陈家杖子金矿地球化学特征及其指示意义     

王喜宽  王宝林  廖蕾  段吉学  龙文华  张宝 《物探与化探》2005,29(4):308-311,315

陈家杖子金矿是通过1∶5万化探工作发现的斑岩型金多金属矿, 其地球化学异常特征可作为在该区寻找类似矿床标志。该矿东部还有形成多金属矿的潜力。在此类土壤覆盖区应采用土壤测量。该金矿的发现反映了在我国中西部地区利用常规方法来发现新矿床的巨大潜力。  相似文献   

新疆葫芦铜镍硫化物矿床的地质特征与成矿时代   总被引：32，自引：1，他引：32  

陈世平  王登红  屈文俊  陈郑辉  高晓理 《新疆地质》2005,23(3):230-233

哈密葫芦铜镍矿是东天山地区典型的与基性-超基性岩有关的岩浆成因块状硫化物矿床.对其中含铜镍硫化物的基性-超基性岩用Re-Os等时线法定年,获得(283±13)Ma的等时线年龄.这表明,葫芦与东天山其他铜镍矿床乃至喀拉通克和箐布拉克铜镍硫化物矿床一样,主要形成于海西期,同位素年代学界定的成岩成矿时间大致在320~280 Ma,表明海西晚期在新疆北部为一个与基性-超基性岩有关的铜镍矿床成矿高峰期.  相似文献   

DMS and SO2 at Baring Head, New Zealand: Implications for the Yield of SO2 from DMS     

Warren J. de Bruyn  Mike Harvey  Jill M. Cainey  Eric S. Saltzman 《Journal of Atmospheric Chemistry》2002,41(2):189-209

Atmospheric dimethyl sulfide (DMS) and sulfur dioxide (SO₂) concentrations were measured at Baring Head, New Zealandduring February and March 2000. Anti-correlated DMS and SO₂ diurnalcycles, consistent with the photochemical production of SO₂ from DMS, were observed in clean southerly air off the ocean. The data is used to infer a yield of SO₂ from DMS oxidation. The estimated yields are highly dependent on assumptions about the DMS oxidation rate. Fitting the measured data in a photochemical box model using model-generated OH levels and the Hynes et al. (1986) DMS + OH rate constant suggests that theSO₂ yield is 50–100%, similar to current estimates for the tropical Pacific.However, the observed amplitude of the DMS diurnal cycle suggests that the oxidation rate is higher than that used by the model, and therefore, that theSO₂ yield is lower in the range of 20–40%.  相似文献   

大西洋洋中脊TAG热液区中块状硫化物的Os同位素研究   总被引：7，自引：0，他引：7  

曾志刚  翟世奎  杜安道 《沉积学报》2002,20(3):394-398

新测得TAG热液区中5件海底块状硫化物样品的锇含量及其同位素组成,187Os/186Os比值在2.305～7.879之间,均值为5.986,介于现代海水和上部洋壳岩石的锇同位素组成之间,表明该区海底块状硫化物中锇是海水和上部洋壳来源锇混合的产物.在海底热液循环过程中,海水的混入对该区热液流体的Os浓度及其同位素组成产生了明显的影响。  相似文献   

Cu–Fe Bearing Zinc Sulfide from Laloki Stratabound Massive Sulfide Deposit, Papua New Guinea: Chemical Characterization     

Banda J. KULANGE  Yoshimichi KAJIWARA  Kosei KOMURO 《Resource Geology》2002,52(1):67-72

Abstract: A strange, unidentified, Cu-Fe bearing zinc sulfide occurs in the Laloki massive sulfide deposit, Papua New Guinea. The mineral is optically uniform in texture but is chemically variable and zoned even within a single grain. Copper contents vary from 0.1 up to 8.85 wt%. Iron reaches 18.31 wt% at maximum and decreases as Cu increases. It is remarkable, however, that the total Fe+Cu remains essentially unchanged between roughly 18 and 20 wt%. Zn and S are least variable, giving 45.85–47.84 wt% and 33.48–34.58 wt%, respectively. Other trace elements such as Cd and Mn are in general less than 0.2 wt%. It is strongly suggested that the mineral in question constitutes a unique Fe-Cu substitutional solid solution series belonging essentially to the Zn–Fe–Cu–S system.
The ideal chemical formula of the solid solution series can well be presented as Zn₁₀(Fe, Cu)₅S₁₅ or Zn₂(Fe, Cu)S₃, where Fe is always greater than Cu. It is intriguing that chalcopyrite blebs are recognizable restrictively only in nearby portions of the Cu-rich end member with the ideal composition close to Zn₁₀Fe₃Cu₂S_15. It has been confirmed by vacuum-sealed heating experiments that this mineral is decomposed to produce chalcopyrite and Fe-bearing normal sphalerite at temperatures below 200C. This would provide another evidence for the existence of such distinct phase as suggested here.  相似文献   

