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Hydrothermal alteration of olivine greatly influences geodynamics and the recycling of volatiles (such as water and carbon) in subduction zones. Silica is an important component of geological fluids, and its influence on the hydrothermal alteration of olivine remains poorly constrained. In this study, we performed experiments at 300–515°C and 3.0 kbar (1 bar=10 5 Pa) by reacting well homogenized mixtures of olivine and silica powders with saline solutions (0.5 mol L −1 NaCl). Silica greatly influences the reaction pathways, reaction rates, and molecular hydrogen (H 2 ) formation during olivine hydrothermal alteration. In experiments at 300°C and 3.0 kbar with mixtures of olivine and 10 wt% silica, olivine was replaced by serpentine and talc. The proportions of serpentine and talc were determined according to standard curves based on infrared spectroscopy analyses. Around 6.5% serpentine and 12% talc were produced after an experimental duration of 7 days, which had no change after a longer period (14 days). Compared to the kinetics in silica-free systems, the rates of olivine hydrothermal alteration in experiments with 10 wt% silica are much lower. The overall reaction is: 4.5Forsterite+5.5SiO 2,aq +4H 2 O=Serpentine+2Talc. With the addition of more silica (20 wt% and 40 wt%), olivine was transformed into talc. The rates of reaction were much faster, e.g., for experiments with olivine and 20 wt% silica, 43% of talc was produced after 14 days, which increased to 77% for experiments with 40 wt% silica over the same period. The overall reaction is: 3Forsterite+5SiO 2,aq +2H 2 O=2Talc. In experiments at 400–505°C and 3.0 kbar, the promoting effect of silica on olivine hydrothermal alteration was also observed, which is closely associated with a decrease in Gibbs free energies of olivine hydrothermal alteration. At 300°C and 3.0 kbar, silica decreased H 2 formed during olivine hydrothermal alteration by around an order of magnitude, resulting in an increase in oxygen fugacity. Based on measured H 2 , we calibrated oxygen fugacities, ranging from 0.96 to 3.41 log units below FMQ (fayalite-magnetite-quartz buffer assemblage). This study suggests that the infiltration of SiO 2 -bearing fluids into peridotites greatly influences redox conditions and the rates of olivine hydrothermal alteration.

We provide new constraints for the fluid flow system at the origin of two F-Ba deposits located at the unconformity between the south of the Paris Basin and the northern edge of the French Massif Central. We used microthermometry and bulk crush-leach analyses to determine isotope ratios of mineralizing fluids (δ18O, δD, δ37Cl), together with cation and anion composition of fluid inclusions hosted by fluorite. Chlorinity and Cl/Br molar ratios (212–521) indicate the involvement of a brine, whose origin likely corresponds to Triassic evaporated seawater compatible with supratidal dolomitic facies preserved nearby. Microthermometry reveals high Ca/Na ratios, suggesting that the brine composition evolved from hydrothermal alteration of the Variscan basement and partial dissolution and replacement of the host sedimentary rocks. δ37Cl values are lower than the expected value of evaporated seawater, suggesting Cl isotope fractionation by ion filtration in clay-rich horizons. Fluorite crystallized at minimum temperatures of 70 to 110 °C, 10–40 °C warmer than the host Triassic sedimentary rocks. Ascending brines were expelled during the Early Cretaceous and experienced a drop in pressure and temperature, together with possible mixing with the SO4-rich pore water of the sedimentary rocks, causing precipitation of silica, followed by fluorite and barite, forming a stratabound deposit similar to those found in many areas in Western Europe.

Kaolin-group minerals occur in nature as the result of high-sulfidation acid sulfate, sulfur-poor HCl-, HF- and H2CO3-rich acidic fluid-related hydrothermal alterations and in situ geochemical weathering. These minerals possess different crystallographic and chemical properties that determine their application areas, mainly in the ceramic and paper industries, and as nanocomposite materials. The physicochemical properties of hydrothermal kaolin deposits are the result of the type of parent rock, the effect of the regional tectonism-associated magmatism, and the chemical features of hydrothermal fluids that interact with the deep basement rocks. However, understanding these geothermal systems is one of the most challenging issues due to the rich mineralogical assemblages, complex geochemistry and isotopic data of hydrothermal alteration zones. This study evaluates the formation of hydrothermal-origin kaolin-group minerals by considering their characteristics of hydrothermal alteration, isotopic compositions and differences in characteristic properties of low- and high-sulfidation occurrences; this paper also addresses mineralogical and structural differences between hypogene and supergene kaolin formations, and kaolin–alunite–pyrophyllite association, and it provides examples of worldwide occurrences. The study of the mineralogical assemblages, geochemistry and isotopic data of the hydrothermal alteration zones is one of the most challenging subjects in terms of gaining a detailed understanding of the geothermal systems. Silicification processes are subsequent to late-stage alteration after the completion of kaolinization processes, erasing existing hydrothermal mineralogical and geochemical traces and making interpretation difficult. In the early stages involving magmatic–hydrothermal-origin acidic geothermal fluids, the latter comes from the disproportionation of SO2 (+H2O) and H2S oxidation to H2SO4 in hydrothermal environments. In the later stages, due to spatial and temporal changes over time in the chemistry of geothermal fluids, the system comes to have a more alkali–chloride composition, with neutral pH waters frequently saturated with amorphous silica which characteristically precipitate as siliceous sinter deposits containing large amounts of opal-A.

