Polycyclic aromatic hydrocarbon and n-alkane pollution characteristics and structural and functional perturbations to the microbial community: a case-study of historically petroleum-contaminated soil

Characterization of the typical petroleum pollutants, polycyclic aromatic hydrocarbons (PAHs) and n-alkanes, and indigenous microbial community structure and function in historically contaminated soil at petrol stations is critical. Five soil samples were collected from a petrol station in Beijing, China. The concentrations of 16 PAHs and 31 n-alkanes were measured by gas chromatography-mass spectrometry. The total concentrations of PAHs and n-alkanes ranged from 973 ± 55 to 2667 ± 183 μg/kg and 6.40 ± 0.38 to 8.65 ± 0.59 mg/kg (dry weight), respectively, which increased with depth. According to the observed molecular indices, PAHs and n-alkanes originated mostly from petroleum-related sources. The levels of ΣPAHs and the total toxic benzo[a]pyrene equivalent (ranging from 6.41 to 72.54 μg/kg) might exert adverse biological effects. Shotgun metagenomic sequencing was employed to investigate the indigenous microbial community structure and function. The results revealed that Proteobacteria and Actinobacteria were the most abundant phyla, and Nocardioides and Microbacterium were the important genera. Based on COG and KEGG annotations, the highly abundant functional classes were identified, and these functions were involved in allowing microorganisms to adapt to the pressure from contaminants. Five petroleum hydrocarbon degradation-related genes were annotated, revealing the distribution of degrading microorganisms. This work facilitates the understanding of the composition, source, and potential ecological impacts of residual PAHs and n-alkanes in historically contaminated soil.

     

Removal of SO2 from smelting flue gas by using copper tailings with MnSO4: factors optimization by response surface methodology

Environmental Science and Pollution Research - The abatement of SO2 and the utilization of copper tailings are identified as two attention-attracting environmental issues in the copper smelter. In...     

The permeability of dredged material-bentonite backfills

Environmental Science and Pollution Research - Extensive attention has been paid to the treatment and disposal of dredged material, and there is a need to clarify the feasibility of recycling...     

SBR加载不同粒径磁性活性炭对其污泥颗粒化进程的影响机制

在相同序批式活性污泥反应器(SBR)中分别加载1.5 g·L~(-1)的80、140、200、和300目不同粒径的磁性活性炭(反应器编号依次为2、3、4、5号),同时以不投加磁性活性炭的SBR反应器(1号)作为对照组,研究各反应器污泥体积指数(SVI)、粒径分布特征、胞外聚合物(EPS)中胞外蛋白(PN)、胞外多糖(PS)的含量变化规律以及除污性能.结果表明,不同粒径磁性活性炭对污泥颗粒化进程有一定的影响,粒径过大、过小对促进污泥颗粒化进程的强化作用不明显,当磁性活性炭的粒径为140目和200目时,活性污泥很容易以其作为"成核"载体快速形成好氧颗粒污泥,并且形成的颗粒污泥结构紧密,沉降速率快.采用高斯函数分析污泥粒径分布和标准偏差发现,反应器运行的第50 d,3号和4号反应器内污泥平均粒径均达到了780μm以上,明显高于其他反应器,标准偏差分别为318.9μm和362.3μm,两反应器内形成的颗粒污泥粒径较均匀,处理系统较稳定.与此同时,投加不同粒径的磁性活性炭均有利于促进污泥胞外蛋白质PN含量的增加,对胞外多糖PS的含量影响不大;但合适的磁性活性炭粒径(140目和200目)越有利于污泥PN的分泌,颗粒化程度明显的3号和4号反应器的PN/PS比值均高于其他3个反应器.磁性炭基好氧颗粒污泥的形成符合"惰性内核模型".此外,3号、4号反应器对废水TN和TP的去除率分别达到50%和60%以上,均高于其他反应器.     

