Hard X-ray spectrum of Mkn 421 during the active phase

Spectral measurement of Mkn 421 were made in the hard X-ray energy band of 20–200 keV using a high sensitivity, large area scintillation counter telescope on November 21, 2000 and these coincided with the onset of an active X-ray phase as seen in the ASM counting rates on board RXTE. The observed spectrum can not be fitted to a single power law similar to the PDS data of BeppoSAX. The data can be fitted both by a two component power-law function or a combination of an exponential function with a power law component at the high energies above 80 keV. We identify these components with those arising from the synchrotron self compton and the high energy power-law tail arising from the upgrading of the thermal photons due to multiple Compton scattering a la Cyg X-1. A comparison with the earlier data clearly suggests a spectral variability in the hard X-ray spectrum of the source. We propose a continuously flaring geometry for the source as the underlying mechanism for energy release.     

大西洋中脊热液硫化物的矿物学研究

利用１９８９年在大西洋热液活动区采集的块状硫化物样品，采用矿相显微镜、电子显微镜和电子探针等手段，进行了矿物共生组合、矿物形态与成分标型及其演化特征研究。结果表明，大西洋热液成矿作用可以划分为热液期与沉积期两个成矿期，和石英－黄铁矿阶段、黄铁矿阶段、多金属硫化物阶段、胶状黄铁矿阶段和非晶质ＳｉＯ２阶段等５个成矿阶段；不同成矿阶段黄铁矿的共生矿物和矿物特征不同，在晶体形态上具有从单形晶－聚形晶－胶状     

山西省基础地理信息数据库的技术研究

山西省基础地理信息数据库是山西省空间数据基础设施建设的重要组成部分,主要介绍数据库建设的技术方案和关键技术.     

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

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.     

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

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.     

Structure cristalline d'une ménéghinite naturelle pauvre en cuivre,Cu0,58Pb12,72(Sb7,04Bi0,24)S24Crystal structure of a Cu-poor natural meneghinite,Cu0.58Pb12.72(Sb7.04Bi0.24)S24

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.     

略阳煎茶岭铜镍硫化物矿床Re—Os同位素年龄及其地质意义

采用矿石Re-Os同位素方法对陕西省煎茶岭硫化镍矿床矿石进行了成矿年代学研究,获得了878士27 Ma(1σ)的等时线年龄,首次厘定了该矿床成矿时代为新元古代,成岩成矿基本同时.通过对878 Ma硫化镍矿石初始Re-Os同位素体系的γOs计算和Re/Os值分析表明,其yOs和Re/Os值变化范围大,深部条带状矿石的Re/Os值仅为0.05,yOs为-6.70;块状矿石的Re/Os值范围为4.24～24.43,γOs为-15.37～+280.65,说明成矿过程中有壳源物质的混染;两件样品的γOs为负值(-15.37,-6.70),可能指示其超镁铁质岩浆来源于Re亏损地幔.煎茶岭超基性岩体年龄及其镍矿石的Re-Os等时线年龄与扬子克拉通北缘火山岩浆活动时间相对应,它们是扬子克拉通西北缘晋宁期构造岩浆成矿作用的产物.     

中子活化分析在铼—锇法年龄测定中的应用

同位素稀释中子活化分析铼与感耦等离子体质谱法测定锇相结合，应用于辉钼矿及铜＿镍硫化物矿物的铼＿锇年龄测定，取得了满意的结果，扩大了铼＿锇测年法的应用范围。     

Metallogenic model of the copper deposit

The copper deposits in the mid-lower reaches of the Changjiang River consist mainly of porphyry, skarn and massive sulphide deposits. According to the geological background, the types of ore deposits and the mineralization, the metallogenic model of the copper deposits is discussed. It is pointed out that the ore-forming hydrothermal fluids came mainly from magmatic water and were related to the intermediate-acid intrusions, and that the formation of skarn arid massive sulphide deposits coincided with the mineralization of porphyry deposits. Project supported by Doctorate Foundation of the State Education Commission of China.     

内蒙古镁铁质-超镁铁质岩型铜镍矿床成矿条件与找矿远景分析

按构造环境控岩控矿特点,划分区内铜镍型矿成矿(岩)带,分析成矿条件,研究了与该类矿床成矿有关的镁铁质岩、超镁铁质岩分布规律及铜镍硫化物成矿特征,提出了找矿方向和建议.