Porphyry Type Research Articles

Exploring the dynamic mechanical response and mesoscopic characteristics of typical frozen rock in Yulong Copper Mine

Dynamic mechanical characteristic testing at low temperatures was conducted for the typical porphyry and sandstone specimens of Yulong Copper Mine in Tibet, China. The stress and strain characteristics of the specimens at different temperatures were analyzed. A dynamic constitutive model was developed by considering the initial damage. Furthermore, microscopic damage characteristics during the water-saturated rock freezing process were investigated using the PFC3D software, revealing the mechanisms of frost heave damage to rocks. The results indicated that the water-ice phase transition either enhanced or deteriorated the specimen strength at low temperatures. Specifically, freezing at −10°C and −20°C enhanced the strength of sandstone. However, freezing at −10°C enhanced the porphyry specimens, and freezing at −20°C caused significant frost swelling injury. The new constitutive equation effectively fitted the dynamic stress and strain curves for both specimens, highlighting their differences. The maximum contact force and particle contact in the frozen rock PFC3D model were affected by rock and water particle deformations. The frost swelling deformation of water particles had a more pronounced impact on specimen damage and was related to the temperature. A specific freezing temperature existed at which the increase in saturated rock strength corresponded to the maximum specimen strength at that temperature.

Element Migration of Mineralization-Alteration Zones and Its Geological Implication in the Beiya Porphyry–Skarn Deposit, Northwestern Yunnan, China

Porphyry and the associated skarn-type deposit is one of the most important types of ore deposits worldwide, which usually exhibit significant zoning of mineralization-alteration, but the research on element migration in these mineralization-alteration zones is relatively weak. The Beiya porphyry–skarn gold-polymetallic deposit is a super-large Cenozoic deposit located in the Sanjiang metallogenic belt, northwestern Yunnan, China. In this paper, through a detailed analysis of mineralization and alteration zoning and its element migration regularity, the findings are as follows: (1) Three types of hydrothermal alteration—porphyry alteration, contact alteration, and wall-rock alteration—are developed, and porphyry alteration includes potassic, phyllic, propylitic, and argillic alteration; (2) five types of mineralization—porphyry-type Cu–Au–(Mo), skarn-type Au–Fe–(Cu), hydrothermal vein-type Au–Fe, distal hydrothermal-type Pb-polymetallic, and oxidizing-leaching enriched-type Au—occur in a diversity of forms, which are dominantly controlled by structures and lithologies; (3) concentric-banded mineralization-alteration zones are exhibited centrally from the alkaline porphyry outward or upward, namely [porphyry alteration] potassic → phyllic → propylitic → argillic → [contact alteration] skarnitization–marbleization → [wall-rock alteration] marbleization–silicification–calcitization; (4) porphyry-type mineralization predominantly forms within potassic and phyllic zones, while skarn-type mineralization occurs in contact alteration zones, and proximal and distal hydrothermal (vein)-type mineralization are commonly distributed in marbleization–silicification–calcitization alteration zones; and (5) element migration analysis demonstrates a significantly lateral and vertical zoning in the metallogenic element association of Cu–Mo → Cu–Au → Au–Fe–Cu → Au–Fe → Pb–Zn–Au–Ag–Fe from alkaline porphyry outward to the wall-rock. The mineralization-alteration zoning model indicates the Beiya deposit has similar mineralization and alteration zone characteristics to the typical porphyry copper system; and element migration within mineralization-alteration zones provides new scientific information for understanding the metallogenic regularity and prospecting at Beiya, as well as the similar types of deposits in the Sanjiang metallogenic belt and elsewhere in the world.

Formation conditions and geochemistry of the Tütün Tepeleri (Baskil-Elazig/Türkiye) Fe-oxide-Cu-Au (IOCG) mineralization

The Tütün Tepeleri Fe-Oxide-Cu-Au (IOCG) mineralization is located in the Eastern Taurus Mountains (Baskil-Elazığ/Turkey) and it is associated with Baskil magmatites (diorite, gabbro and tonalite) cut by Late Cretaceous Bilaser Tepe magmatites (quartized diorite, granite, granodiorite, tonalite porphyry, monzosyenite, monzonite, aplite and diorite porphyry). Baskil Magmatites are Coniacian-Santonian (82–86 Ma), calc-alkaline in character and I-type. Bilaser Tepe Magmatics are Campanian (73–74 Ma) and represent an extensional environment after the collision of oceanic arc and the Taurus platform. In this study, the Sodic-calcic alteration zone in the Tütün Tepeleri region, which was determined as Porphyry type mineralization by different researchers, was determined for the first time and the mineralizations were evaluated in terms of Fe-Oxide-Cu-Au (IOCG) deposits. Three types of alteration zones have been identified in the region, including the sodic-calcic alteration zone. These are sodic-calcic (tremolite-actinolite, albite, epidote, chlorite, magnetite), potassic (biotite, quartz, chlorite, K-feldspar, anhydrite) and sericitic (sericite, carbonate, quartz, chlorite, illite) alterations. Sodic-calcic alteration is more widespread in the region than >1 km2, reaches thicknesses of 500 m, and is occasionally overlain by potassic alterations, just like similar Fe-Oxide-Cu-Au (IOCG) deposits in the world. Tütün Tepeleri mineralizations are in the form of rare magnetite veins with intense magnetite dispersion within the sodic-calcic alteration developed in diorites. Mineral paragenesis is in the form of magnetite, molybdenite, pyrite, arsenopyrite, chalcopyrite, sphalerite, galena, hematite, malachite and azurite, and Ti content in magnetites is determined as 0.13–0.64%. Fe content is 20.13% on average. Formation temperatures in fluid inclusions measured in ore-bearing quartz veins are 320.3 °C on average and salinity is 11.32% NaCl equivalent on average. Isotope analysis results of these mineralizations show δ34Spyrite = 6–8.9; δ34Sc.pyrite = 3.8–5.5; δ18Oquartz was determined in the range of 10.8–13.2 and δD = (−37) – (−53). When the alteration types determined with isotope analysis results showing that the mineralization occurred in a magmatic-hydrothermal system, the low Ti content in the magnetites, the formation temperature and salinity values are evaluated together, it was anticipated that Tütün Tepeleri mineralization is an example of Fe-Oxide-Cu-Au (IOCG) deposits formed in a hydrothermal-magmatic system.

