Primate evolution – in and out of Africa

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Primate evolution – in and out of Africa Caro-Beth Stewart, Todd R Disotell  Current Biology  Volume 8, Issue 16, Pages R582-R588 (July 1998) DOI: 10.1016/S0960-9822(07)00367-3

Figure 1 Potential contacts between Africa and Eurasia during the past 40 million years, based upon geological and faunal evidence (after [28,29]). (a) Late Eocene, approximately 40 million years ago. The Tethys seaway prevents migration between Africa and Eurasia. Uplifting in the western region of the Arabian peninsula coincides with the rifting of the future Red Sea. (b) Early Miocene, approximately 20 million years ago. The Red Sea begins to form, while potential land bridges exist between Africa and Eurasia. (c) Late Miocene, approximately 10 million years ago. The Red Sea continues to grow, and potential connections between Africa and Eurasia exist along the Indian Ocean margin. Current Biology 1998 8, R582-R588DOI: (10.1016/S0960-9822(07)00367-3)

Figure 2 A synthetic hypothesis of catarrhine primate evolution. The branching order shown for the living species is well-supported by numerous molecular phylogenetic studies (for example [6–12,18,24,25]). We present the dates of divergence calculated by Goodman and colleagues [11], on the understanding that these are still rough estimates and more precise measurements are needed, especially for the Old World monkeys. The fossil species (genus names in italics) were placed on this tree by parsimony analyses of relatively large morphological datasets [4,11,14,15]. Known dates for fossils [1,2,21] are indicated by the thicker lines; these lines are attached to the tree as determined by the parsimony analyses, although the dates of the attachment points are our best guesses. Species found in Africa are in red and species found in Eurasia are in black. The continental locations of the ancestral lineages were inferred by parsimony using the computer program MacClade [30]. The intercontinental dispersal events required, at a minimum, to explain the distribution of the living and fossil species are indicated by the arrows. Current Biology 1998 8, R582-R588DOI: (10.1016/S0960-9822(07)00367-3)

Figure 3 Two dispersal scenarios for the hominoids, both assuming an African origin for the catarrhines. As in Figure 2, species found in Africa are in red and species found in Eurasia are in black, and arrows indicate the intercontinental dispersal events required to explain the distribution of the living and fossil species. Scenario A: separate dispersal events from Africa to Eurasia for each of the Eurasian hominoid clades. Scenario B: the common ancestor of all living apes dispersed out of Africa, and later the common ancestor of the modern African apes (gorillas, chimpanzees and humans) dispersed back into Africa. For just the living species (top trees), these two scenarios are equally parsimonious, in that each requires two dispersal events (arrows). When the fossil lineages shown in Figure 2 are included, scenario B is favored, as scenario A now requires a minimum of six independent dispersal events, whereas scenario B still requires only two (bottom trees). Note that the exact branching order of the Eurasian fossil species does not matter for this argument, so long as the fossils do not all branch with the gibbon or orangutan clades; we emphasize this by not naming the fossils in this figure. Current Biology 1998 8, R582-R588DOI: (10.1016/S0960-9822(07)00367-3)