh more than five times as much as a Short-faced Tumbler. The eggs differ in size and shape. According to Parmentier,[[40]] some races use much straw in building their nests, and others use little; but I cannot hear of any recent corroboration of this statement. The length of time required for hatching the eggs is uniform in all the breeds. The period at which the characteristic plumage of some breeds is acquired, and at which certain changes of colour supervene, differs. The degree to which the young birds are clothed with down when first hatched is different, and is correlated in a singular manner with the colour of the plumage. The manner of flight, and certain inherited movements, such as clapping the wings, tumbling either in the air or on the ground, and the manner of courting the female, present the most singular differences. In disposition the several races differ. Some races are very silent; others coo in a highly peculiar manner.
Although many different races have kept true in character during several centuries, as we shall hereafter more fully see, yet there is far more individual variability in the most constant breeds than in birds in a state of nature. There is hardly any exception to the rule that those characters vary most which are now most valued and attended to by fanciers, and which consequently are now being improved by continued selection. This is indirectly admitted by fanciers when they complain that it is much more difficult to breed high fancy pigeons up to the proper standard of excellence than the so-called toy pigeons, which differ from each other merely in colour; for particular colours when once acquired are not liable to continued improvement or augmentation. Some characters become attached, from quite unknown causes, more strongly to the male than to the female sex; so that we have in certain races, a tendency towards the appearance of secondary sexual characters,[[41]] of which the aboriginal rock-pigeon displays not a trace.
REFERENCES
[1] The Hon. C. Murray has sent me some very valuable specimens from Persia; and H.M. Consul, Mr. Keith Abbott, has given me information on the pigeons of the same country. I am deeply indebted to Sir Walter Elliot for an immense collection of skins from Madras, with much information regarding them. Mr. Blyth has freely communicated to me his stores of knowledge on this and all other related subjects. The Rajah Sir James Brooke sent me specimens from Borneo, as has H.M. Consul, Mr. Swinhoe, from Amoy in China, and Dr. Daniell from the west coast of Africa.
[2] Mr. B. P. Brent, well known for his various contributions to poultry literature, has aided me in every way during several years: so has Mr. Tegetmeier, with unwearied kindness. This latter gentleman, who is well known for his works on poultry, and who has largely bred pigeons, has looked over this and the following chapters. Mr. Bult formerly showed me his unrivalled collection of Pouters, and gave me specimens. I had access to Mr. Wicking’s collection, which contained a greater assortment of kinds than could anywhere else be seen; and he has always aided me with specimens and information given in the freest manner. Mr. Haynes and Mr. Corker have given me specimens of their magnificent Carriers. To Mr. Harrison Weir I am likewise indebted. Nor must I by any means pass over the assistance received from Mr. J. M. Eaton, Mr. Baker, Mr. Evans, and Mr. J. Baily, jun., of Mount-street—to the latter gentleman I have been indebted for some valuable specimens. To all these gentlemen I beg permission to return my sincere and cordial thanks.
[3] ‘Les Pigeons de Volière et de Colombier’ Paris 1824. During forty-five years the sole occupation of M. Corbié was the care of the pigeons belonging to the Duchess of Berry. Bonizzi has described a large number of coloured varieties in Italy: ‘Le variazioni dei colombi Domestici,’ Padova, 1873.
[4] ‘Coup d’Oeil sur l’Ordre des Pigeons’ par Prince C. L. Bonaparte, Paris, 1855. This author makes 288 species, ranked under 85 genera.
[5] As I so often refer to the size of the C. livia, or rock-pigeon, it may be convenient to give the mean between the measurements of two wild birds, kindly sent me by Dr. Edmondstone from the Shetland Islands.
| Inches | |
| From feathered base of beak to end of tail: | 14·25 |
| From feathered base of beak to oil-gland: | 9·50 |
| From tip of beak to end of tail: | 15·02 |
| Of tail-feathers: | 4·62 |
| From tip to tip of wing: | 26·75 |
| Of folded wing: | 9·25 |
| Beak: | |
| Length from tip of beak to feathered base: | ·77 |
| Thickness, measured vertically at distal end of nostrils: | ·23 |
| Breadth, measured at same place: | ·16 |
| Feet: | |
| From end of middle toe (without claw) to distal end of tibia: | 2·77 |
| From end of middle toe to end of hind toe (without claws): | 2·02 |
| Weight: 14-1/4 ounces. |
[6] This drawing was made from a dead bird. The six following figures were drawn with great care by Mr. Luke Wells from living birds selected by Mr. Tegetmeier. It may be confidently asserted that the characters of the six breeds which have been figured are not in the least exaggerated.
[7] ‘Das Ganze der Taubenzucht:’ Weimar, 1837, pl. 11 and 12.
[8] Boitard and Corbié, ‘Les Pigeons,’ etc., p. 177, pl. 6.
[9] ‘Die Taubenzucht,’ Ulm, 1824, s. 42.
[10] This treatise was written by Sayzid Mohammed Musari, who died in 1770: I owe to the great kindness of Sir W. Elliot a translation of this curious treatise.
[11] ‘Poultry Chronicle,’ vol. 2, p. 573.
[12] ‘Annals and Mag. of Nat. History,’ vol. xix, 1847, p. 105.
[13] This gland occurs in most birds; but Nitzsch (in his ‘Pterylographie,’ 1840, p. 55) states that it is absent in two species of Columba, in several species of Psittacus, in some species of Otis, and in most or all birds of the Ostrich family. It can hardly be an accidental coincidence that the two species of Columba, which are destitute of an oil-gland, have an unusual number of tail-feathers, namely 16, and in this respect resemble Fantails.
[14] See the two excellent editions published by Mr. J. M. Eaton in 1852 and 1858, entitled ‘A Treatise on Fancy Pigeons.’
[15] English translation, by F. Gladwin, 4th edition, vol. i. The habit of the Lotan is also described in the Persian treatise before alluded to, published about 100 years ago: at this date the Lotans were generally white and crested as at present. Mr. Blyth describes these birds in ‘Annals and Mag. of Nat. Hist.,’ vol. xiv., 1847, p. 104; he says that they “may be seen at any of the Calcutta bird-dealers.”
[16] ‘Journal of Horticulture,’ Oct. 22, 1861, p. 76.
[17] See the account of the House-tumblers kept at Glasgow, in the ‘Cottage Gardener,’ 1858, p. 285. Also Mr. Brent’s paper, ‘Journal of Horticulture,’ 1861, p. 76.
[18] J. M. Eaton, ‘Treatise on Pigeons,’ 1852, p. 9.
[19] J. M. Eaton, ‘Treatise,’ edit. 1858, p. 76.
[20] Neumeister, ‘Taubenzucht,’ tab. 4. fig. i.
[21] Riedel, ‘Die Taubenzucht,’ 1824, s. 26. Bechstein, ‘Naturgeschichte Deutschlands,’ Band iv. s. 36, 1795.
[22] Willughby’s ‘Ornithology,’ edited by Ray.
[23] J. M. Eaton’s edition (1858) of Moore, p. 98.
[24] Pigeon pattu plongeur. ‘Les Pigeons,’ etc., p. 165.
[25] ‘Naturgeschichte Deutschlands,’ Band iv. s. 47.
[26] Mr. W. B. Tegetmeier, ‘Journal of Horticulture,’ Jan. 20, 1863, p. 58.
[27] ‘Coup-d’œil sur L’Ordre des Pigeons,’ par C. L. Bonaparte (‘Comptes Rendus’), 1854-55. Mr. Blyth, in ‘Annals of Nat. Hist.,’ vol. xix., 1847, p. 41, mentions, as a very singular fact, “that of the two species of Ectopistes, which are nearly allied to each other, one should have fourteen tail-feathers, while the other, the passenger pigeon of North America, should possess but the usual number—twelve.”
[28] Described and figured in the ‘Poultry Chronicle,’ vol. iii., 1855, p. 82.
[29] ‘The Pigeon Book,’ by Mr. B. P. Brent, 1859, p. 41.
[30] ‘Die staarhälsige Taube. Das Ganze, etc.,’ s. 21, tab. i. fig. 4.
[31] ‘A Treatise on the Almond-Tumbler,’ by J. M. Eaton, 1852, p. 8, et passim.
[32] ‘A Treatise, etc.,’ p. 10.
[33] Boitard and Corbié ‘Les Pigeons,’ etc., 1824, p. 173.
[34] ‘Le Pigeon Voyageur Belge,’ 1865, p. 87. I have given in my ‘Descent of Man’ (6th edit. p. 466) some curious cases, on the authority of Mr. Tegetmeier, of silver-coloured (i.e. very pale blue) birds being generally females, and of the ease with which a race thus characterised could be produced. Bonizzi (see ‘Variazioni dei Columbi domestici:’ Padova, 1873) states that certain coloured spots are often different in the two sexes, and the certain tints are commoner in females than in male pigeons.
[35] Prof. A. Newton (‘Proc. Zoolog. Soc.,’ 1865, p. 716) remarks that he knows no species which present any remarkable sexual distinction; but Mr. Wallace informs me, that in the sub-family of the Treronidæ the sexes often differ considerably in colour. See also on sexual differences in the Columbidæ, Gould, ‘Handbook to the Birds of Australia,’ vol. ii., pp. 109-149.
[36] I am not sure that I have designated the different kinds of vertebræ correctly: but I observe that different anatomists follow in this respect different rules, and, as I use the same terms in the comparison of all the skeletons, this, I hope, will not signify.
[37] J. M. Eaton’s ‘Treatise,’ edit. 1858, p. 78.
[38] In an analogous, but converse, manner, certain natural groups of the Columbidæ, from being more terrestrial in their habits than other allied groups, have larger feet. See Prince Bonaparte’s ‘Coup d’œil sur l’Ordre des Pigeons.’
[39] It perhaps deserves notice that besides these five birds two of the eight were Barbs, which, as I have shown, must be classed in the same group with the long-beaked Carriers and Runts. Barbs may properly be called short-beaked Carriers. It would, therefore, appear as if, during the reduction of their beaks, their wings had retained a little of that excess of length which is characteristic of their nearest relations and progenitors.
[40] Temminck, ‘Hist. Nat. Gén. des Pigeons et des Gallinacés,’ tom. i., 1813, p. 170.
[41] This term was used by John Hunter for such differences in structure between the males and females, as are not directly connected with the act of reproduction, as the tail of the peacock, the horns of deer, etc.
CHAPTER VI.
PIGEONS—continued.
ON THE ABORIGINAL PARENT-STOCK OF THE SEVERAL DOMESTIC RACES—HABITS OF LIFE—WILD RACES OF THE ROCK-PIGEON—Dovecot-PIGEONS—PROOFS OF THE DESCENT OF THE SEVERAL RACES FROM COLUMBA LIVIA—FERTILITY OF THE RACES WHEN CROSSED—REVERSION TO THE PLUMAGE OF THE WILD ROCK-PIGEON—CIRCUMSTANCES FAVOURABLE TO THE FORMATION OF THE RACES—ANTIQUITY AND HISTORY OF THE PRINCIPAL RACES—MANNER OF THEIR FORMATION—SELECTION—UNCONSCIOUS SELECTION—CARE TAKEN BY FANCIERS IN SELECTING THEIR BIRDS—SLIGHTLY DIFFERENT STRAINS GRADUALLY CHANGE INTO WELL-MARKED BREEDS—EXTINCTION OF INTERMEDIATE FORMS—CERTAIN BREEDS REMAIN PERMANENT, WHILST OTHERS CHANGE—SUMMARY.
The differences described in the last chapter between the eleven chief domestic races and between individual birds of the same race, would be of little significance, if they had not all descended from a single wild stock. The question of their origin is therefore of fundamental importance, and must be discussed at considerable length. No one will think this superfluous who considers the great amount of difference between the races, who knows how ancient many of them are, and how truly they breed at the present day. Fanciers almost unanimously believe that the different races are descended from several wild stocks, whereas most naturalists believe that all are descended from the Columba livia or rock-pigeon.
Temminck[[1]] has well observed, and Mr. Gould has made the same remark to me, that the aboriginal parent must have been a species which roosted and built its nest on rocks; and I may add that it must have been a social bird. For all the domestic races are highly social, and none are known to build or habitually to roost on trees. The awkward manner in which some pigeons, kept by me in a summer-house near an old walnut-tree, occasionally alighted on the barer branches, was evident.[[2]] Nevertheless, Mr. R. Scot Skirving informs me that he often saw crowds of pigeons in Upper Egypt settling on low trees, but not on palms, in preference to alighting on the mud hovels of the natives. In India Mr. Blyth[[3]] has been assured that the wild C. livia, var. intermedia, sometimes roosts in trees. I may here give a curious instance of compulsion leading to changed habits: the banks of the Nile above lat. 28° 30′ are perpendicular for a long distance, so that when the river is full the pigeons cannot alight on the shore to drink, and Mr. Skirving repeatedly saw whole flocks settle on the water, and drink whilst they floated down the stream. These flocks seen from a distance resembled flocks of gulls on the surface of the sea.
If any domestic race had descended from a species which was not social, or which built its nest and roosted in trees,[[4]] the sharp eyes of fanciers would assuredly have detected some vestige of so different an aboriginal habit. For we have reason to believe that aboriginal habits are long retained under domestication. Thus with the common ass we see signs of its original desert life in its strong dislike to cross the smallest stream of water, and in its pleasure in rolling in the dust. The same strong dislike to cross a stream is common to the camel, which has been domesticated from a very ancient period. Young pigs, though so tame, sometimes squat when frightened, and thus try to conceal themselves even on an open and bare place. Young turkeys, and occasionally even young fowls, when the hen gives the danger-cry, run away and try to hide themselves, like young partridges or pheasants, in order that their mother may take flight, of which she has lost the power. The musk-duck (Cairina moschata) in its native country often perches and roosts on trees,[[5]] and our domesticated musk-ducks, though such sluggish birds, “are fond of perching on the tops of barns, walls, etc., and, if allowed to spend the night in the hen-house, the female will generally go to roost by the side of the hens, but the drake is too heavy to mount thither with ease.”[[6]] We know that the dog, however well and regularly fed, often buries, like the fox, any superfluous food; and we see him turning round and round on a carpet, as if to trample down grass to form a bed; we see him on bare pavements scratching backwards as if to throw earth over his excrement, although, as I believe, this is never effected even where there is earth. In the delight with which lambs and kids crowd together and frisk on the smallest hillock, we see a vestige of their former alpine habits.
We have therefore good reason to believe that all the domestic races of the pigeon are descended either from some one or from several species which both roosted and built their nests on rocks, and were social in disposition. As only five or six wild species have these habits, and make any near approach in structure to the domesticated pigeon, I will enumerate them.
Firstly, the Columba leuconota resembles certain domestic varieties in its plumage, with the one marked and never-failing difference of a white band which crosses the tail at some distance from the extremity. This species, moreover, inhabits the Himalaya, close to the limit of perpetual snow; and therefore, as Mr. Blyth has remarked, is not likely to have been the parent of our domestic breeds, which thrive in the hottest countries. Secondly, the C. rupestris, of Central Asia, which is intermediate[[7]] between the C. leuconota and livia; but has nearly the same coloured tail as the former species. Thirdly, the Columba littoralis builds and roosts, according to Temminck, on rocks in the Malayan archipelago; it is white, excepting parts of the wing and the tip of the tail, which are black; its legs are livid-coloured, and this is a character not observed in any adult domestic pigeon; but I need not have mentioned this species or the closely-allied C. luctuosa, as they in fact belong to the genus Carpophaga. Fourthly, Columba guinea, which ranges from Guinea[[8]] to the Cape of Good Hope, and roosts either on trees or rocks, according to the nature of the country. This species belongs to the genus Strictoenas of Reichenbach, but is closely allied to Columba; it is to some extent coloured like certain domestic races, and has been said to be domesticated in Abyssinia; but Mr. Mansfield Parkyns, who collected the birds of that country and knows the species, informs me that this is a mistake. Moreover, the C. guinea is characterised by the feathers of the neck having peculiar notched tips,—a character not observed in any domestic race. Fifthly, the Columba œnas of Europe, which roosts on trees, and builds its nest in holes, either in trees or the ground; this species, as far as external characters go, might be the parent of several domestic races; but, though it crosses readily with the true rock-pigeon, the offspring, as we shall presently see, are sterile hybrids, and of such sterility there is not a trace when the domestic races are intercrossed. It should also be observed that if we were to admit, against all probability, that any of the foregoing five or six species were the parents of some of our domestic pigeons, not the least light would be thrown on the chief differences between the eleven most strongly-marked races.
We now come to the best known rock-pigeon, the Columba livia, which is often designated in Europe pre-eminently as the Rock-pigeon, and which naturalists believe to be the parent of all the domesticated breeds. This bird agrees in every essential character with the breeds which have been only slightly modified. It differs from all other species in being of a slaty-blue colour, with two black bars on the wings, and with the croup (or loins) white. Occasionally birds are seen in Faroe and the Hebrides with the black bars replaced by two or three black spots; this form has been named by Brehm[[9]] C. amaliæ, but this species has not been admitted as distinct by other ornithologists. Graba[[10]] even found a difference in the bars on the right and left wings of the same bird in Faroe. Another and rather more distinct form is either truly wild or has become feral on the cliffs of England and was doubtfully named by Mr. Blyth[[11]] as C. affinis, but is now no longer considered by him as a distinct species. C. affinis is rather smaller than the rock-pigeon of the Scottish islands, and has a very different appearance owing to the wing-coverts being chequered with black, with similar marks often extending over the back. The chequering consists of a large black spot on the two sides, but chiefly on the outer side, of each feather. The wing-bars in the true rock-pigeon and in the chequered variety are, in fact, due to similar though larger spots symmetrically crossing the secondary wing-feather and the larger coverts. Hence the chequering arises merely from an extension of these marks to other parts of the plumage. Chequered birds are not confined to the coasts of England; for they were found by Graba at Faroe; and W. Thompson[[12]] says that at Islay fully half the wild rock-pigeons were chequered. Colonel King, of Hythe, stocked his dovecot with young wild birds which he himself procured from nests at the Orkney Islands; and several specimens, kindly sent to me by him, were all plainly chequered. As we thus see that chequered birds occur mingled with the true rock-pigeon at three distinct sites, namely, Faroe, the Orkney Islands, and Islay, no importance can be attached to this natural variation in the plumage.
Prince C. L. Bonaparte,[[13]] a great divider of species, enumerates, with a mark of interrogation, as distinct from C. livia, the C. turricola of Italy, the C. rupestris of Daouria, and the C. schimperi of Abyssinia; but these birds differ from C. livia in characters of the most trifling value. In the British Museum there is a chequered pigeon, probably the C. schimperi of Bonaparte, from Abyssinia. To these may be added the C. gymnocyclus of G. R. Gray from W. Africa, which is slightly more distinct, and has rather more naked skin round the eyes than the rock-pigeon; but from information given me by Dr. Daniell, it is doubtful whether this is a wild bird, for dovecot-pigeons (which I have examined) are kept on the coast of Guinea.
The wild rock-pigeon of India (C. intermedia of Strickland) has been more generally accepted as a distinct species. It differs chiefly in the croup being blue instead of snow-white; but as Mr. Blyth informs me, the tint varies, being sometimes albescent. When this form is domesticated chequered birds appear, just as occurs in Europe with the truly wild C. livia. Moreover we shall immediately have proof that the blue and white croup is a highly variable character; and Bechstein[[14]] asserts that with dovecot-pigeons in Germany this is the most variable of all the characters of the plumage. Hence it may be concluded that C. intermedia cannot be ranked as specifically distinct from C. livia.
In Madeira there is a rock-pigeon which a few ornithologists have suspected to be distinct from C. livia. I have examined numerous specimens collected by Mr. E. V. Harcourt and Mr. Mason. They are rather smaller than the rock- pigeon from the Shetland Islands, and their beaks are plainly thinner, but the thickness of the beak varied in the several specimens. In plumage there is remarkable diversity; some specimens are identical in every feather (I speak after actual comparison) with the rock-pigeon of the Shetland Islands; others are chequered, like C. affinis from the cliffs of England, but generally to a greater degree, being almost black over the whole back; others are identical with the so-called C. intermedia of India in the degree of blueness of the croup; whilst others have this part very pale or very dark blue, and are likewise chequered. So much variability raises a strong suspicion that these birds are domestic pigeons which have become feral.
From these facts it can hardly be doubted that C. livia, affinis, intermedia, and the forms marked with an interrogation by Bonaparte ought all to be included under a single species. But it is quite immaterial whether or not they are thus ranked, and whether some one of these forms or all are the progenitors of the various domestic kinds, as far as any light can thus be thrown on the differences between the more strongly-marked races. That common dovecot-pigeons, which are kept in various parts of the world, are descended from one or from several of the above-mentioned wild varieties of C. livia, no one who compares them will doubt. But before making a few remarks on dovecot-pigeons, it should be stated that the wild rock-pigeon has been found easy to tame in several countries. We have seen that Colonel King at Hythe stocked his dovecot more than twenty years ago with young wild birds taken at the Orkney Islands, and since then they have greatly multiplied. The accurate Macgillivray[[15]] asserts that he completely tamed a wild rock-pigeon in the Hebrides; and several accounts are on records of these pigeons having bred in dovecots in the Shetland Islands. In India, as Captain Hutton informs me, the wild rock-pigeon is easily tamed, and breeds readily with the domestic kind; and Mr. Blyth[[16]] asserts that wild birds come frequently to the dovecots and mingle freely with their inhabitants. In the ancient ‘Ayeen Akbery’ it is written that, if a few wild pigeons be taken, “they are speedily joined by a thousand others of their kind.”
Dovecot-pigeons are those which are kept in dovecots in a semi- domesticated state; for no special care is taken of them, and they procure their own food, except during the severest weather. In England, and, judging from MM. Boitard and Corbié’s work, in France, the common dovecot- pigeon exactly resembles the chequered variety of C. livia; but I have seen dovecots brought from Yorkshire without any trace of chequering, like the wild rock-pigeon of the Shetland Islands. The chequered dovecots from the Orkney Islands, after having been domesticated by Colonel King for more than twenty years, differed slightly from each other in the darkness of their plumage and in the thickness of their beaks; the thinnest beak being rather thicker than the thickest one in the Madeira birds. In Germany, according to Bechstein, the common dovecot-pigeon is not chequered. In India they often become chequered, and sometimes pied with white; the croup also, as I am informed by Mr. Blyth, becomes nearly white. I have received from Sir. J. Brooke some dovecot-pigeons, which originally came from the S. Natunas Islands in the Malay Archipelago, and which had been crossed with the Singapore dovecots: they were small and the darkest variety was extremely like the dark chequered variety with a blue croup from Madeira; but the beak was not so thin, though decidedly thinner than in the rock- pigeon from the Shetland Islands. A dovecot-pigeon sent to me by Mr. Swinhoe from Foochow, in China, was likewise rather small, but differed in no other respect. I have also received through the kindness of Dr. Daniell, four living dovecot-pigeons from Sierra Leone,[[17]] these were fully as large as the Shetland rock-pigeon, with even bulkier bodies. In plumage some of them were identical with the Shetland rock pigeon, but with the metallic tints apparently rather more brilliant; others had a blue croup, and resembled the chequered variety of C. intermedia of India; and some were so much chequered as to be nearly black. In these four birds the beak differed slightly in length, but in all it was decidedly shorter, more massive, and stronger than in the wild rock-pigeon from the Shetland Islands, or in the English dovecot. When the beaks of these African pigeons were compared with the thinnest beaks of the wild Madeira specimens, the contrast was great; the former being fully one-third thicker in a vertical direction than the latter; so that any one at first would have felt inclined to rank these birds as specifically distinct; yet so perfectly graduated a series could be formed between the above-mentioned varieties, that it was obviously impossible to separate them.
To sum up: the wild Columba livia, including under this name C. affinis, intermedia, and the other still more closely-affined geographical races, has a vast range from the southern coast of Norway and the Faroe Islands to the shores of the Mediterranean, to Madeira and the Canary Islands, to Abyssinia, India, and Japan. It varies greatly in plumage, being in many places chequered with black, and having either a white or blue croup or loins; it varies also slightly in the size of the beak and body. Dovecot-pigeons, which no one disputes are descended from one or more of the above wild forms, present a similar but greater range of variation in plumage, in the size of body, and in the length and thickness of the beak. There seems to be some relation between the croup being blue or white, and the temperature of the country inhabited by both wild and dovecot pigeons; for nearly all the dovecot-pigeons in the northern parts of Europe have a white croup, like that of the wild European rock-pigeon; and nearly all the dovecot-pigeons of India have a blue croup like that of the wild C. intermedia of India. As in various countries the wild rock-pigeon has been found easy to tame, it seems extremely probable that the dovecot-pigeons throughout the world are the descendants of at least two and perhaps more wild stocks; but these, as we have just seen, cannot be ranked as specifically distinct.
With respect to the variation of C. livia, we may without fear of contradiction go one step further. Those pigeon-fanciers who believe that all the chief races, such as Carriers, Pouters, Fantails, etc., are descended from distinct aboriginal stocks, yet admit that the so-called toy-pigeons, which differ from the rock-pigeon in little except colour, are descended from this bird. By toy-pigeons are meant such birds as Spots, Nuns, Helmets, Swallows, Priests, Monks, Porcelains, Swabians, Archangels, Breasts, Shields, and others in Europe, and many others in India. It would indeed be as puerile to suppose that all these birds are descended from so many distinct wild stocks as to suppose this to be the case with the many varieties of the gooseberry, heartsease, or dahlia. Yet these kinds all breed true, and many of them include sub-varieties which likewise transmit their character truly. They differ greatly from each other and from the rock-pigeon in plumage, slightly in size and proportions of body, in size of feet, and in the length and thickness of their beaks. They differ from each other in these respects more than do dovecot-pigeons. Although we may safely admit that dovecot-pigeons, which vary slightly, and that toy- pigeons, which vary in a greater degree in accordance with their more highly-domesticated condition, are descended from C. livia, including under this name the above-enumerated wild geographical races; yet the question becomes far more difficult when we consider the eleven principal races, most of which have been profoundly modified. It can, however, be shown, by indirect evidence of a perfectly conclusive nature, that these principal races are not descended from so many wild stocks; and if this be once admitted, few will dispute that they are the descendants of C. livia, which agrees with them so closely in habits and in most characters, which varies in a state of nature, and which has certainly undergone a considerable amount of variation, as in the toy-pigeons. We shall moreover presently see how eminently favourable circumstances have been for a great amount of modification in the more carefully tended breeds.
The reasons for concluding that the several principal races are not descended from so many aboriginal and unknown stocks may be grouped under the following six heads:—
Firstly.—If the eleven chief races have not arisen from the variation of some one species, together with its geographical races, they must be descended from several extremely distinct aboriginal species; for no amount of crossing between only six or seven wild forms could produce races so distinct as Pouters, Carriers, Runts, Fantails, Turbits, Short-faced Tumblers, Jacobins, and Trumpeters. How could crossing produce, for instance, a Pouter or a Fantail, unless the two supposed aboriginal parents possessed the remarkable characters of these breeds? I am aware that some naturalists, following Pallas, believe that crossing gives a strong tendency to variation, independently of the characters inherited from either parent. They believe that it would be easier to raise a Pouter or Fantail pigeon from crossing two distinct species, neither of which possessed the characters of these races, than from any single species. I can find few facts in support of this doctrine, and believe in it only to a limited degree; but in a future chapter I shall have to recur to this subject. For our present purpose the point is not material. The question which concerns us is, whether or not many new and important characters have arisen since man first domesticated the pigeon. On the ordinary view, variability is due to changed conditions of life; on the Pallasian doctrine, variability, or the appearance of new characters, is due to some mysterious effect from the crossing of two species, neither of which possesses the characters in question. In some few instances it is possible that well-marked races may have been formed by crossing; for instance, a Barb might perhaps be formed by a cross between a long-beaked Carrier, having large eye-wattles, and some short-beaked pigeon. That many races have been in some degree modified by crossing, and that certain varieties which are distinguished only by peculiar tints have arisen from crosses between differently-coloured varieties, is almost certain. On the doctrine, therefore, that the chief races owe their differences to their descent from distinct species, we must admit that at least eight or nine, or more probably a dozen species, all having the same habit of breeding and roosting on rocks and living in society, either now exist somewhere, or formerly existed, but have become extinct as wild birds. Considering how carefully wild pigeons have been collected throughout the world, and what conspicuous birds they are, especially when frequenting rocks, it is extremely improbable that eight or nine species, which were long ago domesticated and therefore must have inhabited some anciently known country, should still exist in the wild state and be unknown to ornithologists.
The hypothesis that such species formerly existed, but have become extinct, is in some slight degree more probable. But the extinction of so many species within the historical period is a bold hypothesis, seeing how little influence man has had in exterminating the common rock-pigeon, which agrees in all its habits of life with the domestic races. The C. livia now exists and flourishes on the small northern islands of Faroe, on many islands off the coast of Scotland, on Sardinia, and the shores of the Mediterranean, and in the centre of India. Fanciers have sometimes imagined that the several supposed parent-species were originally confined to small islands, and thus might readily have been exterminated; but the facts just given do not favour the probability of their extinction, even on small islands. Nor is it probable, from what is known of the distribution of birds, that the islands near Europe should have been inhabited by peculiar species of pigeons; and if we assume that distant oceanic islands were the homes of the supposed parent-species, we must remember that ancient voyages were tediously slow, and that ships were then ill-provided with fresh food, so that it would not have been easy to bring home living birds. I have said ancient voyages, for nearly all the races of the pigeon were known before the year 1600, so that the supposed wild species must have been captured and domesticated before that date.
