Bell, M. A. & Foster, S. A. The Evolutionary Biology of the Threespine Stickleback (Oxford University Press, 1994).
Seebacher, F., Webster, M. M., James, R. S., Tallis, J. & Ward, A. J. W. Morphological differences between habitats are associated with physiological and behavioural trade-offs in stickleback (Gasterosteus aculeatus). R. Soc. Open Sci. 3, 160316 (2016).
Google Scholar
Bolnick, D. I. et al. Phenotype-dependent native habitat preference facilitates divergence between parapatric lake and stream stickleback. Evolution 63, 2004–2016 (2009).
Google Scholar
Svanbäck, R. & Schluter, D. Niche specialization influences adaptive phenotypic plasticity in the threespine stickleback. Am. Nat. 180, 50–59 (2012).
Google Scholar
Caldecutt, W. J. & Adams, D. C. Morphometrics of trophic osteology in the threespine stickleback, Gasterosteus aculeatus. Copeia 1998, 827–838 (1998).
Yershov, P. & Sukhotin, A. Age and growth of marine three-spined stickleback in the White Sea 50 years after a population collapse. Polar Biol. 38, 1813–1823 (2015).
Dorgham, A. S. et al. Morphological variation of threespine stickleback (Gasterosteus aculeatus) on different stages of spawning period. Proc. KarRC RAS 59–73 (2018). https://doi.org/10.17076/them819.
DeFaveri, J. & Merilä, J. Evidence for adaptive phenotypic differentiation in Baltic Sea sticklebacks. J. Evol. Biol. 26, 1700–1715 (2013).
Google Scholar
Shaw, K. A., Scotti, M. L. & Foster, S. A. Ancestral plasticity and the evolutionary diversification of courtship behaviour in threespine sticklebacks. Anim. Behav. 73, 415–422 (2007).
McGee, M. D., Schluter, D. & Wainwright, P. C. Functional basis of ecological divergence in sympatric stickleback. BMC Evol. Biol. 13, 277 (2013).
Google Scholar
Berner, D., Grandchamp, A.-C. & Hendry, A. P. Variable progress toward ecological speciation in parapatry: Stickleback across eight lake-stream transitions. Evolution 63, 1740–1753 (2009).
Google Scholar
Walker, J. A. Ecological morphology of lacustrine threespine stickleback Gasterosteus aculeatus L. (Gasterosteidae) body shape. Biol. J. Linn. Soc. 61, 3–50 (1997).
Hagen, D. W. & Gilbertson, L. G. Geographic variation and environmental selection in Gasterosteus aculeatus L. in the Pacific Northwest America. Evolution 26, 32–51 (1972).
Google Scholar
Smith, C., Zięba, G., Spence, R., Klepaker, T. & Przybylski, M. Three-spined stickleback armour predicted by body size, minimum winter temperature and pH. J. Zool. 311, 13–22 (2020).
Aguirre, W. E. & Bell, M. A. Twenty years of body shape evolution in a threespine stickleback population adapting to a lake environment: Stickleback body shape evolution. Biol. J. Linn. Soc. 105, 817–831 (2012).
Lavin, P. A. & McPhail, J. D. The evolution of freshwater diversity in the threespine stickleback (Gasterosteus aculeatus): Site-specific differentiation of trophic morphology. Can. J. Zool. 63, 2632–2638 (1985).
Matthews, B., Marchinko, K. B., Bolnick, D. I. & Mazumder, A. Specialization of trophic position and habitat use by sticklebacks in an adaptive radiation. Ecology 91, 1025–1034 (2010).
Google Scholar
Lefébure, R., Larsson, S. & Byström, P. A temperature-dependent growth model for the three-spined stickleback Gasterosteus aculeatus. J. Fish Biol. 79, 1815–1827 (2011).
Google Scholar
Foster, S. A. Inference of evolutionary pattern: Diversionary displays of three-spined sticklebacks. Behav. Ecol. 5, 114–121 (1992).
Taylor, E. B. & McPhail, J. D. Evolutionary history of an adaptive radiation in species pairs of threespine sticklebacks (Gasterosteus): Insights from mitochondrial DNA. Biol. J. Linn. Soc. 66, 271–291 (1999).
Hohenlohe, P. A., Bassham, S., Currey, M. & Cresko, W. A. Extensive linkage disequilibrium and parallel adaptive divergence across threespine stickleback genomes. Phil. Trans. R. Soc. B 367, 395–408 (2012).
