XUN Wang

Dr. XUN Wang

orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

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

Representative Publications

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28 July 2016 in Environmental Science & Technology
Verified
Journal Article
Closed access
XWXUN Wang
XUN Wang
ZBZhengduo Bao
Zhengduo Bao
CLChe-Jen Lin
Che-Jen Lin
WYWei Yuan
Wei Yuan
XFXinbin Feng
Xinbin Feng

24 August 2015 in Atmospheric Chemistry and Physics
Verified
Journal Article
Open access
PDF file
XFX. W. Fu
X. W. Fu
Haoran ZhangHaoran Zhang
Haoran Zhang
BYB. Yu
B. Yu
XWXUN Wang
XUN Wang
Che-Jen LinChe-Jen Lin
Che-Jen Lin
Xinbin FengXinbin Feng
Xinbin Feng
China presently contributes the largest amount of anthropogenic mercury (Hg) emission into the atmosphere in the world. Over the past decade, numerous studies have been conducted to characterize the concentration and forms of atmospheric Hg in China, which provide insights into the spatial and temporal distributions of atmospheric Hg through ground-based measurements at widely diverse geographical locations and during cruise and flight campaigns. In this paper, we present a comprehensive review of the state of understanding in atmospheric Hg in China. Gaseous elemental mercury (GEM) and particulate-bound mercury (PBM) measured at the remote sites in China are substantially elevated compared to the background values in the Northern Hemisphere. In Chinese urban areas, the highly elevated GEM, PBM and gaseous oxidized mercury (GOM) were mainly derived from local anthropogenic Hg emissions, whereas regional anthropogenic emissions and long-range transport from domestic source regions are the primary causes of the elevated GEM and PBM concentrations at remote sites. Using 7–9 years of continuous observations at a remote site and an urban site, a slight increase in atmospheric GEM (2.4–2.5 % yr−1) was identified (paired samples test: p < 0.01), which is in agreement with the increasing domestic anthropogenic emissions. Anthropogenic GEM emission quantity in China estimated through the observed GEM / CO concentration ratios ranged from 632 to 1138 t annually over the past decade, 2–3 times larger than published values using emission activity data. Modeling results and filed measurements show dry deposition is the predominant process for removing Hg from the atmosphere, 2.5–9.0 times larger than wet deposition, due to the elevated atmospheric GEM and PBM concentrations that facilitate dry deposition to terrestrial landscapes. Further studies to reconcile the observed and simulated Hg concentrations, to understand the impact of domestic emission reduction on Hg concentration and deposition and to delineate the role of Hg emission and deposition of China in the global Hg biogeochemical cycle, are needed.

3 December 2018 in Environmental Science & Technology
Verified
Journal Article
Closed access
WYWei Yuan
Wei Yuan
JSJonas Sommar
Jonas Sommar
CLChe-Jen Lin
Che-Jen Lin
XWXUN Wang
XUN Wang
KLKai Li
Kai Li
Xinbin FengXinbin Feng
Xinbin Feng

17 August 2016 in Environmental Science & Technology
Verified
Journal Article
Closed access
BYBen Yu
Ben Yu
Xuewu FuXuewu Fu
Xuewu Fu
RYRunsheng Yin
Runsheng Yin
HZHui Zhang
Hui Zhang
XWXUN Wang
XUN Wang
Xinbin FengXinbin Feng
Xinbin Feng

21 August 2019 in Environmental Science & Technology
Verified
Journal Article
Closed access
XWXUN Wang
XUN Wang
WYWei Yuan
Wei Yuan
CLChe-Jen Lin
Che-Jen Lin
LZLeiming Zhang
Leiming Zhang
HZHui Zhang
Hui Zhang
Xinbin FengXinbin Feng
Xinbin Feng

27 June 2019 in Environmental Science & Technology
Verified
Journal Article
Closed access
KLKaiyun Liu
Kaiyun Liu
QWQingru Wu
Qingru Wu
LWLong Wang
Long Wang
Shuxiao WangShuxiao Wang
Shuxiao Wang
TLTonghao Liu
Tonghao Liu
JHJiming Hao
Jiming Hao