Secondly.—The doctrine that the chief domestic races are descended from several aboriginal species, implies that several species were formerly so thoroughly domesticated as to breed readily when confined. Although it is easy to tame most wild birds, experience shows us that it is difficult to get them to breed freely under confinement; although it must be owned that this is less difficult with pigeons than with most other birds. During the last two or three hundred years, many birds have been kept in aviaries, but hardly one has been added to our list of thoroughly reclaimed species: yet on the above doctrine we must admit that in ancient times nearly a dozen kinds of pigeons, now unknown in the wild state, were thoroughly domesticated.
Thirdly.—Most of our domesticated animals have run wild in various parts of the world; but birds, owing apparently to their partial loss of the power of flight, less often than quadrupeds. Nevertheless I have met with accounts showing that the common fowl has become feral in South America and perhaps in West Africa, and on several islands: the turkey was at one time almost feral on the banks of the Parana; and the Guinea-fowl has become perfectly wild at Ascension and in Jamaica. In this latter island the peacock, also, “has become a maroon bird.” The common duck wanders from its home and becomes almost wild in Norfolk. Hybrids between the common and musk-duck which have become wild have been shot in North America, Belgium, and near the Caspian Sea. The goose is said to have run wild in La Plata. The common dovecot-pigeon has become wild at Juan Fernandez, Norfolk Island, Ascension, probably at Madeira, on the shores of Scotland, and, as is asserted, on the banks of the Hudson in North America.[[18]] But how different is the case, when we turn to the eleven chief domestic races of the pigeon, which are supposed by some authors to be descended from so many distinct species! no one has ever pretended that any one of these races has been found wild in any quarter of the world; yet they have been transported to all countries, and some of them must have been carried back to their native homes. On the view that all the races are the product of variation, we can understand why they have not become feral, for the great amount of modification which they have undergone shows how long and how thoroughly they have been domesticated; and this would unfit them for a wild life.
Fourthly.—If it be assumed that the characteristic differences between the various domestic races are due to descent from several aboriginal species, we must conclude that man chose for domestication in ancient times, either intentionally or by chance, a most abnormal set of pigeons; for that species resembling such birds as Pouters, Fantails, Carriers, Barbs, Short-faced Tumblers, Turbits, etc., would be in the highest degree abnormal, as compared with all the existing members of the great pigeon family, cannot be doubted. Thus we should have to believe that man not only formerly succeeded in thoroughly domesticating several highly abnormal species, but that these same species have since all become extinct, or are at least now unknown. This double accident is so extremely improbable that the assumed existence of so many abnormal species would require to be supported by the strongest evidence. On the other hand, if all the races are descended from C. livia, we can understand, as will hereafter be more fully explained, how any slight deviation in structure which first appeared would continually be augmented by the preservation of the most strongly marked individuals; and as the power of selection would be applied according to man’s fancy, and not for the bird’s own good, the accumulated amount of deviation would certainly be of an abnormal nature in comparison with the structure of pigeons living in a state of nature.
I have already alluded to the remarkable fact that the characteristic differences between the chief domestic races are eminently variable; we see this plainly in the great difference in the number of the tail-feathers in the Fantail, in the development of the crop in Pouters, in the length of the beak in Tumblers, in the state of the wattle in Carriers, etc. If these characters are the result of successive variations added together by selection, we can understand why they should be so variable: for these are the very parts which have varied since the domestication of the pigeon, and therefore would be likely still to vary; these variations moreover have been recently, and are still being accumulated by man’s selection; therefore they have not as yet become firmly fixed.
Fifthly.—All the domestic races pair readily together, and, what is equally important, their mongrel offspring are perfectly fertile. To ascertain this fact I made many experiments, which are given in the note below; and recently Mr. Tegetmeier has made similar experiments with the same result.[[19]] The accurate Neumeister asserts that when dovecots are crossed with pigeons of any other breed, the mongrels are extremely fertile and hardy.[[20]] MM. Boitard and Corbié[[21]] affirm, after their great experience, that the more distinct the breeds are which are crossed, the more productive are their mongrel offspring. I admit that the doctrine first broached by Pallas is highly probable, if not actually proved, namely, that closely allied species, which in a state of nature or when first captured would have been in some degree sterile if crossed, lose this sterility after a long course of domestication; yet when we consider the great difference between such races as Pouters, Carriers, Runts, Fantails, Turbits, Tumblers etc., the fact of their perfect, or even increased, fertility when intercrossed in the most complicated manner becomes a strong argument in favour of their having all descended from a single species. This argument is rendered much stronger when we hear (I append in a note[[22]] all the cases which I have collected) that hardly a single well-ascertained instance is known of hybrids between two true species of pigeons being fertile, inter se, or even when crossed with one of their pure parents.
Sixthly.—Excluding certain important characteristic differences, the chief races agree most closely both with each other and with C. livia in all other respects. As previously observed, all are eminently sociable; all dislike to perch or roost, and refuse to build in trees; all lay two eggs, and this is not a universal rule with the Columbidæ; all, as far as I can hear, require the same time for hatching their eggs; all can endure the same great range of climate; all prefer the same food, and are passionately fond of salt; all exhibit (with the asserted exception of the Finnikin and Turner which do not differ much in any other character) the same peculiar gestures when courting the females; and all (with the exception of Trumpeters and Laughers, which likewise do not differ much in any other character) coo in the same peculiar manner, unlike the voice of any other wild pigeon. All the coloured breeds display the same peculiar metallic tints on the breast, a character far from general with pigeons. Each race presents nearly the same range of variation in colour; and in most of the races we have the same singular correlation between the development of down in the young and the future colour of plumage. All have the proportional length of their toes, and of their primary wing-feathers, nearly the same,—characters which are apt to differ in the several members of the Columbidæ. In those races which present some remarkable deviation of structure, such as in the tail of Fantails, crop of Pouters, beak of Carriers and Tumblers, etc., the other parts remain nearly unaltered. Now every naturalist will admit that it would be scarcely possible to pick out a dozen natural species in any family which should agree closely in habits and in general structure, and yet should differ greatly in a few characters alone. This fact is explicable through the doctrine of natural selection; for each successive modification of structure in each natural species is preserved, solely because it is of service; and such modifications when largely accumulated imply a great change in the habits of life, and this will almost certainly lead to other changes of structure throughout the whole organisation. On the other hand, if the several races of the pigeon have been produced by man through selection and variation, we can readily understand how it is that they should still all resemble each other in habits and in those many characters which man has not cared to modify, whilst they differ to so prodigious a degree in those parts which have struck his eye or pleased his fancy.
Besides the points above enumerated, in which all the domestic races resemble C. livia and each other, there is one which deserves special notice. The wild rock-pigeon is of a slaty-blue colour; the wings are crossed by two bars; the croup varies in colour, being generally white in the pigeon of Europe, and blue in that of India; the tail has a black bar close to the end, and the outer webs of the outer tail-feathers are edged with white, except near the tips. These combined characters are not found in any wild pigeon besides C. livia. I have looked carefully through the great collections of pigeons in the British Museum, and I find that a dark bar at the end of the tail is common; that the white edging to the outer tail-feathers is not rare; but that the white croup is extremely rare, and the two black bars on the wings occur in no other pigeon, excepting the alpine C. leuconota and C. rupestris of Asia. Now if we turn to the domestic races, it is highly remarkable, as an eminent fancier, Mr. Wicking, observed to me, that, whenever a blue bird appears in any race, the wings almost invariably show the double black bars.[[23]] The primary wing-feathers may be white or black, and the whole body may be of any colour, but if the wing-coverts are blue, the two black bars are sure to appear. I have myself seen, or acquired trustworthy evidence, as given below,[[24]] of blue birds with black bars on the wing, with the croup either white or very pale or dark blue, with the tail having a terminal black bar, and with the outer feathers externally edged with white or very pale coloured, in the following races, which, as I carefully observed in each case, appeared to be perfectly true: namely, in Pouters, Fantails, Tumblers, Jacobins, Turbits, Barbs, Carriers, Runts of three distinct varieties, Trumpeters, Swallows, and in many other toy-pigeons, which as being closely allied to C. livia, are not worth enumerating. Thus we see that, in purely-bred races of every kind known in Europe, blue birds occasionally appear having all the marks which characterise C. livia, and which concur in no other wild species. Mr. Blyth, also, has made the same observation with respect to the various domestic races known in India.
Certain variations in the plumage are equally common in the wild C. livia, in dovecot-pigeons, and in all the most highly modified races. Thus, in all, the croup varies from white to blue, being most frequently white in Europe, and very generally blue in India.[[25]] We have seen that the wild C. livia in Europe, and dovecots in all parts of the world, often have the upper wing-coverts chequered with black; and all the most distinct races, when blue, are occasionally chequered in precisely the same manner. Thus I have seen Pouters, Fantails, Carriers, Turbits, Tumblers (Indian and English), Swallows, Bald-pates, and other toy-pigeons blue and chequered; and Mr. Esquilant has seen a chequered Runt. I bred from two pure blue Tumblers a chequered bird.
The facts hitherto given refer to the occasional appearance in pure races of blue birds with black wing-bars, and likewise of blue and chequered birds; but it will now be seen that when two birds belonging to distinct races are crossed, neither of which have, nor probably have had during many generations, a trace of blue in their plumage, or a trace of wing-bars and the other characteristic marks, they very frequently produce mongrel offspring of a blue colour, sometimes chequered, with black wing-bars, etc.; or if not of a blue colour, yet with the several characteristic marks more or less plainly developed. I was led to investigate this subject from MM. Boitard and Corbié[[26]] having asserted that from crosses between certain breeds it is rare to get anything but bisets or dovecot pigeons, which, as we know, are blue birds with the usual characteristic marks. We shall hereafter see that this subject possesses, independently of our present object, considerable interest, so that I will give the results of my own trials in full. I selected for experiment races which, when pure, very seldom produce birds of a blue colour, or have bars on their wings and tail.
The Nun is white, with the head, tail, and primary wing-feathers black; it is a breed which was established as long ago as the year 1600. I crossed a male Nun with a female red common Tumbler, which latter variety generally breeds true. Thus neither parent had a trace of blue in the plumage, or of bars on the wing and tail. I should premise that common Tumblers are rarely blue in England. From the above cross I reared several young: one was red over the whole back, but with the tail as blue as that of the rock-pigeon; the terminal bar, however, was absent, but the outer feathers were edged with white: a second and third nearly resembled the first, but the tail in both presented a trace of the bar at the end: a fourth was brownish, and the wings showed a trace of the double bar: a fifth was pale blue over the whole breast, back, croup, and tail, but the neck and primary wing-feathers were reddish; the wings presented two distinct bars of a red colour; the tail was not barred, but the outer feathers were edged with white. I crossed this last curiously coloured bird with a black mongrel of complicated descent, namely, from a black Barb, a Spot, and Almond-tumbler, so that the two young birds produced from this cross included the blood of five varieties, none of which had a trace of blue or of wing and tail-bars: one of the two young birds was brownish-black, with black wing-bars; the other was reddish-dun, with reddish wing-bars, paler than the rest of the body, with the croup pale blue, the tail bluish with a trace of the terminal bar.
Mr. Eaton[[27]] matched two Short-faced Tumblers, namely, a splash cock and kite hen (neither of which are blue or barred), and from the first nest he got a perfect blue bird, and from the second a silver or pale blue bird, both of which, in accordance with all analogy, no doubt presented the usual characteristic marks.
I crossed two male black Barbs with two female red Spots. These latter have the whole body and wings white, with a spot on the forehead, the tail and tail-coverts red; the race existed at least as long ago as 1676, and now breeds perfectly true, as was known to be the case in the year 1735.[[28]] Barbs are uniformly-coloured birds, with rarely even a trace of bars on the wing or tail; they are known to breed very true. The mongrels thus raised were black or nearly black, or dark or pale brown, sometimes slightly piebald with white: of these birds no less than six presented double wing-bars; in two the bars were conspicuous and quite black; in seven some white feathers appeared on the croup; and in two or three there was a trace of the terminal bar to the tail, but in none were the outer tail-feathers edged with white.
I crossed black Barbs (of two excellent strains) with purely-bred, snow-white Fantails. The mongrels were generally quite black, with a few of the primary wing and tail feathers white: others were dark reddish-brown, and others snow-white: none had a trace of wing-bars or of the white croup. I then paired together two of these mongrels, namely, a brown and black bird, and their offspring displayed wing-bars, faint, but of a darker brown than the rest of body. In a second brood from the same parents a brown bird was produced, with several white feathers confined to the croup.
I crossed a male dun Dragon belonging to a family which had been dun- coloured without wing-bars during several generations, with a uniform red Barb (bred from two black Barbs); and the offspring presented decided but faint traces of wing-bars. I crossed a uniform red male Runt with a White trumpeter; and the offspring had a slaty-blue tail with a bar at the end, and with the outer feathers edged with white. I also crossed a female black and white chequered Trumpeter (of a different strain from the last) with a male Almond-tumbler, neither of which exhibited a trace of blue, or of the white croup, or of the bar at end of tail: nor is it probable that the progenitors of these two birds had for many generations exhibited any of these characters, for I have never even heard of a blue Trumpeter in this country, and my Almond-tumbler was purely bred; yet the tail of this mongrel was bluish, with a broad black bar at the end, and the croup was perfectly white. It may be observed in several of these cases, that the tail first shows a tendency to become by reversion blue; and this fact of the persistency of colour in the tail and tail-coverts[[29]] will surprise no one who has attended to the crossing of pigeons.
The last case which I will give is the most curious. I paired a mongrel female Barb-fantail with a mongrel male Barb-spot; neither of which mongrels had the least blue about them. Let it be remembered that blue Barbs are excessively rare; that Spots, as has been already stated, were perfectly characterised in the year 1676, and breed perfectly true; this likewise is the case with white Fantails, so much so that I have never heard of white Fantails throwing any other colour. Nevertheless the offspring from the above two mongrels was of exactly the same blue tint as that of the wild rock-pigeon from the Shetland Islands over the whole back and wings; the double black wing-bars were equally conspicuous; the tail was exactly alike in all its characters, and the croup was pure white; the head, however, was tinted with a shade of red, evidently derived from the Spot, and was of a paler blue than in the rock-pigeon, as was the stomach. So that two black Barbs, a red Spot, and a white Fantail, as the four purely-bred grandparents, produced a bird exhibiting the general blue colour, together with every characteristic mark, the wild Columba livia.
With respect to crossed breeds frequently producing blue birds chequered with black, and resembling in all respects both the dovecot-pigeon and the chequered wild variety of the rock-pigeon, the statement before referred to by MM. Boitard and Corbié would almost suffice; but I will give three instances of the appearance of such birds from crosses in which one alone of the parents or great-grandparents was blue, but not chequered. I crossed a male blue Turbit with a snow-white Trumpeter, and the following year with a dark, leaden-brown, Short-faced Tumbler; the offspring from the first cross were as perfectly chequered as any dovecot-pigeon; and from the second, so much so as to be nearly as black as the most darkly chequered rock-pigeon from Madeira. Another bird, whose great-grandparents were a white Trumpeter, a white Fantail, a white Red-spot, a red Runt, and a blue Pouter, was slaty-blue and chequered exactly like a dovecot-pigeon. I may here add a remark made to me by Mr. Wicking, who has had more experience than any other person in England in breeding pigeons of various colours: namely, that when a blue, or a blue and chequered bird, having black wing- bars, once appears in any race and is allowed to breed, these characters are so strongly transmitted that it is extremely difficult to eradicate them.
What, then, are we to conclude from this tendency in all the chief domestic races, both when purely bred and more especially when intercrossed, to produce offspring of a blue colour, with the same characteristic marks, varying in the same manner, as in Columbia livia? If we admit that these races are all descended from C. livia, no breeder will doubt that the occasional appearance of blue birds thus characterised is accounted for on the well-known principle of “throwing back” or reversion. Why crossing should give so strong a tendency to reversion, we do not with certainty know; but abundant evidence of this fact will be given in the following chapters. It is probable that I might have bred even for a century pure black Barbs, Spots, Nuns, white Fantails, Trumpeters, etc., without obtaining a single blue or barred bird; yet by crossing these breeds I reared in the first and second generation, during the course of only three or four years, a considerable number of young birds, more or less plainly coloured blue, and with most of the characteristic marks. When black and white, or black and red birds, are crossed, it would appear that a slight tendency exists in both parents to produce blue offspring, and that this, when combined, overpowers the separate tendency in either parent to produce black, or white, or red offspring.
If we reject the belief that all the races of the pigeon are the modified descendants of C. livia, and suppose that they are descended from several aboriginal stocks, then we must choose between the three following assumptions: firstly, that at least eight or nine species formerly existed which were aboriginally coloured in various ways, but have since varied in exactly the same manner so as to assume the colouring of C. livia; but this assumption throws not the least light on the appearance of such colours and marks when the races are crossed. Or secondly, we may assume that the aboriginal species were all coloured blue, and had the wing-bars and other characteristic marks of C. livia,—a supposition which is highly improbable, as besides this one species no existing member of the Columbidæ presents these combined characters; and it would not be possible to find any other instance of several species identical in plumage, yet as different in important points of structure as are Pouters, Fantails, Carriers, Tumblers, etc. Or lastly, we may assume that all the races, whether descended from C. livia or from several aboriginal species, although they have been bred with so much care and are so highly valued by fanciers, have all been crossed within a dozen or score of generations with C. livia, and have thus acquired their tendency to produce blue birds with the several characteristic marks. I have said that it must be assumed that each race has been crossed with C. livia within a dozen, or, at the utmost, within a score of generations; for there is no reason to believe that crossed offspring ever revert to one of their ancestors when removed by a greater number of generations. In a breed which has been crossed only once, the tendency to reversion will naturally become less and less in the succeeding generations, as in each there will be less and less of the blood of the foreign breed; but when there has been no cross with a distinct breed, and there is a tendency in both parents to revert to some long-lost character, this tendency, for all that we can see to the contrary, may be transmitted undiminished for an indefinite number of generations. These two distinct cases of reversion are often confounded together by those who have written on inheritance.
Considering, on the one hand, the improbability of the three assumptions which have just been discussed, and, on the other hand, how simply the facts are explained on the principle of reversion, we may conclude that the occasional appearance in all the races, both when purely bred and more especially when crossed, of blue birds, sometimes chequered, with double wing-bars, with white or blue croups, with a bar at the end of the tail, and with the outer tail-feathers edged with white, affords an argument of the greatest weight in favour of the view that all are descended from Columba livia, including under this name the three or four wild varieties or sub-species before enumerated.
To sum up the six foregoing arguments, which are opposed to the belief that the chief domestic races are the descendants of at least eight or nine or perhaps a dozen species; for the crossing of any less number would not yield the characteristic differences between the several races. Firstly, the improbability that so many species should still exist somewhere, but be unknown to ornithologists, or that they should have become within the historical period extinct, although man has had so little influence in exterminating the wild C. livia. Secondly, the improbability of man in former times having thoroughly domesticated and rendered fertile under confinement so many species. Thirdly, these supposed species having nowhere become feral. Fourthly, the extraordinary fact that man should, intentionally or by chance, have chosen for domestication several species, extremely abnormal in character; and furthermore, the points of structure which render these supposed species so abnormal being now highly variable. Fifthly, the fact of all the races, though differing in many important points of structure, producing perfectly fertile mongrels; whilst all the hybrids which have been produced between even closely allied species in the pigeon-family are sterile. Sixthly, the remarkable statements just given on the tendency in all the races, both when purely bred and when crossed, to revert in numerous minute details of colouring to the character of the wild rock-pigeon, and to vary in a similar manner. To these arguments may be added the extreme improbability that a number of species formerly existed, which differed greatly from each other in some few points, but which resembled each other as closely as do the domestic races in other points of structure, in voice, and in all their habits of life. When these several facts and arguments are fairly taken into consideration, it would require an overwhelming amount of evidence to make us admit that the chief domestic races are descended from several aboriginal stocks; and of such evidence there is absolutely none.
The belief that the chief domestic races are descended from several wild stocks no doubt has arisen from the apparent improbability of such great modifications of structure having been effected since man first domesticated the rock-pigeon. Nor am I surprised at any degree of hesitation in admitting their common parentage: formerly, when I went into my aviaries and watched such birds as Pouters, Carriers, Barbs, Fantails, and Short-faced Tumblers, etc., I could not persuade myself that all had descended from the same wild stock, and that man had consequently in one sense created these remarkable modifications. Therefore I have argued the question of their origin at great, and, as some will think, superfluous length.
Finally, in favour of the belief that all the races are descended from a single stock, we have in Columba livia a still existing and widely distributed species, which can be and has been domesticated in various countries. This species agrees in most points of structure and in all its habits of life, as well as occasionally in every detail of plumage, with the several domestic races. It breeds freely with them, and produces fertile offspring. It varies in a state of nature,[[30]] and still more so when semi-domesticated, as shown by comparing the Sierra Leone pigeons with those of India, or with those which apparently have run wild in Madeira. It has undergone a still greater amount of variation in the case of the numerous toy-pigeons, which no one supposes to be descended from distinct species; yet some of these toy-pigeons have transmitted their character truly for centuries. Why, then, should we hesitate to believe in that greater amount of variation which is necessary for the production of the eleven chief races? It should be borne in mind that in two of the most strongly-marked races, namely, Carriers and Short-faced Tumblers, the extreme forms can be connected with the parent-species by graduated differences not greater than those which may be observed between the dovecot-pigeons inhabiting different countries, or between the various kinds of toy-pigeons,—gradations which must certainly be attributed to variation.
That circumstances have been eminently favourable for the modification of the pigeon through variation and selection will now be shown. The earliest record, as has been pointed out to me by Professor Lepsius, of pigeons in a domesticated condition, occurs in the fifth Egyptian dynasty, about 3000 B.C.;[[31]] but Mr. Birch, of the British Museum, informs me that the pigeon appears in a bill of fare in the previous dynasty. Domestic pigeons are mentioned in Genesis, Leviticus, and Isaiah.[[32]] In the time of the Romans, as we hear from Pliny,[[33]] immense prices were given for pigeons; “nay, they are come to this pass, that they can reckon up their pedigree and race.” In India, about the year 1600, pigeons were much valued by Akbar Khan: 20,000 birds were carried about with the court, and the merchants brought valuable collections. “The monarch of Iran and Turan sent him some very rare breeds. His Majesty,” says the courtly historian, “by crossing the breeds, which method was never practised before, has improved them astonishingly.”[[34]] Akber Khan possessed seventeen distinct kinds, eight of which were valuable for beauty alone. At about this same period of 1600 the Dutch, according to Aldrovandi, were as eager about pigeons as the Romans had formerly been. The breeds which were kept during the fifteenth century in Europe and in India apparently differed from each other. Tavernier, in his Travels in 1677, speaks, as does Chardin in 1735, of the vast number of pigeon-houses in Persia; and the former remarks that, as Christians were not permitted to keep pigeons, some of the vulgar actually turned Mahometans for this sole purpose. The Emperor of Morocco had his favourite keeper of pigeons, as is mentioned in Moore’s treatise, published 1737. In England, from the time of Willughby in 1678 to the present day, as well as in Germany and in France, numerous treatises have been published on the pigeon. In India, about a hundred years ago, a Persian treatise was written; and the writer thought it no light affair, for he begins with a solemn invocation, “in the name of God, the gracious and merciful.” Many large towns, in Europe and the United States, now have their societies of devoted pigeon-fanciers: at present there are three such societies in London. In India, as I hear from Mr. Blyth, the inhabitants of Delhi and of some other great cities are eager fanciers. Mr. Layard informs me that most of the known breeds are kept in Ceylon. In China, according to Mr. Swinhoe of Amoy, and Dr. Lockhart of Shangai, Carriers, Fantails, Tumblers, and other varieties are reared with care, especially by the bonzes or priests. The Chinese fasten a kind of whistle to the tail-feathers of their pigeons, and as the flock wheels through the air they produce a sweet sound. In Egypt the late Abbas Pacha was a great fancier of Fantails. Many pigeons are kept at Cairo and Constantinople, and these have lately been imported by native merchants, as I hear from Sir W. Elliot, into Southern India, and sold at high prices.
The foregoing statements show in how many countries, and during how long a period, many men have been passionately devoted to the breeding of pigeons. Hear how an enthusiastic fancier at the present day writes: “If it were possible for noblemen and gentlemen to know the amazing amount of solace and pleasure derived from Almond Tumblers, when they begin to understand their properties, I should think that scarce any nobleman or gentleman would be without their aviaries of Almond Tumblers.”[[35]] The pleasure thus taken is of paramount importance, as it leads amateurs carefully to note and preserve each slight deviation of structure which strikes their fancy. Pigeons are often closely confined during their whole lives; they do not partake of their naturally varied diet; they have often been transported from one climate to another; and all these changes in their conditions of life would be likely to cause variability. Pigeons have been domesticated for nearly 5000 years, and have been kept in many places, so that the numbers reared under domestication must have been enormous: and this is another circumstance of high importance, for it obviously favours the chance of rare modifications of structure occasionally appearing. Slight variations of all kinds would almost certainly be observed, and, if valued, would, owing to the following circumstances, be preserved and propagated with unusual facility. Pigeons, differently from any other domesticated animal, can easily be mated for life, and, though kept with other pigeons, rarely prove unfaithful to each other. Even when the male does break his marriage-vow, he does not permanently desert his mate. I have bred in the same aviaries many pigeons of different kinds, and never reared a single bird of an impure strain. Hence a fancier can with the greatest ease select and match his birds. He will also see the good results of his care; for pigeons breed with extraordinary rapidity. He may freely reject inferior birds, as they serve at an early age as excellent food.
History of the principal Races of the Pigeon.[[36]]
Before discussing the means and steps by which the chief races have been formed, it will be advisable to give some historical details, for more is known of the history of the pigeon, little though this is, than of any other domesticated animal. Some of the cases are interesting as proving how long domestic varieties may be propagated with exactly the same or nearly the same characters; and other cases are still more interesting as showing how slowly but steadily races have been greatly modified during successive generations. In the last chapter I stated that Trumpeters and Laughers, both so remarkable for their voices, seem to have been perfectly characterised in 1735; and Laughers were apparently known in India before the year 1600. Spots in 1676, and Nuns in the time of Aldrovandi, before 1600, were coloured exactly as they now are. Common Tumblers and Ground Tumblers displayed in India, before the year 1600, the same extraordinary peculiarities of flight as at the present day, for they are well described in the ‘Ayeen Akbery.’ These breeds may all have existed for a much longer period; we know only that they were perfectly characterised at the dates above given. The average length of life of the domestic pigeon is probably about five or six years; if so, some of these races have retained their character perfectly for at least forty or fifty generations.
Pouters.—These birds, as far as a very short description serves for comparison, appear to have been well characterised in Aldrovandi’s time,[[37]] before the year 1600. Length of body and length of leg are at the present time the two chief points of excellence. In 1735 Moore said (see Mr. J. M. Eaton’s edition)—and Moore was a first-rate fancier—that he once saw a bird with a body 20 inches in length, “though 17 or 18 inches is reckoned a very good length;” and he has seen the legs very nearly 7 inches in length, yet a leg 6½ or 6¾ long “must be allowed to be a very good one.” Mr. Bult, the most successful breeder of Pouters in the world, informs me that at present (1858) the standard length of the body is not less than 18 inches; but he has measured one bird 19 inches in length, and has heard of 20 and 22 inches, but doubts the truth of these latter statements. The standard length of the leg is now 7 inches, but Mr. Bult has recently measured two of his own birds with legs 7½ long. So that in the 123 years which have elapsed since 1735 there has been hardly any increase in the standard length of the body; 17 or 18 inches was formerly reckoned a very good length, and now 18 inches is the minimum standard; but the length of leg seems to have increased, as Moore never saw one quite 7 inches long; now the standard is 7, and two of Mr. Bult’s birds measured 7½ inches in length. The extremely slight improvement in Pouters, except in the length of the leg, during the last 123 years, may be partly accounted for by the neglect which they suffered, as I am informed by Mr. Bult, until within the last 20 or 30 years. About 1765[[38]] there was a change of fashion, stouter and more feathered legs being preferred to thin and nearly naked legs.
Fantails.—The first notice of the existence of this breed is in India, before the year 1600, as given in the ‘Ayeen Akbery;’[[39]] at this date, judging from Aldrovandi, the breed was unknown in Europe. In 1677 Willughby speaks of a Fantail with 26 tail-feathers; in 1735 Moore saw one with 36 feathers; and in 1824 MM. Boitard and Corbié assert that in France birds can easily be found with 42 tail-feathers. In England, the number of the tail-feathers is not at present so much regarded as their upward direction and expansion. The general carriage of the bird is likewise now much valued. The old descriptions do not suffice to show whether in these latter respects there has been much improvement: but if Fantails with their heads and tails touching had formerly existed, as at the present time, the fact would almost certainly have been noticed. The Fantails which are now found in India probably show the state of the race, as far as carriage is concerned, at the date of their introduction into Europe; and some, said to have been brought from Calcutta, which I kept alive, were in a marked manner inferior to our exhibition birds. The Java Fantail shows the same difference in carriage; and although Mr. Swinhoe has counted 18 and 24 tail-feathers in his birds, a first-rate specimen sent to me had only 14 tail-feathers.
