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首页> 外文期刊>Aquaculture >Stable isotopes and fatty acids as tracers of the assimilation of salmon fish feed in blue mussels (Mytilus edulis)
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Stable isotopes and fatty acids as tracers of the assimilation of salmon fish feed in blue mussels (Mytilus edulis)

机译:稳定的同位素和脂肪酸作为蓝贻贝(Mytilus edulis)鲑鱼饲料同化的示踪剂

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Stable isotopes and fatty acids were used to trace the assimilation of salmon feed (pellets) into the tissues of the blue mussel, Mytilus edulis. The stable isotope (t p#pdC and t p#eN) and fatty acid signatures of mussel digestive gland and mantle tissue were investigated using a 28day laboratory feeding experiment. Mussels were fed natural seston and compared to others with the same diet but supplemented with salmon pellets, before the mantle tissue and digestive gland of individuals were analysed. Mussel digestive gland responded more strongly than mantle tissue to both t p#pdC and the fatty acid signature of the feed. The t p#eN exhibited a 2 change in the direction of salmon pellets in both tissues, and were not significantly dissimilar from salmon pellets after 28days indicating signature incorporation. There was a large increase in the lipid content of digestive gland, and the amount of fatty acids increased from 4 to 12% after feeding with salmon pellets. The fatty acid profile of the digestive gland reflected the fatty acid profile of the salmon pellets. Several fatty acids could be used as lipid biomarkers of the assimilation of salmon pellets, including 18:1 (n-9), 18:2 (n-6) and 16:3 (n-4). The ratio of n-3 to n-6 fatty acids could also be used as a tracer. The mantle tissue responded in a much more conservative manner, but showed some response to the altered fatty acid content of the diet towards the end of the experiment. The results of this study demonstrated that the use of digestive gland t p#pdC and fatty acid signatures was valid in tracing the assimilation of salmon pellets into blue mussel populations after 28days of exposure.
机译:稳定的同位素和脂肪酸用于追踪鲑鱼饲料(小丸)对蓝贻贝(Mytilus edulis)组织的吸收。贻贝消化腺和地幔组织的稳定同位素(t p#pdC和t p#eN)和脂肪酸特征使用28天实验室喂养实验进行了研究。在分析个体的地幔组织和消化腺之前,将贻贝饲喂天然seston,并与相同饮食但添加鲑鱼丸的其他贻贝进行比较。贻贝的消化腺对皮膜t p#pdC和饲料中的脂肪酸特征的反应都比地幔组织强烈。在两个组织中,t p#eN在鲑鱼小丸的方向上显示出2个变化,并且在28天后与鲑鱼小丸没有显着不同,表明有特征性掺入。喂鲑鱼颗粒后,消化腺的脂质含量大大增加,脂肪酸含量从4%增加到12%。消化腺的脂肪酸谱反映了鲑鱼颗粒的脂肪酸谱。几种脂肪酸可用作鲑鱼小丸同化的脂质生物标记,包括18:1(n-9),18:2(n-6)和16:3(n-4)。 n-3与n-6脂肪酸的比例也可以用作示踪剂。披风组织的反应更为保守,但在实验结束时对饮食中脂肪酸含量的变化表现出一定的反应。这项研究的结果表明,在暴露28天后,使用消化腺t p#pdC和脂肪酸签名可以有效地追踪鲑鱼颗粒与蓝贻贝种群的同化。

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