Ore Fluids Research Articles

Contrasting Tectonomagmatic Conditions for Coexisting Iron Oxide-Apatite Deposits and Porphyry and Skarn Cu ± Au Deposits in the Middle-Lower Yangtze River Metallogenic Belt, China

Abstract Porphyry Cu ± Mo ± Au and iron oxide-apatite (IOA) deposits rarely occur in spatial and temporal proximity in Phanerozoic arc-related settings, and the formation of these mineral deposit types in an evolving arc setting remains poorly understood. Specifically, the roles of magma composition and the tectonic regime remain the subject of some debate. Here, we systematically estimated the P-T-fO2 conditions and H2O-S-Cl contents for dioritic to granodioritic source magmas for porphyry and skarn Cu ± Au (150–135 Ma) and IOA deposits (~130 Ma) that formed in transpressional and transtensional settings in the Middle-Lower Yangtze River metallogenic belt, China. Our estimates show that, compared to IOA deposits, the porphyry- and skarn-related magmas were relatively felsic, cooler, and more hydrous. These geochemical features are consistent with the tectonic transition from subduction to slab rollback of the paleo-Pacific plate in the East Asia continental margin at <135 Ma and concomitant crustal extension and steepening of the regional geothermal gradient. Apatite data reveal that the silicate melts associated with the porphyry and skarn Cu ± Au and IOA deposits had comparable predegassed S concentrations (~0.13 ± 0.06 wt % vs. ~0.16 ± 0.09 wt % on average), but that IOA-related melts contained higher predegassed Cl/H2O ratios (~0.11 ± 0.03 vs. ~0.04 ± 0.03 for porphyry- and skarn-related magmas) that decreased by one order of magnitude after magmatic degassing. Magmatic fO2 estimated using zircon and amphibole, reported in log units relative to the fayalite-magnetite-quartz (FMQ) redox buffer, gradually increased during cooling of the porphyry- and skarn-related magmas (ΔFMQ +0.7 to +2.5) at 950° to 800°C and decreased to ΔFMQ +1 at 700°C owing to fractionation of Fe2+-rich minerals and subsequent S degassing, respectively. In contrast, the magmatic fO2 values for the IOA-related source magmas varied significantly from ΔFMQ –1.5 to ΔFMQ +2.5 but generally show an increasing trend with cooling from 970° to 700°C that probably resulted from variable degrees of evaporite assimilation, fractionation of Fe2+-rich minerals, and Cl degassing. These results are consistent with the hypothesis that Cl enrichment of the IOA-related source magmas played a determinant role in their formation. We propose that the porphyry and skarn Cu ± Au deposits in the Middle-Lower Yangtze River metallogenic belt formed in a transpressional setting in response to paleo-Pacific flat-slab subduction that favored storage and evolution of S-rich hydrous ore-forming magmas at variable crustal levels. A subsequent extensional setting formed due to slab rollback, leading to rapid degassing of Cl-rich IOA-related magmas. For the latter scenario, assimilation of evaporite by mafic to intermediate magmas would lead to an enrichment of Cl in the predegassed magmas and subsequent exsolution of hypersaline magmatic-hydrothermal fluid enriched in Fe as FeCl2. This Fe-rich ore fluid efficiently transported Fe to the apical parts of the magma bodies and overlying extensional normal faults where IOA mineralization was localized. The concomitant loss of S, H2O, and Cu with Cl by volcanic outgassing may have inhibited sulfide mineralization at lower temperatures.

Genesis of a sediment-hosted vein-type Cu deposit in the Lanping Basin, SW China: New insights from geology and LA–ICP–MS analysis of fluid inclusions

Sediment-hosted Cu deposits, including stratiform and epigenetic vein-type Cu deposits, are the second largest source of Cu worldwide. However, many facets of these vein-type Cu deposits, such as the nature and origin of ore fluids and geodynamic mechanisms that produced these fluids, remain controversial, limiting our interpretations of the ore genesis and hampering the selection of exploration strategies. Numerous sediment-hosted vein-type Cu deposits are present in the Lanping Basin, SW China, of which the Jinman deposit is the largest. Copper orebodies at Jinman consist of Cu-sulfide–quartz–carbonate veins and altered wall-rocks hosted mainly in faults and fracture zones in metamorphosed and deformed clastic rocks. The deposit was formed in three stages, pre-, syn- and post-ore, with the first two stages producing hydrothermal veins. The veins in pre-ore stage consist of quartz + ankerite ± sericite ± pyrite, whereas those in syn-ore stage consist of Cu-sulfides + quartz + carbonate ± sericite. During the syn-ore stage, tennantite, quartz, and ankerite crystallized early, then bornite was precipitated, followed by chalcopyrite and chalcocite and finally calcite. Only minor sericite was formed during the post-ore stage. Two major types of fluid inclusions—CO2-rich and aqueous inclusions—are present in both pre- and syn-ore quartz, whereas only aqueous inclusions are present in syn-ore calcite. In pre- and syn-ore quartz and calcite, CO2-rich inclusions have higher homogenization temperatures (275–323 °C) and pressures (307–3495 bar) and lower salinities (0.22–2.7 wt% NaCl eqv.) than aqueous inclusions (164–299 °C, 6.5–80.4 bar and 3.7–20.9 wt% NaCl eqv.). However, the small variations in Cs/Na and Cs/(Na + K) ratios [log Cs/Na = –3.3 ∼ –1.9, log Cs/(Na + K) = –3.3 ∼ –2.1] of the fluid inclusions suggest a same source for the ore fluids. We propose that during both stages, CO2-rich inclusions resulted from unmixing of initial deep-seated, single-phase CO2-rich fluids, whereas aqueous inclusions likely represent the fluids that evolved from these unmixed fluids by extensive CO2 degassing. This interpretation, combined with microthermometric results of CO2-rich inclusions, suggests a mesothermal, low-salinity H2O–NaCl–CO2 ore fluid system. The fluid inclusions from Jinman have similar compositions to those of metamorphic fluids, suggesting a metamorphic origin for the ore-forming fluids. The evolution of fluid compositions suggests that fluid degassing likely acted as a major mechanism for Cu precipitation. We propose that the ore fluids were generated through metamorphic devolatilization of basement of the Lanping Basin in the Biluoxueshan–Chongshan metamorphic zone under a compressional or transpressional regime caused by Cenozoic India–Asia collision. The Jinman deposit has many similarities to orogenic gold deposits worldwide and thus can be thought of as an orogenic deposit. Based on a compilation of the geological characteristics of global sediment-hosted epigenetic vein-type Cu deposits, we suggest that other sediment-hosted epigenetic vein-type Cu deposits with similar genesis to the Jinman deposit are likely present in other regions worldwide. This highlights the exploration potential of this type of deposit in these regions and the need for further research.

