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。     

城市固体废弃物综合处理厂微生物气溶胶污染特性

以鄂尔多斯市某城市固体废弃物综合处理厂的生活垃圾预处理区、餐厨预处理区、粪便预处理区及联合厌氧发酵区为对象,研究不同功能区的微生物气溶胶污染特性。研究结果表明,不同功能区空气异养细菌和真菌的浓度存在显著性差异(p<0.05),尤以生活垃圾集料间产生的异养细菌和真菌浓度最高。对照空气微生物评价标准,不同功能区产生的异养细菌和真菌大都有不同程度的污染。粒径分析表明,不同功能区异养细菌粒径主要集中在第1、2、3、4级,各功能区之间无显著性差异(p>0.05),与细菌粒径分布不同,不同功能区真菌粒径主要分布在第3级和第4级,也无明显差异(p>0.05)。     

矿化垃圾中的微生物区系与酶活性变化特征研究

选择某市郊城市生活垃圾填埋场为研究对象,对填埋时间分别达6、8、10年的矿化垃圾中的微生物区系与酶活性变化特征进行了比较。结果表明,表层(0～50 cm)和底层(100～150 cm)矿化垃圾中的微生物数量和酶活性变化幅度大于中层(50～100cm);填埋达6、8、10年后的各层矿化垃圾中的细菌数量明显低于对照,放线菌数量则明显高于对照,而真菌数量在表层和中层中高于对照或与对照相当,在底层则低于对照,各层中的脲酶、碱性磷酸酶、碱性磷酸酶活性则明显高于对照或与对照相当;总体来说,相同填埋深度的矿化垃圾中,填埋达6～8年的细菌、真菌、放线菌数量和脲酶、碱性磷酸酶、酸性磷酸酶活性的变化幅度要大于填埋8～10年的,且均在填埋8～10年趋于稳定。     

北京市某城市污水处理厂微生物气溶胶污染特性研究

以北京市某城市污水处理厂的格栅间、曝气池、污泥浓缩池和污泥脱水间为对象,研究不同功能区的空气微生物浓度、粒径分布及微生物组成.结果表明:(1)该污水处理厂4个功能区空气异养细菌浓度平均值为3.3×104cfu/m3,范围为1.0×102～4.3×105cfu/m3；真菌浓度平均值为6.1×103cfu/m3,范围为7.5×10～7.6×104cfu/m3.异养细菌和真菌浓度存在显著性差异,尤以曝气池上空最高,其次是污泥脱水间,浓度最低的区域为格栅间和污泥浓缩池.各功能区均存在不同程度的异养细菌和真菌污染.(2)该污水处理厂不同功能区逸散出的异养细菌分布比例最高的为第2～5级,真菌主要分布在第3～5级.4个功能区空气中粒径为2.10～4.70μm(第3、4级)的异养细菌和真菌粒子分别占到了总数的37％～40％和46％～56％,而粒径为0.65～2.10μm(第5、6级)的异养细菌和真菌粒子则分别占到了总数的30％～33％和31％～37％,说明该污水处理厂不同功能区内的空气微生物存在一定的健康风险,可能对人呼吸道构成感染威胁.(3)假单孢菌(Pseudomonas)为该污水处理厂不同功能区均检出的优势异养细菌,而优势真菌种属为毛霉(Mucor)和曲霉(Aspergillus).     

厌氧陈腐垃圾模拟柱对渗滤液COD和NH_3-N的处理特性

通过实地钻取阿苏卫填埋场陈腐垃圾,真实模拟填埋场压实工艺,制作2种不同压实密度的陈腐垃圾模拟柱,对比研究其对渗滤液COD、NH3-N处理效果。结果表明,当模拟柱压实密度为1.09 t/m3时,渗滤液垂直运动明显;回灌此模拟柱水力负荷分别为18.6、28、37.2和46.5 L/t时,COD去除效果稳定,平均去除率达82.4%,最高去除率可达90.1%;出水NH3-N浓度均值为549.3 mg/L,且介于415～700 mg/L间变化。自循环回灌COD去除率最高仅为11.5%,NH3-N去除率最高仅为11.8%,两者去除效果不明显。因此,北方平原型填埋场进一步完善填埋工艺,使填埋场垂直方向渗透系数分布均匀,充分利用陈腐垃圾堆体的自降解能力,才是处理渗滤液污染的关键。     

