Please use this identifier to cite or link to this item: https://repositorio.accefyn.org.co/handle/001/870 Cómo citar
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPáramo, Jorge-
dc.contributor.authorNúñez Ricardo, Samuel-
dc.date.accessioned2021-10-15T19:49:21Z-
dc.date.available2021-10-15T19:49:21Z-
dc.date.issued2015-09-12-
dc.identifier.urihttps://repositorio.accefyn.org.co/handle/001/870-
dc.description.abstractCon el fin de presentar información biológica de los camarones de profundidad de importancia comercial para una eventual pesquería en el mar Caribe colombiano, en el presente estudio se propuso suministrar información sobre la estructura de tallas, la talla media de madurez y la razón de sexos de los camarones de profundidad Aristaeomorpha foliacea, Pleoticus robustus y Penaeopsis serrata. Las muestras se recolectaron con pesca de arrastre en profundidades entre los 200 y los 550 m (estratos de profundidad de 100 m) en el Caribe colombiano. Se registró la longitud total, el peso total, el sexo y el número de individuos por especie en cada estación. La talla media de madurez sexual se modeló ajustando la función logística de la proporción de especímenes maduros con un intervalo de 5 mm de la longitud total. Se encontraron diferencias estadísticamente significativas en las tallas y pesos entre los sexos para las tres especies de camarones de aguas profundas, lo que reveló el dimorfismo sexual. La proporción sexual en todos los camarones de profundidad mostró diferencias significativas (p=0,000) entre el número de hembras y machos por clase de talla al compararla con una constante de referencia de 50 % de razón sexual. La relación entre la razón sexual con la talla y la distribución de la frecuencia demostró claramente una predominancia de hembras en los grupos de menor talla en A. foliacea y P. robustus. Sin embargo, en P. serrata la proporción de sexos fue igual en los grupos con las menores tallas.spa
dc.description.abstractWe present biological information of commercially important deep-sea shrimps for a potentially new fishery in the Colombian Caribbean Sea. To do so, our study aimed at providing information on the size structure, the size at sexual maturity and the sex ratio of the deep-sea shrimps Aristaeo morphafoliacea, Pleoticus robustus, Penaeopsis serrata. The samples were collected by trawling in depths ranging between 200 and 550 m (100 m strata intervals) in the Colombian Caribbean Sea. We recorded the total weight, total length, sex and number of individuals per species from each station. The size at sexual maturity was determined by adjusting the logistic function of the proportion of mature specimens to 5 mm intervals of the total length. We found statistically significant differences in size and weight between sexes for the three species, thus revealing sexual dimorphism. The sex ratio in all deep-sea shrimp showed statistically significant differences (p=0,000) between the number of females and males by size class when compared to a 50% constant reference sex ratio. The relationship between the sex ratio and the size frequency distribution clearly showed a predominance of females in the smaller size groups in P. robustus and A. foliacea. However, in P. serrata the sex ratio was equal in the smaller sizes.eng
dc.format.extent8 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isospaspa
dc.publisherAcademia Colombiana de Ciencias Exactas, Físicas y Naturalesspa
dc.rightsCreative Commons Attribution-NonCommercial-ShareAlike 4.0 Internationalspa
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/spa
dc.titleEstructura de tallas, talla media de madurez sexual y razón sexual de camarones de aguas profundas de importancia comercial en el Caribe colombianospa
dc.typeArtículo de revistaspa
dcterms.audienceEstudiantes, Profesores, Comunidad científicaspa
dcterms.referencesBaeza, J.A., Piantoni, C. 2010. Sexual system, sex ratio, and group living in the shrimp Thor amboinensis (De Man): Relevance to resource-monopolization and sex-allocation theories. Biol. Bull. 219:151-165.spa
