Alteration Minerals Research Articles

Greenstone of Calabria: A multi-analytical characterization of heritage metabasite from Southern Italy

This paper reports the results of a multi-analytical investigation on metabasite rocks exploited and marketed since pre-historical times as “Pietra Verde (i.e. Greenstone) of Calabria”, southern Italy and employed as building as well as ornamental stone materials. Our contribution focuses on petrographic and mineralogical features, relating them to petrophysical-mechanical properties. Achieved results confirmed the good mechanical performance of metabasite from Calabria in terms of compression strength and deformability, making it suitable also for building structural elements and foundations. The absence of alteration minerals and of noticeable porosity and microfractures contributes to the good petrophysical and physical-mechanical features of such rocks. This study represents a contribution to the very little literature available on this rock type, even in the frame of its use as sustainable georesource as well as of promoting geotourism across historical sites.

Multi-Sensor Satellite Remote-Sensing Data for Exploring Carbonate-Hosted Pb-Zn Mineralization: Akhlamad Area, Razavi Khorasan, North East Iran

The exploration of Pb-Zn mineralization in carbonate complexes during field campaign is a challenging process that consumes high expenses and time to discover high prospective zones for a detailed exploration stage. In this study, multi-sensor remote-sensing imagery from Landsat-8, Sentinel-2, and ASTER were utilized for Pb-Zn mineralization prospectivity mapping in the Akhlamad carbonate complex area, Razavi Khorasan, NE Iran. Due to the presence of carbonate formations and various evidence of Pb-Zn mineralization, this area was selected. Band composition, band ratio, principal component analysis (PCA), and SAM techniques for mapping alteration minerals as well as lineament analysis were implemented. Subsequently, a fuzzy logic model for identifying the prospective zones of Pb-Zn mineralization using multi-sensor remote-sensing satellite images was designed. The weight of each exploratory layer was determined using the fuzzy hierarchical method and the integration process of the information layers was performed using fuzzy operators. Finally, the existing mineral indications were used to evaluate and validate the obtained mineral potential map. The outcome of this investigation suggested several high-potential zones for Pb-Zn exploration in the study area.

Hydrocarbon-degrading Shewanella algae shows oxidative deterioration corrosion at the aluminium alloy & coating interface

In this investigation, microbial adhesion expedites formation and alteration of aluminous minerals within aviation fuel tank systems. The corrosion mechanisms of two uncoated aluminium alloys and three types of coating-pretreated aluminium alloys by hydrocarbon-degrading Shewanella algae are examined. NO3- reduction of microorganisms induces corrosion acceleration of LY12 aluminium alloy (1.48 g*m−2*h−1) and corrosion inhibition of 7B04 aluminium alloy. CLSM and SEM observation of coating morphology highlight the microbial deterioration behaviors of coatings (pitting, swelling, and peeling). It inspires material selection and surface coating of microbial corrosion protection of aluminium alloy in marine and aerial environments.

Paragenetic and geological setting of the Starra iron oxide copper–gold deposits, Mount Isa Inlier, Queensland, Australia: constraints on IOCG deposit models

The five Starra iron oxide copper–gold (IOCG) deposits, which are located in the Cloncurry district of the Mount Isa Inlier, NW Queensland, are hosted in a N-trending zone of deformed iron-rich metasedimentary rocks that are underlain by two mineralogically distinct mafic–intermediate meta-igneous rocks. Copper–Au mineralisation is subdivided into two stages—an early main stage that transitioned from a magnetite-dominated Cu substage comprising chalcopyrite, pyrite, biotite and chlorite, to a hematite–muscovite-bearing Cu–Au substage with chalcopyrite, bornite and rare chalcocite, as well as Au–Ag-tellurides and native Au. This second stage was followed by a subordinate but nonetheless important carbonate–quartz–barite vein stage with minor but locally high-grade Cu–Au mineralisation characterised by abundant chalcocite and bornite, minor native bismuth and wittichenite (Cu3BiS3), together with minor Au–Ag telluride minerals. Bornite in these carbonate–quartz–barite veins contains considerable amounts of Au (>10 ppm), which appears to be deported either as lattice substitution in the bornite crystal structure or as homogeneously distributed Au0 nanoparticles. An earlier, coarse-grained mafic intrusion was affected by early Na–Ca alteration, whereas a second mafic intrusion lacks evidence of Na–Ca alteration but was exposed to K–Fe alteration and subsequent mineralisation at Starra 222. Mushketovite (magnetite after specular hematite) is only observed in ironstone lodes proximal to the mafic–intermediate rocks. The close spatial and mineralogical associations of the mafic–intermediate bodies and the ironstone lodes point to a stronger link between magmatic activity and IOCG mineralisation than has previously been recognised at Starra. Remobilisation of gold by late-stage hydrothermal fluids aided by the relatively low fluid temperatures during the main pulse of Cu–Au mineralisation refined gold grades at Starra, making it a relatively gold-rich IOCG deposit. We show that the Cu–Au deposits of the Starra trend feature mineralogical and geochemical elements common to both Cloncurry IOCG deposits (e.g. abundant magnetite) and IOCG deposits of the Tennant Creek district (e.g. Au–Cu–Bi mineralisation; hematite–bornite–chalcocite assemblages), making them a unique and important member of this complex family of deposits.

