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Biological and Physical Factors Controlling the Spatial Distribution of the Intertidal Alga Gelidium Pristoides in the Eastern Cape, South Africa

Published online by Cambridge University Press:  11 May 2009

A. R. Carter
Affiliation:
Plant Sciences Department, Rhodes University, Grahamstown 6140, South Africa Sea Fisheries Research Institute, Private Bag X2, Roggebaai 8012, South Africa To whom all correspondence should be addressed
R. J. Anderson
Affiliation:
Plant Sciences Department, Rhodes University, Grahamstown 6140, South Africa Sea Fisheries Research Institute, Private Bag X2, Roggebaai 8012, South Africa To whom all correspondence should be addressed

Extract

Gelidium pristoides dominates the lower and mid-eulittoral zones of rocky shores in the eastern Cape, South Africa. A disproportionately high percentage of the plants is attached to barnacle and limpet shells, or restricted to rock crevices. Our experiments at Port Alfred indicate that this distribution is caused by grazing by the limpet Patella oculus and/or strength of attachment of the plants to the different substrata. Exclusion of limpets caused an approximately four-fold increase in the cover of G. pristoides on rock, and an increase from almost 0 to 80% cover on sterilised (dead) limpet shells. Measurements showed G. pristoides to be more than 50% more strongly attached to barnacle and limpet shells than to rock. The distribution of G. pristoides on the various substrata is largely determined by limpet grazing and possibly the different strengths of attachment to the different substrata. The upper distribution limit of G. pristoides is set by physical effects of emersion and was largely unaffected by limpet exclusion. Competition with other algae is important in setting the lower limit: in the sublittoral fringe, although limpet exclusion enhanced recruitment, juveniles were later displaced by articulated corallines, and adult transplants senesced because of encrusting coralline epiphytes.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1991

