Environmental decentralization,environmental public service,and public health: evidence from 289 cities in China

Environmental Geochemistry and Health - Effective supply of environmental public services (EPS) is important to guarantee the mitigation of residential pollution exposure risk. This study analyzes...     

液液萃取-气相色谱法测定水质可萃取性石油烃C10~C40

建立了以环己烷为萃取剂、气相色谱法(氢火焰离子化检测器,FID)测定水质样品中可萃取性石油烃(C_(10)～C_(40))的分析方法。以正构烷烃混合标准溶液为定性和定量校准标准,以色谱峰面积总和与混合标准溶液总浓度建立校准曲线进行外标法定量。方法检出限为0.01 mg/L,经验证方法精密度和准确度良好。同时,分别以气相色谱法和红外光度法测定了地表水、污水处理厂出水、海水和化工废水等实际样品,对比实验结果表明,在可萃取性石油烃C_(10)～C_(40)的碳数范围内,气相色谱法的测试结果与红外光度法无明显差异,有较好的可比性。     

智能手机应用程序使用与操作的驾驶分心风险影响研究*

为研究智能手机应用程序操作方式与使用行为对驾驶分心影响的问题,探讨智能手机程序操作方式对驾驶分心影响的优劣关系,基于结构方程模型提出4个因果关系假设,构建涵盖程序使用、驾驶分心、驾驶绩效等潜变量的智能手机使用行为影响的结构方程模型。通过收集线下问卷的方式进行调查,搭建模拟场景,设计6项实验方案,通过驾驶模拟实验方式收集相关数据,建立相对偏差矩阵。研究结果表明:手机通话功能的使用（路径系数0.472）对驾驶分心影响显著,手机导航功能使用（路径系数0.256）、手机音乐功能使用（路径系数0.249）对驾驶分心影响不显著。语音交互方式均优于手动操作方式,其中语音交互启动导航方式（F3=0.019）的影响最小。研究结果可对道路驾驶情况下智能手机应用使用与操作方式的研究起推动作用。     

Formation pathways of brominated products from benzophenone-4 chlorination in the presence of bromide ions

The brominated products, formed in chlorination treatment of benzophenone-4 in the presence of bromide ions, were identified, and the formation pathways were proposed.Under disinfection conditions, benzophenone-4 would undertake electrophilic substitution generating mono- or di-halogenated products, which would be oxidized to esters and further hydrolyzed to phenol derivatives. The generated catechol intermediate would be transformed into furan-like heterocyclic product. The product species were p H-dependent,while benzophenone-4 elimination was chlorine dose-dependent. When the chlorination treatment was performed on ambient water spiked with benzophenone-4 and bromide ions, most of brominated byproducts could be detected, and the acute toxicity significantly increased as well.     

Expression of sulfur uptake assimilation-related genes in response to cadmium, bensulfuron-methyl and their co-contamination in rice roots

The responses of sulfur （S） uptake assimilation-related genes＇ expression in roots of two rice cultivars to cadmium （Cd）, bensulfuron-methyl （BSM） and their co-contamination （Cd＋BSM） were investigated by gene-chip microarray analysis and quantitative real-time PCR （QRT-PCR） technology. Treatments of Cd and Cd＋BSM induced expression of sulfate transporter and permease genes, and promoted sulfate uptake in rice roots. Cd＋BSM could alleviate Cd toxicity to cv. Fengmeizhan seedlings, probably due to Cd＋BSM promoting greater S absorption by seedlings. Cd and Cd＋BSM induced expression of sulfate assimilation-related genes, and thus activated the sulfur assimilation pathway. Cd and Cd＋BSM induced expression of phytochelatin synthase and metallothionein genes, and induced expression of glutathione S-transferases （GSTs）, glutathione synthase （GS） and S- containing antioxidation enzyme genes, which detoxified Cd2＋. It is suggested that （to cope with the toxicity of Cd, BSM and their co-contamination） the S uptake and assimilation pathway was activated in rice roots by increased expression of related genes, thus enhancing the supply of organic S for synthesis of Cd or BSM resistance-related substances.     

填埋场中铁的生物化学循环对反硝化的影响

在模拟填埋体系中,以填埋场稳定的垃圾为接种物,通过控制有机物和硝氮负荷,研究了铁的生物化学循环对反硝化的影响.结果表明,垃圾填埋场内蕴藏着能实现铁的厌氧氧化还原并同步还原硝氮的复合功能菌群.通过改变有机物和硝氮的负荷,可使得填埋场内持续进行着铁的氧化还原循环和同步氮素转化.从氮素转化产物来看,铁的循环体系中氨氮浓度比传统的反硝化体系低4 mmol·L-1.填埋场内铁的生物化学循环过程对于原位脱氮具有极大贡献.     