Google Scholar
Walker, J. A. & Bell, M. A. Net evolutionary trajectories of body shape evolution within a microgeographic radiation of threespine sticklebacks (Gasterosteus aculeatus). J. Zool. 252, 293–302 (2000).
Kristjánsson, B. K., Skúlason, S. & Noakes, D. L. G. Rapid divergence in a recently isolated population of threespine stickleback (Gasterosteus aculeatus L.). Evol. Ecol. Res. 4, 659–672 (2002).
Wund, M. A., Baker, J. A., Clancy, B., Golub, J. L. & Foster, S. A. A test of the “flexible stem” model of evolution: Ancestral plasticity, genetic accommodation, and morphological divergence in the threespine stickleback radiation. Am. Nat. 172, 449–462 (2008).
Google Scholar
Arif, S., Aguirre, W. E. & Bell, M. A. Evolutionary diversification of opercle shape in Cook Inlet threespine stickleback. Biol. J. Linn. Soc. 97, 832–844 (2009).
Terekhanova, N. V. et al. Fast evolution from precast bricks: Genomics of young freshwater populations of threespine stickleback Gasterosteus aculeatus. PLoS Genet. 10, e1004696 (2014).
Google Scholar
Miller, S. E., Roesti, M. & Schluter, D. A single interacting species leads to widespread parallel evolution of the stickleback genome. Curr. Biol. 29, 530–537 (2019).
Google Scholar
Ab Ghani, N. I., Herczeg, G. & Merilä, J. Effects of perceived predation risk and social environment on the development of three-spined stickleback (Gasterosteus aculeatus) morphology. Biol. J. Linn. Soc. 118, 520–535 (2016).
DeFaveri, J. & Merilä, J. Local adaptation to salinity in the three-spined stickleback?. J. Evol. Biol. 27, 290–302 (2014).
Google Scholar
Jakubavičiūtė, E., De Blick, Y., Dainys, J., Ložys, L. & Olsson, J. Morphological divergence of three-spined stickleback in the Baltic Sea—Implications for stock identification. Fish. Res. 204, 305–315 (2018).
Yanos, C. L. et al. Predator biomass and vegetation influence the coastal distribution of threespine stickleback morphotypes. Ecol. Evol. 00, 1–12 (2021).
Fang, B., Merilä, J., Ribeiro, F., Alexandre, C. M. & Momigliano, P. Worldwide phylogeny of three-spined sticklebacks. Mol. Phylogenet. Evol. 127, 613–625 (2018).
Google Scholar
Ortí, G., Bell, M. A., Reimchen, T. E. & Meyer, A. Global survey of mitochondrial DNA sequences in the threespine sticklebacks: Evidence for recent migrations. Evolution 48, 608–622 (1994).
Google Scholar
Mäkinen, H. S. & Merilä, J. Mitochondrial DNA phylogeography of the three-spined stickleback (Gasterosteus aculeatus) in Europe: Evidence for multiple glacial refugia. Mol. Phylogenet. Evol. 46, 167–182 (2008).
Google Scholar
Thomson, R. E. Oceanography of the British Columbia Coast (Department of Fisheries and Oceans, 1981).
Emmett, R. et al. Geographic signatures of North American west coast estuaries. Estuaries 23, 765 (2000).
Google Scholar
Dallimore, A. & Jmieff, D. Canadian west coast fjords and inlets. Geol. Soc. Spec. Pub. 344, 143–162 (2010).
Schoch, G. C., Albert, D. M. & Shanley, C. S. An estuarine habitat classification for a complex fjordal island archipelago. Estuaries Coasts 37, 160–176 (2014).
Rudnick, D. L. & Ferrari, R. Compensation of horizontal temperature and salinity gradients in the ocean mixed layer. Science 283, 526–529 (1999).
Google Scholar
Barrett, R. D. H., Rogers, S. M. & Schluter, D. Environment specific pleiotropy facilitates divergence at the Ectodysplasin locus in threespine stickleback. Evolution 63, 2831–2837 (2009).
Google Scholar
McCairns, R. J. S. & Bernatchez, L. Plasticity and heritability of morphological variation within and between parapatric stickleback demes. J. Evol. Biol. 25, 1097–1112 (2012).
Google Scholar
Webster, M. M., Atton, N., Hart, P. J. B. & Ward, A. J. W. Habitat-specific morphological variation among threespine sticklebacks (Gasterosteus aculeatus) within a drainage basin. PLoS ONE 6, e21060 (2011).
Google Scholar
Spoljaric, M. A. & Reimchen, T. E. 10 000 years later: evolution of body shape in Haida Gwaii three-spined stickleback. J. Fish. Biol. 70, 1484–1503 (2007).
