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Anatomy of a Neotropical insect radiation

BACKGROUND: Much evolutionary theory predicts that diversity arises via both adaptive radiation (diversification driven by selection against niche-overlap within communities) and divergence of geographically isolated populations. We focus on tropical fruit flies (Blepharoneura, Tephritidae) that rev...

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Autores principales: Winkler, Isaac, Scheffer, Sonja J., Lewis, Matthew L., Ottens, Kristina J., Rasmussen, Andrew P., Gomes-Costa, Géssica A., Huerto Santillan, Luz Maria, Condon, Marty A., Forbes, Andrew A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853117/
https://www.ncbi.nlm.nih.gov/pubmed/29540154
http://dx.doi.org/10.1186/s12862-018-1146-9
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author Winkler, Isaac
Scheffer, Sonja J.
Lewis, Matthew L.
Ottens, Kristina J.
Rasmussen, Andrew P.
Gomes-Costa, Géssica A.
Huerto Santillan, Luz Maria
Condon, Marty A.
Forbes, Andrew A.
author_facet Winkler, Isaac
Scheffer, Sonja J.
Lewis, Matthew L.
Ottens, Kristina J.
Rasmussen, Andrew P.
Gomes-Costa, Géssica A.
Huerto Santillan, Luz Maria
Condon, Marty A.
Forbes, Andrew A.
author_sort Winkler, Isaac
collection PubMed
description BACKGROUND: Much evolutionary theory predicts that diversity arises via both adaptive radiation (diversification driven by selection against niche-overlap within communities) and divergence of geographically isolated populations. We focus on tropical fruit flies (Blepharoneura, Tephritidae) that reveal unexpected patterns of niche-overlap within local communities. Throughout the Neotropics, multiple sympatric non-interbreeding populations often share the same highly specialized patterns of host use (e.g., flies are specialists on flowers of a single gender of a single species of host plants). Lineage through time (LTT) plots can help distinguish patterns of diversification consistent with ecologically limited adaptive radiation from those predicted by ecologically neutral theories. Here, we use a time-calibrated phylogeny of Blepharoneura to test the hypothesis that patterns of Blepharoneura diversification are consistent with an “ecologically neutral” model of diversification that predicts that diversification is primarily a function of time and space. RESULTS: The Blepharoneura phylogeny showed more cladogenic divergence associated with geography than with shifts in host-use. Shifts in host-use were associated with ~ 20% of recent splits (< 3 Ma), but > 60% of older splits (> 3 Ma). In the overall tree, gamma statistic and maximum likelihood model fitting showed no evidence of diversification rate changes though there was a weak signature of slowing diversification rate in one of the component clades. CONCLUSIONS: Overall patterns of Blepharoneura diversity are inconsistent with a traditional explanation of adaptive radiation involving decreases in diversification rates associated with niche-overlap. Sister lineages usually use the same host-species and host-parts, and multiple non-interbreeding sympatric populations regularly co-occur on the same hosts. We suggest that most lineage origins (phylogenetic splits) occur in allopatry, usually without shifts in host-use, and that subsequent dispersal results in assembly of communities composed of multiple sympatric non-interbreeding populations of flies that share the same hosts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-018-1146-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-58531172018-03-22 Anatomy of a Neotropical insect radiation Winkler, Isaac Scheffer, Sonja J. Lewis, Matthew L. Ottens, Kristina J. Rasmussen, Andrew P. Gomes-Costa, Géssica A. Huerto Santillan, Luz Maria Condon, Marty A. Forbes, Andrew A. BMC Evol Biol Research Article BACKGROUND: Much evolutionary theory predicts that diversity arises via both adaptive radiation (diversification driven by selection against niche-overlap within communities) and divergence of geographically isolated populations. We focus on tropical fruit flies (Blepharoneura, Tephritidae) that reveal unexpected patterns of niche-overlap within local communities. Throughout the Neotropics, multiple sympatric non-interbreeding populations often share the same highly specialized patterns of host use (e.g., flies are specialists on flowers of a single gender of a single species of host plants). Lineage through time (LTT) plots can help distinguish patterns of diversification consistent with ecologically limited adaptive radiation from those predicted by ecologically neutral theories. Here, we use a time-calibrated phylogeny of Blepharoneura to test the hypothesis that patterns of Blepharoneura diversification are consistent with an “ecologically neutral” model of diversification that predicts that diversification is primarily a function of time and space. RESULTS: The Blepharoneura phylogeny showed more cladogenic divergence associated with geography than with shifts in host-use. Shifts in host-use were associated with ~ 20% of recent splits (< 3 Ma), but > 60% of older splits (> 3 Ma). In the overall tree, gamma statistic and maximum likelihood model fitting showed no evidence of diversification rate changes though there was a weak signature of slowing diversification rate in one of the component clades. CONCLUSIONS: Overall patterns of Blepharoneura diversity are inconsistent with a traditional explanation of adaptive radiation involving decreases in diversification rates associated with niche-overlap. Sister lineages usually use the same host-species and host-parts, and multiple non-interbreeding sympatric populations regularly co-occur on the same hosts. We suggest that most lineage origins (phylogenetic splits) occur in allopatry, usually without shifts in host-use, and that subsequent dispersal results in assembly of communities composed of multiple sympatric non-interbreeding populations of flies that share the same hosts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-018-1146-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-14 /pmc/articles/PMC5853117/ /pubmed/29540154 http://dx.doi.org/10.1186/s12862-018-1146-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Winkler, Isaac
Scheffer, Sonja J.
Lewis, Matthew L.
Ottens, Kristina J.
Rasmussen, Andrew P.
Gomes-Costa, Géssica A.
Huerto Santillan, Luz Maria
Condon, Marty A.
Forbes, Andrew A.
Anatomy of a Neotropical insect radiation
title Anatomy of a Neotropical insect radiation
title_full Anatomy of a Neotropical insect radiation
title_fullStr Anatomy of a Neotropical insect radiation
title_full_unstemmed Anatomy of a Neotropical insect radiation
title_short Anatomy of a Neotropical insect radiation
title_sort anatomy of a neotropical insect radiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853117/
https://www.ncbi.nlm.nih.gov/pubmed/29540154
http://dx.doi.org/10.1186/s12862-018-1146-9
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