Geographic Differences in Ecological Processes on Coral Reefs



Although basic ecological processes are generally consistent on a local scale, there are geographic differences in geological processes, the physical environment, and dimensions of the areas involved that change the nature of coral-reef systems. The structure of reefs is affected by plate tectonics, e.g., there is a greater prevalence of atolls in the central Pacific and Indian Oceans than in the Atlantic or eastern Pacific. The vast dimensions of the Pacific Ocean produces a sharp gradient of decrease from west to east in species, generic, class, and habitat diversity across the Pacific that is not so pronounced in the smaller western Atlantic and Indian Oceans. Diseases are generally contained within distantly separated archipelagoes in the Pacific but quickly spread across the relatively small and interconnected greater Caribbean. The differences in sediment input into the oceans (2 % west coasts of continents, 82 % east coasts) and the degree to which river output affects biogeographic patterns (eastern vs western coasts of continents), show the overwhelming global influences of trade winds and the Coriolis effect on coral reefs. The relative prevalence of corals and other sessile photosymbiotic invertebrates compared to sessile heterotrophic invertebrates can be affected on a geographic scale as well as locally by the strength and dependability of nutrient input. Adult coral colonies can persevere in areas with substantial nutrient input such as upwelling, but recruitment in these areas is extraordinarily difficult in competition with algae and heterotrophic invertebrates in areas with abundant nutrients. The effects of disturbances and effects of altering the system, for example by reducing the stock of grazers, can be substantially greater in areas of high nutrient input.


Trophic Diversity Nutrient Coriolis Upwelling 


  1. Aleem AA (1972) Effect of river outflow management on marine life. Mar Biol 15:200–208CrossRefGoogle Scholar
  2. Babcock R, Davies P (1991) Effects of sediment on settlement of Acropora millepora. Coral Reefs 9:205–208CrossRefGoogle Scholar
  3. Barnes H (1956) Balanus balanoides (L.) in the Firth of Clyde: the development and annual variation of the larval population, and the causative factors. J Anim Ecol 25:72–84CrossRefGoogle Scholar
  4. Barnes RSK, Hughes RN (1988) An introduction to marine ecology. Blackwell Sci Publ, Oxford, 351 ppGoogle Scholar
  5. Bellwood DR, Hughes TP, Folke C, Nyström M (2004) Confronting the coral reef crisis. Nature 429:827–833CrossRefPubMedGoogle Scholar
  6. Birkeland C (1977) The importance of rate of biomass accumulation in early successional stages of benthic communities to the survival of coral recruits. Proc 3rd Int Coral Reef Symp, Miami 1: Biology: 15–21Google Scholar
  7. Birkeland C (1982) Terrestrial runoff as a cause of outbreaks of Acanthaster planci (Echinodermata: Asteroidea). Mar Biol 69:175–185CrossRefGoogle Scholar
  8. Birkeland C (ed) (1987) Comparison between Atlantic and Pacific tropical marine coastal ecosystems: community structure, ecological processes, and productivity. UNESCO Reports in Marine Science 46, 262 ppGoogle Scholar
  9. Birkeland C (1989) The influence of echinoderm on coral-reef communities. In: Jangoux M, Lawrence JM (eds) Echinoderm studies. AA Balkema, Rotterdam, pp 1–79Google Scholar
