distinguish the male from the female by the tints of the former being a little more intense. Nor does he know of any striking difference in external structure between the sexes, excepting the prominences which become developed during the breeding-season on the front legs of the male, by which he is enabled to hold the female. (47. The male alone of the Bufo sikimmensis (Dr. Anderson, ‘Proc. Zoolog. Soc.’ 1871, p. 204) has two plate-like callosities on the thorax and certain rugosities on the fingers, which perhaps subserve the same end as the above-mentioned prominences.) It is surprising that these animals have not acquired more strongly-marked sexual characters; for though cold-blooded their passions are strong. Dr. Gunther informs me that he has several times found an unfortunate female toad dead and smothered from having been so closely embraced by three or four males. Frogs have been observed by Professor Hoffman in Giessen fighting all day long during the breeding-season, and with so much violence that one had its body ripped open.
Frogs and toads offer one interesting sexual difference, namely, in the musical powers possessed by the males; but to speak of music, when applied to the discordant and overwhelming sounds emitted by male bull-frogs and some other species, seems, according to our taste, a singularly inappropriate expression. Nevertheless, certain frogs sing in a decidedly pleasing manner. Near Rio Janeiro I used often to sit in the evening to listen to a number of little Hylae, perched on blades of grass close to the water, which sent forth sweet chirping notes in harmony. The various sounds are emitted chiefly by the males during the breeding-season, as in the case of the croaking of our common frog.
this fact the vocal organs of the males are more highly-developed than those of the females. In some genera the males alone are provided with sacs which open into the larynx. (49. J. Bishop, in ‘Todd’s Cyclopaedia of Anatomy and Physiology,’ vol. iv. p. 1503.) For instance, in the edible frog (Rana esculenta) “the sacs are peculiar to the males, and become, when filled with air in the act of croaking, large globular bladders, standing out one on each side of the head, near the corners of the mouth.” The croak of the male is thus rendered exceedingly powerful; whilst that of the female is only a slight groaning noise.
(50. Bell, ibid. pp. 112-114.) In the several genera of the family the vocal organs differ considerably in structure, and their development in all cases may be attributed to sexual selection.
REPTILES.
CHELONIA.
Tortoises and turtles do not offer well-marked sexual differences. In some species, the tail of the male is longer than that of the female.
In some, the plastron or lower surface of the shell of the male is slightly concave in relation to the back of the female. The male of the mud-turtle of the United States (Chrysemys picta) has claws on its front feet twice as long as those of the female; and these are used when the sexes unite. (51. Mr. C.J. Maynard, ‘The American Naturalist,’ Dec. 1869, p. 555.) With the huge tortoise of the Galapagos Islands (Testudo nigra) the males are said to grow to a larger size than the females: during the pairing-season, and at no other time, the male utters a hoarse bellowing noise, which can be heard at the distance of more than a hundred yards; the female, on the other hand, never uses her voice. (52. See my ‘Journal of Researches during the Voyage of the With the Testudo elegans of India, it is said “that the combats of the males may be heard at some distance, from the noise they produce in butting against each other.” (53. Dr. Gunther, ‘Reptiles of British CROCODILIA.
The sexes apparently do not differ in colour; nor do I know that the males fight together, though this is probable, for some kinds make a prodigious display before the females. Bartram (54. ‘Travels through Carolina,’ etc., 1791, p. 128.) describes the male alligator as striving to win the female by splashing and roaring in the midst of a lagoon, “swollen to an extent ready to burst, with its head and tail lifted up, he springs or twirls round on the surface of the water, like an Indian chief rehearsing his feats of war.” During the season of love, a musky odour is emitted by the submaxillary glands of the crocodile, and pervades their haunts. (55. Owen, ‘Anatomy of OPHIDIA.
Dr. Gunther informs me that the males are always smaller than the females, and generally have longer and slenderer tails; but he knows of no other difference in external structure. In regard to colour, be can almost always distinguish the male from the female, by his more strongly-pronounced tints; thus the black zigzag band on the back of the male English viper is more distinctly defined than in the female.
