Fluid Evolution Research Articles

Scheelite as a microtextural and geochemical tracer of multistage ore-forming processes in skarn mineralization: A case study from the giant Xintianling W deposit, South China

The Xintianling deposit is one of the largest skarn-type scheelite deposit in China. Recent discoveries of quartz-vein-type scheelite mineralization within the deposit have raised questions about its origin and the evolution of ore-forming fluids, hindering a comprehensive understanding of the ore-forming process. We investigate the microtextures, trace elements, and oxygen isotope compositions of scheelite from different stages in both skarn-type and quartz-vein-type W mineralizations. Combined with apatite geochemistry and U–Pb dating, we determine the timing of quartz-vein-type mineralization and the evolution of magmatic-hydrothermal system. Based on detailed petrological observation, three types (seven subtypes) of scheelite and two types of apatite are identified. The Mo contents and Eu/Eu* ratios of scheelite, along with the Ce/Ce* ratios of apatite indicate the oxygen fugacity of fluids during the skarn metallogenic episode is generally higher than that during the quartz-vein metallogenic episode. Furthermore, the Y/Ho ratios and REE patterns of scheelite indicate the presence of at least three significant stages of fluid influx and fluid-rock interactions throughout entire ore-forming process. The O isotope compositions of scheelite in the quartz-vein-type metallogenic episode reveal that the ore-forming fluids are originated from a magmatic source, and meteoric water was mixed into the system, leading to the precipitation of the latest stage of scheelite. The apatites closely coexist with scheelite, from the early and the late stages of quartz-vein metallogenic episode, yield consistent U–Pb ages within error of 160.4 ± 2.4 Ma and 158.4 ± 1.3 Ma, respectively, indicating a close genetic link between quartz-vein-type W mineralization and the fine-grained porphyritic biotite granite. Our study highlights the significance of pulsed fluid exsolution and the combined effects of multiple mechanisms, including fluid-rock interaction, fluid mixing, and physicochemical condition changes, in the formation of large W deposits.

Evolution of fluid redox in a fault zone of the Pic de Port Vieux thrust in the Pyrenees Axial Zone (Spain)

Abstract. In mountain ranges, crustal-scale faults localize multiple episodes of deformation. It is therefore common to observe current or past geothermal systems along these structures. Understanding the fluid circulation channelized in fault zones is essential to characterize the thermochemical evolution of associated hydrothermal systems. We present a study of a palaeo-system of the Pic de Port Vieux thrust fault. This fault is a second-order thrust associated with the Gavarnie thrust in the Axial Zone of the Pyrenees. The study focused on phyllosilicates which permit the constraint of the evolution of temperature and redox of fluids at the scale of the fault system. Combined X-ray absorption near-edge structure (XANES) spectroscopy and electron probe microanalysis (EPMA) on synkinematic chlorite, closely linked to microstructural observations, were performed in both the core and damage zones of the fault zone. Regardless of the microstructural position, chlorite from the damage zone contains iron and magnesium (Fetotal / (Fetotal + Mg) about 0.4), with Fe3+ accounting for about 30 % of the total iron. Chlorite in the core zone is enriched in total iron, but individual Fe3+/Fetotal ratios range from 15 % to 40 %, depending on the microstructural position of the grain. Homogeneous temperature conditions about 280–290 °C have been obtained by chlorite thermometry. A scenario is proposed for the evolution of fluid–rock interaction conditions at the scale of the fault zone. It involves the circulation of a single hydrothermal fluid with homogeneous temperature but several redox properties. A highly reducing fluid evolves due to redox reactions involving progressive dissolution of hematite, accompanied by crystallization of Fe2+-rich and Fe3+-rich chlorite in the core zone. This study shows the importance of determining the redox state of iron in chlorite to calculate their temperature of formations and to consider the fluid evolution at the scale of a fault.

Origin of porosity in evaporite platform dolostone in the middle Cambrian Shaelek Formation, NW Tarim Basin, China: constraints from petrology, mineralogy and geochemistry

The extensive middle Cambrian evaporite platform dolostone represents a significant area for hydrocarbon exploration in the Tarim Basin with recent advances indicating promising exploration prospects. However, owing to its considerable depth and the limited exploration, the genesis and distribution of evaporite-related dolostone reservoirs from the middle Cambrian remain poorly understood. This study includes detailed field investigations along with petrological, mineralogical and geochemical analyses to characterise the secondary porosity of the middle Cambrian Shaelek Formation evaporite platform dolostone and to explore the origin of the diagenetic fluids responsible for these features. The results show that gypsum dissolution vugs are the main secondary porosity in the evaporite platform dolostone reservoirs, with their development and distribution strongly controlled by sedimentary facies. Meteoric dissolution during the penecontemporaneous period is responsible for this secondary porosity. The frequent fluctuation in sea-levels and the transient exposure of the dolostone reservoirs provide favourable conditions for the dissolution of unstable gypsum. The multiple stages of calcite filling in the vugs result from supersaturated precipitation from fluids during the late stage of meteoric diagenesis. Variations in δ13C, δ18O and rare earth element compositions between the two types of calcite reflect different stages of fluid evolution and varying degrees of water–rock reaction. The vug-filling fluorite is of non-hydrothermal genesis but results from the highly evaporative concentrated seawater and terrigenous input. The highly concentrated F– in evaporative seawater, combined with F– from fluvial input (if any) during subaerial exposure, most likely provides the F– necessary for fluorite precipitation. A model of reservoir formation and evolution has been established that will be beneficial for hydrocarbon exploration and prediction of the deeply buried Cambrian evaporite platform dolostone reservoir.

