湖南宝山矿床花岗岩类硫-铅同位素和流体包裹体研究及其成因意义   总被引：2，自引：0，他引：2  

丁腾  马东升  陆建军  章荣清  谢银财 《矿床地质》2016,35(4):663-676

宝山铜铅锌多金属矿床是湖南重要的铅锌生产基地。矿床内矽卡岩型铜(钼)矿化受侏罗纪花岗闪长斑岩的控制,而主要的铅锌矿体则产于远离岩体的碳酸盐地层中,且缺乏可靠的矿化年龄限制。为了查明宝山铅锌矿体与花岗闪长斑岩之间的成因关系,文章对宝山花岗岩类中浸染状黄铁矿的硫同位素和钾长石的铅同位素,以及铅锌矿石萤石脉石的流体包裹体进行了测试和研究,并与前人报道的铅锌硫化物矿石的硫、铅同位素进行了对比,尝试为宝山铅锌矿化的物质来源及成因提供依据。研究表明,花岗闪长斑岩中浸染状黄铁矿的δ34S值为+1.5‰~+3.5‰,与铅锌矿石硫化物(方铅矿、闪锌矿及黄铁矿)相一致;同时,花岗岩类中钾长石的铅同位素组成206Pb/204Pb、207Pb/204Pb和208Pb/204Pb分别为18.4789~18.7668、15.6835~15.7220和38.7903~39.1035,具有壳源的特征,且与铅锌矿石硫化物的铅同位素分布范围相吻合。宝山矿床的硫、铅同位素特征表明,花岗闪长斑岩应是铅锌矿化的主要硫源及金属来源。宝山矿床铅锌矿石萤石中的流体包裹体具有低温(130~150℃)、低盐度(8%)的特征,可能是岩浆热液演化到晚期的产物。结合已有的有关资料加以对比和分析,研究认为,宝山铅锌矿床的成矿物质应来源于花岗闪长岩的岩浆期后热液,在热液演化晚期迁移到远端地层中沉淀,形成了宝山的主要铅锌矿体。  相似文献   

The behavior of a multilayered porous thermo-elastic medium with anisotropic thermal diffusivity and permeability     

《Computers and Geotechnics》2016

With the aid of integral transform techniques, this paper presents an extended precise integration solution for thermal consolidation problems of a multilayered porous thermo-elastic medium with anisotropic thermal diffusivity and permeability due to a heat source. From the fundamental governing equations, ordinary differential equations are derived by employing Laplace–Hankel transforms. By applying the extended precise integration method, equations in the transformed domain can be solved, and the actual solutions are further obtained by adopting a numerical inverse transformation. The accuracy and feasibility of the proposed theory is demonstrated by contrastive analysis with existing studies. Finally, several examples are carried out to investigate the influence of heat source’s type, axial distance, burial depth of heat source, ratio of thermo-permeability, permeability anisotropy, thermal diffusivity anisotropy and stratification on the thermal consolidation process.  相似文献   

国内外前寒武纪条带状铁建造研究现状   总被引：4，自引：0，他引：4  

代堰锫  朱玉娣  张连昌  王长乐  陈超  修迪 《地质论评》2016,62(3):735-757

条带状铁建造(BIFs)主要发育于早前寒武纪时期(3.8~1.8Ga),记录了早期地球演化的重要信息且蕴含丰富的铁矿石资源。本文梳理总结了国内外BIF相关领域的研究认识及存在问题:1统计对比显示,BIF沉积事件与地幔柱、地壳增生等重大地质事件相关;2稀土元素及Nd同位素示踪表明,Fe来源于海水与海底高温热液的混合溶液,其中高温热液与海水比例为1:1000;3 BIFs缺乏负Ce异常且富集重Fe同位素,暗示沉积时古海洋整体处于缺氧环境以避免Fe~(2+)发生氧化;4一些重要科学问题尚未解决,例如Si的主要来源、沉淀机制及条带成因等;5华北克拉通BIFs多形成于约2.54Ga,BIF类型、形成时代与富矿成因等问题有待深入研究。本文认为,加强国内外典型BIFs的对比研究并适当应用现代先进测试技术,有利于探索BIF沉积的精细过程及古老克拉通的早期演化。  相似文献   

