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- Title
Variable effects of spatial resolution on modeling of nitrogen oxides.
- Authors
Li, Chi; Martin, Randall V.; Cohen, Ronald C.; Bindle, Liam; Zhang, Dandan; Chatterjee, Deepangsu; Weng, Hongjian; Lin, Jintai
- Abstract
The lifetime and concentration of nitrogen oxides (NO x) are susceptible to nonlinear production and loss and to the resolution of a chemical transport model (CTM). This is due to the strong spatial gradients of NO x and the dependence of its own chemical loss on such gradients. In this study, we use the GEOS-Chem CTM in its high-performance implementation (GCHP) to investigate NO x simulations over the eastern United States across a wide range of spatial model resolutions (six different horizontal grids from 13 to 181 km). Following increasing grid size, afternoon surface NO x mixing ratios over July 2015 generally decrease over the Great Lakes region (GL) and increase over the southern states of the US region (SS), yielding regional differences (181 km vs. 13 km) of -16 % (in the GL) to 7 % (in the SS); meanwhile, hydrogen oxide radicals (HO x) increase over both regions, consistent with their different chemical regimes (i.e., NO x -saturated in the GL and NO x -limited in the SS). Nighttime titration of ozone by surface nitric oxide (NO) was found to be more efficient at coarser resolutions, leading to longer NO x lifetimes and higher surface mixing ratios of nitrogen dioxide (NO 2) over the GL in January 2015. The tropospheric NO 2 column density at typical afternoon satellite overpass time has spatially more coherent negative biases (e.g., -8 % over the GL) at coarser resolutions in July, which reversed the positive biases of surface NO x over the SS. The reduced NO x aloft (>1 km altitude) at coarser resolutions was attributable to the enhanced HO x that intrudes into the upper troposphere. Application of coarse-resolution simulations for interpreting satellite NO 2 columns will generally underestimate surface NO 2 over the GL and overestimate surface NO 2 over the SS in summer, but it will uniformly overestimate NO x emissions over both regions. This study significantly broadens understanding of factors contributing to NO x resolution effects and the role of fine-resolution data in accurately simulating and interpreting NO x and its relevance to air quality.
- Subjects
UNITED States; SPATIAL resolution; PRODUCTION losses; NITROGEN dioxide; NITRIC oxide; NITROGEN oxides; TROPOSPHERIC ozone; CHEMICAL models
- Publication
Atmospheric Chemistry & Physics, 2023, Vol 23, Issue 5, p3031
- ISSN
1680-7316
- Publication type
Article
- DOI
10.5194/acp-23-3031-2023