The theory of sexual selection was formulated by Darwin, even in the first edition of the “Origin of Species,” but was developed at much greater length in “The Descent of Man.” “This form of selection depends, not on a struggle for existence in relation to other organic beings or to external conditions, but on a struggle between the individuals of one sex, generally the males, for the possession of the other sex. The result is not death to the unsuccessful competitor, but few or no offspring. Sexual selection is, therefore, less rigorous than natural selection. Generally the most vigorous males, those which are best fitted for their place in nature, will leave most progeny. But in many cases victory depends, not so much on general vigor, as on having special weapons, confined to the male sex. A hornless stag or spurless cock would have a poor chance of leaving numerous offspring. Sexual selection, by always allowing the victor to breed, might surely give indomitable courage, length to the spur, and strength to the wing to strike in the spurred leg in nearly the same manner as the brutal cock-fighter by the careful selection of his best cocks.” It is important to notice that the theory of sexual selection is admittedly an extension of the selection principle into a new field. Having accounted for domesticated animals and plants by artificial selection, and for the adaptations of wild species by natural selection, there remained only to account for the secondary sexual differences between the sexes by the principle of sexual selection.

There are two ways in which Darwin supposes sexual selection to act: (1) through competition of the individuals of the same sex with each other,—the strongest or best-equipped for fighting or for finding the individuals of the other sex gaining an advantage; (2) through selection by the individuals of one sex of certain preferred individuals of the other sex.

The first category is natural selection applied to the members of one sex in competition with each other, although the result does not lead to the death of the unsuccessful individual, but excludes it from leaving progeny. In the second category a new element is introduced, namely, the selective power of the individuals of one sex, usually the female. It is this part that adds a distinctly new element to Darwin’s other two theories of selection, and it is this part that we naturally think of as the theory of sexual selection par excellence. Darwin makes, however, no sharp distinction between these two sides of his theory, but includes both under the heading of sexual selection.

In order to get the theory itself before us in as concrete form as possible, let us examine some of the cases that Darwin has given to show how he supposes the process to be carried out.

“There are many other structures and instincts which must have been developed through sexual selection—such as the weapons of offence and the means of defence of the males for fighting with and driving away their rivals—their courage and pugnacity—their various ornaments—their contrivances for producing vocal or instrumental music—and their glands for emitting odors, most of these latter structures serving only to allure or excite the female. It is clear that these characters are the result of sexual and not of ordinary selection, since unarmed, unornamented, or unattractive males would succeed equally well in the battle for life and in leaving a numerous progeny, but for the presence of better-endowed males. We may infer that this would be the case, because the females, which are unarmed and unornamented, are able to survive and procreate their kind. Secondary sexual characters of the kind just referred to will be fully discussed in the following chapters, as being in many respects interesting, but especially as depending on the will, choice, and rivalry of the individuals of either sex. When we behold two males fighting for the possession of the female, or several male birds displaying their gorgeous plumage, and performing strange antics before an assembled body of females, we cannot doubt that, though led by instinct, they know what they are about, and consciously exert their mental and bodily powers.”

This general statement gives an idea of the class of phenomena that Darwin proposes to explain by the theory of sexual selection. The close resemblance between this process and that of artificial selection may be gathered from the following statement:—

“Just as man can improve the breed of his game-cocks by the selection of those birds which are victorious in the cockpit, so it appears that the strongest and most vigorous males, or those provided with the best weapons, have prevailed under nature, and have led to the improvement of the natural breed or species. A slight degree of variability leading to some advantage, however slight, in reiterated deadly contests would suffice for the work of sexual selection; and it is certain that secondary sexual characters are eminently variable. Just as man can give beauty, according to his standard of taste, to his male poultry, or more strictly can modify the beauty originally acquired by the parent species, can give to the Sebright bantam a new and elegant plumage, an erect and peculiar carriage—so it appears that female birds in a state of nature have, by a long selection of the more attractive males, added to their beauty or other attractive qualities. No doubt this implies powers of discrimination and taste on the part of the female which will at first appear extremely improbable; but by the facts to be adduced hereafter, I hope to be able to show that the females actually have these powers. When, however, it is said that the lower animals have a sense of beauty, it must not be supposed that such sense is comparable with that of a cultivated man, with his multiform and complex associated ideas. A more just comparison would be between the taste for the beautiful in animals, and that in the lowest savages, who admire and deck themselves with any brilliant, glittering, or curious object.”

Darwin did not close his eyes to the difficulties which the theory had to contend against. One of the most formidable of these objections is described in the following words: “Our difficulty in regard to sexual selection lies in understanding how it is that the males which conquer other males, or those which prove the most attractive to the females, leave a greater number of offspring to inherit their superiority than their beaten and less attractive rivals. Unless this result does follow, the characters which give to certain males an advantage over others could not be perfected and augmented through sexual selection. When the sexes exist in exactly equal numbers, the worst-endowed males will (except where polygamy prevails) ultimately find females, and leave as many offspring, as well fitted for their general habits of life, as the best-endowed males. From various facts and considerations, I formerly inferred that with most animals, in which secondary sexual characters are well developed, the males considerably exceeded the females in number; but this is not by any means always true. If the males were to the females as two to one, or as three to two, or even in a somewhat lower ratio, the whole affair would be simple; for the better-armed or more attractive males would leave the largest number of offspring. But after investigating, as far as possible, the numerical proportion of the sexes, I do not believe that any great inequality in number commonly exists. In most cases sexual selection appears to have been effective in the following manner.

“Let us take any species, a bird for instance, and divide the females inhabiting a district into two equal bodies, the one consisting of the more vigorous and better-nourished individuals, and the other of the less vigorous and healthy. The former, there can be little doubt, would be ready to breed in the spring before the others; and this is the opinion of Mr. Jenner Weir, who has carefully attended to the habits of birds during many years. There can also be no doubt that the most vigorous, best-nourished and earliest breeders would on an average succeed in rearing the largest number of fine offspring. The males, as we have seen, are generally ready to breed before the females; the strongest, and with some species the best-armed of the males, drive away the weaker; and the former would then unite with the more vigorous and better-nourished females, because they are the first to breed. Such vigorous pairs would surely rear a larger number of offspring than the retarded females, which would be compelled to unite with the conquered and less powerful males, supposing the sexes to be numerically equal; and this is all that is wanted to add, in the course of successive generations, to the size, strength and courage of the males, or to improve their weapons.”

I shall comment later on the points here raised, but we should not let this opportunity pass without noticing, that even if the pairing were to follow according to the method here imagined, still the argument breaks down at the critical point, for there is no evidence that the more precocious females would rear a larger number of offspring than the more normal females, or even those that breed somewhat later.

The greater eagerness of the males which has been observed in so many different classes of animals is accounted for as follows:—

“But it is difficult to understand why the males of species, of which the progenitors were primordially free, should invariably have acquired the habit of approaching the females, instead of being approached by them. But in all cases, in order that the males should seek efficiently, it would be necessary that they should be endowed with strong passions; and the acquirement of such passions would naturally follow from the more eager leaving a larger number of offspring than the less eager.”

Thus we are led to the rather complex conclusion, that the more eager males will leave more descendants, and those that are better endowed with ornaments will be the ones selected. But unless it can be shown that there is some connection between greater eagerness and better ornamentation, it might often occur that the less ornamented were the more eager individuals, in which case there would be an apparent conflict between the two acquirements.

After giving some cases of the greater variability of the males, in respect to characters that are not connected with sexual selection, and presumably not the result of any kind of selection, Darwin concludes: “Through the action of sexual and natural selection male animals have been rendered in very many instances widely different from their females; but independently of selection the two sexes, from differing constitutionally, tend to vary in a somewhat different manner. The female has to expend much organic matter in the formation of her ova, whereas the male expends much force in fierce contests with his rivals, in wandering about in search of the female, in exerting his voice, pouring out odoriferous secretions, etc.: and this expenditure is generally concentrated within a short period. The great vigor of the male during the season of love seems often to intensify his colors, independently of any marked difference from the female. In mankind, and even as low down in the organic scale as in the Lepidoptera, the temperature of the body is higher in the male than in the female, accompanied in the case of man by a slower pulse. On the whole, the expenditure of matter and force by the two sexes is probably nearly equal, though effected in very different ways and at different rates.”

Again: “From the causes just specified, the two sexes can hardly fail to differ somewhat in constitution, at least during the breeding season; and although they may be subjected to exactly the same conditions, they will tend to vary in a different manner. If such variations are of no service to either sex, they will not be accumulated and increased by sexual or natural selection. Nevertheless, they may become permanent if the exciting cause acts permanently; and in accordance with a frequent form of inheritance they may be transmitted to that sex alone in which they first appeared. In this case, the two sexes will come to present permanent, yet unimportant, differences of character. For instance, Mr. Allen shows that with a large number of birds inhabiting the northern and southern United States, the specimens from the south are darker-colored than those from the north; and this seems to be the direct result of the difference in temperature, light, etc., between the two regions. Now, in some few cases, the two sexes of the same species appear to have been differently affected; in the AgelÆus phoeniceus the males have had their colors greatly intensified in the south; whereas with Cardinalis virginianus it is the females which have been thus affected: with Quiscalus major the females have been rendered extremely variable in tint, whilst the males remain nearly uniform.”

The admissions contained in this statement would seem to jeopardize the entire question, for, if it is admitted that, on account of the difference in the constitution of the two sexes, the influence of the surrounding conditions would produce a different effect on them, it would seem that there is no need whatsoever for the theory of sexual selection. What Darwin is probably attempting to show is that the material for the further action of sexual selection is already given; but the question may well be asked, if the external conditions have done so much, why may they not have gone farther and produced the entire result?

