Is the amphibian tree of life really fatally flawed?

Autores
Frost, Darrel R.; Grant, Taran; Faivovich, Julián; Bain, Raoul H.; Haas, Alexander; Haddad, Celio F. B.; de Sa, Rafael O.; Channing, Alan Ernest; Wilkinson, Mark; Donnellan, Stephen C.; Raxworthy, Christopher J.; Campbell, Jonathan A.; Blotto Acuña, Boris Leonardo; Moler, Paul; Drewes, Robert C.; Nussbaum, Ronald A.; Lynch, John D.; Green, David M.; Wheeler, Ward C.
Año de publicación
2008
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Wiens (2007, Q. Rev. Biol. 82, 55–56) recently published a severe critique of Frost et al.'s (2006, Bull. Am. Mus. Nat. Hist. 297, 1–370) monographic study of amphibian systematics, concluding that it is “a disaster” and recommending that readers “simply ignore this study”. Beyond the hyperbole, Wiens raised four general objections that he regarded as “fatal flaws”: (1) the sampling design was insufficient for the generic changes made and taxonomic changes were made without including all type species; (2) the nuclear gene most commonly used in amphibian phylogenetics, RAG‐1, was not included, nor were the morphological characters that had justified the older taxonomy; (3) the analytical method employed is questionable because equally weighted parsimony “assumes that all characters are evolving at equal rates”; and (4) the results were at times “clearly erroneous”, as evidenced by the inferred non‐monophyly of marsupial frogs. In this paper we respond to these criticisms. In brief: (1) the study of Frost et al. did not exist in a vacuum and we discussed our evidence and evidence previously obtained by others that documented the non‐monophyletic taxa that we corrected. Beyond that, we agree that all type species should ideally be included, but inclusion of all potentially relevant type species is not feasible in a study of the magnitude of Frost et al. and we contend that this should not prevent progress in the formulation of phylogenetic hypotheses or their application outside of systematics. (2) Rhodopsin, a gene included by Frost et al. is the nuclear gene that is most commonly used in amphibian systematics, not RAG‐1. Regardless, ignoring a study because of the absence of a single locus strikes us as unsound practice. With respect to previously hypothesized morphological synapomorphies, Frost et al. provided a lengthy review of the published evidence for all groups, and this was used to inform taxonomic decisions. We noted that confirming and reconciling all morphological transformation series published among previous studies needed to be done, and we included evidence from the only published data set at that time to explicitly code morphological characters (including a number of traditionally applied synapomorphies from adult morphology) across the bulk of the diversity of amphibians (Haas, 2003, Cladistics 19, 23–90). Moreover, the phylogenetic results of the Frost et al. study were largely consistent with previous morphological and molecular studies and where they differed, this was discussed with reference to the weight of evidence. (3) The claim that equally weighted parsimony assumes that all characters are evolving at equal rates has been shown to be false in both analytical and simulation studies. (4) The claimed “strong support” for marsupial frog monophyly is questionable. Several studies have also found marsupial frogs to be non‐monophyletic. Wiens et al. (2005, Syst. Biol. 54, 719–748) recovered marsupial frogs as monophyletic, but that result was strongly supported only by Bayesian clade confidence values (which are known to overestimate support) and bootstrap support in his parsimony analysis was < 50%. Further, in a more recent parsimony analysis of an expanded data set that included RAG‐1 and the three traditional morphological synapomorphies of marsupial frogs, Wiens et al. (2006, Am. Nat. 168, 579–596) also found them to be non‐monophyletic. Although we attempted to apply the rule of monophyly to the naming of taxonomic groups, our phylogenetic results are largely consistent with conventional views even if not with the taxonomy current at the time of our writing. Most of our taxonomic changes addressed examples of non‐monophyly that had previously been known or suspected (e.g., the non‐monophyly of traditional Hyperoliidae, Microhylidae, Hemiphractinae, Leptodactylidae, Phrynobatrachus , Ranidae, Rana , Bufo ; and the placement of Brachycephalus within “Eleutherodactylus ”, and Lineatriton within “Pseudoeurycea ”), and it is troubling that Wiens and others, as evidenced by recent publications, continue to perpetuate recognition of non‐monophyletic taxonomic groups that so profoundly misrepresent what is known about amphibian phylogeny.
