Temporal and spatial patterns of micropollutants in urban receiving waters

Based on a monitoring program over the course of a year, we characterize the temporal and spatial distribution of selected micropollutants in an urban watershed within the city of Leipzig, Germany. Micropollutants revealed a ubiquitous presence in untreated and treated wastewater, surface water and groundwater. The loads of 4-nonylphenol in the effluents of the municipal wastewater treatment plant followed a seasonal trend, whereas the loads of all other micropollutants were highly variable and not correlated to seasons. In the surface water, load seasonality of caffeine, galaxolide and tonalide resulted from a rapid removal with increased water temperature. The loads of 4-nonylphenol and of caffeine in the colder months increased when rainfall occurred. In the groundwater, complex spatial and temporal patterns were apparent and were related to varying input, retardation and removal processes. As a consequence, an assessment of micropollutants in urban waters should consider different micropollutants' temporal and spatial variability.     

Hg concentrations and related risk assessment in coral reef crustaceans, molluscs and fish from New Caledonia

There is a dramatic lack of data on Hg levels in marine organisms from tropical areas, and in particular from New Caledonia. For the first time, this study reports the total Hg concentrations in the tissues of several marine taxa from the New Caledonian lagoon. Seafood from both wild and farmed populations was considered. Hg concentrations varied over three orders of magnitudes according to factors including species, age (size/weight), trophic level, lifestyle and geographical origin. Taking into account the edible tissues, estimations of the amount of flesh that should be consumed by a 60-kg person to reach the Hg Provisional Tolerable Weekly Intake (PTWI) reveal acceptable risk for Human health in general. However, a risk was clearly identified in one site of the lagoon (i.e. Grande Rade) where high Hg concentrations were measured. These concentrations were higher than values reported in the current literature.     

膜生物反应器中溶解性微生物产物特性的研究进展

溶解性微生物产物是制约生物处理出水达标和回用的主要污染物,处理工艺和操作条件的不同可能造成其特性差异。阐述了溶解性微生物产物的定义和产生机制,对膜生物反应器中溶解性微生物产物的组成、分子质量分布、亲水／疏水性、螯合性和毒性进行了概述,分析了影响其产生、特性和去除的因素。由于膜的截留作用使溶解性微生物产物在膜生物反应器中积累,容易引起膜污染。可以通过优化操作条件,减少溶解性微生物产物的产生,提高出水水质,有效地抑制膜污染。     

矿业权集聚、经济增长与区域贫困减缓

本文基于泰尔指数法,计算并测度了中国资源富集区的城乡收入差距与行业(矿业)收入差距,然后结合矿业权集聚度的测度结果和中国资源税改革的变动特征,建立面板数据回归模型,考察了2004—2014年中国资源富集区矿业权集聚与经济增长、贫困减缓的长期关系。本文的主要结论是:资源税对矿业权集聚水平和矿业经济增长具有正向刺激作用,但矿业经济增长并不利于地区经济的整体改进,也不利于区域贫困减缓。资源税低水平征收对"资源诅咒"和"区域贫困"具有传导效应,进而对资源富集区的贫困减缓形成阻滞作用。另外,矿业权集聚对地区贫困的影响存在异质性,异质性揭示了区域资源性收益分配存在的差异。短期来看,矿业权集聚使中央企业惠及更多,是引致"富饶中的贫困"怪圈的重要原因;但长期来看,随着矿业权集聚度的提升,地方政府获得的累积性资源性收益不断上升,渐次增强了地方政府通过社会保障支出实施收入调节的能力,总体上有利于区域贫困的减缓。因此,为实现资源富集区的精准扶贫,资源主管部门在制定减贫措施前,应根据不同区域特点区别对待,短期内应着力于调整资源性收益分配机制,赋予地方更多资源性收益,并加大对社会的保障性支出;长期来看,应探索建立合理有效的资源税体制,促进经济增长方式的多样化,并鼓励科技创新,进一步提高社会群体的受教育程度,从根本上改变区域贫困产生的内生性环境和外生性环境。     

农药混配制剂环境风险评估现状与展望

本文综述了欧洲和美国农药混配制剂的环境风险评估方法。详细介绍了欧洲食品安全局(EFSA)评估体系中的2种方法,即,基础的"整体测试法"和近年来提倡的"基于组分的方法"。"基于组分的方法"的特点是以浓度加和模型(CA模型)作为默认假设进行初级评估,以独立作用模型(IA模型)等作为高级评估手段的农药混配制剂环境风险评估方法。此外,本文还介绍了模型偏差率(MDR)、毒性相似度及毒力单元(TU)等概念以及混配制剂风险评估流程。本文的目的旨在为建立我国农药混配制剂的环境风险评估方法体系提供参考。     

Degradation products of profenofos as identified by high-field FTICR mass spectrometry: Isotopic fine structure approach

