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Faunal composition within algal mats and adjacent habitats on Likuri Island, Fiji Islands

Published online by Cambridge University Press:  17 November 2008

Andrea C. Alfaro*
Affiliation:
School of Applied Sciences, Auckland University of Technology, Private Bag 92006, Auckland 1020, New Zealand
W. Lindsey Zemke-White
Affiliation:
School of Applied Sciences, Auckland University of Technology, Private Bag 92006, Auckland 1020, New Zealand
Winifereti Nainoca
Affiliation:
School of General Studies, Fiji Institute of Technology, Samabula Campus, Suva, Fiji Islands
*
Correspondence should be addressed to: A.C. Alfaro, School of Applied Sciences, Auckland University of Technology, Private Bag 92006, Auckland 1020, New Zealand email: [email protected]

Abstract

The faunal composition within three mono-specific algal habitats was investigated at Likuri Island, southern Viti Levu, Fiji Islands. Gracilaria maramae was the dominant alga within algal drift mat, seagrass bed, and rocky substrate habitats at the study site. This algal species exhibits two distinctive morphologies depending on whether it is attached or loose-lying. When attached to seagrass blades or rocky substrates, this alga has long straight branches stemming from a single holdfast, while detached individuals develop curled tendrils that re-attach to adjacent substrates. Re-attachment behaviour and high growth rates result in a dense mat of drift algae, which provides a suitable micro-habitat for macro-invertebrates. The sources of algal fragments that contribute to the algal mat appear to be nearby seagrass beds and rocky substrates, where this species may settle directly from spores. Storm events may detach these algae, although pulling experiments showed that the attachment to rocky substrates is 5 times stronger than the attachment to seagrass blades. Results from the macro-faunal samples indicate that the loose-lying algal mat habitat had the highest abundance and biodiversity of organisms, followed by the seagrass bed, and then the rocky substrate habitat. The ability of loose G. maramae fragments to re-attach, along with their high growth rate, may provide a unique micro-habitat for highly abundant and diverse faunal assemblages, which in turn may sustain adjacent near-shore communities. This study highlights the ecological importance of floating algal mats to coastal ecosystems, which should be considered in future management strategies throughout the Fiji Islands.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2008

