Search Results (8)

The Gacun deposit is a typical Volcanic Hosted Massive Sulfide (VHMS) associated with Late Triassic seafloor calc-alkaline felsic volcanics. Studies of zircon ages, petrology, major and trace element geochemistry, and Sr-Nd-Hf isotope geochemistry of volcanic rocks from the Northern Yidun arc were undertaken in this paper. We reshaped the Gacun magmatic system activity time, defined the origin of magma evolution, and proposed a metallogenic model of the deposit. Whole-rock major element compositions of the magmatic rocks in the Northern Yidun island arc indicate that they are a complete basalt–andesite–dacite–rhyolite assemblage, showing three obvious stages of composition evolution. They are enriched in large-ion lithophile and light rare earth elements, but depleted in high field-strength and heavy rare earth elements, with weak-to-negligible Eu anomalies (obvious in rhyolite). These geochemical features indicate that the Northern Yidun island arc is a magmatic arc based on ancient continental crust. The Ganzi–Litang oceanic subduction induced mantle melting and produced calc-alkaline basaltic magma, while the MASH processes at the bottom of the crust produced andesitic magma. Part of the andesite magma erupted to form andesite lava. The remaining part was mixed with magma produced via anatexis of ancient crust (approximately 20%–40% of the ancient crustal component), forming the ore-bearing rhyolite. Zircon U-Pb age data defines Gacun magmatic–hydrothermal mineralization sequence of events: At 238 Ma, arc magmatism led to the formation of andesite in the eastern part of the deposit. At 233 Ma, in the arc zone (the western part of Gacun deposit), a large-scale bimodal magmatism formed the main ore-bearing rock series of Gacun deposit, rhyolitic volcanic rocks. At 221 Ma, volcanic eruptions tended to end and sub-volcanic intrusion occurred, forming a lava dome, which was located under the ore-bearing rhyolitic volcanic rocks. The lava dome acted as a thermal engine and promoted hydrothermal circulation. The hydrothermal activity reached a peak at 217 ± 1 Ma, and the Gacun VHMS deposit was formed. Full article

This review paper aims to integrate geological, tectonic and metallogenetic data, including new data, and propose a regional model for the gold (and base metal) mineralization in the south Amazonian Craton to support the mineral exploration concerning magmatic–hydrothermal deposits. The Proterozoic evolution of the Amazonian Craton comprises the accretion of terrains to the Archean Carajás Mineral Province. In the Tapajós and Juruena mineral provinces, located at the south part of the Amazonian craton, a long-lived ocean–continent subduction event produced ca. 2.0 to 1.77 Ga continental magmatic arcs. Extensive lava flows, volcaniclastic, sedimentary, and plutonic rocks were originated during at least four major orogenic magmatic events (ca. 2.1, 1.9, 1.88, and 1.80 Ga) and two post- to anorogenic events (ca. 1.87 and 1.77 Ga). Gold mineralization occurs in: (i) alluvial/colluvial occurrences, (ii) orogenic carbonate–sulfide-rich quartz veins in shear zones, (iii) stockworks, veins, and dissemination in granites, (iv) contact of basic dikes, (v) well-preserved high-, intermediate- and low-sulfidation epithermal mineralization, and (vi) porphyry-like and intrusion-related gold systems associated with late- to post-orogenic epizonal granites. The estimated historical gold production, mainly in secondary deposits, is over 27 Moz at the Tapajós and 6 Moz at the Juruena provinces. A total resource of over 5 Moz Au is currently defined in several small to large primary gold deposits. Andesite to rhyolite, volcaniclastic, and clastic sedimentary rocks (1.96–1.88 Ga) host epithermal (high-, intermediate-, and low-sulfidation) Au–(Ag–Pb–Zn) mineralization, whereas Au–Cu and Cu–Mo–Au mineralization is hosted in sub-volcanic tonalitic to granitic plutons. Advanced argillic alteration (alunite, pyrophyllite, enargite) associated with high-sulfidation mineralization occurs in ring volcanoes around nested volcanic calderas. This zone grades outward to propylitic or chlorite alteration, often covered by silica caps with vuggy silica. Lava flows and volcaniclastic rocks within faults or associated with volcanic edifices and rhyolitic domes host low- and intermediate-sulfidation mineralization. Low-sulfidation alteration zones typically have adularia and illite or sericite. Chalcopyrite, sphalerite, galena, pyrite, digenite, and manganiferous calcite are related to intermediate-sulfidation gold mineralization. Late- to post-orogenic evolved oxidized I-type granitoids host alkalic-type epithermal and porphyry-like gold mineralization. Porphyry-style hydrothermal alteration is analogous to those of modern systems, with inner sodic and potassic (potassic feldspar ± biotite or biotite) alterations grading to propylitic, muscovite-sericite, chlorite–sericite, and chlorite alterations. Potassic alteration zones are the locus of Cu–Mo mineralization, and gold-rich zones occur in muscovite/sericite–quartz–pyrite alteration. The Paleoproterozoic epithermal and porphyry-like mineralization in these large provinces defines a new frontier for the exploration of world-class gold deposits in the worldwide Proterozoic arc-related magmatic terrains. Full article

