Stable isotopes and fatty acids as tracers of the assimilation of salmon fish feed in blue mussels ( Mytilus edulis)
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 ( δ 13C and δ 15N) and fatty acid signatures of mussel digestive gland and mantle tissue were investigated using a 28 day laboratory fe...
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description | 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 (
δ
13C and
δ
15N) and fatty acid signatures of mussel digestive gland and mantle tissue were investigated using a 28
day 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
δ
13C and the fatty acid signature of the feed. The
δ
15N exhibited a 2‰ change in the direction of salmon pellets in both tissues, and were not significantly dissimilar from salmon pellets after 28
days 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
δ
13C and fatty acid signatures was valid in tracing the assimilation of salmon pellets into blue mussel populations after 28
days of exposure. |
doi_str_mv | 10.1016/j.aquaculture.2009.10.002 |
format | Article |
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Mytilus edulis. The stable isotope (
δ
13C and
δ
15N) and fatty acid signatures of mussel digestive gland and mantle tissue were investigated using a 28
day 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
δ
13C and the fatty acid signature of the feed. The
δ
15N exhibited a 2‰ change in the direction of salmon pellets in both tissues, and were not significantly dissimilar from salmon pellets after 28
days 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
δ
13C and fatty acid signatures was valid in tracing the assimilation of salmon pellets into blue mussel populations after 28
days of exposure.</description><identifier>ISSN: 0044-8486</identifier><identifier>EISSN: 1873-5622</identifier><identifier>DOI: 10.1016/j.aquaculture.2009.10.002</identifier><identifier>CODEN: AQCLAL</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Agnatha. Pisces ; Animal aquaculture ; Animal productions ; Aquaculture ; assimilation (physiology) ; Biochemistry ; Biological and medical sciences ; body composition ; coastal water ; digestive gland ; environmental impact ; environmental indicators ; fatty acid composition ; Fatty acids ; feed composition ; feeds ; fish culture ; fish farms ; fish feeding ; Fundamental and applied biological sciences. Psychology ; General aspects ; Integrated multi-trophic aquaculture (IMTA) ; isotope labeling ; Isotopes ; lipid content ; mantle tissue ; mariculture ; metabolic studies ; Mollusks ; mussels ; Mytilus edulis ; principal component analysis ; Salmo salar ; Salmon ; Salmon farming ; Salmon pellets ; stable isotopes ; tissue distribution ; Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution ; δ13C ; δ15N</subject><ispartof>Aquaculture, 2010-01, Vol.298 (3), p.202-210</ispartof><rights>2009 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Elsevier Sequoia S.A. Jan 7, 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-d384213ea54183205528472d0f4b9944a7aa32d51f3f81c9ceb89a986b733e563</citedby><cites>FETCH-LOGICAL-c402t-d384213ea54183205528472d0f4b9944a7aa32d51f3f81c9ceb89a986b733e563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0044848609008291$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22288481$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Redmond, Kirsten J.</creatorcontrib><creatorcontrib>Magnesen, Thorolf</creatorcontrib><creatorcontrib>Hansen, Pia Kupka</creatorcontrib><creatorcontrib>Strand, Øivind</creatorcontrib><creatorcontrib>Meier, Sonnich</creatorcontrib><title>Stable isotopes and fatty acids as tracers of the assimilation of salmon fish feed in blue mussels ( Mytilus edulis)</title><title>Aquaculture</title><description>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 (
δ
13C and
δ
15N) and fatty acid signatures of mussel digestive gland and mantle tissue were investigated using a 28
day 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
δ
13C and the fatty acid signature of the feed. The
δ
15N exhibited a 2‰ change in the direction of salmon pellets in both tissues, and were not significantly dissimilar from salmon pellets after 28
days 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
δ
13C and fatty acid signatures was valid in tracing the assimilation of salmon pellets into blue mussel populations after 28
days of exposure.</description><subject>Agnatha. Pisces</subject><subject>Animal aquaculture</subject><subject>Animal productions</subject><subject>Aquaculture</subject><subject>assimilation (physiology)</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>body composition</subject><subject>coastal water</subject><subject>digestive gland</subject><subject>environmental impact</subject><subject>environmental indicators</subject><subject>fatty acid composition</subject><subject>Fatty acids</subject><subject>feed composition</subject><subject>feeds</subject><subject>fish culture</subject><subject>fish farms</subject><subject>fish feeding</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>Integrated multi-trophic aquaculture (IMTA)</subject><subject>isotope labeling</subject><subject>Isotopes</subject><subject>lipid content</subject><subject>mantle tissue</subject><subject>mariculture</subject><subject>metabolic studies</subject><subject>Mollusks</subject><subject>mussels</subject><subject>Mytilus edulis</subject><subject>principal component analysis</subject><subject>Salmo salar</subject><subject>Salmon</subject><subject>Salmon farming</subject><subject>Salmon pellets</subject><subject>stable isotopes</subject><subject>tissue distribution</subject><subject>Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution</subject><subject>δ13C</subject><subject>δ15N</subject><issn>0044-8486</issn><issn>1873-5622</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqNkM2KFDEUhQtRsB19BqMg6KLa_FVVaimNfzDiYpx1uJW6cdKkq3pyk4F-e9P0IC5dJTn5cm74muaN4FvBRf9xv4X7Aq7EXBJuJedjzbecyyfNRphBtV0v5dNmw7nWrdGmf968INpzzvu-E5sm32SYIrJAa16PSAyWmXnI-cTAhbmeieUEDhOx1bN8hzWhcAgRcliXc0YQD3XnA90xjzizsLApFmSHQoSR2Hv245RDLMRwLjHQh5fNMw-R8NXjetXcfvn8a_etvf759fvu03XrNJe5nZXRUiiETgujJO86afQgZ-71NI5awwCg5NwJr7wRbnQ4mRFG00-DUtj16qp5e-k9pvW-IGW7X0ta6kgreW2SveAVGi-QSytRQm-PKRwgnazg9uzY7u0_ju3Z8fmqOq5v3z0OAHIQfYLFBfpbIKU01bmo3OsL52G18DtV5vZGcqG4GESv5FiJ3YWowvAhYLLkAi4O55DQZTuv4T_-8wcUDqFb</recordid><startdate>20100107</startdate><enddate>20100107</enddate><creator>Redmond, Kirsten J.