Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/25451
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dc.contributor.authorPochelon, Patricia N.pt_PT
dc.contributor.authorda Silva, Teresa Lopespt_PT
dc.contributor.authorReis, Albertopt_PT
dc.contributor.authordos Santos, Antoninapt_PT
dc.contributor.authorQueiroga, Henriquept_PT
dc.contributor.authorCalado, Ricardopt_PT
dc.date.accessioned2019-02-27T16:12:51Z-
dc.date.available2019-02-27T16:12:51Z-
dc.date.issued2011-
dc.identifier.issn0025-3162pt_PT
dc.identifier.urihttp://hdl.handle.net/10773/25451-
dc.description.abstractThe present study investigated the existence of inter-individual and within-brood variability in the fatty acid (FA) profile of developing embryos of Nephrops norvegicus. In all surveyed females (n = 5), the quantitatively most important FAs were as follows: 22:6n-3 (20.8 ± 3.9% average of total FA ± standard error), 18:1n-9 (19.5 ± 2.0%), 16:0 (15.2 ± 3.4%), 20:5n-3 (10.2 ± 1.4%), 16:1n-7 (8.9 ± 1.6%), and 18:1n-7 (5.7 ± 1.3%). Differences in FA profiles of embryos in the same clutch were assessed using brooding chamber side (left and right) and pleopod (1st and 2nd, 3rd and 4th, and 5th) as predictive factors. There were no significant differences in the FA composition of embryos sampled from both sides of the brooding chamber in 4 of the 5 surveyed females. However, all females exhibited significant differences in the FA profiles of embryos sampled from different pleopods. Both saturated FA (SFA) and highly unsaturated FA (HUFA) present in developing embryos exhibited marked differences along the breeding chamber. Overall, FA reserves appeared to vary significantly within broods, which can ultimately be reflected on early larval survival. A potential cause for the within-brood variation recorded in the FA profile of developing embryos include (1) differential female investment during ovarian maturation, mainly due to variation in food quality/availability; (2) differential lipid catabolism during the incubation period of developing embryos, as a consequence of embryos position within the female’s brooding chamber; or (3) differential female investment during ovarian maturation amplified by differential lipid catabolism during the incubation period.pt_PT
dc.description.sponsorshipThe authors thank Susana Pereira for their help during the sampling and processing of Norway lobster embryos and Carla Santos during the biochemical analysis.pt_PT
dc.language.isoengpt_PT
dc.publisherSpringerpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F27615%2F2006/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/POCI/59426/PTpt_PT
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/82177/PTpt_PT
dc.rightsrestrictedAccesspt_PT
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectFatty acid composition pt_PT
dc.subjectEmbryonic development pt_PT
dc.subjectFatty acid profile pt_PT
dc.subjectBrooding chamber pt_PT
dc.subjectSpiny lobster pt_PT
dc.titleInter-individual and within-brood variability in the fatty acid profiles of Norway lobster, Nephrops norvegicus (L.) embryospt_PT
dc.typearticlept_PT
dc.description.versionpublishedpt_PT
dc.peerreviewedyespt_PT
degois.publication.firstPage2825pt_PT
degois.publication.issue12pt_PT
degois.publication.lastPage2833pt_PT
degois.publication.titleMarine Biologypt_PT
degois.publication.volume158pt_PT
dc.identifier.doi10.1007/s00227-011-1781-9pt_PT
dc.identifier.essn1432-1793pt_PT
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