Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Global warming decreases connectivity among coral populations

Abstract

Global warming is killing corals; however, the effects of warming on population connectivity, a process fundamental to reef recovery, are largely unexplored. Using a high-resolution (as high as 200 m), empirically calibrated biophysical model of coral larval dispersal for the southern Great Barrier Reef, we show that the increased larval mortality and reduced competency duration under a 2 °C warming alter dispersal patterns, whereas projected changes in large-scale currents have limited effects. Overall, there was on average a 7% decrease in the distance larvae disperse (among-reef interquartile range (IQR), −10% to −4%), an 8% decrease in the number of connections into each reef (IQR, −11% to −3%) and a 20% increase in local retention (IQR, 0% to +49%). Collectively, these shifts imply that 2 °C of warming will reduce inter-reef connectivity, hampering recovery after disturbances and reducing the spread of warm-adapted genes. Such changes make protections more effective locally, but may require reducing spacing between protected areas.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Maps showing the effects of a 2 °C increase in water temperature across the southern Great Barrier Reef, Australia, by reef.
Fig. 2: Relative change in recovery times in the 29 °C scenario (2050–2100) compared to the 27 °C scenario (current) following disturbance.

Similar content being viewed by others

Data availability

Yearly connectivity matrices and the processed data used to construct Figs. 1a–e and 2 are available at https://doi.org/10.5061/dryad.4f4qrfjbk. Larval survival and competency is provided in the Appendix 1 (Supplementary Fig. 1) and can be obtained from the authors on request.

Code availability

The SLIM model source code can be found at https://git.immc.ucl.ac.be/dg/dg. Larval dynamics modelling is provided in the Appendix 1, and references therein, and can be obtained from the authors on request.

References

  1. Cesar, H., Burke, L. & Pet-Soede L. The Economics of Worldwide Coral Reef Degradation (Cesar Environmental Economics Consulting, 2003).

  2. Pandolfi, J. M. et al. Global trajectories of the long-term decline of coral reef ecosystems. Science 301, 955–958 (2003).

    Article  CAS  Google Scholar 

  3. Hoegh-Guldberg, O., Poloczanska, E. S., Skirving, W. & Dove, S. Coral reef ecosystems under climate change and ocean acidification. Front. Mar. Sci. 4, 158 (2017).

    Article  Google Scholar 

  4. Hughes, T. P. et al. Global warming transforms coral reef assemblages. Science 359, 80–83 (2018).

    Article  CAS  Google Scholar 

  5. Grottoli, A. G., Rodrigues, L. J. & Juarez, C. Lipids and stable carbon isotopes in two species of Hawaiian corals, Porites compressa and Montipora verrucosa, following a bleaching event. Mar. Biol. 145, 621–631 (2004).

    Article  CAS  Google Scholar 

  6. Grottoli, A. G. et al. The cumulative impact of annual coral bleaching can turn some coral species winners into losers. Glob. Change Biol. 20, 3823–3833 (2014).

    Article  Google Scholar 

  7. Underwood, J. N., Smith, L. D., van Oppen, M. J. H. & Gilmour, J. P. Ecologically relevant dispersal of corals on isolated reefs: implications for managing resilience. Ecol. Appl. 19, 18–29 (2009).

    Article  Google Scholar 

  8. Nozawa, Y. & Harrison, P. L. Effects of elevated temperature on larval settlement and post-settlement survival in scleractinian corals, Acropora solitaryensis and Favites chinensis. Mar. Biol. 152, 1181–1185 (2007).

    Article  Google Scholar 

  9. Heyward, A. J. & Negri, A. P. Plasticity of larval pre-competency in response to temperature: observations on multiple broadcast spawning coral species. Coral Reefs 29, 631–636 (2010).

    Article  Google Scholar 

  10. Figueiredo, J., Baird, A. H., Harii, S. & Connolly, S. R. Increased local retention of reef coral larvae as a result of ocean warming. Nat. Clim. Change 4, 498–502 (2014).

