Southern Great Xing Research Articles

Formation of the Lianhuashan Cu deposit in the southern Great Xing’an Range, NE China: Constraints from fluid inclusions, whole-rock geochemistry, zircon U–Pb geochronology, and H–O–S–Pb isotopes

The medium-sized Lianhuashan Cu sulfide deposit is located in the southern Xing’an Range of Inner Mongolia, NE China. The zoned massive sulfide vein ores are hosted mainly in the Permian Dashizhai Formation, and the ore veins are controlled by NW–NNW-trending structures. The ore-forming process comprises four stages: arsenopyrite–quartz (I); chalcopyrite–pyrite–quartz (II); pyrite–chalcopyrite–sphalerite–galena–quartz (III); and ore-barren sulfide–quartz–carbonate (IV). Three types of fluid inclusions (FIs), namely vapor-rich two-phase (LV-type), liquid-rich two-phase (VL-type), and daughter mineral-bearing three-phase (SL-type), are distinguished. Stage I, II and III contain all types of FIs (LV-, VL-, and SL-type), with homogenization temperatures (Th) of 268–462°C, 230–382°C and 180–340°C and salinities of 3.4–52.3, 3.4–44.5 and 3.7–39.9 wt% NaCl eqv., respectively, whereas stage IV has only VL-type FIs, with Th = 152–232°C and salinity = 3.4–7.9 wt%. Fluid geochemical data show that the Lianhuashan ore fluids were of medium–high temperature (236–382 °C), high-salinity (31.5–44.5 wt%), and relatively oxidizing conditions, typical of a NaCl-H2O system. The microthermometric and H–O isotope data (δ18OH2O = − 9.0 to 6.1 ‰; δD = − 149.0 to − 99.0 ‰) indicate that the ore fluids were initially magmatic with later meteoric water incursion. The sulfide S (δ34S = − 2.9–3.8 ‰) and Pb (206Pb/204Pb = 17.954 − 18.492, 207Pb/204Pb = 15.427 − 15.739, 208Pb/ 204Pb = 37.815 − 38.357) isotopes support that the metals were magmatic-derived. Fluid boiling, cooling, and meteoric water mixing were likely the main ore precipitation mechanism at Lianhuashan.We suggest that Cu minerals at Lianhuashan were precipitated with boiling at ∼ 1km depth. For the ore-forming granodiorite porphyry (zircon U-Pb age: 252.8 ± 1.8 Ma), geochemical data indicate that the primary magma was formed by partial melting of the thickened or delaminated lower crust. Integrating the available age, geological, and geochemical evidence, we suggest that mineralization at Lianhuashan is spatial–temporal and genetically associated with the granodiorite porphyry, and was formed in a volcanic arc setting after the Paleo-Asian Ocean closure.

Transcrustal magmatic systems in NE China: Insights from Early Cretaceous metaluminous–peraluminous–peralkaline rock associations in the southern Great Xing’an Range

The generation and evolution of crustal-scale magmatic systems are important in revealing the continental crust differentiation. In the Bayangeer-Aliwula area of Inner Mongolia, metaluminous–peraluminous–peralkaline rock assemblages provide a rare opportunity to evaluate Early Cretaceous magmatic systems. This study presents new geochemical data, including whole-rock and zircon geochemistry, zircon U–Pb dating, and Hf–O isotopic analysis of rocks formed between 132 and 121 Ma. The metaluminous rocks exhibit low SiO2 (55.35–65.65 wt%), low Rb/Sr (0.08–0.24) and (La/Yb)N (4.88–7.58) ratios, and positive εHf(t) values (+4.9 to +8.7). These features, along with enrichment in large-ion lithophile elements and depletion in Nb and Ta, suggest formation via partial melting of fluid-metasomatised lithospheric mantle. By contrast, peraluminous rocks have high SiO2 (69.37–80.58 wt%), a high differentiation index (DI = 88–95), and Fe-index (0.84–0.95), resembling highly fractionated I-type granites. They show high Rb/Sr (0.77–3.35) and (La/Yb)N (5.79–22.75) ratios, and positive εHf(t) values (+6.7 to +10.8), combined with the modelling results, indicating origin from partial melting of K-rich mafic lower crust followed by magma fractionation. Peralkaline rocks display typical ferroan A-type granite characteristics (Zr + Nb + Ce + Y = 906–4292 ppm; Fe-index = 0.96–0.99), with high SiO2 (74.02–77.50 wt%), high Rb/Sr (6.17–121.38), and (La/Yb)N ratios (2.19–17.72), and positive εHf(t) values (+3.1 to +9.6). Zircon geochemistry characteristics suggest that peralkaline and peraluminous felsic melts are different batches extracted from the same magma reservoir. Further analysis, including hyperbola diagrams and zircon oxygen isotope compositions, suggests peralkaline magma formation through the mixing of altered oceanic crust fluids and peraluminous melts after melt extraction. During Early Cretaceous, the transcrustal magmatic system provides a reasonable explanation for the petrogenesis of various contemporaneous rocks in the study area in southern Great Xing’an Range.