Structure cristalline d'une ménéghinite naturelle pauvre en cuivre,Cu_0,58Pb_12,72(Sb_7,04Bi_0,24)S₂₄Crystal structure of a Cu-poor natural meneghinite,Cu_0.58Pb_12.72(Sb_7.04Bi_0.24)S₂₄     

Yves Moëlo  Pierre Palvadeau  Nicolas Meisser  Alain Meerschaut 《Comptes Rendus Geoscience》2002,334(8):529-536

Cu-poor meneghinite from La Lauzière Massif (Savoy, France) has the composition (electron microprobe) (in wt%): Pb 59.50, Sb 20.33, Bi 1.19, Cu 0.87, Ag 0.05, Fe 0.03, S 17.62, Se 0.05, Total 99.64. Its crystal structure (X-ray on a single crystal) was solved with R1=0.0506, wR2=0.1026, with an orthorhombic symmetry, space group Pnma, and a=24.080(5) Å, b=4.1276(8) Å, c=11.369(2) Å, V=1130.0(4) Å³, Z=4. Relatively to the model of Euler and Hellner (1960), this structure shows a significantly lower site occupancy factor for the tetrahedral Cu site (0.146 against 0.25). Among the five other metallic sites, Bi appears in the one with predominant Sb. Developed structural formula: Cu_0.15Pb₂(Pb_0.53Sb_0.47)(Pb_0.46Sb_0.54)(Sb_0.75Pb_0.19Bi_0.06)S₆; the reduced one: Cu_0.58Pb_12.72(Sb_7.04Bi_0.24)S₂₄. The formation of such a Cu-poor variety seems to be related to specific paragenetic conditions (absence of coexisting galena), or to crystallochemical constraints (minor Bi). To cite this article: Y. Moëlo et al., C. R. Geoscience 334 (2002) 529–536.  相似文献   

阿尔泰可可塔勒铅锌矿床围岩蚀变及成因   总被引：2，自引：3，他引：2  

姜俊 《矿产与地质》2003,17(6):679-682,734

可可塔勒铅锌矿床受火山喷发中心和沉积洼地控制，铅锌沉淀于海进阶段的局限还原卤水池中；矿下存在大型蚀变带，构成成矿流体对流循环过程中的水-岩作用带；后期造山挤压过程使地层和矿体倒转，矿床最终定位于麦兹倒转向斜之北东倒转翼的东南近转折部位。指出该矿床属海底火山喷流沉积改造型块状硫化物铅锌矿床。  相似文献   

大洋多金属结核中1nm锰矿相的相变及其主要控制因素研究   总被引：1，自引：3，他引：1  

冯旭文  钱江初  张培志 《矿物学报》2003,23(2):109-114

多金属结核样品在室温中放置或加热干燥后 ,其中的 1nm锰矿相会部分或全部地相变为 0 7nm锰矿相 ,这说明 0 7nm锰矿相可能不是多金属结核的原生锰矿相 ,而仅仅是 1nm锰矿相的相变产物。研究结果表明 :1nm锰矿相结构中的Cu2 + 、Co2 + 、Ni2 + 等金属阳离子的含量与其结构稳定性有正相关关系 ,即金属离子含量越高 ,其结构越稳定 ,1nm锰矿相越不易相变为 0 7nm锰矿相 ,反之亦然 ;另外 ,不同金属阳离子稳定 1nm锰矿相结构的能力也不同 ,结核中几种主要金属阳离子对 1nm锰矿相结构的稳定能力从大到小为 :Ni2 + >Cu2 + >Co2 + >Zn2 + >Ca2 + =Mg2 + 。  相似文献   

夏塞地区银、锡多金属矿成矿规律新认识     

李建兵  杨更  江元生 《四川地质学报》2003,23(3):146-149

夏塞地区是西南三江(金沙江、澜仓江、怒江)地区东缘的一个重要成矿带，带内银、锡矿产责源十分丰富。本文认为其成矿物质来源于花岗岩体和地层，构造和岩体是区内的主要控矿因素，地壳演化与成矿作用关系十分密切，矿床类型为分布于岩体内接触带的矽卡岩型矿床和分布于岩体外接触带的热液型矿床。  相似文献   

云南白秧坪银多金属矿床微量元素地球化学特征   总被引：1，自引：0，他引：1       下载免费PDF全文

王峰  何明友 《沉积与特提斯地质》2003,23(4):103-107

云南白秧坪银多金属矿床是滇西兰坪盆地内新发现的矿床，属东特提斯—喜马拉雅成矿域的一部分。矿床主要产于下白垩统景星组石英砂岩、粉砂岩中。本文从微量元素地球化学研究入手，与滇西喜马拉雅期富碱岩体相比较，它们具有相同的物质来源区，这种源区被认为是壳—幔物质混合的一种“EMⅡ型”富集地幔源。  相似文献