Correction to: Multiphase evolution of fluids in the Rudnik hydrothermal-skarn deposit (Serbia): new constraints from study of quartz-hosted fluid inclusions

Correction to: Multiphase evolution of fluids in the Rudnik hydrothermal-skarn deposit (Serbia): new constraints from study of quartz-hosted fluid inclusions

Magmatic evolution and sources of metals and fluids in the large granite-related Xiasai vein-type Ag–Pb–Zn(–Sn) deposit, northern Yidun terrane, SW China

The Xiasai Ag–Pb–Zn–(Sn) deposit in the northern Yidun terrane (eastern Tethys), hosted in Late Triassic metasandstones, is genetically associated with Late Cretaceous granites. We present chemical and Sr–Nd–Pb–Li–B isotope data of Late Cretaceous granites and their mafic microgranular enclaves (MME), late aplites, and Late Triassic metasedimentary rocks. The narrow range of 87Sr/86Sr99 (0.70627–0.70953) and εNd99 (–6.1 to –5.2) values of most Late Cretaceous granites reflects a mixed source with contributions from the mantle and Paleoproterozoic felsic crust. These granites have high SiO2 contents (>69 wt%) and strong depletions in Sr, Ba, and Eu. Major and trace element contents correlate with the fractionation index 1/TiO2, indicating that they experienced extensive fractionation. Local late aplite dikes were derived from similar source rocks, but seem to be younger.The Pb isotopic compositions reflect that the metal Pb was derived from the granite with variable contributions from the Late Triassic sedimentary rocks. Weakly and moderately altered metasandstones have similar δ7Li and δ11B values as most granites (δ7Li: 0.00 to 2.68 ‰; δ11B values: –14.93 to –12.36 ‰), indicating magmatic fluid sources. The magmatic fluids resulted in the initial enrichment of Sn, Cu, Pb, and Zn. Strong alteration of feldspar and biotite resulted in the metasandstones in negligible change of Li concentrations, significant loss of Sr, Na2O, CaO, MgO, and Fe2O3, but significant addition of B. This alteration lowered δ7Li from 1.01 to –3.65 ‰ and lowered δ11B from –9.43 to –19.18 ‰. The low δ7Li values and extremely low δ11B values reflect external fluids from the Late Triassic sedimentary wall rocks, which interacted with granites and mobilized metals (e.g., Sn, Ag, Pb, and Zn) from the granite and/or the sedimentary wall rocks. The location of the Xiasai deposit is controlled by regional NNW-trending faults induced by Late Cretaceous extension.

Deciphering ore-forming fluid evolution processes of the Yuerya gold deposit, eastern Hebei, China: Insights from pyrite texture, trace element and sulfur isotope compositions

The Yuerya gold deposit, a representative gold deposit associated with Mesozoic granites in the eastern Hebei region, is located in the eastern Hebei-western Liaoning gold ore-concentrated area, the northern margin of the North China Plate. The orebody is mainly preserved in the Yanshanian granite and its contact zone with the carbonate rocks of the Gaoyuzhuang Formation, and the main ore mineral is pyrite. Based on the pyrite texture, geochemical characteristics of the in-situ trace element analysis, and sulfur isotope, the pyrite in the mining area is classified into five generations (Py1, Py2, Py3, Py4a, and Py4b). Five generations of pyrite all have an average Te/Se ratio > 1, and their average Co/Ni ratios are 1087.27, 43.97, 4.17, 12.62, and 4.99, respectively, indicating that the ore-forming fluid predominantly originates from magmatic-hydrothermal. In-situ sulfur isotopic analysis using LA–MC–ICP–MS shows that the δ34S values of the five generations of pyrites ranged from 0.3 ‰ to 9.6 ‰; the mean values are 3.8 ‰ (Py1, n = 4), 4.2 ‰ (Py2, n = 10), 2.6 ‰ (Py3, n = 18), 4.0 ‰ (Py4a, n = 20) and 4.6 ‰ (Py4b, n = 29), respectively. Approximately 32 % of the results exceed 5.0 ‰, surpassing the values indicative of a magmatic-hydrothermal source. Thermodynamic simulations reveal that the fluctuations in the oxidation state of the ore-forming fluid is not the predominant cause of δ34S enrichment in the pyrite. Our studies suggest that sulfur is primarily derived from mantle-crust mixtures, with some contributions from the wallrock of the Gaoyuzhuang Formation. The results from LA–ICP–MS trace element analysis of pyrites reveal a significant enrichment of As-Bi-Te-Tl alongside Au in the ore-forming fluid. Additionally, the results of ore-forming elements in three typical cross sections of different wallrocks in the mining area also show that Au, Ag, As, and Pb are closely related. Therefore, it is considered that the over-enrichment of As could be an important factor leading to the precipitation of Au. Pyrite undergoes expansion of the mineral lattice parameters or lattice dislocation due to the substitution of S with As, creating space for the growth of solid-solution Au. Subsequently, some of the solid-solution Au within pyrite is liberated through internal oscillations, forming the visible gold particles.