  10. Birkeland C, Amesbury SS (1988) Fish-transect surveys to determine the influences of neighboring habitats on fish community structure in the tropical Pacific. In: Dahl AL (ed) Regional co-operation on environmental protection of the marine and coastal areas of the Pacific, vol 97, UNEP Regional Seas Reports and Studies., pp 195–202Google Scholar
  11. Birkeland C, Rowley D, Randall RH (1982) Coral recruitment patterns at Guam. Proc 4th Internat Coral Reef Symp, Manila 2: 339–344Google Scholar
  12. Birkeland C, Nelson SG, Wilkins S deC, Gates P (1985) Effects of fish grazing on coral reef community metabolism. Proc 5th Int Coral Reef Congr, Tahiti 4: 47–51Google Scholar
  13. Birkeland C, Randall RH, Wass RC, Smith B, Wilkins S (1987) Biological resource assessment of the Fagatele Bay National Marine Sanctuary. US Department of Commerce, NOAA, National Ocean Service, Washington, DC, 232 ppGoogle Scholar
  14. Birrell CL, McCook LJ, Willis BL (2005) Effects of algal turfs and sediment on coral settlement. Mar Pollut Bull 51:408–414CrossRefPubMedGoogle Scholar
  15. Bonilla J, Senior W, Bugden J, Zafiriou O, Jones R (1993) Seasonal distribution of nutrients and primary productivity on the eastern continental shelf of Venezuela as influenced by the Orinoco River. J Geophys Res 98:2245–2257CrossRefGoogle Scholar
  16. Bowen BW, Rocha LA, Toonen RJ, Karl SA et al (2013) The origins of tropical marine biodiversity. Trends Ecol Evol 28:359–366CrossRefPubMedGoogle Scholar
  17. Brodie J (1995) The problems of nutrients and eutrophication in the Australian marine environment. In: Zann LP, Sutton DC (eds) The state of the marine environment report for Australia, Technical Annex 2. Great Barrier Reef Marine Park Authority, Townsville, pp 1–29Google Scholar
  18. Brodie J, Fabricius K, De’ath G, Okaji K (2005) Are increased nutrient inputs responsible for more outbreaks of crown-of-thorns starfish? An appraisal of the evidence. Mar Pollut Bull 51:266–278CrossRefPubMedGoogle Scholar
  19. Buddemeier RW, Hopley D (1988) Turn-ons and turn-offs: causes and mechanisms of the initiation and termination of coral reef growth. Proc 6th Int Coral Reef Symp, Townsville 1: 253–26Google Scholar
  20. Carpenter RC (1997) Invertebrate predators and grazers. In: Birkeland C (ed) Life and death of coral reefs. Chapman & Hall, New York, pp 198–229CrossRefGoogle Scholar
  21. Chevalier JP (1982) Reef Scleractinia of French Polynesia. Proc 4th Int Coral Reef Symp, Manila 2: 177–182Google Scholar
  22. Chuanmin H, Montgomery ET, Schmitt RW, Müller-Harger FE (2004) The dispersal of the Amazon and Orinoco River water in the tropical Atlantic and Caribbean Sea: observations from space and S-PALACE floats. Deep-Sea Res II 51:1151–1171CrossRefGoogle Scholar
  23. Coley PD, Bryant JP, Chapin FS III (1985) Resource availability and plant antiherbivore defense. Science 230:895–899CrossRefPubMedGoogle Scholar
  24. Crossland CJ (1988) Latitudinal comparisons of coral reef structure and function. Proc 6th Int Coral Reef Symp, Townsville 1: 221–226Google Scholar
  25. Darnaude AM (2005) Fish ecology and terrestrial carbon use in coastal areas: implications for marine fish production. J Anim Ecol 74:864–876CrossRefGoogle Scholar
  26. DeCarlo TM, Cohen AL, Barkley HC, Cobban Q, Young C, Shamberger KE, Brainard RE, Golbuu Y (2015) Coral macrobioerosion is accelerated by ocean acidification and nutrients. Geology 43:7–10CrossRefGoogle Scholar
