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 Sanbao Mn–Ag (Zn-Pb) deposit located in the Laojunshan ore district is one of the most important deposits that has produced most Ag and Mn metals in southeastern Yunnan Province, China. Few studies are available concerning the distribution and mineralization of Ag, restricting further resource exploration. In this study, detailed mineralogy, chronology, and geochemistry are examined with the aim of revealing Ag occurrence and its associated primary base-metal and supergene mineralization. Results show that manganite and romanèchite are the major Ag-bearing minerals. Cassiterite from the Mn–Ag ores yielded a U–Pb age of 436 ± 17 Ma, consistent with the Caledonian age of the Nanwenhe granitic pluton. Combined with other geochemical proxies (Zn-Pb-Cu-Sn), the Sanbao Mn–Ag deposit may originally be of magmatic hydrothermal origin, rather than sedimentary. The Ag-rich (Zn-Pb (Sn)-bearing) ore-forming fluids generated during the intrusion of the granite flowed through fractures and overprinted the earlier Mn mineralization. Secondary Ag (and possibly other base-metals) enrichment occurred through later supergene weathering and oxidation. Full article

Whole-rock and apatite geochemical analyses and zircon U–Pb dating were carried out on the lamprophyres in the world-class Zhuxi W–Cu skarn deposit in northern Jiangxi, South China, in order to understand their origin of mantle sources and their relationship with the deposit, as well as metallogenic setting. The results show the lamprophyres were formed at ca. 157 Ma, just before the granite magmatism and mineralization of the Zhuxi deposit. These lamprophyres have from 58.98–60.76 wt% SiO₂, 2.52–4.96 wt% K₂O, 5.92–6.41 wt% Fe₂O_3t, 3.75–4.19 wt% MgO, and 3.61–5.06 wt% CaO, and enrichment of light rare earth elements (LREE) and large-ion lithophile elements (LILE), and depletion of high-field-strength elements (HFSE). Apatites in the lamprophyres are enriched in LREE and LILE, Sr, S, and Cl, and have ⁸⁷Sr/⁸⁶Sr ratios ranging from 0.7076 to 0.7078. The conclusions demonstrate that the lithospheric mantle under the Zhuxi deposit was metasomatized during Neoproterozoic subduction. Late Jurassic crustal extension caused upwelling of the asthenospheric mantle and consecutively melted the enriched lithospheric mantle and then crustal basement, corresponding to the formation of lamprophyres and mineralization-related granites in the Zhuxi deposit, respectively. Full article

The Sisson Brook deposit is a low-grade, large-tonnage W-Mo deposit with notable Cu located in west-central New Brunswick, Canada, and is one of several W-Mo deposits in New Brunswick associated with fluids sourced from granitic plutons emplaced during the Devonian Acadian Orogeny. The younger Devonian-aged stockwork and replacement scheelite-wolframite-molybdenite (and chalcopyrite) mineralization straddles the faulted boundary between Cambro-Ordovician metasedimentary rocks with Ordovician felsic volcaniclastic rocks and the Middle Silurian Howard Peak Granodiorite, with dioritic and gabbroic phases. U-Pb dating of magmatic titanite in the host dioritic phase of the Howard Peak Granodiorite using LA ICP-MS resulted in a ²⁰⁴Pb-corrected concordant age of 432.1 ± 1.9 Ma. Petrologic examination of selected mineralization combined with elemental mapping of vein selvages using micro-XRF and metasomatic titanite and ilmenite grains using LA ICP-MS indicates that saturation of titaniferous phases influenced the distribution of scheelite versus wolframite mineralization by altering the aFe/aCa ratio in mineralizing fluids. Ilmenite saturation in Ti-rich host rocks lowered the relative aFe/aCa and led to the formation of scheelite over wolframite. Altered magmatic titanite and hydrothermal titanite also show increased W and Mo concentrations due to interaction with and/or saturation from mineralizing fluids. Full article

