Shaocai Yu

Prof. Dr. Shaocai Yu

Research Center for Air Pollution and Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058, China

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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8 February 2019 in Science
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DRDaniel Rosenfeld
Daniel Rosenfeld
YZYannian Zhu
Yannian Zhu
MWMinghuai Wang
Minghuai Wang
YZYoutong Zheng
Youtong Zheng
TGTom Goren
Tom Goren
Shaocai YuShaocai Yu
Shaocai Yu
Reflections on cloud effects: How much impact does the abundance of cloud condensation nuclei (CCN) aerosols above the oceans have on global temperatures? Rosenfeld et al. analyzed how CCN affect the properties of marine stratocumulus clouds, which reflect much of the solar radiation received by Earth back to space (see the Perspective by Sato and Suzuki). The CCN abundance explained most of the variability in the radiative cooling. Thus, the magnitude of radiative forcing provided by these clouds is much more sensitive to the presence of CCN than current models indicate, which suggests the existence of other compensating warming effects. Science , this issue p. eaav0566 ; see also p. 580

22 July 2021 in Environmental Chemistry Letters
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MLMengying Li
Mengying Li
Shaocai YuShaocai Yu
Shaocai Yu
XCXue Chen
Xue Chen
ZLZhen Li
Zhen Li
YZYibo Zhang
Yibo Zhang
JSJohn H. Seinfeld
John H. Seinfeld

30 November 2017 in Environmental Chemistry Letters
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Khalid MehmoodKhalid Mehmood
Khalid Mehmood
SCShucheng Chang
Shucheng Chang
Shaocai YuShaocai Yu
Shaocai Yu
LWLiqiang Wang
Liqiang Wang
PLPengfei Li
Pengfei Li
JSJohn H. Seinfeld
John H. Seinfeld

4 May 2015 in Proceedings of the National Academy of Sciences
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PLPengfei Li
Pengfei Li
RYRenchang Yan
Renchang Yan
Shaocai YuShaocai Yu
Shaocai Yu
SWSi Wang
Si Wang
WLWeiping Liu
Weiping Liu
HBHuiming Bao
Huiming Bao

12 June 2020 in Environmental Chemistry Letters
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LWLiqiang Wang
Liqiang Wang
MLMengying Li
Mengying Li
Shaocai YuShaocai Yu
Shaocai Yu
XCXue Chen
Xue Chen
ZLZhen Li
Zhen Li
JSJohn H. Seinfeld
John H. Seinfeld
The outbreak of coronavirus named COVID-19, initially identified in Wuhan, China in December 2019, has spread rapidly at the global scale. Most countries have rapidly stopped almost all activities including industry, services and transportation of goods and people, thus decreasing air pollution in an unprecedented way, and providing a unique opportunity to study air pollutants. While satellite data have provided visual evidence for the global reduction in air pollution such as nitrogen dioxide (NO2) worldwide, precise and quantitative information is missing at the local scale. Here we studied changes in particulate matter (PM2.5, PM10), carbon monoxide (CO), NO2, sulfur dioxide (SO2) and ozone (O3) at 10 urban sites in Hangzhou, a city of 7.03 million inhabitants, and at 1 rural site, before city lockdown, January 1–23, during city lockdown, January 24-February 15, and during resumption, February 16–28, in 2020. Results show that city lockdown induced a sharp decrease in PM2.5, PM10, CO, and NO2 concentrations at both urban and rural sites. The NO2 decrease is explained by reduction in traffic emissions in the urban areas, and by lower regional transport in rural areas during lockdown, as expected. SO2 concentrations decreased from 6.3 to 5.3 μg m−3 in the city, but increased surprisingly from 4.7 to 5.8 μg m−3 at the rural site: this increase is attributed both to higher coal consumption for heating and emissions from traditional fireworks of the Spring Eve and Lantern Festivals during lockdown. Unexpectedly, O3 concentrations increased by 145% from 24.6 to 60.6 μg m−3 in the urban area, and from 42.0 to 62.9 μg m−3 in the rural area during the lockdown. This finding is explained by the weakening of chemical titration of O3 by NO due to reductions of NOx fresh emissions during the non-photochemical reaction period from 20:00 PM to 9:00 AM (local time). During the lockdown, compared to the same period in 2019, the daily average concentrations in the city decreased by 42.7% for PM2.5, 47.9% for PM10, 28.6% for SO2, 22.3% for CO and 58.4% for NO2, which is obviously explained by the absence of city activities. Overall, we observed not only the expected reduction in some atmospheric pollutants (PM, SO2, CO, NO2), but also unexpected increases in SO2 in the rural areas and of ozone (O3) in both urban and rural areas, the latter being paradoxically due to the reduction in nitrogen oxide levels. In other words, the city lockdown has improved air quality by reducing PM2.5, PM10, CO, and NO2, but has also decreased air quality by augmenting O3 and SO2.

