Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: McGee, Matthew D, Schluter, Dolph, Wainwright, Peter C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
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
_version_ 1782299285030699008
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
work_keys_str_mv AT mcgeematthewd functionalbasisofecologicaldivergenceinsympatricstickleback
AT schluterdolph functionalbasisofecologicaldivergenceinsympatricstickleback
AT wainwrightpeterc functionalbasisofecologicaldivergenceinsympatricstickleback