杭州市区大气能见度变化趋势及其与主要污染物相关性分析

利用2004-2006年地面气象观测资料和同期环境空气质量自动监测数据,分析了杭州市区大气能见度变化趋势及其与主要污染物的相关性.结果表明,杭州市区能见度的日分布特征为14时最好,8时最差;季节变化特征为夏季>春季>秋季>冬季,全年仅7月能见度超过10 km;SO2、NO2、PM10浓度均随能见度增高而逐渐降低;影响能见度的首要因子为相对湿度和PM2.5,能见度与PM2.5浓度具有较好的相关性.     

江苏省污染减排与空气质量变化相关性分析

利用2000—2007年大气污染物排放量数据和同期环境空气质量监测数据,分析了江苏省主要大气污染物减排与环境空气质量变化的相关性。结果表明,近年来江苏省SO2排放量与环境空气中SO2浓度存在正相关,而烟尘和粉尘排放总量与空气中可吸入颗粒物的浓度呈现出弱的负相关关系。对江苏省经济发展和环境关系的进一步分析揭示,江苏省环境库兹涅茨曲线呈现出倒U型关系,表明江苏省已经进入经济环境双赢区间,但近年来政策对经济环境关系的影响突出。该研究对中国十二五环境管理政策的制定有着重要的参考意义。     

浙东沿海城市大气颗粒物污染特征及来源解析研究

对2009年夏季浙东沿海地区环境空气质量进行监测,监测大气颗粒物(TSP、PM10、PM2.5、PM1.0)浓度,分析颗粒物污染特征、水溶性离子及无机元素组成,运用化学质量平衡受体模型(CMB模型)对浙东沿海地区大气TSP来源进行解析.结果表明,浙东沿海地区的大气颗粒物主要以细颗粒物为主,颗粒物中主要的水溶性离子为SO2-4、NH+4、Ca2+,土壤尘是该地区大气TSP的主要来源,北仑、乐清和奉化TSP中土壤尘的分担率分别达到55.49%、42.52%、40.70%,各监测点TSP来源具有一定的地域特征.     

萧山区环境空气质量变化及其影响因素分析

利用杭州市萧山区环境空气的监测资料,采用空气综合污染指数、空气污染指数(API)、Daniel趋势检验等评价和分析方法,研究了萧山区"十一五"期间(2005—2010年)环境空气质量的变化趋势及其影响因素。结果显示:(1)PM10是萧山区环境空气中的首要污染物。SO2、PM10浓度以及空气综合污染指数先升高后降低,总体呈现不显著下降趋势,整体环境空气质量在2007年后逐年改善。(2)空气中NO2污染负荷系数逐年上升,NO2/SO2和污染物相关性分析结果表明,萧山区空气污染特征正处于由煤烟型向汽车尾气型转变的初期阶段。(3)萧山区月均API呈现出7-9月4-6月1-3月10-12月的变化特征。(4)在持续快速增长、能源消耗逐年增加的情况下,萧山区环境空气质量的改善说明节能减排、产业升级、污染源综合治理、能源清洁使用等措施对改善环境空气质量起到了关键作用。     

鞍山市大气中挥发性有机物的污染特征研究

对鞍山市不同功能区(工业区、工业区附近、居住区和对照区)的大气进行分季节(夏、冬季)采样,分析该市大气中挥发性有机物(VOCs)的污染水平和季节变化特征.结果表明,夏、冬季的大气中的VOCs浓度变化差异显著,总体来说夏季大气中的VOCs浓度高于冬季;夏季大气中苯系物、挥发性卤代烃浓度分别是冬季的1.1～2.7、1.4～...     

乌鲁木齐市能源结构调整对冬季SO2浓度空间分布变化的影响

乌鲁木齐市冬季大气污染严重,SO2浓度不断增加,且超标频率增多,已成为不容忽视的环境问题.2012年乌鲁木齐市实施“煤改气”工程,旨在改善乌鲁木齐市的大气环境质量.为研究工程的实施对SO2浓度的控制起到的作用,选用冬季污染最为严重的时段(1-2月),对“煤改气”前后城市不同区域的SO2日均浓度变化进行了分析.结果显示,“煤改气”对SO2浓度的降低效果显著,但降低幅度在区域间存在差异,“煤改气”后冬季SO2日均浓度在空间上呈现出由南向北逐渐增加的态势,南面SO2日均浓度基本达标,而北面SO2浓度虽有降低,但超标频率依然较高,值得当地政府在环境治理过程中关注.     