24 October 2014 in Atmospheric Chemistry and Physics
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Shaocai YuShaocai Yu
Shaocai Yu
RMR. Mathur
R. Mathur
JPJ. Pleim
J. Pleim
DWD. Wong
D. Wong
RGR. Gilliam
R. Gilliam
XLX. Liu
X. Liu
This study implemented first, second and glaciation aerosol indirect effects (AIE) on resolved clouds in the two-way coupled Weather Research and Forecasting Community Multiscale Air Quality (WRF–CMAQ) modeling system by including parameterizations for both cloud drop and ice number concentrations on the basis of CMAQ-predicted aerosol distributions and WRF meteorological conditions. The performance of the newly developed WRF–CMAQ model, with alternate Community Atmospheric Model (CAM) and Rapid Radiative Transfer Model for GCMs (RRTMG) radiation schemes, was evaluated with observations from the Clouds and the See http://ceres.larc.nasa.gov/. Earth's Radiant Energy System (CERES) satellite and surface monitoring networks (AQS, IMPROVE, CASTNET, STN, and PRISM) over the continental US (CONUS) (12 km resolution) and eastern Texas (4 km resolution) during August and September of 2006. The results at the Air Quality System (AQS) surface sites show that in August, the normalized mean bias (NMB) values for PM2.5 over the eastern US (EUS) and the western US (WUS) are 5.3% (−0.1%) and 0.4% (−5.2%) for WRF–CMAQ/CAM (WRF–CMAQ/RRTMG), respectively. The evaluation of PM2.5 chemical composition reveals that in August, WRF–CMAQ/CAM (WRF–CMAQ/RRTMG) consistently underestimated the observed SO42- by −23.0% (−27.7%), −12.5% (−18.9%) and −7.9% (−14.8%) over the EUS at the Clean Air Status Trends Network (CASTNET), Interagency Monitoring of Protected Visual Environments (IMPROVE) and Speciated Trends Network (STN) sites, respectively. Both configurations (WRF–CMAQ/CAM, WRF–CMAQ/RRTMG) overestimated the observed mean organic carbon (OC), elemental carbon (EC) and and total carbon (TC) concentrations over the EUS in August at the IMPROVE sites. Both configurations generally underestimated the cloud field (shortwave cloud forcing, SWCF) over the CONUS in August due to the fact that the AIE on the subgrid convective clouds was not considered when the model simulations were run at the 12 km resolution. This is in agreement with the fact that both configurations captured SWCF and longwave cloud forcing (LWCF) very well for the 4 km simulation over eastern Texas, when all clouds were resolved by the finer resolution domain. The simulations of WRF–CMAQ/CAM and WRF–CMAQ/RRTMG show dramatic improvements for SWCF, LWCF, cloud optical depth (COD), cloud fractions and precipitation over the ocean relative to those of WRF default cases in August. The model performance in September is similar to that in August, except for a greater overestimation of PM2.5 due to the overestimations of SO42-, NH4+, NO3-, and TC over the EUS, less underestimation of clouds (SWCF) over the land areas due to the lower SWCF values, and fewer convective clouds in September. This work shows that inclusion of indirect aerosol effect treatments in WRF–CMAQ represents a significant advancement and milestone in air quality modeling and the development of integrated emissions control strategies for air quality management and climate change mitigation.