“生物有效性测量”与“全沉积物毒性识别评估(TIE)”联用有效识别出沉积物中主要致毒污染物

沉积物中污染物种类繁多,准确判断其中产生生物毒性的主要来源是个难点,本文作者先采用TIE法初步判断出主要致毒污染物为有机物和重金属(毒性描述阶段(相I)),传统的毒性单位分析结果显示Cr、Cu、Ni、Pb和Zn主要致毒重金属,而为氯氰菊酯、氯氟氰菊酯、溴氰菊酯和氟虫腈为主要致毒有机物中(毒性鉴定阶段(相II))。采用4步分级提取法和Tenax提取法分析了重金属和有机物的生物有效性。生物有效性毒性单位分析更加准确地锁定了毒性主要贡献重金属为Zn、Ni和Pb,毒性主要贡献有机物为氯氰菊酯、氯氟氰菊酯和氟虫腈。沉积物的稀释降低了重金属的毒性并使其毒性贡献鉴定变得复杂,生物有效性测量可以有效地提高TIE结果的准确性。
精选自Xiaoyi Yi, Huizhen Li, Ping Ma and Jing You. Identifying the causes of sediment-associated toxicity in urban waterways in South China: Incorporating bioavailabillity-based measurements into whole-sediment toxicity identification evaluation. Environmental Toxicology and Chemistry: Volume 34, Issue 8, pages 1744–1750, August 2015. DOI: 10.1002/etc.2970
详情请见http://onlinelibrary.wiley.com/doi/10.1002/etc.2970/full     

Toxiwasp∗

TOXIWASP combines most of the kinetic structure of EXAMS 2 with the transport capabilities of WASP (Water Analysis Simulation Program). TOXIWASP uses variable chemical degradation rates from chemical properties and the environmental conditions of the aquatic ecosystem. These rates are reduced from pseudo first‐order rates to first‐order rates including the processes hydrolysis, biotransfor‐mation, phototransformation, oxidation, and volatilisation. Assuming ultimate local equilibrium, and using a chemical dependent partition coefficient as well as spatially varying environmental carbon fractions, sorption onto sediments and biomass is calculated. Environmental alternations could be specified in any time scale by providing monitoring data.

TOXIWASP generates total sediment and chemical concentrations every time step in every segment, including surface water, subsurface water, surface bed and subsurface bed. Advection, dispersion, mass loading, sedimentation, and scour affect sediment concentration in the water column and in the bed sediment concentrations depend on burial and erosion. In addition chemical concentrations are influenced by degradation, sediment‐water dispersion, and percolation. Lateral transport of chemical within the bed is neglected and transport data are not calculated in the program. TOXIWASP is developed to model stratified lakes, reservoirs, large rivers, estuaries, and coastal waters. As for EXAMS 2 (Burns et al.²) the TOXIWASP user has to accept the model's inability to connect the water body to a chemically contaminated atmosphere.     

Release of heavy metals from a river sediment by a synthetic polymer and an agricultural residue: Variation with time of contact

A comparative study of the solubilization of Fe, Zn, Cu and Mn from a river sediment by solutions of a residue from agricultural industry and a synthetic polymer (SP) is presented. The agricultural residue shows a higher mobilising effect than the SP. The presence of the latter causes in most cases an initial solubilization and a readsorption afterwards, with a tendency to an equilibrium for long reaction times. The effect of the agricultural residue is not uniform for all metals studied, with a significant formation of metal‐organic complexes for Cu and Zn. In the presence of the SP, the proportion of complexes formed is significant only for Zn.     

高分子重金属絮凝剂的制备及含铜废水处理

以聚乙烯亚胺和二硫化碳制备聚乙烯亚胺基黄原酸钠(PEX),研究了PEX对废水中浊度及铜的去除效果.实验证明,在含铜废水中投加PEX,铜和浊度均可被去除,显示了其除浊与除重金属的双重功能.PEX与投加氧化钙的化学沉淀法相比:适用的废水pH值在5.0-6.0之间,低于化学沉淀法所必需的pH值;出水中残余铜远低于化学沉淀法;生成的矾花较大,易于沉降分离,化学沉淀法生成的沉淀细小,难于分离.研究还表明,PEX为两性聚合电解质,在较低的pH值下,分子上的氨基带正电荷,发挥电中和作用达到絮凝除浊效果;在较高的pH值下,分子上的黄原酸基和氨基均可与重金属离子发生配位及螯合反应,从而达到去除重金属离子的效果.     

污灌水重金属污染阻控材料与技术研究

文章综述了具有纳米结构的粘土矿物(高岭土、蒙脱土和海泡石)、硫化物材料和纳米复合材料的制备及其从水中吸附去除重金属离子机理的研究进展.此外,还比较了多种可应用于重金属源头阻控的技术方案,讨论了适用于农业灌溉重金属阻控的装置组成和净化材料类型等.最后对有待进一步解决的问题和阻控技术发展方向进行了展望.     