Geology and ore fluids geochemistry of the Hamzeh–Gharanin orogenic gold deposit, NW Iran

The Hamzeh–Gharanin gold deposit (HGD) is located in the Qolqoleh–Kasnazan shear zone in the northwest of Sanandaj–Sirjan Zone (SSZ) and 40 km SW of Saqez. The main rock units are an assemblage of the Precambrian metasedimentary (pelitic) rocks and the Cretaceous phyllite associated with marble interlayers. The post–Cretaceous intrusive granitoids with NW–SE trends intruded within these two units. Mineralization occurs mainly within the NE–SW extensional veines and veinlets in proto–mylonitic, mylonitic and ultra–mylonitic rocks. Hydrothermal alterations consist of sericitization, carbonatization, silicification and chloritization. The main ore minerals include pyrite, chalcopyrite, arsenopyrite, pyrrhotite, sphalerite, galena, gold, magnetite and hematite. The fluid inclusions study from quartz minerals associated with the mineralization shows four different phases: single vapor phase (V; type I), single liquid phase (L; type II), liquid–vapor biphasic (LV; type III) and three phases (LLV; type IV). Microthermometric studies were performed on types III and IV of fluid inclusions. Homogenization temperatures (Th) for Types III and IV inclusions vary between 138 and 310 °C (mean 230 °C) and 250–335 °C (mean 300 °C) and their salinity varies between 0.52 and 13.87 and 4.79 to 9.58 (wt% NaCl), respectively. Moreover, the density of Types III and IV inclusions vary from 0.71 to 0.927 g/cm3 and 0.700–0.870 g/cm3, respectively. The oxygen (in quartz: 4.58–7.80 ‰; mean 5.82 ‰) and δ34S (in pyrite: 5.54–6.28 ‰; mean 5.91‰) isotope compositions of the mineralizing fluids indicate an insignificant meteoric water input during hydrothermal evolution and a magmatic origin of sulfur in the deposit which is broadly similar to those of orogenic gold deposits worldwide.

Gold source and deposition in the Sanakham gold deposit, SW Laos: Constrains from textures, trace element geochemistry and in-situ sulfur isotopes of pyrite

The Luang Prabang (Laos) – Loei (Thailand) metallogenetic belt is endowed with major porphyry-skarn, and epithermal gold deposits. The Sanakham gold deposit is a newly discovered hydrothermal vein-type orogenic gold deposits (10.6 t Au @ 3.05 g/t) in the belt, and consist of a series of quartz-sulfide veins that are controlled by secondary structures of the regional NNE-trending brittle-ductile shear zone. Its mineralization can be divided into four stages: (I) quartz–pyrite–arsenopyrite, (II) quartz–pyrite–pyrrhotite–chalcopyrite, (III) quartz–pyrite–base-metal sulfide, and (IV) quartz–carbonate. Three pyrite generations were identified: py1 (stage I) as disseminated euhedral to subhedral coarse grains; py2 (stage II) as subhedral to anhedral fine grains occur around the cataclastic and corrosion textures in py1; py3 (stage III) as subhedral to anhedral fine grains occurred in sulfide veins or veinlets that overprint the existing quartz-sulfides. All three generations of pyrite have low trace-element contents including very low lattice-bound gold (py1: 0.040 ppm; py2: 0.098 ppm; py3: 0.028 ppm) and arsenic (py1: 227 ppm; py2: 133 ppm; py3: 13.3 ppm) contents. Visible gold grains are sited in textures of pyrite grains that relate to brittle cataclastic deformation. Considering the relatively low contents of pyrite in the ores of Sanakham, it is impossible to derive the high-gold grade orebodies through local remobilization of originally lattice-bound gold in pyrite. The py2 might be formed during hydrothermal overprinting and dissolution of py1 led by continuous supply of ore fluids with relatively higher contents of Au, Ag, Cu, Sb, Te, Pb, and Bi. A reduction reaction related to reduced carbon species in wallrock is an assignable cause for gold deposition, even though the fluid-rock interaction and fluid immiscibility processes might be important. The Au- and As-poor pyrites have similar δ34S values (py1: –2.58 to –0.83 ‰; py2: –2.17 ‰ to + 0.25 ‰; py3: –1.24 to –0.60 ‰ ppm) that close to 0 ‰, indicating the sulfur may have been originated from magmatic or mantle sources. Therefore, we propose that the Sankham gold deposit is a member of the orogenic deposit class, but notably characterized by the low concentrations of invisible gold in the relatively As-poor pyrite lattice.

