Sources of sedimentary lipids deduced from stable carbon-isotope analyses of individual compounds
COMPOUND-specific isotope analysis by gas chromatography combined with isotope-ratio mass spectrometry (GC-IRMS) provides a new tool with which to study the carbon cycle at the molecular scale. Previous studies using this technique have been concerned with oceanic systems. Here we demonstrate that t...
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Veröffentlicht in: | Nature (London) 1991-08, Vol.352 (6334), p.425-427 |
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description | COMPOUND-specific isotope analysis by gas chromatography combined with isotope-ratio mass spectrometry (GC-IRMS) provides a new tool with which to study the carbon cycle at the molecular scale. Previous studies using this technique have been concerned with oceanic systems. Here we demonstrate that the potential for elucidating terrestrial sedimentary processes is equally important. By comparing the carbon isotope ratios (δ^sup 13^C) of individual n-alkanes from the leaves of lakeside trees with those from the lake sediments, we are able to discriminate between the diverse sources of the sedimentary carbon. The leaf-wax n-alkanes show a large inter-species δ^sup 13^C variation of -30.1 to -38.7[per thousand], which may be the result of genetic differences in plant adaptation and physiology. Values of -30.1 to -35.9[per thousand] were obtained for the corresponding n-alkanes extracted from the lake sediments, indicating that they derive from a mixed input of deciduous leaf waxes. Shorter-chain lipids in the sediments had δ^sup 13^C values of -20 to -22[per thousand], implying that these originate from a different (probably algal) source. Information of this sort goes beyond that which can be deduced from bulk isotope or biomarker analyses alone. [PUBLICATION ABSTRACT] |
doi_str_mv | 10.1038/352425a0 |
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Previous studies using this technique have been concerned with oceanic systems. Here we demonstrate that the potential for elucidating terrestrial sedimentary processes is equally important. By comparing the carbon isotope ratios (δ^sup 13^C) of individual n-alkanes from the leaves of lakeside trees with those from the lake sediments, we are able to discriminate between the diverse sources of the sedimentary carbon. The leaf-wax n-alkanes show a large inter-species δ^sup 13^C variation of -30.1 to -38.7[per thousand], which may be the result of genetic differences in plant adaptation and physiology. Values of -30.1 to -35.9[per thousand] were obtained for the corresponding n-alkanes extracted from the lake sediments, indicating that they derive from a mixed input of deciduous leaf waxes. Shorter-chain lipids in the sediments had δ^sup 13^C values of -20 to -22[per thousand], implying that these originate from a different (probably algal) source. Information of this sort goes beyond that which can be deduced from bulk isotope or biomarker analyses alone. [PUBLICATION ABSTRACT]</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/352425a0</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group</publisher><subject>Analysis ; Carbon ; Carbon cycle ; Carbon isotopes ; Freshwater ; Gas chromatography ; Isotopes ; Lake sediments ; Lakes ; Leaves ; Lipids ; Mass spectrometry ; Sediments ; Water analysis</subject><ispartof>Nature (London), 1991-08, Vol.352 (6334), p.425-427</ispartof><rights>Copyright Nature Publishing Group Aug 1, 1991</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a361t-643093ec3623221c2d58b8bd95e4b15bc0477bc1cb952486c1bbf0c50c1b74a03</citedby><cites>FETCH-LOGICAL-a361t-643093ec3623221c2d58b8bd95e4b15bc0477bc1cb952486c1bbf0c50c1b74a03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Rieley, Gareth</creatorcontrib><creatorcontrib>Collier, Robert J</creatorcontrib><creatorcontrib>Jones, David M</creatorcontrib><creatorcontrib>Eglinton, Geoffrey</creatorcontrib><creatorcontrib>Eakin, Paul A</creatorcontrib><creatorcontrib>Fallick, Anthony E</creatorcontrib><title>Sources of sedimentary lipids deduced from stable carbon-isotope analyses of individual compounds</title><title>Nature (London)</title><description>COMPOUND-specific isotope analysis by gas chromatography combined with isotope-ratio mass spectrometry (GC-IRMS) provides a new tool with which to study the carbon cycle at the molecular scale. Previous studies using this technique have been concerned with oceanic systems. Here we demonstrate that the potential for elucidating terrestrial sedimentary processes is equally important. By comparing the carbon isotope ratios (δ^sup 13^C) of individual n-alkanes from the leaves of lakeside trees with those from the lake sediments, we are able to discriminate between the diverse sources of the sedimentary carbon. The leaf-wax n-alkanes show a large inter-species δ^sup 13^C variation of -30.1 to -38.7[per thousand], which may be the result of genetic differences in plant adaptation and physiology. Values of -30.1 to -35.9[per thousand] were obtained for the corresponding n-alkanes extracted from the lake sediments, indicating that they derive from a mixed input of deciduous leaf waxes. Shorter-chain lipids in the sediments had δ^sup 13^C values of -20 to -22[per thousand], implying that these originate from a different (probably algal) source. Information of this sort goes beyond that which can be deduced from bulk isotope or biomarker analyses alone. [PUBLICATION ABSTRACT]</description><subject>Analysis</subject><subject>Carbon</subject><subject>Carbon cycle</subject><subject>Carbon isotopes</subject><subject>Freshwater</subject><subject>Gas chromatography</subject><subject>Isotopes</subject><subject>Lake sediments</subject><subject>Lakes</subject><subject>Leaves</subject><subject>Lipids</subject><subject>Mass spectrometry</subject><subject>Sediments</subject><subject>Water 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sedimentary lipids deduced from stable carbon-isotope analyses of individual compounds</atitle><jtitle>Nature (London)</jtitle><date>1991-08-01</date><risdate>1991</risdate><volume>352</volume><issue>6334</issue><spage>425</spage><epage>427</epage><pages>425-427</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>COMPOUND-specific isotope analysis by gas chromatography combined with isotope-ratio mass spectrometry (GC-IRMS) provides a new tool with which to study the carbon cycle at the molecular scale. Previous studies using this technique have been concerned with oceanic systems. Here we demonstrate that the potential for elucidating terrestrial sedimentary processes is equally important. By comparing the carbon isotope ratios (δ^sup 13^C) of individual n-alkanes from the leaves of lakeside trees with those from the lake sediments, we are able to discriminate between the diverse sources of the sedimentary carbon. The leaf-wax n-alkanes show a large inter-species δ^sup 13^C variation of -30.1 to -38.7[per thousand], which may be the result of genetic differences in plant adaptation and physiology. Values of -30.1 to -35.9[per thousand] were obtained for the corresponding n-alkanes extracted from the lake sediments, indicating that they derive from a mixed input of deciduous leaf waxes. Shorter-chain lipids in the sediments had δ^sup 13^C values of -20 to -22[per thousand], implying that these originate from a different (probably algal) source. Information of this sort goes beyond that which can be deduced from bulk isotope or biomarker analyses alone. [PUBLICATION ABSTRACT]</abstract><cop>London</cop><pub>Nature Publishing Group</pub><doi>10.1038/352425a0</doi><tpages>3</tpages></addata></record> |
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subjects | Analysis Carbon Carbon cycle Carbon isotopes Freshwater Gas chromatography Isotopes Lake sediments Lakes Leaves Lipids Mass spectrometry Sediments Water analysis |
title | Sources of sedimentary lipids deduced from stable carbon-isotope analyses of individual compounds |
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