Potassic Alteration Zones Research Articles

The origin of Gangjiang adakite-like intrusions and associated porphyry Cu–Mo mineralization in the central Gangdese porphyry Cu belt, southern Tibet

The Gangjiang Cu–Mo deposit is located in the central Gangdese porphyry Cu belt (GPCB), south Tibet. Geological investigation reveals that the Gangjiang deposit is characterized by early potassic alteration, followed by late phyllic and argillic alteration. Late alteration has different degrees of overprinting over the potassic alteration zone. Copper-Mo orebodies are predominantly hosted in the potassic and phyllic alteration zones of the Miocene monzogranite porphyry (MGP) and granodiorite porphyry (GDP). In this study, we present the chemistry and Sr–Nd–Pb–Hf–O isotope compositions of fertile MGP and GDP, barren tonalite porphyrite (TP), and microgranular mafic enclaves (MMEs). Chemical compositions indicate that these intrusions are I-type granites that show high–K calc-alkaline signatures. The negative correlation between Dy/Yb and SiO2 indicates that the intrusions experienced fractionation of amphibole. They have high Sr/Y (>70) and La/Yb (>38) ratios, strong negative Nb–Ta–Ti anomalies, and positive Pb anomalies are typical for arc magma. The high Mg# of various porphyry intrusions (43–65) and MMEs (47–58) indicate the input of mafic components. Various intrusions have whole-rock 87Sr/86Sr(t=13Ma) ratios of 0.70529 to 0.70674, negative εNd(t=13Ma) (−5.0 to −1.2), positive zircon εHf(t) (1.2–9.8), and homogeneous δ18O (5.8–7.1 ‰, mean 6.6 ‰). The MMEs have similar Sr–Nd–Pb–Hf–O isotopic compositions with their host rocks. The features reveal that the Gangjiang adakite-like intrusions and MME samples were derived from the partial melting of the Lhasa Paleoproterozoic crust, with contributions from the juvenile mantle that has been metasomatized by subducted sediments-derived melts. Note, the MGP, GDP, and two types of MMEs have slightly lower δ18O values (down to 4.76 ‰) but higher εNd(t) (up to −1.2) than barren TP, indicating their formation involves more mantle components. Furthermore, the MMEs in the TP and MGP have high Cu contents (up to 1485 ppm), similar to the phenomenon occurs in the Qulong deposit. The Cu-rich MME is probably formed by Cu-refertilization by the underplate arc magma in the juvenile crust. The εHf(t) and εNd(t) values of fertile porphyries increased from the Jiru, Gangjiang, to Qulong deposit indicating increased mantle material additions from the west to the east section of the GPCB. These variations in mantle components have led to an increase in the size of the porphyry Cu deposits from Jiru to Gangjiang, and then to Qulong.

Fluid Inclusion Petrography and Microthermometry of Barren/Mineralized Quartz Veins-Reef of Malanjkhand Cu Deposit, Central India: Implication on Ore and Non-Ore Forming Environment

Quartz reefs and veins of variable thickness have been intruded in host Paleoproterozoic Malanjkhand granites in the mine area and are primarily restricted to phyllic as well as potassic alteration zones. They are mainly of two types: mineralized and barren. Fluid inclusion petrography depicts mainly five types of inclusion which are aqueous biphase, monophase, monocarbonic, H2O-CO2 and polyphase (L+V+H). They are called here Type I, Type II, Type III, Type IV, and Type V, respectively, and are present in both mineralized and barren quartz veins/reefs. All types of inclusion are common except type V, which appears rare in both. However, the sizes of type II and IV are unexpectedly small. The micro thermometry results imply a relatively high temperature (209.4-376.4oC) of fluid entrapment in the mineralized counterpart. However, it is considerably lower (133.9-182.2oC) for the barren counterpart. Although the salinity of fluid appears low for mineralized quartz veins/reef (0.63-0.87 wt.% NaCl equivalent), while for barren counterpart, it is considerably higher (0.92-0.98 wt.% NaCl equivalent). The observed textural and microthermometry results advocate that the Malanjkhand hydrothermal system has resemblances with the porphyry system and indicates probable genetic linkage between barren and mineralized quartz veins/reef. Keywords: Fluid Inclusions, Quartz Veins/Reef, Aqueous Inclusions

Insights into fluid evolution and Re enrichment by mineral micro-analysis and fluid inclusion constraints: Evidence from the Maronia Cu-Mo ± Re ± Au porphyry system in NE Greece

Porphyry-epithermal veins hosting Re-rich molybdenite and rheniite (ReS2) from the Maronia Cu-Mo ± Re ± Au porphyry in Thrace, NE Greece, provide new insights into the hydrothermal processes causing extreme Re enrichment. Quartz trace element chemistry (Al/Ti, Ge/Ti), Ti-in-quartz thermometry, and cathodoluminescence imaging reveal multiple quartz generations in consecutive hydrothermal quartz-sulfide veins associated with potassic, sericitic, and argillic alteration. Fluid inclusions in different quartz generations indicate that phase separation and fluid cooling are the main ore-forming processes in the porphyry stage (~ 500 – 350 °C), whereas mixing of a vapor-rich fluid with metalliferous (e.g., Pb, Zn, Au) meteoric water forms the epithermal veins (~ 280 °C). These processes are recorded by trace element ratios in pyrite that are sensitive to changes in fluid temperature (Se/Te), fluid salinity (As/Sb, Co/As), and mixing between fluids of magmatic and meteoric origin (Se/Ge). Highly variable intra-grain δ34S values in pyrite record S isotope fractionation during SO2 disproportionation and phase separation, emphasizing the importance of in situ δ34S analysis to unravel ore-forming processes. High δ34S (~ 4.5‰) values of sulfides are indicative of low SO42−/H2S fluid ratios buffered by the local host rocks and mixing of the magma-derived fluid with meteoric water. The formation of Re-rich molybdenite (~ 6600 ppm) is favored by cooling and reduction of a magma-derived, high-temperature (~400 °C), oxidized, and Re-rich fluid triggering efficient Re precipitation in early veins in the potassic alteration zone. The systematic temporal fluid evolution therefore reveals that coeval cooling and reduction of oxidized Re-rich fluids cause extreme Re enrichment at the Maronia porphyry system.