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References

REFERENCES

Alfaro, A.C. (2006) Benthic macro-invertebrate community composition within a mangrove/seagrass estuary in northern New Zealand. Estuarine, Coastal and Shelf Science 66, 97110.CrossRefGoogle Scholar
Alfaro, A.C., Jeffs, A.G. and Creese, R. (2004) Bottom-drifting algal/mussel spat associations along a sandy coastal region in northern New Zealand. Aquaculture 241, 269290.CrossRefGoogle Scholar
Bellwood, D.R., Hughes, T.P., Folke, C. and Nystrom, M. (2004) Confronting the coral reef crisis. Nature 429, 827833.CrossRefGoogle ScholarPubMed
Brown, A.C. and McLachlan, A. (1990) Ecology of sandy shores. Amsterdam: Elsevier.Google Scholar
Colombini, I., Aloia, A., Fallaci, M., Pezzoli, G. and Chelazzi, L. (2000) Temporal and spatial use of stranded wrack by the macrofauna of a tropical sandy beach. Marine Biology 136, 531541.CrossRefGoogle Scholar
Connolly, R.M. (1997) Differences in composition of small, motile invertebrate assemblages from seagrass and unvegetated habitats in a southern Australian estuary. Hydrobiologia 346, 137148.CrossRefGoogle Scholar
Davenport, J. and Rees, E.I.S. (1993) Observations on neuston and floating weed patches in the Irish Sea. Estuarine, Coastal and Shelf Science 36, 395411.CrossRefGoogle Scholar
Duarte, C.M. (1999) Seagrass ecology at the turn of the millennium: challenges for the new century. Aquatic Botany 65, 720.CrossRefGoogle Scholar
Edgar, G.J. (1990) The influence of plant structure on the species richness, biomass and secondary production of macrofaunal assemblages associated with Western Australian seagrass beds. Journal of Experimental Marine Biology and Ecology 137, 215240.CrossRefGoogle Scholar
Fabricius, K.E. (2005) Effects of terrestrial runoff on the ecology of corals and coral reefs: review and synthesis. Marine Pollution Bulletin 50, 125146.CrossRefGoogle ScholarPubMed
Friedland, M.T. and Denny, M.W. (1995) Surviving hydrodynamic forces in a wave-swept environment: consequences of morphology in the feather boa kelp, Egregia menziesii (Turner). Journal of Experimental Marine Biology and Ecology 190, 1109–133.CrossRefGoogle Scholar
Griffiths, C.L. and Stenton-Dozey, J.M.E. (1981) The fauna and rate of degradation of stranded kelp. Estuarine, Coastal and Shelf Science 12, 645653.CrossRefGoogle Scholar
Griffiths, C.L., Stenton-Dozey, J.M.E. and Koop, K. (1983) Kelp wrack and the flow of energy through a sandy beach ecosystem. In McLachlan, A. and Erasmus, T. (eds) Sandy beaches as ecosystems. The Hague: W. Junk Publishers, pp. 547556.CrossRefGoogle Scholar
Hily, C., Potin, P. and Floc'h, J. (1992) Structure of subtidal algal assemblages on soft-bottom sediments: fauna/flora interactions and role of disturbances in the Bay of Brest, France. Marine Ecology Progress Series 85, 115130.CrossRefGoogle Scholar
Highsmith, R.C. (1985) Floating and algal rafting as potential dispersal mechanisms in brooding invertebrates. Marine Ecology Progress Series 25, 169179.CrossRefGoogle Scholar
Holmquist, J.G. (1994) Benthic macroalgae as a dispersal for fauna: influence of marine tumbleweed. Journal of Experimental Marine Biology and Ecology 180, 235251.CrossRefGoogle Scholar
Inglis, G. (1989) The colonisation and degradation of stranded Macrocystis pyrifera (L.) C. Ag. by the macrofauna of a New Zealand sandy beach. Journal of Experimental Marine Biology and Ecology 125, 302–217.CrossRefGoogle Scholar
Ingólfsson, A. (1995) Floating clumps of seaweed around Iceland: natural microcosms and a means of dispersal for shore fauna. Marine Biology 122, 1321.CrossRefGoogle Scholar
Jackson, J.B.C. (1997) Reefs since Columbus. Coral Reefs 16S, S23S32.CrossRefGoogle Scholar
Jones, W.E. (1962) The identity of Gracilaria erecta (Grev.). European Journal of Phycology 2, 140144.Google Scholar
Kingsford, M.J. (1992) Drift algae and small fish in coastal waters of northeastern New Zealand. Marine Ecology Progress Series 80, 4155.CrossRefGoogle Scholar
Kingsford, M.J. (1995) Drift algae: a contribution to near-shore habitat complexity in the pelagic environment and an attractant to fish. Marine Ecology Progress Series 116, 297301.CrossRefGoogle Scholar
