Au–Ag–Te Mineralization of the Low‐Sulfidation Epithermal Aginskoe Deposit,Central Kamchatka,Russia

Mineralogic studies of major ore minerals and fluid inclusion analysis in gangue quartz were carried out for the for the two largest veins, the Aginskoe and Surprise, in the Late Miocene Aginskoe Au–Ag–Te deposit in central Kamchatka, Russia. The veins consist of quartz–adularia–calcite gangue, which are hosted by Late Miocene andesitic and basaltic rocks of the Alnei Formation. The major ore minerals in these veins are native gold, altaite, petzite, hessite, calaverite, sphalerite, and chalcopyrite. Minor and trace minerals are pyrite, galena, and acanthine. Primary gold occurs as free grains, inclusions in sulfides, and constituent in tellurides. Secondary gold is present in form of native mustard gold that usually occur in Fe‐hydroxides and accumulates on the decomposed primary Au‐bearing tellurides such as calaverite, krennerite, and sylvanite. K–Ar dating on vein adularia yielded age of mineralization 7.1–6.9 Ma. Mineralization of the deposit is divided into barren massive quartz (stage I), Au–Ag–Te mineralization occurring in quartz‐adularia‐clays banded ore (Stage II), intensive brecciation (Stage III), post‐ore coarse amethyst (Stage IV), carbonate (Stage V), and supergene stages (Stage VI). In the supergene stage various secondary minerals, including rare bilibinskite, bogdanovite, bessmertnovite metallic alloys, secondary gold, and various oxides, formed under intensely oxidized conditions. Despite heavy oxidation of the ores in the deposit, Te and S fugacities are estimated as Stage II tellurides precipitated at the log f Te₂ values ?9 and at log fS₂ ?13 based on the chemical compositions of hypogene tellurides and sphalerite. Homogenization temperature of fluid inclusions in quartz broadly ranges from 200 to 300°C. Ore texture, fluid inclusions, gangue, and vein mineral assemblages indicate that the Aginskoe deposit is a low‐sulfidation (quartz–adularia–sericite) vein system.     

The Arinem Te‐Bearing Gold‐Silver‐Base Metal Deposit,West Java,Indonesia

The vein system in the Arinem area is a gold‐silver‐base metal deposit of Late Miocene (8.8–9.4 Ma) age located in the southwestern part of Java Island, Indonesia. The mineralization in the area is represented by the Arinem vein with a total length of about 5900 m, with a vertical extent up to 575 m, with other associated veins such as Bantarhuni and Halimun. The Arinem vein is hosted by andesitic tuff, breccia, and lava of the Oligocene–Middle Miocene Jampang Formation (23–11.6 Ma) and overlain unconformably by Pliocene–Pleistocene volcanic rocks composed of andesitic‐basaltic tuff, tuff breccia and lavas. The inferred reserve is approximately 2 million tons at 5.7 g t^?1 gold and 41.5 g t^?1 silver at a cut‐off of 4 g t^?1 Au, which equates to approximately 12.5t of Au and 91.4t of Ag. The ore mineral assemblage of the Arinem vein consists of sphalerite, galena, chalcopyrite, pyrite, marcasite, and arsenopyrite with small amounts of pyrrhotite, argentite, electrum, bornite, hessite, tetradymite, altaite, petzite, stutzite, hematite, enargite, tennantite, chalcocite, and covellite. These ore minerals occur in quartz with colloform, crustiform, comb, vuggy, massive, brecciated, bladed and calcedonic textures and sulfide veins. A pervasive quartz–illite–pyrite alteration zone encloses the quartz and sulfide veins and is associated with veinlets of quartz–calcite–pyrite. This alteration zone is enveloped by smectite–illite–kaolinite–quartz–pyrite alteration, which grades into a chlorite–smectite–kaolinite–calcite–pyrite zone. Early stage mineralization (stage I) of vuggy–massive–banded crystalline quartz‐sulfide was followed by middle stage (stage II) of banded–brecciated–massive sulfide‐quartz and then by last stage (stage III) of massive‐crystalline barren quartz. The temperature of the mineralization, estimated from fluid inclusion microthermometry in quartz ranges from 157 to 325°C, whereas the temperatures indicated by fluid inclusions from sphalerite and calcite range from 153 to 218 and 140 to 217°C, respectively. The mineralizing fluid is dilute, with a salinity <4.3 wt% NaCl equiv. The ore‐mineral assemblage and paragenesis of the Arinem vein is characteristically of a low sulfidation epithermal system with indication of high sulfidation overprinted at stage II. Boiling is probably the main control for the gold solubility and precipitation of gold occurred during cooling in stage I mineralization.     

