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Evolutionary and biogeographic history of weasel-like carnivorans (Musteloidea)

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Title: Evolutionary and biogeographic history of weasel-like carnivorans (Musteloidea)
Authors: Sato, Jun J. Browse this author
Wolsan, Mieczyslaw Browse this author
Prevosti, Francisco J. Browse this author
D'Elía, Guillermo Browse this author
Begg, Colleen Browse this author
Begg, Keith Browse this author
Hosoda, Tetsuji Browse this author
Campbell, Kevin L. Browse this author
Suzuki, Hitoshi Browse this author →KAKEN DB
Keywords: Biogeography
Carnivora
Divergence times
Evolution
Mustelidae
Phylogeny
Issue Date: Jun-2012
Publisher: Elsevier
Journal Title: Molecular Phylogenetics and Evolution
Volume: 63
Issue: 3
Start Page: 745
End Page: 757
Publisher DOI: 10.1016/j.ympev.2012.02.025
Abstract: We analyzed a concatenated (8492 bp) nuclear-mitochondrial DNA data set from 44 musteloids (including the first genetic data for Lyncodon patagonicus) with parsimony, maximum likelihood, and Bayesian methods of phylogenetic and biogeographic inference and two Bayesian methods of chronological inference. Here we show that Musteloidea emerged approximately 32.4-30.9 million years ago (MYA) in Asia, shortly after the greenhouse-icehouse global climate shift at the Eocene-Oligocene transition. During their Oligocene radiation, which proceeded wholly or mostly in Asia, musteloids diversified into four primary divisions: the Mephitidae lineage separated first, succeeded by Ailuridae and the divergence of the Procyonidae and Mustelidae lineages. Mustelidae arose approximately 16.1 MYA within the Mid-Miocene Climatic Optimum, and extensively diversified in the Miocene, mostly in Asia. The early offshoots of this radiation largely evolved into badger and marten ecological niches (Taxidiinae, Melinae, Mellivorinae, Guloninae, and Helictidinae), whereas the later divergences have adapted to other niches including those of weasels, polecats, minks, and otters (Mustelinae, Ictonychinae, and Lutrinae). Notably, and contrary to traditional beliefs, the morphological adaptations of badgers, martens, weasels, polecats, and minks each evolved independently more than once within Mustelidae. Ictonychinae (which is most closely related to Lutrinae) arose approximately 9.5-8.9 MYA, most likely in Asia, where it diverged into the Old World Ictonychini (Vormela, Poecilictis, Ictonyx, and Poecilogale) and New World Lyncodontini (Lyncodon and Galictis) lineages. Ictonychini presumably entered Africa during the Messinian Salinity Crisis (at the Miocene-Pliocene transition), which interposed the origins of this clade (approximately 6.5-6.0 MYA) and its African Poecilictis-Ictonyx-Poecilogale subclade (approximately 4.8-4.5 MYA). Lyncodontini originated approximately 2.9-2.6 MYA at the Pliocene-Pleistocene transition in South America, slightly after the emergence of the Panamanian land bridge that provided for the Great American Biotic Interchange. As the genera Martes and Ictonyx (as currently circumscribed) are paraphyletic with respect to the genera Gulo and Poecilogale, respectively, we propose that Pekania and Poecilictis be treated as valid genera and that "Martes" pennanti and "Ictonyx" libyca, respectively, be assigned to these genera.
Type: article (author version)
URI: http://hdl.handle.net/2115/49406
Appears in Collections:環境科学院・地球環境科学研究院 (Graduate School of Environmental Science / Faculty of Environmental Earth Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 鈴木 仁

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