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  • 1
    Keywords: Forschungsbericht ; Mikroplastik ; Verwitterung ; Toxizität ; Meeresökologie
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (16 Seiten, 1,75 MB) , Illustrationen, Diagramme
    Language: German
    Note: Förderkennzeichen BMBF 03F0733A , Verbundnummer 01166606 , Paralleltitel dem englischen Berichtsblatt entnommen , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Sprache der Zusammenfassung: Deutsch, Englisch
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  • 2
    Keywords: Forschungsbericht ; Pazifischer Ozean Nord ; Mikroplastik
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (24 Seiten, 1,41 MB) , Illustrationen, Diagramme
    Language: German
    Note: Förderkennzeichen BMBF 03G0268TA , Verbundnummer 01185052 , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden
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  • 3
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    PANGAEA
    In:  Supplement to: Jahnke, Annika; Berger, Urs; Ebinghaus, Ralf; Temme, Christian (2007): Latitudinal gradient of airborne polyfluorinated alkyl substances in the marine atmosphere between Germany and South Africa (53° N-33° S). Environmental Science and Technology, 41(9), 3055 -3061, https://doi.org/10.1021/es062389h
    Publication Date: 2024-04-27
    Description: Neutral, volatile polyfluorinated alkyl substances (PFAS) were determined in high-volume air samples collected onboard the German research vessel Polarstern during cruise ANT-XXIII/1 between Bremerhaven, Germany (53° N) and Capetown, Republic of South Africa (33° S) in fall 2005. An optimized and validated analytical protocol was used for the determination of several fluorotelomer alcohols (FTOHs) as well as N-alkylated fluorooctane sulfonamides and sulfonamidoethanols (FOSAs/FOSEs). Quantitative analyses were done by gas chromatography-mass spectrometry. This study provides the first concentration data of airborne PFAS from the Southern Hemisphere. Results indicate a strongly decreasing concentration gradient from the European continent toward less industrialized regions. The study confirms that airborne PFAS are mainly restricted to the Northern Hemisphere with a maximum concentration of 190 pg/m**3 (8:2 FTOH) in the first sample collected in the channel between the European mainland and the UK. However, south of the equator, trace amounts of several FTOHs and FOSAs with a maximum of 14 pg/m**3 (8:2 FTOH) could still be detected. Furthermore, a selection of ionic PFAS including perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) were determined in the particulate phase of high-volume air samples by liquid chromatography-mass spectrometry. Levels of ionic PFAS were almost 2 orders of magnitude lower than those of neutral PFAS, with maximum concentrations in the first sample of 2.5 pg/m**3 (PFOS) and 2.0 pg/m**3 (PFOA).
    Keywords: ANT-XXIII/1; CT; Polarstern; PS69; PS69/1-track; Underway cruise track measurements
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 4
    Publication Date: 2024-04-27
    Keywords: 6:2 fluorotelomer sulfonate; ALTITUDE; ANT-XXIII/1; CT; DATE/TIME; Date/time end; High Performance Liquid Chromatography - Mass spectrometry (HPLC-MS); LATITUDE; Latitude 2; LONGITUDE; Longitude 2; Perfluorodecanoate; Perfluorohexane sulfonate; Perfluorononanoate; Perfluorooctane sulfonate; Perfluorooctanoate; Perfluoroundecanoate; Polarstern; PS69; PS69/1-track; Sample code/label; Underway cruise track measurements
    Type: Dataset
    Format: text/tab-separated-values, 111 data points
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  • 5
    Publication Date: 2024-04-27
    Keywords: 10:2 fluorotelomer alcohol; 6:2 fluorotelomer alcohol; 8:2 fluorotelomer alcohol; ALTITUDE; ANT-XXIII/1; CT; DATE/TIME; Date/time end; Gas chromatography - Mass spectrometry (GC-MS); LATITUDE; Latitude 2; LONGITUDE; Longitude 2; N-ethyl fluorooctane sulfonamide; N-ethyl fluorooctane sulfonamidoethanol; N-methyl fluorooctane sulfonamide; N-methyl fluorooctane sulfonamidoethanol; Polarstern; PS69; PS69/1-track; Sample code/label; Underway cruise track measurements
    Type: Dataset
    Format: text/tab-separated-values, 141 data points
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  • 6
    Publication Date: 2018-05-22
    Description: There is a multitude of pollutants that combine persistent and hydrophobic properties. In aquatic environments, they are largely deposited in sediments. The amount and characteristics of the organic carbon determine how strongly they are bound or if they are readily available for partitioning to biota and biouptake. These pollutants can be accumulated by aquatic organisms and biomagnified to higher trophic levels. Hence, it is important to explore the composition, activity and effects of environmental mixtures of pollutants in sediments of different origin, characteristics and pollution history. Sediments from Sweden, the European Arctic (coastal Svalbard vs. open sea), Queensland (Australia) and a French-German river were collected. The freely dissolved concentrations (Cfree) of the chemicals were determined using equilibration with thin coatings of silicone on the inner walls of glass jars with subsequent solvent extraction. Total sediment concentrations (Ctotal) were determined using accelerated solvent extraction. While there is a wide range of pollutants that have been detected in sediments world-wide, traditional chemical analysis cannot cover all compounds and their transformation products. Therefore, in this study, the extracts were dosed into seven cell-based bioassays covering cytotoxicity, activation of metabolic enzymes (binding to the arylhydrocarbon receptor, AhR), specific, receptor-mediated effects such as estrogenicity (ERa); and adaptive stress response (oxidative stress, AREc32). Cytotoxicity was assessed in all bioassays and occurred occasionally. Moreover, four of the seven bioassays were active in this study: AhR, AREc32, the peroxisome proliferator-activated receptor gamma (PPARg) and ERa. The activation of the AhR was by far most responsive and showed a distinct pattern across the sampling locations. The other three assays showed responses only at higher enrichment factors of the extracts, also revealing specific contamination patterns. A comparison between Cfree vs. Ctotal will enable assessing the actual risk (Cfree) vs. the potential hazard of those chemicals that might be released in future scenarios (Ctotal). The presented work calls for more detailed studies at specific sites and testing of additional endpoints with the aim of obtaining a complete picture of mixture effects caused by the freely dissolved and total concentrations of hydrophobic organic chemicals in sediments.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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  • 7