Spatial distribution of heavy metal concentrations in urban, suburban and agricultural soils in a Mediterranean city of Algeria

As part of a larger program aiming at assessing transfer and effects of metals in food webs, this work studied the spatial distribution of Cd, Cr, Cu, Pb, and Zn in 101 sub-surface soils, systematically sampled (1 × 1 km regular grid) over a large area around Annaba, the fourth most-populated city of Algeria. Cd and Cr exhibited only one abnormally high value, with all other concentrations being close to pedogeological background. Some places in the centre of the city were polluted by Pb (up to 823 mg kg⁻¹), probably due to aerial deposition from gasoline exhausts. Zn never exceeded regulatory limits over the whole sampling area. Cu was the only element for which a spatial autocorrelation occurred. A spatial interpolation by cokriging allowed the identification of agricultural activities as the main Cu pollution source. Our approach revealed various anthropogenic pollution sources, more efficiently for large-scale patterns than for local abnormalities.     

Experimental exposure to cadmium affects metallothionein-like protein levels but not survival and growth in wolf spiders from polluted and reference populations

Both local adaptation and acclimation in tolerance mechanisms may allow populations to persist under metal pollution. However, both mechanisms are presumed to incur (energetic) costs and to trade-off with other life-history traits. To test this hypothesis, we exposed Pardosa saltans (Lycosidae) spiderlings originating from metal-polluted and unpolluted sites to a controlled cadmium (Cd) treatment, and compared contents of metal-binding metallothionein-like proteins (MTLPs), internal metal concentrations, and individual survival and growth rates with a reference treatment. While increased MTLP concentrations in offspring originating from both polluted and unpolluted populations upon exposure indicates a plastic tolerance mechanism, survival and growth rates remain largely unaffected, independent of the population of origin. However, MTLP and Cd concentrations were not significantly correlated. We suggest that MTLP production may be an important mechanism enabling P. saltans populations to persist in ecosystems polluted with heavy metals above a certain level.     

RHIZOtest: A plant-based biotest to account for rhizosphere processes when assessing copper bioavailability

The ability of the free ion activity model (FIAM), the terrestrial biotic ligand model (TBLM), the diffusive gradients in thin films (DGT) technique and a plant-based biotest, the RHIZOtest, to predict root copper (Cu) concentration in field-grown durum wheat (Triticum turgidum durum L.) was assessed on 44 soils varying in pH (3.9-7.8) and total Cu (32-184 mg kg⁻¹). None of the methods adequately predicted root Cu concentration, which was mainly correlated with total soil Cu. Results from DGT measurements and even more so FIAM prediction were negatively correlated with soil pH and over-estimated root Cu concentration in acidic soils. TBLM implementation improved numerically FIAM prediction but still failed to predict adequately root Cu concentration as the TBLM formalism did not considered the rhizosphere alkalisation as observed in situ. In contrast, RHIZOtest measurements accounted for rhizosphere alkalisation and were mainly correlated with total soil Cu.     

Metal availability in a highly contaminated, dredged-sediment disposal site: Field measurements and geochemical modeling

Two complementary approaches were used to characterize arsenic and metal mobilizations from a dredged-sediment disposal site: a detailed field study combined with hydrogeochemical modeling. Contaminants in sediments were found to be mainly present as sulfides subject to oxidation. Secondary phases (carbonates, sulfates, (hydr)oxides) were also observed. Oxidative processes occurred at different rates depending on physicochemical conditions and contaminant contents in the sediment. Two distinct areas were identified on the site, each corresponding to a specific contaminant mobility behavior. In a reducing area, Fe and As were highly soluble and illustrated anoxic behavior. In well-oxygenated material, groundwater was highly contaminated in Zn, Cd and Pb. A third zone in which sediments and groundwater were less contaminated was also characterized. This study enabled us to prioritize remediation work, which should aim to limit infiltration and long-term environmental impact.     

Inorganic nanoparticles enhance the production of reactive oxygen species (ROS) during the autoxidation of L-3,4-dihydroxyphenylalanine (L-dopa)

Public concerns over the toxicity of nanoparticles (NPs) are growing due to the rapid development of nanotechnology. An important mechanism of nanotoxicity is oxidative stress resulting from reactive oxygen species (ROS). In this study, the chemical production of ROS by inorganic NPs oxidizing the mammalian phenolic compound, l-3,4-dihydroxyphenylalanine (l-dopa) was evaluated using a ROS sensitive dye, 2′,7′-diclorodihydrofluorescin (DCFH). CeO₂, Fe₂O₃ and Fe⁰ NPs enhanced ROS production during the autoxidation of l-dopa by more than four-fold in reactions that were dependent on O₂. This is the first report of chemical ROS production due to interaction of phenolic compounds with NPs. Mn₂O₃ oxidized DCFH in a reaction that did not require O₂ or l-dopa, suggesting a direct redox reaction between the Mn₂O₃ and the dye. CeO₂, Mn₂O₃ and to a lesser extent Fe⁰ formed clear electron paramagnetic resonance (EPR) signature for hydroxyl radicals when incubated in aerobic aqueous suspensions with spin traps. The results indicate that NPs can generate ROS via chemical reactions with medium components and biomolecules susceptible to oxidation, such as l-dopa. NPs were reactive whereas micron-sized particles were not. The combined assay with l-dopa and DCFH is a method proposed to screen for chemical ROS production by NPs.