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Response of Hawaiian and other Indo-Pacific reef corals to elevated temperature

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Abstract

Loss of symbiotic zooxanthellae, or “bleaching” is one of the first visible signs of thermal stress. Critical threshold temperatures for coral bleaching vary geographically, but can be expressed universally as fixed increments relative to the historical mean local summer maximum. Bleaching can be induced by short-term exposure (i.e. 1–2 days) at temperature elevations of 3°C to 4°C above normal summer ambient or by long-term exposure (i.e. several weeks) at elevations of 1°C to 2°C. Corals in both tropical and subtropical locations live at temperatures close to their lethal limits during the summer months. Temperature elevations above summer ambient, but still below the bleaching threshold, can impair growth and reproduction. Temperature and light interact synergistically; high light accelerates bleaching caused by elevated temperature. Bleaching susceptibility is correlated with respiration rate. Any factor that increases respiration (such as high incident light) accelerates bleaching at higher temperatures. Ultraviolet (UV) radiation is a detrimental factor associated with solar radiation. Increased UV due to thinning of the earth's protective ozone layer may aggravate bleaching and mortality caused by global warming. A warming trend in Hawaiian waters has been observed over the past decade. In 1986, 1987 and 1988 Hawaiian corals were perilously close to their bleaching threshold during the summer months, and localized bleachings did occur. In some cases, local warming of surface water on shallow reef flats exceeded this threshold temperature and caused localized coral bleaching. In other cases, heating of large mesoscale eddies in the lee of the larger islands apparently caused wide-scale bleaching of the most sensitive coral species (Pocillopora meandrina) to depths of 20 m. A continuation of the warming trend in Hawaii would lead to mass bleachings similar to those observed recently in other geographic locations.

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References

  • Brown BE (1987) Worldwide death of corals-natural cyclical events or man-made pollution? Mar Poll Bull 18:9–13

    Google Scholar 

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

    Google Scholar 

  • Buddemeier RW, Smith SV (1988) Coral reef growth in an era of rapidly rising sea level: predictions and suggestions for long-term research. Coral Reefs 7:51–56

    Google Scholar 

  • Chalker BE, Dunlap WC, Oliver JK (1983) Bathymetric adaptations of reef building corals at Davies Reef, Great Barrier Reef, Australia. II. Light saturation curves for photosynthesis and respiration. J Exp Mar Biol Ecol 73:37–56

    Google Scholar 

  • Clausen C, Roth AA (1975) Effect of temperature adaptation on calcification rate in the hermatypic coral Pocillopora damicornis. Mar Biol 33:93–100

    Google Scholar 

  • Coles SL (1975) A comparison of effects of elevated temperature versus temperature fluctuations on reef corals at Kahe Point, Oahu. Pac Sci 29:15–18

    Google Scholar 

  • Coles SL (1984) Colonization of Hawaiian reef corals on new and denuded substrata in the vicinity of a Hawaiian power station. Coral Reefs 3:123–130

    Google Scholar 

  • Coles SL (1985) The effects of elevated temperature on reef coral planula settlement as related to power station entrainment. Proc 5th Int Coral Reef Congr 4:171–176

    Google Scholar 

  • Coles SL (1988) Limitations on reef coral development in the Arabian Gulf. Temperature or algal competition? Proc 6th Int Coral Reef Symp 3:211–216

    Google Scholar 

  • Coles SL, Jokiel PL (1977) Effects of temperature on photosynthesis and respiration in hermatypic corals. Mar Biol 43:209–216

    Google Scholar 

  • Coles SL, Jokiel PL (1978) Synergistic effects of temperature, salinity and light on the hermatypic coral Montipora verrucosa. Mar Biol 49:187–195

    Google Scholar 

  • Coles SL, Jokiel PL, Lewis CR (1976) Thermal tolerance in tropical versus subtropical reef corals. Pac Sci 30:159–166

    Google Scholar 

  • Edmunds PJ, Spencer-Davies P (1988) Post-illumination stimulation of respiration rate in the coral Porites porites. Coral Reefs 7:7–9

    Google Scholar 

  • Edmondson CH (1928) The ecology of an Hawaiian coral reef. Bull Bernice P Bishop Mus 45:1–64

    Google Scholar 

  • Edmondson CH (1946) Behavior of coral planulae under altered saline and thermal conditions. Bernice P Bishop Mus Occ Pap 18:283–304

