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91.
92.
乌拉嘎金矿床地质地球化学特征研究 总被引：8，自引：3，他引：5
乌拉嘎金矿矿体赋存于燕山晚期的斜长花岗斑岩与黑龙江群下亚群接触带附近的近东西向展布的构造角砾岩中,围岩蚀变强烈;金矿化主要受角砾岩带控制。矿床成矿微量元素组合为Au、Hg、As、Sb,且含量均呈向下递增的趋势。LaN／YbN值变化范围为14．146～28．311,稀土元素配分模式为右倾的轻稀土富集型;∑LREE：165．76～62．68;∑HREE：45．82～15．2;LREE／HREE为6．09～4．124,为轻稀土富集型。岩体中流体包裹体以低盐、低压且有天水加入为特征,为典型的浅成低温热液型矿床。 相似文献
93.
新疆哈密卡拉塔格铜(锌)矿红石幅(K46E009008)1∶50 000矿产地质图数据库是根据《固体矿产地质调查技术要求(1∶50 000)》(DD2019-02)和行业其他标准及要求,在充分利用1∶200 000、1∶50 000等区域地质调查工作成果资料的基础上,采用数字填图系统进行野外地质专项填图,并应用室内与室外填编图相结合的方法完成。本数据库将中-上奥陶统荒草坡群大柳沟组、下志留统红柳峡组和卡拉塔格组的建造类型进行了重新划分,把图幅内侵入岩时代划分为志留纪、泥盆纪、二叠纪等3期,建立了岩浆岩演化序列。图幅区内有大中小型矿床和矿点共8个,成矿时代集中分布在志留纪、石炭纪,赋矿围岩为火山碎屑岩和次火山岩,该区优势矿产以铜锌金为主,矿床类型以VMS型和次火山热液脉型矿床为主,分布在图幅东南一带。除金属矿产外,尚有膨润土矿床产出,具有较好的找矿潜力。本数据库包含5个地层单位和3期岩浆岩资料,数据量约为 15.1 MB。这些数据充分反映了该图幅 1∶50 000 矿产地质调查示范性成果,对该区矿产资源研究和勘查等具有参考意义。 相似文献
94.
95.
贵州松桃县木耳溪锰矿为典型的层控型锰矿床,矿体呈层状赋存于南华系下统大塘坡组第一段(Pt2b3d 1)底部的炭质页岩中,产出层位稳定,矿体产状与围岩产状一致。通过统计对比,锰矿层的矿化程度与含锰岩系的厚度呈正比,即当南华系大塘坡组地层厚度大于15m时,有可能成为锰矿的主要找矿方向。 相似文献
96.
97.
河南省商城县汤家坪钼矿床地质和流体包裹体研究 总被引：21，自引：15，他引：6
河南省商城县汤家坪钼矿床产于大别造山带,属于陆-陆碰撞体制的斑岩型矿床。其流体成矿过程可以分为早、中、晚3个阶段,分别以石英-钾长石-磁铁矿-辉钼矿-黄铁矿、石英-多金属硫化物和石英-碳酸盐±黄铁矿组合为标志。石英中可见水溶液包裹体、CO2-H2O型包裹体、纯CO2包裹体和含子晶多相包裹体,但晚阶段石英中只有水溶液包裹体。早阶段和中阶段还发育特殊的含子晶的CO2包裹体,这在以往的斑岩型矿床中鲜有报道。早阶段流体包裹体均一温度>375℃,盐度最高可达62.10％NaCleqv,包裹体内含大量指示氧化条件的赤铁矿子晶以及一些石盐、钾盐、黄铜矿、脆硫锑铅矿子晶。中阶段包裹体均一温度集中在235~335℃,盐度为1.06％~45.87％NaCleqv。除石盐、钾盐子晶外,还含大量黄铜矿、脆硫锑铅矿子晶,表明中阶段还原性较强。晚阶段流体包裹体均一温度集中在115~195℃,盐度较低,介于1.91％~9.98％NaCleqv。中阶段强烈的流体沸腾作用是导致成矿物质快速沉淀的重要机制。总之,初始成矿流体为岩浆热液,以高温、高盐度、高氧化性、富CO2、高金属元素含量为特征;中阶段流体发生沸腾,导致CO2逃逸,氧化性降低,成矿物质快速沉淀;晚阶段流体以低温、低盐度、无子晶、贫CO2为特征,属于大气降水热液。汤家坪钼矿床发育特殊的含子晶的CO2包裹体,可作为大陆碰撞造山带产出富含CO2的斑岩成矿系统的典型实例。 相似文献
98.
The Engineer Mine epithermal precious metal deposit in British Columbia, Canada, is related to Eocene Sloko-Skukum-Group (SSG) volcanism and, according to previous studies, contains roscoelite in intimate association with electrum. Roscoelite, a vanadian mica, is considered characteristic of low-sulfidation epithermal deposits related to alkaline magmatism. This contradicts the fact that the SSG volcanics are subalkaline. In order to address this ambiguity and to accurately classify the style of epithermal mineralization at the Engineer Mine we conducted detailed petrographic, mineralogical, geochronological, fluid inclusion, and stable isotope studies.The principal ore assemblage of the Engineer Mine epithermal veins precipitated in response to boiling during a hydrothermal event at 49.90 Ma ± 0.25 Ma. During this event electrum, arsenopyrite, pyrite ± chalcopyrite ± sphalerite ± löllingite ± tetrahedrite-group phases ± allargentum ± acanthite ± hessite ± dyscrasite ± stibarsen ± galena and an unidentified Ag-rich phase were deposited in conjunction with amorphous silica, platy and rhombic calcite, K-feldspar, and vanadian illite. Fluid inclusion and stable isotope data suggest that the ore-forming fluid was boiling at ∼220 °C during vein mineralization and had an isotopic composition derived from local meteoric water. Based on these results the Engineer Mine is classified as an epithermal low-sulfidation deposit, which shares similarities with alkaline and subalkaline epithermal low-sulfidation deposits. This is attributed to the fact that the SSG volcanic rocks are borderline subalkaline to alkaline in character and that the sedimentary host rocks are vanadium-bearing. These sedimentary rocks contributed the bulk of the vanadium to the Engineer Mine epithermal system. The presence of roscoelite at the Engineer Mine could not be confirmed during this study. The mica referred to as roscoelite in previous publications instead is vanadian illite. To our knowledge the only alkaline low-sulfidation epithermal precious metal deposit that contains V-mica which exclusively qualifies as true roscoelite is the Porgera deposit, Papua New Guinea. 相似文献
99.
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. 相似文献
100.
《Geoforum》2017
Highly alkaline industrial residues (e.g., steel slag, bauxite processing residue (red mud) and ash from coal combustion) have been identified as stocks of potentially valuable metals. Technological change has created demand for metals, such as vanadium and certain rare earth elements, in electronics associated with renewable energy generation and storage. Current raw material and circular economy policy initiatives in the EU and industrial ecology research all promote resource recovery from residues, with research so far primarily from an environmental science perspective. This paper begins to address the deficit of research into the governance of resource recovery from a novel situation where re-use involves extraction of a component from a bulk residue that itself represents a risk to the environment. Taking a political industrial ecology approach, we briefly present emerging techniques for recovery and consider their regulatory implications in the light of potential environmental impacts. The paper draws on EU and UK regulatory framework for these residues along with semi-structured interviews with industry and regulatory bodies. A complex picture emerges of entwined ownerships and responsibilities for residues, with past practice and policy having a lasting impact on current possibilities for resource recovery. 相似文献