Isotopic studies of Pb–Zn–(Ag) and barite Alpine vein deposits in the Iberian Range (NE Spain)

The Iberian Range contains abundant Pb–Zn–(Ag)– and Ba-dominated low temperature veins, mostly formed during the Mesozoic. The hydrothermal activity was related to the extensional regime occurring throughout the Variscan basement of Europe, North Africa and the Appalachians. A stable and radiogenic isotopic study of these veins has identified the reservoir/s of mineralizing components involved in the ore-forming processes. Sulphur isotope ratios indicate that the source of mineralizing components for the base metals veins was a mixture of the Palaeozoic country rocks and Variscan ore deposits. In contrast, either Mesozoic seawater or evaporites supplied most of the sulphur for Ba veins, although a minor contribution of isotopically heavy sulphur derived from the basement is envisaged. The lead isotopic data of galenas define a linear trend in the thorogenic diagram, interpreted in terms of mixing of lead from different reservoirs. The main source is related to local sedimentary country rocks, but a minor contribution from igneous rocks cannot be ruled out. Sr isotope ratios of barites also suggest that most of the components were leached from the basement sequence. When the veins are hosted by carbonate rocks, however, a local source of metals is also available.     

REE and isotope (Sr,S, and Pb) geochemistry to constrain the genesis and timing of the F–(Ba–Pb–Zn) ores of the Zaghouan District (NE Tunisia)

The F–(Ba–Pb–Zn) ore deposits of the Zaghouan District, located in NE Tunisia, occur as open space fillings or stratabound orebodies, hosted in Jurassic, Cretaceous and Tertiary layers. The chondrite-normalized rare earth element (REE) patterns may be split into three groups: (i) “Normal marine” patterns characterizing the wallrock carbonates; (ii) light REE (LREE) enriched (slide-shaped) patterns with respect to heavy REE (HREE), with small negative Ce and Eu anomalies, characteristic of the early ore stages; (iii) Bell-shaped REE patterns displaying LREE depletion, as well as weak negative Ce and Eu anomalies, characterizing residual fluids of subsequent stages. The ⁸⁷Sr/⁸⁶Sr ratios (0.707654–0.708127 ± 8), show that the Sr of the epigenetic carbonates (dolomite, calcite) and ore minerals (fluorite, celestite) are more radiogenic than those of the country (Triassic, Jurassic, Cretaceous, lower Miocene) sedimentary rocks. The uniformity of this ratio, throughout the District, provides evidence for the isotopic homogeneity and, consequently, the identity of the source of the mineralizing fluids. This signature strongly suggests that the radiogenic Sr is carried by Upper Paleozoic basinal fluids.The δ³⁴S values of barite, associated to mineralizations, are close to those of the Triassic sea water (17‰). The δ³⁴S values of sulfide minerals range from − 13.6‰ to + 11.4‰, suggesting two sulfur-reduced end members (BSR/TSR) with a dominant BSR process.Taking account of the homogeneity in the Pb-isotope composition of galenas (18.833–18.954 ± 0.001, 15.679–15.700 ± 0.001 and 38.690–38.880 ± 0.004, for the ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios respectively), a single upper crustal source for base-metals is accepted. The Late Paleozoic basement seems to be the more plausible source for F–Pb–Zn concentrated in the deposits. The genesis of the Zaghouan District ore deposits is considered as the result of the Zaghouan Fault reactivation during the Late Miocene period.     

Stable isotope (O and C) geochemistry of non-sulfide Zn–Pb deposits; case study: Chah-Talkh non-sulfide Zn–Pb deposit (Sirjan,south of Iran)

