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An Improved Retrieval of Tropospheric Nitrogen Dioxide from GOMEWe present a retrieval of tropospheric nitrogen dioxide (NO2) columns from the Global Ozone Monitoring Experiment (GOME) satellite instrument that improves in several ways over previous retrievals, especially in the accounting of Rayleigh and cloud scattering. Slant columns, which are directly fitted without low-pass filtering or spectral smoothing, are corrected for an artificial offset likely induced by spectral structure on the diffuser plate of the GOME instrument. The stratospheric column is determined from NO2 columns over the remote Pacific Ocean to minimize contamination from tropospheric NO2. The air mass factor (AMF) used to convert slant columns to vertical columns is calculated from the integral of the relative vertical NO2 distribution from a global 3-D model of tropospheric chemistry driven by assimilated meteorological data (Global Earth Observing System (GEOS)-CHEM), weighted by altitude dependent scattering weights computed with a radiative transfer model (Linearized Discrete Ordinate Radiative Transfer), using local surface albedos determined from GOME observations at NO2 wavelengths. The AMF calculation accounts for cloud scattering using cloud fraction, cloud top pressure, and cloud optical thickness from a cloud retrieval algorithm (GOME Cloud Retrieval Algorithm). Over continental regions with high surface emissions, clouds decrease the AMT by 20- 30% relative to clear sky. GOME is almost twice as sensitive to tropospheric NO2 columns over ocean than over land. Comparison of the retrieved tropospheric NO2 columns for July 1996 with GEOS-CHEM values tests both the retrieval and the nitrogen oxide radical (NOx) emissions inventories used in GEOS-CHEM. Retrieved tropospheric NO2 columns over the United States, where NOx emissions are particularly well known, are within 18% of GEOS-CHEM columns and are strongly spatially correlated (r = 0.78, n = 288, p less than 0.005). Retrieved columns show more NO2 than GEOS-CHEM columns over the Transvaal region of South Africa and industrial regions of the northeast United States and Europe. They are lower over Houston, India, eastern Asia, and the biomass burning region of central Africa, possibly because of biases from absorbing aerosols.
Document ID
20040111404
Acquisition Source
Langley Research Center
Document Type
Reprint (Version printed in journal)
External Source(s)
Authors
Martin, Randall V.
(Harvard Univ. Cambridge, MA, United States)
Chance, Kelly
(Harvard-Smithsonian Center for Astrophysics Cambridge, MA, United States)
Jacob, Daniel J.
(Harvard Univ. Cambridge, MA, United States)
Kurosu, Thomas P.
(Harvard-Smithsonian Center for Astrophysics Cambridge, MA, United States)
Spurr, Robert J. D.
(Harvard-Smithsonian Center for Astrophysics Cambridge, MA, United States)
Bucsela, Eric
(NASA Goddard Space Flight Center Greenbelt, MD, United States)
Gleason, James F.
(NASA Goddard Space Flight Center Greenbelt, MD, United States)
Palmer, Paul I.
(Harvard Univ. Cambridge, MA, United States)
Bey, Isabelle
(Harvard Univ. Cambridge, MA, United States)
Fiore, Arlene M.
(Harvard Univ. Cambridge, MA, United States)
Date Acquired
August 21, 2013
Publication Date
January 1, 2002
Publication Information
Publication: Journal of Geophysical Research
Publisher: American Geophysical Union
Volume: 107
Issue: D20
ISSN: 0148-0227
Subject Category
Environment Pollution
Funding Number(s)
CONTRACT_GRANT: NAG1-2307
Distribution Limits
Public
Copyright
Other

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