    Article  Google Scholar 

  11. Munday, P. L. et al. Climate change and coral reef connectivity. Coral Reefs 28, 379–395 (2009).

    Article  Google Scholar 

  12. van Gennip, S. J. et al. Going with the flow: the role of ocean circulation in global marine ecosystems under a changing climate. Glob. Change Biol. 23, 2602–2617 (2017).

    Article  Google Scholar 

  13. IPCC Climate Change 2014: Impacts, Adaptation, and Vulnerability (eds Field, C. B. et al.) (Cambridge Univ. Press, 2014).

  14. Nishikawa, A. & Sakai, K. Settlement-competency period of planulae and genetic differentiation of the scleractinian coral Acropora digitifera. Zool. Sci. 22, 391–399 (2005).

    Article  Google Scholar 

  15. Connolly, S. R. & Baird, A. H. Estimating dispersal potential for marine larvae: dynamic models applied to scleractinian corals. Ecology 91, 3572–3583 (2010).

    Article  Google Scholar 

  16. Figueiredo, J., Baird, A. H. & Connolly, S. R. Synthesizing larval competence dynamics and reef-scale retention reveals a high potential for self-recruitment in corals. Ecology 94, 650–659 (2013).

    Article  Google Scholar 

  17. Randall, C. J. & Szmant, A. M. Elevated temperature affects development, survivorship, and settlement of the elkhorn coral, Acropora palmata (Lamarck 1816). Biol. Bull. 217, 269–282 (2009).

    Article  Google Scholar 

  18. Randall, C. J. & Szmant, A. M. Elevated temperature reduces survivorship and settlement of the larvae of the Caribbean scleractinian coral, Favia fragum (Esper). Coral Reefs 28, 537–545 (2009).

    Article  Google Scholar 

  19. Burgess, S. C. et al. Beyond connectivity: how empirical methods can quantify population persistence to improve marine protected-area design. Ecol. Appl. 24, 257–270 (2014).

    Article  Google Scholar 

  20. Woolsey, E. S., Keith, S. A., Byrne, M., Schmidt-Roach, S. & Baird, A. H. Latitudinal variation in thermal tolerance thresholds of early life stages of corals. Coral Reefs 34, 471–478 (2015).

    Article  Google Scholar 

  21. Rodriguez-Lanetty, M., Harii, S. & Hoegh-Guldberg, O. Early molecular responses of coral larvae to hyperthermal stress. Mol. Ecol. 18, 5101–5114 (2009).

    Article  CAS  Google Scholar 

  22. Andutta, F. P., Kingsford, M. J. & Wolanski, E. ‘Sticky water’ enables the retention of larvae in a reef mosaic. Estuar. Coast. Shelf Sci. 54, 655–668 (2012).

    Google Scholar 

  23. Hock, K. et al. Connectivity and systemic resilience of the Great Barrier Reef. PLoS Biol. 15, e2003355 (2017).

    Article  Google Scholar 

  24. Bode, M., Bode, L., Choukroun, S., James, M. K. & Mason, L. B. Resilient reefs may exist, but can larval dispersal models find them? PLoS Biol. 16, e2005964 (2018).

    Article  Google Scholar 

  25. Baird, A. H. & Marshall, P. A. Mortality, growth and reproduction in scleractinian corals following bleaching on the Great Barrier Reef. Mar. Ecol. Prog. Ser. 237, 133–141 (2002).

    Article  Google Scholar 

  26. Hughes, T. P. et al. Global warming transforms coral reef assemblages. Nature 556, 492–496 (2018).

    Article  CAS  Google Scholar 

  27. Strathmann, R. R. et al. Evolution of local recruitment and its consequences for marine populations. Bull. Mar. Sci. 70, 377–396 (2002).

    Google Scholar 

  28. Marshall, D. J., Monro, K., Bode, M., Keough, M. J. & Swearer, S. Phenotype–environment mismatches reduce connectivity in the sea. Ecol. Lett. 13, 128–140 (2010).