dcterms.referencesBelcari, P., Viva, C., Mori, M., De Ranieri, S. 2003. Fishery and biology of Aristaeomorphafoliacea (Risso, 1827) (Crustacea: Decapoda) in the Northern Tyrrenien Sea (western Mediterranean). J. Northw. Atlant. Fish. Sci. 31:195-204.spa
dcterms.referencesBianchi, G. 2008. The concept of the ecosystem approach to fisheries. In: Bianchi, G., Skjoldal, H.R. (editors). The ecosystem approach to fisheries. CAB and FAO, Rome, p. 20-38.spa
dcterms.referencesBorgmann, U. 1987. Models on the slope of, and biomass flow up, the biomass size spectrum. Can J Fish Aquat Sci. 44 (2):136-140.spa
dcterms.referencesBoudreau, P. R., Dickie, L. M. 1992. Biomass spectra of aquatic ecosystems in relation to fisheries yield. Can J Fish Aquat Sci., 49 (8): 1528-1538spa
dcterms.referencesCarlucci, R., D’Onghia, G., Sion, L., Maiorano, P., Tursi, A. 2006. Selectivity parameters and size at first maturity in deep-water shrimps, Aristaeo morphafoliacea (Risso, 1827) and Aristeus antennatus (Risso, 1816), from the North-Western Ionian Sea (Mediterranean Sea). Dev. Hydrobiol. 184: 145-154.spa
dcterms.referencesCalder, W. 2001. Ecological consequences of body size. Encyclopedia of life sciences, John Wiley & Sons Ltd., Chichester. DOI: 10.1038/npg.els.0003208spa
dcterms.referencesCompany J.B., Sarda, F. 1997. Reproductive patterns and populations characteristics of five deep water pandalid shrimps in the western Mediterranean along a depth gradient (150-1100 m). Mar. Ecol. P.S. 148: 49-58.spa
dcterms.referencesCharnov, E.L., Gotshall, D.W., Robinson, J.G. 1978. Sex ratio: Adaptive adjustments to population fluctuations in pandalid shrimp. Science, 200: 204-206.spa
dcterms.referencesCharnov, E. L. & Hannah, R.W. 2002. Shrimp adjust their sex ratio to fluctuating age distributions. Evolutionary Ecology Research. 4: 239-246.spa
dcterms.referencesChiba, S., Yoshino, K., Kanaiwa, M. Kawajiri, T., Goshima, S. 2006. Maladaptive sex ratio adjustment by e sex changing shrimp in selective fishing environments. Journal of Animal Ecology. 82: 632-641.spa
dcterms.referencesChiba, S., Yoshino, K., Kanaiwa, M. Kawajiri, T., Goshima, S. 2006. Maladaptive sex ratio adjustment by e sex changing shrimp in selective fishing environments. Journal of Animal Ecology. 82: 632-641.spa
dcterms.referencesDallagnolo, R., Pérez, J.A.A., Pezzuto, P.R., Wahrlich, R. 2009. The deep-sea shrimp fishery off Brazil (Decapoda: Aristeidae) development and present status. Lat. Am. J. Aquat. Res. 37 (3): 327-346.spa
dcterms.referencesD’onghia, G., Tursi, A., Maiorano, P., Panza, M. 1998. Distribution, biology, and population dynamics of Aristaeo morphafoliacea (Risso, 1827) (Decapoda, Natantia, Aristeidae) in the north-western Ionian Sea (Mediterranean Sea). Crustaceana. 71: 518-544spa
dcterms.referencesFigueiredo, M.J., Figueiredo, I., Machado, P.B. 2001. Deep-water penaeid shrimps (Crustacea: Decapoda) from off the Portuguese continental slope: An alternative future resource? Fish. Res. 51: 321-326.spa
dcterms.referencesGracia A., Vázquez-Bader A.R., Lozano-Álvarez E., Briones-Fourzán, P. 2010. Deep-water shrimp (Crustacea: Penaeoidea) off the Yucatan peninsula (southern Gulf of Mexico): A potential fi shing resource. J. Shellfish Res. 29: 37-43.spa
dcterms.referencesGotelli, N.J., Ellison, A.M. 2004. A primer of ecological statistics. Sinauer Associates. Sunderland, MA.spa
dcterms.referencesGrabowsky, R., Morilhas-Simoes, S., Castilho, A. 2014. Population structure, sex ratio and growth of the seabob shrimp Xiphopenaeus kroyeri (Decapoda, Penaeidae) from coastal waters of southern Brazil. ZooKeys. 457: 253-269spa
dcterms.referencesHaedrich, R.L. & Barnes, S.M. 1997. Ecological consequences of body size. Fish Res. 31: 229-239.spa
dcterms.referencesHolthuis, L.B. 1980. Shrimps and prawns of the world. An annotated catalogue of species of interest to fisheries. (FAO Species Catalogue, 1). FAO Fisheries Synopsis. 125 (1): 1-271.spa
