Publication | Open Access
Global inventory of nitrogen oxide emissions constrained by space‐based observations of NO<sub>2</sub> columns
718
Citations
55
References
2003
Year
EngineeringGreenhouse Gas EmissionAir QualityCarbon AccountingAtmospheric ModelEarth ScienceAtmospheric ScienceSpace‐based ObservationsChemical Transport ModelGreenhouse Gas MeasurementAtmosphere Of EarthBiogeochemistryNo XRadiation MeasurementGome No 2Atmospheric Impact AssessmentAtmospheric ProcessGlobal InventoryAir Pollution
The study uses GOME NO₂ satellite observations to constrain global NOx emissions, integrating top‑down retrievals with bottom‑up inventories for an optimized estimate. A top‑down NOx inventory is derived by linking GOME NO₂ columns to emissions through GEOS‑CHEM relationships, incorporating aerosol scattering/absorption and vertical profile shape factors. The resulting a posteriori estimate (37.7 Tg N yr⁻¹) agrees with bottom‑up inventories overall but shows 50–100 % higher emissions in major urban centers, 25–35 % higher in Japan and South Africa, and up to 50 % lower biomass‑burning emissions, with top‑down errors comparable to bottom‑up errors and half the a priori error.
We use tropospheric NO 2 columns from the Global Ozone Monitoring Experiment (GOME) satellite instrument to derive top‐down constraints on emissions of nitrogen oxides (NO x ≡ NO + NO 2 ), 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 NO x emissions. Our GOME NO 2 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 NO 2 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 NO x emission inventory from the GOME data by using the local GEOS‐CHEM relationship between NO 2 columns and NO x emissions. The resulting NO x emissions for industrial regions are aseasonal, despite large seasonal variation in NO 2 columns, providing confidence in the method. Top‐down errors in monthly NO x 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 NO x 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 NO x 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 NO x emissions are appreciably higher in the western United States, the Sahel, and southern Europe.
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