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1.
Uranium deposits containing molybdenum and fluorite occur in the Central Mining Area, near Marysvale, Utah, and formed in an epithermal vein system that is part of a volcanic/hypabyssal complex. They represent a known, but uncommon, type of deposit; relative to other commonly described volcanic-related uranium deposits, they are young, well-exposed and well-documented. Hydrothermal uranium-bearing quartz and fluorite veins are exposed over a 300 m vertical range in the mines. Molybdenum, as jordisite (amorphous MoS2), together with fluorite and pyrite, increase with depth, and uranium decreases with depth. The veins cut 23-Ma quartz monzonite, 20-Ma granite, and 19-Ma rhyolite ash-flow tuff. The veins formed at 19-18 Ma in a 1 km2 area, above a cupola of a composite, recurrent, magma chamber at least 24 × 5 km across that fed a sequence of 21- to 14-Ma hypabyssal granitic stocks, rhyolite lava flows, ash-flow tuffs, and volcanic domes. Formation of the Central Mining Area began when the intrusion of a rhyolite stock, and related molybdenite-bearing, uranium-rich, glassy rhyolite dikes, lifted the fractured roof above the stock. A breccia pipe formed and relieved magmatic pressures, and as blocks of the fractured roof began to settle back in place, flat-lying, concave-downward, “pull-apart” fractures were formed. Uranium-bearing, quartz and fluorite veins were deposited by a shallow hydrothermal system in the disarticulated carapace. The veins, which filled open spaces along the high-angle fault zones and flat-lying fractures, were deposited within 115 m of the ground surface above the concealed rhyolite stock. Hydrothermal fluids with temperatures near 200 °C, 18OH2O∼−1.5, DH2O∼−130, log f O2 about −47 to −50, and pH about 6 to 7, permeated the fractured rocks; these fluids were rich in fluorine, molybdenum, potassium, and hydrogen sulfide, and contained uranium as fluoride complexes. The hydrothermal fluids reacted with the wallrock resulting in precipitation of uranium minerals. At the deepest exposed levels, wallrocks were altered to sericite; and uraninite, coffinite, jordisite, fluorite, molybdenite, quartz, and pyrite were deposited in the veins. The fluids were progressively oxidized and cooled at higher levels in the system by boiling and degassing; iron-bearing minerals in wall rocks were oxidized to hematite, and quartz, fluorite, minor siderite, and uraninite were deposited in the veins. Near the ground surface, the fluids were acidified by condensation of volatiles and oxidation of hydrogen sulfide in near-surface, steam-heated, ground waters; wall rocks were altered to kaolinite, and quartz, fluorite, and uraninite were deposited in veins. Secondary uranium minerals, hematite, and gypsum formed during supergene alteration later in the Cenozoic when the upper part of the mineralized system was exposed by erosion. Received: 23 June 1997 / Accepted: 15 October 1997  相似文献   

2.
显微镜下矿石薄片鉴定和铀矿物电子探针分析显示,白兴吐铀矿床发育高岭石化、碳酸盐化、黄铁矿化、水云母-绢云母化和赤铁矿化等中低温热液蚀变;矿石的铀矿物主要为铀石,少量沥青铀矿,以及部分含钛铀矿物,矿石普遍富含磷和钛。铀矿物与热液成因的胶状、团块状和莓状黄铁矿、铁白云石、赤铁矿等共生。这些特征表明,该矿床的工业铀矿化与热液作用关系密切。  相似文献   

3.
Despite having been a target for volcanic-hosted massive sulfide (VHMS) deposits since the 1960s, few resources have been defined in the Archean Yilgarn Craton of Western Australia. Exploration challenges associated with regolith and deep cover exacerbate the already-difficult task of exploring for small, deformed deposits in stratigraphically complex, metamorphosed volcanic terranes. We present results of drill-core logging, petrography, whole-rock geochemistry and portable X-ray Fluorescence data from the King Zn deposit, to help refine mineralogical and geochemical halos associated with VHMS mineralisation in amphibolite-facies greenstone sequences of the Yilgarn Craton. The King Zn deposit (2.15?Mt at 3.47?wt% Zn) occurs as a 1–7 m-thick stratiform lens dominated by iron sulfides, in an overturned, metamorphosed volcanic rock-dominated sequence located ～140?km east of Kalgoorlie. The local stratigraphy is characterised by garnet-amphibolite and strongly banded intermediate to felsic schists, with rare horizons of graphitic schist and talc schist. Massive sulfide mineralisation is characterised by stratiform pyrite–pyrrhotite–sphalerite at the contact between quartz–muscovite schists (‘the footwall dacite’), and banded quartz–biotite and amphibole?±?garnet schists of the stratigraphic hanging-wall. A zone of pyrite–(sphalerite) and pyrrhotite–pyrite–(chalcopyrite) veining extends throughout the stratigraphic footwall. Footwall garnet-amphibolites are of sub-alkaline basaltic affinity, with a central zone dominated by chlorite?±?magnetite interpreted to represent the Cu-bearing feeder zone. SiO2, CaO, Fe2O3T, MgO and Cu concentrations are highly variable, reflecting quartz–epidote?±?chlorite?±?magnetite?±?sulfide alteration. Hydrothermal alteration in stratigraphically overlying intermediate to felsic rocks is characterised by a mineral assemblage of quartz–muscovite?±?chlorite?±?albite?±?carbonate. Cordierite and anthophyllite are locally significant and indicative of zones of Mg-metasomatism prior to metamorphism. Increases in SiO2, Fe2O3T, pathfinder elements (e.g. As, Sb, Tl), and depletions of Na2O, CaO, Sr and MgO occur in quartz–muscovite schists approaching massive sulfide mineralisation. Within all strata (including the immediate hanging-wall), the following pathfinder elements are strongly correlated with Zn: Ag, As, Au, Bi, Cd, Eu/Eu*, Hg, In, Ni, Pb, Sb, Se and Tl. These geochemical halos resemble less metamorphosed VHMS deposits across the Yilgarn Craton and suggest that although metamorphism leads to element mobility and mineral segregation at the thin-section scale, assay samples of ～20?cm length are sufficient to vector to mineralisation in amphibolite facies greenstone belts. Recognition of minerals such as Mg-chlorite, muscovite, cordierite, anthophyllite, biotite/phlogopite, and abundant garnet are significant, in addition to Al-rich phases (i.e. kyanite, sillimanite, andalusite and/or staurolite) not identified at King. Chemographic diagrams may be used to identify and distinguish different alteration trends, along with several alteration indices (e.g. Alteration Index, Carbonate–Chlorite–Pyrite Index, Silicification Index) and the abundance of normative corundum and quartz.  相似文献   

