Sediment-hosted Zn–Pb–Cu deposits in the Central African Copperbelt

Stratabound epigenetic sulphide Zn–Pb–Cu ore deposits of the Central African Copperbelt in the Democratic Republic of Congo and Zambia are mostly hosted in deformed shallow marine platform carbonates and associated sedimentary rocks of the Neoproterozoic Katanga Supergroup. Economic orebodies, that also contain variable amounts of minor Cd, Co, Ge, Ag, Re, As, Mo, Ga, and V, occur mainly as irregular pipe-like bodies associated with collapse breccias and faults as well as lenticular bodies subparallel to bedding. Kipushi and Kabwe in the Democratic Republic of the Congo and Zambia, respectively, are the major examples of carbonate-hosted Zn–Pb–Cu mined deposits with important by-products of Ge, Cd, Ag and V in the Lufilian Arc, a major metallogenic province famous for its world-class sediment-hosted stratiform Cu–Co deposits. The carbonate-hosted deposits range in age from Neoproterozoic to early Palaeozoic (680 to 450 Ma). The formation of the relatively older Neoproterozoic deposits is probably related to early collision events during the Lufilian Orogeny, whereas the younger Palaeozoic deposits may be related to post-collisional processes of ore formation. Fluid inclusion and stable isotope data indicate that hydrothermal metal-bearing fluids evolved from formation brines during basin evolution and later tectonogenesis. Ore fluid migration occurred mainly along major thrust zones and other structural discontinuities such as karsts, breccias and faults within the Katangan cover rocks, resulting in ore deposition within favourable structures and reactive carbonates of the Katangan Supergroup.     

Some new data on the genesis of the Linghou Cu–Pb–Zn polymetallic deposit—Based on the study of fluid inclusions and C–H–O–S–Pb isotopes

The Linghou deposit, located near Hangzhou City of Zhejiang Province, eastern China, is a medium-sized polymetallic sulfide deposit associated with granitic intrusion. This deposit is structurally and lithologically controlled and commonly characterized by ore veins or irregular ore lenses. In this deposit, two mineralization events were identified, of which the former produced the Cu–Au–Ag orebodies, while the latter formed Pb–Zn–Cu orebodies. Silicification and calc-silicate (skarn type), phyllic, and carbonate alternation are four principal types of hydrothermal alteration. The early Cu–Au–Ag and late Pb–Zn–Cu mineralizations are characterized by quartz ± sericite + pyrite + chalcopyrite + bornite ± Au–Ag minerals ± magnetite ± molybdenite and calcite + dolomite + sphalerite + pyrite + chalcopyrite + galena, respectively. Calcite clusters and calcite ± quartz vein are formed during the late hydrothermal stage.The NaCl–H₂O–CO₂ system fluid, coexisting with NaCl–H₂O system fluid and showing the similar homogenization temperatures (385 °C and 356 °C, respectively) and different salinities (16.89–21.68 wt.% NaCl eqv. and 7.70–15.53 wt.% NaCl eqv.), suggests that fluid immiscibility occurred during the Cu–Au–Ag mineralization stage and might have given rise to the ore-metal precipitation. The ore-forming fluid of the Pb–Zn–Cu mineralization mainly belongs to the NaCl–H₂O–CO₂ system of high temperature (~ 401 °C) and mid-high salinity (10.79 wt.% NaCl eqv.).Fluids trapped in the quartz-chalcopyrite vein, Cu–Au–Ag ores, Pb–Zn–Cu ores and calcite clusters yielded δ¹⁸O_H2O and δD values varying from 5.54‰ to 13.11‰ and from − 71.8‰ to − 105.1‰, respectively, indicating that magmatic fluids may have played an important role in two mineralization events. The δ¹³C_PDB values of the calcite change from − 2.78‰ to − 4.63‰, indicating that the CO₃^2 − or CO₂ in the ore-forming fluid of the Pb–Zn–Cu mineralization was mainly sourced from the magmatic system, although dissolution of minor marine carbonate may have also occurred during the ore-forming processes. The sulfide minerals have homogeneous lead isotopic compositions with ²⁰⁶Pb/²⁰⁴Pb ranging from 17.958 to 18.587, ²⁰⁷Pb/²⁰⁴Pb ranging from 15.549 to 15.701, and ²⁰⁸Pb/²⁰⁴Pb ranging from 37.976 to 39.052, indicating that metallic elements of the Linghou deposit came from a mixed source involving mantle and crustal components.Based on geological evidence, fluid inclusions, and H–O–C–S–Pb isotopic data, the Linghou polymetallic deposit is interpreted as a high-temperature, skarn-carbonate replacement type. Two types of mineralization are both related to the magmatic–hydrothermal system, with the Cu–Au–Ag mineralization having a close relationship with granodiorite.     