The difference is much plainer in the rattle-snakes of N. America, the male of which, as the keeper in the Zoological Gardens shewed me, can at once be distinguished from the female by having more lurid yellow about its whole body. In S. Africa the Bucephalus capensis presents an analogous difference, for the female “is never so fully variegated with yellow on the sides as the male.” (56. Sir Andrew Smith, ‘Zoology of S.
Africa: Reptilia,’ 1849, pl. x.) The male of the Indian Dipsas cynodon, on the other hand, is blackish-brown, with the belly partly black, whilst the female is reddish or yellowish-olive, with the belly either uniform yellowish or marbled with black. In the Tragops dispar of the same country the male is bright green, and the female bronze-coloured.
(57. Dr. A. Gunther, ‘Reptiles of British India,’ Ray Soc., 1864, pp.
304, 308.) No doubt the colours of some snakes are protective, as shewn by the green tints of tree-snakes, and the various mottled shades of the species which live in sandy places; but it is doubtful whether the colours of many kinds, for instance of the common English snake and viper, serve to conceal them; and this is still more doubtful with the many foreign species which are coloured with extreme elegance. The colours of certain species are very different in the adult and young states. (58. Dr. Stoliczka, ‘Journal of Asiatic Society of Bengal,’ vol. xxxix, 1870, pp. 205, 211.)
During the breeding-season the anal scent-glands of snakes are in 615.); and so it is with the same glands in lizards, and as we have seen with the submaxillary glands of crocodiles. As the males of most animals search for the females, these odoriferous glands probably serve to excite or charm the female, rather than to guide her to the spot where the male may be found. Male snakes, though appearing so sluggish, are amorous; for many have been observed crowding round the same female, and even round her dead body. They are not known to fight together from rivalry. Their intellectual powers are higher than might have been anticipated. In the Zoological Gardens they soon learn not to strike at the iron bar with which their cages are cleaned; and Dr. Keen of Philadelphia informs me that some snakes which he kept learned after four or five times to avoid a noose, with which they were at first easily caught. An excellent observer in Ceylon, Mr. E. Layard, saw (60.
‘Rambles in Ceylon,’ in ‘Annals and Magazine of Natural History,’ 2nd series, vol. ix. 1852, p. 333.) a cobra thrust its head through a narrow hole and swallow a toad. “With this encumbrance he could not withdraw himself; finding this, he reluctantly disgorged the precious morsel, which began to move off; this was too much for snake philosophy to bear, and the toad was again seized, and again was the snake, after violent efforts to escape, compelled to part with its prey. This time, however, a lesson had been learnt, and the toad was seized by one leg, withdrawn, and then swallowed in triumph.”
The keeper in the Zoological Gardens is positive that certain snakes, for instance Crotalus and Python, distinguish him from all other persons. Cobras kept together in the same cage apparently feel some attachment towards each other. (61. Dr. Gunther, ‘Reptiles of British It does not, however, follow because snakes have some reasoning power, strong passions and mutual affection, that they should likewise be endowed with sufficient taste to admire brilliant colours in their partners, so as to lead to the adornment of the species through sexual selection. Nevertheless, it is difficult to account in any other manner for the extreme beauty of certain species; for instance, of the coral-snakes of S. America, which are of a rich red with black and yellow transverse bands. I well remember how much surprise I felt at the beauty of the first coral-snake which I saw gliding across a path in Brazil. Snakes coloured in this peculiar manner, as Mr. Wallace states on the authority of Dr. Gunther (62. ‘Westminster Review,’ July 1st, 1867, p. 32.), are found nowhere else in the world except in S.
America, and here no less than four genera occur. One of these, Elaps, is venomous; a second and widely-distinct genus is doubtfully venomous, and the two others are quite harmless. The species belonging to these distinct genera inhabit the same districts, and are so like each other that no one “but a naturalist would distinguish the harmless from the poisonous kinds.” Hence, as Mr. Wallace believes, the innocuous kinds have probably acquired their colours as a protection, on the principle of imitation; for they would naturally be thought dangerous by their enemies. The cause, however, of the bright colours of the venomous Elaps remains to be explained, and this may perhaps be sexual selection.
