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centre the elaphines spread westward and eastward, resulting in Europe in the red deer, which penetrated southward into north Africa at a time when there was a land connection across the Mediterranean. In the opposite direction, the nearer we get to Bering's Straits the closer is the resemblance to the American wapiti, until the splendid species from the Altai Mountains (_C. canadensis asiaticus_), and Luehdorf's deer (_C. c. luehdorfi_) from Manchuria, are regarded only as sub-species of the eastern American form, which they approach through _C. c. occidentalis_ of Oregon and the northwestern Pacific Coast. This evidence is conclusive in itself, and is further confirmed by the geological record, from which we know that the land connection between Alaska and Kamtschatka was of Pliocene age, while we have no knowledge of the wapiti in America until the succeeding period. While there is not the least doubt that the smaller American deer had an origin identical with those of the old world, the exact point of their separation is not so clear. Two possibilities are open to choice: _Mazama_ may be supposed to have descended from the group to which _Blastomeryx_ belonged, this being a late Miocene genus from Nebraska, with cervine molars, but otherwise much like _Cosoryx,_ which we have seen to be a possible ancestor of the prong-horn; or we may prefer to believe that the differentiation took place earlier in Europe or Asia, from ancestors common to both. But there is a serious dilemma. If we choose the former view, we must conclude that the deciduous antler was independently developed in each of the two continents, and while it is quite probable that approximately similar structures have at times arisen independently, it is not easy to believe that an arrangement so minutely identical in form and function can have been twice evolved. On the second supposition, we have to face the fact that there is very little evidence from palaeontology of the former presence of the American type in Eurasia. But, on the whole, the latter hypothesis presents fewer difficulties and is probably the correct one; in which case two migrations must have taken place, an earlier one of the generalized type to which _Blastomeryx_ and _Cosoryx_ belonged, and a later one of the direct ancestor of _Mazama_. There is little difficulty in the assumption of these repeated migrations, for evidence exists that during a great part of the last half of the T
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