4.
Sedimentary units deposited during the post-rift stage of the Erlian Basin located in northeast China present an alternation of sandstone and mudstone layers. This sedimentological architecture is at the origin of confined permeable reservoirs hosting sandstone-type uranium deposits. The study of the Nuheting deposit offered the opportunity to identify synsedimentary/early diagenetic uranium concentrations and diagenetic mineralization hosted in mudstone-dominated layers of the Erlian Formation, indicating that a stock of uranium was present in the basin prior to the genesis of sandstone-hosted uranium deposits. Therefore, this pre-existing stock may constitute a significant source of uranium for the formation of roll front deposits present in other parts of the Erlian Basin.Detailed petrographic and geochemical study of drill-core samples from the Nuheting deposit led to the characterization of different stages related to the formation of the uranium ore bodies and allowed to propose a new metallogenic model. Uranium mineralization of the Nuheting deposit is mainly hosted in dark gray silty mudstone of wetland depositional environment of the Late Cretaceous Erlian Formation. Petrographic observations and EMP analyses evidenced that a significant amount of uranium was associated with clay minerals (interstratified clays, smectite, chlorite, palygorskyte, illite and kaolinite), either adsorbed on mineral surfaces as U (VI) ions or reduced mainly as UO2 nano to microcrystals disseminated in the clayey matrix, which corresponds to synsedimentary/early diagenetic concentrations. Trace elements on pyrite analyzed by LA-ICPMS, petrographic observations and whole-rock geochemical data led to the characterization of a diagenetic uranium mineralization. High As (1–50 ppm), Mo (10–500 ppm) and Se concentrations in the whole rock and the incorporation of these elements in pyrite highlight reducing conditions within the host-rocks during the diagenesis of the Erlian Formation. During the early diagenetic stage, uranium was either desorbed from clay minerals and organic materials to be reduced or directly reduced and precipitated as P-rich coffinite and pitchblende on pyrite crystals. During the late diagenetic stage, uranium was redistributed in situ and locally deposited mainly as coffinite on pyrites. Finally, an epigenetic stage of cementation was identified with sulfate and carbonate minerals, which may enclose some uranium minerals. This epigenetic stage of fluid circulation may be responsible for a minor uranium remobilization. Therefore, the Nuheting deposit experienced three main stages: (i) a synsedimentary/early diagenetic uranium concentration and mineralization, (ii) a late diagenetic in situ uranium remobilization and deposition on pyrite and (iii) an epigenetic cementation. Rock-Eval pyrolysis indicates that the organic matter contained in host-rocks of the Nuheting deposit is of type IV, inherited from land plant, and do not contain free hydrocarbons (very low S1). Therefore, our results do not support that migrated hydrocarbons were involved as a reducing agent for uranium mineralization.  相似文献   

5.
The Qianjiadian sandstone-type uranium deposit in Songliao Basin has become an ultra-large uranium deposit since its exploration and continuous development. The geological and metallogenic characteristics of this area have been studied widely since its discovery,but the detailed petrological features of its ore-bearing construction and favorable metallogenic conditions still require much detailed research. The mineralization of urnium deposit includes various geological processes resulting in the accumulation of uranium element. The source rock with high uranium concentration and much easier for the leaching of uranium is the basis of uranium mineralization. The later oxidation-reduction,mineral alteration are the key for the uranium deposits. In this paper,the petrological characteristic of lithology sandstone-type uranium deposit is studied by using the micro experimental analysis. It is found that the host rocks are primarily composed of medium-fine grained feldspar lithic sandstone,fine grained feldspar lithic sandstone,boulder-clay-bearing sandstone and glutenin. The amount of quartz and feldspar are close to the rock debris. The debris are mainly composed of rhyolite,rhyolitic tuff,and some trochyte,ayenite-aplite,granite,granite porphyry,andesite,silicalite and mudstone etc. the epigenetic alteration includes the carbonatization and kaolinization is general and intense at the local region,followed by the secondary epigenetic alteration includes pyritization,ferrugination and little baratization. Deep oil and gas infiltrate into the oil-bearing strata causing the oil stains,spots and spillage. The symbiosis of pyrite berry globule and micritic pyrite are common. The uranium element exists in the uranium-bearing minerals(e.g.,asphalt and coffinite)as well as the adsorbed state. The multi-genesis and multi-stages of the metallogenic model is established,i.e.,sedimentary preconcentration stage-interlayer infiltration stage-the oil and gas transformation stage-the oil and gas reduction stage.  相似文献   

