Skip to main content
Log in

The effect of sub-lethal increases in temperature on the growth and population trajectories of three scleractinian corals on the southern Great Barrier Reef

  • Population Ecology
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

To date, coral death has been the most conspicuous outcome of warming tropical seas, but as temperatures stabilize at higher values, the consequences for the corals remaining will be mediated by their demographic responses to the sub-lethal effects of temperature. To gain insight into the nature of these responses, here I develop a model to test the effect of increased temperature on populations of three pocilloporid corals at One Tree Island, near the southern extreme of the Great Barrier Reef (GBR). Using Seriatopora hystrix, S. caliendrum and Pocillopora damicornis as study species, the effects of temperature on growth were determined empirically, and the dynamics of their populations determined under natural temperatures over a 6-month period between 1999 and 2000 [defined as the study year (SY)]. The two data sets were combined in a demographic test of the possibility that the thermal regime projected for the southern GBR in the next 55–83 years—warmer by 3°C than the study year (the SY+3 regime), which is equivalent to 1.4°C warmer than the recent warm year of 1998—would alter coral population trajectories through the effects on coral growth alone; the analyses first were completed by species, then by family after pooling among species. Laboratory experiments showed that growth rates (i.e., calcification) varied significantly among species and temperatures, and displayed curvilinear thermal responses with growth maxima at ∼27.1°C. Based on these temperature-growth responses, the SY+3 regime is projected to: (1) increase annualized growth rates of all taxa by 24–39%, and defer the timing of peak growth from the summer to the autumn and spring, (2) alter the intrinsic rate of population growth (λ) for S. hystrix (λ decreases 26%) and S. caliendrum (λ increases 5%), but not for P. damicornis, and (3) have a minor effect on λ (a 0.3% increase) for the Pocilloporidae, largely because λ varies more among species than it does between temperatures. Ten-year population projections suggest that the effects of a sub-lethal increase in temperature (i.e., the SY+3 regime) are relatively small compared to the interspecific differences in population dynamics, but nevertheless will alter the population size and increase the relative abundance of large colonies at the expense of smaller colonies for all three species, as well as the Pocilloporidae. These effects may play an important role in determining the nuances of coral population structure as seawater warms, and their significance may intensity if the coral species pool is depleted of thermally sensitive species by bleaching.

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
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Andres NG, Rodenhouse NL (1993) Resilience of corals to hurricanes: a simulation model. Coral Reefs 12:167–175

    Article  Google Scholar 

  • Aronson RB, Macintyre IG, Precht WF, Murdoch TJT, Wapnick CM (2002) The expanding scale of species turnover events on coral reefs in Belize. Ecol Monogr 72:233–249

    Google Scholar 

  • Babcock RC (1991) Comparative demography of three species of scleractinian corals using age- and size-dependent classifications. Ecol Monogr 61:225–244

    Article  Google Scholar 

  • Bak RPM, Meesters EH (1999) Population structure as a response of coral communities to global change. Am Zool 39:56–65

    Google Scholar 

  • Barnes DJ (1973) Growth in colonial scleractinians. Bull Mar Sci 23:280–298

    Google Scholar 

  • Barnes DJ, Chalker BE (1990) Calcification and photosynthesis in reef-building corals and algae. In: Dubinsky Z (eds) Ecosystems of the world, vol 25. Coral Reefs. Elsevier, New York, pp 109–131

    Google Scholar 

  • Barnes DJ, Lough JM (1993) On the nature and causes of density banding in massive coral skeletons. J Exp Mar Biol 167:91–108

    Article  Google Scholar 

  • Bellwood DR, Hughes TP, Folke C, Nystrom M (2004) Confronting the coral reef crisis. Nature 429:827–833

    Article  PubMed  CAS  Google Scholar 

  • Berkelmans R, JK Oliver (1999) Large-scale bleaching of corals on the Great Barrier Reef. Coral Reefs 18:55–60

    Article  Google Scholar 

  • Birkeland C (1976) An experimental method of studying corals during early stages of growth. Micronesica 12:319–322

    Google Scholar 

  • Borgiorni L, Shafir S, Angel D, Rinkevich B (2003) Survival, growth and gonad development of two hermatypic corals subjected to in situ fish-farm nutrient enrichment. Mar Ecol Prog Ser 253:137–144

    Article  Google Scholar 

  • Brown BE, Sya’rani L, LeTissier M (1985) Skeletal form and growth in Acropora aspera (Dana) from the Pulau Seribu, Indonesia. J Exp Mar Biol Ecol 86:139–159

    Article  Google Scholar 

  • Bruno JF, Edmunds PJ (1997) Clonal variation for phenotypic plasticity in the coral Madracis mirabilis. Ecology 78:2177–2190

