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Mass mortality ofDiadema antillarum

I. Long-term effects on sea urchin population-dynamics and coral reef algal communities

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Abstract

The mass mortality of the echinoidDiadema antillarum Philippi in 1983/1984 resulted in dramatic changes in the benthic algal community. This study reports data on the population densities of sea urchins prior to and following the mass mortality and data on the biomass, species composition, and rates of primary productivity of algal communities at several study sites in St. Croix, U.S. Virgin Islands. The mass mortality reducedD. antillarum population densities by 95 to 99%. Population densities were reduced further by a second, less severe mortality event in October 1985. Over a period of 2 yr, recruitment ofD. antillarum larvae to the study sites was low and population densities remained at 2 to 30% of their premortality levels. The effects of the mass mortality on the algal community were significant. Algal biomass increased by 22 to 439% across reef zones 16 mo after the die-off. Rates of primary productivity per unit biomass (chlorophylla) remained at approximately 60% of premortality levels in shallow-reef habitats for 25 mo following the die-off. The magnitude of the response of the algal community was positively correlated with the previous population densities ofD. antillarum. The species composition of the algal community also shifted dramatically. Prior to the mass mortality, algal communities were dominated by algal turfs and crustose algae, and macroalgae were either rare or absent. Twenty-five months after the mass mortality, algal turfs covered 40% of the area and macroalgae covered 47%. Many of the macroalgal species are not consumed by herbivores and much of the algae is dislodged by storm waves and is exported from the reef. This represents a transition from a community dominated by a grazing-based food web to one where the majority of primary production may be exported to adjacent communities.

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Literature cited

  • Adey, W. H. (1978). Coral reef morphogenesis: a multidimensional model. Science, N.Y. 202: 831–837

    Google Scholar 

  • Adey, W. H., Steneck, R. S. (1985). Highly productive eastern Caribbean reefs: synergistic effects of biological, physical and geological factors. In: Reaka M. L. (ed.) The ecology of coral reefs. National Oceanic and Atmospheric Administration, Rockville Maryland p. 163–187

    Google Scholar 

  • Bak, R. P. M. (1985). Recruitment patterns and mass mortalities in the sea urchinDiadema antillarum. Proc. 5th int. coral Reef Congress, Tahiti 5: 267–272 [Gabrié, C., et al. (eds.) Antenne Museum — EPHE, Moorea, French Polynesia]

    Google Scholar 

  • Bak, R. P. M., Carpay, M. J. E., de Ruyter van Steveninck, E. D. (1984). Densities of the sea urchinDiadema antillarum before and after mass mortalities on the coral reefs of Curacao. Mar. Ecol. Prog. Ser. 17: 105–108

    Google Scholar 

  • Bauer, J. C. (1980). Observations on geographical variations in population density of the echinoidDiadema antillarum within the western North Atlantic. Bull. mar. Sci. 30: 509–515

    Google Scholar 

  • Breen, P. A., Mann, K. H. (1976). Changing lobster abundance and the destruction of kelp beds by sea urchins. Mar. Biol. 34: 137–142

    Google Scholar 

  • Carpenter, R. C. (1981). Grazing byDiadema antillarum (Philippi) [sic] and its effects on the benthic algal community. J. mar. Res. 39: 749–765

    Google Scholar 

  • Carpenter, R. C. (1985a). Sea urchin mass mortality: effects on reef algal abundance, species composition, and metabolism and other reef herbivores. Proc. 5th int. coral Reef Congr. 4: 53–60 [Gabrié, C., et al. (eds.) Antenne Museum — EPHE, Moorea, French Polynesia]

    Google Scholar 

  • Carpenter, R. C. (1985b). Relationships between primary production and irradiance in coral reef algal communities. Limnol. Oceanogr. 30: 784–793

    Google Scholar 

  • Carpenter, R. C. (1986). Partitioning herbivory and its effects on coral reef algal communities. Ecol. Monogr. 56: 345–363

    Google Scholar 

  • Carpenter, R. C. (1988). Mass mortality of a Caribbean echinoid: immediate effects on community metabolism and other herbivores. Proc. natn. Acad. Sci. U.S.A. 85: 511–514

    Google Scholar 

  • Carpenter, R. C. (1990). Mass mortality ofDiadema antillarum. II. Effects on population densities and grazing intensity of parrotfishes and surgeonfishes. Mar. Biol. 104: 79–86

    Google Scholar 

  • Chapman, A. R. O. (1981). Stability of sea urchin dominated barren grounds following destructive grazing of kelp in St. Margaret's Bay, Eastern Canada. Mar. Biol. 62: 307–311