The study of oxygen and carbon isotopic ratios has gained importance to determine the origin of ore-bearing fluids, carbon origin, and also to determine the formation temperature of non-sulfide Pb and Zn minerals. In order to determine the origin of fluids and carbon existing in Zn carbonate minerals in Chah-Talkh deposit, initially the amounts of δ¹⁸O_SMOW and δ¹³C_PDB changes in various zinc minerals in important deposits in Iran and the world were studied, and then by comparing these values in Chah-Talkh deposit with those of other deposits, the origin of fluids responsible for ore forming, carbon, and formation temperature of Chah-Talkh deposit was determined. The range of δ¹⁸O_SMOW changes in smithsonite mineral in non-sulfide lead and zinc deposits varies from 18.3 to 31.6 ‰, and δ¹⁸O_SMOW in hydrozincite mineral varies from 7.8 to 27 ‰. Due to the impossibility of smithsonite sampling from Chah-Talkh deposit (due to it being fine-grained and dispersed), hydrozincite minerals which have high isotopic similarities with smithsonite are used for the isotopic analysis of carbon and oxygen. The range of δ¹⁸O_SMOW changes in hydrozincite mineral of Chah-Talkh deposit varies from 7.8 to 15.15 ‰, which places in the domain of metamorphic water. The extensiveness of δ¹⁸O_SMOW changes in Chah-Talkh indicates the role of at least two fluids in the formation of non-sulfide minerals. The obtained formation temperature of non-sulfide minerals (hydrozincite) in Chah-Talkh deposit is 70 to 100 °C, which indicates the role of metamorphic fluids in the formation of deposit. Complete weathering of sulfide minerals to a depth of 134 m confirms the role of rising metamorphic fluids in the formation of non-sulfide minerals. The δ¹³C_PDB values of Chah-Talkh deposit are set in the range of atmospheric CO₂ and carbonate rocks, in which the existence of atmospheric CO₂ indicates the role of atmospheric fluids, and the existence of carbonate carbon rock indicates of the role of metamorphic fluids in the precipitation of non-sulfide Zn minerals.     

The ore-forming process of the Maoping Pb–Zn deposit,northeastern Yunnan,China: Constraints from cathodoluminescence (CL) petrography of hydrothermal dolomite

Most Mississippi Valley Type (MVT) Pb–Zn deposits have a common host-rock lithofacies sequence known as the hydrothermal dolomite (HTD) facies; however, the spatial and temporal relationships between dolomitization and Pb–Zn mineralization remain unclear. In this paper, we report a detailed cathodoluminescence (CL) study on the HTD facies of the No. II orebody in the Maoping Pb–Zn deposit in northeastern Yunnan Province, southwestern China. The results indicate that the dolomite in the Carboniferous limestone is part of a spectrum of hydrothermal mineral deposits, and the diagenesis and mineralization processes, in which the acidity of fluids played an important role, can be divided into six steps. A dolomite prototype formed during the first and second steps. In the third step, acid fluids produced by sulfide precipitation interacted with the dolomite prototype, resulting in dissolution and alteration, thus forming cavities. The fluid that formed during the first three steps flowed along open tensional faults. Dolomitization in the first step covered most of the region of later mineralization and gradually extended toward the center of the orebody. In the fourth and fifth steps, vugs and fractures were the main pathways for fluids, with only a small volume of fluid in the fifth step. Dedolomitization occurred in the sixth step and vugs were filled mostly by calcite. However, the fact that voids are present in only a small number of vugs is indicative of fluid exhaustion. Dolomite with growth zoning is characteristic of precipitation by ore-forming fluids accompanied by pulsed filling. There is no significant correlation between vugs and the locus of mineralization. Rather, the vugs indicate that the ore-forming fluids had passed through them, and the locus of massive ore formation was the center of the migrating fluid body. The saddle dolomite was deposited during pauses in sulfide precipitation. Cathodoluminescent zonation of HTD can be used as an aid in understanding the ore-forming process and for mineral prospecting in the Maoping deposit and other MVT deposits.     

Fluid origin of fluorite-rich carbonate-hosted Pb–Zn mineralization of the Himalayan–Zagros collisional orogenic system: A case study of the Mohailaheng deposit,Tibetan Plateau,China