Jacobins.—This breed existed before 1600, but the hood, judging from the figure given by Aldrovandi, did not enclose the head nearly so perfectly as at present: nor was the head then white; nor were the wings and tail so long, but this last character might have been overlooked by the rude artist. In Moore’s time, in 1735, the Jacobin was considered the smallest kind of pigeon, and the bill is said to be very short. Hence either the Jacobin, or the other kinds with which it was then compared, must since that time have been considerably modified; for Moore’s description (and it must be remembered that he was a first-rate judge) is clearly not applicable, as far as size of body and length of beak are concerned, to our present Jacobins. In 1795, judging from Bechstein, the breed had assumed its present character.
Turbits.—It has generally been supposed by the older writers on pigeons, that the Turbit is the Cortbeck of Aldrovandi; but if this be the case, it is an extraordinary fact that the characteristic frill should not have been noticed. The beak, moreover, of the Cortbeck is described as closely resembling that of the Jacobin, which shows a change in the one or the other race. The Turbit, with its characteristic frill, and bearing its present name, is described by Willughby in 1677; and the bill is said to be like that of the bullfinch,—a good comparison, but now more strictly applicable to the beak of the Barb. The sub-breed called the Owl was well known in Moore’s time, in 1735.
Tumblers.—Common Tumblers, as well as Ground Tumblers, perfect as far as tumbling is concerned, existed in India before the year 1600; and at this period diversified modes of flight, such as flying at night, the ascent to a great height, and manner of descent, seem to have been much attended to in India, as at the present time. Belon[[40]] in 1555 saw in Paphlagonia what he describes as “a very new thing, viz. pigeons which flew so high in the air that they were lost to view, but returned to their pigeon-house without separating.” This manner of flight is characteristic of our present Tumblers, but it is clear that Belon would have mentioned the act of tumbling if the pigeons described by him had tumbled. Tumblers were not known in Europe in 1600, as they are not mentioned by Aldrovandi, who discusses the flight of pigeons. They are briefly alluded to by Willughby, in 1687, as small pigeons “which show like footballs in the air.” The short-faced race did not exist at this period, as Willughby could not have overlooked birds so remarkable for their small size and short beaks. We can even trace some of the steps by which this race has been produced. Moore in 1735 enumerates correctly the chief points of excellence, but does not give any description of the several sub-breeds; and from this fact Mr. Eaton infers[[41]] that the Short-faced Tumbler had not then come to full perfection. Moore even speaks of the Jacobin as being the smallest pigeon. Thirty years afterwards, in 1765, in the Treatise dedicated to Mayor, short-faced Almond Tumblers are fully described, but the author, an excellent fancier, expressly states in his Preface (p. xiv.) that, “from great care and expense in breeding them, they have arrived to so great perfection and are so different from what they were 20 or 30 years past, that an old fancier would have condemned them for no other reason than because they are not like what used to be thought good when he was in the fancy before.” Hence it would appear that there was a rather sudden change in the character of the short-faced Tumbler at about this period; and there is reason to suspect that a dwarfed and half-monstrous bird, the parent-form of the several short-faced sub-breeds, then appeared. I suspect this because short-faced Tumblers are born with their beaks (ascertained by careful measurement) as short, proportionally with the size of their bodies, as in the adult bird; and in this respect they differ greatly from all other breeds, which slowly acquire during growth their various characteristic qualities.
Since the year 1765 there has been some change in one of the chief characters of the short-faced Tumbler, namely, in the length of the beak. Fanciers measure the “head and beak” from the tip of the beak to the front corner of the eyeball. About the year 1765 a “head and beak” was considered good,[[42]] which, measured in the usual manner, was 7/8 of an inch in length; now it ought not to exceed 5/8 of an inch; “it is however possible,” as Mr. Eaton candidly confesses,“for a bird to be considered as pleasant or neat even at 6/8 of an inch, but exceeding that length it must be looked upon as unworthy of attention.” Mr. Eaton states that he has never seen in the course of his life more than two or three birds with the “head and beak” not exceeding half an inch in length; “still I believe in the course of a few years that the head and beak will be shortened, and that half-inch birds will not be considered so great a curiosity as at the present time.” That Mr. Eaton’s opinion deserves attention cannot be doubted, considering his success in winning prizes at our exhibitions. Finally in regard to the Tumbler it may be concluded from the facts above given that it was originally introduced into Europe, probably first into England, from the East; and that it then resembled our common English Tumbler, or more probably the Persian or Indian Tumbler, with a beak only just perceptibly shorter than that of the common dovecot-pigeon. With respect to the short-faced Tumbler, which is not known to exist in the East, there can hardly be a doubt that the whole wonderful change in the size of the head, beak, body and feet, and in general carriage, has been produced during the last two centuries by continued selection, aided probably by the birth of a semi- monstrous bird somewhere about the year 1750.
Runts.—Of their history little can be said. In the time of Pliny the pigeons of Campania were the largest known; and from this fact alone some authors assert that they were Runts. In Aldrovandi’s time, in 1600, two sub-breeds existed; but one of them, the short-beaked, is now extinct in Europe.
Barbs.—Notwithstanding statements to the contrary, it seems to me impossible to recognise the Barb in Aldrovandi’s description and figures; four breeds, however, existed in the year 1600 which evidently were allied both to Barbs and Carriers. To show how difficult it is to recognise some of the breeds described by Aldrovandi I will give the different opinions in regard to the above four kinds, named by him C. indica, cretensis, gutturosa, and persica. Willughby thought that the Columba indica was a Turbit, but the eminent fancier Mr. Brent believes that it was an inferior Barb: C. cretensis, with a short beak and a swelling on the upper mandible, cannot be recognised: C. (falsely called) gutturosa, which from its rostrum, breve, crassum, et tuberosum seems to me to come nearest to the Barb, Mr. Brent believes to be a Carrier; and lastly, the C. persica et turcica, Mr. Brent thinks, and I quite concur with him, was a short-beaked Carrier with very little wattle. In 1687 the Barb was known in England, and Willughby describes the beak as like that of the Turbit; but it is not credible that his Barbs should have had a beak like that of our present birds, for so accurate an observer could not have overlooked its great breadth.
English Carrier.—We may look in vain in Aldrovandi’s work for any bird resembling our prize Carriers; the C. persica et turcica of this author comes the nearest, but is said to have had a short thick beak; therefore it must have approached in character a Barb, and have differed greatly from our Carriers. In Willughby’s time, in 1677, we can clearly recognise the Carrier, yet he adds, “the bill is not short, but of a moderate length;” a description which no one would apply to our present Carriers, so conspicuous for the extraordinary length of their beaks. The old names given in Europe to the Carrier, and the several names now in use in India, indicate that Carriers originally came from Persia; and Willughby’s description would perfectly apply to the Bussorah Carrier as it now exists in Madras. In later times we can partially trace the progress of change in our English Carriers: Moore, in 1735, says “an inch and a half is reckoned a long beak, though there are very good Carriers that are found not to exceed an inch and a quarter.” These birds must have resembled or perhaps been a little superior to the Carriers, previously described, now found in Persia. In England at the present day “there are,” as Mr. Eaton[[43]] states, “beaks that would measure (from edge of eye to tip of beak) one inch and three-quarters, and some few even two inches in length.”
From these historical details we see that nearly all the chief domestic races existed before the year 1600. Some remarkable only for colour appear to have been identical with our present breeds, some were nearly the same, some considerably different, and some have since become extinct. Several breeds, such as Finnikins and Turners, the swallow-tailed pigeon of Bechstein and the Carmelite, seem to have originated and to have disappeared within this same period. Any one now visiting a well-stocked English aviary would certainly pick out as the most distinct kinds, the massive Runt, the Carrier with its wonderfully elongated beak and great wattles, the Barb with its short broad beak and eye-wattles, the short-faced Tumbler with its small conical beak, the Pouter with its great crop, long legs and body, the Fantail with its upraised, widely-expanded, well-feathered tail, the Turbit with its frill and short blunt beak, and the Jacobin with his hood. Now, if this same person could have viewed the pigeons kept before 1600 by Akber Khan in India and by Aldrovandi in Europe, he would have seen the Jacobin with a less perfect hood; the Turbit apparently without its frill; the Pouter with shorter legs, and in every way less remarkable—that is, if Aldrovandi’s Pouter resembled the old German kind; the Fantail would have been far less singular in appearance, and would have had much fewer feathers in its tail; he would have seen excellent flying Tumblers, but he would in vain have looked for the marvellous short-faced breeds; he would have seen birds allied to Barbs, but it is extremely doubtful whether he would have met with our actual Barbs; and lastly, he would have found Carriers with beaks and wattle incomparably less developed than in our English Carriers. He might have classed most of the breeds in the same groups as at present; but the differences between the groups were then far less strongly pronounced than at present. In short, the several breeds had at this early period not diverged in so great a degree as now from their aboriginal common parent, the wild rock-pigeon.
Manner of Formation of the chief Races.
We will now consider more closely the probable steps by which the chief races have been formed. As long as pigeons are kept semi-domesticated in dovecots in their native country, without any care in selecting and matching them, they are liable to little more variation than the wild C. livia, namely, in the wings becoming chequered with black, in the croup being blue or white, and in the size of the body. When, however, dovecot-pigeons are transported into diversified countries, such as Sierra Leone, the Malay archipelago, and Madeira, they are exposed to new conditions of life; and apparently in consequence vary in a somewhat greater degree. When closely confined, either for the pleasure of watching them, or to prevent their straying, they must be exposed, even in their native climate, to considerably different conditions; for they cannot obtain their natural diversity of food; and, what is probably more important, they are abundantly fed, whilst debarred from taking much exercise. Under these circumstances we might expect to find, from the analogy of all other domesticated animals, a greater amount of individual variability than with the wild pigeon; and this is the case. The want of exercise apparently tends to reduce the size of the feet and organs of flight; and then, from the law of correlation of growth, the beak apparently becomes affected. From what we now see occasionally taking place in our aviaries, we may conclude that sudden variations or sports, such as the appearance of a crest of feathers on the head, of feathered feet, of a new shade of colour, of an additional feather in the tail or wing, would occur at rare intervals during the many centuries which have elapsed since the pigeon was first domesticated. At the present day such “sports” are generally rejected as blemishes; and there is so much mystery in the breeding of pigeons that, if a valuable sport did occur, its history would often be concealed. Before the last hundred and fifty years, there is hardly a chance of the history of any such sport having been recorded. But it by no means follows from this that such sports in former times, when the pigeon had undergone much less variation, would have been rejected. We are profoundly ignorant of the cause of each sudden and apparently spontaneous variation, as well as of the infinitely numerous shades of difference between the birds of the same family. But in a future chapter we shall see that all such variations appear to be the indirect result of changes of some kind in the conditions of life.
Hence, after a long course of domestication, we might expect to see in the pigeon much individual variability, and occasional sudden variations, as well as slight modifications from the lessened use of certain parts, together with the effects of correlation of growth. But without selection all this would produce only a trifling or no result; for without such aid differences of all kinds would, from the two following causes, soon disappear. In a healthy and vigorous lot of pigeons many more young birds are killed for food or die than are reared to maturity; so that an individual having any peculiar character, if not selected, would run a good chance of being destroyed; and if not destroyed, the peculiarity in question would generally be obliterated by free intercrossing. It might, however, occasionally happen that the same variation repeatedly occurred, owing to the action of peculiar and uniform conditions of life, and in this case it would prevail independently of selection. But when selection is brought into play all is changed; for this is the foundation-stone in the formation of new races; and with the pigeon, circumstances, as we have already seen, are eminently favourable for selection. When a bird presenting some conspicuous variation has been preserved, and its offspring have been selected, carefully matched, and again propagated, and so onwards during successive generations, the principle is so obvious that nothing more need be said about it. This may be called methodical selection, for the breeder has a distinct object in view, namely, to preserve some character which has actually appeared; or to create some improvement already pictured in his mind.
Another form of selection has hardly been noticed by those authors who have discussed this subject, but is even more important. This form may be called unconscious selection, for the breeder selects his birds unconsciously, unintentionally, and without method, yet he surely though slowly produces a great result. I refer to the effects which follow from each fancier at first procuring and afterwards rearing as good birds as he can, according to his skill, and according to the standard of excellence at each successive period. He does not wish permanently to modify the breed; he does not look to the distant future, or speculate on the final result of the slow accumulation during many generations of successive slight changes; he is content if he possesses a good stock, and more than content if he can beat his rivals. The fancier in the time of Aldrovandi, when in the year 1600 he admired his own Jacobins, Pouters, or Carriers, never reflected what their descendants in the year 1860 would become: he would have been astonished could he have seen our Jacobins, our improved English Carriers, and our Pouters; he would probably have denied that they were the descendants of his own once-admired stock, and he would perhaps not have valued them, for no other reason, as was written in 1765, “than because they were not like what used to be thought good when he was in the fancy.” No one will attribute the lengthened beak of the Carrier, the shortened beak of the Short-faced Tumbler, the lengthened leg of the Pouter, the more perfectly enclosed hood of the Jacobin, etc.—changes effected since the time of Aldrovandi, or even since a much later period,—to the direct and immediate action of the conditions of life. For these several races have been modified in various and even in directly opposite ways, though kept under the same climate and treated in all respects in as nearly uniform a manner as possible. Each slight change in the length or shortness of the beak, in the length of leg, etc., has no doubt been indirectly and remotely caused by some change in the conditions to which the bird has been subjected, but we must attribute the final result, as is manifest in those cases of which we have any historical record, to the continued selection and accumulation of many slight successive variations.
The action of unconscious selection, as far as pigeons are concerned, depends on a universal principle in human nature, namely, on our rivalry, and desire to outdo our neighbours. We see this in every fleeting fashion, even in our dress, and it leads the fancier to endeavour to exaggerate every peculiarity in his breeds. A great authority on pigeons,[[44]] says, “Fanciers do not and will not admire a medium standard, that is, half and half, which is neither here nor there, but admire extremes.” After remarking that the fancier of Short-faced Beard Tumblers wishes for a very short beak, and that the fancier of Long-faced Beard Tumblers wishes for a very long beak, he says, with respect to one of intermediate length, “Don’t deceive yourself. Do you suppose for a moment the short or the long-faced fancier would accept such a bird as a gift? Certainly not; the short-faced fancier could see no beauty in it; the long-faced fancier would swear there was no use in it, etc.” In these comical passages, written seriously, we see the principle which has ever guided fanciers, and has led to such great modifications in all the domestic races which are valued solely for their beauty or curiosity.
Fashions in pigeon-breeding endure for long periods; we cannot change the structure of a bird as quickly as we can the fashion of our dress. In the time of Aldrovandi, no doubt the more the pouter inflated his crop, the more he was valued. Nevertheless, fashions do to a certain extent change; first one point of structure and then another is attended to; or different breeds are admired at different times and in different countries. As the author just quoted remarks, “the fancy ebbs and flows; a thorough fancier now-a-days never stoops to breed toy-birds;” yet these very “toys” are now most carefully bred in Germany. Breeds which at the present time are highly valued in India are considered worthless in England. No doubt, when breeds are neglected, they degenerate; still we may believe that, as long as they are kept under the same conditions of life, characters once gained will be partially retained for a long time, and may form the starting-point for a future course of selection.
Let it not be objected to this view of the action of unconscious selection that fanciers would not observe or care for extremely slight differences. Those alone who have associated with fanciers can be thoroughly aware of their accurate powers of discrimination acquired by long practice, and of the care and labour which they bestow on their birds. I have known a fancier deliberately study his birds day after day to settle which to match together and which to reject. Observe how difficult the subject appears to one of the most eminent and experienced fanciers. Mr. Eaton, the winner of many prizes, says, “I would here particularly guard you against keeping too great a variety of pigeons, otherwise you will know a little about all the kinds, but nothing about one as it ought to be known.” “It is possible there may be a few fanciers that have a good general knowledge of the several fancy pigeons, but there are many who labour under the delusion of supposing they know what they do not.” Speaking exclusively of one sub- variety of one race, namely, the short-faced almond tumbler, and after saying that some fanciers sacrifice every property to obtain a good head and beak, and that other fanciers sacrifice everything for plumage, he remarks: “Some young fanciers who are over covetous go in for all the five properties at once, and they have their reward by getting nothing.” In India, as I hear from Mr. Blyth, pigeons are likewise selected and matched with the greatest care. We must not judge of the slight divergences from existing varieties which would have been valued in ancient days, by those which are now valued after the formation of so many races, each with its own standard of perfection, kept uniform by our numerous Exhibitions. The ambition of the most energetic fancier may be fully satisfied by the difficulty of excelling other fanciers in the breeds already established, without trying to form a new one.
A difficulty with respect to the power of selection will perhaps already have occurred to the reader, namely, what could have led fanciers first to attempt to make such singular breeds as Pouters, Fantails, Carriers, etc.? But it is this very difficulty which the principle of unconscious selection removes. Undoubtedly no fancier ever did intentionally make such an attempt. All that we need suppose is that a variation occurred sufficiently marked to catch the discriminating eye of some ancient fancier, and then unconscious selection carried on for many generations, that is, the wish of succeeding fanciers to excel their rivals, would do the rest. In the case of the Fantail we may suppose that the first progenitor of the breed had a tail only slightly erected, as may now be seen in certain Runts,[[45]] with some increase in the number of the tail-feathers, as now occasionally occurs with Nuns. In the case of the Pouter we may suppose that some bird inflated its crop a little more than other pigeons, as is now the case in a slight degree with the œesophagus of the Turbit. We do not know the origin of the common Tumbler, but we may suppose that a bird was born with some affection of the brain, leading it to make somersaults in the air;[[46]] and before the year 1600 pigeons remarkable for their diversified manner of flight were much valued in India, and by the order of the Emperor Akber Khan were sedulously trained and carefully matched.
In the foregoing cases we have supposed that a sudden variation, conspicuous enough to catch a fancier’s eye, first appeared; but even this degree of abruptness in the process of variation is not necessary for the formation of a new breed. When the same kind of pigeon has been kept pure, and has been bred during a long period by two or more fanciers, slight differences in the strain can often be recognised. Thus I have seen first- rate Jacobins in one man’s possession which certainly differed slightly in several characters from those kept by another. I possessed some excellent Barbs descended from a pair which had won a prize, and another lot descended from a stock formerly kept by that famous fancier Sir John Sebright, and these plainly differed in the form of the beak; but the differences were so slight that they could hardly be given by words. Again, the common English and Dutch Tumbler differ in a somewhat greater degree, both in length of beak and shape of head. What first caused these slight differences cannot be explained any more than why one man has a long nose and another a short one. In the strains long kept distinct by different fanciers, such differences are so common that they cannot be accounted for by the accident of the birds first chosen for breeding having been originally as different as they now are. The explanation no doubt lies in selection of a slightly different nature having been applied in each case; for no two fanciers have exactly the same taste, and consequently no two, in choosing and carefully matching their birds, prefer or select exactly the same. As each man naturally admires his own birds, he goes on continually exaggerating by selection whatever slight peculiarities they may possess. This will more especially happen with fanciers living in different countries, who do not compare their stocks or aim at a common standard of perfection. Thus, when a mere strain has once been formed, unconscious selection steadily tends to augment the amount of difference, and thus converts the strain into a sub-breed and this ultimately into a well-marked breed or race.
The principle of correlation of growth should never be lost sight of. Most pigeons have small feet, apparently caused by their lessened use, and from correlation, as it would appear, their beaks have likewise become reduced in length. The beak is a conspicuous organ, and, as soon as it had thus become perceptibly shortened, fanciers would almost certainly strive to reduce it still more by the continued selection of birds with the shortest beaks; whilst at the same time other fanciers, as we know has actually been the case, would in other sub-breeds, strive to increase its length. With the increased length of the beak, the tongue becomes greatly lengthened, as do the eyelids with the increased development of the eye-wattles; with the reduced or increased size of the feet, the number of the scutellæ vary; with the length of the wing, the number of the primary wing-feathers differ; and with the increased length of the body in the pouter the number of the sacral vertebræ is augmented. These important and correlated differences of structure do not invariably characterise any breed; but if they had been attended to and selected with as much care as the more conspicuous external differences, there can hardly be a doubt that they would have been rendered constant. Fanciers could assuredly have made a race of Tumblers with nine instead of ten primary wing-feathers, seeing how often the number nine appears without any wish on their part, and indeed in the case of the white-winged varieties in opposition to their wish. In a similar manner, if the vertebræ had been visible and had been attended to by fanciers, assuredly an additional number might easily have been fixed in the Pouter. If these latter characters had once been rendered constant, we should never have suspected that they had at first been highly variable, or that they had arisen from correlation, in the one case with the shortness of the wings, and in the other case with the length of the body.
In order to understand how the chief domestic races have become distinctly separated from each other, it is important to bear in mind, that fanciers constantly try to breed from the best birds, and consequently that those which are inferior in the requisite qualities are in each generation neglected; so that after a time the less improved parent-stocks and many subsequently formed intermediate grades become extinct. This has occurred in the case of the Pouter, Turbit, and Trumpeter, for these highly improved breeds are now left without any links closely connecting them either with each other or with the aboriginal rock-pigeon. In other countries, indeed, where the same care has not been applied, or where the same fashion has not prevailed, the earlier forms may long remain unaltered, or altered only in a slight degree, and we are thus sometimes enabled to recover the connecting links. This is the case in Persia and India with the Tumbler and Carrier, which there differ but slightly from the rock-pigeon in the proportions of their beaks. So again in Java, the Fantail sometimes has only fourteen caudal feathers, and the tail is much less elevated and expanded than in our improved birds; so that the Java bird forms a link between a first-rate Fantail and the rock-pigeon.
Occasionally a breed may be retained for some particular quality in a nearly unaltered condition in the same country, together with highly modified off-shoots or sub-breeds, which are valued for some distinct property. We see this exemplified in England, where the common Tumbler, which is valued only for its flight, does not differ much from its parent-form, the Eastern Tumbler; whereas the Short-faced Tumbler has been prodigiously modified, from being valued, not for its flight, but for other qualities. But the common-flying Tumbler of Europe has already begun to branch out into slightly different sub-breeds, such as the common English Tumbler, the Dutch Roller, the Glasgow House-tumbler, and the Long-faced Beard Tumbler, etc.; and in the course of centuries, unless fashions greatly change, these sub-breeds will diverge through the slow and insensible process of unconscious selection, and become modified, in a greater and greater degree. After a time the perfectly graduated links which now connect all these sub-breeds together, will be lost, for there would be no object and much difficulty in retaining such a host of intermediate sub-varieties.
The principle of divergence, together with the extinction of the many previously existing intermediate forms, is so important for understanding the origin of domestic races, as well as of species in a state of nature, that I will enlarge a little more on this subject. Our third main group includes Carriers, Barbs, and Runts, which are plainly related to one another, yet wonderfully distinct in several important characters. According to the view given in the last chapter, these three races have probably descended from an unknown race having an intermediate character, and this race from the rock-pigeon. Their characteristic differences are believed to be due to different breeders having at an early period admired different points of structure; and then, on the acknowledged principle of admiring extremes, having gone on breeding, without any thought of the future, as good birds as they could,—Carrier-fanciers preferring long beaks with much wattle,—Barb-fanciers preferring short thick beaks with much eye-wattle,—and Runt-fanciers not caring about the beak or wattle, but only for the size and weight of the body. This process would have led to the neglect and final extinction of the earlier, inferior, and intermediate birds; and thus it has come to pass, that in Europe these three races are now so extraordinarily distinct from each other. But in the East, whence they were originally brought, the fashion has been different, and we there see breeds which connect the highly modified English Carrier with the rock-pigeon, and others which to a certain extent connect Carriers and Runts. Looking back to the time of Aldrovandi, we find that there existed in Europe, before the year 1600, four breeds which were closely allied to Carriers and Barbs, but which competent authorities cannot now identify with our present Barbs and Carriers; nor can Aldrovandi’s Runts be identified with our present Runts. These four breeds certainly did not differ from each other nearly so much as do our existing English Carriers, Barbs, and Runts. All this is exactly what might have been anticipated. If we could collect all the pigeons which have ever lived, from before the time of the Romans to the present day, we should be able to group them in several lines, diverging from the parent rock-pigeon. Each line would consist of almost insensible steps, occasionally broken by some slightly greater variation or sport, and each would culminate in one of our present highly modified forms. Of the many former connecting links, some would be found to have become absolutely extinct without having left any issue, whilst others, though extinct, would be recognised as the progenitors of the existing races.
I have heard it remarked as a strange circumstance that we occasionally hear of the local or complete extinction of domestic races, whilst we hear nothing of their origin. How, it has been asked, can these losses be compensated, and more than compensated, for we know that with almost all domesticated animals the races have largely increased in number since the time of the Romans? But on the view here given, we can understand this apparent contradiction. The extinction of a race within historical times is an event likely to be noticed; but its gradual and scarcely sensible modification through unconscious selection, and its subsequent divergence, either in the same or more commonly in distant countries, into two or more strains, and their gradual conversion into sub-breeds, and these into well- marked breeds are events which would rarely be noticed. The death of a tree, that has attained gigantic dimensions, is recorded; the slow growth of smaller trees and their increase in number excite no attention.
In accordance with the belief in the great power of selection, and of the little direct power of changed conditions of life, except in causing general variability or plasticity of organisation, it is not surprising that dovecot-pigeons have remained unaltered from time immemorial; and that some toy-pigeons, which differ in little else besides colour from the dovecot-pigeon, have retained the same character for several centuries. For when one of these toy-pigeons had once become beautifully and symmetrically coloured,—when, for instance, a Spot had been produced with the crown of its head, its tail, and tail-coverts of a uniform colour, the rest of the body being snow-white,—no alteration or improvement would be desired. On the other hand, it is not surprising that during this same interval of time our highly-bred pigeons have undergone an astonishing amount of change; for in regard to them there is no defined limit to the wish of the fancier, and there is no known limit to the variability of their characters. What is there to stop the fancier desiring to give to his Carrier a longer and longer beak, or to his Tumbler a shorter and shorter beak? nor has the extreme limit of variability in the beak, if there be any such limit, as yet been reached. Notwithstanding the great improvement effected within recent times in the Short-faced Almond Tumbler, Mr. Eaton remarks, “the field is still as open for fresh competitors as it was one hundred years ago;” but this is perhaps an exaggerated assertion, for the young of all highly-improved fancy birds are extremely liable to disease and death.
I have heard it objected that the formation of the several domestic races of the pigeon throws no light on the origin of the wild species of the Columbidæ, because their differences are not of the same nature. The domestic races, for instance do not differ, or differ hardly at all, in the relative lengths and shape of the primary wing-feathers, in the relative length of the hind toe, or in habits of life, as in roosting and building in trees. But the above objection shows how completely the principle of selection has been misunderstood. It is not likely that characters selected by the caprice of man should resemble differences preserved under natural conditions either from being of direct service to each species, or from standing in correlation with other modified and serviceable structures. Until man selects birds differing in the relative length of the wing-feathers or toes, etc., no sensible change in these parts should be expected. Nor could man do anything unless these parts happened to vary under domestication: I do not positively assert that this is the case, although I have seen traces of such variability in the wing-feathers, and certainly in the tail-feathers. It would be a strange fact if the relative length of the hind toe should never vary, seeing how variable the foot is both in size and in the number of the scutellæ. With respect to the domestic races not roosting or building in trees, it is obvious that fanciers would never attend to or select such changes in habits; but we have seen that the pigeons in Egypt, which do not for some reason like settling on the low mud hovels of the natives, are led, apparently by compulsion, to perch in crowds on the trees. We may even affirm that, if our domestic races had become greatly modified in any of the above specified respects, and it could be shown that fanciers had never attended to such points, or that they did not stand in correlation with other selected characters, the fact, on the principles advocated in this chapter, would have offered a serious difficulty.
Let us briefly sum up the last two chapters on the pigeon. We may conclude with confidence that all the domestic races, notwithstanding their great amount of difference, are descended from the Columba livia, including under this name certain wild races. But the differences between the latter throw no light whatever on the characters which distinguish the domestic races. In each breed or sub-breed the individual birds are more variable than birds in a state of nature; and occasionally they vary in a sudden and strongly-marked manner. This plasticity of organisation apparently results from changed conditions of life. Disuse has reduced certain parts of the body. Correlation of growth so ties the organisation together, that when one part varies other parts vary at the same time. When several breeds have once been formed, their intercrossing aids the progress of modification, and has even produced new sub-breeds. But as, in the construction of a building, mere stones or bricks are of little avail without the builder’s art, so, in the production of new races, selection has been the presiding power. Fanciers can act by selection on excessively slight individual differences, as well as on those greater differences which are called sports. Selection is followed methodically when the fancier tries to improve and modify a breed according to a prefixed standard of excellence; or he acts unmethodically and unconsciously, by merely trying to rear as good birds as he can, without any wish or intention to alter the breed. The progress of selection almost inevitably leads to the neglect and ultimate extinction of the earlier and less improved forms, as well as of many intermediate links in each long line of descent. Thus it has come to pass that most of our present races are so marvellously distinct from each other, and from the aboriginal rock-pigeon.
REFERENCES
[1] Temminck ‘Hist. Nat. Gén. des Pigeons,’ etc., tom. i. p. 191.
[2] I have heard through Sir C. Lyell from Miss Buckley, that some half-bred Carriers kept during many years near London regularly settled by day on some adjoining trees, and, after being disturbed in their loft by their young being taken, roosted on them at night.
[3] ‘Annals and Mag. of Nat. Hist.,’ 2nd ser., vol. xx., 1857, p. 509; and in a late volume of the Journal of the Asiatic Society.
