Abstract

Despite the importance of O2 in biogeochemical processes, relatively few environmental studies have incorporated stable isotope information to assess the origins and cycling of this gas. A major limitation to the routine use of δ18O has been the cost and complexity associated with traditional off-line preparation, dual-inlet techniques. A gas chromatograph−isotope ratio mass spectrometry (GC−IRMS) technique providing rapid and precise δ18O−O2 values is presented. The procedure utilizes a 5-A molecular sieve column held at a constant temperature of 50 °C to separate O2 and N2 in time. A precision (± SD) of ±0.3‰ or better for δ18O−O2 is demonstrated on gaseous and dissolved samples spanning an environmentally relevant range in size of 20−700 μM. The potential for utilizing the technique for δ17O−O2 analysis (precision of ±0.5‰) and δ15N−N2 analysis (precision of ±0.2‰) on air samples is also demonstrated. Preliminary results from two unique environments, the subtropical North Pacific and Cornell University...

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.