1株耐冷耐碱好氧反硝化菌的鉴定及其脱氮特性

从贵州冬季水田泥土中分离得到1株好氧反硝化菌,并将其记为菌株B,通过16SrRNA基因测序与形态学分析,将菌株B鉴定为假单胞菌属(Pseudomonas sp.)。对菌株B的好氧反硝化脱氮特性研究表明,该菌在温度低至5℃时对反硝化液体培养基中硝酸盐氮和TN的去除率分别仍达43.16%、27.57%;当pH高达10.0时,菌株B对硝酸盐氮和TN的去除率分别仍达75.10%、67.65%。菌株B的最适培养条件为:温度15℃、pH 7.0、转速150r/min、接菌量1.5×10~(8 )cfu,以丁二酸钠为碳源,碳氮比(C/N,质量比)为15,在此条件下培养48h后,对硝酸盐氮和离心后的TN的去除率分别高达98.60%、93.85%。可见,菌株B是1株耐冷耐碱的好氧反硝化菌,对低温和碱性废水脱氮有较好的应用潜力。     

一株贫营养异养硝化-好氧反硝化细菌的分离鉴定及脱氮特性

从水源水库沉积物中筛选出一株具有较高脱氮效率的异养硝化-好氧反硝化菌SF9。扫描电镜观察其形态特征为(0.2~0.4)μm×(0.4~0.8)μm椭球状,16S r DNA序列分析表明菌株与Delftia lacustris DSM 21246(T)相似性为100%,并分析其系统发育分类地位,对该菌进行贫营养反硝化特性研究。结果表明,该菌在分别以硝氮、亚硝氮及氨氮为唯一氮源时去除率分别达81%、64%和40%。同步硝化反硝化研究表明,该菌在氨氮存在的情况下会优先利用氨氮,在以氨氮与硝氮为氮源时和以氨氮与亚硝氮为氮源时氨氮的去除率分别达81%和74%。将菌株接种到微污染源水(总氮2.34mg/L、C/N为1.2)水体中,总氮72 h去除率达到35%,TOC消耗30%。结果表明,菌株SF9与其他已报道的好氧反硝化菌相比,能耐受更低的C/N比,可作为微污染水源水微生物修复的高效菌剂。     

3株贫营养好氧反硝化细菌的分离鉴定及反硝化特性

贫营养好氧反硝化细菌在水环境能量流动和物质循环过程中扮演着重要的角色。从山东某水源水库沉积物中共驯化分离出216株好氧反硝化细菌,复筛得到3株高效菌株ZN1、ZN2和ZN3。经形态学指标和16S rRNA序列分析,ZN1和ZN3属于铁还原细菌(iron-reducing bacterium),ZN2属于粘液菌属(Zoogloea sp.)。关键酶基因检测表明3株菌均含有周质硝酸盐还原酶基因(nap A)。在30℃、120 r/min条件下,培养47 h后3株菌对培养液中NO3-N的去除率均在80%以上,TN去除率均在40%以上,且无明显的亚硝氮积累。对3株菌分别进行原水适应,以20%的梯度增加原水的比例直至100%原水。原水培养72 h后,3株菌NO3-N去除率为30%~40%,TN去除率为20%~25%。     

耐低温贫营养好氧反硝化菌群脱氮特性及安全性

针对微污染水体强化原位生物脱氮技术同时面临低温、贫营养及好氧问题,对实验室已分离筛选的贫营养好氧反硝化菌和耐低温好氧反硝化菌进行菌源重组,构建出高效耐低温贫营养好氧脱氮功能菌群T1(Y3+F3+H8)和T2(Y3+F4)。研究不同投菌量条件下菌群的脱氮特性,结果表明,投菌量对T1脱氮效果有一定影响,0.1、0.2和1.0 mg/L投量对NO3--N去除率为71%、91%和100%,总氮去除率为56%、34%和52%;T2菌群,当投量为0.2 mg/L时,对NO3--N、总氮去除率最大可达66%和59.48%。对菌群T1、T2进行生物安全性分析,采用次氯酸钠进行消毒,其生物灭活率均达到99.9%以上。     