Linking beryllium mineralization to fluid-rock reactions: A case study of the Madumeng quartz vein-type beryllium mineralization in the Southern Great Xing'an Range, Northeast China

The Southern Great Xing'an Range (SGXR) in Northeast China is a significant polymetallic mineralization belt. Although several beryllium (Be) deposits have been reported in the SGXR, the timing and mechanisms of Be mineralization are poorly understood. To determine the mechanisms of newly-discovered Be mineralization in the Madumeng area, we carried out monazite–zircon–apatite U–Pb dating, whole-rock and mineral geochemical, and monazite Nd isotopic analyses of the beryl-bearing quartz veins and host Late Permian–Early Triassic granite. Monazite from the beryl-bearing quartz veins yielded U–Pb ages of 138–137 Ma, and the host granite yielded zircon and apatite U–Pb ages of 251 ± 1 and 256 ± 27 Ma, which indicate that the Madumeng Be mineralization formed later than the host granite. Monazite in the beryl-bearing veins has similar εNd(t) values (−1.31 to +4.27) to those of Early Cretaceous highly fractionated granite related to Be mineralization in the SGXR, which suggests the ore-forming material was derived from exsolved fluids associated with Early Cretaceous, deep-seated, highly fractionated granites. Fluid-rock reactions had a key role in generating the Madumeng Be mineralization, and the intensity of these reactions was recorded by the whole-rock and mineral geochemistry. The alteration during fluid-rock reactions increased the pH and Ca contents of the fluids. Mica and beryl record the release of Ca and Fe from the granite into the fluid. The released Ca2+ ions combined with F− ions in the fluid, leading to instability of Be–F complexes and subsequent precipitation of beryl. Our findings indicate that the Early Cretaceous was an important period of Be mineralization in the SGXR and highlight the contribution of fluid-rock reactions to Be precipitation in quartz vein-type Be mineralization.

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.

Shear wave splitting and mantle dynamics of the southern Great Xing'an orogenic belt

We deployed a linear seismic array consisting of 50 broadband stations in the southern part of the Great Xing'an orogenic belt to investigate seismic anisotropy in the Songliao Basin, the orogenic belt and the Erlian Basin by making SKS wave splitting measurements. Different features of anisotropy are revealed on the two sides of the north-south gravity lineament. The anisotropy on the east side of the gravity lineament primarily results from mantle flows in the big mantle wedge above the flat Pacific slab in the mantle transition zone, and the SKS fast polarization direction is generally NW-SE, being consistent with the subduction direction of the western Pacific plate. On the west side of the gravity lineament, the SKS splitting is attributed to freezing anisotropy in the stable lithosphere under the Erlian Basin. The SKS splitting delay times show some changes with azimuths of the teleseismic events, but the fast polarization directions are generally the same, indicating that the anisotropies below these seismic stations have the same origin in the continental lithosphere and active flows in the big mantle wedge.

Genesis of Cu-Sn Mineralization in the Shuangjianzishan Super-Large Silver Deposit, Inner Mongolia: Trace Element Constraints from Chalcopyrite and Cassiterite

The Shuangjianzishan silver polymetallic deposit is located in the copper–tin–lead–zinc–silver polymetallic metallogenic belt in the Southern Great Xing’an Range, with silver resources of more than 18,000 t, which is the largest silver polymetallic deposit in Asia. Early studies concluded that the Shuangjianzishan deposit is typically an epithermal Ag-Pb-Zn deposit that lacks a high-temperature mineralization stage. In recent years, with the deepening of research, a large amount of Cu-Sn mineralization has been found in the deep part of the Shuangjianzishan deposit, but it is less studied. The laser-ablation inductively coupled mass spectroscopy (LA-ICP-MS) technique is used to investigate the distribution and substitution of trace elements in chalcopyrite and cassiterite. In this paper, the trace element study of chalcopyrite and cassiterite from the Shuangjianzishan deposit reveals that Sn, In, As, Se, Sb, and Tl mainly exist in chalcopyrite in isomorphic form, while Pb, Bi, and Ni mainly exist in chalcopyrite in the form of mineral inclusions. The enrichment of the high-temperature elements Sn and Se in chalcopyrite, and the deficit of the middle- and low-temperature elements Ga, Sb, etc., reflect that the chalcopyrite in the Shuangjianzishan deposit was formed in a middle- and high-temperature environment, and it also indicates that the early ore-forming hydrothermal solution may be rich in Sn. Fe, In, Co, and Ni mainly exist in cassiterite in isomorphic form, and the content of W in cassiterite is high. There are two main forms, one is isomorphic and the other is wolframite inclusion. Cassiterite has Fe-rich and W-U-poor characteristics, indicating that cassiterite from the Shuangjianzishan deposit was formed under relatively oxidized conditions, and the relative enrichment of elements such as Fe, W, Zr, and Hf indicates that the temperature of cassiterite formation was high. The elemental content and inter-ionic coupling relationships suggest that the cassiterite from the Shuangjianzishan deposit may have an elemental replacement mechanism of W6+ + Fe2+ ↔ 2Sn4+ or Fe3+ + OH− ↔ Sn4+ + O2−. The trace elements in cassiterite of the Shuangjianzishan deposit are rich in Fe and Mn and depleted in Nb and Ta, according to the Fe-W diagram, and the tin mineralization of the Shuangjianzishan deposit belongs to cassiterite–sulfide-type tin mineralization. Chalcopyrite Co/Ni ratios >1 are consistent with the characteristics of chalcopyrite genesis in hydrothermal deposits.

