Now one might feel inclined to ask why the species of the great Mexican lake has not also taken to this mode of life. To this it may be simply replied that the water of this lake never dries up, and that the Axolotls have thus never been reduced to the alternative of undergoing metamorphosis or of perishing. If therefore the conditions of existence in water were more favourable than on land, the tendency to abandon metamorphosis would increase from generation to generation, and the deportment at present observed would finally result, i.e. propagation would take place exclusively in the Axolotl state. As has already been mentioned above, the latest observations of Velasco furnish further confirmation that the Axolotl of the great lake is never met with in the Amblystoma condition, “although it (the Axolotl) is brought daily from Mexico into the market throughout the whole year.” I should not however regard it as a refutation of my view if prolonged investigation should show that this species also (Siredon Humboldtii) occasionally developed into an Amblystoma; on the contrary, it would not at all surprise me if such cases of reversion occurred in Mexico as well as in Europe. The fact that an immense majority of the Amphibians propagate in the Axolotl state would not be thereby affected, and would still require an explanation: this I am still inclined to see in the dryness of the air of the high plains, which is so unfavourably adapted for a life passed entirely on land.


IV.
ON THE MECHANICAL CONCEPTION OF NATURE.


INTRODUCTION.

In the first of the three preceding essays it was attempted to solve the question whether the transformations of a given complex of characters in a certain systematic group could be completely explained by the sole aid of Darwinian principles. It was attempted to trace the origin of the marking and colouring of the Sphinx-caterpillars to individual variability, to the influences of the environment, and to the laws of correlation acting within the organism. These principles as applied to the origin of a certain well-defined, although narrowly restricted range of forms, were tested in order to see whether they were alone sufficient to explain the transformation of the forms.

It appeared that this was certainly the case. In all instances, or at least where the facts necessary to obtain a complete insight were available, the transformations could be traced to these known factors; there remained no inexplicable residual phenomena, and we therefore had no reason for inferring the existence of some still unknown modifying cause lying concealed in the organism. In this region of the marking and colouring of caterpillars, the assumption of a phyletic vital force had to be abandoned, as being superfluous for the explanation of the facts.

In the second essay the attempt was next made with reference to double form-relationship, as presented for observation in metamorphic insects, to draw conclusions as to the causes of the transformations. It appeared here that form- and blood-relationship do not always coincide, since the larvæ of a species, genus, or family, &c., may show quite different form-relationships to their imagines. These facts alone told very decisively against the existence of an internal developmental power, so that the latter had likewise to be set aside by the method of elimination, since the observed incongruences as well as the congruences of form-relationship, found sufficient explanation in the action of the environment on the organism.

This investigation thus also led to the denial of a phyletic vital force.