A significant belt of carbonate-hosted Pb–Zn mineralization occurs in the Himalayan–Zagros collisional orogenic system. Three differing types of these Pb–Zn deposits within this belt have been identified based on variations in gangue mineral assemblages, leading to the classification of carbonate-, quartz- and fluorite-rich classes of Pb–Zn deposits. The third Pb–Zn mineralization (fluorite-rich) type is common in this orogenic system, but little research has been undertaken on it. Here, we focus on the Mohailaheng deposit, a large-sized fluorite-rich carbonate-hosted Pb–Zn deposit (> 100 Mt Pb + Zn ores with average grade of 2.18%–4.23%); the deposit is located in the Sanjiang Cenozoic thrust-fold belt, an important part of the Himalayan–Zagros collisional orogenic system and an area that formed during the early Tertiary India–Eurasia collision. The main orebodies in this deposit are stratabound and are hosted by Carboniferous limestones that are located along secondary faults associated with a regional thrust fault. The main assemblage is a sphalerite + galena + pyrite sulfide assemblage associated with a calcite + fluorite + barite + quartz + dolomite gangue assemblage. Detailed field and experimental work indicates that the deposit formed during three distinct phases of hydrothermal activity. Studies on fluid inclusion and stable isotopes of gangue minerals indicate that two dominant distinct fluids involving the deposit formation. They include (1) a low-temperature (130–140 °C), high-salinity (23–24 wt.% NaCl equivalent) basinal brine containing Na⁺–K⁺–Mg^2 +–Ca^2 +–Cl⁻ ions and abnormally high SO₄^2 − concentrations, which probably derived from Tertiary basins in the regional district, and (2) a low- to moderate-temperature (170–180 °C) and moderate- to high-salinity (19–20 wt.% NaCl equivalent) metamorphic fluid containing Na⁺–K⁺–Mg^2 +–Cl^––SO₄^2 − ions and abnormally high F⁻ and organic matter concentrations, that probably formed during regional metamorphism. Some evaporated seawaters and meteoric fluids were also identified in mixtures with these two dominant fluids. The Pb–Zn mineralization at Mohailaheng formed during three distinct stages, consistent with the regional tectonic history. The first stage involved the formation of favorable lithological and structural traps at Mohailaheng during regional thrusting, leading to the migration of compressed metamorphic waters at depth along a detachment zone, sequestering metals from sediments within the region. Basinal brines at the surface also began to infiltrate down along the secondary faults, dissolving gypsum from the underlying sediments. The second stage was associated with the cessation of thrusting and the onset of strike-slip movements along these thrust faults. Metamorphic fluids containing high concentrations of halogen ions, organic gases, and metals ascended into the structural traps at Mohailaheng along the reactivated thrust faults, causing fluorite, calcite, and some sulfide precipitation. Then, basinal brines rich in SO₄^2 − quickly descended into the structural traps along the reactivated faults, causing reduction of SO₄^2 − by organic matter, and producing significant amounts of H₂S. The reduced sulfur then reacted with the metals in the fluids, causing significant sulfide precipitation. The third stage was associated with metal-depleted fluids, which only resulted in the precipitation of calcite from the diluted basinal brines. Combining these findings with research results on other fluorite-rich carbonate-hosted Pb–Zn deposits in the Himalayan–Zagros orogenic system suggests that this type of carbonate-hosted Pb–Zn deposits can also be classified as Mississippi Valley-type (MVT) deposits, and that the origin of the fluorite in these deposits may be related to multiple hydrothermal fluids involved in the mineralization evolution.     

Genesis of the Assif El Mal Zn–Pb (Cu,Ag) vein deposit. An extension-related Mesozoic vein system in the High Atlas of Morocco. Structural,mineralogical, and geochemical evidence

The Assif El Mal Zn–Pb (Cu–Ag) vein system, located in the northern flank of the High Atlas of Marrakech (Morocco), is hosted in a Cambro-Ordovician volcaniclastic and metasedimentary sequence composed of graywacke, siltstone, pelite, and shale interlayered with minor tuff and mudstone. Intrusion of synorogenic to postorogenic Late Hercynian peraluminous granitoids has contact metamorphosed the host rocks giving rise to a metamorphic assemblage of quartz, plagioclase, biotite, muscovite, chlorite, amphibole, chloritoid, and garnet. The Assif El Mal Zn–Pb (Cu–Ag) mineralization forms subvertical veins with ribbon, fault breccia, cockade, comb, and crack and seal textures. Two-phase liquid–vapor fluid inclusions that were trapped during several stages occur in quartz and sphalerite. Primary inclusion fluids exhibit T _h mean values ranging from 104°C to 198°C. Final ice-melting temperatures range from −8.1°C to −12.8°C, corresponding to salinities of ∼15 wt.% NaCl equiv. Halogen data suggest that the salinity of the ore fluids was largely due to evaporation of seawater. Late secondary fluid inclusions have either Ca-rich, saline (26 wt.% NaCl equiv.), or very dilute (3.5 wt.% NaCl equiv.) compositions and homogenization temperatures ranging from 75°C to 150°C. The δ¹⁸O and δD fluid values suggest an isotopically heterogeneous fluid source involving mixing between connate seawater and black-shale-derived organic waters. Low δ¹³C_VPDB values ranging from −7.5‰ to −7.7‰ indicate a homogeneous carbon source, possibly organic matter disseminated in black shale hosting the Zn–Pb (Cu–Ag) veins. The calculated δ³⁴S_H2S values for reduced sulfur (22.5‰ to 24.3‰) are most likely from reduction of SO₄ ²⁻ in trapped seawater sulfate or evaporite in the host rocks. Reduction of sulfate probably occurred through thermochemical sulfate reduction in which organic matter was oxidized to produce CO₂ which ultimately led to precipitation of saddle dolomite with isotopically light carbon. Lead isotope compositions are consistent with fluid–rock interaction that leached metals from the immediate Cambro-Ordovician volcaniclastic and metasedimentary sequence or from the underlying Paleo-Neoproterozoic crustal basement. Geological constraints suggest that the vein system of Assif El Mal formed during the Jurassic opening of the central Atlantic Ocean.     