Snakes produce other sounds besides hissing. The deadly Echis carinata has on its sides some oblique rows of scales of a peculiar structure with serrated edges; and when this snake is excited these scales are rubbed against each other, which produces “a curious prolonged, almost With respect to the rattling of the rattle-snake, we have at last some definite information: for Professor Aughey states (64. The ‘American Naturalist,’ 1873, p. 85.), that on two occasions, being himself unseen, he watched from a little distance a rattle-snake coiled up with head erect, which continued to rattle at short intervals for half an hour: and at last he saw another snake approach, and when they met they paired. Hence he is satisfied that one of the uses of the rattle is to bring the sexes together. Unfortunately he did not ascertain whether it was the male or the female which remained stationary and called for the other. But it by no means follows from the above fact that the rattle may not be of use to these snakes in other ways, as a warning to animals which would otherwise attack them. Nor can I quite disbelieve the several accounts which have appeared of their thus paralysing their prey with fear. Some other snakes also make a distinct noise by rapidly vibrating their tails against the surrounding stalks of plants; and I have myself heard this in the case of a Trigonocephalus in S. America.
LACERTILIA.
The males of some, probably of many kinds of lizards, fight together from rivalry. Thus the arboreal Anolis cristatellus of S. America is extremely pugnacious: “During the spring and early part of the summer, two adult males rarely meet without a contest. On first seeing one another, they nod their heads up and down three or four times, and at the same time expanding the frill or pouch beneath the throat; their eyes glisten with rage, and after waving their tails from side to side for a few seconds, as if to gather energy, they dart at each other furiously, rolling over and over, and holding firmly with their teeth.
The conflict generally ends in one of the combatants losing his tail, which is often devoured by the victor.” The male of this species is considerably larger than the female (65. Mr. N.L. Austen kept these animals alive for a considerable time; see ‘Land and Water,’ July 1867, p. 9.); and this, as far as Dr. Gunther has been able to ascertain, is the general rule with lizards of all kinds. The male alone of the Cyrtodactylus rubidus of the Andaman Islands possesses pre-anal pores; and these pores, judging from analogy, probably serve to emit an odour.
(66. Stoliczka, ‘Journal of the Asiatic Society of Bengal,’ vol. xxxiv.
1870, p. 166.)
[Fig.33. Sitana minor. Male with the gular pouch expanded (from The sexes often differ greatly in various external characters. The male of the above-mentioned Anolis is furnished with a crest which runs along the back and tail, and can be erected at pleasure; but of this crest the female does not exhibit a trace. In the Indian Cophotis ceylanica, the female has a dorsal crest, though much less developed than in the male; and so it is, as Dr. Gunther informs me, with the females of many Iguanas, Chameleons, and other lizards. In some species, however, the crest is equally developed in both sexes, as in the Iguana tuberculata. In the genus Sitana, the males alone are furnished with a large throat pouch (Fig. 33), which can be folded up like a fan, and is coloured blue, black, and red; but these splendid colours are exhibited only during the pairing-season. The female does not possess even a rudiment of this appendage. In the Anolis cristatellus, according to Mr. Austen, the throat pouch, which is bright red marbled with yellow, is present in the female, though in a rudimental condition. Again, in certain other lizards, both sexes are equally well provided with throat pouches. Here we see with species belonging to the same group, as in so many previous cases, the same character either confined to the males, or more largely developed in them than in the females, or again equally developed in both sexes. The little lizards of the genus Draco, which glide through the air on their rib-supported parachutes, and which in the beauty of their colours baffle description, are furnished with skinny appendages to the throat “like the wattles of gallinaceous birds.” These become erected when the animal is excited. They occur in both sexes, but are best developed when the male arrives at maturity, at which age the middle appendage is sometimes twice as long as the head. Most of the species likewise have a low crest running along the neck; and this is much more developed in the full-grown males than in the females or young males. (67. All the foregoing statements and quotations, in regard to Cophotis, Sitana and Draco, as well as the following facts in regard to Ceratophora and Chamaeleon, are from Dr. Gunther himself, or from his magnificent work on the ‘Reptiles of British India,’ Ray Soc., 1864, pp. 122, 130, 135.)
A Chinese species is said to live in pairs during the spring; “and if one is caught, the other falls from the tree to the ground, and allows itself to be captured with impunity”—I presume from despair. (68. Mr.
[Fig. 34. Ceratophora Stoddartii. Upper figure; lower figure, female.]