    Article  CAS  Google Scholar 

  29. Szmant, A. M. & Gassman, N. J. The effects of prolonged “bleaching” on the tissue biomass and reproduction of the reef coral Montastrea annularis. Coral Reefs 8, 217–224 (1990).

    Article  Google Scholar 

  30. Leis, J. M. Nearshore distributional gradients of larval fish (15 taxa) and planktonic crustaceans (6 taxa) in Hawaii. Mar. Biol. 72, 89–97 (1982).

    Article  Google Scholar 

  31. Kraines, S. B., Yanagi, T., Isobe, M. & Komiyama, H. Wind-wave driven circulation on the coral reef at Bora Bay, Miyako Island. Coral Reefs 17, 133–143 (1998).

    Article  Google Scholar 

  32. Paris, C. B. & Cowen, R. K. Direct evidence of a biophysical retention mechanism for coral reef fish larvae. Limnol. Oceanogr. 49, 1964–1979 (2004).

    Article  Google Scholar 

  33. Keshavmurthy, S., Fontana, S., Mezaki, T., Gonzalez, L. C. & Chen, C. A. Doors are closing on early development in corals facing climate change. Sci. Rep. 4, 5633 (2014).

    Article  CAS  Google Scholar 

  34. Thomas, C. J. et al. Numerical modelling and graph theory tools to study ecological connectivity in the Great Barrier Reef. Ecol. Model. 272, 160–174 (2014).

    Article  Google Scholar 

  35. Holstein, D. M., Paris, C. B., Vaz, A. C. & Smith, T. B. Modeling vertical coral connectivity and mesophotic refugia. Coral Reefs 35, 23–37 (2016).

    Article  Google Scholar 

  36. Hata, T. et al. Coral larvae are poor swimmers and require fine-scale reef structure to settle. Sci. Rep. 7, 2249 (2017).

    Article  Google Scholar 

  37. Gleason, D. F. & Hofmann, D. K. Coral larvae: from gametes to recruits. J. Exp. Mar. Biol. Ecol. 408, 42–57 (2011).

    Article  Google Scholar 

Download references

Acknowledgements

Major funding for this research was provided by the Australian Research Council (DP110101168) (J.F., A.H.B.), a Queensland Government Smart Futures Fellowship (J.F.), the Australian Research Council’s Centre of Excellence for Coral Reef Studies (A.H.B., S.R.C.), Federation Wallonie-Bruxelles ARC grant 10/15-028 (C.J.T.), the Belgian Fund for Scientific Research (FRS-FNRS) (J.L.), and Université catholique de Louvain, Belgium (E.H., E.D., J.L.). High-performance computing resources were provided by the Université catholique de Louvain (CISM/UCL) and the Consortium des Équipements de Calcul Intensif en Fédération Wallonie-Bruxelles (CÉCI) funded by the FRS-FNRS under grant number 2.5020.11 and by the Walloon Region.

Author information

Authors and Affiliations

Authors

Contributions

J.F., C.J.T., S.R.C. and A.H.B. conceptualized the study. J.F. collected the data. J.F. and C.J.T. wrote the original manuscript. S.R.C., A.H.B., E.H. and E.D. edited the article. C.J.T., E.H., E.D. and J.L. developed the model. All authors participated in funding acquisition.

Corresponding author

Correspondence to Joana Figueiredo.

Ethics declarations

Competing interests

The authors declare no competing interests.

Peer review information

Nature Climate Change thanks the anonymous reviewers for their contribution to the peer review of this work.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary Information

Supplementary methods and figures.

Reporting Summary

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Figueiredo, J., Thomas, C.J., Deleersnijder, E. et al. Global warming decreases connectivity among coral populations. Nat. Clim. Chang. 12, 83–87 (2022). https://doi.org/10.1038/s41558-021-01248-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41558-021-01248-7

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing