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The effects of colonization by Sargassum muticum on tidepool macroalgal assemblages

Published online by Cambridge University Press:  06 October 2009

Rosa M. Viejo
Rosa M. Viejo
Affiliation:
Unidad de Ecología, Departamento de Biología de Organismos y Sistemas, Universidad de Oviedo, 33071-Oviedo, Spain.
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Abstract

The impact of colonization by Sargassum muticum (Phaeophyta: Fucales) on the resident macroalgal assemblage in tidepools was investigated in northern Spain. Sargassum muticum was allowed to colonize and spread in some tidepools, and was periodically removed in others. Changes in the abundance of macrophytes were recorded at three sites over two years. The colonization by S. muticum and the subsequent changes induced on the native assemblage was extremely variable among sites. Where the invader colonized profusely, it induced changes in the macroalgal composition of tidepools. The leathery group of macrophytes was significantly affected and changes were also observed in the foliose group. It was suggested that S. muticum may take advantage of their perennial and opportunistic traits in the interaction with groups of algae with different survival strategies. However, the spatial patchiness of the colonization may mitigate the impact of the invasion at local and regional scales.

Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 77 , Issue 2 , May 1997 , pp. 325 - 340
Copyright
Copyright © Marine Biological Association of the United Kingdom 1997

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References

REFERENCES

Ambrose, R.F. & Nelson., B.V., 1982. Inhibition of giant kelp recruitment by an introduced brown alga. Botanica Marina, 25, 265–267.CrossRefGoogle Scholar
Arenas, F., Fernández, C., Rico, J.M., Fernández, E. & Haya, D., 1995. Growth and reproductive strategies of Sargassum muticum (Yendo) Fensholt and Cystoseira nodicaulis (Whit.) Roberts. Scientia Marina, 59, supplement 1, 1–8.Google Scholar
Cebrián, J. & Duarte, CM., 1995. Plant growth-rate dependence of detrital carbon storage in ecosystems. Science, New York, 268, 1606–1608.CrossRefGoogle ScholarPubMed
Critchley, A.T., 1983. The establishment and increase of Sargassum muticum (Yendo) Fensholt populations within the Solent area of southern Britain. I. An investigation of the increase in number of population individuals. Botanica Marina, 26, 539–545.Google Scholar
Critchley, A.T., Farnham, W.F. & Morrell, S.L., 1983. A chronology of new European sites of attachment for the invasive brown alga, Sargassum muticum, 1973–1981. Journal of the Marine Biological Association of the United Kingdom, 63, 799–811.CrossRefGoogle Scholar
Critchley, A.T., Farnham, W.F., Yoshida, T. & Norton, T.A., 1990. A bibliography of the invasive algae Sargassum muticum (Yendo) Fensholt (Fucales; Sargassaceae). Botanica Marina, 33, 551–562.CrossRefGoogle Scholar
Dethier, M.N., 1982. Pattern and process in tidepool algae: factors influencing seasonality and distribution. Botanica Marina, 25, 55–66.CrossRefGoogle Scholar
Dethier, M.N., 1984. Disturbance and recovery in intertidal pools: maintenance of mosaic patterns. Ecological Monographs, 54, 99–118.CrossRefGoogle Scholar
Dethier, M.N., 1994. The ecology of intertidal algal crusts: variation within a functional group. Journal of Experimental Marine Biology and Ecology, 177, 37–71.CrossRefGoogle Scholar
De Wreede, R.E., 1983. Sargassum muticum (Fucales, Phaeophyta): regrowth and interaction with Rhodomela larix (Ceraminales, Rhodophyta). Phycologia, 22, 153–160.CrossRefGoogle Scholar
Drake, J.A., 1991. Community-assembly mechanics and the structure of an experimental species ensemble. American Naturalist, 137, 1–26.CrossRefGoogle Scholar
Druehl, L.D., 1973. Marine transplantations. Science, New York, 179, 12.CrossRefGoogle ScholarPubMed
Enríquez, S., Agusti, S. & Duarte, C.M., 1994. Light absorption by marine macrophytes. Oecologia, 98, 121–129.CrossRefGoogle ScholarPubMed
Farnham, W.F., Fletcher, R.L. & Irvine, L.M., 1973. Attached Sargassum found in Britain. Nature, London, 243, 231–232.CrossRefGoogle Scholar
Fernández, C., Gutierrez, L.M. & Rico, J.M., 1990. Ecology of Sargassum muticum on the north coast of Spain. Preliminary observations. Botanica Marina, 33, 423–428.CrossRefGoogle Scholar
Fernández, C. & Niell, F.X., 1982. Zonación del fitobentos intermareal de la región del Cabo Penñas (Asturias). Investigación Pesquera, Barcelona, 46, 121–144.Google Scholar
