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。     

矿化垃圾混配种植介质的盆栽实验研究

矿化垃圾营养成分和有机质含量较高,但含有重金属和盐分.为了解矿化垃圾的施加比例对植物的生长影响以及植物对矿化垃圾混配种植介质中营养成分的吸收和重金属的富集,将矿化垃圾和本地绿化土按照不同比例混配,研究混配种植介质的理化性质的改善条件、矿化垃圾对植物体内的生物量和叶绿素含量的影响、植物对混配种植介质中营养成分的吸收量以及植物体内各种重金属累积浓度,探索矿化垃圾的最佳施用比例.实验结果表明,矿化垃圾可改善上海本地土壤贫瘠的普遍状况,其添加质量分数在50%～75%合适,对植物生长有利.     

生活垃圾填埋场矿化垃圾分选研究

对上海市老港生活垃圾填埋场填埋龄为1～14年的矿化垃圾进行了分选研究.结果表明,填埋龄在8年以上矿化垃圾细料(粒径＜50 mm)的百分比约占60%,而填埋龄低于5年的矿化垃圾细料比例低于40%.开采出来的垃圾经分选后的产品可得到有效的资源化利用.     

准好氧填埋工艺陈腐垃圾的理化特性变化规律

针对准好氧填埋工艺,研究了实际填埋场1~5年陈腐垃圾的含水率、有机质和腐殖质等理化特性动态变化规律。结果表明,垃圾含水率、电导率、有机质均随着填埋时间的增加呈现明显的降低趋势,且导气管附近垃圾样品(0 m)垃圾含水率、有机质降低速度相对较快,在填埋3年后含水率达到相对稳定的状态,有机质含量的降低主要发生在填埋处置的第2年;垃圾pH值、腐殖质提取率和富里酸含量呈现明显升高的趋势,且距离导气管较远垃圾样品(15 m)pH值升高速度相对较快,在填埋1年左右存在明显的酸化阶段;胡敏酸含量和HA/FA比则呈现出前期升高后期降低的趋势,其中导气管附近垃圾样品(0 m)的变化明显快于距离导气管较远(15 m)的垃圾。     

拉萨污水处理厂污泥对沙化土壤改良效果

以西藏雅鲁藏布江流域沙化土壤为研究对象,采用拉萨污水处理厂脱水污泥进行添加处理,测定了不同污泥掺混量下土壤基本理化性质变化趋势,并与当地农田、草地生态系统土壤进行了比较。结果表明:随着污泥掺混量的增加,沙化土壤的孔隙度逐渐提升(P0.001),土壤密度及容重逐渐降低,在掺混量大于10%时,改良效果趋于减缓;土壤氮、磷、有机质含量呈增加趋势,在掺混量为10%~15%时与对照土壤氮、磷含量相近,在掺混量为20%~30%时,有机质含量与对照相近;土壤最大持水量呈增加趋势,在掺混量为5%~10%时即与对照土壤相近;拉萨污水处理厂污泥重金属含量远低于国家农田土壤标准,且含有一定的植物生长必需元素,是一种理想的沙化土壤改良剂。     

生活垃圾填埋场封场后种植植物中重金属迁移研究

在上海老港生活垃圾填埋场填埋单元封场的覆盖土中掺混了矿化垃圾种植植物,分析Cd、Pb、Cu、Zn 4种重金属在土壤和植物中的迁移变化,研究表明:(1)覆盖土土质从一般耕作土变成肥沃土壤;覆盖土和种植混合土重金属Cd、Pb、Cu、Zn中Cd、Pb含量相近,但种植土的Cu含量略大于覆盖原土,Zn含量远大于覆盖原土;(2)植物能富集土壤和垃圾中的重金属,木本植物的根部富集重金属的能力强于草本植物,但重金属在草本植物根、茎、叶中的迁移速度大于木本植物;(3)植物根、茎、叶的Cu、Zn含量均远大于未受污染土壤种植植物相应部位的Cu、Zn含量,种植的植物不能供家养动物食用,以免通过食物链作用危及人体安全.     

