Precious metal and telluride mineralogy of large volcanic-hosted massive sulfide deposits in the Urals

Summary The study focuses on the mode of occurrence of Au, Ag and Te in ores of the Gaisk, Safyanovsk, Uzelginsk and other volcanic-hosted massive sulfide (VHMS) deposits in the Russian Urals. Minerals containing these elements routinely form fine inclusions within common sulfides (pyrite, chalcopyrite and sphalerite). Gold is mostly concentrated as ‘invisible’ gold within pyrite and chalcopyrite at concentrations of 1–20 ppm. Silver mainly occurs substituted in tennantite (0.1–6 wt.% Ag). In the early stages of mineralization, gold is concentrated into solid solution within the sulfides and does not form discrete minerals. Mineral parageneses identified in the VHMS deposits that contain discrete gold- and gold-bearing minerals, including native gold, other native elements, various tellurides and tennantite, were formed only in the latest stages of mineralization. Secondary hydrothermal stages and local metamorphism of sulfide ores resulted in redistribution of base and precious metals, refining of the common sulfides, the appearance of submicroscopic and microscopic inclusions of Au–Ag alloys (fineness 0.440–0.975) and segregation of trace elements into new, discrete minerals. The latter include Au and Ag compounds combined with Te, Se, Bi and S. Numerous tellurides (altaite, hessite, stützite, petzite, krennerite etc.) are found in the massive sulfide ores of the Urals and appear to be major carriers of gold and PGE in VHMS ores.     

Gold mineralisation in the Surselva region, Canton Grisons, Switzerland

The Tavetsch Zwischenmassif and neighbouring Gotthard Massif in the Surselva region host 18 gold-bearing sulphide occurrences which have been investigated for the present study. In the Surselva region, the main rock constituting the Tavetsch Zwischenmassif (TZM) is a polymetamorphic sericite schist, which is accompanied by subordinate muscovite-sericite gneiss. The entire tectonic unit is affected by a strong vertical schistosity, which parallels its NE-SW elongation. The main ore minerals in these gold occurrences are pyrite, pyrrhotite and arsenopyrite. The mineralisation occurs in millimetric stringers and veinlets, everywhere concordant with the schistosity. Native gold is present as small particles measuring 2–50 μm, and generally associated with pyrite. Average grades are variable, but approximate 4–7 g/t Au, with several occurrences attaining 14 g/t Au. Silver contents of the gold are on the order of 20 wt%. A “bonanza” occurrence consists of a quartz vein coated by 1.4 kg of native gold. The origin of the gold is unknown. On the assumption that the sericite schists are derived from original felsic volcanic tuffs, the gold-bearing sulphides may have been introduced during pre-Alpine magmatism.     

内蒙赤峰红花沟金矿田的金矿物及其微量元素特点

对赤峰西部的红花沟、连花山、索虎沟金矿床的矿物共生组合和金矿物的赋存状态进行了研究，同时对金矿物和寄主硫化物进行了电子探针分析测试。结果表明，从成矿早阶段至晚阶段、从包体金至裂隙金，金矿物的Au／Ag或金成色逐渐降低。总体来讲，金成色高的金矿物，其Fe和Bi含量也高，但不同温度区段形成的金矿物，其局部规律有所不同。对红花沟金矿与银金矿共生的铋硫盐矿物-针硫铋铅矿也进行了详细分析。矿床中富含铋矿物的地方往往也富含金，可作为有意义的找矿标志。     

Sulfur and lead isotope geochemistry of hypogene mineralization at the Barite Hill Gold Deposit, Carolina Slate Belt, southeastern United States: a window into and through regional metamorphism

