“鉴湖环境容量及水质规划”研究通过鉴定

为保护浙江绍兴鉴湖水域水质,由浙江省科委立项研究的《鉴湖环境容量及水质规划》课题,经三年多的工作,业已由绍兴市环境保护科学研究所等四单位研究完成。并于1992年6月25日在绍兴由省环保局主持通过了鉴定。该项目在分析了水域自然环境特征及当前存在的主要环境问题基础上,进行了鉴湖水质现状、污染源调查及发展趋势预测,水域水量及污染物平衡计算。运用入湖污染物与水质关系的数学模型对该水域主要     

再生水补水人工湖水域聚类划分及水质指标时空分布特征

以天津临港生态湿地公园人工湖水质和水文的调查数据为依据,运用相关性分析和聚类分析将研究水体划分为3类水域。研究了不同聚类水域水温、DO、p H、氮磷营养元素以及Chla的时空分布特征。结果显示,DO、硝态氮、TN、TP与流速呈显著正相关,水温、SS与流速呈显著负相关。Chla与水深呈显著正相关,TN、硝态氮与水深呈显著负相关。断面宽度与所有理化指标均没有显著相关性。3种水域在监测期间N/P比(TN/TP)显示湖泊正在从氮营养元素限制型(N/P7)向适宜藻类生长的营养类型过渡。富营养化评价显示,再生水为补水的临港人工湖在监测期间水质已处于中度富营养,主要贡献因子为COD和TP。     

芬兰的水质自动监测

芬兰是北欧的一个多湖国家,全境有大小湖泊六万多个,水系纵横,内陆水域占全国总面积百分之九以上。芬兰又是一个森林之国,森林复盖面积达百分之七十八。利用森林资源,芬兰大力发展造纸及木材加工等工业,由此也引起水质污染问题。为了保护水源,芬兰国家水源局从1972年开始研究发展水质自动监测技术。1975年,世界银行向芬兰贷款两千万美元,用于水质保护科学研究,其中主要研究项目就是建立水质自动监测系统。从1974年至1980年,芬兰水源局水质研究所先后在中部及南部Kokemaeiljoki和Kymijoki河系上建立自动水质监测站、网,目的是监测和防止工业废水、废料、城市污水向水系排放,并研究水质变化规律。经过几年的运行和改进,取得了较好的效果,积累了一定的经验。     

洪泽湖水域的环境演变遥感分析

针对传统水质监测的定点、定剖面采样分析时间及空间的局限性,为对湖泊水质进行全面系统的分析,在前人研究工作的基础上,建立了一种水域水质状况图像识别的主成分监督分类方法,通过对洪泽湖湖区的1991年12月15日和2000年1月7日,两个时相TM遥感图像数据,分别进行主成分变换,并依据不同类型水体的光学特性,分析各主成分图像的构成及其环境意义。研究表明：洪泽湖湖区的水质分布,具有从西向东,从北向南由清洁水（优）向一般水依次递减、逐年下降的特征。其清洁水体主要分布于洪泽湖西部的溧河洼、临淮头、西北部的安河洼和成子湖的北部。从1991--2000年,洪泽湖入湖的工业废水及生活污水量有所减少,湖水受污染程度明显减轻,相对“八五”期间水质污染日益加重的现象,“九五”以后水质逐渐改善。将其分类结果与所收集的洪泽湖历年水质资料对比分析表明：主成分监督分类结果与环境要素吻合较好,且基本反映了其水质环境的变化趋势。     

国外水资源保护区域化和流域化管理发展趋势——探讨我国水资源保护管理体制建设

一、前言 目前国际上水环境保护战略正在从水经济工程战略(即“谁污染谁治理”等环保方针政策)向水环境生态战略(即以资源开发为起点,调节控制物质循环中的污染源,综合协调社会经济和环境生态的平衡,确保其永续的同步发展)过渡.其主要标志是:美国的河系水质规划和环境影响评价;日本的     