Geology and Ore Mineralization Characteristics of the Selodong Prospect, Lombok Island, Indonesia

Abstract The Selodong prospect is located in the southwest sector of Lombok Island which tectonically lies within the W-E trending Sunda-Banda magmatic arc, which hosts various gold-base metal mineralizations including porphyry and epithermal deposits. Lombok Island, particularly southwestern portion of the island is known to hosts gold, silver and copper prospects, including Selodong prospect. The Selodong prospect is divided into several sub-prospect areas which include the Blongas, Montong Botek, Kekalik and Belikat. However, this study only focuses on the Blongas sub-prospect. The study is aimed to discusses the geology, characteristics of alteration and mineralization of the sub-prospect. To achieve the objective, some methods such as mapping and numerous laboratory works were conducted. Petrography to identify alteration minerals, ore microscopy to identify type of ore minerals, and fluid inclusion microthermometry to characterize ore fluid were performed. The geological conditions of the study area are composed of andesite lava, andesite breccia, diorite intrusion and alluvial deposit. Typical porphyry alteration type i.e., potassic is present. Argillic, silicic, advanced argillic, propylitic and phyllic alterations are also identified. The distribution of potassic and some argillic alteration is controlled by lithology, while silicic alteration, advanced argillic, propylitic and some argillic alterations are controlled by geological structures with an NW-SE and NE-SW trending patterns. Propylitic alteration is characterized by chlorite + epidote + calcite ± clay. Argillic alteration is marked by the presence of clay minerals such as clay + quartz. Advanced argillic alteration is typified by quartz + alunite + pyrolusite ± paragonite. Phyllic alteration is typified by sericite + quartz ± clay. Potassic alteration is marked by secondary biotite + quartz ± clay. Silicic alteration is marked by quartz + pyrolusite + epidote. Ore mineralization in the study area is associated with massive and stockwork vein textures. Ore and metalliferous minerals are found as magnetite, chalcopyrite, pyrite, hematite, goethite, jarosite, sphalerite, pyrrhotite, chalcocite and native gold. Generally, homogenization temperatures in the research area range from 543 - >600 °C, with salinity of 26.3 - 73.95 wt.% NaCl eq associated with potassic alteration, whereas homogenization temperatures range from 251 to 349 °C, with salinity of 5.46 - 8.38 wt.% NaCl eq. associated with silicic alteration. Based on those characteristics, the prospect in the study area indicates a porphyry deposit type, which is transition to high sulfidation epithermal.

Contrasting mineralized and barren porphyries in the Zhongdian Arc, insights from biotite and apatite compositions and halogen fugacity.

Copper mineralization in the Pulang (PL) porphyry deposit, Langdu (LD) porphyry-skarn deposit and Songnuo (SN) porphyry prospect in northwestern Yunnan, China, is closely related to the emplacement of quartz monzonite porphyries. The chemical compositions of biotite and apatite from those porphyries were analyzed to calculate the halogen fugacity and to constrain mineralized and barren porphyries. Our data show that biotites from the PL deposit have higher MgO, SiO2, TiO2 and F contents than those from the LD deposit or SN prospect. Compared to those in the LD deposit and SN prospect, the Mg (atoms per formula unit (apfu)) and AlVI (apfu) value in biotite is greater, and the F content is greater and the SO3 and Ce2O3/Y2O3 ratio in apatite are lower in the PL deposit. Ti-biotite thermometry and apatite-biotite geothermometry show that the crystallization temperature of biotite from the PL deposit is higher than that from the SN prospect or LD deposit. The results suggest that oxygen fugacity, magmatic sulfur, and H2O contents cannot be used to efficiently distinguish the PL deposit from the LD deposit and SN prospect. However, the halogen chemistry of biotite from the PL deposit is distinctly different from that of the LD deposit or SN prospect according to the lower IV (F), indicating that mineralized quartz monzonite porphyries in the PL deposit formed during the late magmatic stage, which is in contrast to those in the LD deposit and SN prospect. The mineralized porphyries display a remarkable negative linear relationship (r = -0.96) with the log (f HF/f HCl) and log (f H2O/f HF) ratio, which can be used to distinguish the mineralized and barren porphyries. Compared with other typical porphyry Cu systems, there is a remarkable positive linear relationship between IV (Cl) and log (f H2O/f HCl). In addition, the linear slope and intercept for log (f H2O/f HCl) ratios and the IV (Cl) of biotite from the potassic and phyllic alteration zones are significantly greater than those from other porphyries.