  27. Diaz RJ, Rosenberg R (2008) Spreading dead zones and consequences for marine ecosystems. Science 321:926–929CrossRefPubMedGoogle Scholar
  28. Dodge RE, Lang JC (1983) Environmental correlates of hermatypic coral (Montastrea annularis) growth on the East Flower Gardens Bank, northwest Gulf of Mexico. Limnol Oceanogr 28:228–240CrossRefGoogle Scholar
  29. Doolette JB, Magrath WB (eds) (1990) Watershed development in Asia. Strategies and technologies. World Bank Tech Paper 12, 227 ppGoogle Scholar
  30. Dutterer AC, Mesing C, Cailteux R, Allen MS, Pine WE, Strickland PA (2012) Fish recruitment is influenced by river flows and floodplain inundation at Apalachicola River, Florida. River Res Appl 29:1110–1118CrossRefGoogle Scholar
  31. Earle SA (1972) A review of the marine plants of Panama. Bull Biol Soc Wash 2:69–87Google Scholar
  32. Fabricius KE (2005) Effects of terrestrial runoff on the ecology of corals and coral reefs: review and synthesis. Mar Pollut Bull 50:125–146CrossRefPubMedGoogle Scholar
  33. Fabricius KE, Wild C, Wolanski E, Abele D (2003) Effects of transparent exopolymer particles and muddy terrigenous sediments on the survival of hard coral recruits. Estuar Coast Shelf Sci 57:613–621CrossRefGoogle Scholar
  34. Fabricius KE, Okaji K, De’ath G (2010) Three lines of evidence to link outbreaks of the crown-of-thorns seastar Acanthaster planci to the release of larval food limitation. Coral Reefs 29:593–605CrossRefGoogle Scholar
  35. Geider RJ, Platt T, Raven JA (1986) Size dependence of growth and photosynthesis in diatoms; a synthesis. Mar Ecol Prog Ser 30:93–104CrossRefGoogle Scholar
  36. Gillson J (2011) Freshwater flow and fisheries production in estuarine and coastal systems: where a drop of rain is not lost. Rev Fish Sci 19:168–186CrossRefGoogle Scholar
  37. Gilmour J (1999) Experimental investigation into the effects of suspended sediment on fertilisation, larval survival and settlement in a scleractinian coral. Mar Biol 135:451–462CrossRefGoogle Scholar
  38. Glynn PW (1972) Observations on the ecology of the Caribbean and Pacific coasts of Panama. Bull Biol Soc Wash 2:13–20Google Scholar
  39. Glynn PW (ed) (1990) Global ecological consequences of the 1982–83 El Niño-Southern Oscillation. Elsevier Press, Amsterdam, 563 ppGoogle Scholar
  40. Grigg RW (1982) Darwin Point: a threshold for atoll formation. Coral Reefs 1:29–35CrossRefGoogle Scholar
  41. Grigg RW, Polovina JJ, Atkinson MJ (1984) Model of a coral reef ecosystem. III. Resource limitation, community regulation, fisheries yield and resource management. Coral Reefs 3:23–27CrossRefGoogle Scholar
  42. Gulland JA (1976) Production and catches of fish in the sea. In: Cushing DH, Walsh JJ (eds) The ecology of the seas. WB Saunders Co., Philadelphia, pp 283–314Google Scholar
  43. Hallock P (1987) Fluctuations in the trophic resource continuum; a factor in global biodiversity cycles. Palaeoceanography 2:457–471CrossRefGoogle Scholar
  44. Hallock P, Müller-Harger FE, Halas JC (1993) Coral reef decline. Natl Geogr Res Explor 9:358–378Google Scholar
  45. Hatcher BG (1997) Organic production and decomposition. In: Birkeland C (ed) Life and death of coral reefs. Chapman & Hall, New York, pp 140–174CrossRefGoogle Scholar
  46. Hay ME (1984) Patterns of fish and urchin grazing on Caribbean coral reefs: are previous results typical? Ecology 65:446–454CrossRefGoogle Scholar
