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Mitochondrial phylogenomics of Hemiptera reveals adaptive innovations driving the diversification of true bugs
Hemiptera, the largest non-holometabolous order of insects, represents approximately 7% of metazoan diversity. With extraordinary life histories and highly specialized morphological adaptations, hemipterans have exploited diverse habitats and food sources through approximately 300 Myr of evolution....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597834/ https://www.ncbi.nlm.nih.gov/pubmed/28878063 http://dx.doi.org/10.1098/rspb.2017.1223 |
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author | Li, Hu Leavengood, John M. Chapman, Eric G. Burkhardt, Daniel Song, Fan Jiang, Pei Liu, Jinpeng Zhou, Xuguo Cai, Wanzhi |
author_facet | Li, Hu Leavengood, John M. Chapman, Eric G. Burkhardt, Daniel Song, Fan Jiang, Pei Liu, Jinpeng Zhou, Xuguo Cai, Wanzhi |
author_sort | Li, Hu |
collection | PubMed |
description | Hemiptera, the largest non-holometabolous order of insects, represents approximately 7% of metazoan diversity. With extraordinary life histories and highly specialized morphological adaptations, hemipterans have exploited diverse habitats and food sources through approximately 300 Myr of evolution. To elucidate the phylogeny and evolutionary history of Hemiptera, we carried out the most comprehensive mitogenomics analysis on the richest taxon sampling to date covering all the suborders and infraorders, including 34 newly sequenced and 94 published mitogenomes. With optimized branch length and sequence heterogeneity, Bayesian analyses using a site-heterogeneous mixture model resolved the higher-level hemipteran phylogeny as (Sternorrhyncha, (Auchenorrhyncha, (Coleorrhyncha, Heteroptera))). Ancestral character state reconstruction and divergence time estimation suggest that the success of true bugs (Heteroptera) is probably due to angiosperm coevolution, but key adaptive innovations (e.g. prognathous mouthpart, predatory behaviour, and haemelytron) facilitated multiple independent shifts among diverse feeding habits and multiple independent colonizations of aquatic habitats. |
format | Online Article Text |
id | pubmed-5597834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-55978342017-09-18 Mitochondrial phylogenomics of Hemiptera reveals adaptive innovations driving the diversification of true bugs Li, Hu Leavengood, John M. Chapman, Eric G. Burkhardt, Daniel Song, Fan Jiang, Pei Liu, Jinpeng Zhou, Xuguo Cai, Wanzhi Proc Biol Sci Evolution Hemiptera, the largest non-holometabolous order of insects, represents approximately 7% of metazoan diversity. With extraordinary life histories and highly specialized morphological adaptations, hemipterans have exploited diverse habitats and food sources through approximately 300 Myr of evolution. To elucidate the phylogeny and evolutionary history of Hemiptera, we carried out the most comprehensive mitogenomics analysis on the richest taxon sampling to date covering all the suborders and infraorders, including 34 newly sequenced and 94 published mitogenomes. With optimized branch length and sequence heterogeneity, Bayesian analyses using a site-heterogeneous mixture model resolved the higher-level hemipteran phylogeny as (Sternorrhyncha, (Auchenorrhyncha, (Coleorrhyncha, Heteroptera))). Ancestral character state reconstruction and divergence time estimation suggest that the success of true bugs (Heteroptera) is probably due to angiosperm coevolution, but key adaptive innovations (e.g. prognathous mouthpart, predatory behaviour, and haemelytron) facilitated multiple independent shifts among diverse feeding habits and multiple independent colonizations of aquatic habitats. The Royal Society 2017-09-13 2017-09-06 /pmc/articles/PMC5597834/ /pubmed/28878063 http://dx.doi.org/10.1098/rspb.2017.1223 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolution Li, Hu Leavengood, John M. Chapman, Eric G. Burkhardt, Daniel Song, Fan Jiang, Pei Liu, Jinpeng Zhou, Xuguo Cai, Wanzhi Mitochondrial phylogenomics of Hemiptera reveals adaptive innovations driving the diversification of true bugs |
title | Mitochondrial phylogenomics of Hemiptera reveals adaptive innovations driving the diversification of true bugs |
title_full | Mitochondrial phylogenomics of Hemiptera reveals adaptive innovations driving the diversification of true bugs |
title_fullStr | Mitochondrial phylogenomics of Hemiptera reveals adaptive innovations driving the diversification of true bugs |
title_full_unstemmed | Mitochondrial phylogenomics of Hemiptera reveals adaptive innovations driving the diversification of true bugs |
title_short | Mitochondrial phylogenomics of Hemiptera reveals adaptive innovations driving the diversification of true bugs |
title_sort | mitochondrial phylogenomics of hemiptera reveals adaptive innovations driving the diversification of true bugs |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597834/ https://www.ncbi.nlm.nih.gov/pubmed/28878063 http://dx.doi.org/10.1098/rspb.2017.1223 |
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