Hydrothermal alteration and geochemical proximity indicators to ore at the Metsämonttu Zn–Pb–Cu–Au–Ag deposit, Uusimaa belt, southern Finland

The Paleoproterozoic Metsämonttu Zn–Pb–Cu–Ag–Au deposit (1.5 Mt at 3.5 wt% Zn, 0.8 wt% Pb, 0.3 wt% Cu, 13.2 wt% S, 25 g/t Ag, and 1.4 g/t Au, production 1952–1974) is the largest past-producing mine in the Aijala–Orijärvi area (Orijärvi formation, Aijala member) within the Uusimaa belt, southern Finland. The Aijala member is characterized by 1.9–1.88 Ga felsic-dominated volcanic-sedimentary supracrustal rocks with intercalated sedimentary carbonates and iron formations. The area is underexplored, and little deposit-scale research has been carried out, despite the lateral continuum to the world-class ore district of Bergslagen in south-central Sweden. To better understand the Metsämonttu VMS-related alteration system, we reassessed the previously described metamorphic mineral assemblages and their protolith rock compositions by using mobile and immobile element geochemistry. This resulted in the definition of four metamorphosed alteration mineral assemblages and eight chemostratigraphic rock units. The chemostratigraphic results suggest that the lithological and/or structural setting of the Metsämonttu succession is more complex than previously considered. The stratigraphic footwall is mainly characterized by an extensive cordierite + anthophyllite ± biotite ± phlogopite + pyrite ± pyrrhotite (Mg–Fe–S) assemblage dominated by mafic rocks, designated Mafic B1 and Mafic B2, and Andesite A1. The main sulfide mineralization is hosted by tremolite + diopside ± biotite ± phlogopite ± chlorite skarn (Ca–Mg–K). A sericite-bearing muscovite + quartz ± biotite ± phlogopite + pyrite (K–Si–S) assemblage is composed of felsic to mafic protoliths (Mafic B1–B2, Andesite A1, Dacite A1, Dacite B1, Dacite C1) and extends several tens of meters into the stratigraphic hanging-wall. A quartz + pyrite ± muscovite (Si–S) assemblage represents the immediate ore-proximal alteration and is derived from rocks with a rhyolitic composition (Rhyolite A1).Limited drill core samples near Metsämonttu mineralization, along with restricted surface alteration, pose challenges in studying geochemical variations from distal to ore proximal areas and limits the ability to model the shape and size of the alteration zone. Large mass changes suggest that the alteration was hydrothermal, and due to several protolith compositions, the alteration is interpreted to be predominantly discordant to stratigraphy. A 60-m-wide alteration halo surrounds the Metsämonttu deposit. Major and trace elements, namely MgO, Na2O, K2O, SiO2, Fe2O3, Cu, Zn, Pb, S, Ag, Tl, Hg, Se, Te, Sn, Sb, Rb, and Sr, and the indices modified alteration index (MAI), Ishikawa alteration index (AI), chlorite‑carbonate-pyrite index (CCPI), S/Na2O can be used for chemical vectoring, which can assist regional or near-mine exploration. Elements MnO, Ba, Cd, Bi, As, Ni, Co, W, Ga, Mo, and indices Hashigushi index and advance argillic alteration index (AAAI) were less useful as geochemical exploration indicators.