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References

Anderson, R J., Simons, R.H. & Jarman, N.G., 1989. Commercial seaweeds in southern Africa: A review of utilization and research. South African journal of Marine Science, 8, 277299.CrossRefGoogle Scholar
Beckley, L.E., 1982. Studies on the littoral seaweed epifauna of St Croix Island. 3. Gelidium pristoides (Rhodophyta) and its epifauna. South African Journal of Zoology, 17,310.CrossRefGoogle Scholar
Bolton, J.J., 1986. Marine phytogeography of the Benguela upwelling region on the west coast of southern Africa: a temperature dependent approach. Botanica Marina, 29, 251256.CrossRefGoogle Scholar
Branch, G.M., 1971. The ecology of Patella L. from the Cape Peninsula, South Africa. I. Zonation, movements and feeding. Zoologica Africana, 6, 138.CrossRefGoogle Scholar
Branch, G.M., 1975. Mechanisms reducing the intraspecific competition in Patella spp.: migration, differentiation and territorial behaviour. Journal of Animal Ecology, 44, 575600.CrossRefGoogle Scholar
Branch, G.M. & Newell, R.C., 1978. A comparative study of metabolic energy expenditure in the limpets Patella cochlear, P. oculus and P. granularis. Marine Biology, 49, 351361.CrossRefGoogle Scholar
Carter, A.R. & Anderson, R.J., 1985. Regrowth after experimental harvesting of the agarophyte Celidium pristoides (Gelidiales: Rhodophyta) in the eastern Cape Province. South African Journal of Marine Science, 3, 111118.CrossRefGoogle Scholar
Carter, A.R. & Anderson, R.J., 1986. Seasonal growth and agar contents in Gelidium pristoides (Gelidiales, Rhodophyta) under various harvesting regimes at Port Alfred, South Africa. Botanica Marina, 29, 117123.Google Scholar
Carter, A.R. & Simons, R.H., 1987. Regrowth and production capacity of Gelidium pristoides (Gelidiales, Rhodophyta) under various harvesting regimes at Port Alfred, South Africa. Botanica Marina, 30, 227231.CrossRefGoogle Scholar
Connell, J.H., 1972. Community interactions on marine rocky intertidal shores. Annual Review of Ecology and Systematics, 3, 169192.CrossRefGoogle Scholar
Dayton, P.K., 1971. Competition, disturbance, and community organization: the provisions and subsequent utilization of space in a rocky intertidal community. Ecological Monographs, 41,351 -389.CrossRefGoogle Scholar
Dayton, P.K., 1975. Experimental evaluation of ecological dominance in a rocky intertidal algal community. Ecological Monographs, 45, 137159.CrossRefGoogle Scholar
Edwards, P., 1977. An investigation of the vertical distribution of selected benthic marine algae with a tide-simulating apparatus. Journal of Phycology, 13, 6268.Google Scholar
Eyre, J., Broekhuysen, G.J. & Crichton, M.I., 1938. The South African intertidal zone and its relation to ocean currents. VI. The East London district. Annals of the Natal Museum, 9, 83112.Google Scholar
Harlin, M.M. & Lindbergh, J.M., 1977. Selection of substrata by seaweeds: optimal surface relief. Marine Biology, 40, 3340.CrossRefGoogle Scholar
Harris, S.A., Da Silva, F.M., Bolton, J.J. & Brown, A.C., 1986. Algal gardens and herbivory in a scavenging sandy-beach nassariid whelk. Malacologia, 27, 299305.Google Scholar
Hawkins, S.J., 1981. The influence of season and barnacles on the algal colonization of Patella vulgata exclusion areas. Journal of the Marine Biological Association of the United Kingdom, 61, 115.CrossRefGoogle Scholar
Hawkins, S.J. & Hartnoll, R.G., 1983. Grazing of intertidal algae by marine invertebrates. Oceanography and Marine Biology, an Annual Review, 21, 195282.Google Scholar
Hawkins, S.J. & Hartnoll, R.G., 1985. Factors determining the upper limits of intertidal canopyforming algae. Marine Ecology Progress Series, 20, 265271.CrossRefGoogle Scholar
Hruby, T., 1976. Observations of algal zonation resulting from competition. Estuarine and Coastal Marine Science, 4, 231233.CrossRefGoogle Scholar
Jara, H.F. & Moreno, C.A., 1984. Herbivory and structure in a midlittoral rocky community: a case in southern Chile. Ecology, 65, 2838.Google Scholar
Jernakoff, P., 1983. Factors affecting the recruitment of algae in a midshore region dominated by barnacles. Journal of Experimental Marine Biology and Ecology, 67, 1731.CrossRefGoogle Scholar
Jernakoff, P., 1985. An experimental evaluation of the influence of barnacles, crevices and seasonal patterns of grazing on algal diversity and cover in an intertidal barnacle zone. Journal of Experimental Marine Biology and Ecology, 88, 287–302.CrossRefGoogle Scholar
Jernakoff, P., 1986. Experimental investigation of interactions between the perennial red alga Gelidium pusillum and barnacles on a New South Wales rocky shore. Marine Ecology Progress Series, 28, 259263.Google Scholar
John, D.M. & Pople, W., 1973. The fish grazing of rocky shore algae in the Gulf of Guinea. Journal of Experimental Marine Biology and Ecology, 11, 8190.CrossRefGoogle Scholar
