岩石电子背散射衍射（EBSD）组构分析及应用   总被引：18，自引：1，他引：17  

刘俊来  曹淑云  邹运鑫  宋志杰 《地质通报》2008,27(10):1638-1645

电子背散射衍射（EBSD）技术是现代构造地质学与显微构造分析领域一项崭新的技术,它与现代高分辨率扫描电子显微镜和能谱分析设备结合,可以对块状样品中微米或纳米级尺度的颗粒进行晶体结构分析, 从而使微观结构、微区成分与结晶学数据结合起来,能够更精细地对比研究矿物和岩石显微构造,为岩石显微构造分析开辟了一个全新的领域。分析了EBSD技术的基本原理、系统构成、样品制备和工作程序。介绍了石英组构测量,极细粒物质（微角砾岩）的组构特点,二轴晶矿物（角闪石）的组构、变形机制和金属硫化物组构分析的应用实例,对于应用EBSD系统开展研究存在的一些问题进行了讨论。  相似文献   

Naturally acidic and metalliferous waters at unmined volcanogenic massive sulfide deposits in the Bonnifield mining district, Alaska Range, east-central Alaska     

Robert G. Eppinger Paul H. Briggs Cynthia Dusel-Bacon Stuart A. Giles Larry P. Gough Jane M.Hammarstrom Bernard E. Hubbard 《中国地球化学学报》2006,25(B08):232-232

The Bonnifield district hosts 26 tmmined volcanogenic massive sulfide （VMS） occurrences. Environmental geochemical samples of water and stream sediment were collected at several occurrences, concentrating on the two best-exposed and largest deposits, Red Mountain （RM） and Sheep Creek （SC）. Limited samples were also collected at the poorly exposed WTF deposit. The deposits are Late Devonian to Early Mississippian, and are hosted by felsic metavolcanic and carbonaceous schist members of the Totatlanika Schist or Keevy Peak Fm. Spring and stream waters at RM and SC have pH values commonly 〈3.5 （as low as 2.4 at RM and 2.5 at SC）, high conductivity （up to 11000 μS/cm）, and very high （Is to 100s mg/L） dissolved contents of Al, Cd, Co, Cu, Fe, Ni, and Pb. Waters at RM are characterized by extremely high REE contents （summed REE median 3200 μg/L, n=33）. At both RM and SC, pyrite oxidation and dissolution produce low pH waters that interact with and dissolve bedrock minerals, resulting in acidic, metal-laden, naturally degraded streams that are mostly devoid of aquatic life. Ferricrete is common. In contrast, WTF barely produces a surficial environmental footprint, mostly due to topography and relief. RM and SC are well exposed in the areas of relatively high relief, and both exhibit extensive areas of quartz-sericite-pyrite-alteration. While WTF shares many of the same deposit-and alteration characteristics, it is concealed by tundra in a large, nearly flat area. Surface water at WTF is absent and outcrops are sparse. Even though WTF is roughly the same size as Red Mountain （both around 3 million tonnes） and has similar base- and precious-metal grades, the surficial geochemical manifestation of WTF is minimal. However, exposure through mining of the altered, mineralized rock at WTF potentially could initiate the same processes of pyrite oxidation, acid generation, and mineral dissolution that are observed naturally at RM and SC.  相似文献   

华南下寒武统镍钼矿层中铜铅锌矿物的发现及意义     

陈益平  潘家永  夏菲  郭国林  陈少华  曹双林  严兆斌 《华东地质学院学报》2006,29(1):32-37

华南扬子地块是我国古热水沉积成矿作用最为发育的地区之一,其热水沉积特性最早引起我国学者的关注。华南下寒武统黑色岩系中赋存多个与热水沉积成矿作用相关的大型、超大型重晶石矿床与N i-Mo-U-V多金属富集层。进一步研究分布在华南扬子地块黑色岩系中的金属、非金属矿床成因及其地球化学特征,对认识华南乃至全球晚震旦—早寒武世生物与环境演化有着十分重要的意义。本文对华南下寒武统镍-钼富集层矿石进行电子探针研究,识别出黄铜矿、黝铜矿等铜的独立矿物;闪锌矿等锌的独立矿物;方铅矿、白铅矿等铅的独立矿物。研究表明,在镍-钼矿石中这些矿物的发现为镍-钼矿层是热水沉积作用产物提供了直接的矿物学证据。  相似文献   

红旗岭镁铁-超镁铁岩侵入体及铜镍硫化物矿床的成岩成矿机制   总被引：7，自引：0，他引：7  

杨言辰  孙德有  马志红  许文良 《吉林大学学报(地球科学版)》2005,35(5):593-600

红旗岭铜镍矿床地处华北地台与吉黑地槽系接触带--辉发河断裂北侧.区内出露30多个镁铁-超镁铁质岩体,其中1、7号超镁铁岩体中赋存铜镍硫化物矿(床)体.含矿岩体分相明显,各类岩石均具堆积结构.铜镍矿体呈似板状、脉状、透镜状及囊状赋存于超镁铁岩体底部橄榄辉岩相中.岩石学和地球化学研究表明,7号岩体形成以流动分异为主,1号岩体为重力分异;原始岩浆属拉斑玄武质,块状矿石系压滤作用产物,后续岩浆的补给和混合补充了成矿物质,硫化物不混溶程度受挥发分制约,矿床属岩浆深部熔离分异成因,成矿时代为印支期.  相似文献   

四川昌台农都柯金银矿矿床地质特征及成矿远景     

许远平  姚丽  李继军 《物探化探计算技术》2005,27(3):241-245

农都柯火山岩浅成低温热液型金银矿床系在三江地区义敦岛弧带被首次发现,经初步评价达到中型规模。矿床赋存于流纹质火山碎屑岩中,受北北西向剪切带控制,矿体呈透镜状或似层状,基本顺层产出。围岩蚀变强烈,以硅化为主,次为绢云母化和重晶石化。矿石由黄铁矿、闪锌矿、自然金、辉锑铅矿、砷黝铜矿、辉锑矿、辉锑银铅矿、雄黄、雌黄等组成,为典型的低温热液矿物组合。主矿化温度发生在200℃以下,矿化元素除Ag、Au外,As、Sb、Hg也达到或接近工业品位。通过地球物理、地球化学方法的测量,成矿远景较好。  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