THEORY OF TRANSMUTATION—ABSENCE OF INTERMEDIATE LINKS.

The most obvious and popular of the objections urged against the theory of transmutation may be thus expressed: If the extinct species of plants and animals of the later geological periods were the progenitors of the living species, and gave origin to them by variation and natural selection, where are all the intermediate forms, fossil and living, through which the lost types must have passed during their conversion into the living ones? And why do we not find almost everywhere passages between the nearest allied species and genera, instead of such strong lines of demarcation and often wide intervening gaps?

We may consider this objection under two heads:—

First. To what extent are the gradational links really wanting in the living creation or in the fossil world, and how far may we expect to discover such as are missing by future research?

Secondly. Are the gaps more numerous than we ought to anticipate, allowing for the original defective state of the geological records, their subsequent dilapidation and our slight acquaintance with such parts of them as are extant, and allowing also for the rate of extinction of races and species now going on, and which has been going on since the commencement of the Tertiary period?

First. As to the alleged absence of intermediate varieties connecting one species with another, every zoologist and botanist who has engaged in the task of classification has been occasionally thrown into this dilemma—if I make more than one species in this group, I must, to be consistent, make a great many. Even in a limited region like the British Isles this embarrassment is continually felt.

Scarcely any two botanists, for example, can agree as to the number of roses, still less as to how many species of bramble we possess. Of the latter genus, Rubus, there is one set of forms respecting which it is still a question whether it ought to be regarded as constituting three species or thirty-seven. Mr. Bentham adopts the first alternative and Mr. Babington the second, in their well-known treatises on British plants.

We learn from Dr. Hooker that at the antipodes, both in New Zealand and Australia, this same genus Rubus is represented by several species rich in individuals and remarkable for their variability. When we consider how, as we extend our knowledge of the same plant over a wider area, new geographical varieties commonly present themselves, and then endeavour to imagine the number of forms of the genus Rubus which may now exist, or probably have existed, in Europe and in regions intervening between Europe and Australia, comprehending all which may have flourished in Tertiary and Post-Tertiary periods, we shall perceive how little stress should be laid on arguments founded on the assumed absence of missing links in the flora as it now exists.

If in the battle of life the competition is keenest between closely allied varieties and species, as Mr. Darwin contends, many forms can never be of long duration, nor have a wide range, and these must often pass away without leaving behind them any fossil memorials. In this manner we may account for many breaks in the series which no future researches will ever fill up.