黄河流域水污染风险分区

黄河流域生态环境保护和高质量发展已上升为国家战略,对黄河流域开展水污染风险分区评估具有重要的理论和现实意义.现有研究多集中于突发性水污染风险分区,累积性水污染风险分区鲜有案例.本研究以2019年为基准年,基于环境统计数据、 DEM数据、水质监测断面数据和基础地理数据,以1 km×1 km网格为基本单元,采用环境风险场评估法对黄河流域开展突发性和累积性水污染风险分区评估.结果表明：（1）黄河流域突发性高风险区面积为1 349 km²,占比0.2%,突发性较高风险区面积为3 864 km²,占比0.5%;累积性高风险区面积为5 834 km²,占比0.7%;累积性较高风险区面积为25 382 km²,占比3.1%;（2）兰州市、乌海市、巴彦淖尔市、包头市、宝鸡市、济南市和东营市等部分地区突发性、累积性环境风险均较高;（3）从黄河干流两岸分布来看,黄河干流兰州段、白银段、中卫段、乌海段、巴彦淖尔段、郑州段、德州段和东营段等突发性、累积性环境风险均较高.     

基于网格化的区域突发环境事件风险分区研究

为开展区域环境风险分区研究,文章基于环境统计和基础地理数据,引入地理空间分析法和人口空间离散化方法,充分考虑水系级别及水质的影响,以1 km×1 km网格为基础单元,对石化产业密集型区域的环境风险进行评估。结果表明:(1)研究区环境风险场呈现以石化区为高值中心,向外辐射递减态势,环境风险受体敏感区与环境风险受体分布保持一致。(2)研究区以低风险区为主,其次为中风险区和较高风险区,其中较高风险区面积为4.87 km2,占研究区总面积的1.7%;中风险区面积为42.64 km~2,占研究区总面积的14.6%;低风险区面积为244.52 km~2,占研究区总面积的83.7%,不同等级环境风险呈现以风险源和受体集中区为中心,向周围辐射递减趋势,且在下级行政单元的分布存在差异。(3)研究区环境风险管控的优先次序为Sr24(石化区)、Sr19、Sr20、Sr16、Sr17和Sr10,其中,Sr24和Sr19为较高风险区,属重点优先管控区域。文章旨在优化网格化环境风险分析法,为区域环境风险评估的宏观决策和环境风险分区分级管理提供科学依据。     

关于在长江经济带布局以水质改善为目标的流域生态缓冲体系的思考

生态缓冲带能够有效减缓流域内的人类活动或自然过程对水环境和水生态系统的影响.在长江经济带构建流域生态缓冲体系,对长江生态保护修复具有十分重要的意义.讨论了构建流域生态缓冲体系涉及的生态缓冲带位置选择、缓冲体系所占最低面积比率、宽度划定等一些基本的原则要求;利用卫星遥感影像数据,提取各汇水单元的地形特征、土地利用类型特征、土壤类型、土壤侵蚀强度、水文水系等数据,对长江经济带流域生态缓冲体系进行布局.结果表明:①长江经济带内林草地是主要土地利用类型,占区域总面积的62.46%,但是分布很不均匀,主要集中在西部高地和中下游的丘陵地带,在人口密集、农田密集的区域分布偏少;城镇用地主要集中在长江中下游地区.②土壤类型空间差异显著,浙江省、江苏省、湖南省、江西省及安徽省大部分区域的土壤多是黏性比较大,污染物迁移能力较低;而污染物迁移能力较强的砂质土或者土层较薄的山地草甸土主要分布在四川省北部、西北部.水力侵蚀、风力侵蚀和冻融侵蚀均有分布,且以水力侵蚀为主,建议在中度及以上侵蚀强度区域尽量减少污染源,重点布置缓冲带,增加该区域的缓冲力度.③长江经济带范围内可以利用的中小型湿地、小型河流支浜的面积至少有1.4×104 km2,再结合林草缓冲带,就可以形成一个生态缓冲体系.④在土地利用类型分布结果基础上,叠加土壤侵蚀强度和水系分布,将污染源区、中度及以上侵蚀强度区、水体区作为缓冲对象,建立缓冲体系的重点区域,总面积约14.26×104 km2,占长江经济带总面积的6.95%.对照欧美地区的研究,6.95%的缓冲体系面积占比是偏低的,需要在长江经济带开展深入研究来确定适宜的缓冲体系面积比,推进长江经济带流域生态缓冲体系的构建.      