Geochemistry, Mineralization, and Fluid Inclusion Study of the Bayan-Uul Porphyry Au-Cu-(Mo) Deposit, Central Mongolia

The Bayan-Uul porphyry Au-Cu-(Mo) deposit occurs within the Mongol–Okhotsk Orogenic Belt, which is a part of the Central Asian Orogenic Belt. To understand geotectonic, petrogenesis, mineralization, and ore-forming fluid evolution of the Bayan-Uul deposit, we report petrographic and geochemical analyses of host rocks, mineralogy of ores, and fluid inclusion characteristics. Based on petrographic and mineralogical analyses, Cu, Mo, and Au mineralization occurs as disseminated and sulfide-bearing quartz–tourmaline veins hosted within granodiorites, monzodiorites, and diorite porphyry and tourmaline breccia. Four main alteration assemblages are identified: potassic, phyllic, argillic, and quartz–tourmaline alteration. The ore mineralogy of quartz–tourmaline veinlets are classified into A-type veinlets (quartz + tourmaline + chalcopyrite + magnetite + pyrite ± electrum), B-type veinlets (quartz + tourmaline + molybdenum + chalcopyrite + pyrite), and C-type veinlets (quartz + tourmaline + pyrite ± chalcopyrite). Fluid inclusions are found in quartz–tourmaline veinlets consisting mainly of liquid-rich two-phase (L-type), vapor-rich two-phase (V-type), and solid-bearing multi-phase (S-type) inclusions. The homogenization temperatures for the fluid inclusions in A-type, B-type, and C-type veinlets range from 215 to 490°C, 215 to 500 °C, and 160 to 350 °C and their salinity varies from 5.4 to 43.5 wt.%, 16 to 51.1 wt.%, and 3.4 to 24.1 wt.% NaCl equivalent, respectively. Coexistance of (L-type), (V-type), and (S-type) inclusions support fluid boiling. The δ18O values of ore fluids from different mineralizing A-, B-, and C-type veins are 8.7‰, 10.9‰, and 8.4‰, respectively, and the δ34S values of sulfide minerals range from −1.4‰ to 5.3‰, which indicates magmatic origin.

Spatio-temporal fluid evolution of gold deposit in the Jiaodong Peninsula, China: A case study of the giant Xiling deposit

The Xiling gold deposit (>592 t @ 4.02 g/t) in the eastern Zhaoyuan-Laizhou gold belt of the Jiaodong Peninsula, is currently the largest gold deposit and deepest gold mine in China. This study presents microthermometric fluid inclusions data on quartz gangue, as well as trace element and S isotope data on pyrite from different mineralization stages and depths in the Xiling gold deposit to provide new insights into the spatio-temporal evolution of the ore-forming fluid that led to a giant Early Cretaceous gold deposit in the Jiaodong Peninsula. The δ34S values of pyrite range from 7.5 to 15.2 ‰, but vary temporally and spatially, reflecting a changes in physicochemical conditions as the ore-forming fluid migrated to different crustal levels over time, also suggesting Precambrian basement as the principal sulfur source. Trace element analyses of pyrite revealed that ore-forming metals were scavenged from the wall rock and then incorporated into the pyrite. Fluid inclusions data reveal that the ore-forming H2O-CO2-NaCl ± CH4 fluid had a medium to high temperature (283–401 °C), medium-low salinity (1.91–8.00 wt% NaCl equivalent), analogous to most gold deposits in the Jiaodong Peninsula. Intensive interaction between the ore-forming fluid and wall rock changed the physicochemical conditions of fluid, leading to gold precipitation. The study supports the notion of the ore fluid of Jiaodong-type gold deposit having originated from a metasomatized lithospheric mantle.

Geology and geochronology of the Yingqian granite-type uranium deposit in the Taoshan-Zhuguang Belt, South China

The Yingqian uranium deposit in the Taoshan-Zhuguang belt, South China is a typical granite-type uranium deposit. The geological characteristics and timing of mineralization are not clear, which hinders the understanding of the ore genesis of the Yingqian deposit as well as regional uranium metallogeny in the Taoshan-Zhuguang belt. These scientific problems are examined in this study through detailed field work and petrographic study, as well as geochemical and geochronological analyses on apatite, rutile and zircon. The orebodies of the Yingqian uranium deposit are mostly present in the medium–coarse grained biotite granite and fine grained two-mica granite, and controlled by the NE-trending faults. The principle U-bearing minerals are pitchblende and brannerite, with the presence of metal minerals like pyrite, hematite and minor galena and sphalerite. The predominant hydrothermal alterations are hematitization, fluoritization, illitization, silicification, chloritization and carbonatization. Gangue minerals are mainly quartz, fluorite, illite and calcite. Moreover, four hydrothermal stages can be recognized in the Yingqian deposit, and the second and third stages are the uraniferous ones. The alterations and mineral assemblages indicate ore fluids are acidic, oxidized, and rich in F, P, CO2, which is favorable for dissolving uranium. Abundant apatite and rutile are discovered in the uraniferous third-stage veins. Geochemical analyses indicate that rutile is plotted in the hydrothermal area in the Ti-100 (Fe + Cr + V)-1000 (W) ternary diagram, and apatite is classified as fluorapatite. In-situ LA-ICP-MS dating indicates that the ore-hosting medium–coarse grained biotite granite and fine grained two-mica granite obtain the zircon U-Pb ages of 160.0 ± 0.3 Ma and 164.1 ± 0.6 Ma, which are consistent with many Jurassic granites in the South China Block. The hydrothermal apatite and rutile yield the U-Pb ages of 96.4 ± 11.6 Ma and 85.6 ± 10.8 Ma, respectively, indicating that uranium mineralization is significantly younger than the ore-hosting granites and generally coeval with the regional mafic magmatism. Consequently, the uraniferous fluids in the Yingqian deposit are independent from the magmatic system. Combined with previous research, it is concluded that fluid convection promoted by mantle–crust interaction would leach uranium from various lithologies, and fluid-rock interactions, fluid boiling and cooling are the causes for uranium precipitation.

