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The world-class Huize deposit hosts significant germanium (Ge) resources in the Sichuan–Yunan–Guizhou (SYG) Mississippi Valley-type (MVT) Pb–Zn province of China. The distribution and enrichment mechanism of Ge is still poorly understood. In the main ore-forming stage of Huize, we identified six sphalerite colors from C1 (black) to C6 (white) in transmitted light. Two color sequences are confirmed, including C1 → C2 → C3 → C6 and C1 → C2 → C4 → C5 → C6. We used multiple analytical methods to reveal the Ge distribution and incorporation mechanism into sphalerite and the possible enrichment factors. Our results show that Ge occurs as argutite (GeO2), and in the sphalerite crystal lattice, C1 and C3 sphalerite has up to 593 ppm Ge. Two substitution mechanisms, i.e., Ge4+ + □(vacancy) → 2Zn2+ (e.g., C1 and C2) and Ge4+ + 2Cu+ → 3Zn2+ (e.g., C2, C3, C4, and C5), are inferred from the Huize sphalerite. They show different spatial structures of sphalerite and a weak shift of the white line observed by high-resolution X-ray absorption near-edge structure (XANES) spectroscopy. The trace-element composition of sphalerite suggests that reduced sulfur content of the ore-forming fluid contributes to Ge enrichment, followed by high temperature (> 300 °C). [ABSTRACT FROM AUTHOR]

The Miaoya carbonatite complex in the South Qinling Orogen hosts one of the largest REE-Nb deposits in China. The origin and evolution of REE enrichment in this Silurian intrusion have been extensively studied, whereas Nb mineralization remains less well understood. Here, we report detailed mineralogical and geochemical data on diverse Nb-bearing minerals from the Miaoya carbonatite to explain the development of Nb mineralization in these rocks. Ferrocolumbite is the dominant Nb mineral, which occurs principally as an alteration product of the earlier-crystallized Nb phases (uranopyrochlore, betafite, and fersmite). The ferrocolumbite varieties (Clb-1, Clb-2, Clb-3) inherited some compositional characteristics of its precursors, in particular a trend of decreasing Ta2O5 and UO2 from Clb-1 to Clb-3, which mimics the Ta-U depletion trend from uranopyrochlore to betafite and fersmite. Varieties Clb-1 and Clb-2 and associated calcite and altered uranopyrochlore show evidence of hydrothermal overprint such as positive Eu anomaly. Ferrocolumbite Clb-2 shows slightly higher Eu/Eu* and Zr/Hf ratios and contains fewer relicts of its precursor mineral in comparison with Clb-1, possibly indicating local enrichment of F in the hydrothermal system. Calcite associated with Clb-3 and fersmite shows a trace element signature characteristic of igneous carbonates, suggesting that this mineral paragenesis is least affected by metasomatic overprint with no contribution from external fluids. The study of the Miaoya REE-Nb deposit shows that late-stage metasomatism of carbonatites does not significantly enhance Nb grade in contrast to that of REE mineralization and leads to the formation of a secondary Nb paragenesis with specific trace element characteristics. [ABSTRACT FROM AUTHOR]

The Maogongdong deposit is located in the giant Dahutang W-Cu-(Mo) ore field, northern Jiangxi Province, South China. It is mainly a vein-type deposit, characterized by early W and late Cu-Mo mineralization, and temporally and spatially associated with Late Mesozoic S-type muscovite granites emplaced into a Neoproterozoic granodiorite batholith and the Shuangqiaoshan Group metasedimentary rocks. Fluid inclusions and H–O isotopes suggest that the early ore-forming fluids of the Maogongdong deposit are mainly magmatic water with relatively high temperature (270–410 °C) and moderate-to-low salinity, while the late ore-forming fluids are mixed with meteoric water, with medium-to-low temperature (160–270 °C) and low salinity. Infrared and conventional microthermometric studies of fluid inclusions of the main tungsten mineralization stage show that the homogenization temperatures of primary fluid inclusion assemblages in wolframite (325 to 355 °C) are about 20 °C higher than those of coexisting scheelite and generally 40 °C higher than those in quartz. The δ34S values of sulfides (− 5.2 to − 1.3 ‰) in the sulfide stage are slightly lower than the magmatic sulfur (− 1.7 to 0.6 ‰) in the pre-ore stage, most likely due to an increase in oxygen fugacity. The low carbon isotope values (− 26.2 to − 15.5 ‰) of fluid inclusions in the tungsten mineralization stage show that a large amount of organic carbon was added before mineralization. Fluid cooling and pressure decrease are the main factors of tungsten ore precipitation, while local boiling may also make a contribution. Mixing of the different fluids led to the formation of copper and molybdenum ores. [ABSTRACT FROM AUTHOR]