Darwin makes the following suggestion to account for those cases in which the female is the more highly colored:—

“A few exceptional cases occur in various classes of animals, in which the females instead of the males have acquired well-pronounced secondary sexual characters, such as brighter colors, greater size, strength, or pugnacity. With birds there has sometimes been a complete transposition of the ordinary characters proper to each sex; the females having become the more eager in courtship, the males remaining comparatively passive, but apparently selecting the more attractive females, as we may infer from the results. Certain hen birds have thus been rendered more highly colored or otherwise ornamented, as well as more powerful and pugnacious than the cocks; these characters being transmitted to the female offspring alone.”

Then follows immediately the discussion as to whether a double process of sexual selection may not be supposed to go on at the same time. “It may be suggested that in some cases a double process of selection has been carried on; that the males have selected the more attractive females, and the latter the more attractive males. This process, however, though it might lead to the modification of both sexes, would not make the one sex different from the other, unless indeed their tastes for the beautiful differed; but this is a supposition too improbable to be worth considering in the case of any animal, excepting man. There are, however, many animals in which the sexes resemble each other, both being furnished with the same ornaments, which analogy would lead us to attribute to the agency of sexual selection. In such cases it may be suggested with more plausibility, that there has been a double or mutual process of sexual selection; the more vigorous and precocious females selecting the more attractive and vigorous males, the latter rejecting all except the more attractive females. But from what we know of the habits of animals, this view is hardly probable, for the male is generally eager to pair with any female. It is more probable that the ornaments common to both sexes were acquired by one sex, generally the male, and then transmitted to the offspring of both sexes. If, indeed, during a lengthened period the males of any species were greatly to exceed the females in number, and then during another lengthened period, but under different conditions, the reverse were to occur, a double but not simultaneous process of sexual selection might easily be carried on, by which the two sexes might be rendered widely different.”

The improbability of such a process is so manifest that the suggestion can scarcely be looked upon as anything more than pure speculation. We shall have occasion later to return to the same subject, and point out its bearing more explicitly.

Nearly the whole animal kingdom is passed in review by Darwin from the point of view of the sexual selection theory. There is brought together a large number of extremely interesting facts, and if the theory did no more than merely hold them together, it has served, in this respect, a useful end. We may select some of the most instructive cases by way of illustrating the theory.

In many of the lower animals in which the sexes are separated, and these alone, of course, can be supposed to come within the range of the theory, there are no striking differences between the sexes, in regard to ornamentation, although in other respects differences may exist.

“Moreover it is almost certain that these animals have too imperfect senses and much too low mental powers, to appreciate each other’s beauty or other attractions, or to feel rivalry.

“Hence in these classes or subkingdoms, such as the Protozoa, Coelenterata, Echinodermata, Scolecida, secondary sexual characters, of the kind which we have to consider, do not occur; and this fact agrees with the belief that such characters in the higher classes have been acquired through sexual selection, which depends on the will, desire, and choice of either sex.”

There are some cases, however, in which animals low in the scale show a difference in the ornamentation of the two sexes. A few cases have been recorded in the roundworms, where different shades of the same tint distinguish the sexes. In the annelids the sexes are sometimes so different, that, as Darwin remarks, they have been placed in different genera and even families, “yet the differences do not seem to be of the kind which can be safely attributed to sexual selection.” In regard to the nemertian worms, although they “vie in variety and beauty of coloring with any other group in the invertebrate series,” yet McIntosh states that he “cannot discover that these colors are of any service.” In the copepods, belonging to the group of lower Crustacea, Darwin excludes those cases in which the males alone “are furnished with perfect swimming legs, antennÆ, and sense-organs; the females being destitute of these organs, with their bodies often consisting of a mere distorted mass,” because these extraordinary differences between the two sexes are no doubt related to their widely different habits of life. Nevertheless, it is important to observe that such extreme differences may exist in cases where sexual selection cannot come in, because of the absence of eyes in the female.

In regard to another copepod, Saphirina, Darwin points out that the males are furnished with minute scales, which exhibit beautiful changing colors, and these are absent in the females; yet he states that it would be extremely rash to conclude that these curious organs serve to attract the females. Differences in the sexes are also found in one species of Squilla, and a species of Gelasimus. In the latter case Darwin thinks that the difference is probably due to sexual selection. In addition to these cases, recorded by Darwin, there may be added the two remarkable cases, shown in our Figure 2 A, B, of Calocalanus pavo, the female of which has a gorgeous tail worthy of a peacock, and of Calocalanus plumulosus, in which one of the setÆ of the tail is drawn out into a long featherlike structure. In the former, the male is much more modestly adorned, as shown in Figure 2 C; in the latter species the male is unknown.

In spiders, where as a rule the sexes do not differ much from each other in color, the males are often of a darker shade than the females. “In some species, however, the difference is conspicuous; thus the female of Sparassus smaragdulus is dullish green, whilst the adult male has the abdomen of a fine yellow with three longitudinal stripes of rich red.” Darwin believes that sexual selection must take place in this group, because Canestrini has observed that the males fight for the possession of the females. He has also stated that the males pay court to the female, and that she rejects some of the males who court her, and sometimes devours them, until finally one is chosen. Darwin believed, on this evidence, that the difference in color of the sexes had been acquired by sexual selection, “though we have here not the best kind of evidence—the display by the male of his ornaments.” This evidence has, however, now been supplied through the interesting observations of Mr. and Mrs. Peckham. These accurate observers have studied the courtship of the male, and observed that during the process, he twists and turns his body in such a way as to show to best advantage his colors to the female. From their account this certainly appears to be the result of his movements, but whether this is really the case, and whether the female makes any choice amongst her suitors, according to whether they are more or less brilliantly marked, we are absolutely ignorant. The following account given by Darwin should not pass unnoticed:—

“The male is generally much smaller than the female, sometimes to an extraordinary degree, and he is forced to be extremely cautious in making his advances, as the female often carries her coyness to a dangerous pitch. De Geer saw a male that ‘in the midst of his preparatory caresses was seized by the object of his attentions, enveloped by her in a web and then devoured, a sight which, as he adds, filled him with horror and indignation.’ The Rev. O. P. Cambridge accounts in the following manner for the extreme smallness of the male in the genus Nephila. ‘M. Vinson gives a graphic account of the agile way in which the diminutive male escapes from the ferocity of the female, by gliding about and playing hide and seek over her body and along her gigantic limbs: in such a pursuit it is evident that the chances of escape would be in favor of the smallest males, while the larger ones would fall early victims; thus gradually a diminutive race of males would be selected, until at last they would dwindle to the smallest possible size compatible with the exercise of their generative functions,—in fact probably to the size we now see them, i.e. so small as to be a sort of parasite upon the female, and either beneath her notice, or too agile and too small for her to catch without great difficulty.’”

It is certainly surprising to find Darwin ascribing even this difference in size between the sexes to the action of selection. Is it not a little ludicrous to suppose that the females have reduced the males to a size too small for them to catch?

There are many cases known in the animal kingdom where there is a difference in size between the two sexes, especially in the group of insects; but I doubt very much if they are to be accounted for as the result of sexual selection. In some of these cases Darwin accounts for the larger size of the female, on account of the large number of eggs which she has to carry. In other insects where the male is larger, as in the stag-beetle, the size is ascribed to the conflicts of the males, leading to the survival of the larger individuals. In still other cases, where the males are larger, but do not fight, an explanation is admittedly wanting; but it is suggested that here there would be no necessity for the males to be smaller than the females in order to mature before them (as is supposed to happen in other species), for in these cases the individuals are not short-lived, and there would be ample time for pairing. Again, although the males of nearly all bees are smaller than the females, yet the reverse is true in those forms in which the females are fertilized during the marriage flight. The explanation offered is that in these forms the male carries the female, and this is assumed to require greater size on his part. This loose way of guessing, as to a possible explanation, is characteristic of the whole hypothesis of sexual selection. First one, and then another, guess is made as to the causes of the differences between the sexes. It is not shown in a single one of the instances that the postulated cause has really had anything to do with the differences in question; and the attempt to show that the theory is probable, by pointing out the large number of cases which it appears to account for, is weakened to a very great degree by the number of exceptional cases, for which an equally ready explanation of a different kind is forthcoming. This way of giving loose rein to the imagination has been the bane of the method that has followed hard on the track of Darwin’s hypothesis, and for which his example has been in no small measure responsible. Thus, in the case just quoted, there are no less than four distinct conjectures made to account for the differences in size between the sexes, and each guess involves an entirely different set of processes. Considering the complicated relation of the life of organisms, it may be doubted if any of the imagined processes could bring about the result, and certainly not a single one has been shown to be a real, or a sufficient, cause in the evolutionary process. Neither the actuality of the postulated causes, nor their application to a particular case, has been shown to exist.

In the Diptera, or flies, Wallace records one interesting case of sexual difference in the genus Elaphomyia of New Guinea, in which the males are furnished with horns, which the females lack. Darwin writes:—

“The horns spring from beneath the eyes, and curiously resemble those of a stag, being either branched or palmated. In one of the species, they equal the whole body in length. They might be thought to be adapted for fighting, but as in one species they are of a beautiful pink color, edged with black, with a pale central stripe, and as these insects have altogether a very elegant appearance, it is perhaps more probable that they serve as ornaments.”

Presumably, therefore, Darwin means these colored horns have been acquired by sexual selection.

In the Hemiptera, or bugs, both sexes of some species are “beautifully colored,” and as the members of the group are often unpalatable to other animals, the color in this case is supposed to act as a warning signal.

