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A study of the effects of different XAD-resins, bed volume, flow rate, pH and type of eluent on the extraction of organic mutagens from surface water is presented. XAD-4/8 is as effective as XAD-2 in concentrating organic mutagens from surface water and dimethylsulfoxide (DMSO) is as efficient as acetone in eluting the adsorbed organic mutagens. The latter allows direct testing up to 0.5 ml of DMSO concentrate in the Ames test. Variation of the pH of the water after passing the XAD-4/8, followed by readsorption, shows that the majority of the mutagenic activity due to dissolved organics is adsorbed at neutral pH. Only a minor fraction is readsorbed at pH 3. Further a XAD-4/8 concentrate and a similar concentrate prepared by freeze drying gives similar mutagenic activity. This indicates that many of the organic mutagens are recovered in the XAD-4/8 concentrate.It is concluded that adsorption on XAD-4/8, followed by direct testing of the DMSO eluates in the Ames test, presents a rapid and relatively simple way to detect low concentrations of organic mutagens in surface water. The general suitability of the method is shown for different types of surface water.  相似文献   
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The affinity of dissolved organic matter (DOM) for binding a polycyclic aromatic hydrocarbon, benzo(a)pyrene (BaP), was measured for 11 surface and ground waters and a commercial humic acid. The hydrophobic-acid (HbA) and hydrophobic-neutral (HbN) compositions of the DOM, solution absorptivity at 270nm (ABS270), and DOM molar volumes were determined. Waters enriched in HbA material had a larger molar volume and higher aromatic content (as indicated by the ABS270). There was a good correlation between the size and HbA content of the DOM from the different sources and the Kdom for binding BaP. An excellent predictive relationship (r2 = 0.9) was demonstrated between the ABS270 of a water and the Kdom for binding BaP. Based on these results, it is suggested that binding of BaP to DOM depends not only on the hydrophobicity of DOM, but also on the existence of an open structure within the DOM to provide access of the aqueous solute to hydrophobic domains within the DOM.  相似文献   
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Simultaneous measurements of gaseous hydrogen peroxide and ozone made in southern England are reported. The hydrogen peroxide measurements are the first reported for the United Kingdom and show clear diurnal trends and correlate with ozone measurements. Measurements were made during a photochemical episode when a peak hydrogen peroxide concentration of 2.5 microg m(-3) was recorded with a simultaneous peak of 168 microg m(-3) in the ozone concentration. From observations on the rate of decay in the measured concentrations, an evening-time deposition velocity of 0.28 cm s(-1) was derived for hydrogen peroxide.  相似文献   
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The effects of joint action of SO(2) and HF on three Eucalyptus species were studied by exposing them to combinations of < 13, 122 or 271 microg m(-3) of SO(2) and 0.03, 0.39 or 1.05 microg m(-3) of HF in open top chambers for 120 days. HF and SO(2) reduced the area and weight of immature leaves in all three species, but there were few interactive effects on immature leaves. The response of mature leaves to exposure differed among the species, with the greatest effects on E. calophylla and least effects on E. marginata. The interaction of HF + SO2 had no effect on leaf S concentrations in any of the species, but it reduced leaf F concentrations in E. calophylla and E. gomphocephala. HF increased leaf injury in E. calophylla and E. gomphocephala when simultaneously exposed to 271 microg m(-3) of SO(2), but had no effect at 122 microg m(-3), or on E. marginata. The addition of 271 microg m(-3) of SO(2) increased leaf injury when E. gomphocephala was exposed to 0.39 microg m(-3) of HF and when E. calophylla was exposed to 1.05 microg m(-3) of HF, despite reducing the leaf F concentrations. In some cases the interaction of the pollutants may increase susceptibility to visible injury.  相似文献   
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