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Sökning: AMNE:(NATURVETENSKAP Kemi Miljökemi)

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1.
  • Andersson, Erika, et al. (författare)
  • AhR agonist and genotoxicant bioavailability in a PAH-contaminated soil undergoing biological treatment
  • 2009
  • Ingår i: Environmental Science and Pollution Research. - : Springer Berlin/Heidelberg. - 0944-1344 .- 1614-7499. ; 16:5, s. 521-530
  • Tidskriftsartikel (refereegranskat)abstract
    • Degradation of the 16 US EPA priority PAHs in soil subjected to bioremediation is often achieved. However, the PAH loss is not always followed by a reduction in soil toxicity. For instance, bioanalytical testing of such soil using the chemical-activated luciferase gene expression (CALUX) assay, measuring the combined effect of all Ah receptor (AhR) activating compounds, occasionally indicates that the loss of PAHs does not correlate with the loss of Ah receptor-active compounds in the soil. In addition, standard PAH analysis does not address the issue of total toxicant bioavailability in bioremediated soil.To address these questions, we have used the CALUX AhR agonist bioassay and the Comet genotoxicity bioassay with RTL-W1 cells to evaluate the toxic potential of different extracts from a PAH-contaminated soil undergoing large-scale bioremediation. The extracts were also chemically analyzed for PAH16 and PCDD/PCDF. Soil sampled on five occasions between day 0 and day 274 of biological treatment was shaken with n-butanol with vortex mixing at room temperature to determine the bioavailable fraction of contaminants. To establish total concentrations, parts of the same samples were extracted using an accelerated solvent extractor (ASE) with toluene at 100A degrees C. The extracts were tested as inducers of AhR-dependent luciferase activity in the CALUX assay and for DNA breakage potential in the Comet bioassay.The chemical analysis of the toluene extracts indicated slow degradation rates and the CALUX assay indicated high levels of AhR agonists in the same extracts. Compared to day 0, the bioavailable fractions showed no decrease in AhR agonist activity during the treatment but rather an up-going trend, which was supported by increasing levels of PAHs and an increased effect in the Comet bioassay after 274 days. The bio-TEQs calculated using the CALUX assay were higher than the TEQs calculated from chemical analysis in both extracts, indicating that there are additional toxic PAHs in both extracts that are not included in the chemically derived TEQ.The response in the CALUX and the Comet bioassays as well as the chemical analysis indicate that the soil might be more toxic to organisms living in soil after 274 days of treatment than in the untreated soil, due to the release of previously sorbed PAHs and possibly also metabolic formation of novel toxicants.Our results put focus on the issue of slow degradation rates and bioavailability of PAHs during large-scale bioremediation treatments. The release of sorbed PAHs at the investigated PAH-contaminated site seemed to be faster than the degradation rate, which demonstrates the importance of considering the bioavailable fraction of contaminants during a bioremediation process.It has to be ensured that soft remediation methods like biodegradation or the natural remediation approach do not result in the mobilization of toxic compounds including more mobile degradation products. For PAH-contaminated sites this cannot be assured merely by monitoring the 16 target PAHs. The combined use of a battery of biotests for different types of PAH effects such as the CALUX and the Comet assay together with bioavailability extraction methods may be a useful screening tool of bioremediation processes of PAH-contaminated soil and contribute to a more accurate risk assessment. If the bioremediation causes a release of bound PAHs that are left undegraded in an easily extracted fraction, the soil may be more toxic to organisms living in the soil as a result of the treatment. A prolonged treatment time may be one way to reduce the risk of remaining mobile PAHs. In critical cases, the remediation concept might have to be changed to ex situ remediation methods.
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2.
