Hoda Hallaji, Siqi Ma, Daniel Q. Tong, Lucas R. F. Henneman
{"title":"Neighborhood-Scale O3, NO2, and PM2.5 in Washington, D.C. from a 1 × 1 km2 WRF–SMOKE–CMAQ Framework","authors":"Hoda Hallaji, Siqi Ma, Daniel Q. Tong, Lucas R. F. Henneman","doi":"10.1021/acsestair.6c00155","DOIUrl":null,"url":null,"abstract":"<p>Quantifying air pollution concentrations at fine spatial\r\nscales\r\nis important for resolving intra-urban exposure variability and identifying\r\nsources that disproportionately impact population groups across locations.\r\nWe developed a neighborhood-scale resolution (1 × 1 km<sup>2</sup>) WRF–SMOKE–CMAQ modeling framework to characterize\r\nO<sub>3</sub>, NO<sub>2</sub>, and PM<sub>2.5</sub> concentrations\r\nin Washington, D.C. in 2017. In evaluations against EPA Air Quality\r\nSystem observations and the National Climatic Data Center meteorological\r\ndata, WRF reproduced the temporal variability of temperature and specific\r\nhumidity with reasonable agreement (average <em>r</em> = 0.8\r\nand 0.7, respectively), although biases varied across seasons. CMAQ\r\nreproduced seasonal and diurnal patterns of O<sub>3</sub> and PM<sub>2.5</sub> with r up to 0.7 for hourly O<sub>3</sub>, though NO<sub>2</sub> was negatively biased (−14% to −29%), reflecting\r\nchallenges in resolving near-road gradients. We identified pronounced\r\nintra-urban concentration variability of NO<sub>2</sub>, whose coefficient\r\nof variation was greater than that of O<sub>3</sub> and more than\r\nof three times that of PM<sub>2.5</sub>. O<sub>3</sub> concentrations\r\nwere lower in all months by 4% to 11% in the urban core compared to\r\noutside the urban core due to NO<sub><em>x</em></sub> titration/inhibition.\r\nRelative to 4 × 4 km<sup>2</sup> resolution, 1 × 1 km<sup>2</sup> simulations increased population-weighted exposure (PWE)\r\nfor O<sub>3</sub> (+0.5% to +1.5%) but decreased PWE for NO<sub>2</sub> (−3% to −6%) and PM<sub>2.5</sub> (−1.5% to\r\n−3%). VOC/NO<sub><em>x</em></sub> ratios indicated\r\npredominantly NO<sub><em>x</em></sub>-saturated chemistry\r\nwithin the urban core. This work presents the value and the remaining\r\nchallenges of high-resolution regional air quality modeling in heterogeneous\r\nurban settings.</p>","PeriodicalId":100014,"journal":{"name":"ACS ES&T Air","volume":"3 10","pages":"2640–2653"},"PeriodicalIF":0.0000,"publicationDate":"2026-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS ES&T Air","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsestair.6c00155","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/4 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Quantifying air pollution concentrations at fine spatial
scales
is important for resolving intra-urban exposure variability and identifying
sources that disproportionately impact population groups across locations.
We developed a neighborhood-scale resolution (1 × 1 km2) WRF–SMOKE–CMAQ modeling framework to characterize
O3, NO2, and PM2.5 concentrations
in Washington, D.C. in 2017. In evaluations against EPA Air Quality
System observations and the National Climatic Data Center meteorological
data, WRF reproduced the temporal variability of temperature and specific
humidity with reasonable agreement (average r = 0.8
and 0.7, respectively), although biases varied across seasons. CMAQ
reproduced seasonal and diurnal patterns of O3 and PM2.5 with r up to 0.7 for hourly O3, though NO2 was negatively biased (−14% to −29%), reflecting
challenges in resolving near-road gradients. We identified pronounced
intra-urban concentration variability of NO2, whose coefficient
of variation was greater than that of O3 and more than
of three times that of PM2.5. O3 concentrations
were lower in all months by 4% to 11% in the urban core compared to
outside the urban core due to NOx titration/inhibition.
Relative to 4 × 4 km2 resolution, 1 × 1 km2 simulations increased population-weighted exposure (PWE)
for O3 (+0.5% to +1.5%) but decreased PWE for NO2 (−3% to −6%) and PM2.5 (−1.5% to
−3%). VOC/NOx ratios indicated
predominantly NOx-saturated chemistry
within the urban core. This work presents the value and the remaining
challenges of high-resolution regional air quality modeling in heterogeneous
urban settings.