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Träfflista för sökning "L773:0160 4120 ;srt2:(2005-2009)"

Sökning: L773:0160 4120 > (2005-2009)

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2.
  • Ericson Jogsten, Ingrid, et al. (författare)
  • Perfluorinated chemicals in blood of residents in Catalonia (Spain) in relation to age and gender : a pilot study
  • 2007
  • Ingår i: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 33:5, s. 616-623
  • Tidskriftsartikel (refereegranskat)abstract
    • Fluorinated organic compounds (FOCs) are a group of chemicals widely used as surfactants, lubricants, polymers, and fire-fighting foams. Recent studies have shown the ubiquitous distribution of FOCs in the environment, wildlife, and humans. We here report the results of a pilot study conducted to provide preliminary data on the levels of 13 FOCs in the blood of 48 residents in Catalonia, Spain, in relation to gender and age (25+/-5 and 55+/-5 years). The highest mean concentration was obtained for perfluorooctane sulfonate (PFOS, 7.64 ng/ml), followed by perfluorohexane sulfonate (PFHxS, 3.56 ng/ml) and perfluorooctanoic acid (PFOA, 1.80 ng/ml). Four other FOCs showed mean levels between 0.30 and 0.44 ng/ml, whereas those of the remaining 6 compounds were below the detection limit. Regarding gender, the blood levels of PFHxS and PFOA were significantly higher (p<0.05) in men than in women, while differences according to age were only noted for PFHxS (p<0.05) and perfluorooctane sulfonamide (PFOSA) (p<0.001), for which the levels were higher in the younger (25+/-5 years) group of subjects. A significant correlation between PFOS levels and those of the remaining detected FOCs (except PFDA) was found. In general terms, the current FOC concentrations were lower than those found in recent studies concerning levels of these chemicals in human blood and serum of subjects from different countries.
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3.
  • Fjällborg, Bengt, 1962, et al. (författare)
  • Identification of metal toxicity in sewage sludge leachate
  • 2005
  • Ingår i: Environment International. - : Elsevier BV. - 0160-4120. ; 31:1, s. 25-31
  • Tidskriftsartikel (refereegranskat)abstract
    • Sewage sludge is a source of organic matter and nutrients with the potential for being used as a fertilizer. However, metals in sewage sludge might accumulate in soil after repeated sludge applications, and metal concentrations might reach concentrations that are toxic to microorganisms, soil organisms and/or plants. This toxicity might change with time due to kinetic factors or abiotic factors such as freezing, drying or rainfall. The objective of this study was to determine toxicity of sewage sludge leachate from a lysimeter with 50 cm of sludge applied. Attempts were also made to identify the cause of toxicity of the sludge leachate by toxicity identification and evaluation (TIE) techniques. Sludge leachate was collected monthly during 1 experimental year (August 2001 to August 2002). Metal concentrations were analysed, and the toxicity was determined with Daphnia magna (48-h immobility). The effect of EDTA or sodium thiosulphate addition, filtration through a CM-resin or a Millex-resin on toxicity was also tested. The results showed that toxicity of the sludge leachate apparently varied during the year, and that filtration through the CM-resin reduced most of the toxicity followed by the addition of EDTA. None of the other treatments reduced the toxicity of the sludge leachate. This indicated that one or more metals were responsible for the observed toxicity. Further calculations of toxic units (TU) suggested that Zn contributed most to the toxicity. Results also indicated that Ca concentrations in the sludge leachate reduced the toxicity of Zn.
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6.
  • Hagberg, Jessika, et al. (författare)
  • Chemical and toxicological characterisation of PBDFs from photolytic decomposition of decaBDE in toluene
  • 2006
  • Ingår i: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 32:7, s. 851-857
  • Tidskriftsartikel (refereegranskat)abstract
    • A substantial formation of PBDF congeners was observed during photolytic decomposition of decaBDE in toluene. The decaBDE degradation was monitored by chemical and toxicological analysis and in all, twenty-seven mono- to hexasubstituted polybrominated dibenzofurans (PBDFs) were detected in toluene solutions of decabromodiphenyl ether (decaBDE) after irradiation with UV-A, UV-AB and UV-ABC. The concentration levels of PBDFs formed after 16 h of UV exposure increased with wider spectra and were determined to be 3.5, 4.2 and 14 microg/ml after UV-A, UV-AB and UV-ABC irradiation, respectively. In accordance, bioassay derived TEQs (bio-TEQs), determined with the DR-CALUX assay, increased with a similar pattern. The PBDFs formed after the three UV exposures accounted for 0.31%, 0.35% and 1.2% of the initial amount of decaBDE (molar basis). The PBDF congener patterns were consistent in all three UV experiments which imply that no alterations were induced in the PBDF formation or degradation processes due to differences in UV irradiation. However, these processes tended to increase with wider spectra and increasing radiation energy most likely due to the strong absorbance of for example decaBDE at shorter wavelengths. After total decaBDE decomposition the PBDF formation increased significantly in the UV-ABC experiment. The tetra to hexasubstituted BDFs constituted the majority of detected compounds in all experiments. In all samples, the estimated chemical TEQ indicate that the bio-TEQs observed are largely explained by the presence of non-2,3,7,8-substituted PBDFs with relatively low toxicological potencies.
