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…     

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。     

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。     

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。     

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。     

Effective monitoring of agriculture

An opinion piece published in Nature proposed a global network for agricultural monitoring [J. Sachs, R. Remans, S. Smukler, L. Winowiecki, S. J. Andelman, K. G. Cassman, D. Castle, R. DeFries, G. Denning, J. Fanzo, L. E. Jackson, R. Leemans, J. Leemans, J. C. Milder, S. Naeem, G. Nziguheba, C. A. Palm, J. P. Reganold, D. D. Richter, S. J. Scherr, J. Sircely, C. Sullivan, T. P. Tomich and P. A. Sanchez, Nature, 2010, 466, 558-560.]. Whilst we agree with Sachs et al. that monitoring of agricultural systems is a critically important activity of global significance, especially given increasing problems with global food security and the potential impacts of agriculture on the environment [J. Cribb, The Coming Famine. The Global Food Crisis and What We Can Do to Avoid It, CSIRO Publishing and University of California Press, Melbourne and Oakland, 2010.], we argue in this paper that their generic, mandated monitoring framework has a high probability of failure or at best will be highly inefficient. We base this conclusion on our recently published examination of the factors influencing the success or failure of monitoring programs worldwide [D. B. Lindenmayer and G. E. Likens, Effective Ecological Monitoring, CSIRO Publishing and Earthscan, Melbourne and London, 2010.]. We briefly outline what we believe are three serious flaws in the monitoring framework proposed by Sachs et al. We then suggest an alternative approach that we argue would be more effective, more efficient, and have a greater chance of successfully addressing key issues in sustainable agriculture.     

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.     

Assessment of heavy metals in some wild edible mushrooms collected from Yunnan Province, China

Eight heavy metals (Cu, Zn, Fe, Mn, Cd, Cr, Ni, and Pb) in 14 different wild-growing edible mushroom species (Coprinus comatus, Voluariella volvacea, Pleurotus nebrodensis, Hypsizigus marmoreus, Hericium erinaceus, Agrocybe aegerita, Lenfinus edodes, Collybia velutipes, Agaricus bisporus, Russula albida, Clitocybe conglobata, Pleurotus eryngii, Lepista sordida, and Pleurotus ostreatus) collected from Yunnan province, China, were determined by inductively coupled plasma-atomic emission spectrometry after microwave digestion. All element concentrations were determined on a dry weight basis. The ranges of element concentrations for copper, zinc, iron, manganese, cadmium, chromium, nickel, and lead were 6.8-31.9, 42.9-94.3, 67.5-843, 13.5-113, 0.06-0.58, 10.7-42.7, 0.76-5.1, and 0.67-12.9 mg/kg, respectively. In general, iron content was higher than other metals in all mushroom species. The levels of zinc, cadmium, and lead in some edible mushroom samples were found to be higher than legal limits. The relative standard deviations were found below 10%. The accuracy of procedure was confirmed by certified reference material.     

Chemical monitoring and evaluation of the water quality of the Douro River at the Crestuma-Lever dam

Water taken from the Crestuma-Lever dam on the Douro River was evaluated considering the Portuguese Decree-law no. 236/98 of 1st August, 1998. This paper presents the metrological characteristics, validation of analytical methodologies and the data obtained from seasonal samplings. The test parameters selected are: temperature, pH, chloride, conductivity, carbon dioxide, alkalinity, hardness, oxidability, dissolved oxygen, BOD5, total suspended solids, sulfide, phosphate, silica, ammonium, nitrite, nitrate, sulfate, sodium, potassium, calcium, magnesium, iron, manganese, copper and zinc. From data analysis we can conclude that the water presented the following characteristics: a pH situated in the neutral zone; a median mineralization; a medium hardness; well oxygenated water; and a carbonate hardness exclusively due to bicarbonates. The temperature, pH, dissolved oxygen, ammonia, chlorides, sulfates, copper, zinc and BOD5 were compared with the legal limits presented in annexes XXI and I of Decree-law 236/98. The results relating to total hardness, nitrites, calcium, magnesium, sodium, potassium, aluminium, sulfides and oxidability were compared with the legal values in annex VI as there are no limits relating to these parameters in annexes XXI and I.     

