dc.creatorMacCord F.S.
dc.creatorAmaral A.C.Z.
dc.date2005
dc.date2015-06-26T14:06:14Z
dc.date2015-11-26T15:40:10Z
dc.date2015-06-26T14:06:14Z
dc.date2015-11-26T15:40:10Z
dc.date.accessioned2018-03-28T22:48:40Z
dc.date.available2018-03-28T22:48:40Z
dc.identifier
dc.identifierJournal Of The Marine Biological Association Of The United Kingdom. , v. 85, n. 4, p. 829 - 834, 2005.
dc.identifier253154
dc.identifier10.1017/S002531540501177X
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-22944491462&partnerID=40&md5=c5170f39d2e78d3cb5c75019bb59462b
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/93083
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/93083
dc.identifier2-s2.0-22944491462
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1264314
dc.descriptionSeven hundred and six specimens of Scolelepis cf. chilensis and 551 specimens of Scolelepis goodbodyi were analysed. Individuals of each species were classified according to sex (male, female, and immature individuals). Width (w) and height (h) of setigers 3 and 5, the position of the first and the last gametogenic setigers, the total number of setigers, and the total length of each worm were measured. The area and volume of the setigers were estimated. Discriminant analysis was used to determine whether there were sexually dimorphic features, apart from the presence of gametes. Linear regression analysis was used to evaluate the relationship between each parameter and the number of setigers. Scolelepis cf. chilensis was found to be significantly larger than S. goodbodyi (t=21.71 and t=36.44, P<0.05 for length and number of setigers, respectively). These species also differed in the position of the first gametogenic setiger, which averaged 27 (SD=3) in S. cf. chilensis and 22 (SD=1) in S. goodbodyi (t= 29.18, P<0.05). There were no sexually dimorphic features in either sex of S. cf. chilensis (Wilks' lambda=0.9675, P>0.05, eigenvalue=0.034) or S. goodbodyi (Wilks' lambda=0.8429, P>0.05, eigenvalue=0.186). The total length showed the strongest correlation with the number of setigers in both species (r2=0.887 and 0.850 for S. cf. chilensis and S. goodbodyi, respectively), followed by the width and the volume of setigers.
dc.description85
dc.description4
dc.description829
dc.description834
dc.descriptionAmaral, A.C.Z., Morgado, E.H., Salvador, L.B., Poliquetas bioindicadores de poluição orgânica em praias paulistas (1998) Revista Brasileira de Biologia, 58, pp. 307-316
dc.descriptionAmbrogi, R., Secondary production of Prionospio caspersi (Annelida: Polychaeta: Spionidae) (1990) Marine Biology, 104, pp. 437-442
dc.descriptionAmbrogi, R., Fontana, P., Riccobene, P., Population dynamics and secondary production of the spionid polychaete Prionospio caspersi in front of the Po River Delta (1993) Vie et Milieu, 43, pp. 165-172
dc.descriptionAnderson, R.O., A modified flotation technique for sorting bottom fauna samples (1959) Limnology and Oceanography, 4, pp. 223-225
dc.descriptionBlake, J.A., Life history analysis of five dominant infaunal polychaete species from the continental slope off North Carolina (1993) Journal of the Marine Biological Association of the United Kingdom, 73, pp. 123-141
dc.descriptionBlake, J.A., Family Spionidae Grube, 1850 (1996) The Annelida. Part 3. Vol. 6. Polychaeta: Orbiniidae to Cossuridae, 6, pp. 81-224. , ed. J.A. Blake et al., Santa Barbara: Santa Barbara Museum of Natural History
dc.descriptionBridges, T.S., Reproductive investment in four developmental morphs of Streblospio benedicti (Polychaeta: Spionidae) (1993) Biological Bulletin. Marine Biological Laboratory, Woods Hole, 184, pp. 144-152
dc.descriptionBridges, T.S., Levin, L.A., Cabrera, D., Plaia, G., Effects of sediment amended with sewage, algae, or hydrocarbons on growth and reproduction in two opportunistic polychaetes (1994) Journal of Experimental Marine Biology and Ecology, 177, pp. 99-119