Mobilization and fractionation of Ti-Nb-Ta at the giant Qulong porphyry Cu-Mo mineralization system, Xizang

High field strength elements (HFSE), especially Nb, Ta, and Ti, are commonly considered to be immobile during fluid-rock interaction in ore-forming systems. Hence the mechanisms behind their migration and fractionation associated with mineralization are not often studied. Here, we present a research study of different generations of Nb-Ta-bearing hydrothermal rutile at the giant Qulong porphyry Cu-Mo deposits, Gangdese magmatic belt, Xizang. Based on mineral assemblages and elemental compositions, two distinct groups of rutile can be identified: (1) coarse-grained Rt-1 is found in quartz-biotite-anhydrite veins. It is characterized by high Nb, Fe, Cr, and W contents and formed from the mobilization of HFSE in a relatively oxidized, metal-rich, hypersaline brine during the early high-temperature potassic alteration stage. These rutile grains exhibit suprachondritic Nb/Ta ratios from 20 to 80, that are higher than those of primitive mantle. This may be attributed to the high solubility of HFSE in hypersaline brines, which favors a fractionation of Nb over Ta. (2) Abundant, disseminated, blocky Rt-2 is hosted in monzogranite and monzonitic porphyry, where it forms intergrowths with sericite, chlorite, pyrite, and chalcopyrite. It has relatively low Nb/Ta ratios and formed by alteration of precursor Ti minerals, such as biotite and titanite, during sericite and chlorite alteration stages. This indicates that this generation of rutile was precipitated, together with the ore-forming elements, from moderate-temperature, aqueous fluids. The Nb/Ta variations between the two generations of rutile, reflect the evolution of the mineralizing fluids from an early relatively oxidized, halogen-alkaline-rich composition to late less saline, moderate-temperature fluids. Both Rt-1 and Rt-2 crystallized in these different fluid settings yield 206Pb/238U ages of 16.50 ± 0.32 Ma to 14.70 ± 0.30 Ma, that record the timing of rutile growth and reflect the extended duration of HFSE mobility and final Cu-Mo mineralization. These results suggest that the mobilization and fractionation of HFSE is more common during mineralization in magmatic-hydrothermal metallogenetic systems than often observed, and may thus help elucidate the fluid evolution of magmatic-hydrothermal metallogenetic systems and aid mineral exploration.

Hydrocarbon Accumulation and Overpressure Evolution in Deep–Ultradeep Reservoirs in the Case of the Guole Area of the Tarim Basin

Usually, deep oil and gas accumulation is often controlled by strike–slip faults. However, in the Tarim Basin, deep Ordovician oil and gas accumulations are also found in areas far from the fault zone. The process of oil and gas accumulation in deep reservoirs far from strike–slip fault zones is still unclear at present. The source and evolution of Ordovician fluids were analyzed using inclusion geochemical methods and the U–Pb dating technique. The analysis of rare earth elements and carbon–oxygen–strontium isotopes in the reservoirs showed that the reservoirs were weakly modified by diagenetic fluid. The fluid was derived from the fluid formation during the same period as the seawater, and no oxidizing fluid invaded the reservoir. The late oil and gas reservoirs had good sealing properties. The U–Pb dating results combined with homogenization temperature data revealed that the first-stage oil was charged during the Late Caledonian Period, and the second-stage natural gas was charged during the Middle Yanshanian Period. The evolution of the paleo-pressure showed that the charging of natural gas in the Middle Yanshanian was the main reason for the formation of reservoir overpressure. The strike–slip fault zone was basically inactive in the Middle Yanshanian. During this period, the charged natural gas mainly migrated to the reservoir along the unconformity surface and the open strike–slip fault zone in the upper part of the Ordovician reservoir. The source of the fluid shows that the reservoir in the late stage had good sealing properties, and there was no intrusion of exogenous fluid. The overpressure in the reservoir is well preserved at present.