    Google Scholar 

  • Clark, H. L. (1933). A handbook of the littoral echinoderms of Porto Rico and other West Indian islands. Scientific Survey of Porto Rico and the Virgin Islands. Vol. XVI. New York Academy of Sciences, New York

    Google Scholar 

  • Dean, T. A., Schroeter, S. C., Dixon, J. D. (1984). Effects of grazing by two species of sea urchins (Strongylocentrotus franciscanus andLytechinus anamesus) on recruitment and survival of two species of kelp (Macrocystis pyrifera andPterygophora californica). Mar. Biol. 78: 301–313

    Google Scholar 

  • Duggins, D. O. (1980). Kelp beds and sea otters: an experimental approach. Ecology 61: 447–453

    Google Scholar 

  • Estes, J. A., Palmisano, J. F. (1974). Sea otters: their role in structuring nearshore communities. Science, N.Y. 18: 1058–1060

    Google Scholar 

  • Estes, J. A., Smith, N. S., Palmisano, J. F. (1978). Sea otter predation and community organization in the western Aleutian Islands, Alaska. Ecology 59: 822–833

    Google Scholar 

  • Foster, S. A. (1987). The relative impacts of grazing by Caribbean coral reef fishes andDiadema: effects of habitat and surge. J. exp. mar. Biol. Ecol. 105: 1–20

    Google Scholar 

  • Gladfelter, W. B. (1982). White-band disease inAcropora palmata: implications for the structure and growth of shallow reefs. Bull. mar. Sci. 32: 639–643

    Google Scholar 

  • Hackney, J. M., Carpenter, R. C., Adey, W. H. (1989). Characteristic adaptations to grazing among algal turfs on a Caribbean coral reef. Phycologia 28: 109–119

    Google Scholar 

  • Hatcher, B. G. (1981). The interaction between grazing organisms and the epilithic algal community of a coral reef: a quantitative assessment. Proc. 4th int. coral Reef Symp. 2: 515–524 [Gomez, E. D., et al. (eds.) Marine Sciences Center, University of the Philippines, Quezon City]

    Google Scholar 

  • Hay, M. E. (1984). Patterns of fish and urchin grazing on Caribbean coral reefs: are previous results typical? Ecology 65: 446–454

    Google Scholar 

  • Hay, M. E., Fenical, W., Gustafson, K. (1987). Chemical defense against diverse coral-reef herbivores. Ecology 68: 1581–1591

    Google Scholar 

  • Hay, M. E., Paul, V. J., Lewis, S. M., Gustafson, K., Tucker, J., Trindell, R. (1988). Can tropical seaweeds reduce herbivory by growing at night? Diel patterns of growth, nitrogen content, herbivory, and chemical versus morphological defenses. Oecologia 75: 233–245

    Google Scholar 

  • Hughes, T. P. (1989). Community structure and diversity of coral reefs: the role of history. Ecology 70: 275–279

    Google Scholar 

  • Hughes, T. P., Keller, B. D., Jackson, J. B. C., Boyle, M. J. (1985). Mass mortality of the echinoidDiadema antillarum Philippi in Jamaica. Bull. mar. Sci. 36: 377–384

    Google Scholar 

  • Hughes, T. P., Reed, D. C., Boyle, M. J. (1987). Herbivory on coral reefs: community structure following mass mortalities of sea urchins. J. exp. mar. Biol. Ecol. 113: 39–59

    Google Scholar 

  • Hunte, W., Cote, I., Tomascik, T. (1986). On the dynamics of the mass mortality ofDiadema antillarum in Barbados. Coral Reefs 4: 135–139

    Google Scholar 

  • Hunte, W., Younglao, D. (1988). Recruitment and population recovery in the black sea urchinDiadema antillarum (Echinodermata: Echinoidea) in Barbados. Mar. Ecol. Prog. Ser. 45: 109–119

    Google Scholar 

  • Jackson, J. B. C., Kaufman, K. W. (1987).Diadema antillarum was not a keystone predator in cryptic reef environments. Science, N.Y. 35: 687–689

    Google Scholar 

  • Jackson, J. B. C., Winston, J. E. (1982). Ecology of cryptic reef communities. I. Distribution and abundance of major groups of encrusting organisms. J. exp. mar. Biol. Ecol. 57: 135–147