Quartz fluid inclusions and trace elements in the Lailisigaoer porphyry Mo deposit, Western Tianshan, Xinjiang: Fluid evolution and metallogenic mechanism in magmatic-hydrothermal system

The Lailisigaoer deposit is a typical porphyry Mo deposit located in the late Paleozoic Boluokenu metallogenic belt of Western Tianshan, NW China. This study aims to understand molybdenum mineralization and the dynamics of magmatic-hydrothermal fluid within the porphyry system, focusing on fluid inclusion, cathodoluminescence textures, and trace elemental composition in various generations of quartz. Six vein types in the Lailisigaoer deposit are classified as comb quartz veins with unidirectional solidification texture (UST, QI), actinolite/biotite ± quartz veinlets (M-type, QII), quartz-chalcopyrite vein (A-type, QIII), quartz-molybdenite vein (B-type, QIV), quartz-pyrite vein (D-type, QV) and quartz-carbonate vein (E-type, QVI). Micro thermometry data indicate decreasing homogenization temperatures in primary fluid inclusions from UST to E-type veins. The magmatic-hydrothermal fluids associated with UST and M-, A-, B-, D-, E-type veins underwent a transition from high temperature (342–495℃), high-pressure (∼1.25 kb), and variable salinity (6.7–41.1 wt%NaCl) in the H2O-CO2-NaCl system to low-temperature (142–238℃), low-pressure (∼0.25 kb), and low-salinity (1.6–5.1 wt%NaCl) in the H2O-NaCl system. This evolution is reflected in the proportion of quartz with oscillatory zones decreasing and irregular quartz increasing, indicating a shift from turbulent to stable fluid conditions. Furthermore, a gradual reduction in Ti concentration (from 79 ppm in UST to 1.4 ppm in E-type quartz) suggests a decrease in fluid temperature during the magmatic-hydrothermal evolution. Mineralization primarily occurs in A- and B-type veins, with molybdenum precipitation attributed to fluid immiscibility in a medium–high temperature (240–368 ℃) and high pressure (∼0.95 kb) environment. The A-type veins (mean 31 ppm in Ti concentrations) consist of equigranular (dark-core) (QIII-1) and patchy inhomogeneous CL-gray quartz (QIII-2). The B-type veins (mean 24 ppm in Ti concentrations) are characterized by equigranular (bright-core) inhomogeneous quartz (QIV-1) with growth zones that are cemented by later mosaic homogeneous CL-gray quartz (QIV-2). Based on the quartz-Ti thermometer, the mineralized veins (A- and B-type) were confined to be formed at depths of 2.8–3.6 km, with molybdenum mineralization occurring at 3.4–3.6 km. Molybdenum mineralization initiates during the QIV-1 crystallization period in magmatic-hydrothermal fluids and terminates in the QV-2 generation.

Trace and minor elements in the ore minerals: An assessment of geochemical distribution in overprinting epithermal on porphyry mineralization at Chodarchay, NW Iran