A comparison of black claystones,lignites and dump materials from the Maritsa Iztok Coal Basin,Bulgaria, using organic geochemical proxies     

《Chemie der Erde / Geochemistry》2016,76(3):405-417

Geochemical analysis of dump materials from the opencast Maritsa Iztok mines, Bulgaria, was carried out based on biomarker assemblages of hydrocarbon fractions. Organic matter (OM) and secondary transformations in three representative samples (massive black claystones and materials from the Iztok and Staroselets dump sites) were studied using geochemical proxies.A number of differences were recognised in the respective OM compositions of the samples compared to both published data and between the individual dump samples themselves. The ОM of the studied samples was found to be polar, but also contains some apolar compounds. It consists mainly of resins and asphalthenes. Claystone OM is of the dispersed type, with intense oxidative-reductive interactions in a lacustrine environment resulting in its transformation into an inert material. Dump sample kerogen is of Type II and mixed Type II/III. In all samples, “odd” numbered n-alkanes are found in higher amounts. Diterpenoids (С₁₉, С₂₀) with pimarane, abietane and phyllocladane skeletons are preponderant. Tri- and tetracyclic terpenoids and steranes have been identified in the black claystones OM only. Hopanes are present in low amounts in extractable OM from all three samples. Biomarkers indicate that black claystone OM is formed from aqueous flora, with a minor supply of gymnosperms (mainly G. Sequoia). Iztok Dump OM is structured by higher plants with an aqueous vegetation input. The Staroselets Dump OM formation is assigned to an active microbial reworking of aqueous vegetation and bacteria with a minor coniferous supply. Different geochemical parameters admit anoxic stratified bottom waters for the black claystones with an addition of deep water stagnation for Staroselets sample in a Maritsa Iztok Basin (MIB) aqueous environment.An attempt was also made to track the effect of secondary processes (oxidation, destruction, dearomatisation), temperature, water drainage and wash-out on dump materials. Leaching and weak degradation processes in the MIB dump environment are likely for a time span of ca. 40–50 years, considering the low percentage of short-chain n-alkanes, long-chain prevalence and low Pr/nC₁₇ and Ph/nC₁₈ ratios, with the Iztok Dump sample experiencing more advanced transformations.  相似文献   

湘西北寒武系沉积型镍钼矿成矿物质来源   总被引：1，自引：0，他引：1  

闫友谊 《江苏地质》2016,40(4):560-566

湘西北寒武系含矿丰富,在寒武系下统牛蹄塘组黑色岩系中赋存有磷矿、石煤、钒矿、铀矿,并有有色金属钼、镍矿及铂族元素矿物聚集。通过分析总结前人成果资料,探究镍钼矿成矿地质环境条件是在低温环境、有微生物参与及强还原环境中同生沉积,对寒武系沉积型镍钼矿成矿物质来源提出了明确的看法,即成矿物质来源于海底喷流-热水。  相似文献   