Orogenic Gold Mineralization in the Qolqoleh Deposit, Northwestern Iran

The Qolqoleh gold deposit is located in the northwestern part of the Sanandai‐Sirjan Zone, northwest of Iran. Gold mineralization in the Qolqoleh deposit is almost entirely confined to a series of steeply dipping ductile–brittle shear zones generated during Late Cretaceous–Tertiary continental collision between the Afro‐Arabian and the Iranian microcontinent. The host rocks are Mesozoic volcano‐sedimentary sequences consisting of felsic to mafic metavolcanics, which are metamorphosed to greenschist facies, sericite and chlorite schists. The gold orebodies were found within strong ductile deformation to late brittle deformation. Ore‐controlling structure is NE–SW‐trending oblique thrust with vergence toward south ductile–brittle shear zone. The highly strained host rocks show a combination of mylonitic and cataclastic microstructures, including crystal–plastic deformation and grain size reduction by recrystalization of quartz and mica. The gold orebodies are composed of Au‐bearing highly deformed and altered mylonitic host rocks and cross‐cutting Au‐ and sulfide‐bearing quartz veins. Approximately half of the mineralization is in the form of dissemination in the mylonite and the remainder was clearly emplaced as a result of brittle deformation in quartz–sulfide microfractures, microveins and veins. Only low volumes of gold concentration was introduced during ductile deformation, whereas, during the evident brittle deformation phase, competence contrasts allowed fracturing to focus on the quartz–sericite domain boundaries of the mylonitic foliation, thus permitting the introduction of auriferous fluid to create disseminated and cross‐cutting Au‐quartz veins. According to mineral assemblages and alteration intensity, hydrothermal alteration could be divided into three zones: silicification and sulfidation zone (major ore body); sericite and carbonate alteration zone; and sericite–chlorite alteration zone that may be taken to imply wall‐rock interaction with near neutral fluids (pH 5–6). Silicified and sulfide alteration zone is observed in the inner parts of alteration zones. High gold grades belong to silicified highly deformed mylonitic and ultramylonitic domains and silicified sulfide‐bearing microveins. Based on paragenetic relationships, three main stages of mineralization are recognized in the Qolqoleh gold deposit. Stage I encompasses deposition of large volumes of milky quartz and pyrite. Stage II includes gray and buck quartz, pyrite and minor calcite, sphalerite, subordinate chalcopyrite and gold ores. Stage III consists of comb quartz and calcite, magnetite, sphalerite, chalcopyrite, arsenopyrite, pyrrhotite and gold ores. Studies on regional geology, ore geology and ore‐forming stages have proved that the Qolqoleh deposit was formed in the compression–extension stage during the Late Cretaceous–Tertiary continental collision in a ductile–brittle shear zone, and is characterized by orogenic gold deposits.     

Geochemistry and alteration facies associated with epithermal precious metal mineralization in an active geothermal system,northern Lesbos,Greece

Hydrothermal quartz veins associated with gold and silver mineralization and variable amounts of base metal sulfides have been discovered within an active geothermal system in the Megala Therma area of northern Lesbos. This geothermal system is probably a late evolutionary stage in the formation of this mineralization. The veins are hosted in Upper Miocene volcanic rocks of andesitic composition and consist of quartz, adularia, chlorite, sericite, illite, kaolinite, baryte, small amounts of jarosite and alunite, and native gold, pyrite, galena, sphalerite, chalcopyrite, bornite, chalcocite, covellite and goethite. The principal types of alteration which occur in the studied area are: silicification, propylitization, argillic alteration and potassic, phyllic alteration.     

Geology and Re-Os Geochronology of Mineralization of the Miduk Porphyry Copper Deposit, Iran

The Miduk porphyry copper deposit is located in Kerman province, 85 km northwest of the Sar Cheshmeh porphyry copper deposit, Iran. The deposit is hosted by Eocene volcanic rocks of andesitic–basaltic composition. The porphyry‐type mineralization is associated with two Miocene calc‐alkaline intrusive phases (P1 and P2, respectively). Five hypogene alteration zones are distinguished at the Miduk deposit, including magnetite‐rich potassic, potassic, potassic–phyllic, phyllic and propylitic. Mineralization occurs as stockwork, dissemination and nine generations (magnetite, quartz–magnetite, barren quartz, quartz‐magnetite‐chalcopyrite‐anhydrite, chalcopyrite–anhydrite, quartz‐chalcopyrite‐anhydrite‐pyrite, quartz‐molybdenite‐anhydrite ± chalcopyrite ± magnetite, pyrite, and quartz‐pyrite‐anhydrite ± sericite) of veinlets and veins. Early stages of mineralization consist of magnetite rich veins in the deepest part of the deposit and the main stage of mineralization contains chalcopyrite, magnetite and anhydrite in the potassic zone. The high intensity of mineralization is associated with P2 porphyry (Miduk porphyry). Based on petrography, mineralogy, alteration halos and geochemistry, the Miduk porphyry copper deposit is similar to those of continental arc setting porphyry copper deposits. The Re‐Os molybdenite dates provide the timing of sulfide mineralization at 12.23 ± 0.07 Ma, coincident with U/Pb zircon ages of the P2 porphyry. This evidence indicates a direct genetic relationship between the Miduk porphyry stock and molybdenite mineralization. The Re‐Os age of the Miduk deposit marks the main stage of magmatism and porphyry copper formation in the Central Iranian volcano‐plutonic belt.     

Geochronology and fluid source constraints of the Songligou gold‐telluride deposit,western Henan Province,China: Analysis of genetic implications

The Songligou gold‐telluride deposit, located in Songxian County, western Henan Province, China, is one of many gold‐telluride deposits in the Xiaoqinling‐Xiong'ershan district. Gold orebodies occur within the Taihua Supergroup and are controlled by the WNW F101 Fault, and the fault was cut across by a granite porphyry dike. Common minerals in gold orebodies include quartz, chlorite, epidote, K‐feldspar, calcite, fluorite, sericite, phlogopite, bastnasite, pyrite, galena, chalcopyrite, sphalerite, tellurides, gold, bismuthinite, magnetite, and hematite, and pyrite is the dominant sulfide. Four mineralization stages are recognized, including pyrite‐quartz stage (I), quartz‐pyrite stage (II), gold‐telluride stage (III), and quartz‐calcite stage (IV). This work reports the Rb–Sr age of gold‐telluride‐bearing pyrite and zircon U–Pb age of granite porphyry, as well as S isotope data of pyrite and galena. The pyrite Rb–Sr isochron age is 126.6 ± 2.3 Ma (MSWD = 1.8), and the average zircon U–Pb age of granite porphyry is 166.8 ± 4.1 Ma (MSWD = 4.9). (⁸⁷Sr/⁸⁶Sr) _i values of pyrite and δ³⁴S values of sulfides vary from 0.7104 to 0.7105 and ?11.84 to 0.28‰, respectively. The obtained Rb–Sr isochron age represents the ore formation age of the Songligou gold‐telluride deposit, which is much younger than the zircon U–Pb age of the granite porphyry. Strontium and S isotopes, together with the presence of bastnaesite, suggest that the ore‐forming fluid was derived from felsic magmas with input of a mantle component and subsequently interacted with the Taihua Supergroup. Tellurium was derived from metasomatized mantle and was related to the subduction of the Shangdan oceanic crust and Izanagi plate beneath the North China Craton (NCC). This deposit is a part of the Early Cretaceous large‐scale gold mineralization in east NCC and formed in an extensional tectonic setting.     