Spoljaric, M. A. & Reimchen, T. E. Habitat-dependent reduction of sexual dimorphism in geometric body shape of Haida Gwaii threespine stickleback. Biol. J. Linn. Soc. 95, 505–516 (2008).
Spoljaric, M. A. & Reimchen, T. E. Habitat-specific trends in ontogeny of body shape in stickleback from coastal archipelago: Potential for rapid shifts in colonizing populations. J. Morphol. 272, 590–597 (2011).
Google Scholar
Morris, M. R. J. et al. Gene expression plasticity evolves in response to colonization of freshwater lakes in threespine stickleback. Mol. Ecol. 23, 3226–3240 (2014).
Google Scholar
Ramler, D., Mitteroecker, P., Shama, L. N. S., Wegner, K. M. & Ahnelt, H. Nonlinear effects of temperature on body form and developmental canalization in the threespine stickleback. J. Evol. Biol. 27, 497–507 (2014).
Google Scholar
Mazzarella, A. B., Voje, K. L., Hansson, T. H., Taugbøl, A. & Fischer, B. Strong and parallel salinity-induced phenotypic plasticity in one generation of threespine stickleback. J. Evol. Biol. 28, 667–677 (2015).
Google Scholar
Leinonen, T., Cano, J. M., Mäkinen, H. & Merilä, J. Contrasting patterns of body shape and neutral genetic divergence in marine and lake populations of threespine sticklebacks. J. Evol. Biol. 19, 1803–1812 (2006).
Google Scholar
Schluter, D., Marchinko, K. B., Barrett, R. D. H. & Rogers, S. M. Natural selection and the genetics of adaptation in threespine stickleback. Phil. Trans. R. Soc. B 365, 2479–2486 (2010).
Google Scholar
Rogers, S. M. et al. Genetic signature of adaptive peak shift in threespine stickleback. Evolution 66, 2439–2450 (2012).
Google Scholar
Jamniczky, H. A., Barry, T. N. & Rogers, S. M. Eco-evo-devo in the study of adaptive divergence: Examples from threespine stickleback (Gasterosteus aculeatus). Integr. Comp. Biol. 55, 166–178 (2015).
Google Scholar
Gow, J. L., Rogers, S. M., Jackson, M. & Schluter, D. Ecological predictions lead to the discovery of a benthic–limnetic sympatric species pair of threespine stickleback in Little Quarry Lake, British Columbia. Can. J. Zool. 86, 564–571 (2008).
McPhail, J. D. Genetic evidence for a species pair in Enos Lake, British Columbia. Can. J. Zool. 62, 1402–1408 (1984).
McPhail, J. D. Ecology and evolution of sympatric sticklebacks (Gasterosteus): Origin of the species pairs. Can. J. Zool. 71, 515–523 (1993).
Kimmel, C. B., Aguirre, W., Ullmann, B., Currey, M. & Cresko, W. Allometric change accompanies opercular shape evolution in Alaskan threespine sticklebacks. Behaviour 145, 669–691 (2008).
Wootton, R. J. A Functional Biology of Sticklebacks (Croom Helm, 1984).
Kitano, J., Mori, S. & Peichel, C. L. Sexual dimorphism in the external morphology of the threespine stickleback (Gasterosteus aculeatus). Copeia 2, 336–349 (2007).
Aguirre, W. E., Ellis, K. E., Kusenda, M. & Bell, M. A. Phenotypic variation and sexual dimorphism in anadromous threespine stickleback: Implications for postglacial adaptive radiation. Biol. J. Linn. Soc. 95, 465–478 (2008).
Davenne, E. & Masson, D. Water properties in the Straits of Georgia and Juan de Fuca. 41 http://www.pac.dfo-mpo.gc.ca/sci/osap/projects/straitofgeorgia/JdFG_e.pdf (2001).
Irvine, J. R. & Crawford, W. R. State of the Ocean Report for the Pacific North Coast Integrated Management Area (PNCIMA). 51 (2011).
DFO. Data from British Columbia (BC) Lighthouses. Department of Fisheries and Oceans https://www.dfo-mpo.gc.ca/science/data-donnees/lightstations-phares/index-eng.html (2020).
Palumbi, S. R. Genetic divergence, reproductive isolation, and marine speciation. Annu. Rev. Ecol. Evol. Syst. 25, 547–572 (1994).
Griffin, D. A. & LeBlond, P. H. Estuary/ocean exchange controlled by spring-neap tidal mixing. Estuar. Coast Shelf. Sci. 30, 275–297 (1990).