The Barite Hill gold deposit, at the southwestern end of the Carolina slate belt in the southeastern United States, is one of four gold deposits in the region that have a combined yield of 110 metric tons of gold over the past 10 years. At Barite Hill, production has dominantly come from oxidized ores. Sulfur isotope data from hypogene portions of the Barite Hill gold deposit vary systematically with pyrite–barite associations and provide insights into both the pre-metamorphic Late Proterozoic hydrothermal and the Paleozoic regional metamorphic histories of the deposit. The δ³⁴S values of massive barite cluster tightly between 25.0 and 28.0‰, which closely match the published values for Late Proterozoic seawater and thus support a seafloor hydrothermal origin. The δ³⁴S values of massive sulfide range from 1.0 to 5.3‰ and fall within the range of values observed for modern and ancient seafloor hydrothermal sulfide deposits. In contrast, δ³⁴S values for finer-grained, intergrown pyrite (5.1–6.8‰) and barite (21.0–23.9‰) are higher and lower than their massive counterparts, respectively. Calculated sulfur isotope temperatures for the latter barite–pyrite pairs (Δ=15.9–17.1‰) range from 332–355 °C and probably reflect post-depositional equilibration at greenschist-facies regional metamorphic conditions. Thus, pyrite and barite occurring separately from one another provide pre-metamorphic information about the hydrothermal origin of the deposit, whereas pyrite and barite occurring together equilibrated to record the metamorphic conditions. Preliminary fluid inclusion data from sphalerite are consistent with a modified seawater source for the mineralizing fluids, but data from quartz and barite may reflect later metamorphic and (or) more recent meteoric water input. Lead isotope values from pyrites range for ²⁰⁶Pb/²⁰⁴Pb from 18.005–18.294, for ²⁰⁷Pb/²⁰⁴Pb from 15.567–15.645, and for ²⁰⁸Pb/²⁰⁴Pb from 37.555–38.015. The data indicate derivation of the ore leads from the country rocks, which themselves show evidence for contributions from relatively unradiogenic, mantle-like lead, and more evolved or crustal lead. Geological relationships, and stable and radiogenic isotopic data, suggest that the Barite Hill gold deposit formed on the Late Proterozoic seafloor through exhalative hydrothermal processes similar to those that were responsible for the massive sulfide deposits of the Kuroko district, Japan. On the basis of similarities with other gold-rich massive sulfide deposits and modern seafloor hydrothermal systems, the gold at Barite Hill was probably introduced as an integral part of the formation of the massive sulfide deposit. Received: 17 August 1998 / Accepted: 12 October 2000     

Mineralogical, fluid inclusion, and stable isotope constraints on mechanisms of ore deposition at the Samgwang mine (Republic of Korea)—a mesothermal, vein-hosted gold–silver deposit

The Samgwang mine is located in the Cheongyang gold district (Cheonan Metallogenic Province) of the Republic of Korea. It consists of eight massive, gold-bearing quartz veins that filled NE- and NW-striking fractures along fault zones in Precambrian granitic gneiss of the Gyeonggi massif. Their mineralogy and paragenesis allow two separate vein-forming episodes to be recognized, temporally separated by a major faulting event. The ore minerals occur in quartz and calcite of stage I, associated with fracturing and healing of veins. Hydrothermal wall-rock alteration minerals of stage I include Fe-rich chlorite (Fe/(Fe+Mg) ratios 0.74-0.81), muscovite, illite, K-feldspar, and minor arsenopyrite, pyrite, and carbonates. Sulfide minerals deposited along with electrum during this stage include arsenopyrite, pyrite, pyrrhotite, sphalerite, marcasite, chalcopyrite, galena, argentite, pyrargyrite, and argentian tetrahedrite. Only calcite was deposited during stage II. Fluid inclusions in quartz contain three main types of C–O–H fluids: CO₂-rich, CO₂–H₂O, and aqueous inclusions. Quartz veins related to early sulfides in stage I were deposited from H₂O–NaCl–CO₂ fluids (1,500–5,000 bar, average 3,200) with T _htotal values of 200°C to 383°C and salinities less than about 7 wt.% NaCl equiv. Late sulfide deposition was related to H₂O–NaCl fluids (140–1,300 bar, average 700) with T _htotal values of 110°C to 385°C and salinities less than about 11 wt.% NaCl equiv. These fluids either evolved through immiscibility of H₂O–NaCl–CO₂ fluids as a result of a decrease in fluid pressure, or through mixing with deeply circulated meteoric waters as a result of uplift or unloading during mineralization, or both. Measured and calculated sulfur isotope compositions (δ³⁴S_H2S = 1.5 to 4.8‰) of hydrothermal fluids from the stage I quartz veins indicate that ore sulfur was derived mainly from a magmatic source. The calculated and measured oxygen and hydrogen isotope compositions (δ¹⁸O_H2O = −5.9‰ to 10.9‰, δD = −102‰ to −87‰) of the ore-forming fluids indicate that the fluids were derived from magmatic sources and evolved by mixing with local meteoric water by limited water–rock exchange and by partly degassing in uplift zones during mineralization. While most features of the Samgwang mine are consistent with classification as an orogenic gold deposit, isotopic and fluid chemistry indicate that the veins were genetically related to intrusions emplaced during the Jurassic to Cretaceous Daebo orogeny.     