  • Boström, Björn, et al. (författare)
  • Isotope fractionation and 13C enrichment in soil profiles during the decomposition of soil organic matter
  • 2007
  • Ingår i: Oecologia. - Berlin : Springer. - 0029-8549 .- 1432-1939. ; 153:1, s. 89-98
  • Tidskriftsartikel (refereegranskat)abstract
    • The mechanisms behind the 13C enrichment of organic matter with increasing soil depth in forests are unclear. To determine if 13C discrimination during respiration could contribute to this pattern, we compared d13C signatures of respired CO2 from sieved mineral soil, litter layer and litterfall with measurements of d13C and d15N of mineral soil, litter layer, litterfall, roots and fungal mycelia sampled from a 68-year-old Norway spruce forest stand planted on previously cultivated land. Because the land was subjected to ploughing before establishment of the forest stand, shifts in d13C in the top 20 cm reflect processes that have been active since the beginning of the reforestation process. As 13C-depleted organic matter accumulated in the upper soil, a 1.0 o/oo d13C gradient from –28.5 o/oo in the litter layer to –27.6 o/oo at a depth of 2–6 cm was formed. This can be explained by the 1 o/oo drop in d13C of atmospheric CO2 since the beginning of reforestation together with the mixing of new C (forest) and old C (farmland). However, the isotopic change of the atmospheric CO2 explains only a portion of the additional 1.0& increase in d13C below a depth of 20 cm. The d13C of the respired CO2 was similar to that of the organic matter in the upper soil layers but became increasingly 13C enriched with depth, up to 2.5 o/oo relative to the organic matter. We hypothesise that this 13C enrichment of the CO2 as well as the residual increase in d13C of the organic matter below a soil depth of 20 cm results from the increased contribution of 13C-enriched microbially derived C with depth. Our results suggest that 13C discrimination during microbial respiration does not contribute to the 13C enrichment of organic matter in soils. We therefore recommend that these results should be taken into consideration when natural variations in d13C of respired CO2 are used to separate different components of soil respiration or ecosystem respiration.
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4.
  • Dario, Mårten, et al. (författare)
  • Effects of cement additives on radionuclide mobility
  • 2004
  • Ingår i: Scientific basis for radioactive waste management XXVII. - Warrendale, Pa : Materials Research Society. - 1558997520 ; , s. 639-644
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)
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6.
  • de Boer, J., et al. (författare)
  • United Nations Environment Programme Capacity Building Pilot Project : training and interlaboratory study on persistent organic pollutant analysis under the Stockholm Convention
  • 2008
  • Ingår i: Analytica Chimica Acta. - : Elsevier BV. - 0003-2670 .- 1873-4324. ; 617:1-2, s. 208-215
  • Tidskriftsartikel (refereegranskat)abstract
    • Within the framework of a United Nations Environment Programme (UNEP) Capacity Building Project for training of laboratory staff in developing countries on persistent organic pollutant (POP) analysis, an interlaboratory study was organised following an initial evaluation of the performance of laboratories (reality check) and a series of training sessions. The target compounds were polychlorinated biphenyls (PCB) and organochlorine pesticides (OCP). Seven laboratories from five countries (Ecuador, Uruguay, Kenya, Moldova, and Fiji) participated. Most of the laboratories had no experience in determining PCBs. Although chromatograms improved considerably after the training and installation of new gas chromatographic (GC) columns at participating laboratories, the level of performance in the interlaboratory study was essentially on par with the moderate performance level achieved by European POP laboratories in the 1980s. Only some individual results were within +/-20% of the target values. The relative standard deviations (R.S.D.s) in POP concentrations determined by laboratories in a sediment sample were >200% in a number of cases. The results for a certified herring sample were better with at least some R.S.D. values below 50% and most below 100%. Clean up was as one of the main sources of error. After inspection it was ascertained that training of laboratory staff and investments in simple consumables such as glassware and GC columns would help to improve the quality of the analysis more than major investments in expensive instrumentation. Creating an effective network of POP laboratories at different continents together with a series of interlaboratory studies and workshops is suggested to improve the measurements of POPs in these countries.
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7.
