Some male beetles, which seem ill-fitted for fighting, nevertheless engage in conflicts for the possession of the females. Mr. Wallace (68. ‘The Malay Archipelago,’ vol. ii. 1869, p. 276. Riley, Sixth ‘Report on Insects of Missouri,’ 1874, p. 115.) saw two males of Leptorhynchus angustatus, a linear beetle with a much elongated rostrum, “fighting for a female, who stood close by busy at her boring. They pushed at each other with their rostra, and clawed and thumped, apparently in the greatest rage.” The smaller male, however, “soon ran away, acknowledging himself vanquished.” In some few cases male beetles are well adapted for fighting, by possessing great toothed mandibles, much larger than those of the females. This is the case with the common stag-beetle (Lucanus cervus), the males of which emerge from the pupal state about a week before the other sex, so that several may often be seen pursuing the same female. At this season they engage in fierce conflicts. When Mr. A.H. Davis (69. ‘Entomological Magazine,’ vol. i. 1833, p. 82. See also on the conflicts of this species, Kirby and Spence, ibid. vol. iii. p. 314; and Westwood, ibid. vol. i. p. 187.) enclosed two males with one female in a box, the larger male severely pinched the smaller one, until he resigned his pretensions. A friend informs me that when a boy he often put the males together to see them fight, and he noticed that they were much bolder and fiercer than the females, as with the higher animals. The males would seize hold of his finger, if held in front of them, but not so the females, although they have stronger jaws. The males of many of the Lucanidae, as well as of the above-mentioned Leptorhynchus, are larger and more powerful insects than the females. The two sexes of Lethrus cephalotes (one of the Lamellicorns) inhabit the same burrow; and the male has larger mandibles than the female. If, during the breeding-season, a strange male attempts to enter the burrow, he is attacked; the female does not remain passive, but closes the mouth of the burrow, and encourages her mate by continually pushing him on from behind; and the battle lasts until the aggressor is killed or runs away. (70. Quoted from Fischer, in ‘Dict. Class. d’Hist. Nat.’ tom. x. p. 324.) The two sexes of another Lamellicorn beetle, the Ateuchus cicatricosus, live in pairs, and seem much attached to each other; the male excites the females to roll the balls of dung in which the ova are deposited; and if she is removed, he becomes much agitated. If the male is removed the female ceases all work, and as M. Brulerie believes, would remain on the same spot until she died. (71. ‘Ann. Soc. Entomolog. France,’ 1866, as quoted in ‘Journal of Travel,’ by A. Murray, 1868, p. 135.)

Figure 24: Chiasognathus Grantii, reduced.
Upper figure, male;
lower figure, female.

The great mandibles of the male Lucanidae are extremely variable both in size and structure, and in this respect resemble the horns on the head and thorax of many male Lamellicorns and Staphylinidae. A perfect series can be formed from the best-provided to the worst-provided or degenerate males. Although the mandibles of the common stag-beetle, and probably of many other species, are used as efficient weapons for fighting, it is doubtful whether their great size can thus be accounted for. We have seen that they are used by the Lucanus elaphus of N. America for seizing the female. As they are so conspicuous and so elegantly branched, and as owing to their great length they are not well adapted for pinching, the suspicion has crossed my mind that they may in addition serve as an ornament, like the horns on the head and thorax of the various species above described. The male Chiasognathus grantii of S. Chile–a splendid beetle belonging to the same family–has enormously developed mandibles (Fig. 24); he is bold and pugnacious; when threatened he faces round, opens his great jaws, and at the same time stridulates loudly. But the mandibles were not strong enough to pinch my finger so as to cause actual pain.

Sexual selection, which implies the possession of considerable perceptive powers and of strong passions, seems to have been more effective with the Lamellicorns than with any other family of beetles. With some species the males are provided with weapons for fighting; some live in pairs and shew mutual affection; many have the power of stridulating when excited; many are furnished with the most extraordinary horns, apparently for the sake of ornament; and some, which are diurnal in their habits, are gorgeously coloured. Lastly, several of the largest beetles in the world belong to this family, which was placed by Linnaeus and Fabricius as the head of the Order. (72. Westwood, ‘Modern Classification,’ vol. i. p. 184.)

Stridulating Organs

Beetles belonging to many and widely distinct families possess these organs. The sound thus produced can sometimes be heard at the distance of several feet or even yards (73. Wollaston, ‘On Certain Musical Curculionidae,’ ‘Annals and Mag. of Nat. Hist.’ vol. vi. 1860, p. 14.), but it is not comparable with that made by the Orthoptera. The rasp generally consists of a narrow, slightly-raised surface, crossed by very fine, parallel ribs, sometimes so fine as to cause iridescent colours, and having a very elegant appearance under the microscope. In some cases, as with Typhoeus, minute, bristly or scale-like prominences, with which the whole surrounding surface is covered in approximately parallel lines, could be traced passing into the ribs of the rasp. The transition takes place by their becoming confluent and straight, and at the same time more prominent and smooth. A hard ridge on an adjoining part of the body serves as the scraper for the rasp, but this scraper in some cases has been specially modified for the purpose. It is rapidly moved across the rasp, or conversely the rasp across the scraper.