Fil: Frost, Darrel R.. American Museum of Natural History; Estados Unidos
Fil: Grant, Taran. Pontificia Universidade Católica do Rio Grande do Sul; Brasil
Fil: Faivovich, Julián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Museo Argentino de Ciencias Naturales "Bernardino Rivadavia"; Argentina. Universidade Estadual Paulista Julio de Mesquita Filho; Brasil
Fil: Bain, Raoul H.. American Museum of Natural History; Estados Unidos
Fil: Haas, Alexander. Biocenter Grindel and Zoological Museum Hamburg; Alemania
Fil: Haddad, Celio F. B.. Universidade Estadual Paulista Julio de Mesquita Filho; Brasil
Fil: de Sa, Rafael O.. University of Richmond; Estados Unidos
Fil: Channing, Alan Ernest. University of the Western Cape; Sudáfrica
Fil: Wilkinson, Mark. British Museum (Natural History); Reino Unido
Fil: Donnellan, Stephen C.. South Australia Museum; Australia
Fil: Raxworthy, Christopher J.. American Museum of Natural History; Estados Unidos
Fil: Campbell, Jonathan A.. University of Texas; Estados Unidos
Fil: Blotto Acuña, Boris Leonardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Museo Argentino de Ciencias Naturales "Bernardino Rivadavia"; Argentina
Fil: Moler, Paul. Associate Researcher at the Field Museum; Estados Unidos
Fil: Drewes, Robert C.. California Academy Of Sciences.; Estados Unidos
Fil: Nussbaum, Ronald A.. University of Michigan; Estados Unidos
Fil: Lynch, John D.. Universidad Nacional de Colombia; Colombia
Fil: Green, David M.. McGill University; Canadá
Fil: Wheeler, Ward C.. American Museum of Natural History; Estados Unidos
Materia
PHYLOGENY
AMPHIBIA
TREE OF LIFE
RESPONSE
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/110477

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network_name_str CONICET Digital (CONICET)
spelling Is the amphibian tree of life really fatally flawed?Frost, Darrel R.Grant, TaranFaivovich, JuliánBain, Raoul H.Haas, AlexanderHaddad, Celio F. B.de Sa, Rafael O.Channing, Alan ErnestWilkinson, MarkDonnellan, Stephen C.Raxworthy, Christopher J.Campbell, Jonathan A.Blotto Acuña, Boris LeonardoMoler, PaulDrewes, Robert C.Nussbaum, Ronald A.Lynch, John D.Green, David M.Wheeler, Ward C.PHYLOGENYAMPHIBIATREE OF LIFERESPONSEhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Wiens (2007, Q. Rev. Biol. 82, 55–56) recently published a severe critique of Frost et al.'s (2006, Bull. Am. Mus. Nat. Hist. 297, 1–370) monographic study of amphibian systematics, concluding that it is “a disaster” and recommending that readers “simply ignore this study”. Beyond the hyperbole, Wiens raised four general objections that he regarded as “fatal flaws”: (1) the sampling design was insufficient for the generic changes made and taxonomic changes were made without including all type species; (2) the nuclear gene most commonly used in amphibian phylogenetics, RAG‐1, was not included, nor were the morphological characters that had justified the older taxonomy; (3) the analytical method employed is questionable because equally weighted parsimony “assumes that all characters are evolving at equal rates”; and (4) the results were at times “clearly erroneous”, as evidenced by the inferred non‐monophyly of marsupial frogs. In this paper we respond to these criticisms. In brief: (1) the study of Frost et al. did not exist in a vacuum and we discussed our evidence and evidence previously obtained by others that documented the non‐monophyletic taxa that we corrected. Beyond that, we agree that all type species should ideally be included, but inclusion of all potentially relevant type species is not feasible in a study of the magnitude of Frost et al. and we contend that this should not prevent progress in the formulation of phylogenetic hypotheses or their application outside of systematics. (2) Rhodopsin, a gene included by Frost et al. is the nuclear gene that is most commonly used in amphibian systematics, not RAG‐1. Regardless, ignoring a study because of the absence of a single locus strikes us as unsound practice. With respect to previously hypothesized morphological synapomorphies, Frost et al. provided a lengthy review of the published evidence for all groups, and this was used to inform taxonomic decisions. We noted that confirming and reconciling all morphological transformation series published among previous studies needed to be done, and we included evidence from the only published data set at that time to explicitly code morphological characters (including a