The Descent of Man, Charles Darwin [top 100 books of all time checklist txt] 📗

as we have seen in the eighth chapter, that with certain humming-birds the males greatly exceed the females in number, whilst with other species inhabiting the same country the females greatly exceed the males. If, then, we might assume that during some former lengthened period the males of the Juan Fernandez species had greatly exceeded the females in number, but that during another lengthened period the females had far exceeded the males, we could understand how the males at one time, and the females at another, might have been rendered beautiful by the selection of the brighter coloured individuals of either sex; both sexes transmitting their characters to their young at a rather earlier age than usual. Whether this is the true explanation I will not pretend to say; but the case is too remarkable to be passed over without notice.

We have now seen in all six classes, that an intimate relation exists between the plumage of the young and the adults, either of one sex or both. These relations are fairly well explained on the principle that one sex— this being in the great majority of cases the male—first acquired through variation and sexual selection bright colours or other ornaments, and transmitted them in various ways, in accordance with the recognised laws of inheritance. Why variations have occurred at different periods of life, even sometimes with species of the same group, we do not know, but with respect to the form of transmission, one important determining cause seems to be the age at which the variations first appear.

From the principle of inheritance at corresponding ages, and from any variations in colour which occurred in the males at an early age not being then selected—on the contrary being often eliminated as dangerous—whilst similar variations occurring at or near the period of reproduction have been preserved, it follows that the plumage of the young will often have been left unmodified, or but little modified. We thus get some insight into the colouring of the progenitors of our existing species. In a vast number of species in five out of our six classes of cases, the adults of one sex or of both are bright coloured, at least during the breeding- season, whilst the young are invariably less brightly coloured than the adults, or are quite dull coloured; for no instance is known, as far as I can discover, of the young of dull-coloured species displaying bright colours, or of the young of bright-coloured species being more brilliant than their parents. In the fourth class, however, in which the young and the old resemble each other, there are many species (though by no means all), of which the young are bright-coloured, and as these form old groups, we may infer that their early progenitors were likewise bright. With this exception, if we look to the birds of the world, it appears that their beauty has been much increased since that period, of which their immature plumage gives us a partial record.

ON THE COLOUR OF THE PLUMAGE IN RELATION TO PROTECTION.

It will have been seen that I cannot follow Mr. Wallace in the belief that dull colours, when confined to the females, have been in most cases specially gained for the sake of protection. There can, however, be no doubt, as formerly remarked, that both sexes of many birds have had their colours modified, so as to escape the notice of their enemies; or in some instances, so as to approach their prey unobserved, just as owls have had their plumage rendered soft, that their flight may not be overheard. Mr. Wallace remarks (49. ‘Westminster Review,’ July 1867, p. 5.) that “it is only in the tropics, among forests which never lose their foliage, that we find whole groups of birds, whose chief colour is green.” It will be admitted by every one, who has ever tried, how difficult it is to distinguish parrots in a leaf-covered tree. Nevertheless, we must remember that many parrots are ornamented with crimson, blue, and orange tints, which can hardly be protective. Woodpeckers are eminently arboreal, but besides green species, there are many black, and black-and-white kinds—all the species being apparently exposed to nearly the same dangers. It is therefore probable that with tree-haunting birds, strongly-pronounced colours have been acquired through sexual selection, but that a green tint has been acquired oftener than any other, from the additional advantage of protection.

In regard to birds which live on the ground, every one admits that they are coloured so as to imitate the surrounding surface. How difficult it is to see a partridge, snipe, woodcock, certain plovers, larks, and night-jars when crouched on ground. Animals inhabiting deserts offer the most striking cases, for the bare surface affords no concealment, and nearly all the smaller quadrupeds, reptiles, and birds depend for safety on their colours. Mr. Tristram has remarked in regard to the inhabitants of the Sahara, that all are protected by their “isabelline or sand-colour.” (50. ‘Ibis,’ 1859, vol. i. p. 429, et seq. Dr. Rohlfs, however, remarks to me in a letter that according to his experience of the Sahara, this statement is too strong.) Calling to my recollection the desert-birds of South America, as well as most of the ground-birds of Great Britain, it appeared to me that both sexes in such cases are generally coloured nearly alike. Accordingly, I applied to Mr. Tristram with respect to the birds of the Sahara, and he has kindly given me the following information. There are twenty-six species belonging to fifteen genera, which manifestly have their plumage coloured in a protective manner; and this colouring is all the more striking, as with most of these birds it differs from that of their congeners. Both sexes of thirteen out of the twenty-six species are coloured in the same manner; but these belong to genera in which this rule commonly prevails, so that they tell us nothing about the protective colours being the same in both sexes of desert-birds. Of the other thirteen species, three belong to genera in which the sexes usually differ from each other, yet here they have the sexes alike. In the remaining ten species, the male differs from the female; but the difference is confined chiefly to the under surface of the plumage, which is concealed when the bird crouches on the ground; the head and back being of the same sand- coloured hue in the two sexes. So that in these ten species the upper surfaces of both sexes have been acted on and rendered alike, through natural selection, for the sake of protection; whilst the lower surfaces of the males alone have been diversified, through sexual selection, for the sake of ornament. Here, as both sexes are equally well protected, we clearly see that the females have not been prevented by natural selection from inheriting the colours of their male parents; so that we must look to the law of sexually-limited transmission.