东江源头区典型村庄厨余废水水质分析

在东江源头区选取了3个典型村庄,对其厨余废水的水质进行调查分析。结果表明:东江源头区沿江村庄农户家庭厨余废水中TP、NH 3-N和COD浓度远远超过《城镇污水处理厂污染物排放标准》中一级A标准限值,需经进一步处理后排放;夏秋季节,厨余废水中TP、NH 3-N、COD浓度高于春季;村庄的经济发展水平对厨余废水水质有一定影响,经济发展水平高的村庄排放的厨余废水中污染物的浓度较经济水平较低的村庄厨余废水中污染物的浓度低。     

基于地理加权回归模型评估土地利用对地表水质的影响

针对传统线性回归模型大多忽视空间数据局部变化特征这一缺陷,引入地理加权回归模型(GWR)用于评估土地利用对地表水质的影响,分析了不同子流域内两者关系出现空间变化的规律并阐释了原因.同时,对比了GWR模型与普通最小二乘模型(OLS)的校正R2、Akaike信息准则(AICc)及残差的空间自相关指数(Moran's I),验证了GWR模型在预测精度和处理空间自相关过程中是否优于OLS模型.结果表明,同一土地利用类型对水质的影响随空间位置的改变而发生方向或大小的变化.以温瑞塘河流域总氮(TN)与农用地的关系为例,从GWR模型局部回归系数的方向分析,两者关系表现为农村正、城区负的现象,从大小分析,旧城区TN与农用地回归系数的绝对值高于其它区域;在溶解氧(DO)与人口密度所构建的GWR模型中,两者关系在整个研究区域内均表现为负值,与OLS结果吻合,从回归系数的大小分析,人口密度对DO的作用在郊区及农村更为显著.针对此类关系出现空间变化的原因分析表明,相邻子流域土地利用百分比的改变及水体主要污染源的不同,是导致土地利用对水质作用发生变化的根本因素.最后,对比所构建的80个GWR与OLS模型校正R2、AICc指标,验证了GWR作为一种局部统计模型,其预测精度优于OLS等传统全局模型且更能反映实际空间特征.     

Impact of dissolved organic matter on the photolysis of the ionizable antibiotic norfloxacin

Norfloxacin (NOR), an ionizable antibiotic frequently used in the aquaculture industry, has aroused public concern due to its persistence, bacterial resistance, and environmental ubiquity. Therefore, we investigated the photolysis of different species of NOR and the impact of a ubiquitous component of natural water — dissolved organic matter (DOM), which has a special photochemical activity and normally acts as a sensitizer or inhibiter in the photolysis of diverse organics; furthermore, scavenging experiments combined with electron paramagnetic resonance (EPR) were performed to evaluate the transformation of NOR in water. The results demonstated that NOR underwent direct photolysis and self-sensitized photolysis via hydroxyl radical (·OH) and singlet oxygen (¹O₂) based on the scavenging experiments. In addition, DOM was found to influence the photolysis of different NOR species, and its impact was related to the concentration of DOM and type of NOR species. Photolysis of cationic NOR was photosensitized by DOM at low concentration, while zwitterionic and anionic NOR were photoinhibited by DOM, where quenching of UOH predominated according to EPR experiments, accompanied by possible participation of excited triplet-state NOR and ¹O₂. Photo-intermediate identification of different NOR species in solutions with/without DOM indicated that NOR underwent different photodegradation pathways including dechlorination, cleavage of the piperazine side chain and photooxidation, and DOM had little impact on the distribution but influenced the concentration evolution of photolysis intermediates. The results implied that for accurate ecological risk assessment of emerging ionizable pollutants, the impact of DOM on the environmental photochemical behavior of all dissociated species should not be ignored.     

MFC强化同步短程硝化反硝化工艺的启动

微生物燃料电池(MFC)可在阴极实现反硝化、短程反硝化和同步硝化反硝化并产生电能,但在MFC阴极实现同步短程硝化反硝化的研究尚未见到报道。为了探讨MFC阴极同步短程硝化反硝化工艺的性能,将双室曝气阴极MFC与A/O脱氮工艺结合处理人工模拟低碳氮比废水。通过静置运行15 d使得MFC阴极室亚硝态氮得以积累,氨氧化菌得以富集。随即改为连续运行后第21天成功启动同步短程硝化反硝化MFC;阴极出水氨氮浓度为0.3 mg/L,亚硝态氮浓度为15.9 mg/L,硝态氮浓度为0.6 mg/L,亚硝化率达到95%以上,阴极电极自养反硝化去除率达到50%以上,COD去除率达到85%以上。结果表明,将MFC与同步短程硝化反硝化工艺结合,通过阴极室中氧气得电子获得高p H,可以强化同步短程硝化反硝化工艺,完成生物脱氮的同时回收电能,并具有减少外加碱度的优势。