[4] In works written on the pigeon by fanciers I have sometimes observed the mistaken belief expressed that the species which naturalists called ground-pigeons (in contradistinction to arboreal pigeons) do not perch and build on trees. In these same works by fanciers wild species resembling the chief domestic races are often said to exist in various parts of the world; but such species are quite unknown to naturalists.
[5] Sir R. Schomburgk in ‘Journal R. Geograph. Soc.,’ vol. xiii., 1844, p. 32.
[6] Rev. E. S. Dixon ‘Ornamental Poultry,’ 1848, pp. 63, 66.
[7] ‘Proc. Zoolog. Soc.,’ 1859, p. 400.
[8] Temminck, ‘Hist. Nat. Gén. des Pigeons,’ tom. i.; also ‘Les Pigeons’ par Mme. Knip and Temminck. Bonaparte, however, in his ‘Coup- d’œil’ believes that two closely allied species are confounded together under this name. The C. leucocephala of the West Indies is stated by Temminck to be a rock-pigeon; but I am informed by Mr. Gosse that this is an error.
[9] ‘Handbuch der Naturgesch. Vögel Deutschlands.’
[10] ‘Tagebuch, Reise nach Färo,’ 1830, s. 62.
[11] ‘Annals and Mag. of Nat. Hist.,’ vol. xix., 1847, p. 102. This excellent paper on pigeons is well worth consulting.
[12] ‘Natural History of Ireland,’ Birds, vol. ii. (1850), p. 11. For Graba see previous reference.
[13] ‘Coup-d’œil sur l’Ordre des Pigeons,’ ‘Comptes Rendus,’ 1854-55.
[14] ‘Naturgeschichte. Deutschlands,’ Band. iv. 1795, s. 14.
[15] ‘History of British Birds,’ vol. i. pp. 275-284. Mr. Andrew Duncan tamed a rock-pigeon in the Shetland Islands. Mr. James Barclay, and Mr. Smith of Uyea Sound, both say that the wild rock-pigeon can be easily tamed; and the former gentleman asserts that the tamed birds breed four times a year. Dr. Lawrence Edmondstone informs me that a wild rock-pigeon came and settled in his dovecot in Balta Sound in the Shetland Islands, and bred with his pigeons; he has also given me other instances of the wild rock-pigeon having been taken young and breeding in captivity.
[16] ‘Annals and Mag. of Nat. History,’ vol. xix. 1847, p. 103, and vol. for 1857, p. 512.
[17] Domestic pigeons of the common kind are mentioned as being pretty numerous in John Barbut’s ‘Description of the Coast of Guinea’ (p. 215), published in 1746; they are said, in accordance with the name which they bear, to have been imported.
[18] With respect to feral pigeons—for Juan Fernandez, see Bertero in ‘Annal. des Sc. Nat.,’ tom. xxi. p. 351. For Norfolk Islands, see Rev. E. S. Dixon in the ‘Dovecote,’ 1851, p. 14, on the authority of Mr. Gould. For Ascension I rely on MS. information given me by Mr. Layard. For the banks of the Hudson, see Blyth in ‘Annals of Nat. Hist.,’ vol. xx., 1857, p. 511. For Scotland, see Macgillivray, ‘British Birds,’ vol. i. p. 275; also Thompson’s ‘Nat. Hist. of Ireland, Birds,’ vol. ii. p. 11. For ducks, see Rev. E. S. Dixon, ‘Ornamental Poultry,’ 1847, p. 122. For the feral hybrids of the common and musk-ducks, see Audubon’s ‘American Ornithology,’ and Selys-Longchamp’s ‘Hybrides dans la Famille des Anatides.’ For the goose, Isidore Geoffroy St.-Hilaire, ‘Hist. Nat. Gén.,’ tom. iii. p. 498. For guinea-fowls, see Gosse’s ‘Naturalist’s Sojourn in Jamaica,’ p. 124; and his ‘Birds of Jamaica,’ for fuller particulars. I saw the wild guinea-fowl in Ascension. For the peacock, see ‘A Week at Port Royal,’ by a competent authority, Mr. R. Hill, p. 42. For the turkey I rely on oral information; I ascertained that they were not Curassows. With respect to fowls I will give the references in the next chapter.
[19] I have drawn out a long table of the various crosses made by fanciers between the several domestic breeds but I do not think it worth while publishing. I have myself made for this special purpose many crosses, and all were perfectly fertile. I have united in one bird five of the most distinct races, and with patience I might undoubtedly have thus united all. The case of five distinct breeds being blended together with unimpaired fertility is important, because Gärtner has shown that it is a very general, though not, as he thought, universal rule, that complex crosses between several species are excessively sterile. I have met with only two or three cases of reported sterility in the offspring of certain races when crossed. Pistor (‘Das Ganze der Feldtaubenzucht,’ 1831, s. 15) asserts that the mongrels from Barbs and Fantails are sterile: I have proved this to be erroneous, not only by crossing those hybrids with several other hybrids of the same parentage, but by the more severe test of pairing brother and sister hybrids inter se, and they were perfectly fertile. Temminck has stated (‘Hist. Nat. Gén. des Pigeons,’ tom. i. p. 197) that the Turbit or Owl will not cross readily with other breeds: but my Turbits crossed, when left free with Almond Tumblers and with Trumpeters; the same thing has occurred (Rev. E. S. Dixon, ‘The Dovecote,’ p. 107) between Turbits and Dovecots and Nuns. I have crossed Turbits with Barbs, as has M. Boitard (p. 34), who says the hybrids were very fertile. Hybrids from a Turbit and Fantail have been known to breed inter se (Riedel, ‘Taubenzucht,’ s. 25, and Bechstein, ‘Naturgesch. Deutsch.,’ B. iv. s. 44. Turbits (Riedel, s. 26) have been crossed with Pouters and with Jacobins, and with a hybrid Jacobin-trumpeter (Riedel, s. 27). The latter author has, however, made some vague statements (s. 22) on the sterility of Turbits when crossed with certain other crossed breeds. But I have little doubt that the Rev. E. S. Dixon’s explanation of such statements is correct, viz. that individual birds both with Turbits and other breeds are occasionally sterile.
[20] ‘Das Ganze der Taubenzucht,’ s. 18.
[21] ‘Les Pigeons,’ etc., p. 35.
[22] Domestic pigeons pair readily with the allied C. œnas (Bechstein, ‘Naturgesch. Deutschlands,’ B. iv. s. 3); and Mr. Brent has made the same cross several times in England, but the young were very apt to die at about ten days old; one hybrid which he reared (from C. œnas and a male Antwerp Carrier) paired with a Dragon, but never laid eggs. Bechstein further states (s. 26) that the domestic pigeon will cross with C. palumbus, Turtur risoria, and T. vulgaris, but nothing is said of the fertility of the hybrids, and this would have been mentioned had the fact been ascertained. In the Zoological Gardens (MS. report to me from Mr. James Hunt) a male hybrid from Turtur vulgaris and a domestic pigeon “paired with several different species of pigeons and doves, but none of the eggs were good.” Hybrids from C. œnas and gymnophthalmos were sterile. In Loudon’s ‘Mag. of Nat. Hist.,’ vol. vii. 1834, p. 154, it is said that a male hybrid (from Turtur vulgaris male, and the cream-coloured T. risoria female) paired during two years with a female T. risoria, and the latter laid many eggs, but all were sterile. MM. Boitard and Corbié (‘Les Pigeons,’ p. 235) state that the hybrids from these two turtle-doves are invariably sterile both inter se and with either pure parent. The experiment was tried by M. Corbié “avec une espèce d’obstination;” and likewise by M. Mauduyt, and by M. Vieillot. Temminck also found the hybrids from these two species quite barren. Therefore, when Bechstein (‘Naturgesch. Deutschlands Vögel,’ B. iv. s. 101) asserts that the hybrids from these two turtle-doves propagate inter se equally well with pure species, and when a writer in the ‘Field’ newspaper (in a letter dated Nov. 10th, 1858) makes a similar assertion, it would appear that there must be some mistake; though what the mistake is I know not, as Bechstein at least must have known the white variety of T. risoria: it would be an unparalleled fact if the same two species sometimes produced extremely fertile, and sometimes extremely barren, offspring. In the MS. report from the Zoological Gardens it is said that hybrids from Turtur vulgaris and suratensis, and from T. vulgaris and Ectopistes migratorius, were sterile. Two of the latter male hybrids paired with their pure parents, viz. Turtur vulgaris and the Ectopistes, and likewise with T. risoria and with Columba œnas, and many eggs were produced, but all were barren. At Paris, hybrids have been raised (Isid. Geoffrey Saint-Hilaire, ‘Hist. Nat. Générale,’ tom. iii. p. 180) from Turtur auritus with T. cambayensis and with T. suratensis; but nothing is said of their fertility. At the Zoological Gardens of London the Goura coronata and victoriæ produced a hybrid which paired with the pure G. coronata, and laid several eggs, but these proved barren. In 1860 Columba gymnophthalmos and maculosa produced hybrids in these same gardens.
[23] There is one exception to the rule, namely, in a sub-variety of the Swallow of German origin, which is figured by Neumeister, and was shown to me by Mr. Wicking. This bird is blue, but has not the black wing-bars; for our object, however, in tracing the descent of the chief races, this exception signifies the less as the Swallow approaches closely in structure to C. livia. In many sub-varieties the black bars are replaced by bars of various colours. The figures given by Neumeister are sufficient to show that, if the wings alone are blue, the black wing-bars appear.
[24] I have observed blue birds with all the above-mentioned marks in the following races, which seemed to be perfectly pure, and were shown at various exhibitions. Pouters, with the double black wing-bars, with white croup, dark bar to end of tail, and white edging to outer tail-feathers. Turbits, with all these same characters. Fantails with the same; but the croup in some was bluish or pure blue. Mr. Wicking bred blue Fantails from two black birds. Carriers (including the Bagadotten of Neumeister) with all the marks: two birds which I examined had white, and two had blue croups; the white edging to the outer tail-feathers was not present in all. Mr. Corker, a great breeder, assures me that, if black carriers are matched for many successive generations, the offspring become first ash-coloured, and then blue with black wing-bars. Runts of the elongated breed had the same marks, but the croup was pale blue; the outer tail-feathers had white edges. Neumeister figures the great Florence Runt of a blue colour with black bars. Jacobins are very rarely blue, but I have received authentic accounts of at least two instances of the blue variety with black bars having appeared in England; blue Jacobins were bred by Mr. Brent from two black birds. I have seen common Tumblers, both Indian and English, and Short-faced Tumblers, of a blue colour, with black wing-bars, with the black bar at the end of the tail, and with the outer tail-feathers edged with white; the croup in all was blue, or extremely pale blue, never absolutely white. Blue Barbs and Trumpeters seem to be excessively rare; but Neumeister, who may be implicitly trusted, figures blue varieties of both, with black wing-bars. Mr. Brent informs me that he has seen a blue Barb; and Mr. H. Weir, as I am informed by Mr. Tegetmeier, once bred a silver (which means very pale blue) Barb from two yellow birds.
[25] Mr. Blyth informs me that all the domestic races in India have the croup blue; but this is not invariable, for I possess a very pale blue Simmali pigeon with the croup perfectly white, sent to me by Sir W. Elliot from Madras. A slaty-blue and chequered Nakshi pigeon has some white feathers on the croup alone. In some other Indian pigeons there were a few white feathers confined to the croup, and I have noticed the same fact in a carrier from Persia. The Java Fantail (imported into Amoy, and thence sent me) has a perfectly white croup.
[26] ‘Les Pigeons,’ etc., p. 37.
[27] ‘Treatise on Pigeons,’ 1858, p. 145.
[28] J. Moore’s ‘Columbarium,’ 1735; in J. M. Eaton’s edition, 1852, p. 71.
[29] I could give numerous examples; two will suffice. A mongrel, whose four grandparents were a white Turbit, white Trumpeter, white Fantail, and blue Pouter, was white all over, except a very few feathers about the head and on the wings, but the whole tail and tail-coverts were dark bluish-grey. Another mongrel whose four grandparents were a red Runt, white Trumpeter, white Fantail, and the same blue Pouter, was pure white all over, except the tail and upper tail-coverts, which were pale fawn, and except the faintest trace of double wing-bars of the same pale fawn tint.
[30] It deserves notice, as bearing on the general subject of variation, that not only C. livia presents several wild forms, regarded by some naturalists as species and by others as sub-species or as mere varieties, but that the species of several allied genera are in the same predicament. This is the case, as Mr. Blyth has remarked to me, with Treron, Palumbus, and Turtur.
[31] ‘Denkmäler,’ Abth. ii. Bl. 70.
[32] ‘The ‘Dovecote,’ by the Rev. E. S. Dixon, 1851, pp. 11-13. Adolphe Pictet (in his ‘Les Origines Indo-Européennes,’ 1859, p. 399) states that there are in the ancient Sanscrit language between 25 and 30 names for the pigeon, and other 15 or 16 Persian names; none of these are common to the European languages. This fact indicates the antiquity of the domestication of the pigeon in the East.
[33] English translation, 1601, Book x. ch. xxxvii.
[34] ‘Ayeen Akbery,’ translated by F. Gladwin, 4to edit., vol. i. p. 270.
[35] J. M. Eaton, ‘Treatise on the Almond Tumbler,’ 1851; Preface, p. 6.
[36] As in the following discussion I often speak of the present time, I should state that this chapter was completed in the year 1858.
[37] ‘Ornithologie,’ 1600, vol. ii. p. 360.
[38] ‘A Treatise on Domestic Pigeons,’ dedicated to Mr. Mayor, 1765. Preface, p. 14.
[39] Mr. Blyth has given a translation of part of the ‘Ayeen Akbery’ in ‘Annals and Mag. of Nat. Hist.,’ vol. xix. 1847, p. 104.
[40] ‘L’Histoire de la Nature des Oiseaux,’ p. 314.
[41] ‘Treatise on Pigeons,’ 1852, p. 64.
[42] J. M. Eaton ‘Treatise on the Breeding and Managing of the Almond Tumbler,’ 1851. Compare p. v. of Preface, p. 9, and p. 32.
[43] ‘Treatise on Pigeons,’ 1852, p. 41.
[44] Eaton’s ‘Treatise on Pigeons,’ 1858, p. 86.
[45] See Neumeister’s figure of the Florence Runt, tab. 13 in ‘Das Ganze der Taubenzucht.’
[46] Mr. W. J. Moore gives a full account of the Ground Tumblers of India (‘Indian Medical Gazette,’ Jan. and Feb. 1873), and says the pricking the base of the brain, and giving hydrocyanic acid, together with strychnine, to an ordinary pigeon, brings on convulsive movements exactly like those of a Tumbler. One pigeon, the brain of which had been pricked, completely recovered, and ever afterwards occasionally made somersaults.
CHAPTER VII.
FOWLS.
BRIEF DESCRIPTIONS OF THE CHIEF BREEDS—ARGUMENTS IN FAVOUR OF THEIR DESCENT FROM SEVERAL SPECIES—ARGUMENTS IN FAVOUR OF ALL THE BREEDS HAVING DESCENDED FROM GALLUS BANKIVA—REVERSION TO THE PARENT-STOCK IN COLOUR—ANALOGOUS VARIATIONS—ANCIENT HISTORY OF THE FOWL—EXTERNAL DIFFERENCES BETWEEN THE SEVERAL BREEDS—EGGS—CHICKENS—SECONDARY SEXUAL CHARACTERS—WING-AND TAIL-FEATHERS, VOICE, DISPOSITION, ETC—OSTEOLOGICAL DIFFERENCES IN THE SKULL, VERTEBRÆ, ETC—EFFECTS OF USE AND DISUSE ON CERTAIN PARTS—CORRELATION OF GROWTH.
As some naturalists may not be familiar with the chief breeds of the fowl, it will be advisable to give a condensed description of them.[[1]] From what I have read and seen of specimens brought from several quarters of the world, I believe that most of the chief kinds have been imported into England, but many sub-breeds are probably still unknown here. The following discussion on the origin of the various breeds and on their characteristic differences does not pretend to completeness, but may be of some interest to the naturalist. The classification of the breeds cannot, as far as I can see, be made natural. They differ from each other in different degrees, and do not afford characters in subordination to each other, by which they can be ranked in group under group. They seem all to have diverged by independent and different roads from a single type. Each chief breed includes differently coloured sub-varieties, most of which can be truly propagated, but it would be superfluous to describe them. I have classed the various crested fowls as sub-breeds under the Polish fowl; but I have great doubts whether this is a natural arrangement, showing true affinity or blood relationship. It is scarcely possible to avoid laying stress on the commonness of a breed; and if certain foreign sub-breeds had been largely kept in this country they would perhaps have been raised to the rank of main-breeds. Several breeds are abnormal in character; that is, they differ in certain points from all wild Gallinaceous birds. At first I made a division of the breeds into normal and abnormal, but the result was wholly unsatisfactory.
1. GAME BREED.—This may be considered as the typical breed, as it deviates only slightly from the wild Gallus bankiva, or, as perhaps more correctly named, ferrugineus. Beak strong; comb single and upright. Spurs long and sharp. Feathers closely appressed to the body. Tail with the normal number of 14 feathers. Eggs often pale buff. Disposition indomitably courageous, exhibited even in the hens and chickens. An unusual number of differently coloured varieties exist, such as black and brown-breasted reds, duckwings, blacks, whites, piles, etc., with their legs of various colours.
2. MALAY BREED.—Body of great size, with head, neck, and legs elongated; carriage erect; tail small, sloping downwards, generally formed of 16 feathers; comb and wattle small; ear-lobe and face red; skin yellowish; feathers closely appressed to the body; neck-hackles short, narrow, and hard. Eggs often pale buff. Chickens feather late. Disposition savage. Of Eastern origin.
3. COCHIN, OR SHANGAI BREED.—Size great; wing feathers short, arched, much hidden in the soft downy plumage; barely capable of flight; tail short, generally formed of 16 feathers, developed at a late period in the young males; legs thick, feathered; spurs short, thick; nail of middle toe flat and broad; an additional toe not rarely developed; skin yellowish. Comb and wattle well developed. Skull with deep medial furrow; occipital foramen, sub-triangular, vertically elongated. Voice peculiar. Eggs rough, buff-coloured. Disposition extremely quiet. Of Chinese origin.
4. DORKING BREED.—Size great; body square, compact; feet with an additional toe; comb well developed, but varies much in form; wattles well developed; colour of plumage various. Skull remarkably broad between the orbits. Of English origin.
The white Dorking may be considered as a distinct sub-breed, being a less massive bird.
Fig. 30—Spanish Fowl
5. SPANISH BREED (fig. 30).—Tall, with stately carriage; tarsi long; comb single, deeply serrated, of immense size; wattles largely developed; the large ear-lobes and sides of face white. Plumage black glossed with green. Do not incubate. Tender in constitution, the comb being often injured by frost. Eggs white, smooth, of large size. Chickens feather late but the young cocks show their masculine characters, and crow at an early age. Of Mediterranean origin.
The Andalusians may be ranked as a sub-breed: they are of a slaty-blue colour, and their chickens are well feathered. A smaller, short-legged Dutch sub-breed has been described by some authors as distinct.
Fig. 31—Hamburgh Fowl
6. HAMBURGH BREED (fig 31).—Size moderate; comb flat, produced backwards, covered with numerous small points; wattle of moderate dimensions; ear lobe white; legs blueish, thin. Do not incubate. Skull, with the tips of the ascending branches of the premaxillary and with the nasal bones standing a little separate from each other; anterior margin of the frontal bones less depressed than usual.
There are two sub-breeds; the spangled Hamburgh, of English origin, with the tips of the feathers marked with a dark spot; and the pencilled Hamburgh, of Dutch origin, with dark transverse lines across each feather, and with the body rather smaller. Both these sub-breeds include gold and silver varieties, as well as some other sub-varieties. Black Hamburghs have been produced by a cross with the Spanish breed.
Fig. 32—Polish Fowl
7. CRESTED OR POLISH BREED (fig 32).—Head with a large, rounded crest of feathers, supported on a hemispherical protuberance of the frontal bones, which includes the anterior part of the brain. The ascending branches of premaxillary bones and the inner nasal processes are much shortened. The orifice of the nostrils raised and crescentic. Beak short. Comb absent, or small and of crescentic shape; wattles either present or replaced by a beard-like tuft of feathers. Legs leaden-blue. Sexual differences appear late in life. Do not incubate. There are several beautiful varieties which differ in colour and slightly in other respects.
The following sub-breeds agree in having a crest, more or less developed, with the comb, when present, of crescentic shape. The skull presents nearly the same remarkable peculiarities of structure as in the true Polish fowl.
Sub-breed (a) Sultans.—A Turkish breed, resembling white Polish fowls with a large crest and beard with short and well-feathered legs. The tail is furnished with additional sickle feathers. Do not incubate.[[2]]
Sub-breed (b) Ptarmigans.—An inferior breed closely allied to the last, white, rather small, legs much feathered, with the crest pointed; comb small, cupped; wattles small.
Sub-breed (c) Ghoondooks.—Another Turkish breed having an extraordinary appearance; black and tailless; crest and beard large; legs feathered. The inner processes of the two nasal bones come into contact with each other, owing to the complete abortion of the ascending branches of the premaxillaries. I have seen an allied white, tailless breed from Turkey.
Sub-breed (d) Crève-cœur.—A French breed of large size, barely capable of flight, with short black legs, head crested, comb produced into two points or horns, sometimes a little branched like the horns of a stag; both beard and wattles present. Eggs large. Disposition quiet.[[3]]
Sub-breed (e) Horned fowl.—With a small crest; comb produced into two great points, supported on two bony protuberances.
Sub-breed (f) Houdan.—A French breed; of moderate size, short-legged with five toes, well developed; plumage invariably mottled with black, white, and straw-yellow; head furnished with a crest, on a triple comb placed transversely; both wattles and beard present.[[4]]
Sub-breed (g) Guelderlands.—No comb, head said to be surmounted by a longitudinal crest of soft velvety feathers; nostrils said to be crescentic; wattles well developed; legs feathered; colour black. From North America. The Breda fowl seems to be closely allied to the Guelderland.
8. BANTAM BREED.—Originally from Japan[[5]] characterised by small size alone; carriage bold and erect. There are several sub-breeds, such as the Cochin, Game, and Sebright Bantams, some of which have been recently formed by various crosses. The Black Bantam has a differently shaped skull, with the occipital foramen like that of the Cochin fowl.
9. RUMPLESS FOWLS.—These are so variable in character[[6]] that they hardly deserve to be called a breed. Any one who will examine the caudal vertebræ will see how monstrous the breed is.
10. CREEPERS OR JUMPERS.—These are characterised by an almost monstrous shortness of legs, so that they move by jumping rather than by walking; they are said not to scratch up the ground. I have examined a Burmese variety, which had a skull of rather unusual shape.
11. FRIZZLED OR CAFFRE FOWLS.—Not uncommon in India, with the feathers curling backwards, and with the primary feathers of the wing and tail imperfect; periosteum of bones black.
12. SILK FOWLS.—Feathers silky, with the primary wing and tail-feathers imperfect; skin and periosteum of bones black; comb and wattles dark leaden-blue; ear-lappets tinged with blue; legs thin, often furnished with an additional toe. Size rather small.
13. SOOTY FOWLS.—An Indian breed, having the peculiar appearance of a white bird smeared with soot, with black skin and periosteum. The hens alone are thus characterised.
From this synopsis we see that the several breeds differ considerably, and they would have been nearly as interesting for us as pigeons, if there had been equally good evidence that all had descended from one parent-species. Most fanciers believe that they are descended from several primitive stocks. The Rev. E. S. Dixon[[7]] argues strongly on this side of the question; and one fancier even denounces the opposite conclusion by asking, “Do we not perceive pervading this spirit, the spirit of the Deist?” Most naturalists, with the exception of a few, such as Temminck, believe that all the breeds have proceeded from a single species; but authority on such a point goes for little. Fanciers look to all parts of the world as the possible sources of their unknown stocks; thus ignoring the laws of geographical distribution. They know well that the several kinds breed truly even in colour. They assert, but, as we shall see, on very weak grounds, that most of the breeds are extremely ancient. They are strongly impressed with the great difference between the chief kinds, and they ask with force, can differences in climate, food, or treatment have produced birds so different as the black stately Spanish, the diminutive elegant Bantam, the heavy Cochin with its many peculiarities, and the Polish fowl with its great top-knot and protuberant skull? But fanciers, whilst admitting and even overrating the effects of crossing the various breeds, do not sufficiently regard the probability of the occasional birth, during the course of centuries, of birds with abnormal and hereditary peculiarities; they overlook the effects of correlation of growth—of the long-continued use and disuse of parts, and of some direct result from changed food and climate, though on this latter head I have found no sufficient evidence; and lastly, they all, as far as I know, entirely overlook the all-important subject of unconscious or unmethodical selection, though they are well aware that their birds differ individually and that by selecting the best birds for a few generations they can improve their stocks.
An amateur writes[[8]] as follows: “The fact that poultry have until lately received but little attention at the hands of the fancier, and been entirely confined to the domains of the producer for the market, would alone suggest the improbability of that constant and unremitting attention having been observed in breeding, which is requisite to the consummating in the offspring of any two birds transmittable forms not exhibited by the parents.” This at first sight appears true. But in a future chapter on Selection, abundant facts will be given showing not only that careful breeding, but that actual selection was practised during ancient periods, and by barely civilised races of man. In the case of the fowl I can adduce no direct facts showing that selection was anciently practised; but the Romans at the commencement of the Christian era kept six or seven breeds, and Columella “particularly recommends as the best, those sorts that have five toes and white ears.”[[9]] In the fifteenth century several breeds were known and described in Europe; and in China, at nearly the same period, seven kinds were named. A more striking case is that at present, in one of the Philippine Islands, the semi-barbarous inhabitants have distinct native names for no less than nine sub-breeds of the Game fowl.[[10]] Azara,[[11]] who wrote towards the close of the last century, states that in the interior parts of South America, where I should not have expected that the least care would have been taken of poultry, a black-skinned and black-boned breed is kept, from being considered fertile and its flesh good for sick persons. Now every one who has kept poultry knows how impossible it is to keep several breeds distinct unless the utmost care be taken in separating the sexes. Will it then be pretended that those persons who, in ancient times and in semi-civilised countries took pains to keep the breeds distinct, and who therefore valued them, would not occasionally have destroyed inferior birds and occasionally have preserved their best birds? This is all that is required. It is not pretended that any one in ancient times intended to form a new breed, or to modify an old breed according to some ideal standard of excellence. He who cared for poultry would merely wish to obtain, and afterwards to rear, the best birds which he could; but this occasional preservation of the best birds would in the course of time modify the breed, as surely, though by no means as rapidly, as does methodical selection at the present day, If one person out of a hundred or out of a thousand attended to the breeding of his birds, this would be sufficient; for the birds thus tended would soon become superior to others, and would form a new strain; and this strain would, as explained in the last chapter, slowly have its characteristic differences augmented, and at last be converted into a new sub-breed or breed. But breeds would often be for a time neglected and would deteriorate; they would, however, partially retain their character, and afterwards might again come into fashion and be raised to a standard of perfection higher than their former standard; as has actually occurred quite recently with Polish fowls. If, however, a breed were utterly neglected, it would become extinct, as has recently happened with one of the Polish sub-breeds. Whenever in the course of past centuries a bird appeared with some slight abnormal structure, such as with a lark-like crest on its head, it would probably often have been preserved from that love of novelty which leads some persons in England to keep rumpless fowls, and others in India to keep frizzled fowls. And after a time any such abnormal appearance would be carefully preserved, from being esteemed a sign of the purity and excellence of the breed; for on this principle the Romans eighteen centuries ago valued the fifth toe and the white ear-lobe in their fowls.
Thus from the occasional appearance of abnormal characters, though at first only slight in degree; from the effects of the use and the disuse of parts; possibly from the direct effects of changed climate and food; from correlation of growth; from occasional reversions to old and long-lost characters; from the crossing of breeds, when more than one had been formed; but, above all, from unconscious selection carried on during many generations, there is no insuperable difficulty, to the best of my judgment, in believing that all the breeds have descended from some one parent-source. Can any single species be named from which we may reasonably suppose that all are descended? The Gallus bankiva apparently fulfils every requirement. I have already given as fair an account as I could of the arguments in favour of the multiple origin of the several breeds; and now I will give those in favour of their common descent from G. bankiva.
But it will be convenient first briefly to describe all the known species of Gallus. The G. sonneratii does not range into the northern parts of India; according to Colonel Sykes,[[12]] it presents at different heights of the Ghauts, two strongly marked varieties, perhaps deserving to be called species. It was at one time thought to be the primitive stock of all our domestic breeds, and this shows that it closely approaches the common fowl in general structure; but its hackles partially consist of highly peculiar, horny laminæ, transversely banded with three colours; and I have met no authentic account of any such character having been observed in any domestic breed.[[13]] This species also differs greatly from the common fowl, in the comb being finely serrated, and in the loins being destitute of true hackles. Its voice is utterly different. It crosses readily in India with domestic hens; and Mr. Blyth[[14]] raised nearly 100 hybrid chickens; but they were tender and mostly died whilst young. Those which were reared were absolutely sterile when crossed inter se or with either parent. At the Zoological Gardens, however, some ‘hybrids of the same parentage were not quite so sterile: Mr. Dixon, as he informed me, made, with Mr. Yarrell’s aid, particular inquiries on this subject, and was assured that out of 50 eggs only five or six chickens were reared. Some, however, of these half-bred birds were crossed with one of their parents, namely, a Bantam, and produced a few extremely feeble chickens. Mr. Dixon also procured some of these same birds and crossed them in several ways, but all were more or less infertile. Nearly similar experiments have recently been tried on a great scale in the Zoological Gardens with almost the same result.[[15]] Out of 500 eggs, raised from various first crosses and hybrids, between G. sonneratii, bankiva, and varius, only 12 chickens were reared, and of these only three were the product of hybrids inter se. From these facts, and from the above-mentioned strongly-marked differences in structure between the domestic fowl and G. sonneratii, we may reject this latter species as the parent of any domestic breed.