Figure 25: Necrophorus (from Landois).
r. The two rasps.
Left-hand figure, part of the rasp highly magnified.

These organs are situated in widely different positions. In the carrion-beetles (Necrophorus) two parallel rasps (r, Fig. 25) stand on the dorsal surface of the fifth abdominal segment, each rasp (74. Landois, ‘Zeitschrift fur wissenschaft Zoolog.’ B. xvii. 1867, s. 127.) consisting of 126 to 140 fine ribs. These ribs are scraped against the posterior margins of the elytra, a small portion of which projects beyond the general outline. In many Crioceridae, and in Clythra 4-punctata (one of the Chrysomelidae), and in some Tenebrionidae, etc. (75. I am greatly indebted to Mr. G.R. Crotch for having sent me many prepared specimens of various beetles belonging to these three families and to others, as well as for valuable information. He believes that the power of stridulation in the Clythra has not been previously observed. I am also much indebted to Mr. E.W. Janson, for information and specimens. I may add that my son, Mr. F. Darwin, finds that Dermestes murinus stridulates, but he searched in vain for the apparatus. Scolytus has lately been described by Dr. Chapman as a stridulator, in the ‘Entomologist’s Monthly Magazine,’ vol. vi. p. 130.), the rasp is seated on the dorsal apex of the abdomen, on the pygidium or pro-pygidium, and is scraped in the same manner by the elytra. In Heterocerus, which belongs to another family, the rasps are placed on the sides of the first abdominal segment, and are scraped by ridges on the femora. (76. Schiodte, translated, in ‘Annals and Magazine of Natural History,’ vol. xx. 1867, p. 37.) In certain Curculionidae and Carabidae (77. Westring has described (Kroyer, ‘Naturhist. Tidskrift,’ B. ii. 1848-49, p. 334) the stridulating organs in these two, as well as in other families. In the Carabidae I have examined Elaphrus uliginosus and Blethisa multipunctata, sent to me by Mr. Crotch. In Blethisa the transverse ridges on the furrowed border of the abdominal segment do not, as far as I could judge, come into play in scraping the rasps on the elytra.), the parts are completely reversed in position, for the rasps are seated on the inferior surface of the elytra, near their apices, or along their outer margins, and the edges of the abdominal segments serve as the scrapers. In Pelobius Hermanni (one of Dytiscidae or water-beetles) a strong ridge runs parallel and near to the sutural margin of the elytra, and is crossed by ribs, coarse in the middle part, but becoming gradually finer at both ends, especially at the upper end; when this insect is held under water or in the air, a stridulating noise is produced by the extreme horny margin of the abdomen being scraped against the rasps. In a great number of long-horned beetles (Longicornia) the organs are situated quite otherwise, the rasp being on the meso-thorax, which is rubbed against the pro-thorax; Landois counted 238 very fine ribs on the rasp of Cerambyx heros.

Many beetles are coloured so as to resemble the surfaces which they habitually frequent, and they thus escape detection by their enemies. Other species, for instance diamond-beetles, are ornamented with splendid colours, which are often arranged in stripes, spots, crosses, and other elegant patterns. Such colours can hardly serve directly as a protection, except in the case of certain flower-feeding species; but they may serve as a warning or means of recognition, on the same principle as the phosphorescence of the glow-worm. As with beetles the colours of the two sexes are generally alike, we have no evidence that they have been gained through sexual selection; but this is at least possible, for they have been developed in one sex and then transferred to the other; and this view is even in some degree probable in those groups which possess other well-marked secondary sexual characters. Blind beetles, which cannot of course behold each other’s beauty, never, as I hear from Mr. Waterhouse, jun., exhibit bright colours, though they often have polished coats; but the explanation of their obscurity may be that they generally inhabit caves and other obscure stations.

Some Longicorns, especially certain Prionidae, offer an exception to the rule that the sexes of beetles do not differ in colour. Most of these insects are large and splendidly coloured. The males in the genus Pyrodes (63. Pyrodes pulcherrimus, in which the sexes differ conspicuously, has been described by Mr. Bates in ‘Transact. Ent. Soc.’ 1869, p. 50. I will specify the few other cases in which I have heard of a difference in colour between the sexes of beetles. Kirby and Spence (‘Introduct. to Entomology,’ vol. iii. p. 301) mention a Cantharis, Meloe, Rhagium, and the Leptura testacea; the male of the latter being testaceous, with a black thorax, and the female of a dull red all over. These two latter beetles belong to the family of Longicorns. Messrs. R. Trimen and Waterhouse, jun., inform me of two Lamellicorns, viz., a Peritrichia and Trichius, the male of the latter being more obscurely coloured than the female. In Tillus elongatus the male is black, and the female always, as it is believed, of a dark blue colour, with a red thorax. The male, also, of Orsodacna atra, as I hear from Mr. Walsh, is black, the female (the so-called O. ruficollis) having a rufous thorax.), which I saw in Mr. Bates’s collection, are generally redder but rather duller than the females, the latter being coloured 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 colour 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 Prionidae, in which the sexes differ, are coloured more richly than the males, and this does not accord with the common rule in regard to colour, when acquired through sexual selection.

