THE C-13, C-14 AND O-18 ISOTOPIC COMPOSITION OF CO, CH4, AND CO2 IN THE HIGHER SOUTHERN LATITUDES LOWER STRATOSPHERE

Citation
Cam. Brenninkmeijer et al., THE C-13, C-14 AND O-18 ISOTOPIC COMPOSITION OF CO, CH4, AND CO2 IN THE HIGHER SOUTHERN LATITUDES LOWER STRATOSPHERE, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 100(D12), 1995, pp. 26163-26172
Citations number
53
Categorie Soggetti
Metereology & Atmospheric Sciences
Volume
100
Issue
D12
Year of publication
1995
Pages
26163 - 26172
Database
ISI
SICI code
Abstract
Large air samples were collected in the lower stratosphere (10-12 km) from 43 degrees to 85 degrees S in June 1993, using a special compress or system. For the important trace gases CO, CH4 and CO2, concentratio n and isotopic analyses were carried out and significant correlations were discovered. The (CO)-C-14 isotope is considerably in excess of tr opospheric levels with very high values from 40 to 120 (CO)-C-14 molec ules/cm(3) STP (corresponding to 12,500 percent modern carbon, at 30 p pbv), and is negatively correlated with CO. The linear relationship is used to estimate OH to be 2.9 x 10(5) cm(-3). The O-18/O-16 ratios fo r CO are the lowest ever measured and reflect the inverse kinetic isot ope effect in the oxidation of CO by OH. The C-13/C-12 ratios for CO a re not much different from tropospheric values and confirm that fracti onation is small but also that the in situ contribution from CH4 oxida tion is minor. For CH4 a correlation between delta(13)C and concentrat ion exists from which a fractionation factor for the sink reaction (k( 12)/k(13)) of about 1.012 is calculated, well in excess of results fro m laboratory experiments for OH + CH4. The most plausible explanation presently is the removal of approximately 9% of CH4 by Cl atoms, which , as laboratory experiments have just confirmed, induces a very large fractionation. We also reveal a linear correlation between (CO)-C-14 a nd (CO2)-C-14, precursor and product. Finally, an analysis of potentia l vorticity shows a structure that seems to give an overall agreement with the trace gas variations.