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Coral Reefs

, Volume 15, Issue 2, pp 109–119 | Cite as

Where have all the carbonates gone? A model comparison of calcium carbonate budgets before and after the 1982–1983 El Nino at Uva Island in the eastern Pacific

  • C. M. Eakin
Reports

Abstract

El Nifio related coral mortality and a subsequent increase in crustose coralline algae and sea urchins have resulted in profound changes to the coral reef ecosystem at Uva Island, Panama (Pacific coast). New data and a model are presented that analyze the CaCO3 budget of the reef. The model accounts for production by corals and coralline algae, erosion byDiadema, infauna, fish and other motile organisms, and the retention of sediments as a function of size. The 2.5 ha reef is currently eroding at an average rate of 4,800 kg/y or −0.19 kg/m2/y but there is tremendous variation among reef zones. While deposition in other zones range from +0.1 to 0.4 kg/m2/y, erosion of the seaward reef base averages about −3.65 kg/m2/y. The damselfish/algal lawn symbiosis protects portions of the reef framework, reducing net losses there by 2,000 kg/y (up to 0.33 kg/m2/y). Before the 1982-1983 El Niño, the overall reef was depositional. At that time, estimated production exceeded erosion in most zones, resulting in a net deposition of approximately 8,600 kg/y or 0.34 kg/m2/y.