西南地区某已封场非规范垃圾填埋场垃圾稳定化进程分析

以重庆某非规范填埋场为例,针对西南地区已封场非规范垃圾填埋场的稳定化进程进行了分析。按照场地布局选取4个采样点,在垃圾体上进行钻孔取样,分析不同深度的垃圾样pH值、有机质、含水率、生物可降解度以及垃圾样浸出液和填埋气组成以及各个指标随着填埋深度的变化规律,确定不同深度垃圾体的稳定化程度。结果表明,场内垃圾已呈现矿化垃圾特征;有机质、BDM、浸出液COD以及填埋气CH4含量等4个指标与填埋深度均较好地符合一级降解反应,可以预测垃圾体稳定化临界填埋深度。根据有机质、BDM、浸出液COD以及填埋气CH4含量等4个指标与填埋深度一级降解反应函数预测临界稳定化深度为15 m,与实测值判定的稳定化填埋深度相一致性。在对非规范垃圾填埋场场地利用过程中,需要先对未稳定的上层垃圾进行清理,并在已稳定的底层垃圾体上充填其他稳定介质后利用该地块。     

微生物矿化修复重金属污染土壤

以选矿厂附近土壤为研究对象,分析了土壤中交换态重金属含量,As、Pb、Cd、Zn和Cu的交换态浓度为14.01、4.95、0.64、33.46和12.95 mg/kg。基于生物矿化原理,利用碳酸盐矿化菌生长代谢过程产生的脲酶来分解底物尿素,产生碳酸根离子,固结重金属离子,使得土壤中活泼的重金属离子转变为碳酸盐矿物态,降低其危险。研究了温度、pH和重金属离子对酶活性的影响,发现环境30℃温度有利于促进酶活性;在弱酸性条件下,底物分解量减少15%;重金属离子在低浓度时对脲酶活性影响不大,浓度提高后对酶活性抑制作用没有加剧。将制备好的微生物矿化修复制剂喷洒于1 000 m2的污染土壤中,实验结果发现,土壤中交换态重金属离子含量在0～20 cm范围内明显减少,As、Pb、Cd、Zn和Cu的交换态浓度分别减少至2.37、1.25、0.31、16.67和3.42 mg/kg。     

城市生活污泥和矿化垃圾中氮磷淋失的模拟研究

通过模拟土柱实验,分析了城市生活污泥和矿化垃圾中氮磷的迁移对地下水的影响以及矿化垃圾对氮磷的去除特性.测定项目包括总磷、总氮、硝态氮、pH和电导率(EC).结果表明:施用污泥和矿化垃圾后淋滤液的pH呈下降趋势;EC和总氮都有显著增加;硝态氮增加特别明显,容易造成地下水污染;总磷变化不大,污染地下水的可能性较小.矿化垃圾对氮的去除作用不明显,反而增加了淋滤液中的氮素含量,但对磷的去除效果明显.因此,在利用矿化垃圾取代土壤时,应注意矿化垃圾中氮特别是硝态氮的污染.     

酸性雨持续10～40年将会对日本植物造成有害影响

据户冢绩等研究表明,低于pH3的酸性雨会使植物叶枯萎,妨碍植物生长;但短时间遭受pH4的酸性雨几乎没有直接有害影响。文部省的调查结果预测,如果日本目前pH4的酸性雨持续10～40年将导致土壤恶化,从而影响植物的生育。酸性雨中的硫酸、硝酸根离子溶入森林的土壤中→使土壤酸化→对植物有害的铝离子从土壤中释出→降低植物根的活力→抑制植物的生育,是一个相关过程;据此测算出日本目前的酸性雨保持不变,使10cm土层中释放出对植物有害的5.0ppm铝离子的时     

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.     

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 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.     

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.     

Biochemical interaction of six op delayed neurotoxicants with several neurotargets

Abstract

Five organophosphorous insecticides: Leptophos, EPN, Cyano‐fenphos, trichloronate and salithion proved to cause irreversible ataxia not only to chicken but also to mice and sheep. TOCP was included as a reference. Cyanofenphos blocked the catecholamine B‐receptor binding activity with ³H‐norepinephrine at a level similar to that of the specific inhibitor propranolol in the mouse heart preparation. In the lamb heart preparation, the B‐receptor was more sensitive to Leptophos, salithion and TOCP than to propranolol. The six compounds and their oxons were screened for their in‐vitro inhibition to monamine oxidase (MAO), acetyl cholinesterase (AChE) and neurotoxic esterase (NTE) in the brain of either mouse, lamb or chicken. It is believed that their AChE inhibition stands for their acute toxicity, while NTE inhibition is responsible for their paralytic ataxia.