Skip to main content
Log in

Causes and consequences of sea urchin abundance and diversity in Kenyan coral reef lagoons

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

Large differences in community structure of sea urchins and finfish have been observed in Kenyan reef lagoons. Differences have been attributed to removal of finfish predators through human fishing activities. This study attempted to determine (i) the major sea urchin finfish predators, (ii) the effect of predation on sea-urchin community structure, and (iii) the possible effect of sea urchin increases and finfish decreases on the lagoonal substrate. Six reefs, two protected and four unprotected, were compared for differences in finfish abundance, sea urchin abundance and diversity and substrate cover, diversity and complexity. Comparisons between protected and unprotected reefs indicated that finfish populations were ca. 4 x denser in protected than unprotected reefs. Sea urchin populations were >100 x denser and predation rates on a sea urchin, Echinometra mathaei, were 4 x lower in unprotected than in protected reefs. The balistidae (triggerfish) was the single sea-urchin finfish predator family which had a higher population density in protected than in unprotected reefs. Balistid density was positively correlated with predation rates on tethered E. mathaei (r=0.88; p<0.025) and negatively correlated with total sea-urchin density (r=−0.89; p<0.025) on the six reefs. We conclude from observations that the balistids Balistaphus undulatus and Rhinecanthus aculeatus are the dominant sea-urchin predators. The sea-urchin assemblage had its greatest diversity and species richness at intermediate predation rates and low to intermediate sea-urchin densities. At low predation rates and high sea-urchin density E. mathaei dominated the assemblage's species composition. Preferential predation on the competitive dominant maintains the assemblage's diversity, supporting the compensatory mortality hypothesis (Connell 1978) of coral reef diversity. Protected reefs had greater cover of hard coral, calcareous and coralline algae, and greater substrate diversity and topographic complexity than unprotected reefs which had greater algal turf and sponge cover. Coral cover and topographic complexity were negatively correlated with total sea urchin density. Although experimentation is lacking, these substrate changes may be due to the switch from finfish to sea-urchins as consumers which results from overfishing of finfish. Removal of top invertebrate-eating carnivores appears to have cascading effects on the entire coral reef ecosystem.

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.

Similar content being viewed by others

References

  • Birkeland C (1982) Terrestrial runoff as a cause of outbreaks of Acanthaster planci (Echinodermata: Asteroidea). Mar Biol 69: 175–185

    Google Scholar 

  • Birkeland C (1988) The influence of echinoderms on coral-reef communities. Echinoderm studies. AA Balkema, Rotterdam

    Google Scholar 

  • Campbell AC, Dart JKG, Head SM, Ormond RFG (1973) The feeding activity of Echinostrephus molaris (de Blainville) in the central Red Sea. Mar Behav Physiol 2: 155–169

    Google Scholar 

  • Carpenter RC (1981) Grazing by Diadema antillarum (Philippi) and its effects on the benthic algal community. J Mar Res 39: 749–765

    Google Scholar 

  • Carpenter RC (1985) Sea urchin mass-mortality: effects on reef algal abundance, species composition, and metabolism and other coral reef herbivores. Proc 5th Int Coral Reef Symp 4: 53–59

    Google Scholar 

  • Clark AM, Rowe FWE (1971) Monograph of the shallow-water Indo-West Pacific echinoderms British Museum of Natural History Publication 690. Pitman Press, Bath, England

    Google Scholar 

  • Connell JH (1978) Diversity in tropical rain forests and coral reefs. Science 199: 1302–1310

    Google Scholar 

  • Crame AJ (1986) Late Pleistocene molluscan assemblages from the coral reefs of the Kenyan coast. Coral Reefs 4: 183–196

    Google Scholar 

  • Doherty PJ (1983) Tropical territorial damselfishes: is density limited by aggression or recruitment? Ecology 64: 176–190

    Google Scholar 

  • Downing N, El-Zahr CR (1987) Gut evacuation and filling rates in the rock-boring sea urchin, Echinometra mathaei. Bull Mar Sci 41: 579–584

    Google Scholar 

  • Ebert TA (1982) Longevity, life history, and relative body wall size in sea urchins. Ecol Monogr 52: 353–394

    Google Scholar 

  • Glynn PW, Wellington GM, Birkeland C (1979) Coral reef growth in the Galapagos: limitations by sea urchins. Science 203: 47–49

    Google Scholar 

  • 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: 23–28

    Google Scholar 

  • Hamilton HGH, Brakel WH (1984) Structure and coral fauna of East African reefs. Bull Mar Sci 34: 248–266

    Google Scholar 

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

    Google Scholar 

  • Hay ME (1984b) Predictable spatial escapes from herbivory: how do these affect the evolution of herbivore resistance in tropical marine communities? Oecologia 58: 299–308

    Google Scholar 

  • Hay ME, Taylor PR (1985) Competition between herbivorous fishes and urchins on Caribbean reefs. Oecologia (Berl) 65: 591–598

    Google Scholar 

  • Hay ME, Colburn T, Downing D (1983) Spatial and temporal patterns in herbivory on Caribbean reefs. Oecologia 58: 299–308