The southern Myanmar tin ore district is an important part of the well-known Southeast Asia tin belt (SATB), and hosts numerous economically important primary tin-tungsten ore deposits. However, the timing of formation of these deposits is unclear due to the scarcity of robust age data. The tectonic setting of tin mineralization in this area also needs to be further constrained. Most of the primary tin-tungsten ore deposits in southern Myanmar are typical hydrothermal quartz vein–type, with cassiterite and wolframite as the main ore minerals. Here, we present in situ U–Pb ages of cassiterite and wolframite from nine granite-related hydrothermal Sn–W deposits in southern Myanmar. Cassiterite samples from the Hermyingyi, Thitkhatoe, Thaling Taung, Kalonta, Taungphila, Pagaye, Bawapin, Kanbauk, and Letha Taung deposits yield common lead-corrected weighted mean 206Pb/238U ages of 61.6 ± 0.8 Ma, 61.9 ± 0.6 Ma, 60.4 ± 0.9 Ma, 63.0 ± 0.6 Ma, 62.9 ± 0.6 Ma, 69.5 ± 0.5 Ma, 63.6 ± 0.6 Ma, 61.3 ± 0.6 Ma, and 84.9 ± 0.5 Ma, respectively. Wolframite samples collected from these deposits also yield consistent ages with the cassiterite samples. These ages, combined with available tin mineralization ages from other deposits in the western part of the SATB, define three epochs of Sn metallogeny related to three contrasting geodynamic settings: (1) Early Cretaceous (~ 125–110 Ma) mineralization is related to post-collision slab break-off after collision between the West Burma terrane and the Sibumasu-Tengchong terrane; (2) Late Cretaceous to Paleocene (~ 90–60 Ma) mineralization developed in an Andean-type accretionary setting during subduction of the Neo-Tethys oceanic lithosphere; (3) Early Eocene (~ 50–40 Ma) mineralization may have formed in a post-collision setting after the India-Asia collision. [ABSTRACT FROM AUTHOR]

The Zhaiping Ag–Pb–Zn vein deposit in the Coastal Volcanic Belt of southeastern China, which resulted from subduction of the paleo-Pacific oceanic lithosphere beneath the South China Block, is hosted by Early Cretaceous sub-volcanic rocks (rhyolite porphyry) and younger granite porphyry and quartz porphyry. Three generations of veins have been recognized: (i) pre-ore quartz + pyrite, (ii) syn-ore silver + pyrite + pyrrhotite + base metal sulfides + quartz + sericite, and (iii) post-ore quartz + calcite + fluorite veins. Rubidium–Sr dating of syn-ore pyrite yielded an isochron age of 132.2 ± 2.1 Ma (2σ, MSWD = 2.0, n = 4), which is roughly coincidental with the age of the granite porphyry and quartz porphyry (zircon U–Pb age: ca. 133 Ma). The age data, together with Pb, S, H, and O isotopic compositions, indicate a close temporal and possibly genetic relationship between mineralization and porphyry magmatism at Zhaiping. Geochemical and isotope data demonstrate that the Zhaiping sub-volcanic rocks were derived from partial melting of Proterozoic crustal sources and underwent fractionation of feldspars, monazite, and/or allanite. The 87Sr/86Sr ratios of pre-ore (Aph1) and syn-ore (Aph2) stage apatite are in the ranges of 0.71350 to 0.71441 and 0.71260 to 0.71328, respectively, which are distinct from those of the sub-volcanic intrusive rocks (0.7119–0.7125). The Sr isotope signature, together with lower fluid temperatures (< 360 °C) relative to typical magmatic fluid, points at addition of an external fluid. It is suggested that the sub-volcanic intrusion acted as a heat source that drove the dehydration of, and subsequent fluid circulation within, the host rocks. Lower 87Sr/86Sr ratio but higher Sr content of Aph2 relative to Aph1 possibly indicates continuous fluid–rock interaction and progressive decomposition of feldspar in the host rocks, thus supplying large amounts of Sr and probably Pb to the ore fluid. [ABSTRACT FROM AUTHOR]

