Evol Ecol Res 14: 169-191 (2012)     Full PDF if your library subscribes.

Spatio-temporal patterns in pelvic reduction in threespine stickleback (Gasterosteus aculeatus L.) in Lake Storvatnet

Tom Klepaker1, Kjartan Østbye2,3, Louis Bernatchez4 and L. Asbjørn Vøllestad2

1Department of Biology, Aquatic Behavioural Ecology Research Group, University of Bergen, Bergen, Norway,  2Department of Biology, Centre for Ecological and Evolutionary Synthesis (CEES), University of Oslo, Oslo, Norway, 3Department of Forestry and Wildlife Management, Hedmark University College, Elverum, Norway and  4Institut de Biologie Intégrative et des Systèmes (IBIS), Université Laval, Québec, Canada

Correspondence: T. Klepaker, Department of Biology, Aquatic Behavioural Ecology Research Group, University of Bergen, PO Box 7800, N-5020 Bergen, Norway.
e-mail: tom.klepaker@bio.uib.no

ABSTRACT

Questions: The pelvic girdle with associated spines is an integrated anti-predator defence apparatus, and is assumed to protect against piscivores in the threespine stickleback. On the other hand, it might be costly to produce the pelvic apparatus in ion-poor and mineral-challenging freshwater.

Hypothesis: Stickleback with a reduced pelvic apparatus should use more shelter and be more nocturnal, avoiding predation risk. In contrast, stickleback with a well-developed pelvic apparatus should have reduced mortality during ontogeny in encounters with piscivores and thus have a longer expected lifespan. Given these two life-history strategies, we expect assortative mating as a result of divergent selection.

Organism: Marine and freshwater threespine stickleback (Gasterosteus aculeatus L.).

Places and times: Two representative ancestral marine populations and 36 freshwater populations in northwestern Norway (Lake Storvatnet, the main focus of the study, and three lakes downstream of it). Material was collected from 2006 to 2009.

Analytical methods: We categorized nominal pelvic apparatus development (CPS morphs) in all fish, and measured metrics associated with these categories in a subsample. We also studied temporal, spatial, and habitat variation in the distribution of pelvic morphs in Lake Storvatnet. In this population, and downstream populations, we contrasted the detailed pelvic morphology with the measured genetic diversity (microsatellites), also estimating gene flow. In Lake Storvatnet, we tested for genetic divergence and signs of potential build-up of reproductive isolation via assortative mating among the observed nominal categories of pelvic reduction (CPS).

Results: Pelvic reduction was seen only in Lake Storvatnet, where more than 50% of fish had a reduced pelvis. The distribution of pelvic morphs was stable over time and did not differ between habitats. The proportion of fish with pelvic reduction decreased with age. Freshwater stickleback tended to have a smaller pelvis than marine fish. The Lake Storvatnet stickleback were genetically differentiated from the downstream Lake Gjerhaugsvatn population, and both of these were different from the marine populations, with little gene flow among populations. No apparent genetic structure was found between CPS morphs within Lake Storvatnet. However, genetic factorial correspondence axes were significantly correlated with pelvic principal component axes in Lake Storvatnet, suggesting some phenotype × genetic association.

Conclusion: The weak association between phenotypes and genetic structure observed in this study may reflect the build-up of early steps of reproductive isolation. Given time, such mechanisms may lead to the evolution of assortative mating, which may drive adaptive pelvic morphs (niche peaks), further resulting in genetically divergent populations and pelvic morphs.

Keywords: assortative mating, natural selection, ontogeny, pelvic reduction, regressive evolution, structural mutation dynamics.

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