Geology and Hydrothermal Alteration of the Duobuza Gold‐Rich Porphyry Copper District in the Bangongco Metallogenetic Belt,Northwestern Tibet

The Duobuza gold‐rich porphyry copper district is located in the Bangongco metallogenetic belt in the Bangongco‐Nujiang suture zone south of the Qiangtang terrane. Two main gold‐rich porphyry copper deposits (Duobuza and Bolong) and an occurrence (135 Line) were discovered in the district. The porphyry‐type mineralization is associated with three Early Cretaceous ore‐bearing granodiorite porphyries at Duobuza, 135 Line and Bolong, and is hosted by volcanic and sedimentary rocks of the Middle Jurassic Yanshiping Formation and intermediate‐acidic volcanic rocks of the Early Cretaceous Meiriqie Group. Simultaneous emplacement and isometric distribution of three ore‐forming porphyries is explained as multi‐centered mineralization generated from the same magma chamber. Intense hydrothermal alteration occurs in the porphyries and at the contact zone with wall rocks. Four main hypogene alteration zones are distinguished at Duobuza. Early‐stage alteration is dominated by potassic alteration with extensive secondary biotite, K‐feldspar and magnetite. The alteration zone includes dense magnetite and quartz‐magnetite veinlets, in which Cu‐Fe‐bearing sulfides are present. Propylitic alteration occurs in the host basic volcanic rocks. Extensive chloritization‐silicification with quartz‐chalcopyrite or quartz‐molybdenite veinlets superimposes on the potassic alteration. Final‐stage argillic alteration overlaps on all the earlier alteration. This alteration stage is characterized by destruction of feldspar to form illite, dickite and kaolinite, with accompanying veinlets of quartz + chalcopyrite + pyrite and quartz + pyrite assemblages. Cu coexists with Au, which indicates their simultaneous precipitation. Mass balance calculations show that ore‐forming elements are strongly enriched during the above‐mentioned three alteration stages.     

Mineral Paragenesis of the Lepanto Copper and Gold and the Victoria Gold Deposits, Mankayan Mineral District, Philippines

Abstract: Mineral paragenesis of the alteration, ore and gangue minerals of the Lepanto epithermal copper‐gold deposit and the Victoria gold deposit, Mankayan Mineral District, Northern Luzon, Philippines, is discussed. The principal ore minerals of the Lepanto copper‐gold deposit are enargite and luzonite, with significant presence of tennantite‐tetrahedrite, chalcopyrite, sphalerite, galena, native gold/electrum and gold‐silver tellurides. Pervasive alteration zonations are commonly observed from silicification outward to advanced argillic then to propylitic zone. The ore mineralogy of the Lepanto copper‐gold deposit suggests high f_S2 in the early stages of mineralization corresponding to the deposition of the enargite‐luzonite‐pyrite assemblage. Subsequent decrease in the f_S2 formed the chalcopyrite‐tennantite‐pyrite assemblage. An increase in the f_S2 of the fluids with the formation of the covellite‐digenite‐telluride assemblage caused the deposition of native gold/electrum and gold‐silver tellurides. The principal ore minerals of the Victoria gold deposit are sphalerite, galena, chalcopyrite, tetrahedrite and native gold/electrum. The alteration halos are relatively narrow and in an outward sequence from the ore, silica alteration grades to illitic‐argillic alteration, which in turn grades to propylitic alteration. The Victoria gold mineralization has undergone early stages of silica supersaturation leading to quartz deposition. Vigorous boiling increased the pH of the fluids that led to the deposition of sulfides and carbonates. The consequent decrease in H₂S precipitated the gold. Gypsum and anhydrite mainly occur as overprints that cut the carbonate‐silica stages. The crosscutting and overprinting relationships of the Victoria quartz‐gold‐base metal veins on the Lepanto copper‐gold veins manifest the late introduction of near neutral pH hydrothermal fluids.     

Overprinting porphyry‐type veinlets on the intrusive rocks and phreatomagmatic breccias in the Southwest prospect,southwestern Sto. Tomas II (Philex), Baguio District,Philippines