  47. Highsmith RC (1980) Geographic patterns of coral bioerosion: a productivity hypothesis. J Exp Mar Biol Ecol 46:177–196CrossRefGoogle Scholar
  48. Hodgson G (1990) Tetracycline reduces sedimentation damage to corals. Mar Biol 104:493–496CrossRefGoogle Scholar
  49. Hughes TP (1994) Catastrophes, phase shifts, and large-scale degradation of a Caribbean coral reef. Science 265:1547–1551CrossRefPubMedGoogle Scholar
  50. ISRS (2004) The effects of terrestrial runoff of sediments, nutrients, and other pollutants on coral reefs. Briefing Paper 3, International Society for Reef Studies, 18 ppGoogle Scholar
  51. Ivlev VS (1961) Experimental ecology of the feeding of fishes. Yale University Press, New HavenGoogle Scholar
  52. Jayewardene D (2009) A factorial experiment quantifying the influence of parrotfish density and size on algal reduction on Hawaiian coral reefs. J Exp Mar Biol Ecol 375:64–69CrossRefGoogle Scholar
  53. Jokiel PL, Coles SL (1990) Response of Hawaiian and other Indo-Pacific reef corals to elevated temperature. Coral Reefs 8:155–162CrossRefGoogle Scholar
  54. Kamura S, Choonhabandit S (1986) Distribution of benthic marine algae on the coasts of Khang Khao and Thai Ta Mun, Sichang Islands, the Gulf of Thailand. Galaxea 5:97–114Google Scholar
  55. Kim I-N, Lee K, Gruber N, Karl DM, Bullister JL, Yang S, Kim T-W (2014) Increasing anthropogenic nitrogen in the North Pacific Ocean. Science 346:1102–1106CrossRefPubMedGoogle Scholar
  56. Kinsey DW (1983) Standards of performance in coral reef primary production and carbonate turnover. In: Barnes DJ (ed) Perspectives on coral reefs. Brian Clouston Publ, Manuka, pp 209–220Google Scholar
  57. Kinsey DW, Davies PJ (1979) Effects of elevated nitrogen and phosphorous on coral reef growth. Limnol Oceanogr 24:935–940CrossRefGoogle Scholar
  58. Kuffner IB, Walters LJ, Becerro MA, Paul VJ, Ritson-Williams R, Beach KS (2006) Inhibition of coral recruitment by macroalgae and cyanobacteria. Mar Ecol Prog Ser 323:107–117CrossRefGoogle Scholar
  59. Lewin RA, Cheng L, Alberte RA (1983) Prochloron-ascidian symbioses: photosynthetic potential and productivity. Micrones 19:165–170Google Scholar
  60. Littler MM, Littler DS (1980) The evolution of phallus form and survival strategies in benthic marine macroalgae: held and laboratory tests of a functional form model. Am Nat 116:25–44CrossRefGoogle Scholar
  61. Longhurst AR, Pauly D (1987) Ecology of tropical oceans. Academic, London, 407 ppGoogle Scholar
  62. Maclean J (1984) Red tide – a growing problem in the Indo-Pacific region. ICLARM Newsl 7(4):20Google Scholar
  63. Menasveta P, Wongratana T, Chaitanawisuti, Rungsupa S (1986) Species composition and standing crop of coral reef fishes in the Sichang Islands, Gulf of Thailand. Galaxea 5:115–121Google Scholar
  64. Milliman JD (1992) River sediment discharge to the sea: new analysis of old data. Coastal systems studies and sustainable development. UNESCO Tech Pap Mar Sci 64:56–66Google Scholar
  65. Milliman JD, Meade RH (1983) World-wide delivery of river sediment to the oceans. J Geol 91:1–21CrossRefGoogle Scholar
  66. Milliman JD, Qin YS, Ren ME, Saito Y (1987) Man’s influence on the erosion and transport of sediment by Asian rivers: the Yellow River (Huanghe) example. J Geol 95:751–762CrossRefGoogle Scholar