Jones, N.S. & Kain, J.M., 1967. Subtidal algal colonization following the removal of Echinus. Helgoländer Wissenschaftliche Meeresuntersuchungen, 15, 460466.CrossRefGoogle Scholar
Joubert, C.S.W. & Hanekom, P.B., 1980. A study of feeding in some inshore reef fish of the Natal coast, South Africa. South African Journal of Zoology, 15, 262272.CrossRefGoogle Scholar
Lubchenco, J., 1980. Algal zonation in the New England rocky intertidal community: an experimental analysis. Ecology, 61, 333344.CrossRefGoogle Scholar
Lubchenco, J., 1982. Effects of grazers and algal competitors on fucoid colonization in tide pools. Journal of Phycology, 18, 544550.CrossRefGoogle Scholar
Lubchenco, J., 1983. Littorina and Fucus: effects of herbivores, substratum heterogeneity, and plant escapes during succession. Ecology, 64, 11161123.CrossRefGoogle Scholar
Lubchenco, J. & Gaines, S.D., 1981. A unified approach to marine-plant herbivore interactions. I. Populations and communities. Annual Review of Ecology and Systematics, 12, 405437.Google Scholar
McQuaid, C.D., 1985. Seasonal variation in biomass and zonation of nine intertidal algae in relation to changes in radiation, sea temperature and tidal regime. Botanica Marina, 28, 539544.CrossRefGoogle Scholar
Menge, B.A., 1976. Organization of the New England rocky intertidal community: role of predation, competition and environmental heterogeneity. Ecological Monographs, 46, 355393.Google Scholar
Menge, B.A. & Lubchenco, J., 1981. Community organization in temperate and tropical rocky intertidal habitats: prey refuges in relation to consumer pressure gradients. Ecological Monographs, 51, 429450.CrossRefGoogle Scholar
Menge, B.A., Lubchenco, J. & Ashkenas, L.R., 1985. Diversity, heterogeneity and consumer pressure in a tropical rocky intertidal community. Oecologia, 65, 394405.CrossRefGoogle Scholar
Onraël, A.C. & Robertson, B.L., 1987. Seasonal variation in yield and properties of agar from sporophytic and gametophytic phases of Onikusa pristoides (Turner) Akatsuka (Gelidiaceae: Rhodophyta). Botanica Marina, 30, 491495.CrossRefGoogle Scholar
Paine, R.T. & Vadas, R.L., 1969. The effects of grazing by sea urchins, Strogylocentrotus spp. on benthic algal populations. Limnology and Oceanography, 14, 710719.CrossRefGoogle Scholar
Pomerat, C.M. & Weiss, C.M., 1946. The influence of texture and composition of surfaces on the attachment of sedentary marine organisms. Biological Bulletin, 91, 5765.CrossRefGoogle Scholar
Schonbeck, M. & Norton, T.A., 1978. Factors controlling the upper limits of fucoid algae on the shore. Journal of Experimental Marine Biology and Ecology, 31, 303313.CrossRefGoogle Scholar
Schonbeck, M. & Norton, T. A., 1979. The effects of brief periodic submergence on intertidal fucoid algae. Estuarine and Coastal Marine Science, 8, 205211.CrossRefGoogle Scholar
Schonbeck, M. & Norton, T.A., 1980. Factors controlling the lower limits of fucoid algae on the shore. Journal of Experimental Marine Biology and Ecology, 43, 131150.CrossRefGoogle Scholar
Sousa, W.P., 1979. Experimental investigation of disturbance and ecological succession in a rocky intertidal algal community. Ecological Monographs, 49, 227254.CrossRefGoogle Scholar
Sousa, W.P., Schroeter, S.C. & Gaines, S.D., 1981. Latitudinal variation in intertidal algal community structure: the influence of grazing and vegetative propagation. Oecologia, 48, 297307.CrossRefGoogle ScholarPubMed
Southward, A.J. & Southward, E.C., 1978. Recolonization of rocky shores in Cornwall after use of toxic dispersants to clean up the Torrey Canyon spill. Journal of the Fisheries Research Board of Canada, 35, 682706.CrossRefGoogle Scholar
Stephenson, T.A., Stephenson, A. & Bright, K.M.F., 1938. The South African intertidal zone and its relation to ocean currents. VI. The Port Elizabeth District. Annals of the Natal Museum, 9, 119.Google Scholar
Underwood, A.J., 1981. Structure of a rocky intertidal community in New South Wales: patterns of vertical distribution and seasonal change. Journal of Experimental Marine Biology and Ecology, 51, 5785.CrossRefGoogle Scholar
Underwood, A.J. & Denley, E.J., 1984. Paradigms, explanations, and generalizations in models for the structure of intertidal communities on rocky shores. In Ecological Communities: Conceptual Issues and the Evidence (ed. , D.R. Strong, et al.), pp. 151180. Princeton: Princeton University Press.CrossRefGoogle Scholar
Underwood, A.J. & Jernakoff, P., 1981. Effects of interactions between algae and grazing gastropods on the structure of a lowshore intertidal algal community. Oecologia, 48, 221233.CrossRefGoogle ScholarPubMed
Underwood, A.J. & Jernakoff, P., 1984. The effects of tidal height, wave-exposure, seasonality and rock pools on grazing and the distribution of intertidal macroalgae in New South Wales. Journal of Experimental Marine Biology and Ecology, 75, 7196.CrossRefGoogle Scholar