鄱阳湖沉积物重金属质量基准研究及其生态风险评估

为有效保护鄱阳湖流域水环境质量和水生态系统健康,对鄱阳湖19个采样点的表层沉积物样品及其孔隙水中的4种典型重金属(Cu、Pb、Zn、Cd)含量及赋存形态进行了测定,利用相平衡分配法(EqPA)初步探讨了沉积物重金属质量基准,并以此为评价标准,采用潜在生态风险指数法对鄱阳湖沉积物重金属生态风险进行评估。基于物种敏感度分布(SSD)法确立的重金属水质基准,建立沉积物重金属质量基准低值(SQC-L,Cu、Pb、Zn、Cd的SQC-L分别为57.37、49.40、98.51、2.74mg/kg)和高值(SQC-H,Cu、Pb、Zn、Cd的SQC-H分别为140.86、710.45、189.06、47.20mg/kg),经过对比分析,推荐采用SQC-H和SQC-L为鄱阳湖流域沉积物重金属质量基准。以SQC-L为评价标准,采用潜在生态风险指数法,对鄱阳湖19个采样点的生态风险进行评估,发现鄱阳湖流域受到了一定程度重金属污染,主要集中在南部湖区,具有一定的生态风险。     

乌梁素海表层沉积物重金属分布特征及生态风险评价

采样分析了内蒙古乌梁素海表层沉积物中Cu、Zn、Pb、Cr、Cd、Hg和As的含量、分布特征和富集状况,分别以现代工业化前正常颗粒沉积物中重金属含量的最高背景值和河套地区土壤中重金属含量背景值为参照,采用瑞典科学家Lars Hakanson的潜在生态危害指数法对7种重金属的富集系数和生态危害系数以及各采样点的生态危害指数进行了评价。结果表明,乌梁素海表层沉积物中As和Pb的空间变异性较大;以2种背景值为参比得出的重金属污染水平顺序相近,Hg和As为对乌梁素海生态环境具有潜在影响的主要重金属元素;同时表明,以河套地区土壤重金属背景值为参照更能直观地反映出乌梁素海表层沉积物中重金属的污染程度。     

典型农业活动区土壤重金属污染特征及生态风险评价

联合野外采样和室内分析,以典型农田土壤为研究对象,分析土壤中重金属Cr、Ni、Cu、Zn、Cd、Pb、As和Hg的含量及污染特征,并采用单因子污染指数法、内梅罗污染指数法及潜在生态危害指数法,对农田土壤进行生态风险评价,同时利用主成分因子分析法,提取出3主因子,分析土壤重金属可能来源。结果表明,研究区农田土壤各重金属含量均高于背景值,表层污染程度高于底层;各重金属单因子污染指数对应污染等级均为清洁,内梅罗污染指数为0.46,污染等级为安全。潜在生态风险评估结果显示,研究区土壤重金属污染的潜在生态风险危害程度为中等,各重金属的潜在生态危害程度依次为CdHgAsCuPbNiCrZn。主成分因子分析显示,研究区土壤中Hg、As和Cr主要由工业污染源贡献,土壤中Cd、Pb的污染主要来源于不合理的农业生产活动和居民生活,Ni、Zn和Cu与自然成土过程密切相关。综合评价表明,尽管研究区农田土壤目前重金属污染情况较轻,未达到警戒水平,但由于城市化的发展及长期现代化农业耕作活动造成农田土壤重金属的富集,因此,增强农田土壤安全性生产管理、严控土壤污染源与推行标准农业生产是十分必要的。     

胶州湾表层沉积物重金属污染分布特征及其生态风险评价

根据2009年对胶州湾东岸表层沉积物中重金属调查结果,对重金属含量分布及富集特征进行分析,并采用潜在生态危害指数(RI)法对其生态危害程度进行评价。结果表明,胶州湾东岸表层沉积物中的重金属含量,除7月的Cu、Cr平均含量略低于12月外,其他重金属(Cd、Zn、Pb、As)平均含量7月均高于12月。在表层沉积物中Cd的污染程度最高,7月平均污染指数达1.68。单个重金属潜在生态危害系数(Eir)表明,Cd的Eir大于其他重金属的Eir,其他重金属的Eir均小于轻微危害程度的划分标准,表明对胶州湾东岸生态环境具有潜在影响的重金属主要是Cd,从多个重金属的RI均值看,均小于150,属于轻微生态危害。     

琼北火山岩地区水田和旱地土壤中重金属的累积特征比较

为分析琼北火山岩地区土壤中重金属(As、Cd、Cr、Pb、Ni、Hg)的累积特征,采集旱地和水田的土壤表层样品,并对样品理化性质及重金属含量进行了分析,采用单因子污染指数法和内梅罗综合污染指数法对重金属污染状况进行了评价。结果表明,研究区旱地与水田土壤均呈强酸性-酸性,旱地土壤阳离子交换量(CEC)(4.66 cmol/kg)略大于水田土壤CEC(3.42 cmol/kg),表明旱地土壤保持养分的能力优于水田土壤。与海南土壤背景值比较,研究区旱地和水田土壤中Cd、Cr、Pb和Ni 4种重金属均有不同程度的累积,其中Cd累积程度较重。研究区旱地和水田土壤中Cr与Ni均具有较高的正相关关系,说明旱地和水田土壤中Cr与Ni可能同源,且受基性火山岩地质背景的影响较大。内梅罗综合污染指数评价结果表明,研究区旱地土壤重金属污染明显高于水田土壤,水田土壤重金属为轻度污染,而旱地土壤重金属已达到中度污染,尤其是Cr和Ni污染比较严重,应引起重视。     

