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Composition and Distribution Analysis of Bioaerosols Under Different Environmental Conditions
Published on: January 7, 2019
Characterizing spatiotemporal trends in PM2.5 component exposures across the western United States using daily 1-km
Qingqing He1, Mengyi Li2, Joseph Hotz3
1Department of Environmental & Occupational Health, University of California, Irvine, CA, 92697, United States; School of Resource and Environmental Engineering, Wuhan University of Technology, Wuhan, 430070, China.
Abstract:
Reliable, long-term information on the chemical composition of fine particulate matter (PM2.5) is essential for air quality management and health risk assessment, yet such data are rarely available with both high spatial and temporal resolution across large geographic areas. We developed a spatiotemporal modeling framework using the deep forest algorithm to estimate daily, gap-free PM2.5 component concentrations at 1-km resolution across the western United States from 2002 to 2019. By integrating data from ground-level chemical speciation networks, satellite-derived PM2.5 mass concentrations, CMAQ simulations, and multiple auxiliary predictors, we estimated daily concentrations of sulfate (SO42-), nitrate (NO3-), organic carbon (OC), elemental carbon (EC), and mineral dust (DUST). Model performance showed strong agreement with observations, with cross-validation R2 values of 0.81, 0.89, 0.75, 0.66, and 0.75, and root-mean-squared errors (RMSEs) of 0.30, 0.59, 0.26, 1.52, and 0.59 μg/m3, respectively. The estimated component sum captured the expected fraction of total PM2.5, closely tracking observed total mass with accuracy comparable to the observed component sum (R2 = 0.91 vs. 0.92; RMSE = 2.66 μg/m3; slope = 0.66 for both). Our high-resolution estimates revealed marked spatial variability: SO42-, NO3-, EC, and OC were elevated in urban areas-particularly the Los Angeles-Long Beach-Anaheim region-while DUST was concentrated along the southern California-western Arizona border. The model also captured sharp increases in OC, NO3-, and EC during wildfire events compared to non-fire periods. Over the long term, urban populations experienced 1.5-2 times higher exposure to SO42-, NO3-, EC, and OC than rural populations, with similar DUST exposure levels. All five components showed declining trends over the study period, especially in the southwestern U.S., with total concentrations falling from 12.32 μg/m3 in 2002 to 9.03 μg/m3 in 2019, primarily due to reductions in OC and NO3-. The long-term modeling framework and dataset can support attainment planning, source-specific mitigation, wildfire smoke operations, and health impact assessments.
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