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Seasonal density and distribution of Octopus tehuelchus in the intertidal of North Patagonia

Published online by Cambridge University Press:  17 April 2013

Lorena P. Storero ,
Maite A. Narvarte  and
Raúl A. González
Lorena P. Storero*
Affiliation:
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina Instituto de Biología Marina y Pesquera Almirante Storni (IBMPAS)/Escuela Superior de Ciencias Marinas (ESCiMar), Universidad Nacional del Comahue, San Antonio Oeste, Argentina
Maite A. Narvarte
Affiliation:
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina Instituto de Biología Marina y Pesquera Almirante Storni (IBMPAS)/Escuela Superior de Ciencias Marinas (ESCiMar), Universidad Nacional del Comahue, San Antonio Oeste, Argentina
Raúl A. González
Affiliation:
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina Instituto de Biología Marina y Pesquera Almirante Storni (IBMPAS)/Escuela Superior de Ciencias Marinas (ESCiMar), Universidad Nacional del Comahue, San Antonio Oeste, Argentina
*
Correspondence should be addressed to: Lorena P. Storero, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina email: lorestorero@gmail.com
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Abstract

The abundance and distribution of coastal cephalopods are strongly influenced by the environmental conditions. This study evaluates the seasonal distribution and density of Octopus tehuelchus in three intertidal environments of San Matías Gulf (Patagonia). To estimate and compare density and distribution, monthly transects were carried out, and analysed in relation to the coastlines obtained with satellite images. Densities of O. tehuelchus ranged between 0 and 34 individuals per transect (0–0.11 octopus m−2), and varied between sites. Islote Lobos (IL) had the highest densities (mean octopus per transect 7.32 ± 1.16) followed by El Fuerte (EF) (5.55 ± 0.94) and San Antonio Bay (SAB) (3.40 ± 0.85). Within each site, octopus densities varied between seasons. The highest densities were observed during warm months (SAB = 5.96, EF = 9.52, IL = 14.15) and the lowest during cold ones (SAB = 1.45, EF = 2.6, IL = 3.32). Octopus tehuelchus showed an aggregated spatial distribution, and the nearest neighbour value varied between 0.21 and 0.83 in SAB, 0.27 and 0.78 in EF and 0.23 and 0.53 in IL. Considering the coast lines, the distribution pattern along the intertidal varied seasonally. During warm months this species is widely distributed throughout the intertidal, from the low-tide line to 300 m (in SAB), 500 m (in EL) and 200 m (in IL). On the contrary, during cold months most individuals were found near the low-tide line. These results may be associated with the availability of shelter in the intertidal and the activity and physiology of this species.

Keywords

densitydistributionOctopus tehuelchusPatagonia
Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 93 , Issue 7 , November 2013 , pp. 1895 - 1901
Copyright
Copyright © Marine Biological Association of the United Kingdom 2013 