厦门市空气污染的空间分布及其与影响因素空间相关性分析

基于空间信息技术、克里格插值与空间相关矩阵,研究厦门市SO2、NO2、PM10和PM2.5污染浓度空间分布特征。通过提取人口密度、道路面积比重、建设用地比重、地表温度及植被指数等空气污染影响因素的空间分布数据,划分研究区为生态区、居住区与工业区,定量评价了污染物浓度与影响因素的空间相关性,并识别出各污染物的主要影响因素。结果表明:污染浓度分布总体上呈现出工业区-居住区-生态区递减的空间特征,其主要受工业排放和机动车排放的影响;SO2与除地表温度外的其他影响因数均有较强空间相关性,PM10和PM2.主要与道路面积比重、建设用地比重具有较强相关性,NO2则与道路面积比重的相关性最强,污染浓度与影响因数空间相关性呈现出工业区-居住区-生态区递增趋势;与按照行政区的划分相比,工业区、居住区、生态区的划分显得更为合理。     

唐山市工业区大气污染对小学生肺功能的影响

探讨了工业区大气污染对小学生肺功能的影响。在唐山市工业区和相对清洁区选取452名小学生为研究对象,进行肺功能的测定和问卷调查。用多元回归分析建立模型后,以实测值占预计值的百分比为统计量进行分析。调查结果显示小学生肺功能指标中MVV、V25污染区低于对照区,VC、FEV、V25、V50的异常率高于对照区,且与大气中SO2的浓度有关。     

丽水市大气污染的时空分布特征及与气象要素的相关分析

利用2007-2010年丽水市逐日大气污染物浓度数据和地面气象观测资料,对PM10、SO2、NO23种大气污染物浓度进行了时空分布特征研究,进而探讨了气象要素对大气污染的影响.结果表明:2007-2010年,丽水市主要的3种大气污染物的负荷为PM10＞ NO2 ＞SO2,影响大气环境质量的污染物以PM10为主;总体来说,NO2的月均浓度基本达到《环境空气质量标准》(GB3095-1996)-级标准,冬半年(9-12月、1-2月)SO2的月均浓度仅达到二级标准,而夏半年(3-8月)月均浓度基本达到一级标准,PM10的月均浓度都达到二级标准(0.10 mg/m3);在空间分布上,PM10、NO2的年均浓度都表现出东向西逐渐减少的特征,而SO2年均浓度主要体现为南向北递增的特征,3种大气污染物在空间上都表现为在东部缙云、青田等地的污染相对严重,而在西面的遂昌、龙泉等地的污染程度较轻;各种气象要素对大气污染的影响中,除了气压与3种大气污染物的浓度呈极显著正相关外,其他气象要素都表现为负相关,只是影响程度有所差异.气象要素对大气污染的影响不是单一作用的,而是通过多种气象要素相互配合、相互作用、综合反应来产生作用的.     

济南市环境空气VOCs的化学反应活性及关键活性组分研究

对济南市2010年6月—2012年5月环境空气中55种VOCs监测数据进行分析,研究其反应活性及关键活性组分。结果表明,济南市环境空气VOCs的LOH和OFP的月变化规律与其月浓度变化趋势一致,夏季环境空气VOCs的浓度、LOH和OFP较大,是容易发生复合型大气污染的时段;济南市环境空气VOCs化学活性与其混合比之间具有良好的线性相关性,表明济南市环境空气中VOCs的化学组成具有一定的稳定性;VOCs的平均KOH远远超过乙烯的KOH,MIR与乙烯相当,说明济南市环境空气VOCs的化学反应活性较强;烯烃体积分数远远小于烷烃,但化学反应活性贡献率最高,且顺-二丁烯、丙烯、乙烯、丁烯、反-二丁烯、异戊二烯、苯乙烯、2-甲基-1-戊烯、顺-二戊烯、间,对-二甲苯、邻-二甲苯、甲苯、1,2,4-三甲基苯和环戊烷为济南市关键活性组分,因此,济南市高活性VOCs物种为烯烃,同时芳香烃和环戊烷对环境空气活性的贡献也不容忽视。     

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.     