6.
松辽盆地钱家店砂岩型铀矿床自勘查以来不断获得重大发现,已成为超大型铀矿床。该区矿床地质特征、成矿特点有过不少报道,但就其含矿建造的详细岩石学特征(蚀源区母岩)及有利的成矿条件等还需要随着研究程度的加深不断完善。铀矿的成矿作用包括导致铀元素集中形成铀矿的各种地质作用,其中,铀含量高且容易析出铀的源岩是铀成矿的物质基础,后期的氧化—还原、矿化蚀变是铀矿形成的关键。作者主要利用微观实验分析的方法,通过对钱家店砂岩型铀矿床赋矿岩石岩石学特征的详细分析,提出了矿层岩性主要为中—细粒长石岩屑砂岩、细粒长石岩屑砂岩和含泥砾砂岩和砂砾岩等,并且石英和长石总量与岩屑含量相近,岩屑主要以流纹岩、流纹质凝灰岩为主,次为粗面岩、正长细晶岩、花岗岩、花岗斑岩、安山岩、硅质岩和泥岩等。后生蚀变碳酸盐化、高岭石化较为普遍,局部强烈,其次黄铁矿化、氧化铁化,偶见重晶石化。常见深部油气渗入在赋矿层中出现油渍、油斑、溢散晕圈,共生黄铁矿莓球群及微细粒黄铁矿聚晶。铀的存在形式为铀矿物(沥青油矿、铀石)和吸附状态。分析了多成因—多阶段成矿模式,即沉积预富集阶段—层间渗入成矿阶段—油气改造富集成矿阶段—油气还原护矿阶段。  相似文献   

7.
This report presents mineralogical, geochemical and isotopic data on samples obtained using the Benthic Multi‐coring System (BMS) to drill a submarine hydrothermal deposit developed in a caldera on the summit of the Suiyo Seamount in the Izu–Bonin Island Arc, south of Japan. This deposit is regarded as the first example of Kuroko‐type sulfide mineralization on a volcano at the volcanic front of an island arc. The mineralization and hydrothermal alteration below the 300 × 150‐m area of active venting was investigated to depths of 2–9 m below the sea floor. Drilling beneath the area of active venting recovered a sequence of altered volcanic rocks (dacite lavas, pyroclastic rocks of dacite–rhyolite compositions and pumice) associated with sulfide veining and patches/veins of anhydrite. No massive sulfide was found, however, and the subsea‐floor mineralization to 10 m depth is dominated by anhydrite and clay minerals with some sulfides. Sulfide‐bearing samples contained high Au (up to 42 ppm), Ag (up to 263 ppm), As (up to 1550 ppm), Hg (up to 55 ppm), Sb (up to 772 ppm), and Se (up to 24 ppm). Electron probe microanalyzer indicated that realgar, orpiment, and mimetite were major As‐bearing minerals. The sulfides were also characterized by high Zn (>10%) compared to Cu (<6.3%) and Pb (<0.6%). The δ202Hg/198Hg, δ202Hg/199Hg and δ202Hg/200Hg of the sulfide‐bearing dacite samples and a sulfide chimney decreased with increasing Hg/Zn concentration ratio. The variation of the δ202Hg/198Hg ranged from ?2.8 to +0.5‰ to relative to S‐HG02027. The large range of these δ202Hg/198Hg was greater than might be expected for such a heavy element and may be due to a predominance of kinetic effects. The variation of δ202Hg/198Hg of sulfide‐bearing dacite samples suggested that light Hg isotope in the vapor mixed with oxygenated seawater near sea floor during mineralization. Lead isotope ratios of the sulfide were very similar to those of the dacite lava, suggesting that lead is of magmatic origin. The 87Sr/86Sr ratio (0.70872) of anhydrite was different from that of the dacite lava, and suggests an Sr derivation predominantly from seawater. Hydrothermal alteration of the dacite in the Suiyo hydrothermal field was characterized by Fe‐sulfides, anhydrite, barite, montmorillonite, chlorite/montmorillonite mixed‐layer minerals, mica, and chlorite with little or no feldspar or cristobalite. Hydrothermal clay minerals changed with depth from montmorillonite to chlorite/montmorillonite mixed‐layer minerals to chlorite and mica. Hydrogen isotope ratios of chlorite/montmorillonite and mixed‐layer, mica‐chlorite composites obtained below the active venting sites ranged from ?49 to ?24‰, suggesting seawater as the dominant fluid causing alteration. Oxygen isotope ratios of anhydrite ranged from 9.2 to 10.4‰ and anhydrite formation temperatures were calculated to be 188–207°C. Oxygen isotope ratios ranged from +5.2 to +9.2‰ for montmorillonite, +3.2 to +4.5‰ for chlorite/montmorillonite mixed‐layer minerals, and +2.8 to +3.8‰ in mixtures of chlorite and mica. The formation temperatures of montmorillonite and of the chlorite–mica mixture were 160–250°C and 230–270°C, respectively. The isotope temperatures for clay minerals (220–270°C) and anhydrite (188°C) were significantly lower than the borehole temperature (308.3°C) measured just after the drilling, suggesting that temperature at this site is now higher than when clay minerals and anhydrite were formed.  相似文献   