Contrasting fluids and reservoirs in the contiguous Marcona and Mina Justa iron oxide–Cu (–Ag–Au) deposits,south-central Perú

The Marcona–Mina Justa deposit cluster, hosted by Lower Paleozoic metaclastic rocks and Middle Jurassic shallow marine andesites, incorporates the most important known magnetite mineralization in the Andes at Marcona (1.9 Gt at 55.4% Fe and 0.12% Cu) and one of the few major iron oxide–copper–gold (IOCG) deposits with economic Cu grades (346.6 Mt at 0.71% Cu, 3.8 g/t Ag and 0.03 g/t Au) at Mina Justa. The Middle Jurassic Marcona deposit is centred in Ica Department, Perú, and the Lower Cretaceous Mina Justa Cu (Ag, Au) prospect is located 3–4 km to the northeast. New fluid inclusion studies, including laser ablation time-of-flight inductively coupled plasma mass spectrometry (LA-TOF-ICPMS) analysis, integrated with sulphur, oxygen, hydrogen and carbon isotope analyses of minerals with well-defined paragenetic relationships, clarify the nature and origin of the hydrothermal fluid responsible for these contiguous but genetically contrasted deposits. At Marcona, early, sulphide-free stage M-III magnetite–biotite–calcic amphibole assemblages are inferred to have crystallized from a 700–800°C Fe oxide melt with a δ¹⁸O value from +5.2‰ to +7.7‰. Stage M-IV magnetite–phlogopite–calcic amphibole–sulphide assemblages were subsequently precipitated from 430–600°C aqueous fluids with dominantly magmatic isotopic compositions (δ³⁴S = +0.8‰ to +5.9‰; δ¹⁸O = +9.6‰ to +12.2‰; δD = −73‰ to −43‰; and δ¹³C = −3.3‰). Stages M-III and M-IV account for over 95% of the magnetite mineralization at Marcona. Subsequent non-economic, lower temperature sulphide–calcite–amphibole assemblages (stage M-V) were deposited from fluids with similar δ³⁴S (+1.8‰ to +5.0‰), δ¹⁸O (+10.1‰ to +12.5‰) and δ¹³C (−3.4‰), but higher δD values (average −8‰). Several groups of lower (<200°C, with a mode at 120°C) and higher temperature (>200°C) fluids can be recognized in the main polymetallic (Cu, Zn, Pb) sulphide stage M-V and may record the involvement of modified seawater. At Mina Justa, early magnetite–pyrite assemblages precipitated from a magmatic fluid (δ³⁴S = +0.8‰ to +3.9‰; δ¹⁸O = +9.5‰ to +11.5‰) at 540–600°C, whereas ensuing chalcopyrite–bornite–digenite–chalcocite–hematite–calcite mineralization was the product of non-magmatic, probably evaporite-sourced, brines with δ³⁴S ≥ +29‰, δ¹⁸O = 0.1‰ and δ¹³C = −8.3‰. Two groups of fluids were involved in the Cu mineralization stage: (1) Ca-rich, low-temperature (approx. 140°C) and high-salinity, plausibly a basinal brine and (2) Na (–K)-dominant with a low-temperature (approx. 140°C) and low-salinity probably meteoric water. LA-TOF-ICPMS analyses show that fluids at the magnetite–pyrite stage were Cu-barren, but that those associated with external fluids in later stages were enriched in Cu and Zn, suggesting such fluids could have been critical for the economic Cu mineralization in Andean IOCG deposits.     

山西繁峙义兴寨金矿床金矿物特征研究

义兴寨金矿属于典型的石英脉型金矿床。金矿物以单颗粒的银金矿为主,有少量的自然金。粒度多集中在10～50μm;形态多为浑圆粒状、麦粒状、不规则粒状、角砾状、细脉状等。主要以包体金、粒间金、裂隙金存在于黄铁矿、黄铜矿、石英等颗粒中。利用数量和面积两种统计方法分别对金矿物进行形态、粒度、存在状态的特征统计,显示不同类型金矿物在出现率和面积配分特征上有较大差别。化学成分中普遍含有Fe、S、Cu、Zn、Pb元素,分析得出Fe、S与Au呈不同程度的反相关关系,Pb元素含量相对稳定,Cu、Zn元素变化较大;结合Au、Ag含量与温度关系,显示金矿物形成于中低温环境。成色为510.7~887.9,平均653.6,显示浅成成矿环境。纵向上,从1350 m标高到1070 m标高,金矿物的成色平均值由778.4逐渐降低为651.7,显示逆向分带特征,指示深部1070 m标高以下仍有稳定矿体存在。     