    Google Scholar 

  • Buddemeier RW, Kinzie RA (1976) Coral growth. Ocean Mar Biol Ann Rev 14:183–225

    Google Scholar 

  • Buddemeier RW, Kleypas JA, Aronson RB (2004) Coral reefs and global climate change. Pew center on global climate change report

  • Caswell H (2001) Matrix population models. Sinauer Associates Inc, Sunderland

    Google Scholar 

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

    Article  Google Scholar 

  • Coles SL (1985) The effects of elevated temperature on reef coral planulae settlement as related to power plant entrainment. In: Proceedings of the 5th International Coral Reef Symposium 4:171–17629

  • Connell JH (1973) Population ecology of reef-building corals. In: Jones OA, Endean R (eds) Biology and geology of coral reefs, vol 2. Academic, New York, pp 205–245

    Google Scholar 

  • Davies PS (1989) Short-term growth measurements of corals using an accurate buoyant weighing technique. Mar Biol 101:389–395

    Article  Google Scholar 

  • Done TJ (1987) Simulation of the effects of Acanthaster planci on the population structure of massive corals in the genus Porites: evidence of population resilience? Coral Reefs 6:75–90

    Article  Google Scholar 

  • Done TJ (1988) Simulation of recovery of pre-disturbance size structure in populations of Porites spp. damaged by the crown of thorns starfish Acanthaster planci. Mar Biol 100:51–61

    Article  Google Scholar 

  • Edmunds PJ (2004) Juvenile coral population dynamics track rising seawater temperature on a Caribbean reef. Mar Ecol Prog Ser 269:111–119

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Fong P, Glynn PW (1998) A dynamic size-structure population model: does disturbance control size structure of a population of the massive coral Gardinoseris planulata in the eastern Pacific? Mar Biol 130:663–674

    Article  Google Scholar 

  • Fong P, Glynn PW (2000) A regional model to predict coral population dynamics in response to El Niño-southern oscillations. Ecol Appl 10:842–854

    Google Scholar 

  • Foster AB (1979) Phenotypic plasticity in the reef corals Montastraea annularis (Ellis and Solander) and Siderastrea siderea (Ellis and Solander). J Exp Mar Biol Ecol 39:25–54

    Article  Google Scholar 

  • Gardner TA, Cote IM, Gill JA, Grant A, Watkinson AR (2003) Long-term, region-wide declines in Caribbean corals. Science 301:958–960

    Article  PubMed  CAS  Google Scholar 

  • Hall VR, Hughes TP (1996) Reproductive strategies of modular organisms: comparative studies of reef-building corals. Ecology 77:950–963

    Article  Google Scholar 

  • Harrison PL, Wallace CC (1990) Reproduction, dispersal and recruitment of scleractinian corals. In Dubinsky Z (ed) Ecosystems of the world, vol 25. Coral Reefs. Elsevier, New York, pp 133–207

    Google Scholar 

  • Hoegh-Guldberg O (1988) A method for determining the surface area of corals. Coral Reefs 7:113–116

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Howe SA, Marshall AT (2002) Temperature effects on calcification rate and skeletal deposition in the temperate coral, Plesiastrea versipora (Lamarck). J Exp Mar Biol Ecol 275:63–81

    Article  CAS  Google Scholar 

  • Hughes TP (1984) Population dynamics based on individual size rather than age: a general model with a reef coral example. Am Nat 123:778–795

    Article  Google Scholar 

  • Hughes TP, Jackson JBC (1985) Population dynamics and life histories of foliaceous corals. Ecol Monogr 55:141–166

    Article  Google Scholar 

  • Hughes TP, Tanner JE (2000) Recruitment failure, life histories, and long-term decline of Caribbean corals. Ecology 81:2250–2263

    Google Scholar 

  • Hughes TP, Baird AH, Dinsdale EA, Moltschaniwskyj NA, Pratchett MS, Tanner JE, Willis BL (2000) Supply-side ecology works both ways: the link between benthic adults, fecundity and larval recruits. Ecology 81:2241–2249

    Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

  • IPCC (2001) Third assessment report of the intergovernmental panel on climate change IPCC (WGI & II). Cambridge University Press, Cambridge

    Google Scholar 

  • Jackson JBC (1977) Competition on marine hard substrata: the adaptive significance of solitary and colonial strategies. Am Nat 980:743–767

    Article  Google Scholar 

  • Jackson JBC (1979) Morphological strategies of sessile animals. In Larwood G, Rosen BR (eds) Biology and systematics of colonial organisms. Academic, London, pp 499–555

    Google Scholar 

  • Jones RJ, Ward S, Amri AY, Hoegh-Guldberg O (2000) Changes in quantum yield efficiency of photosystem II of symbiotic dinoflagellates of corals after heat stress, and of bleached corals sampled after the 1998 Great Barrier Reef mass bleaching event. Mar Freshwater Res 51:63–71

