邻苯二甲酸酯降解细菌的多样性、降解机理及环境应用

邻苯二甲酸酯(phthalic acid esters,PAEs)是一类对人体内分泌系统有干扰作用的持续性有机污染物(persistent organic pol utants,POPs)。PAEs在环境介质如水体、底泥和土壤中长期赋存会对生物体产生毒害效应,其分布广、浓度高和难降解等特点是限制有效环境治理的主要因素。作为环境的重要组成部分,微生物对污染物有很强的适应能力和高效的降解能力,这为PAEs的生物修复提供了可能。与物理化学修复法相比,微生物修复技术具有可控性强、修复面广和灵活性高等优势。本文综述了已报道的大部分PAEs降解细菌的种类及其代谢机制,并分析了其在PAEs污染水体和土壤修复中的应用现状与前景,以期为PAEs环境行为与生物修复研究提供参考。     

硝基苯环境效应的研究综述

硝基苯污染威胁着人类和生态系统健康,国外有关硝基苯的环境毒理的研究已经广泛展开,但我国仍处于起步阶段.文章综述了国内外硝基苯环境效应的研究进展,介绍了其基本理化性质、用途、环境基准和标准值、污染的生态毒理效应以及其在生态系统中的迁移转化规律.研究认为环境中的硝基苯属于低毒污染物,但难溶于水,易溶于有机溶剂,难以降解,造成水体和土壤污染的持续时间长,且能够在生物体内积累,产生生物放大效应,因此,高浓度的硝基苯对生态系统和人体健康造成较大的生态风险;不过,阳光中的近紫外线、γ射线、声波振荡以及生物分解等作用可自然环境中硝基苯有降解作用,而生物和物理吸附能降低其浓度,从而降解其毒性.目前,有关自然生态系统中硝基苯迁移转化过程之间协同作用与相互影响的研究还有待于进一步深入.     

硝基苯环境效应的研究综述

硝基苯污染威胁着人类和生态系统健康,国外有关硝基苯的环境毒理的研究已经广泛展开,但我国仍处于起步阶段.文章综述了国内外硝基苯环境效应的研究进展,介绍了其基本理化性质、用途、环境基准和标准值、污染的生态毒理效应以及其在生态系统中的迁移转化规律.研究认为环境中的硝基苯属于低毒污染物,但难溶于水,易溶于有机溶剂,难以降解,造成水体和土壤污染的持续时间长,且能够在生物体内积累,产生生物放大效应,因此,高浓度的硝基苯对生态系统和人体健康造成较大的生态风险;不过,阳光中的近紫外线、γ射线、声波振荡以及生物分解等作用可自然环境中硝基苯有降解作用,而生物和物理吸附能降低其浓度,从而降解其毒性.目前,有关自然生态系统中硝基苯迁移转化过程之间协同作用与相互影响的研究还有待于进一步深入.     

手性农药的环境行为研究进展

手性农药由于其对映体选择性,在环境中具有特殊的归宿.研究其环境行为有助于准确评价生态系统和人体健康的风险性.文章综述了手性农药的研究进展,指出高效液相和气质联用法是不同环境介质中手性农约的主要分离分析方法;利用手性农药的对映体分数可研究农约在土壤-大气,水体-大气间的迁移过程;一些手性农药在土壤、水体和动物体内中发生的选择性降解与累积与微生物或特异性的酶有直接关系,可利用此性质修复被污染的土壤;归纳了在手性农约污染环境风险研究中应注意的问题;加强手性农约在环境中的选择性降解动力学、对映体转化及毒理学机制研究,并最终深人到代谢机理、蛋白和基因水平上,阐述产生手性对映体选择性的根源将是未来研究的方向.     