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References

REFERENCES

Anderson, T.J. (1997) Habitat selection and shelter use by Octopus tetricus. Marine Ecology Progress Series 150, 137–148.CrossRefGoogle Scholar
Anderson, R.C., Hughes, P.D., Mather, J.A. and Steele, C.W. (1999) Determination of the diet of Octopus rubescens Berry, 1953 (Cephalopoda: Octopodidade), through examination of its beer bottle dens in Puget Sound. Malacologia 41, 455–460.Google Scholar
Begon, M., Townsend, C.R. and Harper, J.L. (2006) Ecology: from individuals to ecosystems. Oxford: Blackwell Publishing.Google Scholar
Bellido, J.M., Pierce, G.J. and Wang, J. (2001) Modelling intra-annual variation in abundance of squid Loligo forbesi in Scottish waters using generalised additive models. Fisheries Research 52, 23–39.CrossRefGoogle Scholar
Clarke, P.J. and Evans, F.C. (1954) Distance to nearest neighbour as a measure of spatial relationship in populations. Ecology 35, 445–453.CrossRefGoogle Scholar
Denis, V., Lejeune, J. and Robin, J.P. (2002) Spatio-temporal analysis of commercial trawler data using general additive models: patterns of loliginid squid abundance in the north-east Atlantic. ICES Journal of Marine Science 59, 633–648.CrossRefGoogle Scholar
Guerra, A. (1981) Spatial distribution pattern of Octopus vulgaris. Journal of Zoology 195, 133–146.CrossRefGoogle Scholar
INPE Brasil (2010) http://www.inpe.br/ (accessed 9 March 2013).Google Scholar
Iribarne, O.O. (1990) The ecology and harvest of the small Patagonian octopus, Octopus tehuelchus (d'Orbigny). MSc thesis. University of Washington, USA.CrossRefGoogle Scholar
Iribarne, O.O. (1991a) Intertidal harvest of the Patagonian octopus, Octopus tehuelchus (d'Orbigny). Fisheries Research 12, 375–390.CrossRefGoogle Scholar
Iribarne, O.O. (1991b) Life history and distribution of the small south-western Atlantic octopus, Octopus tehuelchus. Journal of Zoology 223, 549–565.CrossRefGoogle Scholar
Katsanevakis, S. and Verriopoulos, G. (2004) Abundance of Octopus vulgaris on soft sediments. Scientia Marina 68, 553–560.CrossRefGoogle Scholar
Laughlin, R.A. and Livingston, R.J. (1982) Environmental and trophic determinants of the spatial/temporal distribution of the brief squid (Lolliguncula brevis) in the Appalachicola estuary (North Florida, USA). Bulletin of Marine Science 32, 489–497.Google Scholar
Leite, T.S., Haimovici, M., Mather, J. and Lins Oliveira, J.E. (2009) Habitat, distribution, and abundance of the commercial octopus (Octopus insularis) in a tropical oceanic island, Brazil: information for management of an artisanal fishery inside a marine protected area. Fisheries Research 98, 85–91.CrossRefGoogle Scholar
Mather, J.A. (1982a) Factors affecting the spatial distribution of natural populations of Octopus joubini Robson. Animal Behaviour 30, 1166–1170.CrossRefGoogle Scholar
Mather, J.A. (1982b) Choice and competition: their effects on occupancy of shell homes by Octopus joubini. Marine Behaviour and Physiology 8, 285–293.CrossRefGoogle Scholar
Millán, D. (2007) Anuario de estadísticas pesqueras de la provincia de Río Negro. [Statistical yearbook of fisheries in Río Negro Province] San Antonio Oeste, Argentina: Departamento Policía de Pesca Dirección de Pesca, Technical Report 2007.Google Scholar
Morgan, S.G. (1996) Plasticity in reproductive timing by crabs in adjacent tidal regimes. Marine Ecology Progress Series 139, 105–118.CrossRefGoogle Scholar
Narvarte, M.A., González, R. and Sica, M.I. (1996) Estado actual de la pesquería del pulpito patagónico Octopus tehuelchus en el Golfo San Matías. Plan de Manejo Integrado de la Zona Costera Patagónica. GEF/PNUD-WCS/FPN. Technical Report No. 19.Google Scholar
Narvarte, M., González, R. and Fernández, M. (2006) Comparison of Tehuelche octopus (Octopus tehuelchus) abundance between an open-access fishing ground and a marine protected area: evidence from a direct development species. Fisheries Research 79, 112–119.CrossRefGoogle Scholar
