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

if slight, would, however, be difficult to detect, on account of their great variability. Thus, in the first pair of specimens of Necrophorus humator and of Pelobius which I examined, the rasp was considerably larger in the male than in the female; but not so with succeeding specimens. In Geotrupes stercorarius the rasp appeared to me thicker, opaquer, and more prominent in three males than in the same number of females; in order, therefore, to discover whether the sexes differed in their power of stridulating, my son, Mr. F. Darwin, collected fifty-seven living specimens, which he separated into two lots, according as they made a greater or lesser noise, when held in the same manner. He then examined all these specimens, and found that the males were very nearly in the same proportion to the females in both the lots. Mr. F. Smith has kept alive numerous specimens of Monoynchus pseudacori (Curculionidae), and is convinced that both sexes stridulate, and apparently in an equal degree.

Nevertheless, the power of stridulating is certainly a sexual character in some few Coleoptera. Mr. Crotch discovered that the males alone of two species of Heliopathes (Tenebrionidae) possess stridulating organs. I examined five males of H. gibbus, and in all these there was a well- developed rasp, partially divided into two, on the dorsal surface of the terminal abdominal segment; whilst in the same number of females there was not even a rudiment of the rasp, the membrane of this segment being transparent, and much thinner than in the male. In H. cribratostriatus the male has a similar rasp, excepting that it is not partially divided into two portions, and the female is completely destitute of this organ; the male in addition has on the apical margins of the elytra, on each side of the suture, three or four short longitudinal ridges, which are crossed by extremely fine ribs, parallel to and resembling those on the abdominal rasp; whether these ridges serve as an independent rasp, or as a scraper for the abdominal rasp, I could not decide: the female exhibits no trace of this latter structure.

Again, in three species of the Lamellicorn genus Oryctes, we have a nearly parallel case. In the females of O. gryphus and nasicornis the ribs on the rasp of the pro-pygidium are less continuous and less distinct than in the males; but the chief difference is that the whole upper surface of this segment, when held in the proper light, is seen to be clothed with hairs, which are absent or are represented by excessively fine down in the males. It should be noticed that in all Coleoptera the effective part of the rasp is destitute of hairs. In O. senegalensis the difference between the sexes is more strongly marked, and this is best seen when the proper abdominal segment is cleaned and viewed as a transparent object. In the female the whole surface is covered with little separate crests, bearing spines; whilst in the male these crests in proceeding towards the apex, become more and more confluent, regular, and naked; so that three-fourths of the segment is covered with extremely fine parallel ribs, which are quite absent in the female. In the females, however, of all three species of Oryctes, a slight grating or stridulating sound is produced, when the abdomen of a softened specimen is pushed backwards and forwards.

In the case of the Heliopathes and Oryctes there can hardly be a doubt that the males stridulate in order to call or to excite the females; but with most beetles the stridulation apparently serves both sexes as a mutual call. Beetles stridulate under various emotions, in the same manner as birds use their voices for many purposes besides singing to their mates. The great Chiasognathus stridulates in anger or defiance; many species do the same from distress or fear, if held so that they cannot escape; by striking the hollow stems of trees in the Canary Islands, Messrs. Wollaston and Crotch were able to discover the presence of beetles belonging to the genus Acalles by their stridulation. Lastly, the male Ateuchus stridulates to encourage the female in her work, and from distress when she is removed. (79. M. P. de la Brulerie, as quoted in ‘Journal of Travel,’ A. Murray, vol. i. 1868, p. 135.) Some naturalists believe that beetles make this noise to frighten away their enemies; but I cannot think that a quadruped or bird, able to devour a large beetle, would be frightened by so slight a sound. The belief that the stridulation serves as a sexual call is supported by the fact that death-ticks (Anobium tessellatum) are well known to answer each other’s ticking, and, as I have myself observed, a tapping noise artificially made. Mr. Doubleday also informs me that he has sometimes observed a female ticking (80. According to Mr. Doubleday, “the noise is produced by the insect raising itself on its legs as high as it can, and then striking its thorax five or six times, in rapid succession, against the substance upon which it is sitting.” For references on this subject see Landois, ‘Zeitschrift fur wissen. Zoolog.’ B. xvii. s. 131. Olivier says (as quoted by Kirby and Spence, ‘Introduction to Entomology,’ vol. ii. p. 395) that the female of Pimelia striata produces a rather loud sound by striking her abdomen against any hard substance, “and that the male, obedient to this call, soon attends her, and they pair.”), and in an hour or two afterwards has found her united with a male, and on one occasion surrounded by several males. Finally, it is probable that the two sexes of many kinds of beetles were at first enabled to find each other by the slight shuffling noise produced by the rubbing together of the adjoining hard parts of their bodies; and that as those males or females which made the greatest noise succeeded best in finding partners, rugosities on various parts of their bodies were gradually developed by means of sexual selection into true stridulating organs.

CHAPTER XI.

