Cargando…
Signatures of echolocation and dietary ecology in the adaptive evolution of skull shape in bats
Morphological diversity may arise rapidly as a result of adaptation to novel ecological opportunities, but early bursts of trait evolution are rarely observed. Rather, models of discrete shifts between adaptive zones may better explain macroevolutionary dynamics across radiations. To investigate whi...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497661/ https://www.ncbi.nlm.nih.gov/pubmed/31048713 http://dx.doi.org/10.1038/s41467-019-09951-y |
_version_ | 1783415504156753920 |
---|---|
author | Arbour, Jessica H. Curtis, Abigail A. Santana, Sharlene E. |
author_facet | Arbour, Jessica H. Curtis, Abigail A. Santana, Sharlene E. |
author_sort | Arbour, Jessica H. |
collection | PubMed |
description | Morphological diversity may arise rapidly as a result of adaptation to novel ecological opportunities, but early bursts of trait evolution are rarely observed. Rather, models of discrete shifts between adaptive zones may better explain macroevolutionary dynamics across radiations. To investigate which of these processes underlie exceptional levels of morphological diversity during ecological diversification, we use modern phylogenetic tools and 3D geometric morphometric datasets to examine adaptive zone shifts in bat skull shape. Here we report that, while disparity was established early, bat skull evolution is best described by multiple adaptive zone shifts. Shifts are partially decoupled between the cranium and mandible, with cranial evolution more strongly driven by echolocation than diet. Phyllostomidae, a trophic adaptive radiation, exhibits more adaptive zone shifts than all other families combined. This pattern was potentially driven by ecological opportunity and facilitated by a shift to intermediate cranial shapes compared to oral-emitters and other nasal emitters. |
format | Online Article Text |
id | pubmed-6497661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64976612019-05-06 Signatures of echolocation and dietary ecology in the adaptive evolution of skull shape in bats Arbour, Jessica H. Curtis, Abigail A. Santana, Sharlene E. Nat Commun Article Morphological diversity may arise rapidly as a result of adaptation to novel ecological opportunities, but early bursts of trait evolution are rarely observed. Rather, models of discrete shifts between adaptive zones may better explain macroevolutionary dynamics across radiations. To investigate which of these processes underlie exceptional levels of morphological diversity during ecological diversification, we use modern phylogenetic tools and 3D geometric morphometric datasets to examine adaptive zone shifts in bat skull shape. Here we report that, while disparity was established early, bat skull evolution is best described by multiple adaptive zone shifts. Shifts are partially decoupled between the cranium and mandible, with cranial evolution more strongly driven by echolocation than diet. Phyllostomidae, a trophic adaptive radiation, exhibits more adaptive zone shifts than all other families combined. This pattern was potentially driven by ecological opportunity and facilitated by a shift to intermediate cranial shapes compared to oral-emitters and other nasal emitters. Nature Publishing Group UK 2019-05-02 /pmc/articles/PMC6497661/ /pubmed/31048713 http://dx.doi.org/10.1038/s41467-019-09951-y Text en © The Author(s) 2019 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 Arbour, Jessica H. Curtis, Abigail A. Santana, Sharlene E. Signatures of echolocation and dietary ecology in the adaptive evolution of skull shape in bats |
title | Signatures of echolocation and dietary ecology in the adaptive evolution of skull shape in bats |
title_full | Signatures of echolocation and dietary ecology in the adaptive evolution of skull shape in bats |
title_fullStr | Signatures of echolocation and dietary ecology in the adaptive evolution of skull shape in bats |
title_full_unstemmed | Signatures of echolocation and dietary ecology in the adaptive evolution of skull shape in bats |
title_short | Signatures of echolocation and dietary ecology in the adaptive evolution of skull shape in bats |
title_sort | signatures of echolocation and dietary ecology in the adaptive evolution of skull shape in bats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497661/ https://www.ncbi.nlm.nih.gov/pubmed/31048713 http://dx.doi.org/10.1038/s41467-019-09951-y |
work_keys_str_mv | AT arbourjessicah signaturesofecholocationanddietaryecologyintheadaptiveevolutionofskullshapeinbats AT curtisabigaila signaturesofecholocationanddietaryecologyintheadaptiveevolutionofskullshapeinbats AT santanasharlenee signaturesofecholocationanddietaryecologyintheadaptiveevolutionofskullshapeinbats |