dc.descriptionDesrosiers, G., Vincent, B., Retière, C., Boucher, L., Comparison de critères utilisables pour l'étude de la structure des populations du polychète Nereis virens (Sars) (1988) Canadian Journal of Zoology, 66, pp. 1454-1459
dc.descriptionFauchald, K., A morphometric study of eunicid polychaetes from Belize, Western Caribbean Sea (1991) Ophelia, Supplement, 5, pp. 47-53
dc.descriptionGlasby, C.J., Population structure and reproductive biology of Ceratonereis limnetica (Polychaeta: Nereididae) at Lower Portland, Hawkesbury River, Australia (1986) Marine Biology, 90, pp. 589-595
dc.descriptionGould, S.J., Allometry and size in ontogeny and phylogeny (1966) Biological Reviews, 41, pp. 587-640
dc.descriptionGrassle, J.F., Grassle, J.G., Opportunistic life histories and genetic systems in marine benthic polychaetes (1974) Journal of Marine Research, 32, pp. 253-284
dc.descriptionGudmundsson, H., Life history patterns of polychaete species of the family Spionidae (1985) Journal of the Marine Biological Association of the United Kingdom, 65, pp. 93-111
dc.descriptionHsieh, H.L., Larval development and substrate preference at settlement in Pseudopolydora diopatra (Polychaeta: Spionidae) (1994) Invertebrate Reproduction and Development, 25, pp. 205-214
dc.descriptionKnox, C.A., The role of polychaetes in benthic soft-bottom communities (1977) Essays on Polychaetous Annelids in Memory of Dr. Olga Hartman, pp. 547-604. , ed. D.J. Reish and K. Fauchauld, Los Angeles: Allan Hancock Foundation
dc.descriptionLardicci, C., Ceccherelli, G., Rossi, F., Streblospio shrubsolii (Polychaeta: Spionidae): Temporal fluctuations in size and reproductive activity (1997) Cahiers de Biologie Marine, 38, pp. 207-214
dc.descriptionLevin, L.A., Effects of enrichment on reproduction in the opportunistic polychaete Streblospio benedicti (Webster): A mesocosm study (1986) Biological Bulletin. Marine Biological Laboratory, Woods Hole, 171, pp. 143-160
dc.descriptionLevin, L.A., Huggett, D.V., Implications of alternative reproductive modes for seasonality and demography in an estuarine polychaete (1990) Ecology, 71, pp. 2191-2208
dc.descriptionLewis, J.B., Reproduction, larval development and functional relationships of the burrowing, spionid polychaete Dipolydora armata with the calcareous hydrozoan Millepora complanata (1998) Marine Biology, 130, pp. 651-662
dc.descriptionManly, B.F.J., (1998) Multivariate Statistical Methods: A Primer, 2nd Edn., , London: Chapman & Hall
dc.descriptionMarsh, A.G., Tenore, K.R., The role of nutrition in regulating the population dynamics of opportunistic, surface deposit feeders in a mesohaline community (1990) Limnology and Oceanography, 35, pp. 710-724
dc.descriptionMartin, D., Grémare, A., Secondary production of Capitella sp. (Polychaeta: Capitellidae) inhabiting different organically enriched environments (1997) Scientia Marina, 61, pp. 99-109
dc.descriptionMéndez, N., Romero, J., Flos, J., Population dynamics and production of the polychaete Capitella capitata in the littoral zone of Barcelona (Spain, NW Mediterranean) (1997) Journal of Experimental Marine Biology and Ecology, 218, pp. 263-284
dc.descriptionOmena, E.P., Amaral, A.C.Z., Population dynamics and secondary production of Laeonereis acuta (Treadwell, 1923) (Nereididae: Polychaeta) (2000) Bulletin of Marine Science, 67, pp. 421-431
dc.descriptionOmena, E.P., Amaral, A.C.Z., Morphometric study of the nereidid Laeonereis acuta (Annelida: Polychaeta) (2001) Journal of the Marine Biological Association of the United Kingdom, 81, pp. 423-426
dc.descriptionRichards, S.L., Spawning and reproductive morphology of Scolelepis squamata (Spionidae: Polychaeta) (1970) Canadian Journal of Zoology, 48, pp. 1369-1379