盐城海岸带土壤重金属污染风险评价比较研究

以盐城海岸带为研究区,分别采用地质累积指数法、内梅罗指数法和潜在生态危害指数法对土壤重金属污染进行风险评价,分析不同方法在评价同一研究区时结果的差异性。结果表明,研究区Cr、Ni、Zn、Cd质量浓度平均值超过盐城海岸带环境背景值。地质累积指数法显示研究区土壤重金属在中度污染到强污染;内梅罗指数法显示研究区土壤重金属为重度污染;潜在生态危害指数法显示研究区土壤重金属处于中度潜在生态危害程度。3种方法评价结果的严重程度为:内梅罗指数法地质累积指数法潜在生态危害指数法。3种评价方法均有一定缺陷与局限性,相对于单一方法的污染评价,采用多种方法评价土壤重金属污染可使评价结果更加客观。     

江苏省某镇土壤重金属污染评价

为了解江苏省某镇表层土壤重金属污染特征,采集并测定了190个土壤样品的As、Cd、Hg和Pb 4种重金属含量,分析土壤重金属的分布特征,综合运用内梅罗综合污染指数法和污染负荷指数法两种评价方法对土壤重金属污染状况进行评价。结果表明:该镇表层土壤中As、Cd和Pb含量平均值高于土壤背景值,Hg与之相反。4种重金属都是主要受到点源污染的影响,其中As的高含量区主要分布在镇的正西边,Cd和Pb的高含量区主要分布在镇的中心区域,Hg的高含量区主要分布在东部以及东北区域。经内梅罗综合污染指数法评价,安全、警戒线、轻污染、中污染和重污染样点的比例分别为5.79%、32.11%、52.11%、4.74%和5.26%。经污染负荷指数法评价,无污染、轻度污染、中度污染和重度污染样点的比例分别为73.69%、25.26%、1.05%和0%。在内梅罗综合污染指数法和污染负荷指数法评价的结果中,有55.26%的样点评价结果相同,而44.74%的样点不同,但都显示出污染程度从镇中心向四周逐渐降低的变化态势。     

层次分析法与地理信息系统在农田土壤重金属污染评价中的应用

以《土壤环境质量标准》(GB 15618—1995)二级标准作为评价标准,采用以改进层次分析法确定权重的加权平均法对南京市郊典型蔬菜地的土壤重金属污染状况进行了评价。结果表明,研究区土壤中Cu、Pb、Cr的单因子污染指数平均值均小于1,含量超标率均不超过10.32%,而Cd的单因子污染指数平均值达2.15,含量超标率为84.13%,急需对该区土壤和受体做进一步的Cd污染深入调查或风险评估;研究区土壤重金属综合污染指数平均值为1.28,属玷污水平;利用ArcGIS 8.3软件进行土壤重金属污染的空间分布特征分析结果表明,研究区各元素的污染程度为Cd>Pb>Cu>Cr,各元素的污染格局较为相似,城市化活动对土壤污染贡献较大;研究区有81.16%的土壤重金属污染级别为玷污,3.78%处于本底级,15.06%处于安全级。     

广东省主要蔬菜产地土壤中重金属含量调查与评价

调查了广东省20个市(县)52个主要蔬菜产地土壤重金属含量,并以<土壤环境质量标准>(GB 15618-1995)二级标准为评价标准,采用单项污染指数法和综合污染指数法对其进行评价.结果表明,156个蔬菜产地土壤样品中Cd、Hg、As和Cr的超标率分别为9.62%、3.85%、0.64%和0.64%,Pb未出现超标;有8个蔬菜产地土壤重金属处于轻污染,13个蔬菜产地土壤重金属处于警戒限,其余蔬菜产地土壤重金属均在安全范围内.蔬菜产地土壤Cd污染最为普遍和严重,其次是Hg和As,且Cd的变异系数为103.67%,预示蔬菜产地土壤可能受到Cd的点源污染.珠江三角洲地区蔬菜产地土壤重金属含量普遍高于其他地区,粤西和粤北地区个别蔬菜产地土壤重金属超标.     

苕溪流域典型区域重金属污染特征

从苕溪流域景观单元角度研究重金属污染特征,因人类活动是重金属污染的主要来源,所以在苕溪流域内选择采集典型工业区、农业区和城镇生活区附近河道的沉积物,分析各典型区域重金属Pb、Cd、Cr、As、Hg、Cu和Zn的含量特征,并用潜在生态危害指数法评价。结果表明,按照《土壤环境质量标准》,苕溪流域典型工业区主要是Hg、Cu和As的污染,典型农业区和城镇生活区主要是Hg的污染。各元素间的相关性分析表明,在工业区:Zn-As、Zn-Pb和As-Pb之间存在相关关系,说明它们的同源性很高。在农业区:Cu-As、Cu-Cd之间存在显著相关关系,其来源有可能相似。在城镇生活区Zn-As、Zn-Cd之间存在很高的相关性,说明它们有很高的同源性。由多种重金属潜在潜在生态风险评价结果可知:苕溪流域典型工业区、城镇区和农业区的沉积物处于低潜在生态风险。     

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.