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Population features of the invasive kelp Undaria pinnatifida (Phaeophyceae: Laminariales) in Nuevo Gulf (Patagonia, Argentina)

Published online by Cambridge University Press:  15 February 2008

Graciela N. Casas*
Affiliation:
Centro Nacional Patagónico (CENPAT–CONICET), Boulevard Brown s/n-(9120), Puerto Madryn, Argentina
María Luz Piriz
Affiliation:
Centro Nacional Patagónico (CENPAT–CONICET), Boulevard Brown s/n-(9120), Puerto Madryn, Argentina
Elisa R. Parodi
Affiliation:
Universidad Nacional del Sur, Departamento de Biología, Bioquímica y Farmacia, San Juan 670-(8000) Bahía Blanca, Argentina Instituto Argentino de Oceanografía (IADO–CONICET), Camino de la Carrindanga s/n-(8000) Bahía Blanca, Argentina
*
Correspondence should be addressed to: Graciela N. Casas Centro Nacional Patagónico (CENPAT–CONICET), Boulevard Brown s/n-(9120) Puerto MadrynArgentina email: graciela@cenpat.edu.ar

Abstract

The invasive kelp Undaria pinnatifida was observed for the first time in the Nuevo Gulf (Patagonia, Argentina) in December 1992. At the present time, with the exception of sandy bottoms, the coasts of the Nuevo Gulf are almost entirely colonized. From October 1997 to February 2000, the characteristics of this population, i.e. the relationships between morphological features and seawater temperature, the seasonality in sporophyll development and the proportions of different reproductive stages during its life cycle, were analysed. The observations confirmed that the maximal mean densities of sporophytes (149.1 plants m−2) occurred in winter while the mean tallest sporophytes (88.5 cm) and the mean highest biomass (16501 g m−2) were registered in spring and at the beginning of the summer. Coexisting juvenile and mature sporophytes were found. Sporophylls showed also seasonal characteristics, with maximal width in summer. Manipulative experiments conducted for testing the recruitment pattern of Undaria pinnatifida confirmed that the presence of juvenile individuals was uninterrupted. Thus, in this paper, we denote that U. pinnatifida has a constant recruitment, together with high reproductive rates, which are some of the characteristics of an introduced species, which explains why they became a highly invasive species or ‘pest species’, with negative environmental and economic effects.