  67. Muscatine L, Porter JW (1977) Reef corals: mutualistic symbiosis adapted to nutrient-poor environments. Bioscience 27:454–460CrossRefGoogle Scholar
  68. Odum EP, Keunzler EJ, Bunt MX (1958) Uptake of P32 and primary productivity in marine benthic algae. Limnol Oceanogr 3:340–345CrossRefGoogle Scholar
  69. Page HM, Hubbard DM (1987) Temporal and spatial patterns of growth in mussels Mytilus edulis on an offshore platform: relationships to water temperature and food availability. J Exp Mar Biol Ecol 111:159–179CrossRefGoogle Scholar
  70. Paulay G (1997) Diversity and distribution of reef organisms. In: Birkeland C (ed) Life and death of coral reefs. Chapman & Hall, New York, pp 298–353CrossRefGoogle Scholar
  71. Pitcher TJ (1986) Predators and food are the keys to understanding fish shoals: a review of recent experiments. Nat Can Ann Rev Ecol Syst 113:225–233Google Scholar
  72. Pitcher TJ, Magurran AE (1983) Shoal size, patch profitability and information exchange in foraging goldfish. Anim Behav 31:546–555CrossRefGoogle Scholar
  73. Pitcher TJ, Magurran AE, Winfield IJ (1982) Fish in larger shoals find food faster. Behav Ecol Sociobiol 10:149–151CrossRefGoogle Scholar
  74. Ramus J, Venable M (1987) Temporal ammonium patchiness and growth rate in Codium and Ulva (Ulvophyceae). J Phycol 23:518–523CrossRefGoogle Scholar
  75. Richmond RH (1990) Relationships among reproductive mode, biogeographic distribution patters and evolution in scleractinian corals. In: Hoshi M, Yamashita O (eds) Advances in invertebrate reproduction, vol 5. Elsevier, Amsterdam, pp 317–322Google Scholar
  76. Robertson DR (1982) Fish feces as fish food on a Pacific coral reef. Mar Ecol Prog Ser 7:253–265CrossRefGoogle Scholar
  77. Roff G, Mumby PJ (2012) Global disparity in the resilience of coral reefs. Trends Ecol Evol 27:404–419CrossRefPubMedGoogle Scholar
  78. Rose CS, Risk MJ (1985) Increase in Cliona deletrix infestation of Montastrea cavernous heads on an organically polluted portion of the Grand Cayman fringing reef. Mar Ecol 6:345–363CrossRefGoogle Scholar
  79. Ryther JH (1963) Geographic variations in productivity. In: Hill MN (ed) The sea, vol 2. Wiley, New YorkGoogle Scholar
  80. Ryther JH (1969) Photosynthesis and fish production in the sea. Science 166:72–76CrossRefPubMedGoogle Scholar
  81. Sammarco PW (1980) Diadema and its relationship to coral spat mortality: grazing, competition, and biological disturbances. J Exp Mar Biol Ecol 45:245–272CrossRefGoogle Scholar
  82. Sammarco PW (1985) The Great Barrier Reef vs. the Caribbean: comparisons of grazers, coral recruitment patterns, and reef recovery. Proc 5th Int Coral Reef Congr, Tahiti 4: 391–397Google Scholar
  83. Smith SV, Kinsey DW (1976) Calcium carbonate production, coral reef growth and sea level change. Science 194:937–939CrossRefPubMedGoogle Scholar
  84. Smith SV, Kimmerer WJ, Laws EA, Brock RE, Walsh TW (1981) Kaneohe Bay sewage diversion experiment: perspectives on ecosystem response to nutritional perturbation. Pac Sci 35:279–402Google Scholar
  85. Smith JE, Smith CM, Hunter CL (2001) An experimental analysis of the effects of herbivory and nutrient enrichment on benthic community dynamics on a Hawaiian reef. Coral Reefs 19:332–342CrossRefGoogle Scholar
  86. Sutcliffe WH Jr (1972) Some relations of land drainage, nutrients, particulate material, and fish catch in two eastern Canadian bays. J Fish Res Board Can 29:357–362CrossRefGoogle Scholar
