1Research Institute for Global Change, JAMSTEC, Yokohama, 236-0001, Japan
2Institute of Environmental Physics, University of Bremen, 28359 Bremen, Germany
3California Institute of Technology, Pasadena, CA 91125, USA
4National Institute of Water and Atmospheric Research (NIWA), Wellington 6021, New Zealand
5IMK-ASF, Karlsruhe Institute of Technology (KIT), 76344 Eggenstein-Leopoldshafen, Germany
6School of Chemistry, University of Wollongong, NSW, 2522, Australia
7FMI-Arctic Research Center, Tähteläntie 62, 99600, Sodankylä, Finland
8Department of Physics, University of Toronto, Ontario, M5S 1A7, Canada
9National Institute for Environmental Studies (NIES), Tsukuba, 305–8506, Japan
10IMK-IFU, Karlsruhe Institute of Technology (KIT), 82467 Garmisch-Partenkirchen, Germany
Received: 24 Jan 2012 – Published in Atmos. Chem. Phys. Discuss.: 22 Feb 2012
Abstract. We present a comparison of an atmospheric general circulation model (AGCM)-based chemistry-transport model (ACTM) simulation with total column measurements of CO2, CH4 and N2O from the Total Carbon Column Observing Network (TCCON). The model is able to capture observed trends, seasonal cycles and inter hemispheric gradients at most sampled locations for all three species. The model-observation agreements are best for CO2, because the simulation uses fossil fuel inventories and an inverse model estimate of non-fossil fuel fluxes. The ACTM captures much of the observed seasonal variability in CO2 and N2O total columns (~81 % variance, R>0.9 between ACTM and TCCON for 19 out of 22 cases). These results suggest that the transport processes in troposphere and stratosphere are well represented in ACTM. Thus the poor correlation between simulated and observed CH4 total columns, particularly at tropical and extra-tropical sites, have been attributed to the uncertainties in surface emissions and loss by hydroxyl radicals. While the upward-looking total column measurements of CO2 contains surface flux signals at various spatial and temporal scales, the N2O measurements are strongly affected by the concentration variations in the upper troposphere and stratosphere.
Revised: 17 Aug 2012 – Accepted: 20 Aug 2012 – Published: 28 Aug 2012
Citation: Saito, R., Patra, P. K., Deutscher, N., Wunch, D., Ishijima, K., Sherlock, V., Blumenstock, T., Dohe, S., Griffith, D., Hase, F., Heikkinen, P., Kyrö, E., Macatangay, R., Mendonca, J., Messerschmidt, J., Morino, I., Notholt, J., Rettinger, M., Strong, K., Sussmann, R., and Warneke, T.: Technical Note: Latitude-time variations of atmospheric column-average dry air mole fractions of CO2, CH4 and N2O, Atmos. Chem. Phys., 12, 7767-7777, doi:10.5194/acp-12-7767-2012, 2012.