Role of Trade in India’s Rising Atmospheric Mercury Emissions

2021 ◽  
Author(s):  
Jetashree ◽  
Qiumeng Zhong ◽  
Haifeng Zhou ◽  
Yumeng Li ◽  
Yu Liu ◽  
...  
Keyword(s):  
Atmospheric Mercury ◽  
Mercury Emissions

Rapidly changing coal-related city-level atmospheric mercury emissions and their driving forces

2021 ◽  
pp. 125060
Author(s):  
Yaqin Guo ◽  
Lin Xiao ◽  
Bin Chen ◽  
Zhujuan Wu ◽  
Huanxin Chen ◽  
...  
Keyword(s):  
Driving Forces ◽  
Atmospheric Mercury ◽  
Mercury Emissions

scholarly journals Speciated Atmospheric Mercury during Haze and Non-haze Days in an Inland City in China

2016 ◽  
Author(s):  
Qianqian Hong ◽  
Zhouqing Xie ◽  
Cheng Liu ◽  
Feiyue Wang ◽  
Pinhua Xie ◽  
...  
Keyword(s):  
Elemental Mercury ◽  
Atmospheric Mercury ◽  
Central China ◽  
Mercury Emissions ◽  
Gaseous Elemental Mercury ◽  
Enhanced Production ◽  
Mercury Transport ◽  
Haze Pollution ◽  
The Mean ◽  
Haze Days

Abstract. Long-term continuous measurements of speciated atmospheric mercury were conducted at Hefei, a mid-latitude inland city in east central China, from July 2013 to June 2014. The mean concentrations (± standard deviation) of gaseous elemental mercury (GEM), reactive gaseous mercury (RGM) and particle-bound mercury (PBM) were 3.95 ± 1.93 ng m−3, 2.49 ± 2.41 pg m−3 and 23.3 ± 90.8 pg m−3, respectively, during non-haze days, and 4.74 ± 1.62 ng m−3, 4.32 ± 8.36 pg m−3 and 60.2 ± 131.4 pg m−3, respectively, during haze days. Potential source contribution function (PSCF) analysis suggested that the atmospheric mercury pollution during haze days was caused primarily by local mercury emissions, instead of via long-range mercury transport. In addition, the disadvantageous diffussion during haze days will also enhance the level of atmospheric mercury. Compared to the GEM and RGM, change in PBM was more sensitive to the haze pollution. The mean PBM concentration during haze days was 2.5 times that during non-haze days due to elevated concentrations of particulate matter. A remarkable seasonal trend in PBM was observed with concentration decreasing in the following order in response to the frequency of haze days: autumn, winter, spring, summer. A distinct diurnal relationship was found between GEM and RGM during haze days, with the peak values of RGM coinciding with the decline in GEM. Using HgOH as an intermediate product during GEM oxidation, our results suggest that NO2 aggregation with HgOH could explain the enhanced production of RGM during the daytime in haze days. Increasing level of NOx will potentially accelerate the oxidation of GEM despite the decrease of solar radiation.

Gaseous mercury in coastal urban areas

2010 ◽  
Vol 7 (6) ◽  
pp. 537 ◽  
Author(s):  
Anne L. Soerensen ◽  
Henrik Skov ◽  
Matthew S. Johnson ◽  
Marianne Glasius
Keyword(s):  
Urban Areas ◽  
Marine Boundary Layer ◽  
Elemental Mercury ◽  
Atmospheric Mercury ◽  
Mercury Deposition ◽  
Mercury Emissions ◽  
Gaseous Elemental Mercury ◽  
Gaseous Mercury ◽  
Range Transport ◽  
Aquatic Food

Environmental context Mercury is a neurotoxin that bioaccumulates in the aquatic food web. Atmospheric emissions from urban areas close to the coast could cause increased local mercury deposition to the ocean. Our study adds important new data to the current limited knowledge on atmospheric mercury emissions and dynamics in coastal urban areas. Abstract Approximately 50% of primary atmospheric mercury emissions are anthropogenic, resulting from e.g. emission hotspots in urban areas. Emissions from urban areas close to the coast are of interest because they could increase deposition loads to nearby coastal waters as well as contribute to long range transport of mercury. We present results from measurements of gaseous elemental mercury (GEM) and reactive gaseous mercury (RGM) in 15 coastal cities and their surrounding marine boundary layer (MBL). An increase of 15–90% in GEM concentration in coastal urban areas was observed compared with the remote MBL. Strong RGM enhancements were only found in two cities. In urban areas with statistically significant GEM/CO enhancement ratios, slopes between 0.0020 and 0.0087 ng m–3 ppb–1 were observed, which is consistent with other observations of anthropogenic enhancement. The emission ratios were used to estimate GEM emissions from the areas. A closer examination of data from Sydney (Australia), the coast of Chile, and Valparaiso region (Chile) in the southern hemisphere, is presented.