    Google Scholar 

  • Jeffrey, S. W., Humphrey, G. F. (1975). New spectrophotometric equations for determining chlorophyllsa, b, c1, c2 in higher plants, algae, and natural phytoplankton. Biochem. Physiol. Pfl. 167: 191–194

    Google Scholar 

  • Johnson, C. R., Mann, K. H. (1988). Diversity, patterns of adaptation, and stability of Nova Scotia kelp beds. Ecol. Monogr. 58: 129–154

    Google Scholar 

  • Kapraun, D. F., Lemus, A. J., Bula-Meyer, G. (1983). GenusPolysiphonia (Rhodophyta, Ceramiales) in the tropical Western Atlantic. I. Colombia and Venezuela. Bull. mar. Sci. 33: 881–898

    Google Scholar 

  • Klumpp, D. W., McKinnon, D., Daniel, P. (1987). Damselfish territories: zones of high productivity on coral reefs. Mar. Ecol. Prog. Ser. 40: 41–51

    Google Scholar 

  • Lawrence, J. M. (1975). On the relationships between marine plants and sea urchins. Oceanogr. mar. Biol. A. Rev. 13: 213–286

    Google Scholar 

  • Leighton, D. L. (1971). Grazing activities of benthic invertebrates in southern California kelp beds. Nova Hedwigia 32: 421–453

    Google Scholar 

  • Lessios, H. A. (1988a). Mass mortality ofDiadema antillarum in the Caribbean: what have we learned? A. Rev. Ecol. Syst. 19: 371–393

    Google Scholar 

  • Lessios, H. A. (1988b). Population dynamics ofDiadema antillarum (Echinodermata: Echinoidea) following mass mortality in Panamá. Mar. Biol. 99: 515–526

    Google Scholar 

  • Lessios, H. A., Robertson, D. R., Cubit, J. D. (1984). Spread ofDiadema mass mortality through the Caribbean. Science, N.Y. 226: 335–337

    Google Scholar 

  • Levitan, D. R. (1988). Asynchronous spawning and aggregative behavior in the sea urchinDiadema antillarum (Philippi) [sic]. In: Burke, R. D., Mladenov, P. V., Lambert, P., Parsley R. L. (eds.) Echinoderm biology. Proceedings of the 6th International Echinoderm Conference. A. A. Balkema, Rotterdam, p. 181–186

    Google Scholar 

  • Lewis, J. B. (1966). Growth and breeding in the tropical echinoidDiadema antillarum Philippi. Bull. mar. Sci. 16: 151–158

    Google Scholar 

  • Lewis, S. M., Wainwright, P. C. (1985). Herbivore abundances and grazing intensity on a Caribbean coral reef. J. exp. mar. Biol. Ecol. 87: 215–228

    Google Scholar 

  • Liddell, W. D., Ohlhorst, S. L. (1986). Changes in benthic community composition following the mass mortality ofDiadema at Jamaica. J. exp. mar. Biol. Ecol. 95: 271–278

    Google Scholar 

  • Littler, M. M., Littler, D. S. (1980). The evolution of thallus form and survival strategies in benthic marine macroalgae: field and laboratory tests of a functional form hypothesis. Am. Nat. 116: 25–44

    Google Scholar 

  • Littler, M. M., Littler, D. S. (1985). Nondestructive sampling. In: Littler, M. M., Littler, D. S. (eds.) Handbook of phycological methods: macroalgae. Cambridge University Press, Cambridge, p. 161–175

    Google Scholar 

  • Littler, M. M., Taylor, P. R., Littler, D. S. (1983). Algal resistance to herbivory on a Caribbean coral reef. Coral Reefs 2: 111–118

    Google Scholar 

  • Lubchenco, J. L., Gaines, S. D. (1981). A unified approach to marine plant-herbivore interactions. I. Populations and communities. A. Rev. Ecol. Syst. 12: 405–437

    Google Scholar 

  • Morrison, D. (1988). Comparing fish and urchin grazing in shallow and deeper coral reef algal communities. Ecology 69: 1367–1382

    Google Scholar 

  • Norris, J. N., Bucher, K. E. (1982). Marine algae and seagrasses from Carrie Bow Cay, Belize. In: Rutzler, K., Macintyre, I. G. (eds.) The Atlantic Barrier Reef Ecosystem at Carrie Bow Cay, Belize. Smithsonian Institution Press, Washington, D.C., p. 167–238

    Google Scholar 

  • Ogden, J. O. (1977). Carbonate-sediment production by parrotfish and sea urchins on Caribbean reefs. Stud. Geol. Am. Ass. Petrol. Geol., Tulsa 4: 281–288

