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Volume 15, issue 16
Atmos. Chem. Phys., 15, 9455-9476, 2015
https://doi.org/10.5194/acp-15-9455-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.

Special issue: Data collection, analysis and application of speciated atmospheric...

Atmos. Chem. Phys., 15, 9455-9476, 2015
https://doi.org/10.5194/acp-15-9455-2015
© Author(s) 2015. This work is distributed under
the Creative Commons Attribution 3.0 License.

Review article 24 Aug 2015

Review article | 24 Aug 2015

Observations of atmospheric mercury in China: a critical review

X. W. Fu1, H. Zhang1,2, B. Yu1,2, X. Wang1,2, C.-J. Lin1,3,4, and X. B. Feng1 X. W. Fu et al.
  • 1State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang 550002, China
  • 2University of the Chinese Academy of Sciences, Beijing 100049, China
  • 3Department of Civil and Environmental Engineering, Lamar University, Beaumont, Texas 77710, USA
  • 4College of Energy and Environment, South China University of Technology, Guangzhou 510006, China

Abstract. 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.

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