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The relationship between bleaching and mortality of common corals

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Abstract

Reef corals are likely to have many subtle but four gross responses to anomalous warm water. These are (1) not bleach and live (mortality <10%), (2) not bleach and die (mortality >20%), (3) bleach and live, and (4) bleach and die. The frequency of these four possible gross responses was determined for 18 common coral taxa over an exceptionally warm 1998 El Niño where intense bleaching was observed, and mortality determined from line transects averaged 41.2±34.7 (±SD). Field studies included (1) recording the loss of color (bleaching) and observing recently dead individuals among 6,803 colonies during five sampling periods and (2) estimating mortality based on 180 m of line-intercept transects completed 4 months before and near the end of the bleaching episode. There was no clear relationship between the loss of color and either direct observation or transect-based estimates of mortality for the 18 taxa. The morphology of the taxa did not influence color loss but branching and encrusting taxa had higher mortality than massive and submassive taxa. Loss of color and mortality are the most common responses to warm water as only Pavona did not lose color or die and only two taxa, Cyphastrea and Millepora, did not significantly lose color but died. Of the 15 taxa that lost color, five taxa, Astreopora, Favia, Favites, Goniopora, and Leptoria, did not die. These taxa are those most likely to have reduced potential mortality by the loss of pigments and associated algal symbionts. Death of the branching taxa was detected reasonably by direct field observation but some taxa were underestimated when compared with mortality estimates based on line transects. Death of encrusting and massive taxa including Echinopora, Galaxea, Hydnophora, Montipora, Platygyra, and massive Porites was poorly detected from direct observations but they proved to have modest to high mortality (20–80%) based on line transects. There was no single response of these common corals to warm water but these data, collected during an extreme warm-water anomaly, indicate that the loss of color is most frequently a sign of morbidity, particularly for branching and encrusting taxa.

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References

  • Aronson RB, Precht WF, Toscano MA, Koltes KH (2002) The 1998 bleaching event and its aftermath on a coral reef in Belize. Mar Biol 144:435–447

    Article  Google Scholar 

  • Baird AH, Marshall PA (2002) Mortality, growth and reproduction in scleractinian corals following bleaching on the Great Barrier Reef. Mar Ecol Prog Ser 237:133–141

    Google Scholar 

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

    CAS  PubMed  Google Scholar 

  • Berkelmans R, Willis BL (1999) Seasonal and local spatial patterns in the upper thermal limits of corals on the inshore Central Great Barrier Reef. Coral Reefs 18:219–228

    Google Scholar 

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

    Article  Google Scholar 

  • Brown BE, Suharsono (1990) Damage and recovery of coral reefs affected by El Nino related seawater warming in the Thousand Islands, Indonesia. Coral Reefs 8:163–170

    Google Scholar 

  • Brown BE, Le Tissier MDA, Bythell JC (1995) Mechanisms of bleaching deduced from histological studies of reef corals sampled during a natural bleaching event. Mar Biol 122:655–663

    Google Scholar 

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

    Google Scholar 

  • Buddemeier RW, Smith SV (1999) Coral adaptation and acclimatization: a most ingenious paradox. Am Zool 39:1–9

    Google Scholar 

  • Coles SL, Brown BE (2003) Coral bleaching—capacity for acclimitization and adaptation. Adv Mar Biol 46:183–223

    CAS  PubMed  Google Scholar 

  • Davies JM, Dunne RP, Brown BE (1997) Coral bleaching and elevated sea-water temperature in Milne Bay Province, Papua New Guinea, 1996. Mar Freshw Res 48:513–516

    Google Scholar 

  • Douglas AE (2003) Coral bleaching—how and why? Mar Pollut Bull 46:385–392

    Article  CAS  PubMed  Google Scholar 

  • Edmunds PJ, Gates RD, Gleason DF (2003) The tissue composition of Montastraea franksi during a natural bleaching event in the Florida Keys. Coral Reefs 22:54–62

    Google Scholar 

  • Fagoonee I, Wilson HB, Hassell MP, Turner JR (1999) The dynamics of zooxanthellae populations: a long-term study in the field. Science 283:843–845

    Article  CAS  PubMed  Google Scholar 

  • Fitt WK, McFarland FK, Warner ME, Chilcoat GC (2000) Seasonal patterns of tissue biomass and densities of symbiotic dinoflagellates in reef corals and relation to coral bleaching. Limnol Oceanogr 45:677–685

    CAS  Google Scholar 

  • Fitt WK, Brown BE, Warner ME, Dunne RP (2001) Coral bleaching: interpretation of thermal tolerance limits and thermal thresholds in tropical corals. Coral Reefs 20:51–65

    Google Scholar 

  • Gates RD, Edmunds PJ (1999) The physiological mechanisms of acclimatization in tropical reef corals. Am Zool 39:30–43

    Google Scholar 

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

    Google Scholar 

  • Glynn PW (1984) Widespread coral mortality and the 1982/83 El Nino warming event. Environ Conserv 11:133–146

    Google Scholar 

  • Glynn PW (1996) Coral reef bleaching: facts, hypotheses and implications. Global Change Biol 2:495–509

    Google Scholar 

  • Glynn PW (2000) El Nino-Southern Oscillation mass mortalities of reef corals: a model of high temperature marine extinctions? In: Insalaco E, Skelton PW, Palmer TJ (eds) Carbonate platform systems: components and interactions. (Special Publications 178) Geological Society of London, London, pp 117–133