Precipitation of Ag-Pb-Zn ores of the Poshan vein deposit in the Qinling orogen (central China) by dilution of magmatic hydrothermal fluids

Abstract Constraints on the source, nature, and evolution of ore-forming fluids are crucial for better understanding the ore genesis and mechanisms that lead to metal precipitation. Here, we present results of in situ analysis for quartz oxygen isotopes and sulfide sulfur isotopes, combined with apatite U-Pb age and fluid inclusion data, to provide insights into the source and evolution of ore fluids of the Poshan Ag-Pb-Zn vein deposit in the Qinling orogen, central China. Quartz-carbonate-sulfide veins at Poshan are hosted in lower Paleozoic metavolcanic-sedimentary rocks and structurally controlled by fracture zones associated with the Heqianzhuang anticline. The Ag-Pb-Zn mineralization consists of three stages, which are represented by quartz-pyrite-arsenopyrite (stage I), quartz-carbonate-sulfide-silver minerals (stage II), and quartz-calcite ± native silver (stage III). Apatite texturally associated with galena from stage II has a U-Pb age of 125 ± 14 Ma (2σ; mean square of weighted deviates [MSWD] = 0.9), which suggests that the Poshan deposit formed in the Early Cretaceous and thus significantly postdated the Paleozoic and early Mesozoic orogenic deformation of the Qinling orogen. Aqueous-carbonic fluid inclusions from stages I and II have similar total homogenization temperatures of 263–347 °C and calculated salinities of 1.2–5.1 wt% NaCl equivalent, whereas the values for liquid-dominated aqueous inclusions from stage III are 211–245 °C and 0.5–3.0 wt% NaCl equivalent. Five quartz generations are recognized from the three paragenetic stages, including Qz-1 and Qz-2 from stage I, Qz-3 and Qz-4 from stage II, and Qz-5 from stage III. Based on in situ secondary ion mass spectrometry oxygen isotopic analysis of the five quartz generations (Qz-1 to Qz-5), the calculated δ18Ofluid values for the ore fluids are 7.8‰ to 9.2‰ (mean 8.3‰), −3.2‰ to 8.7‰ (mean 5.6‰), −3.5‰ to 7.4‰ (mean 4.6‰), −4.5‰ to 7.6‰ (mean −0.2‰), and −6.4‰ to 1.4‰ (mean −3.8‰). The oxygen isotopic data and trend among the five quartz generations are best interpreted to represent magmatically derived ore fluid being diluted by modified meteoric water to cause mineralization. Fluid mixing is considered to be the principal mechanism that led to Ag-Pb-Zn precipitation at Poshan. Sulfides coexisting with the quartz generations have δ34SV-CDT values of −1.7‰ to 4.4‰, with no systematic variations among different paragenetic stages. These data, combined with apatite U-Pb age and geologic relations, provide additional evidence for a magmatic origin of the Poshan Ag-Pb-Zn deposit, as inferred from the oxygen isotopes. This study highlights the role of fluid dilution in triggering Ag-Pb-Zn deposition, and sheds light on the origin of silver-polymetallic deposits in orogenic belts.

Hyper-enrichment of gold via quartz fracturing and growth of polymetallic melt droplets

Abstract Gold precipitation in hydrothermal systems is traditionally attributed to supersaturation of gold due to decreasing gold complex stability triggered by changes in physicochemical conditions of the ore fluid. However, ultrahigh-grade gold veins in orogenic (shear zone related) gold deposits can contain kilograms per tonne of gold or more, in marked contrast to the typically very low gold concentrations (tens of parts per billion) in fluid. The gold mineral assemblage is commonly restricted to native gold and/or Au-(Ag)-tellurides and occurs in micro-fractures of sheared quartz veins. Textural and compositional characterization of such assemblages, coupled with hydrothermal diamond anvil cell experiments and heating-freezing experiments, provides evidence for an alternative ultrahigh-grade gold enrichment mechanism via growth of polymetallic melt droplets induced by quartz fracturing. We propose that polymetallic melt droplets of Au-Ag-Te-Bi–rich composition form through adsorption-reduction of metal complexes on fractured quartz surfaces, where surface silanol groups and hydrogen serve as reductants. The melt droplets subsequently grow by catalyzing reduction of metal complexes and absorbing metals from fluids percolating in the fractured quartz network. The mobile and reactive polymetallic melt droplets can repeatedly react with the fluid on protracted quartz fracturing and efficiently continue to scavenge gold from multiple pulses of gold-undersaturated ore fluids.

