共查询到7条相似文献,搜索用时 0 毫秒
1.
Christophersen M Broholm MM Mosbaek H Karapanagioti HK Burganos VN Kjeldsen P 《Journal of contaminant hydrology》2005,81(1-4):1-33
An emplaced hydrocarbon source field experiment was conducted in the relatively homogeneous sandy geology of the vadose zone at Airbase Vaerl?se, Denmark. The source (10.2 l of NAPL) consisted of 13 hydrocarbons (n-, iso- and cyclo-alkanes and aromates) and CFC-113 as a tracer. Monitoring in the 107 soil gas probes placed out to 20 m from the centre of the source showed spreading of all the compounds in the pore air and all compounds were measured in the pore air within a few hours after source emplacement. Seven of the fourteen compounds were depleted from the source within the 1 year of monitoring. The organic vapours in the pore air migrated radially from the source. The CFC-113 concentrations seemed to be higher in the deeper soil gas probes compared with the hydrocarbons, indicating a high loss of CFC-113 to the atmosphere and the lack of degradation of CFC-113. For the first days after source emplacement, the transport of CFC-113, hexane and toluene was successfully simulated using a radial gas-phase diffusion model for the unsaturated zone. Groundwater pollution caused by the vadose zone hydrocarbon vapours was only detected in the upper 30 cm of the underlying groundwater and only during the first 3 months of the experiment. Only the most water-soluble compounds were detected in the groundwater and concentrations decreased sharply with depth (approximately one order of magnitude within 10 cm depth) to non-detect at 30 cm depth. The groundwater table varied more than 1 m within the measurement period. However that did not influence the direction of the groundwater flow. Approximately 7 months after source emplacement the groundwater table rose more than 1 m within 1 month. That did not cause additional pollution of the groundwater. 相似文献
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《Atmospheric environment (Oxford, England : 1994)》2001,35(7):1253-1264
The concentrations of the aromatic hydrocarbons benzene, toluene, ethylbenzene and the isomeric xylenes (BTEX) have been determined in the indoor air of 115 private non-smoker homes (∼380 individual rooms) situated in areas with an extreme traffic situation, i.e. in city streets (street canyons) with high traffic density and in rural areas with hardly any traffic at all. The influence of the traffic on the indoor concentration was apparent in the high traffic area. In order to identify other factors influencing the BTEX concentrations, the data and additional questionnaires were analyzed by univariate and multivariate analysis. The analysis was supplemented by some case studies. It is shown that meteorology (the seasons), the type of room (e.g. living room versus bedroom), the ventilation and, in particular, garages in the house strongly influence the indoor concentration of BTEX. Thus, the indoor BTEX level is significantly higher in winter than in summer. Moreover, garages with a connecting door to the living quarters lead to high indoor concentrations of aromatic hydrocarbons in these rooms. In addition, the storage of solvents and hobby materials, and also the presence of smoking guests increase the BTEX level. If rooms are directly heated by coal or wood, the BTEX level is higher compared to the use of gas heating. Surprisingly, no correlation was found between the building materials used and the BTEX level. Case studies were carried out for two homes with an integrated garage (and a connecting door to the living rooms) and for seven homes where redecoration work was carried out during sampling. In both instances, a pronounced increase was observed in the BTEX concentration. 相似文献
3.
Araújo CV Cohin-de-Pinho SJ da S Santos J Delgado F Santana LC Chastinet CB da Silva EM 《Chemosphere》2006,65(4):599-603
The suitability and viability of acute in situ bioassays were investigated in the biomonitoring program of an acidic lake contaminated with sulphur residues. Responses of organisms observed in laboratory and in situ bioassays were also assessed to determine whether or not they were similar and comparable, regarding accuracy and precision. Newborn Poecilia reticulata were employed as test organisms and exposed to the same water samples under in situ and laboratory conditions. Mortality/immobility was the endpoint assessed and dead/immobile organisms were counted at various time intervals during exposure. The mean calculated LT50 values and 95% confidence intervals were 1.61 (1.36-1.87) h in the laboratory bioassays and 0.72 (0.55-0.89) h in the in situ bioassays. Statistical comparison of these values revealed a significant difference (p<0.05). In situ bioassays were more accurate than those carried out in the laboratory, demonstrating higher sensitivity and better reproduction of what occurs in nature, while laboratory bioassays were more precise. 相似文献
4.
《Atmospheric environment (Oxford, England : 1994)》2001,35(29):5007-5018
Aerosol samples were collected from Northwest China desert region (Minqin), coastal suburb (Qingdao) and interior of the Yellow Sea (Qianliyan) in spring and summer of 1995 and 1996. Samples were analysed for major components, carbon and sulphur. The results show that concentrations of aerosols change considerably in time and space. The crustal materials carried by cold front system increase notably the aerosol concentration (mass/unit vol.) over the Yellow Sea but reduce the percentage contribution of pollutants and sea-salt. The sea-salt and regional aerosols become dominant fractions in coastal atmosphere in summer when the dust storms are expired in source region and the Southeast monsoon starts in the Pacific Ocean. 相似文献
5.
Comoretto L Arfib B Talva R Chauvelon P Pichaud M Chiron S Höhener P 《Environmental pollution (Barking, Essex : 1987)》2008,151(3):486-493
A field study on the runoff of pesticides was conducted during the cultivation period in 2004 on a hydraulically isolated rice farm of 120 ha surface with one central water outlet. Four pesticides were studied: Alphamethrin, MCPA, Oxadiazon, and Pretilachlor. Alphamethrin concentrations in runoff never exceeded 0.001 microg L(-1). The three other pesticides were found in concentrations between 5.2 and 28.2 microg L(-1) in the runoff water shortly after the application and decreased thereafter. The data for MCPA compared reasonably well with predictions by an analytical runoff model, accounting for volatilization, degradation, leaching to groundwater, and sorption to soil. The runoff model estimated that runoff accounted for as much as 18-42% of mass loss for MCPA. Less runoff is observed and predicted for Oxadiazon and Pretilachlor. It was concluded that runoff from rice paddies carries important loads of dissolved pesticides to the wetlands in the Ile de Camargue, and that the model can be used to predict this runoff. 相似文献
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Hagen Scherb Kristina Voigt 《Environmental science and pollution research international》2012,19(9):4234-4241