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.     

Soil metal pollution from former Zn–Pb mining assessed by geochemical and magnetic investigations: case study of the Bou Caid area (Tissemsilt,Algeria)

Former zinc and lead mines that have been operating for half a century are located in the massif of Bou Caid (Tissemsilt, Algeria). Hazardous heavy metals emitted from the mines are abundant in the surrounding soil and cause strong metal pollution in the region. This paper investigates the extent of lead and zinc mine activity derived pollution by characterizing both magnetic and geochemical properties of samples collected in the vicinity of the mines. The results of the magnetic study show the coexistence of magnetic minerals such as magnetite, hematite and goethite. Analyses on surface soils and weathered rocks suggest that hematite and goethite have ore-related lithogenic origins. Magnetic susceptibility shows a positive correlation with lead content when present in low-to-medium concentrations (< ~500 mg/kg). At higher lead concentrations, there is no correlation with magnetic susceptibility. The relationship between magnetic susceptibility and zinc content is not straightforward. These observations are explained by the higher affinity of Pb to iron oxides at lower pollution levels and their preferential bonding to carbonates when Pb and Zn contents are extremely high, as demonstrated by Iavazzo et al. (J Geochem Explor 113:56–67, 2012) in a study of former Zn–Pb mine in Morocco. Based on the general features of the spatial maps of field-measured magnetic susceptibility, mass-specific magnetic susceptibility, Pb and Zn contents, it is concluded that field magnetic measurements provide a good qualitative proxy of pollution spread out of the mining galleries, while laboratory measurements afford a more detailed investigation of the links between iron oxides and the main heavy metals in the ore.     

Direct evidence of fluid mixing in the formation of stratabound Pb–Zn–Ba–F mineralisation in the Alston Block, North Pennine Orefield (England)

The North Pennine Orefield Alston Block has produced approximately 4 Mt Pb, 0.3 Mt Zn, 2.1 Mt fluorite, 1.5 Mt barite, 1 Mt witherite, plus a substantial amount of iron ore and copper ore from predominantly vein-hosted mineralisation in Carboniferous limestones. However, a significant proportion of this production (ca. 20%) came from stratabound deposits. Though much is known about the vein mineralisation, the relationship between the veins and the stratabound mineralisation is not well-understood. New petrographic, isotopic and fluid inclusion data derived from samples of stratabound mineralisation allow us to present a unified model that addresses the genesis of both the vein and stratabound styles of mineralisation. The mineralisation can be considered in terms of three episodes:

Metallogenesis at the Terramonte Pb–Zn–Ag quartz vein,Portugal: Geological,mineralogical and geochemical evidences