The Southwest prospect is located at the southwestern periphery of the Sto. Tomas II porphyry copper–gold deposit in the Baguio District, northwestern Luzon, Philippines. The Southwest prospect hosts a copper‐gold mineralization related to a complex of porphyry intrusions, breccia facies, and overlapping porphyry‐type veinlets emplaced within the basement Pugo metavolcanics rocks and conglomerates of the Zigzag Formation. The occurrences of porphyry‐type veinlets and potassic alteration hosted in the complex are thought to be indications of the presence of blind porphyry deposits within the Sto. Tomas II vicinity. The complex is composed of at least four broadly mineralogically similar dioritic intrusive rocks that vary in texture and alteration type and intensity. These intrusions were accompanied with at least five breccia facies that were formed by the explosive brecciation, induced by the magmatic–hydrothermal processes and phreatomagmatic activities during the emplacement of the various intrusions. Hydrothermal alteration assemblages consisting of potassic, chlorite–magnetite, propylitic and sericite–chlorite alteration, and contemporaneous veinlet types were developed on the host rocks. Elevated copper and gold grades correspond to (a) chalcopyrite–bornite assemblage in the potassic alteration in the syn‐mineralization early‐mineralization diorite (EMD) and contemporaneous veinlets and (b) chalcopyrite‐rich mineralization associated with the chalcopyrite–magnetite–chlorite–actinolite±sericite veinlets contemporaneous with the chlorite–magnetite alteration. Erratic remarkable concentrations of gold were also present in the late‐mineralization Late Diorite (LD). High X_Mg of calcic amphiboles (>0.60) in the intrusive rocks indicate that the magmas have been oxidizing since the early stages of crystallization, while a gap in the composition of Al between the rim and the cores of the calcic amphiboles in the EMD and LD indicate decompression at some point during the crystallization of these intrusive rocks. Fluid inclusion microthermometry suggests the trapping of immiscible fluids that formed the potassic alteration, associated ore mineralization, and sheeted quartz veinlets. The corresponding formation conditions of the shallower and deeper quartz veinlets were estimated at pressures of 50 and 30 MPa and temperatures of 554 and 436°C at depths of 1.9 and 1.1 km. Temperature data from the chlorite indicate that the chalcopyrite‐rich mineralization associated with the chlorite–magnetite alteration was formed at a much lower temperature (ca. 290°C) than the potassic alteration. Evidence from the vein offsetting matrix suggests multiple intrusions within the EMD, despite the K‐Ar ages of the potassic alteration in EMD and hornblende in the LD of about the same age at 3.5 ± 0.3 Ma. The K‐Ar age of the potassic alteration was likely to be thermally reset as a result of the overprinting hydrothermal alteration. The constrained K‐Ar ages also indicate earlier formed intrusive rocks in the Southwest prospect, possibly coeval to the earliest “dark diorite” intrusion in the Sto. Tomas II deposit. In addition, the range of δ³⁴S of sulfide minerals from +1.8‰ to +5.1‰ in the Southwest prospect closely overlaps with the rest of the porphyry copper and epithermal deposits in the Sto. Tomas II deposit and its vicinity. This indicates that the sulfides may have formed from a homogeneous source of the porphyry copper deposits and epithermal deposits in the Sto. Tomas II orebody and its vicinity. The evidence presented in this work proves that the porphyry copper‐type veinlets and the adjacent potassic alteration in the Southwest prospect are formed earlier and at a shallower level in contrast with the other porphyry deposits in the Baguio District.     

Geology, Mineralogy, and Formation Environment of the Disseminated Gold-Silver Telluride Bulawan Deposit, Negros Occidental, Philippines

Abstract: The Bulawan deposit is located in the porphyry copper belt of southwest Negros island, Philippines. Propylitic, K–feldspar, sericitic, and carbonate alteration types can be distinguished in the deposit. Propylite alteration occurs mainly in Cretaceous-Eocene andesitic lavas and agglomerates while K–feldspar, sericite and carbonate alteration types occur mostly in the Middle Miocene dacite porphyry breccia pipes and stocks which were intruded into the andesites. K-feldspar zones occur in the inner parts of the sericitized zone. Sericite alteration overprinted the propylitized and K-feldspar alteration zones, at lower temperature than epidote and chlorite in the propylitized zone. Carbonate alteration is associated with the mineralization in the center of the breccia pipes and along faults. Mineralization consists of gold-silver telluride ores that are hosted by the carbonate– and sericite-altered dacite porphyry breccia pipes. The Bulawan ores occur mainly as disseminations, but unlike many epithermal gold deposits, lack classical epithermal colloform and crustiform quartz veins. The ore minerals are sphalerite, galena, chalcopyrite, pyrite and tetrahedite-tennantite with minor amounts of electrum, calaverite, petzite, sylvanite, hessite, tellurobismuthite, coloradoite, altaite, and rucklidgeite. Electrum and telluride minerals are associated mostly with calcite and dolomite-ankerite minerals. Fluid inclusions in quartz and calcite in clasts of propylitized andesite in the breccia pipes homogenize from about 300° to 400°C while fluid inclusions in quartz, calcite and sphalerite within the dacite porphyry breccia pipes homogenize between 300° to 310°C. The ores were formed around 300°C from hydrothermal solutions with salinity of about 6. 6 wt % NaCl equivalent. The presence of sylvanite and calaverite as intergrowths with each other, and the Ag content of calaverite are consistent with the above temperature estimate. Based on paragenesis, the Bulawan deposit formed in a pyrite-stable environment, with pH between 3. 4 and 5. 5, f_O2 between 10^-32 to 10^-30 atm, f_S2 between 10^-9.8 to 10^-7.8 atm, f_Te2 between 10^-8.9 to 10^-6.5 atm, and total sulfur content about 10^-2.8 molal. The dominant reduced sulfur species in the ore solutions may have been H₂S_(aq), and the likely aqueous tellurium species were H₂Te_(aq) and H₂TeO_3(aq). The ore minerals in the Bulawan deposit were probably formed by mixing of slightly saline and low salinity fluids.     

德兴铜厂斑岩铜矿脉体类型、分布规律及其对成矿的指示意义

德兴铜矿是中国东部重要的大型斑岩铜矿,由朱砂红、铜厂和富家坞等3个矿床组成。在详细的野外脉体填图基础上,文章把德兴铜厂斑岩铜矿的成矿脉体划分为A脉、B脉、D脉和H脉等4种类型。研究发现,A脉的形成与钾化蚀变有关,脉体不规则且不连续,以粒状石英±钾长石±黑云母±磁铁矿±少量黄铁矿±少量黄铜矿的矿物组合为特征;B脉的形成与钾质硅酸盐水解有关,脉体较规则且连续,以石英±辉钼矿±黄铜矿±黄铁矿的矿物组合为特征,石英颗粒呈典型的梳状或长柱状对称于脉壁生长;D脉的形成与石英-绢云母化蚀变有关,以黄铁矿±石英±黄铜矿的矿物组合为特征,脉壁发育绢云母晕;H脉的形成与碳酸盐化有关,以方解石±赤铁矿±黄铁矿±黄铜矿的矿物组合为特征。这4种脉体分别记录了成矿流体演化至不同阶段,热液蚀变作用的特点及其与Cu-Mo硫化物沉淀的关系。脉体的宽度-间距定量统计分析表明,脉体宽度(T)服从于幂次分布定律;脉体间距(S)服从于负指数分布或介于对数正态分布与负指数分布之间。脉体宽度分维值D值(0.91~1.35)普遍>1,反映脉体系统的连通性较差,矿化程度较弱。脉体间距变差系数Cν值(0.49~0.92)均<1,说明脉体簇生聚集程度较低,矿化程度较弱;处于脉体聚集中心的脉体,代表着热液流体运移的通道,制约着其他脉体的展布。     

