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  • 1
    Publication Date: 2014-01-24
    Description: [1]  The Study of Houston Atmospheric Radical Precursors (SHARP) was a field campaign developed by the Houston Advanced Research Center (HARC) on behalf of the Texas Environmental Research Consortium (TERC). SHARP capitalized on previous research associated with the Second Texas Air Quality Study (TexAQS II) and the development of the State Implementation Plan (SIP) for the Houston-Galveston-Brazoria (HGB) ozone non-attainment area. These earlier studies pointed to an apparent deficit in ozone production in the SIP attainment demonstration model despite the enhancement of simulated emissions of Highly Reactive Volatile Organic Compounds (HRVOCs) in accordance with the findings of the original Texas Air Quality Study in 2000 (TexAQS I). The scientific hypothesis underlying the SHARP campaign was that there are significant undercounted primary and secondary sources of the radical precursors, formaldehyde and nitrous acid, in both heavily industrialized and more typical urban areas of Houston. These sources, if properly taken into account, could increase the production of ozone in the SIP model and the simulated efficacy of control strategies designed to bring the HGB area into ozone attainment. This overview summarizes the precursor studies and motivations behind SHARP, as well as the overall experimental design and major findings of the 2009 field campaign. These findings include significant combustion sources of formaldehyde at levels greater than accounted for in current point source emission inventories; the underestimate of formaldehyde and nitrous acid emissions, as well as CO/NO x and NO 2 /NO x ratios, by mobile source models; and the enhancement of nitrous acid by atmospheric organic aerosol.
    Print ISSN: 0148-0227
    Topics: Geosciences , Physics
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 2
    Publication Date: 2019
    Description: Abstract Air quality models provide spatial fields of wet deposition (WD) and dry deposition (DD) that explicitly account for the transport and transformation of emissions from thousands of sources. However, many sources of uncertainty in the air quality model including errors in emissions and meteorological inputs (particularly precipitation) and incomplete descriptions of the chemical and physical processes governing deposition, can lead to bias and error in the simulation of WD. We present an approach to bias‐correct Community Multiscale Air Quality (CMAQ) model output over the contiguous United States using observation‐based gridded precipitation data generated by the Parameter‐elevation Regressions on Independent Slopes Model (PRISM), and WD observations at the National Atmospheric Deposition Program National Trends Network (NADP/NTN) sites. A cross‐validation analysis shows that the adjusted annual accumulated WD for NO3‐, NH4+, and SO42‐ from 2002 to 2012 has less bias and higher correlation with observed values than the base model output without adjustment. Temporal trends in observed WD are captured well by the adjusted model simulations across the entire CONUS. Consistent with previous trend analyses, WD NO3‐ and SO42‐ are shown to decrease during this period in the eastern half of the U.S., particularly in the Northeast, while remaining nearly constant in the West. Trends in WD of NH4+ are more spatially and temporally heterogeneous, with some positive trends in the Great Plains and Central Valley of CA and slightly negative trends in the South.
    Print ISSN: 2169-897X
    Electronic ISSN: 2169-8996
    Topics: Geosciences , Physics
    Published by Wiley on behalf of American Geophysical Union (AGU).
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