Temperature Hydrothermal Fluids Research Articles

Evolution of skarn to quartz-vein mineralization: Insights from the Tongshanling Cu–Pb–Zn deposit, South China

The Tongshanling Cu–Pb–Zn deposit, situated within the Qin-Hang intra-continental porphyry-skarn metallogenic belt in South China, presents a valuable case study of intrusion-related ore systems. This deposit is characterized by skarn mineralization closely associated with subsequent quartz-vein sulfide mineralization. While considerable research has been devoted to understanding the origin and evolution of the intrusions and mineralization processes, limited attention has been given to elucidating the relationship between the skarn and quartz-vein mineralization, along with the physicochemical conditions governing their formation. Here, we conducted a comprehensive mineralogical and isotopic investigation of sulfides, and a thorough analysis of fluid inclusion assemblages. We aimed to discern disparities in the sources of ore-forming materials, formation temperature, sulfide fugacity, and precipitation-alteration mechanisms of hydrothermal fluids for these two distinct orebodies. Although same sulfide species including arsenopyrite, pyrite, chalcopyrite, and sphalerite, some silicate minerals such as garnet, chlorite, and epidote are exclusive to the skarn orebodies and absent in the quartz veins.The homogeneous temperatures of fluid inclusions in the skarn orebody, ranging from the early to late stages of evolution, decrease from ∼310 to ∼290 °C. Simultaneously, salinity varies from 5.5 to 3.1 wt% NaCl eqv. In the quartz vein mineral body, the temperature reduction is more pronounced, decreasing from ∼270 to 186 °C, with salinity ranging from 3.6 to 1.4 wt% NaCl eqv. Sphalerite geothermometer indicates that peak hydrothermal fluid temperature in the skarn orebodies (∼300–340 °C) was relatively higher than that in the quartz-vein orebodies (<300 °C). Nevertheless, temperatures in both hydrothermal fluid systems declined as mineral precipitation proceeded, corresponding to a decrease in sulfur fugacity. The final stage of sphalerite represents the lowest temperature, salinity and sulfur fugacity with associated quartz displaying the lowest salinity across the entire hydrothermal fluid spectrum at the Tongshanling deposit, suggestive of meteoric water incorporation. This study delves into the multifaceted history of mineralization at the Tongshanling deposit, providing a fresh perspective on the origin and evolutionary relationships of Cu-polymetallic deposits associated with intrusions, particularly those involving multiple stages of mineralization in skarns and quartz veins, contributing to a better understanding of similar deposits worldwide.

Unveiling the inherent physical-chemical dynamics: Direct measurements of hydrothermal fluid flow, heat, and nutrient outflow at the Tagoro submarine volcano (Canary Islands, Spain)

Tagoro is one of the few submarine volcanoes in the world that has been monitored since its early eruptive stage in 2011 to present day. After six multidisciplinary oceanographic cruises conducted between 2014 and 2023 to gather a comprehensive dataset of georeferenced video-imagery and in situ measurements of hydrothermal flow velocities and hydrothermal fluid samples, we provide a robust characterization of the ongoing hydrothermal fluid velocity, heat flux, and nutrient release, along with an accurate delimitation of the hydrothermal field area. Our results reveal that Tagoro hydrothermal system extends from the main hydrothermal crater up to the summit, covering an area of 7600 m2. This hydrothermal field comprises thousands of small individual vents, displaying diverse morphologies such as crevices and delicate chimney-like structures, irregularly scattered across the dominant diffuse venting surface. Hydrothermal fluid temperatures and velocities at the substratum level reveal a clustered spatial distribution, ranging from 21.0 to 33.3 °C and 1.6–26.8 cm min−1, respectively. Furthermore, our findings indicate a discernible correlation between hydrothermal fluid temperature and vent density, while significant differences were observed between velocities from diffuse and focused areas. Additionally, heat fluxes exceed 200 MW across the entire active region, with heat flux values ranging from 6.06 to 146.87 kW m−2 and dissolve inorganic nutrient concentrations exhibit significant enrichments, comparable to the magnitude of important nutrient sources in the area as upwelling systems or mesoscale structures.