Machine learning model for deep exploration: Utilizing short wavelength infrared (SWIR) of hydrothermal alteration minerals in the Qianchen gold deposit, Jiaodong Peninsula, Eastern China

The Jiaodong Peninsula in the eastern North China Craton is renowned globally as a major gold province. Notably, the Jiaojia orefield is an important gold-producing district in this region, and its depths are inferred to offer substantial prospecting potential, underscoring the need for innovative exploration tools to uncover concealed orebodies. The Qianchen gold deposit in the southern part of the Jiaojia orefield is characterized by the disseminated-stockwork-style orebodies at depths of ca. –1000 to –1800 m, with three mineralization stages, namely (I) pre-ore K-feldspar-quartz stage, (II) quartz-sericite-gold-polymetallic sulfide stage (main Au mineralization stage), and (III) post-ore quartz-calcite stage. Systematic short-wavelength infrared (SWIR) spectral analysis reveals that sericite group minerals developing in Stage II are the predominant and wide-distributed alteration minerals at Qianchen. Their spectral characteristics demonstrate a shift in the Al-OH absorption feature wavelength positions (Pos2200) to longer wavelengths (>2205 nm) within the orebodies. This shift is likely due to strong water–rock interactions leading to Fe and Mg substituting for Al in octahedral sites. Orthogonal partial least squares discriminant analysis (OPLS-DA) indicates that the H2O, OH, and FeOH spectral bands (Variable Importance in the Projection (VIP) ≥ 1) of sericite are crucial for distinguishing between gold ores and barren wall rocks. Additionally, Long Short-Term Memory (LSTM) models demonstrate that spectral data of sericite can be used to predict ore samples with an accuracy of 82 %, validated by receiver operating characteristic analysis (84 %), and blind test results demonstrate that the predicted grade closely aligns with the actual grade. Therefore, it is concluded that SWIR spectral characteristics of sericite group minerals can serve as an effective indicator for prospecting the Qianchen concealed gold mineralization. This study highlights the potential of coupling between machine learning and SWIR spectral data of alteration minerals to uncover the concealed lode gold mineralization.

Exploring in-situ combustion effects on reservoir properties of heavy oil carbonate reservoir

Laboratory modeling of in-situ combustion is crucial for understanding the potential success of field trials in thermal enhanced oil recovery (EOR) and is a vital precursor to scaling the technology for field applications. The high combustion temperatures, reaching up to 480 °C, induce significant petrophysical alterations of the rock, an often overlooked aspect in thermal EOR projects. Quantifying these changes is essential for potentially repurposing thermally treated, depleted reservoirs for CO2 storage.In this study, we depart from conventional combustion experiments that use crushed core, opting instead to analyze the thermal effects on reservoir properties of carbonate rocks using consolidated samples. This technique maintains the intrinsic porosity and permeability, revealing combustion's impact on porosity and mineralogical alterations, with a comparative analysis of these properties pre- and post-combustion. We characterize porosity and pore geometry evolution using low-field nuclear magnetic resonance, X-ray micro-computed tomography, and low-temperature nitrogen adsorption. Mineral composition of the rock and grain-pore scale alterations are analyzed by scanning electron microscopy and X-ray diffraction.The analysis shows a significant increase in carbonate rocks’ porosity, pore size and mineral alterations, and a transition from mixed-wet to a strongly water-wet state. Total porosity of rock samples increased in average for 15%–20%, and formation of new pores is registered at the scale of 1–30 μm size. High-temperature exposure results in the calcite and dolomite decomposition, calcite dissolution and formation of new minerals—anhydrite and fluorite. Increased microporosity and the shift to strongly water-wet rock state improve the prospects for capillary and residual CO2 trapping with greater capacity. Consequently, these findings highlight the importance of laboratory in-situ combustion modeling on consolidated rock over tests that use crushed core, and indicate that depleted combustion stimulated reservoirs may prove to be viable candidates for CO2 storage.

Ore-forming fluid characteristics and ages of the Xinan Cu-Mo deposit at Zijinshan orefield, SE China: New insights for metallogenic mechanism and exploration