利用沉水植物生长期收割进行富营养化水体生态管理的实地研究

在以再生水为补水水源的圆明园玉玲珑水域进行沉水植物收割实验,自2011年4—12月间每隔半个月监测一次水质。结果表明,通过在生长期收割沉水植物,玉玲珑水体TP、SRP、TN、NH4+-N、NO3--N和COD的平均浓度可维持在0.1、0.04、0.86、0.1、0.32和18 mg/L左右,水质保持在Ⅲ类至Ⅳ类地表水之间;与之对照的不收割沉水植物的玉玲珑进水口水域,9月沉水植物开始死亡腐烂,TP、SRP、TN、NH4+-N最高分别可达0.5、0.1、2.4和0.60 mg/L;作为对照的另一以挺水植物为主的水域,水质普遍劣于有大量沉水植物生长的水域,TP、SRP、TN、NH4+-N最高分别可达1.2、0.60、6.1和0.61mg/L。圆明园的实地实验表明,沉水植物有很强的净化水质作用,通过生长期收割,能够进一步强化其水质净化作用,可以作为一项对富营养化水体进行生态管理的有效措施进行推广。     

广州市南沙区水生生态环境现状的调查研究

在广州市南沙区水域采集地表水和水生生物样品,对水质主要理化指标、叶绿素a含量和初级生产力以及水生生物(浮游植物和浮游动物)的种类、数量、多样性和均匀度指数等进行调查,综合评价了南沙区水域水生生态环境质量.结果表明,利用不同指标对南沙区水域进行评价获得的结果基本一致,介于贫营养化至中营养化状态之间,水生生态环境质量状况较好.     

EM对地面水域水质的净化

试验研究了EM对地面水域水质的净化作用，探讨了EM投放方式对水质的净化效果以及对地面水域水质指标的净化选择性及其净化的经济可行性。     

小型景观湖水质模拟及应用研究

由于小型景观水体的体量和再生水补水措施的施行,其水质随环境和入水水质的变化和富营养化过程较大型水体快。由EFDC模型和WASP模型耦合建立小型浅水景观湖生态动力学模型,用实测水质数据进行参数率定与验证,可实现小型景观水体水质变化趋势的模拟,为水质管理提供决策支持。在此基础上,对民主湖在几种水质保障方案下1年的水质变化进行了模拟预测和对比,结果表明,作为富营养化程度表征的叶绿素a在空间和时间分布上均存在一定的规律性,夏季由于温度升高,叶绿素a浓度较高,说明藻类等浮游植物迅速增殖,是水质恶化水华暴发的高发期,而采取加大湖水水力循环和改善入口水质的控制方案,可使水质得到良好保障。     

环境模拟与污染控制国家重点联合实验室中国科学院生态环境研究中心环境水质学实验室

环境水质学实验室由汤鸿霄院士于1989年创建,是环境污染模拟与控制国家联合重点实验室的一个组成部分。实验室目标是面向国家解决水环境污染和饮用水安全保障问题的重大需求和国际水科学技术领域的研究前沿,深入探索天然水体和水处理过程中水质转化的基本规律,发展水处理高新技术,建立并完善环境水质学的学科体系,     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

Radionuclides and trace elements in fish collected upstream and downstream of Los Alamos national laboratory and the doses to humans from the consumption of muscle and bone

Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for ³H, ⁹⁰Sr, ¹³⁷Cs, ^totU, ²³⁸Pu, ^239,240Pu, and ²⁴¹Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of ⁹⁰Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g^‐1 [126E‐02 Bq kg^‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g^‐1 [518E‐02 Bq kg^‐1]). The differences in ⁹⁰Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y^‐1 (1.0 ± 1.0 μSv y^‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y^‐1 (1000 μSv y^‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.     

Book review

The Pesticide Manual ‐ A World Compendium, 8th Edition, C.R. Worthing, Editor and S.B. Walker, Assistant Editor, British Crop Protection Council, BCPC Publications Sales, Bear Farm, Binfield, Bracknell, Berkshire RG12 5QE, England. 1987, 1100 pp., UK £50; Overseas £56. ISBN 0–948404–01–9.     

