Composition and Chemistry
Linking emissions of fossil fuel CO2 and other anthropogenic trace gases using atmospheric 14CO2
Article first published online: 19 APR 2012
DOI: 10.1029/2011JD017048
Copyright 2012 by the American Geophysical Union
Additional Information
How to Cite
, et al. (2012), Linking emissions of fossil fuel CO2 and other anthropogenic trace gases using atmospheric 14CO2, J. Geophys. Res., 117, D08302, doi:10.1029/2011JD017048.
Publication History
- Issue published online: 19 APR 2012
- Article first published online: 19 APR 2012
- Manuscript Accepted: 20 FEB 2012
- Manuscript Revised: 20 JAN 2012
- Manuscript Received: 21 OCT 2011
Keywords:
- HCFCs;
- HFCs;
- carbon dioxide;
- emissions;
- fossil fuel;
- radiocarbon
[1] Atmospheric CO2 gradients are usually dominated by the signal from net terrestrial biological fluxes, despite the fact that fossil fuel combustion fluxes are larger in the annual mean. Here, we use a six year long series of 14CO2 and CO2 measurements obtained from vertical profiles at two northeast U.S. aircraft sampling sites to partition lower troposphere CO2 enhancements (and depletions) into terrestrial biological and fossil fuel components (Cbio and Cff). Mean Cff is 1.5 ppm, and 2.4 ppm when we consider only planetary boundary layer samples. However, we find that the contribution of Cbio to CO2 enhancements is large throughout the year, and averages 60% in winter. Paired observations of Cff and the lower troposphere enhancements (Δgas) of 22 other anthropogenic gases (CH4, CO, halo- and hydrocarbons and others) measured in the same samples are used to determine apparent emission ratios for each gas. We then scale these ratios by the well known U.S. fossil fuel CO2 emissions to provide observationally based estimates of national emissions for each gas and compare these to “bottom up” estimates from inventories. Correlations of Δgas with Cff for almost all gases are statistically significant with median r2for winter, summer and the entire year of 0.59, 0.45, and 0.42, respectively. Many gases exhibit statistically significant winter:summer differences in ratios that indicate seasonality of emissions or chemical destruction. The variability of ratios in a given season is not readily attributable to meteorological or geographic variables and instead most likely reflects real, short-term spatiotemporal variability of emissions.

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