The Chodarchay overprinting epithermal on porphyry mineralization occurs in the Tarom-Hashtjin subzone of the Alborz magmatic arc in northwestern Iran. Rock units include intrusions (phases I and II) and volcano-volcaniclastic rocks. The alteration types consist of potassic, phyllic, argillic, and propylitic. The porphyry type is mostly accompanied by potassic alteration. The Chodarchay Fault implies two extensional and compressional mechanisms. The porphyry type is associated with the extensional and the epithermal type with the compressional stage of the fault. Mineralization occurred mainly inside the Eocene volcanic and volcano-sedimentary rocks; some ores are associated with the Late Eocene quartz monzonite. The mineralization is divided into three zones from depth to surface: 1) Hypogene sulfide zone (deep); 2) Enriched supergene sulfide zone (near-surface); 3) Oxidized and leached zone (surface). The major sulfide minerals consist of chalcopyrite, pyrite, sphalerite, and galena. Based on the results of the new analyses, chalcopyrite hosts Ag as a solid-solution and contains Ag-rich Bi-sulfosalt micro-inclusions. Non-constant Cd/Zn ratio in the chalcopyrite can indicate varying physiochemical conditions during its crystallization. Low As contents in the pyrite caused relatively clean pyrite with very few elements. The Ni concentrations in the pyrite imply that it was sourced from mantle mafic–ultramafic rocks. Sphalerite is the only Au-host mineral among the sulfide minerals as a nano-mineral phase. Solid-solution Ag exists in the sphalerite. The sphalerite Fe/Zn ratios show that it was precipitated between 220 and 280 °C. Silver and Bi have the highest measured concentrations among all analyzed elements in the galena, mainly partitioning within the galena, but Hg and Cd are abundant in the sphalerite. Bornite is one of the major carriers of Ag and Bi. Silver and Bi exhibit considerable variations in the Cu-(Fe) sulfides. A new occurrence of sulfosalt minerals was identified at Chodarchay (N = 14). The discovered Bi-sulfosalts include cuprobismuthite group minerals (cuprobismuthite, hodrushite, and paderaite), aikinite-bismuthinite series (aikinite and friedrichite), emplectite, makovickyite, galenobismutite, gustavite, heyrovskyite, neyite, cupropavanite; and As-Sb-bearing Cu sulfosalts (watanabeite and colusite). This number of sulfosalts had not previously been reported from any of the Tarom or Alborz deposits or mines. The Au-Ag occurrence was reported from the neyite, emplectite, and gustavite. The Ag-rich minerals crystallize from fractionated fluids that cooled during rising. Silver-carrier sulfosalts may have been exsolution from pre-existing Ag-bearing chalcopyrite in the cooling system. Most of the Ag-bearing sulfosalt minerals formed at the margins and fractures of the chalcopyrite, indicating that the cooling started from these points. Thus, Ag at Chodarchay is hosted inside Cu-(Fe) sulfides, the significant part of them being chalcopyrite and Ag-rich sulfosalt micro-inclusions inside the chalcopyrite. The fluid temperature for the Ag and chalcopyrite precipitation is from 200 to 350 °C. Bismuth assemblages precipitated at > 350 °C. The cuprobismuthite group crystallizes at temperatures > 300 °C. The supergene process and rare secondary enrichment of Ag and Au took place in the oxidation zone; this enrichment is dependent on the presence of manganese. Based on the fire-assay results, the concentration of gold is greater at shallower depths.

Molybdenum and gold distribution variances within Iranian copper porphyry deposits

This study aims to differentiate between Cu-Mo and Cu-Au porphyry deposits within Iran through fractal modeling, utilizing the Mo/Au geochemical index as a primary determinant. Employing the Concentration-Number (C-N) fractal model, the Mo and Au values within Iranian copper porphyry deposits were comprehensively classified. The findings from the fractal modeling reveal distinct criteria for separating these deposits. Cu-Mo porphyry deposits are identified by Mo concentrations ≥141 ppm, while Cu-Au porphyry deposits are characterized by Au concentrations ≥398 ppb. The pivotal threshold for the Mo/Au ratio stands at 1585, facilitating the division between these distinct types of porphyry deposits. Within the Urumieh-Dokhtar magmatic arc, numerous Cu-Mo porphyry deposits, exemplified by globally recognized sites like Sarcheshmeh and Sungun, are prevalent. Conversely, Cu-Au porphyry deposits are found in the NW and SW regions of the Urumieh-Dokhtar magmatic arc and eastern Iran, typified by occurrences like Dalli. The study's findings reveal a correlation between geological characteristics and the ages of porphyry deposits, indicating that those formed during the Miocene period and later are predominantly of the Cu-Mo (Copper-Molybdenum) porphyry type.

Mineral Geochemistry of Apatite in the Jiama Porphyry‐Skarn Deposit, Tibet and its Geological Significance

AbstractThe Jiama deposit, a significant porphyry‐skarn‐type copper polymetallic deposit located within the Gangdese metallogenic belt in Tibet, China, exemplifies a typical porphyry metallogenic system. However, the mineral chemistry of its accessory minerals remains under‐examined, posing challenges for resource assessment and ore prospecting. Utilizing electron microprobe analysis and LA‐ICP‐MS analysis, this study investigated the geochemical characteristics of apatite in ore‐bearing granite and monzogranite porphyries, as well as granodiorite, quartz diorite, and dark diorite porphyries in the deposit. It also delved into the diagenetic and metallogenic information from these geochemical signatures. Key findings include: (1) The SiO2 content, rare earth element (REE) contents, and REE partition coefficients of apatite indicate that the dark diorite porphyry possibly does not share a cogenetic magma source with the other four types of porphyries; (2) the volatile F and Cl contents in apatite, along with their ratio, indicate the Jiama deposit, formed in a collisional setting, demonstrates lower Cl/F ratios in apatite than the same type of deposits formed in a subduction environment; (3) compared to non‐ore‐bearing rock bodies in other deposits formed in a collisional setting, apatite in the Jiama deposit exhibits lower Ce and Ga contents. This might indicate that rock bodies in the Jiama deposit have higher oxygen fugacity. Nevertheless, the marginal variation in oxygen fugacity between ore‐bearing and non‐ore‐bearing rock bodies within the deposit suggests oxygen fugacity may not serve as the decisive factor in the ore‐hosting potential of rock bodies in the Jiama deposit.

