Glutathione level after long-term occupational elemental mercury exposure

2008 ◽  
Vol 107 (1) ◽  
pp. 115-123 ◽  
Author(s):  
Alfred Bogomir Kobal ◽  
Marija Prezelj ◽  
Milena Horvat ◽  
Mladen Krsnik ◽  
Darija Gibicar ◽  
...  
Toxics ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 172
Author(s):  
Laura Fantozzi ◽  
Nicoletta Guerrieri ◽  
Giovanni Manca ◽  
Arianna Orrù ◽  
Laura Marziali

We present the first assessment of atmospheric pollution by mercury (Hg) in an industrialized area located in the Ossola Valley (Italian Central Alps), in close proximity to the Toce River. The study area suffers from a level of Hg contamination due to a Hg cell chlor-alkali plant operating from 1915 to the end of 2017. We measured gaseous elemental Hg (GEM) levels by means of a portable Hg analyzer during car surveys between autumn 2018 and summer 2020. Moreover, we assessed the long-term dispersion pattern of atmospheric Hg by analyzing the total Hg concentration in samples of lichens collected in the Ossola Valley. High values of GEM concentrations (1112 ng m−3) up to three orders of magnitude higher than the typical terrestrial background concentration in the northern hemisphere were measured in the proximity of the chlor-alkali plant. Hg concentrations in lichens ranged from 142 ng g−1 at sampling sites located north of the chlor-alkali plant to 624 ng g−1 in lichens collected south of the chlor-alkali plant. A north-south gradient of Hg accumulation in lichens along the Ossola Valley channel was observed, highlighting that the area located south of the chlor-alkali plant is more exposed to the dispersion of Hg emitted into the atmosphere from the industrial site. Long-term studies on Hg emission and dispersion in the Ossola Valley are needed to better assess potential impact on ecosystems and human health.


PEDIATRICS ◽  
1987 ◽  
Vol 79 (6) ◽  
pp. 935-938
Author(s):  
Paul J. Hudson ◽  
Richard L. Vogt ◽  
Jack Brondum ◽  
Linden Witherell ◽  
Gary Myers ◽  
...  

Because evidence of mercury exposure was found among workers of a mercury thermometer-manufacturing plant in March 1984, the Vermont Department of Health studied the workers' children for both exposure to mercury and evidence of mercury toxicity. The median urine mercury level of 23 workers' children was 25 µg/L. This was significantly higher than the level (5 µg/L) among 39 children randomly selected from nonworkers' households in the same community (P < .001). Mercury-in-air levels measured in workers' homes were higher than those measured in control homes. A significant correlation was found between the urine mercury levels of the workers' children and the urine mercury levels of their working parents. No child had frank mercury toxicity. No evidence of neurologic toxicity among exposed children was discovered by a pediatric neurologist who examined these and unexposed children without knowledge of their exposure status. This is the first report demonstrating mercury exposure in children of mercury workers. Although toxic effects of mercury were not demonstrated at these levels of exposure, children of mercury workers are at risk for mercury exposure and potential mercury toxicity.


2013 ◽  
Vol 9 (3) ◽  
pp. 270-273 ◽  
Author(s):  
Maryann Mazer-Amirshahi ◽  
Margit L. Bleecker ◽  
Fermin Barrueto

2014 ◽  
Vol 1 (10) ◽  
pp. 421-425 ◽  
Author(s):  
Johannes Fritsche ◽  
Stefan Osterwalder ◽  
Mats B. Nilsson ◽  
Jörgen Sagerfors ◽  
Staffan Åkerblom ◽  
...  
Keyword(s):  

2014 ◽  
Vol 229 ◽  
pp. S229
Author(s):  
Zeliha Kayaalti ◽  
Dilek Kaya Akyuzlu ◽  
Esma Soylemez ◽  
Engin Tutkun ◽  
Fezile Özdemir ◽  
...  