Origin of the Dongga Au deposit in the giant Xiongcun porphyry Cu–Au district, Tibet, China: Constraints from multiple isotopes (Re, Os, He, Ar, H, O, S, Pb) and fluid inclusions

The Dongga Au deposit (9.55 t Au; average grade = 6.9 g/t [up to 61.6 g/t]) is located in the Xiongcun giant porphyry Cu–Au district of the Gangdese porphyry Cu belt, Tibet. Its mineralization age, ore-forming processes, and relationship to adjacent porphyry mineralization remain unclear. To address this, we conducted a geological, pyrite Re–Os dating, He–Ar–H–O–S–Pb isotopic, and fluid inclusion study of the Dongga deposit. Pyrite samples from ore-bearing chlorite–sulfide veins yielded a weighted-mean Re–Os age of 178.4 ± 2.6 Ma (MSWD=0.01), implying the deposit formed during the Early Jurassic. Fluid inclusion analyses yielded homogenization temperatures of 237–360 °C for quartz–sulfide veins and 125–201 °C for late quartz veins, with corresponding salinities of 2.7–43.8 and 0.9–9.9 wt% NaCleq, respectively. Fluid inclusion analyses of pyrite samples yielded 3He/4He and 40Ar/36Ar values of 0.50–1.08 Ra and 325.1–559.4, respectively, and δD and δ18Ofluid values of –86.2 ‰ to –72.1 ‰ and –5.6 ‰ to 3.9 ‰, respectively. The He–Ar–H–O isotopic data suggest the mineralizing fluids were derived mainly from a crustal source with a small mantle contribution, and also contained a mixture of magmatic and meteoric waters. The S (δ34S = –1.57 ‰ to –0.55 ‰) and Pb (206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb are 18.17–18.41 ‰, 15.55–15.63 ‰ and 38.15–38.37 ‰, respectively) isotopic compositions of pyrite suggest the ore-forming metals were derived from a magma source in the mantle containing minor amounts of subducted sediment. Based on the geology, and isotopic and fluid inclusion data, we infer that mixing between magmatic and meteoric waters was the main trigger of Au precipitation. In addition, based on the geochronological, spatial, and genetic relationships with the adjacent No.2 deposit in the Xiongcun ore district, we propose that the Dongga Au deposit is a sub-epithermal deposit, which represents the transition between porphyry and epithermal deposits. The two deposits constitute a porphyry system and record the continuous evolution of hydrothermal fluids transported outwards in a porphyry system.

Fluid exsolution during disequilibrium crystallization in the border and wall zones of internally zoned pegmatites

Understanding processes that occur during pegmatite crystallization are important for understanding magma evolution and enrichment processes of e.g. strategic and rare metals in pegmatites. Several processes are involved in the formation of pegmatites, and among these the timing of fluid saturation and exsolution is a critical area of investigation. The primary question focuses on if the timing of these processes influences pegmatite crystallization and the concentration of elements. The understanding of the relationship between fluid dynamics and mineralization is essential to develop comprehensive models of pegmatite formation. The unidirectional tourmaline prisms and quartz-tourmaline intergrowths (QTIs), composed of a central tourmaline surrounded by skeletal tourmaline intergrown with quartz are anisotropic textures, linked to disequilibrium crystallization at high degrees of undercooling. This study aims to trace fluid saturation and evolution in the outer zones of internally zoned pegmatites and to provide more accurate temperature constraints for their crystallization, using the Emmons pegmatite (Maine, USA) as a case study. The methodology comprises detailed inclusion petrography, microthermometric analyses, Raman spectroscopy, and LA-ICP-MS analyses. The results indicate that localized fluid saturation occurs early during the magmatic stage of pegmatite crystallization. At this point, the crystallizing mineral assemblages are composed of feldspar, muscovite, quartz, tourmaline, and minor garnet. The exsolved fluid is similar throughout the host tourmalines and is characterized by an H2O-NaCl-CO2-(N2-CH4) composition. Temperatures, which are obtained from primary fluid inclusion isochores vary between 315 °C and 440 °C and confirm that the pegmatite crystallized at undercooled conditions. A decrease in temperature occurs on a centimeter scale between the central tourmaline and the skeletal tourmaline of the QTIs, which could be caused by a nucleation delay within individual boundary layers that are formed around the central tourmaline of the QTI. The higher concentration of water and other incompatible components, including fluxes, in the boundary layer led to fluid exsolution localized at the crystal-melt interface. The increased concentration of fluxes causes a nucleation delay, increasing the degree of undercooling and consequently leading to the skeletal morphologies seen in the QTIs. Furthermore, studied melt inclusions indicate that a compositionally modified melt was present during tourmaline crystallization, confirming the existence of a boundary layer at centimeter to decimeter scale.

Post–peak petrochronology and C–O–H fluid influx in the lower crust: A case study of garnet–orthopyroxene granulites from the Rauer Islands, East Antarctica