Figure 16: Chalcosoma atlas.
Upper figure, male (reduced);
lower figure, female (nat. size).

Figure 17: Copris isidis.

Figure 18: Phanaeus faunus.

Figure 19: Dipelicus cantori.

Figure 20: Onthophagus rangifer, enlarged. (In Figs. 17 to 20 the left-hand figures are males.)

A most remarkable distinction between the sexes of many beetles is presented by the great horns which rise from the head, thorax, and clypeus of the males; and in some few cases from the under surface of the body. These horns, in the great family of the Lamellicorns, resemble those of various quadrupeds, such as stags, rhinoceroses, etc., and are wonderful both from their size and diversified shapes. Instead of describing them, I have given figures of the males and females of some of the more remarkable forms. (Figs. 16 to 20.) The females generally exhibit rudiments of the horns in the form of small knobs or ridges; but some are destitute of even the slightest rudiment. On the other hand, the horns are nearly as well developed in the female as in the male Phanaeus lancifer; and only a little less well developed in the females of some other species of this genus and of Copris. I am informed by Mr. Bates that the horns do not differ in any manner corresponding with the more important characteristic differences between the several subdivisions of the family: thus within the same section of the genus Onthophagus, there are species which have a single horn, and others which have two.

In almost all cases, the horns are remarkable from their excessive variability; so that a graduated series can be formed, from the most highly developed males to others so degenerate that they can barely be distinguished from the females. Mr. Walsh (64. ‘Proceedings of the Entomological Society of Philadephia,’ 1864, p. 228.) found that in Phanaeus carnifex the horns were thrice as long in some males as in others. Mr. Bates, after examining above a hundred males of Onthophagus rangifer (Fig. 20), thought that he had at last discovered a species in which the horns did not vary; but further research proved the contrary.

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 shew marks of friction, as if used for any ordinary work. Some authors suppose (65. Kirby and Spence, ‘Introduction to Entomology,’ vol. iii. P. 300.) 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 Copridae, 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 shewn 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.

Figure 21: Onitis furcifer, male viewed from beneath.

Figure 22: Onitis furcifer.
Left-hand figure, male, viewed laterally.
Right-hand figure, female.
a. Rudiment of cephalic horn.
b. Trace of thoracic horn or crest.

The males of Onitis furcifer (Fig. 21), and of some other species of the genus, are furnished with singular projections on their anterior femora, and with a great fork or pair of horns on the lower surface of the thorax. Judging from other insects, these may aid the male in clinging to the female. Although the males have not even a trace of a horn on the upper surface of the body, yet the females plainly exhibit a rudiment of a single horn on the head (Fig. 22, a), and of a crest (b) on the thorax. That the slight thoracic crest in the female is a rudiment of a projection proper to the male, though entirely absent in the male of this particular species, is clear: for the female of Bubas bison (a genus which comes next to Onitis) has a similar slight crest on the thorax, and the male bears a great projection in the same situation. So, again, there can hardly be a doubt that the little point (a) on the head of the female Onitis furcifer, as well as on the head of the females of two or three allied species, is a rudimentary representative of the cephalic horn, which is common to the males of so many Lamellicorn beetles, as in Phanaeus (Fig. 18).

The old belief that rudiments have been created to complete the scheme of nature is here so far from holding good, that we have a complete inversion of the ordinary state of things in the family. We may reasonably suspect that the males originally bore horns and transferred them to the females in a rudimentary condition, as in so many other Lamellicorns. Why the males subsequently lost their horns, we know not; but this may have been caused through the principle of compensation, owing to the development of the large horns and projections on the lower surface; and as these are confined to the males, the rudiments of the upper horns on the females would not have been thus obliterated.

Figure 23: Bledius taurus, magnified.
Left-hand figure, male;
right-hand figure, female.

The cases hitherto given refer to the Lamellicorns, but the males of some few other beetles, belonging to two widely distinct groups, namely, the Curculionidae and Staphylinidae, are furnished with horns–in the former on the lower surface of the body (66. Kirby and Spence, ‘Introduction to Entomology,’ vol. iii. p. 329.), in the latter on the upper surface of the head and thorax. In the Staphylinidae, the horns of the males are extraordinarily variable in the same species, just as we have seen with the Lamellicorns. In Siagonium we have a case of dimorphism, for the males can be divided into two sets, differing greatly in the size of their bodies and in the development of their horns, without intermediate gradations. In a species of Bledius (Fig. 23), also belonging to the Staphylinidae, Professor Westwood states that, “male specimens can be found in the same locality in which the central horn of the thorax is very large, but the horns of the head quite rudimental; and others, in which the thoracic horn is much shorter, whilst the protuberances on the head are long.” (67. ‘Modern Classification of Insects,’ vol. i. p. 172: Siagonium, p. 172. In the British Museum I noticed one male specimen of Siagonium in an intermediate condition, so that the dimorphism is not strict.) Here we apparently have a case of compensation, which throws light on that just given, of the supposed loss of the upper horns by the males of Onitis.