INSECTS, continued.

ORDER LEPIDOPTERA. (BUTTERFLIES AND MOTHS.)

Courtship of butterflies—Battles—Ticking noise—Colours common to both sexes, or more brilliant in the males—Examples—Not due to the direct action of the conditions of life—Colours adapted for protection—Colours of moths—Display—Perceptive powers of the Lepidoptera—Variability— Causes of the difference in colour between the males and females—Mimicry, female butterflies more brilliantly coloured than the males—Bright colours of caterpillars—Summary and concluding remarks on the secondary sexual characters of insects—Birds and insects compared.

In this great Order the most interesting points for us are the differences in colour between the sexes of the same species, and between the distinct species of the same genus. Nearly the whole of the following chapter will be devoted to this subject; but I will first make a few remarks on one or two other points. Several males may often be seen pursuing and crowding round the same female. Their courtship appears to be a prolonged affair, for I have frequently watched one or more males pirouetting round a female until I was tired, without seeing the end of the courtship. Mr. A.G. Butler also informs me that he has several times watched a male courting a female for a full quarter of an hour; but she pertinaciously refused him, and at last settled on the ground and closed her wings, so as to escape from his addresses.

Although butterflies are weak and fragile creatures, they are pugnacious, and an emperor butterfly (1. Apatura Iris: ‘The Entomologist’s Weekly Intelligence,’ 1859, p. 139. For the Bornean Butterflies, see C. Collingwood, ‘Rambles of a Naturalist,’ 1868, p. 183.) has been captured with the tips of its wings broken from a conflict with another male. Mr. Collingwood, in speaking of the frequent battles between the butterflies of Borneo, says, “They whirl round each other with the greatest rapidity, and appear to be incited by the greatest ferocity.”

The Ageronia feronia makes a noise like that produced by a toothed wheel passing under a spring catch, and which can be heard at the distance of several yards: I noticed this sound at Rio de Janeiro, only when two of these butterflies were chasing each other in an irregular course, so that it is probably made during the courtship of the sexes. (2. See my ‘Journal of Researches,’ 1845, p. 33. Mr. Doubleday has detected (‘Proc. Ent. Soc.’ March 3, 1845, p. 123) a peculiar membranous sac at the base of the front wings, which is probably connected with the production of the sound. For the case of Thecophora, see ‘Zoological Record,’ 1869, p. 401. For Mr. Buchanan White’s observations, the Scottish Naturalist, July 1872, p. 214.)

Some moths also produce sounds; for instance, the males Theocophora fovea. On two occasions Mr. F. Buchanan White (3. ‘The Scottish Naturalist,’ July 1872, p. 213.) heard a sharp quick noise made by the male of Hylophila prasinana, and which he believes to be produced, as in Cicada, by an elastic membrane, furnished with a muscle. He quotes, also, Guenee, that Setina produces a sound like the ticking of a watch, apparently by the aid of “two large tympaniform vesicles, situated in the pectoral region”; and these “are much more developed in the male than in the female.” Hence the sound-producing organs in the Lepidoptera appear to stand in some relation with the sexual functions. I have not alluded to the well-known noise made by the Death’s Head Sphinx, for it is generally heard soon after the moth has emerged from its cocoon.

Giard has always observed that the musky odour, which is emitted by two species of Sphinx moths, is peculiar to the males (4. ‘Zoological Record,’ 1869, p. 347.); and in the higher classes we shall meet with many instances of the males alone being odoriferous.

Every one must have admired the extreme beauty of many butterflies and of some moths; and it may be asked, are their colours and diversified patterns the result of the direct action of the physical conditions to which these insects have been exposed, without any benefit being thus derived? Or have successive variations been accumulated and determined as a protection, or for some unknown purpose, or that one sex may be attractive to the other? And, again, what is the meaning of the colours being widely different in the males and females of certain species, and alike in the two sexes of other species of the same genus? Before attempting to answer these questions a body of facts must be given.

With our beautiful English butterflies, the admiral, peacock, and painted lady (Vanessae), as well as many others, the sexes are alike. This is also the case with the magnificent Heliconidae, and most of the Danaidae in the tropics. But in certain other tropical groups, and in some of our English butterflies, as the purple emperor, orange-tip, etc. (Apatura Iris and Anthocharis cardamines), the sexes differ either greatly or slightly in colour. No language suffices to describe the splendour of the males of some tropical species. Even within the same genus we often find species presenting extraordinary differences between the sexes, whilst others have their sexes closely alike. Thus in the South American genus Epicalia, Mr. Bates, to whom I am indebted for most of the following facts, and for looking over this whole discussion, informs me that he knows twelve species, the two sexes of which haunt the same stations (and this is not always the case with butterflies), and which, therefore, cannot have been differently affected by external conditions. (5. See also Mr. Bates’s paper in ‘Proc. Ent. Soc. of Philadelphia,’ 1865, p. 206. Also Mr. Wallace on the same