煤矿复垦区土壤重金属分布特征与质量评价

为保证煤矿复垦区种植农作物的充填复垦土壤的生态安全,以淮南矿区煤矸石充填复垦地为研究对象,通过对研究区内Cd、Cr、Ni、Pb、Cu、Zn和Hg 7种重金属不同深度含量分析,总结其纵向分布特征,并将研究区土壤重金属含量与淮南市土壤背景值、《土壤环境质量标准》(GB 15618-1995)作比较,分析这7种重金属的污染程度.结果表明,这7种重金属都有不同程度的污染,其中土壤受Cd污染最严重,土壤中重金属垂直方向上无确定分布规律.总体而言,土壤重金属潜在生态风险属于强生态危害.从垂直方向来看,重金属潜在生态风险指数(RD随着深度的增加出现先下降后升高的趋势,其中40～60 cm深度的RI最大.重金属生态危害程度依次为Cd＞ Hg＞ Ni＞ Cu＞ Cr＞ Pb＞ Zn,其中Cd为矿区土壤中最主要的重金属污染生态风险因子.     

鹤壁矿区煤矸石淋滤实验研究

对鹤壁煤矿区第10矿煤矸石进行连续淋溶试验,模拟煤矸石矿井填充后对地下水环境的影响.测定pH值、电导率、F-、总硬度、Zn、Mn、Cr6 、Cd、Cu和Pb等项目,实验结果表明,煤矸石淋出液中F-和Cr6 超标,Mn接近标准,pH值偏高,对地下水环境存在一定影响.其他各元素含量甚微,多未检出.     

模拟酸雨对磷酸二氢钾钝化污染土壤Cu、Cd、Pb和P释放的影响

以磷酸二氢钾(PDP)钝化后的重金属污染土壤为研究对象,通过室内土柱淋溶实验,考察在pH为3.5、4.5和5.6的模拟酸雨作用下土壤Cu、Cd、Pb和P的释放特征。结果表明:PDP处理较对照处理显著增加了淋出液中pH、电导率(EC)和总有机碳(TOC)含量,但不同pH模拟酸雨对对照和PDP处理淋出液pH、EC和TOC含量影响较小。对照处理中,正磷酸盐含量维持在较低水平(0.02~0.13 mg·L~(-1));PDP处理下,正磷酸盐含量在1~3 L和4~12 L分别是《地表水环境质量标准》(GB 3838-2002)五类水标准(总磷含量0.4 mg·L~(-1))的55.1~819倍和9.46~46.6倍,对地表水表现出较大的富营养化风险。PDP处理较对照处理显著降低了淋溶初期淋出液中的Cu、Cd和Pb含量,但是随模拟酸雨pH降低,对照和PDP处理的土壤淋出液中Cu、Pb含量均未表现出显著差异。因此,PDP处理能够显著钝化污染土壤中的Cu、Cd和Pb,但需关注酸雨淋溶下过量磷释放对地表水富营养化的潜在风险。     

施用垃圾堆肥土壤重金属在不同温度和酸雨条件下的淋溶特征

采用淋洗法,研究了垃圾堆肥中重金属在不同温度与模拟酸雨条件下的淋溶特征。结果表明,随着淋洗次数的增加,淋洗液中Cd、Cr、Cu、Ni和Pb的含量都有很大程度的减少。Cd、Cr、Cu和Ni 4种金属在模拟酸雨的情况下淋出量明显高于蒸馏水的情况,增幅都在116%和351%之间,差异显著(P<0.05)或极显著(P<0.01),而酸雨对Pb的淋出影响较小。在酸雨淋洗下,重金属的淋出率在30℃时达到最大,其中Ni随着温度的变化相对较小。而在蒸馏水淋洗下,重金属的淋出率随着温度的变化相对平稳。此外,5种重金属的淋出率明显不同,其中Cr和Ni的淋出率相对较大,Pb最小。     

鹤壁矿区煤矸石淋滤实验研究

对鹤壁煤矿区第10矿煤矸石进行连续淋溶试验,模拟煤矸石矿井填充后对地下水环境的影响.测定pH值、电导率、F^-、总硬度、Zn、Mn、Cr^6＋、Cd、Cu和Pb等项目,实验结果表明,煤矸石淋出液中F^-和Cr^6＋超标,Mn接近标准,pH值偏高,对地下水环境存在一定影响.其他各元素含量甚微,多未检出.     

几种模拟处理方式污泥淋出液重金属与养分特征

为了减少城市污泥重金属对农田的污染,更好地实现污泥农业资源化利用,通过盆栽实验研究不同处理(对照、黑网、附Fe黑网、附Fe黑网+K2SO4及附Fe黑网+玉米)对城市污泥淋出液重金属和养分含量等的影响。结果表明,黑网可降低污泥淋出液的Zn﹑Cd总量,且没有减少污泥淋出液中氮、磷和钾的总量。Fe(OH)3可使淋出液中Zn总量降低,但同时也显著减少了淋出液中的磷总量。K2SO4可降低淋出液中的Cu总量,且促进Fe结合磷的释放。玉米的种植可使污泥的总重降低,同时玉米籽粒和茎叶重金属含量达到饲料标准。综合来看,任何处理每次淋出液的Cu、Zn、Pb、Cd浓度均符合农田灌溉水标准,淋出液氮、磷、钾量占原污泥中氮、磷、钾总量的比例(0.98%～9.88%)远远大于重金属元素(Cu,Zn,Pb,Cd)占原污泥对应重金属总量的比例(0.04%～0.41%),污泥淋出液作为农田灌溉水进行肥水利用将是污泥农业资源化利用的适合途径,同时黑网+玉米处理可能是较理想的污泥综合处理利用方式。     

