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Sökning: WFRF:(Chen Changer)

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1.
  • Wang, Fang, et al. (författare)
  • Emerging contaminants: A One Health perspective
  • 2024
  • Ingår i: Innovation. - 2666-6758. ; 5
  • Forskningsöversikt (refereegranskat)abstract
    • Environmental pollution is escalating due to rapid global development that often prioritizes human needs over planetary health. Despite global efforts to mitigate legacy pollutants, the continuous introduction of new substances remains a major threat to both people and the planet. In response, global initiatives are focusing on risk assessment and regulation of emerging contaminants, as demonstrated by the ongoing efforts to establish the UN's Intergovernmental Science-Policy Panel on Chemicals, Waste, and Pollution Prevention. This review identifies the sources and impacts of emerging contaminants on planetary health, emphasizing the importance of adopting a One Health approach. Strategies for monitoring and addressing these pollutants are discussed, underscoring the need for robust and socially equitable environmental policies at both regional and international levels. Urgent actions are needed to transition toward sustainable pollution management practices to safeguard our planet for future generations.
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2.
  • Chen, Changer Long, et al. (författare)
  • Determination of fragrance ingredients in fish by ultrasound-assisted extraction followed by purge & trap
  • 2017
  • Ingår i: Analytical Methods. - : Royal Society of Chemistry (RSC). - 1759-9660 .- 1759-9679. ; 9:15, s. 2237-2245
  • Tidskriftsartikel (refereegranskat)abstract
    • Fragrance materials are widely used in household and personal care products in applications that can lead to emissions into the aquatic environment. Assessing the potential of fragrance materials to bioaccumulate in fish in in vivo laboratory studies requires a reliable analytical method for determining the concentrations of chemical substances in fish tissue. Here, we present an analytical method for simultaneously measuring a group of model chemicals that are representative of chemicals found in fragrance materials in rainbow trout. This method involves ultrasound-assisted extraction (UAE) followed by enrichment of the fragrance ingredients using a purge & trap system. Nine fragrance ingredients including semi-volatile and volatile compounds were selected as model substances for method development. Homogenised whole rainbow trout subsamples were spiked with these nine model fragrance ingredients, hexachlorobenzene (HCB) and 2,2',5,5'-tetrachlorobiphenyl (PCB52). The targeted chemicals were extracted from the fish tissue using acetonitrile in an ultrasonic bath; after solvent exchange to hexane, they were extracted into the gas phase by heating the samples and purging with nitrogen and trapped on a solid-phase extraction (SPE) cartridge. Finally, these chemicals were eluted with hexane from the SPE column and analysed using gas chromatography-mass spectrometry (GC-MS). The proposed method has been evaluated for blanks, spiked recoveries and precision, which are all acceptable. We believe that the method presented here is generally applicable for analysis of acid-sensitive volatile and semi-volatile organic chemicals in fish and provides the basis to conduct in vivo bioaccumulation studies of fragrance materials.
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3.
  • Kierkegaard, Amelie, et al. (författare)
  • Tissue Distribution of Several Series of Cationic Surfactants in Rainbow Trout (Oncorhynchus mykiss) Following Exposure via Water
  • 2020
  • Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 54:7, s. 4190-4199
  • Tidskriftsartikel (refereegranskat)abstract
    • Bioaccumulation assessment is important for cationic surfactants in light of their use in a wide variety of consumer products and industrial processes. Because they sorb strongly to natural surfaces and to cell membranes, their bioaccumulation behavior is expected to differ from other classes of chemicals. Divided over two mixtures, we exposed rainbow trout to water containing 10 alkyl amines and 2 quaternary alkylammonium surfactants for 7 days, analyzed different fish tissues for surfactant residues, and calculated the tissues' contribution to fish body burden. Mucus, skin, gills, liver, and muscle each contributed at least 10% of body burden for the majority of the test chemicals. This indicates that both sorption to external surfaces and systemic uptake contribute to bioaccumulation. In contrast to the analogue alkylamine bases, the permanently charged quaternary ammonium compounds accumulated mostly in the gills and were nearly absent in internal tissues, indicating that systemic uptake of the charged form of cationic surfactants is very slow. Muscle-blood distribution coefficients were close to 1 for all alkyl amines, whereas liver-blood distribution coefficients ranged from 13 to 90, suggesting that the dominant considerations for sorption in liver are different from those in blood and muscle. The significant fraction of body burden on external surfaces can have consequences for bioaccumulation assessment.