    Article  Google Scholar 

  • Kleypas JA, Buddemeier RW, Archer D, Gattuso JP, Langdon C, Opdyke BN (1999) Geochemical consequences of increased carbon dioxide on coral reefs. Science 284:118–120

    Article  PubMed  CAS  Google Scholar 

  • Knowlton N (2001) The future of coral reefs. Proc Nat Acad Sci USA 98:5419–5425

    Article  PubMed  CAS  Google Scholar 

  • Knutson RA, Buddemeier RW, Smith SV (1972) Coral chronometers: seasonal growth bands in reef corals. Science 177:270–272

    Article  PubMed  Google Scholar 

  • Langdon C (2000) Review of experimental evidence for effects of CO2 on calcification of reef builders.In: Proceedings of the 9th International Coral Reef Symposium 2:1091–1098

  • Lough JM, Barnes DJ (1997) Several centuries of variation in skeletal extension, density and calcification in massive Porites colonies from the Great Barrier Reef: a proxy for seawater temperature and a background of variability against which to identify unnatural variation. J Exp Mar Bio Ecol 211:29–67

    Article  Google Scholar 

  • Lough JM, Barnes DJ (2000) Environmental controls on growth of the massive coral Porites. J Exp Mar Bio Ecol 245:225–243

    Article  PubMed  Google Scholar 

  • Loya Y, Sakai K, Yamazato K, Nakano Y, Sambali H, van Woesik R (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 susceptibility among taxa. Coral Reefs 19:155–163

    Article  Google Scholar 

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

    Article  Google Scholar 

  • McNeil BI, Mateur RJ, Barnes DJ (2004) Coral reef calcification and climate change: the effect of ocean warming. Geophy Res Lett 31: L22309, DOI: 10.1029/2004GL021541

  • McPeek M, Peckarsky BL (1998) Life histories and the strengths of species interactions: combining mortality, growth and fecundity effects. Ecology 79:867–879

    Article  Google Scholar 

  • Meesters EH, Hilterman M, Kardinaal E, Keetman M, deVries M, Bak RPM (2001) Colony size-frequency distributions on scleractinian coral populations: spatial and interspecific variation. Mar Ecol Prog Ser 209:43–54

    Article  Google Scholar 

  • Precht WF, Aronson RB (2004) Climate flickers and range shifts of reef corals. Front Ecol Environ 2:307–314

    Article  Google Scholar 

  • Reynaud S, Leclerq N, Romaine-Lioud S, Ferrier-Lages C, Jaubert J, Gattuso J-P (2003) Interacting effects of CO2 partial pressure and temperature on photosynthesis and calcification in a scleractinian corals. Glob Change Biol 9:1–9

    Article  Google Scholar 

  • Reynaud-Vaganay S, Gattuso JP, Cuif JP, Jaubert J, Juillet-Leclerc A (1999) A novel culture technique for scleractinian corals: application to investigate changes in skeletal δ18O as a function of temperature. Mar Ecol Prog Ser 180:121–130

    Article  CAS  Google Scholar 

  • Tanner JE, Hughes TP, Connell JH (1996) The role of history in community dynamics: a modeling approach. Ecology 77:108–117

    Article  Google Scholar 

  • Veron JEN (1986) Corals of Australia and the Indo-Pacific. University of Hawaii, Honolulu

    Google Scholar 

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

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

This study was carried out under a research permit from the Great Barrier Reef Marine Park Authority (# G99/371) and was funded, in part, by the NSF-International Program (# INT-9910659), and the Graduate Research and International Program of California State University, Northridge (CSUN). The experiments described here comply with the current laws of the country in which they were performed. I would like to thank O. Hoegh-Guldberg for facilitating my visits to Australia, D.J. Barnes (Australian Institute of Marine Sciences) and G. Hendler (Los Angeles Museum of Natural History) for assisting with the CITES permits necessary to transport corals from Australia to the United States, and R.C. Carpenter, R.W. Buddemeier and an anonymous reviewer for comments that improved an earlier draft of this paper. The fieldwork was made possible with the assistance of R. Habeeb, J.A. Idjadi and E.D. Keach, and our visits to One Tree Island benefited greatly from the generosity and natural history knowledge of Pam and Konrad Beinsen. This is contribution number 124 of the CSUN marine biology program.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Peter J. Edmunds.

Additional information

Communicated by Libby Marschall

Rights and permissions

Reprints and permissions

About this article

Cite this article

Edmunds, P.J. The effect of sub-lethal increases in temperature on the growth and population trajectories of three scleractinian corals on the southern Great Barrier Reef. Oecologia 146, 350–364 (2005). https://doi.org/10.1007/s00442-005-0210-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00442-005-0210-5

Keywords

Navigation