2013
DOI: 10.1016/j.ympev.2012.10.015
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Phylogeny and historical demography of Cynops pyrrhogaster (Amphibia: Urodela): Taxonomic relationships and distributional changes associated with climatic oscillations

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Cited by 40 publications
(35 citation statements)
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“…Divergence time between the AM/TK and the ON subclades is estimated as 6.07 (3.81-7.75) MYA in the Calibration I and 3.21 (1.77-4.97) MYA in the Calibration II. The estimated times of divergence between the Amami and Okinawa populations in several amphibians falls within the range from the late Miocene to the early Pleistocene (1.7 [1.1-2.4] MYA for two species of the Odorrana narina complex [Matsui et al, 2005b]; 2.3 [1.5-3.2] MYA for two species of the O. ishikawae species group [Matsui et al, 2005b]; 2.4-8.3 MYA for two species of Babina [Tominaga et al, 2014]; 3.3-6.8 MYA for Cynops ensicauda [Tominaga et al, 2010[Tominaga et al, , 2013; and 3.1-18.0 MYA for Echinotriton andersoni [Honda et al, 2012;Kurabayashi et al, 2012]). Most of these estimations are much older than the formations of straits in the Pleistocene (0.12-1.3 MYA; Kizaki and Oshiro, 1980;Ota, 1998;Kimura, 2003), which have separated the Amami and the Okinawa Groups, and should have induced divergence of the terrestrial animals of the Central Ryukyus into two island group elements.…”
Section: Distribution Patterns and Divergence Historymentioning
confidence: 99%
“…Divergence time between the AM/TK and the ON subclades is estimated as 6.07 (3.81-7.75) MYA in the Calibration I and 3.21 (1.77-4.97) MYA in the Calibration II. The estimated times of divergence between the Amami and Okinawa populations in several amphibians falls within the range from the late Miocene to the early Pleistocene (1.7 [1.1-2.4] MYA for two species of the Odorrana narina complex [Matsui et al, 2005b]; 2.3 [1.5-3.2] MYA for two species of the O. ishikawae species group [Matsui et al, 2005b]; 2.4-8.3 MYA for two species of Babina [Tominaga et al, 2014]; 3.3-6.8 MYA for Cynops ensicauda [Tominaga et al, 2010[Tominaga et al, , 2013; and 3.1-18.0 MYA for Echinotriton andersoni [Honda et al, 2012;Kurabayashi et al, 2012]). Most of these estimations are much older than the formations of straits in the Pleistocene (0.12-1.3 MYA; Kizaki and Oshiro, 1980;Ota, 1998;Kimura, 2003), which have separated the Amami and the Okinawa Groups, and should have induced divergence of the terrestrial animals of the Central Ryukyus into two island group elements.…”
Section: Distribution Patterns and Divergence Historymentioning
confidence: 99%
“…of Tsukuba) and a field ‘Imori-no-Sato’ (Kaizuka/Kamitakai, Toride city, Ibaraki prefecture, Japan; http://imori-net.org/ ) [4] . This population belongs to Kanto group in Northern lineage [12] and is called ‘Toride-Imori’. In this study, sexually mature adult Toride-Imori (total body length: male, ∼9 cm; female, 11–12 cm) which had been reared in the laboratory were used.…”
Section: Methodsmentioning
confidence: 99%
“…The Japanese red‐bellied newt, Cynops pyrrhogaster (Boie, 1826), distributed on the mainland of Japan, has long been studied for geographic variations (Hayashi & Matsui, 1988, 1990; Matsui, 1996; Sawada, 1963a,b; Tominaga et al, 2013, 2015). This species is known to be divided into six morphological/behavioral groups based on morphology and mating behavior (Sawada, 1963a,b; Figure 1a) and five allozyme groups by analyses of enzyme protein polymorphisms (Hayashi & Matsui, 1988, 1990; Matsui, 1996; Figure 1b).…”
Section: Introductionmentioning
confidence: 99%
“…This species is known to be divided into six morphological/behavioral groups based on morphology and mating behavior (Sawada, 1963a,b; Figure 1a) and five allozyme groups by analyses of enzyme protein polymorphisms (Hayashi & Matsui, 1988, 1990; Matsui, 1996; Figure 1b). Moreover, this species comprises five mitochondrial DNA (mtDNA) lineages (Tominaga et al, 2013, 2015; Figure 1c).…”
Section: Introductionmentioning
confidence: 99%
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