Yerranderie a Late Devonian Silver–Gold–Lead Intermediate Sulfidation Epithermal District, Eastern Lachlan Orogen, New South Wales, Australia

Felsic volcanic units of the Early Devonian Bindook Volcanic Complex host the Yerranderie epithermal silver–gold–lead district 94 km west–southwest of Sydney. Mineralization in the district forms part of a fault‐controlled, intermediate sulfidation, epithermal silver–gold–base metal vein system that has significant mineral and alteration zonation. Stage 1 of the mineral paragenesis in the veins developed quartz and carbonate with early pyrite, whereas stage 2 is a crustiform banded quartz–pyrite–arsenopyrite assemblage. Stage 3, the main stage of sulfide deposition, comprises early sphalerite, followed by a tetrahedrite–tennantite–gold assemblage, then a galena–chalcopyrite–native silver–pyrite assemblage, and finally a pyrargyrite–polybasite–pearceite assemblage. Stage 4 involves the deposition of quartz veins with minor (late) pyrite and stage 5 is characterized by siderite that infilled remaining voids. Mineral zonation occurs along the Yerranderie Fault, with bornite being restricted to the Colon Peaks–Silver Peak mine area, whereas arsenopyrite, which is present in both the Colon Peaks–Silver Peak and Wollondilly mine areas, is absent in other lodes along the Yerranderie Fault. The Yerranderie Fault, which hosts the major lodes, is surrounded by a zoned alteration system. With increasing proximity to the fault the intensity of alteration increases and the alteration assemblage changes from an outer quartz–muscovite–illite–(ankerite) assemblage to a quartz–illite–(pyrite–carbonate) assemblage within meters of the fault. ⁴⁰Ar/³⁹Ar dating of muscovite from the alteration zone gave a 372.1 ± 1.9 Ma (Late Devonian) age, which is interpreted to be the timing of the quartz–sulfide vein formation. Sulfur isotope values for sulfides range from 0.1 to 6.2‰ with one outlier of ?5.6 δ³⁴S‰. The results indicate that the initial ore‐forming fluids were reduced, and that sulfur was probably sourced from a magmatic reservoir, either as a direct magmatic contribution or indirectly through dissolution and recycling of sulfur from the host volcanic sequence. The sulfur isotope data suggest the system is isotopically zoned.     

Alteration, zoning model, and mineralogical structure considering lithogeochemical investigation in Northern Dalli Cu–Au porphyry

Dalli Cu–Au porphyry deposit was occurred in the igneous diorite, quartz diorite porphyry (QDP), and volcanic rocks such as porphyritic amphibole andesite, andesite (AND), dacite, and pyroclastics during the late Miocene to Pliocene. Regolith investigations and Advanced Spaceborne Thermal Emission and Reflection Radiometer images were used to identify the anomalous areas. According to lithogeochemical survey (from boreholes and trenches) in Northern Dalli Cu–Au porphyry, the potassic, chlorite, sericite, propylitic, and argillic alterations have been found and mineralization was basically associated with potassic and quartz–sericite alterations. The alteration is dominantly moderate quartz chlorite?±?sericite magnetite with 1–10 mm wide quartz?±?magnetite veinlets. The elevated copper–gold values are correlated with density of stockworking and mineralization. The intensity of the mineralization is high in the contact of QDP and AND with increases in pyrite and chalcopyrite values. Malachite, native Cu, and bornite were used to identify supergene, transition, and hypogene zone. In addition, molybdenum increased near to the center of granodiorite intrusion. And besides, from depth to surface in DDH03 and wall rock to mineralization zones, a sequence of Mo→Cu (Au)→Au (Cu) was recorded and the mineralization temperature cooled down (from high to low). The alteration is characterized by specific pattern and structure in Dalli Cu–Au porphyry deposit. The alteration model was followed from the modified Lowell and Gilbert model. The porphyry is stockworked by quartz veins and by quartz magnetite veins. Vein distribution and ore mineralogy vary between the different alteration zones. Due to the formation of an iron cap in the supergene, especially in the southern hills, supergene grade was higher than hypogene zone. Also, hematite, as a dominant Fe oxide in DDH03 borehole with minor limonite, jarosite, and goethite created thickness about 150–270 m in supergene zone; finally, this finding show a possibility of an extensive mineralization.     