北运河上游非点源污染风险空间分布特征研究

非点源污染是流域水环境污染的重要原因之一,非点源污染风险分区是有效治理水污染的重要前提.本文采用指数函数法改进潜在非点源污染指数（Potential Non-Point Pollution Index,PNPI）模型基于专家评价法主观赋权的不足,并采用改进后的PNPI模型解析北运河上游流域非点源污染风险空间分布特征.结果表明：①指数函数法通过构建土地利用指标、径流指标和距离指标的指数函数描述污染源因子与运输因子之间的关系,能够直观反映研究区内非点源污染风险的空间分布特征;②研究区2017年非点源污染风险呈现出东南高西北低的空间分布特征,极低、低、中等、高和极高风险区面积占比分别为52.4%、0.5%、12.4%、25.1%和9.6%;③研究区非点源污染极高风险区主要集中在人口密集的东南平原区河道两侧,主要土地利用方式为城镇用地;极低风险区则主要分布在人口稀疏且距离河道较远的西北山区,主要土地利用方式为有林地.PNPI模型模拟结果可为北运河上游流域非点源污染防治和生态清洁小流域分区治理提供科学参考.     

基于GIS和LUR模型的西安市PM2.5浓度空间分布模拟研究

基于地理信息系统GIS和土地利用回归LUR模型,模拟西安市PM2.5浓度空间动态分布,结果表明:与PM2.5浓度相关性最高的分别为缓冲区为2 km的水域面积、人口密度和距离水域距离,R 2分别为0.501,0.393和0.280;与PM2.5浓度相关性最低的分别为缓冲区为4 km的水域面积、未利用地面积和耕地面积,R 2分别为0.039、0.021和0.017.未考虑风速建立的LUR模型多元回归的相关系数为0.856,R 2为0.733,考虑风速的相关系数为0.892,R 2为0.796,表明风速对于污染物的分布影响较大,LUR模型模拟效果较好.模拟的PM2.5年均浓度高风险区分布于中部,中风险区分布于中西部,低风险区分布于东南部和西部.     

博斯腾湖流域景观生态风险评价与时空变化

以博斯腾湖流域为研究区,利用eCognition软件对博斯腾湖流域1990年、2000年、2010年和2015年4期Landsat遥感影像分类。基于土地利用类型的生态脆弱度和景观干扰度指数构建景观生态风险评价模型,并利用空间自相关分析方法,开展博斯腾湖流域景观生态风险评价的时空变化研究。结果表明:(1)1990-2015年,博斯腾湖流域景观格局变化明显,主要特征为水域景观面积减少了64.33%,景观优势度降低;林地、耕地和城镇用地增幅显著,三者分别增加了47.96%、44.77%和85.15%;草地仍是流域主导景观类型。流域整体斑块数量减少,景观破碎化程度减弱。(2)低风险区和较低风险区主要分布在流域北部,土地利用以草地为主;高风险区主要分布在流域东南部,土地利用以未利用地为主;较高风险区主要围绕高风险区分布;中等风险区分布比较零散。(3)1990-2015年间,高风险区面积增加了386 263 hm2,低风险区面积减少了217 216 hm2,研究区总体生态风险等级增加,博斯腾湖流域生态质量存在进一步退化的趋势。     

三峡库区突发性水环境风险分区应用研究

流域水环境风险分区是区域风险管理的重要技术支撑,从突发性水环境风险作用及响应控制角度出发,提出了风险分区指标体系和量化分级方法,涵盖风险源危险性、受体敏感性及应急能力等3类要素10项指标;以三峡库区重庆辖区为研究对象,完成了区县级行政单元的突发性水环境风险分区。研究结果表明,三峡库区重庆辖区突发性水环境风险的高风险区主要分布在长寿等8个区县,区域以高风险企业、敏感目标均密集为主要特点;中风险区主要分布在璧山等10个区县,大部分属都市功能拓展区;低风险区主要分布在城口等20个区县,集中在渝东南、渝东北区域。结合分区分级结果,提出了相应的突发性水环境风险管理对策。     