Fluid Flow, Mineralization and Deformation in an Oceanic Detachment Fault: Microtextural, Geochemical and Isotopic Evidence From Pyrite at 13°30′N on the Mid‐Atlantic Ridge

AbstractHydrothermal fluids in ultramafic‐hosted hydrothermal systems associated with oceanic detachment faults can be more oxidizing compared to mafic‐hosted vent sites. These fluids form a mineral assemblage of pyrite, magnetite and hematite. At 13°30′N on the Mid‐Atlantic Ridge, chlorite‐quartz breccias recovered from an exposed fault scarp contain pyrite, with abundant magnetite and hematite, indicating that the redox of the fluids was variable. In primary micron‐scale zonations in pyrite, Ni, Co, and Se have a decoupled relationship, recording fluctuations in the chemical composition and temperature of hydrothermal fluid as the grains grew. Secondary zonations that erase and overprint primary zonations are limited to the grain margin and permeable regions within the grain core. Secondary zonations formed via two processes: (a) grain dissolution followed by overgrowth, and (b) remobilization of metals during oxidizing fluid flow events. In both instances, Ni and Co have been mobilized and concentrated, and are not lost to the hydrothermal fluid. Superimposed on these features is evidence of grain scale deformation related to periods of fault movement along the detachment surface. Sulfur isotope ratios (δ34S) in pyrite systematically decrease from the grain margin to the grain core, indicating that increased amounts of sulfur were derived from thermochemical sulfate reduction of seawater. Thus, pyrite records the evolution of fluid flow and deformation events during exhumation along the detachment surface from ∼1 to 2 km below the seafloor at the base of the lava pile, with temporal fluctuations in fluid redox identified as an important process in controlling Ni and Co enrichment in pyrite.

Intermittent hydrothermal alteration and silicification of black mudstones found in the Middle to Upper Miocene Yagen Formation, Shimokita Peninsula, Northeast Japan

AbstractOrganic geochemical processes in hydrothermal alteration system in terrestrial areas were investigated in the Shimofuro geothermal field, Northeast Japan. This study describes a continuous long mudstone outcrop of the Middle to Late Miocene Yagen Formation on the Shimokita Peninsula, Aomori Prefecture. The outcrop located near Mt.Hiuchi‐dake shows sequential alteration with a color change from black to white. Contents of total organic carbon (TOC) vary from 0.00% to 0.46% according to litho‐color change and become higher for black and lower for gray to white. TOC contents show a negative correlation with SiO2 concentration. These indicate that TOC contents in the outcrop strongly depend on silicification caused by hydrothermal alteration. The mineral assemblages are composed of alunite, kaolinite, illite and pyrite, and indicate distinct alteration zones with acidic to neutral hydrothermal activities. Composition of the minerals formed by the alteration suggests that the temperature of hydrothermal fluid ranged from 150 to 250°C in a high‐sulfidation hydrothermal system. Regarding the extracted hydrocarbons, particularly n‐alkane distributions are significant. Values of Carbon Preference Index (CPI) increase up to 2.8 with increasing alteration and with decreasing TOC contents. This can be explained by two processes, (1) at the site of highly hydrothermal alteration, thermal cracking of organic matter in black mudstone strongly occurred and produced low‐molecular gaseous hydrocarbons, and (2) at the site of inner rock with a distance from the hydrothermal alteration, thermal cracking moderately occurred and produced medium to long chain n‐alkanes which were overlapped with original n‐alkanes. Very low Tmax values were found at the hydrothermal zone. This implies that natural extraction, migration, and precipitation of bituminous organic matter were driven by hydrothermal fluid.

Magnetite geochemistry and mineralogy of iron skarn in the southern Wag Water Belt, Jamaica: Implications for ore genesis

The Mavis Bank iron skarn mineralisation is located within a Paleocene to Eocene rift system typified by terrestrial and marine deposits, and extensive lava flows and subvolcanic intrusions of adakitic composition. Iron occurs primarily as massive, lenticular magnetite bodies at the contact between the intrusions and calcic Fe skarn (metasomatised limestone) which grades into a low-grade marble with disseminated magnetite. Magnetite is also disseminated in shales and lavas located within the main mineralised zones. Skarn mineralogy is poorly developed in both the endoskarn and the exoskarn with only minor occurrence of diopside. Retrograde and alteration minerals, such as epidote, chlorite, and hematite, are more common. Sulphides are rare, highly altered, and dominated by pyrite, pyrrhotite, and minor chalcopyrite. Petrographic analysis, including micro-XRF-EDS mapping of polished thin sections, shows that massive magnetite and calcic Fe skarns have minor disseminated Ti and S phases along with trace amounts of Cu and Co. Scanning electron microscope-backscattered electron (SEM-BSE) imaging of the exoskarn highlights the extent of retrograde alteration and later supergene weathering, and the presence of dissolution and reprecipitation features.The in situ trace element composition of magnetite in massive magnetite and calcic Fe skarn was determined using LA-ICP-MS. The results, when plotted on multi-element and discriminant diagrams, including Ni/(Cr + Mn) vs Ti + V, Ca + Al + Mn vs Ti + V, Ti vs V, and Ti vs Ni/Cr, are generally consistent with the geochemical signatures of skarn deposits worldwide. The mineralogy and trace element signatures suggest that the skarn deposit was formed at relatively shallow levels by low temperature hydrothermal fluids with high fO2 and fS. In addition, δ18O values of 6.6 and 7.1 ‰ obtained from massive magnetite are typical of infiltrative skarns and are consistent with a mixture of magmatic and meteoric water, and limestone oxygen isotope signatures.