Geochemistry and Fluid Inclusions Analysis of Vein Quartz in the Multiple Hydrothermal Systems of Mankayan Mineral District,Philippines

Several high‐sulfidation epithermal gold orebodies in the Mankayan Mineral District were formed in an environment that has been already affected by earlier porphyry‐type mineralization. This study reports the geologic and geochemical characteristics of the Carmen and Florence epithermal orebodies, which are located in the south of the Lepanto main enargite–gold orebody. The gold‐bearing epithermal quartz veins in the Carmen and Florence areas are of two types: (i) the enargite‐rich veins and (ii) the quartz–pyrite–gold (QPG) veins. The two types of veins are mainly hosted by the Cretaceous Lepanto Metavolcanics basement rocks, with minor veins cutting the Pleistocene Imbanguila Dacite Pyroclastics. The mineral assemblages and homogenization temperatures of fluid inclusions indicate that the Carmen and Florence orebodies were deposited by fluids varying from high to very high sulfidation state. The enargite and QPG epithermal veins of Carmen and Florence cut porphyry‐type quartz veinlet stockworks and veins that host polyphase hypersaline fluid inclusions that did not homogenize at or below 400°C. These high‐temperature quartz exhibits distinctly different mineral chemistry from the quartz of the QPG and enargite‐rich epithermal veins. In particular, the Ti content of quartz of the porphyry‐type veinlet stockwork is elevated (>100 ppm), whereas the Ti concentration of the epithermal vein quartz crystals are below detection limits. The Fe concentration of quartz is high in epithermal vein quartz (>300 ppm), whereas nearly undetected in the porphyry‐type stockwork veinlet quartz. Multiple generations of quartz with different mineral chemistry, fluid inclusions morphology, temperature, salinity and bulk gas compositions, and stable isotopic ratios indicate the variable hydrothermal conditions throughout the mineralization history of the Mankayan District. The temperature, pH, sulfidation state, oxidation state, and fluid composition vary among the orebodies in Carmen and Florence areas. Furthermore, the characteristics of earlier alteration affected the apparent characteristics of subsequent mineralization.     

Geochronology and Genesis of the Tiegelongnan Porphyry Cu(Au) Deposit in Tibet: Evidence from U–Pb,Re–Os Dating and Hf,S, and H–O Isotopes

The Tiegelongnan Cu (Au) deposit is the largest copper deposit newly discovered in the Bangong–Nujiang metallogenic belt. The deposit has a clear alteration zoning consisting of, from core to margin, potassic to propylitic, superimposed by phyllic and advanced argillic alteration. The shallow part of the deposit consists of a high sulphidation‐state overprint, mainly comprising disseminated pyrite and Cu–S minerals such as bornite, covellite, digenite, and enargite. At depth porphyry‐type mineralization mainly comprises disseminated chalcopyrite, bornite, pyrite, and a minor vein molybdenite. Mineralization is disseminated and associated with veins contained within the porphyry intrusions and their surrounding rocks. The zircon U–Pb ages of the mineralized diorite porphyry and granodiorite porphyry are 123.1 ± 1.7 Ma (2σ) and 121.5 ± 1.5 Ma (2σ), respectively. The molybdenite Re–Os age is 121.2 ± 1.2 Ma, suggesting that mineralization was closely associated with magmatism. Andesite lava (zircon U–Pb age of 111.7 ± 1.6 Ma, 2σ) overlies the ore‐bodies and is the product of post‐mineralization volcanic activity that played a critical role in preserving the ore‐bodies. Values of ?4.6 ‰ to + 0.8 ‰ δ³⁴S for the metal sulfides (mean ? 1.55 ‰) suggest that S mainly has a deep magmatic source. The H and O isotopic composition is (δD = ?87 ‰ to ?64 ‰; δ¹⁸O_H2O = 5.5 ‰ to 9.0 ‰), indicating that the ore‐forming fluids are mostly magmatic‐hydrothermal, possibly mixed with a small amount of meteoric water. The zircon ε_Hf(t) of the diorite porphyry is 3.7 to 8.3, and the granodiorite porphyry is 1.8 to 7.5. Molybdenite has a high Re from 382.2 × 10^?6 to 1600 × 10^?6. Re and Hf isotope composition show that Tiegelongnan has some mantle source, maybe the juvenile lower crust from crust–mantle mixed source. Metallogenesis of the Tiegelongnan giant porphyry system was associated with intermediate to acidic magma in the Early Cretaceous (~120 Ma). The magma provenance of the Tiegelongnan deposit has some mantle‐derived composition, possibly mixed with the crust‐derived materials.     

Geology of the High Sulfidation Copper Deposits,Monywa Mine,Myanmar

The 50 km² Monywa copper district lies near the Chindwin River within the northward continuation of the Sunda‐Andaman magmatic arc through western Myanmar. There are four deposits; Sabetaung, Sabetaung South, Kyisintaung, and the much larger Letpadaung 7 km to the southeast. Following exploration drilling which began in 1959, production of copper concentrates from a small open pit started at Sabetaung in 1983. Since 1997, when resources totaled 7 million tonnes contained copper in 2 billion tonnes ore, a heap leach–electro‐winning operation has produced over 400,000 t copper cathode from Sabetaung and Sabetaung South. Ore is hosted by mid‐Miocene andesite or dacite porphyry intrusions, and by early mid‐Miocene sandstone and overlying volcaniclastics including eruptive diatreme facies which the porphyries intrude. District‐wide rhyolite dykes and domes with marginal breccias probably post‐date andesite porphyries in the mine area and lack ore‐grade copper. Host rocks to mineralization are altered to phyllic and advanced argillic hydrothermal assemblages within an outer chlorite zone; hypogene alunite is most abundant at Letpadaung and Kyisintaung. Most mineralization is structurally‐controlled with digenite‐chalcocite in breccia dykes, in steeply dipping NE‐trending sheeted veins, and in stockwork and low‐angle sulfide veins. A high‐grade pipe at Sabetaung grades up to 30% Cu, and much of the ore at Sabetaung South is in a NE‐trending zone of mega‐breccia and stockworked sandstone. The hydrothermal alteration, together with replacement quartz, alunite and barite in breccia dykes and veins, the virtual absence of vein quartz, and the presence of chalcopyrite and bornite only as rare veins and as inclusions within the abundant pyrite, indicate that the deposits are high sulfidation. Regional uplift, resistance to erosion and leaching of the altered and mineralized rocks have resulted in porous limonite‐stained leached caps over 200 m thick forming the Letpadaung and Kyisintaung hills. The barren caps pass abruptly downwards at the water table into the highest grade ore at the top of the supergene enrichment zone, within which copper grade, supergene kaolinite and cubic alunite decrease, and pyrite increases with depth; in contrast, marcasite is mostly shallow. Much of the copper to depths exceeding 200 m below the water table occurs as supergene digenite‐chalcocite and minor covellite. Disseminated chalcocite is mostly near‐surface and hence almost certainly supergene. We infer that during prolonged uplift at all four deposits, oxidation of residual pyrite at the water table generated enough acid to leach all the copper from earlier supergene‐enriched ore; below the water table the resulting acid sulfate solutions partly replaced enargite, covellite, chalcopyrite, bornite and pyrite with supergene chalcocite. Undeformed upward‐fining cross‐bedded conglomerates and sands of the ancestral Chindwin River floodplain overlie the margins of the Sabetaung deposits, form a major aquifer up to 40 m thick, and are a potential host for exotic copper mineralization. A mid‐Miocene pluton is inferred to underlie the Monywa deposits, but the possibility of porphyry‐type mineralization within the district is at best highly speculative.     