Patterns of volatile metabolites and nonvolatile trichothecenes produced by isolates of <Emphasis Type="Italic">Stachybotrys,Fusarium, Trichoderma,Trichothecium</Emphasis> and <Emphasis Type="Italic">Memnoniella</Emphasis>

We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.     

Observations on the influence of water and soil pH on the persistence of insecticides

Abstract

The pH‐disappearance rate profiles were determined at ca. 25°C for 24 insecticides at 4 or 5 pH values over the range 4.5 to 8.0 in sterile phosphate buffers prepared in water‐ethanol (99: 1 v/v). Half‐lives measured at pH 8 were generally smaller than at lower pH values. Changes in half lives between pH 8.0 and 4.5 were largest (>1000x) for the aryl carbamates, carbofuran and carbaryl, the oxime carbamate, oxamyl, and the organophosphorus insecticide, trichlorfon. In contrast, half lives of phorate, terbufos, heptachlor, fensulfothion and aldicarb were affected only slightly by pH changes. Under the experimental conditions described half lives at pH8 varied from 1–2 days for trichlorfon and oxamyl to >1 year for fensulfothion and cyper‐methrin. Insecticide persistence on alumina (acid, neutral and basic), mineral soils amended with aluminum sulfate or calcium hydroxide to different pH values and four natural soils of different pH was examined. No correlation was observed between the measured pH of these solids and the rate of disappearance of selected insecticides applied to them. These observations demonstrate the difficulty of extrapolating the pH dependent disappearance behaviour observed in homogeneous solution to partially solid heterogeneous systems such as soil.     

The chemical stability of formulations of some hydrolyzable insecticides in aqueous mixtures with hydrolysis catalysts

Abstract

The active ingredients in commercial formulations of malathion, oxamyl, carbaryl, diazinon, and chlorpyrifos diluted to “spray tank”; concentrations with buffered distilled or natural water of pH 4–9 were stable for at least 24 hr. Formulations of trichlorfon were not stable at pH 7 or above but disappearance rates were slower than for the pure chemical in homogeneous solution. Cupric ion was observed to be an effective catalyst for the hydrolysis of a variety of pure organophosphorus insecticides but did not catalyze hydrolysis of the active ingredients of the formulations examined. Increasing the dilution of the formulation increased the susceptibility of malathion, oxamyl, and carbaryl to hydrolysis.     

Organochlorine compounds in a three-step terrestrial food chain

The concentrations of 15 organochlorine chemicals (PCBs and pesticides) were studied in a Central European oak wood food chain system: Great tit (Parus major), caterpillars (Tortrix viridana, Operophtera brumata, Erannis defoliaria), and oak-leaves (Quercus robur). Juvenile tits receive organochlorines from the mother via egg transfer and, eventually to a greater extent, from the caterpillar food source during nestling period. The concentrations of PCB 153 (2,2′,4,4′,5,5′-hexachlorobiphenyl, the most abundant in this study) was found in leaf material at ca. 1 ng/g, in caterpillars 10 ng/g, and in bird eggs 170 ng/g on an average and on a dry mass basis.     

Radionuclides in deer and elk from Los Alamos national laboratory and the doses to humans from the ingestion of muscle and bone

