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Habitat correlates of the distribution and biomass of Seychelles' reef fishes

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Relationships between quantitative measures of habitat type and the biomass of Chaetodon, Scarus and Parupeneus species were investigated across 35 reef sites in the Inner Seychelles Group. Multiple regression was used to determine the proportion of variance in biomass between sites which could be explained by depth, exposure, vertical relief, topographic complexity, live coral cover, coral rubble cover, rock cover, sand cover, underlying carbonate substrate, underlying sand substrate, underlying rock substrate and an index of fishing intensity. A significant proportion of the variance in biomass was explained by habitat variables and the index of fishing intensity for 7 of 12 Chaetodon species (23–52% of variance explained), 3 of 6 Parupeneus species (33–40%), and 10 of 13 Scarus species (14–46%). Within genera, different groups of habitat variables explained the variance in biomass for different species and, of the variables studied, only the proportion of underlying sand substrate failed to explain a significant proportion of the variance in biomass for any species. Quantitative relationships between the biomass of Chaetodon and habitat were often in accordance with those suggested by previous studies of their ecology, life-history and distribution at other Indo-Pacific locations. However, the habitat associations of the Parupeneus and some Scarus species have not been studied at other locations and clearly warrant further investigation. It was concluded that habitat was an important determinant of the distribution of many Seychelles reef fishes, but that the habitat variables examined were rarely the most important determinant of biomass. However, the inclusion of a procedure to collect habitat data provided a useful means by which to reduce the unexplained variance associated with visual census biomass estimates and therefore improves the possibility of elucidating the effects of other factors on the biomass of Seychelles reef fishes.

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References cited

  • Bell, J.D. & R. Galzin. 1984. Influence of live coral cover on coral-reef fish communities. Mar. Ecol. Prog. Ser. 15: 265–274.

    Google Scholar 

  • Bell, J.D., M. Harmelin-Vivien & R. Galzin. 1985a. Large scale variation in abundance of butterflyfishes (Chaetodontidae) on Polynesian reefs. Proc. Int. Coral Reef Symp. 5 (5): 421–426.

    Google Scholar 

  • Bell, J.D., G.J.S. Craik, D.A. Pollard & B.C. Russell. 1985b. Estimating length frequency distributions of large reef fish underwater. Coral Reefs 4: 41–44.

    Google Scholar 

  • Bellwood, D.R. 1995. Carbonate transport and within-reef patterns of bioerosion and sediment release by parrotfishes (family Scaridae) on the Great Barrier Reef. Mar. Ecol. Prog. Ser. 117: 127–136.

    Google Scholar 

  • Blaber, S.J.M., J.W. Young & M.C. Dunning. 1985. Community structure and zoogeographic affinities of the coastal fishes of the Dampier region of North-western Australia. Aust. J. Mar. Fresh. Res. 36: 247–266.

    Google Scholar 

  • Bouchon-Navaro, Y. & C. Bouchon. 1989. Correlations between chaetodontid fishes and coral communities of the Gulf of Aqaba (Red Sea). Env. Biol. Fish. 25: 47–60.

    Google Scholar 

  • Bouchon-Navaro, Y., C. Bouchon & M. Harmelin-Vivien. 1985. Impact of coral degradation on a chaetodontid fish assemblage (Moorea, French Polynesia). Proc. Int. Coral Reef Symp. 5 (5): 427–432.

    Google Scholar 

  • Carpenter, K.E., R.I. Miclat, V.D. Albaladego & V.T. Corpuz. 1981. The influence of substrate structure on the local abundance and diversity of Philippine reef fishes. Proc. Int. Coral Reef Symp. 4 (2): 497–502.

    Google Scholar 

  • Choat, J.H. & J.E. Randall. 1986. A review of the parrotfishes (family Scaridae) of the Great Barrier Reef of Australia with description of a new species. Rec. Aust. Mus. 38: 175–228.

    Google Scholar 

  • Cox, E.F. 1994. Resource use by corallivorous butterflyfishes (family Chaetodontidae) in Hawaii. Bull. Mar. Sci. 54: 535–545.

    Google Scholar 

  • De Boer, B.A. 1978. Factors influencing the distribution of the damselfish Chromis cyanea (Poey), Pomacentridae, on a reef at Curacao, Netherlands Antilles. Bull. Mar. Sci. 28: 550–565.

