Worldwide biogenic soil NO<sub>x</sub> emissions inferred from OMI NO<sub>2</sub> observations

Biogenic NO<sub>x</sub> emissions from soils are a large natural source with substantial uncertainties in global bottom-up estimates (ranging from 4 to 15 Tg N yr<sup>−1</sup>). We reduce this range in emission estimates, and present a top-down soil NO<sub>x</s...

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Main Authors: G. C. M. Vinken, K. F. Boersma, J. D. Maasakkers, M. Adon, R. V. Martin
Format: Article
Language:English
Published: Copernicus Publications 2014-09-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/14/10363/2014/acp-14-10363-2014.pdf
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spelling doaj-ce91abcd548045e18fe545baafa4d15d2020-11-25T02:04:22ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242014-09-011418103631038110.5194/acp-14-10363-2014Worldwide biogenic soil NO<sub>x</sub> emissions inferred from OMI NO<sub>2</sub> observationsG. C. M. Vinken0K. F. Boersma1J. D. Maasakkers2M. Adon3R. V. Martin4Department of Applied Physics, Eindhoven University of Technology, Eindhoven, the NetherlandsDepartment of Meteorology and Air Quality, Wageningen University, Wageningen, the NetherlandsDepartment of Applied Physics, Eindhoven University of Technology, Eindhoven, the NetherlandsLaboratoire d'Aérologie, UMR CNRS/UPS 5560, Toulouse, FranceDepartment of Physics and Atmospheric Science, Dalhousie University, Halifax, Nova Scotia, CanadaBiogenic NO<sub>x</sub> emissions from soils are a large natural source with substantial uncertainties in global bottom-up estimates (ranging from 4 to 15 Tg N yr<sup>−1</sup>). We reduce this range in emission estimates, and present a top-down soil NO<sub>x</sub> emission inventory for 2005 based on retrieved tropospheric NO<sub>2</sub> columns from the Ozone Monitoring Instrument (OMI). We use a state-of-science soil NO<sub>x</sub> emission inventory (Hudman et al., 2012) as a priori in the GEOS-Chem chemistry transport model to identify 11 regions where tropospheric NO<sub>2</sub> columns are dominated by soil NO<sub>x</sub> emissions. Strong correlations between soil NO<sub>x</sub> emissions and simulated NO<sub>2</sub> columns indicate that spatial patterns in simulated NO<sub>2</sub> columns in these regions indeed reflect the underlying soil NO<sub>x</sub> emissions. Subsequently, we use a mass-balance approach to constrain emissions for these 11 regions on all major continents using OMI observed and GEOS-Chem simulated tropospheric NO<sub>2</sub> columns. We find that responses of simulated NO<sub>2</sub> columns to changing NO<sub>x</sub> emissions are suppressed over low NO<sub>x</sub> regions, and account for these non-linearities in our inversion approach. In general, our approach suggests that emissions need to be increased in most regions. Our OMI top-down soil NO<sub>x</sub> inventory amounts to 10.0 Tg N for 2005 when only constraining the 11 regions, and 12.9 Tg N when extrapolating the constraints globally. Substantial regional differences exist (ranging from −40% to +90%), and globally our top-down inventory is 4–35% higher than the GEOS-Chem a priori (9.6 Tg N yr<sup>−1</sup>). We evaluate NO<sub>2</sub> concentrations simulated with our new OMI top-down inventory against surface NO<sub>2</sub> measurements from monitoring stations in Africa, the USA and Europe. Although this comparison is complicated by several factors, we find an encouraging improved agreement when using the OMI top-down inventory compared to using the a priori inventory. To our knowledge, this study provides, for the first time, specific constraints on soil NO<sub>x</sub> emissions on all major continents using OMI NO<sub>2</sub> columns. Our results rule out the low end of reported soil NO<sub>x</sub> emission estimates, and suggest that global emissions are most likely around 12.9 ± 3.9 Tg N yr<sup>−1</sup>.http://www.atmos-chem-phys.net/14/10363/2014/acp-14-10363-2014.pdf
