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Seasonal and daily variation of mercury evasion at coastal and off shore sites from the Mediterranean Sea

Andersson, Maria, 1980 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,University of Gothenburg
Gårdfeldt, Katarina, 1959 (författare)
Gothenburg University,Göteborgs universitet,Göteborgs miljövetenskapliga centrum, GMV,Institutionen för kemi,Centre for Environment and Sustainability,Department of Chemistry,Chalmers tekniska högskola,Chalmers University of Technology,University of Gothenburg
Wängberg, Ingvar (författare)
Göteborgs universitet,University of Gothenburg
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Sprovieri, F. (författare)
CNR-Institute of Atmospheric Pollution Research, Rende
Pirrone, N. (författare)
CNR-Institute of Atmospheric Pollution Research, Rende
Lindqvist, Oliver, 1943 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,University of Gothenburg
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 (creator_code:org_t)
Elsevier BV, 2007
2007
Engelska.
Ingår i: Marine Chemistry. - : Elsevier BV. - 0304-4203. ; 104:3-4, s. 214-226
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Dissolved gaseous mercury (DGM) was measured continuously using two newly developed techniques and a manual technique. The continuous techniques were based on the equilibrium between the aqueous and gaseous phase (DGM = Hg-extr / H', Hg-extr is the measured mercury concentration in the gas phase, H' is the Henry's Law coefficient at the desired temperature). In order to calculate the annual mercury evasion from the Mediterranean Sea, diurnal and seasonal measurements of DGM, total gaseous mercury in air (TGM), water temperature and wind speed were performed. During August 2003, March-April 2004 and October-November 2004 measurements of these parameters were conducted on board the RV Urania. The continuous measurements of DGM showed a diurnal variation in concentration, at both coastal and off shore sites, with higher concentrations during daytime than nighttime. The concentration difference could be as large as 130 fM between day and night. The degree of saturation was calculated directly from the measurements, S = Hg-extr / TGM and was found to vary between the different seasons. The highest average degree of saturation (850%) and the largest variation in saturation (600-1150%) was observed during the summer. The spring showed the lowest variation (260-360%) and the lowest average degree of saturation (320%). The autumn also showed a large variation in saturation (500-1070%) but a lower average (740%) compared to the summer cruise. This might be explained by the temperature difference between the different seasons, since that parameter varied the most. The flux from the sea surface was calculated using the gas exchange model developed by Nightingale et al. [Nightingale, P.D., Malin, G., Law, C.S., Watson, A.J., Liss, P. S., Liddicoat, M.I., Boutin, J., Upstill-Goddard, R. C., 2000. In situ evaluation of air-sea gas exchange parameterization using novel conservative and volatile tracers. Global Biogeochemical Cycles, 14(l):373-387]. The evasion varied between the different seasons with the highest evasion during the autumn, 24.6 pmol m(-2) h(-1). The summer value was estimated to 22.3 pmol m(-2) h(-1) and the spring to 7.6 pmol m(-2) h(-1). Using this data the yearly evasion from the Mediterranean Sea surface was estimated to 77 tons. (C) 2006 Elsevier B.V. All rights reserved.

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Nyckelord

mercury
evasion
Mediterranean Sea
biogeochemistry
in situ
measurements
gas exchange
DISSOLVED GASEOUS MERCURY
ST-LAWRENCE-RIVER
ELEMENTAL MERCURY
ATMOSPHERIC MERCURY
HUMIC SUBSTANCES
NATURAL-WATERS
AIR EXCHANGE
GAS-EXCHANGE
CO2 FLUXES
WIND-SPEED
NATURAL-WATERS

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