Petrography,geochemistry and geochronology of the host porphyries and associated alteration at the Tuwu Cu deposit,NW China: a case for increased depositional efficiency by reaction with mafic hostrock?

Tuwu is the largest porphyry copper deposit discovered in the Eastern Tianshan Mountains, Xinjiang, China. A newly recognized volcanic complex in the Early Carboniferous Qi’eshan Group at Tuwu consists of basalt, andesite, and diorite porphyry. The plagiogranite porphyry was emplaced into this complex at 332.8±2.5 Ma (U–Pb zircon SIMS determination). Whole-rock element geochemistry shows that the volcanic complex and plagiogranite porphyry formed in the same island arc, although the complex was derived by partial melting of the mantle wedge and the plagiogranite porphyry by partial melting of a subducting slab. The diorite and the plagiogranite porphyries have both been subjected to intense hydrothermal alteration and associated mineralization, but the productive porphyry is the plagiogranite porphyry. Three alteration and mineralization stages, including pre-, syn- and post-ore stages, have been recognized. The pre-ore stage formed a barren propylitic alteration which is widespread in the volcanic complex. The syn-ore stage is divided into three sub-stages: Stage 1 is characterized by potassic alteration with chalcopyrite + bornite + chalcocite; Stage 2 is marked by chlorite–sericite–albite alteration with chalcopyrite ± pyrite ± bornite; Stage 3 is represented by phyllic alteration with chalcopyrite + pyrite ± molybdenite. The post-ore stage produced a barren argillic alteration limited to the diorite porphyry. A specific feature of the Tuwu deposit is that the productive porphyry was emplaced into a very mafic package, and reaction of the resulting fluids with the ferrous iron-rich hostrocks was a likely reason that Tuwu is the largest porphyry in the district.     

Genesis of the Bangbu Orogenic Gold Deposit,Tibet: Evidence from Fluid Inclusion,Stable Isotopes,and Ar-Ar Geochronology

The Bangbu gold deposit is a large orogenic gold deposit in Tibet formed during the AlpineHimalayan collision. Ore bodies(auriferous quartz veins) are controlled by the E-W-trending Qusong-Cuogu-Zhemulang brittle-ductile shear zone. Quartz veins at the deposit can be divided into three types: pre-metallogenic hook-like quartz veins, metallogenic auriferous quartz veins, and postmetallogenic N-S quartz veins. Four stages of mineralization in the auriferous quartz veins have been identified:(1) Stage S1 quartz+coarse-grained sulfides,(2) Stage S2 gold+fine-grained sulfides,(3) Stage S3 quartz+carbonates, and(4) Stage S4 quartz+ greigite. Fluid inclusions indicate the oreforming fluid was CO_2-N_2-CH_4 rich with homogenization temperatures of 170–261°C, salinities 4.34–7.45 wt% Na Cl equivalent. δ~(18)Ofluid(3.98‰–7.18‰) and low δDV-SMOW(-90‰ to-44‰) for auriferous quartz veins suggest ore-forming fluids were mainly metamorphic in origin, with some addition of organic matter. Quartz vein pyrite has δ~(34)SV-CDT values of 1.2‰–3.6‰(an average of 2.2‰), whereas pyrite from phyllite has δ~(34)SV-CDT 5.7‰–9.9‰(an average of 7.4‰). Quartz vein pyrites yield 206Pb/204 Pb ratios of 18.662–18.764, 207Pb/204 Pb 15.650–15.683, and ~(208)Pb/204 Pb 38.901–39.079. These isotopic data indicate Bangbu ore-forming materials were probably derived from the Langjiexue accretionary wedge. 40Ar/39 Ar ages for sericite from auriferous sulfide-quartz veins yield a plateau age of 49.52 ± 0.52 Ma, an isochron age of 50.3 ± 0.31 Ma, suggesting that auriferous veins were formed during the main collisional period of the Tibet-Himalayan orogen(~65–41 Ma).     