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.

Alteration mineralogy, characteristics and shortwave infrared spectroscopy of white mica in the Zijinshan ore field, Fujian Province: Implications for porphyry Cu prospecting

The Zijinshan ore field is situated in the southeastern part of China. in which contains the large Zijinshan high-sulfidation Cu-Au deposit, the Luoboling porphyry Cu-Mo deposit, the Yueyang low-sulfidation Au-Ag deposit, the Longjiangting and the Wuziqilong tansitional Cu deposit, and the Xi’nan porphyry Cu-Mo prospect. Debates on genetic relationship among these deposits, especially the relationship between the Zijinshan Cu-Au deposit and the adjacent Luoboling deposit is a question of importance for further exploration in this ore field. In this contribution, the alteration mineralogy, alteration texture, zonation and mineral chemistry, in combination with shortwave infrared spectroscopy (SWIR) analysis of white mica were used to help focus exploration and assessment of hydrothermal deposits in the Zijinshan ore field.In this study, diaspore-pyrophyllite alteration zone, chlorite-sericite alteration zone and propylitic alteration zone were first identified in the deep drill core of the Zijinshan Cu-Au deposit, which gives way upward to quartz-alunite-kaolinite zone, quartz-alunite zone and the silicic alteration zone. In the Xi’nan Cu-Mo prospect, diaspore-pyrophyllite alteration zone was first recognized in the shallow level with the chlorite-sericite alteration zone and propylitic alteration zone in the deeper level. Andalusite- sericite ± diaspore alteration zone was first recognized in the upper part of the Luoboling Cu-Mo deposit and the deeper part of the Wuziqilong Cu deposit. It indicates that a pervasive occurrence of diaspore -pyrophyllite ± andalusite alteration zones in the Zijinshan ore field, which may potentially represent a transitional environment between the top of porphyry alteration zones and the base of advanced argillic alteration zones. Minerals of the white mica group are extensively distributed in various alteration zones of the Zijinshan ore field. The SWIR analysis of white mica indicated that the wavelength position of the Al-OH (∼2,200 nm; wAlOH) absorption feature increases gradually from the shallow kaolinite-dickite alteration zone to the deep potassic alteration zone. In the advanced argillic alteration zones, the range of wAlOH values of white mica is less than 2205 nm. Conversely, in the porphyry alteration zones, it always exceeds 2205 nm. It is evident that the andalusite-sericite alteration zone with higher wAlOH values (average of 2203 nm) is always proximal to the porphyry mineralization, which may act as indicators for deep porphyry prospecting. The results of electron probe microanalysis (EPMA) reveal that the early enrichment of Mg and depletion of Fe in white mica can be attributed to the preferential incorporation of Fe into iron oxides and iron sulfides in the potassic and propylitic alteration zones. Overall, there is a negative correlation between wAlOH and Al, while wAlOH exhibits a positive correlation with the sum of Fe + Mg + Mn. The distribution characteristics of alteration zones and the variation patterns of the wAlOH of white mica indicate that there are probably several paleo-thermal centers in the deep parts of the Zijinshan ore field, located respectively in the deep parts of the Xi’nan Cu-Mo prospect and the deep part of the Zijinshan Cu-Au deposit and the deep parts of the Wuziqilong Cu deposit, and the latest seems to be more fertile and deserves further exploration.

Modeling remote-sensing and geophysical data to delineate the favorable mineralization localities at Semna area, Central Eastern Desert, Egypt

Semna area is located within the Golden Triangle district in the Central Eastern Desert of Egypt. The study maintains using multisource datasets of remote sensing, aero-spectrometry, aero-magnetic, and field investigations for unraveling the ambiguities associated with the alteration zones at the targeted area. Three remote sensing mapping techniques including; constrained energy minimization, linear spectral unmixing, and mineral indices, were adopted to delineate the alteration zones. The γ-ray spectrometry data of K (%), K/eTh, K/eU, and F-parameter enabled mapping the potassium-enriched localities as indication on possible potassic alteration zones. The surface and subsurface linear structural features were delineated from the digital elevation model and aero-magnetic data, respectively. The outcomes of all the implemented datasets were integrated using GIS overlay modeling, producing an integrated mineralization favorability/potentiality map. Eighteen localities with high potential for mineralization were highlighted. A field study was conducted to the investigated area during which, several alteration indicators were observed, including quartz veins, iron oxides staining, kaolinite, malachite, carbonate, and muscovite (sericite) alteration indicator minerals.