The Pb–Zn–Ag quartz vein from Terramonte cuts the Neoproterozoic–Cambrian schist–greywacke complex. This orebody was partially exploited. The paragenetic sequence consists of four stages containing quartz accompanied mainly by arsenopyrite and pyrite in the first stage, sphalerite in the second stage, galena showing many inclusions of several sulphosalts in the third stage and carbonates in the fourth remobilization stage. Several sulphide and sulphosalt grains are oscillatory zoned. The chemical distinction between lighter and darker zones in backscattered images of arsenopyrite, pyrite, sphalerite and freibergite is due to substitutions in the mineral lattices. But the distinction between these zones in semseyite is due to a higher Pb content and a lower Sb content in the lighter zone than in the darker zone and the metal and metalloid are the main constituents in the solid solution, but are not correlated. The Sb, Ag and Bi substitute for Pb in galena, but did not cause any zoning. Ore deposition was possible due to mixing of a hypersaline fluid with up to 26 wt.% NaCl equivalent (and occasionally with CaCl₂ up to 17 wt.%), which carried the metallic content of the fluid, with an extremely low salinity fluid of presumed meteoric origin that percolated down into the basement. The metals could have been leached from a mixture of mainly metasediments and also previous Sb–Au deposits by fluids that acquire high salinity in one of two probable ways: leaching of salt beds or following seawater evaporation. The entire mineralizing event probably occurred at a relatively low temperature, possibly between 120 and 230 °C. Remobilization of Pb, Zn, Ag, As, Sb and Cu will be due to the tectonic evolution of the opening of the Atlantic Ocean. This vein is probably of Alpine age.     

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.     

A porphyry-skarn metallogenic system in the Lesser Xing’an Range,NE China: Implications from U–Pb and Re–Os geochronology and Sr–Nd–Hf isotopes of the Luming Mo and Xulaojiugou Pb–Zn deposits

The Luming porphyry Mo deposit and the Xulaojiugou skarn Pb–Zn deposit are located in the southeast Lesser Xing’an Range, NE China. They are about 15 km apart, and are both related to monzogranite. Mo orebodies in the Luming deposit are hosted within the medium- to fine-grained monzogranite, while Pb–Zn orebodies in the Xulaojiugou deposit are hosted by the contact zone between the medium-grained monzogranite and the marbles of the early Cambrian Qianshan Formation.LA-ICP-MS zircon U–Pb dating of the ore-related monzogranite in the Luming deposit yields crystallization age of 180.7 ± 1.6 Ma, and the medium-grained and porphyritic monzogranites from the Xulaojiugou deposit yield crystallization ages of 181.2 ± 1.1 Ma and 179.9 ± 1.0 Ma, respectively. Analyses of seven molybdenite samples from the Luming deposit display Re–Os isochron age of 177.9 ± 2.6 Ma. These results indicate that the mineralization in the Luming and Xulaojiugou deposits occurred at about 181–178 Ma. These two deposits are genetically linked and belong to a porphyry-skarn metallogenic system. Combined with the previously reported geochronological data for ore deposits in adjacent areas, we consider that the early Jurassic is an important epoch for Mo and Pb–Zn mineralization in the Lesser Xing’an Range.The monzogranites from the Luming and Xulaojiugou deposits are enriched in and Rb, Th, U, Pb and light rare earth elements (LREEs), and are depleted in Ba, Nb, Ta, P, Ti and Eu. They have positive ε_Hf(t) values of 1.0–4.0 with two-stage Hf model ages (T_DM2) of 868–1033 Ma. Whole-rock Sr and Nd isotopes show restricted ranges of initial compositions, with (⁸⁷Sr/⁸⁶Sr)_i between 0.706346 and 0.707384 and ε_Nd(t) between −3.5 and −1.8. These data indicate that their primary magmas originated from the partial melting of a depleted lithospheric mantle which had been metasomatized by subducted slab-derived fluids/melts. The early Jurassic magmatic–metallogenic events in the Lesser Xing’an Range are interpreted as a response to the subduction of the Paleo-Pacific Plate.     

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.     

The origin of zircon and the significance of U–Pb ages in high-grade metamorphic rocks: a case study from the Variscan orogenic root (Vosges Mountains, NE France)