Norse, E.A. and Crowder, L.B. (2005) Marine conservation biology: the science of maintaining the sea's biodiversity. Washington, DC: Island Press.Google Scholar
Oosthuizen, A. and Smale, M.J. (2003) Population biology of Octopus vulgaris on the temperate south-eastern coast of South Africa. Journal of the Marine Biological Association of the United Kingdom 83, 535–541.CrossRefGoogle Scholar
Osovnikar, P.F., González, R.A. and Narvarte, M.A. (2006) Potencial de los refugios artificiales para el mejoramiento de los stocks de pulpito Octopus tehuelchus en Patagonia. In Salas, S., Cabrera, M.A., Ramos, J., Flores, D. and Sánchez, J. (eds) Memorias Primera Conferencia de Pesquerías Costeras en América Latina y el Caribe. Evaluando, Manejando y Balanceando Acciones. Mérida, México, pp. 107–121.Google Scholar
Pierce, G.J., Bailey, N., Stratoudakis, Y. and Newton, A. (1998) Distribution and abundance of the fished population of Loligo forbesi in Scottish waters: analysis of research cruise data. ICES Journal of Marine Science 55, 14–33.CrossRefGoogle Scholar
Pierce, G.J., Valavanis, V.D., Guerra, A., Jereb, P., Orsi-Relini, L., Bellido, J.M., Katara, I., Piatkowski, U., Pereira, J., Balguerias, E., Sobrino, I., Lefkaditou, E., Wang, J., Santurtun, M., Boyle, P.R., Hastie, L.C., MacLeod, C.D., Smith, J., Viana, M., González, A.F. and Zuur, A.F. (2008) A review of cephalopod–environment interactions in European Seas. Hydrobiologia 612, 49–70.CrossRefGoogle Scholar
Ré, M.E. and Gómez-Simes, E. (1992) Hábitos alimentarios del pulpo (Octopus tehuelchus). Análisis cuali-cuantitativos de la dieta en el intermareal de Puerto Lobos, Golfo San Matías (Argentina). Frente Marítimo 11, 119–128.Google Scholar
Sacau, M., Pierce, G.J., Wang, J., Arkhipkin, A.I., Portela, J., Brickle, P., Santos, M.B., Zuur, A.F. and Cardoso, X. (2005) The spatio-temporal pattern of Argentina shortfin squid Illex argentinus abundance in the southwest Atlantic. Aquatic Living Resources 18, 361–372.CrossRefGoogle Scholar
Scheel, D. (2002) Characteristics of habitats used by Enteroctopus dofleini in Prince William Sound and Cook Inlet, Alaska. Marine Ecology 23, 185–206.CrossRefGoogle Scholar
Scheel, D., Lauster, A. and Vincent, T.L.S. (2007) Habitat ecology of Enteroctopus dofleini from middens and live prey surveys in Prince William Sound, AK. In Landman, N.H. (ed.) Cephalopods present and past: new insights and fresh perspectives. New York: Springer, pp. 434–458.CrossRefGoogle Scholar
Servicio de Hidrografía Naval (2007) http://www.hidro.gov.ar/ (accessed 9 March 2013).Google Scholar
Storero, L.P. (2010) Características ecológicas del pulpito, Octopus tehuelchus, en tres ambientes del Golfo San Matías. Doctoral thesis. Universidad Nacional de Córdoba, Argentina.Google Scholar
Storero, L.P., Ocampo-Reinaldo, M., González, R.A. and Narvarte, M.A. (2010) Growth and life span of the small octopus Octopus tehuelchus in San Matías Gulf (Patagonia): three decades of study. Marine Biology 157, 555–564.CrossRefGoogle Scholar
Storero, L.P., Narvarte, M.A. and González, R.A. (2012) Reproductive traits of the small Patagonian octopus Octopus tehuelchus. Helgoland Marine Research 66, 651–659.CrossRefGoogle Scholar
Storero, L.P., Narvarte, M.A. and González, R.A. (2013) Marine Protected Areas: reserve effect or natural variability? The Patagonian octopus case. Journal of the Marine Biological Association of the United Kingdom 93, 259–266.CrossRefGoogle Scholar
Waluda, C.M., Rodhouse, P.G., Trethan, P.N. and Pierce, G.J. (2001) Remotely sensed mesoscale oceanography and the distribution of Illex argentinus in the South Atlantic. Fisheries Oceanography 10, 207–216.CrossRefGoogle Scholar
Wang, J., Pierce, G.J., Boyle, P.R., Denis, V., Robin, J.P. and Bellido, J.M. (2003) Spatial and temporal patterns of cuttlefish (Sepia officinalis) abundance and environmental influences—a case study using trawl fishery data in French Atlantic coastal, English Channel, and adjacent waters. ICES Journal of Marine Science 60, 1149–1158.CrossRefGoogle Scholar