dcterms.referencesJennings, S. & Dulvy, N.K. 2005. Reference points and reference directions for size-based indicators of community structure. ICES J. Mar. Sci. 62: 397-404.spa
dcterms.referencesKapiris, K. & Thessalou-Legaki, M. 2009. Comparative reproduction aspects of the deep-water shrimps Aristaeo morphafoliacea and Aristeus antennatus (Decapoda, Aristeidae) in the Greek Ionian Sea (Eastern Mediterranean). International Journal of Zoology. Article ID 979512, 9 pages. http://dx.doi.org/10.1155/2009/979512spa
dcterms.referencesKing, M. 2007. Fisheries Biology, Assessment and Management. Wiley-Blackwell. Oxford, UK. 400 p.spa
dcterms.referencesKing, M. 1984. The species and depth distribution of deep water Caridean shrimps (Decapoda, Caridea) near some southwest Pacific Islands. Crustaceana. 47 (2): 174-191.spa
dcterms.referencesKoeller, P., Mohn, R., Etter, M. 2000. Density dependant sex change in Northern shrimp Pandalus borealis on the Scotian Shelf. J. Northw. Atl. Fish. Sci. 27: 107-118.spa
dcterms.referencesLizárraga-Cubedo, H.A., Pierce, GJ., Santos, M.B. 2008. Reproduction of crustaceans in relation to fisheries: 169-222 (en) MENTE, E. (editor) Reproductive biology of crustaceans. Science Publishers, Enfield. 565 pspa
dcterms.referencesLevi, D. & Vacchi, M. 1988. Macroscopic scale for simple and rapid determination of sexual maturity in Aristaeo morphafoliacea (Risso, 1826) (Decapoda: Penaeidae). J Crustacean Biol. 8: 532-538.spa
dcterms.referencesMytilineou, S., Kavadas, C., Politou, Y., Kapiris, K.,Tursi, A., Maiorano, P. 2006. Catch composition on red shrimps’ (Aristaeomorpha foliacea and Aristeus antennatus) grounds in the Eastern Ionian Sea. Dev. Hydrobiol. 184: 155-160.spa
dcterms.referencesMouffok, S., Massuti, E., Boutiba, Z., Guijarro, B., Ordines, F., Fliti, K. 2008. Ecology and fishery of the deep-water shrimp, Aristeus antennatus (Risso, 1816) off Algeria (South-western Mediterranean). Crustaceana. 81 (10): 1177-1199.spa
dcterms.referencesMura, M., Murenu, M., Cau, A. 2002. The occurrence of Penaeopsis serrata Bate 1881 (Decapoda, Penaeidae) in the Middle-West Mediterranean Sea. Crustaceana. 75 (10): 1263-1269.spa
dcterms.referencesPapaconstantinou, C. & Kapiris, K. 2003. The biology of the giant red shrimp (Aristaeomorpha foliacea) at an unexploited fishing ground in the Greek Ionian Sea. Fish. Res., 62: 37-51.spa
dcterms.referencesParamo, J. 2011. Deep-sea fishery in the Colombian Caribbean Sea: Management and conservation strategies for an ecosystem approach to fisheries. PhD Thesis. Universität Bremen, Alemania. 141 p.spa
dcterms.referencesParamo, J., Saint-Paul, U., Moreno, F., Pacheco, M., Almanza, M., Rodríguez, E., Ardila, G., Borda, C., Barreto, C., González, H. 2011. Crustáceos de profundidad en el Caribe colombiano como nuevo recurso pesquero. Informe final. ISBN: 9789584485236. 26 p.spa
dcterms.referencesParamo, J. & Saint-Paul, U. 2012a. Deep-sea shrimps Aristaeomorpha foliacea and Pleoticus robustus (Crustacea: Penaeoidea) in the Colombian Caribbean Sea as a new potential fishing resource. J. Mar. Biol. Ass. U.K. 92 (4): 811-818.spa
dcterms.referencesParamo, J. & Saint-Paul, U. 2012b. Spatial structure of the pink speckled deep-sea shrimp Penaeopsis serrata (Bate, 1881) (Decapoda, Penaeidae) during November-December 2009 in the Colombian Caribbean Sea. Crustaceana. 85 (1): 103-116.spa
dcterms.referencesParamo, J. & Saint-Paul, U. 2012c. Spatial structure of deep sea lobster (Metanephrops binghami) in the Colombian Caribbean Sea. Helg. Mar. Res. 66: 25-31.spa
dcterms.referencesPérez-Farfante, I. 1980. Review of the penaeid shrimp genus Penaeopsis (Crustacea: Decapoda). Fish. Bull., U.S. 77 (4): 721-763.spa
dcterms.referencesPezzuto, R., Pérez, J.A.A., Wahrlich, R. 2006. Deep-sea shrimps (Decapoda: Aristeidae): New targets of the deep-water trawling fishery in Brazil. Braz. J. Oceanog. 54: 123-134.spa