Magmatic-hydrothermal fluid evolution of the tin-polymetallic metallogenic systems from the Weilasituo ore district, Northeast China

The large Weilasituo Sn-polymetallic deposit is a recent exploration discovery in the southern Great Xing’an Range, northeast China. The ore cluster area shows horizontal mineralization zoning, from the inner granite body outward, consisting of high-T Sn–W–Li mineralization, middle-T Cu–Zn mineralization and peripheral low-T Pb–Zn–Ag mineralization. However, the intrinsic genetic relationship between Sn-W-Li mineralization and peripheral vein-type Pb–Zn–Ag–Cu mineralization, the formation mechanism and the deep geological background are still insufficiently understood. Here, we use fluid inclusions, trace elements concentrations in quartz and sphalerite, and H–O isotope studies to determine the genetic mechanism and establish a metallogenic model. Fluid inclusion microthermometry and Laser Raman spectroscopic analysis results demonstrates that the aqueous ore-forming fluids evolved from low-medium salinity, medium–high temperature to low salinity, low-medium temperature fluids. Laser Raman spectroscopic analysis shows that CH4 is ubiquitous in fluid inclusions of all ore stages. Early ore fluids have δ18OH2O (v–SMOW) values from + 5.5 to + 6.2‰ and δD values of approximately − 67‰, concordant with a magmatic origin. However, the late ore fluids shifted toward lower δ18OH2O (v–SMOW) (as low as 0.3‰) and δD values (~ − 136‰), suggesting mixing between external fluids derived from the wall rocks and a contribution from meteoric water. Ti-in-quartz thermometry indicates a magmatic crystallization temperature of around 700 °C at a pressure of 1.5 kbar for the magmatic ore stage. Cathodoluminescence (CL) imaging and trace element analysis of quartz from a hydrothermal vug highlight at least three growth episodes that relate to different fluid pulses; each episode begins with CL-bright, Al-Li-rich quartz, and ends with CL-dark quartz with low Al and Li contents. Quartz from Episode 1 formed from early Sn-(Zn)-rich fluids which were likely derived from the quartz porphyry. Quartz from episodes 2 and 3 formed from Zn-(Sn)-Cu-rich fluid. The early magmatic fluid is characterized by low fS2. The SO2 produced by magma degassing reacted with heated water to form SO42−, causing the shift from low fS2 to high fS2. The SO42− generated was converted to S2– by mixing with CH4-rich, Fe and Zn-bearing external fluid which led to late-stage alteration and dissolution of micas in vein walls, thus promoting crystallization of pyrrhotite, Fe-rich sphalerite and chalcopyrite and inhibiting the precipitation of anhydrite. This study shows that ore formation encompassed multiple episodes involving steadily evolved fluids, and that the addition of external fluids plays an important role in the formation of the later Cu–Zn and Ag–Pb–Zn mineralization in the Weilasituo ore district.

Overview of early cretaceous gold mineralization in the orogenic belt of the eastern margin of the Siberian craton: geological and genetic features

The giant Verkhoyansk-Kolyma gold province, producing more than∼ 3700 t of gold, is one of the most important metallogenic provinces for orogenic gold deposits in the world. The province is located on the eastern margin of the Siberian craton. The main types here are multistage orogenic Au-As and orogenic-like Au-Sb types of mineralization, related to the Late Jurassic-Early Cretaceous metallogeny and the evolution of the convergent margin. These deposits were formed in the environment of late orogeny during two metallogenic stages—the Late Jurassic-Early Cretaceous collision-related (early stage/stage one, 135–150 Ma) and the Early Cretaceous subduction-related (late stage/stage two 114–130 Ma). The common features, differences and genetic nature of the deposits of these two metallogenic stages have been debated for a long time. To improve the understanding of these problematic issues and the genesis of deposits, and control over them by the mantle lithosphere, we consider here the Early Cretaceous orogenic belts of the eastern margin of the Siberian craton. Orogenic belts are related to the development of the paleo-Arctic and paleo-Pacific margins of Siberia. The tectonic, geochronological, mineralogical and geochemical specificity of the deposits of the orogenic belts are shown. A regional metallogenic overview of gold deposits is performed using data on the age of mineralization and the isotopic composition of sulfur sulfides. A preliminary model of the origin of late stage mineralization is proposed in connection with the processes of the Okhotsk-Koryak orogenic belt formation. Increased concentrations of siderophilic and chalcophilic elements, the Ni, Bi minerals presence in the ores, relatively high fineness of gold, predominance of juvenile sulfur in the isotopic composition of sulfide sulfur, аnd the control by large trans-crustal faults as well as spatial and chronological association with initial (dike) magmatism indicate mantle sources of ore fluids. This mineralization within the orogenic belts of the eastern margin of the Siberian craton assumingly appeared due to dehydration of the submerged slab and local upwelling in the mantle in the rear of the active continental margin. The possibility of the gold-bearing fluids existence in such conditions is estimated. The metallogenic specific nature of collision-related and subduction-related orogenic Au is defined. The proposed model can be useful for the analysis of polychronous orogenic Au-As and orogenic-like Au-Sb metallogeny of orogenic belts on craton margins globally.

