Application of pyrite trace element chemistry to exploration for SEDEX style Zn-Pb deposits: McArthur Basin,Northern Territory,Australia

Sedimentary pyrites in black shales contain abundant trace elements that provide information on the chemistry of the seawater at the time of sedimentation. This study focuses on the Barney Creek Formation (~ 1640 Ma) in the McArthur Basin in the Northern Territory of Australia, which is host to one of the world's largest SEDEX Zn-Pb-Ag deposits, and several smaller deposits. Fine-grained sedimentary pyrite has been sampled from three drill holes through the Barney Creek Formation at various distances from SEDEX mineralisation. Samples were selected through the stratigraphy of each hole and analysed by LA-ICPMS for a suite of 14 trace elements. The data show that sedimentary pyrite at the base of the Barney Creek Formation, closest (within 1 km) to SEDEX mineralisation, is strongly enriched in Zn and Tl by one to two orders of magnitude compared to the global average for sedimentary pyrite. In contrast sedimentary pyrite from the hole furthest from SEDEX mineralisation (~ 60 km) contains mean Zn and Tl values equal to, or less than, the global average. Based on the three drill hole pyrite data sets it is concluded that trace elements that are contributed to the basin during hydrothermal exhalation, and adsorbed into contemporaneous sedimentary pyrite, are principally Zn, Tl, Cu, Pb, Ag and As. In contrast, trace elements that are adsorbed into sedimentary pyrite from background seawater are principally Mo, Ni, Co, Se and As. These differences have enabled the development of a SEDEX fertility diagram for sedimentary basins, based on the composition of sedimentary pyrite, that distinguish high Zn, but barren shales, from high zinc SEDEX-related shales. In parallel with the increase in Zn and Tl in sedimentary pyrite approaching mineralisation there is a decrease in Ni, Co and Mo. This means that the ratios Zn/Ni and Tl/Co are particularly good pyrite vectors to SEDEX mineralisation in the McArthur Basin, varying over 4 to 6 orders of magnitude from barren shales to mineralised shales. It is speculated that the reason for the reverse relationship between Ni, Co and Zn, Tl may be caused by hydrothermal exhalations into the water column that effect the ion-exchange pyrite surface complexation processes that alter the uptake of these elements into sedimentary pyrite.Another important conclusion of this study is that hydrothermal exhalations into a sedimentary basin may affect the redox sensitive trace element chemistry of sedimentary pyrite and therefore the trace element chemistry of pyritic black shales. Nickel, Co and Mo all decrease in proximity to hydrothermal vents that form SEDEX deposits, whereas Zn, Tl and Pb increase. Selenium and bismuth are the only redox sensitive trace elements that appear to be unaffected by hydrothermal activity in the McArthur Basin. This has implications on how trace element concentrations of black shales and pyrite are used to reflect past global ocean chemistry.     

Trace Element Record of Pyrite from Diverse Deposits-Examples from the Dabaoshan Polymetallic Deposit of Northern Guangdong,South ChinaEI北大核心CSCD

The Dabaoshan polymetallic deposit, located in the middle Nanling metallogenic belt, is an important and representative W-Mo-Cu-Pb-Zn deposit in the northern Guangdong. The deposit is characterized by a complex combination of ore-forming elements, containing 0.86 Mt Cu, 0.85 Mt Zn, 0.31 Mt Pb, 0.14 Mt WO3 at grades of 0.86%, 12%, 1.77% and 0.12%, respectively. Due to different mineral association and occurrence, mineralization at Dabaoshan can be defined as three types: porphyry W-Mo mineralization, skarn Mo-W mineralization and strata-bound sulfide mineralization. Pyrite from the three-mineralization types has different textures and element compositions. EMPA mapping analysis suggested that distribution of Co, Ni, and As is nearly homogeneous, whilst As in pyrite from the stratabound sulfides shows weak irregular zoning. LA-ICP-MS analyses of pyrite suggested that the three type have distinctive trace element characteristics even though the concentrations of the trace elements are relatively low. Cobalt, Ni, As and Se substitutes Fe and S in pyrite respectively while Cu, Zn, Sn Sb are mainly represented by chalcopyrite, sphalerite, cassiterite and stibnite inclusions enclosed in pyrite. Ni and Ag are rich in the pyrite from the stratabound mineralization. The results suggested that the trace element characteristic of pyrite can be used to: a) study the occurrence of trace element in pyrite; b) imply the chemical-physical conditions; c) trace the regional ore-forming substance and ore forming process. The stratabound mineralization is formed during the volcano eruption during the Devonian then and overprinted by the deep source material and multiple ore-forming fluids in the Yanshanian period. © 2018, Science Press. All right reserved.     