The large Hebaoshan gold deposit (41.5 t Au, average grade: 3.5 g/t) is located in a hitherto poorly documented gold province in the northeastern part of the South China Block. It is hosted by Precambrian metasedimentary rocks that experienced Triassic greenschist- to amphibolite-facies metamorphism. Three hydrothermal stages can be distinguished: quartz + sericite + pyrite + pyrrhotite (stage I), quartz + magnetite + sulfide (stage II), and quartz + carbonate + pyrite + hematite (stage III). Auriferous pyrite samples yielded a Rb-Sr isochron age of 234 ± 3 Ma (2σ, MSWD = 0.24), and ore-related hydrothermal sericite yielded a 40Ar-39Ar plateau age of 226.4 ± 2.0 Ma (2σ, MSWD = 1.01), which are distinctly younger than ca. 430 Ma granitic rocks in the mining district and older than 170–130 Ma granites in the region, ruling out any genetic link between granite emplacement and gold mineralization. The mineralizing fluid system can be described as carbonic-aqueous with low to moderate salinity (2.2–10.1 wt% NaCl equiv.) and medium temperature of 290 to 350 °C (stage I) and 230 to 280 °C (stage II). The δ18O quartz ranges from 13.3 to 15.4 ‰, and the δD values for fluid inclusions in quartz range from − 97 to − 60 ‰. The calcite has C-isotopes ranging from − 6.1 to − 3.8 ‰ and O-isotopes from 2.8 to 13.6 ‰. H-O-C isotope data are consistent with a metamorphic fluid derived from devolatilization of Neoproterozoic basement rocks during regional metamorphism in the Late Triassic Indosinian period. The δ34S values of sulfides for stages I, II, and III are 0.1 to 7.8 ‰, − 10.6 to 5.1 ‰, and − 18.9 to − 14.1 ‰, respectively, indicating an increase in oxygen fugacity during fluid ascent which resulted in more negative sulfur isotope values of sulfides and precipitation of gold. Pyrite separates have 206Pb/204Pb ratios of 17.340 to 17.687, 207Pb/204Pb ratios of 15.539 to 15.604, and 208Pb/204Pb ratios of 37.749 to 38.094. The S-Pb isotope data suggest derivation of S and Pb from the Precambrian metasedimentary country rocks. Auriferous pyrite yielded elevated 3He/4He ratios (0.78–1.46 Ra), which suggest a mantle component as can be expected from fluids derived from a subduction setting. It is concluded that Hebaoshan is an orogenic gold deposit that formed during Triassic flat-slab subduction of the paleo-Pacific plate beneath the South China Block and thus constitutes the first Triassic deposit of this type recognized in the coastal area of Southeast China. [ABSTRACT FROM AUTHOR]

The North Wuyi area is an important metallogenic belt in South China and hosts many Pb–Zn–Ag deposits within the Jurassic–Cretaceous volcanic basins. These deposits are mostly genetically associated with Late Jurassic magmatism. The Cretaceous granitic rocks in the Lizikeng basin, at the eastern part of the North Wuyi area, were investigated for their mineralogical and geochemical characteristics in this study. Three types of granitic rocks, quartz monzonite, granite porphyry, and monzogranite, occur, and zircon U–Pb dating reveals that they all formed during the short period of 133–129 Ma, corresponding to the early Cretaceous volcanic-intrusive activities in South China. The whole-rock geochemistry indicates that all three granitic rocks have I-type affinity. The quartz monzonite and granite porphyry have consistently low whole-rock εNd(t) values of − 10.4 to − 9.6 and zircon εHf(t) values of − 14.2 to − 8.2, and they were likely derived from Proterozoic crustal sources without any significant contribution of mantle-derived material. The monzogranite, which shows also negative but slightly higher εNd(t) and εHf(t) values of − 7.6 to − 7.1 and − 9.3 to − 7.0, respectively, might also be derived from a major Proterozoic crustal source but with some input of mantle magma. The geochemical data show that the monzogranite belongs to tungsten-bearing granite with highly evolved characteristics, and with high Nb and W contents similar to the typical rare-metal and W-bearing granites in South China. A large number of typical hydrothermal rare-metal minerals are identified in the monzogranite, such as W-bearing rutile, niobian rutile, and columbite-group minerals as well as ferberite. The discovery of the early Cretaceous granitic rocks with tungsten mineralization potential indicates that the North Wuyi area is prospective for rare-metal mineralization, which opens a new window for rare-metal prospecting in the volcanic basins, as this type of ore deposit was previously thought to occur in granites from mountain range areas in South China, such as the Nanling Range. [ABSTRACT FROM AUTHOR]