A rare sellaite-bearing orogenic gold deposit at Pianyanzi, Yangtze Craton: Ore genesis as implied from in-situ studies of pyrite

The Pianyanzi gold deposit is situated at the western margin of the Yangtze Craton, and represents a rare sellaite-bearing orogenic gold deposit. This deposit belongs to the Dauduhe gold belt of southwestern China and remains poorly documented. In this paper we present first petrographic and in-situ geochemistrical and sulfur isotope data from pyrite as well as results of multielement mapping. The deposit is dominated by native gold (average gold fineness = 980.8) filling fractures in minerals (e.g., pyrite, quartz, sellaite and hematite) or also emplaced along the contact interface between mineral grains. Pyrite is the most abundant sulfide mineral of this deposit. We identified five generations of pyrite: Py1, Py2a, Py2b, Py3, and Py4. Gold occurs in sellaite- and hematite-bearing mineral assemblages formed simultaneous with the formation of Py2a&b and Py4, respectively. Py1 formed in the Au-poor ore stage, while Py3 formed during the late galena-dominated sulfide stage. All generations of pyrite exhibit low concentrations of gold with an average value of less than 2 ppm. Py2a&b possess distinctive textures and chemical zonation, with trace elements displaying greater variations compared to Py1, Py3 and Py4. The δ34S values vary from −0.52 ‰ to 7.08 ‰, which is consistent with those of orogenic deposits of the Daduhe gold belt. The deep metasomatized mantle lithosphere acted as a potential source of ore fluids. We conclude that the co-precipitation of native gold and sellaite was triggered by the interaction between auriferous fluids and dolomite.

ОСОБЕННОСТИ ФОРМИРОВАНИЯ ЗОЛОТОРУДНОЙ МИНЕРАЛИЗАЦИИ В УСЛОВИЯХ АМФИБОЛИТОВОЙ ФАЦИИ МЕТАМОРФИЗМА: МЕСТОРОЖДЕНИЕ ЫКАН (БАЙКАЛО-ПАТОМСКИЙ ПОЯС)

Black shale deposits whose metamorphic grade exceeds greenschist-facies of regional metamorphosed rocks are considered by most researchers exclusively from the point of view of the potential to mine alluvial gold. The article presents the results of the study on the Ykan deposit located within the epidote-amphibolite facies zone and its comparison with previously studied deposits localized in the greenschist facies alteration zone. It was found that the Ykan gold deposit is lithologically and stratigraphically confined to the contact between carbonaceous phyllite shales and sandstones of the Aunakit Formation in the anticlinal limb, which is one of the main factors controlling ore localization. The ore mineralization of the deposit is represented by the change of the early diathagenetic pyrite (py-I, py-II) → metamorphogenic pyrrhotite (po, cpy, asp) → metamorphogenic-metasomatic pyrite-polymetallic (cpy, asp, py-III, gln, sph, pn, mrc) → post-ore pyrite (py-IV) associations. The ore stage is characterized by the highest possible TP parameters in the early ore metamorphic phase and their decrease in the ore-productive phase. Data on variations in the isotopic composition of sulfur and lead indicate that they were transported into the ore fluid from the host meta-sedimentary strata of the Aunakit Formation. Comparison of the obtained parameters of the Ykan deposit with the previously studied deposits of Sukhoi Log, Golets the Highest, Ugakhan and Krasnyi made it possible to conclude that we are correct in assigning the Ykan deposit to the group of deposits of the Sukholozhsky genetic type.

The world-class carbonate-hosted Fankou Zn-Pb deposit in China. Part II. Alterations: C-O isotopic halos footprint the nature and transfer pathway of ore-fluids, and quantitative water-rock interaction process

The giant Fankou Zn-Pb deposit (more than 10 Mt Zn + Pb metals, grading at 15 %), situated in northern margin of the Quren Basin, is one of the largest Zn-Pb deposits in China. The stratiform orebodies are jointly bounded by both the strata (in the specific layers of Middle to Upper Devonian Donggangling and Tianziling carbonate sequences) and the fault system (a three-order thrusting fault system). Ore textures of carbonate dissolution, replacement-infilling and cementation are widespread in Fankou, analogous to a MVT (Mississippi Valley-type) deposit. Owing to the poorly developed fluid inclusions, the nature of the Fankou ore fluids remains indeterminate. To address this problem, we herein utilize micro-petrography, carbon-oxygen (C-O) isotopes and quantitative isotopic exchange modelling to trace the ore-fluids and water-rock interaction process. A total of ninety-three (93) carbonate samples, covering the majorities of stratigraphic horizons, planar locations, and various alteration intensities, were systematically collected. Micro-petrography reveals the primitively sedimentary bioclastic limestone suffer from heterogeneous dolomitization and carbonatization followed by massive Zn-Pb precipitation. These carbonate samples display a widely-ranged, δ18O- and δ13C-depleted isotope signature (δ18O = 12.57 to 23.82 ‰, δ13C = −7.79 to −0.46 ‰), relative to normal marine carbonates (δ18O = 25 ‰, δ13C = 0 ‰). Further modelling of isotopic exchange indicates a low-temperature (100 to 250 °C), δ18O-depleted (−3 to 7 ‰) and δ13C-depleted (−10 to −7‰) ore fluid equilibrated with the host rock by a relatively low water-rock ratio (W/R = 1 to 10). In terms of space, we identified a relatively decreasing trend of δ18O and δ13C isotopic compositions of carbonates, from southeast to northwest, and from bottom to up. Based upon the previous structural analysis, we interpret that the δ18O and δ13C isotopic distribution patterns are caused by a northwestwards transfer pathway of ore-fluids along the thrusting fault system, and the metalliferous, δ18O- and δ13C-depleted fluids are sourced from the interior of the Quren Basin. Collectively, we clarify the deep southeastern part of the Fankou Zn-Pb deposit and the interiors of the Quren Basin is the favorable exploration target in future.