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

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References

REFERENCES

Akiyama, K. and Kurogi, M. (1982) Cultivation of Undaria pinnatifida (Harvey) Suringar, the decrease in crops from natural plants following crop increase from cultivation. Bulletin of the Tohoku Regional Fisheries Research Laboratory 44, 91100.Google Scholar
Battershill, C., Miller, K. and Cole, R. (1998) The understorey of marine invasions. Seafood New Zealand 6, 3133.Google Scholar
Boudouresque, C.F. and Verlaque, M. (2002) Biological pollution in the Mediterranean Sea: invasive versus introduced macrophytes. Marine Pollution Bulletin 44, 3238.CrossRefGoogle ScholarPubMed
Boudouresque, C.F., Gerbal, M. and Knoepffler-Péguy, M. (1985) L'algue japonnaise Undaria pinnatifida (Phaeophyceae, Laminariales) en Méditerranée. Phycologia 24, 364366.CrossRefGoogle Scholar
Brown, M.T. and Lamare, M.D. (1994) The distribution of Undaria pinnatifida (Harvey) Suringer [sic] within Timaru harbour, New Zealand. Japanese Journal of Phycology (Sôrui) 42, 6370.Google Scholar
Campbell, S.J. and Burridge, T.R. (1998) Occurrence of Undaria pinnatifida (Phaeophyta: Laminariales) in Port Phillip Bay, Victoria, Australia. Marine and Freshwater Research 49, 379381.CrossRefGoogle Scholar
Carlton, J.T. (1996) Pattern, process, and prediction in marine invasion ecology. Biological Conservation 78, 97106.CrossRefGoogle Scholar
Carlton, J.T. (2000) Global change and biological invasions in the oceans. In Mooney, H.A. and Hobbs, R.J. (eds) Invasive species in a changing world. Covelo, CA: Island Press, pp. 3153.Google Scholar
Carlton, J.T. (2001). Introduced species in U.S. coastal waters: environmental impacts and management priorities. Pew Oceans Commission, Arlington, Virginia, 28 pp.Google Scholar
Carlton, J.T. (2003) Community assembly and historical biogeography in the North Atlantic Ocean: the potential role of human-mediated dispersal vectors. Hydrobiologia 503, 18.CrossRefGoogle Scholar
Casas, G.N. (2005). Biology and ecology of Undaria pinnatifida (Phaeophyceae, Laminariales) in Nuevo Gulf (Chubut, Argentina). PhD thesis. Universidad Nacional del Sur, Argentina, 234 pp.Google Scholar
Casas, G.N. and Piriz, M.L. (1996) Surveys of Undaria pinnatifida (Laminariales, Phaeophyta) in Golfo Nuevo, Argentina. Hydrobiologia 326/327, 213215.CrossRefGoogle Scholar
Casas, G.N. and Piriz, M.L. (2001) The threat of bioinvasions on biodiversity of benthic communities: Undaria pinnatifida (Phaeophyta, Laminariales) in Argentina. Applied Phycology Forum, 1–2. [online] Available from http://www.ib.usp.br/opf/argentina.html.Google Scholar
Casas, G., Scrosati, R. and Piriz, M.L. (2004) The invasive kelp Undaria pinnatifida (Phaeophyceae, Laminariales) reduces native seaweed diversity in Nuevo Gulf (Patagonia, Argentina). Biological Invasions 6, 411416.CrossRefGoogle Scholar
Castric-Fey, A., Beaupoil, C., Bouchain, J., Pradier, E. and L'Hardy-Halos, M.Th. (1999) The introduced alga Undaria pinnatifida (Laminariales, Alariaceae) in the rocky shore ecosystem of the St. Malo area: growth rate and longevity of the sporophyte. Botanica Marina 42, 8396.Google Scholar
Curiel, D., Bellemo, G., Marzocchi, M., Scattolin, M. and Parisi, G. (1998) Distribution of introduced Japanese macroalgae Undaria pinnatifida, Sargassum muticum (Phaeophyta) and Antithamnion pectinatum (Rhodophyta) in the Lagoon of Venice. Hydrobiologia 385, 1722.CrossRefGoogle Scholar
Fletcher, R.L. and Manfredi, C. (1995) The occurrence of Undaria pinnatifida (Phaeophyceae, Laminariales) on the South coast of England. Botanica Marina 38, 355358.CrossRefGoogle Scholar
Floc'h, J.Y., Pajot, R. and Wallentinus, I. (1991) The Japanese brown alga Undaria pinnatifida on the coast of France and its possible establishment in European waters. Journal du Conseil International pour l'Exploration de la Mer 47, 379390.CrossRefGoogle Scholar
Floc'h, J.Y., Pajot, R. and Mouret, V. (1996) Undaria pinnatifida (Laminariales, Phaeophyta) 12 years after its introduction into the Atlantic Ocean. Hydrobiologia 326/327, 217222.CrossRefGoogle Scholar