In other cases it is stated, however, that “a small pink and green species” could hardly be distinguished from the buds on the trunks of the lime trees which this insect frequents. In this case the color appears “to be directly protective.” Thus without any means of forming a correct judgment, the color of one animal is supposed to be the result of natural selection, since it resembles its surroundings, but of sexual selection if the color is present or more pronounced in one sex. Where neither view can easily be applied, the color is ascribed in a general way to the nature of the organism.

In respect to the group of Hymenoptera, or bees, Darwin records the following cases:—

“In this order slight differences in color, according to sex, are common, but conspicuous differences are rare except in the family of bees; yet both sexes of certain groups are so brilliantly colored—for instance in Chrysis, in which vermilion and metallic greens prevail—that we are tempted to attribute the result to sexual selection. In the IchneumonidÆ, according to Mr. Walsh, the males are almost universally lighter-colored than the females. On the other hand, in the TenthredinidÆ the males are generally darker than the females. In the SiricidÆ the sexes frequently differ; thus the male of Sirex juvencus is banded with orange, whilst the female is dark purple; but it is difficult to say which sex is the more ornamented.”

In other families of bees, differences in the color of the sexes have been recorded, and since the males have been seen fighting for the possession(?) of the females, and since bees are known to recognize differences in color, Darwin believes that:—

“In some species the more beautiful males appear to have been selected by the females; and in others the more beautiful females by the males. Consequently in certain genera, the males of the several species differ much in appearance, whilst the females are almost indistinguishable; in other genera the reverse occurs. H. MÜller believes that the colors gained by one sex through sexual selection have often been transferred in a variable degree to the other sex, just as the pollen-collecting apparatus of the female has often been transferred to the male, to whom it is absolutely useless.”

Although in beetles the sexes are generally colored alike, yet in some of the longicorns there are exceptions to the rule. “Most of these insects are large and splendidly colored. The males in the genus Pyrodes, which I saw in Mr. Bates’s collection, are generally redder but rather duller than the females, the latter being colored of a more or less splendid golden-green. On the other hand, in one species the male is golden-green, the female being richly tinted with red and purple. In the genus Esmeralda the sexes differ so greatly in color that they have been ranked as distinct species; in one species both are of a beautiful shining green, but the male has a red thorax. On the whole, as far as I could judge, the females of those PrionidÆ, in which the sexes differ, are colored more richly than the males, and this does not accord with the common rule in regard to color, when acquired through sexual selection.”

The great horns that rise from the heads of many male beetles are very striking cases of sexual difference, and Darwin compares them to the horns of stags and of the rhinoceros. They “are wonderful from their size and shapes.” Darwin offers the following conjecture as to their meaning: “The extraordinary size of the horns, and their widely different structure in closely allied forms, indicate that they have been formed for some purpose; but their excessive variability in the males of the same species leads to the inference that this purpose cannot be of a definite nature. The horns do not show marks of friction, as if used for any ordinary work. Some authors suppose that as the males wander about much more than the females, they require horns as a defence against their enemies; but as the horns are often blunt, they do not seem well adapted for defence. The most obvious conjecture is that they are used by the males for fighting together; but the males have never been observed to fight; nor could Mr. Bates, after a careful examination of numerous species, find any sufficient evidence, in their mutilated or broken condition, of their having been thus used. If the males had been habitual fighters, the size of their bodies would probably have been increased through sexual selection, so as to have exceeded that of the females; but Mr. Bates, after comparing the two sexes in above a hundred species of the CopridÆ, did not find any marked difference in this respect amongst well-developed individuals. In Lethrus, moreover, a beetle belonging to the same great division of the lamellicorns, the males are known to fight, but are not provided with horns, though their mandibles are much larger than those of the female.”

“The conclusion that the horns have been acquired as ornaments is that which best agrees with the fact of their having been so immensely, yet not fixedly, developed,—as shown by their extreme variability in the same species, and by their extreme diversity in closely allied species. This view will at first appear extremely improbable; but we shall hereafter find with many animals standing much higher in the scale, namely fishes, amphibians, reptiles and birds, that various kinds of crests, knobs, horns and combs have been developed apparently for this sole purpose.”

It is asking a great deal to suppose that animals, so dull and sluggish as these beetles, are endowed with a sufficient Æsthetic discrimination to select in each generation those males whose horns are a little longer than the average. The resemblance of the horns to those of stags is, as Darwin points out, obvious, but in the latter case also it remains to be proven that they are the result of sexual selection, as Darwin believes to be the case; but the evidence for this belief is not much better, as we shall see in the case of the antlers of deer, than it is in these beetles.

In regard to butterflies, the males and females are both often equally brilliantly colored; in other species the differences in the sexes are very striking. Darwin states:—

“Even within the same genus we often find species presenting extraordinary differences between the sexes, whilst others have their sexes closely alike.” The fine colors of the wings of many moths are also supposed by Darwin to have arisen through sexual selection, although the colors are usually on the lower wings, which are covered during the day by the less ornamented upper wings. It is assumed that, since the moths often begin to fly at dusk, their colors might at this time be seen and appreciated by the other sex. It should not be overlooked, however, that, in the case of some of the most highly colored moths, it is known that the males find the females through the sense of smell. Moreover, although moths are often finely colored, Darwin points out that “it is a singular fact that no British moths which are brilliantly colored, and, as far as I can discover, hardly any foreign species, differ much in color according to sex; though this is the case with many brilliant butterflies.”

Yet Darwin does not hesitate to conclude: “From the several foregoing facts it is impossible to admit that the brilliant colors of butterflies, and of some few moths, have commonly been acquired for the sake of protection. We have seen that their colors and elegant patterns are arranged and exhibited as if for display. Hence I am led to believe that the females prefer or are most excited by the more brilliant males; for on any other supposition the males would, as far as we can see, be ornamented to no purpose. We know that ants and certain lamellicorn beetles are capable of feeling an attachment for each other, and that ants recognize their fellows after an interval of several months. Hence there is no abstract improbability in the Lepidoptera, which probably stand nearly or quite as high in the scale as these insects, having sufficient mental capacity to admire bright colors. They certainly discover flowers by color.”

So far as the evidence of ants having an attachment for each other is concerned, we may eliminate this part of the argument, since the evidence on which the statement is based is now regarded as only showing that ants recognize each other by their sense of smell, which resides in the antennÆ. Hence the so-called fondling means only that the ants are trying by smell to determine the odor of the other individual.

Darwin points out a number of cases in which the females are more brightly colored than the males, and for such cases he reverses the process of selection, supposing that the males have been discriminating, and have not “gladly accepted any female.” No explanation is offered to account for this reversal of instinct, in fact, no evidence to show that such a reversal really exists. Darwin points out that in most cases the male insect carries the female during the period of union, while in two species of butterflies, Colias edusa and hyale, the females carry the males, and the females are here the more highly colored. He suggests that since in this case “the females take the more active part in the final marriage ceremony, so we may suppose that they likewise do so in the wooing; and in this case we can understand how it is that they have been rendered the more beautiful.”

A most significant fact in connection with the difference in sexual coloration of butterflies did not escape Darwin’s attention.

“Whilst reflecting on the beauty of many butterflies, it occurred to me that some caterpillars were splendidly colored; and as sexual selection could not possibly have here acted, it appeared rash to attribute the beauty of the mature insect to this agency, unless the bright colors of their larvÆ could be somehow explained. In the first place, it may be observed that the colors of caterpillars do not stand in any close correlation with those of the mature insect. Secondly, their bright colors do not serve in any ordinary manner as a protection. Mr. Bates informs me, as an instance of this, that the most conspicuous caterpillar which he ever beheld (that of a Sphinx) lived on the large green leaves of a tree on the open llanos of South America; it was about four inches in length, transversely banded with black and yellow, and with its head, legs, and tail of a bright red. Hence it caught the eye of any one who passed by, even at the distance of many yards, and no doubt that of every passing bird.”

Darwin applied to Wallace for a solution of this difficulty, and received the reply that he “thought it probable that conspicuously colored caterpillars were protected by having a nauseous taste; but as their skin is extremely tender, and as their intestines readily protrude from a wound, a slight peck from the beak of a bird would be as fatal to them as if they had been devoured. Hence, as Mr. Wallace remarks, ‘distastefulness alone would be insufficient to protect a caterpillar unless some outward sign indicated to its would-be destroyer that its prey was a disgusting morsel.’ Under these circumstances it would be highly advantageous to a caterpillar to be instantaneously and certainly recognized as unpalatable by all birds and other animals. Thus the most gaudy colors would be serviceable, and might have been gained by variation and the survival of the most easily recognized individuals.”

It need scarcely be pointed out that an occasional peck can scarcely be supposed to have led to the splendid development of color shown by some caterpillars, and Darwin confesses that at first sight this hypothesis appears bold, but nevertheless he believes that it will be found to be true. He adds, “We cannot, however, at present thus explain the elegant diversity in the colors of many caterpillars.”

A most important fact in this connection should not be overlooked, namely, that in the caterpillar stage the sexual organs are so little developed that it is generally impossible at this time to distinguish between the sexes, unless a microscopic examination is made. This gives us, perhaps, a clew as to the difference between the mature sexual forms. These differences are connected with difference of sex itself. This conclusion also fits in well with the fact that during the period when the sexual organs are at the height of their development the individuals are most brilliantly colored. The primary cause of the brilliant color of many animals concerns us here only secondarily, for, since it is known that many of the lower forms are no less brilliantly and elaborately colored than are the sexes of the higher forms, it is not surprising that the sexes themselves sometimes differ in this respect.

Organs for producing sounds of different sorts are present in some insects, and these organs Darwin includes under the head of secondary sexual organs. In the group of Hemiptera, or bugs, the cicadas are the most familiar species that produce sounds. The noise is made by the males; the females are quite mute.

“With respect to the object of the music, Dr. Hartman, in speaking of the Cicada septemdecim of the United States, says, ‘the drums are now (June 6th and 7th, 1851) heard in all directions. This I believe to be the marital summons from the males. Standing in thick chestnut sprouts about as high as my head, where hundreds were around me, I observed the females coming around the drumming males.’ He adds, ‘this season (August, 1868) a dwarf pear-tree in my garden produced about fifty larvÆ of C. pruinosa; and I several times noticed the females to alight near a male while he was uttering his clanging notes.’ Fritz MÜller writes to me from S. Brazil that he has often listened to a musical contest between two or three males of a species with a particularly loud voice, seated at a considerable distance from each other: as soon as one had finished his song, another immediately began, and then another. As there is so much rivalry between the males, it is probable that the females not only find them by their sounds, but that, like female birds, they are excited or allured by the male with the most attractive voice.”

In the flies the following cases are given by Darwin:—

“That the males of some Diptera fight together is certain; for Professor Westwood has several times seen this with the TipulÆ. The males of other Diptera apparently try to win the females by their music: H. MÜller watched for some time two males of an Eristalis courting a female; they hovered above her, and flew from side to side, making a high humming noise at the same time. Gnats and mosquitoes (CulicidÆ) also seem to attract each other by humming; and Professor Mayer has recently ascertained that the hairs on the antennÆ of the male vibrate in unison with the notes of a tuning-fork, within the range of the sounds emitted by the female.”

In the crickets, grasshoppers, and locusts, the males “are remarkable for their musical powers”; and it is generally assumed that the sounds serve to call or to excite the female. In these forms the noise is made by rubbing the wings over each other or the legs against the wing-covers.

In some of these forms both sexes have stridulating organs, and in one case they differ to a certain extent from each other. “Hence we cannot suppose that they have been transferred from the male to the female, as appears to have been the case with the secondary sexual characters of many other animals. They must have been independently developed in the two sexes, which no doubt mutually call to each other during the season of love.”

Some beetles also possess rasping organs in different parts of the body, but they cannot produce much noise by this means.

“We thus see that in the different coleopterous families the stridulating organs are wonderfully diversified in position, but not much in structure. Within the same family some species are provided with these organs, and others are destitute of them. This diversity is intelligible, if we suppose that originally various beetles made a shuffling or hissing noise by the rubbing together of any hard and rough parts of their bodies, which happened to be in contact; and that from the noise thus produced being in some way useful, the rough surfaces were gradually developed into regular stridulating organs. Some beetles as they move, now produce, either intentionally or unintentionally, a shuffling noise, without possessing any proper organs for the purpose.”

Darwin says that he expected from analogy to find in this group also differences in the sexes, but none such were found, although in some cases the males alone possess certain characters or have them more highly developed.

It is important not to forget, when considering all questions connected with sexual selection, that in order for the result to be successful it is not only necessary that the female respond to the noises and music of the other sex, but that she choose the suitor that makes the greatest, or the most pleasing, noise. If the stridulating organs are only used by the animals in finding each other, then the case might be considered as coming under the head of natural selection. If this be granted, then it may be claimed, and apparently Darwin is inclined to adopt this view, that those males that make the most noise will be more likely to be heard, and possibly approached. They will, therefore, be more likely to leave descendants. We have already considered this question when dealing with the theory of natural selection in the preceding chapter and need not go over the ground again. This much may, however, be said again, that even if it is probable that these organs are of use to the animals in finding each other, and this seems not improbable, it does not follow that the organs have been acquired through selection for this purpose.

Darwin finds his best examples of secondary sexual characters in the group of vertebrates, and since in this group the intelligence is of a higher order than in the other groups, the argument that the female chooses the more pleasing suitor is made to appear more plausible.

The elongation of the lower jaw that occurs in a few fishes at the breeding season is regarded as a secondary sexual character. On the other hand, Darwin recognizes the following difficulty in regard to the size of the males:—

“In regard to size, M. Carbonnier maintains that the female of almost all fishes is larger than the male; and Dr. GÜnther does not know of a single instance in which the male is actually larger than the female. With some cyprinodonts the male is not even half as large. As in many kinds of fishes the males habitually fight together, it is surprising that they have not generally become larger and stronger than the females through the effects of sexual selection. The males suffer from their small size, for, according to M. Carbonnier, they are liable to be devoured by the females of their own species when carnivorous, and no doubt by other species. Increased size must be in some manner of more importance to the females, than strength and size are to the males for fighting with other males; and this perhaps is to allow of the production of a vast number of ova.”

The last sentence implies that this particular case is to be explained by the females becoming larger on account of the number of eggs that they are to produce. But why was not the same explanation offered in the case of the spiders? It is this uncertain way of applying any explanation that suggests itself, that puts the whole method in an unfortunate light.

In many species of fish the males are brighter in color than the females. In the case of Callionymus lyra, Darwin states:—

“When fresh caught from the sea the body is yellow of various shades, striped and spotted with vivid blue on the head; the dorsal fins are pale brown with dark longitudinal bands, the ventral, caudal, and anal fins being bluish black. The female, or sordid dragonet, was considered by LinnÆus, and by many subsequent naturalists, as a distinct species; it is of a dingy reddish brown, with the dorsal fin brown and the other fins white. The sexes differ also in the proportional size of the head and mouth, and in the position of the eyes; but the most striking difference is the extraordinary elongation in the male of the dorsal fin. Mr. W. Saville Kent remarks that this ‘singular appendage appears from my observations of the species in confinement, to be subservient to the same end as the wattles, crests, and other abnormal adjuncts of the male in gallinaceous birds, for the purpose of fascinating their mates.’”

In the case of another fish, Cottus scorpius, there is also a great difference between the sexes, and here the males become very brilliant only at the breeding season. In other fishes, in which the sexes are colored alike, the males may become more brilliant during the breeding season. This, too, is explained by Darwin on the assumption that those males that have varied at the breeding season, so as to become more brightly colored, have been chosen in preference to the other males.

A few cases are cited in which it has been observed that the males appear to exhibit themselves before the females, as in the following case of the Chinese Macropus:—

“The males are most beautifully colored, more so than the females. During the breeding season they contend for the possession of the females; and, in the act of courtship, expand their fins, which are spotted and ornamented with brightly colored rays, in the same manner, according to M. Carbonnier, as the peacock. They then also bound about the females with much vivacity, and appear by ‘l’Étalage de leurs vives couleurs chercher À attirer l’attention des femelles, lesquelles ne paraissaient indiffÉrentes À ce manÉge, elles nageaient avec une molle lenteur vers les mÂles et semblaient se complaire dans leur voisinage.’”

In this connection Darwin makes the following general statement:—

“The males sedulously court the females, and in one case, as we have seen, take pains in displaying their beauty before them. Can it be believed that they would thus act to no purpose during their courtship? And this would be the case, unless the females exert some choice and select those males which please or excite them most. If the female exerts such choice, all the above facts on the ornamentation of the males become at once intelligible by the aid of sexual selection.”

While it may readily be granted that display of the male may have for its purpose the excitement of the female, it is another question as to whether she will be more excited by the more beautiful suitor. The attentions of the male may be supposed to have a purpose, even if the female does not choose the more beautiful of her suitors. It is this last proposition, so necessary for the theory of sexual selection, that seems improbable. But even if it were probable, there are, as we shall see, other difficulties to be overcome before we should be justified in accepting Darwin’s statement quoted above, concerning the results of sexual selection.

In regard to those species of fish in which both sexes are equally ornamented, Darwin returns once more to his hypothesis that the color of the male, acquired through sexual selection, may be transmitted to the other sex, and then, as if in doubt on this point, he adds, that it may be the result of the “nature of the tissues and of the surrounding conditions.” He even makes the suggestion, somewhat further on, that the colors may be warning, although it is confessedly unknown that these fish are distasteful to fish-devouring animals.

In amphibians the crest on the back of the male triton, which becomes colored along its edge, is described as a secondary sexual character. The vocal sacs, present in some species of frogs, are found sometimes in both sexes, but more highly developed in the males. In other species, as in the toad, it is the male alone that sings. In the reptiles we find that the two sexes of the turtles are colored alike, and this holds also for the crocodiles. Some male turtles make sounds at the breeding season, and the same is true for the crocodiles, the males of which are said to make a “prodigous display.” In snakes the males are smaller, as a rule, than the females, and the colors are more strongly pronounced, and although some snakes are very brilliantly colored, Darwin puts this down either to protective coloration, or to mimicry of other kinds of snakes. But surely the extremely brilliant colors of many snakes cannot be accounted for in any of these ways. The cause of the color of the venomous kinds, that are supposed to be imitated by the others, “remains to be explained and this may perhaps be sexual selection.”

“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 colors 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 South America, which are of a rich red with black and yellow transverse bands.”

In lizards the erectile crests of the male Anolis, the brilliant throat patches of Sitaria minor, which is colored blue, black, and red, the skinny appendages present on the throat of the little lizards of the genus Draco, which in the beauty of their colors baffle description, are given as cases of sexual adornment. In the last case cited the ornaments are present, however, in both sexes. The remarkable horns in the males of different species of chameleons are imagined to have been acquired through the battle of the males with each other.

In the group of birds we find some of the most striking cases of secondary sexual differences. The spurs, combs, wattles, horns, air-filled sacs, topknots, feathers with naked shafts, plumes, and greatly elongated feathers are all secondary sexual characters. The songs of the males, the rattling together of the quills of the peacock, the drumming of the grouse, and the booming sounds made by the night jars while on the wing, are further examples of secondary sexual differences. The odor of the male of the Australian musk duck is also put in the same category.

