Skip to main content

Advertisement

Log in

Species traits as indicators of coral bleaching

  • Report
  • Published:
Coral Reefs Aims and scope Submit manuscript

Abstract

Coral bleaching as a response to increased sea surface temperature is regularly surveyed, but our understanding of species-specific differences in response is limited. We compiled bleaching response data for multiple warming events in which corals were identified to species and then quantified the relationship between species’ traits and their general bleaching response. Coral family explained more variation between species bleaching responses (11%) than any other individual trait. Other morphological and physiological traits explained between 6.7 and 10.5% of total variation; however, the majority of variation was attributed to differences rather than any coral trait. Some relationships between bleaching response and species traits (e.g., symbiont genotype) vary greatly by study, suggesting that plasticity among individuals related to their history and characteristics of the location or warming event are stronger determinants of bleaching response than species-level traits. Conversely, other traits (e.g., family and growth form) describe enough variation in bleaching responses among species to be useful as predictors of bleaching in species assemblages. Discriminating among higher level coral taxa (family) in conjunction with recording colony growth form would significantly improve the capacity to predict assemblage responses to warming events.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References

  • Baird AH, Bhagooli R, Ralph PJ, Takahashi S (2009) Coral bleaching: the role of the host. Trends in Ecology & Evolution 24:16–20

    Article  Google Scholar 

  • Baker AC (2001) Ecosystems: reef corals bleach to survive change. Nature 411:765–766

    Article  PubMed  CAS  Google Scholar 

  • Baker AC (2003) Flexibility and specificity in coral-algal symbiosis: diversity, ecology, and biogeography of Symbiodinium. Annual Review of Ecology, Evolution, and Systematics 34:661–689

    Article  Google Scholar 

  • Baker AC, Glynn PW, Riegl B (2008) Climate change and coral reef bleaching: an ecological assessment of long-term impacts, recovery trends and future outlook. Estuarine, Coastal and Shelf Science 80:435–471

    Article  Google Scholar 

  • Bartoń K (2013) MuMIn: multi-model inference. R package version 1

  • Bates D, Maechler M, Bolker B, Walker S (2014) lme4: Linear mixed-effects models using Eigen and S4. In: 1.1-7 RPV (ed) R package version 1, no. 7, pp 1–23

  • Berkelmans R, van Oppen MJ (2006) The role of zooxanthellae in the thermal tolerance of corals: a ‘nugget of hope’for coral reefs in an era of climate change. Proceedings of the Royal Society of London B: Biological Sciences 273:2305–2312

    Article  Google Scholar 

  • Boulotte NM, Dalton SJ, Carroll AG, Harrison PL, Putnam HM, Peplow LM, van Oppen MJ (2016) Exploring the Symbiodinium rare biosphere provides evidence for symbiont switching in reef-building corals. The ISME Journal 10:2693

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Brandt M (2009) The effect of species and colony size on the bleaching response of reef-building corals in the Florida Keys during the 2005 mass bleaching event. Coral Reefs 28:911–924

    Article  Google Scholar 

  • Brown B (1997) Coral bleaching: causes and consequences. Coral reefs 16:S129–S138

    Article  Google Scholar 

  • Bruno J, Siddon C, Witman J, Colin P, Toscano M (2001) El Nino related coral bleaching in Palau, western Caroline Islands. Coral Reefs 20:127–136

    Article  Google Scholar 

  • Buddemeier RW, Fautin DG (1993) Coral bleaching as an adaptive mechanism. Bioscience 43:320–326

    Article  Google Scholar 

  • Carpenter KE, Abrar M, Aeby G, Aronson RB, Banks S, Bruckner A, Chiriboga A, Cortés J, Delbeek JC, Devantier L (2008) One-third of reef-building corals face elevated extinction risk from climate change and local impacts. Science 321:560–563

    Article  PubMed  CAS  Google Scholar 

  • Charpentier B (2014) The Role of Colony Size in the Resistance and Tolerance of Scleractinian Corals to Bleaching Caused by Thermal Stress. University of Ottawa