Battery-free temperature logger for deep-sea hydrothermal fluids based on heat pipe heat exchangers and thermoelectric generators.

Long-term in situ measurements of the temperature of hydrothermal fluids have great significance in the research of seafloor hydrothermal activities. Herein, we developed a self-powered battery-free temperature logger for measuring and recording the temperature of hydrothermal fluids. A gravity heat pipe made of titanium alloy was employed as the heat-conducting element of the temperature logger to capture heat from a hydrothermal vent and transfer it to the thermoelectric unit. The thermoelectric generator used herein converted the temperature difference into electrical energy to power the circuit of the temperature logger. Numerical analyses and experiments were performed to investigate the performance of the heat pipe and temperature logger. Results show that the temperature logger can realize self-powered starting at a temperature of >76 °C during a tank test. This paper presents a discussion on a new instrument for temperature measurements of deep-sea hydrothermal fluids.

Organic matter accumulation and hydrothermal effect of the Barney Creek formation in the Glyde Sub-basin, northern Australia

The Glyde Sub-basin is a large petroliferous unit in the McArthur Basin, northern Australia, and it is situated ∼100 km southeast to the world-class McArthur River Zn–Pb hydrothermal deposit. The Paleoproterozoic Barney Creek Formation (BCF) is the hydrocarbon source rock in the sub-basin, and also the host rock for the McArthur River deposit. The controlling factors of organic matter accumulation and the hydrothermal effects on organic matter thermal maturity are not well-constrained for the BCF in the Glyde Sub-basin, hindering petroleum and mineral explorations. To address these issues, rock eval pyrolysis, reflectance measurement, trace element analysis, Nd–Hf and Re–Os isotopic analysis were conducted for the BCF samples taken from the drill-hole GRNT-79-5 in the Glyde Sub-basin. Analysis of trace elements and Nd–Hf isotopic ratios shows that cuttings of the BCF were derived from a mafic-dominant source (La/Ni = 0.89–2.27, La/Cr = 0.63–1.04, La/Sc = 3.16–4.95, La/V = 0.23–0.81, ϵNd = −5.01 to −2.98, ϵHf = −2.27 – 1.8), which may have contributed to a pronounced phosphorous delivery to the basin, resulting in enhanced primary productivity of seawater. Therefore, the high organic matter abundance in the BCF (TOC = 0.86%–5.04%) is most likely controlled by the primary productivity of seawater. The 187Re/188Os ratios (34.954–432.95) of a suite of samples negatively correlate with proportions of kerogen in organic matter (0%–94%), suggesting that burial temperature has reset the Re–Os isotope system. Hydrocarbon generation may have been promoted by hydrothermal fluid flows which relate to the McArthur River mineralization because the Re–Os isotope data yield an isochron age similar to the age of mineralization. The Re–Os isotope data provide direct evidence that the BCF in the Glyde Sub-basin was affected by hydrothermal fluids. However, the co-variation between thermal maturity indicators (Tmax = 436–444 °C; reflectance of solid bitumen = 0.34%–0.66%) and burial depth (97–512 m) suggests that organic matter thermal maturation primarily resulted from burial diagenesis rather than hydrothermal fluid flows. This indicates that temperatures of hydrothermal fluids was not high enough to significantly alter the thermal regime of the studied region.

Tourmalines in the Namacotche Li-Cs-Ta granitic pegmatite group, Mozambique: crystal chemistry and origin

The field work, backscattered electron images and detailed microanalyses of three generations of tourmaline from the Namacotche LCT pegmatites allows de distinction between the compositional magmatic and hydrothermal tourmalines. The generation 1 occurs in the outer intermediate zone of the pegmatite. It consists of zoned crystals with an oscillatory inner core of foitite and schorl, an outer core of schorl and an Fe-rich fluor-elbaite rim. Unzoned Fe-rich fluor-elbaite crystals occur in the inner intermediate zone of the pegmatite. All the crystals are derived by fractionation of a (Al, Li, B)-rich pegmatite melt. However, the rim of zoned crystals and some compositions of unzoned crystals show evidence of hydrothermal fluids, as they plot outside the fractionation trends. The zoned fluor-elbaite crystals of the generation 2 are from the inner intermediate zone of the pegmatite. They have a pink core and a green rim. The rim has higher YFe2+, Na, F contents YFe2+/(YFe2++Licalc.) value and lower Si, YAl, Licalc. and X-site vacancy contents, X-vacancy/(Na+X-vacancy) value than the core. Both zones are hydrothermal. The rim is an overgrowth. The fluor-elbaite gemmy crystals of the generation 3 occur in sheared breccia blasts and clasts with a cookeite matrix. They depend mainly on the fluid-rich hydrothermal environment of low temperatures (280-150ºC). Some from the cycle a may result from the dissolution of magmatic tourmaline crystals of the generation 1 from the sheared outer and inner intermediate zones of the pegmatite due to reaction with late fluids in chemical disequilibrium, followed by growth of tourmaline with low temperature hydrothermal fluids. The evolution from the cycle a to the cycle b and to the cycle c of the generation 3 implies that the hydrothermal reacting fluids were undergoing fractionation and becoming richer in Li and poorer in Fe2+ during the late hydrothermal crystallization of the pegmatites.