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4.
  • Lin, Zhong, et al. (författare)
  • Rhizospheric effects on atrazine speciation and degradation in laterite soils of Pennisetum alopecuroides (L.) Spreng
  • 2018
  • Ingår i: Environmental Science and Pollution Research. - : Springer Science and Business Media LLC. - 0944-1344 .- 1614-7499. ; 25:13, s. 12407-12418
  • Tidskriftsartikel (refereegranskat)abstract
    • Atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazine) is a worldwide-used herbicide and often detected in agricultural soils and groundwater at concentrations above the permitted limit, because of its high mobility, persistence, and massive application. This study applied pot experiments to investigate the atrazine contents and speciation during the phytoremediation process by Pennisetum alopecuroides (L.) Spreng. in laterite soils. From the change of the total atrazine and bioavailable atrazine measured by diffusive gradients in thin film (DGT), P. alopecuroides significantly improved atrazine degradation efficiency from 15.22 to 51.46%, attributing to the increasing bioavailable atrazine in rhizosphere. Only a small amount of atrazine was taken up by P. alopecuroides root and the acropetal translocation from roots to shoots was limited. The atrazine speciation was significantly different between rhizosphere and non-rhizosphere, attributing to the declining pH and organic matters in rhizosphere. The relationship between pH and soil-bound/humus-fixed atrazine illustrated the pH-dependant release of the atrazine from soils and the competition between humus adsorption and uptake by P. alopecuroides. The present study reveals the important roles of soil pH and organic matters in atrazine speciation and availability in laterite soils, and provides new insights in the rhizospheric effects on effective phytoremediation of atrazine.
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5.
  • Peng, Qin, et al. (författare)
  • Assessment of bioavailability of selenium in different plant-soil systems by diffusive gradients in thin-films (DGT)
  • 2017
  • Ingår i: Environmental Pollution. - : Elsevier BV. - 0269-7491 .- 1873-6424. ; 225, s. 637-643
  • Tidskriftsartikel (refereegranskat)abstract
    • Uptake of selenium (Se) by plants largely depend on the availability of Se in soil. Soils and plants were sampled four times within 8 weeks of plant growth in pot experiments using four plant species. Sequential extraction and diffusive gradients in thin-films (DGT) method were employed to measure Se concentrations in potted soils in selenite- or selenate-amended soils. Results showed that DGT-measured Se concentrations (C-DGT-Se) were generally several folds higher for selenate than selenite amended soils, which were obviously affected by the plant species and the duration of their growth. For example, the folds in soil planted with mustard were 1.49-3.47 and those in soils planted with purple cabbage and broccoli, which grew for 3 and 4 weeks after sowing, were 1.06-2.14 and only 0.15-0.62 after 6 weeks of growth. The selenate-amended soil planted with wheat showed an extremely high C-DGT-Se compared with selenite-amended soil, except the last harvest. Furthermore, minimal changes in C-DGT-Se and soluble Se(IV) were found in selenite-amended soils during plant growth, whereas significant changes were observed in selenate-amended soils (p < 0.05). Additionally, Se distribution in various fractions of soil remarkably changed; the soils planted with purple cabbage and broccoli showed the most obvious change followed by wheat and mustard. Soluble Se(VI) and exchangeable Se(VI) were likely the major sources of C-DGT-Se in selenate-amended soils, and soluble Se(IV) was the possible source of C-DCT-Se in selenite-amended soils. In selenate-amended soils, soluble Se(VI) and exchangeable Se(VI) were significantly correlated with Se concentrations in purple cabbage, broccoli, and mustard; in wheat, Se concentration was significantly correlated only with soluble Se(VI) but not with exchangeable Se. C-DGT-Se eventually became positively correlated with Se concentrations accumulated by different plants, indicating that DGT is a feasible method in predicting plant uptake of selenate but not of selenite.
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