Pyrometamorphism is the highest temperature end-member of the sanidinite facies (high-temperature, low-pressure contact metamorphism) and comprises both subsolidus and partial melting reactions which may locally lead to cryptocrystalline-glassy rocks (i.e., porcellanites and buchites). A wide range of pyrometamorphic ejecta, with different protoliths from Stromboli volcano, have been investigated over the last two decades. Among these, a heterogeneous (composite) glassy sample (B1) containing intimately mingled porcellanite and buchite lithotypes was selected to be studied through new FESEM–EDX and QEMSCAN™ mineral mapping investigations, coupled with the already available bulk rock composition data. This xenolith was chosen because of the unique and intriguing presence of abundant Cu–Fe sulphide globules within the buchite glass in contrast with the well-known general absence of sulphides in Stromboli basalts or their subvolcanic counterparts (dolerites) due to the oxygen fugacity of NNO + 0.5–NNO + 1 (or slightly lower) during magma crystallization. The investigated sample was ejected during the Stromboli paroxysm of 5 April 2003 when low porphyritic (LP) and high porphyritic (HP) basalts were erupted together. Both types of magmas are present as coatings of the porcellanite–buchite sample and were responsible for the last syn-eruptive xenoliths’s rim made of a thin crystalline-glassy selvage. The complex petrogenetic history of the B1 pyrometamorphic xenolith is tentatively explained in the framework of the shallow subvolcanic processes and vent system dynamics occurred shortly before (January–March 2003) the 5 April 2003 paroxysm. A multistep petrogenesis is proposed to account for the unique occurrence of sulphide globules in this composite pyrometamorphic xenolith. The initial stage is the pyrometamorphism of an already hydrothermally leached extrusive/subvolcanic vent system wall rock within the shallow volcano edifice. Successively, fragments of this wall rock were subject to further heating by continuous gas flux and interaction with Stromboli HP basalt at temperatures above 1000 °C to partially melt the xenolith. This is an open system process involving continuous exchange of volatile components between the gas flux and the evolving silicate melt. It is suggested that the reaction of plagioclase and ferromagnesian phenocrysts with SO₂ and HCl from the volcanic gas during diffusion into the melt led to the formation of molecular CaCl in the melt, which then was released to the general gas flux. Sulphide formation is the consequence of the reaction of HCl dissolved into the melt from the gas phase, resulting in the release of H₂ into the melt and lowering of f_O2 driving reduction of the dissolved SO₂. Full article

While gold partitioning into hydrothermal fluids responsible for the formation of porphyry and epithermal deposits is currently well understood, its behavior during the differentiation of metal-rich silicate melts is still subject of an intense scientific debate. Typically, gold is scavenged into sulfides during crustal fractionation of sulfur-rich mafic to intermediate magmas and development of native forms and alloys of this important precious metal in igneous rocks and associated ores are still poorly documented. We present new data on gold (Cu-Ag-Au, Ni-Cu-Zn-Ag-Au, Ti-Cu-Ag-Au, Ag-Au) alloys from iron oxide deposits in the Lesser Khingan Range (LKR) of the Russian Far East. Gold alloy particles are from 10 to 100 µm in size and irregular to spherical in shape. Gold spherules were formed through silicate-metal liquid immiscibility and then injected into fissures surrounding the ascending melt column, or emplaced through a volcanic eruption. Presence of globular (occasionally with meniscus-like textures) Cu-O micro-inclusions in Cu-Ag-Au spherules confirms their crystallization from a metal melt via extremely fast cooling. Irregularly shaped Cu-Ag-Au particles were formed through hydrothermal alteration of gold-bearing volcanic rocks and ores. Association of primarily liquid Cu-Ag-Au spherules with iron-oxide mineralization in the LKR indicates possible involvement of silicate-metallic immiscibility and explosive volcanism in the formation of the Andean-type iron oxide gold-copper (IOCG) and related copper-gold porphyry deposits in the deeper parts of sub-volcanic epithermal systems. Thus, formation of gold alloys in deep roots of arc volcanoes may serve as a precursor and an exploration guide for high-grade epithermal gold mineralization at shallow structural levels of hydrothermal-volcanic environments in subduction zones. Full article