Equilibrium and kinetic controls on molecular hydrogen abundance and hydrogen isotope fractionation in hydrothermal fluids

Molecular hydrogen (H2) is among the main components in hydrothermal fluids and exerts a major role in geochemical and biological processes. Nevertheless, the understanding and quantification of factors controlling H2 abundance and isotope composition remain uncertain. Sub-aerial hydrothermal systems provide a unique opportunity to study sources and reactions of H2. Here, we present hydrogen fugacity (fH2) and δD values of H2 and H2O in hydrothermal fluids from such systems worldwide (Greece, Iceland, Kenya and New Zealand), representative of mid-ocean ridge and arc systems and sourced by seawater and meteoric water. The hydrothermal fluid temperatures are 226-359°C, and the fH2, δD-H2 and δD-H2O values are 0.002-3.3 bar, -646 to -391‰ and -94.1 to +11.3‰, respectively. Comparison of measured data with geochemical modeling reveals that H2 is predominantly sourced from the reduction of H2O, enabled through the oxidation of aqueous Fe+II to Fe+III and precipitation of Fe+III-bearing hydrothermal minerals (e.g., epidote). We argue that fH2 in hydrothermal fluids is controlled by metastable mineral-fluid and fluid-fluid equilibria upon progressive rock alteration and depend on temperature, rock-to-water ratio (r/w), source water composition and volcanic gas input. Consequently, fH2 in these systems is not fixed by a sole redox buffer. Our data demonstrate that δD-H2 values of reservoir fluids at depth are controlled by the δD value of the source water and the equilibrium isotope fractionation characteristic of the hydrothermal reservoir temperatures. Attainment of isotopic equilibrium at reservoir conditions is supported by fast isotopic equilibration times at T > 200°C, on the order of minutes to few hours, relative to hydrothermal fluid residence times within the reservoirs of years to decades or even longer. During its ascent to the surface, the isotopic composition of H2 can be modified due to isotopic re-equilibration with H2O. The extent of re-equilibration depends on the interplay between fluid flow velocity, cooling rate and kinetics of D-H exchange between H2 and H2O. For fast flowing well discharges (∼0.1 to >10 m/s), negligible changes occur, whereas for slowly flowing (<0.06 m/s) fumaroles, complete re-equilibration at surface temperatures (∼100°C) is sometimes observed. Based on the extent of hydrogen isotope disequilibrium relative to reservoir conditions, fluid reservoir-to-surface travel times are estimated to range from few minutes to <3 hrs for well fluids and few hours to days for fumarolic vapor.

Alteration of high alkaline and alkaline basaltic rocks: parent rocks in the Lava Durian orchard, Sisaket Province, NE Thailand

Lava Durian Sisaket is the first geographically identified (GI) fruit related to the volcano in Thailand and distributed in three districts of Sisaket Province, the southernmost edge of the Khorat Plateau. The parent rocks of orchards are important for the description of soil and rock relation with respect to mineralogical and geochemical characteristics. This work aims to study lithology, mineralogy, and geochemistry of basaltic rocks, parent rocks of in situ soil in these orchards, and delineate the existing basaltic soil models. The several orchards are covered by reddish-brown to brown in situ soils, weathered from mafic volcanic rocks: porphyritic olivine basalt, vesicular olivine basalt, and nephelinite. The microscopic image analysis, XRD, and MiniSEM-EDS are used to classify mineralogy, while XRF and analysis of large and rare elements in ICP-MS/ICP-OES were used to determine parental rocks geochemistry and alteration. The olivine basalts comprise forsterite microphenocrysts associated with bytownite, diopside, augite, pigeonite, and ilmenite groundmass, while nephelinite is composed of nepheline groundmass and bytownite-labradorite, diopside, augite, pigeonite, and ilmenite crystals. In addition, these basalts display high alteration rates, especially olivine highly altered to iddingsite. According to the geochemical data, Sisaket's basalts were identified as alkali basalt and nepheline basanite with high LILEs and LREEs (La, Nd, Pr, Gd, Eu). The kaolinite, smectite, and illite are altered from felsic minerals, while the chlorite and iddingsite are from mafic minerals. The mineralogical analyses classified secondary phyllosilicates related to low-moderate temperature hydrothermal fluid, very high cation exchange capacity (H+, K+, Ca2+, Mg2+), and tropical weathering. The alkaline and high alkaline basalts, presenting as parent rocks, are one of the parameters that produced good nitisal soil of Sisaket's agricultural areas.