The genetic link between lode and disseminated gold ores and relationship between hypozonal and mesozonal deposits: A case study of the Yanzigou orogenic gold deposit, northwestern Yangtze Craton, China

The process controlling the formation of orogenic lode and disseminated gold ores is the basis for understanding the complexity of the orogenic gold system. The mesozonal Yanzigou gold deposit, located in the Danba ore district of the northwestern Yangtze Craton, is hosted by Devonian carbonaceous slate with coexisting fault-hosted lode and strata-bound disseminated gold ores. Three types of pyrite (PyI-q, PyII-q and Pyd) were formed during two stages of hydrothermal evolution. PyII-q in quartz-polymetallic veins and the rims of Pyd in disseminated ores have the highest Au and As contents, contrasting to distal sedimentary pyrite that have low Au and As contents. This implies that the Devonian host sequences are incapable of providing ore elements to the ore fluid. Pyd and associated quartz have intermediate isotopic values (δ34S = -1.7∼+0.8 ‰; δ18OH2O = 10.6 ∼ 12.7 ‰) between the quartz-vein ores (δ34S = 8.5 ∼ 10.7 ‰; δ18OH2O = 9.0 ∼ 10.1 ‰) and wall-rocks (δ34S ≈ −5‰; δ18OH2O ≈ 12 ‰), implicating a critical role of fluid-rock reaction in the formation of the disseminated gold ores and preservation of original ore fluid characteristics in the lode gold ores. The 40Ar/39Ar dating of hydrothermal muscovite from auriferous quartz veins at Yanzigou yields a total fusion age of 118.4 ± 0.4 Ma, later than ∼ 185 Ma for the nearby hypozonal Danba gold deposit. However, both deposits have common geological, geochemical, and isotopic signatures, suggesting a multi-stage orogenic gold mineralization on the Mesozoic dome margins associated with episodic reactivation of metasomatized mantle lithosphere during the continued crustal uplift.

The Stability Transition From Stable to Unstable Frictional Slip With Finite Pore Pressure

AbstractPore fluids are ubiquitous throughout the lithosphere and are commonly invoked as the cause of induced seismicity and slow earthquakes. We perform lab experiments to address these questions for drained fault conditions and low pore pressure. We shear simulated faults at effective normal stress of 20 MPa and pore pressures Pp from 1 to 4 MPa. We document the full range of lab earthquake behaviors from slow slip to elasto‐dynamic rupture and show that slow slip can be explained by the slip rate dependence of the critical rheologic stiffness without dilatancy hardening or other fluid effects. Our fault permeabilities ranges from 10−18 to 10−17 m2 with an initial porosity of 0.1 and estimated fluid diffusion time ≈1 s. Slow slip and quasi‐dynamic fault motion may arise from high Pp at higher pressures but dilatancy strengthening is not a general requirement.

Shoshonitic pluton and an associated base-metal deposit in the Tarom–Hashtjin metallogenic zone, NW Iran: implication for tectono-magmatic evolution and metallogenic considerations

Petrological, geochemical and zircon U–Pb and Hf isotope studies were carried out on the Hajseyran pluton, along the Tarom–Hashtjin metallogenic zone, as part of the Alborz–Azerbaijan magmatic belt, which is located in the central part of the Alpine–Himalayan orogenic belt. The Hajseyran pluton, which is made up of syenite, monzonite, quartz-monzonite and granite, yields a zircon U–Pb age of 39.20 ± 0.56 Ma (for a quartz-monzonite sample) with shoshonitic features. Enrichment in large ion lithophile elements, depletion in high-field-strength elements and negative anomalies of Nb, Ta and Ti in Chomalou samples suggest a subduction-related arc magmatic setting. The Chomalou epithermal Pb–Zn–Cu deposit occurs close to the Hajseyran pluton with the quartz–base metal sulfide veins predominantly hosted by Eocene volcanic rocks. The ore-forming processes include chalcopyrite and sphalerite–galena formation, with the latter the major mineralisation in this region. Microthermometric results from the liquid–vapour fluid-inclusion assemblages show that the homogenisation temperatures in the first-stage quartz range from 230 to 310 °C, in the sphalerite and second-stage quartz from 161 to 293 °C and in the late-stage quartz from 175 to 262 °C. The salinities of fluids decrease from early-stage quartz to late-stage quartz. The calculated stable isotope values of ore–fluid components (δ18Owater = +3.28‰ to −3.68‰; δ34SH2S = +5.5‰ to +7.8‰) show that magmatic fluids have played a significant role during mineralisation. The Chomalou deposit is interpreted as a volcanic-hosted intermediate-sulfidation type of epithermal mineralisation formed through shallow-level emplacement of the Hajseyran pluton, which formed via partial melting of phlogopite–amphibole-bearing sub-continental lithospheric mantle. The Neotethyan slab roll-back and concomitant asthenospheric upwelling led to the decompression melting of metasomatised sub-continental lithospheric mantle and the formation of several K-rich plutons and associated epithermal deposits in the Alborz–Azerbaijan magmatic belt.