number of traditionally applied synapomorphies from adult morphology) across the bulk of the diversity of amphibians (Haas, 2003, Cladistics 19, 23–90). Moreover, the phylogenetic results of the Frost et al. study were largely consistent with previous morphological and molecular studies and where they differed, this was discussed with reference to the weight of evidence. (3) The claim that equally weighted parsimony assumes that all characters are evolving at equal rates has been shown to be false in both analytical and simulation studies. (4) The claimed “strong support” for marsupial frog monophyly is questionable. Several studies have also found marsupial frogs to be non‐monophyletic. Wiens et al. (2005, Syst. Biol. 54, 719–748) recovered marsupial frogs as monophyletic, but that result was strongly supported only by Bayesian clade confidence values (which are known to overestimate support) and bootstrap support in his parsimony analysis was < 50%. Further, in a more recent parsimony analysis of an expanded data set that included RAG‐1 and the three traditional morphological synapomorphies of marsupial frogs, Wiens et al. (2006, Am. Nat. 168, 579–596) also found them to be non‐monophyletic. Although we attempted to apply the rule of monophyly to the naming of taxonomic groups, our phylogenetic results are largely consistent with conventional views even if not with the taxonomy current at the time of our writing. Most of our taxonomic changes addressed examples of non‐monophyly that had previously been known or suspected (e.g., the non‐monophyly of traditional Hyperoliidae, Microhylidae, Hemiphractinae, Leptodactylidae, Phrynobatrachus , Ranidae, Rana , Bufo ; and the placement of Brachycephalus within “Eleutherodactylus ”, and Lineatriton within “Pseudoeurycea ”), and it is troubling that Wiens and others, as evidenced by recent publications, continue to perpetuate recognition of non‐monophyletic taxonomic groups that so profoundly misrepresent what is known about amphibian phylogeny.Fil: Frost, Darrel R.. American Museum of Natural History; Estados UnidosFil: Grant, Taran. Pontificia Universidade Católica do Rio Grande do Sul; BrasilFil: Faivovich, Julián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Museo Argentino de Ciencias Naturales "Bernardino Rivadavia"; Argentina. Universidade Estadual Paulista Julio de Mesquita Filho; BrasilFil: Bain, Raoul H.. American Museum of Natural History; Estados UnidosFil: Haas, Alexander. Biocenter Grindel and Zoological Museum Hamburg; AlemaniaFil: Haddad, Celio F. B.. Universidade Estadual Paulista Julio de Mesquita Filho; BrasilFil: de Sa, Rafael O.. University of Richmond; Estados UnidosFil: Channing, Alan Ernest. University of the Western Cape; SudáfricaFil: Wilkinson, Mark. British Museum (Natural History); Reino UnidoFil: Donnellan, Stephen C.. South Australia Museum; AustraliaFil: Raxworthy, Christopher J.. American Museum of Natural History; Estados UnidosFil: Campbell, Jonathan A.. University of Texas; Estados UnidosFil: Blotto Acuña, Boris Leonardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Museo Argentino de Ciencias Naturales "Bernardino Rivadavia"; ArgentinaFil: Moler, Paul. Associate Researcher at the Field Museum; Estados UnidosFil: Drewes, Robert C.. California Academy Of Sciences.; Estados UnidosFil: Nussbaum, Ronald A.. University of Michigan; Estados UnidosFil: Lynch, John D.. Universidad Nacional de Colombia; ColombiaFil: Green, David M.. McGill University; CanadáFil: Wheeler, Ward C.. American Museum of Natural History; Estados UnidosWiley Blackwell Publishing, Inc2008-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/110477Frost, Darrel R.; Grant, Taran; Faivovich, Julián; Bain, Raoul H.; Haas, Alexander; et al.; Is the amphibian tree of life really fatally flawed?; Wiley Blackwell Publishing, Inc; Cladistics; 24; 3; 6-2008; 385-3950748-3007CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1111/j.1096-0031.2007.00181.xinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/full/10.1111/j.1096-0031.2007.00181.xinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:24:50Zoai:ri.conicet.gov.ar:11336/110477instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-10 13:24:50.438CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Is the amphibian tree of life really fatally flawed?
title Is the amphibian tree of life really fatally flawed?
spellingShingle Is the amphibian tree of life really fatally flawed?