8.
为了进一步深化铀矿物的富集机理.利用α径迹放射性照相、扫描电镜、电子探针等方法对鄂尔多斯盆地北部铀矿床中铀矿物的赋存状态进行了系统研究.发现该区铀矿物主要为铀石，少量沥青铀矿和含铀钛矿物.沉积-成岩期碎屑铀矿物赋存在碎屑颗粒内部，吸附在锐钛矿周围，为铀储层中预富集的铀.成矿期铀矿物大部分赋存在碎屑颗粒填隙部位，与黄铁矿、碳质碎屑相伴生，与石英颗粒及方解石胶结关系密切；部分吸附在包裹碎屑颗粒的蒙脱石薄膜上.另外发现了，沥青铀矿-赤铁矿-黄铁矿的矿物组合，以及硒铅矿（PbSe）和白硒铁矿（FeSe2）与铀矿物相伴生，并伴有REE含量明显升高.分析得出，沥青铀矿形成于成矿早期，氧化酸性流体与还原碱性流体的过渡界面，偏向于氧化酸性一侧；而铀石主要形成于成矿晚期的还原碱性环境.双重铀源供给、丰富的还原介质、多源流体的耦合，局部的热液流体叠加改造，共同造就了鄂尔多斯盆地北部大矿、富矿的形成.   相似文献   

9.
The Neo-Archean Dominion Reefs (~3.06 Ga) are thin meta-conglomerate layers with concentrations of U- and Th-bearing heavy minerals higher than in the overlying Witwatersrand Reefs. Ore samples from Uranium One Africa’s Rietkuil and Dominion exploration areas near Klerksdorp, South Africa, were investigated for their mineral paragenesis, texture and mineral chemical composition. The ore and heavy mineral assemblages consist of uraninite, other uraniferous minerals, Fe sulphides, Ni–Co sulfarsenides, garnet, pyrite, pyrrhotite, monazite, zircon, chromite, magnetite and minor gold. Sub-rounded uraninite grains occur associated with the primary detrital heavy mineral paragenesis. U–Ti, U–Th minerals, pitchblende (colloform uraninite) and coffinite are of secondary, re-mobilised origin as evidenced by crystal shape and texture. Most of the uranium mineralisation is represented by detrital uraninite with up to 70.2 wt.% UO2 and up to 9.3 wt.% ThO2. Re-crystallised phases such as secondary pitchblende (without Th), coffinite, U–Ti and U–Th phases are related to hydrothermal overprint during low-grade metamorphism and are of minor abundance.  相似文献   

10.
鄂尔多斯砂岩型铀矿床古层间氧化带中铀石的产状和形成   总被引：5，自引：0，他引：5  
鄂尔多斯盆地的东胜铀矿床是一个重要的大型砂岩型铀矿床,业已查明铀石是该铀矿床的主要含铀矿物,铀石的颗粒十分细小.大量的显微镜薄片和电子显微镜观察发现,铀石通常以不规则的集合体产出于蚀变黑云母裂隙和黄铁矿边缘.电子探针分析表明,铀石中w(UO2)变化较大,在50%～70%间.与铀石相关的黑云母已经强烈蚀变,转变为水黑云母、水白云母和绿泥石.黑云母在蚀变过程中K+逐渐流失,直到基本流失殆尽,与原始黑云母相比,水黑云母w(K2O)总体减少了6.54%[占原始蚀变黑云母中w(K2O)的74%],同时w(FeO)减少了7.40%[占原始蚀变黑云母中w(FeO)的29%];水白云母与原始黑云母相比,矿物成分也发生了很大的变化,其中,w(K2O)总体减少了7.87%[占原始蚀变黑云母中w(K2O)的89%],同时w(FeO)减少了19.22%[占原始蚀变黑云母中w(FeO)的76%],w(Al2O3)由16.64%增加至32.72%,增加了16.08%.根据铀石产出的特征和蚀变水黑云母和蚀变水白云母成分特征,探讨了铀酰离子(UO2+2)被还原成U4+和形成铀石[U(SiO 4) 1-x(OH) 4x]的机理,指出古层间氧化带中铀石的形成与黑云母的蚀变以及黄铁矿的形成有着密切的联系.  相似文献   