Chlorite mineralogy, geochemistry and exploration implications: A case study of the Xiaokelehe porphyry Cu-Mo deposit in NE China

The recently discovered Xiaokelehe porphyry Cu-Mo deposit (PCD) is situated in the northern part of the Great Xing’an Range in NE China. At Xiaokelehe, chlorite-illite alteration is characterized by chlorite, illite, disseminated chalcopyrite and pyrite assemblages that are widely developed in the granodiorite porphyry. The illite is altered from plagioclase or K-feldspar, and the chlorite from both igneous and hydrothermal biotite. The chlorite can be divided into three types (Chl1, Chl2 and Chl3): Chl1 is locally developed in the deeper part of the granodiorite porphyry, and is altered from hydrothermal biotite; Chl2 is pervasively distributed in the deeper part of the granodiorite porphyry, and is altered from igneous biotite and associated with abundant disseminated Cu-Fe-sulfide mineralization; Chl3 is widely developed in the shallower part of the granodiorite porphyry, and is altered from igneous biotite. Chl3 is overprinted by phyllic alteration and associated with minor disseminated Cu-Fe-sulfide mineralization. These Xiaokelehe chlorites resemble the chlorites from typical sericite-chlorite-calcic alteration (SCC) in PCDs, and are the first reported SCC-related chlorites in the Great Xing’an Range.Mineral geochemical results show that Chl1 has relatively high FeO, Mn, Ti, Li and Zn contents. Chl2 has relatively high FeO, Mn, Co, Ni, Zn and Sr contents, and Chl3 has relatively high MgO, K and Ni contents. These geochemical differences are likely controlled by temperature (e.g., for Ti), precursor minerals (e.g., for FeO and MgO) and fluid compositions (e.g., for FeO, MgO, Mn, Co and Zn). All Chl1 to Chl3 are classified as trioctahedral chlorite. The Fe-Mg, Tschermark and di-trioctahedral substitution mechanisms may have controlled the chemical differences of the Xiaokelehe chlorites. Empirical thermometer yielded chlorite formation temperatures of 209–314 °C, indicating that the Xiaokelehe chlorites were formed from intermediate-high temperature hydrothermal fluids. Compared with the chlorites from propylitic zones in other PCDs, the Xiaokelehe chlorites have higher FeO, Ti, V, Zn and Ga contents and Fe/(Fe + Mg) ratio, as well as lower MgO, K, Co and Sr contents, which distinguish chlorites in the SCC zone from those in the propylitic zone. Such differences may have also been influenced by temperature, and the protolith and fluid compositions. Compared with typical metamorphic chlorites, the Xiaokelehe chlorites have lower FeO content but higher MgO and Zn contents, of which the Zn difference is likely influenced by the fluid chemistry. We propose that the presence of Chl3 can be used as an effective vector toward mineralized zone. In addition, chlorite Mn and Zn contents in the mineralized zone are clearly higher than those away from it, and thus the chlorite Mn and Zn contents can also be potential exploration vectors at Xiaokelehe.

Depositional Environment and Genesis of the Nabeba Banded Iron Formation (BIF) in the Ivindo Basement Complex, Republic of the Congo: Perspective from Whole-Rock and Magnetite Geochemistry

The Nabeba high-grade iron deposit (Republic of the Congo) is hosted by banded iron formation (BIF) in the Ivindo Basement Complex, which lies in the northwestern part of the Congo Craton. The Nabeba BIF is intercalated with chlorite-sericite-quartz schist and comprises two facies (oxide and a carbonate-oxide). In this study, whole-rock and LA-ICP-MS magnetite geochemistry of the BIF was reported. Magnetite samples from both BIF facies had fairly similar trace element compositions except for the rare earth element plus yttrium (REE + Y) distribution patterns. The high V, Ni, Cr, and Mg contents of the magnetite in the Nabeba BIF could be ascribed to the involvement of external medium-high temperature hydrothermal fluids during their deposition in relatively reduced environment. The Post-Archean Australian Shale (PAAS)-normalized REY patterns of the Nabeba BIF magnetite were characterized by LREE depletion coupled with varying La and positive Eu anomalies. Processing of the information gathered from the geochemical signatures of magnetite and the whole-rock BIF suggested that the Nabeba BIF was formed by the mixing of predominantly anoxic seawater (99.9%) with 0.1% of high-temperature (&gt;250 °C) hydrothermal vent fluids, similar to the formation mechanism of many Archean Algoma-type BIFs reported elsewhere in the world.