The Fukeshan Cu (Mo) deposit is a newfound porphyry deposit in the northern Great Xing’an Range (GXR), northeast China. In this paper, we present results of chalcopyrite Re–Os geochronology, microthermometry of the fluid inclusions (FIs), and isotopic (H–O–S–Pb) compositions of the Fukeshan Cu (Mo) deposit. Its ore-forming process can be divided into sulfide-barren quartz veins (A vein; stage I), quartz + chalcopyrite + pyrite veins (B vein; stage II), quartz + polymetallic sulfide veins (D vein; stage III), and barren quartz + carbonate ± pyrite veins (E vein; stage IV), with Cu mineralization mainly occurred in stage II. Three types of FIs are identified in this deposit: liquid-rich two-phase (L-type) FIs, vapor-rich two-phase (V-type) FIs, daughter mineral-bearing three-phase (S-type) FIs. The homogenization temperatures of primary FIs hosted in quartz of stages I–IV are 381–494 °C, 282–398 °C, 233–340 °C, and 144–239 °C, with salinities of 7.2–58.6, 4.8–9.9, 1.4–7.9, and 0.9–3.9 wt. % NaCl equivalent, respectively. FIs microthermometry and H–O isotope data suggest that the ore-forming fluids were magmatic in origin and were gradually mixed with meteoric water from stages II to IV. Sulfur and lead isotope results indicate that the ore-forming materials of the Fukeshan Cu (Mo) deposit were likely to have originated from Late Jurassic intrusive rocks. The available data suggest that fluid cooling and incursions of meteoric water into the magmatic fluids were two important factors for Cu precipitation in the Fukeshan Cu (Mo) deposit. Chalcopyrite Re–Os dating yielded an isochron age of 144.7 ± 5.4 Ma, which is similar to the zircon U–Pb age of the quartz diorite porphyry, indicating that Late Jurassic quartz diorite porphyry and Cu mineralization occurred contemporaneously. Full article

Eastern Tianshan hosts a number of porphyry Cu deposits. However, these mainly formed in the Jueluotage Belt, in the middle part of Eastern Tianshan. The Tonggou porphyry Cu mineralization is an exception to this, since it is located in the Bogda Orogenic Belt, north of Eastern Tianshan. We obtained new zircon U-Pb ages, whole-rock geochemical data, zircon Hf isotope data, and zircon trace element compositions. LA-ICP-MS zircon U-Pb dating indicates a crystallization age of 302.2–303.0 Ma for the Tonggou mineralized granodiorite (TMG), which suggests that the Tonggou porphyry Cu mineralization formed in the Late Carboniferous period. ε_Hf (t) data (1.8–14.1) for TMG suggests it was sourced from juvenile crustal melts, mixed with some mantle materials. TMG displays low ΣREE, compatible elements (Ba, Sr, Zr, and Hf), Zr/Hf and Nb/Ta ratios, as well as clearly negative Eu anomalies in whole rocks analyses. In addition, TMG is enriched in P, Hf and Th/U ratios in zircon, and has lower crystallization temperatures (734 to 735 °C) than the Daheyan barren granodiorite (DBG) (753 to 802 °C). Whole rock and zircon geochemical analyses show that the TMG was formed by fractional crystallization to a greater extent than the DBG in the Bogda Orogenic Belt. Moreover, zircon grains of the TMG show high Ce⁴⁺/Ce³⁺ ratios (159–286), which are consistent with related values from large porphyry deposits of the Central Asian Orogenic Belt (CAOB). High Ce^4+/Ce³⁺ ratios reflect oxidizing magmas as a result of fractional crystallization, which indicates that the Tonggou deposit has potential to host a large porphyry Cu deposit. Full article

The Lake George antimony mine was at one time North America’s largest producer of antimony. Despite being widely known for the antimony mineralization, the deposit also hosts a range of styles of mineralization such as multiple generations of W-Mo bearing quartz veins as well as a system of As-Au bearing quartz–carbonate veins. In situ U-Pb zircon geochronology, using LA ICP-MS, of the Lake George granodiorite yielded a weighted mean ²⁰⁶Pb/²³⁸U age of 419.6 ± 3.0 Ma. Step heating of phlogopite separated from the lamprophyre dykes produced a ⁴⁰Ar/³⁹Ar plateau segment date of 419.4 ± 1.4 Ma. Single molybdenite crystal analysis for Re-Os geochronology was conducted on two W-Mo-bearing quartz veins, which cross-cut altered granodiorite and altered metasedimentary rocks and yielded two dates of 415.7 ± 1.7 Ma and 416.1 ± 1.7 Ma respectively. ⁴⁰Ar/³⁹Ar geochronology of muscovite from alteration associated with Au-bearing quartz–carbonate veins yielded one representative plateau segment date of 414.1 ± 1.3 Ma. The dates produced in this study revealed that the different magmatic–hydrothermal events at the Lake George mine occurred over approximately a 10-million-year period at the end of the Silurian and the start of the Devonian following the termination of the Acadian orogeny. Full article