11.
The Kristineberg massive sulfide deposit is hosted by metamorphosed volcanic and subvolcanic rocks of the Palaeoproterozoic Skellefte Group. The deposit consists of: (1) two main massive sulfide horizons, the A-ores and B-ores, which dip steeply southwards and are separated by 100–150 m; and (2) the Einarsson Zone, a complex interval of Cu–Au-rich ‘stockwork‘ sulfides and small massive sulfide lenses in altered and deformed rocks near the 1,000 m level. The Einarsson Zone occurs some 20–100 m south of the B-ores. There are no definite younging indicators in the mine sequence. In many areas of the mine, the original host rocks are impossible to identify petrographically due to the abundance of secondary minerals such as quartz, chlorite, muscovite, cordierite, andalusite, phlogopite, pyrite and talc, combined with variably schistose fabrics. Application of immobile-element methods to 600 recent whole-rock chemical analyses has, however, allowed the original rock types to be identified and correlated. Rhyolite X lies immediately north of the A-ore, while andesitic to dacitic to rhyodacitic rocks make up the 100–150 m interval between the A-ore and B-ore, and massive rhyolite A lies immediately south of the B-ore. The felsic rocks are mostly of calc-alkaline affinity, excluding rhyolite X, which is transitional. The mine porphyry, which lies north of the A-ore and forms the marginal phase of the synvolcanic Viterliden Intrusive Complex, is compositionally similar to dacite and rhyodacite. Mass changes calculated for all rock types indicate that most of the volcanic rocks in the mine area are strongly depleted in Na and Ca, and have gained variable amounts of Mg and Fe, whereas Si changes range from negative to positive. Gains in Fe and changes in Si are largest within 5–10 m of the massive sulfide lenses. Cordierite-bearing schists of andesitic to felsic compositions that lie between massive sulfide lenses A and B are not as altered. The Einarsson Zone commonly shows large gains in Fe and Mg, while Si shows large gains to large losses. Immobile-element ratios indicate that very different secondary assemblages in the mine, e.g. andalusite–quartz–muscovite and cordierite–chlorite–talc, can be produced from the same precursor volcanic unit, e.g., rhyolite. Conversely, the same secondary mineral assemblage can be produced from different rocks, e.g. weakly altered andesite and strongly altered rhyolite. The common presence of cordierite + andalusite in the mine area, without anthophyllite, is unusual in the alteration systems of volcanic-hosted massive sulfide deposits, and is proposed to have formed by the metamorphic reaction of the synvolcanic alteration minerals kaolinite and chlorite to produce cordierite. Where kaolinite was in excess of chlorite, andalusite was also formed. We propose that highly acidic alteration fluids locally produced high-Al minerals such as kaolinite that either overprinted, or occurred in place of, a more typical sericite–chlorite–quartz alteration assemblage that otherwise formed near the massive sulfide lenses. Application of lithogeochemical methods to the altered, deformed and metamorphosed Kristineberg rocks has identified specific volcanic contacts with massive sulfide potential, and quantified the effects of synvolcanic hydrothermal alteration. Such an approach can increase the effectiveness of mineral exploration in metamorphosed terrains.  相似文献   

12.
《Ore Geology Reviews》2008,33(3-4):629-650
In the Raposos orogenic gold deposit, hosted by banded iron-formation (BIF) of the Archean Rio das Velhas greenstone belt, the hanging wall rocks to BIF are hydrothermally-altered ultramafic schists, whereas metamafic rocks and their hydrothermal schistose products represent the footwall. Planar and linear structures at the Raposos deposit define three ductile to brittle deformational events (D1, D2 and D3). A fourth group of structures involve spaced cleavages that are considered to be a brittle phase of D3. The orebodies constitute sulfide-bearing D1-related shear zones of BIF in association with quartz veins, and result from the sulfidation of magnetite and/or siderite. Pyrrhotite is the main sulfide mineral, followed by lesser arsenopyrite and pyrite. At level 28, the hydrothermal alteration of the mafic and ultramafic wall rocks enveloping BIF define a gross zonal pattern surrounding the ore zones. Metabasalt comprises albite, epidote, actinolite and lesser Mg/Fe–chlorite, calcite and quartz. The incipient stage includes the chlorite and chlorite-muscovite alteration zone. The least-altered ultramafic schist contains Cr-bearing Mg-chlorite, actinolite and talc, with subordinate calcite. The incipient alteration stage is subdivided into the talc–chlorite and chlorite–carbonate zone. For both mafic and ultramafic wall rocks, the carbonate–albite and carbonate–muscovite zones represent the advanced alteration stage.Rare earth and trace element analyses of metabasalt and its alteration products suggest a tholeiitic protolith for this wall rock. In the case of the ultramafic schists, the precursor may have been peridotitic komatiite. The Eu anomaly of the Raposos BIF suggests that it was formed proximal to an exhalative hydrothermal source on the ocean floor. The ore fluid composition is inferred by hydrothermal alteration reactions, indicating it to having been H2O-rich containing CO2 + Na+ and S. Since the distal alteration halos are dominated by hydrated silicate phases (mainly chlorite), with minor carbonates, fixation of H2O is indicated. The CO2 is consumed to form carbonates in the intermediate alteration stage, in halos around the chlorite-dominated zones. These characteristics suggest variations in the H2O to CO2-ratio of the sulfur-bearing, aqueous-carbonic ore fluid, which interacted at varying fluid to rock ratios with progression of the hydrothermal alteration.  相似文献   

13.
At the Matauri Bay halloysite deposit, economically valuable halloysite-rich clays are hosted by a sanidine rhyolite dome (Ar–Ar dated at 10.1?±?0.03?Ma). The rhyolite dome intrudes an older basalt and is overlain by alluvial sediments and a younger basalt (4.0?±?0.7?Ma). A blanket-like, halloysite-rich zone is restricted to depths of 10–30?m from the present day erosion surface. Primary sanidine and plagioclase phenocrysts in rhyolite are completely leached out in the halloysite-rich zone but are only partially leached out at greater depth. Halloysite was formed by hydrolysis and cation leaching of sanidine and plagioclase phenocrysts and groundmass glass in the rhyolite, resulting in loss of K, Ca, Na and Si and enrichment in OH (LOI 6–10%) and Al2O3 (20–30%) relative to least-altered rhyolite with 1.8% LOI and 14.5% Al2O3. Oxygen and hydrogen isotope data indicate the halloysite is supergene rather than hydrothermal in origin, which is consistent with the absence of pyrite, alunite and other acid-sulphate type hydrothermal minerals, and with the blanket-like alteration profile. The dominance of halloysite over kaolinite was favoured by water-saturated weathering conditions during the late Miocene-Pliocene subtropical weathering regime in Northland.  相似文献   