一株耐盐好氧反硝化细菌的分离鉴定及其脱氮特性

从处理高盐废水的生物接触氧化工艺成熟活性污泥中分离得到一株耐盐好氧反硝化细菌F10.根据形态学特征、生理生化以及16S rRNA基因序列测定分析,初步判定该菌株为盐单胞菌属(Halomonas sp.).菌株能在盐度为3%~7%的培养基中良好的生长及脱氮,最适盐度为3%(以Na Cl计),最适碳源为乙酸钠,最适p H为7~8,最适温度为30℃.该菌株能利用NO-3-N进行反硝化作用,在盐度为3%的反硝化培养基中24 h内对NO-3-N的去除率达到92.6%,36 h基本完全去除。该菌株在3%盐度下表现出良好的异养硝化-好氧反硝化性能,初始硝态氮浓度在270 mg/L时,菌株的脱氮率可达90%以上,氨氮的去除率可达75%以上,脱氮过程中无NO-2-N积累,可实现同步硝化反硝化,具有一定的工程应用价值。     

嗜盐好氧反硝化菌SF16的脱氮特性

从海洋沉积物中分离筛选出一株新型的嗜盐好氧反硝化细菌SF16,经形态观察、生理生化实验、16S r DNA序列分析,鉴定该菌株为魔鬼弧菌(Vibrio diabolicus)。菌株SF16存在周质硝酸盐还原酶(nap A)基因,进一步证实其具有好氧反硝化能力。菌株SF16反硝化适宜条件为盐度3%~5%,碳源为乙酸钠,C/N值10~12,在此条件下,经过48 h培养,NO-3-N浓度从136.43 mg·L-1降至0.39 mg·L-1,且NO-2-N积累量仅为1.96 mg·L-1,总氮去除率高达98.28%。将菌株SF16接种于牡蛎壳填料曝气生物反应器中,用于处理人工合成含盐废水,NO-3-N、TN和COD的去除率分别达到99.87%、97.70%和75.34%。研究结果表明菌株Vibrio diabolicus SF16在含盐废水/富营养化水体处理工程中具有良好应用前景。     

一株异养硝化-好氧反硝化功能菌的分离鉴定及其脱氮特性

从活性污泥中筛选出一株具有异养硝化同时好氧反硝化功能菌N7,经分析鉴定为Acinetobacter calcoaceticus(醋酸钙不动杆菌)。以硫酸铵为氮源、丁二酸钠为碳源,菌株N7对NH+4-N去除率高达99.2%,TN去除率为67.1%,异养硝化效果较好。分别以硝酸钾和亚硝酸钠为氮源,在30℃,150 r·min-1下培养,其TN去除率分别为62.7%和75.0%,表明N7具有良好的好氧反硝化效果。单因素实验结果表明菌株N7的最佳反硝化条件为:温度30℃、转速230 r·min-1、C/N 35、pH 8.1。     

异养硝化-好氧反硝化菌ADN-42的脱氮特性

从大连海域典型繁茂膜海绵(Hymeniacidon perleve)中筛选出1株耐盐异养硝化-好氧反硝化菌,通过形态观察、生理生化实验和16S rRNA基因序列分析,确定其为假单胞菌属(Pseudomonas),命名为ADN-42。其异养硝化-好氧反硝化条件为氯化铵为氮源,柠檬酸三钠为碳源,温度30℃,C/N值为12,摇床转速150 r/min,NH+4-N初始浓度约300 mg/L,盐度为40 g/L Na Cl,在此条件下菌株84 h时NH+4-N去除率为75.4%,无硝态氮产生,亚硝态氮最大积累量为8.3 mg/L;将菌株投加到NH+4-N和NO-2-N混合体系中,混合系统比仅以NH+4-N为氮源的体系的NH+4-N去除速率提高了12.7%;研究结果表明Pseudomonas sp.ADN-42可能是一株有着良好应用前景的高效耐盐异养硝化-好氧反硝化菌。     

一株高效异养硝化-好氧反硝化菌的分离鉴定及脱氮性能

从经驯化的污泥中筛选出一株异养硝化-好氧反硝化细菌,编号为TN-05,通过形态学特征观察,生理生化特征试验和核酸序列分析鉴定其为门多萨假单胞菌（pseudomonasmendocina）。同时对其进行脱氮性能研究,结果表明,TN-05具有较好的异养硝化能力,菌株在培养至48h时对总氮和氨氮去除率均能达95％以上。通过反硝化能力验证实验发现,菌株对NO3-N和N0f—N也分别具有较好的去除效率。将菌株应用于人工合成废水中,发现对废水中氨氮优先利用并能在24h时使去除率接近100％,对硝态氮和亚硝态氮也具有一定的去除效率。因此,菌株TN-05是一株同时具备异养硝化和好氧反硝化能力的高效菌株。     