Constraints of C–O–S–Pb isotope compositions and Rb–Sr isotopic age on the origin of the Tianqiao carbonate-hosted Pb–Zn deposit,SW China

The Tianqiao Pb–Zn deposit in the western Yangtze Block, southwest China, is part of the Sichuan–Yunnan–Guizhou (SYG) Pb–Zn metallogenic province. Ore bodies are hosted in Devonian and Carboniferous carbonate rocks, structurally controlled by a thrust fault and anticline, and carried about 0.38 million tons Pb and Zn metals grading > 15% Pb + Zn. Both massive and disseminated Pb–Zn ores occur either as veinlets or disseminations in dolomitic rocks. They are composed of ore minerals, pyrite, sphalerite and galena, and gangue minerals, calcite and dolomite. δ³⁴S values of sulfide minerals range from + 8.4 to + 14.4‰ and display a decreasing trend from pyrite, sphalerite to galena (δ³⁴S_pyrite > δ³⁴S_sphalerite > δ³⁴S_galena). We interpret that reduced sulfur derived from sedimentary sulfate (gypsum and barite) of the host Devonian to Carboniferous carbonate rocks by thermal–chemical sulfate reduction (TSR). δ¹³C_PDB and δ¹⁸O_SMOW values of hydrothermal calcite range from –5.3 to –3.4‰ and + 14.9 to + 19.6‰, respectively, and fall in the field between mantle and marine carbonate rocks. They display a negative correlation, suggesting that CO₂ in the hydrothermal fluid was a mixture origin of mantle, marine carbonate rocks and sedimentary organic matter. Sulfide minerals have homogeneous and low radiogenic Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb = 18.378 to 18.601, ²⁰⁷Pb/²⁰⁴Pb = 15.519 to 15.811 and ²⁰⁸Pb/²⁰⁴Pb = 38.666 to 39.571) that are plotted in the upper crust Pb evolution curve and overlap with that of Devonian to Carboniferous carbonate rocks and Proterozoic basement rocks in the SYG province. Pb isotope compositions suggest derivation of Pb metal from mixed sources. Sulfide minerals have ⁸⁷Sr/⁸⁶Sr ratios ranging from 0.7125 to 0.7167, higher than Sinian to Permian sedimentary rocks and Permian Emeishan flood basalts, but lower than basement rocks. Again, Sr isotope compositions are supportive of a mixture origin of Sr. They have an Rb–Sr isotopic age of 191.9 ± 6.9Ma, possibly reflecting the timing of Pb–Zn mineralization. C–O–S–Pb–Sr isotope compositions of the Tianqiao Pb–Zn deposit indicate a mixed origin of ore-forming fluids, which have Pb–Sr isotope homogenized before the mineralization. The Permian flood basalts acted as an impermeable layer for the Pb–Zn mineralization hosted in the Devonian–Carboniferous carbonate rocks.     

SHRIMP U–Pb zircon dating of the host rocks of the Cannington Ag–Pb–Zn deposit,southeastern Mt Isa Block,Australia

SHRIMP U–Pb zircon ages are reported from a paragneiss, a pegmatite, a metasomatised metasediment and an amphibolite taken from the upper amphibolite facies host sequence of the Cannington Ag–Pb–Zn deposit at the southeastern margin of the Proterozoic Mt Isa Block. Also reported are ages from a middle amphibolite‐facies metasediment from the Soldiers Cap Group approximately 90 km north of Cannington. The predominantly metasedimentary host rocks of the Cannington deposit were eroded from a terrane containing latest Archaean to earliest Palaeoproterozoic (ca 2600–2300 Ma) and Palaeoproterozoic (ca 1750–1700 Ma) zircon. The ca 1750–1700 Ma group of zircons are consistent with sedimentary provenance from rocks of Cover Sequence 2 age that are now exposed to the north and west of the Cannington deposit. The metasedimentary samples also include a group of zircon grains at ca 1675 Ma, which we interpret as the maximum depositional age of the sedimentary protolith. This is comparable to the maximum depositional age of the metasediment from the Maronan area (ca 1665 Ma) and to previously published data from the Soldiers Cap Group. Metamorphic zircon rims and new zircon grains grew at 1600–1580 Ma during upper amphibolite‐facies metamorphism in metasedimentary and mafic magmatic rocks. Zircon inheritance patterns suggest that sheet‐like pegmatitic intrusions were most likely derived from partial melting of the surrounding metasediments during this period of metamorphism. Some zircon grains from the amphibolite have a morphology consistent with partially recrystallised igneous grains and have apparent ages close to the metamorphic age, although it is not clear whether these represent metamorphic resetting or crystallisation of the magmatic protolith. Pb‐loss during syn‐ to post‐metamorphic metasomatism resulted in partial resetting of zircons from the metasomatised metasediment.     