Mineralogy of the Boroo Gold Deposit in the North Khentei Gold Belt,Central Northern Mongolia

Mineral assemblages and chemical compositions of ore minerals from the Boroo gold deposit in the North Khentei gold belt of Mongolia were studied to characterize the gold mineralization, and to clarify crystallization processes of the ore minerals. The gold deposit consists of low‐grade disseminated and stockwork ores in granite, metasedimentary rocks and diorite dikes. Moderate to high‐grade auriferous quartz vein ores are present in the above lithological units. The ore grades of the former range from about 1 to 3 g/t, and those of the latter from 5 to 10 g/t, or more than 10 g/t Au. The main sulfide minerals in the ores are pyrite and arsenopyrite, both of which are divisible into two different stages (pyrite‐I and pyrite‐II; arsenopyrite‐I and arsenopyrite‐II). Sphalerite, galena, chalcopyrite, and tetrahedrite are minor associated minerals, with trace amounts of bournonite, boulangerite, geerite, alloclasite, native gold, and electrum. The ore minerals in the both types of ores are variable in distribution, abundance and grain size. Four modes of gold occurrence are recognized: (i) “invisible” gold in pyrite and arsenopyrite in the disseminated and stockwork ores, and in auriferous quartz vein ores; (ii) microscopic native gold, 3 to 100 µm in diameter, that occurs as fine grains or as an interstitial phase in sulfides in the disseminated and stockwork ores, and in auriferous quartz vein ores; (iii) visible native gold, up to 1 cm in diameter, in the auriferous quartz vein ores; and (iv) electrum in the auriferous quartz vein ores. The gold mineralization of the disseminated and stockwork ores consists of four stages characterized by the mineral assemblages of: (i) pyrite‐I + arsenopyrite‐I; (ii) pyrite‐II + arsenopyrite‐II; (iii) sphalerite + galena + chalcopyrite + tetrahedrite + bournonite + boulangerite + alloclasite + native gold; and (iv) native gold. In the auriferous quartz vein ores, five mineralization stages are defined by the following mineral assemblages: (i) pyrite‐I; (ii) pyrite‐II + arsenopyrite; (iii) sphalerite + galena + chalcopyrite; (iv) Ag‐rich tetrahedrite‐tennantite + bournonite + geerite + native gold; and (v) electrum. The As–Au relations in pyrite‐II and arsenopyrite suggest that gold detected as invisible gold is mostly attributed to Au⁺¹ in those minerals. By applying the arsenopyrite geothermometer to arsenopyrite‐II in the disseminated and stockwork ores, crystallization temperature and logfs₂ are estimated to be 365 to 300 °C and –7.5 to –10.1, respectively.     

As–Sb–Bi–Au mineralization in the Baogutu gold deposit,Xinjiang, NW China

Here we report the occurrence of some uncommon mineral assemblages including pääkönenite, aurostibite, native arsenic, native antimony, and native bismuth found in the Baogutu gold deposit in the western Junggar, Xinjiang, NW China. The mineralization could be generally subdivided into two types: the gold-bearing quartz-vein type mineralization and disseminated mineralization in the wall rocks. The sulfide minerals in gold lodes commonly include pyrite, arsenopyrite, marcasite, and stibnite. However, the L7 lode in No. 4 orebody and the L1 lode in No. 11 orebody of the Baogutu gold deposit are quite different in terms of their mineral assemblages. The L7 lode contains native arsenic–quartz veins in shallow levels and stibnite–quartz veins at depth. Gold-bearing minerals (electrum, native gold, and rarely aurostibite) mainly coexist with pääkönenite, stibnite, native arsenic, and native antimony. The crystallization of As- and Sb-bearing minerals was likely to have consumed H₂S from the hydrothermal fluid, which probably triggered the precipitation of native gold. The L1 lode consists of several discontinuous sulfide-dominated lensoid orebodies. The massive sulfide ores that produced most of the gold resource are characterized by an intimate association between native bismuth and native gold mineralization.     