    Publication Date: 2018-10-29
    Description: This study investigated whether cell-based bioassays were suitable to characterize profiles of mixture effects of hydrophobic pollutants in multiple sediments covering remote Arctic and tropical sites to highly populated sites in Europe and Australia. The total contamination was determined after total solvent extraction and the bioavailable contamination after silicone-based passive equilibrium sampling. In addition to cytotoxicity, we observed specific responses in cell-based reporter gene bioassays: activation of metabolic enzymes (arylhydrocarbon receptor: AhR, peroxisome proliferator activated receptor gamma: PPARγ) and adaptive stress responses (oxidative stress response: AREc32). No mixture effects were found for effects on the estrogen, androgen, progesterone and glucocorticoid receptors, or they were masked by cytotoxicity. The bioanalytical equivalent concentrations (BEQ) spanned several orders of magnitude for each bioassay. The bioavailable BEQs (passive equilibrium sampling) typically were 10–100 times and up to 420 times lower than the total BEQ (solvent extraction) for the AhR and AREc32 assays, indicating that the readily desorbing fraction of the bioactive chemicals was substantially lower than the fraction bound strongly to the sediment sorptive phases. Contrarily, the bioavailable BEQ in the PPARγ assay was within a factor of five of the total BEQ. We identified several hotspots of contamination in Europe and established background contamination levels in the Arctic and Australia.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 8
    Publication Date: 2022-04-05
    Description: Contaminant analysis in biota extracts can be hampered by matrix interferences caused by, for example, co‐extracted lipids that compromise the quality of the analytical data and require frequent maintenance of the analytical instruments. In the present study, using gas chromatography coupled to high resolution mass spectrometry (GC‐HRMS), we aimed to develop and validate a straightforward, robust, and reproducible cleanup method with acceptable recoveries for diverse compound classes with a wide range of physicochemical properties representative of pollutant screening in biota extracts. We compared Oasis PRiME HLB cartridges, Agilent Captiva EMR‐Lipid cartridges, and “Freeze‐Out” with salmon lipids spiked with 113 target chemicals. The EMR‐Lipid cartridges provided extracts with low matrix effects at reproducible recoveries of the multi‐class target analytes (93 ± 9% and 95 ± 7% for low and high lipid amounts, respectively). The EMR‐Lipid cartridges were further tested with spiked pork lipids submitted to total extraction or silicone‐based passive sampling. Reproducible recoveries were achieved and matrix residuals were largely removed as demonstrated gravimetrically for both types of extracts. Ion suppression of halogenated compounds was not as efficiently removed by the cleanup of total and silicone‐based extracts of pork lipids as for the salmon lipids. However, the samples with clean up provided better instrument robustness than those without cleanup. Hence, EMR‐Lipid cartridges were shown to be efficient as a cleanup method in multi‐class monitoring of biota samples and open up new possibilities as a suitable cleanup method for silicone extracts in biota passive sampling studies using GC‐HRMS analysis. Environ Toxicol Chem 2021;40:2693–2704. © 2021 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.
    Description: H2020 European Research Council http://dx.doi.org/10.13039/100010663
    Keywords: ddc:577.14
    Language: English
    Type: doc-type:article
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  • 9
    Publication Date: 2022-10-25
    Description: Plastic pollution accumulating in an area of the environment is considered “poorly reversible” if natural mineralization processes occurring there are slow and engineered remediation solutions are improbable. Should negative outcomes in these areas arise as a consequence of plastic pollution, they will be practically irreversible. Potential impacts from poorly reversible plastic pollution include changes to carbon and nutrient cycles; habitat changes within soils, sediments, and aquatic ecosystems; co-occurring biological impacts on endangered or keystone species; ecotoxicity; and related societal impacts. The rational response to the global threat posed by accumulating and poorly reversible plastic pollution is to rapidly reduce plastic emissions through reductions in consumption of virgin plastic materials, along with internationally coordinated strategies for waste management.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 10
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    In:  EPIC37th International Marine Debris Conference, Busan, South Korea, 2022-09-18-2022-09-23
    Publication Date: 2023-06-21
    Description: The fate and transport pathways of floating debris are still not completely understood. The material with densities exceeding that of seawater is expected to sink to deeper water layers and eventually reach the seafloor. However, the fate of the plastic waste with lower density is complicated to determine, amongst others, due to complex weathering processes including biofilm formation on its surface. However, several studies have identified accumulation areas at the sea surface. The so-called “Great Pacific Garbage Patch” in the North Pacific Subtropical Gyre is probably the most recognized one among these areas, which likely continues to accumulate plastic rapidly.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Conference , notRev
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