Solid mineral potential evaluation using integrated aeromagnetic and aeroradiometric datasets

The analytical hierarchy process (AHP) was employed to delineate the mineralisation potential across the notable schist belts in northwestern Nigeria. High-resolution aeromagnetic and aeroradiometric datasets were taken into consideration. This was achieved by using advanced signal enhancement techniques to study the structures, identify the hydrothermal alteration zones (that could serve as a pathway for mineralisation), and understand the geologic settings. Amongst the enhancement techniques are first vertical gradient, analytic signal, CET grid analysis and porphyry, Euler deconvolution, and K/Th ratio. The analytic signal reveals lithologic contact, structures and anomalous occurrences that aided the classification of the site into three magneto-lithologic zones: high (> 0.094 nT/m), intermediate (0.028 to 0.094 nT/m), and low magnetic zones (< 0.028 nT/m). The high magnetic zones (HMZ) were considered the main magnetic source outlines, which are inferred to be dominantly intrusive zones for hydrothermal activities. The 3-dimensional Euler deconvolution reveals highly magnetic and intrusive depth sources to be within the range of < 100 to 500 m. The Centre for Exploration Targeting (CET) grid technique revealed the structural distribution from which the lineament density map was produced. The orientations of the prevalent structural anomalies are E-W, NE-SW, WNW-ESE and NW–SE, with similar orientations observed from the first vertical gradient and the analytic signal. The highly dense structural zones coincide with the high magnetic zones and high-frequency amplitudes of the analytic signal and the vertical gradient map, respectively. Additionally, the CET porphyry detects the centres of the intrusive porphyries to be within zones of high lineament density. This reveals that the mineralisation potential of the area is structurally controlled. On the other hand, radioelement maps (eU, eTh, and K%) and ternary maps were used for lithological classification. The radiometric ternary map revealed the highly radioactive zones and the superior concentration of individual radioelements in their respective areas. The K/eTh ratio map delineates highly potassic alteration zones. The AHP model and weighted overlay tool were employed to integrate the analytic signal, lineament density, and K/Th ratio. Consequently, the mineralisation potential of the study site was revealed and classified into high, moderate, and low. This result was validated using known mine sites. There was a total agreement, with 87.5% of mines plotting within the high mineralisation potential class and 12.5% in the moderate class. Promising targets were identified for development.

Ore‐forming process within the Hongyuan reduced porphyry Mo–Cu deposit, West Junggar, NW China

The Hongyuan porphyry Mo–Cu deposit (PMCD) is a rare example of a “reduced” deposit, in contrast to classical oxidized porphyry Cu or Mo–Cu deposits. It is characterized by an ilmenite–series I–type felsic granitoid intrusion, reduced ore‐forming fluids with methane‐rich fluid inclusions, and widely distributed primary pyrrhotite. Mo–Cu mineralization in the Hongyuan PMCD occurs as disseminated in porphyry, granular in miarolitic cavity, and vein‐type in the quartz vein. These three types of mineralization are generally produced in the late magmatic period, magmatic‐hydrothermal transition period, and hydrothermal period, respectively. Molybdenite from miarolitic cavities shows a greater contribution from mantle fluid, as evidenced by mantle He proportions of 37.6%–16.8%. Molybdenite in quartz veins has relatively lower mantle He proportions of 1.63%–10.5%, indicating a predominantly crustal fluid source. The 3He/4He variations of these two groups of molybdenite illustrate an increasing input of crustal fluid during the magmatic to hydrothermal transition. Molybdenite samples from miarolitic cavities and quartz veins yield a Re‐Os model age of 300.5 ± 3.7 Ma, which is consistent with the U–Pb ages of zircons in the wallrock porphyries (300–302 Ma). This further indicates simultaneous diagenesis accompanied by mineralization. The Sr–Nd isotopic compositions (initial 87Sr/86Sr: 0.703404–0.703552; initial 143Nd/144Nd: 0.512585–0.512655; εNd[t]: +6.56 to +7.90) and young T2DM model ages (421–531 Ma) of the Hongyuan porphyries suggest that these rocks were derived from partial melting of the basaltic lower crust. We propose that mantle‐derived fluids rose up and mixed with fluids from the lower crust under an extensional tectonic setting, forming mantle‐like Sr–Nd–He–Ar isotopic compositions. The pre‐mineralization stage of the Hongyuan reduced PMCD is marked by quartz‐molybdenite ± K‐feldspar ± pyrite veins or veinlets and miarolitic cavities in the intensively potassic alteration zone. These veins formed at high temperatures (400–476°C) and high salinities (47.5–56.6 wt.%). The syn‐mineralization stage is the main metallogenic stage represented by numerous quartz‐molybdenite ± pyrrhotite veins associated with moderate to high temperatures (248°C–424°C) and low to high salinities (1.57–50.1 wt.%). The post‐mineralization stage is characterized by low temperatures (104–270°C) and low salinities (0.35–8.81 wt.%). Fluid immiscibility, mixing with meteoric water, ore fluid‐wall rock interactions, and decreasing temperature and salinity have played important roles during molybdenum mineralization.