Volcanogenic-related origin of sulfide-rich quartz veins: evidence from O and S isotopes at the Géant Dormant gold mine, Abitibi belt, Canada

The Géant Dormant gold mine is a sulfide-rich quartz vein gold deposit hosted by a volcano-sedimentary sequence and an associated felsic endogenous dome and dikes. The auriferous quartz-sulfide veins were preceded by two synvolcanic gold-bearing mineralizing events: early sulfidic seafloor-related and later disseminated pyrite in the felsic dome. This deposit differs from classical Archean auriferous quartz vein deposits by the low carbonate and high sulfide contents of the veins and by their formation prior to ductile penetrative deformation. The δ¹⁸O values of quartz associated with seafloor-related auriferous sulfides average 11.9 ± 0.6‰ (n = 3). The seafloor hydrothermal fluids had a δ¹⁸O value of 3.2‰ calculated at 250 °C. The oxygen isotope composition of quartz and chlorite from veins average 12.5 ± 0.3‰ (n = 20) and 5.9 ± 1.1‰ (n = 4) respectively. Assuming oxygen isotope equilibrium between quartz and chlorite, the veins formed at a temperature of ∼275 °C, which is consistent with the calculated temperature of 269 ± 10 °C from chlorite chemistry. The gold-bearing fluids had a δ¹⁸O value of 4.7‰ calculated at 275 °C. The δ³⁴S values of sulfides from the three gold events range from 0.6 to 2.8‰ (n = 32) and are close to magmatic values. Sulfur isotope geothermometry constrains the sulfide precipitation in the gold-bearing veins at a temperature of ∼350 °C. The similarity of the isotope data, the calculated δ¹⁸O of the mineralizing fluids and the likely seawater fluid source suggest that the three mineralizing events are genetically related to a volcanogenic hydrothermal system. The high value of the auriferous fluids (δ¹⁸O = 4.7‰) is attributed to a significant magmatic fluid contribution to the evolved seawater-dominated convective hydrothermal system. The two-stage filling of veins at increasing temperature from quartz-chlorite (275 °C) to sulfides (350 °C) may reflect the progressive maturation of volcanogenic hydrothermal systems. These results, together with field and geochemical data, suggest that formation of gold-rich volcanogenic systems require specific conditions that comprise a magmatic fluid contribution and gold from arc-related felsic rocks, coeval with the mineralizing events. This study shows that some auriferous quartz-vein orebodies in Archean terranes are formed in volcanogenic rather than mesothermal systems. Received: 12 December 1998 / Accepted: 5 July 1999     

甘肃岷县寨上特大型金矿次显微金的赋存状态研究

寨上金矿是一微细浸染型超大型金矿床。通过光学显微镜、人工重砂、电子探针、扫描电镜等显微测试手段对寨上矿区主要载金矿物进行分析测试得出：黄铁矿、白钨矿是最主要的载金矿物之一,石英、褐铁矿、辉铜矿是次要的载金矿物．方解石、菱铁矿、重晶石等不含金。由于受检测手段所限,在含金黄铁矿、白钨矿、石英等矿物中未发现独立金颗粒,所以寨上金矿次显微金呈微包裹体形式存在于载金矿物中或呈类质同象替代的原子形式存在。通过研究主要载金矿物黄铁矿中Au、As的关系得出：Au与As呈正相关关系;从具有增生环带结构黄铁矿的内核向增生体S、Fe呈对数下降趋势,Au、As呈对数上升趋势。对比沉积期、热液期形成的黄铁矿主量、微量元素得出S、Fe变化不大,微量As呈线性递增,而Au呈线性递减。     

冀东峪耳崖金矿床金属矿物特征及其组合意义

峪耳崖金矿床是冀东地区重要的金矿床之一.研究峪耳崖金矿床中金属矿物成分的变化及元素赋存状态,对了解矿床的形成机制及指导找矿具有重要意义.本次工作应用光学显微镜和电子探针(EPMA)对峪耳崖金矿床中的金属矿物进行了研究,并应用氢、氧及硫同位素分析对峪耳崖金矿床的成矿热液来源及硫源进行了探讨.该矿床的载金矿物有石英、黄铁矿、碲铋矿,金矿物为银金矿.其中,黄铁矿的w(S)平均为52.34％,与理论值相比,其普遍亏硫,显示出成矿与热液有关.碲铋矿是本次工作重点研究的载金矿物,与金的产出具关联性.被碲铋矿包裹的银金矿的w(Au)要高于被黄铁矿包裹的银金矿的w(Au).据氢、氧及硫同位素测试结果认为,峪耳崖金矿床的热液来源主要为岩浆水,硫来自深部岩浆源.结合黄铁矿、黄铜矿、闪锌矿、方铅矿、碲铋矿和银金矿等的矿物学特征及组合意义推断,峪耳崖金矿床为中-深成中温岩浆热液矿床,并认为其深部找矿可关注Te、Bi富集异常的区段.     

