Jun Wang

Dr. Jun Wang

University of Iowa, 4133 Seamans Center, Iowa City, IA 52242-1503, USA
orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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6 November 2003 in Geophysical Research Letters
Verified
Journal Article
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Jun WangJun Wang
Jun Wang
SCSundar A. Christopher
Sundar A. Christopher
We explore the relationship between column aerosol optical thickness (AOT) derived from the Moderate Resolution Imaging SpectroRadiometer (MODIS) on the Terra/Aqua satellites and hourly fine particulate mass (PM2.5) measured at the surface at seven locations in Jefferson county, Alabama for 2002. Results indicate that there is a good correlation between the satellite‐derived AOT and PM2.5 (linear correlation coefficient, R = 0.7) indicating that most of the aerosols are in the well‐mixed lower boundary layer during the satellite overpass times. There is excellent agreement between the monthly mean PM2.5 and MODIS AOT (R > 0.9), with maximum values during the summer months due to enhanced photolysis. The PM2.5 has a distinct diurnal signature with maxima in the early morning (6:00 ∼ 8:00AM) due to increased traffic flow and restricted mixing depths during these hours. Using simple empirical linear relationships derived between the MODIS AOT and 24hr mean PM2.5 we show that the MODIS AOT can be used quantitatively to estimate air quality categories as defined by the U.S. Environmental Protection Agency (EPA) with an accuracy of more than 90% in cloud‐free conditions. We discuss the factors that affect the correlation between satellite‐derived AOT and PM2.5 mass, and emphasize that more research is needed before applying these methods and results over other areas.

1 January 2017 in Journal of Quantitative Spectroscopy and Radiative Transfer
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Journal Article
Open access
PZP. Zoogman
P. Zoogman
XLXiong Liu
Xiong Liu
RSR.M. Suleiman
R.M. Suleiman
WPW.F. Pennington
W.F. Pennington
DFD.E. Flittner
D.E. Flittner
KCK. Chance
K. Chance
TEMPO was selected in 2012 by NASA as the first Earth Venture Instrument, for launch between 2018 and 2021. It will measure atmospheric pollution for greater North America from space using ultraviolet and visible spectroscopy. TEMPO observes from Mexico City, Cuba, and the Bahamas to the Canadian oil sands, and from the Atlantic to the Pacific, hourly and at high spatial resolution (~2.1 km N/S×4.4 km E/W at 36.5°N, 100°W). TEMPO provides a tropospheric measurement suite that includes the key elements of tropospheric air pollution chemistry, as well as contributing to carbon cycle knowledge. Measurements are made hourly from geostationary (GEO) orbit, to capture the high variability present in the diurnal cycle of emissions and chemistry that are unobservable from current low-Earth orbit (LEO) satellites that measure once per day. The small product spatial footprint resolves pollution sources at sub-urban scale. Together, this temporal and spatial resolution improves emission inventories, monitors population exposure, and enables effective emission-control strategies.

1 September 2006 in Atmospheric Environment
Verified
Journal Article
Closed access
PGPawan Gupta
Pawan Gupta
SCSundar A. Christopher
Sundar A. Christopher
Jun WangJun Wang
Jun Wang
RGRobert Gehrig
Robert Gehrig
YLYc Lee
Yc Lee
Naresh KumarNaresh Kumar
Naresh Kumar

26 January 2023 in Atmospheric Chemistry and Physics
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Journal Article
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Jing WeiJing Wei
Jing Wei
zhanqing lizhanqing li
zhanqing li
Jun WangJun Wang
Jun Wang
CLCan Li
Can Li
PGPawan Gupta
Pawan Gupta
MCMaureen Cribb
Maureen Cribb
Gaseous pollutants at the ground level seriously threaten the urban air quality environment and public health. There are few estimates of gaseous pollutants that are spatially and temporally resolved and continuous across China. This study takes advantage of big data and artificial-intelligence technologies to generate seamless daily maps of three major ambient pollutant gases, i.e., NO2, SO2, and CO, across China from 2013 to 2020 at a uniform spatial resolution of 10 km. Cross-validation between our estimates and ground observations illustrated a high data quality on a daily basis for surface NO2, SO2, and CO concentrations, with mean coefficients of determination (root-mean-square errors) of 0.84 (7.99 µg m−3), 0.84 (10.7 µg m−3), and 0.80 (0.29 mg m−3), respectively. We found that the COVID-19 lockdown had sustained impacts on gaseous pollutants, where surface CO recovered to its normal level in China on around the 34th day after the Lunar New Year, while surface SO2 and NO2 rebounded more than 2 times slower due to more CO emissions from residents' increased indoor cooking and atmospheric oxidation capacity. Surface NO2, SO2, and CO reached their peak annual concentrations of 21.3 ± 8.8 µg m−3, 23.1 ± 13.3 µg m−3, and 1.01 ± 0.29 mg m−3 in 2013, then continuously declined over time by 12 %, 55 %, and 17 %, respectively, until 2020. The declining rates were more prominent from 2013 to 2017 due to the sharper reductions in anthropogenic emissions but have slowed down in recent years. Nevertheless, people still suffer from high-frequency risk exposure to surface NO2 in eastern China, while surface SO2 and CO have almost reached the World Health Organization (WHO) recommended short-term air quality guidelines (AQG) level since 2018, benefiting from the implemented stricter “ultra-low” emission standards. This reconstructed dataset of surface gaseous pollutants will benefit future (especially short-term) air pollution and environmental health-related studies.

