As the ring-spots became detached from the subdorsal line out of which they had arisen, the latter disappeared more and more completely from the last ontogenetic stage, and receded towards the younger stages of life of the caterpillar—it became historical. This disappearance of the subdorsal may also be explained by the fact that the original longitudinal stripe imitating the linear arrangement of leaves would become meaningless, even if it did not always diminish the effect of the ring-spots. But characters which have become worthless are known in the course of time to become rudimentary, and finally to disappear altogether. I do not believe that disuse alone causes such characters to vanish, although in the case of active organs it may have a large share in this suppression. With markings it cannot, however, be a question of use or disuse—nevertheless they gradually disappear as soon as they become meaningless. I consider this to be the effect of the arrest of the controlling action of natural selection upon these characters (suspension of the so-called “conservative adaptation,” Seidlitz). Any variations may become of value if the character concerned is met with in the necessary state of fluctuation. That this process of extinction does not proceed rapidly, but rather with extreme slowness, is seen in the ontogeny of several species of Deilephila, which retain the now meaningless subdorsal line through a whole series of stages of life.

In another group of Sphinx-larvæ with longitudinal stripes, an eye-spot became developed independently of the subdorsal line, in the position of the caudal horn, which has here vanished with the exception of a small knob-like swelling. This character—which we now see perfected in Pterogon Œnotheræ—undoubtedly serves as a means of causing terror; but whether the incipient stages possessed the same significance, cannot be decided in the isolated case offered by the one species of the genus Pterogon possessing this marking.

In a third group of longitudinally striped caterpillars, the younger genus Chærocampa, eye-spots were developed directly from portions of the subdorsal line, at first only on the fourth and fifth segments. It can be here positively asserted that this character served as a means of alarm from its very commencement. It is certainly for this reason that we see the subdorsal line in the immediate neighbourhood of the spots disappear at an early stage, whilst it is retained on the other segments for a longer period. A portion of the younger (tropical) species of this group then developed similar, or nearly similar, ocelli on the remaining segments by correlation; and it may now have occurred that in solitary cases the eye-spots acquired another significance (C. Tersa?), becoming of use as a disguise by resembling berries or flower-buds. It is also conceivable that the eye-spots may in other cases have been converted into a warning sign of distastefulness.

In all those larvæ which possessed purely terrifying markings, however, not only was the original protective colouring preserved, but in most of them this colour gradually became replaced by a better one (adaptation of the adult larva to the soil). The oblique stripes imitating the leaf-ribs also are by no means lost, but are almost always present, although but feebly developed, and often only temporarily.

The pattern formed by the oblique stripes may also be retained, even with perfect adaptation to the soil, and may be converted to a new use by losing its sharpness, and, instead of imitating definite parts of plants, may become transformed into an irregular and confused marking, and thus best serve to represent the complicated lights and shadows, stripes, spots, &c., cast on the ground under low-growing plants from between the stems and dead leaves.

Just as in the case of ocellated species where caterpillars without eye-spots may retain and newly utilize their older markings, so larvæ having oblique stripes with the most diversely coloured edges may show the same markings in allied (younger?) species, both in a rudimentary and in a transformed condition. These markings may thus contribute to the formation of a latticed or reticulated pattern. Even the oldest marking, the subdorsal line, may still play a part, since its remnants cause certain portions of the complicated pattern to appear more strongly marked (S. Convolvuli). Finally, when an adaptation to a changing environment intersected by lights and shadows is required, new markings may be here added as in other cases, viz., dark streaks extending over the light surface of the whole caterpillar.

In concluding this essay, I may remark that, with respect to the wide and generally important question which gave rise to these investigations, a clearer and simpler result has been obtained than could have been expected, considering the complexity of the characters requiring to be traced to their causes, as well as our still highly imperfect knowledge of ontogenetic and biological facts.

For a long time I believed that it was not possible to trace all the forms of marking and their combinations to those causes which are known to produce transformation; I expected that there would be an inexplicable residue.

But this is not the case. Although it cannot yet be stated at first sight with certainty in every single instance how far any particular element of marking may have a biological value in the species possessing it, nevertheless it has been established that each of the elements of marking occurring in the larvæ of the Sphingidæ originally possessed a decided biological significance, which was produced by natural selection.

In the case of the three chief elements of the markings of the Sphingidæ, it can be further shown that not only the initial stages but also their ultimate perfection—the highest stages of their development, are of decided advantage to their possessors, and have a distinct biological value, so that the gradual development and improvement of these characters can be traced to the action of natural selection.