Epithermal mineralization and ore controls of the Shasta Au-Ag deposit, Toodoggone District, British Columbia, Canada

The Shasta gold-silver deposit, British Columbia, Canada, is an adularia-sericite-type epithermal deposit in which deposition of precious metals coincided with the transition of quartz- to calcite-dominant gangue. Mineralization is associated with stockwork-breccia zones in potassically altered dacitic lapilli tuffs and flows, and consists of pyrite, sphalerite, chalcopyrite, galena, acanthite, electrum and native silver. Pre- and post-ore veins consist solely of quartz and calcite, respectively. Fluid inclusion microthermometry indicates that ore minerals were deposited between 280 ° and 225 °C, from a relatively dilute hydrothermal fluid (˜1.5 wt.% NaCl equivalent). Abundant vapor-rich inclusions in ore-stage calcite are consistent with boiling. Oxygen and hydrogen isotopic data (δ¹⁸O_fluid = −1.5 to −4.1‰; δD_fluid = −148 to −171‰) suggest that the fluid had a meteoric origin, but was ¹⁸O-enriched by interaction with volcanic wallrocks. Initial (˜280 °C) fluid pH and log f O₂ conditions are estimated at 5.3 to 6.0, and −32.5 to −33 bar, respectively; during ore deposition, the fluid became more alkaline and oxidizing. Ore deposition at Shasta is attributed to localization of meteoric hydrothermal fluids by extensional faults; mineralization was controlled by boiling in response to hydraulic brecciation. Calcite and base metal sulfides precipitated due to the increase in pH that accompanied boiling, and the associated decrease in H₂S concentration led to precipitation of gold and silver. Received: 23 February 1995 / Accepted: 16 April 1996     

Mineralogy and geochemistry of El Dorado epithermal gold deposit, El Sauce district, central-northern Chile

Summary The El Dorado Au-Cu deposit is located in an extensive intra-caldera zone of hydrothermal alteration affecting Upper Cretaceous andesites of the Los Elquinos Formation at La Serena (≈ 29°47′S Lat., 70°43′W Long., Chile). Quartz-sulfide veins of economic potential are hosted by N25W and N20E fault structures associated with quartz-illite alteration (+supergene kaolinite). The main ore minerals in the deposit are pyrite, chalcopyrite ± fahlore (As/(As + Sb): 0.06−0.98), with electrum, sphalerite, galena, bournonite-seligmanite (As/(As + Sb): 0.21−0.31), marcasite, pyrrhotite being accessory phases. Electrum, with an Ag content between 32 and 37 at.%, occurs interstitial to pyrite aggregates or along pyrite fractures. Pyrite commonly exhibits chemical zonation with some zones up to 1.96 at.% As. Electron probe microanalyses of pyrite indicate that As-rich zones do not exhibit detectable Au values. Fluid inclusion microthermometry shows homogenization temperatures between 130 and 352 °C and salinities between 1.6 and 6.9 wt.% NaCl eq. Isotope data for quartz, ankerite and phyllosilicates and estimated temperatures show that δ¹⁸O and δD for the hydrothermal fluids were between 3 and 10‰ and between −95 and −75‰, respectively. These results suggest the mineralizing fluids were a mixture of meteoric and magmatic waters. An epithermal intermediate-sulfidation model is proposed for the formation of the El Dorado deposit. Author’s present address: J. Carrillo-Rosúa, Dpto. de Didáctica de las Ciencias Experimentales, Universidad de Granada, Campus de Cartuja, 18071, Granada, Spain     

Gold mineralization without quartz veins in a ductile-brittle shear zone, Macraes Mine, Otago Schist, New Zealand

