The Eastern Arctic Seas and the north-western Pacific are among the most poorly investigated areas as far as Hg cycling in marine systems is concerned. Continuous measurements of gaseous elemental mercury (Hg(0)) concentrations in the marine boundary layer and Hg(0) evasion fluxes from the sea surface were performed in these regions in fall 2018. Atmospheric Hg(0) concentrations of 1.02-2.50 ng/m were measured (average: 1.45 ± 0.12 ng/m; N = 2518). Values in the Far Eastern Seas of Russia were lower compared to previous observations, presumably reflecting а global trend of decreasing atmospheric Hg(0). Concentration-weighted trajectory analysis highlighted three source regions influencing Hg(0) concentrations in the ambient air during the cruise: 1) the north-eastern China and the Yellow Sea region; 2) the Kuril-Kamchatka region of the Pacific Ocean and the region around the Commander and Aleutian Islands; and 3) the Arctic region. In the Arctic, sea-air Hg(0) evasion fluxes were at the same low levels as those observed earlier in the northern sea areas (0.28-1.35 ng/m/h, average, 0.70 ± 0.26 ng/m/h, N = 29). In the Eastern Arctic Seas, Hg(0) evasion fluxes were significantly dependent on river runoff. In the Arctic Ocean, they were negatively correlated with water temperature and positively correlated with salinity, suggesting a proximity to areas with contiguous ice and higher dissolved Hg(0) concentrations in the surface seawater. These findings are consistent with the hypothesis that the Arctic Ocean is a source of atmospheric Hg(0) during late summer and fall.
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http://dx.doi.org/10.1016/j.scitotenv.2020.142003 | DOI Listing |
Environ Pollut
September 2024
University of Hohenheim, Institute of Landscape and Plant Ecology, Department of Plant Ecology, Stuttgart, Germany.
Due to integrated pollution prevention and control measures and the reduced burning of coal, air concentrations of mercury (Hg) are currently levelling off. In the future, however, evasion from land surfaces will probably reverse this trend. Reasons are the rising temperatures and the loss of forest cover caused by calamities, droughts, storms and wildfires.
View Article and Find Full Text PDFEnviron Sci Technol
October 2023
State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang 550081, China.
Environ Sci Technol
July 2023
State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang 550081, China.
Significant knowledge gaps exist regarding the emission of elemental mercury (Hg) from the tropical forest floor, which limit our understanding of the Hg mass budget in forest ecosystems. In this study, biogeochemical processes of Hg deposition to and evasion from soil in a Chinese tropical rainforest were investigated using Hg stable isotopic techniques. Our results showed a mean air-soil flux as deposition of -4.
View Article and Find Full Text PDFEnviron Pollut
September 2023
Department of Mathematics & Geosciences, University of Trieste, Via E. Weiss 2, 34128, Trieste, Italy.
The northern Adriatic Sea is well known for mercury (Hg) contamination mainly due to historical Hg mining which took place in Idrija (Slovenia). The formation of dissolved gaseous mercury (DGM) and its subsequent volatilisation can reduce the amount of Hg available in the water column. In this work, the diurnal patterns of both DGM production and gaseous elemental Hg (Hg) fluxes at the water-air interface were seasonally evaluated in two selected environments within this area, a highly Hg-impacted, confined fish farm (VN: Val Noghera, Italy) and an open coastal zone less impacted by Hg inputs (PR: Bay of Piran, Slovenia).
View Article and Find Full Text PDFProc Natl Acad Sci U S A
January 2023
School of Atmospheric Sciences, Nanjing University, Nanjing, Jiangsu 210023, China.
Human exposure to monomethylmercury (CHHg), a potent neurotoxin, is principally through the consumption of seafood. The formation of CHHg and its bioaccumulation in marine food webs experience ongoing impacts of global climate warming and ocean biogeochemistry alterations. Employing a series of sensitivity experiments, here we explicitly consider the effects of climate change on marine mercury (Hg) cycling within a global ocean model in the hypothesized twenty-first century under the business-as-usual scenario.
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