Cause of the Extinction of Species.—There is good reason to believe that the most effective agent in the extinction of species is the pressure of other species, whether as enemies or merely as competitors. If therefore any portion of the earth is cut off from the influx of new or more highly organised animals, we may there expect to find the remains of groups which have elsewhere become extinct. In islands which have been long separated from their parent continents these conditions are exactly fulfilled, and it is in such places that we find the most striking examples of the preservation of fragments of primeval groups of animals, often widely separated from each other, owing to their having been preserved at remote portions of the area of the once widespread parental group. There are many other ways in which portions of dying out groups may be saved. Nocturnal or subterranean modes of life may save a species from enemies or competitors, and many of the ancient types still existing have such habits. The dense gloom of equatorial forests also affords means of concealment and protection, and we sometimes find in such localities a few remnants of low types in the midst of a general assemblage of higher forms. Some of the most ancient types now living inhabit caves like the Proteus, or bury themselves in mud like the Lepidosiren, or in sand like the Amphioxus, the last being the most primitive of all vertebrates; while the Galeopithecus and Tarsius of the Malay islands and the potto of West Africa, survive amid the higher mammalia of the Asiatic and African continents owing to their nocturnal habits and concealment in the densest forests.
The Rise and Decay of Species and Genera.—The preceding sketch of the mode in which species and genera have arisen, have come to maturity, and then decay, leads us to some very important conclusions as to the mode of distribution of animals. When a species or a genus is increasing and spreading, it necessarily occupies a continuous area which gets larger and larger till it reaches a maximum; and we accordingly find that almost all extensive groups are thus continuous. When decay commences, and the group, ceasing to be in harmony with its environment, is encroached upon by other forms, the continuity may frequently be broken. Sometimes the outlying species may be the first to become extinct, and the group may simply diminish in area while keeping a compact central mass; but more often the process of extinction will be very irregular, and may even divide the group into two or more disconnected portions. This is the more likely to be the case because the most recently formed species, probably adapted to local conditions and therefore most removed from the general type of the group, will have the best chance of surviving, and these may exist at several isolated points of the area once occupied by the whole group. We may thus understand how the phenomenon of discontinuous areas has come about, and we may be sure that when allied species or varieties of the same species are found widely separated from each other, they were once connected by intervening forms or by each extending till it overlapped the other's area.
Discontinuous Specific Areas, why Rare.—But although discontinuous generic areas, or the separation from each other of species whose ancestors must once have occupied conterminous or overlapping areas, is of frequent occurrence, yet undoubted cases of discontinuous specific areas are very rare, except, as already stated, when one portion of a species inhabits an island. A few examples among mammalia have been referred to in our first chapter, but it may be said that these are examples of the very common phenomenon of a species being only found in the station for which its organisation adapts it; so that forest or marsh or mountain animals are of course only found where there are forests, marshes, or mountains. This may be true, and when the separate forests or mountains inhabited by the same species are not far apart there is little that needs explanation; but in one of the cases referred to there was a gap of a thousand miles between two of the areas occupied by the species, and this being too far for the animal to traverse through an uncongenial territory, we are forced to the conclusion that it must at some former period and under different conditions have occupied a considerable portion of the intervening area.
Among birds such cases of specific discontinuity are very rare and hardly ever quite satisfactory. This may be owing to birds being more rapidly influenced by changed conditions, so that when a species is divided the two portions almost always become modified into varieties or distinct species; while another reason may be that their powers of flight cause them to occupy on the average wider and less precisely defined areas than do the species of mammalia. It will be interesting therefore to examine the few cases on record, as we shall thereby obtain additional knowledge of the steps and processes by which the distribution of varieties and species has been brought about.
Discontinuity of the Area of Parus palustris.—Mr. Seebohm, who has travelled and collected in Europe, Siberia, and India, and possesses extensive and accurate knowledge of Palæarctic birds, has recently called attention to the varieties and sub-species of the marsh tit (Parus palustris), of which he has examined numerous specimens ranging from England to Japan.[11] The curious point is that those of Southern Europe and of China are exactly alike, while all over Siberia a very distinct form occurs, forming the sub-species P. borealis.[12] In Japan and Kamschatka other varieties are found, which have been named respectively P. japonicus and P. camschatkensis and another P. songarus in Turkestan and Mongolia. Now it all depends upon these forms being classed as sub-species or as true species whether this is or is not a case of discontinuous specific distribution. If Parus borealis is a distinct species from Parus palustris, as it is reckoned in Gray's Hand List of Birds, and also in Sharpe and Dresser's Birds of Europe, then Parus palustris has a most remarkable discontinuous distribution, as shown in the accompanying map, one portion of its area comprising Central and South Europe and Asia Minor, the other an undefined tract in Northern China, the two portions being thus situated in about the same latitude and having a very similar climate, but with a distance of about 4,000 miles between them. If, however, these two forms are reckoned as sub-species only, then the area of the species becomes continuous, while only one of its varieties or sub-species has a discontinuous area. It is a curious fact that P. palustris and P. borealis are found together in Southern Scandinavia and in some parts of Central Europe, and are said to differ somewhat in their note and their habits, as well as in colouration.
Discontinuity of Emberiza schœniclus.—The other case is that of our reed bunting (Emberiza schœniclus), which ranges over almost all Europe and Western Asia as far as the Yenesai valley and North-west India. It is then replaced by another smaller species, E. passerina, which ranges eastwards to the Lena river, and in winter as far south as Amoy in China; but in Japan the original species appears again, receiving a new name (E. pyrrhulina), but Mr. Seebohm assures us that it is quite indistinguishable from the European bird. Although the distance between these two portions of the species is not so great as in the last example, being about 2,000 miles, in other respects the case is an interesting one, because the forms which occupy the intervening space are recognised by Mr. Seebohm himself as undoubted species.[13]
The European and Japanese Jays.—Another case somewhat resembling that of the marsh tit is afforded by the European and Japanese jays (Garrulus glandarius and G. japonicus). Our common jay inhabits the whole of Europe except the extreme north, but is not known to extend anywhere into Asia, where it is represented by several quite distinct species. (See Map, Frontispiece.) But the great central island of Japan is inhabited by a jay (G. japonicus) which is very like ours, and was formerly classed as a sub-species only, in which case our jay would be considered to have a discontinuous distribution. But the specific distinctness of the Japanese bird is now universally admitted, and it is certainly a very remarkable