2013
DOI: 10.5252/g2013n1a8
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The origin(s) of extant amphibians: a review with emphasis on the “lepospondyl hypothesis”

Abstract: The origins of the extant amphibians (frogs, salamanders, caecilians) remain controversial after over a century of debate. Three groups of hypotheses persist in the current literature: the "temnospondyl hypothesis" (TH) which roots Lissamphibia Haeckel, 1866 (the smallest clade composed of the extant amphibians) within the Paleozoic temnospondyls, the "lepospondyl hypothesis" (LH) which postulates a monophyletic Lissamphibia nested within the Paleozoic lepospondyls, and the "polyphyly hypothesis" (PH), accordi… Show more

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Cited by 85 publications
(132 citation statements)
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References 141 publications
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“…Branch lengths were calculated from estimated divergence times of the different nodes taken from the literature, because characters and clustering methods used to construct trees might have been different and thus might have affected branch lengths. Phylogenetic trees were constructed from Vidal and Hedges [68], Mulcahy et al [69] and Amer and Kumazawa [70] for squamates; Hackett et al [71] for birds; Marjanovic and Laurin [72] and Clack [73] for non-amniote tetrapods; Bennett [74] and Nesbitt [75] for non-dinosaurian archosaurs; Pisani et al [76] and Brusatte et al [77] for tyrannosaurid dinosaurs; Yates [78]–[79]; Sereno [80]; Allain and Aquesbi [81]; Remes et al [82] for Sauropodomorpha and Beck et al [83] and Perelman et al [84] for mammals using Mesquite v. 2.75 [80]. Additional information on node divergence times was taken from Benton et al [85] and Müller and Reisz [86].…”
Section: Methodsmentioning
confidence: 99%
“…Branch lengths were calculated from estimated divergence times of the different nodes taken from the literature, because characters and clustering methods used to construct trees might have been different and thus might have affected branch lengths. Phylogenetic trees were constructed from Vidal and Hedges [68], Mulcahy et al [69] and Amer and Kumazawa [70] for squamates; Hackett et al [71] for birds; Marjanovic and Laurin [72] and Clack [73] for non-amniote tetrapods; Bennett [74] and Nesbitt [75] for non-dinosaurian archosaurs; Pisani et al [76] and Brusatte et al [77] for tyrannosaurid dinosaurs; Yates [78]–[79]; Sereno [80]; Allain and Aquesbi [81]; Remes et al [82] for Sauropodomorpha and Beck et al [83] and Perelman et al [84] for mammals using Mesquite v. 2.75 [80]. Additional information on node divergence times was taken from Benton et al [85] and Müller and Reisz [86].…”
Section: Methodsmentioning
confidence: 99%
“…Dissorophoidea is a large clade that was very successful during the Paleozoic and continues to be so today, as most authors consider some or all three groups of modern amphibians to be part of Dissorophoidea (Anderson, 2008;Anderson et al, 2008b;Milner, 1988Milner, , 1993Schoch and Milner, 2004;Sigurdsen and Green, 2011), but see, for example, Marjanović and Laurin (2013) for a different view. Recent phylogenetic analyses have recovered two distinct subclades within fossil dissorophoids, one comprising the Olsoniformes (dissorophids and trematopids) and one comprising the Xerodromes (amphibamids and branchiosaurids) (Anderson et al, 2008b;Fröbisch and Schoch, 2009;Schoch, 2012;Schoch and Milner, 2014).…”
Section: Introductionmentioning
confidence: 99%
“…). Whereas the analyses of Laurin & Reisz (), Vallin & Laurin (), Marjanović & Laurin () and Marjanović & Laurin () found lepospondyls (and thus microsaurs) to be stem‐amphibians, the present authors agree with Ruta, Coates & Quicke (), Ruta & Coates (), Sigurdsen & Green (), and Schoch () who regard lepospondyls as stem‐amniotes and lissamphibians as derived from temnospondyls, another large group of early non‐amniotic tetrapods.…”
Section: Resultsmentioning
confidence: 99%