In situ trace elements and sulfur isotope analyses of layered sphalerite as a record of ore-forming processes in the world-class Jinding sediment-hosted Zn-Pb Ore Deposit, China

The Jinding deposit is well-known to contain high concentrations of metals Zn, Pb, Cd, Tl, Ag, etc. in the world. The associated critical metals and their substitution mechanisms were wildly concerned. This study investigated and compared sphalerites using a combination of textural, trace element, and sulfur isotopic analyses to give insights into element substitution mechanisms and possible sources of ore-forming fluids and to constrain processes involved in ore genesis of the world-class Jinding sediment-hosted Zn-Pb deposit. LA-ICP-MS analyses reveal chemical zoning in the sphalerites together with the coupling of two main groups of trace elements substitution mechanisms: one is Fe + Ge + Mn + Pb + As + Tl and vacancies to substitute Zn, and the other is Cd + Cu + Ag + Sb to substitute Zn. The incorporation of trace elements is facilitated by the replacement of Zn by Cd and Fe. These two group elements have distinct color oscillatory zonation and are intertwined in the trace element LA-ICP-MS element maps. The sulfur isotopic values show high isotope fractionation in the sphalerite from −28.4 to −0.5 ‰, suggesting a bacteriogenic sulfur origin at Jinding. Sphalerite sample has observed that sulfur isotope is correlated with Fe concentration and anti-correlated with Cd concentration. These variations in isotope fractionation and trace element disequilibrium partitioning were interpreted as the effects of temperature and pH with less influence from sulfur activity. These variability zones of sphalerite alternately enriched in Cd- and Fe-related elements suggested that ore fluids may flow from metal-fertile sedimentary/basement sequences during their ascent, and colloform sphalerite was likely formed by a high degree of supercooling, over-saturation, and rapid mixing between bacteriogenic sulfur and metal-rich in spaces of collapse dome. Based on our observations, we suggested that these variability zones of layered sphalerite alternately enriched in Cd and Fe would likely provide useful insight for a potential economic Zn-Pb and associated critical metals mineral exploration deposit.

Fluid evolution and ore genesis of the Weilasituo Li-Sn-Cu-Zn polymetallic deposit in Inner Mongolia: Evidence from fluid inclusion and C-H-O-Li isotopes

The Weilasituo Li-Sn-Cu-Zn polymetallic deposit is located in the southwestern Great Xing'an Range (GXR), and crypto-explosive breccia-type and hydrothermal vein-type mineralization are developed in the mining area. With the Early Cretaceous amazonite granite as the mineralization center, the greisen-type Li(-Rb) mineralization is developed in the crypto-explosive breccia pipe above the granite, and the quartz vein-type Sn(-W-Mo) and Cu-Zn(-Ag) mineralization is successively developed in the surrounding Paleoproterozoic Xilinguole complex, forming mineralization zoning. The polymetallic metallogeny comprises early Li (Rb) through Sn(-W-Mo) to late Cu-Zn(-Ag) mineralization, and can be divided into six stages: (I) zinnwaldite–topaz–fluorite, (II) quartz–arsenopyrite–cassiterite–sphalerite–wolframite, (III) quartz–molybdenite–polymetallic sulfides, (IV) quartz–arsenopyrite–pyrite–chalcopyrite, (V) quartz–chalcopyrite–pyrrhotite–sphalerite–galena ± pyrite, and (VI) quartz–calcite–fluorite.Fluid inclusions (FIs) in the zinnwaldite, topaz and fluorite of Li(-Rb) ore phase contain high-temperature medium-salinity (348–404℃; 5.09–9.60 wt%) vapor–liquid two–phase aqueous type (vapor–liquid ratio: 35–70 %), similar to intermediate-density (ID) type FIs, and represent a single-phase fluid directly exsolved from the magma; FIs in the Sn(-W-Mo) ore phase quartz contain daughter mineral-bearing three-phase (SVL), vapor (V), vapor-rich two-phase aqueous (LV) and liquid-rich two-phase aqueous (VL) type, reflecting fluid boiling; FIs in the Cu-Zn(-Ag) ore phase quartz contain CH4 ± CO2 two-phase FIs and VL-type FIs, indicating fluid immiscibility. Lithium isotope data show that the Li ore-forming material was crustal derived, while H-O isotope data indicate that the ore fluid was derived from magmatic water and mixed with meteoric water in the late Cu-Zn(-Ag) ore phase; Carbon isotope data suggest that the CH4 and CO2 in the FIs were sourced from the fluid-rock reaction between the hydrothermal fluid and with the Xilinguole Complex graphite-bearing wallrocks. Raman spectroscopy shows that stage Ⅱ-Ⅴ FIs contain CH4 and CO2, whose content increased markedly from the Sn(-W-Mo) to Cu-Zn(-Ag) stage, indicating that CH4 and CO2 are enriched continuously with fluid migration and fluid-rock reaction.We conclude tha the initial single-phase ID Li-Rb-W-Sn-rich fluid was exsolved from the magma, and formed the Li(-Rb) mineralization in the crypto-explosive breccia pipe as the temperature dropped. Subsequently, the fluid entered the faults and the pressure dropped, causing fluid boiling, and triggered the proximal Sn(-W-Mo) vein-type mineralization. With the fluid migration and more water–rock reaction, CH4 and CO2 are continuously enriched and fluid immiscibility occurred, forming the distal Cu-Zn(-Ag) vein-type mineralization.

Fingerprinting the source and complex history of ore fluids of a giant lode gold deposit using quartz textures and in-situ oxygen isotopes

Fingerprinting the source and complex history of ore fluids of a giant lode gold deposit using quartz textures and in-situ oxygen isotopes