Paleolimnological assessment of Grove and Plow Shop Ponds, Ayer, Massachusetts, USA--a superfund site

Three sediment cores from each of severely polluted Grove and Plow Shop Ponds, Ayer, Massachusetts, USA, were dated using (210)Pb, characterized for plant macrofossil assemblages, and analyzed for H(2)O, loss-on-ignition, stable Pb isotopes, and concentrations of As, Ca, Cd, Cr, Cu, Fe, Hg, methyl-Hg, Ni, Pb, and Zn. A core from nearby kettle Spectacle Pond, Littleton, Massachusetts, was similarly characterized (except for plant macrofossil assemblages) to assess the regional air pollution signal in sediment for comparison with the six cores. Accumulation rates for metals (mass per area per year), the anthropogenic component (mass per area per year), and total accumulation of the anthropogenic component (mass per area) indicate that As, Cd, Cr, Cu, Hg, methyl-Hg, Ni, Pb, and Zn have accumulated in sediment as a consequence of point source pollution from within the drainage basins of Grove and Plow Shop Ponds. Three distinct sources of pollution are inferred. As is entering Plow Shop Pond via groundwater in the southwest. Cd, Ni, Pb, and Zn are entering the system predominantly at the eastern end of, or upstream from, Grove Pond. Pb also comes from the northwest corner of Grove Pond, the principal source of Cr, Cu, and Hg. These results are consistent with chemistry of modern surface sediments. The history of pollution extends back more than 100 years. Intra- and inter-core variability of concentrations and accumulation rates indicate that much of the pollution was likely in particulate form with little physical redistribution. Recently, concentrations and accumulation rates have generally decreased substantially for those elements present in excessive concentrations in the past. This is a consequence of accumulation of recent, less polluted sediment. In Spectacle Pond, the nearby reference lake, accumulation rates for As, Cd, Hg, and Pb, adjusted for background values and changes in sedimentation rate, increased above background starting in the late 19th century, peaked about 1980, and declined substantially to 2000. These decreases suggest that the anthropogenic (pollution) component of atmospheric deposition of these elements declined after 1980 by at least 50%(As), 80%(Cd), 80%(Hg), and 80%(Pb).     

Drinking water quality assessment in Southern Sindh (Pakistan)

The southern Sindh province of Pakistan adjoins the Arabian Sea coast where drinking water quality is deteriorating due to dumping of industrial and urban waste and use of agrochemicals and yet has limited fresh water resources. The study assessed the drinking water quality of canal, shallow pumps, dug wells, and water supply schemes from the administrative districts of Thatta, Badin, and Thar by measuring physical, chemical, and biological (total coliform) quality parameters. All four water bodies (dug wells, shallow pumps canal water, and water supply schemes) exceeded WHO MPL for turbidity (24%, 28%, 96%, 69%), coliform (96%, 77%, 92%, 81%), and electrical conductivity (100%, 99%, 44%, 63%), respectively. However, the turbidity was lower in underground water, i.e., 24% and 28% in dug wells and shallow pumps as compared to open water, i.e., 96% and 69% in canal and water supply schemes, respectively. In dug wells and shallow pumps, limits for TDS, alkalinity, hardness, and sodium exceeded, respectively, by 63% and 33%; 59% and 70%, 40% and 27%, and 78% and 26%. Sodium was major problem in dug wells and shallow pumps of district Thar and considerable percent in shallow pumps of Badin. Iron was major problem in all water bodies of district Badin ranging from 50% to 69% and to some extent in open waters of Thatta. Other parameters as pH, copper, manganese, zinc, and phosphorus were within standard permissible limits of World Health Organization. Some common diseases found in the study area were gastroenteritis, diarrhea and vomiting, kidney, and skin problems.     