Sulfide disseminations and hydrothermal alteration haloes in the Gabal Monqul area, Egypt: Field, mineralogical, and remote sensing studies

Field and mineralogical studies are integrated with multispectral and radar satellite data to unravel the occurrence of sulfide dissemination in the Gabal Monqul area (Eastern Desert, Egypt). This study was motivated by the strong belief that the widespread hydrothermal alteration haloes and sulfide disseminations in this area were ambiguously deciphered as a porphyry-style mineralisation. NE-Elongate bodies of silicified and sulfidized rocks frequently occur at the contacts between andesite-dacite, granodiorite, and porphyritic biotite granite intrusions.Hydrothermal alteration zones are best identified and outlined by employing band ratios (BR) and independent component analysis (ICA) techniques for the distinction between ferric and ferrous iron minerals. If fused with the clay and OH-bearing minerals maps, ferric iron oxides may characterise epithermal and porphyry mineralisation in which ore formation occurs under oxidising conditions. Iron-hydroxide, copper hydro-carbonate (malachite), and hydrous copper phosphate (pseudomalachite) are supergene mineral phases.The resultant processed images show that alteration extends beyond unit boundaries and overlaps different crosscutting lithologies. This observation implies that hydrothermal alteration of the host rock represents a secondary overprint, yet gypsum (±anhydrite) and barite in association with iron oxides and pyrite disseminations pinpoint a porphyry-related alteration assemblage. The poor metal endowment in the potassic alteration zones goes against the supergene enrichment typical of the porphyry mineralisation system and is coupled with the lack of hydrothermal breccia bodies, implying a rather epithermal sulfidation genesis. However, a thorough assay program is required to outline the potential metal-rich lithological unit(s) using XRD and remote sensing investigations that point to zonal alteration anomalies.

IDENTIFICATION OF AREAS OF HIGH POTENTIAL-BEARING MINERALIZATIONS, EASTERN DESERT OF EGYPT: INSIGHTS FROM AIRBORNE GAMMA-RAY SPECTROMETRIC DATA.

A major number of mineral deposits are related to hydrothermal processes. Therefore, the mapping of the hydrothermally alteration areas, connected with mineralization, is crucial in the search for metal deposits. To achieve this purpose, areas of hydrothermal alterations are targeted by processing the airborne gamma-ray spectrometric data to detect areas enriched in potassium that may indicate the existence of potassic alteration zones, which are often associated with hydrothermal alterations accompanied by mineral deposits. Data processing and analysis were performed using the K/eTh ratio, deviation of ideal potassium (Kd) and F-parameter. Besides, determining the environmental radiation risk due to the fact that the study area contains many excavation sites for various mining materials and quarries. Hydrothermal alteration indicator maps show five known mineralizations of gold, copper, molybdenum, fluorite and wolframite, which are associated with hydrothermal processes that took place in the study area. It is possible to note the intimate correlation of mineral deposits present in areas with high potassium content. Positive correlation between the computed hydrothermal alteration indicators (K/eTh, Kd and F-parameter), shown on the ternary image map, revealed favorable high and intermediate targets for the detection of various mineral deposits in the study area. On the other hand, the estimated mean values of absorbed dose rate for all rock units were within the permissible range (28-120 nGy h-1), and the mean annual effective dose rate was below the permissible limit of 1.0mSv y-1 for these rocks.

Geology, mineralization and calcite‐rich potassic alteration at the Humpa Leu East (HLE) porphyry Cu‐Au prospect, Hu'u district, Sumbawa Island, Indonesia

AbstractThe Humpa Leu East (HLE) prospect is one of the newly discovered porphyry Cu‐Au prospects in the Hu'u district, Sumbawa Island, Indonesia. The HLE prospect was formed by calc‐alkaline magmatic activity in an active continental margin setting. The prospect is typical calc‐alkaline porphyry Cu‐Au mineralization related to multiphase diorite and quartz diorite porphyry intrusions, which are hosted by andesitic crystalline tuff, volcanic breccia, and andesite lava. Hydrothermal alteration recognized at the surface includes potassic, propylitic, advanced argillic, intermediate argillic, and argillic alteration. Two styles of Cu‐Au mineralization were identified in the HLE prospect, that is, quartz‐sulfide veins and sulfide dissemination, formed in the early, intermediate, and late stages. The early stage is associated with M (magnetite ± bornite ± chalcopyrite), A (quartz + magnetite), and AB (quartz + magnetite + chalcopyrite ± pyrite) veins. These veins were mainly formed in the potassic alteration zone. The intermediate stage is characterized by B (quartz + chalcopyrite + pyrite) and C (chalcopyrite ± pyrite) veins and mainly associated with the chlorite‐sericite and sericite alteration zones. The late stage is mainly associated with D (calcite + gypsum + quartz + pyrite ± chalcopyrite ± sphalerite ± galena) veins with sericite‐chlorite alteration halo. Petrography and electron microprobe analyses indicate that calcite mainly replaced Ca‐rich plagioclase. Fluid inclusion petrography and Raman spectroscopy revealed that monophase vapor inclusions, as well as two‐phase (V + L) and multiphase (V + S + L) fluid inclusions contain CO2 gas. The potassic alteration with significant amounts of calcite is indicative of CO2‐rich fluids, which is uncommon in other porphyry Cu‐Au deposits. On the basis of textural and fluid inclusion analyses, calcite formed by a reaction between Ca‐rich plagioclase and CO2‐rich hydrothermal fluids. The CO2 in the hydrothermal fluids of the HLE prospect was likely derived from the magma.