Garnet–orthopyroxene granulites from the Rauer Islands (East Antarctica) provide a spectacular example to investigate the late fluid evolution, metamorphic duration, and behavior of monazite and zircon in response to metamorphic reactions and fluid–rock interaction. Here, we characterize the secondary fluid inclusions in peritectic garnet and orthopyroxene, which occur as multiphase inclusions along micro–fractures. Inclusions are composed of siderite, pyrophyllite, calcite, quartz and residual CO2, representing stepdaughter phases resulting from the interactions between C–O–H fluid and its hosts at variable temperatures during retrogression. Zircon grains show clear core–rim structure, which yield 206Pb/238U ages of 540–507 Ma and 527–490 Ma, respectively. Index inclusions and internal structures suggest that the cores document the timing of peak and post–peak decompression while the growth of rims corresponds to melt crystallization during the final cooling. The UPb systems in zircons are considered to have not been obviously affected by fluid or melt–mediated modification. The unusual formation of monazites in garnet–orthopyroxene granulites may be linked with the elevated phosphorus budget as a result of apatite dissolution during the prograde melting of the rocks. Detailed investigations suggest that the crystallization of monazites occurred both at peak and post–decompression stages, whose isotopic systematics has been completely reset due to melt–mediated dissolution–precipitation. The spurious dates for monazites (522–495 Ma) are highly coinstantaneous with the dating results for zircon rims, further supporting this view. Therefore, we conclude that the late carbonic fluid influx cannot result in marked U(Th)–Pb resetting in zircon and monazite. Instead, anatectic melt may have played an important role in the disturbance of isotopic systematics in monazites, especially for long–lived high–grade metamorphic terranes. Combined with previously published data, we propose that the Pan–African metamorphic event in the Rauer Islands may have reached the peak at around ∼540 Ma, followed by a protracted post–peak evolution that lasted for at least ∼50 Myr. This study highlights the importance of an integrated investigation of fluid and index mineral inclusions, as well as the chemical signatures of zircon and monazite, to interpret chronological data correctly.

Fluid inclusion and He-Ar-Pb isotope studies of the Dabie-type Leimengou giant porphyry Mo deposit, Qinling Orogen

The Leimengou deposit is a Dabie-type porphyry Mo system in the Leimengou-Qiyugou orefield of Qinling Orogen. Orebodies host within the porphyry and the metasedimentary Taihua Supergroup. However, the characteristics and sources of ore-forming fluid, metal precipitation mechanism, and the sources of mineralizing substances remain unclear. In this contribution, by a comprehensive study comprising an investigation of deposit geology, fluid inclusion microthermometry, and He-Ar-Pb isotope, we discuss the source and evolution of ore-forming fluids and the molybdenum precipitation mechanism of the Leimengou deposit. The mineralizing process is divided into the Stage I quartz ± K-feldspar vein in potassic altered zone, Stage IIa molybdenite ± quartz vein, and Stage IIb molybdenite + quartz + pyrite ± purple fluorite vein in silicification-phyllic altered zone, Stage III quartz + pyrite + sphalerite + galena ± chalcopyrite ± green fluorite ± pink calcite in prophylitic altered zone and Stage IV quartz ± calcite vein in carbonatization zone based on cross-relationship. The Stage IIa and IIb veins characterize the main molybdenum mineralization stages. By microthermometry, CO2-bearing (C-), Water (WV- and WL-), and daughter minerals-bearing (S-) types of inclusions were recognized. The Stage I quartz contains C-type fluid inclusion assemblages (FIAs) with a salinity of 6.3 ± 1.4 wt% NaCl equiv., and a total homogenization temperature (Th, total) of 473 ± 3 °C. This suggests that the early fluids show characteristics of high temperature, CO2-rich, and moderate salinity, distinguishing them from those of Endako-type and Climax-type deposits. C-type and coexisting W-type FIAs from Stage IIa show similar salinity, ranging from 1.9 to 13.0 wt% NaCl equiv. and 1.9 to 14.1 wt% NaCl equiv., with Th, total of 349–376 °C and 327–392 °C, respectively. Moreover, C-type FIAs homogenize to distinct phases and also show similar homogenization temperatures, indicating fluid immiscibility. The FIAs in Stage IIb show an average salinity of 8.3 ± 7.4 wt% NaCl equiv. and a Th, total of 302 ± 14 °C. WL-type and WV-type FIAs coexist, with similar temperatures varying from 308 to 310 °C during this stage, indicating significant fluid boiling. These observations indicate that the decrease in temperature, fluid immiscibility, and decompression boiling collectively led to the precipitation of molybdenite. Trapping pressures are estimated to be 82–231 MPa for Stage IIa and 43–115 MPa for Stage IIb, corresponding to ore-forming depths of approximately 8.4 km and 4.3 km, respectively. Additionally, the He-Ar isotopes obtained from pyrite indicate a clear mixing trend of crustal fluids with mantle fluids at Stage IIb, with mantle-derived fluid components increasing during Stage III. This coincides with the tectonic shift from regional compression to extension, leading to the formation of many Dabie-type Mo deposits, alongside crustal thinning and the upwelling of asthenospheric mantle materials. Futhermore, Pb isotopes from the ore, ore-hosted gneiss, and ore-causative granitoids demonstrate that the Taihua Supergroup gneiss supplied ore-forming materials, suggesting a crustal origin for the Leimengou Mo deposit.