涕灭威农药的残留、毒性及其对生态环境的影响

本文描述了涕灭威农药在土壤、水体和生物中的残留、降解和归趋以及对生物的毒性。涕灭威是一种剧毒农药、在环境中虽能很快降解成亚砜,并能进一步降解成毒性更低的化合物,但它仍有可能造成对地下水的污染和对生物与人体的潜在危害。     

两相分配生物反应器治理高浓度有机污染研究进展

高浓度有机污染物难以进行生物降解的主要原因之一是其会对微生物产生较大毒害作用而抑制微生物生长以及降解过程,而两相分配生物反应器(Two-phase partitioning bioreactor,TPPB)可以有效解决污染物毒性的问题,因而在高浓度有机污染治理中具有较大的应用潜力.本文系统介绍了TPPB类型以及各自的工作原理,即TPPB通过非水相的引入可以溶解系统内大部分有机污染物,减少水相中污染物的浓度,降低其对微生物的毒性,并通过微生物的代谢活动实现污染物的降解,随着降解过程的进行污染物在两相间的分配平衡不断被打破,污染物又不断从非水相进入到水相之中,使得微生物的降解过程持续进行.同时分析了反应过程中的各种影响因素,如传质速率、微生物影响等,进而阐述了该技术在水体、土壤、大气污染治理中的应用,最后根据目前的研究进展,对TPPB技术的工程应用前景进行了展望.     

多溴联苯醚微生物降解过程与机理的研究进展

多溴联苯醚(PBDEs)属溴代阻燃剂,曾因其优良的阻燃性能而广泛应用于电子电器、石油化工和建材纺织等工业产品中.然而,随着大量生产和使用,PBDEs已成为大气、水体、土壤和生物体等多环境介质中普遍检出且极具生态风险的有机污染物.因此,开展微生物降解研究对于典型环境中PBDEs污染风险消除和污染修复,具有重要的科学意义.本文从PBDEs环境归趋行为及其暴露风险出发,综述了PBDEs微生物厌氧降解和好氧降解的最新研究动态,比较分析了两种降解过程的降解特性与影响因素,并针对微生物,尤其是好氧微生物降解机理,阐述了bph A或etb A功能基因及其编码酶对PBDEs好氧降解过程的调控作用,同时就PBDEs微生物高效降解菌种选育、降解机理等方面的研究趋势进行了展望.     

微生物砷代谢机制的研究进展（Progress in Study of Mechanisms of Microbial Arsenic Transformation in Environment）

环境砷污染是一个全球性问题.研究砷的生物地球化学循环可以明确环境中砷的来源及其转化特征,为探索砷污染治理的方法提供参考.越来越多的研究表明,自然界中的微生物在砷的迁移转化过程中发挥了重要作用.根据微生物对砷的代谢机制不同将其分为:砷氧化微生物、砷还原微生物和砷甲基化微生物.砷氧化微生物可以将环境中的As(Ⅲ)氧化为毒性较弱并且容易被铁铝矿物吸附固定的As(Ⅴ),因此对降低环境中的砷毒性具有重要作用;微生物对砷的甲基化作用的产物通常为毒性较低的有机砷,因此也被认为是理想的修复环境砷污染的生物手段之一;然而在还原环境中,砷还原微生物却可以将游离态和结合态的As(Ⅴ)还原为毒性更强的As(Ⅲ),从而加重环境中的砷污染状况.由此可见,明确微生物的砷代谢机制及其对砷污染环境中砷迁移转化的影响,是实现生物修复砷污染环境的必要前提.论文总结了近年来国内外微生物砷代谢机制的研究进展,以期为深入研究微生物代谢砷的机理及其在砷污染治理中的应用提供参考.     

氟喹诺酮类抗生素环境行为及其生态毒理研究进展

氟喹诺酮类抗生素(FQs)是治疗人和动物细菌性感染的高效广谱抗菌药,随着氟喹诺酮类抗生素在禽畜养殖业的广泛使用,由此引起的环境污染受到人们的关注。本文综述了氟喹诺酮类抗生素在水体、土壤/沉积物中的污染现状、吸附降解环境行为及其生态毒理研究进展。FQs抗生素的环境行为和风险应从环境多介质层面进行评估,同时应加强对生态毒性机理以及与其他环境污染物的联合毒性效应的研究。     

结合态雌激素的检测方法及污染现状

结合态雌激素是天然雌激素物质的一种重要赋存形态,在环境中可水解为自由态,产生内分泌干扰效应,因此具有潜在的环境风险,并且会影响天然雌激素污染调查和毒性评估的准确性.本文详细探讨了结合态雌激素特定的化学结构对其检测、转化及环境风险等方面的影响,对比分析了目前常用的几类检测方法的优缺点,并初步总结了其在污水处理设施和环境水体中的污染浓度及归趋,以期为我国开展相关研究工作提供参考.     