  • Crabbe MJC, Smith DJ (2006) Modelling variations in corallite morphology of Galaxea fascicularis coral colonies with depth and light on coastal fringing reefs in the Wakatobi Marine National Park (SE Sulawesi, Indonesia). Computational Biology and Chemistry 30:155–159

    Article  PubMed  CAS  Google Scholar 

  • Done TJ (1999) Coral community adaptability to environmental change at the scales of regions, reefs and reef zones. American Zoologist 39:66–79

    Article  Google Scholar 

  • Dove SG, Hoegh-Guldberg O (2006) The cell physiology of coral bleaching. Science and Management, Coral Reefs and Climate Change, pp 55–71

    Google Scholar 

  • Fabina NS, Putnam HM, Franklin EC, Stat M, Gates RD (2012) Transmission mode predicts specificity and interaction patterns in coral-Symbiodinium networks

  • Fautin DG, Buddemeier RW (2004) Adaptive bleaching: a general phenomenon Coelenterate Biology 2003. Springer, Berlin, pp 459–467

    Book  Google Scholar 

  • Fitt W, Warner M (1995) Bleaching patterns of four species of Caribbean reef corals. The Biological Bulletin 189:298–307

    Article  PubMed  CAS  Google Scholar 

  • Fox J, Weisberg S (2011) An R Companion to Applied Regression. Sage, Thousand Oaks, CA

    Google Scholar 

  • Gilmour J, Smith L, Cook K, Pincock S (2013) Discovering Scott Reef: 20 years of exploration and research. Australian Institute of Marine Science, Cape Ferguson

    Google Scholar 

  • Gleason M (1993) Effects of disturbance on coral communities: bleaching in Moorea, French Polynesia. Coral Reefs 12:193–201

    Article  Google Scholar 

  • Glynn P (1993) Coral reef bleaching: ecological perspectives. Coral reefs 12:1–17

    Article  Google Scholar 

  • Glynn PW (1984) Widespread coral mortality and the 1982–83 El Niño warming event. Environmental Conservation 11:133–146

    Article  Google Scholar 

  • Glynn PW, Maté JL, Baker AC, Calderón MO (2001) Coral bleaching and mortality in Panama and Ecuador during the 1997–1998 El Niño-Southern Oscillation event: spatial/temporal patterns and comparisons with the 1982–1983 event. Bulletin of Marine Science 69:79–109

    Google Scholar 

  • Hoegh-Guldberg O (1999) Climate change, coral bleaching and the future of the world’s coral reefs. Marine and freshwater research 50:839–866

    Article  Google Scholar 

  • Hoegh-Guldberg O, Smith GJ (1989) The effect of sudden changes in temperature, light and salinity on the population density and export of zooxanthellae from the reef corals Stylophora pistillata Esper and Seriatopora hystrix Dana. Journal of Experimental Marine Biology and Ecology 129:279–303

    Article  Google Scholar 

  • Hoeksema BW (1991) Control of bleaching in mushroom coral populations(Scleractinia: fungiidae) in the Java Sea: Stress tolerance and interference by life history strategy. Marine ecology progress series Oldendorf 74:225–237

    Article  Google Scholar 

  • Hoeksema BW (2017) World Register of Marine Species

  • Hoogenboom MO, Frank GE, Chase TJ, Jurriaans S, Alvarez-Noriega M, Peterson K, Critchell K, Berry KL, Nicolet KJ, Ramsby B (2017) Environmental drivers of variation in bleaching severity of Acropora species during an extreme thermal anomaly. Glob Chang Biol 11:2251–2265

    Google Scholar 

  • Hughes TP, Baird AH, Bellwood DR, Card M, Connolly SR, Folke C, Grosberg R, Hoegh-Guldberg O, Jackson J, Kleypas J (2003) Climate change, human impacts, and the resilience of coral reefs. Science 301:929–933