Quartz texture and the chemical composition fingerprint of ore-forming fluid evolution at the Bilihe porphyry Au deposit, NE China

Abstract Quartz is widely distributed in various magmatic-hydrothermal systems and shows variable textures and trace element contents in multiple generations, enabling quartz to serve as a robust tracer for monitoring hydrothermal fluid evolution. This study demonstrates that integrated high-resolution SEM-CL textures and trace element data of quartz can be used to constrain physicochemical fluid conditions and trace the genesis of quartz in porphyry ore-forming systems. The Bilihe deposit is a gold-only porphyry deposit located in the Central Asian orogenic belt, NE China. Four quartz generations were distinguished following a temporal sequence from early-stage dendritic quartz, unidirectional solidification textured quartz (UST quartz), gray banded vein quartz (BQ), to late-stage white calcite vein quartz (CQ), with the Au precipitation being mostly related to dendritic quartz, UST quartz, and BQ. The well-preserved dendritic quartz with sector-zoned CL intensities and euhedral oscillatory growth zones crystallized rapidly during the late magmatic stage. The relatively low Al contents of dendritic quartz were interpreted to be related to contemporaneous feldspar or mica crystallization, while the high-Ti contents indicate high-crystallization temperatures (~750 °C). The comb-layered UST quartz displays heterogeneous, patchy luminescence with weak zoning, hosts coeval melt and fluid inclusions, and retains the chemical characteristics of magmatic dendritic quartz. High-Ti and low-Al contents of UST quartz suggest a formation at relatively high temperatures (~700 °C) and high-pH conditions. Three sub-types can be defined for hydrothermal BQ (BQ1, BQ2, and BQ3) based on contrasting CL features and trace element contents. The Al contents increase from BQ1 to BQ2 followed by a drop in BQ3, corresponding to an initial decrease and subsequent increase in fluid acidity. Temperature estimates of BQ decrease from BQ1 (635 °C) to BQ3 (575 °C), which may, however, be disturbed by high growth rates and/or high-TiO2 activities. The CQ typically displays a CL-bright core and CL-dark rim with oscillating CL intensities and is characterized by the lowest Ti and highest Al, Li, and Sb contents compared to the other quartz types, which suggests a deposition from more acidic and lower temperature fluids (~250 °C). Trace element patterns indicate that a coupled Si4+ ↔ (Al3+) + (K+) element exchange vector is applicable to dendritic quartz, UST quartz, and BQ. By contrast, charge-compensated cation substitution of Si4+ ↔ (Al3+, Sb3+) + (Li+, Rb+) is favored for CQ. The comparison with compiled trace element data of quartz from other porphyry Au, Cu, and Mo deposits worldwide suggests that Ti, Al, Li, K, and Ge concentrations, as well as Al/Ti and Ge/Ti ratios, have the potential to discriminate the metal fertility of porphyry mineralization.

Fluid-mediated Cu and Zn isotope fractionation in subduction zones and implications for arc volcanism: Constraints from high pressure veins within eclogites in the Dabie Orogen

High-pressure (HP) veins in eclogites are the products of fluid-rock interaction and provide insight into the composition and evolution of fluids in subduction zones. We here present the Cu and Zn isotope data for different types of HP veins and their host eclogites from Ganghe and Hualiangting in the Dabie Orogen to reveal the behavior of Cu and Zn isotopes during fluid-rock interaction and fluid evolution. The HP veins include omphacite-epidote (Omp-Ep), epidote-quartz (Ep-Qtz), and kyanite-epidote-quartz (Ky-Ep-Qtz) veins. The Omp-Ep veins first crystallized from eclogite-derived, solute-rich fluids with the Ep-Qtz and Ky-Ep-Qtz veins successively crystallizing from the residual fluids after the Omp-Ep vein formation. The early Omp-Ep veins have variably lower δ65Cu (−1.32 to −1.12‰ at Ganghe, −0.70 to −0.66‰ at Hualiangting) but higher δ66Zn (0.36 to 0.38‰ at Ganghe, 0.40 to 0.41‰ at Hualiangting) relative to the host eclogites (δ65Cu: −0.71 vs. 1.84‰, δ66Zn: 0.22 vs. 0.33‰), indicating CuZn isotope fractionation during slab dehydration in subduction zones with the lighter Cu and heavier Zn isotopes preferentially entering the vein-forming fluids from the eclogites. Systematic increase of δ65Cu from the Omp-Ep (−0.70 to −0.66‰) through Ep-Qtz (0.01‰) to Ky-Ep-Qtz veins (0.46 to 0.95‰) can be attributed to isotope fractionation induced by redox changes during the evolution of metamorphic fluids, as revealed by the negative correlations of δ65Cu with redox-sensitive ratios of Fe3+/ΣFe and (Eu/Eu*)N in those veins. Additionally, the higher δ66Zn of the Omp-Ep veins relative to the Ky-Ep-Qtz veins can be explained by equilibrium isotope fractionation between crystallized minerals and evolved metamorphic fluids. Our results thus demonstrate that CuZn isotope fractionation occurred during the evolution of slab-derived metamorphic fluids in subduction zones. Binary mixing calculations show that fluids derived from dehydration of mafic rocks in subducted slabs, represented by the multistage HP veins in the present study, cannot account for the heavier Cu and lighter Zn isotope compositions in most arc magmas than in mid-ocean ridge basalts. This offset can be resolved by addition of forearc serpentinite-derived fluids enriched in heavy Cu and light Zn isotopes into the mantle source of arc magmas.