This study was performed to identify the degradation products of profenofos “a phenyl organothiophosphate insecticide” in raw water (RW) collected from the entry point of Metropolitan Water Works Authority “Bangkaen, Thailand” and ultrapure water (UPW) with and without TiO₂ under simulated sunlight irradiation. Degradation of profenofos was followed with ultrahigh performance liquid chromatography (UHPLC) and follows pseudo first-order kinetic. Accordingly, high-field FTICR mass spectrometry coupled to an electrospray ionization source was used to reveal the degradation routes of profenofos and the isotopic fine structures (IFS) elucidations to approve the chemical structures of its degradation products. More degradation products were detected in UPW as compared to RW. Consequently, two main degradation pathways namely (i) interactive replacements of bromine and hydrogen by hydroxyl functional groups and (ii) rupture of PO, PS, CBr and CCl bonds were observed. None interactive replacement of chlorine by hydroxyl functional group was detected. Accordingly, mechanistical pathways of the main degradation products were established.     

Photodegradation of quinestrol in waters and the transformation products by UV irradiation

Quinestrol is synthetic estrogen used in contraceptive and hormone replacement therapy and occasionally for treating breast cancer and prostate cancer. It can make its way into the environment through sewage discharge and waste disposal produced by human excretions. In this study, the photodegradation kinetics of quinestrol in various conditions was investigated by UV and solar irradiation. The affecting factors were studied including concentration of hydrogen peroxide, different water types, and the initial concentrations of quinestrol. Concurrently, the transformation products and presumed pathways of quinestrol in distilled water by UV irradiation were identified and proposed. The results showed that the degradation of quinestrol in both irradiation conditions followed the pseudo-first-order kinetics. More rapid degradation was observed by UV irradiation (k = 0.018 min⁻¹) than solar irradiation (k = 0.004 h⁻¹), and the photodegradation rate of quinestrol depended on the concentration of hydrogen peroxide, the initial concentration of quinestrol and water types. The transformation products of quinestrol in distilled water were identified by gas chromatography/mass spectrometry. When exposed to UV irradiation, quinestrol in aqueous solution was rapidly degraded, giving at least ten photodegradation products. The chemical structures of ten degradation products were identified on the basis of mass spectrum interpretation and literature data.     

Fenton 法降解抗生素磺胺间甲氧嘧啶钠

应用Fenton高级氧化技术降解水溶液中抗生素磺胺间甲氧嘧啶钠(SMMS),系统探讨了起始pH、CSMMS、CFe2+、CH2O2和温度等因素对SMMS降解效果的影响。结果表明:CSMMS=4.53 mg/L,pH=4.0,CH2O2=0.49 mmol/L,CFe2+=19.51μmol/L,T=25℃为最佳反应条件。在最佳条件下,87.4%的SMMS可以在120 min内降解。反应动力学研究表明Fenton氧化降解SMMS分为两个阶段,快速反应阶段和慢速反应阶段,并建立了两阶段动力学模型,模型拟合结果较好。研究结果为含有SMMS的污废水处理提供了基础数据和科学参考。     

改性矿物吸附剂抗菌作用

通过对蒙脱石、沸石和蛭石进行改性处理,研究了三者对大肠杆菌（E．coB）和猪链球菌（S．suis）的抗菌作用。结果发现,经过改性处理后三者对细菌的抗菌能力上升,其中以双十八烷基二甲基溴化铵改性蒙脱石（DODMAB．MMT）的抗菌效果最好,对E．coli和S．suis的抗菌率达到95％以上。研究了DODMAB—MMT在体外对E．coli和S．suis的抗菌规律,以及对土壤中微生物的影响。结果表明,同等菌液浓度条件下,DODMAB—MMT对S．suis的抗菌效果好于E．coli。介质温度、pH值和有机物浓度都会对DODMAB—MMT的抗菌效果产生影响,在一定范围内,介质温度越高、pH值偏离中性、有机物含量越低时,抗菌效果越好。低浓度DODMAB—MMT（〈25rtlg／g土壤）对土壤中E．coli和S．suis基本无抗菌作用,高浓度DODMAB—MMT对土壤中的E．coli和S．suis具有抗菌作用。     

Changes in TcpA gene frequency explain 2,4,6-trichlorophenol degradation in mesocosms

Soils are often polluted by chlorophenols in timber production areas in the northern hemisphere. The tcpA gene encodes the first step of 2,4,6-trichlorophenol (246-TCP) degradation. We tested tcpA gene frequency in three natural pristine soils with different 246-TCP degradation capacity. Gene tcpA frequency increased more in spiked than non-spiked 10-L pails containing coniferous humus soil with high degradation capacity, in contrast to soils where degradation was slower. As the soil in each mesocosm originated from a spatially separate field plot, changes in tcpA gene frequency affected 246-TCP degradation over a range of soil origins. This indicates that the abundance of and changes in tcpA gene frequency could be utilized in estimating the efficacy of natural attenuation and biostimulation treatments in controlled conditions.