    Article  PubMed  CAS  Google Scholar 

  • Hughes TP, Anderson KD, Connolly SR, Heron SF, Kerry JT, Lough JM, Baird AH, Baum JK, Berumen ML, Bridge TC (2018) Spatial and temporal patterns of mass bleaching of corals in the Anthropocene. Science 359:80–83

    Article  PubMed  CAS  Google Scholar 

  • Jiménez C, Cortés J, León A, Ruíz E (2001) Coral bleaching and mortality associated with the 1997–98 El Nino in an upwelling environment in the eastern Pacific (Gulf of Papagayo, Costa Rica). Bulletin of Marine Science 69:151–169

    Google Scholar 

  • Knowlton N, Rohwer F (2003) Multispecies microbial mutualisms on coral reefs: the host as a habitat. The American Naturalist 162:S51–S62

    Article  PubMed  Google Scholar 

  • Lesser M, Stochaj W, Tapley D, Shick J (1990) Bleaching in coral reef anthozoans: effects of irradiance, ultraviolet radiation, and temperature on the activities of protective enzymes against active oxygen. Coral Reefs 8:225–232

    Article  Google Scholar 

  • Loya Y, Sakai K, Yamazato K, Nakano Y, Sambali H, van Woesik R (2001) Coral bleaching: the winners and the losers. Ecology letters 4:122–131

    Article  Google Scholar 

  • Madin JS, Anderson KD, Andreasen MH, Bridge TC, Cairns SD, Connolly SR, Darling ES, Diaz M, Falster DS, Franklin EC (2016) The Coral Trait Database, a curated database of trait information for coral species from the global oceans. Scientific Data 3:160017

    Article  PubMed  PubMed Central  Google Scholar 

  • Marshall P, Baird A (2000) Bleaching of corals on the Great Barrier Reef: differential susceptibilities among taxa. Coral Reefs 19:155–163

    Article  Google Scholar 

  • Marshall P, Schuttenberg H (2006) A reef manager’s guide to coral bleaching. Great Barrier Reef Marine Park Authority

  • Mcclanahan T, Baird A, Marshall P, Toscano M (2004) Comparing bleaching and mortality responses of hard corals between southern Kenya and the Great Barrier Reef, Australia. Marine Pollution Bulletin 48:327–335

    Article  PubMed  CAS  Google Scholar 

  • Muir PR, Marshall PA, Abdulla A, Aguirre JD (2017) Species identity and depth predict bleaching severity in reef-building corals: shall the deep inherit the reef? Proc R Soc B 284:20171551

    Article  PubMed  Google Scholar 

  • Muscatine L (1990) The role of symbiotic algae in carbon and energy flux in reef corals. Ecosystems of the world 25:75–87

    Google Scholar 

  • Nakagawa S, Schielzeth H (2013) A general and simple method for obtaining R2 from generalized linear mixed-effects models. Methods in Ecology and Evolution 4:133–142

    Article  Google Scholar 

  • Nakamura T, van Woesik R (2001) Water-flow rates and passive diffusion partially explain differential survival of corals during the 1998 bleaching event. Marine ecology Progress series 212:301–304

    Article  Google Scholar 

  • Obura DO (2001) Can differential bleaching and mortality among coral species offer useful indicators for assessment and management of reefs under stress? Bulletin of Marine Science 69:421–442

    Google Scholar 

  • Oliver T, Palumbi S (2011) Many corals host thermally resistant symbionts in high-temperature habitat. Coral Reefs 30:241–250

    Article  Google Scholar 

  • Oxenford HA, Roach R, Brathwaite A, Nurse L, Goodridge R, Hinds F, Baldwin K, Finney C (2008) Quantitative observations of a major coral bleaching event in Barbados, Southeastern Caribbean. Climatic Change 87:435–449

    Article  Google Scholar 

  • Penin L, Vidal-Dupiol J, Adjeroud M (2013) Response of coral assemblages to thermal stress: are bleaching intensity and spatial patterns consistent between events? Environmental monitoring and assessment 185:5031–5042