The pugnacity of many male birds is well known, and it is imagined that one of the results of the competition of the individuals of the same sex with each other has led to the development of the organs of defence and offence. The males that have been successful in these battles are then supposed to mate with the best females. In this way those secondary sexual differences, connected with the encounters of the males, are supposed to have been formed. Darwin states in this connection:—

“Even with the most pugnacious species it is probable that the pairing does not depend exclusively on the mere strength and courage of the male; for such males are generally decorated with various ornaments, which often become more brilliant during the breeding season, and which are sedulously displayed before the females. The males also endeavor to charm or excite their mates by love-notes, songs, and antics; and the courtship is, in many instances, a prolonged affair. Hence it is not probable that the females are indifferent to the charms of the opposite sex, or that they are invariably compelled to yield to the victorious males.”

Thus a double process of selection is imagined to take place; one, the outcome of a competition of the males with each other, and the other, through a choice of the more successful males by the females, the more beautiful being supposed to be chosen.

It may be well not to lose sight of the fact that unless the selection is severe in each generation, its good effects will be lost, as has been stated in connection with the theory of natural selection. Still more important is the consideration that unless the same variations appear at the same time, in many of the surviving males, the results will be lost through crossing. These statements will show that the difficulties of the theory are by no means small, and when we are asked to believe further that another process still has been superimposed on this one, namely, the selection of the more beautiful males by the females, we can appreciate how great are the difficulties that must be overcome in order that the process may be carried out.

The love-antics and dances of male birds at the breeding season furnish many curious data. The phenomena are imagined by Darwin to be connected with sexual selection, for in the dances the males are supposed to exhibit their ornaments to the females who are imagined to choose the suitor that is most to their taste.

Hudson, who has studied the habits of birds in the field, asks some very pertinent questions in connection with their performances of different kinds. “What relation that we can see or imagine to the passion of love and the business of courtship have these dancing and vocal performances in nine cases out of ten? In such cases, for instance, as that of the scissortail tyrant-bird, and its pyrotechnic displays, when a number of couples leave their nests containing eggs and young to join in a wild aËrial dance; the mad exhibitions of ypecahas and ibises and the jacana’s beautiful exhibition of grouped wings; the triplet dances of the spur-winged lapwing, to perform which two birds already mated are compelled to call in a third bird to complete the set; the harmonious duets of the oven-birds and the duets and choruses of nearly all the wood-hewers, and the wing-slapping aËrial displays of the whistling widgeons,—will it be seriously contended that the female of this species makes choice of the male able to administer the most vigorous and artistic slaps?”

“The believer in the theory would put all these cases lightly aside to cite the case of the male cow-bird practising antics before the female, and drawing a wide circle of melody around her, etc.... And this was in substance what Darwin did.” “How unfair the argument is based on these carefully selected cases gathered from all regions of the globe and often not properly reported is seen when we turn to the book of nature and closely consider the habits and actions of all the species inhabiting any one district.” Hudson concludes that he is convinced that any one who will note the actions of animals for himself will reach the conviction, that “conscious sexual selection on the part of the female is not the cause of music and dancing performances in birds, nor of the brighter colors and ornaments that distinguish the male.”

The differences in color in the sexes of birds are classified by Darwin as follows: (1) when the males are ornamented exclusively or in a much higher degree than the females; (2) when both sexes are highly ornamented; (3) when the female is more brightly colored. A few examples of each sort may be chosen for illustration.

“In regard to color, hardly anything need here be said, for every one knows how splendid are the tints of many birds, and how harmoniously they are combined. The colors are often metallic and iridescent. Circular spots are sometimes surrounded by one or more differently shaded zones, and are thus converted into ocelli. Nor need much be said on the wonderful difference between the sexes of many birds. The common peacock offers a striking instance. Female birds of paradise are obscurely colored and destitute of all ornaments, whilst the males are probably the most highly decorated of all birds, and in so many different ways, that they must be seen to be appreciated. The elongated and golden-orange plumes which spring from beneath the wings of the Paradisea apoda, when vertically erected and made to vibrate, are described as forming a sort of halo, in the centre of which the head ‘looks like a little emerald sun, with its rays formed by the two plumes.’”

Male humming-birds are almost as splendidly colored as are the birds of paradise, some having the feathers modified in a truly extraordinary way. “Almost every part of their plumage has been taken advantage of, and modified; and the modifications have been carried, as Mr. Gould showed me, to a wonderful extreme in some species belonging to nearly every subgroup. Such cases are curiously like those which we see in our fancy breeds, reared by man for the sake of ornament: certain individuals originally varied in one character, and other individuals of the same species in other characters; and these have been seized on by man and much augmented—as shown by the tail of the fantail pigeon, the hood of the jacobin, the beak and wattle of the carrier, and so forth. The sole difference between these cases is that in the one the result is due to man’s selection, whilst in the other, as with humming-birds, birds of paradise, etc., it is due to the selection by the females of the more beautiful males.”

A remarkable bird of South America, the bell-bird, has a peculiar note that “can be distinguished at the distance of nearly three miles and astonishes every one who hears it.... The male is pure white, whilst the female is dusky-green; and white is a very rare color in terrestrial species of moderate size and inoffensive habits. The male, also, as described by Waterton, has a spiral tube, nearly three inches in length, which rises from the base of the beak. It is jet-black, dotted over with minute downy feathers. This tube can be inflated with air, through a communication with the palate; and when not inflated hangs down on one side. The genus consists of four species, the males of which are very distinct, whilst the females, as described by Mr. Sclater in a very interesting paper, closely resemble each other, thus offering an excellent instance of the common rule that within the same group the males differ much more from each other than do the females. In a second species (C. nudicollis) the male is likewise snow-white, with the exception of a large space of naked skin on the throat and round the eyes, which during the breeding season is of a fine green color. In a third species (C. tricarunculatus) the head and neck alone of the male are white, the rest of the body being chestnut-brown, and the male of this species is provided with three filamentous projections half as long as the body—one rising from the base of the beak, and the two others from the corners of the mouth.”

The most familiar case of sexual difference amongst North American birds is that of the scarlet tanager, in which the male is scarlet with jet-black wings, while the female is an inconspicuous yellow-green color. Amongst domesticated animals the peafowl shows the most beautiful case of sexual differences. The magnificent tail of the male can be lifted up, so as to be seen to best advantage when the male faces the observer. Moreover the wild form, living in the forests of India, has the same gorgeous train.

The male Argus pheasant has a remarkable series of spots, or ocelli, on the secondary wing-covers. They are concealed until the male displays them before the female. Darwin states that, while it may seem incredible that such elegant shading and exquisite patterns could have been the outcome of the taste of the female, yet the extraordinary attitude assumed by the male during courtship appears entirely purposeless, unless it be supposed that he is attempting to charm the female by a display of his ornamentation.

Let us pass to the second class of cases, in which both sexes are similarly and brightly colored, and in which the young have a plumage different from the adults. For example, the male and the female of the splendid scarlet ibis are alike, whilst the young are brown. The males and females of many finely colored herons are ornamented alike, and this plumage, Darwin admits, has a nuptial character. He even tries to explain this by the curious assumption, that while the color has been acquired through the selection of the males by the females, the results attained in this way have been transmitted to both sexes. We find here another example of the method so often employed by Darwin. When he meets with facts that are not in conformity with the theory, he proceeds to make a new assumption without establishing its validity. Thus, to assume that in all cases where the sexes are colored differently, the characters acquired by the males have been transmitted only to the same sex, and in those cases where the sexes are colored alike the transmission has been to both sexes, is most arbitrary.

In other cases, which are commoner than the last, the male and female have the same color, and the young in their first plumage resemble the adults. Darwin admits that here the facts are so complex that his conclusions are doubtful. The following account of the tree-sparrow shows how vague are the principles involved in the entire discussion in relation to transmission:—

“Now with the tree-sparrow (P. montanus) both sexes and the young closely resemble the male of the house-sparrow; so that they have all been modified in the same manner, and all depart from the typical coloring of their early progenitor. This may have been effected by a male ancestor of the tree-sparrow having varied, firstly, when nearly mature; or secondly, whilst quite young, and by having in either case transmitted his modified plumage to the females and the young; or, thirdly, he may have varied when adult and transmitted his plumage to both adult sexes, and, owing to the failure of the law of inheritance at corresponding ages, at some subsequent period to his young.”

The further admissions made in the following quotation are also significant:—

“The plumage of certain birds goes on increasing in beauty during many years after they are fully mature; this is the case with the train of the peacock, with some of the birds of paradise, and with the crest and plumes of certain herons, for instance, the Ardea ludovicana. But it is doubtful whether the continued development of such feathers is the result of the selection of successive beneficial variations (though this is the most probable view with birds of paradise) or merely of continuous growth. Most fishes continue increasing in size, as long as they are in good health and have plenty of food; and a somewhat similar law may prevail with the plumes of birds.”

We need not follow Darwin through his discussion of those cases in which the adults have a winter and a summer dress and the young resemble the one or the other in plumage, or are different from either. The discussion of these cases, confessedly very complex, adds nothing to our understanding of the theory, and little but conjecture is offered to account for the facts.

