铜绿山矿区菜地土壤重金属污染特征

以铜绿山矿区菜地为研究对象,测定了土壤和蔬菜中Cu、Zn、Pb、Cd 4种重金属的含量,分析了土壤-蔬菜体系重金属的污染特征和蔬菜对重金属的富集能力。结果表明:矿区菜地土壤中重金属Cu、Zn、Pb、Cd的污染因子分别为10.63、1.12、1.10、0.06,表明Cu污染非常严重,Zn、Pb属轻度污染,Cd无污染;参考《食品中污染物限量》(GB 2762—2017)、《食品中铜限量卫生标准》(GB 15199—94)以及《食品中锌限量卫生标准》(GB 13106—91),蔬菜中Cu、Zn污染较严重且具有普遍性;蔬菜中Cd含量虽均未超出食品安全限值,但明显高于蔬菜根部土壤中的Cd含量;叶菜类、根茎类蔬菜中Pb均未超标,瓜果类蔬菜中Pb超标;蔬菜可食部位对重金属的富集能力为CdZnCuPb;蔬菜中重金属含量与土壤重金属含量总体表现出较弱的相关性,表明蔬菜中重金属的积累不完全决定于土壤重金属的含量,还与土壤中重金属的生物有效性、环境行为及其他环境因素有关。     

污泥蚓粪的土壤改良效果及其重金属健康风险

将污泥蚓粪作为改良剂施用于土壤,研究了污泥蚓粪的最佳配比,并利用健康风险评价模型对生菜(Lactuca sativa L. var. ramosa Hort.)和小白菜(Brassica campestris L. ssp. chinensis(L.)Makino var. communis Tsen et Lee)通过摄食途径进入人体的健康风险进行了评价。结果表明,风干污泥蚓粪占混合基质总质量的10%为最佳配比,该混合基质中铬未检出,镍、铜、锌、砷、镉、铅的质量浓度分别为(5.6±0.3)、(5.9±0.3)、(20.1±2.9)、(5.8±0.7)、(0.25±0.05)、(10.20±1.10)mg/kg,均未超过《土壤环境质量标准》(GB 15168—1995)的二级标准和《农用污泥中污染物控制标准》(GB 4284—84)。该混合基质中生长的生菜和小白菜的重金属检测结果表明,《食品中污染物限量》(GB 2762—2012)中规定的铬、砷、镉和铅均未超标。健康风险评价结果表明,进行评价的铬、镍、铜、锌、砷、镉、铅不具有非致癌风险,砷、镉、铅不具有致癌风险。     

改良剂对Cd污染土壤中小白菜品质的影响

通过小白菜盆栽试验,以啤酒污泥、草木灰及其混合物作为土壤改良剂,以生物量、可溶性糖、维生素C和叶绿素含量为指标,研究了改良剂对小白菜品质的影响,并分析了土壤中Cd赋存形态的变化。结果表明,不同改良剂在性质和改良机制上存在差异,因此改良效果各不相同,其中啤酒污泥和草木灰的混合物的改良效果最好,其次是啤酒污泥,最后是草木灰。虽然3种改良剂均能降低小白菜茎叶中Cd含量和土壤中有效态(水溶态和可交换态)Cd含量,提高小白菜品质,但小白菜茎叶中Cd含量仍超过《食品中污染物限量》(GB 2762—2005)规定的蔬菜中Cd限量值。     

北京、南京、广东地区土壤中铅、锌、镉

铅、锌、镉都是土壤中的痕量元素,它们在天然土壤中含量很低,正常情况下,土壤中含镉为0.01—2ppm,平均为0.35ppm,含铅为2—300ppm,平均为35ppm,含锌为1—900ppm,平均为90ppm。它们都是环境中重要元素,现已证明,铅和镉对动植物都是有害的。锌是动植物的营养元素,但是,在一定条件下,过量的锌对人和动物可能有致癌性。因此,它们在土壤中的含量多少对动植物生长和人体健康有着重要的影响。本文根据中国科学院土壤背景协作组提供的数据,对北京、南京、广东地区土壤中铅、锌、镉的含量水平、元素间的关系等问题进行初步探讨。 一、样品来源及分析方法 根据各地区土壤母质类型,远离污染源以及按野外观察划分自然层次,采集不同类     

