Group 3.—In the species of this group the eye-spots are repeated on all the segments. I am acquainted with seven such Chærocampa larvæ, of which C. Bisecta, Horsfield,[83] shows some affinity to the foregoing group, since the eye-spots on segments 6–11 have not yet attained full perfection. In C. Odenlandiæ, Fabr.,[84] and in C. Alecto from India,[85] the eye-spots appear to be perfectly alike on all the segments; whilst in C. Acteus, Cram.,[86] and in the North American C. Tersa[87] ([Pl. IV]., Fig. 35) they are smaller on the other segments than on the fourth; and in C. Celerio, Linn., from India,[88] the size of the spots diminishes from the head to the tail.
In this group also the subdorsal line is retained in a very variable degree. In some species it appears to have completely vanished (C. Acteus, Celerio); in others it is present as a light stripe extending along all the segments (C. Alecto); whilst in others it is retained as a broad white stripe, which extends only to the fourth segment (C. Tersa, [Fig. 35]). In species possessing eye-spots, the subdorsal line is thus a very variable character. It is, however, an interesting fact that even in the present group, which has made the greatest step forward, the subdorsal line is of general occurrence, because the eye-spots in all these species may have almost a similar development to those of Elpenor and Porcellus. The ontogeny of the tropical species would alone give a definite reply on this point, but unfortunately we are not acquainted with any of the young forms, so that we can but presume that some of them at least would show only in the first stage the simple subdorsal line without eye-spots; that in the second stage the primary pairs of eye-spots would be formed on the fourth and fifth segments, whilst the transference of these spots to the remaining segments would take place in the last stage.
The foregoing assumption is based immediately on the ontogeny of Elpenor and Porcellus; it is supported by the considerable size attained by the eye-spots in many species of the third group, and would receive additional confirmation by observations on the Indian C. Celerio, supposing that Horsfield’s statements do not arise from a confusion of species. This skilful observer, who was the first to breed systematically a large number of tropical larvæ, has given a figure of the Indian caterpillar of C. Celerio, according to which this species possesses eye-spots on all the segments from the fourth to the tenth. The European form of this same species has eye-spots only on segments four and five, a fact which does not appear to have been known to Horsfield, as no mention of it is made in his notice of the Indian species. If the caterpillar figured is really that of Celerio, which I consider to be by no means improbable, not only is it thus shown that in the species of the third group the ocelli on the hind segments have a secondary origin through a repetition of the primary ones of the front segments, but we can also establish that the same species in two different regions may arrive at two different phyletic stages.
If, finally, we sum up the facts taught by the ontogeny of the two German species, and the adult forms of the other species, we can form therefrom a tolerably complete picture of the course of development of the genus Chærocampa. Of the four phyletic stages indicated by the ontogeny of Elpenor and Porcellus, three still form the terminus of the development of existing species. The great differences among the caterpillars of this genus can be very simply explained on the view that they stand at different levels of phyletic development; some species having remained far behind (Group 1), others having advanced further (Group 2), and others having reached the highest point of development (Group 3). The fact that the species of the third group are only tropical accords well with this view, since many facts prove that phyletic development proceeds more rapidly in the tropics than in temperate climates.
The striking markings of the Chærocampa larvæ may, in brief, be stated to originate from a local transformation of two portions of the subdorsal line into eye-spots, and the subsequent transference of these two primary ocelli to the other segments. The eye-spots always originate on segments four and five, and from these the transference mostly occurs backwards, although in certain cases it takes place at the same time forwards. Herein, i.e. in the origin of the eye-spots, there lies a great distinction between the genus Chærocampa and the genus Deilephila, with which it was formerly associated, and in which the origin of a very similar kind of marking can be traced to quite another source.
The Genus Deilephila, Ochsenheimer.
I am acquainted with the caterpillars of nine European and one North American species, these differing in marking to such a wonderful extent that they appear to offer at first sight but little hope of being able to trace them to a common form. These ten species can be separated, according to their markings, into five groups, which I will briefly define before entering upon their ontogeny.
The first group consists of three species, and comprises the commonest and most widely-ranging of all the European species, Deilephila Euphorbiæ, as well as D. Dahlii from Sardinia and Corsica, and D. Nicæa, a species of very restricted range, which appears to occur only in one small district on the French coast of the Mediterranean. These three species agree in marking to the extent of their possessing in the adult form two rows of ring-spots on each side, whilst the subdorsal line is completely absent.
The second group, consisting also of three species, shows a great resemblance to Euphorbiæ, but has only one row of ring-spots. It contains D. Vespertilio, D. Galii, and the Algerian D. Mauritanica.
For the third group I only know one representative, D. Livornica, Esp., which possesses a single row of ring-spots connected by a subdorsal line.