Species Changed through Natural Selection.—In the third class, that of species changed in the process of adaptation, most insular forms belong. As a matter of fact, at some time or another almost every species must be in this category, for isolation is a source of the most potent elements in the initiation and intensification of the minor differences which separate related species. It is not the preservation of the most useful features, but of those which actually existed in the ancestral individuals, which distinguish such species. Natural selection must include not only the process of the survival of the fittest, but also the results of the survival of the existing. This means the preservation through heredity of the traits not of the species alone, but those of the actual individuals set apart to be the first in the line of descent in a new environment. In hosts of cases the persistence of characters rests not on any special usefulness or fitness, but on the fact that individuals possessing these characters have, at one time or another, invaded a certain area and populated it. The principle of utility explains survivals among competing structures. It rarely accounts for qualities associated with geographical distribution.
Extinction of Species.—The extinction of species may be noted here in connection with their extension of range. Prof. Herbert Osborn has recognized five different types of elimination.
1. That extinction which comes from modification or progressive evolution, a relegation to the past as the result of a transmutation into more advanced forms. 2. Extinction from changes of physical environment which outrun the powers of adaptation. 3. The extinction which results from competition. 4. The extinction from extreme specialization and limitation to special conditions the loss of which means extinction. 5. Extinction as a result of exhaustion. As an illustration of No. 1, we may take almost any species which has a cognate species on the further side of some barrier or in the tertiary seas. Thus the trout of the Twin Lakes in Colorado has acquired its present characters in the place of those brought into the lake by its actual ancestors. No. 2 is illustrated by the disappearance of East Indian types (Zanclus, Platax, Toxotes, etc.) in Italy at the end of the Eocene, perhaps for climatic reasons. Extinction through competition is shown in the gradual disappearance of the Sacramento perch (Archoplitis interruptus) after the invasion of the river by catfish and carp. From extreme specialization certain forms have doubtless disappeared, but no certain case of this kind has been pointed out among fishes, unless this be the cause of the disappearance of the Devonian mailed Ostracophores and Arthrodires. It is not likely that any group of fishes has perished through exhaustion of the stock of vigor.
Barriers Checking Movement of Marine Fishes.—The limits of the distribution of individual species or genera must be found in some sort of barrier, past or present. The chief barriers which limit marine fishes are the presence of land, the presence of great oceans, the differences of temperature arising from differences in latitude, the nature of the sea bottom, and the direction of oceanic currents. That which is a barrier to one species may be an agent in distribution to another. The common shore fishes would perish in deep waters almost as surely as on land, while the open Pacific is a broad highway to the albacore or the swordfish.
Again, that which is a barrier to rapid distribution may become an agent in the slow extension of the range of a species. The great continent of Asia is undoubtedly one of the greatest of barriers to the wide movement of species of fish, yet its long shore-line enables species to creep, as it were, from bay to bay, or from rock to rock, till, in many cases, the same species is found in the Red Sea and in the tide-pools or sand-reaches of Japan. In the North Pacific, the presence of a range of half-submerged volcanoes, known as the Aleutian and the Kurile Islands, has greatly aided the slow movement of the fishes of the tide-pools and the kelp. To a school of mackerel or of flying-fishes these rough islands with their narrow channels might form an insuperable barrier.
Fig. 173.—Japanese filefish, Rudarius ercodes Jordan and Snyder. Wakanoura, Japan. Family Monacanthidæ.
Temperature the Central Fact in Distribution.—It has long been recognized that the matter of temperature is the central fact in all problems of geographical distribution. Few species in any group freely cross the frost-line, and except as borne by oceanic currents, not many extend their range far into waters colder than those in which the species is distinctively at home. Knowing the average temperature of the water in a given region we know in general the types of fishes which must inhabit it. It is the similarity in temperature and physical conditions which chiefly explains the resemblance of the Japanese fauna to that of the Mediterranean or the Antilles. This fact alone must explain the resemblance of the Arctic and Antarctic faunæ, there being in no case a barrier in the sea that may not some time be crossed. Like forms lodge in like places.
Agency of Ocean Currents.—We may consider again for a moment the movements of the great currents in the Pacific as agencies in the distribution of species.