  • Engwall, Magnus, et al. (författare)
  • Bioanalys av organiska föroreningars biotillgänglighet : tillämpning i sanerade massor
  • 2009
  • Rapport (populärvet., debatt m.m.)abstract
    • Polycykliska aromatiska kolväten (PAHer) är relativt vanliga i förorenadeområden, särskilt på gamla gasverktomter, bensinstationer och tidigare impregneringsanläggningar.På grund av deras toxicitet så är sanering av PAH-förorenadeområden av hög prioritet. För att minska riskerna med PAH-förorenade jordar,både före och efter sanering, är det viktigt att åstadkomma en heltäckande riskbedömningoch säker klassning av dessa jordmassor. De generella riktvärden förPAH-förorenad mark som används idag är i regel baserade på kemisk analys av 16standard PAHer (PAH16), trots att det ofta förekommer 100-tals PAHer och PAHmetaboliteri jordarna.I detta projekt har vi genom att jämföra kemisk och biologisk analys (H4IIEluc)av ett flertal sanerade PAH-förorenade jordprover studerat om toxicitetenverkligen minskar i proportion till minskningen av PAHer i jordarna. H4IIE-luc ären mekanismspecifik bioanalys som detekterar alla ämnen som aktiverar Ahreceptorn,en av de två viktigaste mekanismerna bakom PAHers toxicitet. Jämförelsenav resultaten visade att den totala toxiciteten i de sanerade jordprovernainte gick att förklara med kemisk analys av PAH16 och att man därmed med dagensanalysmetodik riskerar att missa toxikologiskt relevanta PAHer och andra liknandeämnen. Vidare kemiska identifieringsstudier samt bioanalytiska studier krävs föratt ta reda på om dessa okända ämnen utgör en risk för människa eller miljö.Våra resultat visar på svagheten med kemisk analys av ett mindre antal ämnensom grundval för klassning av renade massor. Det är därför är rimligt att inkluderamekanismspecifika tester i riskbedömning och vid klassning av renade PAHförorenadejordar. Dels för att minimera riskerna som dessa jordar kan utgöra förmänniskor och miljö, dels för att man med en större säkerhet och i större utsträckningskall kunna återanvända sanerade jordmassor.
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8.
  • Ericson Jogsten, Ingrid, et al. (författare)
  • Exposure to perfluorinated compounds in Catalonia, Spain, through consumption of various raw and cooked foodstuffs, including packaged food
  • 2009
  • Ingår i: Food and Chemical Toxicology. - Amsterdam : Elsevier. - 0278-6915 .- 1873-6351. ; 47:7, s. 1577-1583
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study, the role that some food processing and packaging might play as a source of perfluorinated compounds (PFCs) through the diet was assessed. The levels of PFCs were determined in composite samples of veal steak (raw, grilled, and fried), pork loin (raw, grilled, and fried), chicken breast (raw, grilled, and fried), black pudding (uncooked), liver lamb (raw), marinated salmon (home-made and packaged), lettuce (fresh and packaged), pate of pork liver, foie gras of duck, frankfurt, sausages, chicken nuggets (fried), and common salt. Among the 11 PFCs analyzed, only PFHxS, PFOS, PFHxA, and PFOA were detected in at least one composite sample, while the levels of the remaining PFCs (PFBuS, PFHpA, PFNA, PFDA, PFUnDA, and PFDoDA) were under their respective detection limits. PFOS was the compound most frequently detected, being found in 8 of the 20 food items analyzed, while PFHxA was detected in samples of raw veal, chicken nuggets, frankfurt, sausages, and packaged lettuce. According to the results of the present study, it is not sufficiently clear if cooking with non-stick cookware, or packaging some foods, could contribute to a higher human exposure to PFCs.
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9.