Kingsford, M.J. and Choat, J.H. (1985) The fauna associated with drift algae captured with a plankton-mesh purse seine net. Limnology and Oceanography 30, 618630.CrossRefGoogle Scholar
Koop, K. and Field, J.G. (1980) The influence of food availability on population dynamics of a supralittoral isopod, Ligia dilatata Brandt. Journal of Experimental Marine Biology and Ecology 48, 6172.CrossRefGoogle Scholar
Koop, K., Newell, R.C. and Lucas, M.I. (1982) Biodegradation and carbon flow based on kelp (Ecklonia maxima) debris in a sandy beach microcosm. Marine Ecology Progress Series 7, 315326.CrossRefGoogle Scholar
Locke, A. and Corey, S. (1989) Amphipods, isopods and surface currents: a case for passive dispersal in the Bay of Fundy, Canada. Journal of Plankton Research 11, 419430.CrossRefGoogle Scholar
Mandeel, Q.A. (2002) Microfungal community associated with rhizosphere soil of Zygophyllum qatarense in arid habitats of Bahrain. Journal of Arid Environments 50, 665681.CrossRefGoogle Scholar
McManus, J.W. and Polsenberg, J.F. (2004) Coral–algal phase shifts on coral reefs: ecological and environmental aspects. Progress in Oceanography 60, 263279.CrossRefGoogle Scholar
Norkko, J., Bonsdorff, E. and Norkko, A. (2000) Drifting algal mats as an alternative habitat for benthic invertebrates: species specific responses to a transient resource. Journal of Experimental Marine Biology and Ecology 248, 79104.CrossRefGoogle ScholarPubMed
Robertson, A.I. and Hansen, J.A. (1982) Decomposing seaweed: a nuisance or a vital link in coastal food chains? CSIRO Marine Laboratories Report 1979, 7583.Google Scholar
Robertson, A.I. and Lucas, J.S. (1983) Food choice, feeding rates, and the turnover of macrophyte biomass by a surf-zone inhabiting amphipod. Journal of Experimental Marine Biology and Ecology 72, 99124.CrossRefGoogle Scholar
Robertson, A.I. and Mann, K.H. (1982) Population dynamics and life history adaptations of Littorina neglecta Bean in an eelgrass meadow (Zostera marina L.) in Nova Scotia. Journal of Experimental Marine Biology and Ecology 63, 151171.CrossRefGoogle Scholar
Salovius, S. and Bonsdorff, E. (2004) Effects of depth, sediment and grazers on the degradation of drifting filamentous algae (Cladophora glomerata and Pilayella littoralis). Journal of Experimental Marine Biology and Ecology 298, 93109.CrossRefGoogle Scholar
Santelices, B. and Varela, D. (1994) Abiotic control of reattachment in Gelidium chilense (Montagne) Santelices & Montalva (Gelidiales; Rhodophyta). Journal of Experimental Marine Biology and Ecology 177, 145155.CrossRefGoogle Scholar
Sheridan, P. (1997) Benthos of adjacent mangrove, seagrass and non-vegetated habitats in Rookery Bay, Florida, U.S.A. Estuarine, Coastal and Shelf Science 44, 455469.CrossRefGoogle Scholar
Smith, B.D. and Foreman, R.E. (1984) An assessment of seaweed decomposition within a southern Strait of Georgia seaweed community. Marine Biology 84, 197205.CrossRefGoogle Scholar
Stenton-Dozey, J. and Griffiths, C.L. (1983) The fauna associated with kelp stranded on a sandy beach. In McLachlan, A. and Erasmus, T. (eds) Sandy beaches as ecosystems. The Hague: W. Junk Publishers, pp. 557568.CrossRefGoogle Scholar
Stoner, A.W. and Greening, H.S. (1984) Geographic variation in the macro-faunal associates of pelagic Sargassum and some biogeographic implications. Marine Ecology Progress Series 20, 185192.CrossRefGoogle Scholar
Talbot, M.M.B. and Bate, G.C. (1988) The relative quantities of live and detrital organic matter in a beach-surf ecosystem. Journal of Experimental Marine Biology and Ecology 121, 255264.CrossRefGoogle Scholar
Tzetlin, A.B., Mokievsky, V.O., Melnikov, A.N., Saphonov, M.V., Simdyanov, T.G. and Ivanov, I.E. (1997) Fauna associated with detached kelp in different types of subtidal habitats of the White Sea. Hydrobiologia 355, 91100.CrossRefGoogle Scholar
Woodcock, A.H. (1995) Winds subsurface pelagic Sargassum and Langmuir circulations. Journal of Experimental Marine Biology and Ecology 170, 117125.CrossRefGoogle Scholar
Zemke-White, W.L., Speed, S.R. and McClary, D.J. (2005) Beach-cast seaweed: a review. New Zealand Fisheries Assessment Report 2005/44, pp. 47.Google Scholar