    Google Scholar 

  • Driscoll, J.W. & J.L. Driscoll. 1988. Pair behaviour and pair spacing in butterflyfishes (Chaetodontidae). Env. Biol. Fish. 22: 29–37.

    Google Scholar 

  • Findley, J.S. & M.T. Findley. 1985. A search for pattern in butterflyfish communities. Amer. Nat. 126: 800–816.

    Google Scholar 

  • Fowler, A.J. 1990. Spatial and temporal patterns of distribution and abundance of chaetodontid fishes at One Tree Reef, southern GBR. Mar. Ecol. Prog. Ser. 64: 39–53.

    Google Scholar 

  • Galzin, R. 1987. Structure of fish communities of French Polynesian coral reefs. I. Spatial scales. Mar. Ecol. Prog. Ser. 41: 129–136.

    Google Scholar 

  • Grigg, R.W. 1994. Effects of sewage discharge, fishing pressure and habitat complexity on coral ecosystems and reef fishes in Hawaii. Mar. Ecol. Prog. Ser. 103: 25–34.

    Google Scholar 

  • Hobson, E.S. & J.R. Chess. 1978. Trophic relationships among fishes and plankton in the lagoon at Enewetak Atoll, Marshall Islands. U.S. Fish. Bull. 76: 133–153.

    Google Scholar 

  • Holland, K.N., J.D. Peterson, C.G. Lowe & B.M. Wetherbee. 1993. Movements, distribution and growth rates of the white goatfish Mulloides flavolineatus in a fisheries conservation zone. Bull. Mar. Sci. 52: 982–992.

    Google Scholar 

  • Hourigan, T.F., T.C. Tricas & E.S. Reese. 1988. Coral reef fishes as indicators of environmental stress in coral reefs. pp. 107–136. In: D.F. Soule & G.S. Keppel (ed.) Marine Organisms as Indicators, Springer-Verlag, New York.

    Google Scholar 

  • Jennings, S. & J.M. Lock. 1996. Population and ecosystem effects of fishing. In: N.V.C. Polunin & C.M. Roberts (ed.) Tropical Reef Fisheries, Chapman and Hall, London (in press).

    Google Scholar 

  • Jennings, S. & N.V.C. Polunin. 1995. Biased underwater visual census biomass estimates for target-species in tropical reef fisheries. J. Fish Biol. (in press).

  • Jennings, S. & N.V.C. Polunin. 1996. The impacts of fishing on tropical reef ecosystems. Ambio (in press).

  • Jennings, S., A.S. Brierley & J.W. Walker. 1994. The inshore fish assemblages of the Galapagos archipelago. Biol. Cons. 70: 49–57.

    Google Scholar 

  • Jennings, S., E.M. Grandcourt & N.V.C. Polunin. 1995. Effects of fishing on the diversity, biomass and trophic structure of Seychelles' reef fish communities. Coral Reefs (in press).

  • Kaufman, L.S. & J.P. Ebersole. 1984. Microtopography and the organisation of two assemblages of coral reef fishes in the West Indies. J. Exp. Mar. Biol. Ecol. 78: 253–268.

    Google Scholar 

  • Kulbicki, M. 1988. Patterns in the trophic structure of fish populations across the SW lagoon of New Caledonia. Proc. Int. Coral Reef Symp. 6 (2): 89–94.

    Google Scholar 

  • Kulbicki, M., G. Mou Tham, P. Thollot & L. Wantiez. 1993. Length-weight relationships of fish from the lagoon of New Caledonia. Naga 2 + 3: 26–30.

    Google Scholar 

  • Luckhurst, B.E. & K. Luckhurst. 1978. Analysis of the influence of substrate variables on coral reef fish communities. Mar. Biol. 49: 317–323.

    Google Scholar 

  • Ogden, J.C. & N.S. Buckman. 1973. Movements, foraging groups and diurnal migrations of the striped parrotfish Scarus croicensis Bloch (Scaridae). Ecology 54: 587–596.

    Google Scholar 

  • Patton, M.L., R.S. Grove & R.F. Harman. 1985. What do natural reefs tell us about designing artificial reefs in southern California. Bull. Mar. Sci. 37: 279–298.