The Xinan deposit, a newly discovered porphyry Cu-Mo deposit in the Zijinshan orefield, Fujian Province, exhibits distinct alteration and porphyry mineralization stages, including the potassic, propylitic, and phyllic alteration stages. The phyllic stage is further divided into molybdenite, chalcopyrite, and pyrite sub-stages. Molybdenite Re-Os model age (108.3 ± 1.1 Ma) and concomitant sericite 40Ar/39Ar plateau age (109.0 ± 6.0 Ma) indicate that the Xinan Cu-Mo deposit was formed at 109 ∼ 108 Ma. Four types of fluid inclusions have been identified at the Xinan deposit, including vapor-rich, liquid-rich, and opaque daughter mineral-bearing subtypes with minor transparent daughter mineral-bearing subtypes. Fluid inclusion microthermometry measurements reveal that the potassic alteration stage exhibits homogenization temperatures of 375–475 °C and salinities range of 4–20 wt% NaCl eqv., suggesting slight fluid boiling. Chlorite geothermometer suggests temperatures of the propylitic alteration stage range from 261 to 336 °C, averaging at 303 °C. The molybdenite, chalcopyrite, and pyrite sub-stages have homogenization temperatures of 325–400 °C, 325–350 °C, and 300–350 °C, respectively, with corresponding salinities of 2–10 wt% NaCl eqv., 4–8 wt% NaCl eqv., and 2–4 wt% NaCl eqv.. The Laser Raman spectroscopy results show that the fluid inclusions in the Xinan deposit consist of H2O with minor CO2, hematite, chalcopyrite, and halite. The evolution of the ore-forming fluids in the Xinan porphyry Cu-Mo deposit is characterized by a transition from high-temperature, low- to moderate-salinity, oxidized, and CO2-bearing conditions during the potassic alteration stage, to moderate- to high-temperature and low-salinity conditions during the propylitic alteration stage. The subsequent phyllic alteration stage, which overprints on the potassic and partial propylitic alteration stages, is marked by moderate- to high-temperature, low-salinity, and low-oxygen fugacity environments. The primary mechanisms driving mineralization in the Xinan porphyry Cu-Mo deposit are thus identified as the reduction in temperature and oxygen fugacity, coupled with CO2 escape. In contrast to the Luoboling-Jintonghu porphyry Cu-Mo deposit, the ore-forming fluid of the Xinan deposit is characterized by lower temperatures, salinity, and CO2 contents, and reduced fluid boiling. This suggests a relatively subdued porphyry-type mineralization. The lack of a distinct potassic alteration zone in the Xinan Cu-Mo deposit suggests the potential existence of a deeper, higher temperature and salinity porphyry mineralization center beneath this deposit.

Gold occurrence and mineralization in the Paleozoic Heijianshan Fe–Cu (–Au) deposit, Eastern Tianshan

Gold (e.g., electrum) has been reported in the Paleozoic Heijianshan Fe–Cu (–Au) or iron oxide–copper–gold-like (IOCG-like) deposit in the Eastern Tianshan, but relationships between gold occurrence and sulfides are unclear. The Heijianshan Fe–Cu (–Au) (or IOCG-like) deposit underwent five alteration and mineralization stages: Pre-ore epidote alteration (Stage I), syn-ore magnetite/iron mineralization (Stage II) followed by pyrite alteration (Stage III) and Cu (–Au) mineralization (Stage IV), and post-ore late veins (Stage V). This deposit mainly has two types of pyrite (A and B) based on pyrite–hematite and pyrite–pyrrhotite–chalcopyrite assemblages. They are euhedral to subhedral and mainly homogenous, with the former having porous or inclusion-rich domains. Trace elements incorporating into pyrite at Heijianshan are mainly controlled by compositions (e.g., As, Co, and Cu), temperature (e.g., Ni and Se), and oxygen fugacity (fO2; e.g., As and Se) of hydrothermal fluids, respectively. The time-resolved depth-concentration profiles suggest trace elements in pyrite and chalcopyrite occur as solid solution (e.g., Co, Ni, Zn, As, and Se) and micro- to nano-sized mineral inclusions (e.g., Cu, Bi, and Pb). The gold occurrence at Heijianshan is invisible as solid solution in Stage III pyrite and Stage IV chalcopyrite and visible as micron-sized Stage IV electrum. Moreover, incorporation mechanisms of invisible gold are Au3+ substituting iron or copper in pyrite A and chalcopyrite, respectively, and Au+ incorporating into the vacancy or defect positions of pyrite B. Sulfides texture and geochemical compositions when combined with previous in-situ sulfur isotope suggest that pyrite formation was resulted from interaction between external basinal brines and altered host rocks under different temperature and fO2 conditions. Ongoing fluid-rock reaction led to formation of chalcopyrite ± electrum veins as Cu (–Au) mineralization at Heijianshan. This study suggests that the prolonged interaction contributes to sulfide formation and Cu (–Au) mineralization in these Paleozoic Fe–Cu or IOCG-like deposits formed in basin-related setting, and the Aqishan-Yamansu belt, Eastern Tianshan has gold mineralization potential.

