= 11,236 5th " O + 16 + 1,220 + 10,000 = 11,236 and so on for any number of generations.
In the preceding discussion we have given the theory the advantage of the large proportion of 10 per cent of this very exceptional variety arising in its midst year by year, and we have seen that, even under these favourable conditions, it is unable to increase its numbers much above its starting-point, and that it remains wholly dependent on the continued renewal of the variety for its existence beyond a few years.
It appears, then, that this form of inter-specific sterility cannot be increased by natural or any other known form of selection, but that it contains within itself its own principle of destruction.

If it is proposed to get over the difficulty by postulating a larger percentage of the variety annually arising within the species, we shall not affect the law of decrease until we approach equality in the numbers of the two varieties.

But with any such increase of the physiological variety the species itself would inevitably suffer by the large proportion of sterile unions in its midst, and would thus be at a great disadvantage in competition with other species which were fertile throughout.

Thus, natural selection will always tend to weed out any species with too great a tendency to sterility among its own members, and will therefore prevent such sterility from becoming the general characteristic of varying species, which this theory demands should be the case.
On the whole, then, it appears clear that no form of infertility or sterility between the individuals of a species, can be increased by natural selection unless correlated with some useful variation, while all infertility not so correlated has a constant tendency to effect its own elimination.

But the opposite property, fertility, is of vital importance to every species, and gives the offspring of the individuals which possess it, in consequence of their superior numbers, a greater chance of survival in the battle of life.