Garnet geochronology, major and trace element geochemistry of the Huanggangliang Fe-Sn polymetallic deposit, NE China

Cu-Fe (Au), W-Sn (Mo), Pb-Zn (Ag) and other element assemblages are common in many skarn deposits, but examples of Fe and Sn coexistence in nature are relatively rare. The Huanggangliang deposit in the southern Great Xing'an Range is the largest Fe-Sn polymetallic deposit in northern China, and there are five main mining areas (SK Ⅰ–SK Ⅴ) distributed along a SW–NE trend. SK Ⅰ and SK Ⅲ are the two larger mining areas in the Huanggangliang deposit, and their mineral assemblages and wall-rocks are significantly different: cassiterite and metal sulfides are duncommon in SK Ⅰ (andesite), while they are widely distributed in SK Ⅲ (marble). Garnet is widely distributed in SK Ⅰ and SK Ⅲ mining areas, and provides a good opportunity to explore the mechanism of Fe-Sn assemblage differentiation. Three types of garnet are distinguishable (Grt 1, Grt 2 and Grt 3) based on their mineral associations, textures and locations, and they mainly belong to the andradite-grossular solid solution series. The LA–ICP–MS U-Pb ages of the garnets from SK Ⅰ and SK Ⅲ are 136.0 ± 1.2 Ma (n = 25, MSWD = 1.9) and 136.2 ± 2.6 Ma (n = 37, MSWD = 1.8), respectively, suggesting that magmatic-hydrothermal activity in these two mining areas began at the same time. Grt 1 (located deep in SK Ⅰ and SK Ⅲ) and Grt 2 (located shallowly in SK Ⅰ) are mainly andradite, while Grt 3 (located shallowly in SK Ⅲ) is mainly grossular. They are all enriched in high field strength elements (HFSEs) and depleted in large ion lithophile elements (LILEs), and their REE patterns are enriched in light rare earth elements (LREEs) and depleted in heavy rare earth elements (HREEs). However, Grt Ⅰ-1a and 1b (deep garnets in SK Ⅰ) exhibit obvious positive Eu anomalies, while the other garnet types exhibit negative or no obvious Eu anomalies. Additionally, Grt 3 has high contents of V, Sn, U, Th, Zn and Y, and low contents of W and Mo. This pattern implies that the garnets in deep SK Ⅰ may have formed under oxidizing conditions with high temperatures, high oxygen fugacity (fO2) and weak acidity, while the garnets in shallow SK Ⅲ formed under reducing conditions with moderate temperatures, moderate fO2 and near-neutral pH. The garnets in shallow SK Ⅰ and deep SK Ⅲ may have formed under weak oxidation–reduction conditions at moderate to high temperatures, moderate fO2 and weakly acidic to neutral pH conditions. Our newly reported field geological, mineralogical, and geochemical data from garnet suggest that the ore-forming fluids of the Huanggangliang were magmatic-hydrothermal fluids mixed with slightly acidic external fluids, chloride complexes may have been the main transport ligands of REEs. The metallogenic environment may be an important factor leading to the difference of mineral assemblages in the Huanggangliang deposit.