扬子西缘乡城-丽江结合带燕山期斑岩Mo多金属矿床成矿系统   总被引：5，自引：3，他引：2  

刘学龙  李文昌  张娜  赖安琦  李喆  杨富成 《岩石学报》2016,32(8):2281-2302

位于扬子陆块西缘与西南三江造山带结合部位的乡城-丽江地区,北起四川乡城经云南格咱南至丽江地区,在印支期斑岩铜矿带上新发现叠加了燕山期斑岩Mo多金属成矿作用,形成乡城-丽江斑岩Mo矿带。受印支期古特提斯洋盆闭合后地壳缩短与加厚的影响,燕山晚期下地壳发生拆沉作用,导致后碰撞型花岗质岩浆侵位,发育了Mo多金属成矿作用,并构成斑岩成矿系统。岩石地球化学特征表明,燕山晚期含矿斑岩具高硅(SiO_2=66.29%~79.36%)、高碱(K_2O+Na_2O=5.07%~9.24%)、富钾(K_2O/Na_2O=0.71~2.13)的特点,属于高钾钙碱性岩石系列。岩石富集轻稀土元素(LREE),具有负δEu异常;微量元素具富集大离子亲石元素K、U、Th、Rb,亏损高场强元素Nb、Ta、P、Ti的特征;大离子亲石元素的富集和Nb、Ta等高场强元素的亏损,表明形成这些岩体的岩浆主要来自地壳,具有造山带花岗岩的地球化学特征。区内代表性含矿斑岩相似的地球化学组成及分布特征表明,乡城-丽江结合带燕山晚期的成矿斑岩是由同源岩浆分异演化而来。成矿系统的分析表明,燕山晚期主要含矿斑岩成矿物质以壳源为主,但具有少量地幔物质的加入,成岩成矿物质来源具有相似或一致的源区特征。在成矿元素的组合上,由成矿斑岩体向外带表现出W、Mo→W、Mo、Cu→Pb、Zn、Ag的演化趋势。研究表明,本区燕山晚期花岗岩浆的侵入及Mo多金属成矿作用并不是独立或个别的成矿事件,而是纵跨义敦岛弧、甘孜-理塘结合带及扬子西缘的带状成矿活动,属于区内与燕山晚期岩浆侵入作用相关的统一斑岩成矿系统。  相似文献   

混凝土灌注桩桩头渗水的处理及预防措施          下载免费PDF全文

孙立宝 《探矿工程》2016,43(5):86-88

混凝土灌注桩桩头渗水对桩体混凝土受力和基底防水产生影响,对混凝土结构中的钢筋造成腐蚀。结合工程实例,对桩头渗水产生的原因进行分析,主要有操作经验不足、责任心不强,灌注器具不合格,混凝土质量指标不符合要求,灌注接近结束时拔管速度过快、灌注终了超灌高度测量不准,基土含水量高、水压大等;出现桩头渗水可采用人工剔除或注浆封堵处理;介绍了预防措施,包括加强作业人员培训,强化灌注器具检查,严控混凝土质量,重点监管终灌时的状态,做好基坑内降水工作等。  相似文献   

Molybdenum Mass Fractions and Isotopic Compositions of International Geological Reference Materials          下载免费PDF全文

Pei‐Pei Zhao  Jie Li  Le Zhang  Zhi‐Bing Wang  De‐Xin Kong  Jin‐Long Ma  Gang‐Jian Wei  Ji‐Feng Xu 《Geostandards and Geoanalytical Research》2016,40(2):217-226

The double‐spike method with multi‐collector inductively coupled plasma‐mass spectrometry was used to measure the Mo mass fractions and isotopic compositions of a set of geological reference materials including the mineral molybdenite, seawater, coral, as well as igneous and sedimentary rocks. The long‐term reproducibility of the Mo isotopic measurements, based on two‐year analyses of NIST SRM 3134 reference solutions and seawater samples, was ≤ 0.07‰ (two standard deviations, 2s, n = 167) for δ^98/95Mo. Accuracy was evaluated by analyses of Atlantic seawater, which yielded a mean δ^98/95Mo of 2.03 ± 0.06‰ (2s, n = 30, relative to NIST SRM 3134 = 0‰) and mass fraction of 0.0104 ± 0.0006 μg g^?1 (2s, n = 30), which is indistinguishable from seawater samples taken world‐wide and measured in other laboratories. The comprehensive data set presented in this study serves as a reference for quality assurance and interlaboratory comparison of high‐precision Mo mass fractions and isotopic compositions.  相似文献   

High Precision Sr‐Nd‐Hf‐Pb Isotopic Compositions of USGS Reference Material BCR‐2          下载免费PDF全文

Jason Jweda  Louise Bolge  Cornelia Class  Steven L. Goldstein 《Geostandards and Geoanalytical Research》2016,40(1):101-115

