in the latter portion of the Miocene or early in the Pliocene period.[[151]]

It is clear, therefore, that if Madagascar had once formed part of Africa, but had been separated from it before Africa was united to Europe and Asia, it would not contain any of those kinds of animals which then first entered the country. But, besides the African mammals, we know that some birds now confined to Africa then inhabited Europe, and we may therefore fairly assume that all the more important groups of birds, reptiles, and insects, now abundant in Africa but absent from Madagascar, formed no part of the original African fauna, but entered the country only after it was joined to Europe and Asia.

Early History of Africa and Madagascar.—We have seen that Madagascar contains an abundance of mammals, and that most of them are of types either peculiar to, or existing also in, Africa; it follows that that continent must have had an earlier union with Europe, Asia, or America, or it could never have obtained any mammals at all.

Now these ancient African mammals are Lemurs, Insectivora, and small Carnivora, chiefly Viverridæ; and all these groups are known to have inhabited Europe in Eocene and Miocene times; and that the union was with Europe rather than with America is clearly proved by the fact that even the insectivorous Centetidæ, now confined to Madagascar and the West Indies, inhabited France in the Lower Miocene period, while the Viverridæ, or civets, which form so important a part of the fauna of Madagascar as well as of Africa, were abundant in Europe throughout the whole Tertiary period, but are not known to have ever lived in any part of the American continent. We here see the application of the principle which we have already fully proved and illustrated (Chapter IV., p. [60]), that all extensive groups have a wide range at the period of their maximum development; but as they decay their area of distribution diminishes or breaks up into detached fragments, which one after another disappear till the group becomes extinct. Those animal forms which we now find isolated in Madagascar and other remote portions of the globe all belong to ancient groups which are in a decaying or nearly extinct condition, while those which are absent from it belong to more recent and more highly-developed types, which range over extensive and continuous areas, but have had no opportunity of reaching the more ancient continental islands.

Anomalies of Distribution and How to Explain Them.—If these considerations have any weight, it follows that there is no reason whatever for supposing any former direct connection between Madagascar and the Greater Antilles merely because the insectivorous Centetidæ now exist only in these two groups of islands; for we know that the ancestors of this family must once have had a much wider range, which almost certainly extended over the great northern continents. We might as reasonably suppose a land-connection across the Pacific to account for the camels of Asia having their nearest existing allies in the llamas and alpacas of the Peruvian Andes, and another between Sumatra and Brazil, in order that the ancestral tapir of one country might have passed over to the other. In both

these cases we have ample proof of the former wide extension of the group. Extinct camels of numerous species abounded in North America in Miocene, Pliocene, and even Post-pliocene times, and one has also been found in North-western India, but none whatever among all the rich deposits of mammalia in Europe. We are thus told, as clearly as possible, that from the North American continent as a centre the camel tribe spread westward, over now-submerged land at the shallow Behring Straits and Kamschatka Sea, into Asia, and southward along the Andes into South America. Tapirs are even more interesting and instructive. Their remotest known ancestors appear in Western Europe in the early portion of the Eocene period; in the latter Eocene and the Miocene other forms occur both in Europe and North America. These seem to have become extinct in North America, while in Europe they developed largely into many forms of true tapirs, which at a much later period found their way again to North, and thence to South, America, where their remains are found in caves and gravel deposits. It is an instructive fact that in the Eastern continent, where they were once so abundant, they have dwindled down to a single species, existing in small numbers in the Malay Peninsula, Sumatra, and Borneo only; while in the Western continent, where they are comparatively recent immigrants, they occupy a much larger area, and are represented by three or four distinct species. Who could possibly have imagined such migrations, and extinctions, and changes of distribution as are demonstrated in the case of the tapirs, if we had only the distribution of the existing species to found an opinion upon? Such cases as these—and there are many others equally striking—show us with the greatest distinctness how nature has worked in bringing about the examples of anomalous distribution that everywhere meet us; and we must, on every ground of philosophy and common sense, apply the same method of interpretation to the more numerous instances of anomalous distribution we discover among such groups as reptiles, birds, and insects, where we rarely have any direct evidence of their past migrations through the discovery of

fossil remains. Whenever we can trace the past history of any group of terrestrial animals, we invariably find that its actual distribution can be explained by migrations effected by means of comparatively slight modifications of our existing continents. In no single case have we any direct evidence that the distribution of land and sea has been radically changed during the whole lapse of the Tertiary and Secondary periods, while, as we have already shown in our fifth chapter, the testimony of geology itself, if fairly interpreted, upholds the same theory of the stability of our continents and the permanence of our oceans. Yet so easy and pleasant is it to speculate on former changes of land and sea with which to cut the gordian knot offered by anomalies of distribution, that we still continually meet with suggestions of former continents stretching in every direction across the deepest oceans, in order to explain the presence in remote parts of the globe of the same genera even of plants or of insects—organisms which possess such exceptional facilities both for terrestrial, aërial, and oceanic transport, and of whose distribution in early geological periods we generally know little or nothing.

The Birds of Madagascar, as Indicating a Supposed Lemurian Continent.—Having thus shown how the distribution of the land mammalia and reptiles of Madagascar may be well explained by the supposition of a union with Africa before the greater part of its existing fauna had reached it, we have now to consider whether, as some ornithologists think, the distribution and affinities of the birds present an insuperable objection to this view, and require the adoption of a hypothetical continent—Lemuria—extending from Madagascar to Ceylon and the Malay Islands.

There are about one hundred and fifty land birds known from the island of Madagascar, of which a hundred and twenty-seven are peculiar; and about half of these peculiar species belong to peculiar genera, many of which are extremely isolated, so that it is often difficult to class them in any of the recognised families, or to determine their affinities to any living birds.[[152]] Among the other moiety,