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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....

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Autores principales: Li, Hu, Leavengood, John M., Chapman, Eric G., Burkhardt, Daniel, Song, Fan, Jiang, Pei, Liu, Jinpeng, Zhou, Xuguo, Cai, Wanzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2017
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.
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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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