Occurrence,distribution and dynamics of perchlorate in soil,water, fertilizers,vegetables and fruits and associated human exposure in Chile

Environmental Geochemistry and Health - Perchlorate (ClO4?) has been identified as a persistent environmental contaminant of concern. Perchlorate exposure is a potential health concern...     

Uptake and transformation of perchlorate by vascular plants

Phytoremediation is a promising new method that uses green plants to cleanse soil and water contaminated with organic or inorganic pollutants. In this study, the uptake and transformation of sodium perchlorate (NaClO₄) using four vascular plant species were examined in batch experiments. The species include two trees, cabbage gum (Eucalyptus amplifolia) and eastern cottonwood (Populus deltoides), a herbaceous wetland plant, perennial glasswort (Salicornia virginica), and a herbaceous aquatic plant, waterweed (Elodea canadensis). Perchlorate was depleted from solution in the presence of all but one species (waterweed). Depletion was calculated as a first‐order kinetics reaction with k values in the range of 0–0.013 per day and accumulation of perchlorate was between 3.2 and 3138 mg/kg. Perchlorate and transformation metabolites (chlorate, chlorite, chloride) were observed in all plant tissues (e.g., roots, stems, leaves) analyzed. Results suggest that significant influences on perchlorate uptake include: (1) plant species present, (2) concentration of perchlorate, (3) sand versus hydroponic treatments, (4) the presence or absence of plant nutrients or competing ions, (5) stage of plant maturity.     

Determination of trace perchlorate in water: a simplified method for the identification of potential interferences

Background

Perchlorate contamination of water and food poses potential health risks to humans due to the possible interference of perchlorate with the iodide uptake into the thyroid gland. Perchlorate has been found in food and drinking, surface, or swimming pool waters in many countries, including the United States, Canada, France, Germany, and Switzerland, with ion chromatography (IC) being the preferred analytical method. The standardization of a robust ion chromatographic method is therefore of the high interest for public health and safety. This article summarizes the experiments and results obtained from analyzing untreated samples, considering the sample’s electrical conductance as guidance for direct sample injection as described in EPA 314.0.

Results

The suitability of ion chromatography with suppressed conductivity detection was tested for water samples in order to check the influence of matrix effects on the perchlorate signal of untreated samples. A sample injection volume of 750 μL was applied to the selected 2 mm?IC?column. The IC?determination of perchlorate at low µg/L levels is challenged by the presence of high loads of matrix ions (e.g., chloride, nitrate, carbonate, and sulfate at 100 mg/L and above). Perchlorate recovery is impaired with the increasing matrix ion concentrations, and its chromatographic peak is asymmetric particularly at low perchlorate concentrations. The identification of the individual maximum concentration of interfering anions like chloride, nitrate, and sulfate that influence perchlorate recovery helps to reduce the number of sample preparation steps or an obligatory measurement of the electrical conductivity of the sample. Within the scope of this study, samples containing less than 125 mg/L of either anion did not need sample preparation.

Conclusion

The identification of the maximum concentration of interfering anions like chloride, nitrate, and sulfate influencing perchlorate recovery provides a simplified alternative to the EPA 314.0 method. This approach reduces unnecessary sample preparation steps while allowing a reliable prognosis of possible interferences and maintaining result quality. This study was performed to support the development of a respective international standard, which is being established by the International Organization for Standardization (ISO). The results of the study are also intended to be used as guidance for interested laboratories to optimize the analytical workflow for trace perchlorate determination.

     

支持人居环境健康发展的自然调和理论研究

人类聚居的城市环境和建筑环境，与人类自然气象环境之间持续着动态的自然调和作用，当然调和理论是支持人居环境可持续发展的基础理论之一；文中圈定了自然调和理论研究的框架体系；介绍了面向人居环境的可持续发展所进行的自然调和技术研究进展；剖析了自然调和理论问题研究的科学性。     

水体中金属(氧化物)纳米颗粒的环境行为与污染控制研究进展

金属(氧化物)纳米材料在生产和使用过程中,可以通过各种途径进入到水环境中,对水生生物、生态环境和人体健康产生威胁.理解纳米颗粒在水体中的环境行为,对于评估纳米材料的归趋及其对环境和人体的健康风险至关重要.本文概述了金属(氧化物)纳米颗粒的性质、来源和毒性危害,汇总了表征纳米颗粒浓度、粒径及形貌的分析方法与技术,分析了它们在水环境中的环境行为以及影响其稳定性的主要环境因素,并总结了水体中金属(氧化物)纳米颗粒的去除方法和效果的最新研究进展.随着金属(氧化物)纳米材料的广泛应用,未来有必要加强对自然水体中纳米颗粒环境行为的研究,并系统开展纳米颗粒健康风险评估工作,为预测纳米材料进入水环境后的归趋和风险提供科学依据.     

