Heuer, Verena et al. (2006): Online delta (super 13) C analysis of volatile fatty acids in sediment/porewater systems by liquid chromatography-isotope ratio-mass spectrometry

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Identifier:
2011-015348
georefid

Creator:
Heuer, Verena
German Research Foundation-Research Center Ocean Margins, Organic Geochemistry Group, Bremen, Germany
author

Elvert, Marcus
Thermo Electron Corporation, Germany
author

Tille, Stefanie
author

Krummen, Michael
author

Mollar, Xavier Prieto
author

Hmelo, Laura R.
author

Hinrichs, Kai-Uwe
author

Identification:
Online delta (super 13) C analysis of volatile fatty acids in sediment/porewater systems by liquid chromatography-isotope ratio-mass spectrometry
2006
Limnology and Oceanography, Methods
American Society of Limnology and Oceanography, Waco, TX, United States
4
346-357
Volatile fatty acids (VFAs) are central intermediates of anaerobic metabolism and present in aquatic environments such as marine sediments. Conceptually, the isotopic composition of volatile fatty acids is presumed to be sensitive to the specific biogeochemical processes involved in their production and consumption. However, due to generally low environmental concentrations, our knowledge on isotopic variability of VFAs is limited. We report the development and application of a new protocol for compound-specific carbon isotopic analysis of VFAs in marine porewaters and other aqueous liquids. This new protocol involves reversed-phase separation of volatile fatty acids with an aqueous mobile phase by high performance liquid chromatography (HPLC) combined with chemical oxidation of the effluents by the Finnigan (super TM) LC IsoLink interface (Krummen et al. 2004) and subsequent online transfer of the resulting CO (sub 2) into an isotope ratio mass spectrometer. We obtained reproducible and accurate results for pure Na-acetate dissolved in artificial seawater at concentrations as low as 2 mu M, whereas minimum concentrations in marine porewaters were 10 mu M. Our technique extends the previously accessible concentration range and the fully automated online operation allows for systematic analysis of large sample sets. These technical improvements make carbon isotopic analysis of selected VFAs a realistic perspective for many sedimentary environments. Our initial survey of acetate in porewaters and fluids obtained from incubations of marine sediments has revealed an unexpectedly large range of isotopic compositions from -5 ppm to -85 ppm and provides strong support for process-specific information encoded in the isotopic compositions of VFAs.
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Isotope geochemistry; accuracy; acetates; anaerobic environment; aquatic environment; C-13/C-12; carbon; carbon dioxide; carboxylic acids; chemical analysis; chromatography; esters; fatty acids; isotope ratios; isotopes; liquid chromatography; mass spectroscopy; metabolism; methods; organic acids; organic compounds; pore water; sea water; sediments; spectroscopy; stable isotopes; volatile organic compounds; volatiles;

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