Potassium silicate alteration in porphyry copper‑gold deposits: a case study at the giant maar-diatreme hosted Grasberg deposit, Indonesia

Potassium silicate alteration is a hallmark of the porphyry copper deposits that supply two thirds of the world's annual copper demand. These deposits formed in the cores of calc-alkaline to alkaline volcanic systems from the flux of magmatic gas that transported copper and other metals from source to the surface. The giant 3.2 Ma Grasberg CuAu deposit formed within a maar-diatreme complex following a resurgence in magmatism. The defined resources of this deposit occur from a few hundred metres depth to 1.7 km below the paleosurface which, uniquely in this deposit, is partially preserved as a section of maar tuffs.Potassium silicate alteration has commonly been interpreted as being the result of the addition of potassium to the porphyry copper host rocks via pervasive interaction with a large volume of a potassium-rich brine that is commonly presumed to be of magmatic origin. However, the data reported here show that alteration at the deposit scale is essentially isochemical with respect to the major rock-forming components and that only sulphur and the economic metals (Cu, Mo, Au, etc.) are added by flux of reactive magmatic gas containing SO2 and HCl from source intrusions at depth. Silicate solubilities are very low so that only a minor fraction of the total alkalis in the host rock are extracted by alteration reactions and then discharged at the paleo-surface. Reaction of the magmatic gas phase with plagioclase results in the coupled deposition of anhydrite (CaSO4) and disproportionation of SO2 to release H2S. The in-situ release of H2S immediately scavenges Cu and other chalcophile metals from the continuing magmatic gas flux to form the Cu-, Fe- and other sulphides that, in sufficient concentration, make up the economic reserve available to mining.The sequestration of Ca into anhydrite, along with deposition of silica into early quartz veins, increases the concentration of the other major components (K2O, Na2O, MgO, etc) in the remaining silicate assemblage within the porous host rock. The result is the development of intermingled potassium-enriched silicate and sulphur-rich (anhydrite-sulphide) sub-assemblages that constitute the mineralised phyllic or potassic alteration zones. These crystallise according to their pressure and depth into alteration assemblages dominated by potassic phyllosilicates, quartz and pyrite in the phyllic alteration zone, and alkali feldspar and phlogopitic-biotite plus minor andalusite and corundum in the central potassic zone. Dissolution and recrystallisation of primary magmatic biotite in the host rock releases K as well as Fe, the latter (along with amphibole and feldspar) providing iron for the formation of chalcopyrite, bornite and pyrite. The in-situ release of H2S through anhydrite formation, immediately scavenges Cu and other chalcophile metals from the continuing magmatic gas flux to form the CuFe sulphides that, in sufficient concentration, make up the economic reserve available to mining. Understanding of the alteration processes during porphyry copper formation also provides insights into gas-solid reactions processes inside active magmatic arc volcanoes but the magnitude of copper mineralisation is dependent on the original metal content of the source of the magmatic gas phase.

Дундговь болон Хэрлэнгийн төмрийн металлогений бүсэд тархсан төмрийн ордууд

Iron Oxide Apatite and Iron Oxide Copper Gold deposits generally consist of Fe and Cu-Au ore, and some deposits occasionally are recognized P, REE, Co, Ag and U. IOCG deposits are divided into magnetite and hematite subtypes by general ore mineral. Magnetite type IOCG has Na-Ca or, Na and potassic alteration zones, ore bodies are breccia and veins in shapes, ore-forming fluid was δ18O light supplied by magmatic and metamorphic waters. Hematite IOCG has a little potassic alteration zone, and ore bodies are formed breccia and lens in shapes in sericitic-chloritic alteration zone. Ore-forming fluid was δ18O heavy supplied by magma with a significant contribution of meteoric water. Banded Iron Formation is divided into Algoma, Superior and Rapitan sub types. The Algoma type BIF has δ18O of primary silica changed from +8‰ to +20‰ at temperatures below 100°C during diagenesis, indicating that although O isotope exchange occurs during diagenesis, low concentrations of rare earth and trace elements in siliceous shale do not change in ocean water-derived fluids. The Rapitan type, when the Earth’s oceans were almost completely covered by ice and cut off from the atmosphere, the ferruginous quartzite was deposited in the water at a time when the oceans were re-oxygenated. Prominent deposits of superior-type ferruginous quartzite occur in Paleoproterozoic sedimentary basins or in shallow-water sedimentary rocks of the continental shelf (Dartsagt, Ereen). Iron skarn deposits are divided into calcic, magnesian, and scapolite (albite) by their general chemical composition. Calcic iron skarn is developed at contact of carbonate bearing rocks and basic intrusion, and ore consists of magnetite, chalcopyrite, cobaltite, and pyrrhotite. Host rocks of magnesian iron skarn are typically dolomite, or limestone, quartzite, and schist associated with dolomitic. Ore minerals are recognized as magnetite, chalcopyrite, pyrite, sphalerite, arsenopyrite, and pyrrhotite in these type deposits (Bargilt). Host rocks are andesite, tuff, limestone, argillite at the scapolite (albite) iron skarn, then magnetite, hematite, pyrite, marcasite, chalcopyrite, sphalerite, pyrrhotite, and arsenopyrite are ore minerals.

