地面水监测优化布点的探索

本文提出,地面水监测网的优化布点,应该从测点的宏观位置、微观位置、典型位置三个层次上予以优化。文中用AG法确定宏观位置,用水质模型和混合长度经验公式确定微观位置,用统计模型确定典型位置,三者互相补充,互相印证,从而达到监测网优化设计的目的。这种方法成功地用于松花湖监测网的优化设计,可使原来的77个监测断面减少到3个,提高了环境的效率和效益。     

河流断面高锰酸盐指数采样点代表性的确定

按《江苏省地面水环境监测技术规范》(以下简称规范 )要求 ,对水面宽度小于 50ｍ的河流 ,一般只在河流中泓水深 0 5ｍ处布设一个采样点 ,用该采样点上监测的高锰酸盐指数 ,代表该监测断面上的高锰酸盐指数浓度。但由横洛间水质监测断面(以下简称断面 ) 1 996年丰水期和平水期的监测资料分析表明 ,选用中泓水深 0 5ｍ处采样点上监测的高锰酸盐指数 ,代表该断面上的高锰酸盐指数浓度有些不当 ,故对高锰酸盐指数采样点的代表性问题进行讨论。1　采样点设置为适应地区排污总量核算的需要 ,于 1 996年在横洛间断面进行水样加密监测试验。横洛间…     

废水总量控制监测中主要污染物的采样技术研究

对总量控制监测中主要污染物ＣＯＤｃｒ、Ｐｂ、Ｃｄ在废水中的分布规律及采样点位布设进行了研究,在此基础上,提出了采用采样点位优化选择的办法以提高废水样品的空间代表性。     

江苏省“十四五”地表水监测网优化调整思路与实践

分析了江苏省“十三五”地表水监测网状况及存在的问题,根据新形势下水环境管理和水生态保护的新要求,提出了该省“十四五”地表水监测网优化调整思路及预期目标。比对评估表明,优化调整后的地表水监测网实现了“三提升,一突破”,河湖覆盖率、跨界水体覆盖率和重点区域监控密度明显提升,农业面源监测有所突破,在助力发现水质薄弱区域、推动重点区域有效截污控源、促进化解跨界地区污染纠纷等方面具有实践成效。     

环境监测数据分析和监测网设计中SPSS 10.0的应用

SPSS10.0是目前功能齐全、便于应用的优秀统计软件。文章介绍了该软件在环境监测数据分析和监测网设计中的应用。文中简述了该软件的功能及优点，并通过实例，展示其在环境监测数据分析和监测网设计中的应用，这对于优化监测数据分析结果和监测网的设计均有较好的借鉴作用。     

太湖蓝藻预警采样点位布设与采样层次的研究

蓝藻水华的聚集和分布与气象条件有着密切的关系.根据近几年蓝藻预警监测及科研的实践,分析了风向对蓝藻迁移的影响,以及不同深度的藻密度变化情况.以此为依据,对太湖蓝藻监测时采样点位布设与采样层次选择的方案进行了比较研究,并提出了优化方案,为环太湖地区的相关部门更好地开展蓝藻预警监测工作提供了科学依据.     

废水污染物总量监测中采样方法的研究

通过对21家有代表性的废水污染源进行现场采样、排放曲线分析、采样频率优化的研究,确定总量监测中采样频率优化结果,为污染源总量控制监测提供技术指导。     

城市空气质量管理体系的监测技术及模式

无论在任何地点的污染物浓度都是来自不同范围内不同排放源贡献的加和。一个采样点的污染物浓度是以下几种浓度的加和:自然界的背景浓度;地区的背景浓度;采样点周边的城市平均浓度;附近排放源,如街道、点源(工厂、供热厂)等的影响。1　监测网络的设计设计监测系统网络的两种方案:(1)对城市,在人为划定的固定网格的交叉点附近设置采样点。如果交叉点靠近某个排放源,则需要仔细调整采样点的位置。这种方法导致大量的采样点,并为绘制空气污染等浓度曲线提供了可能性。其空间分配率就是网络大小的尺度。(2)采样点有选择地置于最具代表性的地方。…     

污染源废水排放总量监测中采样频次的确定

实施污染物总量控制计划和跨世纪绿色工程规划,是“九五”环保目标的重要内容。废水采样频次的确定,在目前情况睛是实行污染物总量控制监测的关键。文章应用数理统计抽样误差原理确定其采样频次,在废水排放总量监测中有一一的实用价值,可供广大监测人员参考。     