Study on Process Mineralogy of the Combined Copper Oxide Ore in Tibet and Acid Leaching Behavior with Calcium Fluoride

The Yulong copper deposit in Tibet is a typical porphyry copper deposit, with about 30 million tons of copper oxide ore in the surface layer. However, more than 40% of the copper resources are in a combination state, resulting in an extraction efficiency of only 50% for copper via the hydrometallurgical process. In this study, the process mineralogy of the combined copper oxide ore was systematically investigated and a calcium fluoride-enhanced leaching process is proposed to increase the leaching efficiency of the combined copper ore. The process mineralogy of the combined copper oxide ore was analyzed using various testing techniques, including chemical analysis, X-ray diffraction, and a process mineralogy parameter testing system (Mineral Liberation Analysis). The results revealed that limonite accounted for 86.12% of the sample, and 63.51% of the copper resource existed in the form of combined copper oxide in limonite. However, it is difficult for the uniformly distributed combined copper oxide in limonite to sufficiently make contact with sulfuric acid, which is the leaching agent, resulting in low copper leaching efficiency. The enhanced leaching behavior of the combined copper oxide ores was also investigated, thereby determining effective and economical enhanced leaching conditions. Under optimal conditions, at a grinding fineness ratio of −0.074 mm (accounting for 85%), liquid-solid ratio of 4:1, sulfuric acid concentration of 50 g/L, temperature of 30 °C, CaF2 dosage of 1% of the ore mass, and leaching time of 4 h, the copper leaching efficiency increased to 60.57%, which was 7.34% higher than that of atmospheric pressure leaching. Finally, the enhanced leaching slag was analyzed using an electron probe microanalyzer. It indicated that fluorine ions can erode the combined copper oxide ore and facilitate the diffusion of hydrogen ions inside the limonite, thereby achieving a strengthening effect.

Zircon U-Pb and Whole-Rock Geochemistry of the Aolunhua Mo-Associated Granitoid Intrusion, Inner Mongolia, NE China

The Aolunhua Mo deposit is a typical porphyry deposit, which is located in the middle southern section of the Da Hinggan Range metallogenic belt. Here, we report LA-ICP-MS zircon U-Pb age data from the Mo-associated granitoid, together with the element geochemistry of the zircons, discussing the source material of the ore-forming rock of the deposit. The zircon data constrain the crystallization age of the granite porphyry as 135.0 ± 1.0 Ma, correlating it with the widespread Yanshanian intermediate–felsic magmatic activity. The Th/U ratio of the zircon is greater than 0.1, with a significant positive Ce anomaly (Ce* = 1.72–188.71) and a negative Eu anomaly (Eu* = 0.05–0.57). The zircons show depleted LREE and enriched HREE patterns, as well as low La and Pr contents, suggesting crystallization from crust-derived magmas. Based on the geology of the ore deposit and the age data, in combination with the regional geodynamic evolution, we infer that the Aolunhua Mo deposit was formed near the peak stage of Sn poly-metallic metallogenesis in the Da Hinggan Range region at around 140 Ma, associated with a tectonic setting, characterized by the transition from compression to extension. Based on a comparison with the newly found Mo deposits along the banks of the Xilamulun River, we propose that the Tianshan–Linxi is an important Mo-metallogenic belt. It also suggests an increased likelihood for the occurrence of Mo along the north bank of the Xilamulun River.

Tracing metal source of copper-rich tungsten mineralization: Evidence from individual fluid inclusion analysis of the Huangsha Cu-rich W deposit in South China

The Huangsha Cu-rich W deposit, located in the northeast part of the Nanling region, is a typical large-size wolframite-quartz vein-type W deposit with considerable reserves of copper. Wolframite and chalcopyrite usually distribute in the same quartz veins, while field and petrographic observation show that wolframite commonly precipitates earlier than coexisting quartz and sulfides. Veined quartz can be divided into three successive generations (Q1, Q2, and Q3) based on SEM-CL imaging, and only Q2 is strictly coeval with chalcopyrite and other sulfides. Primary two-phase aqueous (type Lw) fluid inclusions are identified from wolframite with homogenization temperatures of 292 to 327 ℃ and salinities of 6.9 to 9.9 wt% NaCl equiv. Pseudosecondary two-phase aqueous (type Lq) and vapor-rich (type Vq) fluid inclusions are recognized from Q2, supporting the occurrence of fluid immiscibility. Homogenization temperatures of type Lq inclusions in Q2 range from 200 to 258 ℃ with salinities of 4.3 to 7.7 wt% NaCl equiv. LA-ICP-MS analysis shows that all inclusions contain Na and K as the major cations. For all the detected elements, type Lw inclusions in wolframite have higher concentration ratios X/Na than type Lq inclusions to varying degrees. The ore-forming fluid in both W and Cu mineralization stages share the same characteristics of high B concentrations, consistent Rb/Cs ratios and evolving nature of ore metals, indicating that W and Cu were sourced from the same magmatic fluid but precipitated in different mineralization stages. The variation of fluid Sr concentration likely indicates fluid-rock interaction during precipitation of wolframite, whereas the deposition of chalcopyrite is possibly influenced by fluid cooling and immiscibility. Compared with typical porphyry Cu systems and W/Sn mineralized systems worldwide, the ore-forming fluid in the W mineralization stage at Huangsha shows considerably higher mineralization potential of Cu, which is consistent with the geological fact. The Cu contents in initial W ore-forming fluids may serve as an indicator in identifying Cu-rich W deposits.

