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Assortative mating and self-fertilization differ in their contributions to reinforcement, cascade speciation, and diversification

Cascade speciation and reinforcement can evolve rapidly when traits are pleiotropic and act as both signal/cue in nonrandom mating. Here, we examine the contribution of two key traits—assortative mating and self-fertilization—to reinforcement and (by extension) cascade speciation. First, using a pop...

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Autores principales: Castillo, Dean M., Gibson, Amanda K., Moyle, Leonie C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804227/
https://www.ncbi.nlm.nih.gov/pubmed/29491904
http://dx.doi.org/10.1093/cz/zow004
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author Castillo, Dean M.
Gibson, Amanda K.
Moyle, Leonie C.
author_facet Castillo, Dean M.
Gibson, Amanda K.
Moyle, Leonie C.
author_sort Castillo, Dean M.
collection PubMed
description Cascade speciation and reinforcement can evolve rapidly when traits are pleiotropic and act as both signal/cue in nonrandom mating. Here, we examine the contribution of two key traits—assortative mating and self-fertilization—to reinforcement and (by extension) cascade speciation. First, using a population genetic model of reinforcement we find that both assortative mating and self-fertilization can make independent contributions to increased reproductive isolation, consistent with reinforcement. Self-fertilization primarily evolves due to its 2-fold transmission advantage when inbreeding depression (d) is lower (d < 0.45) but evolves as a function of the cost of hybridization under higher inbreeding depression (0.45 < d < 0.48). When both traits can evolve simultaneously, increased self-fertilization often prohibits the evolution of assortative mating. We infer that, under specific conditions, mating system transitions are more likely to lead to increased reproductive isolation and initiate cascade speciation, than assortative mating. Based on the results of our simulations, we hypothesized that transitions to self-fertilization could contribute to clade-wide diversification if reinforcement or cascade speciation is common. We tested this hypothesis with comparative data from two different groups. Consistent with our hypothesis, there was a trend towards uniparental reproduction being associated with increased diversification rate in the Nematode phylum. For the plant genus Mimulus, however, self-fertilization was associated with reduced diversification. Reinforcement driving speciation via transitions to self-fertilization might be short lived or unsustainable across macroevolutionary scales in some systems (some plants), but not others (such as nematodes), potentially due to differences in susceptibility to inbreeding depression and/or the ability to transition between reproductive modes.
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spelling pubmed-58042272018-02-28 Assortative mating and self-fertilization differ in their contributions to reinforcement, cascade speciation, and diversification Castillo, Dean M. Gibson, Amanda K. Moyle, Leonie C. Curr Zool Special Column Cascade Reinforcement Cascade speciation and reinforcement can evolve rapidly when traits are pleiotropic and act as both signal/cue in nonrandom mating. Here, we examine the contribution of two key traits—assortative mating and self-fertilization—to reinforcement and (by extension) cascade speciation. First, using a population genetic model of reinforcement we find that both assortative mating and self-fertilization can make independent contributions to increased reproductive isolation, consistent with reinforcement. Self-fertilization primarily evolves due to its 2-fold transmission advantage when inbreeding depression (d) is lower (d < 0.45) but evolves as a function of the cost of hybridization under higher inbreeding depression (0.45 < d < 0.48). When both traits can evolve simultaneously, increased self-fertilization often prohibits the evolution of assortative mating. We infer that, under specific conditions, mating system transitions are more likely to lead to increased reproductive isolation and initiate cascade speciation, than assortative mating. Based on the results of our simulations, we hypothesized that transitions to self-fertilization could contribute to clade-wide diversification if reinforcement or cascade speciation is common. We tested this hypothesis with comparative data from two different groups. Consistent with our hypothesis, there was a trend towards uniparental reproduction being associated with increased diversification rate in the Nematode phylum. For the plant genus Mimulus, however, self-fertilization was associated with reduced diversification. Reinforcement driving speciation via transitions to self-fertilization might be short lived or unsustainable across macroevolutionary scales in some systems (some plants), but not others (such as nematodes), potentially due to differences in susceptibility to inbreeding depression and/or the ability to transition between reproductive modes. Oxford University Press 2016-04 2016-02-29 /pmc/articles/PMC5804227/ /pubmed/29491904 http://dx.doi.org/10.1093/cz/zow004 Text en © The Author (2016). Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Special Column Cascade Reinforcement
Castillo, Dean M.
Gibson, Amanda K.
Moyle, Leonie C.
Assortative mating and self-fertilization differ in their contributions to reinforcement, cascade speciation, and diversification
title Assortative mating and self-fertilization differ in their contributions to reinforcement, cascade speciation, and diversification
title_full Assortative mating and self-fertilization differ in their contributions to reinforcement, cascade speciation, and diversification
title_fullStr Assortative mating and self-fertilization differ in their contributions to reinforcement, cascade speciation, and diversification
title_full_unstemmed Assortative mating and self-fertilization differ in their contributions to reinforcement, cascade speciation, and diversification
title_short Assortative mating and self-fertilization differ in their contributions to reinforcement, cascade speciation, and diversification
title_sort assortative mating and self-fertilization differ in their contributions to reinforcement, cascade speciation, and diversification
topic Special Column Cascade Reinforcement
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804227/
https://www.ncbi.nlm.nih.gov/pubmed/29491904
http://dx.doi.org/10.1093/cz/zow004
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