    Google Scholar 

  • Fadlallah YH, Lindo RT (1988) Contrasting cycles of reproduction in Stylophora pistillata from the Red Sea and the Arabian Gulf, with emphasis on temperature. Proc 6th Int Coral Reef Symp 3:225–230

    Google Scholar 

  • Fisk DA, Done TJ (1985) Taxonomic and bathymetric patterns of bleaching in corals, Myrmidon Reef (Queensland). Proc 5th Int Coral Reef Congr 6:149–154

    Google Scholar 

  • Franzisket L (1970) The atrophy of hermatypic reef corals maintained in darkness and their subsequent regeneration in light. Int Rev Ges Hydrobiol 55:1–12

    Google Scholar 

  • Glynn PW (1983) Extensive bleaching and death of reef corals on the Pacific Coast of Panama. Environ Conserv 10:149–154

    Google Scholar 

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

    Google Scholar 

  • Glynn PW (1985) Corallivore population sizes and feeding effects following El Niño (1982–83) associated coral mortality in Panama. Proc 5th Int Coral Reef Congr 4:183–188

    Google Scholar 

  • Glynn PW, Cortes J, Guzman HM, Richmond RH (1988) El Niño (1982–83) associated coral mortality and relationship to sea surface temperature deviations in the tropical eastern Pacific. Proc 6th Int Coral Reef Symp 3:231–243

    Google Scholar 

  • Harriott VJ (1983) Reproductive seasonality, settlement, and postsettlement mortality of Pocillopora damicornis (Linnaeus), at Lizard Island, Great Barrier Reef. Coral Reefs 2:151–157

    Google Scholar 

  • Harriott VJ (1985) Mortality rates of scleractinian corals before and during a mass bleaching event. Mar Ecol Prog Ser 21:81–88

    Google Scholar 

  • Harrigan JF (1972) The planula larva of Pocillopora damicornis. Lunar periodicity of swarming and substratum behavior. PhD thesis, University of Hawaii, Honolulu

  • Houck JE, Buddemeier RW, Smith SV, Jokiel PL (1977) The response of coral growth rate and skeletal strontium content to light intensity and water temperature. Proc 3rd Int Coral Reef Symp 2:425–431

    Google Scholar 

  • Hudson JH (1981) Response of Montastrea annularis to environmental change in the Florida Keys. Proc 4th Int Coral Reef Symp 2:233–240

    Google Scholar 

  • Jaap WC (1979) Observations on zooxanthellae expulsion at Middle Sambo Reef Florida Keys. Bull Mar Sci 29:414–422

    Google Scholar 

  • Jaap WC (1985) An epidemic zooxanthellae expulsion during 1983 in the lower Florida Keys coral reefs: Hyperthermic etiology. Proc 5th Int Coral Reef Congr 6:143–148

    Google Scholar 

  • Jokiel PL (1985) Lunar periodicity of planulae release in the reef coral Pocillopora damicornis in relation to various environmental causes. Proc 5th Int Coral Reef Congr 4:307–312

    Google Scholar 

  • Jokiel PL (1988) Is photoadaptation a critical process in the development, function and maintenance of reef communities. Proc 6th Int Coral Reef Symp 1:181–192

    Google Scholar 

  • Jokiel PL, Coles SL (1977) Effects of heated effluent on hermatypic corals at Kahe Point, Oahu. Pac Sci 28:1–18

    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 

  • Jokiel PL, Guinther EB (1978) Effects of temperature on reproduction in the hermatypic coral Pocillopora damicornis. Bull Mar Sci 28:786–789

    Google Scholar 

  • Jokiel PL, Morrissey JI (1986) Influence of size on primary production in the reef coral Pocillopora damicornis and the macroalga Acanthophora spicifera. Mar Biol 91:15–26

    Google Scholar 

  • Jokiel PL, Townsley SJ (1974) Biology of the polyclad Prosthiostomium (Prosthiostomium) sp., a new coral parasite from Hawaii. Pac Sci 28:361–373

    Google Scholar 

  • Jokiel PL, York RH Jr (1984) Solar ultraviolet photobiology of the reef coral Pocillopora damicornis and symbiotic zooxanthellae. Bull Mar Sci 32:301–315

    Google Scholar 

  • Jokiel PL, Coles SL, Guinther EB, Key GS, Smith SV, Townsley SJ (1975) Effects of thermal loading on the Hawaiian nearshore marine biota. US Environmental Protection Agency Final Report Project 1805 DDN. Office of Research and Monitoring, US EPA, Washington, 285 pp