The Nuocang Pb-Zn deposit is a newly discovered polymetallic skarn deposit in the southern Lhasa subterrane, western Gangdese, Tibet. The skarn occurs at the contact between the limestone of Angjie Formation and the Linzizong volcanic rocks of Dianzhong Formation (LDF), and the subvolcanic granite porphyry intruding those formations; the contact metasomatic skarn is well zoned mineralogically and texturally, as well as geochemically. The skarn minerals predominantly consist of an anhydrous to hydrous calc-silicate sequence pyroxene–garnet–epidote. The endoskarn mainly consists of an assemblage of pyroxene, garnet, ilvaite, epidote, and quartz, whereas the exoskarn is characterized proximal to distally, by decreasing garnet, and increasing pyroxene, ilvaite, epidote, chlorite, muscovite, quartz, calcite, galena, and sphalerite. Geochemical analyses suggest that the limestone provided the Ca for all the skarn minerals and the magmatic volatiles were the main source for Si (except the skarnified hornfels/sandstone, and muscovite-epidote-garnet-pyroxene skarn possibly from the host sandstones), with Fe and Mn and other mineralizing components. During the hydrothermal alteration, the garnet-pyroxene skarn and pyroxene-rich skarn gained Si, Fe, Mn, Pb, Zn, and Sn, but lost Ca, Mg, K, P, Rb, Sr, and Ba. However, the skarnified hornfels/sandstone, and muscovite-epidote-garnet-pyroxene skarn gained Fe, Ca, Mn, Sr, Zr, Hf, Th, and Cu, but lost Si, Mg, K, Na, P, Rb, Ba, and Li. The REEs in the skarn were sourced from magmatic fluids during the prograde stage. Skarn mineral assemblages and geochemistry indicate the skarn in the Nuocang deposit were formed in a disequilibrated geochemical system by infiltrative metasomatism of magmatic fluids. During the prograde stage, garnet I (And_97.6Gro_1.6) firstly formed, and then a part of them incrementally turned into garnet II (And_64.4Gro_33.8) and III (And_70.22Gro_29.1). The subsequent substitution of Fe for Al in the garnet II and III indicates the oxygen fugacity of the fluid became more reduced, then resulted in formation of significant pyroxene. However, the anisotropic garnet IV (And_38.5Gro_59.8) usually replaced the pyroxene. In the retrograde stage, the temperature decreased and oxygen fugacity increased, but hydrolysis increased with epidote, ilvaite, chlorite I, and muscovite forming with magnetite. The continuing decreasing temperature and mixing with meteoric water lead to Cu, Pb, and Zn saturation as sulfides. After the sulfides deposition, the continued mixing with large amounts of cold meteoric water would decrease its temperature, and increase its pH value (neutralizing), promoting the deposition of significant amounts of calcite and chlorite II. The geological, mineralogical, and geochemical characteristics of Nuocang skarn, suggest that the Nuocang deposit is of a Pb-Zn polymetallic type. Compared to the other typical skarn-epithermal deposits in the Linzizong volcanic area, it indicates that the Nuocang deposit may have the exploration potential for both skarn and epithermal styles of mineralization. Full article

The Busang mineral prospect in Kalimantan, Indonesia, was reported to host a large Au resource until 1997 when it was revealed that drill core samples had been deliberately and systematically contaminated (“salted”) with extraneous Au to falsify resource estimates. One month before the fraud was uncovered, Dr. G. Milligan, then professor emeritus of geology, visited the site to collect a suite of core samples for academic study that was deemed representative of the host rocks, alteration, and mineralization of the Busang Southeast Zone. These samples were re-examined here by optical microscopy, electron microprobe (EMPA), whole-rock geochemistry, and fluid inclusion microthermometry to characterize the subsurface geology and hydrothermal mineralization, and to assess reasons why the system is of uneconomic character. The host rocks were variably altered calc-alkaline porphyritic subvolcanic diorites, typical of the lithological units along the mineralized trend in the Kalimantan Gold Belt. Early hydrothermal mineralization with quartz-sulfide (pyrite, chalcopyrite, Cu-sulfosalts) stockwork veinlets associated with pervasive phyllic and propylitic alteration was overprinted by crudely banded quartz-carbonate-sulfide/sulfosalt (pyrite, sphalerite, chalcopyrite, galena, tennantite-tetrahedrite, bournonite-seligmannite) veins. The stockwork veins were associated with up to 140 ppb bulk rock Au, some of which was hosted by Cu-sulfosalts. Microthermometry on quartz-hosted aqueous fluid inclusion assemblages (FIA; n = 13) and single inclusions (non-FIA; n = 20) in quartz-carbonate-sulfide/sulfosalt veins yielded an overall range in homogenization temperatures (T_h) between 179 °C and 366 °C and bulk salinities between 1.1 wt.% to 8.6 wt.% NaCl equivalent, with much smaller data ranges for individual FIA (e.g., FIA 3; 239.1 °C to 240.5 °C and 0.5 wt.% to 1.4 wt.% NaCl equivalent). Primary FIA along growth zones in quartz were identified, providing constraints on fluid characteristics at the time of quartz growth. Carbonate-hosted FIA (n = 3) and single inclusions (non-FIA; n = 3) in the same veins yielded T_h between 254 °C and 343 °C and bulk salinities of 1.1 wt.% to 11.6 wt.% NaCl equivalent. Likewise, data ranges for individual FIA were much smaller. Many of the geological characteristics of the Busang Southeast Zone were compatible with a telescoped, intermediate-sulfidation epithermal system, having formed from diluted magmatic fluids that precipitated weak base metal mineralization. However, the system was unproductive with respect to Au and Ag, at least within the studied area. Of note, vein textures and fluid inclusion characteristics indicative of boiling or efficient fluid mixing—processes both considered critical for the formation of economic lode gold deposits—were absent in the samples. Full article