回灌对垃圾填埋初期渗滤液化学需氧量的影响

通过模拟柱实验 ,研究了回灌对垃圾填埋场初期渗滤液 CODCr的影响。研究结果表明 ,模拟降雨雨水的渗入且无渗滤液回灌的参照柱 ,其渗滤液出水 CODCr最高 ,一般在 70 0 0 0 mg/L 左右 ;模拟渗滤液原液回灌 ,从第 4周起因脂肪酸的积累导致渗滤液的 p H低于 6,从而抑制了微生物的生化反应 ;模拟好氧生物处理后渗滤液的回灌 ,能加速垃圾层 CODCr的溶出和甲烷化阶段的建立 ,且此时渗滤液的 CODCr变化规律符合指数方程 ;当垃圾层建立甲烷化阶段后 ,回灌 CODCr在 2 0 0 0 0 m g/L 左右的渗滤液 ,仍可促使垃圾中有机物迅速转化为气态物     

柴油机尾气中微粒粒径分布特征的实验研究

柴油机尾气中的微粒粒径大小分布范围广泛,不同直径的微粒所占的比例以及对环境和人身健康造成的危害各不相同,因此对微粒粒径特征进行研究更具有实际意义。本研究分别采用滤膜称重法和光散射法对厦工XG951Ⅲ装载机配置的国Ⅲ柴油发动机怠速工况下的尾气进行测试,研究了微粒的质量浓度分布、数量浓度分布以及质量浓度与数量浓度分布的关系。研究结果表明,从微粒质量上看,可吸入微粒(PM10)占微粒总量(TSP)的74.0%,可入肺微粒(PM2.5)占可吸入微粒的48.1%;2.5μm以下粒径范围内的微粒质量浓度是2.5~10μm粒径范围内微粒质量浓度的将近3倍,是10~100μm粒径范围内微粒质量浓度的52倍;2.5~10μm粒径范围的微粒质量浓度是10~100μm粒径范围内微粒质量浓度的18倍。数量上,在不同的数量级上,微粒数量浓度随粒径变化差距很明显,尤其是1μm以下的微粒较多。另外,质量浓度的粒径分布滞后于数量浓度。因此PM2.5排放标准中应考虑以个数浓度代替质量浓度为标准。     

二氧化钛气溶胶颗粒在石英玻璃纤维上的沉积

利用雾化挥发发生原理制备二氧化钛气溶胶,将二氧化钛气溶胶颗粒负载在石英玻璃纤维上,制备二氧化钛-石英玻璃纤维功能性空气过滤材料。实验研究了二氧化钛气溶胶发生相关参数、石英玻璃纤维直径分布、透过率曲线、最易透过粒径,并对二氧化钛气溶胶颗粒在石英玻璃纤维上的负载过程和负载形态进行了探讨。研究结果表明,发生的二氧化钛气溶胶具有可控的粒径分布和较好的分散性;中值粒径128 nm的二氧化钛气溶胶颗粒能够稳定负载在3μm的石英玻璃纤维上;二氧化钛在石英玻璃纤维上的沉积量受沉积时间的影响,沉积过程中阻力开始变化不大,随后在沉积饱和点后阻力迅速增大,滤料填充度越高沉积饱和点出现时间越早;二氧化钛粒子在纤维表面的负载形态除颗粒、团簇外,还有三维的树枝状空间结构。     

某生活垃圾卫生填埋场渗滤液的梯度分离与表征

目前,渗滤液中污染物的粒度分布及其在渗滤液污染控制中的作用日益受到关注。通过系列微滤膜(1.2μm及0.45μm)对某生活垃圾卫生填埋场渗滤液各处理单元的渗滤液进行梯度分离,发现悬浮物对COD、浊度的影响较大;COD主要在胶体态和可溶解态间分配,不同渗滤液中的分配情况不同;磷主要与胶体、悬浮物以各种形式结合而存在;细胶粒和溶解态等小分子对TN的贡献大;不同粒度物质对pH的影响不明显;总残渣在可溶态组分中所占比例较大。膜微滤处理渗滤液可以有效的去除一部分物质,使COD、TP、TN、浊度、电导率都有不同程度的降低,pH逐渐升高,但对总N、残渣的去除效果不好。     