锰矿区土-水界面污染流中重金属来源分析

基于对湘潭锰矿红旗矿区土-水界面重金属污染流的采样分析,通过相关性和主成分分析法,研究了锰矿区土-水界面重金属污染流中的锰、镍、铜、锌、镉、铅重金属的来源以及同源性。结果表明:6种重金属的差异性、离散程度、变异性较大;锰—镍、锰—锌、锰—镉、锰—铅、镍—锌、铜—锌、铜—铅、锌—镉、锌—铅、铅—镉呈极显著正相关,镍与锰以外的其他重金属相关性都较低;3个主成分的贡献率分别为58.300%、16.628%、11.115%,累积贡献率达到了81.543%,并且6种重金属在主成分1的载荷非常高。结合矿区的周边环境和自身特点,表明6种重金属的主要共同来源为矿区内的矿业活动,并且工业活动、交通运输、农业活动等也对矿区造成了一定程度的重金属污染。     

钢丝绳产业区废水重金属对土壤与蔬菜的影响及生态风险评价

选取钢丝绳产业区某较发达的一乡镇为研究区域，对其周边土壤及蔬菜的污染状况进行调查和实验研究，结果表明：（1）钢丝绳产业区废水重金属对附近土壤并未产生较大污染，蔬菜重金属元素锌的安全率为100％，铅仅为55％。（2）钢丝绳产业区叶类蔬菜中铅的含量最高，豆类蔬菜中却是锌的含量最高，根茎类蔬菜中铅和锌的含量均较低。     

土壤中铜、镉、锌的示波极谱法测定

极谱法对于矿石及金属的测定已应用很广.近年来随着极谱技术的发展,出现了阳极溶出伏安法测定土壤及水中铜镉、锌、铅的方法.本实验是在氨性底液中用示波极谱法同时连测铜、镉、锌. 实验部分 1.仪器试剂 JP—1A型示波极谱仪,用三电极及常     

某废弃铅冶炼场地周边蔬菜重金属污染水平及来源解析

于某废弃铅冶炼场地周边菜地采集69份蔬菜样品,通过测定蔬菜样品中的As、Cd、Cr、Hg、Pb含量评价重金属污染水平,并对污染来源进行解析。结果表明,萝卜中As、Cd、Cr、Hg、Pb的整体水平分别为0.040、0.022、0.359、0.003、0.220mg/kg;白菜中的整体水平分别为0.026、0.022、0.307、0.004、0.158mg/kg;大葱中的整体水平分别为0.014、0.017、0.204、0.002、0.104mg/kg,蔬菜样品中Cr、Pb存在超过《食品安全国家标准食品中污染物限量》(GB 2762—2017)限值的现象,超标率分别为17.65%～46.15%、3.85%～86.77%;蔬菜中5种重金属的富集系数为CdHgPbCrAs,蔬菜中Cr、Pb为中度或重度污染,其中白菜比萝卜和大葱更易受到污染;工业排放源是周边地区蔬菜重金属含量的主要来源,其对萝卜、白菜和大葱重金属的贡献率分别为65.4%、35.5%、97.3%。     

公路两侧土壤中铅和镉污染以及存在形态分布的分析

测定了土壤中铅、镉总量,并采用五级连续浸提法和石墨炉原子吸收分光光度法对北京市3条典型公路两侧的土壤样品中铅和镉的存在形态分布进行了测定.结果表明,所选3条公路出京方向右侧的土壤铅和镉污染严重,其铅、镉总量分别是北京地区土壤铅和镉含量背景值的1.62～6.69、5.97～18.74倍.土壤中铅主要以铁锰氧化物结合态、碳酸盐结合态、有机结合态和残渣态等形式存在,镉主要以铁锰氧化物结合态和残渣态形式存在,而活性强的离子交换态浓度均较低.不容忽视的是,铅和镉的碳酸盐结合态在碱性条件下稳定,但是具有遇酸释放的隐患.     

