That there never was a universal ocean since the planet was inhabited, or, rather, since the oldest groups of strata yet known to contain organic remains were formed, is proved by the presence of terrestrial plants or by indications of shores in all the older formations; and if this conclusion was not established, yet no geologist could deny that, since the first small portion of the earth was laid dry, there have been many entire changes in the species of plants and animals inhabiting the land.
But, without dwelling on the above and other refuted theories, let us inquire whether some hypothesis cannot be substituted as simple as that of Linnæus, to which the phenomena now ascertained in regard to the distribution both of aquatic and terrestrial species may be referred. The following may, perhaps, be reconcileable with known facts:—Each species may have had its origin in a single pair, or individual, where an individual was sufficient, and species may have been created in succession at such times and in such places as to enable them to multiply and endure for an appointed period, and occupy an appointed space on the globe.
In order to explain this theory, let us suppose every living thing to be destroyed in the western hemisphere, both on the land and in the ocean, and permission to be given to man to people this great desert, by transporting into it animals and plants from the eastern hemisphere, a strict prohibition being enforced against introducing two original stocks of the same species.
Now it is easy to show that the result of such a mode of colonizing would correspond exactly, so far as regards the grouping of animals and plants, with that now observed throughout the globe. In the first place, it would be necessary for naturalists, before they imported species into particular localities, to study attentively the climate and other physical conditions of each spot. It would be no less requisite to introduce the different species in succession, so that each plant and animal might have time and opportunity to multiply before the species destined to prey upon it was admitted. Many herbs and shrubs, for example, must spread far and wide before the sheep, the deer, and the goat could be allowed to enter, lest they should devour and annihilate the original stocks of many plants, and then perish themselves for want of food. The above-mentioned herbivorous animals in their turn must be permitted to make considerable progress before the entrance of the first pair of wolves or lions. Insects must be allowed to swarm before the swallow could be permitted to skim through the air, and feast on thousands at one repast.
It is evident that, however equally in this case our original stocks were distributed over the whole surface of land and water, there would nevertheless arise distinct botanical and zoological provinces, for there are a great many natural barriers which oppose common obstacles to the advance of a variety of species. Thus, for example, almost all the animals and plants naturalized by us, towards the extremity of South America, would be unable to spread beyond a certain limit, towards the east, west, and south; because they would be stopped by the ocean, and a few of them only would succeed in reaching the cooler latitudes of the northern hemisphere, because they would be incapable of bearing the heat of the tropics, through which they must pass. In the course of ages, undoubtedly, exceptions would arise, and some species might become common to the temperate and polar regions, or both sides of the equator; for I have before shown that the powers of diffusion conferred on some classes are very great. But we might confidently predict that these exceptions would never become so numerous as to invalidate the general rule.
Some of the plants and animals transplanted by us to the coast of Chili and Peru would never be able to cross the Andes, so as to reach the eastern plains; nor, for a similar reason, would those first established in the Pampas, or the valleys of the Amazon and the Orinoco, ever arrive at the shores of the Pacific.
In the ocean an analogous state of things would prevail; for there, also, climate would exert a great influence in limiting the range of species, and the land would stop the migrations of aquatic tribes as effectually as the sea arrests the dispersion of the terrestrial. As certain birds, insects, and the seeds of plants, can never cross the direction of prevailing winds, so currents form natural barriers to the dissemination of many oceanic races. A line of shoals may be as impassable to deep-water species, as are the Alps and the Andes to plants and animals peculiar to plains; while deep abysses may prove insuperable obstacles to the migrations of the inhabitants of shallow waters.
Supposed centres, or foci, of creation.—It is worthy of observation, that one effect of the introduction of single pairs of each species must be the confined range of certain groups in spots, which, like small islands, or solitary inland lakes, have few means of interchanging their inhabitants with adjoining regions. Now this congregating in a small space of many peculiar species, would give an appearance of centres or foci of creation, as they have been termed, as if they were favourite points where the creative energy has been in greater action than in others, and where the numbers of peculiar organic beings have consequently become more considerable.
I do not mean to call in question the soundness of the inferences of some botanists, as to the former existence of certain limited spots whence species of plants have been propagated, radiating, as it were, in all directions from a common centre. On the contrary, I conceive these phenomena to be the necessary consequences of the plan of nature before suggested, operating during the successive mutations of the surface, some of which the geologist can prove to have taken place subsequently to the period when many species now existing were created. In order to exemplify how this arrangement of plants may have been produced, let us imagine that, about three centuries before the discovery of St. Helena (itself of submarine volcanic origin), a multitude of new islands had been thrown up in the surrounding sea, and that these had each become clothed with plants emigrating from St. Helena, in the same manner as the wild plants of Campania have diffused themselves over Monte Nuovo. Whenever the first botanist investigated the new archipelago, he would, in all probability, find a different assemblage of plants in each of the islands of recent formation; but in St. Helena itself, he would meet with individuals of every species, belonging to all parts of the archipelago, and some, in addition, peculiar to itself, viz., those which had not been able to obtain a passage into any one of the surrounding new-formed lands. In this case it might be truly said that the original island was the primitive focus, or centre, of a certain type of vegetation; whereas, in the surrounding islands, there would be a smaller number of species, yet all belonging to the same group.
But this peculiar distribution of plants would not warrant the conclusion that, in the space occupied by St. Helena, there had been a greater exertion of creative power than in the spaces of equal area occupied by the new adjacent lands; because, within the period in which St. Helena had acquired its peculiar vegetation, each of the spots supposed to be subsequently converted into land may have been the birth-place of a great number of marine animals and plants, which may have had time to scatter themselves far and wide over the southern Atlantic.