Constrains of eruption environment and hydrothermal fluid on the Permian pyroclastic reservoirs in the Sichuan Basin, SW China

A breakthrough has been recently made in the hydrocarbon exploration of the Permian pyroclastic rocks in the Jianyang Area, western Sichuan Basin, China. With an aim to decipher the impacts of the eruption environment, the temperature of hydrothermal fluids, and the paleo-salinity on the formation of authigenic mineral assemblage and pores, this study implements comprehensive petrographic and geochemical studies through the integrated core and thin section analyses. The data presented demonstrate that the Permian volcanic intervals are intensively affected by an event of Emei taphrogeny. During basaltic magma upward migration, fractional crystallization of anorthose results in slightly-alkaline magma. The specific pyroclastic rocks are formed by the eruption of slightly-alkaline magma in the sea or a salt lake and subsequent hydrothermal alteration. During deposition and diagenesis, the authigenic mineral association is constrained jointly by the sodium-rich and high salinity water environment, and mid-high temperature, high-salinity hydrothermal fluid. Specifically, the sodium-rich hydrothermal fluid, which may sustain till the late diagenesis stage, caused pervasive albitization of pyroclastic rocks, then leading to mineral transformation and formation of a series of mineral associations. Therefore, zeolitization of volcanic glass and vesicle-infillings of zeolite is an essential condition for later mineral transformation and dissolution. Albitization of analcite, recrystallization induced by deep hydrothermal fluids, and both meteoric and deep burial dissolution expanding the micro-pore space ultimately formed porous pyroclastic reservoirs.

Laser ablation ICP–MS trace element composition of native gold from the Abitibi greenstone belt, Timmins, Ontario

Trace elements in native gold provide a “fingerprint” that tends to be unique to individual gold deposits. Fingerprinting can distinguish gold sources and potentially yield insights into geochemical processes operating during gold deposit formation. Native gold grains come from three historical gold ore deposits: Hollinger, McIntyre (quartz-veined ore), and Aunor near Timmins, Ontario, at the western end of the Porcupine gold camp and the southwestern part of the Abitibi greenstone belt. Laser ablation – inductively coupled plasma – mass spectrometry (LA–ICP–MS) trace element concentrations were determined on 20–25 µm wide, 300 µm long rastor trails in ∼60 native gold grains. Analyses used Ag as an internal standard with Ag and Au determined by a scanning electron microscope with an energy dispersive spectrometer. The London Bullion Market AuRM2 reference material served as the external standard for 21 trace element analytes (Al, As, Bi, Ca, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Pd, Pt, Rh, Sb, Se, Si, Sn, Te, Ti, Zn; Se generally below detection in samples). Trace elements in native gold associate according to Goldschmidt’s classification of elements strongly suggesting that element behaviour in native Au is not random. Such element behaviour suggests that samples from each Timmins deposit formed under similar but slightly variable geochemical conditions. Chalcophile and siderophile elements provide the most compelling fingerprints of the three ore deposits and appear to be mostly in solid solution in Au. Lithophile elements are not very useful for distinguishing these deposits and element concentrations may be controlled by microinclusions such as tourmaline. The deposits show low Ag contents, which is consistent with mesothermal Au. Hollinger and McIntyre deposits have similar trace element abundances with higher Ag, Pb, Bi, Sb, and Pd and generally low Cu; however, Cu concentrations in McIntyre are higher than in Hollinger. In contrast, Aunor shows comparatively low Ag, Bi, Sb, Pb, and Pd and higher Au/Ag consistent with higher hydrothermal fluid temperatures. Gold grain signatures reflect the chemical characteristics of the host rock superimposed on a chemical signature inherited from the mineralizing fluid. The association of Pb–Bi–Cu bearing phases such as galena and chalcopyrite with gold apparently enriched in these elements supports precipitation from hydrothermal fluids carrying the elements.

The relationship of volcanic facies and temperature range derived from the associated clay mineral in Gunung Endut, Banten

Gunung Endut located in Lebak, Banten is one of the prospected areas of geothermal energy resource on the island of Java, Indonesia. The presence of clay mineral in the surface can help to determine the hydrothermal fluid temperature circulating in Gunung Endut. Based on the collected samples, petrography analysis revealed the presence of clay minerals while diffraction method confirmed the presence of dickite, montmorillonite, kaolinite, pyrophyllite, chlorite, diaspore and illite. There are three different temperature range from each volcanic facies. It is predicted that clay minerals at their temperature range in Gunung Endut are formed based on the type of rocks and the topography of the research area.