Study on the reduction of atmospheric mercury emissions from mine waste enriched soils through native grass cover in the Mt. Amiata region of Italy

2013 ◽  
Vol 125 ◽  
pp. 69-74 ◽  
Author(s):  
L. Fantozzi ◽  
R. Ferrara ◽  
F. Dini ◽  
L. Tamburello ◽  
N. Pirrone ◽  
...  
Keyword(s):  
Mine Waste ◽  
Atmospheric Mercury ◽  
Grass Cover ◽  
Native Grass ◽  
Mercury Emissions

Atmospheric mercury emissions from mine wastes and surrounding geologically enriched terrains

2003 ◽  
Vol 43 (3) ◽  
pp. 339-351 ◽  
Author(s):  
Sexauer M. Gustin ◽  
M. Coolbaugh ◽  
M. Engle ◽  
B. Fitzgerald ◽  
R. Keislar ◽  
...  
Keyword(s):  
Atmospheric Mercury ◽  
Mine Wastes ◽  
Mercury Emissions

scholarly journals Trans-provincial health impacts of atmospheric mercury emissions in China

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Long Chen ◽  
Sai Liang ◽  
Maodian Liu ◽  
Yujun Yi ◽  
Zhifu Mi ◽  
...  
Keyword(s):  
Atmospheric Mercury ◽  
Health Impacts ◽  
Mercury Emissions

scholarly journals Effects of Brownfield Remediation on Total Gaseous Mercury Concentrations in an Urban Landscape

Sensors ◽  
2020 ◽  
Vol 20 (2) ◽  
pp. 387
Author(s):  
Linghui Meng ◽  
Charles T. Driscoll ◽  
Mario Montesdeoca ◽  
Huiting Mao
Keyword(s):  
Urban Areas ◽  
Urban Landscape ◽  
Urban Ecosystems ◽  
Atmospheric Mercury ◽  
Soil Restoration ◽  
Total Gaseous Mercury ◽  
Annual Average ◽  
Mercury Emissions ◽  
Gaseous Mercury ◽  
Parking Lot

In order to obtain a better perspective of the impacts of brownfields on the land–atmosphere exchange of mercury in urban areas, total gaseous mercury (TGM) was measured at two heights (1.8 m and 42.7 m) prior to 2011–2012 and after 2015–2016 for the remediation of a brownfield and installation of a parking lot adjacent to the Syracuse Center of Excellence in Syracuse, NY, USA. Prior to brownfield remediation, the annual average TGM concentrations were 1.6 ± 0.6 and 1.4 ± 0.4 ng · m − 3 at the ground and upper heights, respectively. After brownfield remediation, the annual average TGM concentrations decreased by 32% and 22% at the ground and the upper height, respectively. Mercury soil flux measurements during summer after remediation showed net TGM deposition of 1.7 ng · m − 2 · day − 1 suggesting that the site transitioned from a mercury source to a net mercury sink. Measurements from the Atmospheric Mercury Network (AMNet) indicate that there was no regional decrease in TGM concentrations during the study period. This study demonstrates that evasion from mercury-contaminated soil significantly increased local TGM concentrations, which was subsequently mitigated after soil restoration. Considering the large number of brownfields, they may be an important source of mercury emissions source to local urban ecosystems and warrant future study at additional locations.

scholarly journals Diatom ooze—A large marine mercury sink

Science ◽  
2018 ◽  
Vol 361 (6404) ◽  
pp. 797-800 ◽  
Author(s):  
Sara Zaferani ◽  
Marta Pérez-Rodríguez ◽  
Harald Biester
Keyword(s):  
High Resolution ◽  
Southern Ocean ◽  
Marine Sediment ◽  
Crucial Role ◽  
Anthropogenic Pollution ◽  
Atmospheric Mercury ◽  
Mercury Accumulation ◽  
Accumulation Rates ◽  
Sediment Data

The role of algae for sequestration of atmospheric mercury in the ocean is largely unknown owing to a lack of marine sediment data. We used high-resolution cores from marine Antarctica to estimate Holocene global mercury accumulation in biogenic siliceous sediments (diatom ooze). Diatom ooze exhibits the highest mercury accumulation rates ever reported for the marine environment and provides a large sink of anthropogenic mercury, surpassing existing model estimates by as much as a factor of 7. Anthropogenic pollution of the Southern Ocean began ~150 years ago, and up to 20% of anthropogenic mercury emitted to the atmosphere may have been stored in diatom ooze. These findings reveal the crucial role of diatoms as a fast vector for mercury sequestration and diatom ooze as a large marine mercury sink.

scholarly journals Atmospheric Mercury in China Studied with Differential Absorption Lidar

2020 ◽  
Vol 237 ◽  
pp. 03003
Author(s):  
Guangyu Zhao ◽  
Zheng Duan ◽  
Ming Lian ◽  
Sune Svanberg
Keyword(s):  
Environmental Pollutant ◽  
Atmospheric Mercury ◽  
Guizhou Province ◽  
Differential Absorption ◽  
Differential Absorption Lidar ◽  
Mercury Emissions ◽  
Mining Areas ◽  
Main Producer ◽  
Mercury Mining ◽  
Atomic Mercury

Mercury is a very serious environmental pollutant which is intensely studied by many researchers. China is a main producer and consumer of mercury. We have pursued extensive monitoring of atomic mercury using the differential absorption lidar (DIAL) technique, based on a newly constructed mobile monitoring system. Mercury levels in major cities (Guangzhou, Zhengzhou, Xi´a n) were measured, as well as in mercury mining areas in Wanshan, Guizhou province. Further, mercury emissions from the Emperor Qin Mausoleum in Xi´an were investigated together with archaeologists.

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