The Yubileinoe Porphyry Gold–Copper Deposit (Western Kazakhstan): Geological Position and Conditions of Formation

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.

Distinctive Features of the Major and Trace Element Composition of Biotite from Igneous Rocks Associated with Various Types of Mineralization on the Example of the Shakhtama Intrusive Complex (Eastern Transbaikalia)

This article presents data on the composition of biotite from igneous rocks of the Shakhtama complex, which are associated with various types of mineralization in Eastern Transbaikalia: Au-Cu-Fe-skarn, skarn-porphyry, Mo-porphyry, rare-metal–greisen, Au-polymetallic and Au-Bi. The major element and halogen contents were determined by EPMA. The content of trace elements was determined by means of LA-ICP-MS. As a result, the specific traits of the composition of the biotite of igneous rocks associated with specific types of mineralization of the Eastern Transbaikalia were determined. The biotites of rare-metal–greisen deposits are characterized by the maximum content of fluorine (>2 wt. %) and low chlorine content (<0.04 wt. %). In addition, such biotites are characterized by high XFe (>0.47). Within Eastern Transbaikalia, igneous rocks developed at the Bystrinsky deposit are potentially ore-bearing for the “classic” porphyry type of mineralization. They have the highest values of IV(F/Cl) (4.9–7.1) and IV(F) (2–2.8) and the lowest values of Log(XMg/XFe) (0.1–0.4). The trace element composition clearly distinguishes biotites from rare-metal–greisen deposits and is identified by the highest contents (ppm) Ga > 65, Li > 600, Sn > 20, Mn > 2000, Cs > 50, Zn > 600. Biotites of Au-polymetallic and Au-Bi deposits occupy an average position between rare-metal–greisen and Mo-porphyry ones. Biotites of Mo-porphyry deposits differ in minimum values (ppm) of Sn < 3, Zn < 160, and low values of Li (150–290), V (290–440), and Ga (39–48). In general, the chemical composition of biotites shows that the degree of igneous rock fractionation of deposits increases in the series: porphyry–skarn–polymetallic–rare-metal.

Mineral chemistry and apatite Sr isotope signatures record overprinting mineralization in the Duobaoshan porphyry Cu deposit, Heilongjiang Province, NE China

Porphyry copper deposits can be deformed by subsequent magmatic-tectonic-metamorphic evolution, resulting in the remobilization of pre-existing ores and the consequent overprinting mineralization. This process might potentially increase the ore grade and/or resource. We focus on the Duobaoshan porphyry Cu (Mo) deposit, two periods were identified in this study, i.e., porphyry period (including Stage 1: potassic alteration; 2: propylitic alteration, and 3: chlorite-sericite alteration and porphyry mineralization) and overprinting period (including Stage 4–1: ductile–brittle deformation; Stage 4–2 and Stage 4–3: overprinting mineralization). Metal sulfide veins occur along the schist in Stage 4–2 and Stage 4–3, features that differ from the typical porphyry mineralization of Stage 3 (veinlets, stockworks, and dissemination). Here, we present in situ Sr isotope data for apatite and compositions of chlorite, epidote, and apatite to reveal the source and nature of fluids and mechanism of precipitation during overprinting mineralization. The in situ 87Sr/86Sr ratios of apatite from Stages 3, which range from 0.7030 to 0.7046, are slightly higher than those observed in the Ordovician granodiorite. Meanwhile, the Sr isotope ratios for apatite from Stages 4–2 and 4–3 are 07033–0.7040 and 0.7013–0.7045 respectively. These ratios broadly consistent with those of the surrounding Ordovician granodiorite and basaltic andesite, suggesting that the ore-forming fluids for all these stages originated from magmatic sources. Chlorite in Stage 4–2 has a higher Mn, Co, Ni, Zn content compared to chlorite in Stage 3, 4–3, whereas epidote and apatite in Stage 4–2 have higher Ca, Sr, Pb content compared to those in Stage 3, 4–3, implying that the fluids in Stage 4–2 underwent strongly water–rock reactions and extracted metal elements from surrounding rocks. Copper was only detected in Stage 4–3 chlorite (15.13–500.20 ppm) and epidote (7.91–19.29 ppm), indicating a high concentration of copper in the fluid, and due to the pre-existing magnetite dissolution, chlorite, epidote, and apatite in Stage 4–3 exhibit high V and Fe relative to other stages. Fluid mixing likely occurred during Stage 3, leading to the precipitation of copper. Strong water-reaction in Stage 4–2 produce changes in fluid natures that facilitate sulfide deposition during this stage. While in Stage 4–3, copper precipitation is controlled by a combination of rising pH and changing sulfur content and valence. Our study highlights that in the Duobaoshan deposit, late magmatic-hydrothermal fluids remobilized pre-existing ore bodies, and the copper precipitation mechanisms differed during the main copper mineralization events.

