Factors affecting the concentration and distribution of gaseous elemental mercury in the urban atmosphere of downtown Toronto

2018 ◽  
Vol 192 ◽  
pp. 24-34 ◽  
Author(s):  
Daniel Prete ◽  
Matthew Davis ◽  
Julia Lu
Keyword(s):  
Elemental Mercury ◽  
Urban Atmosphere ◽  
Factors Affecting ◽  
Gaseous Elemental Mercury

scholarly journals Effect of sources and meteorological conditions on the concentration and distribution of gaseous elemental mercury in the urban atmosphere

2021 ◽  
Author(s):  
Daniel Prete
Keyword(s):  
Rural Areas ◽  
Elemental Mercury ◽  
Average Concentration ◽  
Meteorological Conditions ◽  
Urban Atmosphere ◽  
Mercury Vapour ◽  
Data Set ◽  
Gaseous Elemental Mercury ◽  
Regional Sources ◽  
High Mercury

Atmospheric gaseous elemental mercury (GEM) and meteorological parameters were monitored at two sites in downtown Toronto, Canada from Oct. 2015 to Oct. 2016 using Tekran 2537A mercury vapour analyzers. The average concentration was found to be 1.78 ± 0.89 ng/m3 for Kerr Hall North (KHN) and 1.46 ± 0.54 ng/m3 for Jorgenson Hall (JOR) site. Analysis of the data reveals that sporadic events of high mercury concentration are related to local sources. Comparing this data set with that collected in 2004 revealed that the average atmospheric GEM concentration in downtown Toronto dropped from 4.5 ng/m3 to 1.78 ng/m3. Decreases in GEM were also observed over the same period in rural areas as measured by CAMNet. The decrease might be a result of policy change, as three key national and provincial environmental policies have been enacted since 2004. The data collected in Toronto suggest GEM concentration and distribution are influenced by local and regional sources, meteorological conditions, and changes in environmental policy.

scholarly journals A comparison of methyl and gaseous elemental mercury in the urban atmosphere

2021 ◽  
Author(s):  
Elaine Cairns
Keyword(s):  
Urban Areas ◽  
Elemental Mercury ◽  
Point Sources ◽  
Urban Atmosphere ◽  
Mercury Vapour ◽  
Mercury Species ◽  
Gaseous Elemental Mercury ◽  
Location Function ◽  
Air Circulation ◽  
The City

This study was carried out to compare the levels of mercury species, i.e., elemental mercury (Hg°) and methyl mercury (MeHg), in indoor and outdoor air in urban areas in Canada. Offices, laboratories for undergraduate studies, and laboratories for research, in a public building located in the downtown core of the city of Toronto, were selected. Hg° was measured using an automated mercury vapour analyzer. MeHg in the air was collected using a carbotrap, and the trapped MeHg was thermally desorbed and analyzed using a CVAFS. The results showed that both indoor MeHg and Hg° levels were related to location function and air circulation. Outdoor MeHg levels were significantly elevated, ranging between 21 and 41% of total mercury (THg) levels, compared to those reported from previous studies. Outdoor Hg° fluctuations were not found to be significantly related to temperature or sunlight exposure, and outdoor MeHg levels were connected to soil and vegetation abundance. Average indoor Hg° levels were found to be between 1.4 and 15 times higher than outdoor levels, whereas MeHg indoor levels were not consistently higher than outdoor levels. Although the mercury concentrations in the indoor environment are still lower than the safety standard for Hg° and organic mercury, they are comparable to those observed near point sources. Thus, indoor air can be a source of mercury to the atmosphere.

scholarly journals A comparison of methyl and gaseous elemental mercury in the urban atmosphere

2021 ◽  
Author(s):  
Elaine Cairns
Keyword(s):  
Urban Areas ◽  
Elemental Mercury ◽  
Point Sources ◽  
Urban Atmosphere ◽  
Mercury Vapour ◽  
Mercury Species ◽  
Gaseous Elemental Mercury ◽  
Location Function ◽  
Air Circulation ◽  
The City

This study was carried out to compare the levels of mercury species, i.e., elemental mercury (Hg°) and methyl mercury (MeHg), in indoor and outdoor air in urban areas in Canada. Offices, laboratories for undergraduate studies, and laboratories for research, in a public building located in the downtown core of the city of Toronto, were selected. Hg° was measured using an automated mercury vapour analyzer. MeHg in the air was collected using a carbotrap, and the trapped MeHg was thermally desorbed and analyzed using a CVAFS. The results showed that both indoor MeHg and Hg° levels were related to location function and air circulation. Outdoor MeHg levels were significantly elevated, ranging between 21 and 41% of total mercury (THg) levels, compared to those reported from previous studies. Outdoor Hg° fluctuations were not found to be significantly related to temperature or sunlight exposure, and outdoor MeHg levels were connected to soil and vegetation abundance. Average indoor Hg° levels were found to be between 1.4 and 15 times higher than outdoor levels, whereas MeHg indoor levels were not consistently higher than outdoor levels. Although the mercury concentrations in the indoor environment are still lower than the safety standard for Hg° and organic mercury, they are comparable to those observed near point sources. Thus, indoor air can be a source of mercury to the atmosphere.

scholarly journals Effect of sources and meteorological conditions on the concentration and distribution of gaseous elemental mercury in the urban atmosphere

2021 ◽  
Author(s):  
Daniel Prete
Keyword(s):  
Rural Areas ◽  
Elemental Mercury ◽  
Average Concentration ◽  
Meteorological Conditions ◽  
Urban Atmosphere ◽  
Mercury Vapour ◽  
Data Set ◽  
Gaseous Elemental Mercury ◽  
Regional Sources ◽  
High Mercury

