Anthropogenic mercury migration from Asia to the open ocean

Abstract To evaluate the path of anthropogenic mercury (Hg) from Asia to the Pacific Ocean, we report mercury stable isotopes in zooplankton from the East China Sea to the Bay of Bengal, and in the Philippine Sea and the Central Pacific. Here, we find that zooplankton mercury concentration decreases and δ 202 Hg and Δ 199 Hg increase with distances away from Asia, depicting anthropogenic mercury dilution. Anomalies of even mass-number isotopes (Δ 200 Hg), used to decipher between near-surface and tropospheric oxidation, suggest that 40–48% of anthropogenic Hg(0) is initially oxidized at the marine boundary layer or via terrestrial vegetation, and >50% of anthropogenic Hg(0) is circulated to the upper atmosphere for oxidation and removal to the Pacific. The fact that both near-surface and atmospheric Hg(0) oxidation supplies bioavailable Hg(II) strengthens the case for mitigating Hg(0) emissions. Recently reported climate-projected increase in riverine mercury fluxes may also benefit by reducing anthropogenic Hg(0) available for vegetative uptake.

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Publication Details

Journal
Communications Earth & Environment
Published
2025-08-16
DOI
https://doi.org/10.1038/s43247-025-02555-z
Citations
1
Primary Topic
Mercury impact and mitigation studies
Type
article
Field-Weighted Citation Impact
1.20

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Anthropogenic mercury migration from Asia to the open ocean

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Mercury impact and mitigation studies
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Anthropogenic mercury migration from Asia to the open ocean

Dong‐Jin Kang, Laura C. Motta, Seung Hyeon Lim, Joel D. Blum, Sae Yun Kwon, Youn‐Ho Lee
article en
1 citations

Abstract

Abstract To evaluate the path of anthropogenic mercury (Hg) from Asia to the Pacific Ocean, we report mercury stable isotopes in zooplankton from the East China Sea to the Bay of Bengal, and in the Philippine Sea and the Central Pacific. Here, we find that zooplankton mercury concentration decreases and δ 202 Hg and Δ 199 Hg increase with distances away from Asia, depicting anthropogenic mercury dilution. Anomalies of even mass-number isotopes (Δ 200 Hg), used to decipher between near-surface and tropospheric oxidation, suggest that 40–48% of anthropogenic Hg(0) is initially oxidized at the marine boundary layer or via terrestrial vegetation, and >50% of anthropogenic Hg(0) is circulated to the upper atmosphere for oxidation and removal to the Pacific. The fact that both near-surface and atmospheric Hg(0) oxidation supplies bioavailable Hg(II) strengthens the case for mitigating Hg(0) emissions. Recently reported climate-projected increase in riverine mercury fluxes may also benefit by reducing anthropogenic Hg(0) available for vegetative uptake.

Communications Earth & EnvironmentVol. 6(1)
Pohang University of Science and Technology (KR), Korea Institute of Ocean Science and Technology (KR), University of Michigan (US), Woods Hole Oceanographic Institution (US), Korea University of Science and Technology (KR)
National Research Foundation, Ministry of Oceans and Fisheries, National Research Foundation of Korea, Korea Institute of Ocean Science and Technology, Korea Institute of Marine Science and Technology promotion, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 19%
Mercury impact and mitigation studies
1.20
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