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Adaptive potential of a Pacific salmon challenged by climate change

Abstract

Pacific salmon provide critical sustenance for millions of people worldwide and have far-reaching impacts on the productivity of ecosystems. Rising temperatures now threaten the persistence of these important fishes1,2, yet it remains unknown whether populations can adapt. Here, we provide the first evidence that a Pacific salmon has both physiological and genetic capacities to increase its thermal tolerance in response to rising temperatures. In juvenile chinook salmon (Oncorhynchus tshawytscha), a 4 °C increase in developmental temperature was associated with a 2 °C increase in key measures of the thermal performance of cardiac function3,4. Moreover, additive genetic effects significantly influenced several measures of cardiac capacity, indicative of heritable variation on which selection can act. However, a lack of both plasticity and genetic variation was found for the arrhythmic temperature of the heart, constraining this upper thermal limit to a maximum of 24.5 ± 2.2 °C. Linking this constraint on thermal tolerance with present-day river temperatures and projected warming scenarios5, we predict a 17% chance of catastrophic loss in the population by 2100 based on the average warming projection, with this chance increasing to 98% in the maximum warming scenario. Climate change mitigation is thus necessary to ensure the future viability of Pacific salmon populations.

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Figure 1: Mean increase in maximum heart rate (fHmax) among all offspring from the +0 °C (black line) and +4 °C (grey line) treatment groups of Quinsam River chinook salmon (O. tshawytscha).
Figure 2: Norms of reaction among paternal half-sib families of Quinsam River chinook salmon (O. tshawytscha).

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References

  1. Farrell, A. P. et al. Pacific salmon in hot water: Applying aerobic scope models and biotelemetry to predict the success of spawning migrations. Phys. Biochem. Zool. 81, 697–708 (2008).

    Article  CAS  Google Scholar 

  2. Crozier, L. G., Zabel, R. W. & Hamlett, A. F. Predicting differential effects of climate change at the population level with life-cycle models of spring chinook salmon. Glob. Change Biol. 14, 236–249 (2008).

    Article  Google Scholar 

  3. Casselman, M. T., Anttila, K. & Farrell, A. P. Using maximum heart rate as a rapid screening tool to determine optimum temperature for aerobic scope in Pacific salmon Oncorhynchus spp. J. Fish Biol. 80, 358–377 (2012).

    Article  CAS  Google Scholar 

  4. Anttila, K., Casselman, M. T., Schulte, P. M. & Farrell, A. P. Optimum temperature in juvenile salmonids: Connecting subcellular indicators to tissue function and whole-organism thermal optimum. Physiol. Biochem. Zool. 86, 245–256 (2013).

    Article  CAS  Google Scholar 

  5. Christensen, J. H. et al. in Climate Change 2013: The Physical Science Basis (eds Stocker, T. F. et al.) 1217–1308 (Cambridge Univ. Press, 2013).

    Google Scholar 

  6. Dillon, M. E., Wang, G. & Huey, R. B. Global metabolic impacts of recent climate warming. Nature 467, 704–706 (2010).

    Article  CAS  Google Scholar 

  7. Angilletta, M. J. Thermal Adaptation: A Theoretical and Empirical Synthesis (Oxford Univ. Press, 2009).

    Book  Google Scholar 

  8. Somero, G. N. The physiology of climate change: How potentials for acclimatization and genetic adaptation will determine ‘winners’ and ‘losers’. J. Exp. Biol. 213, 912–920 (2010).

    Article  CAS  Google Scholar 

  9. Crozier, L. G. & Hutchings, J. A. Plastic and evolutionary responses to climate change in fish. Evol. Appl. 7, 68–87 (2014).

    Article  Google Scholar 

  10. Munday, P. L., Warner, R. R., Monro, K., Pandolfi, J. M. & Marshall, D. J. Predicting evolutionary responses to climate change in the sea. Ecol. Lett. 16, 1488–1500 (2013).

    Article  Google Scholar 

  11. Pörtner, H. O. & Knust, R. Climate change affects marine fishes through the oxygen limitation of thermal tolerance. Science 315, 95–97 (2007).

    Article  Google Scholar 

  12. Pörtner, H. O. & Farrell, A. P. Physiology and climate change. Science 322, 690–692 (2008).

    Article  Google Scholar 

  13. Clark, T. D., Sandblom, E. & Jutfelt, F. Aerobic scope measurements of fishes in an era of climate change: Respirometry, relevance and recommendations. J. Exp. Biol. 216, 2771–2782 (2013).

    Article  Google Scholar 

  14. Clark, T. D., Sandblom, E. & Jutfelt, F. Response to Farrell and to Pörtner and Giomi. J. Exp. Biol. 216, 4495–4497 (2013).

    Article  Google Scholar 

  15. Farrell, A. P. Environment, antecedents and climate change: Lessons from the study of temperature physiology and river migration of salmonids. J. Exp. Biol. 212, 3771–3780 (2009).