Atmospheric gaseous elemental mercury (GEM) and meteorological parameters were monitored at two sites in downtown Toronto, Canada from Oct. 2015 to Oct. 2016 using Tekran 2537A mercury vapour analyzers. The average concentration was found to be 1.78 ± 0.89 ng/m3 for Kerr Hall North (KHN) and 1.46 ± 0.54 ng/m3 for Jorgenson Hall (JOR) site. Analysis of the data reveals that sporadic events of high mercury concentration are related to local sources. Comparing this data set with that collected in 2004 revealed that the average atmospheric GEM concentration in downtown Toronto dropped from 4.5 ng/m3 to 1.78 ng/m3. Decreases in GEM were also observed over the same period in rural areas as measured by CAMNet. The decrease might be a result of policy change, as three key national and provincial environmental policies have been enacted since 2004. The data collected in Toronto suggest GEM concentration and distribution are influenced by local and regional sources, meteorological conditions, and changes in environmental policy.

scholarly journals Air Concentrations of Gaseous Elemental Mercury and Vegetation–Air Fluxes within Saltmarshes of the Tagus Estuary, Portugal

Atmosphere ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 228
Author(s):  
Rute Cesário ◽  
Nelson J. O’Driscoll ◽  
Sara Justino ◽  
Claire E. Wilson ◽  
Carlos E. Monteiro ◽  
...  
Keyword(s):  
Leaf Area ◽  
Elemental Mercury ◽  
Ambient Air ◽  
Tagus Estuary ◽  
Contaminated Site ◽  
Gaseous Elemental Mercury ◽  
Mercury Flux ◽  
Sarcocornia Fruticosa ◽  
Air Concentrations

In situ air concentrations of gaseous elemental mercury (Hg(0)) and vegetation–atmosphere fluxes were quantified in both high (Cala Norte, CN) and low-to-moderate (Alcochete, ALC) Hg-contaminated saltmarsh areas of the Tagus estuary colonized by plant species Halimione portulacoides (Hp) and Sarcocornia fruticosa (Sf). Atmospheric Hg(0) ranged between 1.08–18.15 ng m−3 in CN and 1.18–3.53 ng m−3 in ALC. In CN, most of the high Hg(0) levels occurred during nighttime, while the opposite was observed at ALC, suggesting that photoreduction was not driving the air Hg(0) concentrations at the contaminated site. Vegetation–air Hg(0) fluxes were low in ALC and ranged from −0.76 to 1.52 ng m−2 (leaf area) h−1 for Hp and from −0.40 to 1.28 ng m−2 (leaf area) h−1 for Sf. In CN, higher Hg fluxes were observed for both plants, ranging from −9.90 to 15.45 ng m−2 (leaf area) h−1 for Hp and from −8.93 to 12.58 ng m−2 (leaf area) h−1 for Sf. Mercury flux results at CN were considered less reliable due to large and fast variations in the ambient air concentrations of Hg(0), which may have been influenced by emissions from the nearby chlor-alkali plant, or historical contamination. Improved experimental setup, the influence of high local Hg concentrations and the seasonal activity of the plants must be considered when assessing vegetation–air Hg(0) fluxes in Hg-contaminated areas.

scholarly journals An Integrated Investigation of Atmospheric Gaseous Elemental Mercury Transport and Dispersion Around a Chlor-Alkali Plant in the Ossola Valley (Italian Central Alps)

Toxics ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 172
Author(s):  
Laura Fantozzi ◽  
Nicoletta Guerrieri ◽  
Giovanni Manca ◽  
Arianna Orrù ◽  
Laura Marziali
Keyword(s):  
Elemental Mercury ◽  
Background Concentration ◽  
Dispersion Pattern ◽  
Central Alps ◽  
Gaseous Elemental Mercury ◽  
Mercury Transport ◽  
Close Proximity ◽  
Potential Impact ◽  
Hg Accumulation

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.

scholarly journals Occurrence of Volcanogenic Inorganic Mercury in Wild Mice Spinal Cord: Potential Health Implications

2021 ◽  
Author(s):  
A. Navarro-Sempere ◽  
M. García ◽  
A. S. Rodrigues ◽  
P. V. Garcia ◽  
R. Camarinho ◽  
...  
Keyword(s):  
Spinal Cord ◽  
Inorganic Mercury ◽  
Elemental Mercury ◽  
Potential Health ◽  
Wild Mice ◽  
Gaseous Elemental Mercury ◽  
Lumbar Level ◽  
Quantification Analysis ◽  
Spinal Cord Potential ◽  
Cord Potential

AbstractMercury accumulation has been proposed as a toxic factor that causes neurodegenerative diseases. However, the hazardous health effects of gaseous elemental mercury exposure on the spinal cord in volcanic areas have not been reported previously in the literature. To evaluate the presence of volcanogenic inorganic mercury in the spinal cord, a study was carried out in São Miguel island (Azores, Portugal) by comparing the spinal cord of mice exposed chronically to an active volcanic environment (Furnas village) with individuals not exposed (Rabo de Peixe village), through the autometallographic silver enhancement histochemical method. Moreover, a morphometric and quantification analysis of the axons was carried out. Results exhibited mercury deposits at the lumbar level of the spinal cord in the specimens captured at the site with volcanic activity (Furnas village). A decrease in axon calibre and axonal atrophy was also observed in these specimens. Given that these are relevant hallmarks in the neurodegenerative pathologies, our results highlight the importance of the surveillance of the health of populations chronically exposed to active volcanic environments.

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