Keywords

Coral Reef CaCO3 Sedimentology Pacific Coast Carbonate Budget 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Bagnold RA (1966) An approach to the sediment transport problem from general physics. US Geological Survey Prof Pap 422-I, 32pGoogle Scholar
  2. Brock RE (1979) An experimental study on the effects of grazing by parrotfishes and role of refuges in benthic community structure. Mar Biol 51(4):381–388Google Scholar
  3. Cloud PE Jr (1959) Geology of Saipan, Mariana Islands; part 4. US Geol Survey Prof Paper 280-K:361-445Google Scholar
  4. Chave KE, Smith SV, Roy KJ (1972) Carbonate production by coral reefs. Mar Geol 12:123–140Google Scholar
  5. Colgan MW (1990) El Nifio and the history of eastern Pacific reef building. In: Glynn PW (ed) Global ecological consequences of the 1982-83 El Nifio-Southern Oscillation. Elsevier Oceanography Series. Elsevier Press, pp 183-232Google Scholar
  6. Day RW, Quinn GP (1989) Comparisons of treatments after an analysis of variance in ecology. Ecol Monogr 59(4):433–463Google Scholar
  7. Eakin CM (1987) Damselfishes and their algal lawns:a case of plural mutualism. Symbiosis 4 (1-3):275–288Google Scholar
  8. Eakin CM (1988) Avoidance of damselfish lawns by the sea urchinDiadema mexicanum at Uva Island, Panama. Proc 6th Intl Coral Reef Symp 2:21–26Google Scholar
  9. Eakin CM (1991) The damselfish-algal lawn symbiosis and its influence on the bioerosion of an El Niño impacted coral reef, Uva Island, pacific Panama. PhD dissertation, Univ of Miami 158pGoogle Scholar
  10. Eakin CM (1992) Post-El Nifio panamanian reefs:less accretion, more erosion and damselfish protection. Proc 7th Intl Coral Reef Symp 1:387–396Google Scholar
  11. Eakin CM, Smith DB, Glynn PW, D'Croz L, Gil J (1989) Extreme tidal exposures, cool upwelling and coral mortality in the eastern Pacific (Panama). Assoc Mar Labs Carib 22:insertGoogle Scholar
  12. Gattuso J-P, Pichon M, Delesalle B, Frankignoulle M (1993) Community metabolism and air-sea CO2 fluxes in a coral sea reef ecosystem (Moorea, French Polynesia). Mar Ecol Progr Ser, 96(3):259–268Google Scholar
  13. Ginsburg RN (1983) Geological and biological roles of cavities in coral reefs. In: Barnes DJ (ed) Perspective on coral reefs. Brain Clouston Publisher, Manuka, ACT, Australia, pp 148–153Google Scholar
  14. Glynn PW (1976) Some physical and biological determinants of coral community structure in the eastern Pacific. Ecol Monogr 46(4): 431–456Google Scholar
  15. Glynn PW (1977) Coral growth in upwelling and nonupwelling areas off the Pacific coast of Panama. J Mar Res 35(3):567–585Google Scholar
  16. Glynn PW (1984) Widespread coral mortality and the 1982-83 El Niño warming event. Environ Conserv 11(2):133–146Google Scholar
  17. Glynn PW (1985a) Corallivore population sizes and feeding effects following El Niño (1982-83) associated coral mortality in Panama. Proc 5th Intl Coral Reef Congress. Tahiti 4:183–188Google Scholar
  18. Glynn PW (1985b) E1 Niño-associated disturbance to coral reefs and post disturbance mortality byAcanthaster planci. Mar Ecol Prog Ser 26:295–300Google Scholar
  19. Glynn PW (1988) El Niño warming, coral mortality and reef framework destruction by echinoid bioerosion in the eastern Pacific. Galaxea 7:129–160Google Scholar
  20. Glynn PW (1990) Coral mortality and disturbances to coral reefs in the tropical eastern Pacific. In: Glynn PW (ed) Global Ecological Consequences of the 1982-83 El Niño-Southern Oscillation. Elsevier Oceanography Series, Elsevier Press, Amsterdam, pp 55–126Google Scholar
  21. Glynn PW (1991.) Coral bleaching in the 1980s and possible connection with global warming. Trends Ecol Evol 6: 175–179Google Scholar
  22. Glynn PW, Cortes J, Guzmán 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 Intl Coral Reef Symp 3:237–243Google Scholar
  23. Glynn PW, Gassman NJ, Eakin CM, Cortes J, Smith DB, Guzmán HM (1991) Reef coral reproduction in the eastern Pacific:Costa Rica, Panama and Galápagos Islands (Ecuador), Part l. Pocilloporidae. Mar Biol 109:355–368Google Scholar
  24. Glynn PW, Macintyre IG (1977) Growth rate and age of coral reefs on the Pacific coast of Panama. Proc Third Intl Coral Reef Symp 2:251–259Google Scholar
  25. Glynn PW, Stewart RH, McCosker JE (1972) Pacific coral reefs of Panama: structure, distribution and predators. Sonderdruck aus der Geol Rundschau Band 61(2):483–519Google Scholar