    Article  CAS  Google Scholar 

  16. Logan, C. A., Kost, L. E. & Somero, G. N. Latitudinal differences in Mytilus californianus thermal physiology. Mar. Ecol. Prog. Ser. 450, 93–105 (2012).

    Article  Google Scholar 

  17. Iftikar, F. I. et al. Could thermal sensitivity of mitochondria determine species distribution in a changing climate? J. Exp. Biol. 217, 2348–2357 (2014).

    Article  Google Scholar 

  18. Weng, K. C. et al. Satellite tagging and cardiac physiology reveal niche expansion in salmon sharks. Science 310, 104–106 (2005).

    Article  CAS  Google Scholar 

  19. Eliason, E. J. et al. Differences in thermal tolerance among sockeye salmon populations. Science 332, 109–112 (2011).

    Article  CAS  Google Scholar 

  20. Crozier, L. G. & Zabel, R. W. Climate impacts at multiple scales: Evidence for differential population responses in juvenile chinook salmon. J. Anim. Ecol. 75, 1100–1109 (2006).

    Article  Google Scholar 

  21. Lynch, M. & Walsh, B. Genetics and Analysis of Quantitative Traits (Sinauer Associates, 1998).

    Google Scholar 

  22. Chen, Z. et al. Optimum and maximum temperatures of sockeye salmon (Oncorhynchus nerka) populations hatched at different temperatures. Can. J. Zool. 91, 265–274 (2013).

    Article  Google Scholar 

  23. Anttila, K. et al. Atlantic salmon show capability for cardiac acclimation to warm temperatures. Nature Commun. 5, 4252 (2014).

    Article  CAS  Google Scholar 

  24. Heath, D. D., Heath, J. W., Bryden, C. A., Johnson, R. M. & Fox, C. W. Rapid evolution of egg size in captive salmon. Science 299, 1738–1740 (2003).

    Article  CAS  Google Scholar 

  25. Muñoz, N. J. et al. Indirect genetic effects underlie oxygen-limited thermal tolerance within a coastal population of chinook salmon. Proc. R. Soc. B 281, 20141082 (2014).

    Article  Google Scholar 

  26. Shiels, H. A. & Farrell, A. P. The effect of temperature and adrenaline on the relative importance of the sarcoplasmic reticulum in contributing Ca2+ to force development in isolated ventricular trabeculae from rainbow trout. J. Exp. Biol. 200, 1607–1621 (1997).

    CAS  Google Scholar 

  27. Castilho, P. C., Landeira-Fernandez, A. M., Morrissette, J. & Block, B. A. Elevated Ca2+ ATPase (SERCA2) activity in tuna hearts: Comparative aspects of temperature dependence. Comp. Biochem. Physiol. 148, 124–132 (2007).

    Article  Google Scholar 

  28. Jensen, L. F. et al. Local adaptation in brown trout early life-history traits: Implications for climate change adaptability. Proc. R. Soc. B 275, 2859–2868 (2008).

    Article  Google Scholar 

  29. Meier, K. et al. Local adaptation at the transcriptome level in brown trout: Evidence from early life-history temperature genomic reaction norms. PLoS ONE 9, e85171 (2014).

    Article  Google Scholar 

  30. Donelson, J. M., Munday, P. L., McCormick, M. I. & Pitcher, C. R. Rapid transgenerational acclimation of a tropical reef fish to climate change. Nature Clim. Change 2, 30–32 (2012).

    Article  Google Scholar 

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Acknowledgements

We thank A. Heath and the staff at Yellow Island Aquaculture Ltd for their support with fish husbandry, A. Berchtold for assisting with the heart rate experiment, D. MacKinlay and the staff at the Fisheries and Oceans Canada Quinsam River salmon hatchery for their help with gamete collection, and S. Garner for help with the climate change susceptibility model. This study was supported by Discovery grants to B.D.N. and A.P.F. from the Natural Science and Engineering Research Council of Canada. A.P.F. holds a Canada Research Chair in Fish Physiology, Culture and Conservation. All experiments followed ethical guidelines from the Canadian Council on Animal Care as reviewed and approved by the Animal Use Subcommittees at the University of Western Ontario (protocol no. 2010-214) and the University of British Columbia (protocol no. 810-022).

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All authors designed the experiment; N.J.M. conducted the experiment and data analyses; J.W.H. contributed materials and logistical support during the experiment; N.J.M., A.P.F. and B.D.N. wrote the paper. All authors provided intellectual input, and read and approved the manuscript.

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Correspondence to Bryan D. Neff.

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The authors declare no competing financial interests.

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Muñoz, N., Farrell, A., Heath, J. et al. Adaptive potential of a Pacific salmon challenged by climate change. Nature Clim Change 5, 163–166 (2015). https://doi.org/10.1038/nclimate2473

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