Anthropogenic short-lived halogens increase human exposure to mercury contamination due to enhanced mercury oxidation over continents

Author:

Fu Xiao1,Sun Xianyi1,Travnikov Oleg2ORCID,Li Qinyi345ORCID,Qin Chuang1,Cuevas Carlos A.3ORCID,Fernandez Rafael P.6ORCID,Mahajan Anoop S.7ORCID,Wang Shuxiao8ORCID,Wang Tao4ORCID,Saiz-Lopez Alfonso3ORCID

Affiliation:

1. Institute of Environment and Ecology, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China

2. Department of Environmental Sciences, Jožef Stefan Institute, Ljubljana 1000, Slovenia

3. Department of Atmospheric Chemistry and Climate, Institute of Physical Chemistry Blas Cabrera, Spanish National Research Council, Madrid 28006, Spain

4. Department of Civil and Environmental Engineering, The Hong Kong Polytechnic University, Hong Kong 999077, China

5. Environment Research Institute, Shandong University, Qingdao 266237, China

6. Institute for Interdisciplinary Science, National Research Council, School of Natural Sciences, National University of Cuyo, Mendoza M5502JMA, Argentina

7. Centre for Climate Change Research, Indian Institute of Tropical Meteorology, Ministry of Earth Sciences, Pashan, Pune 411008, India

8. State Key Joint Laboratory of Environmental Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 100084, China

Abstract

Mercury (Hg) is a contaminant of global concern, and an accurate understanding of its atmospheric fate is needed to assess its risks to humans and ecosystem health. Atmospheric oxidation of Hg is key to the deposition of this toxic metal to the Earth’s surface. Short-lived halogens (SLHs) can provide halogen radicals to directly oxidize Hg and perturb the budget of other Hg oxidants (e.g., OH and O 3 ). In addition to known ocean emissions of halogens, recent observational evidence has revealed abundant anthropogenic emissions of SLHs over continental areas. However, the impacts of anthropogenic SLHs emissions on the atmospheric fate of Hg and human exposure to Hg contamination remain unknown. Here, we show that the inclusion of anthropogenic SLHs substantially increased local Hg oxidation and, consequently, deposition in/near Hg continental source regions by up to 20%, thereby decreasing Hg export from source regions to clean environments. Our modeling results indicated that the inclusion of anthropogenic SLHs can lead to higher Hg exposure in/near Hg source regions than estimated in previous assessments, e.g., with increases of 8.7% and 7.5% in China and India, respectively, consequently leading to higher Hg-related human health risks. These results highlight the urgent need for policymakers to reduce local Hg and SLHs emissions. We conclude that the substantial impacts of anthropogenic SLHs emissions should be included in model assessments of the Hg budget and associated health risks at local and global scales.

Funder

深圳市科技创新委员会 | Natural Science Foundation of Shenzhen Municipality

GDSTC | Natural Science Foundation of Guangdong Province

MOST | National Natural Science Foundation of China

Scientific Research Start-up Funds from Tsinghua Shenzhen International Graduate School

Publisher

Proceedings of the National Academy of Sciences

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