Geochemistry and magnetite mineral properties in a porphyry copper prospect in A‐type granitoids: A case study from the Karbi Hills of Northeast India

This paper discusses the porphyry copper mineralization in A‐type granitoids from the Precambrian shield of the Karbi Hills (Mikir Hills), NE India. The prospective zone lies in the Kuthori‐Bagori of Kaziranga locality of the north Karbi Hills. The host granitoids are characterized by intermediate to high SiO2 (66.30–72.97 wt.%), Na2O (up to 4.90 wt.%), Ba (up to 1,943 ppm), Zr (up to 410 ppm), Y (up to 70 ppm) and Al2O3 (up to 14.77 wt.%) with low concentrations of CaO (up to 1.53 wt.%), and Cu (up to 32.41 ppm) which suggest a consistent granodiorite‐monzogranite host composition, an intraplate emplacement, A‐type chemistry, shoshonitic to high‐K calc‐alkaline and a predominant metaluminous character. Minerals in the investigated granitoids show hypogene alteration features similar to ideal porphyry style mineralization. Remnants of early chalcopyrite‐bornite‐magnetite (Magnetite‐I) veins have been preserved in the distant propylitic zone. The central core zone of potassic alteration shows the dominance of pyrite‐chalcopyrite‐magnetite (Magnetite‐II) assemblages. Mineral chemistry confirms the presence of two types of magnetites: magmatic (Mag‐I) and hydrothermal (Mag‐II). Mag‐I is octahedral, less commonly cubic, or irregular. It has a porous core with trellis‐type ilmenite exsolution lamellae. Mag‐II is non‐porous, devoid of ilmenite exsolution lamellae, has irregular to distinctly octahedral crystal habit and contains micro‐inclusions of pyrite, chalcopyrite, aluminosilicates, manganite and apatite. The progressive chemical purification of igneous magnetite, exacerbated by hydrothermal re‐equilibration, has resulted in a significant reduction in trace element contents such as Ti, Al, Mg, Zn and Cr, and a significant increase in iron content from 89 to ~94 wt.%. A combination of [Ni/(Cr + Mn) vs. Ti + V], and [(Ca + Al + Mn) vs. Ti + V] variation diagrams and upper threshold concentrations for the Kuthori‐Bagori ore effectively separates Mag‐I and Mag‐II. Our field, petrographic and geochemical data indicate that the Kuthori‐Bagori of Kaziranga granitoid of the Karbi Hills (Mikir Hills) in NE India is an ideal location for porphyry copper mineralization.

Mapping of favourable mining areas in the Tiouit area by multispectral remote sensing and airborne gamma-ray spectrometry coupled with geochemical data (Eastern Anti-Atlas, Morocco)

ABSTRACT The current investigation concern Tiouit region in order to perceive potential mining zones. Remote sensing data were the main component to process. In order to spot geochemical anomalies associated with the target zones, multispectral ASTER data, gamma-ray spectrometry, and stream sediment data were used. Crosta and SAM applications granted to map a spatial distribution of propylitic, phyllic, clay, and ferruginous alteration zones. The normalized ratios let the delineation of potassic alteration zones, including the Tiouit gold mine characterized by an intense alteration in the Ikniwn granodiorite. Thus, the potassic alteration zones are consistently co-located with the tectonic structures materialized by strong fracturing densities. The stream sediment geochemical investigation revealed that the cited areas have an important potential of mineralization, with high concentrations of As (136 g/t), Cu (91 g/t), Pb (141 g/t), Zn (392 g/t), Ag (3 g/t), Mo (11 g/t), Mn (0.2 g/t), and Fe (10.63 %).

Phase separation and fluid mixing revealed by trace element signatures in pyrite from porphyry systems

Porphyry deposits host various trace elements in economic amounts, but the hydrothermal processes causing their fractionation and enrichment are still not fully understood, but vital to target the most prospective mineralisation. We present the first micro-analytical study on the trace element composition of pyrite from the Koloula Cu-Au porphyry in the young and thin (<25 km) Solomon Islands arc. A statistical evaluation of the trace element data of pyrite indicates that mineral inclusions obscure the chemical signature of the mineralisation processes. The filtered pyrite data, from which the inclusions were excluded, correlate with variations in temperature and salinity, as defined by fluid inclusions from several alteration zones. Trace element ratios in pyrite show systematic variations with fluid temperature and salinity (Co/Ni, Se/Te), phase separation (Co/Ni, Co/As) and mixing of magmatic fluids and meteoric waters (Se/Ge). The mineralisation in the potassic alteration zone was controlled by the formation of a hypersaline liquid (Co/As > 1, Co/Ni > 50) from a magma-derived fluid (Se/Ge ~ 100) at lithostatic pressure conditions and temperatures of up to 700 °C (Se/Te > 50). This was followed by a transition to hydrostatic pressure conditions due to open-fracture continuity towards the paleo-surface, marking the onset of boiling in the chlorite-sericite to sericitic alteration zone (Co/As < 1), where minor proportions of meteoric water were involved (Se/Ge < 100). The shallowest part of the mineralisation is controlled by lower temperature (<300 °C, Se/Te < 50) vapour-rich fluids (Co/As < 1) that condensed into meteoric waters in an epithermal transition zone (Co/Ni < 50, Se/Ge < 100). Trace element systematics in pyrite from progressive alteration zones therefore preserve the time-space evolution of porphyry (-epithermal) systems in young and thin oceanic island arcs.

