To explore the variation of mercury in the atmosphere in Suzhou, continuous monitoring of gaseous element mercury (GEM), gaseous oxidized mercury (GOM), and particulate bound mercury (PBM) was conducted from January 1 to December 31, 2018, in Suzhou. The weights trajectory analysis method (CWT) and concentration rose were used to analyze the atmospheric mercury sources and concentration variation. The results showed that during the monitoring period, the concentration ranges of GEM, GOM, and PBM in Suzhou were 0-53.3 ng·m, 0-256 pg·m, and 0-5208 pg·m, respectively. The corresponding annual average concentrations of the three mercury species were (2.57±2.09) ng·m, (5.27±15.7) pg·m, and (16.0±157) pg·m, respectively. GEM was the main component of atmospheric mercury in Suzhou. During the monitoring period, the average concentration of GEM in Suzhou was highest in winter, higher in spring than in autumn, and lowest in summer. According to the CWT, the mercury-containing air mass in spring and winter predominantly originated from inland; in summer, it mainly originated from the local area, the Yellow Sea, and the East China Sea, and in autumn from inland, the Yellow Sea, and the Bohai Sea. The wind and mercury rose charts showed that atmospheric mercury concentrations were higher from inland and lower from the ocean. During the monitoring period, the average concentrations of GEM and PBM in Suzhou were lower during the day than the night. The diurnal variation of GEM and PBM was significantly and strongly correlated with solar radiation, humidity, and air temperature. The average concentration of GOM showed multiple peaks and valleys in one day. Some peaks were caused by fuel oil combustion emissions, and some by O oxidation with GEM.
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http://dx.doi.org/10.13227/j.hjkx.201910076 | DOI Listing |
Nat Commun
January 2025
Department of Earth and Environmental Sciences, Tulane University, New Orleans, LA, 70118, USA.
Mercury (Hg) contamination poses a persistent threat to the remote Arctic ecosystem, yet the mechanisms driving the pronounced summer rebound of atmospheric gaseous elemental Hg (Hg) and its subsequent fate remain unclear due to limitations in large-scale seasonal studies. Here, we use an integrated atmosphere-land-sea-ice-ocean model to simulate Hg cycling in the Arctic comprehensively. Our results indicate that oceanic evasion is the dominant source (~80%) of the summer Hg rebound, particularly driven by seawater Hg release facilitated by seasonal ice melt (~42%), with further contributions from anthropogenic deposition and terrestrial re-emissions.
View Article and Find Full Text PDFEnviron Pollut
January 2025
College of Meteorology and Oceanography, National University of Defense Technology, Changsha, 410073, China.
Understanding the composition of mercury (Hg) in the atmosphere is important for confirming its sources and to preventing and reduce the production. To explore the morphological distribution characteristics of wet Hg concentrations in Xi'an Shaanxi Province, China, total Hg (THg), dissolved Hg (DTHg), reactive Hg (RTHg) and particulate-bound Hg (PTHg) (Hg insoluble in water) were measured at 72 precipitation in Xi'an from September 2020 to July 2022, and their average concentrations were 3.035 ± 3.
View Article and Find Full Text PDFSci Total Environ
January 2025
Trent University, Peterborough, Ontario, Canada.
Arctic rivers may be the largest net sources of mercury (Hg) to the Arctic Ocean, yet riverine sources of Hg remain poorly characterized compared to atmospheric processes. This article reviews the current state of knowledge on Hg inputs to the Mackenzie River and Valley in Northern Canada from six point and non-point sources. Point sources include the locations of mines, fossil fuel extraction facilities, and retrogressive permafrost thaw slumps.
View Article and Find Full Text PDFJ Hazard Mater
January 2025
Department of Civil, Urban, Earth, and Environmental Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea. Electronic address:
The source-receptor relationship of atmospheric mercury is a critical environmental concern. However, comprehensive evaluations of mercury pollution based on spatially resolved and time-averaged data have not yet been conducted in Korea. In this study, the spatio-temporal variations of total gaseous mercury (TGM) and mercury isotopes were examined using passive air samplers at 30 sites in Ulsan over one year.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
Key Laboratory of Geographic Information Science (Ministry of Education), School of Geographic Sciences, East China Normal University, Shanghai 200241, China.
Mercury (Hg) is a neurotoxic pollutant that is ubiquitous on the planet and receives global concern because of its adverse health effects. Particle-bound Hg formation in the atmosphere stems mainly from the adsorption of reactive gaseous Hg on aerosol particles, particularly sea salt aerosol. However, the observed comparable abundance of Hg over Hg in the marine atmosphere has not been reproduced by traditional statistics-based schemes, which were constructed by continental observations.
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