不同运行模式下改良型CAST工艺处理生活污水的除磷性能

实验采用改良型CAST工艺,以生活污水为研究对象,考察了C/P、回流比及温度等不同运行模式对系统除磷性能的影响.结果表明,常温条件下进水C/P由50升至100,系统除磷率均值从15%迅速升至95.6%,除磷性能显著提高;继而降低C/P至75,除磷性能因进水碳源不足再度下降,除磷率均值为51.4%,且长期投加易降解碳源引发系统污泥膨胀并导致污泥大量流失.C/P较低情况下,回流比由25%降低至12.5%,除磷性能提高2.3倍,继续降低回流比至0,除磷性能反而下降;温度实验研究则表明,低温系统(14℃±1℃),除磷率稳定维持在90%以上,而高温短程硝化系统(27℃±1℃)除磷率仅为14.1%,可见低温更有利于系统磷的去除.吸磷小试发现,常温系统污泥以O_2、NO_3~-和NO_2~-为电子受体均能进行吸磷,而低温系统污泥能以O_2、NO_3~-为电子受体进行吸磷,高温系统污泥则仅能以O_2为电子受体进行少量吸磷.此外,实验还发现,系统短期闲置导致的污泥"饥饿"有利于系统除磷率的提高.     

应用相平衡分配法建立湘江衡阳段沉积物重金属质量基准

采集湘江衡阳段29个站点的表层沉积物样品,测定沉积物中4种重金属(Cu、Pb、Zn和Cd)含量及赋存形态、以及孔隙水中重金属含量,根据相平衡分配法的基本理论,考虑参与沉积物-水相平衡分配的重金属组成,实测法计算重金属的沉积物-水相平衡分配系数(Kp),分别引用美国EPA制定保护水生生物不受重金属慢性毒性影响的基本连续浓度(CCC)和我国地表水环境质量标准(GB 3838-2002)Ⅰ类水质标准,建立两种湘江衡阳段沉积物重金属质量基准(SQC)进行对比分析,其中基于美国CCC建立的湘江衡阳段沉积物重金属质量基准与国内外研究成果相比可比性较好,4种重金属(Cu、Pb、Zn和Cd)的SQC值分别为64.62、55.57、1 360.40和2.34μg.g-1,此SQC具有保护长期生活于沉积物中的底栖生物不受重金属慢性毒性影响的意义.通过单因子评价法将湘江衡阳段沉积物中重金属总量与沉积物质量基准值(SQC)进行比较,结果表明,湘江衡阳段沉积物中Cd和Pb含量水平对底栖生物具有较大的慢性毒性影响,Cd污染不容忽视.     

西大海湖沉积物营养盐垂直分布特征变化分析

通过对西大海湖心柱状沉积岩芯有机质(OM)、总氮(TN)、总磷(TP)、磷形态和粒度指标的测试和分析,探讨其垂向分布特征及影响因素.结果表明,营养盐中OM、TN和TP的含量分别为0.633%~2.756%、0.150%~0.429%和648.00~1 480.67 mg·kg-1.Ca-P是TP的主要部分,占TP含量66.04%.1843~1970年间,Ca-P、IP、OM含量变化较小,Fe/Al-P、OP、TP、TN含量波动较大;1970~1996年间,Ca-P、IP、TP含量变化均呈减小趋势,Fe/Al-P、OP、OM含量不同程度上先减少后增加,TN波动较大;1996~2009年营养元素含量相对波动较大,Fe/Al-P、OP和OM的平均含量是3个阶段中最高的.西大海湖沉积岩芯营养元素污染来源以工业废水、生活污水和化肥农药的流失为主.沉积物中C/N比值显示有机质主要来源于水生生物.沉积物粒度组成以黏土和细粉砂为主.相关性研究表明,Ca-P、IP与TP均呈显著的正相关关系,表明Ca-P对IP、TP的增长贡献大.     

