Oecologia

, Volume 80, Issue 3, pp 331–340

Complex interactions in the control of coral zonation on a Caribbean reef flat

  • M. M. Littler
  • P. R. Taylor
  • D. S. Littler
Original Papers
  • 317 Downloads

Summary

This study uses short-term assays and long-term transplant experiments to document the potential importance of fish predation and herbivory to the distribution and abundance of reef-building corals in a Caribbean back-reef system. Experimental manipulations of fish access reveal that the zonal patterns of the two reef-building corals Porites astreoides and P. porites f. furcata, dominant on shallow back-reef habitats, are strongly associated with the feeding intensity of parrotfishes. Differential palatability of the two corals to parrotfishes, the proximity of protective cover for large grazers and the availability of small refugia to harbor a cryptic grazer fauna are suggested as major features contributing to the observed patterns. A model predicting the interactions of various algivore/corallivore guilds on the relative dominance of Porites and algal populations is presented.

Key words

Algivore/corallivore guilds Caribbean Fish-coral interactions Porites Reef zonation 

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References

  1. Antonius A (1982) Coral reef pathology: a review. Proc 4th Int Coral Reef Symp 2:3–6Google Scholar
  2. Bakus GJ (1967) The feeding habits of fishes and primary production at Eniwetok, Marshall Islands. Micronesica 3:135–149Google Scholar
  3. Banner AH (1974) Kaneohe Bay, Hawaii: urban pollution and a coral reef ecosystem. Proc 2nd Int Coral Reef Symp 2:685–702Google Scholar
  4. 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 1:15–21Google Scholar
  5. Burke RB (1982) Reconnaissance study of the geomorphology and benthic communities of the outer barrier reef platform, Belize. In: Rützler K, Macintyre IG (eds) The Atlantic barrier reef ecosystem at Carrie Bow Cay, Belize, I. Structure and communities. Smithsonian Institution Press, Washington, DC, Smith-sonian Contrib Mar Sci 12:509–526Google Scholar
  6. Cairns SD (1982) Stony corals (Cnidaria: Hydrozoa, Scleractinia) of Carrie Bow Cay, Belize. In: Rützler K, Macintyre IG (eds) The Atlantic barrier reef ecosystem at Carrie Bow Cay, Belize. I. Structure and communities. Smithsonian Institution press, Washington, DC, Smithsonian Contrib Mar Sci 12:271–302Google Scholar
  7. Coen LD (1988) Herbivory by crabs and the control of algal epibionts on Caribbean host corals. Oecologia 75:198–203Google Scholar
  8. Frydl P (1977) The geological effect of grazing by parrotfish (Scaridae) on a Barbados coral reef. M.Sc. thesis. McGill University, Montreal, CanadaGoogle Scholar
  9. Geister J (1977) The influence of wave exposure on the ecological zonation of Caribbean coral reefs. Proc 3rd Inter Coral Reef Symp 1:23–29Google Scholar
  10. Glynn PW (1973) Aspects of the ecology of coral reefs in the western Atlantic region. In: Jones OA, Endean R (eds) Biology and geology of coral reefs. Academic Press, New York, pp 271–324Google Scholar
  11. Glynn PW (1976) Some physical and biological determinants of coral community structure in the eastern Pacific. Ecol Monogr 46:431–456Google Scholar
  12. Glynn PW, Stewart RH, McCosker JE (1972) Pacific coral reefs of Panama: structure, distribution and predators. Geol Rundsch 61:483–519Google Scholar
  13. Gygi RA (1975) Sparisoma viride (Bonnaterre), the stoplight parrotfish, a major sediment producer on coral reefs of Bernuda. Ecolgae Geol Helv 68:327–359Google Scholar
  14. Hatcher BG (1982) The interaction between grazing organisms and the epilithic algal community of a coral reef: a quantitative assessment. Proc 4th Int Coral Reef Symp 2:515–524Google Scholar
  15. Hay ME (1981) Spatial patterns of grazing intensity on a Caribbean barrier reef: herbivory and algal distribution. Aquat Bot 11:97–109Google Scholar
  16. Hay ME (1984) Patterns of fish and urchin grazing on Caribbean coral reefs: are previous results typical? Ecology 65:446–454Google Scholar
  17. Hay ME, Colburn T, Downing D (1983) Spatial and temporal patterns in herbivory on a Caribbean fringing reef: the effects on plant distribution. Oecologia 58:299–308Google Scholar
  18. Hiatt RW, Strasburg DW (1960) Ecological relationships of the fish fauna on coral reefs of the Marshall Islands. Ecol Monogr 30:65–127Google Scholar
  19. James NP, Ginsburg RN, Marszalek DS, Choquette PW (1976) Facies and fabric specificity of early subsea cements in shallow Belize (British Honduras) reefs. J Sediment Petrol 46:523–544Google Scholar
  20. Kaufman L (1977) The three spot damselfish: effects on benthic biota of Caribbean coral reefs. Proc 3rd Int Coral Reef Symp 1:559–564Google Scholar
  21. Lessios HA, Glynn PW, Robertson DR (1983) Mass mortalities of coral reef organisms. Science 222:715Google Scholar
  22. Lewis SM (1986) The role of herbivorous fishes in the organization of a Caribbean reef community. Ecol Monogr 56:183–200Google Scholar