Ore-forming process of the Xiaoyuzan gold deposit in the Western Tianshan, Northwest China: Constraints from mineralogy and S isotopes of sulfides

The Xiaoyuzan deposit is a typical intermediate-sulfidation epithermal Au deposit in the Boluokenu metallogenetic belt. The orebodies are hosted by the Lower Carboniferous Dahalajunshan Formation volcanic rocks and controlled by the NW- and NNW-striking faults. The metal minerals present in the ores mainly include pyrite, sphalerite, galena, chalcopyrite, and tetrahedrite. The non-metallic minerals are primarily composed of quartz, calcite, and sericite. Three ore-forming stages are distinguished based on mineral assemblages, wall-rock alteration, and vein crosscutting relationships, including the quartz-pyrite stage (I) with silicification and propylitization, quartz-sulfide stage (II) with phyllic alteration, and quartz-carbonate stage (Ⅲ) with carbonatization. Three different types of pyrite are classified: coarse-grained PyI with cubic from the wall rock, fine-grained PyII with a crystal form of pentagonal dodecahedron in the quartz-sulfide veins, and coarse-grained cubic PyⅢ in the quartz-carbonate veins. The in-situ δ34S value range of sulfides from stage I, stage II and stage Ⅲ are 5.0 ‰ to 5.5 ‰, 4.3 ‰ to 6.5 ‰ and 5.7 ‰ to 6.2 ‰, respectively. The composition of S isotopes indicates that the source of the sulfur is magmatic in origin, with main contribution from the host rock. All the types of pyrite are relatively enriched with Sb, Cu, Ag, Pb, Bi, and As. The composition of pyrite suggests that the Au in the pyrite present as lattice gold (Au+1). The gradual decrease in Co contents from in PyⅠ, PyⅡ to PyⅢ indicates a gradual decrease in temperature during fluid evolution. The contents of trace elements in sphalerite are relatively low, with Fe, Mn, Cd, and Cu being relatively enriched. Using the sphalerite geothermometer (GGIMFis), the calculated temperature falls within the range of 303.0 to 334.3 °C. Pyrite II is characterized by the occurrence of oscillatory zones, suggesting rhythmic changes in fluid physicochemical conditions and compositions. Although coexisting of liquid-rich and vapor-rich aqueous inclusions were locally observed in stage II quartz according to previous studies, the absence of crustiform/colloidal/lattice bladed quartz in the main stage suggests that slight or gentle fluid boiling has occurred. In summary, it is proposed that fluid-rock reactions made great contribution for the precipitation of gold and sulfides in the Xiaoyuzan deposit.

Embracing differences in organizations: ‘differences work’ as a new theoretical perspective

ABSTRACT The paper presents an expansion of the perspective on ‘differences’ by proposing a novel theoretical concept: ‘differences work’. Differences work is the subjective and intersubjective effort that is put in place to approach differences from a dynamic stance, to encompass the different processes – identity, relational, and cultural – intertwined in experiencing ourselves and the relationship with differences. The concept is illustrated in its cognitive and emotional components. The paper contributes to developing new sensitivities to the in-situ work on differences, advising to investigate empirically how differences work deploys. The paper suggests methodologies for digging into dialogues and conversations, for entering the self-constructions and others’ counter-constructions of differences, and for observing their dynamic and fluid evolution as it happens. The new concept enriches the possibility of going beyond category-oriented policies and orientations in organizations, which are generally aimed at proposing activities not always sufficient to represent all the differences circulating in organizations.

Amphibole geochemistry in the Haobugao skarn Zn-Fe-Sn deposit in the southern Great Xing’an Range: Implications for the ore-forming process

The Haobugao Zn-Fe-Sn deposit is a typical skarn deposit in the southern Great Xing’an Range of NE China. Despite many advances in understanding its genesis, the detailed ore-forming processes of Zn, Fe and Sn are still unclear. Amphibole, a rock-forming mineral, has been well studied as an indicator of diverse magmatic and metamorphic processes; however, the geochemistry of hydrothermal amphibole has previously received less attention. The Haobugao deposit contains two generations of hydrothermal amphibole (Amp-I and Amp-Ⅱ), which provides a good opportunity to use amphibole geochemistry to trace the mineralization process. Early Amp-I coexists with cassiterite, magnetite and quartz, whereas late Amp-II coexists with quartz and sulfides and can be further divided into two subgroups: Amp-Ⅱa (in skarn) and Amp-Ⅱb (in the country rocks of siltstone). The oxygen isotopic compositions of the fluid (δ18Ofluid 2.9‰) responsible for the Amp-I formation indicate that the amphiboles formed from mixed magmatic fluid with meteoric water. Amp-I is LREE-depleted and HREE-enriched with obvious negative Eu anomalies. Amp-Ⅱ is generally slightly LREE-depleted with negative or positive Eu anomalies and positive Ce anomalies. The incorporation of trace and rare elements is mainly controlled by the fluid composition. Detailed petrological observations and amphibole geochemistry, combined with previous research results, confirm that Sn, Fe, Pb and Zn mineralization occurred during a single mineralization event. From the oxide to the quartz sulfide stage, the ore-forming fluid evolved from high-temperature and oxidized conditions with enrichment of Sn, Li, Be and REEs to low-temperature and reduced or oxidized conditions with enrichment of Cu, Co and Zn. The concentrations of Cu, Co and Zn in different amphiboles vary with the mineral crystallization sequence. This study shows that amphibole geochemistry can be useful for tracing fluid evolution and mineralization processes in hydrothermal systems.