Aluminum-phosphate-sulfates (APS) of the alunite supergroup occur in igneous rocks within zones of advanced argillic and silicic alteration in porphyry and epithermal ore environments. In this study we report on the presence of woodhouseite-rich APS in ash from the 27 September 2014 hydrothermal eruption of Ontake volcano. Scanning electron microscope coupled with energy dispersive X-ray spectrometer (SEM-EDS) and field emission (FE)-SEM-EDS observations show two types of occurrence of woodhouseite: (a) as cores within chemically zoned alunite-APS crystals (Zoned-alunite-woodhouseite-APS), and (b) as a coherent single-phase mineral in micro-veinlets intergrown with similar micro-veinlets of silica minerals (Micro-wormy-vein woodhouseite-APS). The genetic environment of APS minerals at Ontake volcano is that of a highly acidic hydrothermal system existing beneath the volcano summit, formed by condensation in magmatic steam and/or ground waters of sulfur-rich magmatic volatiles exsolved from the magma chamber beneath Mt. Ontake. Under these conditions, an advanced argillic alteration assemblage forms, which is composed of silica, pyrophyllite, alunite and kaolinite/dickite, plus APS, among other minerals. The discovery of woodhouseite in the volcanic ash of the Ontake 2014 hydrothermal eruption represents the first reported presence of APS within an active volcano. Other volcanoes in Japan and elsewhere with similar phreatic eruptions ejecting altered ash fragments will likely contain APS minerals derived from magmatic-hydrothermal systems within the subvolcanic environment. The presence of APS minerals within the advanced argillic zone below the summit vent of Ontake volcano, together with the prior documentation of phyllic and potassically altered ash fragments, provides evidence for the existence within an active volcano in Japan of an alteration column comparable to that of porphyry copper systems globally. Full article

The Konos Hill prospect in NE Greece represents a telescoped Mo–Cu–Re–Au porphyry occurrence overprinted by deep-level high-sulfidation mineralization. Porphyry-style mineralization is exposed in the deeper parts of the system and comprises quartz stockwork veins hosted in subvolcanic intrusions of granodioritic composition. Ore minerals include pyrite, molybdenite, chalcopyrite, and rheniite. In the upper part of the system, intense hydrothermal alteration resulted in the formation of a silicified zone and the development of various advanced argillic alteration assemblages, which are spatially related to N–S, NNW–SSE, and E–W trending faults. More distal and downwards, advanced argillic alteration gradually evolves into phyllic assemblages dominated by quartz and sericite. Zunyite, along with various amounts of quartz, alunite, aluminum phosphate–sulfate minerals (APS), diaspore, kaolinite, and minor pyrophyllite, are the main minerals in the advanced argillic alteration. Mineral-chemical analyses reveal significant variance in the SiO₂, F, and Cl content of zunyite. Alunite supergroup minerals display a wide compositional range corresponding to members of the alunite, beudantite, and plumbogummite subgroups. Diaspore displays an almost stoichiometric composition. Mineralization in the lithocap consists of pyrite, enargite, tetrahedrite/tennantite, and colusite. Bulk ore analyses of mineralized samples show a relative enrichment in elements such as Se, Mo, and Bi, which supports a genetic link between the studied lithocap and the underlying Konos Hill porphyry-style mineralization. The occurrence of advanced argillic alteration assemblages along the N–S, NNW–SSE, and E–W trending faults suggests that highly acidic hydrothermal fluids were ascending into the lithocap environment. Zunyite, along with diaspore, pyrophyllite, and Sr- and Rare Earth Elements-bearing APS minerals, mark the proximity of the hypogene advanced argillic alteration zone to the porphyry environment. Full article