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dc.contributor.authorYúfera, Manueles_ES
dc.contributor.authorFernández-Díez, Cristinaes_ES
dc.contributor.authorPascual Vázquez, Emilioes_ES
dc.contributor.authorSarasquete, Carmenes_ES
dc.contributor.authorMoyano, Francisco Javieres_ES
dc.contributor.authorDíaz, M.es_ES
dc.contributor.authorAlarcón, Francisco Javieres_ES
dc.contributor.authorGarcía-Gallego, Manueles_ES
dc.contributor.authorParra-Olea, Gabrielaes_ES
dc.date.accessioned2011-12-01T11:41:15Z-
dc.date.available2011-12-01T11:41:15Z-
dc.date.issued2000-09-
dc.identifier.citationAquaculture Nutrition 6(3): 143-152 (2000)es_ES
dc.identifier.issn1353-5773-
dc.identifier.urihttp://hdl.handle.net/10261/43006-
dc.description10 páginas, 4 figuras, 2 tablas. The definitive version is available at www.blackwell-synergy.comes_ES
dc.description.abstractThe development of an inert food to replace live prey during the early stages of marine fish larvae requires research in different fields and therefore a precise work strategy. Our research on this subject has been carried out in successive steps using the gilthead seabream Sparus aurata. The first step was the design of a food particle that would be well accepted and ingested by free-swimming marine larval fish during the first developmental stages. We chose microencapsulation by polymerization of the dietary protein as the most appropriate method for making the particles; different types of microcapsules were made using a basic diet containing only the major dietary components. In the second step, our aim was to keep the larvae alive in a routine rearing system in 300-L tanks, using exclusively this kind of food, long enough to detect any changes in growth, survival, or anatomical and histological status of the larvae, in order to verify whether the technological changes were positive. The third step focused on diet formulation and searching for clues to inefficient assimilation and growth. The use of ‘in vitro’ digestibility techniques allowed us to detect the inhibitory effect of some diet ingredients on larval proteases and to determine more suitable sources of protein. We now have a microcapsule able to efficiently support growth and development of S. aurata larvae, at least during the first 2 weeks of life, although the larvae still need to feed on rotifers during the first 2–4 days of exogenous feeding. This microcapsule will make it possible to make advances in determining the specific nutritional requirements of larval fish.es_ES
dc.description.sponsorshipThis work was supported by the Comisión Interministerial de Ciencia y Tecnología, Spain (CICYT, MAR97–0924-C02–01 and MAR97–0924-C02–02).es_ES
dc.language.isoenges_ES
dc.publisherBlackwell Publishinges_ES
dc.rightsclosedAccesses_ES
dc.subjectDigestive systemes_ES
dc.subjectLarval fishes_ES
dc.subjectMicroencapsulated dietses_ES
dc.subjectProteaseses_ES
dc.subjectSparus aurataes_ES
dc.titleTowards an inert diet for first-feeding gilthead seabream Sparus aurata L. larvaees_ES
dc.typeartículoes_ES
dc.identifier.doi10.1046/j.1365-2095.2000.00110.x-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1046/j.1365-2095.2000.00110.xes_ES
dc.identifier.e-issn1365-2095-
dc.relation.csices_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeartículo-
item.cerifentitytypePublications-
item.grantfulltextnone-
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