Google Scholar
Vaz, N., Dias, J. M., Leitão, P. & Martins, I. Horizontal patterns of water temperature and salinity in an estuarine tidal channel: Ria de Aveiro. Ocean Dyn. 55, 416–429 (2005).
Google Scholar
Rybkina, E. V., Ivanova, T. S., Ivanov, M. V., Kucheryavyy, A. V. & Lajus, D. L. Habitat preference of three-spined stickleback juveniles in experimental conditions and in wild eelgrass. J. Mar. Biol. Ass. UK 97, 1437–1445 (2017).
Flynn, S., Cadrin, C. & Filatow, D. Estuaries in British Columbia. 6 (2006).
Kelly, J. R., Proctor, H. & Volpe, J. P. Intertidal community structure differs significantly between substrates dominated by native eelgrass (Zostera marina L.) and adjacent to the introduced oyster Crassostrea gigas (Thunberg) in British Columbia, Canada. Hydrobiologia 596, 57–66 (2008).
Fagherazzi, S. et al. Ecogeomorphology of Salt Marshes. In The Ecogeomorphology of Tidal Marshes (eds Blum, L. K. & Marani, M.) 182–200 (American Geophysical Union, 2004).
Campbell, A. Vegetation-environment relationships and plant community classification and ordination in British Columbia coastal salt marshes. Master’s Thesis. (University of British Columbia, 1986).
Kjerfve, B. Comparative oceanography of coastal lagoons. in Estuarine Variability (ed. Wolfe, D. A.) 63–81 (Academic Press, 1986). https://doi.org/10.1016/B978-0-12-761890-6.50009-5.
Barnes, R. S. K. & de Villiers, C. J. Animal abundance and food availability in coastal lagoons and intertidal marine sediments. J. Mar. Biol. Ass. UK 80, 193–202 (2000).
Saimoto, R. K. Life history of marine stickleback in Oyster Lagoon, British Columbia. Master’s Thesis. (University of British Columbia, 1993).
King, R. W. The threespine stickleback adaptive radiation: Salinity, plasticity, and the important of ancestry. Doctoral Dissertation. (Clark University, 2016).
Ahnelt, H. Imprecise naming: the anadromous and the sea spawning threespine stickleback should be discriminated by names. Biologia 73, 389–392 (2018).
Morris, M. R. J., Bowles, E., Allen, B. E., Jamniczky, H. A. & Rogers, S. M. Contemporary ancestor? Adaptive divergence from standing genetic variation in Pacific marine threespine stickleback. BMC Evol. Biol. 18, 113 (2018).
Google Scholar
Kim, S.-Y., Costa, M. M., Esteve-Codina, A. & Velando, A. Transcriptional mechanisms underlying life-history responses to climate change in the three-spined stickleback. Evol. Appl. 10, 718–730 (2017).
Google Scholar
Sambrook, R. J. Interactions between threespine stickleback (Gasterosteus aculeatus linnæus) and juvenile Chinook salmon (Oncorhynchus tshawytscha Walbaum) in an estuarine marsh. Master’s Thesis. (University of British Columbia, 1990). https://doi.org/10.14288/1.0098704.
Jakubavičiūtė, E., Bergström, U., Eklöf, J. S., Haenel, Q. & Bourlat, S. J. DNA metabarcoding reveals diverse diet of the three-spined stickleback in a coastal ecosystem. PLoS ONE 12, e0186929 (2017).
Google Scholar
Kennedy, G. J. A. & Strange, C. D. The distribution of salmonids in upland streams in relation to depth and gradient. J. Fish Biol. 20, 579–591 (1982).
Macdonald, J. S., Birtwell, I. K. & Kruzynski, G. M. Food and habitat utilization by juvenile salmonids in the Campbell River estuary. Can. J. Fish. Aquat. Sci. 44, 1233–1246 (1987).
Everest, F. H. & Chapman, D. W. Habitat selection and spatial interaction by juvenile chinook salmon and steelhead trout in two Idaho streams. J. Fish. Res. Bd. Can. 29, 91–100 (2011).
McPhail, J. D. Speciation and the evolution of reproductive isolation in the sticklebacks (Gasterosteus) of south-western British Columbia. In The Evolutionary Biology of the Threespine Stickleback (eds Bell, M. A. & Foster, S. A.) 399–471 (Oxford University Press, 1994).
Kimmel, C. B. et al. Independent axes of genetic variation and parallel evolutionary divergence of opercle bone shape in threespine stickleback. Evolution 66, 419–434 (2012).