  87. Sutcliffe WH Jr (1973) Correlations between seasonal river discharge and local landings of American lobster (Homarus americanus) and Atlantic halibut (Hippoglossus hippoglossus) in the Gulf of St. Lawrence. J Fish Res Board Can 30:856–859CrossRefGoogle Scholar
  88. Tsuchiya M, Nakasone Y, Moordee R, Manthachitra V (1986) Distribution of subtidal macrobenthic animals around the Sichang islands, the Gulf of Thailand. Galaxea 5:75–96Google Scholar
  89. Twilley RR, Kemp WM, Staver KW, Stevenson JC, Boynton WR (1985) Nutrient enrichment of estuarine submersed vascular plant communities. 1. Algal growth acid effects on production of plants and associated communities. Mar Ecol Prog Ser 23:179–191CrossRefGoogle Scholar
  90. van Moorsel GWNM (1988) Early maximum growth of stony corals (Scleractinia) after settlement on artificial substrata on a Caribbean reef. Mar Ecol Prog Ser 50:127–135CrossRefGoogle Scholar
  91. Vermeij GJ (1978) Biogeography and adaptation, patterns of marine life. Harvard University Press, Cambridge, MA, 332 ppGoogle Scholar
  92. Veron JEN (1993) A biogeographic database of hermatypic corals. Species of the central Indo-Pacific, genera of the world. Aust Inst Mar Sci Monogr Ser 10:1–433Google Scholar
  93. Veron JEN (1995) Corals in space and time. The biogeography and evolution of the Scleractinia. University of New South Wales Press, Sydney, 321 ppGoogle Scholar
  94. Wallace CC (1985) Seasonal peaks and annual fluctuation in recruitment of juvenile scleractinian corals. Mar Ecol Prog Ser 21:289–298CrossRefGoogle Scholar
  95. Werner EE, Hall DJ (1974) Optimal foraging and the size selection of prey be the bluegill sunfish (Lepomis macrochirus). Ecology 55:1042–1052CrossRefGoogle Scholar
  96. Wilkinson CR (1983) Role of sponges in coral reef structural processes. In: Barnes DJ (ed) Perspectives on coral reefs. Brian Clouston Publ, Manuka, pp 263–274Google Scholar
  97. Wilkinson CR (1986) The nutritional spectrum in coral reef benthos or sponging off one another for dinner. Oceanus 29:68–75Google Scholar
  98. Wilkinson CR (1987) Interocean differences in size and nutrition of coral reef sponge populations. Science 236:1654–1657CrossRefPubMedGoogle Scholar
  99. Wilkinson CR, Cheshire AC (1990) Comparisons of sponge populations across the barrier reefs of Australia and Belize: evidence for higher productivity in the Caribbean. Mar Ecol Prog Ser 67:285–294CrossRefGoogle Scholar
  100. Wisshak M, Schönberg CHL, Form A, Freiwald A (2012) Ocean acidification accelerates reef bioerosion. PLoS One 7:e45124PubMedCentralCrossRefPubMedGoogle Scholar
  101. Wolf NG (1987) Schooling tendency and foraging benefit in the ocean surgeonfish. Behav Ecol Sociobiol 21:59–63CrossRefGoogle Scholar
  102. Wolff WJ, Gueye A, Meijboo A, Piersma T, Sall MA (1987) Distribution, biomass, recruitment and productivity of Anadara senillis (L.) (Mollusca: Bivalvia) on the Banc d’Arguin, Mauritania. Neth J Sea Res 21:243–253CrossRefGoogle Scholar
  103. Wulff J (2012) Ecological interactions and the distribution, abundance, and diversity of sponges. Adv Mar Biol 61:273–344CrossRefPubMedGoogle Scholar

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© Springer Science+Business Media Dordrecht 2015

Authors and Affiliations

  1. 1.Department of BiologyUniversity of Hawaii at ManoaHonoluluUSA

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