Grosholz, E. (2002) Ecological and evolutionary consequences of coastal invasions. Trends in Ecology and Evolution 17, 2227.CrossRefGoogle Scholar
Hay, C.H. (1990) The dispersal of sporophytes of Undaria pinnatifida by coastal shipping in New Zealand, and implications for further dispersal of Undaria in France. British Phycological Journal 25, 301313.CrossRefGoogle Scholar
Hay, C.H. and Luckens, P.A. (1987) The Asian kelp Undaria pinnatifida (Phaeophyta, Laminariales) found in a New Zealand harbour. New Zealand Journal of Botany 25, 329332.CrossRefGoogle Scholar
Hay, C.H. and Villouta, E. (1993) Seasonality of the adventive Asian kelp Undaria pinnatifida in New Zealand. Botanica Marina 36, 461476.CrossRefGoogle Scholar
Kolar, C.S. and Lodge, D.M. (2001) Progress in invasion biology: predicting invaders. Trends in Ecology and Evolution 16, 199204.CrossRefGoogle ScholarPubMed
Martín, J.P. and Cuevas, J.M. (2006) First record of Undaria pinnatifida (Laminariales, Phaeophyta) in Southern Patagonia, Argentina. Biological Invasions 8, 13991402.CrossRefGoogle Scholar
Nyberg, C.D. and Wallentinus, I. (2005) Can species traits be used to predict marine macroalgal introductions? Biological Invasions 7, 265279.CrossRefGoogle Scholar
Oh, S-H. and Koh, C-H. (1996) Growth and photosynthesis of Undaria pinnatifida (Laminariales, Phaeophyta) on a cultivation ground in Korea. Botanica Marina 39, 389393.CrossRefGoogle Scholar
Piriz, M.L. and Casas, G. (1994) Occurrence of Undaria pinnatifida in Golfo Nuevo, Argentina. Applied Phycology Forum 10, 4.Google Scholar
Piriz, M.L. and Casas, G. (2001) Introduction of species and its impact on biodiversity. The Undaria pinnatifida case (Phaeophyta, Laminariales). In Alveal, K. and Antezana, T. (eds) Sustainability of biodiversity. Chile: Universidad de Concepción. [In Spanish.], pp. 679692.Google Scholar
Ricciardi, A. and Rasmussen, J.B. (1998) Predicting the identity and impact of future biological invaders: a priority for aquatic resource management. Canadian Journal of Fisheries and Aquatic Sciences 55, 17591765.CrossRefGoogle Scholar
Saito, Y. (1975) Undaria. In Tokida, J. and Hirose, H. (eds) Advances of phycology in Japan. Jena: VEB Gustav Fischer Verlag, pp. 304320.Google Scholar
Sanderson, J.C. (1990) A preliminary survey of the distribution of the introduced macroalga, Undaria pinnatifida (Harvey) Suringer [sic] on the East Coast of Tasmania, Australia. Botanica Marina 33, 153157.CrossRefGoogle Scholar
Sanderson, J.C. and Barrett, N. (1989) A survey of the distribution of the introduced Japanese macroalga Undaria pinnatifida (Harvey) Suringer [sic] in Tasmania. Technical Report. Department of Sea Fisheries, Hobart, Tasmania, No. 38, 35 pp.Google Scholar
Schaffelke, B., Campbell, M.L. and Hewitt, C.L. (2005) Reproductive phenology of the introduced kelp Undaria pinnatifida (Phaeophyceae, Laminariales) in Tasmania, Australia. Phycologia 44, 8494.CrossRefGoogle Scholar
Silva, P.C., Woodfield, R.A., Cohen, A.N., Harris, L.H. and Goddard, J.H.R. (2002) First report of the Asian kelp Undaria pinnatifida in the Northeastern Pacific Ocean. Biological Invasions 4, 333338.CrossRefGoogle Scholar
Skriptsova, A., Khomenko, V. and Isakov, V. (2004) Seasonal changes in growth rate, morphology and alginate content in Undaria pinnatifida at the northern limit in the Sea of Japan (Russia). Journal of Applied Phycology 16, 1721.CrossRefGoogle Scholar
Stuart, M.D., Hurd, C.L. and Brown, M.T. (1999) Effects of seasonal growth rate on morphological variation of Undaria pinnatifida (Alariaceae, Phaeophyceae). Hydrobiologia 398/399, 191199.CrossRefGoogle Scholar
Thornber, C.S., Kinlan, B.P., Graham, M.H. and Stachowicz, J.J. (2004) Population ecology of the invasive kelp Undaria pinnatifida in California: environmental and biological controls on demography. Marine Ecology Progress Series 268, 6980.CrossRefGoogle Scholar
Wallentinus, I. (1999) Undaria pinnatifida (Harvey) Suringar. In Gollasch, S. et al. (ed.) Case histories on introduced species: their general biology, distribution, range expansion and impact. Department of Fishery Biology, Institute for Marine Science, University of Kiel, Germany, pp. 1119.Google Scholar