    Google Scholar 

  • Polunin, N.V.C. 1984. Marine fishes of the Seychelles. pp. 171–191. In: D.R. Stoddart (ed.) Biogeography and Ecology of the Seychelles Islands, Dr W. Junk, Publishers, The Hague.

    Google Scholar 

  • Polunin, N.V.C. & C.M. Roberts 1993. Greater biomass and value of target coral-reef fishes in two small Caribbean marine reserves. Mar. Ecol. Prog. Ser. 100: 67–76.

    Google Scholar 

  • Randall, J.E. & J. van Egmond. 1994. Marine fishes from the Seychelles: 108 new records. Zool. Verh., Leiden 297: 43–83.

    Google Scholar 

  • Randall, J.E., G.R. Allen & R.C. Steene. 1990. Fishes of the Great Barrier Reef and Coral Sea. Crawford House Press, Bathurst. 507 pp.

    Google Scholar 

  • Risk, M.J. 1972. Fish diversity on a coral reef in the Virgin Islands. Atoll Res. Bull. 153: 1–6.

    Google Scholar 

  • Roberts, C.M. & R.F.G. Ormond. 1987. Habitat complexity and coral reef fish diversity and abundance on Red Sea fringing reefs. Mar. Ecol. Prog. Ser. 41: 1–8.

    Google Scholar 

  • Russ, G.R. 1984a. Distribution and abundance of herbivorous grazing fishes in the central Great Barrier Reef: 1. Level of variability across the entire continental shelf. Mar. Ecol. Prog. Ser. 20: 23–34.

    Google Scholar 

  • Russ, G.R. 1984b. 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: 35–44.

    Google Scholar 

  • Russ, G.R. 1991. Coral reef fisheries: effects and yields. pp. 601–635. In: P.F. Sale (ed.) The Ecology of Fishes on Coral Reefs, Academic Press, San Diego.

    Google Scholar 

  • Sale, P.F. 1991. Reef fish communities: open nonequilibrial systems, pp. 564–598. In: P.F. Sale The Ecology of Fishes on Coral Reefs, Academic Press, San Diego.

    Google Scholar 

  • Samoilys, M. & G.M. Carlos. 1992. Development of an underwater visual census method for assessing shallow water reef fish stocks in the south-west Pacific. Queensland Department of Primary Industries, Cairns. 100 pp.

    Google Scholar 

  • Sano, M., M. Shimizu & Y. Nose. 1987. Long-term effects of destruction of hermatypic corals by Acanthaster planci infestation on reef fish communities at Iriomote Island, Japan. Mar. Ecol. Prog. Ser. 37: 191–199.

    Google Scholar 

  • Sutton, M. 1985. Patterns of spacing in a coral reef fish in two habitats on the Great Barrier Reef. Anim. Behav. 33: 1332–1337.

    Google Scholar 

  • Talbot, F.H. 1965. A description of the coral structure of Tutia Reef (Tanganyika Territory, East Africa) and its fish fauna. J. Zool. 145: 431–470.

    Google Scholar 

  • Thresher, R.E. 1983. Environmental correlates of the distribution of planktivorous fishes in the One Tree Reef lagoon. Mar. Ecol. Prog. Ser. 10: 137–145.

    Google Scholar 

  • Tricas, T.C. 1989. Determinants of feeding territory size in the corallivorous butterflyfish, Chaetodon multicinctus. Anim. Behav. 37: 830–840.

    Google Scholar 

  • Watson, R.A., G.M. Carlos & M.A. Samoilys. 1995. Bias introduced by the non-random movement of fish in visual transect surveys. Ecol. Model. 77: 205–214.

    Google Scholar 

  • Williams, D.McB. 1982. Patterns in the distribution of fish communities across the central Great Barrier Reef. Coral Reefs 1: 35–43.

    Google Scholar 

  • Williams, D.McB. 1991. Patterns and processes in the distribution of coral reef fishes. pp. 437–474. In: P.F. Sale. (ed.) The Ecology of Fishes on Coral Reefs, Academic Press, San Diego.

    Google Scholar 

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Jennings, S., Boullé, D.P. & Polunin, N.V.C. Habitat correlates of the distribution and biomass of Seychelles' reef fishes. Environ Biol Fish 46, 15–25 (1996). https://doi.org/10.1007/BF00001693

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