Short-Wavelength Infrared Characteristics and Indications of Exploration of the Jiawula Silver–Lead–Zinc Deposit in Inner Mongolia

For the Jiawula lead–zinc deposit, as easily accessible resources become depleted, mines are becoming deeper to replenish ore reserves. Identifying large, continuous, and high-grade ore bodies in deep areas has become a daunting problem. Moreover, separating lead–zinc-bearing complex ore bodies from waste material and extracting them from associated minerals are also difficult. Thus, pioneering exploratory strategies and technological methodologies are required to make breakthroughs in mineral discovery. Based on extensive-scale structural lithofacies mapping, this paper uses short-wave infrared (SWIR) spectroscopy technology to investigate hydrothermal alteration minerals in the mining area. It has identified a total of 16 hydroxyl-bearing alteration minerals, including chlorite, muscovite, illite, calcite, ankerite, kaolinite, and smectite. These minerals establish zoning characteristics around the ore bodies and on their flanks. They comprise a segmented assemblage that follows the pattern of comb-textured quartz–illite–chlorite–carbonate → muscovite–illite–chlorite–ankerite → illite–smectite–chlorite → chlorite–kaolinite–calcite. Deep-zone illitization with a lower Al–OH absorbance peak wavelength (<2206 nm) and higher crystallinity indices (>1.1) and chloritization with higher Fe–OH absorbance peak wavelengths (>2254) and higher crystallinity indices (>3.0) are indicators of potential hydrothermal centers in the deeper regions. By finding hydrothermal centers and connecting their spatial distribution with existing ore bodies, a pertinent relationship between diabase + andesite, Fe-chlorite + illite, and high-grade mineralization has been established. They correspond well with the lithology-alteration mineralization. This research provides a basis for predicting the positioning of concealed ore bodies deep inside a mine or at the periphery.

The Molecular Mechanisms Underlying the Systemic Effects Mediated by Parathormone in the Context of Chronic Kidney Disease.

Chronic kidney disease (CKD) stands as a prominent non-communicable ailment, significantly impacting life expectancy. Physiopathology stands mainly upon the triangle represented by parathormone-Vitamin D-Fibroblast Growth Factor-23. Parathormone (PTH), the key hormone in mineral homeostasis, is one of the less easily modifiable parameters in CKD; however, it stands as a significant marker for assessing the risk of complications. The updated "trade-off hypothesis" reveals that levels of PTH spike out of the normal range as early as stage G2 CKD, advancing it as a possible determinant of systemic damage. The present review aims to review the effects exhibited by PTH on several organs while linking the molecular mechanisms to the observed actions in the context of CKD. From a diagnostic perspective, PTH is the most reliable and accessible biochemical marker in CKD, but its trend bears a higher significance on a patient's prognosis rather than the absolute value. Classically, PTH acts in a dichotomous manner on bone tissue, maintaining a balance between formation and resorption. Under the uremic conditions of advanced CKD, the altered intestinal microbiota majorly tips the balance towards bone lysis. Probiotic treatment has proven reliable in animal models, but in humans, data are limited. Regarding bone status, persistently high levels of PTH determine a reduction in mineral density and a concurrent increase in fracture risk. Pharmacological manipulation of serum PTH requires appropriate patient selection and monitoring since dangerously low levels of PTH may completely inhibit bone turnover. Moreover, the altered mineral balance extends to the cardiovascular system, promoting vascular calcifications. Lastly, the involvement of PTH in the Renin-Angiotensin-Aldosterone axis highlights the importance of opting for the appropriate pharmacological agent should hypertension develop.