There are other and much more remarkable differences between the sexes of certain lizards. The male of Ceratophora aspera bears on the extremity of his snout an appendage half as long as the head. It is cylindrical, covered with scales, flexible, and apparently capable of erection: in the female it is quite rudimental. In a second species of the same genus a terminal scale forms a minute horn on the summit of the flexible appendage; and in a third species (C. Stoddartii, fig. 34) the whole appendage is converted into a horn, which is usually of a white colour, but assumes a purplish tint when the animal is excited.
In the adult male of this latter species the horn is half an inch in length, but it is of quite minute size in the female and in the young.
These appendages, as Dr. Gunther has remarked to me, may be compared with the combs of gallinaceous birds, and apparently serve as ornaments.
[Fig. 35. Chamaeleo bifurcus. Upper figure, male; lower figure, female.
Fig. 36. Chamaeleo Owenii. Upper figure, male; lower figure, female.]
In the genus Chamaeleon we come to the acme of difference between the sexes. The upper part of the skull of the male C. bifurcus (Fig. 35), an inhabitant of Madagascar, is produced into two great, solid, bony projections, covered with scales like the rest of the head; and of this wonderful modification of structure the female exhibits only a rudiment. Again, in Chamaeleo Owenii (Fig. 36), from the West Coast of Africa, the male bears on his snout and forehead three curious horns, of which the female has not a trace. These horns consist of an excrescence of bone covered with a smooth sheath, forming part of the general integuments of the body, so that they are identical in structure with those of a bull, goat, or other sheath-horned ruminant.
Although the three horns differ so much in appearance from the two great prolongations of the skull in C. bifurcus, we can hardly doubt that they serve the same general purpose in the economy of these two animals. The first conjecture, which will occur to every one, is that they are used by the males for fighting together; and as these animals are very quarrelsome (69. Dr. Buchholz, ‘Monatsbericht K. Preuss.
Akad.’ Jan. 1874, p. 78.), this is probably a correct view. Mr. T.W.
Wood also informs me that he once watched two individuals of C. pumilus fighting violently on the branch of a tree; they flung their heads about and tried to bite each other; they then rested for a time and afterwards continued their battle.
With many lizards the sexes differ slightly in colour, the tints and stripes of the males being brighter and more distinctly defined than in the females. This, for instance, is the case with the above Cophotis and with the Acanthodactylus capensis of S. Africa. In a Cordylus of the latter country, the male is either much redder or greener than the female. In the Indian Calotes nigrilabris there is a still greater difference; the lips also of the male are black, whilst those of the female are green. In our common little viviparous lizard (Zootoca vivipara) “the under side of the body and base of the tail in the male are bright orange, spotted with black; in the female these parts are pale-greyish-green without spots.” (70. Bell, ‘History of British Reptiles,’ 2nd ed., 1849, p. 40.) We have seen that the males alone of Sitana possess a throat-pouch; and this is splendidly tinted with blue, black, and red. In the Proctotretus tenuis of Chile the male alone is marked with spots of blue, green, and coppery-red. (71. For Proctotretus, see ‘Zoology of the Voyage of the “Beagle”; Reptiles,’ by Mr. Bell, p. 8. For the Lizards of S. Africa, see ‘Zoology of S.
Africa: Reptiles,’ by Sir Andrew Smith, pl. 25 and 39. For the Indian Calotes, see ‘Reptiles of British India,’ by Dr. Gunther, p. 143.) In many cases the males retain the same colours throughout the year, but in others they become much brighter during the breeding-season; I may give as an additional instance the Calotes maria, which at this season has a bright red head, the rest of the body being green. (72. Gunther figure.)
Both sexes of many species are beautifully coloured exactly alike; and there is no reason to suppose that such colours are protective. No doubt with the bright green kinds which live in the midst of vegetation, this colour serves to conceal them; and in N. Patagonia I saw a lizard (Proctotretus multimaculatus) which, when frightened, flattened its body, closed its eyes, and then from its mottled tints was hardly distinguishable from the surrounding sand. But the bright colours with which so many lizards are ornamented, as well as their various curious appendages, were probably acquired by the males as an attraction, and then transmitted either to their male offspring alone, or to both sexes. Sexual selection, indeed, seems to have played almost as important a part with reptiles as with birds; and the less conspicuous colours of the females in comparison with the males cannot be accounted for, as Mr. Wallace believes to be the case with birds, by the greater exposure of the females to danger during incubation.
