Abstract
Mercury (Hg) is a ubiquitous environmental toxicant that has caused global concern due to its persistence and bioaccumulation in the environment. Wet deposition is a crucial Hg input for both terrestrial and aquatic environments and is a significant indicator for evaluating the effectiveness of anthropogenic Hg control. Rainwater samples were collected from May 2014 to October 2018 in Chongming Island to understand the multi-year Hg wet deposition characteristics. The annual Hg wet deposition flux ranged from 2.6 to 9.8 μg m−2 yr−1 (mean: 4.9 μg m−2 yr−1). Hg wet deposition flux in Chongming was comparable to the observations at temperate and subtropical background sites (2.0–10.2 μg m−2 yr−1) in the northern hemisphere. Hg wet deposition flux decreased from 8.6 μg m−2 yr−1 in 2014–2015 to 3.8 μg m−2 yr−1 in 2016 and was attributed to a decrease in the volume-weighted mean (VWM) Hg concentration (−4.1 ng L−1 yr−1). The reduced VWM Hg was explained by the decreasing atmospheric Hg and anthropogenic emissions reductions. The annual Hg wet deposition flux further decreased from 3.8 μg m−2 in 2016 to 2.6 μg m−2 in 2018. The reduction of warm season (April–September) rainfall amounts (356–845 mm) mainly contributed to the Hg wet deposition flux reduction during 2016–2018. The multi-year monitoring results suggest that long-term measurements are necessary when using wet deposition as an indicator to reflect the impact of anthropogenic efforts on mercury pollution control and meteorological condition variations.
Highlights
Mercury (Hg) is a pollutant of global concern due to its long residence time and neurotoxicity.Once emitted in the atmosphere, Hg can be transported in long distances and cause ecological damage globally [1]
The mean volume-weighted mean (VWM) Hg concentration (7.6 ng L−1 ) in Chongming was within the range of temperate and subtropical background observation sites in East
The seasonal variation of Hg wet deposition flux was characterized by a maximum in June and a minimum in December, induced by the variation of rainfall amounts
Summary
Mercury (Hg) is a pollutant of global concern due to its long residence time and neurotoxicity. Once emitted in the atmosphere, Hg can be transported in long distances and cause ecological damage globally [1]. Atmospheric Hg exists in three forms: gaseous elemental mercury (GEM), gaseous oxidized mercury (GOM), and particulate-bound mercury (PBM). GEM contributes to 95–99% of atmospheric Hg with a residence time of 0.5–2 years [2]. GOM and PBM represent less than 5%. Of atmospheric Hg, they impact the global Hg cycling by rapid dry deposition and wet scavenging such as rainfall [3,4]. Hg deposition could represent its pollution characteristics and help us understand Hg
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