    Google Scholar 

  • Ogden, J. O., Brown, R. A., Salesky, N. (1973). Grazing by the echinoidDiadema antillarum Philippi: formation of halos around West Indian patch reefs. Science, N.Y. 182: 715–717

    Google Scholar 

  • Paine, R. T., Vadas, R. L. (1969). The effects of grazing by sea urchinsStrongylocentrotus spp. on benthic algal populations. Limnol. Oceanogr. 14: 710–719

    Google Scholar 

  • Paul, V. J., Hay, M. E. (1986). Seaweed susceptibility to herbivory: chemical and morphological correlates. Mar. Ecol. Prog. Ser. 33: 255–264

    Google Scholar 

  • Pearse, J. S., Hines, A. H. (1979). Expansion of a Central California kelp forest following the mass mortality of sea urchins. Mar. Biol. 51: 83–91

    Google Scholar 

  • Ruyter van Steveninck, E. D. de, Bak, R. P. M. (1986). Changes in abundance of coral-reef bottom components related to mass mortality of the sea urchinDiadema antillarum. Mar. Ecol. Prog. Ser. 34: 87–94

    Google Scholar 

  • Sammarco, P. W. (1980).Diadema and its relationship to coral spat mortality: grazing, competition and biological disturbance. J. exp. mar. Biol. Ecol. 45: 245–272

    Google Scholar 

  • Sammarco, P. W. (1982). Effects of grazing byDiadema antillarum Philippi (Echinodermata: Echinoidea) on algal diversity and community structure. J. exp. mar. Biol. Ecol. 65: 83–105

    Google Scholar 

  • Sammarco, P. W., Levinton, J. S., Ogden, J. O. (1974). Grazing and control of community structure byDiadema antillarum Philippi (Echinodermata: Echinoidea): a preliminary study. J. mar. Res. 32: 47–53

    Google Scholar 

  • Scheibling, R. (1986). Increased macroalgal abundance following mass mortalities of sea urchins (Strongylocentrotus droebachiensis) along the Atlantic coast of Nova Scotia. Oecologia 68: 186–198

    Google Scholar 

  • Scott, F. J., Russ, G. R. (1987). Effects of grazing on species composition of the epilithic algal community on coral reefs of the Great Barrier Reef. Mar. Ecol. Prog. Ser. 39: 293–304

    Google Scholar 

  • Steneck, R. S. (1983). Quantifying herbivory on coral reefs: just scratching the surface and still biting off more than we can chew. In: Reaka, M. L. (ed.) The ecology of deep and shallow coral reefs. National Oceanic and Atmospheric Administration, Rockville, Maryland, p. 103–111

    Google Scholar 

  • Steneck, R. S., Watling, L. (1982). Feeding capabilities and limitation of herbivorous molluscs: a functional group approach. Mar. Biol. 68: 299–319

    Google Scholar 

  • Targett, N. M., Targett, T. E., Vrolijk, N. H., Ogden, J. C. (1986). Effect of macrophyte secondary metabolites on feeding preferences of the herbivorous parrotfishSparisoma radians. Mar. Biol. 92: 141–148

    Google Scholar 

  • Taylor, W. R. (1960). Marine algae of the eastern tropical and subtropical coasts of the Americas. University of Michigan Press, Ann Arbor

    Google Scholar 

  • Vadas, R. L., Elner, R. W., Garwood, P. E., Babb, I. G. (1986). Experimental evaluation of aggregation behavior in the sea urchinStrongylocentrotus droebachiensis. A reinterpretation. Mar. Biol. 90: 433–448

    Google Scholar 

  • Wharton, W. G., Mann, K. H. (1981). Relationship between destructive grazing by the sea urchin,Strongylocentrotus droebachiensis, and the abundance of American lobster,Homarus americanus, on the Atlantic coast of Nova Scotia. Can. J. Fish. aquat. Sciences 38: 1339–1349

    Google Scholar 

  • Williams, S. L., Carpenter, R. C. (1988). Nutrient-limited primary productivity of coral reef algal turfs: potential contribution of ammonium excreted byDiadema antillarum. Mar. Ecol. Prog. Ser. 47: 145–152

    Google Scholar 

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  1. Department of Biology, California State University, 91330, Northridge, California, USA

    R. C. Carpenter

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Communicated by M. G. Hadfield, Honolulu

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Carpenter, R.C. Mass mortality ofDiadema antillarum . Mar. Biol. 104, 67–77 (1990). https://doi.org/10.1007/BF01313159

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