Pb isotopic constraints on the formation of the Dikulushi Cu–Pb–Zn–Ag mineralisation, Kundelungu Plateau (Democratic Republic of Congo)

Base metal–Ag mineralisation at Dikulushi and in other deposits on the Kundelungu Plateau (Democratic Republic of Congo) developed during two episodes. Subeconomic Cu–Pb–Zn–Fe polysulphide ores were generated during the Lufilian Orogeny (c. 520 Ma ago) in a set of E–W- and NE–SW-oriented faults. Their lead has a relatively unradiogenic and internally inhomogeneous isotopic composition (²⁰⁶Pb/²⁰⁴Pb = 18.07–18.49), most likely generated by mixing of Pb from isotopically heterogeneous clastic sources. These sulphides were remobilised and enriched after the Lufilian Orogeny, along reactivated and newly formed NE–SW-oriented faults into a chalcocite-dominated Cu–Ag mineralisation of high economic interest. The chalcocite samples contain only trace amounts of lead and show mostly radiogenic Pb isotope signatures that fall along a linear trend in the ²⁰⁷Pb/²⁰⁴Pb vs. ²⁰⁶Pb/²⁰⁴Pb diagram (²⁰⁶Pb/²⁰⁴Pb = 18.66–23.65; ²⁰⁷Pb/²⁰⁴Pb = 15.72–16.02). These anomalous characteristics reflect a two-stage evolution involving admixture of both radiogenic lead and uranium during a young fluid event possibly c. 100 Ma ago. The Pb isotope systematics of local host rocks to mineralisation also indicate some comparable young disturbance of their U–Th–Pb systems, related to the same event. They could have provided Pb with sufficiently radiogenic compositions that was added to less radiogenic Pb remobilised from precursor Cu–Pb–Zn–Fe polysulphides, whereas the U most likely originated from external sources. Local metal sources are also suggested by the ²⁰⁸Pb/²⁰⁴Pb–²⁰⁶Pb/²⁰⁴Pb systematics of combined ore and rock lead, which indicate a pronounced and diversified lithological control of the immediate host rocks on the chalcocite-dominated Cu–Ag ores. The Pb isotope systematics of polysulphide mineralisation on the Kundelungu Plateau clearly record a diachronous evolution.     

Heavy metal contamination in the vicinity of the Daduk Au–Ag–Pb–Zn mine in Korea

The heavy metal contamination and seasonal variation of the metals in soils, plants and waters in the vicinity of an abandoned metalliferous mine in Korea were studied. Elevated levels of Cd, Cu, Pb and Zn were found in tailings with averages of 8.57, 481, 4,450 and 753 mg/kg, respectively. These metals are continuously dispersed downstream and downslope from the tailings by clastic movement through wind and water. Thus, significant levels of the elements in waters and sediments were found up to 3.3 km downstream from the mining site, especially for Cd and Zn. Enriched concentrations of heavy metals were also found in various plants grown in the vicinity of the mining area, and the metal concentrations in plants increased with those in soils. In a study of seasonal variation on the heavy metals in paddy fields, relatively high concentrations of heavy metals were found in rice leaves and stalks grown under oxidizing conditions rather than a reducing environment (P<0.05).     

Ore-forming material sources of the Jurassic Cu–Pb–Zn mineralization in the Qin–Hang ore belt,South China: Constraints from S–Pb isotopes

The Qin–Hang ore belt in South China, which serves as the boundary between the Yangtze and Cathaysia blocks, is marked by extensive Jurassic porphyry-skarn-metasomatic Cu–Pb–Zn polymetallic mineralization. In this contribution, S and Pb isotopic compositions of the Baoshan Cu–Pb–Zn deposit in the western portion of the Qin–Hang ore belt were analyzed to determine the ore-forming material sources in the area. This is coupled by the first systematic collection, compilation and interpretation of previously published S and Pb isotopic data of multiple sulfide minerals to reveal the metal origin and accumulation mechanism of the Cu–Pb–Zn mineralization from the significant deposits in the region (i.e., Dexing, Qibaoshan, Shuikoushan, Baoshan, Huangshaping, Tongshanling and Dabaoshan). The results show that Cu mineralization is characterized by low and narrow δ³⁴S (‰) range of values (–5 to 6) and Pb isotopic ratios (²⁰⁸Pb/²⁰⁴Pb = 38.0–39.0, ²⁰⁷Pb/²⁰⁴Pb = 15.4–15.8, and ²⁰⁶Pb/²⁰⁴Pb = 17.7–18.7), which are consistent with those of local porphyries. In contrast, the Pb–Zn mineralization reveals higher and more variable δ³⁴S (‰) values (–4 to 18) and Pb isotopic ratios (²⁰⁸Pb/²⁰⁴Pb = 38.0–39.5, ²⁰⁷Pb/²⁰⁴Pb = 15.3–16.0, and ²⁰⁶Pb/²⁰⁴Pb = 18.0–19.0) that correspond to wall-rock and basement rock compositions in the region. This indicates that the sulfur and lead that formed the Cu mineralization in the Qin–Hang ore belt was mainly sourced from regional magmatism with mantle contributions, whereas the sulfur and lead for the Pb–Zn mineralization was likely derived from the host sedimentary rocks and Proterozoic metamorphic basement rocks, respectively. The S and Pb isotopic data, combined with the geochemical signatures of mineralization-related porphyries, suggest that the Cu was sourced from the deeper levels along with mantle-derived magmas. In contrast, the Pb–Zn probably originated from the crust, with partial melting of the crystalline basement in the Cathaysia Block. Consequently, a three-stage genetic model is proposed to explain the ore-forming processes of the Qin–Hang Cu-polymetallic belt in South China.     

