How modern humans dispersed into Eurasia and Australasia, including the number of separate expansions and their timings, is highly debated [ 1, 2 ]. Two categories of models are proposed for the dispersal of non-Africans: (1) single dispersal, i.e., a single major diffusion of modern humans across Eurasia and Australasia [ 3–5 ]; and (2) multiple dispersal, i.e., additional earlier population expansions that may have contributed to the genetic diversity of some present-day humans outside of Africa [ 6–9 ]. Many variants of these models focus largely on Asia and Australasia, neglecting human dispersal into Europe, thus explaining only a subset of the entire colonization process outside of Africa [ 3–5, 8, 9 ]. The genetic diversity of the first modern humans who spread into Europe during the Late Pleistocene and the impact of subsequent climatic events on their demography are largely unknown. Here we analyze 55 complete human mitochondrial genomes (mtDNAs) of hunter-gatherers spanning ∼35,000 years of European prehistory. We unexpectedly find mtDNA lineage M in individuals prior to the Last Glacial Maximum (LGM). This lineage is absent in contemporary Europeans, although it is found at high frequency in modern Asians, Australasians, and Native Americans. Dating the most recent common ancestor of each of the modern non-African mtDNA clades reveals their single, late, and rapid dispersal less than 55,000 years ago. Demographic modeling not only indicates an LGM genetic bottleneck, but also provides surprising evidence of a major population turnover in Europe around 14,500 years ago during the Late Glacial, a period of climatic instability at the end of the Pleistocene.
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RBINS Staff Publications 2016
Plesiadapidae are among the most successful mammal families of the Paleocene, but in North America they disappear abruptly around the Paleocene-Eocene boundary. In contrast, in Europe, they survive a few million years into the Eocene, although only as the genus Platychoerops. The latest Paleocene deposits of Petit-P^atis (Paris Basin, France) have produced three new plesiadapid species, one of each genus known in Europe: Plesiadapis ploegi, sp. nov., Platychoerops boyeri, sp. nov., and Chiromyoides mauberti, sp. nov. Each of these new species is represented by the very characteristic upper incisor, thus ascertaining their concomitant presence and in particular the spatial and temporal coexistence of Plesiadapis and Platychoerops. Plesiadapis ploegi, sp. nov., is morphologically intermediate between Plesiadapis tricuspidens and Platychoerops russelli, with a tricuspid I1 typical of Plesiadapis and a semimolariform p4 closer to Platychoerops. Its relatively high morphological variability is illustrated. Platychoerops boyeri, sp. nov., has the simple derived I1 of all Platychoerops and a p4 slightly more molariform than that of Ples. ploegi. Chiromyoides mauberti, sp. nov., is closest to Chiromyoides campanicus, but it is smaller and has a particular I1 with multiple posterocones. The systematic position of ‘Platychoerops’ georgei is discussed; this taxon is considered a chimera, and its type I1 belongs to either Chiromyoides or Plesiadapis. Cladistic analysis highlights the paraphyly or polyphyly of all genera of Plesiadapidae. Finally, there is some indication of morphological convergences between European and North American plesiadapids, which may be the result of similar environmental changes on both continents just before the Paleocene-Eocene boundary.
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RBINS Staff Publications 2018