Ceylon possesses a fowl peculiar to the island, viz. G. stanleyii; this species approaches so closely (except in the colouring of the comb) to the domestic fowl, that Messrs. Layard and Kellaert[[16]] would have considered it, as they inform me, as one of the parent-stocks, had it not been for its singularly different voice. This bird, like the last, crosses readily with tame hens, and even visits solitary farms and ravishes them. Two hybrids, a male and female, thus produced, were found by Mr. Mitford to be quite sterile: both inherited the peculiar voice of G. stanleyii. This species, then, may in all probability be rejected as one of the primitive stocks of the domestic fowl.
Java and the islands eastward as far as Flores are inhabited by G. varius (or furcatus), which differs in so many characters—green plumage, unserrated comb, and single median wattle—that no one supposes it to have been the parent of any one of our breeds; yet, as I am informed by Mr. Crawfurd,[[17]] hybrids are commonly raised between the male G. varius and the common hen, and are kept for their great beauty, but are invariably sterile: this, however, was not the case with some bred in the Zoological Gardens. These hybrids were at one time thought to be specifically distinct, and were named G. æneus. Mr. Blyth and others believe that the G. temminckii[[18]] (of which the history is not known) is a similar hybrid. Sir J. Brooke sent me some skins of domestic fowls from Borneo, and across the tail of one of these, as Mr. Tegetmeier observed, there were transverse blue bands like those which he had seen on the tail-feathers of hybrids from G. varius, reared in the Zoological Gardens. This fact apparently indicates that some of the fowls of Borneo have been slightly affected by crosses with G. varius, but the case may possibly be one of analogous variation. I may just allude to the G. giganteus, so often referred to in works on poultry as a wild species; but Marsden[[19]] the first describer, speaks of it as a tame breed; and the specimen in the British Museum evidently has the aspect of a domestic variety.
The last species to be mentioned, namely, Gallus bankiva, has a much wider geographical range than the three previous species; it inhabits Northern India as far west as Sinde, and ascends the Himalaya to a height of 4000 ft.; it inhabits Burmah, the Malay peninsula, the Indo-Chinese countries, the Philippine Islands, and the Malayan archipelago as far eastward as Timor. This species varies considerably in the wild state. Mr. Blyth informs me that the specimens, both male and female, brought from near the Himalaya, are rather paler coloured than those from other parts of India; whilst those from the Malay peninsula and Java are brighter coloured than the Indian birds. I have seen specimens from these countries, and the difference of tint in the hackles was conspicuous. The Malayan hens were a shade redder on the breast and neck than the Indian hens. The Malayan males generally had a red ear-lappet, instead of a white one as in India; but Mr. Blyth has seen one Indian specimen without the white ear-lappet. The legs are leaden blue in the Indian, whereas they show some tendency to be yellowish in the Malayan and Javan specimens. In the former Mr. Blyth finds the tarsus remarkably variable in length. According to Temminck[[20]] the Timor specimens differ as a local race from that of Java. These several wild varieties have not as yet been ranked as distinct species; if they should, as is not unlikely, be hereafter thus ranked, the circumstance would be quite immaterial as far as the parentage and differences of our domestic breeds are concerned. The wild G. bankiva agrees most closely with the black-breasted red Game-breed, in colouring and in all other respects, except in being smaller, and in the tail being carried more horizontally. But the manner in which the tail is carried is highly variable in many of our breeds, for, as Mr. Brent informs me, the tail slopes much in the Malays, is erect in the Games and some other breeds, and is more than erect in Dorkings, Bantams, etc. There is one other difference namely, that in G. bankiva, according to Mr. Blyth, the neck-hackles when first moulted are replaced during two or three months not by other hackles, as with our domestic poultry, but by short blackish feathers.[[21]] Mr. Brent, however, has remarked that these black feathers remain in the wild bird after the development of the lower hackles, and appear in the domestic bird at the same time with them: so that the only difference is that the lower hackles are replaced more slowly in the wild than in the tame bird; but as confinement is known sometimes to affect the masculine plumage, this slight difference cannot be considered of any importance. It is a significant fact that the voice of both the male and female G. bankiva closely resembles, as Mr. Blyth and others have noted, the voice of both sexes of the common domestic fowl; but the last note of the crow of the wild bird is rather less prolonged. Captain Hutton, well known for his researches into the natural history of India, informs me that he has seen several crossed fowls from the wild species and the Chinese bantam; these crossed fowls bred freely with bantams, but unfortunately were not crossed inter se. Captain Hutton reared chickens from the eggs of the Gallus bankiva; and these, though at first very wild, afterwards became so tame that they would crowd round his feet. He did not succeed in rearing them to maturity; but as he remarks, “no wild gallinaceous bird thrives well at first on hard grain.” Mr. Blyth also found much difficulty in keeping G. bankiva in confinement. In the Philippine Islands, however, the natives must succeed better, as they keep wild cocks to fight with their domestic game-birds.[[22]] Sir Walter Elliot informs me that the hen of a native domestic breed of Pegu is undistinguishable from the hen of the wild G. bankiva; and the natives constantly catch wild cocks by taking tame cocks to fight with them in the woods.[[23]] Mr. Crawfurd remarks that from etymology it might be argued that the fowl was first domesticated by the Malays and Javanese.[[24]] It is also a curious fact, of which I have been assured by Mr. Blyth, that wild specimens of the Gallus bankiva, brought from the countries east of the Bay of Bengal, are far more easily tamed than those of India; nor is this an unparalleled fact, for, as Humboldt long ago remarked, the same species sometimes evinces a more tameable disposition in one country than in another. If we suppose that the G. bankiva was first tamed in Malaya and afterwards imported into India, we can understand an observation made to me by Mr. Blyth, that the domestic fowls of India do not resemble the wild G. bankiva of India more closely than do those of Europe.
From the extremely close resemblance in colour, general structure, and especially in voice, between Gallus bankiva and the Game fowl; from their fertility, as far as this has been ascertained, when crossed; from the possibility of the wild species being tamed, and from its varying in the wild state, we may confidently look at it as the parent of the most typical of all the domestic breeds, namely, the Game fowl. It is a significant fact, that almost all the naturalists in India, namely Sir W. Elliot, Mr. S. N. Ward, Mr. Layard, Mr. J. C. Jerdon, and Mr. Blyth,[[25]] who are familiar with G. bankiva, believe that it is the parent of most or all our domestic breeds. But even if it be admitted that G. bankiva is the parent of the Game breed, yet it may be urged that other wild species have been the parents of the other domestic breeds; and that these species still exist, though unknown, in some country, or have become extinct. The extinction, however, of several species of fowls, is an improbable hypothesis, seeing that the four known species have not become extinct in the most ancient and thickly peopled regions of the East. There is, in fact, not one other kind of domesticated bird, of which the wild parent-form is unknown, that is become extinct. For the discovery of new, or the rediscovery of old species of Gallus, we must not look, as fanciers often look, to the whole world. The larger gallinaceous birds, as Mr. Blyth has remarked,[[26]] generally have a restricted range: we see this well illustrated in India, where the genus Gallus inhabits the base of the Himalaya, and is succeeded higher up by Gallophasis, and still higher up by Phasianus. Australia, with its islands, is out of the question as the home for unknown species of the genus. It is, also, as improbable that Gallus should inhabit South America[[27]] as that a humming-bird should be found in the Old World. From the character of the other gallinaceous birds of Africa, it is not probable that Gallus is an African genus. We need not look to the western parts of Asia, for Messrs. Blyth and Crawfurd, who have attended to this subject, doubt whether Gallus ever existed in a wild state even as far west as Persia. Although the earliest Greek writers speak of the fowl as a Persian bird, this probably merely indicates its line of importation. For the discovery of unknown species we must look to India, to the Indo-Chinese countries, and to the northern parts of the Malay Archipelago. The southern portion of China is the most likely country; but as Mr. Blyth informs me, skins have been exported from China during a long period, and living birds are largely kept there in aviaries, so that any native species of Gallus would probably have become known. Mr. Birch, of the British Museum, has translated for me passages from a Chinese Encyclopædia published in 1609, but compiled from more ancient documents, in which it is said that fowls are creatures of the West, and were introduced into the East (i.e. China) in a dynasty 1400 B.C. Whatever may be thought of so ancient a date, we see that the Indo-Chinese and Indian regions were formerly considered by the Chinese as the source of the domestic fowl. From these several considerations we must look to the present metropolis of the genus, namely, to the south-eastern parts of Asia, for the discovery of species which were formerly domesticated, but are now unknown in the wild state; and the most experienced ornithologists do not consider it probable that such species will be discovered.
In considering whether the domestic breeds are descended from one species, namely, G. bankiva, or from several, we must not quite overlook, though we must not exaggerate, the importance of the test of fertility. Most of our domestic breeds have been so often crossed, and their mongrels so largely kept, that it is almost certain, if any degree of infertility had existed between them, it would have been detected. On the other hand, the four known species of Gallus when crossed with each other, or when crossed, with the exception of G. bankiva, with the domestic fowl, produce infertile hybrids.
Finally, we have not such good evidence with fowls as with pigeons, of all the breeds having descended from a single primitive stock. In both cases the argument of fertility must go for something; in both we have the improbability of man having succeeded in ancient times in thoroughly domesticating several supposed species,—most of these supposed species being extremely abnormal as compared with their natural allies,—all being now either unknown or extinct, though the parent-form of no other domesticated bird has been lost. But in searching for the supposed parent-stocks of the various breeds of the pigeon, we were enabled to confine our search to species having peculiar habits of life; whilst with fowls there is nothing in their habits in any marked manner distinct from those of other gallinaceous birds. In the case of pigeons, I have shown that purely-bred birds of every race and the crossed offspring of distinct races frequently resemble, or revert to, the wild rock-pigeon in general colour and in each characteristic mark. With fowls we have facts of a similar nature, but less strongly pronounced, which we will now discuss.
Reversion and Analogous Variation.—Purely-bred Game, Malay, Cochin, Dorking, Bantam, and, as I hear from Mr. Tegetmeier, Silk fowls, may frequently or occasionally be met with, which are almost identical in plumage with the wild G. bankiva. This is a fact well deserving attention, when we reflect that these breeds rank amongst the most distinct. Fowls thus coloured are called by amateurs black-breasted reds. Hamburghs properly have a very different plumage; nevertheless, as Mr. Tegetmeier informs me, “the great difficulty in breeding cocks of the golden-spangled variety is their tendency to have black breasts and red backs. The males of white Bantams and white Cochins, as they come to maturity, often assume a yellowish or saffron tinge; and the longer neck hackles of black Bantam cocks,”[[28]] when two or three years old, not uncommonly become ruddy; these latter Bantams occasionally “even moult brassy-winged, or actually red-shouldered.” So that in these several cases we see a plain tendency to reversion to the hues of G. bankiva, even during the lifetime of the individual bird. With Spanish, Polish, pencilled Hamburgh, silver-spangled Hamburgh fowls, and with some other less common breeds, I have never heard of a black-breasted red bird having appeared.
From my experience with pigeons, I made the following crosses. I first killed all my own poultry, no others living near my house, and then procured, by Mr. Tegetmeier’s assistance, a first-rate black Spanish cock, and hens of the following pure breeds,—white Game, white Cochin, silver-spangled Polish, silver-spangled Hamburgh, silver-pencilled Hamburgh, and white Silk. In none of these breeds is there a trace of red, nor when kept pure have I ever heard of the appearance of a red feather; though such an occurrence would perhaps not be very improbable with white Games and white Cochins. Of the many chickens reared from the above six crosses the majority were black, both in the down and in the first plumage; some were white, and a very few were mottled black and white. In one lot of eleven mixed eggs from the white Game and white Cochin by the black Spanish cock, seven of the chickens were white, and only four black. I mention this fact to show that whiteness of plumage is strongly inherited, and that the belief in the prepotent power in the male to transmit his colour is not always correct. The chickens were hatched in the spring, and in the latter part of August several of the young cocks began to exhibit a change, which with some of them increased during the following years. Thus a young male bird from the silver-spangled Polish hen was in its first plumage coal-black, and combined in its comb, crest, wattle, and beard, the characters of both parents; but when two years old the secondary wing-feathers became largely and symmetrically marked with white, and, wherever in G. bankiva the hackles are red, they were in this bird greenish-black along the shaft, narrowly bordered with brownish-black, and this again broadly bordered with very pale yellowish-brown; so that in general appearance the plumage had become pale-coloured instead of black. In this case, with advancing age there was a great change, but no reversion to the red colour of G. bankiva.
A cock with a regular rose comb derived either from the spangled or pencilled silver Hamburgh was likewise at first quite black; but in less than a year the neck-hackles, as in the last case, became whitish, whilst those on the loins assumed a decided reddish-yellow tint; and here we see the first symptom of reversion; this likewise occurred with some other young cocks, which need not here be described. It has also been recorded[[29]] by a breeder, that he crossed two silver-pencilled Hamburgh hens with a Spanish cock, and reared a number of chickens, all of which were black, the cocks having golden and the hens brownish hackles; so that in this instance likewise there was a clear tendency to reversion.
Two young cocks from my white Game hen were at first snow white; of these, one subsequently assumed male orange-coloured hackles, chiefly on the loins, and the other an abundance of fine orange-red hackles on the neck, loins, and upper wing-coverts. Here again we have a more decided, though partial, reversion to the colours of G. bankiva. This second cock was in fact coloured like an inferior “pile Came cock;”—now this sub-breed can be produced, as I am informed by Mr. Tegetmeier, by crossing a black-breasted red Game cock with a white Game hen, and the “pile” sub-breed thus produced can afterwards be truly propagated. So that we have the curious fact of the glossy-black Spanish cock and the black-breasted red Game cock when crossed with white Game hens producing offspring of nearly the same colours.
I reared several birds from the white Silk hen by the Spanish cock: all were coal-black, and all plainly showed their parentage in having blackish combs and bones; none inherited the so-called silky feathers, and the non-inheritance of this character has been observed by others. The hens never varied in their plumage. As the young cocks grew old, one of them assumed yellowish-white hackles, and thus resembled in a considerable degree the cross from the Hamburgh hen; the other became a gorgeous bird, so much so that an acquaintance had it preserved and stuffed simply from its beauty. When stalking about it closely resembled the wild Gallus bankiva, but with the red feathers rather darker. On close comparison one considerable difference presented itself, namely, that the primary and secondary wing-feathers were edged with greenish-black, instead of being edged, as in G. bankiva, with fulvous and red tints. The space, also, across the back, which bears dark-green feathers, was broader, and the comb was blackish. In all other respects, even in trifling details of plumage, there was the closest accordance. Altogether it was a marvellous sight to compare this bird first with G. bankiva, and then with its father, the glossy green-black Spanish cock, and with its diminutive mother, the white Silk hen. This case of reversion is the more extraordinary as the Spanish breed has long been known to breed true, and no instance is on record of its throwing a single red feather. The Silk hen likewise breeds true, and is believed to be ancient, for Aldrovandi, before 1600, alludes probably to this breed, and described it as covered with wool. It is so peculiar in many characters that some writers have considered it as specifically distinct; yet, as we now see, when crossed with the Spanish fowl, it yields offspring closely resembling the wild G. bankiva.
Mr. Tegetmeier has been so kind as to repeat, at my request, the cross between a Spanish cock and Silk hen, and he obtained similar results; for he thus raised, besides a black hen, seven cocks, all of which were dark-bodied with more or less orange-red hackles. In the ensuing year he paired the black hen with one of her brothers, and raised three young cocks, all coloured like their father, and a black hen mottled with white.
The hens from the six above-described crosses showed hardly any tendency to revert to the mottled-brown plumage of the female G. bankiva: one hen, however, from the white Cochin, which was at first coal-black, became slightly brown or sooty. Several hens, which were for a long time snow-white, acquired as they grew old a few black feathers. A hen from the white Game, which was for a long time entirely black glossed with green, when two years old had some of the primary wing feathers greyish-white, and a multitude of feathers over her body narrowly and symmetrically tipped or laced with white. I had expected that some of the chickens whilst covered with down would have assumed the longitudinal stripes so general with gallinaceous birds; but this did not occur in a single instance. Two or three alone were reddish-brown about their heads. I was unfortunate in losing nearly all the white chickens from the first crosses; so that black prevailed with the grandchildren; but they were much diversified in colour, some being sooty, others mottled, and one blackish chicken had its feathers oddly tipped and barred with brown.
I will here add a few miscellaneous facts connected with reversion, and with the law of analogous variation. This law implies, as stated in a previous chapter, that the varieties of one species frequently mock distinct but allied species; and this fact is explained, according to the views which I maintain, on the principle of allied species having descended from one primitive form. The white Silk fowl with black skin and bones degenerates, as has been observed by Mr. Hewitt and Mr. R. Orton, in our climate; that is, it reverts to the ordinary colour of the common fowl in its skin and bones, due care having been taken to prevent any cross. In Germany[[30]] a distinct breed with black bones, and with black, not silky plumage, has likewise been observed to degenerate.
Mr. Tegetmeier informs me that, when distinct breeds are crossed, fowls are frequently produced with their feathers marked or pencilled by narrow transverse lines of a darker colour. This may be in part explained by direct reversion to the parent-form, the Bankiva hen; for this bird has all its upper plumage finely mottled with dark and rufous brown, with the mottling partially and obscurely arranged in transverse lines. But the tendency to pencilling is probably much strengthened by the law of analogous variation, for the hens of some other species of Gallus are more plainly pencilled, and the hens of many gallinaceous birds belonging to other genera, as the partridge, have pencilled feathers. Mr. Tegetmeier has also remarked to me that, although with domestic pigeons we have so great a diversity of colouring, we never see either pencilled or spangled feathers; and this fact is intelligible on the law of analogous variation, as neither the wild rock pigeon nor any closely allied species has such feathers. The frequent appearance of pencilling in crossed birds probably accounts for the existence of “cuckoo” sub-breeds in the Game, Polish, Dorking, Cochin, Andalusian, and Bantam breeds. The plumage of these birds is slaty-blue or grey, with each feather transversely barred with darker lines, so as to resemble in some degree the plumage of the cuckoo. It is a singular fact, considering that the male of no species of Gallus is in the least barred, that the cuckoo-like plumage has often been transferred to the male, more especially in the cuckoo Dorking; and the fact is all the more singular, as in gold- and silver-pencilled Hamburghs, in which pencilling is characteristic of the breed, the male is hardly at all pencilled, this kind of plumage being confined to the female.
Another case of analogous variation is the occurrence of spangled sub-breeds of Hamburgh, Polish, Malay, and Bantam fowls. Spangled feathers have a dark mark, properly crescent-shaped, on their tips; whilst pencilled feathers have several transverse bars. The spangling cannot be due to reversion to G. bankiva; nor does it often follow, as I hear from Mr. Tegetmeier, from crossing distinct breeds; but it is a case of analogous variation, for many gallinaceous birds have spangled feathers,—for instance, the common pheasant. Hence spangled breeds are often called “pheasant”-fowls. Another case of analogous variation in several domestic breeds is inexplicable; it is, that the chickens, whilst covered with down, of the black Spanish, black Game, black Polish, and black Bantam, all have white throats and breasts, and often have some white on their wings.[[31]] The editor of the ‘Poultry Chronicle’[[32]] remarks that all the breeds which properly have red ear-lappets occasionally produce birds with white ear-Tappets. This remark more especially applies to the Game breed, which of all comes nearest to the G. bankiva; and we have seen that with this species living in a state of nature, the ear-lappets vary in colour, being red in the Malayan countries, and generally, but not invariably, white in India.
In concluding this part of my subject, I may repeat that there exists one widely-ranging, varying, and common species of Gallus, namely, G. bankiva, which can be tamed, produces fertile offspring when crossed with common fowls, and closely resembles in its whole structure, plumage, and voice the Game breed; hence it may be safely ranked as the parent of this, the most typical domesticated breed. We have seen that there is much difficulty in believing that other, now unknown, species have been the parents of the other domestic breeds. We know that all the breeds are most closely allied, as shown by their similarity in most points of structure and in habits, and by the analogous manner in which they vary. We have also seen that several of the most distinct breeds occasionally or habitually closely resemble in plumage G. bankiva, and that the crossed offspring of other breeds, which are not thus coloured, show a stronger or weaker tendency to revert to this same plumage. Some of the breeds, which appear the most distinct and the least likely to have proceeded from G. bankiva, such as Polish fowls, with their protuberant and little ossified skulls, and Cochins, with their imperfect tail and small wings, bear in these characters the plain marks of their artificial origin. We know well that of late years methodical selection has greatly improved and fixed many characters; and we have every reason to believe that unconscious selection, carried on for many generations, will have steadily augmented each new peculiarity, and thus have given rise to new breeds. As soon as two or three breeds were once formed, crossing would come into play in changing their character and in increasing their number. Brahma Pootras, according to an account lately published in America, offer a good instance of a breed, lately formed by a cross, which can be truly propagated. The well-known Sebright Bantams offer another and similar instance. Hence it may be concluded that not only the Game-breed but that all our breeds are probably the descendants of the Malayan or Indian variety of G. bankiva. If so, this species has varied greatly since it was first domesticated; but there has been ample time, as we shall now show.
History of the Fowl.—Rütimeyer found no remains of the fowl in the ancient Swiss lake-dwellings; but, according to Jeitteles,[[33]] such have certainly since been found associated with extinct animals and prehistoric remains. It is, therefore a strange fact that the fowl is not mentioned in the Old Testament, nor figured on the ancient Egyptian monuments. It is not referred to by Homer or Hesiod (about 900 B.C.); but is mentioned by Theognis and Aristophanes between 400 and 500 B.C. It is figured on some of the Babylonian cylinders, between the sixth and seventh centuries B.C., of which Mr. Layard sent me an impression; and on the Harpy Tomb in Lycia, about 600 B.C.: so that the fowl apparently reached Europe in a domesticated condition somewhere about the sixth century B.C. It had travelled still farther westward by the time of the Christian era, for it was found in Britain by Julius Cæsar. In India it must have been domesticated when the Institutes of Manu were written, that is, according to Sir W. Jones, 1200 B.C., but, according to the later authority of Mr. H. Wilson, only 800 B.C., for the domestic fowl is forbidden, whilst the wild is permitted to be eaten. If, as before remarked, we may trust the old Chinese Encyclopædia, the fowl must have been domesticated several centuries earlier, as it is said to have been introduced from the West into China 1400 B.C.
Sufficient materials do not exist for tracing the history of the separate breeds. About the commencement of the Christian era, Columella mentions a five-toed fighting breed, and some provincial breeds; but we know nothing about them. He also alludes to dwarf fowls; but these cannot have been the same with our Bantams, which, as Mr. Crawfurd has shown, were imported from Japan into Bantam in Java. A dwarf fowl, probably the true Bantam, is referred to in an old Japanese Encyclopædia, as I am informed by Mr. Birch. In the Chinese Encyclopædia published in 1596, but compiled from various sources, some of high antiquity, seven breeds are mentioned, including what we should now call Jumpers or Creepers, and likewise fowls with black feathers, bones, and flesh. In 1600 Aldrovandi describes seven or eight breeds of fowls, and this is the most ancient record from which the age of our European breeds can be inferred. The Gallus turcicus certainly seems to be a pencilled Hamburgh; but Mr. Brent, a most capable judge, thinks that Aldrovandi “evidently figured what he happened to see, and not the best of the breed.” Mr. Brent, indeed, considers all Aldrovandi’s fowls as of impure breed; but it is a far more probable view that all our breeds have been much improved and modified since his time; for, as he went to the expense of so many figures, he probably would have secured characteristic specimens. The Silk fowl, however, probably then existed in its present state, as did almost certainly the fowl with frizzled or reversed feathers. Mr. Dixon[[34]] considers Aldrovandi’s Paduan fowl as “a variety of the Polish,” whereas Mr. Brent believes it to have been more nearly allied to the Malay. The anatomical peculiarities of the skull of the Polish breed were noticed by P. Borelli in 1656. I may add that in 1737 one Polish sub-breed, viz., the Golden-spangled, was known; but judging from Albin’s description, the comb was then larger, the crest of feathers much smaller, the breast more coarsely spotted, and the stomach and thighs much blacker: a Golden-spangled Polish fowl in this condition would now be of no value.
Differences in External and Internal Structure between the Breeds: Individual Variability.—Fowls have been exposed to diversified conditions of life, and as we have just seen there has been ample time for much variability and for the slow action of unconscious selection. As there are good grounds for believing that all the breeds are descended from Gallus bankiva, it will be worth while to describe in some detail the chief points of difference. Beginning with the eggs and chickens, I will pass on to their secondary sexual characters, and then to their differences in external structure and in the skeleton. I enter on the following details chiefly to show how variable almost every character has become under domestication.
Eggs.—Mr. Dixon remarks[[35]] that “to every hen belongs an individual peculiarity in the form, colour, and size of her egg, which never changes during her life-time, so long as she remains in health, and which is as well known to those who are in the habit of taking her produce, as the hand-writing of their nearest acquaintance.” I believe that this is generally true, and that, if no great number of hens be kept, the eggs of each can almost always be recognised. The eggs of differently sized breeds naturally differ much in size; but apparently, not always in strict relation to the size of the hen: thus the Malay is a larger bird than the Spanish, but she produces not such large eggs; white Bantams are said to lay smaller eggs than other Bantams;[[36]] white Cochins, on the other hand, as I hear from Mr. Tegetmeier, certainly lay larger eggs than buff Cochins. The eggs, however, of the different breeds vary considerably in character; for instance, Mr. Ballance states[[37]] that his Malay “pullets of last year laid eggs equal in size to those of any duck, and other Malay hens, two or three years old, laid eggs very little larger than a good sized Bantam’s egg. Some were as white as a Spanish hen’s egg, and others varied from a light cream-colour to a deep rich buff, or even to a brown.” The shape also varies, the two ends being much more equally rounded in Cochins than in Games or Polish. Spanish fowls lay smoother eggs than Cochins, of which the eggs are generally granulated. The shell in this latter breed, and more especially in Malays is apt to be thicker than in Games or Spanish; but the Minorcas, a sub-breed of Spanish, are said to lay harder eggs than true Spanish.[[38]] The colour differs considerably,—the Cochins laying buff-coloured eggs; the Malays a paler variable buff; and Games a still paler buff. It would appear that darker-coloured eggs characterise the breeds which have lately come from the East, or are still closely allied to those now living there. The colour of the yolk, according to Ferguson, as well as of the shell, differs slightly in the sub-breeds of the Game. I am also informed by Mr. Brent that dark partridge-coloured Cochin hens lay darker coloured eggs than the other Cochin sub-breeds. The flavour and richness of the egg certainly differ in different breeds. The productiveness of the several breeds is very different. Spanish, Polish, and Hamburgh hens have lost the incubating instinct.
Chickens.—As the young of almost all gallinaceous birds, even of the black curassow and black grouse, whilst covered with down, are longitudinally striped on the back,—of which character, when adult, neither sex retains a trace,—it might have been expected that the chickens of all our domestic fowls would have been similarly striped.[[39]] This could, however, hardly have been expected, when the adult plumage in both sexes has undergone so great a change as to be wholly white or black. In white fowls of various breeds the chickens are uniformly yellowish white, passing in the black-boned Silk fowl into bright canary-yellow. This is also generally the case with the chickens of white Cochins, but I hear from Mr. Zurhost that they are sometimes of a buff or oak colour, and that all those of this latter colour, which were watched, turned out males. The chickens of buff Cochins are of a golden-yellow, easily distinguishable from the paler tint of the white Cochins, and are often longitudinally streaked with dark shades: the chickens of silver-cinnamon Cochins are almost always of a buff colour. The chickens of the white Game and white Dorking breeds, when held in particular lights, sometimes exhibit (on the authority of Mr. Brent) faint traces of longitudinal stripes. Fowls which are entirely black, namely, Spanish, black Game, black Polish, and black Bantams, display a new character, for their chickens have their breasts and throats more or less white, with sometimes a little white elsewhere. Spanish chickens also, occasionally (Brent), have, where the down was white, their first true feathers tipped for a time with white. The primordially striped character is retained by the chickens of most of the Game sub-breeds (Brent, Dixon); by Dorkings; by the partridge and grouse-coloured sub-breeds of Cochins (Brent), but not, as we have seen, by the sub-breeds; by the pheasant-Malay (Dixon), but apparently not (at which I am much surprised) by other Malays. The following breeds and sub-breeds are barely, or not at all, longitudinally striped: viz., gold and silver pencilled Hamburghs, which can hardly be distinguished from each other (Brent) in the down, both having a few dark spots on the head and rump, with occasionally a longitudinal stripe (Dixon) on the back of the neck. I have seen only one chicken of the silver-spangled Hamburgh, and this was obscurely striped along the back. Gold-spangled Polish chickens (Tegetmeier) are of a warm russet brown; and silver-spangled Polish chickens are grey, sometimes (Dixon) with dashes of ochre on the head, wings, and breast. Cuckoo and blue-dun fowls (Dixon) are grey in the down. The chickens of Sebright Bantams (Dixon) are uniformly dark brown, whilst those of the brown-breasted red Game Bantam are black, with some white on the throat and breast. From these facts we see that young chickens of the different breeds, and even of the same main breed, differ much in their downy plumage; and, although longitudinal stripes characterise the young of all wild gallinaceous birds, they disappear in several domestic breeds. Perhaps it may be accepted as a general rule that the more the adult plumage differs from that of the adult G. bankiva, the more completely the chickens have lost their stripes.