Mineralogical evidence for the role of deep magmatic fluids in beryllium enrichment in magmatic-hydrothermal systems

Vein-type and greisen-type beryllium (Be) mineralization is closely associated with the magmatic-hydrothermal evolution in highly fractionated granites. However, the source of ore-forming fluids and their role in the migration and enrichment of Be is poorly understood. Although whole rock Ba-Rb isotope researches highlight that even deep magmatic fluids beneath the shallow magmatic-hydrothermal systems could provide rare metals and promote mineralization, it is still challenging to determine the influences of such fluids via using conventional geochemical indicators. Here we present zircon-monazite-xenotime-wolframite U-Pb ages, whole-rock geochemistry, monazite Nd isotopes, as well as muscovite and beryl geochemistry for the Zhujiayingzi quartz vein-type Be mineralization in the southern Great Xing’an Range (SGXR), Northeast (NE) China, and introduce the neighboring Nasigatu gresien-type Be mineralization for comparison. Geochronological results reveal that the Zhujiayingzi beryl-wolframite-bearing quartz veins formed in the Early Cretaceous (149–147 Ma), much younger than the host Permian (270–267 Ma) crystal tuffs, but coeval with the Nasigatu highly fractionated alkali-feldspar granite (144–139 Ma). Similar muscovite-beryl compositions and monazite Nd isotopes, combining with their close temporal-spatial relationships indicate that the Zhujiayingzi and Nasigatu Be mineralization have consistent hydrothermal assemblages and enrichment processes. Higher silica, K, and lower Al contents of muscovites from Be-rich veins (M2) and greisens (M4) than those recorded in barren crystal tuffs (M1) and alkali-feldspar granite samples (M3) at both Zhujiayingzi and Nasigatu are consistent with the evolution of the Early Cretaceous granitic magma, proving the involvement of shallow magmatic fluids exsolved from the Nasigatu-like highly evolved granitic melts. However, ore-related M2 and M4 samples have higher Mg (>1 wt%) and Ti contents than those of M1 and M3 samples, which violates the conventional hydrothermal evolution trend. Trace element compositions as well as K/Rb, K/Cs, and Rb/Sr ratios of four-type muscovites, together with the core-rim geochemical variations of muscovites at Zhujiayingzi and beryls at Nasigatu, indicate the existence of deep magmatic fluids rather than fluid-rock interaction to account for the anomalous mineralogical evidence. Such deep magmatic fluids were exsolved from large silicic magmatic reservoirs beneath the shallow magmatic-hydrothermal system, and thus likely display low evolution degrees and high Mg-Ti contents. They can not only provide heat and promote fluid-mineral interactions, but also can efficiently extract and transport Be enriched in deep crystal mushes at different depths. Thus we invoke that the Early Cretaceous Be mineralization in the SGXR was achieved under the combined action of both shallow and deep magmatic fluids derived from the crystal mush-dominated transcrustal magmatic system.

Zircon in tin granite as tracer for fluid metasomatism and Sn mineralization

Most tin deposits in the world are genetically related to tin granite and form during complex magmatic-hydrothermal processes. Zircon is a common accessory mineral in granite and related ore systems and can host a number of ore metals, such as Sn, W, Nb, Ta, U and Th, in its crystal lattice. However, whether metal enrichment/depletion can trace ore-forming processes is still unclear. Here, we report that the metal concentrations in various types of zircons from the Mopanshan tin granites in the southern Great Xing'an Range (Northern China) can be used as good indicators of fluid metasomatism and Sn mineralization. Two lithological zones are developed in the Mopanshan pluton, including porphyritic syenogranite (PG) in the center and fine-grained syenogranite (FG) at the margin. Zircons in the PG (PGZ-1, PGZ-2, and PGZ-3) are all magmatic in origin, while zircons in the FG can be categorized into magmatic zircons (FGZ-1 and FGZ-2) and metasomatic zircons (FGZ-3). The PGZ-1 and FGZ-1 grains are transparent prismatic crystals with bright oscillatory zonation, whereas the PGZ-2 grains are murky crystals with dark oscillatory zonation. PGZ-3 and FGZ-2 grains occur as overgrowths of previously formed zircon (PGZ-1, PGZ-2, and FGZ-1) or as brown individual crystals, showing dark and homogeneous cathodoluminescence (CL) textures. The metasomatic FGZ-3 grains are translucent-opaque porous crystals with vermicular CL zonation and commonly replace FGZ-2. The trace element compositions of magmatic zircons are completely melt controlled, providing a record of magmatic evolution as a constant decrease in Zr/Hf ratios and a gradual increase in Th, U, Nb, and Ta contents. Moreover, the structure of magmatic zircons transforms from a crystalline state to an amorphous state as a consequence of radioactive decay of U and Th. A coupled dissolution-reprecipitation process is proposed for the formation of metasomatic FGZ-3. The reactive fluid is the magmatic fluid that exsolved from the melt in the late magmatic stage. The magmatic fluid replaced biotite and rare earth phosphates (mainly monazite and apatite) enclosed within biotite, resulting in significant amounts of Nb, Ta, Sn, P, Al, Ca, Fe, and REEs, which subsequently reacted with the FGZ-2 zircons to leach Th, U, Y, and HREEs. Eventually, REEs, Y, Th, and U in the fluid combined with P to form monazite and xenotime, while the other elements partially precipitated with the crystallization of the FGZ-3 zircons. Although the alteration of biotite only released approximately 190 ppm of Sn into the fluid, this is still a significant Sn source for the Sn deposits surrounding the Mopanshan pluton, taking the granite size (∼50 km2) and the volume proportion of biotite (∼5%) into account. Furthermore, based on previous studies on tourmaline from the Mopanshan granite and regional geochemistry, it may be inferred that the addition of wall rock components may also play an important role in Sn mineralization.

