Simultaneous stable isotope analysis of methane and nitrous oxide on ice core samples

Methane and nitrous oxide are important greenhouse gases which show a strong increase in atmospheric mixing ratios since pre-industrial time as well as large variations during past climate changes. The understanding of their biogeochemical cycles can be improved using stable isotope analysis. Howeve...

Full description

Bibliographic Details
Published in:Atmospheric Measurement Techniques
Main Authors: C. J. Sapart, C. van der Veen, I. Vigano, M. Brass, R. S. W. van de Wal, M. Bock, H. Fischer, T. Sowers, C. Buizert, P. Sperlich, T. Blunier, M. Behrens, J. Schmitt, B. Seth, T. Röckmann
Format: Article in Journal/Newspaper
Language:English
Published: Copernicus Publications 2011
Subjects:
Online Access:https://doi.org/10.5194/amt-4-2607-2011
https://doaj.org/article/d5e148b36e824c00a9db8621d6e6efd0
Description
Summary:Methane and nitrous oxide are important greenhouse gases which show a strong increase in atmospheric mixing ratios since pre-industrial time as well as large variations during past climate changes. The understanding of their biogeochemical cycles can be improved using stable isotope analysis. However, high-precision isotope measurements on air trapped in ice cores are challenging because of the high susceptibility to contamination and fractionation. Here, we present a dry extraction system for combined CH 4 and N 2 O stable isotope analysis from ice core air, using an ice grating device. The system allows simultaneous analysis of δD(CH 4 ) or δ 13 C(CH 4 ), together with δ 15 N(N 2 O), δ 18 O(N 2 O) and δ 15 N(NO + fragment) on a single ice core sample, using two isotope mass spectrometry systems. The optimum quantity of ice for analysis is about 600 g with typical "Holocene" mixing ratios for CH 4 and N 2 O. In this case, the reproducibility (1σ ) is 2.1‰ for δD(CH 4 ), 0.18‰ for δ 13 C(CH 4 ), 0.51‰ for δ 15 N(N 2 O), 0.69‰ for δ 18 O(N 2 O) and 1.12‰ for δ 15 N(NO + fragment). For smaller amounts of ice the standard deviation increases, particularly for N 2 O isotopologues. For both gases, small-scale intercalibrations using air and/or ice samples have been carried out in collaboration with other institutes that are currently involved in isotope measurements of ice core air. Significant differences are shown between the calibration scales, but those offsets are consistent and can therefore be corrected for.