  • Glynn PW, Mate JL, Baker AC, Calderon MO (2001) Coral bleaching and mortality in Panama and Ecuador during the 1997–98 El Nino-Southern Oscillation event: spatial/temporal patterns and comparisons with the 1982–1983 event. Bull Mar Sci 69:79–109

    Google Scholar 

  • Goreau T, McClanahan T, Hayes R, Strong A (2000) Conservation of coral reefs after the 1998 global bleaching event. Conserv Biol 14:5–15

    Article  Google Scholar 

  • Goreau TJ (1990) Coral bleaching in Jamaica. Nature 343:417

    PubMed  Google Scholar 

  • Goreau TJ (1992) Bleaching and reef community change in Jamaica: 1951–1991. Am Zool 32:683–695

    Google Scholar 

  • Goreau TJ, Macfarlane AH (1990) Reduced growth rate of Montastrea annularis following the 1987–1988 coral-bleaching event. Coral Reefs 8:211–215

    Google Scholar 

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

    Google Scholar 

  • Hoegh-Guldberg O, Salvat B (1995) Periodic mass-bleaching and elevated sea temperatures: bleaching of outer reef slope communities in Moorea, French Polysnesia. Mar Ecol Prog Ser 121:181–190

    Google Scholar 

  • Hoegh-Guldberg O, Jones RJ, Ward S, Loh WK (2002) Is coral bleaching really adaptive? Nature 415:601–602

    Article  CAS  PubMed  Google Scholar 

  • Jokiel PL, Coles SL (1977) Effects of temperature on the mortality and growth of Hawaiian reef corals. Mar Biol 43:201–208

    Google Scholar 

  • Jones RJ, Hoegh-Guldberg O, Larkum AWD, Schreiber U (1998) Temperature-induced bleaching of corals begins with impairment of the CO2 fixation mechanism in zooxanthellae. Plant Cell Environ 21:1219–1230

    CAS  Google Scholar 

  • Kinzie RA (1999) Sex, symbiosis and coral communities. Am Zool 39:80–91

    Google Scholar 

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

    Article  Google Scholar 

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

    Google Scholar 

  • McClanahan TR (1997) Primary succession of coral-reef algae: differing patterns on fished versus unfished reefs. J Exp Mar Biol Ecol 218:77–102

    Article  Google Scholar 

  • McClanahan TR (2000) Bleaching damage and recovery potential of Maldivian coral reefs. Mar Pollut Bull 40:587–597

    Google Scholar 

  • McClanahan TR, Maina J (2003) Response of coral assemblages to the interaction between natural temperature variation and rare warm-water events. Ecosystems 6:551–563

    Google Scholar 

  • McClanahan TR, Mangi S (2000) Spillover of exploitable fishes from a marine park and its effect on the adjacent fishery. Ecol Appl 10:1792–1805

    Google Scholar 

  • McClanahan TR, Muthiga NA, Mangi S (2001) Coral and algal response to the 1998 coral bleaching and mortality: interaction with reef management and herbivores on Kenyan reefs. Coral Reefs 19:380–391

    Article  Google Scholar 

  • McPhaden MJ (1999) Genesis and evolution of the 1997–98 El Nino. Science 283:950–954

    Article  CAS  PubMed  Google Scholar 

  • Mumby PJ, Chisholm JRM, Edwards AJ, Clark CD, Roark EB, Andrefouet S, Jaubert J (2001) Unprecedented bleaching-induced mortality in Porites spp. at Rangiroa Atoll, French Polynesia. Mar Biol 139:183–189

    Article  Google Scholar 

  • Riegl B (2002) Effects of the 1996 and 1998 positive sea-surface temperature anomalies on corals, coral diseases and fish in the Arabian Gulf (Dubai, UAE). Mar Biol 140:29–40

    Article  Google Scholar 

  • Rowan R, Knowlton N, Baker A, Jara J (1997) Landscape ecology of algal symbionts creates variation in episodes of coral bleaching. Nature 388:265–269

    CAS  PubMed  Google Scholar 

  • Sall J, Lehman A, Creighton L (2001) JMP start statistics. Duxbury/Thomson Learning, Pacific Grove, Calif.

  • Sheppard C, Rayner NA (2002) Utility of the Hadley Centre sea ice and sea surface temperature data set (HadISST1) in two widely contrasting coral reef areas. Mar Pollut Bull 44:303–308

    Article  CAS  PubMed  Google Scholar 

  • Ware JR, Fautin DG, Buddemeier RW (1996) Patterns of coral bleaching: modeling the adaptive bleaching hypothesis. Ecol Model 84:199–214

    Article  Google Scholar 

  • Webster PJ, Moore AM, Loschnigg JP, Leben RR (1999) Coupled ocean-atmosphere dynamics in the Indian Ocean during 1997–1998. Nature 401:356–360

    CAS  Google Scholar 

Download references

Acknowledgements

Research was supported by the Wildlife Conservation Society and permission to undertake field work in Kenya and the parks was provided by Kenya’s Office of the President and Kenya Wildlife Services. I am grateful to R. Arthur, H. Machano Ali, and S. Mangi for assistance with the line transects and J. Maina for preparing the figures.

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Correspondence to T. R. McClanahan.

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Communicated by P.W. Sammarco, Chauvin

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McClanahan, T.R. The relationship between bleaching and mortality of common corals. Marine Biology 144, 1239–1245 (2004). https://doi.org/10.1007/s00227-003-1271-9

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