长春市郊区蔬菜有机磷农药残留与健康风险评价

为了明晰长春市郊区蔬菜有机磷农药残留现况,原位采集7种214个蔬菜样品,采用气相色谱法(GC-FPD)对11种有机磷农药进行分析测定,并采用目标危险系数(THQ)法等对其风险进行了预测研究.结果表明,样品可食用部分有机磷农药含量超过与低于最大残留限量(MRL)的比率分别为23.4%和68.7%,仅7.9%样品未检出有机磷农药.有机磷农药检出率顺序依次为:二嗪农(82.2%)甲拌磷(45.8%)乐果(29.4%)甲基对硫磷(27.6%)氧化乐果(23.8%)敌敌畏(22.9%)杀螟硫磷(21%)倍硫磷(18.7%)对硫磷(18.2%)甲胺磷(17.3%)马拉硫磷(12.1%).叶菜类蔬菜有机磷超标率高于根茎类和茄果类蔬菜.不同种类蔬菜有机磷农药超标率顺序依次为:葱(82.5%)萝卜(37.5%)辣椒(17.2%)白菜(14.3%)黄瓜(3.2%)茄子(2.9%)西红柿(0%).49.5%蔬菜中检测到1种以上有机磷农药.目标平均危险系数(ave THQ)均小于1,ave HI为0.462.因此,从蔬菜有机磷农药平均含量看,目前蔬菜中的有机磷农药不会对市民造成明显的健康风险.     

含13种有机氯农药土壤标准样品的研制

采用分级稀释混合法将来自不同采样点的含不同种类和浓度的有机氯农药(OCPs)的样品进行混合制得含13种OCPs的土壤标准样品。根据GB/T 15000《标准样品工作导则》系列标准对土壤标准样品进行均匀性检验、稳定性检验,并和16家实验室协作定值。实验结果表明:土壤标准样品中13种OCPs指标均匀性良好,保证土壤标准样品足够均匀的最小取样量为0.50 g;在室温(不超过30℃)避光贮存条件下,在为期12个月的稳定性检验期间,该土壤标准样品中13种OCPs稳定性良好。该土壤标准样品中13种OCPs指标的含量范围为0.08~5.23μg/g,扩展不确定度为0.014~0.82μg/g,基本满足我国土壤、沉积物等环境样品中OCPs的质量控制检测需求。     

微滤-反渗透深度处理高盐度农药废水

采用微滤+反渗透双膜组合工艺深度处理农药废水,通过均匀试验考察进水温度、操作压力、回收率和p H等因素对无机盐去除率的影响,建立回归方程,对最佳控制参数进行快速寻优,并在优化工况下运行。试验结果表明:各因素的影响程度依次为操作压力>进水水温>回收率>p H;最佳控制参数:操作压力为577 k Pa,进水温度为20℃,p H值为6~9,回收率为50%;在此工艺条件下,可使废水的ρ(COD)降至29.1 mg/L以下,去除率达80.2%,ρ(NH3-N)降至4.7 mg/L以下,去除率达69.4%,脱盐率、Cl-去除率、SO2-4去除率分别达97.7%,97.6%、97.8%,浊度基本完全去除,出水水质满足GB/T 19923—2005《城市污水再生利用工业用水水质》标准。     

ERα和ERβ介导的有机磷农药雌激素效应差异分析

雌激素受体（Estrogen Receptor,ER）ERα和ERβ能与雌激素特异性结合,它们在结构上的差异性可能影响与类雌激素的相互作用,这进而会影响其功能.因此,针对10种有机磷农药对ERα和ERβ的雌激素效应差异,采用分子对接方法比较分析了它们与ERα、ERβ相互作用的差异并筛选出与ERα和ERβ相互作用的最佳结合模式.结果发现,10种有机磷农药分子与ERα配体结合域（Ligand Binding Domain,LBD）精氨酸（Arg394）、赖氨酸（Lys449）、色氨酸（Trp393）形成氢键;而部分农药分子与ERβLBD精氨酸（Arg346）、亮氨酸（Leu343）、赖氨酸（Lys401）形成氢键.有机磷农药配体与ERαLBDArg394、Lys449、苯丙氨酸（Phe445）、脯氨酸（Pro324）、Leu387、谷氨酸（Glu353）、甘氨酸（Gly390）等存在疏水作用,与ERβLBD氨基酸Arg346、Glu305、Leu343、蛋氨酸（Met336）、组氨酸（His279）、丙氨酸（Ala302）等存在疏水作用.采用量子化学从头算进一步分析了10种有机磷农药分子表面静电势的差异.研究发现,有机磷农药分子与ERα和ERβ受体不同的相互作用是导致雌激素效应差异的重要原因.     

Removal technology for pesticide contaminants in potable water

Abstract

Granular activated carbon adsorption is one of the reliable and effective means of removing organochlorine pesticides from water. Continuous stirred tank and fix bed reactor systems were used for the screening of indigenous granular activated carbons in the removal of organochlorine pesticides from water at low microgram levels in simulated samples. The carbon dose reguired to treat raw water at initial concentrations of 5–10 ug/1 of Y‐HCH, p,p'‐DDT and p,p'‐DDE to <2 ug/1 potable level was computed. Data leads to the development of a tap attachable water treatment unit for pesticides removal for applications on domestic scale.     

The greenhouse work environment: a modifier of occupational pesticide exposure?