2015 ◽  
Vol 8 (8) ◽  
pp. 8113-8156
Author(s):  
S. Osterwalder ◽  
J. Fritsche ◽  
M. B. Nilsson ◽  
C. Alewell ◽  
J. Sommar ◽  
...  

Abstract. The fate of anthropogenic emissions of mercury (Hg) to the atmosphere is influenced by the exchange of elemental Hg with the earth surface. This exchange which holds the key to a better understanding of Hg cycling from local to global scales has been difficult to quantify. To advance and facilitate research about land–atmosphere Hg interactions, we developed a dual-intake, single analyzer Relaxed Eddy Accumulation (REA) system. REA is an established technique for measuring turbulent fluxes of trace gases and aerosol particles in the atmospheric surface layer. Accurate determination of gaseous elemental mercury (GEM) fluxes has proven difficult to technical challenges presented by extremely small concentration differences (typically < 0.5 ng m−3) between updrafts and downdrafts. To address this we present an advanced REA design that uses two inlets and two pair of gold cartridges for semi-continuous monitoring of GEM fluxes. They are then analyzed sequentially on the same detector while another pair of gold cartridges takes over the sample collection. We also added a reference gas module for repeated quality-control measurements. To demonstrate the system performance, we present results from field campaigns in two contrasting environments: an urban setting with a heterogeneous fetch and a boreal mire during snow-melt. The observed emission rates were 15 and 3 ng m−2 h−1. We claim that this dual-inlet, single detector approach is a significant development of the REA system for ultra-trace gases and can help to advance our understanding of long-term land–atmosphere GEM exchange.


2019 ◽  
Author(s):  
Stefan Osterwalder ◽  
Werner Eugster ◽  
Iris Feigenwinter ◽  
Martin Jiskra

Abstract. Direct measurements of the net ecosystem exchange (NEE) of gaseous elemental mercury (Hg0) are crucial to improve the understanding of global Hg cycling und ultimately human and wildlife Hg exposure. The lack of long-term, ecosystem-scale measurements causes large uncertainties in Hg0 flux estimates. Today it remains unclear whether terrestrial ecosystems are net sinks or sources of atmospheric Hg0. Here we show a detailed validation of the eddy covariance technique for direct Hg0 flux measurements (Eddy Mercury) based on a Lumex mercury monitor RA-915AM. The flux detection limit derived from a zero-flux experiment in the laboratory was 0.22 ng m−2 h−1 (maximum) with a 50 % cut-off at 0.074 ng m−2 h−1. The statistical estimate of the Hg0 flux detection limit under real-world outdoor conditions at the site was 5.9 ng m−2 h−1 (50 % cut-off). We present the first successful eddy covariance NEE measurements of Hg0 over a low-Hg level soil (41–75 ng Hg g−1 topsoil [0–10 cm]) in summer 2018 at a managed grassland at the Swiss FluxNet site in Chamau, Switzerland (CH-Cha). We measured a net summertime re-emission over a period of 34 days with a median Hg0 flux of 2.5 ng m−2 h−1 (−0.6 to 7.4 ng m−2 h−1, range between 25th and 75th percentiles). We observed a distinct diel cycle with higher median daytime fluxes (8.4 ng m−2 h−1) than nighttime fluxes (1.0 ng m−2 h−1). Drought stress during the measurement campaign in summer 2018 induced partial stomata closure of vegetation which led to a midday depression in CO2 uptake which did not recover during the afternoon. Thus, the cumulative net CO2 uptake was only 8 % of the net CO2 uptake during the same period in the previous year 2017. We suggest that partial stomata closure dampened Hg0 uptake by vegetation, resulting in a NEE of Hg0 dominated by soil re-emission. Finally, we give suggestions to further improve the precision and handling of the Eddy Mercury system in order to assure its suitability for long-term NEE measurements of Hg0 over natural background surfaces with low soil Hg concentrations (


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