Global inventory of nitrogen oxide emissions constrained by space‐based observations of NO2 columns
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Open Access
- 5 September 2003
- journal article
- research article
- Published by American Geophysical Union (AGU) in Journal of Geophysical Research: Atmospheres
- Vol. 108 (D17)
- https://doi.org/10.1029/2003jd003453
Abstract
We use tropospheric NO2 columns from the Global Ozone Monitoring Experiment (GOME) satellite instrument to derive top‐down constraints on emissions of nitrogen oxides (NOx ≡ NO + NO2), and combine these with a priori information from a bottom‐up emission inventory (with error weighting) to achieve an optimized a posteriori estimate of the global distribution of surface NOx emissions. Our GOME NO2 retrieval improves on previous work by accounting for scattering and absorption of radiation by aerosols; the effect on the air mass factor (AMF) ranges from +10 to −40% depending on the region. Our AMF also includes local information on relative vertical profiles (shape factors) of NO2 from a global 3‐D chemical transport model (GEOS‐CHEM); assumption of a globally uniform shape factor, as in most previous retrievals, would introduce regional biases of up to 40% over industrial regions and a factor of 2 over remote regions. We derive a top‐down NOx emission inventory from the GOME data by using the local GEOS‐CHEM relationship between NO2 columns and NOx emissions. The resulting NOx emissions for industrial regions are aseasonal, despite large seasonal variation in NO2 columns, providing confidence in the method. Top‐down errors in monthly NOx emissions are comparable with bottom‐up errors over source regions. Annual global a posteriori errors are half of a priori errors. Our global a posteriori estimate for annual land surface NOx emissions (37.7 Tg N yr−1) agrees closely with the GEIA‐based a priori (36.4) and with the EDGAR 3.0 bottom‐up inventory (36.6), but there are significant regional differences. A posteriori NOx emissions are higher by 50–100% in the Po Valley, Tehran, and Riyadh urban areas, and by 25–35% in Japan and South Africa. Biomass burning emissions from India, central Africa, and Brazil are lower by up to 50%; soil NOx emissions are appreciably higher in the western United States, the Sahel, and southern Europe.Keywords
This publication has 54 references indexed in Scilit:
- A database of spectral surface reflectivity in the range 335–772 nm derived from 5.5 years of GOME observationsJournal of Geophysical Research: Atmospheres, 2003
- Sources and chemistry of nitrogen oxides over the tropical PacificJournal of Geophysical Research: Atmospheres, 2003
- Interannual and seasonal variability of biomass burning emissions constrained by satellite observationsJournal of Geophysical Research: Atmospheres, 2003
- An improved retrieval of tropospheric nitrogen dioxide from GOMEJournal of Geophysical Research: Atmospheres, 2002
- Global chlorine emissions from biomass burning: Reactive Chlorine Emissions InventoryJournal of Geophysical Research: Atmospheres, 1999
- Derivation of aerosol properties from satellite measurements of backscattered ultraviolet radiation: Theoretical basisJournal of Geophysical Research: Atmospheres, 1998
- Global distribution of UV‐absorbing aerosols from Nimbus 7/TOMS dataJournal of Geophysical Research: Atmospheres, 1997
- Global gridded inventories of anthropogenic emissions of sulfur and nitrogenJournal of Geophysical Research: Atmospheres, 1996
- Origin of ozone and NOx in the tropical troposphere: A photochemical analysis of aircraft observations over the South Atlantic basinJournal of Geophysical Research: Atmospheres, 1996
- Black carbon formation by savanna fires: Measurements and implications for the global carbon cycleJournal of Geophysical Research: Atmospheres, 1996