With respect to the period of life at which the characters proper to each breed first appear, it is obvious that such structures as additional toes must be formed long before birth. In Polish fowls, the extraordinary protuberance of the anterior part of the skull is well developed before the chickens come out of the egg;[[40]] but the crest, which is supported on the protuberance, is at first feebly developed, nor does it attain its full size until the second year. The Spanish cock is pre-eminent for his magnificent comb, and this is developed at an unusually early age; so that the young males can be distinguished from the females when only a few weeks old, and therefore earlier than in other breeds; they likewise crow very early, namely, when about six weeks old. In the Dutch sub-breed of the Spanish fowl the white ear-lappets are developed earlier than in the common Spanish breed.[[41]] Cochins are characterised by a small tail, and in the young cocks the tail is developed at an unusually late period.[[42]] Game fowls are notorious for their pugnacity; and the young cocks crow, clap their little wings, and fight obstinately with each other, even whilst under their mother’s care.[[43]] “I have often had,” says one author,[[44]] “whole broods, scarcely feathered, stone-blind from fighting; the rival couples moping in corners, and renewing their battles on obtaining the first ray of light.” The weapons and pugnacity of all male gallinaceous birds evidently serve the purpose of gaining possession of the females; so that the tendency in our Game chickens to fight at an extremely early age is not only useless, but injurious, as they suffer much from their wounds. The training for battle during an early age may be natural to the wild Gallus bankiva; but as man during many generations has gone on selecting the most obstinately pugnacious cocks, it is more probable that their pugnacity has been unnaturally increased, and unnaturally transferred to the young male chickens. In the same manner, it is probable that the extraordinary development of the comb in the Spanish cock has been unintentionally transferred to the young cocks; for fanciers would not care whether their young birds had large combs, but would select for breeding the adults which had the finest combs, whether or not developed at an early period. The last point which need here be noticed is that, though the chickens of Spanish and Malay fowls are well covered with down, the true feathers are acquired at an unusually late age; so that for a time the young birds are partially naked, and are liable to suffer from cold.
Secondary Sexual Characters.—The two sexes in the parent-form, the Gallus bankiva, differ much in colour. In our domestic breeds the difference is never greater, but is often less, and varies much in degree even in the sub-breeds of the same main breed. Thus in certain Game fowls the difference is as great as in the parent-form, whilst in the black and white sub-breeds there is no difference in plumage. Mr. Brent informs me that he has seen two strains of black-breasted red Games, of which the cocks could not be distinguished, whilst the hens in one were partridge-brown and in the other fawn-brown. A similar case has been observed in the strains of the brown-breasted red Game. The hen of the “duck-winged Game” is “extremely beautiful,” and differs much from the hens of all the other Game sub-breeds; but generally, as with the blue and grey Game and with some sub-varieties of the pile-game, a moderately close relation may be observed between the males and females in the variation of their plumage.[[45]] A similar relation is also evident when we compare the several varieties of Cochins. In the two sexes of gold and silver-spangled and of buff Polish fowls, there is much general similarity in the colouring and marks of the whole plumage, excepting of course in the hackles, crest, and beard. In spangled Hamburghs, there is likewise a considerable degree of similarity between the two sexes. In pencilled Hamburghs, on the other hand, there is much dissimilarity; the pencilling which is characteristic of the hens being almost absent in the males of both the golden and silver varieties. But, as we have already seen, it cannot be given as a general rule that male fowls never have pencilled feathers, for Cuckoo Dorkings are “remarkable from having nearly similar markings in both sexes.”
It is a singular fact that the males in certain sub-breeds have lost some of their secondary masculine characters, and from their close resemblance in plumage to the females, are often called hennies. There is much diversity of opinion whether these males are in any degree sterile; that they sometimes are partially sterile seems clear,[[46]] but this may have been caused by too close interbreeding. That they are not quite sterile, and that the whole case is widely different from that of old females assuming masculine characters, is evident from several of these hen-like sub-breeds having been long propagated. The males and females of gold and silver-laced Sebright Bantams can be barely distinguished from each other, except by their combs, wattles, and spurs, for they are coloured alike, and the males have not hackles, nor the flowing sickle-like tail-feathers. A hen-tailed sub-breed of Hamburghs was recently much esteemed. There is also a breed of Game-fowls, in which the males and females resemble each other so closely that the cocks have often mistaken their hen-feathered opponents in the cock-pit for real hens, and by the mistake have lost their lives.[[47]] The cocks, though dressed in the feathers of the hen, “are high-spirited birds, and their courage has been often proved:” an engraving even has been published of one celebrated hen-tailed victor. Mr. Tegetmeier[[48]] has recorded the remarkable case of a brown-breasted red Game cock which, after assuming its perfect masculine plumage, became hen-feathered in the autumn of the following year; but he did not lose voice, spurs, strength, nor productiveness. This bird has now retained the same character during five seasons, and has begot both hen-feathered and male-feathered offspring. Mr. Grantley F. Berkeley relates the still more singular case of a celebrated strain of “polecat Game fowls,” which produced in nearly every brood a single hen-cock. “The great peculiarity in one of these birds was that he, as the seasons succeeded each other, was not always a hen-cock, and not always of the colour called the polecat, which is black. From the polecat and hen-cock feather in one season he moulted to a full male-plumaged black-breasted red, and in the following year he returned to the former feather.”[[49]]
I have remarked in my ‘Origin of Species’ that secondary sexual characters are apt to differ much in the species of the same genus, and to be unusually variable in the individuals of the same species. So it is with the breeds of the fowl, as we have already seen, as far as the colour of plumage is concerned, and so it is with the other secondary sexual characters. Firstly, the comb differs much in the various breeds,[[50]] and its form is eminently characteristic of each kind, with the exception of the Dorkings, in which the form has not been as yet determined on by fanciers, and fixed by selection. A single, deeply-serrated comb is the typical and most common form. It differs much in size, being immensely developed in Spanish fowls; and in a local breed called Red-caps, it is sometimes “upwards of three inches in breadth at the front, and more than four inches in length, measured to the end of the peak behind.”[[51]] In some breeds the comb is double, and when the two ends are cemented together it forms a “cup-comb;” in the “rose-comb” it is depressed, covered with small projections, and produced backwards; in the horned and creve-coeur fowl it is produced into two horns; it is triple in the pea-combed Brahmas, short and truncated in the Malays, and absent in the Guelderlands. In the tasselled Game a few long feathers rise from the back of the comb: in many breeds a crest of feathers replaces the comb. The crest, when little developed, arises from a fleshy mass, but, when much developed, from a hemispherical protuberance of the skull. In the best Polish fowls it is so largely developed, that I have seen birds which could hardly pick up their food; and a German writer asserts[[52]] that they are in consequence liable to be struck by hawks. Monstrous structures of this kind would thus be suppressed in a state of nature. The wattles, also, vary much in size, being small in Malays and some other breeds; in certain Polish sub-breeds they are replaced by a great tuft of feathers called a beard.
The hackles do not differ much in the various breeds, but are short and stiff in Malays, and absent in Hennies. As in some orders male birds display extraordinarily-shaped feathers, such as naked shafts with discs at the end, etc., the following case may be worth giving. In the wild Gallus bankiva and in our domestic fowls, the barbs which arise from each side of the extremities of the hackles are naked or not clothed with barbules, so that they resemble bristles; but Mr. Brent sent me some scapular hackles from a young Birchen Duckwing Game cock, in which the naked barbs became densely re-clothed with barbules towards their tips; so that these tips, which were dark coloured with a metallic lustre, were separated from the lower parts by a symmetrically-shaped transparent zone formed of the naked portions of the barbs. Hence the coloured tips appeared like little separate metallic discs.
The sickle-feathers in the tail, of which there are three pair, and which are eminently characteristic of the male sex, differ much in the various breeds. They are scimitar-shaped in some Hamburghs, instead of being long and flowing as in the typical breeds. They are extremely short in Cochins, and are not at all developed in Hennies. They are carried, together with the whole tail, erect in Dorkings and Gaines; but droop much in Malays and in some Cochins. Sultans are characterised by an additional number of lateral sickle-feathers. The spurs vary much, being placed higher or lower on the shank; being extremely long and sharp in Games, and blunt and short in Cochins. These latter birds seem aware that their spurs are not efficient weapons; for though they occasionally use them, they more frequently fight, as I am informed by Mr. Tegetmeier, by seizing and shaking each other with their beaks. In some Indian Game cocks, received by Mr. Brent from Germany, there are, as he informs me, three, four, or even five spurs on each leg. Some Dorkings also have two spurs on each leg;[[53]] and in birds of this breed the spur is often placed almost on the outside of the leg. Double spurs are mentioned in an ancient Chinese Encyclopædia. Their occurrence may be considered as a case of analogous variation, for some wild gallinaceous birds, for instance, the Polyplectron, have double spurs.
Judging from the differences which generally distinguish the sexes in the Gallinaceæ, certain characters in our domestic fowls appear to have been transferred from the one sex to the other. In all the species (except in Turnix), when there is any conspicuous difference in plumage between the male and female, the male is always the most beautiful; but in golden-spangled Hamburghs the hen is equally beautiful with the cock, and incomparably more beautiful than the hen in any natural species of Gallus; so that here a masculine character has been transferred to the female. On the other hand, in Cuckoo Dorkings and in other cuckoo breeds the pencilling, which in Gallus is a female attribute, has been transferred to the male: nor, on the principle of analogous variation, is this transference surprising, as the males in many gallinaceous genera are barred or pencilled. With most of these birds head ornaments of all kinds are more fully developed in the male than in the female; but in Polish fowls the crest or top-knot, which in the male replaces the comb, is equally developed in both sexes. In the males of certain other sub-breeds, which from the hen having a small crest, are called lark-crested, “a single upright comb sometimes almost entirely takes the place of the crest.”[[54]] From this latter case, and more especially from some facts presently to be given with respect to the protuberance of the skull in Polish fowls, the crest in this breed must be viewed as a feminine character which has been transferred to the male. In the Spanish breed the male, as we know, has an immense comb, and this has been partially transferred to the female, for her comb is unusually large, though not upright. In Game fowls the bold and savage disposition of the male has likewise been largely transferred to the female;[[55]] and she sometimes even possesses the eminently masculine character of spurs. Many cases are on record of fertile hens being furnished with spurs; and in Germany, according to Bechstein,[[56]] the spurs in the Silk hen are sometimes very long. He mentions also another breed similarly characterised, in which the hens are excellent layers, but are apt to disturb and break their eggs owing to their spurs.
Mr. Layard[[57]] has given an account of a breed of fowls in Ceylon with black skin, bones, and wattle, but with ordinary feathers, and which cannot “be more aptly described than by comparing them to a white fowl drawn down a sooty chimney; it is, however,” adds Mr. Layard, “a remarkable fact that a male bird of the pure sooty variety is almost as rare as a tortoise-shell tom-cat.” Mr. Blyth found the same rule to hold good with this breed near Calcutta. The males and females, on the other hand, of the black-boned European breed, with silky feathers, do not differ from each other; so that in the one breed, black skin and bones and the same kind of plumage are common to both sexes, whilst in the other breed, these characters are confined to the female sex.
At the present day all the breeds of Polish fowls have the great bony protuberance on their skulls, which includes part of the brain and supports the crest, equally developed in both sexes. But formerly in Germany the skull of the hen alone was protuberant: Blumenbach,[[58]] who particularly attended to abnormal peculiarities in domestic animals, states, in 1805, that this was the case; and Bechstein had previously, in 1793 observed the same fact. This latter author has carefully described the effects on the skull of a crest not only in the case of fowls, but of ducks, geese, and canaries. He states that with fowls, when the crest is not much developed, it is supported on a fatty mass; but when much developed, it is always supported on a bony protuberance of variable size. He well describes the peculiarities of this protuberance; he attended also to the effects of the modified shape of the brain on the intellect of these birds, and disputes Pallas’ statement that they are stupid. He then expressly remarks that he never observed this protuberance in male fowls. Hence there can be no doubt that this extraordinary character in the skulls of Polish fowls was formerly in Germany confined to the female sex, but has now been transferred to the males, and has thus become common to both sexes.
External Differences, not connected with the Sexes, between the Breeds and between individual Birds.
The size of the body differs greatly. Mr. Tegetmeier has known a Brahma to weigh 17 pounds; a fine Malay cock 10 pounds; whilst a first-rate Sebright Bantam weighs hardly more than 1 pound. During the last 20 years the size of some of our breeds has been largely increased by methodical selection, whilst that of other breeds has been much diminished. We have already seen how greatly colour varies even within the same breed; we know that the wild G. bankiva varies slightly in colour; we know that colour is variable in all our domestic animals; nevertheless some eminent fanciers have so little faith in variability, that they have actually argued that the chief Game sub-breeds, which differ from each other in nothing but colour, are descended from distinct wild species! Crossing often causes strange modification of colour. Mr. Tegetmeier informs me that when buff and white Cochins are crossed, some of the chickens are almost invariably black. According to Mr. Brent, black and white Cochins occasionally produce chickens of a slaty-blue tint; and this same tint results, as Mr. Tegetmeier tells me, from crossing white Cochins with black Spanish fowls, or white Dorkings with black Minorcas.[[59]] A good observer[[60]] states that a first-rate silver-spangled Hamburgh hen gradually lost the most characteristic qualities of the breed, for the black lacing to her feathers disappeared, and her legs changed from leaden-blue to white: but what makes the case remarkable is, that this tendency ran in the blood for her sister changed in a similar but less strongly marked manner; and chickens produced from this latter hen were at first almost pure white, “but on moulting acquired black colours and some spangled feathers with almost obliterated markings;” so that a new variety arose in this singular manner. The skin in the different breeds differs much in colour, being white in common kinds, yellow in Malays and Cochins, and black in Silk fowls; thus mocking, as M. Godron[[61]] remarks the three principal types of skin in mankind. The same author adds that, as different kinds of fowls living in distant and isolated parts of the world have black skin and bones, this colour must have appeared at various times and places.
The shape and carriage of the body, and the shape of the head differ much. The beak varies slightly in length and curvature, but incomparably less than with pigeons. In most crested fowls the nostrils offer a remarkable peculiarity in being raised with a crescentic outline. The primary wing-feathers are short in Cochins; in a male, which must have been more than twice as heavy as G. bankiva, these feathers were in both birds of the same length. I have counted, with Mr. Tegetmeier’s aid, the primary wing-feathers in thirteen cocks and hens of various breeds; in four of them, namely in two Hamburghs, a Cochin, and Game bantam, there were 10, instead of the normal number 9; but in counting these feathers I have followed the practice of fanciers, and have not included the first minute primary feather, barely three-quarters of an inch in length. These feathers differ considerably in relative length, the fourth, or the fifth, or the sixth, being the longest; with the third either equal to, or considerably shorter than the fifth. In wild gallinaceous species the relative length and number of the main wing and tail-feathers are extremely constant.
The tail differs much in erectness and size, being small in Malays and very small in Cochins. In thirteen fowls of various breeds which I have examined, five had the normal number of 14 feathers, including in this number the two middle sickle-feathers; six others (viz., a Caffre cock, Gold-spangled Polish cock, Cochin hen, Sultan hen, Game hen and Malay hen had 16; and two (an old Cochin cock and Malay hen) had 17 feathers. The rumpless fowl has no tail and in one which I possessed there was no oil-gland; but this bird though the os coccygis was extremely imperfect, had a vestige of a tail with two rather long feathers in the position of the outer caudals. This bird came from a family where, as I was told, the breed had kept true for twenty years; but rumpless fowls often produce chickens with tails.[[62]] An eminent physiologist[[63]] has recently spoken of this breed as a distinct species; had he examined the deformed state of the os coccyx he would never have come to this conclusion; he was probably misled by the statement, which may be found in some works, that tailless fowls are wild in Ceylon; but this statement, as I have been assured by Mr. Layard and Dr. Kellaert who have so closely studied the birds of Ceylon, is utterly false.
The tarsi vary considerably in length, being relatively to the femur considerably longer in the Spanish and Frizzled, and shorter in the Silk and Bantam breeds, than in the wild G. bankiva; but in the latter, as we have seen, the tarsi vary in length. The tarsi are often feathered. The feet in many breeds are furnished with additional toes. Golden-spangled Polish fowls are said[[64]] to have the skin between their toes much developed: Mr. Tegetmeier observed this in one bird, but it was not so in one which I examined. Prof. Hoffmann has sent me a sketch of the feet of a fowl of the common breed at Giessen, with a web extending between the three toes, for about a third of their length. In Cochins the middle toe is said[[65]] to be nearly double the length of the lateral toes, and therefore much longer than in G. bankiva or in other fowls; but this was not the case in two which I examined. The nail of the middle toe in this same breed is surprisingly broad and flat, but in a variable degree in two birds which I examined; of this structure in the nail there is only a trace in G. bankiva.
The voice differs slightly, as I am informed by Mr. Dixon, in almost every breed. The Malays[[66]] have a loud, deep, somewhat prolonged crow, but with considerable individual difference. Colonel Sykes remarks that the domestic Kulm cock in India has not the shrill clear pipe of the English bird, and “his scale of notes appears more limited.” Dr. Hooker was struck with the “prolonged howling screech” of the cocks in Sikhim.[[67]] The crow of the Cochin is notoriously and ludicrously different from that of the common cock. The disposition of the different breeds is widely different, varying from the savage and defiant temper of the Game-cock to the extremely peaceable temper of the Cochins. The latter, it has been asserted, “graze to a much greater extent than any other varieties.” The Spanish fowls suffer more from frost than other breeds.
Before we pass on to the skeleton, the degree of distinctness of the several breeds from G. bankiva ought to be noticed. Some writers speak of the Spanish as one of the most distinct breeds, and so it is in general aspect; but its characteristic differences are not important. The Malay appears to me more distinct, from its tall stature, small drooping tail with more than fourteen tail-feathers, and from its small comb and wattles; nevertheless, one Malay sub-breed is coloured almost exactly like G. bankiva. Some authors consider the Polish fowl as very distinct; but this is a semi-monstrous breed, as shown by the protuberant and irregularly perforated skull. The Cochin, from its deeply furrowed frontal bones, peculiarly shaped occipital foramen, short wing-feathers, short tail containing more than fourteen feathers, broad nail to the middle toe, fluffy plumage, rough and dark-coloured eggs, and especially from its peculiar voice, is probably the most distinct of all the breeds. If any one of our breeds has descended from some unknown species, distinct from G. bankiva, it is probably the Cochin; but the balance of evidence does not favour this view. All the characteristic differences of the Cochin breed are more or less variable, and may be detected in a greater or lesser degree in other breeds. One sub-breed is coloured closely like G. bankiva. The feathered legs, often furnished with an additional toe, the wings incapable of flight, the extremely quiet disposition, indicate a long course of domestication; and these fowls come from China, where we know that plants and animals have been tended from a remote period with extraordinary care, and where consequently we might expect to find profoundly modified domestic races.
Osteological Differences.—I have examined twenty-seven skeletons and fifty-three skulls of various breeds, including three of G. bankiva: nearly half of these skulls I owe to the kindness of Mr. Tegetmeier, and three of the skeletons to Mr. Eyton.
Fig. 33—Occipital Foramen of the Skulls of Fowls
The Skull differs greatly in size in different breeds, being nearly twice as long in the largest Cochins, but not nearly twice as broad, as in Bantams. The bones at the base, from the occipital foramen to the anterior end (including the quadrates and pterygoids), are absolutely identical in shape in all the skulls. So is the lower jaw. In the forehead slight differences are often perceptible between the males and females, evidently caused by the presence of the comb. In every case I take the skull of G. bankiva as the standard of comparison. In four Games, in one Malay hen, in an African cock, in a Frizzled cock from Madras, in two black-boned Silk hens, no differences worth notice occur. In three Spanish cocks, the form of the forehead between the orbits differs considerably; in one it is considerably depressed, whilst in the two others it is rather prominent, with a deep medial furrow; the skull of the hen is smooth. In three skulls of Sebright Bantams the crown is more globular, and slopes more abruptly to the occiput, than in G. bankiva. In a Bantam or Jumper from Burmah these same characters are more strongly pronounced, and the supra-occiput is more pointed. In a black Bantam the skull is not so globular, and the occipital foramen is very large, and has nearly the same sub-triangular outline presently to be described in Cochins; and in this skull the two ascending branches of the premaxillary are overlapped in a singular manner by the processes of the nasal bone, but, as I have seen only one specimen, some of these differences may be individual. Of Cochins and Brahmas (the latter a crossed race approaching closely to Cochins) I have examined seven skulls; at the point where the ascending branches of the premaxillary rest on the frontal bone the surface is much depressed, and from this depression a deep medial furrow extends backwards to a variable distance; the edges of this fissure are rather prominent, as is the top of the skull behind and over the orbits. These characters are less developed in the hens. The pterygoids, and the processes of the lower jaw, are broader, relatively to the size of the head, than in G. bankiva; and this is likewise the case with Dorkings when of large size. The fork of the hyoid bone in Cochins is twice as wide as in G. bankiva, whereas the length of the other hyoid bones is only as three to two. But the most remarkable character is the shape of the occipital foramen: in G. bankiva (A) the breadth in a horizontal line exceeds the height in a vertical line, and the outline is nearly circular; whereas in Cochins (B) the outline is sub-triangular, and the vertical line exceeds the horizontal line in length. This same form likewise occurs in the black Bantam above referred to, and an approach to it may be seen in some Dorkings, and in a slight degree in certain other breeds.
Fig. 34—Skulls of Fowls
Of Dorkings I have examined three skulls, one belonging to the white-sub-breed; the one character deserving notice is the breadth of the frontal bones, which are moderately furrowed in the middle; thus in a skull which was less than once and a half the length of that of G. bankiva, the breadth between the orbits was exactly double. Of Hamburghs I have examined four skulls (male and female) of the pencilled sub-breed, and one (male) of the spangled sub-breed; the nasal bones stand remarkably wide apart, but in a variable degree; consequently narrow membrane-covered spaces are left between the tips of the two ascending branches of the pre-maxillary bones, which are rather short, and between these branches and the nasal bones. The surface of the frontal bone, on which the branches of the premaxillary rest, is very little depressed. These peculiarities no doubt stand in close relation with the broad, flattened rose-comb characteristic of the Hamburgh breed.
Fig. 35—Longitudinal sections of Skulls of Fowls
I have examined fourteen skulls of Polish and other crested breeds. Their differences are extraordinary. First for nine skulls of different sub-breeds of English Polish fowls. The hemispherical protuberance of the frontal bones[[68]] may be seen in fig. 34, in which (B) the skull of a white-crested Polish fowl is shown obliquely from above, with the skull (A) of G. bankiva in the same position. In fig. 35 longitudinal sections are given of the skull of a Polish fowl, and, for comparison, of a Cochin of the same size. The protuberance in all Polish fowls occupies the same position but differs much in size. In one of my nine specimens it was extremely slight. The degree to which the protuberance is ossified varies greatly, larger or smaller portions of bone being replaced by membrane. In one specimen there was only a single open pore; generally, there are many variously shaped open spaces, the bone forming an irregular reticulation. A medial, longitudinal, arched ribbon of bone is generally retained, but in one specimen there was no bone whatever over the whole protuberance, and the skull, when cleaned and viewed from above, presented the appearance of an open basin. The change in the whole internal form of the skull is surprisingly great. The brain is modified in a corresponding manner, as is shown in the two longitudinal sections, which deserve attentive consideration. The upper and anterior cavity of the three into which the skull may be divided, is the one which is so greatly modified; it is evidently much larger than in the Cochin skull of the same size, and extends much further beyond the interorbital septum, but laterally is less deep. This cavity, as I hear from Mr. Tegetmeier, is entirely filled with brain. In the skull of the Cochin and of all ordinary fowls a strong internal ridge of bone separates the anterior from the central cavity; but this ridge is quite absent in the Polish skull here figured. The shape of the central cavity is circular in the Polish, and lengthened in the Cochin skull. The shape of the posterior cavity, together with the position, size, and number of the pores for the nerves, differ much in these two skulls. A pit deeply penetrating the occipital bone of the Cochin is entirely absent in this Polish skull, whilst in another specimen it was well developed. In this second specimen the whole internal surface of the posterior cavity likewise differs to a certain extent in shape. I made sections of two other skulls,—namely, of a Polish fowl with the protuberance singularly little developed, and of a Sultan in which it was a little more developed; and when these two skulls were placed between the two above figured (fig. 35), a perfect gradation in the configuration of each part of the internal surface could be traced. In the Polish skull, with a small protuberance, the ridge between the anterior and middle cavities was present, but low; and in the Sultan this ridge was replaced by a narrow furrow standing on a broad raised eminence.
Fig. 36—Skulls of Horned Fowl
It may naturally be asked whether these remarkable modifications in the form of the brain affect the intellect of Polish fowls; some writers have stated that they are extremely stupid, but Bechstein and Mr. Tegetmeier have shown that this is by no means generally the case. Nevertheless Bechstein[[69]] states that he had a Polish hen which “was crazy, and anxiously wandered about all day long.” A hen in my possession was solitary in her habits, and was often so absorbed in reverie that she could be touched; she was also deficient in the most singular manner in the faculty of finding her way, so that, if she strayed a hundred yards from her feeding-place, she was completely lost, and would then obstinately try to proceed in a wrong direction. I have received other and similar accounts of Polish fowls appearing stupid or half-idiotic.[[70]]
To return to the skull of Polish fowls. The posterior part, viewed externally, differs little from that of G. bankiva. In most fowls the posterior-lateral process of the frontal bone and the process of the squamosal bone run together and are ossified near their extremities: this union of the two bones, however, is not constant in any breed; and in eleven out of fourteen skulls of crested breeds, these processes were quite distinct. These processes, when not united, instead of being inclined anteriorly, as in all common breeds, descend at right angles to the lower jaw; and in this case the longer axis of the bony cavity of the ear is likewise more perpendicular, than in other breeds. When the squamosal process is free instead of expanding at the tip, it is reduced to an extremely fine and pointed style, of variable length. The pterygoid and quadrate bones present no differences. The palatine bones are a little more curved upwards at their posterior ends. The frontal bones, anteriorly to the protuberance, are, as in Dorkings, very broad, but in a variable degree. The nasal bones either stand far apart, as in Hamburghs, or almost touch each other, and in one instance were ossified together. Each nasal bone properly sends out in front two long processes of equal lengths, forming a fork; but in all the Polish skulls, except one, the inner process was considerably, but in a variable degree, shortened and somewhat upturned. In all the skulls, except one, the two ascending branches of the premaxillary, instead of running up between the processes of the nasal bones and resting on the ethmoid bone, are much shortened and terminate in a blunt, somewhat upturned point. In those skulls in which the nasal bones approach quite close to each other or are ossified together, it would be impossible for the ascending branches of the premaxillary to reach the ethmoid and frontal bones; hence we see that even the relative connection of the bones has been changed. Apparently in consequence of the branches of the premaxillary and of the inner processes of the nasal bones being somewhat upturned, the external orifices of the nostrils are upraised and assume a crescentic outline.
I must still say a few words on some of the foreign Crested breeds. The skull of a crested, rumpless, white Turkish fowl was very slightly protuberant, and but little perforated; the ascending branches of the premaxillary were well developed. In another Turkish breed, called Ghoondooks, the skull was considerably protuberant and perforated; the ascending branches of the premaxillary were so much aborted that they projected only 1/15th of an inch; and the inner processes of the nasal bone were so completely aborted, that the surface where they should have projected was quite smooth. Here then we see these two bones modified to an extreme degree. Of Sultans (another Turkish breed) I examined two skulls; in that of the female the protuberance was much larger than in the male. In both skulls the ascending branches of the premaxillary were very short, and in both the nasal portion of the inner processes of the nasal bones were ossified together. These Sultan skulls differed from those of English Polish fowls in the frontal bones, anteriorly to the protuberance, not being broad.
The last skull which I need describe is a unique one, lent to me by Mr. Tegetmeier: it resembles a Polish skull in most of its characters, but has not the great frontal protuberance; it has, however, two rounded knobs of a different nature, which stand more in front, above the lachrymal bones. These curious knobs, into which the brain does not enter, are separated from each other by a deep medial furrow; and this is perforated by a few minute pores. The nasal bones stand rather wide apart, with their inner processes, and the ascending branches of the premaxillary, upturned and shortened. The two knobs no doubt supported the two great horn-like projections of the comb.