The extreme to which even conjecture can be carried may be gathered from the following quotation, taken from the section dealing with cases in which the young in their first plumage differ from each other according to sex, the young males resembling more or less closely the adult males, and the young females more or less closely the adult females:

“Two humming-birds belonging to the genus Eustephanus, both beautifully colored, inhabit the small island of Juan Fernandez, and have always been ranked as specifically distinct. But it has lately been ascertained that the one which is of a rich chestnut-brown color with a golden-red head, is the male, whilst the other, which is elegantly variegated with green and white with a metallic-green head, is the female. Now the young from the first somewhat resemble the adults of the corresponding sex, the resemblance gradually becoming more and more complete.

“In considering this last case, if as before we take the plumage of the young as our guide, it would appear that both sexes have been rendered beautiful independently; and not that one sex has partially transferred its beauty to the other. The male apparently has acquired his bright colors through sexual selection in the same manner as, for instance, the peacock or pheasant in our first class of cases; and the female in the same manner as the female RhynchÆa or Turnix in our second class of cases. But there is much difficulty in understanding how this could have been effected at the same time with the two sexes of the same species. Mr. Salvin states, 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-colored 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.”

The third group of cases include those in which the females are more brightly colored, or more ornamented, than the males. These cases are rare, and the differences between the sexes are never so great as when the male is the more highly colored. Wallace thinks that since in these cases the male incubates the eggs his less conspicuous colors have been acquired through natural selection. In the genus Turnix the female is larger than the male, and lacks the black on the throat and neck, and the plumage as a whole is lighter than that of the male. The natives assert that the females after laying their eggs associate in flocks, and leave the males to do the incubating; and from other evidence Darwin thinks that this is true.

In three species of painted snipe the females “are not only larger but much more richly colored than the males,” and the trachea is more convoluted in some species. “There is also reason to believe that the male undertakes the duty of incubation.” In the dotterel plover the female is larger and somewhat more strongly colored. The males take at least a share in the incubation. In the common cassowary the female is larger and the skin of the head more brightly colored than in the male. The female is pugnacious during the breeding season and the male sits on the eggs. The female emu is large and has a crest. She is more courageous and pugilistic and makes a deep, hollow, guttural boom. The male is more docile and can only hiss or croak. He not only incubates the eggs, but defends the young against their own mother. “So that with this emu we have a complete reversal not only of the parental and incubating instincts, but of the usual moral qualities of the two sexes; the females being savage, quarrelsome, and noisy, the males gentle and good. The case is very different with the African ostrich, for the male is somewhat larger than the female and has finer plumes with more strongly contrasted colors; nevertheless he undertakes the whole duty of incubation.”

Darwin attempts to explain these reversals of instincts on the assumption that the males have turned the tables on the females, and have themselves done the selecting; and incidentally, it may be pointed out in passing, they have had to pay the penalty by incubating the eggs.

In the group of mammals, Darwin thinks that the male wins the female by conquering other males rather than by charming her through his display. The males, even when unarmed, engage in desperate conflicts with each other, and sometimes kill, but more often only wound, their fellows. The secondary sexual characters of the males have been acquired, therefore, by natural selection applied to one sex, and less frequently through the choice of the female. Since we are here more especially concerned with the latter class of phenomena, we may examine only a few cases under the first head.

The horns of stags are used by them in their conflicts with each other; the tusks of the elephant make this animal the most dangerous in the world, when in must. The horns of bulls, the canine teeth of many mammals, the tusks of the walrus, are further examples of organs which have been, according to Darwin, acquired through the competitions of the males with each other.

The voices of mammals are used for various purposes, “as a signal of danger, as a call from one member of the troup to another, and from the mother to her lost offspring, or from the latter for protection.”

“Almost all male animals use their voices much more during the rutting season than at any other time; and some, as the giraffe and porcupine, are said to be completely mute excepting at this season. As the throats (i.e. the larynx and thyroid bodies) of stags periodically become enlarged at the beginning of the breeding season, it might be thought that their powerful voices must be somehow of high importance to them; but this is very doubtful. From information given to me by two experienced observers, Mr. McNeill and Sir P. Egerton, it seems that young stags under three years old do not roar or bellow; and that the old ones begin bellowing at the commencement of the breeding season, at first only occasionally and moderately, whilst they restlessly wander about in search of the females. Their battles are prefaced by loud and prolonged bellowing, but during the actual conflict they are silent. Animals of all kinds which habitually use their voices utter various noises under any strong emotion, as when enraged and preparing to fight; but this may merely be the result of nervous excitement, which leads to the spasmodic contraction of almost all the muscles of the body, as when a man grinds his teeth and clenches his fists in rage or agony. No doubt stags challenge each other to mortal combat by bellowing; but those with the more powerful voices, unless at the same time the stronger, better-armed, and more courageous, would not gain any advantage over their rivals.”

“Some writers suggest that the bellowing serves as a call to the female; but the experienced observers above quoted inform me that female deer do not search for the male, though the males search eagerly for the females, as indeed might be expected from what we know of the habits of other male quadrupeds. The voice of the female, on the other hand, quickly brings to her one or more stags, as is well known to the hunters who in wild countries imitate her cry.

“As the case stands, the loud voice of the stag during the breeding season does not seem to be of any special service to him, either during his courtship or battles, or in any other way. But may we not believe that the frequent use of the voice, under the strong excitement of love, jealousy, and rage, continued during many generations, may at last have produced an inherited effect on the vocal organs of the stag, as well as of other male animals? This appears to me, in our present state of knowledge, the most probable view.”

Here once more we find that Darwin makes use, as a sort of last resort, of the principle of the inheritance of acquired characters. As long as the theory of selection, in any of its forms, appears to offer a satisfactory solution, we find the facts used in support of this theory, but as soon as a difficulty arises the Lamarckian theory is brought to the front. It is this shifting, as we have already more than once pointed out, that shows how little real basis there is for the theory of sexual selection.

The male gorilla has a tremendous voice, and he has, as has also the orang, a laryngeal sac. One species of gibbon has the power of producing a correct octave of musical notes.

“The vocal organs of the American Mycetes caraya are one-third larger in the male than in the female, and are wonderfully powerful. These monkeys in warm weather make the forests resound at morning and evening with their overwhelming voices. The males begin the dreadful concert, and often continue it during many hours, the females sometimes joining in with their less powerful voices. An excellent observer, Rengger, could not perceive that they were excited to begin by any special cause; he thinks that, like many birds, they delight in their own music, and try to excel each other. Whether most of the foregoing monkeys have acquired their powerful voices in order to beat their rivals and charm the females—or whether the vocal organs have been strengthened and enlarged through the inherited effects of long-continued use without any particular good being thus gained—I will not pretend to say; but the former view, at least in the case of the Hylobates agilis, seems the most probable.”

The odor of some mammals is confined to, or more developed, in the males; but in some forms, as in the skunk, it is present in both sexes. In the shrew mice, abdominal scent glands are present, but since these mice are rejected by birds of prey, their glands probably serve to protect them; “nevertheless the glands become enlarged in the males during the breeding season.” In many other quadrupeds the scent glands are of the same size in both sexes, and their function is unknown.

“In other species the glands are confined to the males, or are more developed than in the females; and they almost always become more active during the rutting season. At this period the glands on the sides of the face of the male elephant enlarge, and emit a secretion having a strong musky odor. The males, and rarely the females, of many kinds of bats have glands and protrudable sacs situated in various parts; and it is believed that these are odoriferous.

“The rank effluvium of the male goat is well known, and that of certain male deer is wonderfully strong and persistent. Besides the general odor, permeating the whole body of certain ruminants (for instance, Bos moschatus) in the breeding season, many deer, antelopes, sheep, and goats, possess odoriferous glands in various situations, more especially on their faces. The so-called tear-sacs, or suborbital pits, come under this head. These glands secrete a semifluid fetid matter which is sometimes so copious as to stain the whole face, as I have myself seen in an antelope. They are ‘usually larger in the male than in the female, and their development is checked by castration.’ According to Desmarest they are altogether absent in the female of Antilope subgutturosa. Hence, there can be no doubt that they stand in close relation with the reproductive functions. They are also sometimes present, and sometimes absent, in nearly allied forms. In the adult male musk-deer (Moschus moschiferus), a naked space round the tail is bedewed with an odoriferous fluid, whilst in the adult female and in the male until two years old, this space is covered with hair, and is not odoriferous.” Darwin believes in these cases that the odor serves to attract the females. He admits that here, “active and long-continued use cannot have come into play as in the case of the vocal organs.” He concludes, therefore, that “the odor emitted must be of considerable importance to the male, inasmuch as large and complex glands, furnished with muscles for everting the sac, and for closing or opening the orifice, have in some cases been developed. The development of these organs is intelligible through sexual selection, if the most odoriferous males are the most successful in winning the females, and in leaving offspring to inherit their gradually perfected glands and colors.”

There is sometimes a difference in the mammals in the hair of the two sexes both in amount and in color. In some species of goats the males have a beard, in others it is present in both sexes. The bull, but not the cow, has curly hair on the forehead. In some monkeys the beard is confined to the male, as in the orang; in other species it is only larger in the males.

“The males of various members of the ox family (BovidÆ), and of certain antelopes, are furnished with a dewlap, or great fold of skin on the neck, which is much less developed in the female.

“Now, what must we conclude with respect to such sexual differences as these? No one will pretend that the beards of certain male goats, or the dewlap of the bull, or the crests of hair along the backs of certain male antelopes, are of any use to them in their ordinary habits.

“Must we attribute all these appendages of hair or skin to mere purposeless variability in the male? It cannot be denied that this is possible; for in many domesticated quadrupeds, certain characters, apparently not derived through reversion from any wild parent form, are confined to the males, or are more developed in them than in the females—for instance, the hump on the male zebu cattle of India, the tail of fat-tailed rams, the arched outline of the forehead in the males of several breeds of sheep, and, lastly, the mane, the long hairs on the hind-legs, and the dewlap of the male of the Berbura goat.”