collection DOAJ
language English
format Article
sources DOAJ
author G. C. M. Vinken
K. F. Boersma
J. D. Maasakkers
M. Adon
R. V. Martin
spellingShingle G. C. M. Vinken
K. F. Boersma
J. D. Maasakkers
M. Adon
R. V. Martin
Worldwide biogenic soil NO<sub>x</sub> emissions inferred from OMI NO<sub>2</sub> observations
Atmospheric Chemistry and Physics
author_facet G. C. M. Vinken
K. F. Boersma
J. D. Maasakkers
M. Adon
R. V. Martin
author_sort G. C. M. Vinken
title Worldwide biogenic soil NO<sub>x</sub> emissions inferred from OMI NO<sub>2</sub> observations
title_short Worldwide biogenic soil NO<sub>x</sub> emissions inferred from OMI NO<sub>2</sub> observations
title_full Worldwide biogenic soil NO<sub>x</sub> emissions inferred from OMI NO<sub>2</sub> observations
title_fullStr Worldwide biogenic soil NO<sub>x</sub> emissions inferred from OMI NO<sub>2</sub> observations
title_full_unstemmed Worldwide biogenic soil NO<sub>x</sub> emissions inferred from OMI NO<sub>2</sub> observations
title_sort worldwide biogenic soil no<sub>x</sub> emissions inferred from omi no<sub>2</sub> observations
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2014-09-01
description Biogenic NO<sub>x</sub> emissions from soils are a large natural source with substantial uncertainties in global bottom-up estimates (ranging from 4 to 15 Tg N yr<sup>−1</sup>). We reduce this range in emission estimates, and present a top-down soil NO<sub>x</sub> emission inventory for 2005 based on retrieved tropospheric NO<sub>2</sub> columns from the Ozone Monitoring Instrument (OMI). We use a state-of-science soil NO<sub>x</sub> emission inventory (Hudman et al., 2012) as a priori in the GEOS-Chem chemistry transport model to identify 11 regions where tropospheric NO<sub>2</sub> columns are dominated by soil NO<sub>x</sub> emissions. Strong correlations between soil NO<sub>x</sub> emissions and simulated NO<sub>2</sub> columns indicate that spatial patterns in simulated NO<sub>2</sub> columns in these regions indeed reflect the underlying soil NO<sub>x</sub> emissions. Subsequently, we use a mass-balance approach to constrain emissions for these 11 regions on all major continents using OMI observed and GEOS-Chem simulated tropospheric NO<sub>2</sub> columns. We find that responses of simulated NO<sub>2</sub> columns to changing NO<sub>x</sub> emissions are suppressed over low NO<sub>x</sub> regions, and account for these non-linearities in our inversion approach. In general, our approach suggests that emissions need to be increased in most regions. Our OMI top-down soil NO<sub>x</sub> inventory amounts to 10.0 Tg N for 2005 when only constraining the 11 regions, and 12.9 Tg N when extrapolating the constraints globally. Substantial regional differences exist (ranging from −40% to +90%), and globally our top-down inventory is 4–35% higher than the GEOS-Chem a priori (9.6 Tg N yr<sup>−1</sup>). We evaluate NO<sub>2</sub> concentrations simulated with our new OMI top-down inventory against surface NO<sub>2</sub> measurements from monitoring stations in Africa, the USA and Europe. Although this comparison is complicated by several factors, we find an encouraging improved agreement when using the OMI top-down inventory compared to using the a priori inventory. To our knowledge, this study provides, for the first time, specific constraints on soil NO<sub>x</sub> emissions on all major continents using OMI NO<sub>2</sub> columns. Our results rule out the low end of reported soil NO<sub>x</sub> emission estimates, and suggest that global emissions are most likely around 12.9 ± 3.9 Tg N yr<sup>−1</sup>.
url http://www.atmos-chem-phys.net/14/10363/2014/acp-14-10363-2014.pdf
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