From the foregoing facts we see in how astonishing a manner some of the bones of the skull vary in Crested fowls. The protuberance may certainly be called in one sense a monstrosity, as being wholly unlike anything observed in nature: but as in ordinary cases it is not injurious to the bird, and as it is strictly inherited, it can hardly in another sense be called a monstrosity. A series may be formed commencing with the black-boned Silk fowl, which has a very small crest with the skull beneath penetrated only by a few minute orifices, but with no other change in its structure; and from this first stage we may proceed to fowls with a moderately large crest, which rests, according to Bechstein, on a fleshy mass, but without any protuberance in the skull. I may add that I have seen a similar fleshy or fibrous mass beneath the tuft of feathers on the head of the Tufted duck; and in this case there was no actual protuberance in the skull, but it had become a little more globular. Lastly, when we come to fowls with a largely developed crest, the skull becomes largely protuberant and is perforated by a multitude of irregular open spaces. The close relation between the crest and the size of the bony protuberance is shown in another way; for Mr. Tegetmeier informs me that if chickens lately hatched be selected with a large bony protuberance, when adult they will have a large crest. There can be no doubt that in former times the breeder of Polish fowls attended solely to the crest, and not to the skull; nevertheless, by increasing the crest, in which he has been wonderfully successful, he has unintentionally made the skull protuberant to an astonishing degree; and through correlation of growth, he has at the same time affected the form and relative connexion of the premaxillary and nasal bones, the shape of the orifice of the nose, the breadth of the frontal bones, the shape of the post-lateral processes of the frontal and squamosal bones, the direction of the axis of the bony cavity of the ear, and lastly the internal configuration of the whole skull together with the shape of the brain.
Fig. 37—Sixth Cervical Verterbra of Fowls
Vertebræ.—In G. bankiva there are fourteen cervical, seven dorsal with ribs, apparently fifteen lumbar and sacral, and six caudal vertebræ;[[71]] but the lumbar and sacral are so much anchylosed that I am not sure of their number, and this makes the comparison of the total number of vertebræ in the several breeds difficult. I have spoken of six caudal vertebræ, because the basal one is almost completely anchylosed with the pelvis; but if we consider the number as seven, the caudal vertebræ agree in all the skeletons. The cervical vertebræ are, as just stated, in appearance fourteen; but out of twenty-three skeletons in a fit state for examination, in five of them, namely, in two Games, in two pencilled Hamburghs, and in a Polish, the fourteenth vertebra bore ribs, which, though small, were perfectly developed with a double articulation. The presence of these little ribs cannot be considered as a fact of much importance, for all the cervical vertebræ bear representatives of ribs; but their development in the fourteenth vertebra reduces the size of the passages in the transverse processes, and makes this vertebra exactly like the first dorsal vertebra. The addition of these little ribs does not affect the fourteenth cervical alone, for properly the ribs of the first true dorsal vertebra are destitute of processes; but in some of the skeletons in which the fourteenth cervical bore little ribs the first pair of true ribs had well-developed processes. When we know that the sparrow has only nine, and the swan twenty-three cervical vertebræ,[[72]] we need feel no surprise at the number of the cervical vertebræ in the fowl being, as it appears, variable.
There are seven dorsal vertebræ bearing ribs; the first dorsal is never anchylosed with the succeeding four, which are generally anchylosed together. In one Sultan fowl, however, the two first dorsal vertebræ were free. In two skeletons, the fifth dorsal was free; generally the sixth is free (as in G. bankiva), but sometimes only at its posterior end, where in contact with the seventh. The seventh dorsal vertebra, in every case excepting in one Spanish cock, was anchylosed with the lumbar vertebræ. So that the degree to which these middle dorsal vertebræ are anchylosed is variable.
Seven is the normal number of true ribs, but in two skeletons of the Sultan fowl (in which the fourteenth cervical vertebra was not furnished with little ribs) there were eight pairs; the eighth pair seemed to be developed on a vertebra corresponding with the first lumbar in G. bankiva; the sternal portion of both the seventh and eighth ribs did not reach the sternum. In four skeletons in which ribs were developed on the fourteenth cervical vertebra, there were, when these cervical ribs are included, eight pairs; but in one Game cock, in which the fourteenth cervical was furnished with ribs, there were only six pairs of true dorsal ribs; the sixth pair in this case did not have processes, and thus resembled the seventh pair in other skeletons; in this Game cock, as far as could be judged from the appearance of the lumbar vertebræ, a whole dorsal vertebra with its ribs was missing. We thus see that the ribs (whether or not the little pair attached to the fourteenth cervical vertebra be counted) vary from six to eight pair. The sixth pair is frequently not furnished with processes. The sternal portion of the seventh pair is extremely broad in Cochins, and is completely ossified. As previously stated, it is scarcely possible to count the lumbo-sacral vertebræ; but they certainly do not correspond in shape or number in the several skeletons. The caudal vertebræ are closely similar in all the skeletons, the only difference being whether or not the basal one is anchylosed to the pelvis; they hardly vary even in length, not being shorter in Cochins, with their short tail-feathers, than in other breeds; in a Spanish cock, however, the caudal vertebræ were a little elongated. In three rumpless fowls the caudal vertebræ were few in number, and anchylosed together into a misformed mass.
In the individual vertebræ the differences in structure are very slight. In the atlas the cavity for the occipital condyle is either ossified into a ring, or is, as in Bankiva, open on its upper margin. The upper arc of the spinal canal is a little more arched in Cochins, in conformity with the shape of the occipital foramen, than in G. bankiva. In several skeletons a difference, but not of much importance, may be observed, which commences at the fourth cervical vertebra, and is greatest at about the sixth, seventh, or eighth vertebra; this consists in the hæmal descending processes being united to the body of the vertebra by a sort of buttress. This structure may be observed in Cochins, Polish, some Hamburghs, and probably other breeds; but is absent, or barely developed, in Game, Dorking, Spanish, Bantam, and several other breeds examined by me. On the dorsal surface of the sixth cervical vertebra in Cochins three prominent points are more strongly developed than in the corresponding vertebra of the Game fowl or G. bankiva.
Pelvis.—This differs in some few points in the several skeletons. The anterior margin of the ilium seems at first to vary much in outline, but this is chiefly due to the degree to which the margin in the middle part is ossified to the crest of the vertebræ; the outline, however, does differ in being more truncated in Bantams, and more rounded in certain breeds, as in Cochins. The outline of the ischiadic foramen differs considerably, being nearly circular in Bantams, instead of egg-shaped as in the Bankiva, and more regularly oval in some skeletons, as in the Spanish. The obturator notch is also much less elongated in some skeletons than in others. The end of the pubic bone presents the greatest difference; being hardly enlarged in the Bankiva; considerably and gradually enlarged in Cochins, and in a lesser degree in some other breeds; and abruptly enlarged in Bantams. In one Bantam this bone extended very little beyond the extremity of the ischium. The whole pelvis in this latter bird differed widely in its proportions, being far broader proportionally to its length than in Bankiva.
Fig. 38—Extremity of the Furcula of Fowls
Sternum.—This bone is generally so much deformed that it is scarcely possible to compare its shape strictly in the several breeds. The form of the triangular extremity of the lateral processes differs considerably, being either almost equilateral or much elongated. The front margin of the crest is more or less perpendicular and varies greatly, as does the curvature of the posterior end, and the flatness of the lower surface. The outline of the manubrial process also varies, being wedge-shaped in the Bankiva, and rounded in the Spanish breed. The furculum differs in being more or less arched, and greatly, as may be seen in the accompanying outlines, in the shape of the terminal plate; but the shape of this part differed a little in two skeletons of the wild Bankiva. The coracoid presents no difference worth notice. The scapula varies in shape, being of nearly uniform breadth in Bankiva, much broader in the middle in the Polish fowl, and abruptly narrowed towards the apex in the two Sultan fowls.
I carefully compared each separate bone of the leg and wing, relatively to the same bones in the wild Bankiva, in the following breeds, which I thought were the most likely to differ; namely, in Cochin, Dorking, Spanish, Polish, Burmese Bantam, Frizzled Indian, and black-boned Silk fowls; and it was truly surprising to see how absolutely every process, articulation, and pore agreed, though the bones differed greatly in size. The agreement is far more absolute than in other parts of the skeleton. In stating this, I do not refer to the relative thickness and length of the several bones; for the tarsi varied considerably in both these respects. But the other limb-bones varied little even in relative length.
Finally, I have not examined a sufficient number of skeletons to say whether any of the foregoing differences, except in the skull, are characteristic of the several breeds. Apparently some differences are more common in certain breeds than in others,—as an additional rib to the fourteenth cervical vertebra in Hamburghs and Games, and the breadth of the end of the pubic bone in Cochins. Both skeletons of the Sultan fowl had eight dorsal vertebræ, and the end of the scapula in both was somewhat attenuated. In the skull, the deep medial furrow in the frontal bones and the vertically elongated occipital foramen seem to be characteristic of Cochins; as is the great breadth of the frontal bones in Dorkings; the separation and open spaces between the tips of the ascending branches of the premaxillaries and nasal bones, as well as the front part of the skull being but little depressed, characterise Hamburghs; the globular shape of the posterior part of the skull seems to be characteristic of laced Bantams; and lastly, the protuberance of the skull with the ascending branches of the premaxillaries partially aborted, together with the other differences before specified, are eminently characteristic of Polish and other Crested fowls.
But the most striking result of my examination of the skeleton is the great variability of all the bones except those of the extremities. To a certain extent we can understand why the skeleton fluctuates so much in structure; fowls have been exposed to unnatural conditions of life, and their whole organisation has thus been rendered variable; but the breeder is quite indifferent to, and never intentionally selects, any modification in the skeleton. External characters, if not attended to by man, such as the number of the tail and wing feathers and their relative lengths, which in wild birds are generally constant,—fluctuate in our domestic fowls in the same manner as the several parts of the skeleton. An additional toe is a “point” in Dorkings, and has become a fixed character, but is variable in Cochins and Silk fowls. The colour of the plumage and the form of the comb are in most breeds, or even sub-breeds, eminently fixed characters; but in Dorkings these points have not been attended to, and are variable. When any modification in the skeleton is related to some external character which man values, it has been, unintentionally on his part, acted on by selection, and has become more or less fixed. We see this in the wonderful protuberance of the skull, which supports the crest of feathers in Polish fowls, and which by correlation has affected other parts of the skull. We see the same result in the two protuberances which support the horns in the horned fowl, and in the flattened shape of the front of the skull in Hamburghs consequent on their flattened and broad “rose-combs.” We know not in the least whether additional ribs, or the changed outline of the occipital foramen, or the changed form of the scapula, or of the extremity of the furculum, are in any way correlated with other structures, or have arisen from the changed conditions and habits of life to which our fowls have been subjected; but there is no reason to doubt that these various modifications in the skeleton could be rendered, either by direct selection, or by the selection of correlated structures, as constant and as characteristic of each breed, as are the size and shape of the body, the colour of the plumage, and the form of the comb.
Effects of the Disuse of Parts.
Judging from the habits of our European gallinaceous birds, Gallus bankiva in its native haunts would use its legs and wings more than do our domestic fowls, which rarely fly except to their roosts. The Silk and the Frizzled fowls, from having imperfect wing-feathers, cannot fly at all; and there is reason to believe that both these breeds are ancient, so that their progenitors during many generations cannot have flown. The Cochins, also, from their short wings and heavy bodies, can hardly fly up to a low perch. Therefore in these breeds, especially in the two first, a considerable diminution in the wing-bones might have been expected, but this is not the case. In every specimen, after disarticulating and cleaning the bones, I carefully compared the relative length of the two main bones of the wing to each other, and of the two main bones of the leg to each other, with those of G. bankiva; and it was surprising to see (except in the case of the tarsi) how exactly the same relative length had been retained. This fact is curious, from showing how truly the proportions of an organ may be inherited, although not fully exercised during many generations. I then compared in several breeds the length of the femur and tibia with the humerus and ulna, and likewise these same bones with those of G. bankiva; the result was that the wing-bones in all the breeds (except the Burmese Jumper, which has unnaturally short legs, are slightly shortened relatively to the leg-bones; but the decrease is so slight that it may be due to the standard specimen of G. bankiva having accidentally had wings of slightly greater length than usual; so that the measurements are not worth giving. But it deserves notice that the Silk and Frizzled fowls, which are quite incapable of flight, had their wings less reduced relatively to their legs than in almost any other breed! We have seen with domesticated pigeons that the bones of the wings are somewhat reduced in length, whilst the primary feathers are rather increased in length, and it is just possible, though not probable, that in the Silk and Frizzled fowls any tendency to decrease in the length of the wing-bones from disuse may have been checked through the law of compensation, by the decreased growth of the wing-feathers, and consequent increased supply of nutriment. The wing-bones, however, in both these breeds, are found to be slightly reduced in length when judged by the standard of the length of the sternum or head, relatively to these same parts in G. bankiva.
The actual weight of the main bones of the leg and wing in twelve breeds is given in the two first columns in Table I. The calculated weight of the wing-bones relatively to the leg-bones, in comparison with the leg and wing-bones of G. bankiva, are given in the third column,—the weight of the wing-bones in G. bankiva being called a hundred.[[73]]
Table I.
| Names of Breeds. | Actual Weight of Femur and Tibia. | Actual Weight of Humerus and Ulna. | Weight of Wing- bones relatively to the Leg-bones in comparison with these same bones in G. bankiva. | |
| Grains. | Grains. | |||
| Gallus bankiva (wild male) | 86 | 54 | 100 | |
| 1 | Cochin (male) | 311 | 162 | 83 |
| 2 | Dorking (male) | 557 | 248 | 70 |
| 3 | Spanish (Minorca) (male) | 386 | 183 | 75 |
| 4 | Gold-Spangled Polish (male) | 306 | 145 | 75 |
| 5 | Game, black-breasted (male) | 293 | 143 | 77 |
| 6 | Malay (female) | 231 | 116 | 80 |
| 7 | Sultan (male) | 189 | 94 | 79 |
| 8 | Indian Frizzled (male) | 206 | 88 | 67 |
| 9 | Burmese Jumper (female) | 53 | 36 | 108 |
| 10 | Hamburgh (pencilled) (male) | 157 | 104 | 106 |
| 11 | Hamburgh (pencilled) (female) | 114 | 77 | 108 |
| 12 | Silk (black-boned) (female) | 88 | 57 | 103 |
In the eight first birds, belonging to distinct breeds, in this table, we see a decided reduction in the weight of the bones of the wing.
In the Indian Frizzled fowl, which cannot fly, the reduction is carried to the greatest extent, namely, to thirty-three per cent of their proper proportional weight. In the next four birds, including the Silk hen, which is incapable of flight, we see that the wings, relatively to the legs, are slightly increased in weight; but it should be observed that, if in these birds the legs had become from any cause reduced in weight, this would give the false appearance of the wings having increased in relative weight. Now a reduction of this nature has certainly occurred with the Burmese Jumper, in which the legs are abnormally short, and in the two Hamburghs and Silk fowl, the legs, though not short, are formed of remarkably thin and light bones. I make these statements, not judging by mere eyesight, but after having calculated the weights of the leg-bones relatively to those of G. bankiva, according to the only two standards of comparison which I could use, namely, the relative lengths of the head and sternum; for I do not know the weight of the body in G. bankiva, which would have been a better standard. According to these standards, the leg-bones in these four fowls are in a marked manner far lighter than in any other breed. It may therefore be concluded that in all cases in which the legs have not been through some unknown cause much reduced in weight, the wing-bones have become reduced in weight relatively to the leg-bones, in comparison with those of G. bankiva. And this reduction of weight may, I apprehend, safely be attributed to disuse.
To make Table I quite satisfactory, it ought to have been shown that in the eight first birds the leg-bones have not actually increased in weight out of due proportion with the rest of the body; this I cannot show, from not knowing, as already remarked, the weight of the wild Bankiva.[[74]] I am indeed inclined to suspect that the leg-bones in the Dorking, No. 2 in the table, are proportionally too heavy; but this bird was a very large one, weighing 7 pounds 2 ounces, though very thin. Its leg-bones were more than ten times as heavy as those of the Burmese Jumper! I tried to ascertain the length both of the leg-bones and wing-bones relatively to other parts of the body and skeleton: but the whole organisation in these birds, which have been so long domesticated, has become so variable, that no certain conclusions could be reached. For instance, the legs of the above Dorking cock were nearly three-quarters of an inch too short relatively to the length of the sternum, and more than three-quarters of an inch too long relatively to the length of the skull, in comparison with these same parts in G. bankiva.
Table II.
| Names of Breeds. | Length of Sternum. | Depth of Crest of Sternum | Depth of Crest relatively to the length of the Sternum, in comparison with G. bankiva. | |
| Inches. | Inches | |||
| Gallus bankiva (male) | 4·20 | 1·40 | 100 | |
| 1 | Cochin (male) | 5·83 | 1·55 | 78 |
| 2 | Dorking (male) | 6·95 | 1·97 | 84 |
| 3 | Spanish (male) | 6·10 | 1·83 | 90 |
| 4 | Polish (male) | 5·07 | 1·50 | 87 |
| 5 | Game (male) | 5·55 | 1·55 | 81 |
| 6 | Malay (female) | 5·10 | 1·50 | 87 |
| 7 | Sultan (male) | 4·47 | 1·36 | 90 |
| 8 | Frizzled hen (male) | 4·25 | 1·20 | 84 |
| 9 | Burmese Jumper (female) | 3·06 | 0·85 | 81 |
| 10 | Hamburgh (male) | 5·08 | 1·40 | 81 |
| 11 | Hamburgh (female) | 4·55 | 1·26 | 81 |
| 12 | Silk fowl (female) | 4·49 | 1·01 | 66 |
In Table II in the two first columns we see in inches and decimals the length of the sternum, and the extreme depth of its crest to which the pectoral muscles are attached. In the third column we have the calculated depth of the crest, relatively to the length of the sternum, in comparison with these same parts in G. bankiva.[[75]]
By looking to the third column we see that in every case the depth of the crest relatively to the length of the sternum, in comparison with G. bankiva, is diminished, generally between 10 and 20 per cent. But the degree of reduction varies much, partly in consequence of the frequently deformed state of the sternum. In the Silk fowl, which cannot fly, the crest is 34 per cent less deep than what it ought to have been. This reduction of the crest in all the breeds probably accounts for the great variability, before referred to, in the curvature of the furculum, and in the shape of its sternal extremity. Medical men believe that the abnormal form of the spine so commonly observed in women of the higher ranks results from the attached muscles not being fully exercised. So it is with our domestic fowls, for they use their pectoral muscles but little, and, out of twenty-five sternums examined by me, three alone were perfectly symmetrical, ten were moderately crooked, and twelve were deformed to an extreme degree. Mr. Romanes, however, believes that the malformation is due to fowls whilst young resting their sternums on the sticks on which they roost.
Finally, we may conclude with respect to the various breeds of the fowl, that the main bones of the wing have probably been shortened in a very slight degree; that they have certainly become lighter relatively to the leg-bones in all the breeds in which these latter bones are not unnaturally short or delicate; and that the crest of the sternum, to which the pectoral muscles are attached, has invariably become less prominent, the whole sternum being also extremely liable to deformity. These results we may attribute to the lessened use of the wings.
Correlation of Growth.—I will here sum up the few facts which I have collected on this obscure, but important, subject. In Cochin and Game fowls there is perhaps some relation between the colour of the plumage and the darkness of the egg-shell. In Sultans the additional sickle-feathers in the tail are apparently related to the general redundancy of the plumage, as shown by the feathered legs, large crest, and beard. In two tailless fowls which I examined the oil-gland was aborted. A large crest of feathers, as Mr. Tegetmeier has remarked, seems always accompanied by a great diminution or almost entire absence of the comb. A large beard is similarly accompanied by diminished or absent wattles. These latter cases apparently come under the law of compensation or balancement of growth. A large beard beneath the lower jaw and a large top-knot on the skull often go together. The comb when of any peculiar shape, as with Horned, Spanish, and Hamburgh fowls, affects in a corresponding manner the underlying skull; and we have seen how wonderfully this is the case with Crested fowls when the crest is largely developed. With the protuberance of the frontal bones the shape of the internal surface of the skull and of the brain is greatly modified. The presence of a crest influences in some unknown way the development of the ascending branches of the premaxillary bone, and of the inner processes of the nasal bones; and likewise the shape of the external orifice of the nostrils. There is a plain and curious correlation between a crest of feathers and the imperfectly ossified condition of the skull. Not only does this hold good with nearly all crested fowls, but likewise with tufted ducks, and as Dr. Gunther informs me with tufted geese in Germany.
Lastly, the feathers composing the crest in male Polish fowls resemble hackles, and differ greatly in shape from those in the crest of the female. The neck, wing-coverts, and loins in the male bird are properly covered with hackles, and it would appear that feathers of this shape have spread by correlation to the head of the male. This little fact is interesting; because, though both sexes of some wild gallinaceous birds have their heads similarly ornamented, yet there is often a difference in the size and shape of feathers forming their crests. Furthermore, there is in some cases, as in the male Gold and in the male Amherst pheasants (P. pictus and amherstiæ), a close relation in colour, as well as in structure, between the plumes on the head and on the loins. It would therefore appear that the same law has regulated the state of the feathers on the head and body, both with species living under natural conditions, and with birds which have varied under domestication.
REFERENCES
[1] I have drawn up this brief synopsis from various sources, but chiefly from information given me by Mr. Tegetmeier. This gentleman has kindly looked through this chapter; and from his well-known knowledge, the statements here given may be fully trusted. Mr. Tegetmeier has likewise assisted me in every possible way in obtaining for me information and specimens. I must not let this opportunity pass without expressing my cordial thanks to Mr. B. P. Brent, a well-known writer on poultry, for continuous assistance and the gift of many specimens.
[2] The best account of Sultans is by Miss Watts in ‘The Poultry Yard,’ 1856, p. 79. I owe to Mr. Brent’s kindness the examination of some specimens of this breed.
[3] A good description, with figures, is given of this sub-breed in the ‘Journal of Horticulture,’ June 10, 1862, p. 206.
[4] A description, with figures, is given of this breed in ‘Journal of Horticulture,’ June 3, 1862, p. 186. Some writers describe the comb as two-horned.
[5] Mr. Crawfurd ‘Descript. Dict. of the Indian Islands,’ p. 113. Bantams are mentioned in an ancient native Japanese Encyclopædia, as I am informed by Mr. Birch of the British Museum.
[6] ‘Ornamental and Domestic Poultry,’ 1848.
[7] ‘Ornamental and Domestic Poultry,’ 1848.
[8] Ferguson’s ‘Illustrated Series of Rare and Prize Poultry,’ 1854, p. vi. Preface.
[9] Rev. E. S. Dixon in his ‘Ornamental Poultry,’ p. 203, gives an account of Columella’s work.
[10] Mr. Crawfurd ‘On the Relation of the Domesticated Animals to Civilization,’ separately printed, p. 6; first read before the Brit. Assoc. at Oxford 1860.
[11] ‘Quadrupèdes du Paraguay,’ tom. ii. p. 324.
[12] ‘Proc. Zoolog. Soc.,’ 1832, p. 151.
[13] These feathers have been described by Dr. W. Marshall ‘Der Zoolog. Garten,’ April 1874, p. 124. I examined the feathers of some hybrids raised in the Zoological Gardens between the male G. sonneratii and a red game-hen, and they exhibited the true character of those of G. sonneratii, except that the horny laminæe were much smaller.
[14] See also an excellent letter on the Poultry of India, by Mr. Blyth, in ‘Gardener’s Chronicle,’ 1851, p. 619.
[15] Mr. S. J. Salter, in ‘Natural History Review,’ April 1863, p. 276.
[16] See also Mr. Layard’s paper in ‘Annals and Mag. of Nat. History,’ 2nd series, vol. xiv. p. 62.
[17] See also Mr. Crawfurd’s ‘Descriptive Dict. of the Indian Islands,’ 1856, p. 113.
[18] Described by Mr. G. R. Gray, ‘Proc. Zoolog. Soc.,’ 1849, p. 62.
[19] The passage from Marsden is given by Mr. Dixon in his ‘Poultry Book,’ p. 176. No ornithologist now ranks this bird as a distinct species.
[20] ‘Coup-d’œeil général sur l’Inde Archipélagique,’ tom. iii. (1849) p. 177; see also Mr. Blyth in ‘Indian Sporting Review,’ vol. ii. p. 5, 1856.
[21] Mr. Blyth, in ‘Annals and Mag. of Nat. Hist.,’ 2nd ser., vol. i. (1848), p. 455.
[22] Crawfurd, ‘Desc. Dict. of Indian Islands,’ 1856, p. 112.
[23] In Burmah, as I hear from Mr. Blyth, the wild and tame poultry constantly cross together, and irregular transitional forms may be seen.
[24] Ibid. p. 113.
[25] Mr. Jerdon, in the ‘Madras Journ. of Lit. and Science,’ vol. xxii. p. 2, speaking of G. bankiva, says, “unquestionably the origin of most of the varieties of our common fowls.” For Mr. Blyth see his excellent article in ‘Gardener’s Chron.,’ 1851, p. 619; and in ‘Annals and Mag. of Nat. Hist.,’ vol. xx., 1847, p. 388.
[26] ‘Gardener’s Chronicle,’ 1851, p. 619.
[27] I have consulted an eminent authority, Mr. Sclater, on this subject, and he thinks that I have not expressed myself too strongly. I am aware that one ancient author, Acosta, speaks of fowls as having inhabited S. America at the period of its discovery; and more recently, about 1795, Olivier de Serres speaks of wild fowls in the forests of Guiana; these were probably feral birds. Dr. Daniell tells me, he believes that fowls have become wild on the west coast of Equatorial Africa; they may, however, not be true fowls, but gallinaceous birds belonging to the genus Phasidus. The old voyager Barbut says that poultry are not natural to Guinea. Capt. W. Allen (‘Narrative of Niger Expedition,’ 1848, vol. ii. p. 42) describes wild fowls on Ilha dos Rollas, an island near St. Thomas’s on the west coast of Africa; the natives informed him that they had escaped from a vessel wrecked there many years ago; they were extremely wild and had “a cry quite different to that of the domestic fowl,” and their appearance was somewhat changed. Hence it is not a little doubtful, notwithstanding the statement of the natives, whether these birds really were fowls. That the fowl has become feral on several islands is certain. Mr. Fry, a very capable judge, informed Mr. Layard, in a letter, that the fowls which have run wild on Ascension “had nearly all got back to their primitive colours, red, and black cocks, and smoky-grey hens.” But unfortunately we do not know the colour of the poultry which were turned out. Fowls have become feral on the Nicobar Islands (Blyth in the ‘Indian Field,’ 1858, p. 62), and in the Ladrones (Anson’s Voyage). Those found in the Pellew Islands (Crawfurd) are believed to be feral; and lastly, it is asserted that they have become feral in New Zealand, but whether this is correct I know not.
[28] Mr. Hewitt, in ‘The Poultry Book,’ by W. B. Tegetmeier, 1866, p. 248.
[29] ‘Journal of Horticulture,’ Jan. 14th, 1862, p. 325.
[30] ‘Die Hühner- und Pfauenzucht,’ Ulm, 1827, s. 17. For Mr. Hewitt’s statement with respect to the white Silk fowl see the ‘Poultry Book,’ by W. B. Tegetmeier, 1866, p. 222. I am indebted to Mr. Orton for a letter on the same subject.
[31] Dixon ‘Ornamental and Domestic Poultry,’ p. 253, 324, 335. For game fowls, see Ferguson on ‘Prize Poultry,’ p. 260.
[32] ‘Poultry Chronicle,’ vol. ii. p. 71.
[33] ‘Die vorgeschichtlichen Alterthümer,’ II. Theil, 1872, p. 5. Dr. Pickering, in his ‘Races of Man,’ 1850, p. 374, says that the head and neck of a fowl is carried in a Tribute-procession to Thoutmousis III. (1445 B.C.); but Mr. Birch of the British Museum doubts whether the figure can be identified as the head of a fowl. Some caution is necessary with reference to the absence of figures of the fowl on the ancient Egyptian monuments, on account of the strong and widely prevalent prejudice against this bird. I am informed by the Rev. S. Erhardt that on the east coast of Africa, from 4° to 6° south of the equator, most of the pagan tribes at the present day hold the fowl in aversion. The natives of the Pellew Islands would not eat the fowl nor will the Indians in some parts of S. America. For the ancient history of the fowl see also Volz ‘Beiträge zur Culturgeschichte,’ 1852, s. 77; and Isid. Geoffroy St.-Hilaire, ‘Hist. Nat. Gén.,’ tom. iii. p. 61. Mr. Crawfurd has given an admirable history of the fowl in his paper ‘On the Relation of Domesticated Animals to Civilisation,’ read before the Brit. Assoc. at Oxford in 1860, and since printed separately. I quote from him on the Greek poet Theognis, and on the Harpy Tomb described by Sir C. Fellowes. I quote from a letter of Mr. Blyth’s with respect to the Institutes of Manu.
[34] ‘Ornamental and Domestic Poultry,’ 1847, p. 185; for passages translated from Columella, see p. 312. For Golden Hamburghs see Albin’s ‘Natural History of Birds,’ 3 vols., with plates 1731-38.
[35] ‘Ornamental and Domestic Poultry,’ p. 152.
[36] Ferguson on ‘Rare Prize Poultry,’ p. 297. This writer, I am informed, cannot generally be trusted. He gives, however, figures and much information on eggs. See pp. 34 and 235 on the eggs of the Game fowl.
[37] See ‘Poultry Book,’ by Mr. Tegetmeier, 1866, pp. 81 and 78.
[38] ‘The Cottage Gardener,’ Oct. 1855, p. 13. On the thinness of the eggs of Game-fowls see Mowbray on Poultry, 7th edit., p. 13.
[39] My information, which is very far from perfect, on chickens in the down, is derived chiefly from Mr. Dixon’s ‘Ornamental and Domestic Poultry.’ Mr. B. P. Brent has also communicated to me many facts by letter, as has Mr. Tegetmeier. I will in each case mark my authority by the name within brackets. For the chickens of white Silk-fowls see Tegetmeier’s ‘Poultry Book,’ 1866, p. 221.