The Koldar Massif in southeastern Kazakhstan is a geologically complex area with potential for porphyry copper and rare-metal mineralization. This study applies a multi-scale remote sensing approach to delineate hydrothermal alteration zones using medium-resolution ASTER imagery and very high-resolution WorldView-3 data. Image processing techniques—including false color composites (FCCs), band ratios (BRs), and the Spectral Angle Mapper (SAM)—were employed across the VNIR and SWIR bands to detect alteration minerals such as kaolinite, illite, montmorillonite, chlorite, epidote, calcite, quartz, and muscovite. These minerals correspond to argillic, propylitic, and phyllic alteration zones. While ASTER supported regional-scale mapping, WorldView-3 enabled detailed analysis at the Aidarly deposit. Validation was performed using copper occurrences, lithogeochemical anomaly contours, and ore body boundaries. The results show a strong spatial correlation between the mapped alteration zones and known mineralization patterns. Importantly, this study reports the identification of a previously undocumented hydrothermal zone north of the Aidarly deposit, detected using WorldView-3 data. This zone exhibits concentric phyllic and argillic alterations, similar to those at Aidarly, and may represent an extension of the mineralized system. Unlike earlier studies on the Aktogay deposit based on ASTER and Landsat-8, this work focuses on the Aidarly deposit and introduces higher-resolution analysis and SAM-based classification, offering improved spatial accuracy and target delineation. The proposed methodology provides a reproducible and scalable workflow for early-stage mineral exploration in underexplored regions, especially where field access is limited. These results highlight the value of high-resolution remote sensing in detecting concealed porphyry copper systems in structurally complex terrains.

The Igla Ahmr region in the Central Eastern Desert (CED) of Egypt comprises mainly syenogranites and alkali feldspar granites, with a few tonalite xenoliths. The mineral potential maps were presented in order to convert the concentrations of total rare earth elements (REEs) and associated elements such as Zr, Nb, Ga, Y, Sc, Ta, Mo, U, and Th into mappable exploration criteria based on the line density, five alteration indices, random forest (RF) machine learning, and the weighted sum model (WSM). According to petrography and geochemical analysis, random forest (RF) gives the best result and represents new locations for rare metal mineralization compared with the WSM. The studied tonalites resemble I-type granites and were crystallized from mantle-derived magmas that were contaminated by crustal materials via assimilation, while the alkali feldspar granites and syenogranites are peraluminous A-type granites. The tonalites are the old phase and are considered a transitional stage from I-type to A-type, whereas the A-type granites have evolved from the I-type ones. Their calculated zircon saturation temperature TZr ranges from 717 °C to 820 °C at pressure < 4 kbar and depth < 14 km in relatively oxidized conditions. The A-type granites have high SiO2 (71.46–77.22 wt.%), high total alkali (up to 9 wt.%), Zr (up to 482 ppm), FeOt/(FeOt + MgO) ratios > 0.86, A/CNK ratios > 1, Al2O3 + CaO < 15 wt.%, and high ΣREEs (230 ppm), but low CaO and MgO and negative Eu anomalies (Eu/Eu* = 0.24–0.43). These chemical features resemble those of post-collisional rare metal A-type granites in the Arabian-Nubian Shield (ANS). The parent magma of these A-type granites was possibly derived from the partial melting of the I-type tonalitic protolith during lithospheric delamination, followed by severe fractional crystallization in the upper crust in the post-collisional setting. Their rare metal-bearing minerals, including zircon, apatite, titanite, and rutile, are of magmatic origin, while allanite, xenotime, parisite, and betafite are hydrothermal in origin. The rare metal mineralization in the Igla Ahmr granites is possibly attributed to: (1) essential components of both parental peraluminous melts and magmatic-emanated fluids that have caused metasomatism, leading to rare metal enrichment in the Igla Ahmr granites during the interaction between rocks and fluids, and (2) structural control of rare metals by the major NW–SE structures (Najd trend) and conjugate N–S and NE–SW faults, which all are channels for hydrothermal fluids that in turn have led to hydrothermal alteration. This explains why rare metal mineralization in granites is affected by hydrothermal alteration, including silicification, phyllic alteration, sericitization, kaolinitization, and chloritization.