Little need here be said, except as to colour. In the Ephemeridae the sexes often differ slightly in their obscure tints (49. B.D. Walsh, the ‘Pseudo-neuroptera of Illinois,’ in ‘Proceedings of the Entomological Society of Philadelphia,’ 1862, p. 361.); but it is not probable that the males are thus rendered attractive to the females. The Libellulidae, or dragon-flies, are ornamented with splendid green, blue, yellow, and vermilion metallic tints; and the sexes often differ. Thus, as Prof. Westwood remarks (50. ‘Modern Classification,’ vol. ii. p. 37.), the males of some of the Agrionidae, “are of a rich blue with black wings, whilst the females are fine green with colourless wings.” But in Agrion Ramburii these colours are exactly reversed in the two sexes. (51. Walsh, ibid. p. 381. I am indebted to this naturalist for the following facts on Hetaerina, Anax, and Gomphus.) In the extensive N. American genus of Hetaerina, the males alone have a beautiful carmine spot at the base of each wing. In Anax junius the basal part of the abdomen in the male is a vivid ultramarine blue, and in the female grass-green. In the allied genus Gomphus, on the other hand, and in some other genera, the sexes differ but little in colour. In closely-allied forms throughout the animal kingdom, similar cases of the sexes differing greatly, or very little, or not at all, are of frequent occurrence. Although there is so wide a difference in colour between the sexes of many Libellulidae, it is often difficult to say which is the more brilliant; and the ordinary coloration of the two sexes is reversed, as we have just seen, in one species of Agrion. It is not probable that their colours in any case have been gained as a protection. Mr. MacLachlan, who has closely attended to this family, writes to me that dragon-flies–the tyrants of the insect-world–are the least liable of any insect to be attacked by birds or other enemies, and he believes that their bright colours serve as a sexual attraction. Certain dragon-flies apparently are attracted by particular colours: Mr. Patterson observed (52. ‘Transactions, Ent. Soc.’ vol. i. 1836, p. lxxxi.) that the Agrionidae, of which the males are blue, settled in numbers on the blue float of a fishing line; whilst two other species were attracted by shining white colours.

It is an interesting fact, first noticed by Schelver, that, in several genera belonging to two sub-families, the males on first emergence from the pupal state, are coloured exactly like the females; but that their bodies in a short time assume a conspicuous milky-blue tint, owing to the exudation of a kind of oil, soluble in ether and alcohol. Mr. MacLachlan believes that in the male of Libellula depressa this change of colour does not occur until nearly a fortnight after the metamorphosis, when the sexes are ready to pair.

Certain species of Neurothemis present, according to Brauer (53. See abstract in the ‘Zoological Record’ for 1867, p. 450.), a curious case of dimorphism, some of the females having ordinary wings, whilst others have them “very richly netted, as in the males of the same species.” Brauer “explains the phenomenon on Darwinian principles by the supposition that the close netting of the veins is a secondary sexual character in the males, which has been abruptly transferred to some of the females, instead of, as generally occurs, to all of them.” Mr. MacLachlan informs me of another instance of dimorphism in several species of Agrion, in which some individuals are of an orange colour, and these are invariably females. This is probably a case of reversion; for in the true Libellulae, when the sexes differ in colour, the females are orange or yellow; so that supposing Agrion to be descended from some primordial form which resembled the typical Libellulae in its sexual characters, it would not be surprising that a tendency to vary in this manner should occur in the females alone.

Although many dragon-flies are large, powerful, and fierce insects, the males have not been observed by Mr. MacLachlan to fight together, excepting, as he believes, in some of the smaller species of Agrion. In another group in this Order, namely, the Termites or white ants, both sexes at the time of swarming may be seen running about, “the male after the female, sometimes two chasing one female, and contending with great eagerness who shall win the prize.” (54. Kirby and Spence, ‘Introduction to Entomology,’ vol. ii. 1818, p. 35.) The Atropos pulsatorius is said to make a noise with its jaws, which is answered by other individuals. (55. Houzeau, ‘Les Facultes Mentales,’ etc. Tom. i. p. 104.)

Order, Hymenoptera

That inimitable observer, M. Fabre (56. See an interesting article, ‘The Writings of Fabre,’ in ‘Nat. Hist. Review,’ April 1862, p. 122.), in describing the habits of Cerceris, a wasp-like insect, remarks that “fights frequently ensue between the males for the possession of some particular female, who sits an apparently unconcerned beholder of the struggle for supremacy, and when the victory is decided, quietly flies away in company with the conqueror.” Westwood (57. ‘Journal of Proceedings of Entomological Society,’ Sept. 7, 1863, p. 169.) says that the males of one of the saw-flies (Tenthredinae) “have been found fighting together, with their mandibles locked.” As M. Fabre speaks of the males of Cerceris striving to obtain a particular female, it may be well to bear in mind that insects belonging to this Order have the power of recognising each other after long intervals of time, and are deeply attached. For instance, Pierre Huber, whose accuracy no one doubts, separated some ants, and when, after an interval of four months, they met others which had formerly belonged to the same community, they recognised and caressed one another with their antennae. Had they been strangers they would have fought together. Again, when two communities engage in a battle, the ants on the same side sometimes attack each other in the general confusion, but they soon perceive their mistake, and the one ant soothes the other. (58. P. Huber, ‘Recherches sur les Moeurs des Fourmis,’ 1810, pp. 150, 165.)

