2020
DOI: 10.1655/herpetologica-d-19-00046.1
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Geographic Variation in the Acoustic Signals of Dendropsophus nanus (Boulenger 1889) (Anura: Hylidae)

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Cited by 3 publications
(2 citation statements)
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“…The roles of environmental factors in acoustic divergence, especially habitat-or climate-driven call divergence, have been examined in some frogs with the expectation that acoustic signals evolve to increase the transmission efficiency within the habitats in which they are emitted (e.g. Bosch & De la Riva 2004;Annibale et al 2020;Röhr et al 2020;Zhao et al 2021). Anuran calls are relatively simple, and many studies on these simple signals have suggested that their geographic variation is correlated with the acoustic characteristics of different habitats.…”
Section: Discussionmentioning
confidence: 99%
“…The roles of environmental factors in acoustic divergence, especially habitat-or climate-driven call divergence, have been examined in some frogs with the expectation that acoustic signals evolve to increase the transmission efficiency within the habitats in which they are emitted (e.g. Bosch & De la Riva 2004;Annibale et al 2020;Röhr et al 2020;Zhao et al 2021). Anuran calls are relatively simple, and many studies on these simple signals have suggested that their geographic variation is correlated with the acoustic characteristics of different habitats.…”
Section: Discussionmentioning
confidence: 99%
“…This has been the case with taxa (cryptic) that share many similarities, but whose distinctions (mostly linked to colour, warts or tubercles, or sometimes by acoustic [not immune to variability] and genetic analysis) can be ambiguous and conceptually confusing. Additionally, those distinctions have not even been tested under any experimental model of diversification dynamics ( Ajmal Ali et al, 2014 ; Annibale et al, 2020 ; Schindel & Miller, 2005 ; Van Holstein & Foley, 2020 ), where patterns of trait richness are equivalent to the rates of intraspecific population divergence (and would thus reinforce the divergence hypotheses). This is mainly the case for species of the P. goyana and P. cristiceps groups ( Martins & Giaretta, 2011 ); but why not then for the P. biggibosa , P. boei and P. appendiculata groups, whose taxonomic histories depend on variable phenetic traits, while evidence of pre- or post-zygotic barriers or their biogeographies continue to be elusive?…”
Section: Discussionmentioning
confidence: 99%