Google Scholar
Østbye, K. et al. The temporal window of ecological adaptation in postglacial lakes: A comparison of head morphology, trophic position and habitat use in Norwegian threespine stickleback populations. BMC Evol. Biol. 16, 102 (2016).
Google Scholar
Aguirre, W. E. & Akinpelu, O. Sexual dimorphism of head morphology in three-spined stickleback Gasterosteus aculeatus. J. Fish Biol. 77, 802–821 (2010).
Google Scholar
Reimchen, T. E. & Nosil, P. Variable predation regimes predict the evolution of sexual dimorphism in a population of threespine stickleback. Evolution 58, 1274 (2004).
Google Scholar
Pistore, A. Ontogeny of population-specific phenotypic variation in the threespine stickleback. Master’s Thesis. (University of Calgary, 2018).
Yurtseva, A. O. et al. Aging three-spined sticklebacks Gasterosteus aculeatus: Comparison of estimates from three structures. J. Fish Biol. 95, 802–811 (2019).
Google Scholar
Picard, P. Jr., Dodson, J. J. & FitzGerald, G. J. Habitat segregation among the age groups of Gasterosteus aculeatus (Pisces: Gasterosteidae) in the middle St. Lawrence estuary, Canada. Can. J. Zool. 68, 1202–1208 (1990).
Reimchen, T. E., Bergström, C. A. & Nosil, P. Natural selection and the adaptive radiation of Haida Gwaii stickleback. Evol. Ecol. Res. 15, 241–269 (2013).
Raeymaekers, J. A. M., Delaire, L. & Hendry, A. P. Genetically based differences in nest characteristics between lake, inlet, and hybrid threespine stickleback from the Misty system, British Columbia, Cananda. Evol. Ecol. Res. 11, 905–919 (2009).
Di Poi, C., Lacasse, J., Rogers, S. M. & Aubin-Horth, N. Evolution of stress reactivity in stickleback. Evol. Ecol. Res. 17, 395–405 (2016).
Weber, J. N., Bradburd, G. S., Stuart, Y. E., Stutz, W. E. & Bolnick, D. I. Partitioning the effects of isolation by distance, environment, and physical barriers on genomic divergence between parapatric threespine stickleback. Evolution 71, 342–356 (2017).
Google Scholar
Rohlf, F. J. Package: tpsUtil, tps file utility program. Version 1. 61. Department of Ecology and Evolution, State University of New York at Stony Brook, Stony Brook, NY. (2015).
Rohlf, F. J. Package: tpsDig, digitize landmarks and outlines. Version 2. 05. Department of Ecology and Evolution, State University of New York at Stony Brook, Stony Brook, NY. (2005).
Adams, D. C., Collyer, M. L. & Kaliontzopoupou, A. Geomorph: Software for geometric morphometric analysis (2020).
Zelditch, M. L., Swiderski, D. L. & Sheets, H. D. Geometric Morphometrics for Biologists: A Primer (Elsevier Academic Press, 2012).
Google Scholar
Galipaud, M., Gillingham, M. A. F., David, M. & Dechaume-Moncharmont, F.-X. Ecologists overestimate the importance of predictor variables in model averaging: A plea for cautious interpretations. Methods Ecol. Evol. 5, 983–991 (2014).
Scheipl, F., Greven, H. & Kuechenhoff, H. Size and power of tests for a zero random effect variance or polynomial regression in additive and linear mixed models. Comput. Stat. Data Anal. 52, 3283–3299 (2008).
Google Scholar
Robinson, J. James Robinson’s functions. Version 0. 0. 0. 1. Retrieved from https://rdrr.io/github/jpwrobinson/funk/. (2019).
Bartoń, K. R Package: MuMIn: Multi-model inference. Version 1. 43. 17. Retrieved from https://CRAN.R-project.org/package=MuMIn. (2020).
Frank, A. Diagnosing collinearity in mixed models from lme4 R package, vif.mer function [R script]. Retrieved from https://raw.githubusercontent.com/aufrank/R-hacks/master/mer-utils.R. GitHub https://raw.githubusercontent.com/aufrank/R-hacks/master/mer-utils.R. (2011).
Lakens, D. Calculating and reporting effect sizes to facilitate cumulative science: a practical primer for t-tests and ANOVAs. Front. Psychol. https://doi.org/10.3389/fpsyg.2013.00863 (2013).
Google Scholar
Kilkenny, C., Browne, W. J., Cuthill, I. C., Emerson, M. & Altman, D. G. Improving bioscience research reporting: The ARRIVE guidelines for reporting animal research. PLoS Biol. 8, e1000412 (2010).
Google Scholar
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