    Google Scholar 

  • Jones RS, Randall RH (1973) A study of biological impact caused by natural and man-induced changes on a tropical reef. Univ Guam Mar Lab Tech Rept 7:1–184

    Google Scholar 

  • Kinsman DJJ (1964) Reef coral tolerance of high temperatures and salinities. Nature 202:1280–1282

    Google Scholar 

  • Kinzie RA III, Jokiel PL, York RH Jr (1984) Effects of light of altered spectral composition on coral zooxanthellae associations and on zooxanthellae in vitro. Mar Biol 78:239–248

    Google Scholar 

  • Lang LC, Wicklund RI, Dill RF (1988) Depth-and habitat-related bleaching of reef organisms near Lee Stocking Island, Exuma Cays, Bahamas. Proc 6th Int Coral Reef Symp 3:269–214

    Google Scholar 

  • Lasker HR, Peters EC, Coffroth MA (1984) Bleaching of reef coelenterates in the San Blas Islands, Panama. Coral Reefs 3:183–190

    Google Scholar 

  • Lobel PS, Robinson AR (1986) Transport and entrapment of fish larvae by ocean mesoscale eddies and currents in Hawaiian waters. Deep Sea Res 33:483–500

    Google Scholar 

  • Marcus J, Thorhaug A (1981) Pacific versus Atlantic responses of the subtropical hermatypic coral Porites spp. to temperature and salinity effects. Proc 4th Int Coral Reef Symp 2:15–20

    Google Scholar 

  • Neudecker S (1981) Growth and survival of scleractinian corals exposed to thermal effluents at Guam. Proc 4th Int Coral Reef Symp 1:173–180

    Google Scholar 

  • Oliver J (1985) Recurrent seasonal bleaching and mortality of corals on the Great Barrier Reef. Proc 5th Int Coral Reef Congr 4:201–206

    Google Scholar 

  • Patzert WC (1969) Eddies in Hawaiian waters. Haw Inst Geophys Rept HIG-69-8 Honolulu

  • Ramanathan V (1988) The greenhouse theory of climate change: a test by an inadvertent global experiment. Science 240:293–299

    Google Scholar 

  • Revkin AC (1988) Endless summer: living with the greenhouse effect. Discover 9:50–61

    Google Scholar 

  • Richmond RH (1985) Variations in the population biology of Pocillopora damicornis across the Pacific Ocean. Proc 5th Int Coral Reef Congr 6:101–106

    Google Scholar 

  • Seckel GR, Yong MYY (1977) Koko Head, Oahu, sea-surface temperatures and salinities, 1965–1973, and Christmas Island seasurface temperatures, 1954–73. Fish Bull 75:767–787

    Google Scholar 

  • Shinn EA (1972) Coral reef recovery in Florida and the Persian Gulf. Rept from Environmental Conservation Dept, Shell Oil Co, Houston, Texas

  • Vaughan TW (1914) Reef corals of the Bahamas and of Southern Florida. Carnegie Inst Wash Yearbook 13:222–226

    Google Scholar 

  • Williams EH, Bunkley-Williams L (1988) Circumtropical coral reef bleaching in 1987–88. Proc 6th Int Coral Reef Symp 3:313–318

    Google Scholar 

  • Williams EH Jr, Goenaga C, Vicente V (1987) Mass bleachings on Atlantic coral reefs. Science 237:877–878

    Google Scholar 

  • Yonge CM, Nicholls AG (1931) Studies on the physiology of corals. IV. The structure, distribution and physiology of the zooxanthellae. Sci Rep Gr Barrier Reef Exped 1928–29 1:135–176

    Google Scholar 

Download references

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Authors and Affiliations

  1. Hawaii Institute of Marine Biology, University of Hawaii, P.O. Box 1346, 96744, Kaneohe, Hawaii, USA

    P. L. Jokiel

  2. King Fahd University of Petroleum, 31261, Dhahran, Saudi Arabia

    S. L. Coles

  3. Minerals Research Institute, 31261, Dhahran, Saudi Arabia

    S. L. Coles

Authors
  1. P. L. Jokiel
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  2. S. L. Coles
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Jokiel, P.L., Coles, S.L. Response of Hawaiian and other Indo-Pacific reef corals to elevated temperature. Coral Reefs 8, 155–162 (1990). https://doi.org/10.1007/BF00265006

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