重金属复合污染土壤稳定化研究及效果评价

用自制稳定化试剂CTS-AC01试剂对广西河池某砒霜厂遗址As、Cd、Pb、Zn复合污染土壤进行稳定化研究并进行效果评价。结果表明:(1)CTS-AC01试剂可以降低土壤中重金属的毒性特征浸出程序(TCLP)浸出液浓度,使As、Cd、Pb、Zn的稳定效率分别达到87.7%、93.7%、90.9%、99.5%;(2)经过20次模拟淋溶,淋溶液中As、Cd、Pb、Zn的质量浓度分别为0.199、0、0、0.017mg/L,除As浓度超过《地表水环境质量标准》(GB 3838—2002)的Ⅴ类水质标准外,其他3种重金属均已达标;(3)通过土壤中重金属形态分析发现,稳定化主要是将可交换态和氧化结合态向残渣态转化,但20次模拟淋溶对土壤中重金属形态的影响不大,更长期的淋溶作用有待进一步研究。     

辽宁省红透山铜矿区土壤中重金属迁移特征研究

采用柱淋溶实验模拟辽宁省红透山铜矿区土壤中重金属的淋溶迁移特征,研究了淋溶液pH、电导率(EC)和重金属含量的变化及其相关性,分析了重金属在淋溶前后的总量和形态变化,并初步探讨其生态与健康风险.结果表明,在1～3次淋溶中,淋溶液pH迅速下降,土样中的部分酸性物质被快速溶出,在第3次淋溶之后,淋溶液pH缓慢上升;淋溶初期淋溶液EC大幅度、迅速降低,此后随着淋溶次数的增加EC缓慢降低;Fe、Mn、Cu、As、Cd均能从土样中溶出进入淋溶液,其中Fe、Mn、Cu、As的溶出主要在淋溶初期,而Cd除了在初期有所溶出外,在淋溶后期还存在二次溶出释放阶段;淋溶后土样中绝大部分重金属总量均有所下降,各重金属的解吸率为Cd＞As＞Fe＞Cu＞Mn＞Zn,其中以Cd、As含量下降最为明显,而Zn基本未溶出;淋溶前后土样中重金属的活性态(弱酸提取态(BCR-1)、可还原态(BCR-2)、可氧化态(BCR-3))含量发生了不同程度的变化,Fe的活性态含量在淋溶后变化很小,Mn、As的活性态含量在淋溶后有所上升,而Cu、Cd的活性态含量在淋溶后有所下降;随着淋溶的进行,土壤中各重金属的赋存形态发生了一定变化,从而可能引起其生态与健康风险的改变.     

植物处理污泥对华南红壤淋出液重金属的影响

利用2年的盆栽试验,研究了植物处理对污泥农用后华南红壤淋出液重金属的减少效果.设置了对照、无植物污泥处理、单种污泥处理和套种污泥处理.结果表明,不同处理污泥施用于红壤表层后,每次淋出的土壤淋出液中Cu浓度均达到《地表水环境质量标准》(GB 3838-2002)V类标准,但Zn、Cd和Pb浓度则不是每次均达到V类标准.土壤淋出液中Zn、Cd浓度超出V类标准限值时,单种污泥处理对其影响较小,且单种污泥处理土壤淋出液中Zn、Cd浓度分别为无植物污泥处理的12.6％～77.5％和21.5％～53.5％.3个施污泥处理的土壤淋出液中Pb浓度没有明显差异.与无植物污泥处理相比,套种植物处理可以显著降低污泥对土壤淋出液中Zn、Cd、Cu和Pb总量的影响,分别占无植物污泥处理的51.6％、35.4％、51.7％和59.1％,同时显著降低土壤淋出液体积(降低了20.3％);单种植物处理仅显著降低污泥对土壤淋出液中Zn、Cd和Cu总量的影响,分别占无植物污泥处理的51.0％、39.6％、62.8％.     

嗜酸氧化亚铁硫杆菌淋溶煤矸石过程中铁锰铬形态的释放特征

为研究微生物作用下煤矸石中重金属形态的淋溶释放特征,以湖南湘潭某煤矿矸石为研究对象,分析了接种嗜酸氧化亚铁硫杆菌(Acidithiobacillus ferrooxidans)的淋溶液中铁、锰和铬金属离子浓度与矸石中相应金属形态的相互关系。结果表明:新鲜煤矸石中铁锰铬的背景值对其释放特性存在影响,接种微生物对矸石中的3种金属释放有促进作用,从其释放浓度来看,FeMnCr;矸石中铁主要以残渣态形式存在,而锰主要以铁锰氧化物结合态存在,经微生物的淋溶释放作用后铁的铁锰氧化态和残渣态减少,而Mn的可交换态减少,但是残存态增多,Cr的各种形态变化不太明显;淋溶液中金属离子浓度和矸石中相应金属形态的相关分析和逐步回归分析结果表明,接种微生物的淋溶液中铁离子浓度与铁的有机结合态和残渣态存在显著相关关系,而锰离子浓度主要与矸石中锰的可交换态存在非常显著的相关关系。     

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.