    Google Scholar 

  • Hutchings PA (1986) Biological destruction of coral reefs: a review. Coral Reefs 4: 239–252

    Google Scholar 

  • Khamala CPM (1971) Ecology of Echinometra mathaei (Echinoidea: Echinodermata) at Diani Beach, Kenya. Mar Biol 2: 167–172

    Google Scholar 

  • Kohn AJ, Leviten PJ (1976) Effect of habitat complexity on population density and species richness in tropical intertidal predatory gastropod assemblages. Oecologia 25: 119–210

    Google Scholar 

  • Lessios HA, Robertson DR, Cubit JD (1984) Spread of Diadema mass mortalities through the Caribbean. Science 226: 335–337

    Google Scholar 

  • Lewis SA (1986) The role of herbivorous fishes in the community organization of a Caribbean reef community. Ecol Monogr 51: 183–200

    Google Scholar 

  • Lubchenco J (1978) Plant species diversity in a marine intertidal community: importance of herbivore food preference and algal competitive abilities. Am Nat 112: 23–39

    Google Scholar 

  • McClanahan TR (1988a) Coexistence in a sea urchin guild and its implications to coral reef diversity and degradation. Oecologia 77: 210–218

    Google Scholar 

  • McClanahan TR (1988b) Seasonality in East Africa's coastal waters. Mar Ecol Prog Ser 44: 191–199

    Google Scholar 

  • McClanahan TR (1989) Kenyan coral reef-associated gastropod fauna: a comparison between protected and unprotected reefs. Mar Ecol Prog Ser 53: 11–20

    Google Scholar 

  • McClanahan TR, Muthiga NA (1988) Changes in Kenyan coral reef community structure and function due to exploitation. Hydrobiologia 166: 269–276

    Google Scholar 

  • McClanahan TR, Muthiga NA (1989) Patterns of predation on a sea urchin, Echinometra mathaei (de Blainville), on Kenyan coral reefs. J Exp Mar Biol Ecol 126: 77–94

    Google Scholar 

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

    Google Scholar 

  • Neudecker S (1979) Effects of grazing and browsing fishes on the zonation of corals in Guam. Ecology 60: 666–672

    Google Scholar 

  • Ogden JC (1977) Carbonate-sediment production by parrot fish and sea urchins on Caribbean reefs. In: Forst S, Weiss M (eds) Caribbean reef systems: Holocene and ancient. Am Ass Petrol Geol Special paper 4, pp 281–288

  • Paine RT (1966) Food web complexity and species diversity. Am Nat 100: 65–75

    Google Scholar 

  • Robertson DR, Gaines SD (1986) Interference competition structures habitat use in a local assemblage of coral reef surgeon-fishes. Ecology 67: 1372–1383

    Google Scholar 

  • Routledge RD (1979) Diversity indices: which ones are admissible? J Theor Biol 76: 502–515

    Google Scholar 

  • Sammarco PW (1980) Diadema and its relationship to coral spat mortality: grazing, competition, and biological disturbance. J Exp Mar Biol Ecol 45: 245–272

    Google Scholar 

  • Scoffin TP, Stern CW, Boucher D, Fryal P, Hawkins CM, Hunter IG, MacGeachy JK (1980) Calcium carbonate budget of a fringing reef on the west coast of Barbados II. Erosion, sediments and internal structure. Bull Mar Sci 30: 475–508

    Google Scholar 

  • Shulman MJ (1985) Variability in recruitment of coral reef fishes. J Exp Mar Biol Ecol 89: 205–219

    Google Scholar 

  • Simpson EH (1949) Measurements of diversity. Nature 163: 688

    Google Scholar 

  • Smith JLB (1965) The sea fishes of southern Africa. Central News Agency, South Africa

    Google Scholar 

  • Wellington GM (1982) Depth zonation of corals in the Gulf of Panama: control of facilitation by resident reef fishes. Ecol Monogr 52: 223–241

    Google Scholar 

  • Wilkinson CR, Sammarco PW (1983) Effects of fish grazing and damselfish territoriality. II. Nitrogen fixation. Mar Ecol Prog Ser 13: 15–19

    Google Scholar 

  • Wilkinson CR, Williams D McB, Sammarco PW, Hogg RW, Trott LA (1984) Rates of nitrogen fixation on coral reefs across the continental shelf of the central Great Barrier Reef. Mar Biol 80: 255–262

    Google Scholar 

  • Williams AH (1981) An analysis of competitive interaction in a patchy back-reef environment. Ecology 62: 1107–1120

    Google Scholar 

  • Williams SL, Carpenter RC (1988) Nitrogen-limited primary productivity of coral reef algal turfs: potential contribution of ammonium excreted by Diadema antillarum. Mar Ecol Prog Ser 47: 145–152

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

McClanahan, T.R., Shafir, S.H. Causes and consequences of sea urchin abundance and diversity in Kenyan coral reef lagoons. Oecologia 83, 362–370 (1990). https://doi.org/10.1007/BF00317561

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00317561

Key words

Navigation