| 1. |
- Agrell, Cecilia, et al.
(författare)
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PCB congeners in precipitation, wash out ratios and depositional fluxes within the Baltic Sea region, Europe
- 2002
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Ingår i: Atmospheric Environment. - 1352-2310. ; 36:2, s. 371-383
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Tidskriftsartikel (refereegranskat)abstract
- Concentrations of PCB congeners were determined in precipitation and the annual and seasonal depositional fluxes were calculated for 16 (mostly rural) stations around the Baltic Sea during 1990-1993. The concentrations of individual congeners in precipitation were found to be influenced by atmospheric concentrations of PCBs, ambient temperature, precipitation volume and physico-chemical properties of the compounds. Median levels of PCBs in precipitation differed one order of magnitude between stations. When analyzing all data together to obtain regional trends, concentrations of PCBs in precipitation decreased with increasing temperature. This relationship was the same for all stations but differed in the magnitude of the slope for individual congeners. Low chlorinated PCB congeners showed steeper slopes for the temperature relationship than did high chlorinated congeners, a result explained by high atmospheric concentrations of the low chlorinated congeners during low temperatures. Annual wash out ratios were between 31 and 72 x 103 and tended to be higher for the high chlorinated congeners. Wash out ratios decreased with increasing temperature for all congeners except PCB-33. At snow scavenging events, the wash out ratio of PCBs increased with a factor of 2. Latitudinal trends for PCB concentrations in precipitation and deposition were generally not statistically significant. The calculated yearly deposition of PCBs to the Baltic Sea was 390 and 5-18 kg for individual congeners, with PCB-138 having the highest flux. Deposition of PCB congeners varied seasonally, with a factor between 2 and 3, and was generally highest during fall. Relatively higher deposition of low chlorinated congeners compared to high chlorinated congeners was found during winter. (C) 2002 Elsevier Science Ltd. All rights reserved.
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| 2. |
- Backe, Cecilia, et al.
(författare)
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Polychlorinated biphenyls in the air of southern Sweden - spatial and temporal variation
- 2000
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Ingår i: Atmospheric Environment. - 1352-2310. ; 34:9, s. 1481-1486
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Tidskriftsartikel (refereegranskat)abstract
- Polychlorinated biphenyls in the lower atmosphere were studied over a regional area covering approximately 11000 km(2) in southern Sweden. Sampling were performed in 1992-1993, continuously during one year, where samples from 11 sampling-sites (in all 260 samples) were analysed. PCB concentrations ranged over two order of magnitudes, 7-983 pg m(-3). Differences in PCB concentrations among the sampling sites revealed a large number of high-concentration outliers, mainly originating from one suburban site. Smaller differences in PCB concentrations between sites probably originated from varying geographical and meteorological conditions, that affected exchange processes between air and surfaces differently at the sampling sites. (C) 2000 Elsevier Science Ltd. All rights reserved.
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| 3. |
- ter Schure, Arnout, et al.
(författare)
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Polybrominated diphenyl ethers in precipitation in Southern Sweden (Skane, Lund)
- 2002
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Ingår i: Atmospheric Environment. - 1352-2310. ; 36:25, s. 4015-4022
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Tidskriftsartikel (refereegranskat)abstract
- The presence of polybrominated diphenyl ether (PBDE) flame retardants in total deposition (wet + dry) was assessed with the simultaneous use of three bulk samplers during a 2 week period. The particle associated and the 'dissolved' phase were separated during sampling. Volume weighted mean (VWM) concentrations of SigmaPBDE (9 congeners) in rain were 209 pg l(-1). Total deposition rates were 2 +/- 1 ng SigmaPBDE m(-2) day(-1). The total PBDE deposition was dominated by decaBDE(209) and thereafter 2,2'4,4'-tetraBDE(47) and 2,2'4,4',5-pentaBDE(99). Concentrations of particle associated and 'dissolved' PBDEs in total deposition were used to calculate filter/adsorbent ratios (F/A). We found that 65 +/- 18% of the total PBDEs were particle associated. Low F/A ratios for higher brominated congeners (Br > 5) were observed. This is contradictory with predictions based on the PBDEs' physico-chemical properties and was attributed to sampling artefacts, such as particle size distribution, and/or non-equilibrium processes. There was a negative relationship between the particulate SigmaPBDE concentration and rain volume suggesting a dilution effect and the importance of particle scavenging for wet deposition of PBDEs. (C) 2002 Elsevier Science Ltd. All rights reserved.
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| 4. |
- Agrell, Cecilia, et al.
(författare)
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Polybrominated diphenyl ethers (PBDES) at a solid waste incineration plant I: Atmospheric concentrations
- 2004
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 38:30, s. 5139-5148
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Tidskriftsartikel (refereegranskat)abstract
- In the first of two papers, the atmospheric poly brominated diphenyl ether (PBDE) concentrations at a municipal solid waste incineration (MSW) plant with electronic recycling is compared with that at an industrial urban reference site producing asphalt and concrete. In the second paper, atmospheric deposition and washout behaviour is presented (Atmos. Environ. (2004a)). PBDEs (BDE28, -47, -66, -100, -154, -153, -183, -209) in the gaseous and particulate phase were measured with high resolution in time during the colder parts of the year to minimise the influence of potential historical pollution at the sites through volatilisation. This also means that reported levels are lower compared to other reported data. Results of BDE47 (TetraBDE) and BDE209 (DecaBDE) as representatives of "old" vs. "new" PBDEs as well as SigmaPBDE, excluding BDE209, are presented. Median SigmaPBDE, BDE47 and BDE209 concentration were 6.3, 2.1 and 10.4 pg m(-3) at the MSW and 3.5, 1.7 and 6.5 pg m-3 at the reference site. The total concentrations (gaseous and particulate phase) were significantly higher at the MSW compared to the reference site for SigmaPBDE and BDE47 but not for BDE209. The same results were obtained regarding concentrations in the gaseous phase. Particle concentrations were significantly higher at the MSW for SigmaPBDE, BDE47 and BDE209. Within each site, the gaseous-phase concentration was significantly higher than the particulate-phase concentration except for BDE209 at the MSW. Thus, the proportion of BDE209 detected in the particulate phase was higher at the MSW compared to the reference site. Together with the results of the second paper, we suggest that treatment of waste is presently a source of "old" PBDEs to the environment, whereas the rather similar BDE209 concentrations at the two sites are more a result of proximity to potential diffuse sources.