Pb–Pb Age of Carbonate Rocks of the Kamo Group,Baikit Anteclise of the Siberian Platform

Doklady Earth Sciences - The first direct Pb–Pb dating of carbonate rocks of the Kamo Group has been carried out. The Pb–Pb age of carbonates of the lower units (the Madra, Jurubchen,...     

The Hakkari nonsulfide Zn–Pb deposit in the context of other nonsulfide Zn–Pb deposits in the Tethyan Metallogenic Belt of Turkey

The Hakkari nonsulfide zinc deposit is situated close to the southeastern border of Turkey. Here both sulfide and nonsulfide Zn ≫ Pb ores are hosted in carbonate rocks of the Jurassic Cudi Group with features typical of carbonate-hosted supergene nonsulfide zinc mineralization. The regional strike extent of the mineralized district is at least 60 km. The age of the supergene deposit has not been determined, but it is probable that the main weathering happened during Upper Tertiary, possibly between Upper Miocene and Lower Pliocene. The Hakkari mineralization can be compared to other carbonate-hosted Zn–Pb deposits in Turkey, and an interpretation made of its geological setting. The zinc mineral association at Hakkari typically comprises smithsonite and hemimorphite, which apparently replace both sulfide minerals and carbonate host rock. Two generations of smithsonite are present: the first is relatively massive, the second occurs as concretions in cavities as a final filling of remnant porosity. Some zinc is also hosted within Fe–Mn-(hydr)oxides. Lead is present in cerussite, but also as partially oxidized galena. Lead can also occur in Mn-(hydr)oxides (max 30% PbO). The features of the supergene mineralization suggest that the Hakkari deposit belongs both to the “direct replacement” and the “wall-rock replacement” types of nonsulfide ores. Mineralization varies in style from tabular bodies of variable thickness (< 0.5 to 13 m) to cross-cutting breccia zones and disseminated ore minerals in pore spaces and fracture planes. At Hakkari a As–Sb–Tl(≫ Hg) geochemical association has been detected, which may point to primary sulfide mineralization, quite different from typical MVT.     

U–Pb and Th–Pb dating of apatite by LA-ICPMS

Apatite is a common U- and Th-bearing accessory mineral in igneous and metamorphic rocks, and a minor but widespread detrital component in clastic sedimentary rocks. U–Pb and Th–Pb dating of apatite has potential application in sedimentary provenance studies, as it likely represents first cycle detritus compared to the polycyclic behavior of zircon. However, low U, Th and radiogenic Pb concentrations, elevated common Pb and the lack of a U–Th–Pb apatite standard remain significant challenges in dating apatite by LA-ICPMS, and consequently in developing the chronometer as a provenance tool.This study has determined U–Pb and Th–Pb ages for seven well known apatite occurrences (Durango, Emerald Lake, Kovdor, Mineville, Mud Tank, Otter Lake and Slyudyanka) by LA-ICPMS. Analytical procedures involved rastering a 10 μm spot over a 40 × 40 μm square to a depth of 10 μm using a Geolas 193 nm ArF excimer laser coupled to a Thermo ElementXR single-collector ICPMS. These raster conditions minimized laser-induced inter-element fractionation, which was corrected for using the back-calculated intercept of the time-resolved signal. A Tl–U–Bi–Np tracer solution was aspirated with the sample into the plasma to correct for instrument mass bias. External standards (Ple?ovice and 91500 zircon, NIST SRM 610 and 612 silicate glasses and STDP5 phosphate glass) along with Kovdor apatite were analyzed to monitor U–Pb, Th–Pb, U–Th and Pb–Pb ratiosCommon Pb correction employed the ²⁰⁷Pb method, and also a ²⁰⁸Pb correction method for samples with low Th/U. The ²⁰⁷Pb and ²⁰⁸Pb corrections employed either the initial Pb isotopic composition or the Stacey and Kramers model and propagated conservative uncertainties in the initial Pb isotopic composition. Common Pb correction using the Stacey and Kramers (1975) model employed an initial Pb isotopic composition calculated from either the estimated U–Pb age of the sample or an iterative approach. The age difference between these two methods is typically less than 2%, suggesting that the iterative approach works well for samples where there are no constraints on the initial Pb composition, such as a detrital sample. No ²⁰⁴Pb correction was undertaken because of low ²⁰⁴Pb counts on single collector instruments and ²⁰⁴Pb interference by ²⁰⁴Hg in the argon gas supply.Age calculations employed between 11 and 33 analyses per sample and used a weighted average of the common Pb-corrected ages, a Tera–Wasserburg Concordia intercept age and a Tera–Wasserburg Concordia intercept age anchored through common Pb. The samples in general yield ages consistent (at the 2σ level) with independent estimates of the U–Pb apatite age, which demonstrates the suitability of the analytical protocol employed. Weighted mean age uncertainties are as low as 1–2% for U- and/or Th-rich Palaeozoic–Neoproterozoic samples; the uncertainty on the youngest sample, the Cenozoic (31.44 Ma) Durango apatite, ranges from 3.7–7.6% according to the common Pb correction method employed. The accurate and relatively precise common Pb-corrected ages demonstrate the U–Pb and Th–Pb apatite chronometers are suitable as sedimentary provenance tools. The Kovdor carbonatite apatite is recommended as a potential U–Pb and Th–Pb apatite standard as it yields precise and reproducible ²⁰⁷Pb-corrected, ²³²Th–²⁰⁸Pb, and common Pb-anchored Tera–Wasserburg Concordia intercept ages.     