In these cases and in others that Darwin cites, which seem clearly to indicate that some of these secondary sexual characters are not the result of sexual selection, he concludes, “that they must be due to simple variability, together with sexually limited inheritance.

“Hence it appears reasonable to extend this same view to all analogous cases with animals in a state of nature. Nevertheless I cannot persuade myself that it generally holds good, as in the case of the extraordinary development of hair on the throat and fore-legs of the male Ammotragus, or in that of the immense beard of the male Pithecia. Such study as I have been able to give to nature makes me believe that parts or organs which are highly developed, were acquired at some period for a special purpose. With those antelopes in which the adult male is more strongly colored than the female, and with those monkeys in which the hair on the face is elegantly arranged and colored in a diversified manner, it seems probable that the crests and tufts of hair were gained as ornaments; and this I know is the opinion of some naturalists. If this be correct, there can be little doubt that they were gained, or at least modified through sexual selection; but how far the same view may be extended to other mammals is doubtful.”

The astonishing colors in some of the monkeys cannot be passed over without comment.

“In the beautiful Cercopithecus diana, the head of the adult male is of an intense black, whilst that of the female is dark gray; in the former the fur between the thighs is of an elegant fawn-color, in the latter it is paler.

“In the Cercopithecus cynosurus and griseoviridis one part of the body, which is confined to the male sex, is of the most brilliant blue or green, and contrasts strikingly with the naked skin on the hinder part of the body, which is vivid red.

“Lastly, in the baboon family, the adult male of Cynocephalus hamadryas differs from the female not only by his immense mane, but slightly in the color of the hair and of the naked callosities. In the drill (C. leucophÆus) the females and young are much paler-colored, with less green, than the adult males. No other member in the whole class of mammals is colored in so extraordinary a manner as the adult male mandrill (C. mormon). The face at this age becomes of a fine blue, with the ridge and tip of the nose of the most brilliant red. According to some authors, the face is also marked with whitish stripes, and is shaded in parts with black, but the colors appear to be variable. On the forehead there is a crest of hair, and on the chin a yellow beard. ‘Toutes les parties supÉrieures de leurs cuisses et le grand espace nu de leurs fesses sont Également colorÉs du rouge le plus vif, avec un mÉlange de bleu qui ne manque rÉellement pas d’ÉlÉgance.’ When the animal is excited all the naked parts become much more vividly tinted.”

Darwin sums up the evidence in regard to the differences in color between the male and female in the following statement:—

“I have now given all the cases known to me of a difference in color between the sexes of mammals. Some of these may be the result of variations confined to one sex and transmitted to the same sex, without any good being gained, and therefore without the aid of selection. We have instances of this with our domesticated animals, as in the males of certain cats being rusty-red, whilst the females are tortoise-shell colored. Analogous cases occur in nature: Mr. Bartlett has seen many black varieties of the jaguar, leopard, vulpine phalanger, and wombat; and he is certain that all or nearly all these animals, were males. On the other hand, with wolves, foxes, and apparently American squirrels, both sexes are occasionally born black. Hence it is quite possible that with some mammals a difference in color between the sexes, especially when this is congenital, may simply be the result, without the aid of selection, of the occurrence of one or more variations, which from the first were sexually limited in their transmission. Nevertheless it is improbable that the diversified, vivid, and contrasted colors of certain quadrupeds, for instance, of the above monkeys and antelopes, can thus be accounted for.”

Finally, the case of man must be considered from the point of view of sexual selection, for Darwin claims that man has acquired a number of his secondary sexual characters in this way. For instance, the beard is an excellent case of a secondary sexual character. Darwin’s interpretation is that the beard has been retained, or even developed, through the selection by the females of those males that had this outgrowth best developed. Conversely, the absence of hair on the face of the female is supposed by Darwin to have been brought about by men selecting those women having less hair on their faces. The greater intellect, energy, courage, pugnacity, and size of man are the outcome of the competition of the males with each other, since the individual excelling in these qualities will be able to select the most desirable wife, or wives, and it is assumed will, therefore, leave more descendants. The standard of beauty has been kept up by men selecting the most beautiful women in each generation (the fate of the other married women is ignored), and this beauty is supposed to have been transmitted primarily to their daughters, but also to their sons.

Although all these forms of selection are imagined to be acting in man, either alternately or simultaneously, yet Darwin recognizes in man a number of checks to the action of sexual selection: amongst savages, the so-called communal marriages; second, infanticide, generally of the young females, which appears in some races to be practised to an astonishing degree; third, early betrothals; fourth, the holding of women as slaves.

When we recall that selection to be effective can only be carried out under very exacting conditions, we cannot but be appalled at the demands made here on our credulity. The choice of the women has produced the beard of man, the choice of man the absence of a beard in women; the competition of the males with each other is leading at the same time to the development of at least half a dozen qualities that are supposed to be male specialities, and while all this is going on the results are being checked sometimes by one means, sometimes by another. Moreover, even this is not all that we are asked to accept, for there are several other qualities of the male that are put down as secondary sexual characters. For example, let us examine what Darwin has to say in regard to the development of the voice, and of singing in man.

In man the vocal cords are about a third longer than in woman and his voice deeper. Emasculation arrests the development of the vocal apparatus, and the voice remains like that of a woman. This difference between the sexes, Darwin thinks, is due probably to long-continued use by the male “under the excitement of love, rage, and jealousy.” In other words, an appeal is again made to the Lamarckian theory, and in this case to explain the origin of an organ that conforms to all the requirements of the secondary sexual characters.

“The capacity and love for singing, or music, though not a sexual character in man,” in the sense of being confined to one sex, yet is supposed to have arisen through sexual selection in the following way: “Human song is generally admitted to be the basis or origin of instrumental music. As neither the enjoyment nor the capacity of producing musical notes are faculties of the least use to man in reference to his daily habits of life, they must be ranked amongst the most mysterious with which he is endowed.”

Man is supposed to have possessed this faculty of song from a very remote time, and even the most savage races make musical sounds, although we do not enjoy their music, or they ours.

“We see that the musical faculties, which are not wholly deficient in any race, are capable of prompt and high development, for Hottentots and Negroes have become excellent musicians, although in their native countries they rarely practise anything that we should consider music. Hence the capacity for high musical development, which the savage races of man possess, may be due either to the practice by our semi-human progenitors of some rude form of music, or simply to their having acquired the proper vocal organs for a different purpose. But in this latter case we must assume, as in the above instance of parrots, and as seems to occur with many animals, that they already possessed some sense of melody.”

Darwin sums up the evidence in the two following statements, the insufficiency of which to explain the phenomena is I think only too obvious: “All these facts in respect to music and impassioned speech become intelligible to a certain extent, if we assume that musical tones and rhythm were used by our half-human ancestors, during the season of courtship, when animals of all kinds are excited not only by love, but by the strong passions of jealousy, rivalry, and triumph. From the deeply laid principle of inherited associations, musical tones in this case would be likely to call up vaguely and indefinitely the strong emotions of a long past age.” Thus the difficulty is shifted to the shoulders of our long-lost savage ancestors; or even, in fact, to our simian forefathers, as the following paragraph indicates:—

“As the males of several quadrumanous animals have their vocal organs much more developed than in the females, and as a gibbon, one of the anthropomorphous apes, pours forth a whole octave of musical notes and may be said to sing, it appears probable that the progenitors of man, either the males or females or both sexes, before acquiring the power of expressing their mutual love in articulate language, endeavored to charm each other with musical notes and rhythm. So little is known about the use of the voice by the Quadrumana during the season of love, that we have no means of judging whether the habit of singing was first acquired by our male or female ancestors. Women are generally thought to possess sweeter voices than men, and as far as this serves as any guide, we may infer that they first acquired musical powers in order to attract the other sex. But if so, this must have occurred long ago, before our ancestors had become sufficiently human to treat and value their women merely as useful slaves. The impassioned orator, bard, or musician, when with his varied tones and cadences he excites the strongest emotions in his hearers, little suspects that he uses the same means by which his half-human ancestors long ago aroused each other’s ardent passions during their courtship and rivalry.”

We have now examined in some detail the evidence that Darwin has brought forward in support of his hypothesis of sexual selection. A running comment has been made while considering the individual cases, but it may be well to sum up the matter by briefly indicating the reasons why the hypothesis seems incompetent to explain the facts.

General Criticism of the Theory of Sexual Selection

1. Some of the objections that apply to the theory of natural selection apply also with equal force to the theory of sexual selection in so far as the results in both cases are supposed to be the outcome of the selection of individual, or fluctuating, variations. If these variations appear in only a few individuals, their perpetuation is not possible, since they will soon disappear through crossing. It would be, of course, preposterous to suppose that at any one time only those few individuals pair and leave descendants that have the secondary sexual characters developed to the highest point, but if something of this sort does not occur, the extreme of fluctuating variations cannot be maintained. Even if half of the individuals are selected in each generation, the accumulation of a variation in a given direction could not go very far. The assumption, however, that only half of all the individuals that reach maturity breed, and that all of these are chosen on account of the special development of their secondary sexual characters, seems preposterous. Furthermore, if it is assumed that the high development of the new character appears in a large number of individuals, then it is not improbable that its continued appearance might be accounted for without bringing in, at all, the hypothesis of sexual selection.

