There are, however, many individual functions of the Arthropods the exercise of which depends on the simultaneous change of several skeletal parts; as, for instance, many of the 'singing' or vocal apparatuses in insects. In quite recent times such vocal organs have been discovered in ants, in which they consist of a small striated region on the surface of the third abdominal segment, and a sharp ridge on the segment in front; the latter is rubbed against the former by the movements of the two segments. Quite a similar 'stridulating organ' has long been known in the bee-ant (_Mutilla_), and the whistling sound produced by it is easily heard by our ears; moreover August Forel has heard it in the large wood-ant (_Camponotus ligniperdus_), and has described it as an 'alarm-signal,' which the animals give each other on the approach of danger--an observation which has recently been confirmed by Wasmann and extended by Robert Wroughton in regard to Indian ants. All these arrangements for producing sound depend always on two organs, of which one resembles the bow, the other the strings of a violin; the one is of no value without the other, and they must therefore have developed simultaneously, yet they cannot have arisen through use, and the inheritance of the results of use, because they are both dead chitinous parts, which are never strengthened by rubbing against each other with the movements of the abdomen, but are rather worn away. [Illustration: FIG. 91 (repeated). Hind-leg of a Grasshopper (_Stenobothrus protorma_), after Graber. _fe_, femur. _ti_, tibia. _ta_, tarsal joints. _schr_, the stridulating ridge.] The same is true of the chirping organs of grasshoppers, beetles, and crickets; in all cases they consist of two different parts, which together produce a sound, and which therefore must have arisen simultaneously, and the origin of which cannot be referred to the inheritance of the results of exercise, but rather to selection. It is thus possible that co-adaptation of at least two parts may take place even when the hypothetical Lamarckian principle is altogether excluded. When I say that we have here a case of two parts adapted to each other, that is, strictly speaking, understating the case, for, in the crickets and locusts, for instance, there is a whole series of peg-like chitinous papillæ (Fig. 86), the so-called 'bridge,' each of which must have arisen by itself through variation of the corresponding spot of skin. At least I can see no ground for the assumption that the chitinous surfaces on which the 'bridge' is now placed would necessarily, from internal reasons, have varied precisely in the line of the bridge as it has done.