污染场地土壤初步调查布点及采样方法探讨

结合我国污染场地的普遍特征以及场地初步调查的基本目标,从布点前期准备、布点原则、布点程序和布点方法等方面详细探讨了污染场地土壤初步调查的点位布设方法;并从采样准备、采集方法、采集程序以及现场记录等环节探讨了现场样品采集的注意事项和要求,以期为污染场地环境调查的土壤监测和采样提供借鉴。     

Community air monitoring for pesticides. Part 3: using health-based screening levels to evaluate results collected for a year

The CA Department of Pesticide Regulation (CDPR) and the CA Air Resources Board monitored 40 pesticides, including five degradation products, in Parlier, CA, to determine if its residents were exposed to any of these pesticides and, if so, in what amounts. They included 1,3-dichloropropene, acrolein, arsenic, azinphos-methyl, carbon disulfide, chlorpyrifos and its degradation product, chlorthalonil, copper, cypermethrin, diazinon and its degradation product, dichlorvos, dicofol, dimethoate and its degradation product, diuron, endosulfan and its degradation product, S-ethyl dipropylcarbamothioate (EPTC), formaldehyde, malathion and its degradation product, methyl isothiocyanate (MITC), methyl bromide, metolachlor, molinate, norflurazon, oryzalin, oxyfluorfen, permethrin, phosmet, propanil, propargite, simazine, SSS-tributylphosphorotrithioate, sulfur, thiobencarb, trifluralin, and xylene. Monitoring was conducted 3 days per week for a year. Twenty-three pesticides and degradation products were detected. Acrolein, arsenic, carbon disulfide, chlorpyrifos, copper, formaldehyde, methyl bromide, MITC, and sulfur were detected in more than half the samples. Since no regulatory ambient air standards exist for these pesticides, CDPR developed advisory, health-based non-cancer screening levels (SLs) to assess acute, subchronic, and chronic exposures. For carcinogenic pesticides, CDPR assessed risk using cancer potency values. Amongst non-carcinogenic agricultural use pesticides, only diazinon exceeded its SL. For carcinogens, 1,3-dichloropropene concentrations exceeded its cancer potency value. Based on these findings, CDPR has undertaken a more comprehensive evaluation of 1,3-dichloropropene, diazinon, and the closely related chlorpyrifos that was frequently detected. Four chemicals—acrolein, arsenic, carbon disulfide, and formaldehyde—sometimes used as pesticides were detected, although no pesticidal use was reported in the area during this study. Their presence was most likely due to vehicular or industrial emissions.     

Heavy metals in water, sediments and wetland plants in an aquatic ecosystem of tropical industrial region, India

Concentrations of heavy metals (Cu, Cr, Fe, Pb, Zn, Hg, Ni, and Cd) and macronutrients (Mn) were measured in industrial effluents, water, bottom sediments, and wetland plants from a reservoir, Govind Ballabh (G.B.) Pant Sagar, in Singrauli Industrial region, India. The discharge point of a thermal power plant, a coal mine, and chlor-alkali effluent into the G.B. Pant Sagar were selected as sampling sites with one reference site in order to compare the findings. The concentrations of heavy metals in filtered water, sieved sediment samples (0.4-63 microm), and wetland plants were determined with particle-induced X-ray emission. The collected plants were Aponogeton natans, L. Engl. & Krause, Cyperus rotundus, L., Hydrilla verticillata, (L.f.) Royle, Ipomoea aquatica, Forssk., Marsilea quadrifolia, L., Potamogeton pectinatus, L., Eichhornia crassipes, (Mart.) Solms Monogr., Lemna minor, L., Spirodela polyrhiza (L.) Schleid. Linnaea, Azolla pinnata, R.Br., Vallisneria spiralis, L., and Polygonum amphibium, L. In general, metal concentration showed a significant positive correlation between industrial effluent, lake water, and lake sediment (p < 0.01). Likewise, significant positive correlation was recorded with metals concentration in plants and lake ambient, which further indicated the potential of aforesaid set of wetland macrophytes for pollution monitoring.     