In all parts of the world both sexes of many soft-billed birds, especially those which frequent reeds or sedges, are obscurely coloured. No doubt if their colours had been brilliant, they would have been much more conspicuous to their enemies; but whether their dull tints have been specially gained for the sake of protection seems, as far as I can judge, rather doubtful. It is still more doubtful whether such dull tints can have been gained for the sake of ornament. We must, however, bear in mind that male birds, though dull-coloured, often differ much from their females (as with the common sparrow), and this leads to the belief that such colours have been gained through sexual selection, from being attractive. Many of the soft-billed birds are songsters; and a discussion in a former chapter should not be forgotten, in which it was shewn that the best songsters are rarely ornamented with bright tints. It would appear that female birds, as a general rule, have selected their mates either for their sweet voices or gay colours, but not for both charms combined. Some species, which are manifestly coloured for the sake of protection, such as the jack-snipe, woodcock, and night-jar, are likewise marked and shaded, according to our standard of taste, with extreme elegance. In such cases we may conclude that both natural and sexual selection have acted conjointly for protection and ornament. Whether any bird exists which does not possess some special attraction, by which to charm the opposite sex, may be doubted. When both sexes are so obscurely coloured that it would be rash to assume the agency of sexual selection, and when no direct evidence can be advanced shewing that such colours serve as a protection, it is best to own complete ignorance of the cause, or, which comes to nearly the same thing, to attribute the result to the direct action of the conditions of life.

Both sexes of many birds are conspicuously, though not brilliantly coloured, such as the numerous black, white, or piebald species; and these colours are probably the result of sexual selection. With the common blackbird, capercailzie, blackcock, black scoter-duck (Oidemia), and even with one of the birds of paradise (Lophorina atra), the males alone are black, whilst the females are brown or mottled; and there can hardly be a doubt that blackness in these cases has been a sexually selected character. Therefore it is in some degree probable that the complete or partial blackness of both sexes in such birds as crows, certain cockatoos, storks, and swans, and many marine birds, is likewise the result of sexual selection, accompanied by equal transmission to both sexes; for blackness can hardly serve in any case as a protection. With several birds, in which the male alone is black, and in others in which both sexes are black, the beak or skin about the head is brightly coloured, and the contrast thus afforded adds much to their beauty; we see this in the bright yellow beak of the male blackbird, in the crimson skin over the eyes of the blackcock and capercailzie, in the brightly and variously coloured beak of the scoter-drake (Oidemia), in the red beak of the chough (Corvus graculus, Linn.), of the black swan, and the black stork. This leads me to remark that it is not incredible that toucans may owe the enormous size of their beaks to sexual selection, for the sake of displaying the diversified and vivid stripes of colour, with which these organs are ornamented. (51. No satisfactory explanation has ever been offered of the immense size, and still less of the bright colours, of the toucan’s beak. Mr. Bates (‘The Naturalist on the Amazons,’ vol. ii. 1863, p. 341) states that they use their beaks for reaching fruit at the extreme tips of the branches; and likewise, as stated by other authors, for extracting eggs and young birds from the nests of other birds. But, as Mr. Bates admits, the beak “can scarcely be considered a very perfectly-formed instrument for the end to which it is applied.” The great bulk of the beak, as shewn by its breadth, depth, as well as length, is not intelligible on the view, that it serves merely as an organ of prehension. Mr. Belt believes (‘The Naturalist in Nicaragua,’ p. 197) that the principal use of the beak is as a defence against enemies, especially to the female whilst nesting in a hole in a tree.) The naked skin, also, at the base of the beak and round the eyes is likewise often brilliantly coloured; and Mr. Gould, in speaking of one species (52. Rhamphastos carinatus, Gould’s ‘Monograph of Ramphastidae.’), says that the colours of the beak “are doubtless in the finest and