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7.
  • Jaspers, Veerle L B, et al. (författare)
  • Preen oil as the main source of external contamination with organic pollutants onto feathers of the common magpie (Pica pica).
  • 2008
  • Ingår i: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 34:6, s. 741-8
  • Tidskriftsartikel (refereegranskat)abstract
    • We investigated the possible sources of contamination with organic pollutants, such as polychlorinated biphenyls (PCBs), /p/,/p/'-dichlorodiphenyltrichloroethane (DDT) and metabolites, and polybrominated diphenyl ethers (PBDEs), in and onto tail feathers of a large songbird, the common magpie (Pica pica). Although feathers are potentially useful as a non-destructive biomonitor for organic pollutants, concentrations may be influenced by external contamination onto the feather surface. In a first approach, a group of magpies was captured after the completion of moult. The third tail feather was pulled out and a blood sample was taken. Most PCBs, DDTs and some PBDEs could be quantified in one single tail feather, indicating that the applicability of feathers goes beyond monitoring with predatory birds, as shown previously. Nevertheless, correlations between levels in serum and feathers were found significant in three cases only (i.e. CB 170, CB 180 and CB 187). This finding may be attributed to different factors, such as varying diet, condition, sample size or external contamination. In a second approach, cadavers of magpies were collected throughout Flanders. The preen gland was removed and the first, third and fifth tail feathers were pulled out at both sides. No significant differences were found among tail feathers within an individual. We compared three washing procedures to remove external contamination with organic pollutants from these feathers: deionised water, acetone and a surfactant/acetone solution. Right feathers were washed and left feathers were kept as control. Concentrations in the resulting washes were found highest in the acetone solutions. Furthermore, feathers washed with acetone or with a surfactant/acetone solution had significantly lower mean concentrations than the control feathers. Highest correlations with levels in preen gland were obtained for the control feathers. Consequently, the source of external contamination with organic pollutants onto feathers seems to be endogenous, originating from the preen gland. This is in great contrast to the extensive airborne pollution that has been reported for most heavy metals. In summary, the results of the current study highlight the usefulness of feathers for non-destructive biomonitoring of organic pollutants.
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8.
  • Karlsson, Marie, et al. (författare)
  • Levels of brominated flame retardants in blood in relation to levels in household air and dust
  • 2007
  • Ingår i: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 33:1, s. 62-69
  • Tidskriftsartikel (refereegranskat)abstract
    • Levels of tri- to decabrominated diphenyl ethers (BDEs), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE) and 1,2-bis(pentabromophenyl)ethane (DeBDethane) were determined in air, sedimentary dust and human plasma from five households in Sweden. The levels of the individual BDEs in the plasma samples were in the same order of magnitude as in other studies of the general population in Scandinavia, and varied between non-detectable (< 0.41 ng g− 1 l.w.) to 17 ng g− 1 (l.w.). BDE#28 and #47 were present in all air samples, with mean values of 0.015 and 0.12 ng m− 3, respectively, except for one sample where the BDE#47 concentration was below the limit of detection (< 0.17 ng m− 3). BDE#209 was found in one of the five air samples at a concentration of 0.26 ng m− 3. DeBDethane was also detected in one sample, in which the BDE#209 level was below LOD (< 0.021 ng m− 3), at a level of 0.023 ng m− 3. All the target compounds were found in the sedimentary dust samples at levels from 0.51 to 1600 ng g− 1, the highest concentration representing BDE#209. The most abundant components in plasma, air and dust were BDE#47, #99 and #209. In the plasma samples BDE#207 and #206 were also present at similar concentrations as BDE#47. In the sedimentary dust samples, DeBDethane was also among the most abundant BFRs. A positive relationship was found for the sumBDE concentrations in dust and plasma, although the relationship was strongly dependent on one of the five observations. BFR levels in dust and air were not dependent on the house characteristics such as living area, floor material or number of electronic devices.
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10.
  • Kärrman, Anna, et al. (författare)
  • Identification and pattern of perfluorooctane sulfonate (PFOS) isomers in human serum and plasma
  • 2007
  • Ingår i: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 33:6, s. 782-788
  • Tidskriftsartikel (refereegranskat)abstract
    • Human serum and plasma from Sweden (n=17), the United Kingdom (the UK) (n=13) and Australia (n=40) were analyzed by high performance liquid chromatography coupled to mass spectrometry. The objective was to identify different perfluorooctane sulfonate (PFOS) isomers. Similar isomer patterns typical for the electrochemical fluorination (ECF) process were found for all samples. The linear PFOS (L-PFOS) was the major isomer found (58-70%) followed by the monosubstituted PFOS isomers 1/6-CF(3)-PFOS (18-22%) and 3/4/5-CF(3)-PFOS (13-18%). Disubstituted isomers were also detected. The percentage of L-PFOS found in the serum and plasma samples was lower compared to a standard PFOS product (76-79%). The pattern of PFOS isomers in human serum and plasma may be suggestive concerning potential isomeric discrimination since PFOS is only produced by ECF. Possibilities for such isomer discrimination are discussed. Significant higher content of L-PFOS (68%) in Swedish samples compared to Australia and the UK (59%) was also found, which may suggest differences in exposure sources for humans.
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