Assessment of Atmospheric Deposition of Heavy Metals and Other Elements in Belgrade Using the Moss Biomonitoring Technique and Neutron Activation Analysis

This study aimed at assessing atmospheric deposition of heavy metals and other elements using the moss genera Brachythecium sp. (B. rutabulum and B. salebrosum) and Eurhynchium sp. (E. hians and E. striatum) collected in autumn 2004 in the urban area of Belgrade. The concentrations of 36 elements (Na, Mg, Al, Cl, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Zn, As, Se, Br, Rb, Sr, Mo, Sb, I, Cs, Ba, La, Ce, Sm, Tb, Dy, Hf, Ta, W, Hg, Th, U) were determined in moss and local topsoil samples by instrumental neutron activation analysis. The concentration of elements in moss positively correlated to those obtained for topsoil. High enrichment factors for As, Zn, Mo, Br, Sb, Se, Hg and Cl, calculated to continental crust composition, gave an evidence for anthropogenic impact on urban area, mainly due to intensive vehicular traffic and fossil fuel combustion. The concentration of elements in moss, characteristic for fossil fuel combustion, obtained in this study were substantially lower than in the previous investigation (2000) conducted in the area of Belgrade. The level of concentrations for V, Cr, Ni, and As in moss from this study correlated to those measured for neighboring countries, and were several times higher than the base-level data from low polluted areas. The level of accumulated elements in both investigated moss genera were similar and all studied species could be combined for biomonitoring purposes in urban areas.     

Characterization of atmospheric aerosols in the city of S?o Paulo, Brazil: comparisons between polluted and unpolluted periods

The objective of this study was to determine the size and composition of atmospheric aerosols in the downtown area of the city of S?o Paulo, Brazil, for a polluted and an unpolluted period. Aerosols were sampled with a portable air sampler (PAS), Micro-Orifice Uniform Deposit Impactor (MOUDI), and Scanning Mobility Particle Sizer. At the study site, air quality is poor, especially during the winter, high concentrations of pollutants being emitted primarily by the light- and heavy-duty vehicle fleet. We analyzed mass, black carbon (BC), Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sn, Zr, and Pb. During the polluted period, diurnal PM₁₀ was higher than nocturnal PM₁₀, whereas the inverse was true during the unpolluted period. The FPM was rich in BC, S, and Pb, whereas CPM was rich in Al, Si, Ca, Ti, and Fe. Mass balance was performed by category: ammonium sulfate, sodium chloride, crustal material, BC, and other. The PAS-determined FPM was mainly BC. The MOUDI-determined FPM crustal material explained more mass than did ammonium sulfate and BC during the polluted period, whereas ammonium sulfate had the largest mass during the unpolluted period. Crustal material was the major CPM component, followed by ammonium sulfate and BC. During the unpolluted period, FPM concentrations were lower, whereas those of ammonium sulfate were relatively higher, especially at night, and particle number was inversely proportional to particle size. Aerosol growth was more intense during the polluted period.     

Analysis of trace elements (Cu, Cd, and Zn) in the muscle, gill, and liver tissues of some fish species using anodic stripping voltammetry

Heavy metal (Cu, Cd, Zn) concentration of the muscle, gill, and liver of Otolithes rubber, Pampus argenteus, Parastromateus niger, Scomberomorus commerson, and Onchorynchus mykiss are determined by anodic stripping voltammetry method. The results show that the concentration of Cu, Cd, and Zn varied between 0.44 and not detected, 0.585 and 0.001, and 0.450 and 0.005?μg/g, respectively. It is interesting that in O. mykiss, the mean value of copper concentration was more than other marine organisms of this study, while in P. niger, the mean value of copper was minimum. The results of this study indicate that in the different tissues of fish species (O. rubber, P. argenteus, P. niger, S. commerson, and O. mykiss), the concentrations of Cu, Cd, and Zn were significantly lower than the permissible FAO/WHO levels.     

Coal cleaning residues and Fe-minerals implications

In the present investigation, a study was undertaken to understand the origin of Fe-minerals presents in Brazilian coal mining and to understand the environmental implication and the chemical heterogeneity in the study area. Coal cleaning residue samples rich in clays, quartz, sulphides, carbonates, sulphates, etc. were sampled from Lauro Muller, Urussanga, Treviso, Siderópolis, and Criciúma cities in the Santa Catarina State and a total of 19 samples were collected and Mössbauer, XRD, SEM/EDX, and TEM analyses were conducted on the samples. The major Fe-minerals identified are represented by the major minerals chlorite, hematite, illite, and pyrite, while the minor minerals include, ankerite, chalcopyrite, goethite, hematite, jarosite, maghemite, magnetie, marcasite, melanterite, natrojarosite, oligonite, pyrrhotite, rozenite, schwertmannite, siderite, and sideronatrile. Pyrite is relatively abundant in some cases, making up to around 10% of the mineral matter in several samples. The sulphates minerals such as jarosite and others, probably represent oxidation products of pyrite, developed during exposure or storage.     