</creator><creator>Magnesen, Thorolf</creator><creator>Hansen, Pia Kupka</creator><creator>Strand, Øivind</creator><creator>Meier, Sonnich</creator><general>Elsevier B.V</general><general>Amsterdam: Elsevier Science</general><general>Elsevier</general><general>Elsevier Sequoia S.A</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QR</scope><scope>7ST</scope><scope>7TN</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope></search><sort><creationdate>20100107</creationdate><title>Stable isotopes and fatty acids as tracers of the assimilation of salmon fish feed in blue mussels ( Mytilus edulis)</title><author>Redmond, Kirsten J. ; Magnesen, Thorolf ; Hansen, Pia Kupka ; Strand, Øivind ; Meier, Sonnich</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-d384213ea54183205528472d0f4b9944a7aa32d51f3f81c9ceb89a986b733e563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Agnatha. Pisces</topic><topic>Animal aquaculture</topic><topic>Animal productions</topic><topic>Aquaculture</topic><topic>assimilation (physiology)</topic><topic>Biochemistry</topic><topic>Biological and medical sciences</topic><topic>body composition</topic><topic>coastal water</topic><topic>digestive gland</topic><topic>environmental impact</topic><topic>environmental indicators</topic><topic>fatty acid composition</topic><topic>Fatty acids</topic><topic>feed composition</topic><topic>feeds</topic><topic>fish culture</topic><topic>fish farms</topic><topic>fish feeding</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects</topic><topic>Integrated multi-trophic aquaculture (IMTA)</topic><topic>isotope labeling</topic><topic>Isotopes</topic><topic>lipid content</topic><topic>mantle tissue</topic><topic>mariculture</topic><topic>metabolic studies</topic><topic>Mollusks</topic><topic>mussels</topic><topic>Mytilus edulis</topic><topic>principal component analysis</topic><topic>Salmo salar</topic><topic>Salmon</topic><topic>Salmon farming</topic><topic>Salmon pellets</topic><topic>stable isotopes</topic><topic>tissue distribution</topic><topic>Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution</topic><topic>δ13C</topic><topic>δ15N</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Redmond, Kirsten J.</creatorcontrib><creatorcontrib>Magnesen, Thorolf</creatorcontrib><creatorcontrib>Hansen, Pia Kupka</creatorcontrib><creatorcontrib>Strand, Øivind</creatorcontrib><creatorcontrib>Meier, Sonnich</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Chemoreception Abstracts</collection><collection>Environment Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Aquaculture</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Redmond, Kirsten J.</au><au>Magnesen, Thorolf</au><au>Hansen, Pia Kupka</au><au>Strand, Øivind</au><au>Meier, Sonnich</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stable isotopes and fatty acids as tracers of the assimilation of salmon fish feed in blue mussels ( Mytilus edulis)</atitle><jtitle>Aquaculture</jtitle><date>2010-01-07</date><risdate>2010</risdate><volume>298</volume><issue>3</issue><spage>202</spage><epage>210</epage><pages>202-210</pages><issn>0044-8486</issn><eissn>1873-5622</eissn><coden>AQCLAL</coden><abstract>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 (
δ
13C and
δ
15N) and fatty acid signatures of mussel digestive gland and mantle tissue were investigated using a 28
day 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
δ
13C and the fatty acid signature of the feed. The
δ
15N exhibited a 2‰ change in the direction of salmon pellets in both tissues, and were not significantly dissimilar from salmon pellets after 28
days 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
δ
13C and fatty acid signatures was valid in tracing the assimilation of salmon pellets into blue mussel populations after 28
days of exposure.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.aquaculture.2009.10.002</doi><tpages>9</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals |
subjects | Agnatha. Pisces Animal aquaculture Animal productions Aquaculture assimilation (physiology) Biochemistry Biological and medical sciences body composition coastal water digestive gland environmental impact environmental indicators fatty acid composition Fatty acids feed composition feeds fish culture fish farms fish feeding Fundamental and applied biological sciences. Psychology General aspects Integrated multi-trophic aquaculture (IMTA) isotope labeling Isotopes lipid content mantle tissue mariculture metabolic studies Mollusks mussels Mytilus edulis principal component analysis Salmo salar Salmon Salmon farming Salmon pellets stable isotopes tissue distribution Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution δ13C δ15N |
title | Stable isotopes and fatty acids as tracers of the assimilation of salmon fish feed in blue mussels ( Mytilus edulis) |
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