Hostname: page-component-cd9895bd7-gbm5v Total loading time: 0 Render date: 2024-12-26T19:08:24.492Z Has data issue: false hasContentIssue false
  • English
  • Français

Macrobenthos–sediment relationships in a sandy bottom community off Mar del Plata, Argentina

Published online by Cambridge University Press:  23 June 2010

Florencia Arrighetti  and
Pablo E. Penchaszadeh
Florencia Arrighetti*
Affiliation:
Laboratorio de Invertebrados, DBBE, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab. II C1428EHA, Buenos Aires, Argentina CONICET, Museo Argentino de Ciencias Naturales, Avenida Angel Gallardo 470, C1405DJR, Buenos Aires, Argentina
Pablo E. Penchaszadeh
Affiliation:
Laboratorio de Invertebrados, DBBE, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab. II C1428EHA, Buenos Aires, Argentina CONICET, Museo Argentino de Ciencias Naturales, Avenida Angel Gallardo 470, C1405DJR, Buenos Aires, Argentina
*
Correspondence should be addressed to: F. Arrighetti, Laboratorio de Invertebrados, DBBE Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab. II C1428EHA, Buenos Aires, Argentina email: flora@bg.fcen.uba.ar
Get access Rights & Permissions [Opens in a new window]

Abstract

The aim of this study is to characterize the different macrozoobenthos communities in Mar del Plata waters (south-western Atlantic) on the basis of their abundance and habitat, and to determine how sediment characteristics, like the grain-size composition, affect macrobenthic community structure. Multivariate techniques indicated that benthic communities and sediments in the surveyed area were included into the following five well-defined groups: (1) a medium sand assemblage dominated by the bivalve Crassinella marplatensis and Diplodonta patagonica, the echinoderm Encope emarginata, the tanaidacean Bacescapseudes sp. and the polychaete Armandia loboi; (2) a medium to very fine sand assemblage dominated by ostracods, the tanaidacean Bacescapseudes sp., amphipods and polychaetes of the family Nephtyidae; (3) a fine to very fine sand assemblage dominated by the tanaidacean Bacescapseudes sp.; (4) a silt and fine sand assemblage dominated by polychaetes particularly Scolelepis sp. and individuals of the family Nephtyidae; and (5) a fine sand assemblage dominated by amphipods and the tanaidacean Bacescapseudes sp. These results revealed the patchy distribution of macrobenthic assemblages as a result of sediment characteristics and serve as baseline information for this area strongly subjected to trawling perturbations.