CHAPTER XIII.
SECONDARY SEXUAL CHARACTERS OF BIRDS.
and seasonal—Double and single annual moults—Display of ornaments by the males.
Secondary sexual characters are more diversified and conspicuous in birds, though not perhaps entailing more important changes of structure, than in any other class of animals. I shall, therefore, treat the subject at considerable length. Male birds sometimes, though rarely, possess special weapons for fighting with each other. They charm the female by vocal or instrumental music of the most varied kinds. They are ornamented by all sorts of combs, wattles, protuberances, horns, air-distended sacks, top-knots, naked shafts, plumes and lengthened feathers gracefully springing from all parts of the body. The beak and naked skin about the head, and the feathers, are often gorgeously coloured. The males sometimes pay their court by dancing, or by fantastic antics performed either on the ground or in the air. In one instance, at least, the male emits a musky odour, which we may suppose serves to charm or excite the female; for that excellent observer, Mr. Ramsay (1. ‘Ibis,’ vol. iii. (new series), 1867, p.
414.), says of the Australian musk-duck (Biziura lobata) that “the smell which the male emits during the summer months is confined to that sex, and in some individuals is retained throughout the year; I have never, even in the breeding-season, shot a female which had any smell of musk.” So powerful is this odour during the pairing-season, that it can be detected long before the bird can be seen. (2. Gould, ‘Handbook of the Birds of Australia,’ 1865, vol. ii. p. 383.) On the whole, birds appear to be the most aesthetic of all animals, excepting of course man, and they have nearly the same taste for the beautiful as we have.
This is shewn by our enjoyment of the singing of birds, and by our women, both civilised and savage, decking their heads with borrowed plumes, and using gems which are hardly more brilliantly coloured than the naked skin and wattles of certain birds. In man, however, when cultivated, the sense of beauty is manifestly a far more complex feeling, and is associated with various intellectual ideas.
Before treating of the sexual characters with which we are here more particularly concerned, I may just allude to certain differences between the sexes which apparently depend on differences in their habits of life; for such cases, though common in the lower, are rare in the higher classes. Two humming-birds belonging to the genus Eustephanus, which inhabit the island of Juan Fernandez, were long thought to be specifically distinct, but are now known, as Mr. Gould informs me, to be the male and female of the same species, and they differ slightly in the form of the beak. In another genus of humming-birds (Grypus), the beak of the male is serrated along the margin and hooked at the extremity, thus differing much from that of the female. In the Neomorpha of New Zealand, there is, as we have seen, a still wider difference in the form of the beak in relation to the manner of feeding of the two sexes. Something of the same kind has been observed with the goldfinch (Carduelis elegans), for I am assured by Mr. J. Jenner Weir that the bird-catchers can distinguish the males by their slightly longer beaks. The flocks of males are often found feeding on the seeds of the teazle (Dipsacus), which they can reach with their elongated beaks, whilst the females more commonly feed on the seeds of the betony or Scrophularia. With a slight difference of this kind as a foundation, we can see how the beaks of the two sexes might be made to differ greatly through natural selection. In some of the above cases, however, it is possible that the beaks of the males may have been first modified in relation to their contests with other males; and that this afterwards led to slightly changed habits of life.
LAW OF BATTLE.
Almost all male birds are extremely pugnacious, using their beaks, wings, and legs for fighting together. We see this every spring with our robins and sparrows. The smallest of all birds, namely the humming-bird, is one of the most quarrelsome. Mr. Gosse (3. Quoted by Mr. Gould, ‘Introduction to the Trochilidae,’ 1861, page 29.) describes a battle in which a pair seized hold of each other’s beaks, and whirled round and round, till they almost fell to the ground; and M. Montes de Oca, in speaking or another genus of humming-bird, says that two males rarely meet without a fierce aerial encounter: when kept in cages “their fighting has mostly ended in the splitting of the tongue of one of the two, which then surely dies from being unable to feed.” (4.
