Haoran Zhang

Prof. Dr. Haoran Zhang

The University of Tokyo
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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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.

1 November 2021 in Journal of Computational Physics
Verified
Journal Article
Open access
YCYuntian Chen
Yuntian Chen
DHDou Huang
Dou Huang
DZDongxiao Zhang
Dongxiao Zhang
JZJunsheng Zeng
Junsheng Zeng
NWNanzhe Wang
Nanzhe Wang
JYJinyue Yan
Jinyue Yan

1 January 2020 in Applied Energy
Verified
Journal Article
Closed access
JZJianqin Zheng
Jianqin Zheng
Haoran ZhangHaoran Zhang
Haoran Zhang
YDYuanhao Dai
Yuanhao Dai
Bohong WangBohong Wang
Bohong Wang
TZTaicheng Zheng
Taicheng Zheng
XSXuan Song
Xuan Song

1 May 2019 in Applied Energy
Verified
Journal Article
Closed access
KFKai Fang
Kai Fang
QZQifeng Zhang
Qifeng Zhang
YLYin Long
Yin Long
YYYoshikuni Yoshida
Yoshikuni Yoshida
Lu SunLu Sun
Lu Sun
SLShuai Li
Shuai Li

1 June 2018 in Applied Energy
Verified
Journal Article
Closed access
Haoran ZhangHaoran Zhang
Haoran Zhang
Xuan SongXuan Song
Xuan Song
TXTianqi Xia
Tianqi Xia
MYMeng Yuan
Meng Yuan
ZFZipei Fan
Zipei Fan
YLYongtu Liang
Yongtu Liang

1 March 2019 in Health & Place
Verified
Journal Article
Closed access
TXTianqi Xia
Tianqi Xia
Xuan SongXuan Song
Xuan Song
Haoran ZhangHaoran Zhang
Haoran Zhang
XSXiaoya Song
Xiaoya Song
HKHiroshi Kanasugi
Hiroshi Kanasugi
RSRyosuke Shibasaki
Ryosuke Shibasaki