Hydrothermal Alteration Zones Mapping Using Sentinel 2 MSI and Terra Aster Data in The Uruguay Mine, Minas do Camaquã District

Objective: This work has as main objective to evaluate the usage of data from the Terra ASTER multispectral sensor, as well as data from Sentinel 2 MSI for the identification of hydrothermal alteration zones in the Uruguay Mine. Another objective of this work was to map a not-so-great scale deposit that present a hydrothermal pattern associated in a tropical country. Method: Were applied principal component analysis and entropy analysis technique to the ASTER surface reflectance data and principal components only to the surface reflectance MSI data. The field spectra provided were obtained with the ASD FieldSpec-3 High-Resolution spectroradiometer. The samples collected contained spectral features characteristic of minerals such as ferric chlorite, hematite, goethite and illite (Phengite). Result and Conclusion: The ASTER data resulted in a good radial highlighted pattern at the mine location indicating that the processing was able to map the target spectral patterns. The MSI data were processed to map the ferric minerals and presented a pattern highlighting the mine contours and slopes, demonstrating the possible occurrence of minerals containing the aimed spectral features. The entropy usage as an intensity factor applied to intensity-hue-saturation (IHS) fusion on ASTER data improved the reliability of the results, by highlighting the pixels with deepest absorbance features, reducing the uncertainty associated with the process. The results were considered good since both processes showed correspondence in the location of the mine. Implication of the research: This work contributes for the understanding of spectroscopy analysis of alteration minerals related to copper mineralization, and techniques of remote sensing to map them. Originality/value: Good results of the application of principal component analysis in the studied area and application of entropy concept in spectral analysis.

Water weakening and the compressive brittle strength of carbonates: Influence of fracture toughness and static friction

Water is ubiquitous within the pore space of rocks and has been shown to affect their physical and mechanical behaviour. Indeed, water can act on the rock strength via mechanical (i.e., reducing the effective stresses) or chemical effects (e.g., mineral dissolution, mineral alteration, subcritical crack growth, etc.). As rock macroscopic strength is controlled by both fracture toughness and friction at the grain-scale, these parameters should also be affected in presence of water. While some recent studies have measured the effect of water on both fracture toughness and frictional parameters to constrain the water weakening of porous rock compressive strength, the physical parameters, or rock characteristics, that influence this weakening are as of yet unclear. Here, we report a series of laboratory experiments in order to determine the influence of a water-saturated, as opposed to dry, environment on five limestones’ strengths. The uniaxial compressive strength, the mode-I fracture toughness and the static friction parameters are of interest. The experiments show that, for the tested limestones, water-saturated conditions provoke a reduction of the uniaxial compressive strength by up to 53 %. This reduction is accompanied by a reduction of the mode-I fracture toughness by up to 34 % and of the static friction by up to 16 %. Even though the water weakening of the uniaxial compressive strength is not influenced by the sample porosity, the mode-I fracture toughness reduction in the presence of water is accentuated for high-porosity limestones. Additionally, low porosity limestones appear to promote higher static friction reductions in water-saturated environments.

ALTERATION AND MINERALIZATION STUDIES IN THE JEBLOGAN AREA, KARANGTENGAH, WONOGIRI, CENTRAL JAVA

The research area is located in Jeblogan, Karangtengah, Wonogiri, Central Java. This study aims to investigate the hydrothermal alteration and mineralization. Geological structures present in the research area include faults and fractures. These faults are well-developed trending NE-SW, NW-SE, and N-S as pathways for fluid ascent to the surface, thereby influencing alteration patterns. Mineral alteration assemblages in the research area, based on petrographic, mineragraphy, and XRD analysis, result from hydrothermal processes and include mineral assemblage zones such as Quartz ± Silica ± Pyrite, Alunite + Pyrophyllite ± Zunyite ± Quartz ± Hematite, Illite + Halloysite ± Smectite ± Kaolinite ± Quartz, and Chlorite + Calcite + Epidote ± Pyrite. Mineralization found in the research area includes Chalcopyrite, Sphalerite, Pyrite, Chalcocite, and Galena. Based on the characteristic parameters of the deposit type and laboratory analysis, the deposit type at the research location is low-sulfidation epithermal deposit and intermediate-sulfidation deposit.

Prospecting Prediction for the Yulong Metallogenic Belt in Tibet Based on Remote Sensing Alteration Information and Structural Interpretation

The Yulong porphyry copper belt in eastern Tibet is located in the middle of Tethys–Himalayan metallogenic mega-province, which is one of the three major porphyry copper metallogenic mega-provinces. The Yulong copper belt belongs to the super porphyry copper belt and represents one of the most important copper mineralization prospecting areas in China. A significant quantity of research data shows that this study area belongs to the environment of intracontinental collision and compression, with a complex geological structure, magmatic rock development and excellent metallogenic geological background. However, because this area is located in an alpine and high-altitude area, it is difficult to carry out any traditional field geological surveys, and the existing studies of both prospecting and prediction are relatively weak. This study focused on information extraction for alteration minerals in the Yulong metallogenic belt and its surroundings based on multispectral data and hyperspectral data, establishing a spectral library of alteration minerals in this area. Based on Sentinel-1A radar data and Landsat-8 OLI color synthesis data, the linear structure of the study area was interpreted. On this basis, the information extraction results relating to alteration minerals obtained from multi-source remote sensing data, linear structure interpretation results and the geochemical exploration data of the study area were superimposed to comprehensively analyze the metallogenic geological conditions and mineralization characteristics in the area, establish remote sensing prospecting indicators there and optimize the potential areas for prospecting, providing technical support for the next step of prospecting and exploration in the area.