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.

Zircon Hf Isotope Mapping for Understanding Crustal Architecture and Its Controls on Mineralization during Early Cretaceous in the Southern Great Xing’an Range, NE China

Zircon Hf Isotope Mapping for Understanding Crustal Architecture and Its Controls on Mineralization during Early Cretaceous in the Southern Great Xing’an Range, NE China

Linking beryllium enrichment to crystal-melt separation in granitic magmatic systems: Insights from high-silica granites in the southern Great Xing’an Range, NE China

High-silica granites are significant carriers of highly incompatible elements and are closely associated with mineralization of the rare metal beryllium. Thus, understanding their origin and evolution is of paramount importance for comprehending the evolution of the continental crust and enrichment processes of beryllium. This study presents zircon U-Pb ages, whole-rock major and trace element compositions, and Nd-Hf-O isotopic data for Early Cretaceous high-silica granite porphyries, monazite U-Pb ages and Nd isotopic data for beryllium-rich quartz veins, and whole-rock and apatite Nd isotopic data for Permian tuffs in the Dongshanwan W-Mo-Be deposit in the southern Great Xing’an Range, northeastern China. Our aim is to elucidate the link between mineralization and magmatism and to further our insight into the processes of crystal-melt separation and the mechanisms driving beryllium enrichment in granitic magmatic systems. Zircon U-Pb dating of the high-silica granite porphyry yields a weighted mean 206Pb/238U age of 141 ± 1 Ma, which is consistent with the age of hydrothermal monazite (ca. 140 Ma) from the beryllium-rich quartz veins. Hydrothermal monazite from the intra-granite porphyry quartz vein has positive εNd(t) values (+0.76 to +1.63) that overlap broadly with whole-rock Nd isotopic compositions of the host granite porphyry [εNd(t) = +1.24 to +1.61]. These characteristics indicate that the Dongshanwan beryllium mineralization was temporally and genetically associated with magmatic-hydrothermal activity of the Dongshanwan high-silica granite porphyries. Our systematic studies suggest that both the Dongshanwan high-silica granite porphyries and coeval Be-barren high-silica granites in the study area are high-K calc-alkaline I-type granites. They originated from a shared magmatic system and formed by the partial melting of a predominantly juvenile medium- to high-K basaltic crustal source, with a minor addition of old crustal components. Rayleigh fractionation modeling indicates that the granitic magma underwent a two-stage crystal-melt separation process. During the first stage, the fractional crystallization of a large proportion of plagioclase, in which beryllium is compatible, not only effectively inhibited beryllium enrichment in the differentiated melt, but also removed a large amount of Ca. During the second stage, minerals in which beryllium is incompatible dominated the fractionating assemblage owing to the low Ca contents in the magma, resulting in a surge in beryllium concentration in the differentiated melt. Our findings reveal that beryllium cannot be appreciably enriched in calc-alkaline granitic magmatic systems until plagioclase fractionation has substantially removed Ca from the system.

Trace elements and growth patterns in quartz from the Alubaogeshan granite in the Maodeng Mo-Bi-Sn-Cu deposit, southern Great Xing’an Range, NE China

The Maodeng Mo-Bi-Sn-Cu deposit is located in the southern segment of the Great Xing’an Range in northeastern China. The Alubaogeshan complex is the major intrusion in this region, which is composed of porphyritic monzogranite (PMG), granite porphyry (GP), and alkali feldspar granite (AFG). We conducted SEM-CL and LA-ICP-MS analyses to examine internal textures and trace elements of quartz from three facies, aiming to uncover the petrogenetic connections among the different lithologies. Quartz phenocrysts from PMG and GP exhibit smudged pre-resorption core, and post-resorption quartz overgrowths with higher Ti concentration and CL intensity, whereas quartz from AFG shows a taxitic structure, with an outward decrease in Ti concentration and CL intensity. There is a positive correlation between CL intensity and Ti content in magmatic quartz. The Al/Ti and Ge/Ti ratios in quartz indicate that the degrees of differentiation of PMG and GP are comparable and relatively low, while that of AFG is high. Trace element contents also exhibit characteristic evolution during magmatic differentiation, with the higher Al, Be, Ge, Rb, and B, and the lower Ti contents in quartz from the highly evolved AFG, and the higher Ti values in quartz from the less evolved PMG. A strong correlation between Al and Li concentrations suggests that Li+ is a primary charge compensator of Al3+ substituting for Si4+ in quartz, with the remaining Al3+ equilibrating with H+. The entry of Al into quartz is mainly controlled by crystallization temperature in the less evolved granite, but magmatic differentiation exerts a key role in the highly evolved granite. Magma differentiation is a primary factor influencing Ge incorporation into quartz. Quartz crystals from PMG and GP display textural and chemical evidence of high-Ti, -CL, and -temperature overgrowth, indicating multiple recharges of mafic magma into the felsic magma chamber. This process could have supplied abundant metals to the granitic magma system and contributed to the formation of the Maodeng deposit.