采煤沉陷区耕地土壤微生物数量及酶活性的空间特征

通过野外调查和采样分析,研究了焦作矿区韩王矿沉陷区不同沉陷部位和不同深度耕地的土壤微生物数量及酶活性特征。研究结果表明:与对照区比较,沉陷区耕地土壤微生物数量、酶活性赋存特征及微生物类群组成比例发生了明显变化。沉陷区表层(0~5 cm)、上层(5~10 cm)、中层(10~20 cm)土壤微生物总数、细菌数量均明显减少,而下层(20~40 cm)土壤微生物总数、细菌、真菌、放线菌数量均明显升高。沉陷区表层、上层土壤细菌数量所占微生物总数比例分别降低了20.64%和13.17%,而放线菌数量所占比例分别升高了20.69%和12.66%。沉陷区表层土壤脲酶、蔗糖酶、磷酸酶、脱氢酶、过氧化氢酶和多酚氧化酶活性分别降低了1.5%、17.5%、22.0%、35.3%、20.4%和5.4%。不同沉陷部位的土壤微生物数量及部分酶活性指标空间异质性显著(p0.05)。沉陷区土壤真菌、放线菌数量、蔗糖酶、磷酸酶、脱氢酶、过氧化氢酶、多酚氧化酶活性较对照区均具有不同的垂向分布特征。表明采煤引发的地表沉陷使耕地土壤微生物数量及酶活性在水平和垂直方向上均发生了显著变化,而这些变化是导致沉陷区耕地退化、生产力降低的重要原因。     

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.     

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.     

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.     

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.     

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.     

Knowledge transfer initiative between molecular biologists and environmental researchers and regulators

A Natural Environment Research Council (NERC) funded Knowledge Transfer (KT) workshop was held in the United Kingdom (UK) to identify the needs and opportunities in the application of molecular biology and ‘omics’ techniques to environmental monitoring and risk assessment. Attendees highlighted a lack of effective communication between end-users and researchers as well as difficulties with data interpretation as reasons behind the slow uptake of molecular biology and omics techniques. A number of promising areas in which new techniques could be implemented at a practical level in the very near future were identified, thereby raising the profile of these recent technologies and providing vital proof of concept work. Molecular taxonomy, bacterial source tracking and pre-screening of chemicals for potential toxicities were all viewed as areas in which omics and molecular techniques could have immediate value, with the aim of reducing cost, increasing efficiency and providing more comprehensive data of improved quality.     

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.     

Sorption and predicted mobility of herbicides in Baltic soils

This study was undertaken to determine sorption coefficients of eight herbicides (alachlor, amitrole, atrazine, simazine, dicamba, imazamox, imazethapyr, and pendimethalin) to seven agricultural soils from sites throughout Lithuania. The measured sorption coefficients were used to predict the susceptibility of these herbicides to leach to groundwater. Soil-water partitioning coefficients were measured in batch equilibrium studies using radiolabeled herbicides. In most soils, sorption followed the general trend pendimethalin > alachlor > atrazine～ amitrole～ simazine > imazethapyr > imazamox > dicamba, consistent with the trends in hydrophobicity (log K_ow) except in the case of amitrole. For several herbicides, sorption coefficients and calculated retardation factors were lowest (predicted to be most susceptible to leaching) in a soil of intermediate organic carbon content and sand content. Calculated herbicide retardation factors were high for soils with high organic carbon contents. Estimated leaching times under saturated conditions, assuming no herbicide degradation and no preferential water flow, were more strongly affected by soil textural effects on predicted water flow than by herbicide sorption effects. All herbicides were predicted to be slowest to leach in soils with high clay and low sand contents, and fastest to leach in soils with high sand content and low organic matter content. Herbicide management is important to the continued increase in agricultural production and profitability in the Baltic region, and these results will be useful in identifying critical areas requiring improved management practices to reduce water contamination by pesticides.