The Xianghualing skarn Sn deposit in the southwestern part of the southern Hunan Metallogenic Belt is a large Sn deposit in the Nanling area. In this paper, the garnet has been analyzed by laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) to obtain the concentrations of the major and trace elements. The results reveal that the garnets from the Xianghualing deposit mainly belong to andradite-grossular (grandite) solid solution and are typically richer in Al than in Fe. They show enrichment in heavy rare earth elements (HREEs) and notably lower light rare earth elements (LREEs), and commonly negative Eu anomalies, indicative of a relatively reduced formation environment. The garnets have high Sn concentrations between 2313 ppm and 5766 ppm. It is also evident that there is a positive correlation between Sn and Fe, suggesting that Sn⁴⁺ substitutes into the garnets through substituting for Fe³⁺ in the octahedral position. Combined with previous studies, it can be recognized that the Sn concentrations of garnet in skarn Sn deposits are generally high, whereas the W concentrations are relatively low. This is just the opposite in garnets from skarn W deposits that typically have high W, but low Sn concentrations. In polymetallic skarn deposits with both economic Sn and W, the concentrations of both metals in garnets are relatively high, although varying greatly. Therefore, the Sn and W concentrations in garnets can be used to evaluate a skarn deposit’s potential to produce Sn and (or) W mineralization, which is helpful in exploration. Full article

The Wulandele molybdenum deposit is a porphyry-type Mo deposit in the Dalaimiao area of northern Inner Mongolia, China. Molybdenite Re-Os dating yields a model age of 134.8 ± 1.9 Ma, with the fine-grained monzogranite most closely related to the mineralization. The lithogeochemical data show that the monzogranite is weakly peraluminous, high-K calc-alkaline series, with reduced to slightly oxidized, highly fractionated I-type granite characteristics. The relatively low initial ⁸⁷Sr/⁸⁶Sr (range from 0.705347 to 0.705771), weakly negative ε_Nd(t) (range from −2.0 to −1.3), and crust-mantle mixing of Pb isotopes suggest that the monzogranite originated from the partial melting of mafic juvenile lower continental crust derived from the depleted mantle, with a minor component of ancient continental crust. Combined with the regional tectonic evolution, we argue that the partial melting, then injection, of the monzogranite melt was probably triggered by collapse or delamination of the thickened lithosphere, which was mainly in response to the post-orogenic extensional setting of the Mongol–Okhotsk belt; this is possibly coupled with a back-arc extension related to Paleo-Pacific plate subduction. The extensively fractional crystallization of the monzogranite melt is the crucial enrichment process, resulting in magmatic hydrothermal Mo mineralization in the Wulandele deposit, and the Cretaceous granitoids are generally favorable to form Mo mineralization in the Dalaimiao area. Full article

The Lyhamyar deposit is a large Sb deposit in the Southern Shan Plateau, Eastern Myanmar. The deposit is located in the Early Silurian Linwe Formation, occurring as syntectonic quartz-stibnite veins. The ore body forms an irregular staircase shape, probably related to steep faulting. Based on the mineral assemblages and cross-cutting relationships, the deposit shows two mineralization stages: (1) the pre-ore sedimentary and diagenetic stage, and (2) the main-ore hydrothermal ore-forming stage (including stages I, II, and III), i.e., (i) early-ore stage (stage I) Quartz-Stibnite, (ii) late-ore stage (stage II) Quartz-calcite-Stibnite ± Pyrite, and (iii) post-ore stage (stage III) carbonate. The ore-forming fluid homogenization temperatures from the study of primary fluid inclusions in quartz and calcite indicate that the ore-forming fluid was of a low temperature (143.8–260.4 °C) and moderate to high-salinity (2.9–20.9 wt. % NaCl equivalent). Hydrogen and oxygen isotopes suggest that the ore-forming fluids of the Lyhamyar deposit were derived from circulating meteoric water mixed with magmatic fluids that underwent isotopic exchange with the surrounding rocks. Sulfur in Lyhamyar was dominated by thermochemical sulfate reduction (TSR) with dominant magmatic source sulfur. The lead isotope compositions of the stibnite indicate that the lead from the ore-forming metals was from the upper crustal lead reservoir and orogenic lead reservoir. On the basis of the integrated geological setting, ore geology, fluid inclusions, (H-O-S-Pb) isotope data, and previous literature, we propose a new ore-deposit model for the Lyhamyar Sb deposit: It was involved in an early deposition of pyrite in sedimentary and diagenetic stages and later Sb mineralization by mixing of circulating meteoric water with ascending magmatic fluids during the hydrothermal mineralization stage. Full article