生物脱氮好氧阶段不同反应过程N_2O产量

在成功实现生活污水短程生物脱氮的基础上,采用体积为3 L的小试反应器,利用在线DO监测手段控制DO=1.0 mg·L~(-1),通过投加Na NO2的方式控制系统初始NO~(-2)-N=40 mg·L~(-1),以丙烯基硫脲(ATU)抑制NH+4-N的氧化过程,考察了生物脱氮好氧阶段不同反应过程中N_2O的产生量。结果表明,除缺氧反硝化细菌的反硝化过程外,好氧条件下,氨氧化菌(AOB)能够以NH+4-N作为电子供体,NO~(-2)-N作为电子受体,进行反硝化脱氮过程,其反硝化产物为N_2O。生物脱氮好氧阶段AOB的好氧反硝化和异养菌的缺氧反硝化反应中,N_2O的产量分别占分别占进水总氮(NH+4-N+NO~(-2)-N)的7.23%和7.80%。好氧阶段NH+4-N和NO~(-2)的氧化过程中,几乎没有N_2O的产生。     

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.     

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.     

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.     

土壤中砷的化学平衡

本文比较详细地综述了砷的化学特性,环境背景值及来源和循环,土壤中砷的三大化学平衡即沉淀溶解平衡,氧化还原平衡,吸附解吸平衡,以及微生物对砷的转化。     

Elemental uptake by edible herbs and lettuce (Latuca sativa)

The total concentration of toxic elements (aluminum, cadmium, chromium and lead) and selected macro and micro elements (iron, manganese, copper and zinc) are reported in six leafy edible vegetation species, namely lettuce, spinach, cabbage, chards and green and red types of Amaranth herbs. Although spinach and chards had greater than 125 mv of iron, both the amaranthus herbs recorded > than 320 μ g g^{? 1} dry weight. In both the spinach and chard species, the Mn and Zn levels were appreciable recording > 225 μ g g^{? 1} and 150 μ g g^{? 1} dry weight, respectively. Aluminum concentrations were (in μ g g^{? 1} dry weight) lettuce (10), cabbage (11), spinach (167), chards (65), amaranthus green (293) and amaranthus red (233). All the micro and macro elements and the toxic elements (Ni, Cr, Cd and Pb) elements analyzed, were below the recommended maximum permitted levels (RMI) in vegetables. Further the elemental uptake and distribution of the nine elements, at three growth stages of the lettuce plant grown on soil bed under controlled conditions are detailed. In the soil, except for iron (16%), greater than 33% of the other cations were in exchangeable form. Generally in the lettuce plant, roots retained much of the iron (> 224 μ g g^{? 1}) and aluminum (> 360 μ g g^{? 1}), while leaves had less than 200 μ g g^{? 1} of iron and 165 μ g g^{? 1} of Al. Although the concentrations of elements marginally decreased with growth, the lettuce leaves had significant amounts of Mn (30 μ g g^{? 1}), Zn (50 μ g g^{? 1}) and Cu (3.6 μ g g^{? 1}). Some presence of lead in leaves (2.0 μ g g^{? 1}) was noticed, but all the toxic and other elements analyzed were well below the RMI values for the vegetables.     

The dissipation of nonlyphenol in stream and pond water under simulated field conditions

Abstract

The dissipation of 1.0 ppm nonylphenol in stream and pond water, incubated in flasks at 16°C under simulated field conditions up to 44 days indicated that the half‐life was 2.5 days if the flasks were open, and 16 days if they were closed. A transformed product was detected in the closed flasks.

Translocation of nonylphenol in water occurred when treated water samples were incubated in the presence of sediment. After 10 days, nonylphenol was detected only in the sediment, but not in water (detection limit = 10 ppb). About 80% of the nonylphenol was degraded in 71 days, but no degradation occurred if the water and the sediment were autoclaved prior to incubation.