1NOAA/ESRL, 325 Broadway, Boulder, CO 80305, USA
2INSTAAR, University of Colorado at Boulder, Boulder, CO 80309-0450, USA
3CIRES, University of Colorado at Boulder, Boulder, CO 80309-0216, USA
4Lawrence Berkeley Laboratory, 1 Cyclotron Rd, Berkeley, CA 94720, USA
5Dept. of Land, Air and Water Resources, University of California, Davis, CA 95616-8627, USA
6Lawrence Livermore National Laboratories, Center for Accelerator Mass Spectrometry, Livermore, CA 94551, USA
7KalScott Engineering, 811 E 28th St, Lawrence, KS 66046, USA
Abstract. Direct quantification of fossil fuel CO2 (CO2ff) in atmospheric samples can be used to examine several carbon cycle and air quality questions. We collected in-situ CO2, CO, and CH4 measurements and flask samples in the boundary layer and free troposphere over Sacramento, California, USA, during two aircraft flights over and downwind of this urban area during spring of 2009. The flask samples were analyzed for Δ14CO2 and CO2 to determine the recently added CO2ff mole fraction. A suite of additional greenhouse gases including hydrocarbons and halocarbons were measured in the same samples. Strong correlations were observed between CO2ff and numerous trace gases associated with urban emissions. From these correlations we estimate emission ratios between CO2ff and these species, and compare these with bottom-up inventory-derived estimates. Recent county level inventory estimates for carbon monoxide (CO) and benzene from the California Air Resources Board CEPAM database are in good agreement with our measured emission ratios, whereas older emissions inventories appear to overestimate emissions of these gases. For most other trace species, there are substantial differences between our measured emission ratios and those derived from available emission inventories. For the first flight, we combine in situ CO measurements with the measured CO:CO2ff emission ratio of 14±2 ppbCO/ppmCO2 to derive an estimate of CO2ff mole fraction throughout this flight, and also estimate the biospheric CO2 mixing ratio (CO2bio) from the difference of total and fossil CO2. The resulting CO2bio varies substantially between air in the urban plume and the surrounding boundary layer air. Finally, we use the in situ estimates of CO2ff mole fraction to infer total fossil fuel CO2 emissions from the Sacramento region, using a mass balance approach. However the resulting emissions are uncertain to within a factor of two due to uncertainties in wind speed and boundary layer height. Nevertheless, this first attempt to estimate urban-scale CO2ff from atmospheric radiocarbon measurements shows that CO2ff can be used to verify and improve emission inventories for many poorly known anthropogenic species, separate biospheric CO2, and indicates the potential to constrain the CO2ff emissions if transport uncertainties are reduced.