dcterms.referencesPolitou, Ch-Y., Kapiris, K., Maiorano, P., Capezzuto, F., Dokos, J. 2004. Deep-sea Mediterranean biology: The case of Aristaeomorpha foliacea (Risso, 1827) (Crustacea: Decapoda: Aristidae). Sci. Mar. 68 (3): 129-139.spa
dcterms.referencesPongtippatee, P., Laburee, K., Thaweethamsewee, P., Hiranphan, R., Asuvapongpatana, S., Weerachatyanukul, W., Srisawat, T., Withayachumnarnkul, B. 2012. Triploid Penaeus monodon: Sex ratio and growth rate. Aquaculture. 356-357: 7-13.spa
dcterms.referencesRagonese, S., Bertolino, F., Branchini, M.L. 1997. Biometric relationships of the red shrimp, Aristaeomorpha foliacea Risso 1827, in the Strait of Sicily (Mediterranean Sea). Sci. Mar. 61 (3): 367-377.spa
dcterms.referencesRagonese, S., Branchini, M.L., Di Stefano, L. 2002. Trawl cod-end selectivity for deepwater red shrimp (Aristoaeomorphafoliacea, Risso 1827) in the strait of Sicily (Mediterranean Sea). Fish. Res. 57: 131-144.spa
dcterms.referencesRochet M.J. & Trenkel, V. 2003. Which community indicators can measure the impact of fishing? A review and proposals. Can. J. Fish. Aquat. Sci. 60: 86-99.spa
dcterms.referencesRice, J. 2003. Environmental health indicators. Ocean. Coast. Manag. 46 (3): 235-259.spa
dcterms.referencesShin, Y.J., Rochet, M.J., Jennings, S., Field, J.G. Gislason, H. 2005. Using size-based indicators to evaluate the ecosystem effects of fishing. ICES J. Mar. Sci. 62: 384-396.spa
dcterms.referencesSiegel, V., Damm, U., Neudecker, T. 2008. Sex-ratio, seasonality and long-term variation in maturation and spawning of the brown shrimp Crangon crangon (L.) in the German Bight (North Sea). Helgol. Mar. Res. 62 (4): 339-349.spa
dcterms.referencesTavares, M. 2002. Shrimps: 251-291 (en) CARPENTER, K. E. (editor) The living marine resources of the western central Atlantic, species identification guide for fisheries purposes. FAO, Rome. 600 p.spa
dcterms.referencesYemane, D., Field, J.G., Leslie, R.W. 2008. Indicators of change in the size structure of fish communities: A case study from the south coast of South Africa. Fish. Res. 93: 163-172.spa
dcterms.referencesWenner, A.M. 1972. Sex ratio as a function of size in marine Crustacea. Amer. Naturalist. 106: 321-351.spa
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessspa
dc.type.driverinfo:eu-repo/semantics/articlespa
dc.type.versioninfo:eu-repo/semantics/publishedVersionspa
dc.rights.creativecommonsAtribución-NoComercial 4.0 Internacional (CC BY-NC 4.0)spa
dc.identifier.doihttps://doi.org/10.18257/raccefyn.242-
dc.subject.proposalEstructura de tallasspa
dc.subject.proposalSize structureeng
dc.subject.proposalRazón sexualspa
dc.subject.proposalSex ratioeng
dc.subject.proposalTalla media de madurezspa
dc.subject.proposalSize at 50% maturityeng
dc.subject.proposalCamarones de aguas profundasspa
dc.subject.proposalDeep-sea shrimpseng
dc.subject.proposalCaribe colombianospa
dc.subject.proposalColombian Caribbeaneng
dc.type.coarhttp://purl.org/coar/resource_type/c_6501spa
dc.relation.ispartofjournalRevista de la Academia Colombiana de Ciencias Exactas, Físicas y Naturalesspa
dc.relation.citationvolume39spa
dc.relation.citationstartpage408spa
dc.relation.citationendpage415spa
dc.publisher.placeBogotá, Colombiaspa
dc.contributor.corporatenameAcademia Colombiana de Ciencias Exactas,Físicas y Naturalesspa
dc.contributor.corporatenameCiencia y Tecnología Pesquera Tropical” (CITEPT), Santa Marta, Colombiaspa
dc.contributor.corporatenamePrograma de Biología, Universidad del Magdalenaspa
dc.coverage.regionCaribe Colombiano-
dc.relation.citationissue152spa
dc.type.contentDataPaperspa
dc.type.redcolhttp://purl.org/redcol/resource_type/ARTspa
oaire.accessrightshttp://purl.org/coar/access_right/c_abf2spa
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
Appears in Collections:BA. Revista de la Academia Colombiana de Ciencias Exactas Físicas y Naturales

Files in This Item:
File Description SizeFormat 
11. Estructura de tallas, talla media de madurez sexual.pdfCiencias naturales2.2 MBAdobe PDFThumbnail
View/Open


This item is licensed under a Creative Commons License Creative Commons