Removal and bioaccumulation of anthropogenic, halogenated transient tracers in an anoxic fjord   总被引：1，自引：0，他引：1  

Toste Tanhua  K. Anders Olsson   《Marine Chemistry》2005,94(1-4):27

The persistence of the anthropogenic halogenated tracers, CFC-11 (CCl₃F), CFC-12 (CCl₂F₂), CFC-113 (CCl₂FCClF₂), carbon tetrachloride (CCl₄) and methyl chloroform (CH₃CCl₃) in oxygen-depleted waters was investigated in the anoxic fjord Framvaren in southern Norway. A model for the ventilation of the water in the fjord was created based on tritium and CFC-12 profiles. The results suggest that CFC-12 is stable in this environment, although still affected by particulate scavenging, while the other four halocarbon species shows signs of significant removal in the oxic/anoxic interface. The first-order removal coefficients were calculated to be 0.35, 0.19, 1.23 and 0.31 year⁻¹ for CFC-11, CFC-113, CCl₄ and CH₃CCl₃, respectively. Significant downward flux of halogenated tracers by sinking organic matter is suggested by the model; the tracers are subsequently released to the water column by the remineralisation of the particles. This process acts as a sink of halogenated tracers in the surface waters, whereas it is a source for the deep waters. Our results points to bioaccumulation factors (BF) for the CFC tracers in the order of 4.4–5.4 (log BF), which is 100–600 times those previously reported. This might be of significance to near-shore, semi-enclosed, basins with a high flux of organic matter, but would still have little importance in open ocean basins.  相似文献   

Model analysis of the measured concentration of organic gases in the Norwegian Arctic     

Ivar S. A. Isaksen  Øystein Hov  Stuart A. Penkett  Arne Semb 《Journal of Atmospheric Chemistry》1985,3(1):3-27

A 2-D meridional model for the chemistry and transport in the troposphere is used to study the seasonal variation of the concentration of organic gases like C₂H₂, C₂H₆, C₃H₈, C₆H₆, C₇H₈. CHCl₃ and C₂Cl₄ at high latitudes. The anthropogenic sources for these species were estimated, and the temporal and latitudinal distribution of OH and O₃ was calculated using a complex photochemical reaction system. There is fair agreement between the calculated annual variation and the measured concentrations for C₂H₂, C₂H₆, C₃H₈, C₇H₈ and C₂Cl₄ at Spitsbergen during July 1982 and March/April 1983, with a distinct late winter maximum and summer minimum. For CHCl₃, the direct anthropogenic source is minor compared to indirect anthropogenic or natural sources. For benzene, emission in car exhaust is important, but other anthropogenic sources are required for the calculations to agree with the measurements. Measured C₂H₄ and C₃H₆ concentrations are much higher than the calculated ones based on anthropogenic emissions, and show opposite seasonal trends. This indicates biogenic sources for these compounds.A buildup of PAN (300 pptv) is calculated at high latitudes during winter. This makes it the dominant source for NO_x as the temperature increases in the spring. NO_x is found to be a limiting factor for O₃ production at high latitudes during spring.  相似文献   

Occurrence of volatile organic compounds (VOCs) in Liverpool Bay, Irish Sea   总被引：4，自引：0，他引：4  

Bravo-Linares CM  Mudge SM  Loyola-Sepulveda RH 《Marine pollution bulletin》2007,54(11):1742-1753

Surface seawater samples were collected in the Irish Sea and Liverpool Bay area from the R.V. Prince Madog during the period of 25-31 of March 2006. VOCs were purged with nitrogen, pre-concentrated on a SPME fibre and analysed immediately on a GC-MS. Target compounds quantified were halogenated (0.2-1400 ng L(-1)), BTEXs and mono-aromatics (1.5-2900 ng L(-1)), aliphatic hydrocarbons and others (0.6-15,800 ng L(-1)). Day and night sampling was performed at a single station and suggested that factors such as sunlight and tide affect the presence of many of these compounds. Sample variability was high due to the variable weather conditions at the station. Poor correlations were found between marine phytopigments and selected VOCs. Principal component analysis (PCA) analysis showed that chlorinated compounds such as 1,2-dichloroethane, 1,1,1-trichloroethane, trichloroethene, tetrachloroethene and carbon tetrachloride, predominantly from anthropogenic sources, originated from the River Mersey. Other brominated and iodinated compounds quantified were more likely to be from biogenic sources including novel marine compounds such as 2-chloropropane, 1-bromoethane and 1-chlorobutane.  相似文献