29 June 2022 in Environmental Science & Technology
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Journal Article
Open access
Jing WeiJing Wei
Jing Wei
SLSong Liu
Song Liu
zhanqing lizhanqing li
zhanqing li
WTWei Tan
Wei Tan
KQKai Qin
Kai Qin
Jun WangJun Wang
Jun Wang
Nitrogen dioxide (NO2) at the ground level poses a serious threat to environmental quality and public health. This study developed a novel, artificial intelligence approach by integrating spatiotemporally weighted information into the missing extra-trees and deep forest models to first fill the satellite data gaps and increase data availability by 49% and then derive daily 1 km surface NO2 concentrations over mainland China with full spatial coverage (100%) for the period 2019-2020 by combining surface NO2 measurements, satellite tropospheric NO2 columns derived from TROPOMI and OMI, atmospheric reanalysis, and model simulations. Our daily surface NO2 estimates have an average out-of-sample (out-of-city) cross-validation coefficient of determination of 0.93 (0.71) and root-mean-square error of 4.89 (9.95) μg/m3. The daily seamless high-resolution and high-quality dataset "ChinaHighNO2" allows us to examine spatial patterns at fine scales such as the urban-rural contrast. We observed systematic large differences between urban and rural areas (28% on average) in surface NO2, especially in provincial capitals. Strong holiday effects were found, with average declines of 22 and 14% during the Spring Festival and the National Day in China, respectively. Unlike North America and Europe, there is little difference between weekdays and weekends (within ±1 μg/m3). During the COVID-19 pandemic, surface NO2 concentrations decreased considerably and then gradually returned to normal levels around the 72nd day after the Lunar New Year in China, which is about 3 weeks longer than the tropospheric NO2 column, implying that the former can better represent the changes in NOx emissions.

27 January 2020 in Atmospheric Chemistry and Physics
Verified
Journal Article
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XPXiaohua Pan
Xiaohua Pan
CICharles Ichoku
Charles Ichoku
MCMian Chin
Mian Chin
HBHuisheng Bian
Huisheng Bian
ADAnton Darmenov
Anton Darmenov
GCGe Cui
Ge Cui
Aerosols from biomass burning (BB) emissions are poorly constrained in global and regional models, resulting in a high level of uncertainty in understanding their impacts. In this study, we compared six BB aerosol emission datasets for 2008 globally as well as in 14 regions. The six BB emission datasets are (1) GFED3.1 (Global Fire Emissions Database version 3.1), (2) GFED4s (GFED version 4 with small fires), (3) FINN1.5 (FIre INventory from NCAR version 1.5), (4) GFAS1.2 (Global Fire Assimilation System version 1.2), (5) FEER1.0 (Fire Energetics and Emissions Research version 1.0), and (6) QFED2.4 (Quick Fire Emissions Dataset version 2.4). The global total emission amounts from these six BB emission datasets differed by a factor of 3.8, ranging from 13.76 to 51.93 Tg for organic carbon and from 1.65 to 5.54 Tg for black carbon. In most of the regions, QFED2.4 and FEER1.0, which are based on satellite observations of fire radiative power (FRP) and constrained by aerosol optical depth (AOD) data from the Moderate Resolution Imaging Spectroradiometer (MODIS), yielded higher BB aerosol emissions than the rest by a factor of 2–4. By comparison, the BB aerosol emissions estimated from GFED4s and GFED3.1, which are based on satellite burned-area data, without AOD constraints, were at the low end of the range. In order to examine the sensitivity of model-simulated AOD to the different BB emission datasets, we ingested these six BB emission datasets separately into the same global model, the NASA Goddard Earth Observing System (GEOS) model, and compared the simulated AOD with observed AOD from the AErosol RObotic NETwork (AERONET) and the Multiangle Imaging SpectroRadiometer (MISR) in the 14 regions during 2008. In Southern Hemisphere Africa (SHAF) and South America (SHSA), where aerosols tend to be clearly dominated by smoke in September, the simulated AOD values were underestimated in almost all experiments compared to MISR, except for the QFED2.4 run in SHSA. The model-simulated AOD values based on FEER1.0 and QFED2.4 were the closest to the corresponding AERONET data, being, respectively, about 73 % and 100 % of the AERONET observed AOD at Alta Floresta in SHSA and about 49 % and 46 % at Mongu in SHAF. The simulated AOD based on the other four BB emission datasets accounted for only ∼50 % of the AERONET AOD at Alta Floresta and ∼20 % at Mongu. Overall, during the biomass burning peak seasons, at most of the selected AERONET sites in each region, the AOD values simulated with QFED2.4 were the highest and closest to AERONET and MISR observations, followed closely by FEER1.0. However, the QFED2.4 run tends to overestimate AOD in the region of SHSA, and the QFED2.4 BB emission dataset is tuned with the GEOS model. In contrast, the FEER1.0 BB emission dataset is derived in a more model-independent fashion and is more physically based since its emission coefficients are independently derived at each grid box. Therefore, we recommend the FEER1.0 BB emission dataset for aerosol-focused hindcast experiments in the two biomass-burning-dominated regions in the Southern Hemisphere, SHAF, and SHSA (as well as in other regions but with lower confidence). The differences between these six BB emission datasets are attributable to the approaches and input data used to derive BB emissions, such as whether AOD from satellite observations is used as a constraint, whether the approaches to parameterize the fire activities are based on burned area, FRP, or active fire count, and which set of emission factors is chosen.