Frost, Darrel R.
PHYLOGENY
AMPHIBIA
TREE OF LIFE
RESPONSE
title_short Is the amphibian tree of life really fatally flawed?
title_full Is the amphibian tree of life really fatally flawed?
title_fullStr Is the amphibian tree of life really fatally flawed?
title_full_unstemmed Is the amphibian tree of life really fatally flawed?
title_sort Is the amphibian tree of life really fatally flawed?
dc.creator.none.fl_str_mv Frost, Darrel R.
Grant, Taran
Faivovich, Julián
Bain, Raoul H.
Haas, Alexander
Haddad, Celio F. B.
de Sa, Rafael O.
Channing, Alan Ernest
Wilkinson, Mark
Donnellan, Stephen C.
Raxworthy, Christopher J.
Campbell, Jonathan A.
Blotto Acuña, Boris Leonardo
Moler, Paul
Drewes, Robert C.
Nussbaum, Ronald A.
Lynch, John D.
Green, David M.
Wheeler, Ward C.
author Frost, Darrel R.
author_facet Frost, Darrel R.
Grant, Taran
Faivovich, Julián
Bain, Raoul H.
Haas, Alexander
Haddad, Celio F. B.
de Sa, Rafael O.
Channing, Alan Ernest
Wilkinson, Mark
Donnellan, Stephen C.
Raxworthy, Christopher J.
Campbell, Jonathan A.
Blotto Acuña, Boris Leonardo
Moler, Paul
Drewes, Robert C.
Nussbaum, Ronald A.
Lynch, John D.
Green, David M.
Wheeler, Ward C.
author_role author
author2 Grant, Taran
Faivovich, Julián
Bain, Raoul H.
Haas, Alexander
Haddad, Celio F. B.
de Sa, Rafael O.
Channing, Alan Ernest
Wilkinson, Mark
Donnellan, Stephen C.
Raxworthy, Christopher J.
Campbell, Jonathan A.
Blotto Acuña, Boris Leonardo
Moler, Paul
Drewes, Robert C.
Nussbaum, Ronald A.
Lynch, John D.
Green, David M.
Wheeler, Ward C.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv PHYLOGENY
AMPHIBIA
TREE OF LIFE
RESPONSE
topic PHYLOGENY
AMPHIBIA
TREE OF LIFE
RESPONSE
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Wiens (2007, Q. Rev. Biol. 82, 55–56) recently published a severe critique of Frost et al.'s (2006, Bull. Am. Mus. Nat. Hist. 297, 1–370) monographic study of amphibian systematics, concluding that it is “a disaster” and recommending that readers “simply ignore this study”. Beyond the hyperbole, Wiens raised four general objections that he regarded as “fatal flaws”: (1) the sampling design was insufficient for the generic changes made and taxonomic changes were made without including all type species; (2) the nuclear gene most commonly used in amphibian phylogenetics, RAG‐1, was not included, nor were the morphological characters that had justified the older taxonomy; (3) the analytical method employed is questionable because equally weighted parsimony “assumes that all characters are evolving at equal rates”; and (4) the results were at times “clearly erroneous”, as evidenced by the inferred non‐monophyly of marsupial frogs. In this paper we respond to these criticisms. In brief: (1) the study of Frost et al. did not exist in a vacuum and we discussed our evidence and evidence previously obtained by others that documented the non‐monophyletic taxa that we corrected. Beyond that, we agree that all type species should ideally be included, but inclusion of all potentially relevant type species is not feasible in a study of the magnitude of Frost et al. and we contend that this should not prevent progress in the formulation of phylogenetic hypotheses or their application outside of systematics. (2) Rhodopsin, a gene included by Frost et al. is the nuclear gene that is most commonly used in amphibian systematics, not RAG‐1. Regardless, ignoring a study because of the absence of a single locus strikes us as unsound practice. With respect to previously hypothesized morphological synapomorphies, Frost et al. provided a lengthy review of the published evidence for all groups, and this was used to inform taxonomic decisions. We noted that confirming and reconciling all morphological transformation series published among previous studies needed to be done, and we included evidence from the only published data set at that time to explicitly code morphological characters (including a number of traditionally applied synapomorphies from adult morphology) across the bulk of the diversity of amphibians (Haas, 2003, Cladistics 19, 23–90). Moreover, the phylogenetic results of the Frost et al. study were largely consistent