公路地表灰尘及径流中颗粒物附着重金属对比研究

对北京城区北三环上北太平桥以西约300 m处路段地表灰尘及径流中不同粒径颗粒物附着重金属载荷进行对比研究.结果表明:(1)随着颗粒物粒径的增大,地表灰尘中颗粒物附着重金属浓度总体上逐渐降低;地表灰尘中<40.00 μm颗粒物附着重金属浓度最高;重金属载荷分布集中度不强,但主要集中在地表灰尘中<300.00 μm的颗粒物L.(2)地表径流中大部分重金属附着在<125.00 μm颗粒物上;0.45～10.00 μm颗粒物附着重金属载荷最高;0.45～40.00 μm颗粒物附着重金属载荷平均为77.1%.(3)地表灰尘中<40.00 μm的颗粒物的潜在水环境风险不太突出,但是其实际水环境影响却起主导作用.(4)进入水体的小粒径颗粒物质量分数升高是地表灰尘和径流重金届载荷随颗粒物粒径分布不同的重要原因之一;大气湿沉降对小粒径颗粒物重金属载荷可能会有一定的影响.     

北京春节期间大气颗粒物污染及影响

利用2006年春节期间的大气颗粒物浓度及粒径谱分布资料,结合大气能见度及NO2监测数据,分析了北京市鞭炮燃放禁改限后大气颗粒物污染的变化规律,以及对大气消光作用的影响.结果表明:春节期间特别是除夕夜大量鞭炮的集中燃放导致了大气颗粒物浓度的急剧升高,主要以细粒子为主;颗粒物浓度的升高致使大气能见度明显降低,鞭炮燃放最集中的时段,能见度低于2 km;燃放鞭炮产生的颗粒物是造成大气消光作用的主要因素.估算了北京市鞭炮燃放的颗粒物排放量,2006年除夕0:00～1:00市区排放了大约3.0×104kg PM10,官园监测点PM10小时最高质量浓度超过了800 μg/m3.元宵节夜间燃放鞭炮产生的颗粒物半衰期为2.4 h.     

燃煤电厂烟气中颗粒物粒径分布特征研究

采用冲击式尘粒分级仪对某燃煤电厂1、3机组静电除尘器进、出口烟气进行监测,分析了烟气中颗粒物排放规律和静电除尘器对不同粒径颗粒物的去除率.结果表明,除尘前烟气中以大粒径颗粒物为主,小粒径颗粒物含量相对较低.静电除尘器对不同粒径颗粒物的去除率差别较大,1、3机组的静电除尘器对平均粒径(d50)≥3.56 μm的颗粒物的去除率均达到99.99%,对d50为1.01 μm的颗粒物的去除率则分别为92.75%、95.69%.除尘后烟气中PM2.5和PM10所占比例迅速增加,燃煤电厂排放的烟气中颗粒物以PM2.5为主.     

烟草烟雾对室内空气颗粒物浓度的影响

采用电称冲击低压系统(ELPI)将无烟室和吸烟室内的空气颗粒物(0.03～10.00 μm)分成12级,对其粒子数和质量浓度进行测定.结果表明,吸烟室PM0.03～10.00的日平均粒子数和质量浓度分别是无烟室的1.50、1.13倍.烟草烟雾对室内颗粒物粒子数的影响集中在0.03～1.00 μm粒径段;对室内颗粒物质量浓度的影响表现为双模态结构,峰值分别在0.20～0.70、5.00～8.20 μm粒径段.烟草烟雾颗粒物的粒子数和质量浓度随烟雾消散时间的增加而减少,粒径越小,减小的越明显;烟草烟雾颗粒物在室内消散缓慢,会在长时间内造成影响,应引起足够关注.     

新型多级冲击采样器切割粒径的标准粒子实验分析

大气溶胶对环境污染、气候变化以及人体健康有着重要的影响,大气溶胶的采集和分析已成为当前大气环境研究领域中的一个重要课题.论述的新型多级冲击采样器能够实现大气溶胶颗粒物按空气动力学粒径的大小7级分离采集,提供大致均匀的平面样品以进行后续的物理、化学分析,同时保证各分级切割粒径的稳定性.利用振动孔溶胶发生器产生均匀、粒径大致相同、单分散相的1.5～17μm空气动力学粒径标准粒子,对新型多级冲击采样器前三级的切割粒径和收集效率进行鉴定性分析实验,结果表明,能够满足对大气溶胶颗粒物分级采集的要求.     