Systematic exploration has delineated significant gold mineralization in the River Reef Zone and the presence of a siliceous body at Watuputih Hill, which is a Poboya gold prospect in Central Sulawesi, Indonesia. The mineralization is hosted within the Palu Metamorphic Complex. The host rocks consist of granite, biotite gneiss, and biotite schist, which is intercalated by feldspar porphyroblastic biotite schist and amphibolitic schist. The X-ray fluorescence (XRF) analysis of the granite and biotite gneiss suggests that the granitic rocks can be characterized as magnesian arc calc-alkaline rocks, with a weakly peraluminous composition. Alteration minerals were analyzed by a combination of petrographic and X-ray diffraction (XRD). In the River Reef Zone, the hydrothermal alteration zones can be sorted by their proximity to the primary fluid conduit and divided into inner, high-T, and low-T propylitic zones. In Watuputih Hill, the hydrothermal alteration can be divided into advanced argillic and argillic zones. The hydrothermal alteration assemblages indicated that the fluid was at a near-neutral pH in the River Reef Zone, whereas the fluid was acidic within Watuputih Hill. Because the hill is relatively distant from the River Reef Zone, the presence of these zones at Watuputih Hill may be indicative of another mineralization system beneath the hill.

Detailed mineralogical analyses in areas with surface hydrothermal alteration zones associated with recent volcanism (<1 Ma) in the Central Andean Volcanic Zone could provide key information to unravel the presence of hidden geothermal systems. In the Cordón de Inacaliri Volcanic Complex, a geothermal field with an estimated potential of ~1.08 MWe·km−2 has been recently discovered. In this work, we focus on the hydrothermal alteration zones and discharge products of this area, with the aim to reconstruct the geological processes responsible for the space-time evolution leading to the geothermal records. We identified (1) discharge products associated with acid fluids that could be related to: (i) acid-sulfate alteration with alunite + kaolinite + opal CT + anatase, indicating the presence of a steam-heated blanket with massive fine-grained silica (opal-CT), likely accumulated in mud pots where the intersection of the paleowater table with the surface occurred; (ii) argillic alteration with kaolinite + hematite + halloysite + smectite + I/S + illite in the surrounding of the acid-sulfate alteration; and (2) discharge products associated with neutral-alkaline fluids such as: (i) discontinuous pinnacle-like silica and silica deposits with laterally developed coarse stratification which, together with remaining microorganisms, emphasize a sinter deposit associated with alkaline/freshwater/brackish alkaline-chlorine water bodies and laterally associated with (ii) calcite + aragonite deriving from bicarbonate waters. The scarce presence of relics of sinter deposits, with high degree crystallinity phases and diatom remnants, in addition to alunite + kaolinite + opal CT + anatase assemblages, is consistent with a superimposition of a steam-heated environment to a previous sinter deposit. These characters are also a distinguishing feature of paleosurface deposits associated with the geothermal system of the Cordón de Inacaliri Volcanic Complex. The presence of diatoms in heated freshwater bodies at 5100 m a.s.l. in the Atacama Desert environment could be related with the last documented deglaciation in the area (~20–10 ka), an important factor in the recharge of the hidden geothermal systems of the Pabelloncito graben.

Recent studies have suggested that a chromian spinel can be formed under natural hydrothermal conditions; however, the required conditions, process, and associated redistribution of Cr are still poorly understood. Here, chromian spinel formation was performed by Fe-Cr hydroxides alteration with an Fe2+(aq) supply at 150, 170, and 200 °C and 5 MPa simulating the diagenetic process. The flow-through system enabled the Fe2+(aq) supply to be leached from the magnetite by an acidic solution to synthesize Fe-Cr hydroxides as the starting material with two reaction cells, flow lines, heaters, and a high-performance liquid chromatography (HPLC) pump. The accuracy of the temperature measurement was confirmed based on the amorphous silica solubility. Mineralogical analysis of solid samples recovered from the reaction cell indicated that the chromian spinel was formed between 150 and 170 °C from Fe-Cr hydroxides through goethite with a simultaneous hematite formation, while Mössbauer spectra showed that a large quantity of Fe-Cr ferrihydrites still remained after the experiments probably because of the Cr addition to the stability of ferrihydrites. The Cr/Fe ratio of the chromian spinel was smaller than that of the bulk of the Fe-Cr ferrihydrites and equivalent to Cr-rich magnetite, suggesting a redistribution of Cr during the transformation from goethite to synthesized spinel under the hydrothermal conditions.