with previous morphological and molecular studies and where they differed, this was discussed with reference to the weight of evidence. (3) The claim that equally weighted parsimony assumes that all characters are evolving at equal rates has been shown to be false in both analytical and simulation studies. (4) The claimed “strong support” for marsupial frog monophyly is questionable. Several studies have also found marsupial frogs to be non‐monophyletic. Wiens et al. (2005, Syst. Biol. 54, 719–748) recovered marsupial frogs as monophyletic, but that result was strongly supported only by Bayesian clade confidence values (which are known to overestimate support) and bootstrap support in his parsimony analysis was < 50%. Further, in a more recent parsimony analysis of an expanded data set that included RAG‐1 and the three traditional morphological synapomorphies of marsupial frogs, Wiens et al. (2006, Am. Nat. 168, 579–596) also found them to be non‐monophyletic. Although we attempted to apply the rule of monophyly to the naming of taxonomic groups, our phylogenetic results are largely consistent with conventional views even if not with the taxonomy current at the time of our writing. Most of our taxonomic changes addressed examples of non‐monophyly that had previously been known or suspected (e.g., the non‐monophyly of traditional Hyperoliidae, Microhylidae, Hemiphractinae, Leptodactylidae, Phrynobatrachus , Ranidae, Rana , Bufo ; and the placement of Brachycephalus within “Eleutherodactylus ”, and Lineatriton within “Pseudoeurycea ”), and it is troubling that Wiens and others, as evidenced by recent publications, continue to perpetuate recognition of non‐monophyletic taxonomic groups that so profoundly misrepresent what is known about amphibian phylogeny.
Fil: Frost, Darrel R.. American Museum of Natural History; Estados Unidos
Fil: Grant, Taran. Pontificia Universidade Católica do Rio Grande do Sul; Brasil
Fil: Faivovich, Julián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Museo Argentino de Ciencias Naturales "Bernardino Rivadavia"; Argentina. Universidade Estadual Paulista Julio de Mesquita Filho; Brasil
Fil: Bain, Raoul H.. American Museum of Natural History; Estados Unidos
Fil: Haas, Alexander. Biocenter Grindel and Zoological Museum Hamburg; Alemania
Fil: Haddad, Celio F. B.. Universidade Estadual Paulista Julio de Mesquita Filho; Brasil
Fil: de Sa, Rafael O.. University of Richmond; Estados Unidos
Fil: Channing, Alan Ernest. University of the Western Cape; Sudáfrica
Fil: Wilkinson, Mark. British Museum (Natural History); Reino Unido
Fil: Donnellan, Stephen C.. South Australia Museum; Australia
Fil: Raxworthy, Christopher J.. American Museum of Natural History; Estados Unidos
Fil: Campbell, Jonathan A.. University of Texas; Estados Unidos
Fil: Blotto Acuña, Boris Leonardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Museo Argentino de Ciencias Naturales "Bernardino Rivadavia"; Argentina
Fil: Moler, Paul. Associate Researcher at the Field Museum; Estados Unidos
Fil: Drewes, Robert C.. California Academy Of Sciences.; Estados Unidos
Fil: Nussbaum, Ronald A.. University of Michigan; Estados Unidos
Fil: Lynch, John D.. Universidad Nacional de Colombia; Colombia
Fil: Green, David M.. McGill University; Canadá
Fil: Wheeler, Ward C.. American Museum of Natural History; Estados Unidos
description Wiens (2007, Q. Rev. Biol. 82, 55–56) recently published a severe critique of Frost et al.'s (2006, Bull. Am. Mus. Nat. Hist. 297, 1–370) monographic study of amphibian systematics, concluding that it is “a disaster” and recommending that readers “simply ignore this study”. Beyond the hyperbole, Wiens raised four general objections that he regarded as “fatal flaws”: (1) the sampling design was insufficient for the generic changes made and taxonomic changes were made without including all type species; (2) the nuclear gene most commonly used in amphibian phylogenetics, RAG‐1, was not included, nor were the morphological characters that had justified the older taxonomy; (3) the analytical method employed is questionable because equally weighted parsimony “assumes that all characters are