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Space Occupation by the Polychaetous Annelid Perinereis Cultrifera: Influence of Substratum Heterogeneity and Intraspecific Interactions on Burrow Structure

Published online by Cambridge University Press:  11 May 2009

P. Scaps ,
S. Brenot ,
C. Retiere  and
G. Desrosiers
P. Scaps
Affiliation:
Laboratoire maritime, Muséum National d'Histoire Naturelle, 17, avenue George V, BP 28, 35 801 Dinard, France.
S. Brenot
Affiliation:
Laboratoire maritime, Muséum National d'Histoire Naturelle, 17, avenue George V, BP 28, 35 801 Dinard, France.
C. Retiere
Affiliation:
Laboratoire maritime, Muséum National d'Histoire Naturelle, 17, avenue George V, BP 28, 35 801 Dinard, France.
G. Desrosiers
Affiliation:
Centre d'Océanographie de Rimouski, Département d'Océanographie, Université du Québec á Rimouski, 310, allée des Urs, ulines, Rimouski (Québec), G5L 3A1, Canada.
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Extract

Spatial analysis, laboratory experiments and field observations in the intertidal zone of La Ranee Estuary (northern coast of Brittany, France) of the infaunal polychaete Perinereis cultrifera indicate that the distribution and the abundance of this species appear to be related to the availability of cobbles. Individuals build U-shaped galleries with a surface gutter network protected by a cobble which acts as a roof. The study of spatio-temporal evolution of P. cultrifera burrows showed experimentally that density is important in space-sharing modalities within the sediment. Effects of increased density lead to modifications in the shape and size of the burrows. The absence of connections between burrows, as observed in ‘sandwich aquaria’ and in resin casts, suggest that the gallery is defended against intruders. The study of the distance between individuals in the laboratory did not reveal a regular distribution pattern. These results probably mean that the area around the burrow opening is not defended and, therefore, does not constitute a territory. Perinereis cultrifera is probably competing for burrow space while food may be shared. Territoriality is certainly the main factor involved in the organization and the spatial arrangements of individuals within a population.

Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 78 , Issue 2 , May 1998 , pp. 435 - 449
Copyright
Copyright © Marine Biological Association of the United Kingdom 1998