Hydrothermal Alteration and Cu-Au Mineralization at Nena High Sulfidation-type Deposit, Frieda River, Papua New Guinea

Abstract. The Nena Cu‐Au deposit, located in the Frieda River mineral district of northwestern mainland Papua New Guinea, is a composite structurally‐lithologically controlled high sulfidation (HS) system. Its hydrothermal alteration and Cu‐Au mineralization are presented in this paper. Initially propylitized andesitic volcanics veined by epithermal quartz were pervasively superimposed by zoned HS alteration. The zonation grades from vuggy silica core to sulfur‐rich, pyritic silica‐alunite halo followed by pyrophyllite‐dickite‐kaolinite interval and finally to thin illite‐smectite margin, suggesting progressive decrease in temperature and increase in pH. This zonation is enveloped by chlorite‐epidote‐calcite‐gypsum alteration. The acid altered rocks were then invaded by multiple phases of pyrite, subsequently crosscut by quartz, vein alunite and barite. Then sequential deposition of bladed covellite, enargite, luzonite and stibioluzonite occurred from the NW to the SE portions of the deposit, forming a zonation suggestive of progressive decrease in temperature, sulfur fugacity and sulfidation stage. Most ore mineralization occurs in the vuggy silica core. Gold mineralization commenced from the transition of enargite to luzonite and continued throughout the stibioluzonite stage. Associated with gold deposition are Au‐rich pyrite, tennantite‐tetrahedrite, chalcopyrite‐bornite, native tellurium, electrum, calaverite, bismuthinite and galena. Native sulfur occupied the remaining cavities and represents the waning stage of the hydrothermal system. Fluid inclusions studies distinguished magmatic (>300–350d?C, 9–15 wt% NaCl equiv.) and meteoric (<150–200d?C, 1–2 wt% NaCl equiv.) fluids (Holzberger et al., 1996). Temperatures and salinities of fluid inclusions from barite associated with Cu sulfides show a general decrease from NW (330d?C, 9–15 wt% NaCl equiv.) to SE (172d?C, 10 wt% NaCl equiv.) parts of the deposit, indicating gradual entrainment of ground water (Hitchman and Espi, 1997). Interaction of magmatic fluids with meteoric water accompanied by changes in temperature, salinity, acidity and oxidation state of the resultant fluids is interpreted to have been the main cause of metal precipitation. Finally, supergene processes generated Au zone with an underlying chalcocite‐covellite‐digenite blanket over the primary sulfides at depth. Gold occurs as lattice constituent in scorodite, limonite‐goethite and jarosite. Chalcocite is more abundant and widespread than other Cu sulfides. Acidic fluids deposited powdery alunite and kaolinite, vein alunite and amorphous silica. Weakly secondary biotite‐quartz altered porphyry located below the known HS Cu‐Au deposit contains chalcopyrite‐bornite and is overprinted by quartz‐alunite‐pyro‐phyllite‐pyrite assemblage. This feature indicates close temporal, spatial and genetic relation between the two deposit types.     

Evolution of Hydrothermal System at the Dizon Porphyry Cu-Au Deposit, Zambales, Philippines

Abstract. Evolution of hydrothermal system from initial porphyry Cu mineralization to overlapping epithermal system at the Dizon porphyry Cu‐Au deposit in western central Luzon, Zambales, Philippines, is documented in terms of mineral paragen‐esis, fluid inclusion petrography and microthermometry, and sulfur isotope systematics. The paragenetic stages throughout the deposit are summarized as follows; 1) stockwork amethystic quartz veinlets associated with chalcopyrite, bornite, magnetite and Au enveloped by chlorite alteration overprinting biotite alteration, 2) stockwork quartz veinlets with chalcopyrite and pyrite associated with Au and chalcopyrite and pyrite stringers in sericite alteration, 3) stringer quartz veinlets associated with molybdenite in sericite alteration, and 4) WNW‐trending quartz veins associated with sphalerite and galena at deeper part, while enargite and stibnite at shallower levels associated with advanced argillic alteration. Chalcopyrite and bornite associated with magnetite in quartz veinlet stockwork (stage 1) have precipitated initially as intermediate solid solution (iss) and bornite solid solution (bnss), respectively. Fluid inclusions in the stockwork veinlet quartz consist of gas‐rich inclusions and polyphase inclusions. Halite in polyphase inclusions dissolves at temperatures ranging from 360d?C to >500d?C but liquid (brine) and gas (vapor) do not homogenize at <500d?C. The maximum pressure and minimum temperature during the deposition of iss and bnss with stockwork quartz veinlets are estimated to be 460 bars and 500d?C. Fluid inclusions in veinlet stockwork quartz enveloped in sericite alteration (stage 2) consist mainly of gas‐rich inclusions and polyphase inclusions. In addition to the possible presence of saturated NaCl crystals at the time of entrapment of fluid inclusions that exhibit the liquid‐vapor homogenization temperatures lower than the halite dissolution temperatures in some samples, wide range of temperatures of halite dissolution and liquid‐vapor homogenization of polyphase inclusions from 230d?C to >500d?C and from 270d?C to >500d?C, respectively, suggests heterogeneous entrapment of gaseous vapor and hypersaline brine. The minimum pressure and temperature are estimated to be about 25 bars and 245d?C. Fluid inclusions in veinlet quartz associated with molybdenite (stage 3) are dominated by gas‐rich inclusions accompanied with minor liquid‐rich inclusions that homogenize at temperatures between 350d?C and 490d?C. Fluid inclusions in vuggy veinlet quartz associated with stibnite (stage 4) consist mainly of gas‐rich inclusions with subordinate polyphase inclusions that do not homogenize below 500d?C. Fluid inclusions in veinlet quartz associated with galena and sphalerite (stage 4) are composed of liquid‐rich two‐phase inclusions, and they homogenize into liquid phase at temperatures ranging widely from 190d?C to 300d?C (suggesting boiling) and the salinity ranges from 1.0 wt% to 3.4 wt% NaCl equivalent. A pressure of about 15 bars is estimated for the dilute aqueous solution of 190d?C from which veinlet quartz associated with galena and sphalerite precipitated. In addition to a change in temperature‐pressure regime from lithostatic pressure during the deposition of iss and bnss with stockwork quartz veinlets to hydrostatic pressure during fracture‐controlled quartz veinlet associated with galena and sphalerite, a decrease in pressure is supposed to have occurred due to unroofing or removal of the overlying piles during the temperature decrease in the evolution of hydrothermal system. The majority of the sulfur isotopic composition of sulfides ranges from ±0 % to +5 %. Sulfur originated from an iso‐topically uniform and homogeneous source, and the mineralization occurred in a single hydrothermal system.