14.
The Alligator Rivers Uranium Field (ARUF) includes the mined and unmined Jabiluka, Ranger, Koongarra and Nabarlek unconformity-related uranium deposits and several small prospects including the newly discovered King River prospect. Uranium mineralisation is hosted by a variety of metamorphosed Nimbuwah Domain lithologies that are unconformably overlain by the Kombolgie Subgroup, a basin package of unmetamorphosed arenites and mafic volcanics. All of the uranium deposits and prospects preserve an identical alteration assemblage that is subdivided into a distal and proximal alteration zone. The distal alteration zone comprises an assemblage of sericite and chlorite that replace albite and amphibole. In some cases, this alteration can be traced >1000 m from the proximal alteration zone that is dominated by uraninite, hematite, chlorite and sericite. Uranium precipitated in the basement as uraninite at 1680 Ma at around 200°C from a fluid having δ18Ofluid values of 3.0±2.8‰ and δDfluid values of ?28±13‰ VSMOW reflecting an evolved marine source. These geochemical properties are indistinguishable from those recorded by diagenetic illite and chlorite that were collected from the Kombolgie Subgroup sandstones across the ARUF. The illite and chlorite formed in diagenetic aquifers, and where these aquifers intersected favourable basement rocks, such as those containing graphite or other reductants, U was precipitated as uraninite. Therefore, it is proposed that the Kombolgie Subgroup is the source for fluids that formed the deposits. A post-ore alteration assemblage dominated by chlorite, but also comprising quartz±dolomite±sulfide veins cut the uranium mineralisation at all deposits and has historically been recorded as part of the syn-ore mineralisation event. However, these minerals formed anywhere between 1500 to 630 Ma from fluids that have distinctly lower δ18Ofluid values around 1.5‰ and lower δDfluid values around ?45‰ reflecting a meteoric water origin. Despite unconformity-related uranium deposits having a large alteration halo, they remain difficult to find. The subtle alteration of albite to sericite several hundred metres from mineralisation occurs in isolation of any increase in trace elements such as U and radiogenic Pb and can be difficult or impossible to identify in hand specimen. Whole rock geochemical data indicate that Pearce Element Ratio (PER) analysis and General Element Ratio (GER) analysis may vector into this subtle alteration because it does not rely on an increase in trace elements to identify proximity to ore. PER and GER plots, Al/Ti vs (2Ca + Na + K)/Ti, Na/Al vs (Na + K)/Al, K/Al vs (Na + K)/Al and (Fe + Mg)/Al vs (Na + K)/Al provide a visual guide that readily distinguish unaltered from altered samples. A plot of (Na + K)/Al and (Fe + Mg)/Al on the x-axis against the concentration of trace elements on the y-axis reveals that U, Pb, Mo, Cu, B, Br, Ce, Y, Li, Ni, V and Nd are associated with the most intensely altered samples. The lithogeochemical vectors should aid explorers searching for uranium mineralisation in a prospective basin environment, but exploration must first focus on the characteristics of the basin to assess its mineralisation potential. A holistic model that describes the evolution of the Kombolgie Subgroup from deposition through diagenesis to formation of the uranium deposits in the underlying basement rocks is presented and has application to other basins that are considered prospective for unconformity-related uranium deposits. The model outlines that explorers will need to consider the thickness of the sedimentary pile, its lithological composition relative to depositional setting, the depth to which the sediments were buried during diagenesis and the degree of diagenesis achieved, which may be time dependant, before deciding on the prospectivity of the basin.  相似文献   

15.
The Bianbianshan deposit, the unique gold-polymetal (Au-Ag-Cu-Pb-Zn) veined deposit of the polymetal metallogenic belt of the southern segment of Da Hinggan Mountains mineral province, is located at the southern part of the Hercynian fold belt of the south segment of Da Hinggan Mountains mineral province, NE China. Ores at the Bianbianshan deposit occur within Cretaceous andesite and rhyolite in the form of gold-bearing quartz veins and veinlet groups containing native gold, electrum, pyrite, chalcopyrite, galena and sphalerite. The deposit is hosted by structurally controlled faults associated with intense hydrothermal alteration. The typical alteration assemblage is sericite + chlorite + calcite + quartz, with an inner pyrite - sericite - quartz zone and an outer seicite - chlorite - calcite - epidote zone between orebodies and wall rocks. δ34 S values of 17 sulfides from ores changing from –1.67 to +0.49‰ with average of –0.49‰, are similar to δ34 S values of magmatic or igneous sulfide sulfur. 206Pb/204Pb, 207Pb/204Pb and 208Pb/ 204Pb data of sulfide from ores range within 17.66–17.75, 15.50–15.60, and 37.64–38.00, respectively. These sulfur and lead isotope compositions imply that ore-forming materials might mainly originate from deep sources. H and O isotope study of quartz from ore-bearing veins indicate a mixed source of deep-seated magmatic water and shallower meteoric water. The ore formations resulted from a combination of hydrothermal fluid mixing and a structural setting favoring gold-polymetal deposition. Fluid mixing was possibly the key factor resulting in Au-Ag-Cu-Pb-Zn deposition in the deposit. The metallogenesis of the Bianbianshan deposit may have a relationship with the Cretaceous volcanic-subvolcanic magmatic activity, and formed during the late stage of the crust thinning of North China.  相似文献   

16.