Evaluation of magnetite as an indicator mineral for porphyry Cu exploration: a case study using bedrock and stream sediments at the Casino porphyry Cu–Au–Mo deposit, Yukon, Canada

The trace element composition of detrital magnetite grains recovered from six local streams around the Casino high-grade porphyry Cu–Au–Mo deposit, west-central Yukon, is compared with igneous and magmatic-hydrothermal magnetite recovered from mineralized and unmineralized host rocks at the deposit. Linear discriminant analysis of 12 elements (Mg, Al, Ti, V, Mn, Co, Cr, Ni, Cu, Zn, Ga and Ge) and plots of Ti v. Ni/Cr are used to discriminate between magmatic-hydrothermal magnetite from the potassic alteration zone and igneous magnetite from granodiorite and quartz monzonite hosting the deposit. Magmatic-hydrothermal magnetite with a trace element composition similar to that from the potassic alteration zone at Casino is identifiable in stream sediments draining the deposit. Copper in magmatic-hydrothermal magnetite, present as minute inclusions of sulfide minerals such as chalcopyrite or substituted within the magnetite crystal lattice, is a strong indicator of Cu mineralization. We show that the chemical compositions of magnetite recovered from stream sediments can be used to explore for porphyry systems. Thematic collection: This article is part of the Applications of Innovations in Geochemical Data Analysis collection available at: https://www.lyellcollection.org/cc/applications-of-innovations-in-geochemical-data-analysis Supplementary material: Laser ablation data for major, minor and trace elements in magnetite from bedrock and stream sediment samples from Casino are available at https://doi.org/10.6084/m9.figshare.c.5896900

Evolution of ore-forming fluids in a post-collisional porphyry Cu-Au system: A case study from the Bučim deposit, Republic of North Macedonia

The Bučim porphyry Cu-Au deposit is situated in the westernmost part of the Serbo-Macedonian Massif, Republic of North Macedonia. The deposit is hosted by Precambrian gneisses with tectonically imbedded rare lenses of Palaeozoic amphibolites. The mineralization is spatially associated with intrusions of andesitic to trachyandesitic magmatic bodies. The geochemical signature of the intrusions and their radiogenic age suggest that the Bučim porphyry Cu-Au deposit represents a product of the Oligocene/Early Miocene post-collisional magmatic activity. The Vršnik intrusion, the youngest among four intrusions at the Bučim deposit, has not been subjected to later magmatic overprints and was therefore selected for studying the evolution of ore-forming fluids in post-collisional porphyry Cu-Au systems.The Cu-Au mineralization is spatially associated with hydrothermal alteration assemblages within and around the Vršnik intrusion. The infiltration of hot, near-neutral, oxidized, and highly saline and metal-rich aqueous solutions developed a mineralized potassic alteration zone. The fluid inclusion study suggests the formation temperature and pressure of 600-645⁰C and 0.675 kbar, respectively. This alteration zone is characterized by the replacement of amphibole with biotite and crystallization of hydrothermal biotite, magnetite, and hematite within the fine-grained groundmass of the intrusion. The oxidation of ferrous to ferric iron in this alteration zone has been recognized as a possible trigger for sulfate reduction and the consequent deposition of sulfide mineralization.The fluid inclusion study reflects that the barren phyllic alteration zone represents a product of infiltration of hot and saline fluids with a high metal-transport capability. Anyhow, sericitization and silicification suggest a low pH that might have played a significant role in preventing Cu deposition. The stable isotope composition of carbonates associated with the phyllic alteration zone point to a contribution of magmatic CO2.The mineralized chlorite alteration zone is mainly well developed along the contact between the intrusion and surrounding gneisses and reflects conditions of a high water/rock ratio. The fluid inclusion assemblages composed exclusively of vapor-rich inclusions indicate fluid flashing, probably associated with the transition from the lithostatic to hydrostatic regime at the point when the system cooled down to approximately 400⁰C. The liquid + vapor fluid inclusion assemblages point to dilution and cooling episodes, apparently related to mixing of ore-bearing fluids and meteoric water. The decrease in temperature as well as the decrease in the fluid salinity are associated with the mobility of metals transported in forms of their chloride complexes, including Cu, Au and Ag.The barren argillic alteration zone was developed under the influence of relatively cold and diluted fluids, with very limited capability for transport of metals. The water/rock ratio was relatively high but lower comparing the chlorite alteration zone.The presented study revealed that development of hydrothermal alteration zones and evolution of ore-forming fluids in post-collisional porphyry Cu-Au systems are comparable with those known from subduction-related magmatic arcs.

The Kultuma Au–Cu–Fe-Skarn Deposit (Eastern Transbaikalia): Magmatism, Zircon Geochemistry, Mineralogy, Age, Formation Conditions and Isotope Geochemical Data