[40] As I hear from Mr. Tegetmeier; see also ‘Proc. Zoolog. Soc.,’ 1856, p. 366. On the late development of the crest see ‘Poultry Chronicle,’ vol. ii. p. 132.
[41] On these points, see ‘Poultry Chronicle,’ vol. iii. p. 166; and Tegetmeier’s ‘Poultry Book,’ 1866, pp. 105 and 121.
[42] Dixon, ‘Ornamental and Domestic Poultry,’ p. 273.
[43] Ferguson on ‘Rare and Prize Poultry,’ p. 261.
[44] Mowbray on Poultry, 7th edit., 1834, p. 13.
[45] See the full description of the varieties of the Game-breed in Tegetmeier’s ‘Poultry Book,’ 1866, p. 131. For Cuckoo Dorkings, p. 97.
[46] Mr. Hewitt in Tegetmeier’s ‘Poultry Book,’ 1866, pp. 246 and 156. For hen-tailed game-cocks, see p. 131.
[47] ‘The Field,’ April 20th, 1861. The writer says he has seen half-a-dozen cocks thus sacrificed.
[48] ‘Proceedings of Zoolog. Soc.,’ March 1861, p. 102. The engraving of the hen-tailed cock just alluded to was exhibited before the Society.
[49] ‘The Field,’ April 20th, 1861.
[50] I am much indebted to Mr. Brent for an account, with sketches, of all the variations of the comb known to him, and likewise with respect to the tail as presently to be given.
[51] The ‘Poultry Book,’ by Tegetmeier, 1866, p. 234.
[52] ‘Die Hühner-und Pfauenzucht,’ 1827, s. 11.
[53] ‘Poultry Chronicle,’ vol. i. p. 595. Mr. Brent has informed me of the same fact. With respect to the position of the spurs in Dorkings see ‘Cottage Gardener,’ Sept. 18th, 1860, p. 380.
[54] Dixon, ‘Ornamental and Domestic Poultry,’ p. 320.
[55] Mr. Tegetmeier informs me that Game hens have been found so combative, that it is now generally the practice to exhibit each hen in a separate pen.
[56] ‘Naturgeschichte Deutschlands,’ Band iii. (1793), s. 339, 407.
[57] On the Ornithology of Ceylon in ‘Annals and Mag. of Nat. History,’ 2nd series, vol. xiv. (1854), p. 63.
[58] ‘Handbuch der vergleich. Anatomie,’ 1805, p. 85, note. Mr. Tegetmeier, who gives in ‘Proc. Zoolog. Soc.,’ Nov. 25th, 1856, a very interesting account of the skulls of Polish fowls, not knowing of Bechstein’s account, has disputed the accuracy of Blumenbach’s statement. For Bechstein see ‘Naturgeschichte Deutschlands,’ Band iii. (1793), s. 399, note. I may add that at the first exhibition of Poultry at the Zoological Gardens in May, 1845, I saw some fowls, called Friezland fowls, of which the hens were crested, and the cocks furnished with a comb.
[59] ‘Cottage Gardener,’ Jan. 3rd, 1860, p. 218.
[60] Mr. Williams, in a paper read before the Dublin Nat. Hist. Soc., quoted in ‘Cottage Gardener,’ 1856, p. 161.
[61] ‘De l’Espèce,’ 1859, p. 442. For the occurrence of black-boned fowls in South America, see Roulin in ‘Mém. de l’Acad. des Sciences,’ tom. vi. p. 351; and Azara, ‘Quadrupèdes du Paraguay,’ tom. ii. p. 324. A frizzled fowl sent to me from Madras had black bones.
[62] Mr. Hewitt, in Tegetmeier’s ‘Poultry Book,’ 1866, p. 231.
[63] Dr. Broca, in Brown-Séquard’s ‘Journal de Phys.,’ tom. ii. p. 361.
[64] Dixon’s ‘Ornamental Poultry,’ p. 325.
[65] ‘Poultry Chronicle,’ vol. i. p. 485. Tegetmeier’s ‘Poultry Book,’ 1866, p. 41. On Cochins grazing, ibid., p. 46.
[66] Ferguson on ‘Prize Poultry,’ p. 87.
[67] Col. Sykes in ‘Proc. Zoolog. Soc.,’ 1832, p. 151. Dr. Hooker’s ‘Himalayan Journals,’ vol. i. p. 314.
[68] See Mr. Tegetmeier’s account with woodcuts of the skull of Polish fowls in ‘Proc. Zoolog. Soc.,’ Nov. 25th, 1856. For other references, see Isid. Geoffroy Saint-Hilaire, ‘Hist. Gén. des Anomalies,’ tom. i. p. 287. M. C. Dareste suspects (‘Recherches sur les Conditions de la Vie,’ etc., Lille 1863, p. 36) that the protuberance is not formed by the frontal bones, but by the ossification of the dura mater.
[69] ‘Naturgeschichte Deutschlands,’ Band iii. (1793), s. 400.
[70] The ‘Field,’ May 11th, 1861. I have received communications to a similar effect from Messrs. Brent and Tegetmeier.
[71] It appears that I have not correctly designated the several groups of vertebræ, for a great authority, Mr. W. K. Parker (‘Transact. Zoolog. Soc.,’ vol. v. p. 198), specifies 16 cervical, 4 dorsal, 15 lumbar, and 6 caudal vertebræ in this genus. But I have used the same terms in all the following descriptions.
[72] Macgillivray, ‘British Birds,’ vol. i. p. 25.
[73] It may be well to explain how the calculation has been made for the third column. In G. bankiva the leg-bones are to the wing-bones as 86 : 54, or as (neglecting decimals) 100 : 62;—in Cochins as 311 : 162, or as 100 : 52;—in Dorkings as 557 : 248, or as 100 : 44; and so on for the other breeds. We thus get the series of 62, 52, 44 for the relative weights of the wing-bones in G. bankiva, Cochins, Dorkings, etc. And now taking 100, instead of 62, for the weight of the wing-bones in G. bankiva, we get, by another rule of three, 83 as the weight of the wing-bones in Cochins; 70 in the Dorkings; and so on for the remainder of the third column in the table.
[74] Mr. Blyth (in ‘Annals and Mag. of Nat. Hist.,’ 2nd series, vol. i., 1848, p. 456) gives 3¼ pounds as the weight of a full-grown male G. bankiva; but from what I have seen of the skins and skeletons of various breeds, I cannot believe that my two specimens of G. bankiva could have weighed so much.
[75] The third column is calculated on the same principle as explained in footnote 73 above.
CHAPTER VIII.
DUCK—GOOSE—PEACOCK—TURKEY—GUINEA-FOWL—CANARY-BIRD—GOLD-FISH—RIVER-BEES—SILK-MOTHS.
DUCKS, SEVERAL BREEDS OF—PROGRESS OF DOMESTICATION—ORIGIN OF FROM THE COMMON WILD-DUCK—DIFFERENCES IN THE DIFFERENT BREEDS—OSTEOLOGICAL DIFFERENCES—EFFECTS OF USE AND DISUSE ON THE LIMB-BONES.
GOOSE, ANCIENTLY DOMESTICATED—LITTLE VARIATION OF—SEBASTOPOL BREED.
PEACOCK, ORIGIN OF BLACK-SHOULDERED BREED.
TURKEY,BREEDS OF—CROSSED WITH THE UNITED STATES SPECIES—EFFECTS OF CLIMATE ON.
GUINEA-FOWL, CANARY-BIRD, GOLD-FISH, HIVE-BEES.
SILK-MOTHS, SPECIES AND BREEDS OF—ANCIENTLY DOMESTICATED—CARE IN THEIR SELECTION—DIFFERENCES IN THE DIFFERENT RACES—IN THE EGG, CATERPILLAR, AND COCOON STATES—INHERITANCE OF CHARACTERS—IMPERFECT WINGS—LOST INSTINCTS—CORRELATED CHARACTERS.
I will, as in previous cases, first briefly describe the chief domestic breeds of the duck:—
BREED 1. Common Domestic Duck.—Varies much in colour and in proportions, and differs in instincts and disposition from the wild duck. There are several sub-breeds:—(1) The Aylesbury, of great size, white, with pale-yellow beak and legs; abdominal dermal sack largely developed. (2) The Rouen, of great size, coloured like the wild duck, with green or mottled beak; dermal sack largely developed. (3) Tufted Duck, with a large top-knot of fine downy feathers, supported on a fleshy mass, with the skull perforated beneath. The top-knot in a duck which I imported from Holland was two and a half inches in diameter. (4) Labrador (or Canadian, or Buenos Ayres, or East Indian); plumage entirely black; beak broader, relatively to its length, than in the wild duck; eggs slightly tinted with black. This sub-breed perhaps ought to be ranked as a breed; it includes two sub-varieties, one as large as the common domestic duck, which I have kept alive, and the other smaller and often capable of flight.[[1]] I presume it is this latter sub-variety which has been described in France[[2]] as flying well, being rather wild, and when cooked having the flavour of the wild duck; nevertheless this sub-variety is polygamous, like other domesticated ducks and unlike the wild duck. These black Labrador ducks breed true; but a case is given by Dr. Turral of the French sub-variety producing young with some white feathers on the head and neck, and with an ochre-coloured patch on the breast.
BREED 2. Hook-billed Duck.—This bird presents an extraordinary appearance from the downward curvature of the beak. The head is often tufted. The common colour is white, but some are coloured like wild ducks. It is an ancient breed, having been noticed in 1676.[[3]] It shows its prolonged domestication by almost incessantly laying eggs, like the fowls which are called everlasting layers.[[4]]
BREED 3. Call Duck.—Remarkable from its small size, and from the extraordinary loquacity of the female. Beak short. These birds are either white, or coloured like the wild duck.
BREED 4. Penguin Duck.—This is the most remarkable of all the breeds, and seems to have originated in the Malayan archipelago. It walks with its body extremely erect, and with its thin neck stretched straight upwards. Beak rather short. Tail upturned, including only 18 feathers. Femur and metatarsus elongated.
Almost all naturalists admit that the several breeds are descended from the common wild duck (Anas boschas); most fanciers, on the other hand, take as usual a very different view.[[5]] Unless we deny that domestication, prolonged during centuries, can affect even such unimportant characters as colour, size, and in a slight degree proportional dimensions and mental disposition, there is no reason whatever to doubt that the domestic duck is descended from the common wild species, for the one differs from the other in no important character. We have some historical evidence with respect to the period and progress of the domestication of the duck. It was unknown[[6]] to the ancient Egyptians, to the Jews of the Old Testament, and to the Greeks of the Homeric period. About eighteen centuries ago Columella[[7]] and Varro speak of the necessity of keeping ducks in netted enclosures like other wild fowl, so that at this period there was danger of their flying away. Moreover, the plan recommended by Columella to those who wish to increase their stock of ducks, namely, to collect the eggs of the wild bird and to place them under a hen, shows, as Mr. Dixon remarks, “that the duck had not at this time become a naturalised and prolific inmate of the Roman poultry-yard.” The origin of the domestic duck from the wild species is recognised in nearly every language of Europe, as Aldrovandi long ago remarked, by the same name being applied to both. The wild duck has a wide range from the Himalayas to North America. It crosses readily with the domestic bird, and the crossed offspring are perfectly fertile.
Both in North America and Europe the wild duck has been found easy to tame and breed. In Sweden this experiment was carefully tried by Tiburtius; he succeeded in rearing wild ducks for three generations, but, though they were treated like common ducks, they did not vary even in a single feather. The young birds suffered from being allowed to swim about in cold water,[[8]] as is known to be the case, though the fact is a strange one, with the young of the common domestic duck. An accurate and well-known observer in England[[9]] has described in detail his often repeated and successful experiments in domesticating the wild duck. Young birds are easily reared from eggs hatched under a bantam; but to succeed it is indispensable not to place the eggs of both the wild and tame duck under the same hen, for in this case “the young wild ducks die off, leaving their more hardy brethren in undisturbed possession of their foster-mother’s care. The difference of habit at the onset in the newly-hatched ducklings almost entails such a result to a certainty.” The wild ducklings were from the first quite tame towards those who took care of them as long as they wore the same clothes, and likewise to the dogs and cats of the house. They would even snap with their beaks at the dogs, and drive them away from any spot which they coveted. But they were much alarmed at strange men and dogs. Differently from what occurred in Sweden, Mr. Hewitt found that his young birds always changed and deteriorated in character in the course of two or three generations; notwithstanding that great care was taken to prevent their crossing with tame ducks. After the third generation his birds lost the elegant carriage of the wild species, and began to acquire the gait of the common duck. They increased in size in each generation, and their legs became less fine. The white collar round the neck of the mallard became broader and less regular, and some of the longer primary wing-feathers became more or less white. When this occurred, Mr. Hewitt destroyed nearly the whole of his stock and procured fresh eggs from wild nests; so that he never bred the same family for more than five or six generations. His birds continued to pair together, and never became polygamous like the common domestic duck. I have given these details, because no other case, as far as I know, has been so carefully recorded by a competent observer of the progress of change in wild birds reared for several generations in a domestic condition.
From these considerations there can hardly be a doubt that the wild duck is the parent of the common domestic kind; nor need we look to other species for the parentage of the more distinct breeds, namely, Penguin, Call, Hook-billed, Tufted, and Labrador ducks. I will not repeat the arguments used in the previous chapters on the improbability of man having in ancient times domesticated several species since become unknown or extinct, though ducks are not readily exterminated in the wild state;—on some of the supposed parent-species having had abnormal characters in comparison with all the other species of the genus, as with Hook-billed and Penguin ducks;—on all the breeds, as far as is known being fertile together;[[10]]—on all the breeds having the same general disposition, instinct, etc. But one fact bearing on this question may be noticed: in the great duck family, one species alone, namely, the male of A. boschas, has its four middle tail-feathers curled upwardly; now in every one of the above-named domestic breeds these curled feathers exist, and on the supposition that they are descended from distinct species, we must assume that man formerly hit upon species all of which had this now unique character. Moreover, sub-varieties of each breed are coloured almost exactly like the wild duck, as I have seen with the largest and smallest breeds, namely Rouens and Call ducks, and, as Mr. Brent states,[[11]] is the case with Hook-billed ducks. This gentleman, as he informs me, crossed a white Aylesbury drake and a black Labrador duck, and some of the ducklings as they grew up assumed the plumage of the wild duck.
With respect to Penguins, I have not seen many specimens, and none were coloured precisely like the wild duck; but Sir James Brooke sent me three skins from Lombok and Bali, in the Malayan archipelago; the two females were paler and more rufous than the wild duck, and the drake differed in having the whole under and upper surface (excepting the neck, tail-coverts, tail, and wings) silver-grey, finely pencilled with dark lines, closely like certain parts of the plumage of the wild mallard. But I found this drake to be identical in every feather with a variety of the common breed procured from a farm-yard in Kent, and I have occasionally elsewhere seen similar specimens. The occurrence of a duck bred under so peculiar a climate as that of the Malayan archipelago, where the wild species does not exist, with exactly the same plumage as may occasionally be seen in our farm-yards, is a fact worth notice. Nevertheless the climate of the Malayan archipelago apparently tends to cause the duck to vary much, for Zollinger,[[12]] speaking of the Penguin breed, says that in Lombok “there is an unusual and very wonderful variety of ducks.” One Penguin drake which I kept alive differed from those of which the skins were sent me from Lombok, in having its breast and back partially coloured with chestnut-brown, thus more closely resembling the Mallard.
From these several facts, more especially from the drakes of all the breeds having curled tail-feathers, and from certain sub-varieties in each breed occasionally resembling in general plumage the wild duck, we may conclude with confidence that all the breeds are descended from A. boschas.
I will now notice some of the peculiarities characteristic of the several breeds. The eggs vary in colour; some common ducks laying pale-greenish and others quite white eggs. The eggs which are first laid during each season by the black Labrador duck, are tinted black, as if rubbed with ink. A good observer assured me that one year his ducks of this breed laid almost perfectly white eggs. Another curious case shows what singular variations sometimes occur and are inherited; Mr. Hansell[[13]] relates that he had a common duck which always laid eggs with the yolk of a dark-brown colour like melted glue; and the young ducks, hatched from these eggs, laid the same kind of eggs, so that the breed had to be destroyed.
Fig 39—Skulls of Ducks, viewed laterally.
A. Wild Duck. B. Hook-billed Duck.
The Hook-billed duck is highly remarkable (see fig. 39, of skull); and its peculiar beak has been inherited at least since the year 1676. This structure is evidently analogous with that described in the Bagadotten carrier pigeon. Mr. Brent[[14]] says that, when Hook-billed ducks are crossed with common ducks, “many young ones are produced with the upper mandible shorter than the lower, which not unfrequently causes the death of the bird.” With ducks a tuft of feathers on the head is by no means a rare occurrence; namely, in the True-tufted breed, the Hook-billed, the common farm-yard kind, and in a duck having no other peculiarity which was sent to me from the Malayan archipelago. The tuft is only so far interesting as it affects the skull, which is thus rendered slightly more globular, and is perforated by numerous apertures. Call ducks are remarkable from their extraordinary loquacity: the drake only hisses like common drakes; nevertheless, when paired with the common duck, he transmits to his female offspring a strong quacking tendency. This loquacity seems at first a surprising character to have been acquired under domestication. But the voice varies in the different breeds; Mr. Brent[[15]] says that Hook-billed ducks are very loquacious, and that Rouens utter a “dull, loud, and monotonous cry, easily distinguishable by an experienced ear.” As the loquacity of the Call duck is highly serviceable, these birds being used in decoys, this quality may have been increased by selection. For instance, Colonel Hawker says, if young wild ducks cannot be got for a decoy, “by way of make-shift, select tame birds which are the most clamorous, even if their colour should not be like that of wild ones.”[[16]] It has been erroneously asserted that Call ducks hatch their eggs in less time than common ducks.[[17]]
The Penguin duck is the most remarkable of all the breeds; the thin neck and body are carried erect; the wings are small; the tail is upturned; and the thigh-bones and metatarsi are considerably lengthened in proportion with the same bones in the wild duck. In five specimens examined by me there were only eighteen tail-feathers instead of twenty as in the wild duck; but I have also found only eighteen and nineteen tail-feathers in two Labrador ducks. On the middle toe, in three specimens, there were twenty-seven or twenty-eight scutellæ, whereas in two wild ducks there were thirty-one and thirty-two. The Penguin when crossed transmits with much power its peculiar form of body and gait to its offspring; this was manifest with some hybrids raised in the Zoological Gardens between one of these birds and the Egyptian goose,[[18]] (Anser ægyptiacus) and likewise with some mongrels which I raised between the Penguin and Labrador duck. I am not much surprised that some writers should maintain that this breed must be descended from an unknown and distinct species; but from the reasons already assigned, it seems to me far more probable that it is the descendant, much modified by domestication under an unnatural climate, of Anas boschas.
Osteological Characters.—The skulls of the several breeds differ from each other and from the skull of the wild duck in very little except in the proportional length and curvature of the premaxillaries. These latter bones in the Call duck are short, and a line drawn from their extremities to the summit of the skull is nearly straight, instead of being concave as in the common duck; so that the skull resembles that of a small goose. In the Hook-billed duck (fig. 39), these same bones as well as the lower jaw curve downwards in a most remarkable manner, as represented. In the Labrador duck the premaxillaries are rather broader than in the wild duck; and in two skulls of this breed the vertical ridges on each side of the supra-occipital bone are very prominent. In the Penguin the premaxillaries are relatively shorter than in the wild duck; and the inferior points of the paramastoids more prominent. In a Dutch tufted duck, the skull under the enormous tuft was slightly more globular and was perforated by two large apertures; in this skull the lachrymal bones were produced much further backwards, so as to have a different shape and nearly to touch the post. lat. processes of the frontal bones, thus almost completing the bony orbit of the eye. As the quadrate and pterygoid bones are of such complex shape and stand in relation with so many other bones, I carefully compared them in all the principal breeds; but excepting in size they presented no difference.
Fig 40—Cervical Verterbræ of Ducks.
Vertebræ and Ribs.—In one skeleton of the Labrador duck there were the usual fifteen cervical vertebræ and the usual nine dorsal vertebræ bearing ribs; in the other skeleton there were fifteen cervical and ten dorsal vertebræ with ribs; nor, as far as could be judged, was this owing merely to a rib having been developed on the first lumbar vertebra; for in both skeletons the lumbar vertebræ agreed perfectly in number, shape, and size with those of the wild duck. In two skeletons of the Call duck there were fifteen cervical and nine dorsal vertebræ; in a third skeleton small ribs were attached to the so-called fifteenth cervical vertebra, making ten pairs of ribs; but these ten ribs do not correspond, or arise from the same vertebra, with the ten in the above-mentioned Labrador duck. In the Call duck, which had small ribs attached to the fifteenth cervical vertebra, the hæmal spines of the thirteenth and fourteenth (cervical) and of the seventeenth (dorsal) vertebræ corresponded with the spines on the fourteenth, fifteenth, and eighteenth vertebræ of the wild duck: so that each of these vertebræ had acquired a structure proper to one posterior to it in position. In the eighth cervical vertebra of this same Call duck (fig. 40, B), the two branches of the hæmal spine stand much closer together than in the wild duck (A), and the descending hæmal processes are much shortened. In the Penguin duck the neck from its thinness and erectness falsely appears (as ascertained by measurement) to be much elongated, but the cervical and dorsal vertebræ present no difference; the posterior dorsal vertebræ, however, are more completely anchylosed to the pelvis than in the wild duck. The Aylesbury duck has fifteen cervical and ten dorsal vertebræ furnished with ribs, but the same number of lumbar, sacral, and caudal vertebræ, as far as could be traced, as in the wild duck. The cervical vertebræ in this same duck (fig. 40, D) were much broader and thicker relatively to their length than in the wild (C); so much so, that I have thought it worth while to give a sketch of the twelfth cervical vertebra in these two birds. From the foregoing statements we see that the fifteenth cervical vertebra occasionally becomes modified into a dorsal vertebra, and when this occurs all the adjoining vertebræ are modified. We also see that an additional dorsal vertebra bearing a rib is occasionally developed, the number of the cervical and lumbar vertebræ apparently remaining the same as usual.
I examined the bony enlargement of the trachea in the males of the Penguin, Call, Hook-billed, Labrador, and Aylesbury breeds; and in all it was identical in shape.
The pelvis is remarkably uniform; but in the skeleton of the Hook-billed duck the anterior part is much bowed inwards; in the Aylesbury and some other breeds the ischiadic foramen is less elongated. In the sternum, furculum, coracoids, and scapulæ, the differences are so slight and so variable as not to be worth notice, except that in two skeletons of the Penguin duck the terminal portion of the scapula was much attenuated.
In the bones of the leg and wing no modification in shape could be observed. But in the Penguin and Hook-billed ducks, the terminal phalanges of the wing are a little shortened. In the former, the femur, and metatarsus (but not the tibia) are considerably lengthened, relatively to the same bones in the wild duck, and to the wing-bones in both birds. This elongation of the leg-bones could be seen whilst the bird was alive, and is no doubt connected with its peculiar upright manner of walking. In a large Aylesbury duck, on the other hand, the tibia was the only bone of the leg which relatively to the other bones was slightly lengthened.
On the effects of the increased and decreased Use of the Limbs.—In all the breeds the bones of the wing (measured separately after having been cleaned) relatively to those of the leg have become slightly shortened, in comparison with the same bones in the wild duck, as may be seen in Table I.
Table I
| Name of Breed | Length of Femur, Tibia, and Meta- tarsus together | Length of Humerus, Radius, and Meta- carpus together | Or as |
| Inches | Inches | ||
| Wild mallard | 7·14 | 9·28 | 100 : 129 |
| Aylesbury | 8·64 | 10·43 | 100 : 120 |
| Tufted (Dutch) | 8·25 | 9·83 | 100 : 119 |
| Penguin | 7·12 | 8·78 | 100 : 123 |
| Call | 6·20 | 7·77 | 100 : 125 |
| Length of same Bones | Length of all the Bones of Wing | ||
| Inches | Inches | ||
| Wild duck (another specimen) | 6·85 | 10·07 | 100 : 147 |
| Common domestic duck | 8·15 | 11·26 | 100 : 138 |
In Table I we see, by comparison with the wild duck, that the reduction in the length of the bones of the wing, relatively to those of the legs, though slight, is universal. The reduction is least in the Call duck, which has the power and the habit of frequently flying.
In weight there is a greater relative difference between the bones of the leg and wing, as may be seen in Table II:—
Table II
| Name of Breed | Weight of Femur, Tibia, and Metatarsus | Weight of Humerus, Radius, and Metacarpus | Or as |
| Grains | Grains | ||
| Wild mallard | 54 | 97 | 100 : 179 |
| Aylesbury | 164 | 204 | 100 : 124 |
| Hooked-bill | 107 | 160 | 100 : 149 |
| Tufted (Dutch) | 111 | 148 | 100 : 133 |
| Penguin | 75 | 90.5 | 100 : 120 |
| Labrador | 141 | 165 | 100 : 117 |
| Call | 57 | 93 | 100 : 163 |
| Weight of all the Bones of the Leg and Foot | Weight of all the Bones of the Wing | ||
| Grains | Grains | ||
| Wild (another specimen) | 66 | 115 | 100 : 173 |
| Common domestic duck | 127 | 158 | 100 : 124 |
In these domesticated birds, the considerably lessened weight of the bones of the wing (i.e. on an average, twenty-five per cent of their proper proportional weight), as well as their slightly lessened length, relatively to the leg-bones, might follow, not from any actual decrease in the wing-bones, but from the increased weight and length of the bones of the legs. Table IIIa shows that the leg-bones relatively to the weight of the entire skeleton have really increased in weight; but Table IIIb shows that according to the same standard the wing-bones have also really decreased in weight; so that the relative disproportion shown in the foregoing tables between the wing and leg-bones, in comparison with those of the wild duck, is partly due to the increase in weight and length of the leg-bones, and partly to the decrease in weight and length of the wing-bones.
Table III
| Name of Breed | Weight of entire Skeleton. (N.B. One Metatarsus and Foot was removed from each skeleton, as it had been accidentally lost in two cases.) | Weight of Femur, Tibia, and Metatarsus | Or as |
| Grains | Grains | ||
| Wild mallard | 839 | 54 | 1000 : 64 |
| Aylesbury | 1925 | 164 | 1000 : 85 |
| Tufted (Dutch) | 1404 | 111 | 1000 : 79 |
| Penguin | 871 | 75 | 1000 : 86 |
| Call (from Mr. Fox) | 717 | 57 | 1000 : 79 |
| Weight of Skeleton as above. | Weight of Humerus, Radius and Metacarpus. | ||
| Grains | Grains | ||
| Wild mallard | 839 | 97 | 1000 : 115 |
| Aylesbury | 1925 | 204 | 1000 : 105 |
| Tufted (Dutch) | 1404 | 148 | 1000 : 105 |
| Penguin | 871 | 90 | 1000 : 103 |
| Call (from Mr. Baker) | 914 | 100 | 1000 : 109 |
| Call (from Mr. Fox) | 717 | 92 | 1000 : 129 |
With respect to Table III, I may first state that I tested them by taking another skeleton of a wild duck and of a common domestic duck, and by comparing the weight of all the bones of the leg with all those of the wings, and the result was the same. In the first of these tables we see that the leg-bones in each case have increased in actual weight. It might have been expected that, with the increased or decreased weight of the entire skeleton, the leg-bones would have become proportionally heavier or lighter; but their greater weight in all the breeds relatively to the other bones can be accounted for only by these domestic birds having used their legs in walking and standing much more than the wild, for they never fly, and the more artificial breeds rarely swim. In the second table we see, with the exception of one case, a plain reduction in the weight of the bones of the wing, and this no doubt has resulted from their lessened use. The one exceptional case, namely, in one of the Call ducks, is in truth no exception, for this bird was constantly in the habit of flying about; and I have seen it day after day rise from my grounds, and fly for a long time in circles of more than a mile in diameter. In this Call duck there is not only no decrease, but an actual increase in the weight of the wing-bones relatively to those of the wild-duck; and this probably is consequent on the remarkable lightness and thinness of all the bones of the skeleton.
Lastly, I weighed the furculum, coracoids, and scapula of a wild duck and of a common domestic duck, and I found that their weight, relatively to that of the whole skeleton, was as one hundred in the former to eighty-nine in the latter; this shows that these bones in the domestic duck have been reduced eleven per cent of their due proportional weight. The prominence of the crest of the sternum, relatively to its length, is also much reduced in all the domestic breeds. These changes have evidently been caused by the lessened use of the wings.
It is well known that several birds, belonging to different Orders, and inhabiting oceanic islands, have their wings greatly reduced in size and are incapable of flight. I suggested in my ‘Origin of Species’ that, as these birds are not persecuted by any enemies, the reduction of their wings had probably been caused by gradual disuse. Hence, during the earlier stages of the process of reduction, such birds would probably have resembled our domesticated ducks in the state of their organs of flight. This is the case with the water-hen (Gallinula nesiotis) of Tristan d’Acunha, which “can flutter a little, but obviously uses its legs, and not its wings, as a mode of escape.” Now Mr. Sclater[[19]] finds in this bird that the wings, sternum, and coracoids are all reduced in length, and the crest of the sternum in depth, in comparison with the same bones in the European water-hen (G. chloropus). On the other hand, the thigh-bones and pelvis are increased in length, the former by four lines, relatively to the same bones in the common water-hen. Hence in the skeleton of this natural species nearly the same changes have occurred, only carried a little further, as with our domestic ducks, and in this latter case I presume no one will dispute that they have resulted from the lessened use of the wings and the increased use of the legs.