Ultrapotassic plutons as a source of uranium of vein-type U-deposits (Moldanubian Zone, Bohemian Massif): insights from SIMS uraninite U–Pb dating and trace element geochemistry

The Bohemian Massif hosts significant hydrothermal U-deposits associated with shear zones in the high-grade metamorphic basement. But there is a lack of evidence of a genetic link between mineralization and U-fertile igneous rocks. This contribution provides constraints on the major U source of the vein-type U-deposits, the timing of ore formation and the metallogenetic model. The anomalous trace element signatures of the low-temperature hydrothermal deposits (high Zr, Y, Nb, Ti, ∑REE) and their close spatial relation with ultrapotassic rocks of the durbachite series point to a HFSE and REE enriched source rock. The durbachites have high U content (13.4–21.5 ppm) mainly stored in magmatic uraninite and other refractory minerals (e.g., thorite, zircon, allanite) that became metamict over a time interval sufficient to release U from their crystal structure, as suggested by the time gap between emplacement of the durbachites (EMP uraninite U–Pb age ~ 338 Ma) and hydrothermal activity (SIMS uranium ore U–Pb age ~ 270 Ma). Airborne radiometric data show highly variable Th/U ratios (1.5–6.0), likely reflecting a combination between (1) crystallization of magmatic uraninite, (2) hydrothermal alteration, and (3) leaching and mobilization of U along NW–SE-trending fault zones, manifested by elevated Th/U values in the radiometric map. The presence of rare magmatic uraninite in durbachites suggests almost complete uraninite dissolution; EMP imaging coupled with LA-ICP-MS analyses of refractory accessory phases revealed extensive mobilization of U together with HFSE and REE, providing direct evidence for metal leaching via fluid-driven alteration of radiation-damaged U-rich minerals. The large-scale HFSE and REE mobilization, demonstrated by the unusual trace element signatures of the U-deposits, was likely caused by low-temperature (270–300 °C), highly alkaline aqueous solutions containing F-, P-, and K-dominated complexing ligands. The first SIMS U–Pb age of 270.8 ± 7.5 Ma obtained so far for U-mineralization from the Bohemian Massif revealed a main Permian U mineralizing event, related to crustal extension, exhumation of the crystalline basement, and basin formation, as recorded by U–Pb apatite dates (280–290 Ma) and AFT thermal history models of the durbachites. The Permo-Carboniferous sedimentary cover probably represented a source of oxidized basinal brines infiltrating the basement-hosted durbachite plutons and triggering massive metal leaching. The interaction between basin-derived brines and durbachites resulted in significant modification of the chemical composition of the hydrothermal system (K and F release during biotite chloritization, P liberation through monazite alteration), leading to the formation of ore-bearing fluids responsible for the metallogenesis of the basement-hosted unconformity-related U-deposits in shear zones in the Bohemian Massif.

Nephrolithiasis in Renal Tubular Acidosis: Pathophysiology, Diagnosis, and Management Strategies

Renal tubular acidosis (RTA) encompasses a group of disorders characterized by impaired kidney acid-base regulation, resulting in metabolic acidosis. Nephrolithiasis, the formation of kidney stones, represents a significant complication of RTA. Despite its clinical importance, the relationship between RTA and nephrolithiasis remains complex and poorly understood. This review provides a comprehensive overview of nephrolithiasis in RTA, focusing on its pathophysiology, diagnostic challenges, and management strategies. Mechanisms underlying kidney stone formation in RTA, including altered urinary pH, electrolyte abnormalities, and mineral metabolism disturbances, are explored in detail. Clinical manifestations and diagnostic considerations specific to nephrolithiasis in RTA patients are discussed, emphasizing the importance of a comprehensive metabolic evaluation and imaging procedures for accurate diagnosis. Current therapeutic approaches for treating kidney stones in RTA patients, including dietary modifications, pharmacological interventions, and surgical interventions, are reviewed. By elucidating the intricate interplay between RTA and nephrolithiasis, this review aims to enhance clinical understanding and guide optimal management strategies for patients with this challenging renal disorder.