Gould, ibid. p. 52.) With waders, the males of the common water-hen (Gallinula chloropus) “when pairing, fight violently for the females: they stand nearly upright in the water and strike with their feet.” Two were seen to be thus engaged for half an hour, until one got hold of the head of the other, which would have been killed had not the observer interfered; the female all the time looking on as a quiet spectator. (5. W. Thompson, ‘Natural History of Ireland: Birds,’ vol.
ii. 1850, p. 327.) Mr. Blyth informs me that the males of an allied bird (Gallicrex cristatus) are a third larger than the females, and are so pugnacious during the breeding-season that they are kept by the natives of Eastern Bengal for the sake of fighting. Various other birds are kept in India for the same purpose, for instance, the bulbuls (Pycnonotus hoemorrhous) which “fight with great spirit.” (6. Jerdon, [Fig. 37. The Ruff or Machetes pugnax (from Brehm’s ‘Thierleben’).]
The polygamous ruff (Machetes pugnax, Fig. 37) is notorious for his extreme pugnacity; and in the spring, the males, which are considerably larger than the females, congregate day after day at a particular spot, where the females propose to lay their eggs. The fowlers discover these spots by the turf being trampled somewhat bare. Here they fight very much like game-cocks, seizing each other with their beaks and striking with their wings. The great ruff of feathers round the neck is then erected, and according to Col. Montagu “sweeps the ground as a shield to defend the more tender parts”; and this is the only instance known to me in the case of birds of any structure serving as a shield. The ruff of feathers, however, from its varied and rich colours probably serves in chief part as an ornament. Like most pugnacious birds, they seem always ready to fight, and when closely confined, often kill each other; but Montagu observed that their pugnacity becomes greater during the spring, when the long feathers on their necks are fully developed; and at this period the least movement by any one bird provokes a general battle. (7. Macgillivray, ‘History of British Birds,’ vol. iv.
1852, pp. 177-181.) Of the pugnacity of web-footed birds, two instances will suffice: in Guiana “bloody fights occur during the breeding-season between the males of the wild musk-duck (Cairina moschata); and where these fights have occurred the river is covered for some distance with feathers.” (8. Sir R. Schomburgk, in ‘Journal of Royal Geographic Society,’ vol. xiii. 1843, p. 31.) Birds which seem ill-adapted for fighting engage in fierce conflicts; thus the stronger males of the pelican drive away the weaker ones, snapping with their huge beaks and giving heavy blows with their wings. Male snipe fight together, “tugging and pushing each other with their bills in the most curious manner imaginable.” Some few birds are believed never to fight; this is the case, according to Audubon, with one of the woodpeckers of the United States (Picu sauratus), although “the hens are followed by even half a dozen of their gay suitors.” (9. ‘Ornithological Biography,’ vol. i. p. 191. For pelicans and snipes, see vol. iii. pp. 138, 477.)
The males of many birds are larger than the females, and this no doubt is the result of the advantage gained by the larger and stronger males over their rivals during many generations. The difference in size between the two sexes is carried to an extreme point in several Australian species; thus the male musk-duck (Biziura), and the male Cincloramphus cruralis (allied to our pipits) are by measurement actually twice as large as their respective females. (10. Gould, With many other birds the females are larger than the males; and, as formerly remarked, the explanation often given, namely, that the females have most of the work in feeding their young, will not suffice.
In some few cases, as we shall hereafter see, the females apparently have acquired their greater size and strength for the sake of conquering other females and obtaining possession of the males.
The males of many gallinaceous birds, especially of the polygamous kinds, are furnished with special weapons for fighting with their rivals, namely spurs, which can be used with fearful effect. It has been recorded by a trustworthy writer (11. Mr. Hewitt, in the ‘Poultry Book’ by Tegetmeier, 1866, p. 137.) that in Derbyshire a kite struck at a game-hen accompanied by her chickens, when the cock rushed to the rescue, and drove his spur right through the eye and skull of the aggressor. The spur was with difficulty drawn from the skull, and as the kite, though dead, retained his grasp, the two birds were firmly locked together; but the cock when disentangled was very little injured. The invincible courage of the game-cock is notorious: a gentleman who long ago witnessed the brutal scene, told me that a bird had both its legs broken by some accident in the cockpit, and the owner laid a wager that if the legs could be spliced so that the bird could stand upright, he would continue fighting. This was effected on the spot, and the bird fought with undaunted courage until he received his death-stroke. In Ceylon a closely allied, wild species, the Gallus Stanleyi, is known to fight desperately “in defence of his seraglio,” so that one of the combatants is frequently found dead. (12. Layard, ‘Annals and Magazine of Natural History,’ vol. xiv. 1854, p. 63.) An Indian partridge (Ortygornis gularis), the male of which is furnished with strong and sharp spurs, is so quarrelsome “that the scars of former fights disfigure the breast of almost every bird you kill.” (13.