Genesis of the Supergiant Shuangjianzishan Ag–Pb–Zn Deposit in the Southern Great Xing’an Range, NE China: Constraints from Geochronology, Isotope Geochemistry, and Fluid Inclusion

The supergiant Shuangjianzishan (SJS) Ag–Pb–Zn deposit, located in the southern Great Xing’an Range (SGXR), is the largest Ag deposit in China. The SJS deposit can be divided into two ore blocks: the Shuangjianzishan ore block and the Xinglongshan ore block. Given the importance of the Xinglongshan ore block in the SJS deposit, our work is focused on the Xinglongshan ore block. The vein orebodies in the Xionglongshan ore block mainly occur in the NW-, NNW-, and NNE-trending fault zones, and its mineralization is mainly related to a deep concealed syenogranite. Here, we present new geochronology, isotope geochemistry, and fluid inclusion data for the Xinglongshan ore block and provide additional insights into the metallogenic mechanism of the deposit. The dating results show that the syenogranite related to the mineralization formed at approximately 137 Ma, which is coherent with some previous age determinations in sulfides from the ore deposit. The mineralization of the Xinglongshan ore block can be divided into four stages: sphalerite–arsenopyrite–pyrite–chalcopyrite–quartz stage (stage I), sphalerite–galena–pyrite–silver-bearing mineral–quartz stage (stage II), sphalerite–galena–silver-bearing mineral–quartz–calcite stage (stage III), and weakly mineralized quartz–calcite stage (stage IV). Four types of fluid inclusions (FIs) have been identified within quartz and calcite veins: liquid-rich, gas-rich, pure-liquid, and pure-gas FIs. The homogenization temperatures in the four stages exhibit a gradual decrease, with stage I ranging from 253 to 302 °C, stage II from 203 to 268 °C, stage III from 184 to 222 °C, and stage IV from 153 to 198 °C, respectively. The salinity for stages I, II, III, and IV falls within the ranges of 3.4–6.6 wt% NaCl eqv., 2.6–7.2 wt% NaCl eqv., 2.9–7.0 wt% NaCl eqv., and 1.2–4.8 wt% NaCl eqv., respectively, indicative of a low-salinity ore-forming fluid. The δ18Owater and δD values of the ore-forming fluid span from −13.9‰ to 7.4‰ and −145‰ to −65‰, with δ13CV-PDB values between −11.0‰ and −7.9‰. These values suggest that the ore-forming fluid predominantly originated from a mixture of magmatic and meteoric water. The 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios of sulfides range from 18.278 to 18.361, 15.530 to 15.634, and 38.107 to 38.448, respectively. These ratios imply that the ore-forming material was primarily derived from the Early Cretaceous granitic magma, which resulted from the mixing of depleted mantle- and crustal-derived magmas. The fluid mixing was the dominant mechanism for mineral precipitation. The Xinglongshan ore block belongs to a magmatic-hydrothermal vein-type deposit related to the Early Cretaceous syenogranite, and the Shuangjianzishan ore block belongs to an intermediate sulfidation epithermal deposit related to coeval subvolcanic rocks. The Ag–Pb–Zn mineralization at Shuangjianzishan is genetically related to the Early Cretaceous volcanic–intrusive complex.

Fluid evolution and genesis of the Changchunling Pb–Zn deposit in the Southern Great Xing'an Range, Northeast China: Constraints from fluid inclusions and H–O–S–Pb isotopes

