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High-resolution measurements of sulphur isotope variations in sediment pore-waters by laser ablation multicollector inductively coupled plasma mass spectrometry

Research output: Contribution to Journal/MagazineJournal articlepeer-review

<mark>Journal publication date</mark>6/01/2012
<mark>Journal</mark>Chemical Geology
Issue numbern/a
Number of pages8
Pages (from-to)278-285
Publication StatusPublished
<mark>Original language</mark>English


A novel combination of the technique of diffusive gradients in thin films (DGT) and laser ablation high-resolution multicollector inductively coupled plasma mass spectrometry was developed to study sulphur isotope variations of dissolved pore-water sulphide in freshwater and marine sediments. The technique enables two-dimensional mapping of isotopic variations (δ34S) in dissolved sulphide captured as solid Ag2S in DGT polyacrylamide gels.
Measurements can be performed at a spatial resolution (~100 μm) relevant to microbiological processes and formation of individual iron sulphide grains in surface sediments. Values of δ34S measured in BaSO4–DGT gel isotope standards (δ34S=9.28±0.36‰ to 9.33±0.57‰) are within 1‰ of the accepted value determined
with conventional analytical techniques (δ34S=10.13±0.29‰). Sulphur isotope measurements were performed in sediments from a eutrophic lake (Esthwaite Water, UK) contained in laboratory mesocosms.
Bacterial sulphate reduction and sulphide formation in this sediment are predominantly localized to discrete, mm-sized microniches, where oxidation of labile organic matter such as fresh algae and faecal pellets drives the reduction of sulphate. The results emphasize the importance of microniches as localized, highly dynamic reaction sites in sediments, where significant shifts in δ34S of up to +20‰ relative to the local background were measured across microniches. The improved spatial resolution for pore-water sulphur isotope measurements, compared to that of conventional sampling and analytical techniques, is essential for improving our understanding of the global biogeochemical cycling of sulphur as well as trace metal–sulphide interactions in
modern sediments.