Abundances and modes of occurrence of trace elements in the Çan coals (Miocene), Çanakkale-Turkey

This study presents the concentrations and modes of occurrence of trace elements in 81 coal samples from the Çan basin of northwestern Turkey. The concentration of trace elements in coal were determined by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry. Additionally, traditional coal parameters were studied by proximate, ultimate, X-ray diffraction, and petrographic analyses. Twenty trace elements, including As, B, Ba, Be, Cd, Cu, Co, F, Hg, Mo, Ni, Pb, Sb, Se Sn, Th, Tl, U, V, and Zn, receive much attention due to their related environmental and human health concerns. The Çan coals investigated in this study are lignite to sub-bituminous coal, with a broad range of ash yields and sulphur contents. The trace element concentrations show variety within the coal seams in the basin, and the affinities vary among locations. The concentrations of B, Ba, Be, Cd, Cu, Co, F, Hg, Mo, Ni, Pb, Sb, Se, Sn, Tl, and Zn in Çan coals are within the Swaine's worldwide concentration range, with the exception of As, Th, U, and V. On the other hand, compared with world coals, the Çan basin coals have higher contents of As, B, Cu, Co, Mo, Pb, Th, U, V, and Zn. Based on statistical analyses, most of the trace elements, except for U, show an affinity to ash yield. Elements including As, Cd, Hg, Se, Cu, Mo, Ni, and Zn, show a possible association with pyrite; however, the elements Se, B, and Mo can be have both organic and inorganic associations.     

滇东南都龙超大型锡锌多金属矿床黄铁矿LA-ICPMS微量元素组成研究

滇东南马关都龙是一个以锡锌为主,共-伴生铟、铜、铅、钨、铁、银等多种元素的锡锌多金属超大型矿床。虽然前人从矿物学、矿床地球化学、年代学等不同角度开展了较多的研究,该矿床锡锌多金属矿化为燕山晚期岩浆热液活动的产物已是不争的事实,但关于该矿床是否存在热水沉积作用及其与锡锌多金属成矿作用的关系依然存在较大争议。本文选取都龙矿区广泛存在的黄铁矿作为主要研究对象,在矿相学基础上利用LA-ICPMS对不同阶段黄铁矿的微量元素组成开展了系统的研究。野外及显微鉴定结果表明,矿区存在四种类型(期次)的黄铁矿,即:鲕状黄铁矿Py1;穿切或交代Py1的细脉状黄铁矿Py2;与闪锌矿等硫化物共生的自形黄铁矿Py3;包裹早期黄铁矿或闪锌矿等硫化物的他形黄铁矿Py4。LA-ICPMS分析结果表明,该矿床黄铁矿中富集多种微量元素,其中Co、Ni、As、Ge等元素以类质同象的形式存在黄铁矿晶格中,而其余元素多以显微矿物包体形式赋存于黄铁矿中。上述四期黄铁矿微量元素组成存在较大差别,Py1相对富集Zn和As,而其余微量元素含量较低,Co与Ni含量较低,Co/Ni比值远低于1.00,其微量元素组成与典型沉积作用形成黄铁矿基本一致; Py2与Py1具有相似的微量元素组成特征,其Co/Ni比值接近Py1变化范围; Py3和Py4除富集Zn、As外,Mn、Co、Ni、Cu、Sb、Pb、Bi元素含量也相对较高,其Co/Ni比值相对较高,多大于1,与典型岩浆热液型黄铁矿微量元素组成相似,而与沉积型黄铁矿差异明显。结合各阶段黄铁矿产出地质特征,对比不同类型黄铁矿微量元素组成,本研究认为:Py1鲕状黄铁矿为热水沉积作用形成; Py2为Py1变质改造形成的细脉状黄铁矿,其微量元素继承了Py1; Py3为岩浆热液活动形成的自形黄铁矿; Py4为岩浆热液活动晚期形成的他形黄铁矿,Ag和Bi组成作为区分不同成因类型黄铁矿的化学指标的潜力。矿区早期沉积作用形成鲕状黄铁矿过程可能为后期成矿作用提供了部分硫源及少量Zn等成矿物质,海西-印支期区域变质改造作用对矿区成矿作用影响不大,而燕山晚期岩浆热液活动才是矿区锡多金属大规模成矿作用的主导因素。     