Source to sink tracking of selected human pharmaceuticals from two Oslo city hospitals and a wastewater treatment works

The occurrence of twenty pharmaceutical compounds was quantitatively determined in effluents from two major Oslo city hospitals, Rikshospitalet and Ullev?l, along with influent, sludge and final effluent from the city's VEAS wastewater treatment works (WTW). Composite hospital effluents were collected over a twelve week period and were showed to contain paracetamol, metoprolol, diclofenac, ibuprofen, 17beta-Estradiol, estriol, estrone, oxytetracycline, tetracycline, doxycycline, chlorotetracycline, demeclocycline, trimethoprim, ciprofloxacin, sulfamethoxazole, cyclophosphamide and ifosfamide. Three pharmaceuticals were not detected above the limit of detection; cefuroxime, 17alpha-ethinylestradiol and meclocycline. Composite influent, sludge and effluent samples were collected from VEAS WTW over a seven week period. The influent into VEAS WTW contained all of the same selected substances detected in the hospital effluents, except for oxytetracycline, chlorotetracycline, demeclocycline, cyclophosphamide and ifosfamide. The percentage of pharmaceuticals entering the works from the hospitals was <10% for all of the selected compounds. VEAS sludge samples contained a different profile of substances reflecting their physico-chemical properties. Hydrophobic antibiotics, such as oxytetracycline, tetracycline and ciprofloxacin, were detected in all of the collected sludge samples. Their absence in the collected influent samples suggests that they enter the works bound to effluent particles, with the dissolved fraction observed in the hospital effluents partitioning onto particulate matter within the sewerage network. The final effluent from VEAS WTW contained reduced concentrations of many pharmaceuticals, including paracetamol, ibuprofen and sulfamethoxazole. For other compounds, such as metoprolol, diclofenac and trimethoprim, there were often higher concentrations in the effluent than the influent. These effluent concentrations represent median inputs varying from low g day(-1) (e.g. paracetamol and ibuprofen) to nearly 200 g day(-1) (e.g. metoprolol and trimethoprim) into Oslofjord. A simple risk assessment showed that the antibiotic ciprofloxacin may at times pose an acute risk to the Oslofjord aquatic environment.     

Major and trace elements’ concentrations in hard and soft tissues of kutum, <Emphasis Type="Italic">Rutilus kutum</Emphasis>, from the Caspian Sea and their potential use as biomonitoring tools

The potential use of different hard and soft parts (otolith, scale, eye lens, dorsal spine, vertebral bone, muscle, and liver) of Rutilus kutum for biomonitoring of 13 major and trace elements (Br, Ca, Cl, Cu, Fe, K, Mg, Mn, Na, P, S, Sr, and Zn) was evaluated, for the first time. The specimens were sampled from three sampling sites in the Southern Caspian Sea in May 2016. Twenty specimens were collected from each site. The elements’ concentrations in the samples were measured by proton-induced X-ray emission (PIXE). In all the hard tissues, except for eye lens, Ca was the most abundant element, whereas Fe was among the least abundant elements. The orders of element occurrence in the two soft tissues were largely similar. Ca, Fe, S, Cl, and K could be detected in all the selected tissues, while Br was detectable only in otolith. Minor similarities among the tissues were identified in the case of eye lens (concerning P, S, and Zn) and liver (in terms of Cl, Fe, and K), whereas, in the case of Sr and Ca, otolith shows the maximum distance. In general, it can be concluded that all the studied hard parts, except for eye lens, may offer alternatives for biomonitoring of Ca, Cl, Fe, K, and S in the southern Caspian Sea. The scales and spines represent a potential non-lethal alternative to the other hard parts.     

Metal concentrations in deciduous tree leaves from urban areas in Poland

Accumulation of metals in deciduous tree foliage fromurban areas in western-south Poland was monitored duringthe vegetation season of 2000 year. Concentrations of Al,Ba, Ca, Cd, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Sr, Ti and Znwere measured in birch, willow, linden and maple leavesusing the ICP-AES method. Seasonal variations of metalconcentrations and their relations with sampling sitewere investigated. The most dynamic accumulation of Al,Cd, Cr, Ni and Pb was observed for examined species. Thehighest differences in element concentrations forinvestigated sites were found for Ba, Cd, Mn and Ni.Interelement correlations were investigated. In allfoliar samples synergistic relationships between Al–Crand Ca-Sr were found. Statistically significant negativecorrelations were observed only for Cd and Ti in birch leaves.