AbstractThe southern Great Xing'an Range (SGXR), an important polymetallic metallogenic province in the eastern Central Asian Orogenic Belt (CAOB) in Northeast China, containing numerous ore deposits of Cu, Fe, Pb, Zn, Au, and so forth. The Changchunling Pb–Zn deposit, located in the eastern segment of the SGXR, is primarily hosted by a Permian conglomerate and siltstone unit. The paragenetic sequence of the deposit can be divided into three stages involving arsenopyrite–quartz (stage I); pyrite–sphalerite–galena–quartz (stage II); and barren quartz–carbonate (stage III). Fluid inclusion (FIs) microthermometric studies revealed that only liquid‐rich aqueous inclusions (VL‐type FIs) are observed in the ore‐bearing quartz veins. The FIs of stages I, II, and III yield homogenization temperatures of 190–314, 170–268, and 140–195°C with salinities of 9.73–13.44, 7.86–10.74, and 4.94–5.99 wt% NaCl eqv., respectively. The ore‐forming fluids are characterized by low temperature and low salinity of the H2O–NaCl fluid system. The δ18OH2O and δD values range from −11.8‰ to 0‰ and −120.4‰ to −99.9‰, respectively, indicating that the source of the fluids was primarily derived from a mixed fluid of magmatic water and meteoric water. Fluid cooling, mixing and fluid‐rock reactions were the major ore precipitation mechanisms at Chanchunling. Sulfur‐lead isotopes of pyrite and sphalerite (δ34S = 2.3‰–3.7‰, 206Pb/204Pb = 18.259–18.285, 207Pb/204Pb = 15.544–15.57, and 208Pb/204Pb = 38.136–38.215) indicate that ore metals had a magmatic source. Integrating the available geological, mineralization, fluid inclusion, and H–O–S–Pb isotope evidence, we conclude that the Changchunling Pb–Zn deposit is an epithermal system, which shares many similar features with the regional Pb–Zn polymetallic deposit.

Geochronology and geochemistry of the Beidashan pluton in the southern Great Xing'an Range, Northeast China: Implication for its petrogenesis and metallogenic potential

Geochronology and geochemistry of the Beidashan pluton in the southern Great Xing'an Range, Northeast China: Implication for its petrogenesis and metallogenic potential

Silver Behavior During Magmatic and Magmatic-Hydrothermal Evolution of a Highly Evolved Reduced Granitic System Related to the Giant Shuangjianzishan Ag-Pb-Zn-(Sn) Epithermal Deposit, Northeast China

Abstract Magmatic-related epithermal silver-rich polymetallic deposits are among the most important sources of Ag in the world, and they are found associated with magmatic systems with striking differences. Most of the time, they are associated either with I-type oxidized (magnetite-series granite) intermediate to evolved intrusions or with S-type/A-type reduced (ilmenite-series granite) highly evolved intrusions. To better understand these associations, the Ag evolution has been tracked during the magmatic differentiation and the magmatic-hydrothermal transition stage of A-type highly evolved porphyritic granites associated with the giant Shuangjianzishan Ag-Pb-Zn-(Sn) epithermal deposit, the largest known Ag deposit of Asia (145 million tonnes at 128.5 g/t Ag and 2.2 wt % Pb + Zn) located in the largest known metallogenic province for Ag in China (the southern Great Xing’an Range). At the Shuangjianzishan deposit, the porphyritic granite complex consists of three temporally distinct intrusions—a coarse-grained monzogranite porphyry, a fine-grained syenogranite porphyry, and a fine-grained syenogranite—having crystallized at ~2 kbar and ~750°C and recording a continuous magmatic differentiation trend. The silicate melt that generated the last highly differentiated intrusion (fine-grained syenogranite) is interpreted as the source of the mineralizing fluids forming the Shuangjianzishan Ag-Pb-Zn-(Sn) epithermal deposit, as it is the only intrusive unit that reached fluid saturation, as indicated by cotrapped fluid and melt inclusions in quartz phenocrysts and by the occurrences of unidirectional solidification textures (USTs). Silver evolution in the different porphyritic granite facies was reconstructed with laser ablation-inductively coupled plasma-mass spectrometry analyses of quartz-hosted silicate melt inclusions, amphibole-hosted magmatic sulfide inclusions, and chemical modeling. The silicate melt forming the porphyritic granite complex was sulfide saturated during the first crystallization stage, as shown by the occurrence of Ag-rich monosulfide solid solution (MSS) inclusions hosted in amphibole phenocrysts from the coarse-grained monzogranite porphyry and from mafic microgranular enclaves hosted in the coarse-grained monzogranite porphyry. However, these Ag-rich MSSs had only a minimal impact on the Ag budget of the magmatic system, as shown by the increase of the Ag concentration (~100–1,000 ppb) in quartz-hosted silicate melt inclusions during the further evolution of the system until fluid exsolution was reached. These results combined with mass balance modeling suggest that Ag and Sn are efficiently transferred to the evolving residual melt during crystallization and crystal-melt segregation. The results of this study indicate that highly Ag endowed epithermal polymetallic deposits can be formed from the exsolution of Ag-rich mineralizing fluids from relatively low volume, highly evolved, reduced melts, similar to those responsible for the formation of Sn-rich greisen deposits.