Pyrite geochemistry in the Toarcian Posidonia Shale of south‐west Germany: Evidence for contrasting trace‐element patterns of diagenetic and syngenetic pyrites

Authigenic pyrite grains from a section of the Lower Toarcian Posidonia Shale were analysed for their trace‐element contents and sulphur‐isotope compositions. The resulting data are used to evaluate the relationship between depositional conditions and pyrite trace‐element composition. By using factor analysis, trace‐elements in pyrite may be assigned to four groups: (i) heavy metals (including Cu, Ni, Co, Pb, Bi and Tl); (ii) oxyanionic elements (As, Mo and Sb); (iii) elements partitioned in sub‐microscopic sphalerite inclusions (Zn and Cd); and (iv) elements related to organic or silicate impurities (Ga and V). Results indicate that trace‐element contents in pyrite depend on the site and mechanism of pyrite formation, with characteristic features being observed for diagenetic and syngenetic pyrites. Diagenetic pyrite formed within anoxic sediments generally has a high heavy metals content, and the degree of pyritization of these elements increases with increasing oxygen deficiency, similar to the degree of pyritization of reactive Fe. The highest gradient in the increase of the degree of trace element pyritization with bottom‐water oxygenation was found for the elements Ni < Cu < Mo = As < Tl. In contrast, syngenetic pyrite formed within a euxinic water column typically is enriched in As, Mo and Sb, but is low in heavy metals, and the geochemical variation reflects changes in sea water composition.     

冀北张家口地区汉诺坝玄武岩中麻粒岩捕虏体的硫化物相

捕虏体麻粒岩是了解下地壳形成和演化的重要样品。汉诺坝新生代玄武岩中的二辉麻粒岩捕虏体样品中富含各种硫化物相,主要类型有:①孤立产出的球状出溶硫化物;②矿物颗粒之间或颗粒内的粗晶硫化物;③次生硫化物包裹体群;④裂隙充填硫化物。电子探针分析表明,硫化物的矿物成分均为贫镍磁黄铁矿,(Ni+Co+Cu)/Fe(原子比)远小于0.2;(Fe+Cu+Co+Ni)/S(原子比)比地幔岩的磁黄铁矿小,多小于0.875,反映了一种S过饱和环境。各种产状的磁黄铁矿中Au、Ag都有一定的含量,其平均值分别为0.19%～0.22%(Au)、0.01%～0.02%(Ag),反映下地壳的麻粒岩化与金矿化的成因联系。磁黄铁矿的Ni、Co、Cu含量与S正相关,说明微量重金属元素与S具有同源的关系,由于地幔去气伴随S而进入下地壳。     

山西高凡银金矿床黄铁矿的微量元素标型特征及其应用

高凡银金矿床黄铁矿的微量元素研究发现富Au、Ag、Pb、Zn、As、Sb,贫Co、Ni、Se,且S/Se较大,S/As和Fe/(Pb+Zn)较小,As/(Co+Ni)、(Pb+Zn)/(Co+Ni)>10。同时高凡矿田中的滩上铜钼矿化点的黄铁矿则显示相反的特征。总结出一套区分两类矿化黄铁矿微量元素的标型特征,对高凡矿田和五台地区各矿化点的判别和评价中显示了一定的适用性,可作为本区寻找同类金银矿床的找矿标型特征。     

Crystallographic and chemical variations during pyritization in the upper Barremian and lower Aptian dark claystones from the Lower Saxonian Basin (NW Germany)