  • Ericson Jogsten, Ingrid, et al. (författare)
  • Human exposure to perfluorinated chemicals through the diet : intake of perfluorinated compounds in foods from the Catalan (Spain) market
  • 2008
  • Ingår i: Journal of Agricultural and Food Chemistry. - : American Chemical Society (ACS). - 0021-8561 .- 1520-5118. ; 56:5, s. 1787-1794
  • Tidskriftsartikel (refereegranskat)abstract
    • The aim of this study was to determine the dietary intake of perfluorinated chemicals (PFCs) by the population of Tarragona County (Catalonia, Spain). PFC levels were determined in 36 composite samples of foodstuffs randomly purchased in various locations. Exposure to PFCs through the diet was estimated for various age/gender groups. Perfluorooctane sulfonate (PFOS), perfluorocarboxylate perfluorooctanoate (PFOA), and perfluoroheptanoic acid (PFHpA) were the only detected PFCs in foodstuffs. On average, for a standard adult man (70 kg of body weight), the dietary intake of PFOS was estimated to be 62.5 or 74.2 ng/day (assuming ND=0 or ND=1/2 LOD, respectively). Fish, followed by dairy products and meats, were the main contributors to PFOS intake. For an adult man, the intake of PFOS (1.07 ng/kg/day) and those of PFOA and PFHpA were lower than that recently reported for Canada (4.0 ng/kg/day), and considerably lower than that previously found in the United Kingdom, the only two countries where, to date, results concerning this issue have been reported. A correlation between dietary intake and blood levels of PFOS is suggested. However, the current results do not justify dietary intake as the main route of exposure governing blood concentrations of other PFCs.
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10.
  • Ericson Jogsten, Ingrid, et al. (författare)
  • Levels of perfluorochemicals in water samples from Catalonia, Spain : is drinking water a significant contribution to human exposure?
  • 2008
  • Ingår i: Environmental Science and Pollution Research. - Heidelberg, Germany : Springer Science and Business Media LLC. - 0944-1344 .- 1614-7499. ; 15:7, s. 614-619
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND, AIM, AND SCOPE: In recent years, due to a high persistence, biomagnification in food webs, presence in remote regions, and potential toxicity, perfluorochemicals (PFCs) have generated a considerable interest. The present study was aimed to determine the levels of perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), and other PFCs in drinking water (tap and bottled) and river water samples from Tarragona Province (Catalonia, Spain). MATERIALS AND METHODS: Municipal drinking (tap) water samples were collected from the four most populated towns in the Tarragona Province, whereas samples of bottled waters were purchased from supermarkets. River water samples were collected from the Ebro (two samples), Cortiella, and Francolí Rivers. After pretreatment, PFC analyses were performed by HPLC-MS. Quantification was done using the internal standard method, with recoveries between 68% and 118%. RESULTS: In tap water, PFOS and PFOA levels ranged between 0.39 and 0.87 ng/L (0.78 and 1.74 pmol/L) and between 0.32 and 6.28 ng/L (0.77 and 15.2 pmol/L), respectively. PFHpA, PFHxS, and PFNA were also other detected PFCs. PFC levels were notably lower in bottled water, where PFOS could not be detected in any sample. Moreover, PFHpA, PFHxS, PFOA, PFNA, PFOS, PFOSA, and PFDA could be detected in the river water samples. PFOS and PFOA concentrations were between <0.24 and 5.88 ng/L (<0.48 and 11.8 pmol/L) and between <0.22 and 24.9 ng/L (<0.53 and 60.1 pmol/L), respectively. DISCUSSION: Assuming a human water consumption of 2 L per day, the daily intake of PFOS and PFOA by the population of the area under evaluation was calculated (0.78-1.74 and 12.6 ng, respectively). It was found that drinking water might be a source of exposure to PFCs as important as the dietary intake of these pollutants. CONCLUSIONS: The contribution of drinking water (tap and bottled) to the human daily intake of various PFCs has been compared for the first time with data from dietary intake of these PFCs. It was noted that in certain cases, drinking water can be a source of exposure to PFCs as important as the dietary intake of these pollutants although the current concentrations were similar or lower than those reported in the literature for surface water samples from a number of regions and countries. RECOMMENDATIONS AND PERSPECTIVES: Further studies should be carried out in order to increase the knowledge of the role of drinking water in human exposure to PFCs.
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