石油污染土壤的植物与微生物修复技术

石油污染土壤的生物修复技术具有成本低、简便高效、对环境影响小等优点,正逐步成为石油污染治理研究的热点领域,具有广阔的发展前景.介绍了我国的石油污染概况及生物修复技术在石油污染治理中的应用,重点对石油污染土壤的微生物修复、植物修复、植物一微生物联合修复技术的研究进展及各自的优点、局限性进行了综述,并提出了石油污染土壤生物修复技术研究的重点领域.     

利用植物修复污染土壤研究进展

本文介绍了植物修复技术的概念及其内涵，回顾了植物修复技术的研究历史，对该项技术的国内外研究现状与未来发展方向进行了讨论。同时指出，植物修复技术优点与其局限性。文中还对利用植物修复重金属污染的土壤应该考虑的因素作了简单的讨论     

植物修复--大面积低剂量放射性污染的新治理技术

放射性污染是当今难以治理的环境污染问题,对于大面积低剂量的放射性污染,植物修复是种较适用的新型治理技术.系统阐述了植物修复技术的概念与内容,对放射性污染植物修复技术研究现状与进展、植物修复的优缺点进行了重点评述,并对这技术在未来放射性污染治理中的应用与研究提出了建议.     

多环芳烃的毒性及其治理技术研究

多环芳烃（PAHs）是一类长久存在于环境中，具有致癌、致畸与致突变等特性的环境优先污染物。文中概括介绍了PAHs的来源、毒性及毒理，重点阐述了目前国内外对PAHs污染采取的处理方法及治理技术，包括微生物修复、植物修复和微生物-植物联合修复等。     

植物修复及重金属在植物体内形态分析综述

植物修复是重金属污染土壤治理的重要方法,因其具有高效、经济及生态协调性等优势而广受关注。当前相关研究主要包括超积累植物体内重金属的迁移转化与形态分析方法,土壤修复后植物的减量化、无害化和资源化利用等方面。实验研究及修复工程中存在的问题主要体现为:(1)基础研究方面,目前对植物超积累重金属的分子机制、调控原理等方面的研究不够完善;(2)应用技术方面,修复植物的规模化种植、适用的栽培技术、收获物安全处置及资源化利用方面仍是植物修复技术发展的瓶颈。因此,目前需要深入研究超积累植物吸收、运输和积累重金属的生理机制,利于植物生长的农业措施以及用于修复的植物收获后的相应处理技术。同时,应结合重金属在植物体内的形态,对修复后的植物进行合理的减量化、无害化、资源化处理,以便于更加科学合理地选择土壤重金属修复植物,大规模推广植物修复技术的应用。     

重金属污染土壤淋洗技术的基础研究与工程应用进展

随着城市结构调整,工业企业易地搬迁后遗留下大量污染场地,严重威胁人居环境,亟待开展土壤修复.土壤淋洗技术具有工艺简单、处理范围广、修复效率高和治理费用相对低廉等优点,是目前修复重金属污染土壤最有效的技术之一,同时对于有机物污染土壤也具有显著修复效果.经过大量资料、文献调研,系统梳理土壤淋洗技术在国内的研究现状,结合实际...     

植物修复重金属污染土壤的强化措施

植物修复技术作为一种新兴的绿色环保技术,有着高效、经济和生态协调等特点而成为当前研究的热点领域,而且由于其修复的彻底性和环境友好性而在治理污染土壤实地过程得到广泛应用.概述了当前植物修复研究的基本类型和修复机理,并着重从生物技术、农艺措施和物理化学等强化手段上阐述了利用超富集植物修复污染土壤,以进一步提高超富集植物的修复效率,为大规模治理重金属污染土壤和商业化应用提供技术途径和科学依据.     

重金属污染土壤的植物修复技术与其他技术联用的进展与前景

随着工业和经济的发展,土壤重金属污染越来越严重,因此重金属污染土壤的修复迫在眉睫.植物修复技术因其经济、环保等优点已经成为国内外研究的热点,但存在修复植物稀少的问题.将其他技术与植物修复技术联用可能是突破植物修复这一局限性的关键举措之一.介绍了基因工程技术与植物修复技术联用的研究进展;总结了微生物技术与植物修复技术联用...     

甲基叔丁基醚的污染治理技术研究进展

甲基叔丁基醚(MTBE)是一种无铅汽油添加剂,其广泛使用造成了土壤和地下水污染;同时对人类有可疑致癌作用,因此成为人们关注的焦点.对近年来国外MTBE的污染治理技术研究进展进行了综述,并对主要方法进行了对比.在适宜的微生物存在条件下,MTBE的生物降解是可以发生的;植物修复技术可用于地下水和土壤污染治理;物理化学方法种类繁多,包括吸附和高级氧化等,其处理效率高成本也较高;新的处理技术如渗透性活性障壁PRB、膜分离/催化技术等也在研究之中.     

人工湿地植物对重金属铅的抗性

随着含铅废水污染引起的生态安全问题日益加重,以及处理要求的日益严格,含铅废水的处理已成为目前研究和工程实践的重点。由于植物修复技术操作管理方便,成本低廉,处理效率高和选择性强等优点,植物修复已成为处理含铅废水的较有潜力的和行之有效的优化技术。实验参照水体重金属污染现状,模拟设置不同铅浓度的水体,通过盆栽水培实验及实验室分析测试,分别研究了重金属铅对芦苇、香蒲、鸭跖草这3种植物生长的影响、分析各种植物对铅的抗性的表现及重金属在植物体内的积累和分布,为人工湿地植物的选择提供科学依据。     

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.     

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.