In the Lower Saxonian Basin, cores from three drill holes provide a cross-section from the basin centre towards the margin through the upper Barremian/lowermost Aptian pyritic claystones and marls. Microscopic analyses distinguish six types of pyrite (I: ‘cones and tubes’, II: ‘tubes’, III: ‘isometric crystal aggregates’, IV: ‘pseudomorphs of fossils’, V: ‘star-like concretions’, and VI: ‘filiform pyrite-marcasite intergrowths’) which are associated with subordinate amounts of Fe carbonate, chalcopyrite, sphalerite and wurtzite. The crystal morphology of these sulphides shows a clear-cut diagenetic sequence from pyrite crystals dominated by the octahedron to those dominated by the cube. Among these early to late diagenetic pyrites, the conversion of crystal habits is accompanied by a striking variation in trace element contents, some of which have extremely low values (e.g. Au, Se, Te, Tl, Co). In this context, classification of crystal habits and analyses of As and Ni establishes a sequence of pyritization which may help define a basin zonation for these argillaceous sedimentary rocks, categorized as ‘normal facies’—oxygenated bottom waters—interrupted by short episodes of bottom water oxygen depletion (‘bituminous facies’). Substitution of the cube for the octahedron in the Fe bisulphide aggregates led to a continuous removal of As and Ni from the pyrite, attesting to a steady decrease of those elements in the pore fluids with time. By contrast, within each type of pyrite, As and Ni contents increase from the margin towards the centre of the basin, owing to pre-concentration of both elements in the basinal sediments, which are more abundant in organic matter. Some other elements, however, such as Mn, Cu, Sb and Ag, do not follow this trend and are unrelated to the lattice transformation of the Fe bisulphides. Their sometimes anomalously high quantities in Fe bisulphides are controlled by the host rock chemistry (presence of volcaniclastic material) and accessory minerals intergrown with pyrite (e.g. chalcopyrite). Pyrite I through III formed in tubular hollows of burrowing organisms, and type IV in tests of fossils. Types V and VI did not result from replacement or void filling but were generated by diffusion of sulphate along inhomogeneties, such as bedding planes, shrinkage cracks or water escape structures.     

Time-resolved,defect-hosted,trace element mobility in deformed Witwatersrand pyrite

The Pb isotopic composition of rocks is widely used to constrain the sources and mobility of melts and hydrothermal fluids in the Earth's crust. In many cases, the Pb isotopic composition appears to represent mixing of multiple Pb reservoirs. However, the nature, scale and mechanisms responsible for isotopic mixing are not well known. Additionally, the trace element composition of sulphide minerals are routinely used in ore deposit research, mineral exploration and environmental studies, though little is known about element mobility in sulphides during metamorphism and deformation. To investigate the mechanisms of trace element mobility in a deformed Witwatersrand pyrite(FeS_2), we have combined electron backscatter diffraction(EBSD) and atom probe microscopy(APM). The results indicate that the pyrite microstructural features record widely different Pb isotopic compositions, covering the entire range of previously published sulphide Pb compositions from the Witwatersrand basin. We show that entangled dislocations record enhanced Pb, Sb, Ni, Tl and Cu composition likely due to entrapment and short-circuit diffusion in dislocation cores. These dislocations preserve the Pb isotopic composition of the pyrite at the time of growth(~3 Ga) and show that dislocation intersections, likely to be common in deforming minerals, limit trace element mobility. In contrast, Pb, As, Ni, Co, Sb and Bi decorate a highangle grain boundary which formed soon after crystallisation by sub-grain rotation recrystallization.Pb isotopic composition within this boundary indicates the addition of externally-derived Pb and trace elements during greenschist metamorphism at ~2 Ga. Our results show that discrete Pb reservoirs are nanometric in scale, and illustrate that grain boundaries may remain open systems for trace element mobility over 1 billion years after their formation.     