Greenschist facies schist which hosts the Macraes Mine in East Otago, New Zealand has been pervasively altered by post-metamorphic (lower greenschist facies) fluids over a 120 m thick section perpendicular to foliation. Metamorphic titanite has been replaced by rutile, and epidote has been replaced by a variety of metamorphic minerals including siderite, chlorite, muscovite and calcite. The early stages of this alteration occurred during development of a ductile cleavage associated with kilometre scale recumbent folding. The cleavage was widely overprinted by a subparallel set of spaced (mm scale) microshears which are locally enriched in rutile and hydrothermal graphite. Strain was then concentrated into narrow (m scale) zones where more intensely deformed portions of the rock are crossed and highly disrupted by closely spaced (100 μm scale) microshears. The highly strained rocks show a combination of mylonitic and cataclastic microstructures, including crystal-plastic grain size reduction and recrystallization of micas to form a new foliation. Muscovite has grown at the expense of albite in the mylonitic cataclasites. Hydrothermal alteration was accompanied by addition of pyrite, arsenopyrite and gold without development of quartz veins. Gold precipitated with sulphides during reduction of the fluid by hydrothermal graphite. The whole altered rock sequence was later cut sporadically by mesothermal quartz veins which contain gold, scheelite, rutile, pyrite and arsenopyrite. This deposit displays a continuum of post-metamorphic processes and hydrothermal fluid flow which occurred during uplift of the schist belt. Received: 4 December 1997 / Accepted: 21 September 1998     

The Existence of the Negative Charge of Gold in Sulphide Minerals and Its Formation Mechanism1;

Abstract: Through a study, particularly an X-ray photoelectron spectroscopy (XPS or ESCA) analysis, of gold-bearing arsenopyrite and pyrite in Carlin-type gold deposits of Guangxi, China, and hydrothermally synthesized gold-bearing pyrite and marcasite, the authors have found that these minerals contain “invisible gold” whose binding energy is lower than that of native gold (Au°). Therefore they suggest that gold occurs in a negative charge state in these sulphide minerals as it replaces some sulphur and is combined with sulphur with the covalent bond. This paper also preliminarily discusses the possibility of its formation from the chemistry and geochemistry of gold, crystal chemistry of arsenopyrite, pyrite and marcasite and geochemical environment.     

Oxidized and reduced mineral assemblages in greenstone belt rocks of the St. Ives gold camp, Western Australia: vectors to high-grade ore bodies in Archaean gold deposits?

Hydrothermal sulfide–oxide–gold mineral assemblages in gold deposits in the Archaean St. Ives gold camp in Western Australia indicate extremely variable redox conditions during hydrothermal alteration and gold mineralization in space and time. Reduced alteration assemblages (pyrrhotite–pyrite) occur in deposits in the southwest of the camp (e.g., Argo, Junction deposits) and moderately to strongly oxidized assemblages (magnetite–pyrite, hematite–pyrite) occur in deposits in the Central Corridor in the northeast (e.g., North Orchin, Revenge deposits). Reduced mineral assemblages flank the Central Corridor of oxidized deposits and, locally, cut across it along E–W trending faults. Oxidized mineral assemblages in the Central Corridor are focused on gravity lows which are interpreted to reflect abundant felsic porphyritic intrusions at about 1,000 m below present surface. Hydrothermal magnetite predates and is synchronous with early phases of gold-associated albite–carbonate–pyrite–biotite–chlorite hydrothermal alteration. Later-stage, gold-associated pyrite is in equilibrium with hematite. The spatial distribution and temporal sequence of iron sulfides and oxides with gold indicate the presence of at least two spatially restricted but broadly synchronous hydrothermal fluids with contrasting redox states. Sulfur isotope constraints support the argument that the different mineral assemblages reflect differences in redox conditions. The δ ³⁴S values for pyrite for the St. Ives gold camp range between −8.4‰ and +5.1‰ with the negative values occurring in oxidized magnetite-rich domains and slightly negative or positive values occurring in reduced, pyrrhotitic domains. Preliminary spatial and paragenetic analysis of the distribution of iron sulfides and oxides in the St. Ives camp suggests that gold grades are highest where the redox state of the hydrothermal alteration assemblages switches from relatively reduced pyrrhotite–pyrite to relatively oxidized magnetite–pyrite and hematite–pyrite both in space and time. Gold deposition is inferred to have occurred where fluids of contrasting redox state mixed.     

Hydrothermal fluid evolution and structural control of the Guarim gold mineralisation, Tapajós Province, Amazonian Craton, Brazil