Abstract

Greenhouses are enclosed structures which have various characteristics that enhance crop productivity, but the implications for workers’ pesticide exposure and uptake are not well understood. A narrative literature review was conducted to explore the mechanism/s of interactions between greenhouse characteristics and occupational pesticide exposure. Using a “work”, “worker” and “workplace” conceptual framework, the greenhouse environment (hot and humid microclimate, limited space and dense crop arrangements) combines with work characteristics (high work and pesticide use intensity, multi-tasking, predominantly manual spraying techniques and quick reentry to treated farms) to potentially increase occupational pesticide exposure, compared with open field farming. Greenhouse environments, are variable but have been shown to influence pesticide availability, route, pathways and frequency of exposure, deposition and distribution on a worker’s body as well as use and performance of exposure control methods. Training programs can emphasize the differences in exposure potential between greenhouse and open field farming. Development of tailored guidelines for exposure control strategies to better suit the level of uniqueness of greenhouse agriculture seems warranted.     

Effects of soil composition on solid phase microextraction determination of triazine and organophosphorus pesticides

The influence of organic matter and clay contents on headspace solid phase microextraction (HS-SPME) determination of triazine and organophosphorus pesticides in different soils was studied. The results of the study showed that content of soil organic matter dominantly participated in sorption of triazines (simazine, atrazine and prometryn) to soil, while sorption of organophosphorus pesticides (phorate and tebupirimfos) could not be explained only by contents of dominant soil sorption components (soil organic matter and clay). Sorption of all pesticides studied to different soil types was similar at their lower concentrations while the influence of soil composition was expressed at higher concentration levels. Except for phorate, the obtained sorption trends were different from those obtained by direct SPME mode (DM-SPME) and exhaustive liquid-solid extraction (LSE) method. These results indicated that most likely co-extractants from the analyzed medium complicated evaporation and diffusion of the pesticides to the PDMS fiber during HS-SPME sampling.     

细胞色素P450酶代谢新烟碱类农药N-脱烷基反应的机制研究：以噻虫嗪为例

生物转化是影响有机污染物毒性的重要过程,细胞色素P450酶在其中起着关键作用.新烟碱类农药对于哺乳动物毒性较低,但是经过P450酶的转化后,可能会产生毒性增强的代谢产物,提高环境和健康风险.本研究以噻虫嗪（TMX）为例,采用计算模拟的方法研究P450酶催化下TMX的代谢路径和产物,探讨该类污染物N-脱烷基的反应机制.计算结果表明,P450酶代谢TMX有两条不同路径：一条是经过两次O-亚甲基羟基化后通过水桥开环生成毒性减小的噻虫胺（CLO）;另一条是通过氢提取/羟基反弹羟基化甲基的过程,然后经水桥转移氢质子发生N-脱甲基反应,生成去甲基噻虫嗪（dm-TMX）,据前人实验报道该产物会导致肝肿瘤发生率的增加,具有明显的健康风险.鉴于其他烷基胺类化合物具有类似的代谢机理,进一步通过C—H键解离能(BDE_C-H)与氢提取反应的活化能（ΔE^*）建立了N-脱烷基化反应活性的预测模型,R²=0.932,平均绝对误差MAE=1.75 kcal·mol^-1,模型的稳健性良好,可以快速有效地为该类污染物的代谢活性研究提供...     

Organohalogen compounds in blubber of Indo-Pacific bottlenose dolphin (Tursiops aduncus) and spinner dolphin (Stenella longirostris) from Zanzibar, Tanzania

Blubber samples of Indo-Pacific bottlenose (Tursiops aduncus) and spinner (Stenella longirostris) dolphins from Zanzibar, East Africa, were analyzed for a wide range of organohalogen compounds. Methoxylated polybrominated diphenyl ethers (MeO-BDEs), presumably biogenic, were found at higher concentrations than anthropogenic organochlorine pesticides (OCPs). Only traces of industrial pollutants, such as polychlorinated biphenyls, were detected. The OCP levels found off Zanzibar were lower than those reported from other regions while MeO-BDE levels were higher. The relative composition of the OCPs indicated recent use of lindane (γ-hexachlorocyclohexane) and aged residues of DDT and technical HCH. Placental transfer was estimated to 2.5% and 0.5% of the total burden of OCPs and MeO-BDEs, respectively. Overall transfer from mother to calf in Indo-Pacific bottlenose dolphins was estimated to 72% and 85% for the OCPs and MeO-BDEs burdens, respectively. Health effects of MeO-BDEs are not known, but structural similarities with well-known environmental toxins are cause for concern.     

Organochlorine pesticides accumulation and degradation products in vegetation samples of a contaminated area in Galicia (NW Spain)

The content of 21 organochlorine pesticides were studied in vegetation samples of a highly contaminated area by isomers of hexachlorocyclohexane (HCH) located close to a former industrial area in Galicia (NW Spain). Five species of plants were collected at different points of the contaminated area and the different parts of the plants were separated in order to study differences in accumulation capabilities. Samples were extracted employing microwave energy followed by a clean-up step using solid phase extraction and finally determined by GC–ECD. The results obtained show that the most abundant pesticides are HCHs isomers, being the main isomers β-HCH and -HCH in all samples whereas δ-HCH and γ-HCH were at lower levels. Some other pesticides such as p,p′-DDT, p,p′-DDD and p,p′-DDE were also present in much lower amount in some of the samples. Several degradation products of HCH were also identified in some samples by GC–MS.