    Article  PubMed  Google Scholar 

  • R Development Core Team (2015) R: a language and environment for statistical computing R Foundation for Statistical Computing. Austria, Vienna

    Google Scholar 

  • Salih A, Larkum A, Cox G, Kühl M, Hoegh-Guldberg O (2000) Fluorescent pigments in corals are photoprotective. Nature 408:850–853

    Article  PubMed  CAS  Google Scholar 

  • Shenkar N, Fine M, Loya Y (2005) Size matters: bleaching dynamics of the coral Oculina patagonica. Marine Ecology Progress Series 294:181–188

    Article  Google Scholar 

  • Spencer T, Teleki KA, Bradshaw C, Spalding MD (2000) Coral bleaching in the southern Seychelles during the 1997–1998 Indian Ocean warm event. Marine Pollution Bulletin 40:569–586

    Article  CAS  Google Scholar 

  • Stat M, Gates RD (2010) Clade D Symbiodinium in scleractinian corals: a “nugget” of hope, a selfish opportunist, an ominous sign, or all of the above? Journal of Marine Biology 2011

  • Stimson J, Sakai K, Sembali H (2002) Interspecific comparison of the symbiotic relationship in corals with high and low rates of bleaching-induced mortality. Coral Reefs 21:409–421

    Google Scholar 

  • Todd P, Ladle R, Lewin-Koh N, Chou L (2004) Genotype x environment interactions in transplanted clones of the massive corals Favia speciosa and Diploastrea heliopora. Marine Ecology Progress Series 271:167–182

    Article  Google Scholar 

  • Todd PA (2008) Morphological plasticity in scleractinian corals. Biological Reviews 83:315–337

    Article  PubMed  Google Scholar 

  • van Oppen MJ, Lough JM (2008) Coral bleaching: patterns, processes, causes and consequences. Springer Science & Business Media

  • van Woesik R, Irikawa A, Anzai R, Nakamura T (2012) Effects of coral colony morphologies on mass transfer and susceptibility to thermal stress. Coral Reefs 31:633–639

    Article  Google Scholar 

  • Walther G-R, Post E, Convey P, Menzel A, Parmesan C, Beebee TJ, Fromentin J-M, Hoegh-Guldberg O, Bairlein F (2002) Ecological responses to recent climate change. Nature 416:389–395

    Article  PubMed  CAS  Google Scholar 

  • West JM, Salm RV (2003) Resistance and resilience to coral bleaching: implications for coral reef conservation and management. Conservation Biology 17:956–967

    Article  Google Scholar 

  • Wiedenmann J, D’angelo C, Smith EG, Hunt AN, Legiret F-E, Postle AD, Achterberg EP (2013) Nutrient enrichment can increase the susceptibility of reef corals to bleaching. Nature Climate Change 3:160

    Article  CAS  Google Scholar 

  • Wooldridge SA (2014) Differential thermal bleaching susceptibilities amongst coral taxa: re-posing the role of the host. Coral Reefs 33:15–27

    Article  Google Scholar 

Download references

Acknowledgements

We would like to thank B. J. Neilson, Hawaii Division of Aquatic Resources for providing access to coral bleaching survey data and D. Huang for advice and assistance. This research was supported by the International Macquarie University Research Excellence Scholarship (TLM). The findings and conclusions in this article are those of the author(s) and do not necessarily represent the views of the US Fish and Wildlife Service.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Toni L. Mizerek.

Ethics declarations

Conflict of interest

On behalf of all authors, the corresponding author states that there is no conflict of interest.

Additional information

Topic Editor Simon Davy

Electronic supplementary material

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mizerek, T.L., Baird, A.H. & Madin, J.S. Species traits as indicators of coral bleaching. Coral Reefs 37, 791–800 (2018). https://doi.org/10.1007/s00338-018-1702-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00338-018-1702-1

Keywords

Navigation