In this Order slight differences in colour, 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 coloured–for instance in Chrysis, in which vermilion and metallic greens prevail–that we are tempted to attribute the result to sexual selection. In the Ichneumonidae, according to Mr. Walsh (59. ‘Proceedings of the Entomological Society of Philadelphia,’ 1866, pp. 238, 239.), the males are almost universally lighter-coloured than the females. On the other hand, in the Tenthredinidae the males are generally darker than the females. In the Siricidae 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 Tremex columbae the female is much brighter coloured than the male. I am informed by Mr. F. Smith, that the male ants of several species are black, the females being testaceous.

In the family of Bees, especially in the solitary species, as I hear from the same entomologist, the sexes often differ in colour. The males are generally the brighter, and in Bombus as well as in Apathus, much more variable in colour than the females. In Anthophora retusa the male is of a rich fulvous-brown, whilst the female is quite black: so are the females of several species of Xylocopa, the males being bright yellow. On the other hand the females of some species, as of Andraena fulva, are much brighter coloured than the males. Such differences in colour can hardly be accounted for by the males being defenceless and thus requiring protection, whilst the females are well defended by their stings. H. Muller (60. ‘Anwendung der Darwinschen Lehre auf Bienen,’ Verh. d. n. V. Jahrg. xxix.), who has particularly attended to the habits of bees, attributes these differences in colour in chief part to sexual selection. That bees have a keen perception of colour is certain. He says that the males search eagerly and fight for the possession of the females; and he accounts through such contests for the mandibles of the males being in certain species larger than those of the females. In some cases the males are far more numerous than the females, either early in the season, or at all times and places, or locally; whereas the females in other cases are apparently in excess. 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 (Muller, p. 42), the males of the several species differ much in appearance, whilst the females are almost indistinguishable; in other genera the reverse occurs. H. Muller believes (p. 82) that the colours 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. (61. M. Perrier in his article ‘la Selection sexuelle d’apres Darwin’ (‘Revue Scientifique,’ Feb. 1873, p. 868), without apparently having reflected much on the subject, objects that as the males of social bees are known to be produced from unfertilised ova, they could not transmit new characters to their male offspring. This is an extraordinary objection. A female bee fertilised by a male, which presented some character facilitating the union of the sexes, or rendering him more attractive to the female, would lay eggs which would produce only females; but these young females would next year produce males; and will it be pretended that such males would not inherit the characters of their male grandfathers? To take a case with ordinary animals as nearly parallel as possible: if a female of any white quadruped or bird were crossed by a male of a black breed, and the male and female offspring were paired together, will it be pretended that the grandchildren would not inherit a tendency to blackness from their male grandfather? The acquirement of new characters by the sterile worker-bees is a much more difficult case, but I have endeavoured to shew in my ‘Origin of Species,’ how these sterile beings are subjected to the power of natural selection.)

Mutilla Europaea makes a stridulating noise; and according to Goureau (62. Quoted by Westwood, ‘Modern Classification of Insects,’ vol. ii. p. 214.) both sexes have this power. He attributes the sound to the friction of the third and preceding abdominal segments, and I find that these surfaces are marked with very fine concentric ridges; but so is the projecting thoracic collar into which the head articulates, and this collar, when scratched with the point of a needle, emits the proper sound. It is rather surprising that both sexes should have the power of stridulating, as the male is winged and the female wingless. It is notorious that Bees express certain emotions, as of anger, by the tone of their humming; and according to H. Muller (p. 80), the males of some species make a peculiar singing noise whilst pursuing the females.

Figure 13: Chlorocoelus Tanana (from Bates). a,b. Lobes of opposite wing-covers.

In the Locustidae the opposite wing-covers differ from each other in structure (Fig. 13), and the action cannot, as in the last family, be reversed. The left wing, which acts as the bow, lies over the right wing which serves as the fiddle. One of the nervures (a) on the under surface of the former is finely serrated, and is scraped across the prominent nervures on the upper surface of the opposite or right wing. In our British Phasgonura viridissima it appeared to me that the serrated nervure is rubbed against the rounded hind-corner of the opposite wing, the edge of which is thickened, coloured brown, and very sharp. In the right wing, but not in the left, there is a little plate, as transparent as talc, surrounded by nervures, and called the speculum. In Ephippiger vitium, a member of this same family, we have a curious subordinate modification; for the wing-covers are greatly reduced in size, but “the posterior part of the pro-thorax is elevated into a kind of dome over the wing-covers, and which has probably the effect of increasing the sound.” (37. Westwood ‘Modern Classification of Insects,’ vol. i. p. 453.)

We thus see that the musical apparatus is more differentiated or specialised in the Locustidae (which include, I believe, the most powerful performers in the Order), than in the Achetidae, in which both wing-covers have the same structure and the same function. (38. Landois, ‘Zeitschrift fur wissenschaft Zoolog.’ B. xvii. 1867, ss. 121, 122.) Landois, however, detected in one of the Locustidae, namely in Decticus, a short and narrow row of small teeth, mere rudiments, on the inferior surface of the right wing-cover, which underlies the other and is never used as the bow. I observed the same rudimentary structure on the under side of the right wing-cover in Phasgonura viridissima. Hence we may infer with confidence that the Locustidae are descended from a form, in which, as in the existing Achetidae, both wing-covers had serrated nervures on the under surface, and could be indifferently used as the bow; but that in the Locustidae the two wing-covers gradually became differentiated and perfected, on the principle of the division of labour, the one to act exclusively as the bow, and the other as the fiddle. Dr. Gruber takes the same view, and has shewn that rudimentary teeth are commonly found on the inferior surface of the right wing. By what steps the more simple apparatus in the Achetidae originated, we do not know, but it is probable that the basal portions of the wing-covers originally overlapped each other as they do at present; and that the friction of the nervures produced a grating sound, as is now the case with the wing-covers of the females. (39. Mr. Walsh also informs me that he has noticed that the female of the Platyphyllum concavum, “when captured makes a feeble grating noise by shuffling her wing-covers together.”) A grating sound thus occasionally and accidentally made by the males, if it served them ever so little as a love-call to the females, might readily have been intensified through sexual selection, by variations in the roughness of the nervures having been continually preserved.

Figure 14: Hind-leg of Stenobothrus pratorum: r, the stridulating ridge; lower figure, the teeth forming the ridge, much magnified (from Landois).

Figure 15: Pneumora (from specimens in the British Museum).
Upper figure, male;
lower figure, female.

In the last and third family, namely the Acridiidae or grasshoppers, the stridulation is produced in a very different manner, and according to Dr. Scudder, is not so shrill as in the preceding Families. The inner surface of the femur (Fig. 14, r) is furnished with a longitudinal row of minute, elegant, lancet-shaped, elastic teeth, from 85 to 93 in number (40. Landois, ibid. s. 113.); and these are scraped across the sharp, projecting nervures on the wing-covers, which are thus made to vibrate and resound. Harris (41. ‘Insects of New England,’ 1842, p. 133.) says that when one of the males begins to play, he first “bends the shank of the hind-leg beneath the thigh, where it is lodged in a furrow designed to receive it, and then draws the leg briskly up and down. He does not play both fiddles together, but alternately, first upon one and then on the other.” In many species, the base of the abdomen is hollowed out into a great cavity which is believed to act as a resounding board. In Pneumora (Fig. 15), a S. African genus belonging to the same family, we meet with a new and remarkable modification; in the males a small notched ridge projects obliquely from each side of the abdomen, against which the hind femora are rubbed. (42. Westwood, ‘Modern Classification,’ vol i. p. 462.) As the male is furnished with wings (the female being wingless), it is remarkable that the thighs are not rubbed in the usual manner against the wing-covers; but this may perhaps be accounted for by the unusually small size of the hind-legs. I have not been able to examine the inner surface of the thighs, which, judging from analogy, would be finely serrated. The species of Pneumora have been more profoundly modified for the sake of stridulation than any other orthopterous insect; for in the male the whole body has been converted into a musical instrument, being distended with air, like a great pellucid bladder, so as to increase the resonance. Mr. Trimen informs me that at the Cape of Good Hope these insects make a wonderful noise during the night.

In the three foregoing families, the females are almost always destitute of an efficient musical apparatus. But there are a few exceptions to this rule, for Dr. Gruber has shewn that both sexes of Ephippiger vitium are thus provided; though the organs differ in the male and female to a certain extent. 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. In most other Locustidae (but not according to Landois in Decticus) the females have rudiments of the stridulatory organs proper to the male; from whom it is probable that these have been transferred. Landois also found such rudiments on the under surface of the wing-covers of the female Achetidae, and on the femora of the female Acridiidae. In the Homoptera, also, the females have the proper musical apparatus in a functionless state; and we shall hereafter meet in other divisions of the animal kingdom with many instances of structures proper to the male being present in a rudimentary condition of the female.

Landois has observed another important fact, namely, that in the females of the Acridiidae, the stridulating teeth on the femora remain throughout life in the same condition in which they first appear during the larval state in both sexes. In the males, on the other hand, they become further developed, and acquire their perfect structure at the last moult, when the insect is mature and ready to breed.

From the facts now given, we see that the means by which the males of the Orthoptera produce their sounds are extremely diversified, and are altogether different from those employed by the Homoptera. (43. Landois has recently found in certain Orthoptera rudimentary structures closely similar to the sound-producing organs in the Homoptera; and this is a surprising fact. See ‘Zeitschrift fur wissenschaft Zoolog.’ B. xxii. Heft 3, 1871, p. 348.) But throughout the animal kingdom we often find the same object gained by the most diversified means; this seems due to the whole organisation having undergone multifarious changes in the course of ages, and as part after part varied different variations were taken advantage of for the same general purpose. The diversity of means for producing sound in the three families of the Orthoptera and in the Homoptera, impresses the mind with the high importance of these structures to the males, for the sake of calling or alluring the females. We need feel no surprise at the amount of modification which the Orthoptera have undergone in this respect, as we now know, from Dr. Scudder’s remarkable discovery (44. ‘Transactions, Entomological Society,’ 3rd series, vol. ii. (‘Journal of Proceedings,’ p. 117).), that there has been more than ample time. This naturalist has lately found a fossil insect in the Devonian formation of New Brunswick, which is furnished with “the well-known tympanum or stridulating apparatus of the male Locustidae.” The insect, though in most respects related to the Neuroptera, appears, as is so often the case with very ancient forms, to connect the two related Orders of the Neuroptera and Orthoptera.

I have but little more to say on the Orthoptera. Some of the species are very pugnacious: when two male field-crickets (Gryllus campestris) are confined together, they fight till one kills the other; and the species of Mantis are described as manoeuvring with their sword-like front-limbs, like hussars with their sabres. The Chinese keep these insects in little bamboo cages, and match them like game-cocks. (45. Westwood, ‘Modern Classification of Insects,’ vol. i. p. 427; for crickets, p. 445.) With respect to colour, some exotic locusts are beautifully ornamented; the posterior wings being marked with red, blue, and black; but as throughout the Order the sexes rarely differ much in colour, it is not probable that they owe their bright tints to sexual selection. Conspicuous colours may be of use to these insects, by giving notice that they are unpalatable. Thus it has been observed (46. Mr. Ch. Horne, in ‘Proceedings of the Entomological Society,’ May 3, 1869, p. xii.) that a bright-coloured Indian locust was invariably rejected when offered to birds and lizards. Some cases, however, are known of sexual differences in colour in this Order. The male of an American cricket (47. The Oecanthus nivalis, Harris, ‘Insects of New England,’ 1842, p. 124. The two sexes of OE. pellucidus of Europe differ, as I hear from Victor Carus, in nearly the same manner.) is described as being as white as ivory, whilst the female varies from almost white to greenish-yellow or dusky. Mr. Walsh informs me that the adult male of Spectrum femoratum (one of the Phasmidae) “is of a shining brownish-yellow colour; the adult female being of a dull, opaque, cinereous brown; the young of both sexes being green.” Lastly, I may mention that the male of one curious kind of cricket (48. Platyblemnus: Westwood, ‘Modern Classification,’ vol. i. p. 447.) is furnished with “a long membranous appendage, which falls over the face like a veil;” but what its use may be, is not known.

Every one who has wandered in a tropical forest must have been astonished at the din made by the male Cicadae. The females are mute; as the Grecian poet Xenarchus says, “Happy the Cicadas live, since they all have voiceless wives.” The noise thus made could be plainly heard on board the “Beagle,” when anchored at a quarter of a mile from the shore of Brazil; and Captain Hancock says it can be heard at the distance of a mile. The Greeks formerly kept, and the Chinese now keep these insects in cages for the sake of their song, so that it must be pleasing to the ears of some men. (23. These particulars are taken from Westwood’s ‘Modern Classification of Insects,’ vol. ii. 1840, p. 422. See, also, on the Fulgoridae, Kirby and Spence, ‘Introduct.’ vol. ii. p. 401.) The Cicadidae usually sing during the day, whilst the Fulgoridae appear to be night-songsters. The sound, according to Landois (24. ‘Zeitschrift fur wissenschaft Zoolog.’ B. xvii. 1867, ss. 152-158.), is produced by the vibration of the lips of the spiracles, which are set into motion by a current of air emitted from the tracheae; but this view has lately been disputed. Dr. Powell appears to have proved (25. ‘Transactions of the New Zealand Institute,’ vol. v. 1873, p. 286.) that it is produced by the vibration of a membrane, set into action by a special muscle. In the living insect, whilst stridulating, this membrane can be seen to vibrate; and in the dead insect the proper sound is heard, if the muscle, when a little dried and hardened, is pulled with the point of a pin. In the female the whole complex musical apparatus is present, but is much less developed than in the male, and is never used for producing sound.

With respect to the object of the music, Dr. Hartman, in speaking of the Cicada septemdecim of the United States, says (26. I am indebted to Mr. Walsh for having sent me this extract from ‘A Journal of the Doings of Cicada septemdecim,’ by Dr. Hartman.), “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 (Aug. 1868) a dwarf pear-tree in my garden produced about fifty larvae of Cic. pruinosa; and I several times noticed the females to alight near a male while he was uttering his clanging notes.” Fritz Muller 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.

I have not heard of any well-marked cases of ornamental differences between the sexes of the Homoptera. Mr. Douglas informs me that there are three British species, in which the male is black or marked with black bands, whilst the females are pale-coloured or obscure.

Order, Orthoptera (Crickets and Grasshoppers)

The males in the three saltatorial families in this Order are remarkable for their musical powers, namely the Achetidae or crickets, the Locustidae for which there is no equivalent English name, and the Acridiidae or grasshoppers. The stridulation produced by some of the Locustidae is so loud that it can be heard during the night at the distance of a mile (27. L. Guilding, ‘Transactions of the Linnean Society,’ vol. xv. p. 154.); and that made by certain species is not unmusical even to the human ear, so that the Indians on the Amazons keep them in wicker cages. All observers agree that the sounds serve either to call or excite the mute females. With respect to the migratory locusts of Russia, Korte has given (28. I state this on the authority of Koppen, ‘Uber die Heuschrecken in Sudrussland,’ 1866, p. 32, for I have in vain endeavoured to procure Korte’s work.) an interesting case of selection by the female of a male. The males of this species (Pachytylus migratorius) whilst coupled with the female stridulate from anger or jealousy, if approached by other males. The house-cricket when surprised at night uses its voice to warn its fellows. (29. Gilbert White, ‘Natural History of Selborne,’ vol. ii. 1825, p. 262.) In North America the Katy-did (Platyphyllum concavum, one of the Locustidae) is described (30. Harris, ‘Insects of New England,’ 1842, p. 128.) as mounting on the upper branches of a tree, and in the evening beginning “his noisy babble, while rival notes issue from the neighbouring trees, and the groves resound with the call of Katy-did-she-did the live-long night.” Mr. Bates, in speaking of the European field-cricket (one of the Achetidae), says “the male has been observed to place himself in the evening at the entrance of his burrow, and stridulate until a female approaches, when the louder notes are succeeded by a more subdued tone, whilst the successful musician caresses with his antennae the mate he has won.” (31. ‘The Naturalist on the Amazons,’ vol. i. 1863, p. 252. Mr. Bates gives a very interesting discussion on the gradations in the musical apparatus of the three families. See also Westwood, ‘Modern Classification of Insects,’ vol. ii. pp. 445 and 453.) Dr. Scudder was able to excite one of these insects to answer him, by rubbing on a file with a quill. (32. ‘Proceedings of the Boston Society of Natural History,’ vol. xi. April 1868.) In both sexes a remarkable auditory apparatus has been discovered by Von Siebold, situated in the front legs. (33. ‘Nouveau Manuel d’Anat. Comp.’ (French translat.), tom. 1, 1850, p. 567.)

Figure 11: Gryllus campestris (from Landois).
Right-hand figure, under side of part of a wing-nervure, much magnified, showing the teeth, st.
Left-hand figure, upper surface of wing-cover, with the projecting, smooth nervure, r, across which the teeth (st) are scraped.

Figure 12: Teeth of Nervure of Gryllus domesticus (from Landois).

In the three Families the sounds are differently produced. In the males of the Achetidae both wing-covers have the same apparatus; and this in the field-cricket (see Gryllus campestris, Fig. 11) consists, as described by Landois (34. ‘Zeitschrift fur wissenschaft. Zoolog.’ B. xvii. 1867, s. 117.), of from 131 to 138 sharp, transverse ridges or teeth (st) on the under side of one of the nervures of the wing-cover. This toothed nervure is rapidly scraped across a projecting, smooth, hard nervure (r) on the upper surface of the opposite wing. First one wing is rubbed over the other, and then the movement is reversed. Both wings are raised a little at the same time, so as to increase the resonance. In some species the wing-covers of the males are furnished at the base with a talc-like plate. (35. Westwood, ‘Modern Classification of Insects,’ vol. i. p. 440.) I here give a drawing (Fig. 12) of the teeth on the under side of the nervure of another species of Gryllus, viz., G. domesticus. With respect to the formation of these teeth, Dr. Gruber has shewn (36. ‘Ueber der Tonapparat der Locustiden, ein Beitrag zum Darwinismus,’ ‘Zeitschrift fur wissenschaft. Zoolog.’ B. xxii. 1872, p. 100.) that they have been developed by the aid of selection, from the minute scales and hairs with which the wings and body are covered, and I came to the same conclusion with respect to those of the Coleoptera. But Dr. Gruber further shews that their development is in part directly due to the stimulus from the friction of one wing over the other.

Figure 13: Chlorocoelus Tanana (from Bates). a,b. Lobes of opposite wing-covers.

In the Locustidae the opposite wing-covers differ from each other in structure (Fig. 13), and the action cannot, as in the last family, be reversed. The left wing, which acts as the bow, lies over the right wing which serves as the fiddle. One of the nervures (a) on the under surface of the former is finely serrated, and is scraped across the prominent nervures on the upper surface of the opposite or right wing. In our British Phasgonura viridissima it appeared to me that the serrated nervure is rubbed against the rounded hind-corner of the opposite wing, the edge of which is thickened, coloured brown, and very sharp. In the right wing, but not in the left, there is a little plate, as transparent as talc, surrounded by nervures, and called the speculum. In Ephippiger vitium, a member of this same family, we have a curious subordinate modification; for the wing-covers are greatly reduced in size, but “the posterior part of the pro-thorax is elevated into a kind of dome over the wing-covers, and which has probably the effect of increasing the sound.” (37. Westwood ‘Modern Classification of Insects,’ vol. i. p. 453.)