The Lamont‐Doherty Earth Observatory radiogenic isotope group has been systematically measuring Sr‐Nd‐Pb‐Hf isotopes of USGS reference material BCR‐2 (Columbia River Basalt 2), as a chemical processing and instrumental quality control monitor for isotopic measurements. BCR‐2 is now a widely used geochemical inter‐laboratory reference material (RM), with its predecessor BCR‐1 no longer available. Recognising that precise and accurate data on RMs is important for ensuring analytical quality and for comparing data between different laboratories, we present a compilation of multiple digestions and analyses made on BCR‐2 during the first author's dissertation research. The best estimates of Sr, Nd and Hf isotope ratios and measurement reproducibilities, after filtering at the 2s level for outliers, were ⁸⁷Sr/⁸⁶Sr = 0.705000 ± 11 (2s, 16 ppm, n = 21, sixteen digestions, one outlier), ¹⁴³Nd/¹⁴⁴Nd = 0.512637 ± 13 (2s, 25 ppm, n = 27, thirteen digestions, one outlier) and ¹⁷⁶Hf/¹⁷⁷Hf = 0.282866 ± 11 (2s, 39 ppm, n = 25, thirteen digestions, no outliers). Mean Nd and Hf values were within error of those reported by Weis et al. (2006, 2007) in their studies of RMs; mean Sr values were just outside the 2s uncertainty range of both laboratories. Moreover, a survey of published Sr‐Nd‐Hf data shows that our results fall within the range of reported values, but with a smaller variability. Our Pb isotope results on acid leached BCR‐2 aliquots (n = 26, twelve digestions, two outliers) were ²⁰⁶Pb/²⁰⁴Pb = 18.8029 ± 10 (2s, 55 ppm), ²⁰⁷Pb/²⁰⁴Pb = 15.6239 ± 8 (2s, 52 ppm), ²⁰⁸Pb/²⁰⁴Pb = 38.8287 ± 25 (2s, 63 ppm). We confirm that unleached BCR‐2 powder is contaminated with Pb, and that sufficient leaching prior to digestion is required to achieve accurate values for the uncontaminated Pb isotopic compositions.  相似文献   

An Investigation of Digestion Methods for Trace Elements in Bauxite and Their Determination in Ten Bauxite Reference Materials Using Inductively Coupled Plasma‐Mass Spectrometry          下载免费PDF全文

Wen Zhang  Liang Qi  Zhaochu Hu  Cunjiang Zheng  Yongsheng Liu  Haihong Chen  Shan Gao  Shenghong Hu 《Geostandards and Geoanalytical Research》2016,40(2):195-216

Trace elements from samples of bauxite deposits can provide useful information relevant to the exploration of the ore‐forming process. Sample digestion is a fundamental and critical stage in the process of geochemical analysis, which enables the acquisition of accurate trace element data by ICP‐MS. However, the conventional bomb digestion method with HF/HNO₃ results in a significant loss of rare earth elements (REEs) due to the formation of insoluble AlF₃ precipitates during the digestion of bauxite samples. In this study, the digestion capability of the following methods was investigated: (a) ‘Mg‐addition’ bomb digestion, (b) NH₄HF₂ open vessel digestion and (c) NH₄F open vessel digestion. ‘Mg‐addition’ bomb digestion can effectively suppress the formation of AlF₃ and simultaneously ensure the complete decomposition of resistant minerals in bauxite samples. The addition of MgO to the bauxite samples resulted in (Mg + Ca)/Al ratios ≥ 1. However, adding a large amount of MgO leads to significant blank contamination for some transition elements (V, Cr, Ni and Zn). The NH₄HF₂ or NH₄F open vessel digestion methods can also completely digest resistant minerals in bauxite samples in a short period of time (5 hr). Unlike conventional bomb digestion with HF/HNO₃, the white precipitates and the semi‐transparent gels present in the NH₄HF₂ and NH₄F digestion methods could be efficiently dissolved by evaporation with HClO₄. Based on these three optimised digestion methods, thirty‐seven trace elements including REEs in ten bauxite reference materials (RMs) were determined by ICP‐MS. The data obtained showed excellent inter‐method reproducibility (agreement within 5% for REEs). The relative standard deviation (% RSD) for most elements was < 6%. The concentrations of trace elements in the ten bauxite RMs showed agreement with the limited certified (Li, V, Cr, Cu, Zn, Ga, Sr, Zr and Pb) and information values (Co, Ba, Ce and Hf) available. New trace element data for the ten RMs are provided, some of which for the first time.  相似文献