Brownfield areas are important targets of exploration; however, the extensive drilling present in these areas has not fully exploited their prospective potential. The appropriate use of drill hole cores in these areas can play an important role in deep exploration. We present a case study of iron oxide-copper-gold (IOCG) Furnas Southeast deposit, located in the Carajás Mineral Province, Brazil. This deposit has disseminated chalcopyrite, bornite and gold mineralization associated with a silicic (Si), potassic (K), calcic (Na), sodic-calcic (Na-Ca) hydrothermal alteration, and intense iron metasomatism with massive magnetite (Fe) alteration. Petrophysical hand-held equipment measurements were carried out on drill core samples with the purpose of studying the potential roles that magnetic susceptibility properties can play in high-grade mineralization. The results indicate that the geological complexity of the IOCG deposit is readily reflected in the extensive variation of the measurements. The statistical analysis shows how the detailed characterization of this physical property carried out for this mineral association could effectively define and describe ore, and the magnetic susceptibility footprints of hydrothermal alteration zones. Furthermore, we were able to perform a magnetic susceptibility 3D modeling of diamagnetic, paramagnetic, and ferrimagnetic responses strictly correlated with known orebody. Thus, petrophysical analyses can form a quantitative geological criterion for ore delineation.

In the Uralian Fold Belt, there are quite numerous and well-studied porphyry copper (±Mo) deposits corresponding to the traditional “diorite” (most) or “monzonite” (Talitsa, Verkhneuralskoe) models. Along with them, there are relatively small but gold-rich massifs of porphyric granitoids, including the large Yubileinoe porphyry Au–Cu deposit, which is located at the southernmost extremity of the Urals. In this study, two main types of regional hydrothermal–metasomatic alteration were distinguished based on applying quantitative petrography and areal multielement geochemical studies in the scale of the ore district: (1) an earlier synvolcanic secondary alteration of volcanics, similar to those observed in volcanic massive sulfide-bearing fields (albitization, propylitic, and listvenitic alteration) and (2) a later plutonogenic alteration of the porphyry type. The plutonogenic hydrothermal–metasomatic (HM) complex is represented by K-feldspathization, hornfels and skarn alteration at the progressive phase, and propylitization, sericitization, and beresitization at the regressive phase. They are caused by hydrothermal alteration in the apical part of the stock, composed of the mineralizing Frasnian granite porphyry complex that hosts the Yubileinoe gold deposit. A lateral series of geochemical zonality (from the periphery of volcanotectonic structures to their center) has been established for the volcanogenic stage of hydrothermal activity: CrNiCo → PbZnCuCrNi → AuAg (CrNi) → BaAuAg. A large positive anomaly of the lithochalcophilic type was found for the HM plutonogenic complex in the ore field of the Yubileinoe deposit. The concentric zonality of this anomaly is characterized by the development of Ag, W, Sn, Pb, As, and Sb halos at its periphery, and Au, Cu, Bi and Mo at its focus (“core”). The stable and radiogenic isotope geochemical data for most of the porphyry copper deposits of the Urals indicate the predominant mantle source of their rocks and ore matter. Their paleotectonic position is reconstructed as a mature stage of intraoceanic island arcs. Unlike many other porphyry objects in the Urals, the totality of geochemical, isotope–geochemical and geological features of the Yubileinoe deposit indicate the predominantly crustal magma source. According to these features, this deposit is closer to Andean-type porphyry deposits, and its position can be reconstructed as an active margin of the Mugodzhar microcontinent, i.e., a suprasubduction regime, transitional from a mature island arc to the marginal continental one. According to the complex of features, this deposit in the Urals is a close analogue of the porphyry gold deposits of the Maricunga Belt in Chile. The magmatic complexes from the Silurian (Wenlock) to the Devonian (Frasnian) age, which are parental to the porphyry gold–copper systems of the Urals, correspond to the early phase of the Wilson cycle. This phase is the most ore-productive with the formation of giant Cr and Fe–Ti–V deposits associated with ultramafic–mafic complexes. It is likely that the differentiation of mafic magmas in the large-volume chambers occurring in the lower part of the lithosphere causes the appearance (as an extreme member) of diorite melts with a noticeable enrichment in gold and copper.