Cargando…

Evolutionary morphology of the lizard chemosensory system

Foraging mode plays a pivotal role in traditional reconstructions of squamate evolution. Transitions between modes are said to spark concerted changes in the morphology, physiology, behaviour, and life history of lizards. With respect to their sensory systems, species that adopt a sit-and-wait strat...

Descripción completa

Detalles Bibliográficos
Autores principales: Baeckens, Simon, Herrel, Anthony, Broeckhoven, Chris, Vasilopoulou-Kampitsi, Menelia, Huyghe, Katleen, Goyens, Jana, Van Damme, Raoul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583331/
https://www.ncbi.nlm.nih.gov/pubmed/28871144
http://dx.doi.org/10.1038/s41598-017-09415-7
_version_ 1783261301083996160
author Baeckens, Simon
Herrel, Anthony
Broeckhoven, Chris
Vasilopoulou-Kampitsi, Menelia
Huyghe, Katleen
Goyens, Jana
Van Damme, Raoul
author_facet Baeckens, Simon
Herrel, Anthony
Broeckhoven, Chris
Vasilopoulou-Kampitsi, Menelia
Huyghe, Katleen
Goyens, Jana
Van Damme, Raoul
author_sort Baeckens, Simon
collection PubMed
description Foraging mode plays a pivotal role in traditional reconstructions of squamate evolution. Transitions between modes are said to spark concerted changes in the morphology, physiology, behaviour, and life history of lizards. With respect to their sensory systems, species that adopt a sit-and-wait strategy are thought to rely on visual cues primarily, while actively hunting species would predominantly use chemical information. The morphology of the tongue and the vomeronasal-organs is believed to mirror this dichotomy. Still, support for this idea of concerted evolution of the morphology of the lizard sensory system merely originates from studies comparing only a few, distantly related taxa that differ in many aspects of their biology besides foraging mode. Hence, we compared vomeronasal-lingual morphology among closely related lizard species (Lacertidae). Our findings show considerable interspecific variation indicating that the chemosensory system of lacertids has undergone substantial change over a short evolutionary time. Although our results imply independent evolution of tongue and vomeronasal-organ form, we find evidence for co-variation between sampler and sensor, hinting towards an ‘optimization’ for efficient chemoreception. Furthermore, our findings suggest species’ degree of investment in chemical signalling, and not foraging behaviour, as a leading factor driving the diversity in vomeronasal-lingual morphology among lacertid species.
format Online
Article
Text
id pubmed-5583331
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-55833312017-09-06 Evolutionary morphology of the lizard chemosensory system Baeckens, Simon Herrel, Anthony Broeckhoven, Chris Vasilopoulou-Kampitsi, Menelia Huyghe, Katleen Goyens, Jana Van Damme, Raoul Sci Rep Article Foraging mode plays a pivotal role in traditional reconstructions of squamate evolution. Transitions between modes are said to spark concerted changes in the morphology, physiology, behaviour, and life history of lizards. With respect to their sensory systems, species that adopt a sit-and-wait strategy are thought to rely on visual cues primarily, while actively hunting species would predominantly use chemical information. The morphology of the tongue and the vomeronasal-organs is believed to mirror this dichotomy. Still, support for this idea of concerted evolution of the morphology of the lizard sensory system merely originates from studies comparing only a few, distantly related taxa that differ in many aspects of their biology besides foraging mode. Hence, we compared vomeronasal-lingual morphology among closely related lizard species (Lacertidae). Our findings show considerable interspecific variation indicating that the chemosensory system of lacertids has undergone substantial change over a short evolutionary time. Although our results imply independent evolution of tongue and vomeronasal-organ form, we find evidence for co-variation between sampler and sensor, hinting towards an ‘optimization’ for efficient chemoreception. Furthermore, our findings suggest species’ degree of investment in chemical signalling, and not foraging behaviour, as a leading factor driving the diversity in vomeronasal-lingual morphology among lacertid species. Nature Publishing Group UK 2017-09-04 /pmc/articles/PMC5583331/ /pubmed/28871144 http://dx.doi.org/10.1038/s41598-017-09415-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Baeckens, Simon
Herrel, Anthony
Broeckhoven, Chris
Vasilopoulou-Kampitsi, Menelia
Huyghe, Katleen
Goyens, Jana
Van Damme, Raoul
Evolutionary morphology of the lizard chemosensory system
title Evolutionary morphology of the lizard chemosensory system
title_full Evolutionary morphology of the lizard chemosensory system
title_fullStr Evolutionary morphology of the lizard chemosensory system
title_full_unstemmed Evolutionary morphology of the lizard chemosensory system
title_short Evolutionary morphology of the lizard chemosensory system
title_sort evolutionary morphology of the lizard chemosensory system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583331/
https://www.ncbi.nlm.nih.gov/pubmed/28871144
http://dx.doi.org/10.1038/s41598-017-09415-7
work_keys_str_mv AT baeckenssimon evolutionarymorphologyofthelizardchemosensorysystem
AT herrelanthony evolutionarymorphologyofthelizardchemosensorysystem
AT broeckhovenchris evolutionarymorphologyofthelizardchemosensorysystem
AT vasilopouloukampitsimenelia evolutionarymorphologyofthelizardchemosensorysystem
AT huyghekatleen evolutionarymorphologyofthelizardchemosensorysystem
AT goyensjana evolutionarymorphologyofthelizardchemosensorysystem
AT vandammeraoul evolutionarymorphologyofthelizardchemosensorysystem