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Functional basis of ecological divergence in sympatric stickleback
BACKGROUND: The evolution of ecological divergence in closely related species is a key component of adaptive radiation. However, in most examples of adaptive radiation the mechanistic basis of ecological divergence remains unclear. A classic example is seen in the young benthic and limnetic stickleb...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890603/ https://www.ncbi.nlm.nih.gov/pubmed/24380474 http://dx.doi.org/10.1186/1471-2148-13-277 |
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author | McGee, Matthew D Schluter, Dolph Wainwright, Peter C |
author_facet | McGee, Matthew D Schluter, Dolph Wainwright, Peter C |
author_sort | McGee, Matthew D |
collection | PubMed |
description | BACKGROUND: The evolution of ecological divergence in closely related species is a key component of adaptive radiation. However, in most examples of adaptive radiation the mechanistic basis of ecological divergence remains unclear. A classic example is seen in the young benthic and limnetic stickleback species pairs of British Columbia. In each pair the benthic species feeds on littoral macroinvertebrates whereas the limnetic feeds on pelagic zooplankton. Previous studies indicate that in both short-term feeding trials and long-term enclosure studies, benthics and limnetics exhibit enhanced performance on their own resource but fare more poorly on the other species’ resource. We examined the functional basis of ecological divergence in the stickleback species pair from Paxton Lake, BC, using biomechanical models of fish feeding applied to morphological traits. We examined the consequences of morphological differences using high speed video of feeding fish. RESULTS: Benthic stickleback possess morphological traits that predict high suction generation capacity, including greatly hypertrophied epaxial musculature. In contrast, limnetic stickleback possess traits thought to enhance capture of evasive planktonic prey, including greater jaw protrusion than benthics and greater displacement advantage in both the lower jaw-opening lever system and the opercular four-bar linkage. Kinematic data support the expectations from the morphological analysis that limnetic stickleback exhibit faster strikes and greater jaw protrusion than benthic fish, whereas benthics exert greater suction force on attached prey. CONCLUSIONS: We reveal a previously unknown suite of complex morphological traits that affect rapid ecological divergence in sympatric stickleback. These results indicate that postglacial divergence in stickleback involves many functional systems and shows the value of investigating the functional consequences of phenotypic divergence in adaptive radiation. |
format | Online Article Text |
id | pubmed-3890603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38906032014-01-15 Functional basis of ecological divergence in sympatric stickleback McGee, Matthew D Schluter, Dolph Wainwright, Peter C BMC Evol Biol Research Article BACKGROUND: The evolution of ecological divergence in closely related species is a key component of adaptive radiation. However, in most examples of adaptive radiation the mechanistic basis of ecological divergence remains unclear. A classic example is seen in the young benthic and limnetic stickleback species pairs of British Columbia. In each pair the benthic species feeds on littoral macroinvertebrates whereas the limnetic feeds on pelagic zooplankton. Previous studies indicate that in both short-term feeding trials and long-term enclosure studies, benthics and limnetics exhibit enhanced performance on their own resource but fare more poorly on the other species’ resource. We examined the functional basis of ecological divergence in the stickleback species pair from Paxton Lake, BC, using biomechanical models of fish feeding applied to morphological traits. We examined the consequences of morphological differences using high speed video of feeding fish. RESULTS: Benthic stickleback possess morphological traits that predict high suction generation capacity, including greatly hypertrophied epaxial musculature. In contrast, limnetic stickleback possess traits thought to enhance capture of evasive planktonic prey, including greater jaw protrusion than benthics and greater displacement advantage in both the lower jaw-opening lever system and the opercular four-bar linkage. Kinematic data support the expectations from the morphological analysis that limnetic stickleback exhibit faster strikes and greater jaw protrusion than benthic fish, whereas benthics exert greater suction force on attached prey. CONCLUSIONS: We reveal a previously unknown suite of complex morphological traits that affect rapid ecological divergence in sympatric stickleback. These results indicate that postglacial divergence in stickleback involves many functional systems and shows the value of investigating the functional consequences of phenotypic divergence in adaptive radiation. BioMed Central 2013-12-31 /pmc/articles/PMC3890603/ /pubmed/24380474 http://dx.doi.org/10.1186/1471-2148-13-277 Text en Copyright © 2013 McGee et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 McGee, Matthew D Schluter, Dolph Wainwright, Peter C Functional basis of ecological divergence in sympatric stickleback |
title | Functional basis of ecological divergence in sympatric stickleback |
title_full | Functional basis of ecological divergence in sympatric stickleback |
title_fullStr | Functional basis of ecological divergence in sympatric stickleback |
title_full_unstemmed | Functional basis of ecological divergence in sympatric stickleback |
title_short | Functional basis of ecological divergence in sympatric stickleback |
title_sort | functional basis of ecological divergence in sympatric stickleback |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890603/ https://www.ncbi.nlm.nih.gov/pubmed/24380474 http://dx.doi.org/10.1186/1471-2148-13-277 |
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