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Oviposition traits generate extrinsic postzygotic isolation between two pine sawfly species

BACKGROUND: Although empirical data indicate that ecological speciation is prevalent in nature, the relative importance of different forms of reproductive isolation and the traits generating reproductive isolation remain unclear. To address these questions, we examined a pair of ecologically diverge...

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Autores principales: Bendall, Emily E., Vertacnik, Kim L., Linnen, Catherine R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5248504/
https://www.ncbi.nlm.nih.gov/pubmed/28103815
http://dx.doi.org/10.1186/s12862-017-0872-8
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author Bendall, Emily E.
Vertacnik, Kim L.
Linnen, Catherine R.
author_facet Bendall, Emily E.
Vertacnik, Kim L.
Linnen, Catherine R.
author_sort Bendall, Emily E.
collection PubMed
description BACKGROUND: Although empirical data indicate that ecological speciation is prevalent in nature, the relative importance of different forms of reproductive isolation and the traits generating reproductive isolation remain unclear. To address these questions, we examined a pair of ecologically divergent pine-sawfly species: while Neodiprion pinetum specializes on a thin-needled pine (Pinus strobus), N. lecontei utilizes thicker-needled pines. We hypothesized that extrinsic postzygotic isolation is generated by oviposition traits. To test this hypothesis, we assayed ovipositor morphology, oviposition behavior, and host-dependent oviposition success in both species and in F1 and backcross females. RESULTS: Compared to N. lecontei, N. pinetum females preferred P. strobus more strongly, had smaller ovipositors, and laid fewer eggs per needle. Additionally, we observed host- and trait-dependent reductions in oviposition success in F1 and backcross females. Hybrid females that had pinetum-like host preference (P. strobus) and lecontei-like oviposition traits (morphology and egg pattern) fared especially poorly. CONCLUSIONS: Together, these data indicate that maladaptive combinations of oviposition traits in hybrids contribute to extrinsic postzygotic isolation between N. lecontei and N. pinetum, suggesting that oviposition traits may be an important driver of divergence in phytophagous insects. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0872-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-52485042017-01-25 Oviposition traits generate extrinsic postzygotic isolation between two pine sawfly species Bendall, Emily E. Vertacnik, Kim L. Linnen, Catherine R. BMC Evol Biol Research Article BACKGROUND: Although empirical data indicate that ecological speciation is prevalent in nature, the relative importance of different forms of reproductive isolation and the traits generating reproductive isolation remain unclear. To address these questions, we examined a pair of ecologically divergent pine-sawfly species: while Neodiprion pinetum specializes on a thin-needled pine (Pinus strobus), N. lecontei utilizes thicker-needled pines. We hypothesized that extrinsic postzygotic isolation is generated by oviposition traits. To test this hypothesis, we assayed ovipositor morphology, oviposition behavior, and host-dependent oviposition success in both species and in F1 and backcross females. RESULTS: Compared to N. lecontei, N. pinetum females preferred P. strobus more strongly, had smaller ovipositors, and laid fewer eggs per needle. Additionally, we observed host- and trait-dependent reductions in oviposition success in F1 and backcross females. Hybrid females that had pinetum-like host preference (P. strobus) and lecontei-like oviposition traits (morphology and egg pattern) fared especially poorly. CONCLUSIONS: Together, these data indicate that maladaptive combinations of oviposition traits in hybrids contribute to extrinsic postzygotic isolation between N. lecontei and N. pinetum, suggesting that oviposition traits may be an important driver of divergence in phytophagous insects. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0872-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-19 /pmc/articles/PMC5248504/ /pubmed/28103815 http://dx.doi.org/10.1186/s12862-017-0872-8 Text en © The Author(s). 2017 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
Bendall, Emily E.
Vertacnik, Kim L.
Linnen, Catherine R.
Oviposition traits generate extrinsic postzygotic isolation between two pine sawfly species
title Oviposition traits generate extrinsic postzygotic isolation between two pine sawfly species
title_full Oviposition traits generate extrinsic postzygotic isolation between two pine sawfly species
title_fullStr Oviposition traits generate extrinsic postzygotic isolation between two pine sawfly species
title_full_unstemmed Oviposition traits generate extrinsic postzygotic isolation between two pine sawfly species
title_short Oviposition traits generate extrinsic postzygotic isolation between two pine sawfly species
title_sort oviposition traits generate extrinsic postzygotic isolation between two pine sawfly species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5248504/
https://www.ncbi.nlm.nih.gov/pubmed/28103815
http://dx.doi.org/10.1186/s12862-017-0872-8
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