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Sympatric speciation in structureless environments
BACKGROUND: Darwin and the architects of the Modern Synthesis found sympatric speciation difficult to explain and suggested it is unlikely to occur. Increasingly, evidence over the past few decades suggest that sympatric speciation can occur under ecological conditions that require at most intraspec...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770699/ https://www.ncbi.nlm.nih.gov/pubmed/26922946 http://dx.doi.org/10.1186/s12862-016-0617-0 |
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author | Getz, Wayne M. Salter, Richard Seidel, Dana Paige van Hooft, Pim |
author_facet | Getz, Wayne M. Salter, Richard Seidel, Dana Paige van Hooft, Pim |
author_sort | Getz, Wayne M. |
collection | PubMed |
description | BACKGROUND: Darwin and the architects of the Modern Synthesis found sympatric speciation difficult to explain and suggested it is unlikely to occur. Increasingly, evidence over the past few decades suggest that sympatric speciation can occur under ecological conditions that require at most intraspecific competition for a structured resource. Here we used an individual-based population model with variable foraging strategies to study the evolution of mating behavior among foraging strategy types. Initially, individuals were placed at random on a structureless resource landscape, with subsequent spatial variation induced through foraging activity itself. The fitness of individuals was determined by their biomass at the end of each generational cycle. The model incorporates three diallelic, codominant foraging strategy genes, and one mate-choice or m-trait (i.e. incipient magic trait) gene, where the latter is inactive when random mating is assumed. RESULTS: Under non-random mating, the m-trait gene promotes increasing levels of either disassortative or assortative mating when the frequency of m respectively increases or decreases from 0.5. Our evolutionary simulations demonstrate that, under initial random mating conditions, an activated m-trait gene evolves to promote assortative mating because the system, in trying to fit a multipeak adaptive landscape, causes heterozygous individuals to be less fit than homozygous individuals. CONCLUSION: Our results extend our theoretical understanding that sympatric speciation can evolve under nicheless or gradientless resource conditions: i.e. the underlying resource is monomorphic and initially spatially homogeneous. Further the simplicity and generality of our model suggests that sympatric speciation may be more likely than previously thought to occur in mobile, sexually-reproducing organisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0617-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4770699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47706992016-03-01 Sympatric speciation in structureless environments Getz, Wayne M. Salter, Richard Seidel, Dana Paige van Hooft, Pim BMC Evol Biol Research Article BACKGROUND: Darwin and the architects of the Modern Synthesis found sympatric speciation difficult to explain and suggested it is unlikely to occur. Increasingly, evidence over the past few decades suggest that sympatric speciation can occur under ecological conditions that require at most intraspecific competition for a structured resource. Here we used an individual-based population model with variable foraging strategies to study the evolution of mating behavior among foraging strategy types. Initially, individuals were placed at random on a structureless resource landscape, with subsequent spatial variation induced through foraging activity itself. The fitness of individuals was determined by their biomass at the end of each generational cycle. The model incorporates three diallelic, codominant foraging strategy genes, and one mate-choice or m-trait (i.e. incipient magic trait) gene, where the latter is inactive when random mating is assumed. RESULTS: Under non-random mating, the m-trait gene promotes increasing levels of either disassortative or assortative mating when the frequency of m respectively increases or decreases from 0.5. Our evolutionary simulations demonstrate that, under initial random mating conditions, an activated m-trait gene evolves to promote assortative mating because the system, in trying to fit a multipeak adaptive landscape, causes heterozygous individuals to be less fit than homozygous individuals. CONCLUSION: Our results extend our theoretical understanding that sympatric speciation can evolve under nicheless or gradientless resource conditions: i.e. the underlying resource is monomorphic and initially spatially homogeneous. Further the simplicity and generality of our model suggests that sympatric speciation may be more likely than previously thought to occur in mobile, sexually-reproducing organisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-016-0617-0) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-29 /pmc/articles/PMC4770699/ /pubmed/26922946 http://dx.doi.org/10.1186/s12862-016-0617-0 Text en © Getz et al. 2016 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 Getz, Wayne M. Salter, Richard Seidel, Dana Paige van Hooft, Pim Sympatric speciation in structureless environments |
title | Sympatric speciation in structureless environments |
title_full | Sympatric speciation in structureless environments |
title_fullStr | Sympatric speciation in structureless environments |
title_full_unstemmed | Sympatric speciation in structureless environments |
title_short | Sympatric speciation in structureless environments |
title_sort | sympatric speciation in structureless environments |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770699/ https://www.ncbi.nlm.nih.gov/pubmed/26922946 http://dx.doi.org/10.1186/s12862-016-0617-0 |
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