evolving at equal rates”; and (4) the results were at times “clearly erroneous”, as evidenced by the inferred non‐monophyly of marsupial frogs. In this paper we respond to these criticisms. In brief: (1) the study of Frost et al. did not exist in a vacuum and we discussed our evidence and evidence previously obtained by others that documented the non‐monophyletic taxa that we corrected. Beyond that, we agree that all type species should ideally be included, but inclusion of all potentially relevant type species is not feasible in a study of the magnitude of Frost et al. and we contend that this should not prevent progress in the formulation of phylogenetic hypotheses or their application outside of systematics. (2) Rhodopsin, a gene included by Frost et al. is the nuclear gene that is most commonly used in amphibian systematics, not RAG‐1. Regardless, ignoring a study because of the absence of a single locus strikes us as unsound practice. With respect to previously hypothesized morphological synapomorphies, Frost et al. provided a lengthy review of the published evidence for all groups, and this was used to inform taxonomic decisions. We noted that confirming and reconciling all morphological transformation series published among previous studies needed to be done, and we included evidence from the only published data set at that time to explicitly code morphological characters (including a number of traditionally applied synapomorphies from adult morphology) across the bulk of the diversity of amphibians (Haas, 2003, Cladistics 19, 23–90). Moreover, the phylogenetic results of the Frost et al. study were largely consistent with previous morphological and molecular studies and where they differed, this was discussed with reference to the weight of evidence. (3) The claim that equally weighted parsimony assumes that all characters are evolving at equal rates has been shown to be false in both analytical and simulation studies. (4) The claimed “strong support” for marsupial frog monophyly is questionable. Several studies have also found marsupial frogs to be non‐monophyletic. Wiens et al. (2005, Syst. Biol. 54, 719–748) recovered marsupial frogs as monophyletic, but that result was strongly supported only by Bayesian clade confidence values (which are known to overestimate support) and bootstrap support in his parsimony analysis was < 50%. Further, in a more recent parsimony analysis of an expanded data set that included RAG‐1 and the three traditional morphological synapomorphies of marsupial frogs, Wiens et al. (2006, Am. Nat. 168, 579–596) also found them to be non‐monophyletic. Although we attempted to apply the rule of monophyly to the naming of taxonomic groups, our phylogenetic results are largely consistent with conventional views even if not with the taxonomy current at the time of our writing. Most of our taxonomic changes addressed examples of non‐monophyly that had previously been known or suspected (e.g., the non‐monophyly of traditional Hyperoliidae, Microhylidae, Hemiphractinae, Leptodactylidae, Phrynobatrachus , Ranidae, Rana , Bufo ; and the placement of Brachycephalus within “Eleutherodactylus ”, and Lineatriton within “Pseudoeurycea ”), and it is troubling that Wiens and others, as evidenced by recent publications, continue to perpetuate recognition of non‐monophyletic taxonomic groups that so profoundly misrepresent what is known about amphibian phylogeny.
publishDate 2008
dc.date.none.fl_str_mv 2008-06
dc.type.none.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/110477
Frost, Darrel R.; Grant, Taran; Faivovich, Julián; Bain, Raoul H.; Haas, Alexander; et al.; Is the amphibian tree of life really fatally flawed?; Wiley Blackwell Publishing, Inc; Cladistics; 24; 3; 6-2008; 385-395
0748-3007
CONICET Digital
CONICET
url http://hdl.handle.net/11336/110477
identifier_str_mv Frost, Darrel R.; Grant, Taran; Faivovich, Julián; Bain, Raoul H.; Haas, Alexander; et al.; Is the amphibian tree of life really fatally flawed?; Wiley Blackwell Publishing, Inc; Cladistics; 24; 3; 6-2008; 385-395
0748-3007
CONICET Digital
CONICET
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