In Archean greenstone belts, magmatism is dominated by intrusive and volcanic rocks with tholeiitic affinities, as well as tonalite- and granodiorite-dominated large-volume batholiths, i.e., tonalite–trondhjemite–granodiorite (TTG) suites. These intrusions are associated with poorly documented mineralization (Cu-Au porphyries) that, in the Neoarchean Abitibi Subprovince (>2.79 to ~2.65 Ga), Superior Province, Canada, are associated with diorite bearing plutons, i.e., tonalite–trondhjemite–diorite (TTD) suites. The importance of TTG versus TTD suites in the evolution of greenstone belts and of their magmatic-hydrothermal systems and related mineralization is unconstrained. The aim of this study was to portray the chemistry and distribution of these suites in the Abitibi Subprovince. The study used data compiled by the geological surveys of Québec and Ontario to evaluate the chemistry of TTG and TTD suites and uncovered two coeval magmas that significantly differentiated (fractional crystallization mostly): 1) a heavy rare earth elements (HREE)-depleted tonalitic magma from high pressure melting of an hydrated basalt source; and 2) a hybrid HREE-undepleted magma that may be a mixture of mantle-derived (tholeiite) and tonalitic melts. The HREE-depleted rocks (mostly tonalite and granodiorite) display chemical characteristics of TTG suites (HREE, Ti, Nb, Ta, Y, and Sr depletion, lack of mafic unit, Na-rich), while the other rocks (tonalite and diorite) formed TTD suites. Tonalite-dominated magmatism, in the Abitibi Subprovince, comprises crustal melts as well as a significant proportion of mantle-derived magmas and this may be essential for Cu-Au magmatic-hydrothermal mineralizing systems. Full article

Ore-forming fluids in the auriferous district of the Central gold belt in Peninsular Malaysia were studied for their temperature, salinity, and relationship to the surrounding geology. Microthermometric analysis carried out showed homogenisation temperatures range from 210 to 348 °C (Tersang), between 194 and 348 °C (Selinsing), and from 221 to 346 °C (Penjom). Salinities range from 2.41 to 8.95 wt % NaCl equiv (Tersang), between 1.23 and 9.98 wt % NaCl equiv (Selinsing), and from 4.34 to 9.34 wt % NaCl equiv (Penjom). Laser Raman studies indicated that at the Tersang gold deposit, most inclusions are either pure or nearly pure CO₂-rich (87–100 mol %), except for one inclusion, which contains CH₄ gas (13 mol %). In addition, at Selinsing, most inclusions are CO₂-rich (100 mol %). However, an inclusion was found containing CO₂ (90 mol %), with minor N₂ and CH₄. Additionally, at the Penjom gold deposit, most fluid inclusions are CO₂-rich (91–100 mol %), whereas one fluid inclusion is N₂-rich (100 mol %) and another one has minor N₂ and CH₄. At a basin scale, homogenisation temperatures against salinity suggests an isothermal mixing of fluids. Most fluids are CO₂-rich and are interpreted to be of metamorphic origin. The evidence further indicates involvement of magmatic fluids that is supported by the association of sandstone and carbonaceous black shales with magmatic rocks, such as rhyolite, rhyolite-dacite, and trachyte-andesite at the Tersang and Penjom orogenic gold deposits. Full article

