Abstract
Sea urchins of the genus Diadema play an important role as controlers of algal growth in coral reef and rocky reef communities, but high densities cause bioerosion of the reef framework. Between January 2006 and February 2007 (except April, July and August), population densities and mean test diameter of Diadema mexicanum were determined at Isla Montosa, La Entrega, Isla Cacaluta and San Agustín, Bahías de Huatulco, Mexico. Mean density of the sea urchins was relatively constant through time at all localities: lowest at San Agustín (0.26±0.13 ind.m-2) and highest at La Entrega (4.17±1.4 ind.m-2). There were significant differences between La Entrega and other localities. Mean test diameter ranged between 4.41±0.88 cm (Isla Cacaluta) and 4.72±0.27 (San Agustin), and did no vary significantly between localities, but there were monthly variations. Test diameter agrees with other studies. The calculated amount of CaCO3 removed by D. mexicanum showed variations between localities. The lowest rate of bioerosion occurred at San Agustín (0. 25 kg.m-2.yr-1 ), and the highest at La Entrega (4 kg.m-2.yr-1). The recent urchin population decrease means a reduction in their removal of coral CaCO3: 5.55% to 2.36% at Isla Cacaluta, 5.08% to 1.40% at San Agustin and 16.59% to 3.08% at Isla Montosa. The only locality where bioerosion increased was La Entrega, from 27.04 % to 33.05 %. This reduction of urchin activities could be beneficial for coral reef growing and recovery from stress, nevertheless it could also signify an increase in algal biomass and competition with corals for light and space. We recommend a permanent monitoring and evaluation of population densities of D. mexicanum and fishes, as well as coral and algal cover at the area, to discern if changes in sea urchin densities in Bahias de Huatulco are a continuous phenomenon, or part of a natural cycle of increments and reductions. Rev. Biol. Trop. 56 (Suppl. 3): 255-263. Epub 2009 January 05.References
Bak, R.P.M. 1994. Sea urchin bioerosion on coral reefs: place in the carbonate budget and relevant variables. Coral Reefs 13: 99-104.
Bauer, J.C. 1980. Observations on geographical variations in population density of the echinoid Diadema antillarum within the western north Atlantic. Bull. Mar. Sci. 30: 509-515.
Birkeland, C. 1989. The influence of echinoderms on coralreef communities, p. 1-79. In. M. Jangoux and J.M. Lawrence (eds.). Echinoderm Studies. A.A. Balkema, Rotterdam.
Carpenter, R.C. 1984. Predator and population density control of homing behavior in the Caribbean echinoid Diadema antillarum. Mar. Biol. 82: 101-108.
Carpenter, R.C. 1990. Mass mortality of Diadema antillarum. I. Long-term effects on sea urchin populationdynamics and coral reef algal communities. Mar. Biol. 104: 67-77.
De Ruyter van Stevenick, E.D. & R.P.M. Bak. 1986. Changes in abundance of coral-reef bottom components related to mass mortal.ity of the sea urchin Diadema antillarum. Mar. Ecol. Prog. Ser. 34:87-94.
Eakin, C.M. 1992. Post-El Niño panamanian reefs: less accretion, more erosion and Damselfish protection. Proc. 7th Int. Coral Reefs Symp. 1: 387-396.
Eakin, C.M. 1996. Where have all the carbonates gone? A model comparison of calcium carbonate budgets before and after the 1982-83 El Niño at Uva Island in the eastern Pacific. Coral Reefs 15: 109-119.
Glynn, P.W. 1988. El Niño-Southern Oscillation 1982-1983: Near shore population, community, and ecosystem responses. Annu. Rev. Ecol. Syst. 19: 309-345.
Glynn, P.W. & G.E. Leyte-Morales. 1997. Coral reefs of Huatulco, west Mexico: reef development in upwelling Gulf of Tehuantepec. Rev. Biol. Trop. 45: 1033-1047.
Glynn, P.W., G.M. Wellington & C. Birkeland. 1979. Coral reef growth in the Galápagos: Limitation by sea urchins. Science 203: 47-49.
Guzmán, H.M. 1988. Distribución y abundancia de organismos coralívoros en los arrecifes coralinos de la Isla del Caño, Costa Rica. Rev. Biol. Trop. 36: 191-207.
Guzmán, H.M. & J. Cortés. 1992. Cocos Island coral reefs after the 1982-83 El Niño disturbance. Rev. Biol. Trop. 40: 309-324.
Guzmán, H. M. & J. Cortés. 2007. Reef recovery 20 years after the 1982–1983 El Niño massive mortality. Mar. Biol. 151: 401-411
Hay, M.E. 1984. Patterns of fish and urchin grazing on Caribbean coral reefs: are previous results typical? Ecology 65: 446-454.
Hay, M.E. & P.R. Taylor. 1985. Competition between herviborous fishes and urchins on Caribbean reefs. Oecologia 65: 591-598.
Herrera-Escalante, T., R.A. López-Pérez & G.E. Leyte- Morales. 2005. Bioerosion caused by the sea urchin Diadema mexicanum (Echinodermata: Echinoidea) at Bahias de Huatulco, Western Mexico. Rev. Biol. Trop. 53 (Supl. 3): 263-273.
Hughs, T.P. 1989. Community structure and diversity of coral reefs: The role of history. Ecology 70: 275-279.
Knowlton, N. 2001. Sea urchin recovery from mass mortality: new hope for Caribbean Coral reefs? Proc. Nat. Acad. Sci. 98: 4822-4824.
Lessios, H.A. 1988. Mass mortality of Diadema antillarum in the Caribbean: what have we learned? Ann. Rev. Ecol. Syst. 19: 371-393.
