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3-D imaging reveals four extraordinary cases of convergent evolution of acoustic communication in crickets and allies (Insecta)
When the same complex trait is exhibited by closely related species, a single evolutionary origin is frequently invoked. The complex stridulatory apparatus present in the forewings of extant crickets, mole crickets, katydids, and prophalangopsids, is currently interpreted as sharing a single common...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541040/ https://www.ncbi.nlm.nih.gov/pubmed/28769067 http://dx.doi.org/10.1038/s41598-017-06840-6 |
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author | Desutter-Grandcolas, Laure Jacquelin, Lauriane Hugel, Sylvain Boistel, Renaud Garrouste, Romain Henrotay, Michel Warren, Ben H. Chintauan-Marquier, Ioana C. Nel, Patricia Grandcolas, Philippe Nel, André |
author_facet | Desutter-Grandcolas, Laure Jacquelin, Lauriane Hugel, Sylvain Boistel, Renaud Garrouste, Romain Henrotay, Michel Warren, Ben H. Chintauan-Marquier, Ioana C. Nel, Patricia Grandcolas, Philippe Nel, André |
author_sort | Desutter-Grandcolas, Laure |
collection | PubMed |
description | When the same complex trait is exhibited by closely related species, a single evolutionary origin is frequently invoked. The complex stridulatory apparatus present in the forewings of extant crickets, mole crickets, katydids, and prophalangopsids, is currently interpreted as sharing a single common origin due to their similarity and unique function. An alternative hypothesis of convergent evolution in these ensiferan groups has challenged this common view, but remained controversial because of competing interpretations of wing venation. Here we propose another hypothesis for the widely and long debated homology of ensiferan stridulatory apparatus, performing the first 3D reconstruction of hidden structures at the wing bases. This approach allowed defining the homology of each vein from its very origin rather than after its more distal characteristics, which may be subjected to environmental pressure of selection. The stridulatory apparatus involves different veins in these four singing clades. In light of the most recent phylogenetic evidence, this apparatus developed four times in Ensifera, illustrating extraordinary convergent evolutions between closely related clades, by far exceeding the number of evolutionary steps ever proposed for calling ability in this group. |
format | Online Article Text |
id | pubmed-5541040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55410402017-08-07 3-D imaging reveals four extraordinary cases of convergent evolution of acoustic communication in crickets and allies (Insecta) Desutter-Grandcolas, Laure Jacquelin, Lauriane Hugel, Sylvain Boistel, Renaud Garrouste, Romain Henrotay, Michel Warren, Ben H. Chintauan-Marquier, Ioana C. Nel, Patricia Grandcolas, Philippe Nel, André Sci Rep Article When the same complex trait is exhibited by closely related species, a single evolutionary origin is frequently invoked. The complex stridulatory apparatus present in the forewings of extant crickets, mole crickets, katydids, and prophalangopsids, is currently interpreted as sharing a single common origin due to their similarity and unique function. An alternative hypothesis of convergent evolution in these ensiferan groups has challenged this common view, but remained controversial because of competing interpretations of wing venation. Here we propose another hypothesis for the widely and long debated homology of ensiferan stridulatory apparatus, performing the first 3D reconstruction of hidden structures at the wing bases. This approach allowed defining the homology of each vein from its very origin rather than after its more distal characteristics, which may be subjected to environmental pressure of selection. The stridulatory apparatus involves different veins in these four singing clades. In light of the most recent phylogenetic evidence, this apparatus developed four times in Ensifera, illustrating extraordinary convergent evolutions between closely related clades, by far exceeding the number of evolutionary steps ever proposed for calling ability in this group. Nature Publishing Group UK 2017-08-02 /pmc/articles/PMC5541040/ /pubmed/28769067 http://dx.doi.org/10.1038/s41598-017-06840-6 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 Desutter-Grandcolas, Laure Jacquelin, Lauriane Hugel, Sylvain Boistel, Renaud Garrouste, Romain Henrotay, Michel Warren, Ben H. Chintauan-Marquier, Ioana C. Nel, Patricia Grandcolas, Philippe Nel, André 3-D imaging reveals four extraordinary cases of convergent evolution of acoustic communication in crickets and allies (Insecta) |
title | 3-D imaging reveals four extraordinary cases of convergent evolution of acoustic communication in crickets and allies (Insecta) |
title_full | 3-D imaging reveals four extraordinary cases of convergent evolution of acoustic communication in crickets and allies (Insecta) |
title_fullStr | 3-D imaging reveals four extraordinary cases of convergent evolution of acoustic communication in crickets and allies (Insecta) |
title_full_unstemmed | 3-D imaging reveals four extraordinary cases of convergent evolution of acoustic communication in crickets and allies (Insecta) |
title_short | 3-D imaging reveals four extraordinary cases of convergent evolution of acoustic communication in crickets and allies (Insecta) |
title_sort | 3-d imaging reveals four extraordinary cases of convergent evolution of acoustic communication in crickets and allies (insecta) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541040/ https://www.ncbi.nlm.nih.gov/pubmed/28769067 http://dx.doi.org/10.1038/s41598-017-06840-6 |
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