The Kultuma deposit is among the largest and most representative Au–Cu–Fe–skarn deposits situated in Eastern Transbaikalia. However, its genetic classification is still a controversial issue. The deposit is confined to the similarly named massif of the Shakhtama complex, which is composed mainly of quartz monzodiorite-porphyry and second-phase monzodiorite-porphyry. The magmatic rocks are characterized by a low Fe2O3/FeO ratio, low magnetic susceptibility and belong to meta-aluminous, magnesian high-potassic calc-alkalic reduced granitoids of type I. The results of 40Ar-39Ar and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) U-Pb dating showed that the formation of magmatic rocks proceeded during the Late Jurassic time: 161.5–156.8 Ma. Relatively low Ce/Ce*, Eu/Eu* and Dy/Yb ratios in the zircons indicate that the studied magmatic rocks were formed under relatively reduced conditions and initially contained a rather low amount of magmatic water. A mineralogical–geochemical investigation allowed us to outline five main stages (prograde skarn, retrograde skarn, potassic alteration, propylitic (hydrosilicate) alteration and late low-temperature alteration) of mineral formation, each of them being characterized by a definite paragenetic mineral association. The major iron, gold and copper ores were formed at the stage of retrograde skarn and potassic alteration, while the formation of polymetallic ores proceeded at the stage of propylitic alteration. The obtained timing of the formation of retrograde skarn (156.3 Ma) and magmatic rocks of the Shakhtama complex, along with the direct geological observations, suggest their spatial–temporal and genetic relationship. The data obtained on the age of magmatic rocks and ore mineralization are interpreted as indicating the formation of the Kultuma deposit that proceeded at the final stages of collision. Results of the investigation of the isotope composition of S in sulfide minerals point to their substantial enrichment with the heavy sulfur isotope (δ34S from 6.6 to 16‰). The only exclusion with anomalous low δ34S values (from 1.4 to 3.7‰) is pyrrhotite from retrograde skarns of the Ochunogda region. These differences are, first of all, due to the composition of the host rocks. Results of the studies of C and O isotope composition allow us to conclude that one of the main sources of carbon was the host rocks of the Bystrinskaya formation, while the changes in the isotope composition of oxygen are mainly connected with decarbonization processes and the interactions of magmatic fluids, host rocks and meteoric waters. The fluids that are responsible for the formation of the mineral associations of retrograde skarns and the zones of potassic alteration at the Kultuma deposit were reduced, moderately hot (~360–440 °C) and high-pressure (estimated pressure is up to 2.4 kbar). The distinguishing features of the fluids in the zones of potassic alteration at the Ochunogda region are a lower concentration and lower estimated pressure values (~1.7 kbar). The propylitic alteration took place with the participation of reduced lower-temperature (~280–320 °C) and lower-pressure (1–1.2 kbar) fluids saturated with carbon dioxide, which were later on diluted with meteoric waters to become more water-rich and low-temperature (~245–260 °C). The studies showed that the main factors that affected the distribution and specificity of mineralization are magmatic, lithological and structural–tectonic ones. Results of the studies allow us to classify the Kultuma deposit as a Au–Cu–Fe–skarn deposit related to reduced intrusion.

Geochronology, geochemistry and Sr-Nd-Hf isotopes of the Heihuashan granite porphyry, NE China, and implications for Cu-Mo mineralization

Heihuashan is a newly discovered porphyry Cu-Mo prospect in Heilongjiang Province, northeastern China, with considerable Cu and Mo mineralization. Until now the ages of the Cu-Mo ores and the causative granite porphyry, the magma origin and characteristics, as well as the mineralization potential at depth are still unclear. In this contribution, whole rock geochemical and Sr-Nd isotopic compositions, zircon U-Pb ages and Hf isotopes, and molybdenite Re-Os dating, are presented to constrain the timing of the magmatism and mineralization, and the petrogenesis of the causative intrusion. The results also provide an opportunity for evaluating the potential of the deep Cu-Mo mineralization.Zircon U-Pb dating using LA-ICP-MS yields a crystallization age of 146.4 ± 1.8 Ma for the Heihuashan granite porphyry, which is consistent with the molybdenite Re-Os isochron age of 143.7 ± 3.1 Ma. These results indicate that the porphyry Cu-Mo mineralization at Heihuashan occurred at late Jurassic to early Cretaceous. The whole rockgeochemicaldatasuggest that the ore-related intrusion is mildly peraluminous and belongs to the high-Kcalc-alkalineseries, I-type granitoids. The granite porphyry samples are enriched in Rb, Ba, Th, U, and Sr, but depleted in Nb and Ta, showing typical arc magma affinities. They also have initial 87Sr/86Sr ratios of 0.70546–0.70550 and εNd(t) values between +0.4 and +0.7. The zircon εHf(t) values for the granitic intrusion range from +3.5 to +9.2, with two-stage Hf model ages of 977–614 Ma. The geochemical and Sr-Nd-Hf isotopic compositions suggest that the parental magma was dominantly derived from the slab-metasomatized mantle, which could have mixed with some lower crust components.The Fe2O3/FeO ratios of the Heihuashan granite porphyry are relatively high, ranging from 0.52 to 1.17, indicating a high magmatic oxidation state. This is also supported by the high zircon Ce/Ce*, Eu/Eu* and Ce/Nd ratios (33–2433, 0.22–0.70 and 2.4–44.0, respectively) and the high magmatic ΔFMQ values (+0.1 to +3.5 with an average of +2.1) calculated using the zircon trace elements. The intrusion has relatively high Sr/Y ratios (40–94) and displays negligible Eu anomalies (Eu/Eu* = 0.68–1.07); the zircons from the intrusion have high (Eu/Eu*)/Y (mostly > 0.0001) and (Ce/Nd)/Y ratios (mostly > 0.01), but low Dy/Yb ratios (generally < 0.4). These suggest that the fractionation of hornblende rather than plagioclase is dominant during the magma crystallization, which reveals a high magmatic water content. The above results indicate that the ore-related magma at Heihuashan is oxidized and hydrous, both of which are critical for porphyry Cu-Mo mineralization. The Heihuashan granite porphyry is geochemically similar to other Cu-related intrusions in NE China and also comparable to many porphyry Cu (-Mo) systems worldwide, implying a high Cu-Mo mineralization potential. Considering the surface and shallow levels at Heihuashan are characterized dominantly by sericite alteration, we suggest exploration and drilling focusing on the deeper levels beneath the currently mineralized domains, where major potassic alteration zones, likely associated with more extensive Cu-Mo mineralization, could be discovered.