Fletcher, R.L. & Fletcher, S.M., 1975. Studies on the recently introduced brown alga Sargassum muticum (Yendo) Fensholt. I. Ecology and reproduction. Botanica Marina, 18, 149–156.Google Scholar
Fritsch, F.E., 1977. The structure and reproduction of algae. Cambridge University Press.Google Scholar
Haya, D., 1988. Biologia y ecologia de Paracentrotus lividus en la zona intermareal. Thesis Doctoral. Universidad de Oviedo, Spain.Google Scholar
Herbold, B. & Moyle, P.B., 1986. Introduced species and vacant niches. American Naturalist, 128, 751–760.CrossRefGoogle Scholar
Jephson, N.A. & Gray, P.W.G., 1977. Aspects of the ecology of Sargassum muticum (Yendo) Fensholt, in the Solent region of the British Isles. I. The growth cycle and epiphytes. In Biology ofbenthic organisms. Proceedings of the 11th European Symposium in marine biology (ed. Keegan, B.F. et al. ), pp. 367–375. Oxford: Pergamon Press.Google Scholar
Johansen, H.W., 1981. Coralline algae, a first synthesis. Florida: CRC Press Inc.Google Scholar
Kooistra, W.H.C.F., Joosten, A.M.T. & Hoek, C. van den, 1989. Zonation patterns in intertidal pools and their possible causes: a multivariate approach. Botanica Marina, 32, 9–26.CrossRefGoogle Scholar
Littler, M.M., 1980. Morphological form and photosynthetic performances of marine macroalgae: tests of a functional/form hypothesis. Botanica Marina, 23, 161–165.CrossRefGoogle 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 model. American Naturalist, 116, 25–44.CrossRefGoogle Scholar
Lodge, D.M., 1993. Biological invasions: lessons for ecology. Trends in Ecology and Evolution, 8, 133–137.CrossRefGoogle ScholarPubMed
Mann, K.H., 1973. Seaweeds: their productivity and strategy for growth. Science, New York, 182, 975–981.CrossRefGoogle ScholarPubMed
McCook, L.J. & Chapman, A.R.O., 1992. Vegetative regeneration of Fucus rockweed canopy as a mechanism of secondary succession on an exposed rocky shore. Botanica Marina, 35, 35–46.CrossRefGoogle Scholar
McKone, J., 1993. Statistical analysis of experiments conducted at multiple sites. Oikos, 67, 184–186.CrossRefGoogle Scholar
Metaxas, A. & Scheibling, R.E., 1993. Community structure and organization of tidepools. Marine Ecology Progress Series, 98, 187–198.CrossRefGoogle Scholar
Norton, T.A., 1976. Why is Sargassum muticum so invasive? British Phycological Journal, 11, 197–198.Google Scholar
Norton, T.A., 1977. Ecological experiments with Sargassum muticum. Journal of the Marine Biological Association of the United Kingdom, 57, 33–43.CrossRefGoogle Scholar
Paula, E.J. & Eston, V.R., 1987. Are there other Sargassum species potentially as invasive as S. muticum? Botanica Marina, 30, 405–410.CrossRefGoogle Scholar
Rice, W.R., 1989. Analysing tables of statistical tests. Evolution, 43, 223–225.CrossRefGoogle Scholar
Ricklefs, R.E. & Schluter, D., 1993. Species diversity: regional and historical influences. In Species diversity in ecological communities. Historical and geographical perspectives (ed. Ricklefs, R.E. and Schluter, D.), pp. 350–363. Chicago: University of Chicago Press.Google Scholar
Rueness, T., 1989. Sargassum muticum and other introduced Japanese macroalgae: biological pollution of European coasts. Marine Pollution Bulletin, 20, 173–176.CrossRefGoogle Scholar
Steneck, R.S., 1986. The ecology of coralline algal crusts: convergent patterns and adaptative strategies. Annual Review of Ecology and Systematics, 17, 273–306.CrossRefGoogle Scholar
Steneck, R.S. & Dethier, M.N., 1994. A functioning group approach to the structure of algal-dominated communities. Oikos, 69, 476–498.CrossRefGoogle Scholar
Underwood, A.J. & Fairweather, P.G., 1989. Supply-side ecology and benthic marine assemblages. Trends in Ecology and Evolution, 4, 16–20.CrossRefGoogle ScholarPubMed
Vadas, R.L., Wright, W.A. & Miller, S.L., 1990. Recruitment of Ascophyllum nodosum: wave-action as a source of mortality. Marine Ecolgy Progress Series, 61, 263–272.CrossRefGoogle Scholar
Vermeij, G.J., 1991. When biotas meet: understanding biotic interchange. Science, New York, 253, 1099–1104.CrossRefGoogle ScholarPubMed
Viejo, R.M., Arrontes, J. & Andrew, N.L., 1995. An experimental evaluation of the effect of wave action on the distribution of Sargassum muticum in northern Spain. Botanica Marina, 38, 437–441.CrossRefGoogle Scholar
Walker, T.D. & Valentine, J.W., 1984. Equilibrium models of evolutionary species diversity and the number of empty niches. American Naturalist, 124, 887–899.CrossRefGoogle Scholar
Winer, B.J., 1971. Statistical principles in experimental design, USA: McGraw-Hill, Inc.Google Scholar