Distribution of trace elements in sulfides from Deyin hydrothermal field, Mid-Atlantic Ridge – Implications for its mineralizing processes

Knowledge about the trace element distribution in sulfides is the key for understanding the trace metal inventory during the formation of the volcanic massive sulfide deposits on the seafloor. The distribution of trace metals in sulfides reflects changes in the physicochemical conditions and precipitation processes during precipitation. Hydrothermal black smoker samples of this study originate from the southern Mid-Atlantic (TVG02, TVG06) and can be classified into two types: (1) (Fe-Zn) sulfides consisting predominantly of pyrite and sphalerite, with minor chalcopyrite, isocubanite, and galena and (2) (Fe-Cu) sulfides, which contain mainly pyrite and chalcopyrite, with rare isocubanite and sphalerite. The sulfide samples were analyzed by electron microprobe for major elements, and by laser ablation inductively coupled plasma mass spectrometry, focused ion beam technique and transmission electron microscopy for in situ trace elements. The data reveal complex hydrothermal processes in high- and low- temperature fluids. Colloform and dendritic pyrite from (Fe-Zn) sulfides are enriched in Mn, Tl, As, V, Pb, and Zn, indicating precipitating from a rapid mixture of low temperature fluids (100–250 °C) with seawater. A continuous enrichment of incompatible elements (Pb and Zn) at the interface of growing pyrite with fluid finally leads to the nucleation and precipitation of sphalerite and galena, and results in the enrichment of As, Hg, Pb, Au, Ag, and Cd in sphalerite micro-inclusions which are hosted in colloform pyrite at low temperature. Galena inclusions occur in the pores and the interstices of sphalerite grains and formed by the enrichment of Pb in the hydrothermal fluid at low-temperature (<250 °C). High Cu, As, Ag, Au, and Sb concentrations in colloform sphalerite indicate a medium to low formation temperature (350–200 °C). Copper, Sb, Se, and Sn enrichments in coarse-grained sphalerite indicate medium temperature hydrothermal fluids. Idiomorphic pyrite and chalcopyrite have high Se and Co contents and indicate precipitaion from high-temperature (>300 °C) fluids.

Experimental partitioning of osmium between pyrite and fluid: Constraints on the mid-ocean ridge hydrothermal flux of osmium to seawater

This study presents experimental, geochemical modeling, and field data focusing on the partitioning of osmium (Os) between pyrite and fluid upon precipitation at conditions representative of mid-ocean ridge hydrothermal environments. Dissolved Os partitions strongly into pyrite upon precipitation at experimental conditions, 350 °C and 50 MPa, with a representative relative Os/Fe partition coefficient, DPyrite-FluidOs/Fe, between 10 and 15. Integrating the experimentally determined DPyrite-FluidOs/Fe into a geochemical model indicates that a significant amount of Os is retained within the subseafloor due to sulfide precipitation induced by mixing of conductively heated seawater with pristine high temperature hydrothermal fluids that are enriched in dissolved metals, such as Os and Fe. Comparison with existing Os concentration and isotopic data of hydrothermal fluids and sulfide minerals from a wide range of hydrothermal systems with the experimental and modeling constraints suggest that modern high temperature hydrothermal systems are a minor source of unradiogenic Os to the modern global ocean dissolved Os budget due to the majority of Os being sequestered into sulfide minerals formed within and on the seafloor.

Emplacement of sharp-walled sulfide veins during the formation and reactivation of impact-related structures at the Broken Hammer Mine, Sudbury, Ontario

Broken Hammer is a hybrid Cu–Ni–Platinum Group Element (PGE) footwall deposit located in Archean basement rocks below the impact-induced Sudbury Igneous Complex (SIC), Canada. The deposit consists of massive chalcopyrite veins surrounded by thin epidote, actinolite, and quartz selvedges and low-sulfide, high-PGE mineralization consisting of disseminated chalcopyrite (&lt;5%) and platinum group minerals, associated with Ni-bearing chlorite overprinting alteration patches of epidote, actinolite, and quartz. The veins are grouped into five steeply-dipping sets, striking northeast-, southwest-, southeast-, south-, and east–west, which were emplaced along impact-related fractures that were reactivated multiple times during stabilization of the crater floor. Early reactivation of the fractures created pathways for the migration of hydrothermal fluids from which quartz and chlorite precipitated sealing the fractures. Renewed slip shattered the quartz–chlorite veins into fragments that were incorporated in massive sulfide veins that crystallized from fractionated sulfide melts or from high temperature (400–500 °C) hydrothermal fluids, which migrated outward into the basement rocks from a cooling and crystallizing SIC melt sheet. Hydrothermal fluids syn-genetic with the epidote–actinolite–quartz alteration distributed the PGE into the footwall rocks, or late hydrothermal fluids associated with the Ni-bearing chlorite leached Ni and PGMs from the sulfide veins and redistributed them to form low-sulfide, high-PGE zones in the footwall rocks. During post-impact tectonic events, slip at temperatures below the brittle–ductile transition for chalcopyrite (&lt;200 °C to 250 °C) produced striations along the vein margins. The Broken Hammer deposit exemplifies how Cu–Ni–PGE footwall deposits formed by the reactivation of impact-related fractures that provided conduits for the migration of melts and hydrothermal fluids.