Coupling Between Exhumation and Subduction: A Case Study From the Southern Great Xing'an Range, NE Asia

AbstractThe link between subduction and continental exhumation is explored using high‐resolution thermal histories from southern Great Xing'an Range (GXR), NE Asia and integrated with a regional low‐temperature thermochronology data synthesis from the NE Asian continental margin. The GXR thermal histories are constrained by multiple thermo‐, geochronometers (zircon, titanite, apatite U‐Pb, zircon, apatite (U‐Th)/He and apatite fission track). These data yield a large range in U‐Pb ages (292–119 Ma) with enhanced exhumation mainly during the early Cretaceous (ca. 155–110 Ma) in an extensional regime linked to roll‐back of the Paleo‐Pacific Ocean and consequent lithospheric thinning and delamination. Integrated with Cretaceous‐Cenozoic low‐temperature thermochronological data from the NE Asian continent margin, three regional phases of exhumation are recognized, which can be linked to changes in the geometry and kinematics of the subduction systems of the Paleo‐Pacific and Pacific oceans, demonstrating coupling between the subducting plate and the continental margin at active plate boundaries.

Petrogenesis and Tectonic Setting of Early Cretaceous A-Type Granite from the Southern Great Xing’an Range, Northeastern China: Geochronological, Geochemical, and Hf Isotopic Evidence

The southern Great Xing’an Range is located in the eastern Central Asian Orogenic Belt, where voluminous igneous rocks developed during the Late Mesozoic period. The east slope of the southern Great Xing’an Range has been the topic of numerous debates on the level of influence of the Mongol-Okhotsk and the Paleo-Pacific regimes in the Late Mesozoic period. Therefore, this area is a suitable region in which to study the temporal changes in magma sources and tectono-magmatic evolution. In this paper, whole-rock geochemical data, zircon U-Pb geochronology, and zircon Hf isotope studies were carried out on the granitoids in the east slope area of the southern Great Xing’an Range. LA-ICP-MS zircon U-Pb dating revealed the ages of four granitoid samples: 135.0 ± 0.6 Ma, 130.7 ± 1.4 Ma, 130.4 ± 1.0 Ma, and 127.6 ± 0.8 Ma, respectively. The Hf isotope values 176Hf/177Hf = 0.282751–0.283015, εHf (t) = +2.0~+11.5, and T2DM = 583~1442 Ma suggest that the magma was generated by partial melting of Meso- and Neoproterozoic accreted and thickened low crust. The whole-rock geochemical data implied that these granitoids are A-type granite and their formation is closely linked to the subduction of the Paleo-Pacific Ocean plate. These geochemical, isotopic, and geochronological data suggest that the Early Cretaceous magmatism in the east slope area of the southern Great Xing’an Range formed in an extensional back-arc tectonic setting associated with the slab roll-back of the Paleo-Pacific plate subduction.

Contribution discrepancy of two distinct wall rocks to wolframite mineralization from Dongshanwan quartz-vein tungsten deposit, Southern Great Xing’an Range, China

The Southern Great Xing’an Range is a significant polymetallic metallogenic belt in Northeast China. The ages of granite related to tungsten mineralization have been well quantified, however, the timing and mechanism of quartz vein-type wolframite deposition remain unclear. Therefore, our study focused on the Dongshanwan tungsten deposit, representing a typical wolframite-bearing quartz vein-type deposit in the Southern Great Xing’an Range. Quartz vein-type tungsten mineralization was mainly contained in the Early Cretaceous granite porphyry, with few exceptions in the Permian tuff. Representative wolframite samples were collected from intragranitic (Wol-I) and intra-tuff (Wol-II) quartz veins for wolframite U–Pb dating, electron probe microanalysis (EPMA), and trace elemental analysis. Wolframite U–Pb dating recognized an Early Cretaceous mineralization event at 139–141 Ma, consistent with the previous Dongshanwan granite’s ages (∼142 Ma) but much younger than tuff (∼260 Ma). All the wolframite samples belonged to the ferberite series (FeO/MnO = 4.0–6.9), which indicates a link to the highly fractionated granite. Wol-I showed high contents of Nb, Ta, Sc, and HREEs and a strongly negative Eu anomaly (0.02–0.29), while these elements in Wol-II were approximately one order of magnitude lower than in Wol-I and the Eu anomaly was highly variable (0.17–1.02). The redox characteristics reflected by the Eu anomaly of wolframite may correspond to the variations in oxygen fugacity. Based on petrology, geochemistry, and element mass migration, this study suggests that the granite porphyry and tuff in the Dongshanwan deposit contributed differently to the wolframite precipitation even if the ore-forming fluids were of a common magmatic-hydrothermal origin. The exsolved fluid reserved in the closed system interacts with granite to achieve continuous enrichment in Nb, Ta, Sn, and REEs and accepts external Fe supply from granite alteration to precipitate Wol-I. In contrast, the fluids in relatively open and non-granitic systems have lower Nb, Ta, Sn, and REEs than the former, and Fe supply depends on the alteration of tuff. The abundance of fluorite and the non-CHARAC (CHArge-and-RAdius-Controlled) behavior of Y/Ho and Zr/Hf in the wolframite suggested that fluorine plays an important role in the migration and enrichment of tungsten and other elements during tungsten mineralization.