基于城市规划的开封市地质环境风险评价

随着城市化进程的加快,城市地质环境风险评价作为缓解日益严峻的人地矛盾,科学合理地利用地质环境的有效措施,对城市的规划和可持续发展有着十分重要的指导意义。针对开封市的城市规划,将不同类型功能区作为评价对象,建立了地质环境危险性和社会经济易损性评价指标体系,并采用通用的风险评价模型对开封市地质环境风险进行了评价。评价结果显示:开封市高风险区面积占1.21%;次高风险区面积占11.89%;次低、低风险区面积占86.9%。根据评价分区结果,提出了功能优化和风险防控建议。     

查干湖汇水区面源污染风险识别及管控

面源污染是我国流域面临的主要水环境问题,为了识别面源污染高风险区和潜在风险路径,实现流域水环境保护,以查干湖水质目标为约束条件,构建4类关键“源”景观.选取高程、坡度、土地利用类型、污染强度、距居民点距离、距公路距离、距铁路距离、距水体距离等8个评价因子构建阻力面,对查干湖汇水区面源污染风险区和风险路径进行识别,提出管控分区和治理措施.结果表明:①查干湖汇水区关键“源”景观有4类,分别为面源污染单位面积高负荷区、坡度>3°区域、污染传输通道和临湖区域,面积共126.33 km2.②查干湖汇水区面源污染高风险区即面源污染重点管控区,占汇水区总面积的27.10%,主要位于乾安灌区有字泡区域、查干湖及周边泡沼沿岸.区内现有耕地不再增加,同时对坡度较大的区域退耕还湿、退耕还草,并设置污染降解设施.③查干湖汇水区面源污染较高风险区即面源污染一般管控区,占汇水区总面积的20.23%.该区鼓励开展有机农业,发展生态旅游.④查干湖北岸和东南岸、库里泡周边设置一定宽度的植被缓冲带,汇水区设置生态降解渠道333.41 km,生态湿地节点9个.研究显示,污染排放强度是查干湖汇水区面源污染风险的主要威胁因素,需要重点加强查干湖汇水区乾安灌区有字泡、湖区北岸及东南岸的面源污染管控.      

长江经济带水质目标管理平台总体设计

为强化长江经济带资源整合与共享,集成统一规范的大数据平台,基于“十一五”“十二五”国家水体污染控制与治理科技重大专项数据和模型库资源,以面向服务的架构(SOA)和模块化设计为支撑,遵循“五横两纵四统一”的平台架构设计思路,应用大数据挖掘、云计算等现代信息技术,构建长江经济带水质目标管理平台.平台基于长江经济带水生态环境功能分区,兼顾不同类别水质目标管理技术的协调性、衔接性和适应性,对水质目标管理相关信息进行跟踪、模拟、分析和三维可视化表达,在水生态环境功能分区管理、数据汇交与信息共享、容量总量管理、风险评估与预警等方面实现业务化运行,实现全景式水质达标形势研判、一体化风险联防联控.平台已在国家长江生态环境保护修复联合研究中心进行业务化运行,将有效提升长江经济带水环境综合管理能力,同时可为其他重要流域水质目标管理提供信息化工作参考.      

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Effects of chitosan on growth of an aquatic plant (Hydrilla verticillata) in polluted waters with different chemical oxygen demands

Effects of chitosan on a submersed plant, Hydrilla verticillata, were investigated. Results indicated that H. venicillata could prevent ultrastructure phytotoxicities and oxidativereaction from polluted water with high chemical oxygen demand (COD). Superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in H. verticillata treated with 0.1% chitosan in wastewater increased with high COD (980 mg/L) and decreased with low COD (63 mg/L), respectively. Ultrastructural analysis showed that the stroma and grana of chloroplast basically remained normal. However, plant cells from the control experiment (untreated with chitosan) were vacuolated and the cell interval increased. The relict of protoplast moved to the center, with cells tending to disjoint. Our findings indicate that wastewater with high COD concentration can cause a substantial damage to submersed plant, nevertheless, chitosan probably could alleviate the membrane lipid peroxidization and ultrastructure phytotoxicities, and protect plant cells from stress of high COD concentration polluted water.     

