Science (N.S.) 19(483) 549-550 (1904)
NATURAL SELECTION IN KINETIC EVOLUTION*
O. F. Cook
WASHINGTON, D. C.,
March 11, 1904.
*Read before the Biological Society of Washington, March 19, 1904.
|†The Popular Science Monthly, March, 1904, p. 451.|
THAT there are species, varieties, mutations or hybrids which differ in one, two, or three characters, as commonly assumed in discussions of Mendel's laws, is a misleading assumption. To speak of a species as having developed in one direction or as having a single peculiar character may be permissible for taxonomic purposes, but in evolutionary studies it is careless to forget that the diversity is general, if not complete. The diversity of varieties and species is like that of individuals, but greater. Evolution, which is a continuous summary or integration of this individual diversity, is not a simple process, but highly multiplex; as much so, indeed, as the lines of descent in which the life of the species goes forward. A composite general direction is maintained by the species because the multitudinous strands of individual descent are bound together by interbreeding. The variations take place in particular threads, but evolution signifies rather the progressive change of the whole organic network.†
|*Mutations, like hybrids, are sometimes completely sterile, and they may have at the same time an increased vegetative vigor. The vegetative vigor of many mutative varieties of domesticated plants has doubtless delayed the recognition of their abnormal evolutionary status, though the abnormality of infertile hybrids has long been appreciated. It is paradoxical, indeed, that the increased vigor which accompanies normal variations and crosses should also attend degenerative changes, but there is room for this apparent contradiction in so complex and many-sided a process as evolution.|
The evolution of a new type means changes in many directions and of many kinds, in the germ cells and in the various tissues and organs, as well as in the external form of the complex cell-colony which we are accustomed to look upon as a single individual. Each cell, tissue, organ and feature is undergoing evolution, and for normal and permanent progress these manifold developments must keep together. When single lines or slender strands of descent are separated from the main network the congruence of type is lost. The normal variation and individual diversity of the species having been eliminated, the evolutionary coordination of cells, organs and functions breaks down, and abrupt changes or aberrations of heredity appear. These degenerative mutations may not differ in their essential nature from normal variations, but the conditions of their appearance are abnormal, and the results often disastrous.*
A domestic variety may be 'improved' by the further increase of the one or two characters or qualities which render it valuable, but a new specific or generic type is the compound or resultant of many variations in many characters. By close selection which restricts evolutionary progress to a narrow line of descent a 'single character' may push out farther in a decade than the natural multiplex evolution would carry it in a century or a millennium, but such a specialization weakens and unbalances the organism, and is a process of degeneration rather than a constructive evolution. Selective inbreeding and other forms of isolation accentuate single characters, but the interbreeding of normally diverse individuals (symbasis) weaves new types out of the variations of many lines of descent.
|†Very recent examples
of the latter tendency are found in Professor Morgan's ‘Evolution and
Adaptation' and also in Dr. D. T. MacDougal's review of this work (Torreya, 3: 185, December, 1903). Professor Morgan refers (p. 368) with approval to an admission by Darwin that
selection can not explain dimorphism in plants because it can not be an
advantage to a plant to be able to breed with only half of the members of its
species. The same reasoning would apply, however, to all the phenomena of
sexual separation, of which the dimorphism of bisexual plants may be an
incipient stage. It seems obvious, too, that to breed successfully with half of
the individuals of a species is an important advantage over the alternative of
breeding less effectively with all of them. The partial or complete sterility
of some dimorphic plants to the pollen of others of their own caste may be due
to impotency rather than to adaptation, and a dimorphism by which this fatal
result could be avoided would certainly be favored by selection.
*Except as selection implies inbreeding, by which mutations are induced.
The neglect of this distinction vitiates much evolutionary literature, both that which treats selection as an actuating 'force,' and that which rejects selection for 'discontinuous variation' or 'the mutation theory.'† It is true that many variations of inbred domesticated plants and animals are very abruptly discontinuous, and that such changes are not caused by selection,* but these facts in no way militate against others equally obvious, that the natural evolution of new types is a relatively slow and gradual process, and that selection may easily influence the direction of this continuous vital motion. The older selective hypothesis was only half erroneous. Selection does not set stationary organisms in motion, but it often guides spontaneous change. It does not explain evolution or vital motion in general, but it does explain adaptation, or motion in some particular direction, as when one species differs from it relatives in special characters which enable it to exist in a special environment. That all adaptations are mere coincidences is as improbable as that all characters represent useful adaptations.
Selection is not, as many 'Darwinians' have maintained, the true, efficient cause of evolution; the vital motion of species proceeds whether selection is operative or not. Species do not acquire characters from the environment, but merely in accordance with it. At any point in the evolutionary journey, selection may determine whether certain characters shall be acquired or not; it is an obstacle in the environmental road over which the species would travel, instead of being the source of power of the organic automobile. By preventing motion in one direction selection may be said, of course, to cause advance in another, but it is apparent that this causality is negative and passive, or a mere figure of speech. Selection may explain why a particular character is accentuated in a particular species, but it is no more a cause of the developmental progress of the species than the turns of the road are the motive power of the vehicle. Segregation enables species to attain differential characters, and selection assists their accommodation to environment, but both these possibilities rest on the more fundamental fact that organic evolution goes forward without external causation in groups of diverse, interbreeding individuals. If a species stood still selection could effect nothing except its partial extinction. In the recognition of a continuous and universal evolutionary motion the kinetic theory supplies the long-sought explanation of selective influence. By ceasing to look upon selection as a mysterious evolutionary cause we are able to ascribe to it a practical and easily comprehensible evolutionary function.