Zircon U-Pb Ages, Petrogenesis, and Tectono-Magmatic Evolution of Late Jurassic–Early Cretaceous S-Type Granitoid in Wujinshan Area of Northwestern Zhejiang, South China

Northwest Zhejiang area (NWZJ) is one of the important parts of the large Qingzhou-Hangzhou mineralized belt in South China formed during the Late Jurassic–Early Cretaceous period. Through the study of zircon LA-ICPMS U-Pb dating, whole-rock geochemistry, and Sr-Nd isotopes for the Wujinshan granitoid in NWZJ, two distinct S-type granitic rocks of porphyry type granodiorite and granite were identified, and the two ages of 146.4 ± 1.5 Ma for granodiorite porphyry and 141.9 ± 1.4 Ma for granite porphyries were obtained. These rocks exhibited a geochemical affinity for S-type granitoid, and the two magmatic ages indicate that these rocks were intruded in two magmatic pulses. The Late Jurassic granodiorite porphyry showed moderate SiO2 (64.38–67.89 wt.%) with higher K2O + Na2O (6.22–6.78 wt.%), lower K2O/Na2O (0.57–0.96), moderate Zr (170–215 ppm), high Sr (302–475 ppm), and low Mg# (31–32) contents. The Early Cretaceous granite porphyries contained high SiO2 (69.68–74.85 wt.%), variable K2O + Na2O (4.60–6.99), high K2O/Na2O (1.72–23.53), slightly higher Zr (160–255 ppm), variable Sr (25–412 ppm), and very low to intermediate Mg# (13–44). The granodiorites had intermediate ∑REE (149–177 ppm), while granite samples showed moderate to high ∑REE content (147–271 ppm), and both rocks showed negative Eu anomalies (0.18–0.29). We propose that these two rocks were predominantly generated by the partial melting of Mesoproterozoic metamorphic basement and underwent variable degrees of fractionation and evolution. The Late Jurassic granodiorite porphyry was formed by the partial melting of Mesoproterozoic metamorphic basement with slab-derived melts or basaltic lower crust input following fractional crystallization, while the Early Cretaceous granite porphyries were generated by the partial melting of Mesoproterozoic metamorphic basement and crystal fractionation with variable magma mixing and assimilation in the upper crust. Tectonically, the Wujinshan granitoid formed in a volcanic arc setting largely affected by the subduction and slab rollback of the paleo-Pacific Plate.

The Role of Reductive Carbonaceous Surrounding Rocks in the Formation of Porphyry Mo Deposits

Porphyry Mo deposits are the most important type of Mo resource. They result from a high oxygen fugacity of the parent magma, which acts as an effective indicator for evaluating the mineralization. In the ore-forming system of porphyry Mo deposits, sulfur exists mainly as sulfate in highly oxidized magma but as sulfide in ores. What triggers the reduction in the mineralization system that leads to sulfide precipitation has not yet been determined. Most of the previous studies have focused on the origin and evolution of the ore-forming parent magma, and the effects of reductive surrounding rocks on porphyry mineralization have been ignored. In this study, a comprehensive geological–geochemical investigation and review have been performed on the typical porphyry Mo deposits, the Nannihu-Sandaozhuang, Yuchiling, and Shapingou deposits in China, and the Mt. Emmons deposits in America. Black carbonaceous sedimentary layers commonly surround porphyry Mo ores, which are widely altered and discolored during mineralization. CH4 is commonly present in fluid inclusions in the main mineralization stage, and the δ13CV-PDB values of calcite and fluid inclusions from the altered surrounding rocks and ore minerals are generally low and significantly different from those of marine sedimentary carbonate rocks, indicating that the involvement of reductive components from carbonaceous surrounding rocks might be key to the redox state transformation leading to mineral precipitation. On the other hand, the CH4 produced by the thermal decomposition of organic matter or carbonaceous reaction with H2O can diffuse into the ore-forming system along the structural fractures and reduce the SO42− in the ore-forming hydrothermal fluids to form sulfide precipitation without direct contact between the intrusion and the carbonaceous surrounding rocks. Moreover, the CH4 content controls the location of the orebody formation with the high content producing orebodies mainly in the porphyry intrusion, while the low CH4 content results in the orebodies mainly occurring at the contact zone between the porphyry and carbonaceous surrounding rocks. Compared to the magmatic stage of mineralization, the involvement of reductive components in the carbonaceous surrounding rocks during the hydrothermal stage is more favorable for forming giant/large Mo deposits. The highly oxidized porphyry with reductive carbonaceous surrounding rocks or Fe-rich volcanic rocks offers a new indicator for efficiently evaluating porphyry Mo mineralization.