胶东焦家金成矿带2420~3206 m垂深金矿物和黄铁矿微量元素特征

在胶东莱州吴一村地区完成的3266.06 m深钻,是目前焦家金成矿带最深见矿钻孔,研究钻孔揭露的深部矿石中金矿物及黄铁矿微量元素特征,对探讨深部成矿作用演化具有重要意义。笔者采取深钻中2420~3206 m垂深的岩（矿）芯样品进行了详细的岩相学和矿相学研究,结合扫描电镜和电子探针微区分析,研究了矿石中金矿物的赋存状态和成分。对不同成矿阶段形成的黄铁矿进行了LA-ICPMS微量元素分析。研究结果表明,深部矿石中载金矿物主要为黄铁矿,其次为石英、黄铜矿、方铅矿,可见金主要以自然金和银金矿的形式存在,以晶隙金和裂隙金为主,其次为包体金。与浅部金矿床比较,深部金的成色较高。黄铁矿分为6种类型,第Ⅰ成矿阶段形成富Co型黄铁矿Py1,第Ⅱ成矿阶段形成富Ni型黄铁矿Py2a和Py2b,第Ⅲ成矿阶段形成富Au、As型黄铁矿Py3a和富Au、Ag、Pb、Bi型黄铁矿Py3b,第Ⅳ成矿阶段形成贫微量元素黄铁矿Py4。其中,Py1和Py2a发生强烈破碎,裂隙表面对热液中的Au络合物产生吸附作用,对金沉淀富集起重要作用。黄铁矿中Co、Ni、As等微量元素主要以类质同象形式赋存,而Au、Ag、Cu、Pb、Zn、Bi等主要以纳米级、微米级矿物包体形式赋存。Pb+Bi、Cu+Pb+Zn、Te+Bi与Au+Ag呈明显正相关,而Au与As相关性较差。黄铁矿中Co、Ni含量较低,而Au+Ag+As或Au+Ag+Pb+Bi+Cu含量较高指示成矿有利。另外,黄铁矿中Co、Ni含量较高,并且破碎强烈,成矿相关元素含量较高也指示成矿有利。     

云浮黄铁矿利用过程中微量毒害元素的环境化学活动性

为了解云浮黄铁矿利用过程中微量毒害元素的环境地球化学行为，客观评价它们对环境质量的影响，利用元素结合形态的连续提取实验方法，分析了云浮黄铁矿及其工业废渣中Co,Ni,Cu,Zn,As,Se,Cd,Sn,Sb,Pb和Tl等11种毒害元素的形态及化学活动性。结果表明，黄铁矿中大部分微量毒害元素都有着极强的化学活动性，各元素活动态浸出比例依次为Co96.3%,Se91.9%,Cu90.3%,Cd90.0%,Pb89.7%,Zn88.6%,Sb82.5%,Ni80.6%，Sn70%,Tl55.1%和As31.9％，元素As和Tl主要赋存于硫化物和硅酸盐矿物相中，另有少量的Cu,Pb和Sb可能赋存于碳酸盐矿物相中，其他元素则主要赋存于硫化物矿物相中。与黄铁矿相比，飞灰和灰渣中各元素可交换态和碳酸盐结合态所占的比例明显减少。废渣中各元素的化学活动性表现出很大的差别，其中Cu,Zn和Cd的化学活动性最强，活性态浸出比例在90％以上；其次是Co,Ni,Se,Pb和Tl，浸出比例在50％左右；Sb,As和Sn的稳定性较高，浸出比例分别为1％、5％和14％左右；飞灰中微量毒害元素的活动性均高于灰渣。     

湖南桃江响涛源锰矿地球化学特征及其成因意义

湖南响涛源锰矿位于湘中桃江成锰盆地。盆地内发育一组NNW向同沉积断裂,形成了一系列断陷槽,控制了沉积岩相的分布,其中黑色页岩、含锰灰岩、碳酸锰矿为成矿最佳的岩性组合。矿石的化学组分多样,Co、Ni、Pb、Mo和Ba等丰度较高,Co/Ni、SiO2/Al2O3、(Fe+Mn)/Ti、Al/(Fe+Mn+Al)、Fe/Ti比值以及Co/Zn-(Cu+Ni+Co)和Fe-Mn-(Cu+Ni+Co)图解揭示锰矿成矿过程中有海底热水的参与;稀土元素配分模式、Ce、Eu异常表示锰矿形成于被动大陆边缘环境,并具有热水沉积特征;碳同位素结果显示出富集碳的轻同位素的特征,反映了响涛源锰矿成矿过程中深部热水沉积及生物作用的特征;氧同位素计算古温度为湘中响涛源锰矿床的低温热水沉积成因提供了有利的佐证。     