Metallogeny of the northeastern Gangdese Pb–Zn–Ag–Fe–Mo–W polymetallic belt in the Lhasa terrane,southern Tibet

The northeastern Gangdese Pb–Zn–Ag–Fe–Mo–W polymetallic belt (NGPB), characterized by skarn and porphyry deposits, is one of the most important metallogenic belts in the Himalaya–Tibetan continental orogenic system. This belt extends for nearly four hundred kilometers along the Luobadui–Milashan Fault in the central Lhasa subterrane, and contains more than 10 large ore deposits with high potential for development. Three major types of mineralization system have been identified: skarn Fe systems, skarn/breccia Pb–Zn–Ag systems, and porphyry/skarn Mo–Cu–W systems. In this study, we conducted a whole-rock geochemical, U–Pb zircon geochronological, and in situ zircon Hf isotopic study of ore-forming rocks in the NGPB, specifically the Jiangga, Jiaduopule, and Rema skarn Fe deposits, and the Yaguila Pb–Zn–Ag deposit. Although some of these deposits (porphyry Mo systems) formed during the post-collisional stage (21–14 Ma), the majority (these three systems) developed during the main (‘soft collision’) stage of the India–Asia continental collision (65–50 Ma). The skarn Fe deposits are commonly associated with granodiorites, monzogranites, and granites, and formed between 65 and 50 Ma. The ore-forming intrusions of the Pb–Zn–Ag deposits are characterized by granite, quartz porphyry, and granite porphyry, which developed in the interval of 65–55 Ma. The ore-forming porphyries in the Sharang Mo deposit, formed at 53 Ma. The rocks from Fe deposits are metaluminous, and have relatively lower SiO₂, and higher CaO, MgO, FeO contents than the intrusions associated with Mo and Pb–Zn–Ag mineralization, while the Pb–Zn–Ag deposits are peraluminous, and have high SiO₂ and high total alkali concentrations. They all exhibit moderately fractionated REE patterns characterized by lower contents of heavy REE relative to light REE, and they are enriched in large-ion lithophile elements and relatively depleted in high-field-strength elements. Ore-forming granites from Fe deposits display ⁸⁷Sr/⁸⁶Sr_(i) = 0.7054–0.7074 and ε_Nd(t) = − 4.7 to + 1.3, whereas rocks from the Yaguila Pb–Zn–Ag deposit have ⁸⁷Sr/⁸⁶Sr_(i) = 0.7266–0.7281 and ε_Nd(t) = − 13.5 to − 13.3. In situ Lu–Hf isotopic analyses of zircons from Fe deposits show that ε_Hf(t) values range from − 7.3 to + 6.6, with T_DM(Hf)^C model ages of 712 to 1589 Ma, and Yaguila Pb–Zn–Ag deposit has ε_Hf(t) values from − 13.9 to − 1.3 with T_DM(Hf)^C model ages of 1216 to 2016 Ma. Combined with existing data from the Sharang Mo deposit, we conclude that the ore-forming intrusions associated with the skarn Fe and porphyry Mo deposits were derived from partial melting of metasomatized lithospheric mantle and rejuvenated lower crust beneath the central Lhasa subterrane, respectively. Melting of the ancient continental material was critical for the development of the Pb–Zn–Ag system. Therefore, it is likely that the source rocks play an important role in determining the metal endowment of intrusions formed during the initial stage of the India–Asia continental collision.     

