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     

Geochemistry of Flooded Underground Mine Workings Influenced by Bacterial Sulfate Reduction

Unlike the majority of the water in the flooded mine complex of Butte Montana, which includes the highly acidic Berkeley pit lake, groundwater in the flooded West Camp underground mine workings has a circum-neutral pH and contains at least 8 μM aqueous sulfide. This article examines the geochemistry and stable isotope composition of this unusual H₂S-rich mine water, and also discusses problems related to the colorimetric analysis of sulfide in waters that contain FeS_(aq) cluster compounds. The West Camp mine pool is maintained at a constant elevation by continuous pumping, with discharge water that contains elevated Mn (90 μM), Fe (16 μM), and As (1.3 μM) but otherwise low metal concentrations. Dissolved inorganic carbon in the mine water is in chemical and isotopic equilibrium with rhodochrosite in the mineralized veins. The mine water is under-saturated with mackinawite and amorphous FeS, but is supersaturated with Cu- and Zn-sulfides. However, voltammetry studies show that much of the dissolved sulfide and ferrous iron are present as FeS_(aq) cluster molecules: as a result, the free concentration of the West Camp water is poorly constrained. Concentrations of dissolved sulfide determined by colorimetry were lower than gravimetric assays obtained by AgNO₃ addition, implying that the FeS_(aq) clusters are not completely extracted by the Methylene Blue reagent. In contrast, the clusters are quantitatively extracted as Ag₂S after addition of AgNO₃. Isotopic analysis of co-existing aqueous sulfide and sulfate confirms that the sulfide was produced by sulfate-reducing bacteria (SRB). The H₂S-rich mine water is not confined to the immediate vicinity of the extraction well, but is also present in flooded mine shafts up to 3 km away, and in samples bailed from mine shafts at depths up to 300 m below static water level. This illustrates that SRB are well established throughout the southwestern portion of the extensive (>15 km³) Butte flooded mine complex.     

甘肃金川铜镍矿床Ⅰ矿区深部边部地质-地电化学-地球物理多元信息成矿预测

在综合研究分析金川铜镍矿区前人资料的基础上,经现场地质调查、收集地质资料,总结了矿区的成矿规律,有针对性地在Ⅰ矿区的北东侧开展了地质-地球电化学-地球物理多元信息的深部边部成矿预测。根据地电化学数据的统计结果,对矿区元素共生组合和成矿作用、成矿期次等地球化学特征进行了探讨,以此确定了地电化学综合异常;在掌握矿区岩石、矿石物性特征的情况下,通过地球物理勘探推测在Ⅰ号矿体与F1断裂之间存在一隐伏的超基性岩体。最终对矿区进行地质-地电化学-地球物理特征的综合分析,圈定了测区的找矿远景区。     

狼山-渣尔泰山成矿带铁铜铅锌多金属硫化物矿床特征研究

狼山-渣尔泰山多金属成矿带位于华北地台北缘西段的中元古代被动陆缘裂陷槽内,其产出的多处大型-超大型铜、铅、锌、铁多金属硫化物矿床的矿床特征具相似性和可对比性。通过分析该成矿带的区域地质背景、含矿建造特征及其产出的典型矿床（东升庙、炭窑口、霍各乞、甲生盘）的矿床地质特征,得出该成矿带内铜铅锌铁多金属硫化物矿床的以下特征：①盆地控矿特征十分明显;②成矿过程中伴有与成矿作用关系密切的同生断裂活动和同沉积期火山活动;③成矿元素具分带性和规律性组合的特征;④各典型矿床具鲜明的“时控”、“层控”和“岩控”特点;⑤成矿作用具有间歇性和多期演化成矿的特征;⑥含矿建造具有典型地球化学剖面结构序列特征;⑦矿体的产状与含矿岩系一致,且相应类型的矿石对应相应的容矿岩性。     

Relative contribution of magmatic and post-magmatic processes in the genesis of the Thompson Mine Ni-Co sulfide ores,Manitoba, Canada