下庄竹山下铀矿床黄铁矿元素地球化学特征及其表征意义

竹山下铀矿床是粤北下庄铀矿田内大型铀矿床之一,铀矿化类型为"交点"型和硅化带型。在详细的野外地质调查基础上,对竹山下铀矿床4种不同类型黄铁矿进行元素含量分析及硫同位素测试,结果表明:"交点"型矿石中黄铁矿相对富集Pb、 Cu、 Co、 As、 Ni、 Se、 Bi、 U、 Sb、 Zn等微量元素;"交点"型铀矿化形成于中深部高温环境,成矿热液具有地幔流体特征,成矿过程硫来源与该区花岗岩中黄铁矿的硫来源一致或者相似,花岗岩中的黄铁矿可能为该期成矿事件的产物;竹山下矿床在垂向上表现出越往深部硫逸度越低的特征;"交点"型和硅化带型中黄铁矿具有相似的微量元素配分曲线,表明二者具有相同的成矿热液来源,且与辉绿岩中黄铁矿配分曲线相似,表明该区成矿热液具有深源性。     

江西相山铀矿田深部多金属矿化中黄铁矿微量元素地球化学特征

在对相山铀矿田的深部勘查过程中陆续发现了一批铅、锌、银、铜多金属矿化,利用ICP-MS方法对多金属矿化中的重要金属矿物黄铁矿进行了微量元素分析。结果表明,黄铁矿中富集Co、Ni、Cu、Zn、Cd、Sb、Tl、Pb、Bi等微量元素。对比黄铁矿与矿区出露的主要岩浆岩和基底变质岩的LREE/HREE、(La/Yb)N、Y/Ho、Zr/Hf和Nb/Ta特征参数,结果表明多金属成矿流体在上升运移过程中受到变质基底的强烈混染。LREE富集,Hf/Sm、Nb/La和Th/La值小于1的特征表明多金属矿化成矿流体并非为富F流体,与铀成矿流体具有较大差异。微量元素Co含量与Co/Ni特征值显示矿化形成于中低温环境,成矿物质主要来自于基底变质岩。     

吉林延边金苍矿化带黄铁矿地球化学特征及找矿意义

金苍是吉林延边中生代火山岩成矿带内的一个重要矿化区,矿化带内发育黄铁矿化,包括脉状细粒黄铁矿和浸染状粗粒黄铁矿2种类型,对这2种黄铁矿分别进行了主元素和微量元素分析。结果表明:2类黄铁矿主元素含量低于标准黄铁矿,属于硫亏损型,表现出深部、高温的形成环境;黄铁矿微量元素差异较大,为2个成矿期产物;Au及Ag的含量较低,以Cu、Pb、Zn为主,高温Ni相对Co的含量较高,反映其形成温度较高。黄铁矿既存在Co、Ni对Fe的类质同象替代,也存在As、Sb对S的类质同象替代。在与典型热液型金矿床黄铁矿对比后,显示金苍矿化带中黄铁矿不是与火山热液型金成矿有关的成分标型,更多地体现出Cu等金属的成矿特征。黄铁矿的成分地球化学特征不仅能较好地了解矿物的形成环境,而且可以为矿产勘查提供重要的找矿标志。     

川北广元田坝子剖面含铀沥青脉的发现及其地质意义

通过野外地质调查,在四川盆地西北部广元市青川县田坝子剖面发现了多处具铀异常(≈70×10-6)的含铀沥青脉.对含铀沥青脉开展了矿物学、元素地球化学、光谱学研究,并与研究区典型砂岩型铀矿床(303矿床)中的"有机质"开展了对比研究.研究表明,含铀沥青脉中含有大量的微粒状矿物,包括微米级的石英、重晶石、黄铜矿、闪锌矿、方铅...     