雪冰中痕量高氯酸盐的在线富集方法

利用一维离子色谱建立了高氯酸盐的在线富集方法,以期为建立定量检测南极雪冰中痕量高氯酸盐的离子色谱-串联质谱法奠定基础.选用高容量、强亲水性的IonPac AS20阴离子交换柱进行分离,以淋洗液自动发生器在线产生的KOH作为淋洗液,等梯度淋洗.考虑到南极雪冰样品量十分有限,选定5 mL为富集体积,对应的富集时间为10 min.高氯酸盐质量浓度在0.5—50μg.L-1范围内,方法具有良好的线性（相关系数为0.9995）,检出限（以S/N=3计）为0.05μg.L-1.将浓度为0.5μg.L-1的标准溶液连续11次富集进样,所得峰面积的相对标准偏差（RSD）为4.7%.以人工配制的仅含有高氯酸盐的溶液实施了加标回收实验,回收率在85%—108%之间.     

Toxic metals status in human blood and breast milk samples in an integrated steel plant environment in Central India

Owing to its unique nutritional and immunological characteristics, human milk is the most important food source for infants. Breast milk can, however, also be a pathway of maternal excretion of toxic elements. Selected toxic elements (As, Pb, Mn,a Hg and Cd) were determined in human breast milk and blood samples obtained from 120 subjects related to an integrated steel plant environment located in central India. Samples of breast milk and blood from subjects living outside the steel plant environment were also analyzed for comparative study. Higher levels of these toxic elements were found in blood samples as compared to breast milk samples. Plant workers showed the higher presence of these metals in their breast milk and blood samples compared to the residents of the area and the subjects living outside the industrial environment, respectively. Mn, Pb and Hg have shown a higher tendency to associate with blood and breast milk than As and Cd. The order of occurrence of these metals in blood and milk samples thus found is Mn > Pb > Hg > As > Cd.     

Understanding and addressing the environmental risk of microplastics

Over the past decades, the plastic production has been dramatically increased. Indeed, a category of small plastic particles mainly with the shapes of fragments, fibers, or spheres, called microplastics (particles smaller than 5 mm) and nanoplastics (particles smaller than 1 μm) have attracted particular attention. Because of its wide distribution in the environment and potential adverse effects to animal and human, microplastic pollution has been reported as a serious environment problem receiving increased attention in recent years. As one of the commonly detected emerging contaminants in the environment, recent evidence indicates that the concentration of microplastics show an increasing trend, for the reason that up to 12.7 million metric tons of plastic litter is released into aquatic environment from land-based sources each year. Furthermore, microplastic exposure levels of model organisms in laboratory studies are usually several orders of magnitude higher than those found in environment, and the microplastics exposure conditions are also different with those observed in the environment. Additionally, the detection of microplastics in feces indicates that they can be excreted out of the bodies of animal and human. Hence, great uncertainties might exist in microplastics exposure and health risk assessment based on current studies, which might be exaggerated. Policies reduce microplastic emission sources and hence minimize their environmental risks are determined. To promote the above policies, we must first overcome the technical obstacles of detecting microplastics in various samples.     

The role of primary and secondary air pollutants in atmospheric pollution: Athens urban area as a case study

The question to what extent primary and secondary air pollutants are relevant to atmospheric pollution and their effects on human health and the quality of the environment can be answered in a straight-forward manner: atmospheric processes, including oxidation procedures, particle formation and equilibria, determine the fate of primary emissions and, in most cases, the secondary products of these processes are the more important ones concerning their effects on human health and the quality of the environment. The formation of secondary products represents the critical property determining the establishment of certain air standards, rather than the actually emitted substance, although there are notable exceptions. In this paper, a review concerning transformation of primary pollutants as studied in the atmosphere of Athens is used to enlighten matters that may need further attention by the responsible authorities and stakeholders for the control and reduction of atmospheric pollution.