Hydrothermal Vapor‐Phase Fluids on the Seafloor: Evidence From In Situ Observations

AbstractSubseafloor phase separation is a common and significant process in hydrothermal systems and may result in a large of fluid composition differences. The temperatures of hydrothermal fluids are generally considered to be below the associated fluid boiling temperature due to mixing with ambient seawater and the phase separation process. However, we report here shimmering water with temperatures up to 383.3 °C observed in a hot overturned lake at the Yokosuka site, Okinawa Trough, East China Sea, where in situ Raman spectra suggest the presence of a superheated vapor phase. Hydrothermal vents similar to the low‐density hydrothermal system found at the Yokosuka site have also been observed in many other regions. Therefore, much more attention should be given to the impacts of low‐density hydrothermal fluid emanations on marine environments and resource distributions.

Multiple sulfur sources for the volcanic hosted massive sulfides in Betul Belt, Central India: Evidence from the sulfide ore chemistry and sulfur isotope geochemistry

This work provides an overview of the geological, petrological, and geochemical data available on the three volcanic-hosted massive sulfides (VHMS) deposits (Ghisi, Biskhan, and Jangaldehri) in Betul Belt, Central Indian Tectonic Zone. Sulfur isotope geochemistry was used for the first time from the Betul Belt to constrain the source of sulfur for a better understanding of the ore genesis process. Mineralization is hosted in a felsic dominant bimodal volcano-sedimentary sequence associated with syn-genetic hydrothermal alteration, i.e., intense Mg–Ca alteration (actinolite-tremolite-anthophyllite) and Al–Fe alteration zone (gahnite-garnet-biotite-staurolite) followed by regional metamorphism. Field observations, drill core logging, and petrography studies reveal different modes of mineralization, i.e., dissemination, stringers, and semi-massive sulfides vein, comprises of chalcopyrite, sphalerite, pyrite, galena with lesser pyrrhotite, are paragenetically distinct in three deposits. The petrography, SEM-EPMA studies show the presence of chalcopyrite disease in Fe-rich sphalerite at Biskhan and Jangaldehri in the east and absence of the same texture at Ghisi in the west. This difference reveals the variable physio-chemical nature of the hydrothermal fluid and partial melting of sulfides during subsequent metamorphism.Cu–Fe mineralization was deposited from high-temperature hydrothermal fluids with less sulfur activity at Biskhan-Jangaldehri. Later Zn–Cu–Pb mineralization was formed from lower temperature hydrothermal fluids with higher sulfur activity. The δ34S values of sulfides (sphalerite, chalcopyrite, and pyrite) from three deposits show a wide range of sulfur values (δ34S) from −12.87 to + 19.31‰ (n = 27), consistent with heterogeneous sourcing of S, probably combining magmatic source along with the reduction of seawater sulfate. Variation in the sulfur isotopic compositions of sulfide was the result of dilution and cooling of the metalliferous fluid at different stages after interaction with meteoric, seawater and hydrothermal fluids, which caused the deposition of base metal sulfides.Sulfides from Ghisi in the west display both +ve and −ve values (−12.88 to + 0.38‰; n = 10), suggest sulfur predominantly derived by thermochemical reduction of seawater sulfate with minor input of magmatic sulfur reduction lead to polymetallic Zn–Cu–Pb mineralization. The gradual increasing in the δ34S values (more + ve values +18.65 to +19.31‰; n = 8) from west to east at Biskhan and Jangaldehri (+ 5.01 to + 8.3‰, n = 9) may be due to involvement of both the leaching of igneous basement rocks and chemical process of seawater sulfates by thermochemical reduction (TSR) from deep water levels lead to Zn–Cu mineralization. This δ34S variation occurs in three deposits of the Betul Belt due to modifications of the primary mineralization during subsequent stages of ore formation and metamorphism, indicating a complex fluid evolution history for VHMS deposits in Betul Belt, Central India, where S derived from a heterogeneous source by multiple geological processes. This situation is more akin to many established VHMS deposits of ancient and modern submarine hydrothermal systems.