Genesis of the Angeer Yinwula Pb–Zn deposit,Inner Mongolia,China: constraints from fluid inclusions,C–H–O–S–Pb isotope systematics,and zircon U–Pb geochronology

Arabian Journal of Geosciences - Soil toxic metal pollution is one of the most prominent environmental problems in the rapid industrialization of societies because of the considerable harm caused...     

Ore genesis of the Tianbaoshan carbonate-hosted Pb–Zn deposit,Southwest China: geologic and isotopic (C–H–O–S–Pb) evidence

The Tianbaoshan Pb–Zn deposit, part of the Sichuan–Yunnan–Guizhou (SYG) Pb–Zn metallogenic province, is located in the western Yangtze Block and contains 2.6 million tonnes of 10–15 wt.% Pb + Zn metals. Ore bodies occur as vein or tubular types and are hosted in Sinian (late Proterozoic) carbonate rocks and are structurally controlled by the SN-trending Anninghe tectonic belt and NW-trending concealed fractures. The deposits are simple in mineralogy, with sphalerite, galena, pyrite, chalcopyrite, arsenopyrite, freibergite, and pyrargyrite as ore minerals and dolomite, calcite, and quartz as gangue minerals. These phases occur as massive, brecciated, veinlet, and dissemination in dolostone of the upper Sinian Dengying Formation. Hydrogen and oxygen isotope compositions of hydrothermal fluids range from –47.6 to –51.2‰ and –1.7 to +3.7‰, respectively. These data suggest that H₂O in hydrothermal fluids had a mixed origin of metamorphic and meteoric waters. Carbon and oxygen isotope compositions range from –6.5 to –4.9‰ and +19.3 to +20.2‰, respectively. These compositions plot in the field between mantle and marine carbonate rocks with a negative correlation, suggesting that CO₂ in the ore-forming fluids had multiple sources, including the Permian Emeishan flood basalts, Sinian-to-Permian marine carbonate rocks, and organic matters in Cambrian-to-Permian sedimentary rocks. Sulphur isotope compositions range from –0.4 to +9.6‰, significantly lower than Cambrian-to-Permian seawater sulphate (+15 to +35‰) and sulphate (+15 to +28‰) from evaporates in Cambrian-to-Permian strata, implicating that the S was derived from host-strata evaporates by thermal–chemical sulphate reduction. ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios range from 18.110 to 18.596, 15.514 to 15.878, and 38.032 to 39.221, respectively, which plot in field of the upper crust Pb evolution curve, unlike those of Proterozoic basement rocks, Sinian dolostone, Devonian-to-Permian carbonate rocks, and the Permian Emeishan flood basalts, implying complex derivation of Pb metal in the ore-forming fluids. Geological and isotopic studies of the Tianbaoshan Pb–Zn deposit reveal that constituents in the hydrothermal fluids were derived from multiple sources and that fluid mixing was a possible metallogenic mechanism. The studied deposit is not distal magmatic–hydrothermal, sedimentary exhalative (SEDEX), or Mississippi Valley (MVT) types, rather, it represents a unique ore deposit type, named in this article the SYG type.     

Metallogeny of precious and base metal mineralization in the Murchison Greenstone Belt, South Africa: indications from U–Pb and Pb–Pb geochronology

The 3.09 to 2.97 Ga Murchison Greenstone Belt is an important metallotect in the northern Kaapvaal Craton (South Africa), hosting several precious and base metal deposits. Central to the metallotect is the Antimony Line, striking ENE for over 35?km, which hosts a series of structurally controlled Sb–Au deposits. To the north of the Antimony Line, hosted within felsic volcanic rocks, is the Copper–Zinc Line where a series of small, ca. 2.97 Ga Cu–Zn volcanogenic massive sulfide (VMS)-type deposits occur. New data are provided for the Malati Pump gold mine, located at the eastern end of the Antimony Line. Crystallizations of a granodiorite in the Malati Pump Mine and of the Baderoukwe granodiorite are dated at 2,964?±?7 and 2,970?±?7?Ma, respectively (zircon U–Pb), while pyrite associated with gold mineralization yielded a Pb–Pb age of 2,967?±?48?Ma. Therefore, granodiorite emplacement, sulfide mineral deposition and gold mineralization all happened at ca. 2.97?Ga. It is, thus, suggested that the major styles of orogenic Au–Sb and the Cu–Zn VMS mineralization in the Murchison Greenstone Belt are contemporaneous and that the formation of meso- to epithermal Au–Sb mineralization at fairly shallow levels was accompanied by submarine extrusion of felsic volcanic rocks to form associated Cu–Zn VMS mineralization.     

