河南省方城县宋家庄金矿地质特征及控矿因素分析

本文通过对河南省方城县宋家庄金矿矿床地质特征、矿石类型及控矿因素进行分析,认为熊耳群的火山岩为该金矿提供了"矿源层",下汤-拐河深大断裂为含矿热液提供了通道,燕山期的火山活动为"矿源层"中金活化、运移、富集提供了动力。宋家庄金矿体的形成与区域地层、构造、岩浆活动关系密切。     

豫、晋、陕相邻地区西阳河群(熊耳群)火山岩特征、形成构造环境及其地质遗产意义

本文介绍了豫、晋、陕相邻地区西阳河群(熊耳群)火山岩的基本特征、形成构造环境及其地质遗产意义。西阳河群火山岩的结构、构造及沉积夹层特征表明,西阳河群火山岩经历了从陆相到海相、从海相再到陆相的演变过程。虽然它具有较明显的岛弧型火山岩特征,但它并不属于与俯冲作用直接相关的活动大陆边缘产物。研究表明,西阳河群火山岩源于遭受俯冲带组分改造的地幔源区,形成于夭折的三叉裂谷环境。西阳河群火山岩的发育规模和保存完好性十分罕见,其独特的岩石学特征和火山地貌景观,极具科学价值和美学观赏价值,是建立各级地质公园的重要地区。     

河南范疙瘩金矿床矿体定位的构造控制

范疙瘩金矿位于熊耳山断隆的东南部,马超营断裂带的北侧,金矿体产于北西向M14断裂带内.本文通过研究断裂构造的方向、规模、分布特征,分析断裂活动历史及矿体产出特征,总结成矿规律.金矿体严格受M14断裂控制,离断裂越远金矿化越弱,M14断裂带倾向上引张部位及断裂分支复合部位是金元素的富集地段,是成矿有利部位.     

广东省揭西县金坑铜锡铅锌多金属矿床成因探讨

广东省揭西县金坑铜锡铅锌多金属矿床位于惠阳—梅县新华夏构造带之莲花山深断裂带内。通过野外地质调查及室内综合研究,认为该矿床为构造动力变质热液型铜锡铅锌矿床,具有矿化范围广、规模大、矿脉发育、金属矿物品位变化大、成矿多期多阶段性的特征;地层岩性、构造、岩浆岩是该矿床的主要控矿因素,NE—NNE向新华夏裂隙带、片理化带及其配套断裂是该矿床的主要容矿构造,动力变质带是该矿床的重要控矿因素。莲花山深断裂带具有"金坑式"矿床的找矿潜力。     

安徽省霍山县东溪-南关岭金矿地质特征与成矿条件

东溪-南关岭金矿为北淮阳东段发现的第一个原生金矿,产于磨子潭-晓天中生代火山盆地边缘,容矿围岩为安山质-英安质火山岩,矿化和蚀变受桐柏-桐城深大断裂带的次级构造带控制。该金矿发育陡倾斜的脉状矿体和缓倾斜的似层状矿体,成因类型为冰长石-绢云母型浅成低温热液金矿。火山岩盆地之下的变质基底可能起到了初始矿源层作用,桐柏-桐城断裂带及其次级构造破碎带为重要的导岩导矿构造,早白垩世强烈的岩浆活动提供了热源、动力源和部分矿源。参照国内外类似金矿的特征,认为本区成矿地质条件良好,有可能隐伏着与石英正长岩体有关的细脉浸染型矿化,晓天火山盆地具有良好的找矿前景。     

新疆吉拉拜金矿床地质特征及成因

吉拉拜金矿位于新疆布尔津县北约 40km处的哈巴河黑云母斜长花岗岩体内北西向断裂带中 ,研究表明该金矿为石英脉型金矿 ,稀土元素研究表明 ,矿化蚀变岩石与黑云母斜长花岗岩具有相似的变化特征 ,流体包裹体均一测温表明成矿温度为 12 0～ 36 0℃ ,有两个峰值 ,一个峰值位于 2 70～ 30 0℃范围 ,另一峰值位于 15 0～ 2 30℃范围内 ,表明岩浆期后热液和断裂活动对成矿均起作用。含金脉石英的氢氧同位素组成研究表明 ,矿化早阶段 ,成矿热液中以变质热液及岩浆热液为主 ,随着矿化作用的后移 ,成矿溶液中自然会加入越来越多的大气降水 ,导致其氢氧同位素组成向大气降水线方向漂移。研究结果显示 ,哈巴河岩体为该金矿提供成矿物质 ,成矿流体是由哈巴河岩体的岩浆期后热液、动力变质热液及大气降水共同组成 ,北西向断裂带是这些成矿热液的运移通道。该北西向断裂带为逆冲压扭性质。该逆冲压扭断裂中的局部弱应力部位是成矿物质有利的沉淀富集场所。吉拉拜金矿床含金石英脉就是沿北西向逆冲压扭性断层中局部张性部位产出。哈巴河岩体中北西向断裂带及其中的石英脉都很发育 ,具有很好的找矿前景     

苏北变质地质的几个问题

本文运用构造一地层法重新厘定了苏北变质地层层序,系统研究了变质岩群序列及其接触关系、区域变质岩和变质作用、混合岩及混合岩化作用、变质变形序列和构造演化等几个主要问题。新建了东海群和“石桥群”。在特征变质矿物的研究基础上,确定了东海群是中压低角闪岩相为主,海州群和“石桥群”属高压高绿片岩相到低绿片岩相,各群都具多期变质变形。     

康滇地区某些铁矿浆矿床的矿物特征

<正> 康滇地区产于前震旦纪火山岩系中的富铁矿,对其成因一直是一个有争议的问题。如云南大红山铁矿,曾提出过变质-热液富化火山矿床、火山沉积变质-热液交代矿床、火山喷溢溶浆矿床等:位于金沙江北岸的四川莱园子铁矿,产于会理群力马河组更长磁铁玄武岩中,是一个小而富的磁铁矿床。也提出过沉积变质、火山沉积和接触交代等成因论述。通过对这     

福建省“尤德地体”的成矿特征和找矿远景

“尤德地体”位于闽中裂谷带南端 ,与紫金山金矿处于同一成矿带。在“尤德地体”中 ,目前已发现元古界麻源群变质岩和侏罗系长林组、南园组 ,火山岩中均存在韧性剪切带型矿床和热液交代充填矿床。区域构造、地层含矿性、物化探重砂异常等表明其找矿前景很好。找矿工作重点应紧扣层控矿床 ,大断裂带 ,斑岩型金矿和红土型金矿     

广东省揭西县金坑铜锡铅锌矿床地质、地球化学特征及成因

广东省揭西县金坑铜锡铅锌矿位于惠阳—梅县新华夏构造体系之莲花山深大断裂带,矿体受断裂控制,呈脉状产于上侏罗统高基坪群火山岩层间滑动带。通过对该矿床地质及地球化学特征研究,认为该矿床成矿物质来源主要是地壳同熔型花岗岩,热液来源与花岗岩关系密切,是岩浆期后热液裂隙充填(交代)型矿床。     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.