Keywords

macrobenthosgrain size compositionpatchy distributionsouth-western Atlantic
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 90 , Issue 5 , August 2010 , pp. 933 - 939
Copyright
Copyright © Marine Biological Association of the United Kingdom 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Bremec, C.S. and Giberto, D. (2006) Polychaete assemblages in the Argentinean biogeographical province, between 34° and 38°S. Scientia Marina 70, 249–257.CrossRefGoogle Scholar
Bremec, C.S. and Roux, A. (1997) Resultados del análisis de una campaña de investigación pesquera sobre comunidades bentónicas asociadas a bancos de mejillón (Mytilus edulis platenses D'Orb.) en costas de Buenos Aires, Argentina. Revista de Investigación y Desarrollo Pesquero 11, 153–166.Google Scholar
Capitoli, R., Bremec, C.S., Elías, R. and Giberto, D. (2004) Polychaetes assemblages from the South Brazilian Shelf. VIII International Polychaete Conference, 45 pp.Google Scholar
Chapman, P.M., Anderson, B., Carr, S., Engle, V., Green, R., Hameedi, J., Harmon, M., Haverland, P., Hyland, J., Ingersoll, C., Long, E., Rodgers, J. Jr., Salazar, M., Sibley, P.K. and Windom, H. (1997) General guidelines for using the sediment quality triad. Marine Pollution Bulletin 34, 368–372.CrossRefGoogle Scholar
Clarke, K.R. and Warwick, R.M. (1994) Change in marine communities: an approach to statistical analysis and interpretation, second edition. Plymouth: PRIMER-E.Google Scholar
Elías, R. (1992) Quantitative benthic structure in Blanca Bay and their relationship with organic enrichment. Marine Ecology 13, 189–201.CrossRefGoogle Scholar
Elías, R. and Bremec, C.S. (1994) Biomonitoring of water quality using benthic communities in Blanca Bay (Argentina). The Science of the Total Environment 158, 45–49.CrossRefGoogle Scholar
Elías, R., Bremec, C.S. and Vallarino, E.A. (2001) Polychaetes assemblages in a southern shallow shelf affected by seawage discharge. Revista Chilena de Historia Natural 74, 523–531.CrossRefGoogle Scholar
Elías, R., Rivero, M.S. and Vallarino, E.A. (2003). Sewage impact on the composition and distribution of Polychaeta associated to intertidal mussel beds of the Mar del Plata rocky shore. Argentina. Iheringia, Serie Zoologica 93, 309–318.CrossRefGoogle Scholar
Guerrero, R.A. and Piola, A.R. (1997) Masas de agua en la plataforma continental. In Boschi, E.E. (ed.) El Mar y sus Recursos Pesqueros. Mar del Plata: Instituto Nacional de Investigación y Desarrollo Pesquero, pp 107–118.Google Scholar
Hensley, R.H. (1996) Preliminary survey of benthos from the Nephrops norvegicus mud grounds in the north-western Irish Sea. Marine Ecology Progress Series 66, 285–299.Google Scholar
Holme, N.A. and Wilson, J.B. (1985) Faunas associated with longitudinal furrows and sand ribbons in a tide-swept area in the English Channel. Journal of the Marine Biological Association of the United Kingdom 65, 1051–1072.CrossRefGoogle Scholar
López Gappa, J.J., Tablado, A. and Magaldi, N.H. (1993) Seasonal changes in an intertidal community affected by sewage pollution. Environmental Pollution 82, 157–165.CrossRefGoogle Scholar
Mannino, A. and Montagna, P.A. (1997) Small-scale spatial variation of macrobenthic community structure. Estuaries 20, 159–173.CrossRefGoogle Scholar
Nanami, A., Saito, H., Akita, T., Motomatsu, K. and Kuwahara, H. (2005) Spatial distribution and assemblage structure of macrobenthic invertebrates in a brackish lake in relation to environmental variables. Estuarine, Coastal and Shelf Science 63, 167–176.CrossRefGoogle Scholar
Newell, R.C., Seiderer, L.J. and Robinson, J.E. (2001) Animal–sediment relationships in coastal deposits of the eastern English Channel. Journal of the Marine Biological Association of the United Kingdom 81, 1–9.CrossRefGoogle Scholar
Olivier, S.R., Bastida, R. and Torti, M.R. (1968) Resultados de las campañas oceanográficas Mar del Plata I–V. Contribución al trazado de una carta bionómica del área de Mar del Plata. Las asociaciones del sistema litoral entre 12 y 70 m de profundidad. Boletín Instituto de Biología Marina 16, 1–85.Google Scholar
Pardo, E.V. and Amaral, A.C.Z. (2004) Feeding behavior of Scolelepis sp. (Polychaeta: Spionidae). Brazilian Journal of Oceanography 52, 74–79.CrossRefGoogle Scholar
Peeters, E.T.H.M., Gylstra, R. and Vos, J.H. (2004) Benthic macroinvertebrate community structure in relation to food and environmental variables. Hydrobiologia 519, 103–115.CrossRefGoogle Scholar
Perillo, G.M.E., Gómez, E.A., Aliotta, S. and Galíndez, D.E. (1985) Granus: un programa FORTRAN para el análisis estadístico y gráfico de muestras de sedimentos. Revista Asociación Argentina Mineralogía, Petrología y Sedimentología 16, 1–5.Google Scholar
Pinel-Alloul, B., Méthot, G., Lapierre, L. and Willsie, A. (1996) Macroinvertebrate community as a biological indicator of ecological and toxicological factors in Lake Saint-Francois (Québec). Environmental Pollution 91, 65–87.CrossRefGoogle ScholarPubMed
Rhoads, D.C. and Young, D.K. (1970) The influences of deposit-feeding organisms on sediment stability and community trophic structure. Journal of Marine Research 28, 150–178.Google Scholar
Sanders, H.L. (1958) Benthic studies in Buzzards Bay. I. Animal sediment relationships. Limnology and Oceanography 3, 245–258.CrossRefGoogle Scholar
Seiderer, L.J. and Newell, R.C. (1999) Analysis of the relationship between sediment composition and benthic community structure in coastal deposits: implications for marine aggregate dredging. ICES Journal of Marine Science 56, 757–765.CrossRefGoogle Scholar
Scelzo, M.A., Martinez Arca, J. and Lucero, N.M. (2002) Diversidad, densidad y biomasa de la macrofauna componente de los fondos de pesca ‘camarón-langostino’ frente a Mar del Plata, Argentina (1998–1999). Revista de Investigación y Desarrollo Pesquero 15, 43–65.Google Scholar
Snelgrove, P.V.R. and Butman, C.A. (1994) Animal–sediment relationships revisited: cause versus effects. Oceanography and Marine Biology: an Annual Review 32, 111–177.Google Scholar
Warwick, R.M. and Davies, J.R. (1997) The distribution of sublittoral macrofauna communities in the Bristol Channel in relation to the substrate. Estuarine, Coastal and Shelf Science 5, 97–103.Google Scholar
Wilson, W.H. (1990) Competition and predation in marine soft-sediment communities. Annual Review of Ecology, Evolution and Systematics 21, 221–241.CrossRefGoogle Scholar