微波消解-电感耦合等离子体质谱法同时测定废水中20种元素

采用微波消解-电感耦合等离子体质谱法,同时测定了废水中Be、V、Cr、Mn、Co、Ni、Cu、Zn、As、Se、Mo、Ag、Cd、Sb、Ba、Hg、Tl、Pb、Th、U等20种元素,比较了5种不同消解体系对废水样品的加标回收结果,确定采用硝酸+过氧化氢消解体系。Hg在0.050μg/L～2.00μg/L、其他元素在5.00μg/L～500μg/L范围内线性良好,检出限为0.01μg/L～0.2μg/L,国家有证标准物质的测定结果符合要求,废水样品平行测定的RSD为2.6%～6.5%,加标回收率为84%～110%。     

山西省大气降水水质评价

为了解山西省大气降水水质状况、主要污染物及区域分布规律，山西省水文部门于1984年开始对大气降水进行监测。在全省9个地市布设测点，分别为：太原市、大同市、长治市、榆次市、临汾市以及吕梁、忻州、阳泉、运城地区。监测项目为H^2 、电导率、Ca^2 、Mg^2 、K^2 、Na^2 、NH4^2 、SO4^2-、NO3^-、Cl^-、CO3^-、HCO3^-、F^-。结果表明，除吕梁、忻州地区外。山西省各地市均有酸雨发生，但酸雨发生的频率不高，全省年平均为3．3％；酸雨的酸性程度也不高，对生态可造成明显影响的降水次数不多；山西省酸雨为典型的硫酸型，酸雨中硫酸与硝酸的质量浓度比值远高于全国平均值。     

地面水中氨,硝酸盐,亚硝酸盐,氯化物,正磷酸盐,总硬度和硅酸盐的同时测定

用AQUA800辨别分析仪同时测定地面水中的氨、硝酸盐、亚硝酸盐、氯化物、正磷酸盐、总硬度和硅酸盐,是一种简便、迅速、准确、可靠的测定方法,样品无需预处理,精密度试验其变异系数分别为1．24％、2．18％、2．02％、2．67％、2．35％、3．57％、4．78％,加标回收率分别为103．5％、101．0％、95．0％、99．2％、97．6％、101．5％、98．0％,方法检测限分别为氨0．022mg／L,硝酸盐0．015mp／L,亚硝酸盐0．002tug／L,氯化物0．47mg／L,正磷酸盐0．015mg／L,总硬度17．6mg／L,硅酸盐0．55mg/L,能满足地面水中辨别分析仪同时测定氨、硝酸盐、亚硝酸盐点化物、正磷酸盐、总硬度和硅酸盐分析测定的要求。     

Statistical apportionment and risk assessment of selected metals in sediments from Rawal Lake (Pakistan)

The present study was carried out in order to evaluate the statistical apportionment and risk assessment of selected metals (Ca, Cd, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Na, Pb, Sr, and Zn) in freshly deposited sediments in Rawal Lake, Pakistan. Composite sediment samples were collected, oven-dried, grounded, homogenized, and processed to assess the water-soluble and acid extractable concentrations of the metals in the water extract and acid extract of the sediments using flame atomic absorption spectrophotometer. Statistical methods were used to identify the possible sources of the metals. Sediment quality guidelines and potential acute toxicity were used to evaluate the ecotoxicological sense of selected metals. Non-carcinogenic health risk assessment was also carried out to determine the potential adverse health risks to the inhabitants. Relatively higher concentration was noted for Ca, Fe, Mg, Na, K, Mn, and Sr in the sediment samples. Principal component analysis and cluster analysis revealed anthropogenic contributions of Cd, Pb, Cr, Mn, Fe, and Li in the sediments. Enrichment factors of the metals in sediments showed severe to moderate enrichment of Cd, Pb, Ca, Fe, Li, Mn, and Sr. Geoaccumulation indices and contamination factors evidenced significant contamination by Cd and Pb, although, on the whole, low degree of contamination was noted. The levels of some metals exceeded the sediment quality guidelines, which revealed frequently adverse biological effects to the dwelling biota in the aquatic ecosystem. The sediments were found to be significantly contaminated by Cd, Pb, Cr, Mn, Fe, and Li.