| Literature DB >> 19813280 |
T Hansen1, A Burmeister, U Sommer.
Abstract
Conventional simultaneous CNS stable isotope abundance measurements of solid samples usually require high sample amounts, up to 1 mg carbon, to achieve exact analytical results. This rarely used application is often impaired by high C:S element ratios when organic samples are analyzed and problems such as incomplete conversion into sulphur dioxide occur during analysis. We introduce, as a technical innovation, a high sensitivity elemental analyzer coupled to a conventional isotope ratio mass spectrometer, with which CNS-stable isotope ratios can be determined simultaneously in samples with low carbon content (<40 microg C corresponding to approximately 100 microg dry weight). The system includes downsized reactors, a temperature program-controlled gas chromatography (GC) column and a cryogenic trap to collect small amounts of sulphur dioxide. This modified application allows for highly sensitive measurements in a fully automated operation with standard deviations better than +/-0.47 per thousand for delta15N and delta34S and +/-0.12 per thousand for delta13C (n = 127). Samples collected from one sampling site in a Baltic fjord within a short time period were measured with the new system to get a first impression of triple stable isotope signatures. The results confirm the potential of using delta34S as a stable isotope tracer in combination with delta15N and delta13C measurements to improve discrimination of food sources in aquatic food webs. Copyright 2009 John Wiley & Sons, Ltd.Entities:
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Year: 2009 PMID: 19813280 DOI: 10.1002/rcm.4267
Source DB: PubMed Journal: Rapid Commun Mass Spectrom ISSN: 0951-4198 Impact factor: 2.419