粤北大宝山铜多金属矿区黄铁矿与磁黄铁矿EPMA和LA-ICP-MS原位微区组分特征及其对矿床成因机制约束

粤北大宝山铜多金属矿床一直存在燕山期岩浆热液成因和海西期火山喷流成因之争,争议的焦点在于块状、似层状硫化物矿体的成因。本文在全面开展矿区地质调查和钻探查证的基础上,对块状、似层状和脉状硫化物矿石中的黄铁矿和磁黄铁矿开展EPMA和LA-ICP-MS原位分析。测试结果表明,不同产状黄铁矿的平均分子式相似,分别为FeS_(1.98)、FeS_(1.99)和FeS_(1.98),似层状和脉状硫化物中磁黄铁矿的平均化学式为Fe_(0.886)S和Fe_(0.874)S,属形成温度相对较低单斜磁黄铁矿。与花岗岩岩浆热液标型黄铁矿相比,不同产状的黄铁矿和磁黄铁矿中Co、Ni、Mn、Se和Ge等元素以类质同象形式赋存,它们含量较低但稳定,Cu、Pb、Zn、Ag、Bi和Tl及Ga主要以微细矿物子晶形式存在,其含量丰富,但变化明显。从块状、似层状到脉状硫化物矿体,黄铁矿和磁黄铁矿中Co、Zn和Se的含量及Co/Ni值降低,而Cu、Pb、Ag、Bi等元素的含量明显升高。结合矿区次英安斑岩的产状和含矿性特征表明,大宝山矿床块状、似层状和脉状硫化物矿体都是次英安斑岩深部岩浆房产出的含矿流体在不同赋矿环境中的产物。     

复杂的山东昌乐新生代玄武岩辉石岩捕虏体及其岩石圈演化意义

紧邻郯庐断裂带分布的山东昌乐新生代玄武岩含有丰富的辉石岩捕虏体。根据辉石岩的主、微量元素特征,可以将它们大致分为3类。Ⅰ类和Ⅱ类样品的岩石地球化学特征分别与河北汉诺坝-阳原新生代玄武岩中的Cr系列和Al系列辉石岩捕虏体相对应,都属壳-幔过渡带或岩石圈顶部地幔的分离结晶产物,其中Ⅱ类辉石岩还包含有陆壳物质组成,更可能是壳幔过渡带来源。Ⅲ类辉石岩在岩石地球化学特征上与汉诺坝的石榴石辉石岩相似,但不同的样品则分别表现出与洋岛玄武岩或正常洋中脊玄武岩相似的特征。丰富的昌乐玄武岩中辉石岩捕虏体所表现出来的复杂成因来源,与相对简单的上地幔特征相比,该区新生代时的顶部岩石圈地幔和壳-幔过渡带组成异常复杂,说明岩石圈减薄过程中自下而上的新生地幔物质对古老岩石圈的置换作用。     

塔里木盆地中新生代海侵和海相地层研究的新进展

中新生代海侵是塔里木盆地地质发展史上的重要事件之一。通过对新近发现的古生物化石和海相地层资料研究，本文提出了早白垩世、晚白垩世、古近纪的海侵范围的新认识。同时，依据露头和钻井资料提出了中新世海水分布的新范围。这些新成果对厘定塔里木盆地中新生代地层时代，建立整个盆地中新生代地层格架和油气远景分析具有重要意义。     

山东莱州曲家金矿黄铁矿微量元素对成矿过程的指示

曲家金矿位于我国重要的蚀变岩型金矿矿集区之焦家金矿带的中段，矿床赋存标高为-726～-1 334 m。为研究黄铁矿的演化及其对金成矿过程的指示，运用LA-ICP-MS分析黄铁矿原位微量元素含量，结合岩相学观察和点群分析对黄铁矿进行了分类。发现黄铁矿中Co、Ni、As等微量元素主要以类质同像形式赋存，而Au、Ag、Cu、Zn、Pb、Bi等元素主要以纳米级、微米级矿物包裹体形式赋存。黄铁矿主要分为5种类型：富Co型Py1,富Ni型Py2,富Au、As型Py3,富Au、Ag、Pb、Bi型Py4及“干净”型Py5。黄铁矿微量元素特征指示成矿物质可能主要来源于前寒武纪变质基底岩石和中生代岩浆岩，少量来源于地幔，成矿热液可能属变质热液、岩浆热液和浅部大气降水的混合成因。不同类型黄铁矿反映成矿热液由富Co、Ni经富As、Au向富Pb、Bi、Au、Ag演化。Py1和Py2形成后受构造活动影响发生强烈破碎，裂隙表面对热液中金络合物增强的吸附作用促使金在裂隙中沉淀，对金的富集成矿可能起重要作用。Co、Ni含量较低，同时Au、Ag、As、Pb、Bi等元素含量较高的黄铁矿与成矿作用有密切关系。另外，黄铁矿中C...