The genesis of Earth's largest rare earth element (REE) deposit, Bayan Obo (China), has been intensely debated, in particular whether the host dolomite marble is of sedimentary or igneous origin. The protracted (Mesoproterozoic to Paleozoic) and intricate (magmatic to metasomatic) geological processes complicate geochemical interpretations. In this study, we present a comprehensive petrographic and in situ, high-spatial resolution Sr-Pb isotopic and geochemical investigation of the host dolomite from the Bayan Obo marble. Based on petrographic evidence, the dolomite marble is divided into three facies including coarse-grained (CM), fine-grained (FM), and heterogeneous marble (HM). All carbonates are ferroan dolomite with high SrO and MnO contents (> 0.15 wt.%), consistent with an igneous origin. Trace element compositions of these dolomites are highly variable both among and within individual samples, with CM dolomite displaying the strongest LREE enrichment. In situ 206Pb/204Pb and 207Pb/204Pb ratios of the dolomite are generally consistent with mantle values. However, initial 208Pb/204Pb ratios define a large range from 35.45 to 39.75, which may result from the incorporation of radiogenic Pb released from decomposition of monazite and/or bastnäsite during Early Paleozoic metasomatism. Moreover, in situ Sr isotope compositions of dolomite indicate a large range (87Sr/86Sr = 0.70292–0.71363). CM dolomite is characterized by a relatively consistent, unradiogenic Sr isotope composition (87Sr/86Sr = 0.70295–0.70314), which is typical for Mesoproterozoic mantle. The variation of 87Sr/86Sr ratios together with radiogenic 206Pb/204Pb signatures for dolomite within FM and HM possibly represents recrystallization during Early Paleozoic metasomatism with the contribution of radiogenic Sr and Pb from surrounding host rocks. Therefore, our in situ geochemical data support a Mesoproterozoic igneous origin for the ore-bearing dolomite marble in the Bayan Obo deposit, which subsequently underwent intensive metasomatism during the Early Paleozoic. [ABSTRACT FROM AUTHOR]

The Pengshan Sn and Pb-Zn polymetallic deposits are located in the south margin of the Jiujiang-Ruichang (Jiurui) district of the Middle-Lower Yangtze River Metallogenic Belt in South China. Four large deposits include Huangjinwa, Zengjialong, Jianfengpo, and Zhangshiba, the former three are Sn-dominant deposits which occur as stratiform orebodies in the contact zones of the Pengshan granites and within the country rock strata, whereas Zhangshiba consists of stratiform Pb-Zn orebodies within the Precambrian metasedimentary strata. In this study, we present results on zircon U-Pb ages, major and trace elements, and mineral chemistry as well as Sr-Nd-Hf isotope data of the granites, Pb and S isotopes of both the Sn-dominant and Pb-Zn dominant deposits, and U-Pb dating of cassiterite from the Pengshan district. SHRIMP and LA-ICP-MS zircon U-Pb dating shows that the Pengshan granites were emplaced in the Early Cretaceous (129-128 Ma), which is in good agreement with the U-Pb dating (130-128 Ma) of cassiterite from the Jianfengpo Sn deposit. The Pengshan granites consist mainly of weakly peraluminous highly fractionated I-type affinity granitic rocks. Detailed elemental and isotopic data suggest that the granites formed by partial melting of Mesoproterozoic metamorphic basement materials with minor input of mantle-derived melts. The mineral chemistry of biotite demonstrates that the Pengshan granitic magma had a low oxygen fugacity, thereby precluding the tin dominantly partitioning into the rock-forming silicate minerals and favoring accumulation in the exsolved residual liquid during magma crystallization stages. Sulfur isotopes show a relatively heavy sulfur isotopic composition from 5.8 to 17.6 ‰, and no difference for sulfur isotopes between the Sn deposits (5.8-13.4 ‰, Huangjinwa, Zengjialong, Jianfengpo) and the Pb-Zn deposit (mostly 7.1-13.0 ‰, except for one 17.6 ‰, Zhangshiba). The sulfur isotope data of pyrite from the host sedimentary rocks show relatively higher δS values of 22.7-28.7 ‰. Lead isotopes indicate that the granites have higher Pb/Pb, Pb/Pb, and Pb/Pb ratios than the host Precambrian metasedimentary rocks, and the sulfide minerals from the orebodies fall in between them. Again, there is no difference for Pb isotopes between the Sn deposits (Huangjinwa, Zengjialong, Jianfengpo) and the Zhangshiba Pb-Zn deposit. The coincidence in S and Pb isotope compositions for Sn and Pb-Zn deposits suggests that similar sources for these mineralization, possibly derived from a mixed source of the granitic magmas and the Precambrian metasedimentary rocks. These data therefore favor of a magmatic-hydrothermal origin for both the Sn and Pb-Zn polymetallic mineralization in the Pengshan district. [ABSTRACT FROM AUTHOR]