Lesssios, H.A., J.D. Cubit, R.D. Robertson, M.J. Shulman, M.R. Parker, S.D. Garrity & S.C. Levings. 1984. Mass mortality of Diadema antillarum on the Caribbean coast of Panama. Coral Reefs 3: 173-182.
Lessios, H.A., B.D. Kessing & J.S. Pearse. 2001. Population structure and speciation in tropical seas: global phylogeography of the sea urchin Diadema. Evolution, 55: 955-975.
Levitan, D.R. 1988. Density-dependant size regulation and negative growth in the sea urchin Diadema antillarum Philippi. Oecologia 76: 627-629.
Levitan, D.R. 1989. Density-dependant size regulation Diadema antillarum: Effects on fecundity and survivorship. Ecology 70: 1414-1424.
Levitan, D.R. 1991. Skeletal changes in the test and jaws of the sea urchin Diadema antillarum in response to food limitation. Mar. Biol.111: 431-435.
Levitan, D.R. 1995. The ecology of fertilization in freespawing invertebrates. p. 123-156. In L. McEdward (ed.). Ecology of Marine Invertebrate Larvae. CRC, Florida.
Liddell, W.D. & S.L. Ohlhorst. 1986. Changes in benthic community composition following the mass mortality of Diadema at Jamaica. J. Exp. Mar. Biol. Ecol. 95: 271-278.
Lirman, D., P.W. Glynn, A.C. Baker & G.E. Leyte-Morales. 2001. Combined effects of three sequential storms on the Huatulco coral reef tract, Mexico. Bull. Mar. Sci. 69: 267-278.
López-Pérez, R.A., L.M. Hernández-Ballesteros & T. Herrera-Escalante. 2002. Cambio en la dominancia de la comunidad arrecifal en Chachacual, Bahías de Huatulco, Oaxaca. Ciencia y Mar 16: 33-38.
López-Pérez, R.A & L.M. Hernández-Ballesteros. 2004. Coral community structure and dynamics in the Huatulco area, western Mexico. Bull. Mar. Sci. 75: 453-472.
McClanahan, T. R. 2007. Response of the coral reef benthos and herbivory to fishery closure management and the 1998 ENSO disturbance. Oecologia DOI 10.1007/s00442-007-0890-0.
McClanahan, T.R., A.T. Kamukuru, N.A. Muthiga, M. Gilagabher & D. Obura. 1996. Effect of sea urchin reductions on algae, coral, and fish populations. Conserv. Biol. 10: 136-154.
Muthiga, N.A., T.R. McClanahan. 2007. Ecology of Diadema, p. 205-219. In J.M. Lawrence (ed.). Edible Sea Urchins: Biology and Ecology. Elsevier, Amsterdam, The Netherlands.
Ogden, J.C. 1976. Some aspects of hervibore-plant relationship on Caribbean reefs and seagrass beds. Aquatic Botany 2: 103-116.
Ogden, J.C. & P.S. Lobel. 1978. The role of herviborous fishes and urchins in coral reefs communities. Env. Bio. Fish. 3: 49-63.
Ogden, J.C., R.A. Brown & N. Salesky. 1973. Grazing by the echinoid Diadema antillarum philippi: formation of halos around West Indian patch reefs. Science 182: 715-716.
Reyes-Bonilla H. 2003. Coral reefs of the Pacific coast of Mexico, p. 387–418. In J. Cortés (ed). Latin American Coral Reefs. Elsevier, Amsterdam.
Reyes-Bonilla, H. & L.E. Calderón-Aguilera. 1999. Population density, distribution and consuption rates of three corallivores at Cabo Pulmo reef., Gulf of California, Mexico. Mar. Ecol. 20: 347-357.
Reyes-Bonilla, H., J.D. Carriquiry, G.E. Leyte-Morales & A.L. Cupul-Magaña. 2002. Effects of El Niño Southern Oscilation and the anti-El Niño event (1997-1999) on coral reefs of the western coast of Mexico. Coral Reefs 21: 368-372.
Sammarco, P.W. 1980. Diadema and its relationship to coral spat mortality: grazing competition and biological disturbance. J. Mar. Res. 32: 254-272.
Sammarco, P.W. 1982a. Echinoid grazing as a structuring force in coral communities: whole reef manipulations. J. Exp. Mar. Biol. Ecol. 61: 31-35.
Sammarco, P.W. 1982b. Effects of grazing by Diadema antillarum Philippi (Echinodermata: Echinoidea) on algal diversity and community structure. J. Exp. Mar. Biol. Ecol., 65: 83-105.
Solandt, J.L. & A.C. Campbell. 2001. Macroalgal feeding characteristics of the sea urchin Diadema antillarum Philippi at Discovery Bay, Jamaica. Carib. J. Sci. 37: 227-238.
Tuya, F., J.A. Martín, G.M. Reuss & A. Luque. 2001. Food preferences of the sea urchin Diadema antillarum in Gran Canaria (Canary Islands, central-east Atlantic Ocean). J. Mar. Biol. Ass.UK., 81: 845-849.
Tuya, F., R. Haroun, A. Boyra & P. Sánchez-Jerez. 2005. Sea urchin Diadema antillarum: different functions in the structure and dynamics of reefs on both sides of the Atlantic. Mar. Ecol. Prog. Ser. 302: 307-310.
Vicente, V.P. & C. Goenaga. 1984. Mortandades masivas del erizo de mar Diadema antillarum (Philippi) en Puerto Rico. Centro para Estudios Energéticos y Ambientales, Div. Ecología Marina, Reporte CEER-M-195, Univ. Puerto Rico, Puerto Rico.
Comments
This work is licensed under a Creative Commons Attribution 4.0 International License.
Copyright (c) 2008 Revista de Biología Tropical