Abstract

This paper summarizes radionuclide concentrations (³H, ⁹⁰Sr, ¹³⁷Cs, ²³⁸Pu, ^239,240Pu, ²⁴¹Am, and ^totU) in muscle and bone tissue of mule deer (Odocoileus hemionus) and Rocky Mountain elk (Cervus elaphus) collected from Los Alamos National Laboratory (LANL), Los Alamos, New Mexico, lands from 1991 through 1998. Also, the committed effective dose equivalent (CEDE) and the risk of excess cancer fatalities (RECF) to people who ingest muscle and bone from deer and elk collected from LANL lands were estimated. Most radionuclide concentrations in muscle and bone from individual deer (n = 11) and elk (n = 22) collected from LANL lands were either at less than detectable quantities (where the analytical result was smaller than two counting uncertainties) and/or within upper (95%) level background (BG) concentrations. As a group, most radionuclides in muscle and bone of deer and elk from LANL lands were not significantly higher (p<0.10) than in similar tissues from deer (n = 3) and elk (n = 7) collected from BG locations. Also, elk that had been radio collared and tracked for two years and spent an average time of 50% on LANL lands were not significantly different in most radionuclides from road kill elk that have been collected as part of the environmental surveillance program. Overall, the upper (95%) level net CEDEs (the CEDE plus two sigma for each radioisotope minus background) at the most conservative ingestion rate (50 lbs of muscle and 13 lbs of bone) were as follows: deer muscle = 0.22 mrem y^‐1 (2.2 μSv y^‐1), deer bone = 3.8 mrem y^‐1 (38 μSv y^‐1), elk muscle = 0.12 mrem y^‐1 (1.2 μSv y^‐1), and elk bone = 1.7 mrem y^‐1 (17 μSv y^‐1). All CEDEs were far below the International Commission on Radiological Protection guideline of 100 mrem y^‐1 (1000 μSv y^‐1), and the highest muscle plus bone net CEDE corresponded to a RECF of 2E‐06, which is far below the Environmental Protection Agency upper level guideline of 1E‐04.     

Radionuclides in pinon pine (Pinus edulis) nuts from los alamos national laboratory lands and the dose from consumption

Abstract

One of the dominant tree species growing within and around the eastern portion of Los Alamos National Laboratory (LANL), Los Alamos, NM, lands is the pinon pine (Pinus edulis). Pinon pine is used for firewood, fence posts, and building materials and is a source of nuts for food—the seeds are consumed by a wide variety of animals and are also gathered by people in the area and eaten raw or roasted. This study investigated the (1) concentration of ³H, ¹³⁷Cs, ⁹⁰Sr, ^totU, ²³⁸Pu, ^{239, 240}Pu, and²⁴¹ Am in soils (0‐ to 12‐in. [31 cm] depth underneath the tree), pinon pine shoots (PPS), and pinon pine nuts (PPN) collected from LANL lands and regional background (BG) locations, (2) committed effective dose equivalent (CEDE) from the ingestion of nuts, and (3) soil to PPS to PPN concentration ratios (CRs). Most radionuclides, with the exception of ³H in soils, were not significantly higher (p < 0.10) in soils, PPS, and PPN collected from LANL as compared to BG locations, and concentrations of most radionuclides in PPN from LANL have decreased over time. The maximum net CEDE (the CEDE plus two sigma minus BG) at the most conservative ingestion rate (10 lb [4.5 kg]) was 0.0018 mrem (0.018 μSv); this is far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem (1000 μSv). Soil‐to‐nut CRs for most radionuclides were within the range of default values in the literature for common fruits and vegetables.     

Degradation and sorption of imidacloprid in dissimilar surface and subsurface soils

Degradation and sorption/desorption are important processes affecting the leaching of pesticides through soil. This research characterized the degradation and sorption of imidacloprid (1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine) in Drummer (silty clay loam) and Exeter (sandy loam) surface soils and their corresponding subsurface soils using sequential extraction methods over 400 days. By the end of the incubation, approximately 55% of imidacloprid applied at a rate of 1.0 mg kg^?1 degraded in the Exeter sandy loam surface and subsurface soils, compared to 40% of applied imidacloprid within 300 days in Drummer surface and subsurface soils. At the 0.1 mg kg^?1 application rate, dissipation was slower for all four soils. Water-extractable imidacloprid in Exeter surface soil decreased from 98% of applied at day 1 to > 70% of the imidacloprid remaining after 400 d, as compared to 55% in the Drummer surface soil at day 1 and 12% at day 400. These data suggest that imidacloprid was bioavailable to degrading soil microorganisms and sorption/desorption was not the limiting factor for biodegradation. In subsurface soils > 40% of ¹⁴C-benzoic acid was mineralized over 21 days, demonstrating an active microbial community. In contrast, cumulative ¹⁴CO₂ was less than 1.5% of applied ¹⁴C-imidacloprid in all soils over 400 d. Qualitative differences in the microbial communities appear to limit the degradation of imidacloprid in the subsurface soils.