2. But even supposing that the females select the most beautiful males, then, since in the vast majority of higher animals the males and the females are in equal numbers, the others will also be able to unite with each other in pairs after this first selection has taken place. Nothing will therefore be gained in the next generation. It is interesting to see how Darwin attempts to meet this argument. He tries to show in the case of birds, that there are always unpaired individuals, but since the few facts that he has been able to collect show that there are as many additional females as males, the argument proves too much. A few species are polygamous, one male having a number of female birds; but on this basis we can only account, at best, for the development through competition of the organs of offence and defence used to keep away the weaker males. Yet it is just amongst these birds that we often find the ornamental characters well developed. In fact, since all the females in such cases are selected, and since they will transmit the characters of all the males, it is evident that the secondary sexual characters could not be formed in the way imagined.

3. If the female fails to select only the more ornamental males, no result will follow. It has not been shown that she is capable of making such a choice, and in the lower forms particularly, it does not seem probable that this is done. The argument that Darwin often employs, namely, that unless she does select, the display of the males before her is meaningless, is not to the point. So far as we can detect the “cause” of the display of the male, it appears to be due to his own excitement; and even if we go so far as to admit that the “purpose” is to attract the other sex, it still does not in the least follow that the most ornamental male is selected, and unless this occurs the display has no bearing on the hypothesis of sexual selection.

4. The two forms of sexual selection, namely, competition of the males with one another (really one form of natural selection), and the selection of the most ornamental or gifted individuals, are both used by Darwin to explain secondary sexual characters, the one for organs of offence and defence, and the other for ornamental characters. If we fully appreciate the difficulties that any theory of selection meets with, we shall realize how extraordinarily complex the action must be, when two such processes are carried out at the same time, or even during alternating periods.

5. It has been objected to Darwin’s theory of sexual selection, that he suddenly reverses its mode of action to explain those cases in which the female is the stronger and more ornamented sex; but if, as Darwin shows, the instincts of the male have also changed, and have become more like those of the female, I can see no inherent difficulty in this way of applying the theory. A much more serious objection, it seems to me, is that the male is supposed to select the female for one set of characteristics, and the female to select the male for another set. It sounds a little strange to suppose that women have caused the beard of man to develop by selecting the best-bearded individuals, and the compliment has been returned by the males selecting the females that have the least amount of beard. It is also assumed that the results of the selection are transmitted to one sex only. Unless, in fact, the character in question were from the beginning peculiar to only one sex as to its inheritance, the two sexes might go on forever selecting at cross-purposes, and the result would be nothing.

6. The development, or the presence, of the Æsthetic feeling in the selecting sex is not accounted for on the theory. There is just as much need to explain why the females are gifted with an appreciation of the beautiful, as that the beautiful colors develop in the males. Shall we assume that still another process of selection is going on, as a result of which those females are selected by the males that appreciate their unusual beauty, or that those females whose taste has soared a little higher than that of the average (a variation of this sort having appeared) select males to correspond, and thus the two continue heaping up the ornaments on one side and the appreciation of these ornaments on the other? No doubt an interesting fiction could be built up along these lines, but would any one believe it, and, if he did, could he prove it?

Darwin assumes that the appreciation on the part of the female is always present, and he thus simplifies, in appearance, the problem, but he leaves half of it unexplained.

7. It has been pointed out, that it is important to distinguish between the possible excitement of the female by the display or antics of the male, and the selection of the more beautiful or agile performer. Darwin himself records a few cases, which plainly show that the more beautiful is not always the more successful. It has also been suggested that the battles of the males are sometimes sham performances, and even when they are real, if the less vigorous do not remain to be destroyed but run away, they live to find mates of their own. In fact, the conduct of the males at the breeding season appears to be much more the outcome of their own excitement than an attempt to attract the females.

8. There is another side to the question, the importance of which is so great, that it is surprising that Darwin has not taken any notice of it. If, in order to bring about, or even maintain, the results of sexual selection, such a tremendous elimination of individuals must take place, it is surprising that natural selection would not counteract this by destroying those species in which a process, so useless for the welfare of the species, is going on. It is curious that this has not been realized by those who believe in both of these two hypotheses.

9. What has just been said applies also with almost equal force to the development of such structures as the horns of deer, bison, antelopes, and the brilliant colors of many insects and birds. If in nature, competition between species takes place on the scale that the Darwinian theory of natural selection postulates, such forms, if they are much exposed, would be needlessly reduced in numbers in the process of acquiring these structures. So many individuals would have been at such a disadvantage in breeding, that if competition is as severe as the theory of natural selection postulates, these species could hardly be expected to compete successfully with other species in which sexual selection was not taking place.

10. Darwin admits that, in certain cases, external conditions may have acted directly to produce the colors in certain forms, and if these were not injurious he thinks they might have become constant. Such cases are left unexplained in the sense that they are not supposed to be adaptations to anything in particular. That colors produced in this way might afterward be found useful, irrespective of how they arose, is admitted as one of the ways in which sexual differences may have arisen.

11. It is baffling to find Darwin resorting to the Lamarckian explanation in those cases in which the improbability of the hypothesis of sexual selection is manifest. If either principle is true, we should expect it to apply to all phenomena of the same sort; yet Darwin makes use of the Lamarckian principle, in the hypothesis of sexual selection, only when difficulties arise.

12. In attempting to explain the development of the musical sense in man, it is clear that the hypothesis of sexual selection fails to give a satisfactory explanation. To suppose that the genius of a Beethoven or of a Mozart could have been the result of a process of sexual selection is too absurd to discuss. Neither the power of appreciation nor of expression in music could possibly have been the outcome of such a process, and it does not materially help the problem to refer it back to a troop of monkeys making the woods hideous with their cries.

We come now to some of the special cases to which Darwin’s hypothesis has been applied.

13. In one case at least, it is stated that a bird living on the ground might have acquired the color of the upper surface of the body through natural selection, while the under surface of the males of the same species might have become ornamented through the action of sexual selection. Thus in one and the same individual the two processes are supposed to have been at work, and it does not lessen the difficulty very much by supposing the two processes to have been carried out at different times, because it is evident that what had been gained at one time by one process might become lost while the color of certain parts was being acquired through the other process.

14. Darwin points out that “the plumage of certain birds goes on increasing in beauty during many years after they are fully mature,” as in the peacock, and in some of the birds of paradise, and with the plumes and crests of some herons. This is explained as possibly merely the result of “continued growth.” The improbability of selection is manifest in these cases, but if “continued growth” can accomplish this much, why may not the whole process be also the outcome of such growth? At any rate, whatever the explanation is, it is important to find a case of a secondary sexual character that the hypothesis obviously is insufficient to explain.

15. It is admitted in a number of cases, as in the stag for instance, that, although the larynx of the male is enlarged, this is not, in all probability, the outcome of sexual selection, but in other forms this same enlargement is ascribed to the selection process.

16. It is admitted that in none of the highly colored British moths is there much difference according to sex, although when a difference of color is found in butterflies this is put down to the action of sexual selection. If such wonderful colors as those of moths can arise without the action of selection, why make a special explanation for those cases in which this difference is associated with sex?

17. It is well known that birds sing at other times of the year than at the breeding season, and an attempt is made to account for this in that birds take pleasure in practising those instincts that they make use of at other times, as the cat plays with the captive mouse. Does not this suggest that, if they had certain instincts, they would be more likely to employ them at the times when their vitality or excitement is at its highest without regard to the way in which they have come by them?

18. The color of the iris of the eyes of many species of hornbills is said to be an intense crimson in the males, and white in the females. In the male condor the eye is yellowish brown, and in the female a bright red. Darwin admits that it is doubtful if this difference is the result of sexual selection, since in the latter case the lining of the mouth is black in the males, and flesh-colored in the females, which does not affect the external beauty. Yet if these colors were more extensive and on the exterior, there can be little doubt that they would have been explained as due to sexual selection.

19. When the females in certain species of birds differ more from each other than they do from their respective males, the case is compared to “those inexplicable ones, which occur independently of man’s selection in certain sub-breeds of the game-fowl, in which the females are very different, whilst the males can hardly be distinguished.” Here then is a case of difference in color associated with sex, but not the outcome of sexual selection.

20. The long hairs on the throat of the stag are said possibly to be of use to him when hunted, since the dogs generally seize him by the throat, “but it is not probable that the hairs were specially developed for this purpose; otherwise the young and the females would have been equally protected.” Here also is a sexual difference that can scarcely be ascribed to selection.

Some cases of differences in color between the sexes “may be the result of variations confined to one sex, and transmitted to the same sex without any good being gained, and, therefore, without the aid of selection. We have instances of this with our domesticated animals, as in the males of certain cats being rusty-red while the females are tortoise-shell colored. Analogous cases occur in nature: Mr. Bartlett has seen many black varieties of the jaguar, leopard, vulpine phalanger, and wombat; and he is certain that all or nearly all of these animals were males.” If changes of this sort occur, associated with one sex, why is there any need of a special explanation in other cases of difference?

In the light of the many difficulties that the theory of sexual selection meets with, I think we shall be justified in rejecting it as an explanation of the secondary sexual differences amongst animals. Other attempts to explain these differences have been equally unsuccessful. Thus Wallace accounts for them as due to the excessive vigor of the male, but Darwin’s reply to Wallace appears to show that this is not the cause of the difference. He points out that, while the hypothesis might appear plausible in the case of color, it is not so evident in the case of other secondary sexual characters, such, for instance, as the musical apparatus of the males of certain insects, and the difference in the size of the larynx of certain birds and mammals.

Darwin’s theory served to draw attention to a large number of most interesting differences between the sexes, and, even if it prove to be a fiction, it has done much good in bringing before us an array of important facts in regard to differences in secondary sexual characters. More than this I do not believe it has done. The theory meets with fatal objections at every turn.

In a later chapter the question will be more fully discussed as to the sense in which these secondary sexual differences may be looked upon as adaptations.