Erebia (Erebia) pawloskii Ménétriés, 1859
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https://doi.org/10.5281/zenodo.16642576 |
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https://doi.org/10.5281/zenodo.16802242 |
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https://treatment.plazi.org/id/4D7E87DA-4B77-7200-FF2D-FF14AC77FD21 |
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Felipe |
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Erebia (Erebia) pawloskii Ménétriés, 1859 |
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Erebia (Erebia) pawloskii Ménétriés, 1859 is confirmed as a species distinct from Erebia theano (Tauscher, 1806) and Erebia stubbendorfii Ménétriés, 1847
Nuclear genome phylogeny reveals that Erebia (Erebia) theano (Tauscher, 1806) (type locality in Altai Mts.) ( Fig. 3a View Fig brown), Erebia (Erebia) stubbendorfii Ménétriés, 1847 (type locality Russia: Kansk) ( Fig. 3a View Fig olive), and Erebia (Erebia) pawloskii Ménétriés, 1859 (type locality in Russia: Sakha) ( Fig. 3a View Fig purple, blue, magenta, green, dark blue, and cyan, with the nominate in blue), form strongly supported (100% ultrafast bootstrap ( Minh et al. 2013)) clades genetically differentiated at the species level, e.g., their Fst values are: 0.36 ( E. theano and E. stubbendorfii ), 0.36 ( E. theano and E. pawloskii ), and 0.28 ( E. stubbendorfii and E. pawloskii ). Therefore, genomic analysis supports the three distinct species hypothesis ( Lukhtanov and Lukhtanov 1994; Gorbunov 2001) and suggests that the name stubbendorfii should not be applied to E. pawloskii . Curiously, mitochondrial genome phylogeny is different, and reveals two major haplotypes for these species, split by geography: the Old World haplotype (including the North Slope of Alaska, USA) and the New World haplotype (the rest of Alaska, Canada, and the US) ( Fig. 3b View Fig ). Similar evolutionary scenarios, likely resulting from mitochondrial introgression, are known in other butterfly groups, such as Junonia Hübner, [1819] (Gemmell and Marcus 2015) , and offer a cautionary lesson against relying solely on mitochondrial data (e.g., COI barcodes) to address species delimitation.
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