Evaluation of trichloroethene recovery processes in heterogeneous aquifer cells flushed with biodegradable surfactants

The ability of two biodegradable surfactants, polyoxyethylene (20) sorbitan monooleate (Tween 80) and sodium dihexyl sulfosuccinate (Aerosol MA), to recover a representative dense non-aqueous-phase liquid (DNAPL), trichloroethene (TCE), from heterogeneous porous media was evaluated through a combination of batch and aquifer cell experiments. An aqueous solution containing 3.3% Aerosol MA, 8% 2-propanol and 6 g/l CaCl(2) yielded a weight solubilization ratio (WSR) of 1.21 g TCE/g surfactant, with a corresponding liquid-liquid interfacial tension (IFT) of 0.19 dyn/cm. Flushing of aquifer cells containing a TCE-DNAPL source zone with approximately two pore volumes of the AMA formulation resulted in substantial (>30%) mobilization of TCE-DNAPL. However, a TCE mass recovery of 81% was achieved when the aqueous-phase flow rate was sufficient to displace the mobile TCE-DNAPL toward the effluent well. Aqueous solutions of Tween 80 exhibited a greater capacity to solubilize TCE (WSR=1.74 g TCE/g surfactant) and exerted markedly less reduction in IFT (10.4 dyn/cm). These data contradict an accepted empirical correlation used to estimate IFT values from solubilization capacity, and indicate a unique capacity of T80 to form concentrated TCE emulsions. Flushing of aquifer cells with less than 2.5 pore volumes of a 4% T80 solution achieved TCE mass recoveries ranging from 66 to 85%, with only slight TCE-DNAPL mobilization (<5%) occurring when the total trapping number exceeded 2 x 10(-5). These findings demonstrate the ability of Tween 80 and Aerosol MA solutions to efficiently recover TCE from a heterogeneous DNAPL source zone, and the utility of the total trapping number as a design parameter for a priori prediction of DNAPL mobilization and bank angle formation when flushing with low-IFT solutions. Given their potential to stimulate microbial reductive dechlorination at low concentrations, these surfactants are well-suited for remedial action plans that couple aggressive mass removal followed by enhanced bioremediation to treat chlorinated solvent source zones.     

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.     

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.     

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.     

The variation of street air levels of PAH and other mutagenic PAC in relation to regulations of traffic emissions and the impact of atmospheric processes

The occurrence of particle associated PAH and other mutagenic PAC was determined in 1996 in the street air of Copenhagen. In addition, particle extracts were tested for mutagenicity. The measurements were compared with previous measurements in 1992/1993. The levels had decreased in this period. The decrease was caused by an implementation of light diesel fuels for buses and the exchange of older petrol-driven passenger cars with catalystequipped new ones. About 65% of the reduction was caused by the application of the light diesel fuels. Under special conditions, chemical processes in the atmosphere produced many more mutagens than the direct emissions. The concentrations of S-PAC and N-PAC were 10 times lower than those of PAH, while the levels of oxy-PAH were in the same order of magnitude as those of PAH. Benzanthrone, an oxy-PAH, is proposed to be formed in the atmosphere in addition to direct emissions. Benzo(a)pyrene, often applied as an air quality criteria indicator, was photochemically degraded in the atmosphere. A strong increase in the mutagenic activities was observed to coincide with a depletion of benzo(a)pyrene.     

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.     

Teratological effects of pesticides in vertebrates: a review

Abstract

In the last decades, the use and misuse of pesticides in the agriculture have increased, having a severe impact on ecosystems and their fauna. Although the various effects of pesticides on biodiversity have been already documented in several studies, to our knowledge no consistent overview of the impact of pesticides in vertebrates, both terrestrial and aquatic, is available. In this review, we try to present a concise compilation of the teratogenic effects of pesticides on the different classes of vertebrates – mammals, birds, reptiles, amphibians and fish.     

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.