Most of the granite-related Sn–W deposits in Myanmar are located in the Western Granitoid Province (WGP) of Southeast Asia. The Tagu deposit in the southern part of the WGP is a granite related Sn–W deposit. The biotite granite is composed of quartz, feldspars (plagioclase, orthoclase, and microcline), and micas (muscovite and biotite) and belongs to S-type peraluminous granite. Abundances of large-ion lithophile elements (LILEs), such as Rb, K, and Pb, coupled with the deficiency of high-field-strength elements (HFSEs), such as Nb, P, and Ti, indicate that the parental magma for the Tagu granite was derived from the lower continental crust at syn-collisional setting. Mineralized veins consist of early-formed oxide ore minerals, such as cassiterite and wolframite, which were followed by the formation of sulfide minerals. Three main types of fluid inclusions were distinguished from the mineralized quartz veins hosted by granite and metasedimentary rocks: Type-A—two phases, liquid (L) + vapor (V) aqueous inclusions; Type-B—two phases, vapor (V) + liquid (L) vapor-rich inclusions; And type-C—three phases, liquid + CO₂-liquid + CO₂-vapor inclusions. Quartz in the veins hosted in granite corresponding with earlier deposition contains type-A, type-B, and type-C fluid inclusions, whereas that in the veins hosted in metasedimentary rocks corresponding with later deposition contains only type-A fluid inclusions. The homogenization temperatures of type-A inclusions range from 140 °C to 330 °C (mode at 230 °C), with corresponding salinities from 1.1 wt.% to 8.9 wt.% NaCl equivalent for quartz veins hosted in metasedimentary rocks, and from 230 °C to 370 °C (mode at 280 °C), with corresponding salinities from 2.9 wt.% to 10.6 wt.% NaCl equivalents for quartz veins hosted in granite. The homogenization temperatures of type-B vapor-rich inclusions in quartz veins in granite range from 310 °C to 390 °C (mode at 350 °C), with corresponding salinities from 6.7 wt.% to 12.2 wt.% NaCl equivalent. The homogenization temperatures of type-C H₂O–CO₂–NaCl inclusions vary from 270 °C to 405 °C (mode at 330 °C), with corresponding salinities from 1.8 wt.% to 5.6 wt.% NaCl equivalent. The original ascending ore fluid was probably CO₂-bearing fluid which evolved into two phase fluid by immiscibility due to pressure drop in the mineralization channels. Furthermore, the temperature and salinities of two-phase aqueous fluids were later most likely decreased by the mixing with meteoric water. The salinities of the type-B vapor-rich inclusions are higher than those of the type-C CO₂-rich inclusions, which may have resulted from CO₂ separation from the fluids. The escape of gases can lead to an increase in the salinity of the residual fluids. Therefore, the main ore-forming mechanisms of the Tagu Sn–W deposit are characterized by fluid immiscibility during an early stage, and fluid mixing with meteoric water in the late stage at a lower temperature. Full article

Active subaerial geothermal systems are regarded as modern analogues of low- to intermediate-sulfidation epithermal Au–Ag deposits, where minor amounts of Cu are mostly present as chalcopyrite. Although trace element data concerning sulfides are scarce in active geothermal systems at convergent settings, studies in several other environments have demonstrated that chalcopyrite is a relevant host of Ag and other trace elements. Here, we focus on the active Cerro Pabellón geothermal system in the Altiplano of northern Chile, where chalcopyrite-bearing samples were retrieved from a 561 m drill core that crosscuts the high-enthalpy geothermal reservoir at depth. A combination of EMPA and LA-ICP-MS data shows that chalcopyrite from Cerro Pabellón is silver-rich (Ag > 1000 ppm) and hosts a wide range of trace elements, most notably Se, Te, Zn, Sb, As, and Ni, which can reach 100 s of ppm. Other elements detected include Co, Pb, Cr, Ga, Ge, Sn, Cd, and Hg but are often present in low concentrations (<100 ppm), whereas Au, Bi, Tl, and In are generally below 1 ppm. Chalcopyrite shows a distinct geochemical signature with depth, with significantly higher Ag concentrations in the shallow sample (494 m) and increasing Cd and In contents towards the bottom of the studied drill core (549 m). These differences in the trace element contents of chalcopyrite are interpreted as related to temperature gradients during the waning stages of boiling at Cerro Pabellón, although further studies are still needed to assess the precise partitioning controls. Our data provide evidence that chalcopyrite may play a relevant role as a scavenger of certain metals and a monitor of fluid changes in hydrothermal systems. 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