dc.descriptionSantos, P.J.P., Morphodynamical influence of a temporary freshwater stream on the population dynamics of Scolelepis gaucha (Polychaeta: Spionidae) on a sandy beach in southern Brazil (1991) Bulletin of Marine Science, 48, pp. 657-664
dc.descriptionSantos, P.J.P., Population dynamics and production of Scolelepis gaucha (Polychaeta: Spionidae) on the sandy beaches of southern Brazil (1994) Marine Ecology Progress Series, 110, pp. 159-165
dc.descriptionSardá, R., Martin, D., Populations of Streblospio (Polychaeta: Spionidae) in temperate zones: demography and production (1993) Journal of the Marine Biological Association of the United Kingdom, 73, pp. 769-784
dc.descriptionSeitz, R.D., Schaffner, L.C., Population ecology and secondary production of the polychaete Loimia medusa (Terebellidae) (1995) Marine Biology, 121, pp. 701-711
dc.descriptionShimizu, R.M., (1997) Ecologia Populacional de Scolelepis Squamata (Müller, 1806) (Polychaeta: Spionidae) e Callichirus Major (Say, 1818) (Crustacea: Decapoda: Thalassinidae) Da Praia de Barequeçaba (São Sebastião, SP), , PhD thesis, University of São Paulo, São Paulo, Brazil
dc.descriptionSouza, J.R.B., Borzone, C.A., Population dynamics and secondary production of Scolelepis squamata (Polychaeta: Spionidae) in an exposed sandy beach, southern Brazil (2000) Bulletin of Marine Science, 67, pp. 221-233
dc.descriptionSteimle, F.W., Kinner, P., Howe, S., Leathem, W., Polychaete population dynamics and production in the New York Bight associated with variable levels of sediment contamination (1990) Ophelia, 31, pp. 105-123
dc.descriptionTeissier, G., Relative growth (1960) The Physiology of Crustacea, 1, pp. 537-560. , ed. T.H. Waterman, New York: Academic Press
dc.descriptionVázquez, F.C., Rojas, D.A., Estimación de la producción secundaria de Paraprionospio pinnata (Spionidae, Polychaeta) frente a Bahía de Concepción, Chile (1980) Boletim Do Instituto Oceanográfico, São Paulo, 29, pp. 79-82
dc.descriptionWarwick, R.M., Price, R., Macrofauna production in an estuarine mudflat (1975) Journal of the Marine Biological Association of the United Kingdom, 55, pp. 1-18
dc.descriptionWarwick, R.M., George, C.L., Davies, J.R., Annual macrofauna production in a Venus community (1978) Estuarine and Coastal Marine Science, 7, pp. 215-241
dc.descriptionWilliams, J.D., Reproduction and larval development of Polydora robi (Polychaeta: Spionidae), an obligate commensal of hermit crabs from the Philippines (2001) Invertebrate Biology, 120, pp. 237-247
dc.descriptionWilson, W.H., Sexual reproductive modes in polychaetes: Classification and diversity (1991) Bulletin of Marine Science, 48, pp. 500-516
dc.descriptionYokoyama, H., Effects of temperature on the feeding activity and growth rate of the spionid polychaete Paraprionospio sp. (form A) (1988) Journal of Experimental Marine Biology and Ecology, 123, pp. 41-60
dc.descriptionZajac, R.N., Population ecology of Polydora ligni (Polychaeta: Spionidae). I. Seasonal variation in population characteristics and reproductive activity (1991) Marine Ecology Progress Series, 77, pp. 197-206
dc.descriptionZajac, R.N., Population ecology of Polydora ligni (Polychaeta: Spionidae). II. Seasonal demographic variation and its potential impact on life history evolution (1991) Marine Ecology Progress Series, 77, pp. 207-220
dc.descriptionZettler, M.L., Population dynamics, growth and production of the neozoon Marenzelleria cf. viridis (Verril, 1873) (Polychaeta: Spionidae) in a coastal water of the southern Baltic Sea (1997) Aquatic Ecology, 31, pp. 177-186
dc.languageen
dc.publisher
dc.relationJournal of the Marine Biological Association of the United Kingdom
dc.rightsfechado
dc.sourceScopus
dc.titleMorphometric Analyses Of Two Species Of Scolelepis (polychaeta: Spionidae)
dc.typeArtículos de revistas


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