Metallogenesis and ore-forming time of the Changtuxili Mn–Ag–Pb–Zn deposit in Inner Mongolia: Evidence from C–O–S isotopes and U–Pb geochronology

This paper reports new geochronological (U–Pb) and isotope (C, O, and S) data to investigate the timing of mineralization and mode of ore genesis for the recently discovered Changtuxili Mn–Ag–Pb–Zn deposit, located on the western slopes of the southern Great Hinggan Range in NE China. The mineralization is hosted by intermediate–acidic lavas and pyroclastic rocks of the Baiyingaolao Formation. Three stages of mineralization are identified: quartz–pyrite (Stage I), galena–sphalerite–tetrahedrite–rhodochrosite (Stage II), and quartz–pyrite (Stage III). δ¹³C and δ¹⁸O values for carbonate from the ore vary from −8.51‰ to −4.96‰ and 3.97‰ to 15.90‰, respectively, which are indicative of a low-temperature alteration environment. δ³⁴S_V-CDT values of sulfides range from −1.77‰ to 4.16‰ and show a trend of equilibrium fractionation (δ³⁴S_Py ​> ​δ³⁴S_Sp ​> ​δ³⁴S_Gn). These features indicate that pyrite, sphalerite, and galena precipitated during the period of mineralization. The alteration mineral assemblage and isotope data indicate that the weakly acidic to weakly alkaline ore-forming fluid was derived largely from meteoric water and the ore-forming elements C and S originated from magma. During the mineralization, a geochemical barrier was formed by changes in the pH of the ore-forming fluid, leading to the precipitation of rhodochrosite. On the basis of the mineralization characteristics, new isotope data, and comparison with adjacent deposits, we propose that the Changtuxili Mn–Ag–Pb–Zn deposit is an intermediate-to low-sulfidation epithermal deposit whose formation was controlled by fractures and variability in the pH of the ore-forming fluid. The surrounding volcanic rocks yield zircon U–Pb ages of 160−146 ​Ma (Late Jurassic), indicating that the mineralization is younger than 146 ​Ma.     

Geology and chronology of the Zhaofayong carbonate-hosted Pb–Zn ore cluster: Implication for regional Pb–Zn metallogenesis in the Sanjiang belt,Tibet

Mississippi Valley type (MVT) Pb–Zn deposits can occur in orogenic thrust belts. However, the relationship between MVT ore-forming processes and thrusting is unclear. The 1500-km-long Sanjiang Metallogenic Belt in Tibetan Plateau is an important thrust-controlled MVT ore province with 860 Mt at 0.76–2.3% Pb, 0.3–6.1% Zn. The Zhaofayong MVT ore cluster in the Changdu area is a typical sample. The orebodies in this ore cluster are hosted in limestone, controlled by secondary faults to regional thrusts and forming along these faults. Two Pb–Zn mineralization stages in this cluster are recognized. Stage I is characterized by coarse and euhedral galena + sphalerite + calcite + fluorite + barite and Stage II by fine grained sphalerite + galena + pyrite + calcite. Sm–Nd isotopic dating of calcite forming in Stage I yields isochron ages of 41.1–38.1 Ma, suggesting the mineralization formed during extension following the first regional compression in the Changdu area. The connection between Stage I mineralization and the regional thrusting in the Changdu area can extend to the whole Sanjiang belt. Two stages of regional Pb–Zn mineralization are recognized between 65 Ma and 30 Ma and between 30 Ma and 16 Ma in the belt. The two Pb–Zn mineralization stages are consistent with those regional episodic thrusting activities and both of them immediately occurred after the episodic thrusting. An interpretation of the regional Pb–Zn mineralization is that regional compression forced the movement of hydrothermal fluids along regional thrust-nappe detachment faults and subsequent post-thrust extension caused the migration of hydrothermal fluids to the ore forming locations. The two mineralization stages in the Sanjiang Belt indicate complex processes related to India–Eurasia collision and the gradually younger mineralization ages from southeast to northwest indicate the collision follows the same direction.     

U–Pb zircon ages,geochemical and Sr–Nd–Pb isotopic constraints on the dating and origin of intrusive complexes in the Sulu orogen,eastern China

TPost-orogenic intrusive complexes from the Sulu belt of eastern China consist of pyroxene monzonites and dioritic porphyrites. We report new U–Pb zircon ages, geochemical data, and Sr–Nd–Pb isotopic data for these rocks. Laser ablation-inductively coupled plasma-mass spectrometry U–Pb zircon analyses yielded a weighted mean ²⁰⁶Pb/²³⁸U age of 127.4 ± 1.2 Ma for dioritic porphyrites, consistent with crystallization ages (126 Ma) of the associated pyroxene monzonites. The intrusive complexes are characterized by enrichment in light rare earth elements and large ion lithophile elements (i.e. Rb, Ba, Pb, and Th) and depletion in heavy rare earth elements and high field strength elements (i.e. Nb, Ta, P, and Ti), high (⁸⁷Sr/⁸⁶Sr)_i ranging from 0.7083 to 0.7093, low ?_Nd(t) values from ?14.6 to ? 19.2, ²⁰⁶Pb/²⁰⁴Pb = 16.65–17.18, ²⁰⁷Pb/²⁰⁴Pb = 15.33–15.54, and ²⁰⁸Pb/²⁰⁴Pb = 36.83–38.29. Results suggest that these intermediate plutons were derived from different sources. The primary magma-derived pyroxene monzonites resulted from partial melting of enriched mantle hybridized by melts of foundered lower crustal eclogitic materials before magma generation. In contrast, the parental magma of the dioritic porphyrites was derived from partial melting of mafic lower crust beneath the Wulian region induced by the underplating of basaltic magmas. The intrusive complexes may have been generated by subsequent fractionation of clinopyroxene, potassium feldspar, plagioclase, biotite, hornblende, ilmenite, and rutile. Neither was affected by crustal contamination. Combined with previous studies, these findings provide evidence that a Neoproterozoic batholith lies beneath the Wulian region.     