PRISMA Hyperspectral Remote Sensing Data for Mapping Alteration Minerals in Sar-e-Châh-e-Shur Region, Birjand, Iran

Remote sensing satellite imagery consistently provides valuable and frequent information, enabling the exploration of mineral resources across immense, remote and harsh domains. Recent developments in spaceborne hyperspectral remote sensing have opened avenues to support diverse remote sensing applications, particularly in the realm of mineral exploration. This study evaluates the capabilities of the PRecursore IperSpettrale della Missione Applicativa (PRISMA) hyperspectral satellite data for mapping alteration minerals using the Matched Filtering Unmixing (MFU) approach in the Sar-e-châh-e-shur, Birjand, Iran. Minerals such as richterite, augite, psilomelane, ilmenite, kaolinite, smectite, mirabilite, muscovite, and chlorite were identified using the vertex component analysis (VCA) technique. Subsequently, alteration mineral maps of the study area were generated using a matched filtering technique. Additionally, through the integration of X-ray diffraction (XRD) analysis, thin section examination, geochemical study of stream sediments, and interpretation of geological maps, potential alteration mineralization zones were delineated in the study area. Ultimately, the validation process, which included comparing the maps with the findings derived from the PRISMA remote sensing study, was conducted using the normal score equation. Thus, our results yielded a normalized score of 3.42 out of 4, signifying an 85.71% agreement with the regional geological characteristics of the study area. The results of this investigation highlight the substantial potential of the PRISMA dataset for systematic alteration mineral mapping and consequent exploration of ore minerals, specifically in challenging and inaccessible terrains.

Extracting geological and alteration information and predicting antimony ore based on multisource remote sensing data in Huangyangling, Xinjiang

Introduction: China has the world’s largest amount of antimony resources and plays a vital role in the global antimony industry. The Huangyangling area in Xinjiang belongs to the Lazhulong-Huangyangling antimony mineralization belt; this area is rich in antimony ore resources, with potential for discovery of additional ore. This high-elevation mountainous area is located in the northwestern region of the northern Tibetan Plateau, with a harsh natural environment and poor transportation access; thus, the use of traditional geological exploration methods is limited, and remote sensing technology provides unique advantages.Methods: Using Landsat 8 OLI and Gaofen-6 (GF-6) data, we extracted stratigraphic, lithologic and fault information from the study area through information enhancement processing of the images. Based on Landsat 8 OLI, Sentinel-2 and ASTER images and the use of remote sensing image preprocessing and interference information masking, the spectral characteristics of limonite, as well as hydroxyl, carbonate, and silicified alteration minerals were utilized; the characteristics included reflection or absorption in specific spectral bands. The spectral characteristics were then combined with principal component analysis (PCA) and the band ratio method to extract the alteration information for the study area.Results: The stratigraphy and boundaries between stratigraphic and lithologic units extracted in this study were defined, and numerous small faults were identified based on a comparison with 1:250,000 geologic maps. And the overall distribution trends of the indicators of alteration extracted in this study were located along fault zones; additionally, the hydroxyl and carbonate alteration anomalies matched well with known deposits (occurrences). Thus, the alteration information is a good indication of antimony ore bodies. Based on the geological interpretation, alteration information extraction and geochemical exploration data, four prospecting areas were identified.Discussion: The method of extracting geological and hydrothermal alteration information by remote sensing has practical significance because it provides the possibility for geological work and mineral exploration in difficult high-elevation environments.

Lithogeochemistry of the Nesjavellir geothermal field, SW Iceland—Implications for elemental mass movement in active geothermal systems

The lithogeochemistry of altered basalts was investigated to assess elemental mass changes in the active meteoric water dominated geothermal system at Nesjavellir, SW Iceland. The study revealed that elemental mass changes upon hydrothermal alteration is rather limited and the extent of metasomatism is controlled by the type of alteration minerals. Large mass movement was detected in volatiles (C and S), likely derived from magma degassing. The geothermal system at Nesjavellir may thus provide an ideal locality to investigate the natural sequestration of deep-sourced volatiles and deliver insights in quantifying the input of mantle degassing on the budget of geothermal systems.