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| 5. |
- Larsson, Per
(författare)
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Atmospheric deposition of persistent pollutants governs uptake in freshwater zooplankton
- 1989
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310 .- 1873-2844 .- 0004-6981. ; 23:10, s. 2151-2158
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Tidskriftsartikel (refereegranskat)abstract
- The atmospheric fallout of PCBs, ∑DDT and γ-HCH (lindane) to a pond in southern Sweden was studied in relation to uptake by freshwater Zooplankton. The extent of the atmospheric deposition of PCBs and lindane was reflected in the uptake by the Zooplankton; high deposition in the spring and autumn resulted in high uptake by the organisms while a lower uptake during summer was a result of lower deposition. The atmospheric deposition of ∑DDT was dominated by p,p-DDT, p,p-DDE and o,p-DDT, while p,p-DDE and p,p-DDD were dominant in Zooplankton. These differences in ∑DDT composition are probably attributed to microbial conversion; as a result, levels in the Zooplankton appeared not to be governed by atmospheric deposition. The availability of the previously airborne, persistent pollutants to Zooplankton was a function of the compounds chemical properties, e.g. water solubility, and the form of deposition. The results show that atmospheric deposition is an important route by which persistent pollutants are transported to Holarctic, aquatic ecosystems.
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| 6. |
- Larsson, Per, et al.
(författare)
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Atmospheric transport of chlorinated hydrocarbons to Sweden 1985 compared to 1973
- 1989
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310 .- 1873-2844 .- 0004-6981. ; 23:8, s. 1699-1711
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Tidskriftsartikel (refereegranskat)abstract
- The atmospheric fallout of DDT and DDE (ΣDDT) over Sweden has decreased during the last decade. Today long-range transport from southern sources outside the country dominates the inflow. This was reflected in a decreasing south-to-north gradient of the compounds in atmospheric deposition and in the lower atomosphere. The fallout of PCBs was similar in 1984–1985 and 1972–1973, and today local contamination by combustion is more prominent than it was 10 years ago, even though PCB restrictions have been in force during the interim. Since PCB deposition is higher in the coastal areas than in the inland regions, other sources, such as volatilization from the seas and long-range transport also contribute to PCBs in fallout. The levels of PCB and ΣDDT in the lower atmosphere were positively correlated with temperature. Consequently, the compounds tended to be in the gas phase during the warmer summer period whereas during winter they were more liable to be adsorbed to particles, partition to airborne water and contribute in fallout. From each sampling station a chromatographic 'fingerprint' of pollutants in airborne fallout and in the lower atmosphere was obtained. The fingerprint was the combined result of the station's location and climate. The results show that considerable amounts of chlorinated pollutants are being transported to and within Sweden via the atmosphere.
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| 7. |
- ter Schure, Arnout, et al.
(författare)
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Polybrominated diphenyl ethers at a solid waste incineration plant II: atmospheric deposition
- 2004
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 38:30, s. 5149-5155
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Tidskriftsartikel (refereegranskat)abstract
- In the second of two papers, the atmospheric polybrominated diphenyl ethers (PBDE) deposition (wet and dry) at a municipal solid waste incineration (MSW) plant with electronics recycling is compared with that at an industrial urban reference site (URS) producing asphalt and concrete. Results of BDE209 and SigmaPBDE excluding BDE209 as representatives of "new" vs. "old" PBDEs are presented. Volume weighted mean SigmaPBDE and BDE209 concentrations at the MSW were 6.2 and 14.4 ng l(-1), and at the URS were 2.5 and 14.1 ng l(-1). Median SigmaPBDE and BDE209 deposition fluxes were 21.3, 63.8 and 7.0, 14.7 ng m(-2) day(-1) at the MSW and URS, respectively. The concentrations in precipitation and the deposition fluxes were significantly higher at the MSW compared to the URS. Measured total washout- ratios (W-T) were dependent on particle scavenging and the median WT for all congeners was 5.4x 10(5). Median dry particle deposition velocities ranged from 0.4 to 49 cm s(-1), depending on congener, showing that PBDEs are effectively removed from the atmosphere by particle deposition. PBDE fluxes increased at the reference site when winds were blowing from west south-west, i.e. from the direction of the MSW. PBDE deposition and washout ratios were not influenced by temperature or rain volume, suggesting a constant emission from the MSW regardless of weather conditions. Together with the results of paper I (Agrell et al., 2004, Atmospheric Environment, this issue) we therefore suggest that treatment of waste, e.g. electronics recycling, is more a source of "old" PBDEs to the environment, whereas the rather similar BDE209 concentrations at the two urban sites are more a result of proximity to potential diffuse sources. (C) 2004 Elsevier Ltd. All rights reserved.
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