Removal of cadmium using MnO2 loaded D301 resin

MnO2 loaded weak basic anion exchange resin D301 （Anion exchange resin, macroreticular weak basic styrene） as adsorbent has been prepared and applied to the removal of cadmium. The adsorption characteristics have been investigated with respect to effect of pH, equilibrium isotherms, removal kinetic data, and interference of the coexisting ions. The results indicated that the Cd^2＋ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions. The saturate adsorption capacity of the Cd^2＋ was 77.88 mg/g. The adsorption process followed the pseudo first-order kinetics. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm.     

Effect of coagulation pretreatment on the fouling of ultrafiltration membrane

The purpose of this study is to understand the effect and mechanism of preventing membrane fouling, by coagulation pretreatment, in terms of fractional component and molecular weight of natural organic matter （NOM）. A relatively higher molecular weight （MW） of hydrophobic compounds was responsible for a rapid decline in the ultrafiltration flux. Coagulation could effectively remove the hydrophobic organics, resulting in the increase of flux. It was found that a lower MW of neutral hydrophilic compounds, which could remove inadequately by coagulation, was responsible for the slow declining flux. The fluxes in the filtration of coagulated water and supernatant water were compared and the results showed that a lower MW of neutral hydrophilic compounds remained in the supernatant water after coagulation could be rejected by a membrane, resulting in fouling. It was also found that the coagulated flocs could absorb neutral hydrophilic compounds effectively. Therefore, with the coagulated flocs formed on the membrane surface, the flux decline could be improved.     

Penetration analysis of elements and bioleaching treatment of spent refractory for recycling

Acidithiobacillus ferrooxidans ATCC23270 and Acidithiobacillus thiooxidans TM-32 were used for bioleaching of spent refractories of aluminium and copper melting furnaces for their recycling.Firstly,penetration of elements into aluminium melting furnace refractory was investigated and it was found that up to 7 cm from surface was contaminated.Comparison on leaching efficiency by the strains ATCC23270 and TM-32 found that the strain ATCC23270 could treat larger amount of the refractories than the strain TM-32 could do.In the experiment of bioleaching of spent refractory aluminium melting furnace by the strain ATCC23270,high leaching efficiency were obtained on Al,Si,and Ca,and extremely low leaching performance was,however,shown on the rest of elements i.e.,Na,Mn,and Zn.Under the strain TM-32 use,relatively high leaching performance was recognized on Al,Si,Ca,Na,Mn,and Zn.In the experiment of bioleaching for spent refractory copper melting furnace,almost the same leaching trends were shown on Cu,Zn,Al,and Si under the strains ACTT23270 and TM-32 uses.     

Simultaneous removal of ammonium and phosphate by zeolite synthesized from coal fly ash as influenced by acid treatment

Zeolite synthesized from fly ash （ZFA） without modification is not efficient for the purification of NH4＋ and phosphate at low concentrations that occur in real effluents, despite the high potential removal capacity. To develop an effective technique to enhance the removal efficiency of ammonium and phosphate at low concentrations, ZFA was modified with acid treatment and the simultaneous removal of ammonium and phosphate in a wide range of concentration was investigated. It was seen that when compared with untreated ZFA, only the treatment by 0.01 mol/L of H2SO4 significantly improved the removal efficiency of ammonium at low initial concentrations. The behavior was well explained by the pH effect. Treatment by more concentrated H2SO4 led to the deterioration of the ZFA structure and a decrease in the cation exchange capacity. Treatment by 0.01 mol/L H2SO4 improved the removal efficiency of phosphate by ZFA at all initial P concentrations, while the treatment by concentrated H2SO4 （≥0.9 mol/L） resulted in a limited maximum phosphate immobilization capacity （PIC）. It was concluded that through a previous mild acid treatment （e.g. 0.01 mol/L of H2SO4）, ZFA can be used in the simultaneous removal of NH4＋ and P at low concentrations simulating real effluent.