Endeavour 42 is a structurally controlled Au deposit with similarities to adularia‐sericite deposits. It is the largest of four gold prospects discovered in the Late Ordovician Lake Cowal volcanic complex, adjacent to the Gilmore Fault Zone, in central New South Wales, Australia. The Lake Cowal volcanic complex consists of calc‐alkaline to shoshonitic volcanic rocks and related sedimentary rocks that were deposited in a relatively deep‐water environment. The volcanic and sedimentary rocks of the Lake Cowal volcanic complex were intruded by diorite and granodiorite. Low‐grade porphyry Cu (0.2–0.35% Cu) mineralisation is developed in parts of the granodiorite intrusion. The gold deposits are developed north of the porphyry Cu mineralisation and occur within a north‐south corridor adjacent to a north‐south‐oriented body of diorite. The Endeavour 42 deposit is hosted by three volcanic units and a diorite. The stratigraphic units at Endeavour 42, consistently strike 215° and dip 50°NW, and comprise an upper unit dominated by redeposited pyroclastic debris and a lower conglomerate unit with clasts of reworked volcanic rocks. Separating these units is a sequence of trachyandesite lava and hyaloclastite breccias. Laminated mudstone and siltstone throughout the sequence are indicative of a relatively deep‐water, below wave‐base, environment. Porphyritic dykes, which are typically associated with zones of faulting, cross‐cut both the volcano‐sedimentary sequence and the diorite. The major fault orientations are 290° and 340°, forming subparallel conjugate fault sets. Both sets of faults are mineralised, contain deformed porphyritic dykes and are associated with sericitic alteration. Endeavour 42 is a sulfide‐poor gold deposit with free native Au and Au associated with pyrite and sphalerite. Minor galena, pyrrhotite and chalcopyrite are also observed. Irregular pyrite veinlets and carbonate‐sulfide veinlets occur in the upper unit of re‐deposited pyroclastic debris. Auriferous veins are parallel‐sided dilatant veins with quartz‐sulfide‐carbonate‐adularia. These veins display a consistent strike of 305° and a dip of 35°SW. Alteration and mineralisation were influenced by host‐rock composition and rheology. A pervasive alteration assemblage of chlorite‐carbonate‐hematite‐epidote is developed throughout the Lake Cowal volcanic complex. This is overprinted by sericite‐silica‐carbonate alteration around fault zones and dykes, with patchy and pervasive alteration of this type developed in the lava sequence and upper volcani‐clastic unit, reflecting permeability and probable alteration zoning. In the lower clastic unit, the diorite and, in parts of the lava sequence, a chlorite‐carbonate‐pyrite assemblage partially overprints sericite‐silica alteration, suggesting an evolving fluid composition, changing physico‐chemical conditions or a different alteration fluid. Age dating of the intrusive phases and sericitic alteration associated with mineralisation at Endeavour 42 yields ages of 465.76 ± 1 and 438.6 ± 0.5 Ma, respectively, suggesting that mineralisation post‐dates the Lake Cowal intrusive event and is related to intrusion of magma during the 440 Ma mineralising event, an important period in the eastern Lachlan Fold Belt.  相似文献   

17.
The Blue Dot gold deposit, located in the Archean Amalia greenstone belt of South Africa, is hosted in an oxide (± carbonate) facies banded iron formation (BIF). It consists of three stratabound orebodies; Goudplaats, Abelskop, and Bothmasrust. The orebodies are flanked by quartz‐chlorite‐ferroan dolomite‐albite schist in the hanging wall and mafic (volcanic) schists in the footwall. Alteration minerals associated with the main hydrothermal stage in the BIF are dominated by quartz, ankerite‐dolomite series, siderite, chlorite, muscovite, sericite, hematite, pyrite, and minor amounts of chalcopyrite and arsenopyrite. This study investigates the characteristics of gold mineralization in the Amalia BIF based on ore textures, mineral‐chemical data and sulfur isotope analysis. Gold mineralization of the Blue Dot deposit is associated with quartz‐carbonate veins that crosscut the BIF layering. In contrast to previous works, petrographic evidence suggests that the gold mineralization is not solely attributed to replacement reactions between ore fluid and the magnetite or hematite in the host BIF because coarse hydrothermal pyrite grains do not show mutual replacement textures of the oxide minerals. Rather, the parallel‐bedded and generally chert‐hosted pyrites are in sharp contact with re‐crystallized euhedral to subhedral magnetite ± hematite grains, and the nature of their coexistence suggests that pyrite (and gold) precipitation was contemporaneous with magnetite–hematite re‐crystallization. The Fe/(Fe+Mg) ratio of the dolomite–ankerite series and chlorite decreased from veins through mineralized BIF and non‐mineralized BIF, in contrast to most Archean BIF‐hosted gold deposits. This is interpreted to be due to the effect of a high sulfur activity and increase in fO2 in a H2S‐dominant fluid during progressive fluid‐rock interaction. High sulfur activity of the hydrothermal fluid fixed pyrite in the BIF by consuming Fe2+ released into the chert layers and leaving the co‐precipitating carbonates and chlorites with less available ferrous iron content. Alternatively, the occurrence of hematite in the alteration assemblage of the host BIF caused a structural limitation in the assignment of Fe3+ in chlorite which favored the incorporation of magnesium (rather than ferric iron) in chlorite under increasing fO2 conditions, and is consistent with deposits hosted in hematite‐bearing rocks. The combined effects of reduction in sulfur contents due to sulfide precipitation and increasing fO2 during progressive fluid‐rock interactions are likely to be the principal factors to have caused gold deposition. Arsenopyrite–pyrite geothermometry indicated a temperature range of 300–350°C for the associated gold mineralization. The estimated δ34SΣS (= +1.8 to +2.5‰) and low base metal contents of the sulfide ore mineralogy are consistent with sulfides that have been sourced from magma or derived by the dissolution of magmatic sulfides from volcanic rocks during fluid migration.  相似文献   

