It has already been shown that Darwin clearly perceived that the very general occurrence of some degree of infertility between allied species cannot possibly be attributed to the _direct_ agency of natural selection. His explanation was that the slight structural modifications entailed by the transformation of one specific type into another, so react upon the highly delicate reproductive system of the changing type as to render it in some degree infertile with its parent type. Now the theory of physiological selection begins by traversing this view. It does not, however, deny that in _some_ cases the morphological may be the prior change; but it strenuously denies that this must be so in _all_ cases. Indeed, according to my statement in 1886, the theory inclines to the view that, _as a rule_, the physiological change is prior. At the same time, the theory, as I have always stated it, maintains that it is immaterial whether, "in the majority of instances," the physiological change has been prior to the morphological, or vice versa; since in either case the physiological change will equally make for divergence of character. To show this clearly the best way will be to consider the two cases separately, taking first that in which the physiological change has priority. In this case our theory regards any morphological changes which afterwards supervene as due to the independent variability which will sooner or later arise under the physiological isolation thus secured. But to whatever causes the subsequent morphological changes may be due, the point to notice is that they are as a general rule, consequent upon the physiological change. For in whatever _degree_ such infertility arises between two sections of a species occupying the same area, in that _degree_ is their interbreeding prevented, and, therefore, opportunity is given for a subsequent divergence of type, whether by the influence of independent variability alone, or also by that of natural selection, as now acting more or less independently on each of the partially separated groups. In short, all that was said in the foregoing chapters with respect to isolation in general, here applies to physiological isolation in particular; and by supposing such isolation to have been the prior change, we can as well understand the subsequent appearance of morphological divergence on continuous areas, as in other forms of isolation we can understand such divergence on discontinuous areas, seeing that even a moderate degree of cross-infertility may be as effectual for purposes of isolation as a high mountain-chain, or a thousand miles of ocean.