14 research outputs found

    Fluxes of gaseous elemental mercury on a Mediterranean coastal grassland

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    Coastal rural areas can be a source of elemental mercury, but the potential influence of their topographic and climatic particularities on gaseous elemental mercury (GEM) fluxes have not been investigated extensively. In this study, gaseous elemental mercury was measured over Mediterranean coastal grassland located in Northern Greece from 2014 to 2015 and GEM fluxes were evaluated utilizing Monin–Obukhov similarity theory. The GEM fluxes ranged from –50.30 to 109.69 ng m−2 h−1 with a mean value equal to 10.50 ± 19.14 ng m−2 h−1. Concerning the peak events, with high positive and low negative GEM fluxes, those were recorded from the morning until the evening. Rain events were a strong contributing factor for enhanced GEM fluxes. The enhanced turbulent mixing under daytime unstable conditions led to greater evasion and positive GEM fluxes, while, during nighttime periods, the GEM evasion is lower, indicating the effect of atmospheric stability on GEM fluxes. The coastal grassland with its specific characteristics influences the GEM fluxes and this area could be characterized as a source of elemental mercury. This study is one of the rare efforts in the research community to estimate GEM fluxes in a coastal natural site based on aerodynamic gradient method

    Greenhouse gases in cold water filaments in the Arabian Sea during the Southwest Monsoon

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    The distribution of partial pressure of carbon dioxide and the concentrations of nitrous oxide and methane were investigated in a cold water filament near the coastal upwelling region off Oman at the beginning of the southwest monsoon in 1997. The results suggest that such filaments are regions of intense biogeochemical activity which may affect the marine cycling of climatically relevant trace gase

    Nitrous oxide cycling in the Arabian Sea

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    Depth profiles of dissolved nitrous oxide (N2O) were measured in the central and western Arabian Sea during four cruises in May and July–August 1995 and May–July 1997 as part of the German contribution to the Arabian Sea Process Study of the Joint Global Ocean Flux Study. The vertical distribution of N2O in the water column on a transect along 65°E showed a characteristic double-peak structure, indicating production of N2O associated with steep oxygen gradients at the top and bottom of the oxygen minimum zone. We propose a general scheme consisting of four ocean compartments to explain the N2O cycling as a result of nitrification and denitrification processes in the water column of the Arabian Sea. We observed a seasonal N2O accumulation at 600–800 m near the shelf break in the western Arabian Sea. We propose that, in the western Arabian Sea, N2O might also be formed during bacterial oxidation of organic matter by the reduction of IO3 − to I−, indicating that the biogeochemical cycling of N2O in the Arabian Sea during the SW monsoon might be more complex than previously thought. A compilation of sources and sinks of N2O in the Arabian Sea suggested that the N2O budget is reasonably balanced

    Decomposition Kinetics of Non-Volatile Alkanes on Urban Aerosol

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    The decomposition kinetics of non-volatile n-alkanes that were collected in an urban environment were studied. The quartz filters that they were collected on were exposed in two reactors, in dark and natural light conditions, for four days. Ambient air that was passed through the reactors continuously, ensured a supply of exogenic oxidants to the surface of the filters. The lifetimes of the non-volatile n-alkanes were experimentally determined to be in the order of 3–6 days. The results from the light reactor exhibited approximately a 10% decrease in their lifetime. The results obtained for the prevailing atmospheric conditions and for the duration of the experiments, were in agreement with values from the literature

    The Effect of Students, Computers, and Air Purifiers on Classroom Air Quality

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    Indoor air pollutant sources are crucial in assessing IAQ, especially when outdoor air pollutant concentrations are low. In the present study, PM mass concentrations in a range of five sizes; CO, CO2, O3, NO, NO2, and TVOC concentrations; along with temperature and relative humidity were monitored in three indoor locations of a university. The monitoring took place in a building dedicated to teaching undergraduates. The first two locations, a professor’s office and a computer centre (laboratory), were not refurbished. The classroom under study is refurbished and now is airtight, as are all of the classrooms in this building. Air purifiers were installed in all of the classrooms to prevent the transmission of infectious pollutants. In all monitored locations, people were the main indoor source of PM, CO2, and TVOC. The operation of twelve computers in the small laboratory did not contribute to the air pollution, at least for the examined pollutants. The air purifier decreased the PM concentrations, but not the gaseous air pollutants

    The Effect of Students, Computers, and Air Purifiers on Classroom Air Quality

    No full text
    Indoor air pollutant sources are crucial in assessing IAQ, especially when outdoor air pollutant concentrations are low. In the present study, PM mass concentrations in a range of five sizes; CO, CO2, O3, NO, NO2, and TVOC concentrations; along with temperature and relative humidity were monitored in three indoor locations of a university. The monitoring took place in a building dedicated to teaching undergraduates. The first two locations, a professor’s office and a computer centre (laboratory), were not refurbished. The classroom under study is refurbished and now is airtight, as are all of the classrooms in this building. Air purifiers were installed in all of the classrooms to prevent the transmission of infectious pollutants. In all monitored locations, people were the main indoor source of PM, CO2, and TVOC. The operation of twelve computers in the small laboratory did not contribute to the air pollution, at least for the examined pollutants. The air purifier decreased the PM concentrations, but not the gaseous air pollutants
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