微气泡臭氧催化氧化-生化耦合工艺深度处理煤化工废水

采用微气泡臭氧催化氧化-生化耦合工艺对煤化工废水生化出水进行深度处理,考察耦合系统处理性能及不同臭氧投加量和进水COD量比值的影响.结果表明,微气泡臭氧催化氧化处理能够有效降解废水中难降解含氮芳香族污染物,去除部分COD并释放氨氮,显著提高废水可生化性,臭氧利用率接近100%,无需进行臭氧尾气处理;同时为生化处理提供充足溶解氧(DO),实现生化处理对COD和氨氮的进一步有效去除,生化处理无需曝气.在系统出水回流比为30%、臭氧投加量和进水COD量之比为0.44 mg·mg~(-1)的运行条件下,耦合系统处理性能较好.微气泡臭氧催化氧化处理对COD去除率为42.5%,臭氧消耗量与COD去除量比值为1.38 mg·mg~(-1),臭氧利用率为98.0%;生化处理对COD去除率为42.3%;耦合系统整体COD去除率为66.7%,最终平均出水COD浓度为91.5 mg·L~(-1),估算整体臭氧消耗量与COD去除量比值为0.68 mg·mg~(-1),具有较优的技术经济性能.     

Effect of oxide nanoparticles on the morphology and fluidity of phospholipid membranes and the role of hydrogen bonds

Engineered oxide nanoparticles (NPs) are widely applied in insulators, catalyzers, paints, cosmetic products, textiles and semiconductors. Their attachment on cell membrane may lead to cytotoxicity. The effects of Al₂O₃, Fe₂O₃, SiO₂, TiO₂ and ZnO NPs on membrane integrity and fluidity were studied using giant or small unilamellar vesicles in this study. Al₂O₃ and SiO₂ NPs disrupted the oppositely charged membrane, indicating the important role of electrostatic attraction. However, Fe₂O₃, TiO₂ and ZnO NPs did not cause serious membrane disruption as Al₂O₃ and SiO₂ NPs. Membrane fluidity was evaluated by the generalized polarity (GP) values of Laurdan fluorescent emission. SiO₂ NPs induce the membrane gelation of both positively and negatively charged membrane. Al₂O₃ and ZnO NPs induced the gelation of the oppositely charged membrane, but did not cause obvious membrane gelation to the like charged membrane. The phospholipid molecular structural changes after NP exposure were analyzed by Fourier transform infrared (FT-IR) spectroscopy. FT-IR spectra revealed the hydrogen bond formation between NPs and the carbonyl/phosphate groups of phospholipids. Al₂O₃ and SiO₂ NPs showed strongest evidence of hydrogen bonding on their FT-IR spectra. It was consistent with the microscopic observation and fluorescent data that Al₂O₃ and SiO₂ NPs caused more serious membrane disruption and gelation. This study on membrane damage provides further knowledge on the cytotoxicity of nanomaterials and the safety of NP application.     

基于环境因子和邻近信息的土壤属性空间分布预测

为探索乡镇尺度上土壤属性空间分布预测的最佳方法,以江西省万年县齐埠镇为例,借助四方位搜索法、地统计学和遥感影像分析技术提取环境因子（地形因子和植被覆盖指数）和邻近信息[w（有机质）与w（速效钾）],构建OK法（普通克里金法）、RK1法（仅基于环境因子的回归克里金法）以及RK2法（基于环境因子和邻近信息的回归克里金法）对齐埠镇耕地表层（0~20 cm）土壤w（有机质）、w（速效钾）空间分布进行预测.结果表明:齐埠镇土壤w（有机质）平均值为35.03 g/kg,w（速效钾）平均值为96.73 mg/kg,均为中等空间变异性.对62个样点进行建模,16个测试样点进行独立验证的误差分析表明,RK2法对土壤w（有机质）、w（速效钾）预测结果的均方根误差、平均绝对误差和平均相对误差较OK法分别降低了18.05%、18.01%、21.77%和7.25%、9.49%、9.84%;较RK1法分别降低了22.48%、20.91%、22.02%和9.27%、12.61%、13.52%.研究显示,RK2法明显提高了土壤w（有机质）、w（速效钾）空间分布模拟精度,并且存在改进和提高的空间.