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
Hauptverfasser: Rieley, Gareth, Collier, Robert J, Jones, David M, Eglinton, Geoffrey, Eakin, Paul A, Fallick, Anthony E
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container_end_page 427
container_issue 6334
container_start_page 425
container_title Nature (London)
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creator Rieley, Gareth
Collier, Robert J
Jones, David M
Eglinton, Geoffrey
Eakin, Paul A
Fallick, Anthony E
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. 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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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ispartof Nature (London), 1991-08, Vol.352 (6334), p.425-427
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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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