The Ni-Co-(PGE) sulfide deposits of the Thompson Nickel Belt (TNB) in Northern Manitoba, Canada are part of the fifth largest nickel camp in the world based on contained nickel; past production from the TNB deposits is 2500 kt Ni. The Thompson Deposit is located on the eastern and southern flanks of the Thompson Dome structure, which is a re-folded nappe structure formed during collision of the Trans-Hudson Orogen with the Canadian Shield at 1.9–1.7 Ga. The Thompson Deposit is almost entirely hosted by P2 member sulfidic metasedimentary rocks of the Paleoproterozoic Ospwagan Group. Variably serpentinised and altered dunites, peridotites and pyroxenites contain disseminated sulfides and have a spatial association with sediment-hosted Ni sulfides which comprise the bulk of the ore types. These rocks formed from rift-related komatiitic magmas that were emplaced at 1.88 Ga, and subsequently deformed by boudinage, thinning, folding, and stacking.Disseminated sulfide mineralization in the large serpentinised peridotite and dunite intrusions that host the Birchtree and Pipe Ni-Co sulfide deposits typically has 4–6 wt% Ni in 100% sulfide. The disseminated sulfides in the less abundant and much smaller boudinaged serpentinised peridotite and dunite bodies associated with the Thompson Deposit have 7–10 wt% Ni in 100% sulfide. The majority of Thompson Mine sulfides are hosted in the P2 member of the Pipe Formation which is a sulfidic schist developed from a shale prololith; the mineralization in the schist includes both low Ni tenor (<1 wt% Ni in sulfide) and barren sulfide (<200 ppm Ni) and a Ni-enriched sulfide with 1–18 wt% Ni in 100% sulfide. The semi-massive and massive sulfide ores show a similar range in Ni tenor to the metasediment-hosted mineralization, but there are discrete populations with maximum Ni tenors of ∼8, 11 and 13 wt% Ni in 100% sulfide. The variations in Ni tenor are related to the Ni/Co ratio (high Ni/Co correlates with high Ni tenor sulfide) and this relationship is produced by the different Ni/Co ratios in sulfides with a range in proportions of pyrrhotite and pentlandite. Geological models of the ore deposit, host rocks, and sulfide geochemical data in three dimensions reveal that the Thompson Deposit forms an anastomosing domain on the south and east flanks of a first order D3 structure which is the Thompson Dome. In detail, a series of second order doubly-plunging folds on the eastern and southern flank control the geometry of the mineral zones. The position of these folds on the flank of the Thompson Dome is a response to the anisotropy of the host rocks during deformation; ultramafic boudins and layers of massive quartzite in ductile metasedimentary rocks control the geometry of the doubly-plunging F3 structures. The envelope of mineralization is almost entirely contained within the P2 member of the Pipe formation, so the deposit is clearly folded by the first order and second order D3 structures. The sulfides with highest Ni tenor (typically >13 wt% Ni in sulfide) define a systematic trend that mirrors the configuration of the second order doubly-plunging F3 structures on the flanks of the Dome. Although moderate to high Ni tenor mineralization is sometimes localized in fold hinges, more typically the highest Ni tenor mineralization is located on the flanks of the fold structures.There is no indication of the mineralogical and geochemical signatures of sedimentary exhalative or hydrothermal processes in the genesis of the Thompson ores. The primary origin of the mineralization is undoubtedly magmatic and this was a critical stage in the development of economic mineralization. Variations in metal tenor in disseminated sulfides contained in ultramafic rock indicate a higher magma/sulfide ratio in the Thompson parental magma relative to Birchtree and Pipe. The variation in Ni tenor of the semi-massive and massive sulfide broadly supports this conclusion, but the variations in metal tenor in the Thompson ores was likely created partly during deformation. The sequence of rocks was modified by burial and loading of the crust (D2 events) to a peak temperature of 750 °C and pressure of 7.5 kbar. The third major phase of deformation (D3) was a sinistral transpression (D3 event) which generated the dome and basin configuration of the TNB. These conditions allowed for progressive deformation and reformation of pyrrhotite and pentlandite into monosulfide solid solution as pressure and temperature increased; this process is termed sulfide kinesis. Separation of the ductile monosulfide solid solution from granular pentlandite would result in an effective separation of Ni during metamorphism, and the monosulfide solid solution would likely be spread out in the stratigraphy to form a broad halo around the main deposit to produce the low Ni tenor sulfide. Reformation of pentlandite and pyrrhotite after the peak D2 event would explain the broad footprint of the mineral system. The effect of the D3 event at lower pressure and temperature would have been to locally redistribute, deform, and repeat the lenses of sulfide.The understanding of the relationships between petrology, stratigraphy, structure, and geochemistry has assisted in formulating a predictive exploration model that has triggered new discoveries to the north and south of the mine, and provides a framework for understanding ore genesis in deformed terrains and the future exploration of the Thompson Nickel Belt.     

现代海底热液成矿作用

从现代块状硫化物矿床成矿特征对比角度,总结分析了世界现代海底喷流的块状硫化物成矿堆积,综述了现代海底块状硫化物成矿主要形成于洋壳和岛弧环境的实际观察结果,突出强调了洋壳环境和岛弧或陆壳环境两种成矿环境对成矿类型分类的意义。对上地幔部分熔融岩浆来源与地壳物质可能带入、火山喷发岩浆系列的演化和对热液成矿作用的控制进行了讨论,对比分析了岩浆流体对成矿的重要贡献和控制作用,以及成矿热液循环体系形成的条件和模式。     

小红石砬子银铅锌矿床地质特征及找矿标志

本文试图通过小红石砬子银铅锌矿床产于火山穹窿构造环境、控矿与海相火山-沉积建造有关、热液蚀变种类与矿体在金属矿化、元素分布空间上具有分带性等特征,论证该矿床属于位于火山穹窿构造环境中的火山成因块状硫化物矿床。进而推测同处于吉中弧形构造带中的地局子、新立屯、二道林子、圈岭等赋存于上古生界二叠系火山-沉积建造中的多金属硫化物矿床也应同属于与火山作用有关的块状硫化物矿床。在此基础上提出有关省内地槽区块状硫化物多金属矿床的几点找矿评价标志。     

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.     

西澳州Cattle Creek地区铜镍硫化物矿床成矿潜力探讨

西澳州Catlle Creek地区位于金伯利地块西缘霍尔斯克里克(Halls Creek)活动带上,附近发育有深大断裂。研究区内发现多处基性-超基性小岩体及岩脉且存在两处矿化点(带),存在两处1∶5万土壤地球化学甲类综合异常区,二者均主要由Cu、Ni、Au、Mo、Co等元素组成,多个浓集中心,异常套合较好,Cu、Ni的极大值均超过或接近边界品位,甚至工业品位,二者与矿化等信息套合良好。岩体中岩石样品主量元素特征显示其具有辉长岩-苏长岩的成矿专属性特征;在AFM图解上,岩石样品显示原始岩浆为高MgO拉斑玄武岩系列。微量元素原始地幔标准化蛛网图表明岩体岩浆演化过程中发生过明显的陆壳物质同化混染作用。稀土元素配分图反映出成岩过程中有相似的分异演化过程,并表明岩浆在演化过程中存在明显橄榄石分离结晶作用。研究区与萨凡纳矿床具有很高的可对比性,同时符合古大陆内小岩体成矿系统理论。表明研究区具较高的成矿潜力。