Regional distribution of cadmium minerals and risk assessment for potential cadmium pollution of soil in China

系统地分析和评价了中国镉矿的区域分布及长期采选冶活动所带来的土壤镉污染风险.研究结果表明,截至2005年底,中国累计探明镉资源储量约为719.47kt,保有镉资源储量约为587.37 kt,且多与铅矿、锌矿等以共、伴生形式存在.中国镉矿主要分布在中部、西南部及华东地区,这些地区的镉资源探明储量占中国累计探明总储量的88.0％,保有储量占中国总保有储量的87.1％.据统计,中国镉采出量约为136.10 kt,主要集中在西南地区,其镉采出量占中国总采出量的59.4％.镉污染事件主要发生在镉矿相对丰富及采选冶活动较密集的云南、广东、湖南、贵州等地区,大部分矿冶区及周边土壤呈现重度镉污染,农作物中含镉量超出《食品中污染物限量》(GB2762-2005)中限值.     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Kinetic and structural relationships of transition monomeric and oligomeric carboxyl- and choline-esterases

The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric CE's (mCE). The rabbit liver mCE was not a subunit of the oligomeric CE (oCE), although the oCE also hydrolyzed choline esters at a very low rate. The complex kinetics of the mCE's, mBuChE's, oCE's, and of the oligomeric BuChE's of horse and human serum could be interpreted according to a single reaction scheme involving an allosteric site and the equation derived from it. Thus activation and inhibition at high substrate concentrations, together with sigmoidal activity versus substrate concentration plots, all of which characterize the reactions of these esterases, could be interpreted by a single scheme and equation. Structural and kinetic comparisons showed a progressive transition of properties from the oCE's through the mCE's to the oBuChE's. One of the purified mCE's was from horse serum, and it exhibited physical and kinetic properties unlike those of the liver mCE's or oCE's.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Sorption and desorption behavior of chloroanilines and chlorophenols on montmorillonite and kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Bacterial and archaeal diversity in oil fields and reservoirs and their potential role in hydrocarbon recovery and bioprospecting

Environmental Science and Pollution Research - Hydrocarbon is a primary source of energy in the current urbanized society. Considering the increasing demand, worldwide oil productions are declining...     

Sources and fate of PCDD and PCDF

PCDD and PCDF were found in urban air particulates from St. Louis and Washington, D.C., and in sediments from the Great Lakes and Siskiwit Lake, Isle Royale. The similarity between the PCDD and PCDF found in air particulates and sediment samples and the presence of PCDD and PCDF in sediment from Siskiwit Lake (a location which can receive only atmospheric inputs) suggest that these compounds are emitted to the atmosphere from combustion sources. The historical input of PCDD and PCDF to dated sediment cores shows a strong increase since 1940, and this suggests that the incineration of chlorinated organic compounds is an important source of PCDD and PCDF to the environment.     

畜禽养殖业污染与循环经济

解决畜禽养殖业的污染问题要以充分利用资源为根本出发点，通过对污染全过程控制及废物综合利用，达到畜禽粪便的减量化、无害化、资源化，走循环经济的发展道路。     

Isocyanatocyclohexane and isothiocyanatocyclohexane levels in urban and industrial areas and possible emission-related activities

Isocyanatocyclohexane and isothiocyanatocyclohexane are becoming relevant compounds in urban and industrial air, as they are used in important amounts in automobile industry and building insulation, as well as in the manufacture of foams, rubber, paints and varnishes. Glass multi-sorbent tubes (Carbotrap, Carbopack, Carboxen) were connected to LCMA-UPC pump samplers for the retention of iso- and isothiocyanatocyclohexanes. The analysis was performed by automatic thermal desorption (ATD) coupled with capillary gas chromatography (GC)/mass spectrometry detector (MSD). TD-GC/MS was chosen as analytical method due to its versatility and the possibility of analysis of a wide range of volatility and polarity VOC in air samples. The method was satisfactory sensitive, selective and reproducible for the studied compounds. The concentrations of iso- and isothioisocyanatocyclohexanes were evaluated in different urban, residential and industrial locations from extensive VOC air quality and odour episode studies in several cities in the Northeastern edge of Spain. Around 200–300 VOC were determined qualitatively in each sample. Higher values of iso- and isothiocyanatocyclohexane were found in industrial areas than in urban or residential locations. The concentrations ranged between n.d.−246 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively, for industrial areas. On the other hand, urban and residential locations showed concentrations ranging between n.d.−164 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively. The site location (urban or industrial), the kind and nearness of possible iso- and isothiocyanatocyclohexane emission activities (industrial or building construction) and the changes of wind regimes throughout the year have been found the most important factors influencing the concentrations of these compounds in the different places.