  23. Lewis SM, Wainwright PC (1985) Herbivore abundance and grazing intensity on a Caribbean coral reef. J Exp Mar Biol Ecol 87:215–228Google Scholar
  24. Lewis SM, Norris JN, Searles RB (1987) The regulation of morphological plasticity in tropical reef algae by herbivory. Ecology 68:636–641Google Scholar
  25. Littler MM, Littler DS (1984) A relative-dominance model for biotic reefs. In: Advances in reef sciences. Proceedings of the Joint Meeting of the Atlantic Reef Committee and the International Society of Reef Studies, Miami, FloridaGoogle Scholar
  26. Littler MM, Littler DS (1985) Non-destructive sampling. In: Littler MM, Littler DS (eds) Handbook of phycological methods. Ecological field methods: macroalgae. Cambridge University Press, Cambridge, pp 161–175Google Scholar
  27. Littler MM, Littler DS (1988) Structure and role of algae in tropical reef communities. In: Lembi CA, Waaland JR (eds) Algae and human affairs. Cambridge University Press, Cambridge, pp 29–55Google Scholar
  28. Littler MM, Littler DS, Taylor PR (1983a) Evolutionary strategies in a tropical barrier reef system: functional-form groups of marine macroalgae. J Phycol 19:229–237Google Scholar
  29. Littler MM, Taylor PR, Littler DS (1983b) Algal resistance to herbivory on a Caribbean barrier reef. Coral Reefs 2:111–118Google Scholar
  30. Littler MM, Taylor PR, Littler DS (1986) Plant defense associations in the marine environment. Coral Reefs 5:63–71Google Scholar
  31. Littler MM, Littler DS, Taylor PR (1987) Animal-plant defense associations: effects on the distribution and abundance of tropical reef macrophytes. J Exp Mar Biol Ecol 105:107–121Google Scholar
  32. Macintyre IG (1984) Preburial and shallow-subsurface alteration of modern scleractinian corals. Ealaconpographica Americanica 54:229–244Google Scholar
  33. Macintyre IG, Graus RR, Reinthal PN, Littler MM, Littler DS (1987) The barrier reef sediment apron: Tobacco Reef, Belize. Coral Reefs 6:1–12Google Scholar
  34. Miller AC (1982) Effects of differential fish grazing on the community structure of an intertidal reef flat at Enewetak Atoll, Marshall Islands. Pac Sci 36:467–482Google Scholar
  35. Motoda S (1940) The environment and the life of massive reef coral, Goniastrea aspera Verrill, inhabiting the reef flat in Palao. Palao Tropical Biol Sta Studies 2:61–104Google Scholar
  36. Neudecker S (1979) Effects of grazing and browsing fishes on the zonation of corals in Guam. Ecology 60:666–672Google Scholar
  37. Potts DC (1977) Suppression of coral populations by filamentous algae within damselfish territories. J Exp Mar Biol Ecol 28:207–216Google Scholar
  38. Randall JE (1965) Grazing effect on sea grasses by herbivorous reef fishes in the West Indies. Ecology 46:255–260Google Scholar
  39. Randall JE (1967) Food habits of reef fishes of the West Indies. Stud Trop Oceanogr 5:665–847Google Scholar
  40. Russ G (1984) Distribution and abundance of herbivorous grazing fishes in the central Great Barrier Reef. II. Patterns of zonation of mid-shelf and outershelf reefs. Mar Ecol Prog Ser 20:35–44Google Scholar
  41. Rützler K, Macintyre IG (1982) The habitat distribution and community structure of the barrier reef complex at Carrie Bow Cay, Belize. In: Rützler K, Macintyre IG (eds) The Atlantic barrier reef ecosystem at Carrie Bow Cay, Belize. I. Structure and communities. Smithsonian Institution Press, Washington, DC, Smithsonian Contrib Mar Sci 12:9–45Google Scholar
  42. Sammarco PW (1980) Diadema and its relationship to coral spat mortality: grazing, competition, and biological disturbance. J Exp Mar Biol Ecol 45:245–272Google Scholar
  43. Sammarco PW (1982) Effects of grazing by Diadema antillarum Philippi (Echinodermata: Echinoidea) on algal diversity and community structure. J Exp Mar Biol Ecol 65:83–105Google Scholar
  44. SAS (1985) SAS user's guide: basics. SAS Institute Inc., Cary, North CarolinaGoogle Scholar
  45. Sokal RR, Rohlf FJ (1969) Biometry. Freeman, San FranciscoGoogle Scholar
  46. Taylor PR, Littler MM, Littler DS (1986) Escapes from herbivory in relation to the structure of mangrove island macroalgal communities. Oecologia 69:481–490Google Scholar
  47. Vine PJ (1974) Effects of algal grazing and aggressive behaviour of the fishes Pomacentrus lividus and Acanthurus sohal on coral-reef ecology. Mar Biol 24:131–136Google Scholar
  48. Wellington GM (1982) Depth zonation of corals in the Gulf of Panama: control and facilitation by resident reef fishes. Ecol Monogr 52:223–241Google Scholar

Copyright information

© Springer-Verlag 1989

Authors and Affiliations

  • M. M. Littler
    • 1
  • P. R. Taylor
    • 2
  • D. S. Littler
    • 1
  1. 1.Department of Botany, National Museum of Natural HistorySmithsonian InstitutionWashingtonUSA
  2. 2.Biological Oceanography Program, Division of Ocean SciencesNational Science FoundationWashingtonUSA

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