  26. Hubbard DK, Miller Al, Scaturo D (1990) Production and cycling of calcium carbonate in a shelf-edge reef system (St. Croix, US Virgin Islands): applications to the nature of reef systems in the fossil record. J Sed Petrology 60(3): 335–360Google Scholar
  27. Hunter IG (1977) Sediment production byDiadema antillarum on a Barbados fringing reef. Proc 3rd Intl Coral Reef Symp 2: 105–109Google Scholar
  28. Hutchings PA (1986) Biological destruction of coral reefs: a review. Coral Reefs 4(4):239–252Google Scholar
  29. Inter-agency Committee on Water Resources (1957). The development and calibration of the visual-accumulation tube. Report No. 11 of A study of methods used in measurement and analysis of sediment loads in streams. St. Anthony Falls Hydraulic Laboratory, Minneapolis, MN, 109pGoogle Scholar
  30. Kayanne H, Suzuki A, Saito H (1995) Diurnal changes in the partial pressure of carbon dioxide in coral reef water. Science. 269(5221): 214–216Google Scholar
  31. Kiene WE (1988) A model of bioerosion on the Great Barrier Reef. Proc 6th Intl Coral Reef Symp 3:449–454Google Scholar
  32. Klumpp DW, McKinnon D, Daniel P (1987) Damselfish territories: zones of high productivity on coral reefs. Mar Ecol Prog Ser 40 (1-2):41–51Google Scholar
  33. Land LS (1979) The fate of reef-derived sediment on the north Jamaican Island slope. Mar Geol 29:55–71Google Scholar
  34. Lamberts AE (1978) Coral growth: alizarin method. In: Stoddart DR, Johannes RE (eds) Coral Reefs: research methods, 5. UNESCO, Paris, pp 523–527Google Scholar
  35. Le Campion-Alsumard T, Romano J-C, Peyrot-Clausade M, Le Campion J, Paul R (1993) Influence of some coral reef communities on the calcium carbonate budget of Tiahua reef (Moorea, French Polynesia). Mar Biol 115:685–693Google Scholar
  36. McCave IN (1971) Sand waves in the North Sea off the coast of Holland. Mar Geol 10: 199–225Google Scholar
  37. Ogden JC (1977) Carbonate-sediment production by parrot fish and sea urchins on Caribbean reefs. In: Frost SH, Weiss MP, Saunders JB (eds) Reefs and related carbonates-ecology and sedimentology. American Association of Petroleum Geologists, Tulsa, OK, pp 281–288Google Scholar
  38. Ogden JC, Lobel PS (1978) The role of herbivorous fishes and urchins in coral reef communities. Env Biol Fishes 3(1):49–63Google Scholar
  39. Polunin NVC, Koike I (1987) Temporal focusing of nitrogen release by a periodically feeding herbivorous reef fish. J Exp Biol Ecol 111:285–296Google Scholar
  40. Randall JE (1967) Food habits of reef fishes of the West Indies. In: Bayer FM, et al. (eds) Proceedings of the International Conference on Tropical Oceanography, 5. University of Miami, Institute of Marine Sciences, Miami, pp 665–847Google Scholar
  41. Reaka-Kudla ML, Feingold JS, Glynn PW (1996) Experimental studies of rapid bioerosion of coral reefs in the Galápagos Islands. Coral Reefs 15:101–107Google Scholar
  42. Scoffin TP, Stearn CW, Boucher D, Frydl P, Hawkins CM, Hunter IG, MacGeachy JK (1980) Calcium carbonate budget of a fringing reef on the west coast of Barbados; part II-erosion, sediments and internal structure. Bull Mar Sci 30(2):475–508Google Scholar
  43. Scott PJB, Risk MJ and Carriquiry JD (1988) El Niño, bioerosion and the survival of east Pacific reefs. Proc 6th Intl Coral Reef Symp 2:517–520Google Scholar
  44. Smith SV and Kinsey DW (1978) Calcification and organic carbon metabolism as indicated by carbon dioxide. In: Stoddart DR and Johannes RE (eds) Coral reefs: research methods. UNESCO, Paris, pp 469–484Google Scholar
  45. Sokal RR, Rohlf FJ (1981) Biometry. WH Freeman & Co, San FranciscoGoogle Scholar
  46. Southard JB, Boguchwal LA (1990) Bed configurations in steady unidirectional water flows. Part 2. Synthesis of flume data. J Sed Petr 60(5):658–679Google Scholar
  47. Warless HR, Burton EA, Dravis J (1981) Hydrodynamics of carbonate fecal pellets. J Sed Petr 51(1):27–36Google Scholar
  48. Wilkinson CR (1992) Coral reefs of the world are facing widespread devastation:can we prevent this through sustainable managements practices? Proc 7th Intl Coral Reef Symp 1:11–24Google Scholar
  49. Williams EH and Williams LB (1990) The world-wide coral reef bleaching cycle and related sources of coral mortality. Atoll Res Bull 335:1–71Google Scholar
  50. Zar JH (1984) Biostatistical Analysis. Prentice-Hall, Inc, Englewood Cliffs, NJ, 718Google Scholar

Copyright information

© Springer-Verlag 1996

Authors and Affiliations

  • C. M. Eakin
    • 1
  1. 1.Office of Global ProgramsNational Oceanic and Atmospheric AdministrationSilver SpringUSA

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