Pb isotope variations in hydrogenetic Fe–Mn crusts from the Izu–Bonin fore-arc

Fe–Mn crusts were recovered from the western escarpment of the Bonin Ridge in the Izu–Bonin fore-arc region (dive site #824: 28.612°N, 141.803°E) at water depths of c. 2900 m using the Shinkai 6500 submersible during cruise YK 04–05. Major and trace element data and XRD mineralogy indicate that the crusts are hydrogenetic in origin. We present profiles of variations in Pb isotope composition measured in-situ by laser ablation MC-ICP-MS across two of the crusts. The isotopic variations are systematic and can be matched up between the two crusts, indicating similar growth rates. The crust Pb isotope composition rules out any local source for Pb from within the Izu–Bonin–Mariana arc system, either from hydrothermal activity or through leaching of volcanic detritus. Input of a globally well-mixed volcanic Pb component, either from aerosols or as an absorbed component on aeolian dust, has been proposed as a mechanism to explain the Pb isotope composition of Central Pacific deep water. However, the Izu–Bonin crusts are displaced to lower ²⁰⁶Pb/²⁰⁴Pb and higher ²⁰⁸Pb/²⁰⁴Pb, which requires an additional Pb source. One possibility is that as water is advected from the south, outboard of the Luzon–Ryukyu–Honshu arc system, it is progressively polluted by Pb derived by weathering and erosion of these young island arc volcanic systems. Using a constant Co-flux model, growth rates are estimated at ～ 7–13 mm/Ma, which would suggest that these crusts provide a record of changes in the composition of deep water in the Izu–Bonin fore-arc region of the western Pacific Ocean over the last 4–8 Ma. Over this interval, the main feature has been a progressive decrease in ²⁰⁷Pb/²⁰⁶Pb (0.843 to 0.839) and ²⁰⁸Pb/²⁰⁶Pb (2.088 to 2.080) with time. The interior parts have compositions similar to those of crusts from the Izu–Bonin fore-arc, while the rims have compositions similar to crusts from the central Western Pacific.     

Origin of the Yinshan epithermal-porphyry Cu–Au–Pb–Zn–Ag deposit,southeastern China: insights from geochemistry,Sr–Nd and zircon U–Pb–Hf–O isotopes

The Yinshan deposit is a large epithermal-porphyry polymetallic deposit, and the timing and petrogenesis of ore-hosting porphyries have been hotly debated. We present new results from geochemical, whole-rock Sr–Nd and zircon U–Pb–Hf–O isotopic investigations. Zircon U–Pb data demonstrate that the quartz porphyry, dacitic porphyry, and quartz dioritic porphyry formed at ?172.2 ± 0.4 Ma, ?171.7 ± 0.5 Ma, and ?170.9 ± 0.3 Ma, respectively. Inherited zircon cores show significant age spreads from ?730 to ?1390 Ma. Geochemically, they are high-K calc-alkaline or shoshonitic rocks with arc-like trace element patterns. They have similar whole-rock Nd and zircon Hf isotopic compositions, yet an increasing trend in ?_Nd(t) and ?_Hf(t) values typifies the suite. Older (inherited) zircons of the three porphyries display Hf compositions comparable to those of the Jiangnan Orogen basement rocks. In situ zircon oxygen isotopic analyses reveal that they have similar oxygen isotopic compositions, which are close to those of mantle zircons. Moreover, a decreasing trend of δ¹⁸O values is present. We propose that the ore-related porphyries of the Yinshan deposit were emplaced contemporaneously and derived from partial melting of Neoproterozoic arc-derived mafic (or ultra-mafic) rocks. Modelling suggests that the quartz porphyries, dacitic porphyries, and quartz dioritic porphyries experienced ?25%, ?10%, and ?10% crustal contaminations by Shuangqiaoshan rocks. Our study provides important constraints on mantle–crust interaction in the genesis of polymetallic mineralization associated with Mesozoic magmatism in southeastern China.