Cargando…
The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals
Listeners locate potential mates using species-specific vocal signals. As tetrapods transitioned from water to land, lungs replaced gills, allowing expiration to drive sound production. Some frogs then returned to water. Here we explore how air-driven sound production changed upon re-entry to preser...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324873/ https://www.ncbi.nlm.nih.gov/pubmed/30618379 http://dx.doi.org/10.7554/eLife.39946 |
_version_ | 1783386046412619776 |
---|---|
author | Kwong-Brown, Ursula Tobias, Martha L Elias, Damian O Hall, Ian C Elemans, Coen PH Kelley, Darcy B |
author_facet | Kwong-Brown, Ursula Tobias, Martha L Elias, Damian O Hall, Ian C Elemans, Coen PH Kelley, Darcy B |
author_sort | Kwong-Brown, Ursula |
collection | PubMed |
description | Listeners locate potential mates using species-specific vocal signals. As tetrapods transitioned from water to land, lungs replaced gills, allowing expiration to drive sound production. Some frogs then returned to water. Here we explore how air-driven sound production changed upon re-entry to preserve essential acoustic information on species identity in the secondarily aquatic frog genus Xenopus. We filmed movements of cartilage and muscles during evoked sound production in isolated larynges. Results refute the current theory for Xenopus vocalization, cavitation, and favor instead sound production by mechanical excitation of laryngeal resonance modes following rapid separation of laryngeal arytenoid discs. Resulting frequency resonance modes (dyads) are intrinsic to the larynx rather than due to neuromuscular control. Dyads are a distinctive acoustic signature. While their component frequencies overlap across species, their ratio is shared within each Xenopus clade providing information on species identity that could facilitate both conspecific localization and ancient species divergence. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter). |
format | Online Article Text |
id | pubmed-6324873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63248732019-01-10 The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals Kwong-Brown, Ursula Tobias, Martha L Elias, Damian O Hall, Ian C Elemans, Coen PH Kelley, Darcy B eLife Ecology Listeners locate potential mates using species-specific vocal signals. As tetrapods transitioned from water to land, lungs replaced gills, allowing expiration to drive sound production. Some frogs then returned to water. Here we explore how air-driven sound production changed upon re-entry to preserve essential acoustic information on species identity in the secondarily aquatic frog genus Xenopus. We filmed movements of cartilage and muscles during evoked sound production in isolated larynges. Results refute the current theory for Xenopus vocalization, cavitation, and favor instead sound production by mechanical excitation of laryngeal resonance modes following rapid separation of laryngeal arytenoid discs. Resulting frequency resonance modes (dyads) are intrinsic to the larynx rather than due to neuromuscular control. Dyads are a distinctive acoustic signature. While their component frequencies overlap across species, their ratio is shared within each Xenopus clade providing information on species identity that could facilitate both conspecific localization and ancient species divergence. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter). eLife Sciences Publications, Ltd 2019-01-08 /pmc/articles/PMC6324873/ /pubmed/30618379 http://dx.doi.org/10.7554/eLife.39946 Text en © 2019, Kwong-Brown et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Ecology Kwong-Brown, Ursula Tobias, Martha L Elias, Damian O Hall, Ian C Elemans, Coen PH Kelley, Darcy B The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals |
title | The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals |
title_full | The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals |
title_fullStr | The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals |
title_full_unstemmed | The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals |
title_short | The return to water in ancestral Xenopus was accompanied by a novel mechanism for producing and shaping vocal signals |
title_sort | return to water in ancestral xenopus was accompanied by a novel mechanism for producing and shaping vocal signals |
topic | Ecology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324873/ https://www.ncbi.nlm.nih.gov/pubmed/30618379 http://dx.doi.org/10.7554/eLife.39946 |
work_keys_str_mv | AT kwongbrownursula thereturntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT tobiasmarthal thereturntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT eliasdamiano thereturntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT hallianc thereturntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT elemanscoenph thereturntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT kelleydarcyb thereturntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT kwongbrownursula returntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT tobiasmarthal returntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT eliasdamiano returntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT hallianc returntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT elemanscoenph returntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals AT kelleydarcyb returntowaterinancestralxenopuswasaccompaniedbyanovelmechanismforproducingandshapingvocalsignals |