新型多级冲击采样器切割粒径的标准粒子实验分析

大气溶胶对环境污染、气候变化以及人体健康有着重要的影响,大气溶胶的采集和分析已成为当前大气环境研究领域中的一个重要课题.论述的新型多级冲击采样器能够实现大气溶胶颗粒物按空气动力学粒径的大小7级分离采集,提供大致均匀的平面样品以进行后续的物理、化学分析,同时保证各分级切割粒径的稳定性.利用振动孔溶胶发生器产生均匀、粒径大致相同、单分散相的1.5～17μm空气动力学粒径标准粒子,对新型多级冲击采样器前三级的切割粒径和收集效率进行鉴定性分析实验,结果表明,能够满足对大气溶胶颗粒物分级采集的要求.     

南京市大气气溶胶中颗粒物和正构烷烃特征及来源分析

于2002年夏季（7月）和冬季（12月）采集南京市5个功能区的大气气溶胶（PM2．5和PM10）样品，对两个季节不同功能区颗粒物及其颗粒物中正构烷烃的分布特征和污染来源进行了分析。结果表明，南京市大气颗粒物含量冬季高于夏季，细颗粒高于粗颗粒。正构烷烃的变化规律同颗粒物一致，且主要分布在细颗粒物上。根据各个功能区正构烷烃（C15-C32）的CPI（CPI1、CPI2和CPI3）结果，可知南京市大气气溶胶中正构烷烃由生物源和人为源共同排放产生。％waxCn的结果表明生物源对气溶胶中正构烷烃的贡献率为20％～43％，对南京市大气颗粒物的贡献率为1．66％～4．76％。     

垃圾填埋场微生物气溶胶粒径分布研究

为了了解垃圾填埋场微生物气溶胶粒径分布规律,在北京市某垃圾卫生填埋场填埋区、渗滤液处理区、生活区分别选定监测点,利用安德森六级微生物采样器,对填埋场空气微生物进行了系统的定点取样、测定和分析。研究结果表明,空气细菌粒径分布均为第Ⅰ级(>8.2 μm)最高,填埋区空气细菌粒径呈偏态分布,渗滤液处理区、生活区分别在第Ⅳ级和第Ⅲ级出现第2个峰值。携带细菌的可吸入微粒在渗滤液处理区比例最大。空气真菌与放线菌均在第Ⅳ级分布最高,携带真菌和放线菌的可吸入粒子的比例显著大于细菌(P<0.05)。填埋区不同作业时段空气微生物粒径在各级分布比例基本一致。填埋区细菌气溶胶中值直径为5.7 μm,渗滤液处理区为3.7 μm,生活区为5.3 μm,显著大于真菌气溶胶和放线菌气溶胶的中值直径(P<0.05)。     

六氯苯对水体微型生物群落的影响及其吸附行为

研究了六氯苯(HCB)对微型水生生物群落的影响及其吸附、传递过程.测定了群落的耗氧量和不同粒经颗粒物的生物量及HCB变化.试验结果显示,在6μg/L HCB影响下,群落的呼吸作用受到抑制,生物量减少.试验第1天,30.0%(质量分数,下同)的HCB以溶解态存在,26.3%吸附在0.22～2 μm的颗粒物(以细菌为主)上,22.1%吸附在2～8 μm的颗粒物(以鞭毛虫和藻类为主)上,21.6%吸附在大于8 μm的颗粒物(以藻类和大型原生动物为主)上.48 h后,溶解态的HCB逐渐减少,并由食物链低营养级向高营养级传递.最后74.9%的HCB都吸附在微型生物群落等颗粒物上,只有25.1%的HCB以溶解态存在.     

自由表面流人工湿地微生物气溶胶研究

微生物气溶胶的种类、浓度和粒径分布与人类健康关系密切。采用MD8空气浮游菌采样仪和FA-1型6级筛孔撞击式空气微生物采样器,对人工湿地细菌和真菌气溶胶的数量和粒径分布进行研究。结果表明,人工湿地进水前,细菌和真菌气溶胶平均值较低,分别为64.0、126.0CFU/m3;进水后,细菌气溶胶平均值在6月26日达到最高,为2292.5CFU/m3,真菌气溶胶平均值在8月27日达到最高,为6200.0CFU/m3;易进入肺部的细菌和真菌(粒径为0.65～4.70μm)粒子数分别占粒子总数的22.2%～62.3%、54.2%～87.6%;空气细菌中值直径为1.88～4.13μm,空气真菌中值直径在3.00μm左右波动。空气细菌中革兰氏阳性菌明显多于革兰氏阴性菌,空气真菌主要为酵母菌、镰刀菌属、枝孢属、毛霉属、交链孢属、肉座菌属、枝霉属、青霉属和曲霉属。     

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.     

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.     

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.     

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.