Dolomitization history and fluid evolution of end-ediacaran multi-phase dolomites from the near-surface to deep burial depths in the tarim craton, northwestern China

The deeply buried (>8 km) end-Ediacaran Qigebrak Formation dolostones in the Tarim Basin, China, have significant petroleum potential, but have experienced multi-stage dolomitization that has resulted in the occurrence of diverse dolomite phases. The features and origins of the different dolomite types were merely investigated, which hinders an in-depth understanding of the complex dolomitization processes. This paper presents an integrated petrological, geochemical (C–O–Sr isotope and in situ trace element), fluid inclusion microthermometric, and dolomite U–Pb dating study of outcrop and core samples, to investigate the dolomitization mechanisms, and the nature and evolution of the dolomitizing fluids. The results indicate the occurrence of early dolomitization triggered by seepage–reflux of mesosaline seawater, which retained the primary marine geochemical properties of most of the matrix dolomite. Subsequently, during early diagenesis, fibrous dolomite cement was precipitated from marine porewaters, which have similar geochemical characteristics to the matrix dolomites. Following this, during intermediate-depth burial diagenesis in the Ordovician, fine-to medium-crystalline dolomite cements formed at temperatures of 80–117 °C in association with dissolution–reprecipitation of the matrix and early fibrous cements or diagenetic interactions with clay minerals of the lower Cambrian Yurtus Formation shales. During deep burial diagenesis and dolomitization in the Carboniferous, coarse-crystalline dolomite cements formed at temperatures of 104–138 °C from saline brines enriched in middle rare earth elements. Saddle dolomites, formed by hydrothermal dolomitization (162–184 °C) that was closely related to Permian–Triassic volcanic activity, have positive Eu anomalies and depleted δ18O values, that resulted from the mixing of basinal brines with 87Sr-enriched hydrothermal fluids. This study provides a detailed description of multiple dolomitization events in deep time that affected deeply buried dolostones.

Fluid origin and evolution of the Taolin Pb-Zn deposit in northeastern Hunan Province, South China: Insights from fluid inclusions and H-O-He-Ar isotopes

Situated in northeastern Hunan Province, the vein-type Pb-Zn orebodies at Taolin are mainly hosted in NE-/NEE-trending faults between Dayunshan-Mufushan pluton and Neoproterozoic metasedimentary rocks of the Lengjiaxi Group. Hydrothermal mineralization can be divided into five stages: (1) coarse-grained quartz stage, (2) quartz-fluorite-base metal stage, (3) quartz-barite-fluorite-base metal stage, (4) pale pink and colorless quartz stage, and (5) fine-grained quartz stage. In this research, fluid inclusions as well as stable (H-O) and noble gas (He-Ar) isotope compositions were performed to uncover the nature, origin, and evolution of the ore-forming fluids, ore precipitation mechanisms, and mineralization process of the Taolin deposit. Four types of fluid inclusions, i.e., liquid-rich two-phase inclusions (LV-type), pure liquid phase inclusions (PL-type), vapor-rich two-phase inclusions (VL-type), and pure vapor phase inclusions (PV-type), were distinguished in sphalerite, quartz, and fluorite. Microthermometric analysis of fluid inclusion assemblages in sphalerite, quartz, and fluorite from different stages indicates that from the Stage 1 to Stage 5, the homogenization temperatures vary between 168 and 211 °C, between 151 and 198 °C, between 131 and 180 °C, between 132 and 164 °C, and between 118 and 138 °C, respectively, whereas the fluid salinities vary from 12.4 to 16.9 wt% NaCl equivalent, from 9.7 to 14.6 wt% NaCl equivalent, from 5.6 to 10.3 wt% NaCl equivalent, from 3.6 to 9.7 wt% NaCl equivalent, and from 0.9 to 3.8 wt% NaCl equivalent, respectively. The H-O isotope data of quartz and the He-Ar isotopic compositions of sulfide crystals suggest that the ore-forming fluids were a mixture of crust-derived magmatic hydrothermal fluid and meteoric water. Fluid mixing and cooling were likely the crucial mechanisms for ore precipitation.

Multiphase evolution of fluids in the Rudnik hydrothermal-skarn deposit (Serbia): new constraints from study of quartz-hosted fluid inclusions

Multiphase evolution of fluids in the Rudnik hydrothermal-skarn deposit (Serbia): new constraints from study of quartz-hosted fluid inclusions