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References

Allen, E.J. & Tood, R.A., 1900. The fauna of the Salcombe Estuary. Journal of the Marine Biological Association of the United Kingdom, 6, 150–217.CrossRefGoogle Scholar
Bertran, R., 1984. Selection du substrat et construction d'abris par le jeune homard europeéen (Homarus gammarus). Thése 3éme cycle, Université de Rennes, France.Google Scholar
Boisseau, J., 1962. Contribution la faune du bassin d'Arcachon. I. Annélides polychètes. Procès-Verbaux Société Linnéenne de Bordeaux, 99, 113–126.Google Scholar
Bridges, T.S., Farrar, J.D., Gamble, E.V. & Dillon, T.M., 1996. Intraspecific density effects in Nereis (Neanthes) arenaceodentata Moore (Polychaeta: Annelida). journal of Experimental Marine Biology and Ecology, 195, 221–235.CrossRefGoogle Scholar
Cabioch, L., L'hardy, J.P. & Rullier, F., 1968. Inventaire de la faune marine de Roscoff–Annelides. Editions de la station biologique de Roscoff.Google Scholar
Cazaux, C., 1965. Evolution de Perinereis cultrifera (Grübe) au cours d'un cycle annuel Arcachon. Proces-Verbaux Société Linnéenne de Bordeaux, 101, 1–18.Google Scholar
Cazaux, C., 1970. Recherches sur I'écologie et le développement larvaire des polychètes de la région d'Arcachon. Thèse de doctorat d'état, Université de Bordeaux, France.Google Scholar
Clark, P.J. & Evans, F.C. 1954. Distance to nearest neighbor as a measure of spatial relationships in populations. Ecology, 35, 445–453.CrossRefGoogle Scholar
Durchon, M., 1951. Les modalités de l'essaimage de Perinereis cultrifera Grübe (Annélide Polychète) à Luc-sur-mer (Calvados). Archives de Zoologie Expérimentale et de Génétique, 88, 1–6.Google Scholar
Eales, N.B., 1967. The littoral of the British Isles. Cambridge University Press.Google Scholar
Eckman, J.E., 1979. Small-scale patterns and processes in a soft-substratum intertidal community. Journal of Marine Research, 37, 437–457.Google Scholar
Esnault, G., Retière, C. & Lambert, R., 1990. Food resource partitioning in a population of Nereis diversicolor (Annelida, Polychaeta) under experimental conditions. In Trophic relationships in the marine environment (ed. M., Barnes and R.N., Gibson), pp. 453–467. Aberdeen University. Press.Google Scholar
Esselink, P. & Zwarts, L. 1989. Seasonal trend in burrow depth and tidal variation in feeding activity of Nereis diversicolor. Marine Ecology Progress Series, 56, 243–254.CrossRefGoogle Scholar
Herpin, R., 1925. Recherches biologiques sur la reproduction et le développement de quelques annélides polychètes. Bulletin de la Société de Sciences Naturelles de l'Ouest, 4, 1–250.Google Scholar
Hughes, J.E., 1996 Size-dependent, small-scale dispersion of the capitellid polychaete, Mediomastus ambiseta. Journal of Marine Research, 54, 915–937.CrossRefGoogle Scholar
Inamori, Y. & Kurihara, Y., 1979. Analysis of the environmental factors affecting the life of the brackish polychaete, Neanthes japonica (Izuka) I: the effects of the environmental factors on survival and growth. Bulletin of the Marine Biological Station of Asamushi Tohoku University, 16, 87–100.Google Scholar
Jumars, P.A. & Eckman, J.E., 1983. Spatial structure within deep-sea benthic communities. In The sea. Vol 8. (ed. G.T., Rowe), pp. 399–151. New York: John Wiley & Sons.Google Scholar
Lambert, R., 1986. Etude de la territorialité chez Nereis diversicolor; approche methodologique. Diplôme d'Etudes Approfondies, Université de Rennes I, France.Google Scholar
Lambert, R., 1988. Techniques aquariologiques appliquées à l'étude du comportement de vers marins (annélides polychétes). Bulletin de I'Institut Océanographique de Monaco, 5, 129–132.Google Scholar
Lambert, R. & Retière, C., 1987. Etude de la territorialité chez les adultes de Nereis diversicolor (annélide polychéte). Comptes Rendus de l'Académie des Sciences de Paris, 305, 643–647.Google Scholar
Levin, L.A., 1981. Dispersion, feeding behavior and competition in two spionid polychaetes. Journal of Marine Research, 39, 99–117.Google Scholar
Levin, L.A., 1982. Interference interactions among tube-dwelling polychaetes in a dense infaunal assemblage. Journal of Experimental Marine Biology and Ecology, 65, 107–119.CrossRefGoogle Scholar
Marine Biological Association, 1957. Plymouth marine fauna. Plymouth: Marine Biological Association.Google Scholar
Masson, S., 1992. Etude du régime alimentaire et des modalités d'alimentation du polychéte Nereis diversicolor (O.F. Müller), incluant un examen préliminaire du régime alimentaire du polychète Perinereis cultrifera (Grübe). Mémoire de Maîtrise, Université du Québec Rimouski, Rimouski, Québec.Google Scholar
Miron, G. & Desrosiers, G., 1990. Distributions and population structures of two intertidal estuarine polychaetes in the lower St. Lawrence Estuary with special reference to environmental factors. Marine Biology, 105, 297–306.CrossRefGoogle Scholar
Miron, G., Desrosiers, G., Retière, C. & Lambert, R., 1991a. Dispersion and prospecting behaviour of polychaete Nereis virens (Sars) as a function of density. Journal of Experimental Marine Biology and Ecology, 145, 65–77.CrossRefGoogle Scholar
Miron, G., Desrosiers, G., Retière, C. & Lambert, R., 1991b. Evolution spatio-temporelle du réseau de galeries chez le polychète Nereis virens (Sars) en relation avec la densité. Canadian Journal of Zoology, 69, 39–2.CrossRefGoogle Scholar
Olivier, M., Desrosiers, G., Caron, A., Retière, C. & Caillou, A., 1995. Réponses comportementales des polychètes Nereis diversicolor (O.F. Müller) et Nereis virens (Sars) aux stimuli d'ordre alimentaire: utilisation de la matière organique particulaire (algues et halophytes). Canadian Journal of Zoology, 73, 2307–2317.CrossRefGoogle Scholar
Pesch, C.E., Zajac, R.N., Whitlach, R.B. & Balboni, M.A., 1987. Effects of intraspecific density on life history traits and population growth of Neanthes arenaceodentata. Marine Biology, 96, 545–554.CrossRefGoogle Scholar
Reise, K., 1979. Spatial configurations generated by motile benthic polychaetes. Helgoländer Wissenschaftliche Meeresuntersuchungen, 32, 55–72.CrossRefGoogle Scholar
Retière, C. & Richoux, P., 1973. Ecologie des polychetes des lithoclases intertidales. Cahiers de Biologie Marine, 14, 39–55.Google Scholar
Scaps, P., 1995. Intraspecific agonistic behaviour in the polychaete Perinereis cultrifera (Grübe). Vie et Milieu, 45, 123–128.Google Scholar
Scaps, P., Retière, C., Desrosiers, G. & Miron, G., 1992. Dynamique d'une population de Perinereis cultrifera (Grübe) de la côte Nord Bretagne. Cahiers de Biologie Marine, 33, 477–494.Google Scholar
Scherrer, B., 1984. Biostatistique. Chicoutimi: Gaetan Morin.Google Scholar
Taghon, G.L., 1992. Effects of animal density and supply of deposited and suspended food particles on feeding, growth and small-scale distribution of two spionid polychaetes. Journal of Experimental Marine Biology and Ecology, 162, 77–95.CrossRefGoogle Scholar