Jerdon, ‘Birds of India,’ vol. iii. p. 574.)
The males of almost all gallinaceous birds, even those which are not furnished with spurs, engage during the breeding-season in fierce conflicts. The Capercailzie and Black-cock (Tetrao urogallus and T.
tetrix), which are both polygamists, have regular appointed places, where during many weeks they congregate in numbers to fight together and to display their charms before the females. Dr. W. Kovalevsky informs me that in Russia he has seen the snow all bloody on the arenas where the capercailzie have fought; and the black-cocks “make the feathers fly in every direction,” when several “engage in a battle royal.” The elder Brehm gives a curious account of the Balz, as the love-dances and love-songs of the Black-cock are called in Germany. The bird utters almost continuously the strangest noises: “he holds his tail up and spreads it out like a fan, he lifts up his head and neck with all the feathers erect, and stretches his wings from the body.
Then he takes a few jumps in different directions, sometimes in a circle, and presses the under part of his beak so hard against the ground that the chin feathers are rubbed off. During these movements he beats his wings and turns round and round. The more ardent he grows the more lively he becomes, until at last the bird appears like a frantic creature.” At such times the black-cocks are so absorbed that they become almost blind and deaf, but less so than the capercailzie: hence bird after bird may be shot on the same spot, or even caught by the hand. After performing these antics the males begin to fight: and the same black-cock, in order to prove his strength over several antagonists, will visit in the course of one morning several Balz-places, which remain the same during successive years. (14. Brehm, ‘Thierleben,’ 1867, B. iv. s. 351. Some of the foregoing statements are taken from L. Lloyd, ‘The Game Birds of Sweden,’ etc., 1867, p. 79.)
The peacock with his long train appears more like a dandy than a warrior, but he sometimes engages in fierce contests: the Rev. W.
Darwin Fox informs me that at some little distance from Chester two peacocks became so excited whilst fighting, that they flew over the whole city, still engaged, until they alighted on the top of St. John’s tower.
The spur, in those gallinaceous birds which are thus provided, is generally single; but Polyplectron (Fig. 51) has two or more on each leg; and one of the Blood-pheasants (Ithaginis cruentus) has been seen with five spurs. The spurs are generally confined to the male, being represented by mere knobs or rudiments in the female; but the females of the Java peacock (Pavo muticus) and, as I am informed by Mr. Blyth, of the small fire-backed pheasant (Euplocamus erythrophthalmus) possess spurs. In Galloperdix it is usual for the males to have two spurs, and for the females to have only one on each leg. (15. Jerdon, ‘Birds of India’: on Ithaginis, vol. iii. p. 523; on Galloperdix, p. 541.) Hence spurs may be considered as a masculine structure, which has been occasionally more or less transferred to the females. Like most other secondary sexual characters, the spurs are highly variable, both in number and development, in the same species.
[Fig.38. Palamedea cornuta (from Brehm), shewing the double wing-spurs, and the filament on the head.]
Various birds have spurs on their wings. But the Egyptian goose (Chenalopex aegyptiacus) has only “bare obtuse knobs,” and these probably shew us the first steps by which true spurs have been developed in other species. In the spur-winged goose, Plectropterus gambensis, the males have much larger spurs than the females; and they use them, as I am informed by Mr. Bartlett, in fighting together, so that, in this case, the wing-spurs serve as sexual weapons; but according to Livingstone, they are chiefly used in the defence of the young. The Palamedea (Fig. 38) is armed with a pair of spurs on each wing; and these are such formidable weapons that a single blow has been