Evaluation of the impact of the intensive exploitation of groundwater and the mega-drought based on the hydrochemical and isotopic composition of the waters of the Chacabuco-Polpaico basin in central Chile

A hydrogeochemical and isotopic study has been carried out to understand the hydrogeological functioning of a small alluvial aquifer in central Chile in a context of mega-drought and intensive exploitation of its waters. Additionally, two mine tailings dams from porphyry copper mining are situated in the area. The prolonged mega-drought, which has lasted for over thirteen years, has resulted in a significant decrease in rainfall recharge and a drop of up to 50 m in piezometric levels, although no serious groundwater contamination problems have yet been detected, except for a rise in nitrate contents (ranging between 23 and 45 mg/L NO3) attributed to return irrigation. Groundwaters are calcium-bicarbonate and calcium-sodium-bicarbonate in composition. The values of δ18O and δ2H of the alluvial aquifer indicate fractionation by evaporation that would be explained by the recirculation of water that occurs in the agricultural areas of the basin, where the excess irrigation water that go back to the aquifer presents fractionation by evaporation. The δ34S and δ18O of dissolved sulfate point to pyrite oxidation, which could be related to the pyrite present in the copper porphyry and recognized in the Andes Cordillera. The 87Sr/86Sr isotopic values of the alluvial aquifer waters are close to the isotopic fingerprint of the volcanic rocks of the Abanico Formation. However, the water from the wells located further downstream in the basin and close to the tailing dams show δ34S and δ18O of dissolved sulfate and 87Sr/86Sr consistent with Miocene intrusive mineralogies of the copper porphyry type. The groundwater chemistry does not show water seepage from the tailings dam. Therefore, a minor contribution of minerals related to the intrusive rocks is proposed, which would originate from the movement of fine particles by the wind from the dams to the valley floor. The 14C activities indicate that groundwater is recent.

Petrogenesis and Mo(W) mineralization of deep porphyritic granites in the Laowan ore field, Eastern Qinling, Central China

The Laowan ore field of the Tongbai district is a crucial metallogenic belt within Eastern Qinling, including super large gold (Au) and large molybdenum (Mo) deposits. However, the Au and Mo metallogenic relationship and tectonic setting are still disputed. Petrology, geochemistry, and geochronology were conducted on the 3000 m scientific drilling hole, ZKE1012, south of the Laowan ore field. A concealed porphyritic granite with Mo mineralization was observed at a depth of 1717 m. The concealed porphyry comprises K-feldspar, plagioclase, quartz, biotite and minor magnetite, ilmenite, rutile, apatite, and zircon. Molybdenite, scheelite, pyrite, and chalcopyrite are immersed in the rock as veinlet-dissemination, showing typical porphyry mineralization characteristics. Zircon U–Pb data define that the deep rock was formed at 131.0 ± 2.1 and 133.2 ± 1.0 Ma, consistent with the molybdenite Re–Os age (130 Ma), indicating that the Mo mineralization was related to the porphyry. The rocks are characterized by high silica (SiO2 = 70.5–76.8 wt%), high alkali (Na2O + K2O = 8.55–9.25 wt%), and metaluminous to weakly peraluminous (A/CNK = 0.99–1.09). They are enriched with large ion lithophile elements (Rb, Y, Th, Ce, Sm, and Zr), depleted in Nb, Ba, and Sr, and show negligible Eu anomalies. The deep porphyries belong to I-type granite, and their zircon εHf(t) values are from − 11.2 to − 5.7. Therefore, the concealed porphyritic granite and its mineralization are the product of partial melting of the basements, mixing minor mantle materials caused by the subduction of the Paleo–Pacific Plate to Eurasia in the Early Cretaceous.

Multiple tectonic switches in the Eastern Tianshan, Central Asian Orogenic Belt: Implications for crustal growth and metallogenesis

Subduction zones are crucial sites for inputs of juvenile crust and the generation of porphyry copper deposits by arc magmatic processes that generally involve episodic trench advance and retreat. It is well documented that the generation of juvenile crust is associated with lithospheric extension during the retreat of subduction zones, whereas crustal reworking is associated with lithospheric compression in continental arcs during the advance of subduction zones. However, it remains unclear whether such models can be applied to island arc settings and how they relate to metallogenesis. To address this issue, we examine intermediate–felsic igneous rocks (∼460–300 Ma) of the Dananhu–Harlik island arc in the southern Central Asian Orogenic Belt. Our new and compiled data indicate three magmatic episodes in the Dananhu–Harlik island arc during the northward subduction of the Kangguer oceanic plate, with each involving a tectonic switch from compressional trench advance to extensional retreat. Crustal growth occurred mainly during the compressional stages of trench advance, which is in contrast with typical continental arcs. Tectonic transitions also controlled regional mineralization patterns, and the typical porphyry and related skarn-type deposits formed during subduction zone advance, whereas volcanogenic massive sulfide (VMS) deposits and overprinting mineralization were generated during subduction zone retreat. A combination of all data on tectonic settings and physical–chemical conditions (e.g., temperature, oxygen fugacity, and water content) of the pre-mineralization and ore-related intrusions led us to the conclusion that normal intra-crustal arc magmatic processes, involving sulfide pre-enrichment and reactivation, generated the typical Tuwu–Yandong porphyry Cu deposits in the Dananhu arc without the prerequisite of slab melting. Our study provides an excellent example of crustal growth in an island arc setting as well as metallogenesis during the repeated advance and retreat of a subduction zone.