18.
Hydrothermal ore deposits are typically characterised by footprints of zoned mineral assemblages that extend far beyond the size of the orebody. Understanding the mineral assemblages and spatial extent of these hydrothermal footprints is crucial for successful exploration, but is commonly hindered by the impact of regolith processes on the Earth's surface. Hyperspectral drill core (HyLogger?-3) data were used to characterise alteration mineralogy at the Mt Olympus gold deposit located 35 km southeast of Paraburdoo along the Nanjilgardy Fault within the northern margin of the Ashburton Basin in Western Australia. Mineralogy interpreted from hyperspectral data over the visible to shortwave (400–2500 nm) and thermal (6000–14500 nm) infrared wavelength ranges was validated with X-ray diffraction and geochemical analyses. Spaceborne multispectral (ASTER) and airborne geophysical (airborne electromagnetic, AEM) data were evaluated for mapping mineral footprints at the surface and sub-surface. At the deposit scale, mineral alteration patterns were identified by comparing the most abundant mineral groups detected in the HyLogger data against lithology logging and gold assays. Potential hydrothermal alteration phases included Na/K-alunite, kaolin phases (kaolinite, dickite), pyrophyllite, white mica, chlorite and quartz, representing low-T alteration of earlier greenschist metamorphosed sediments. The respective zoned mineral footprints varied depending on the type of sedimentary host rock. Siltstones were mainly characterised by widespread white-mica alteration with proximal kaolinite alteration or quartz veining. Sandstones showed (1) distal white mica, intermediate dickite, and proximal alunite + kaolinite or (2) widespread white-mica alteration with associated intervals of kaolinite. In both, sandstones and siltstones, chlorite was distal to gold mineralisation. Conglomerates showed distal kaolinite/dickite and proximal white-mica/dickite alteration. Three-dimensional visualisation of the gold distribution and spatially associated alteration patterns around Mt Olympus revealed three distinct categories: (1) several irregular, poddy, SE-plunging zones of >0.5 ppm gold intersected by the Zoe Fault; (2) sulfate alteration proximal to mineralisation, particularly on the northern side of the Mt Olympus open pit; and (3) varying AlIVAlVISiIV–1(Mg,Fe)VI–1 composition of white micas with proximity to gold mineralisation. Chlorite that developed during regional metamorphic or later hydrothermal alteration occurs distal to gold mineralisation. ASTER mineral mapping products, such as the MgOH Group Content used to map chlorite (±white mica) assemblages, showed evidence of correlation to mapped, local structural features and unknown structural or lithological contacts as indicated by inversion modelling of AEM data.  相似文献   

19.
陈路路 《地质与勘探》2017,53(4):632-642
纳岭沟铀矿床位于鄂尔多斯盆地东北部的伊陕单斜构造区,该区含矿主岩为中侏罗统直罗组下段下亚段。本文通过电子探针、能谱及背散射分析等方法,详细研究了该区目的层砂岩的铀矿物类型及其赋存形式,并对其矿物组合特征及期次等进行了探讨。结果表明纳岭沟地区铀矿物主要为铀石,还有少量的含钛含铀矿物、沥青铀矿、铀钍石等。铀矿物与黄铁矿、蚀变钛铁矿、锐钛矿/白钛石、粘土矿物等密切共生,呈毛刺状或微细柱状产于矿物边缘,或呈粒状产于黑云母解理缝中,另外也见产于碎屑颗粒中。结合电子探针及背散射分析,对蚀变黑云母解理缝中黄铁矿及铀石成因、以及蚀变钛铁矿与铀特殊关系进行了初步探讨。另外该区存在高Y和低Y元素两种铀石类型,沥青铀矿可能为原铀矿物蚀变残留,结合矿物蚀变期次,初步认为该区含铀砂岩至少遭受两期不同成矿流体作用,多源流体耦合成矿可能是砂岩型铀成矿的重要机制之一。  相似文献   

20.
长江岩体是诸广南部地区重要的产铀花岗岩体之一,此次研究运用电子探针和扫描电镜对长江岩体新鲜花岗岩和 蚀变花岗岩中的绿泥石和有关含铀矿物进行了精细对比,揭示花岗岩中铀的活化与成矿前期或早期致使花岗岩发生绿泥 石化的还原性热液蚀变作用关系密切,黑云母等的绿泥石化蚀变,使其中包裹的一些含铀副矿物也发生蚀变,导致原来 以类质同象形式存在于副矿物中的惰性铀转变成活性铀,并在绿泥石附近沉淀成铀石等铀含量高且在成矿期低度氧化性 热液作用下容易释放铀的矿物。长江岩体中的副矿物有锆石、磷灰石、褐帘石、铀石-钍石、晶质铀矿、独居石等,其 中,晶质铀矿、铀石、铀钍石中铀含量高且铀容易释放,是长江岩体的主要铀源矿物;独居石中铀含量较高,当其周围 矿物绿泥石化时,独居石蚀变形成直氟碳钙铈矿并释放铀,因而也是长江岩体的潜在铀源矿物;锆石中铀含量虽高,但 因其结构稳定,铀难以释放,因此它不是长江岩体中重要的铀源矿物;磷灰石、褐帘石中铀含量均低于检测限,作为铀 源矿物的可能性很小。  相似文献   

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