Fluid inclusion and structural studies were carried out at the Guarim gold deposit in the Palaeoproterozoic Tapajós province of the Amazonian craton. Guarim is a fault-hosted gold deposit cutting basement granitoids. It consists of a quartz vein, which is massive in its inner portions, grading laterally either to a massive or to cavity-bearing quartz vein associated with hydrothermal breccias. The wallrock alteration comprises chlorite, carbonate, white mica and sulphide minerals, with free gold occurring within quartz grains and spatially associated with sulphide mineral grains. Petrographic, microthermometric and Laser Raman investigations recognised CO₂-rich, mixed H₂O–CO₂, and H₂O fluid inclusions. The coexisting CO₂ and H₂O–CO₂ inclusions were interpreted as primary immiscible fluids that formed the gold-bearing vein. The H₂O inclusions were considered a product of later infiltration of fluids unrelated to the mineralising episode. The mineralising fluid has CO₂ ranging typically from 5–10 mol%, contains traces of N₂, has salinities of ∼5 wt% NaCl equiv., and densities varying between 0.85 and 0.95 g/cm³. The P–T estimations bracket gold deposition between 270–320 °C and 0.86–2.9 kb; ƒ_O2–ƒ_S2–pH estimates suggest a reduced, near-neutral character for the fluid. Variations in the physico-chemical properties, as demonstrated by the fluid inclusion study, resulted from a combination of fluid immiscibility and pressure fluctuation. This interpretation, combined with textural and structural evidence, suggests the emplacement of the mineralised vein in an active fault and at a rather shallow level (4–7 km). The geological and structural setting, deposit-scale textures and structures, wallrock alteration and physico-chemical fluid properties are compatible with those of epizonal to mesozonal orogenic lode gold deposits. Received: 3 March 2000 / Accepted: 21 October 2000     

利用电子探针研究甘肃陇南赵家庄金矿载金矿物特征

应用偏光显微镜与电子探针相结合的手段是研究载金矿物的主要方法。本文采用镜下鉴定和电子探针分析技术,对赵家庄金矿中载金矿物含量、形态特征及其与其他矿物的空间关系开展研究,并对载金矿物进行定性和定量分析,探寻具有找矿意义的载金矿物和总结标志矿物特征。结果表明:研究区金矿石中主要载金矿物为黄铁矿,少量为黄铜矿、闪锌矿,这些载金矿物中Au含量依次为:细晶黄铁矿粗晶黄铁矿草莓状黄铁矿黄铜矿。不同时期的黄铁矿(粗晶黄铁矿、细晶黄铁矿、草莓状黄铁矿)中Au的分布均匀,但存在差异性,主要表现为细晶黄铁矿和草莓状黄铁矿中的Au含量较高(平均含量0. 14%～0. 18%),这种现象表明此类矿物为构造热液期形成,金易富集。Au以两种形式存在,一种是"可见金"包裹于脉石矿物中,或以裂隙金的形式嵌布在矿物晶隙及裂隙中;另一种是"不可见金"以纳米级颗粒金的形式存在于载金矿物中,也是Au的主要存在形式。本研究为后期矿床的成因、成矿过程和成矿机理研究提供了佐证,同时易于根据含金矿物的特征选择合适的选冶方法。     

Petrography, mineralogy and geochemistry of the Zarshuran Carlin-like gold deposit, northwest Iran

Gold mineralisation at Zarshuran, northwestern Iran, is hosted by Precambrian carbonate and black shale formations which have been intruded by a weakly mineralised granitoid. Granitoid intrusion fractured the sedimentary rocks, thereby improving conditions for hydrothermal alteration and mineralisation. Silicification is the principal hydrothermal alteration along with decalcification and argillisation. Three hydrothermal sulphide mineral assemblages have been identified: an early assemblage of pyrrhotite, pyrite and chalcopyrite; then widespread base metal sulphides, lead-sulphosalts and zoned euhedral arsenical pyrite; and finally late network arsenical pyrite, massive and colloform arsenical pyrite, colloform sphalerite, coloradoite, and arsenic–antimony–mercury–thallium-bearing sulphides including orpiment, realgar, stibnite, getchellite, cinnabar, lorandite and a Tl-mineral, probably christite. Most of the gold at Zarshuran is detectable only by quantitative electron microprobe and bulk chemical analyses. Gold occurs mainly in arsenical pyrite and colloform sphalerite as solid solution or as nanometre-sized native gold. Metallic gold is found rarely in hydrothermal quartz and orpiment. Pure microcrystalline orpiment, carbon-rich shale, silicified shale with visible pyrite grains and arsenic minerals contain the highest concentrations of gold. In many ways Zarshuran appears to be similar to the classic Carlin-type sediment-hosted disseminated gold deposits. However, relatively high concentrations of tellurium at Zarshuran, evidenced by the occurrence of coloradoite (HgTe), imply a greater magmatic contribution in the mineralising hydrothermal solutions than is typical of Carlin-type gold deposits. Received: 13 May 1999 / Accepted: 2 February 2000