U–Pb zircon dating is combined with petrology, Zr-in-rutile thermometry and mineral equilibria modelling to discuss zircon petrogenesis and the age of metamorphism in three units of the Variscan Vosges Mountains (NE France). The monotonous gneiss unit shows results at 700–500?Ma, but no Variscan ages. The varied gneiss unit preserves ages between 600 and 460?Ma and a Variscan group at 340–335?Ma. Zircon analyses from the felsic granulite unit define a continuous array of ages between 500 and 340?Ma. In varied gneiss samples, zoned garnet includes kyanite and rutile and is surrounded by matrix sillimanite and cordierite. In a pseudosection, it points to peak conditions of?~16 kbar/850?°C followed by isothermal decompression to 8–10 kbar/820–860?°C. In felsic granulite samples, the assemblage K-feldspar–garnet–kyanite–Zr-rich rutile is replaced by sillimanite and Zr-poor rutile. Modelling these assemblages supports minimum conditions of?~13 kbar/925?°C, and a subsequent P–T decrease to 6.5–8.5 kbar/800–820?°C. The internal structure and chemistry of zircons, and modelling of zircon dissolution/growth along the inferred P–T paths are used to discuss the significance of the U–Pb ages. In the monotonous unit, inherited zircon ages of 700–500?Ma point to sedimentation during the Late Cambrian, while medium-grade metamorphism did not allow the formation of Variscan zircon domains. In both the varied gneiss and felsic granulite units, zircons with a blurred oscillatory-zoned pattern could reflect solid-state recrystallization of older grains during HT metamorphism, whereas zircons with a dark cathodoluminescence pattern are thought to derive from crystallization of an anatectic melt during cooling at middle pressure conditions. The present work proposes that U–Pb zircon ages of ca. 340?Ma probably reflect the end of a widespread HT metamorphic event at middle crustal level.     

U–Pb zircon geochronology of the Ediacaran volcano-sedimentary succession of the NE Saghro inlier (Anti-Atlas,Morocco): Chronostratigraphic correlation on the northwestern margin of Gondwana

We report a new regional correlation for the Ediacaran succession in the Anti-Atlas belt on the northwestern margin of Gondwana, based on U-Pb LA-ICP-MS zircon geochronology of volcanic rocks in the NE edge of the Saghro inlier. The thick volcano-sedimentary succession comprises a diverse suite of rhyolitic-ignimbrite, basaltic to andesitic lava fields, rhyolitic lava, mafic hydroclastic complex, fallout and surge deposits, pyroclastic dyke, interbedded clastic sediment and subvolcanic bodies.Ten volcanic rocks yield crystallization ages ranging from 573 to 547 Ma, consistent with a lower and upper Ouarzazate Supergroup affinity respectively. Inherited zircon ages range from 623 Ma to 600 Ma, analogous to zircon peaks in the older volcano-sedimentary rocks of the Bou Salda, and Saghro groups in the Anti-Atlas, suggesting the continuity of the Saghro Group beneath the Ouarzazate Supergroup at the NE edge of the Saghro inlier.Rocks with a lower Ouarzazate Supergroup affinity include lithic-poor ignimbrites which yield ages of 573.6 ± 1.9 Ma, 571.8 ± 4.2 Ma, 571.3 ± 2.6 Ma, and 567.4 ± 2.9 Ma, two fallout deposits which yield ages of 563.5 ± 2.1 Ma and 569.2 ± 1.9 Ma, a surge deposit dated at 571.6 ± 2.8 Ma and a rhyolite lava dated at 562.5 ± 3.1 Ma. Two lithic-poor ignimbrites from the upper Ouarzazate Supergroup are dated at 557.3 ± 2.6 Ma and 547.9 ± 3.1 Ma.Volcanic activity at the NE edge of the Saghro inlier is related to West African Cadomian orogenic (WACadomian) activity between 620 and 560 Ma. During this period the Saghro and Bou Salda groups were deposited, followed by the lower Ouarzazate Supergroup. Later extension along the Gondwanan margin took place close to Ediacaran – Cambrian boundary, contemporaneous with upper Ouarzazate Supergroup deposition.     

S,O and Pb isotopic evidence on the origin of the İnkaya (Simav-Kütahya) Cu–Pb–Zn–(Ag) Prospect,NW Turkey

The İnkaya Cu–Pb–Zn–(Ag) prospect is a typical example of the hydrothermal mineralization occurring in the Menderes Massif, which crop out in Western Anatolia. The prospect located approximately 20 km west of Simav (Kütahya-Turkey) in northern part of the Menderes Massif have been characterized through the detailed examinations involving geological, mineralogical, whole-rock geochemistry, fluid inclusion, stable isotope and lead isotope.The İnkaya Cu–Pb–Zn–(Ag) prospect is located along an E–W-trending fault in the Cambrian Simav Metamorphics, which consist of quartz–muscovite schist, quartz–biotite schist, muscovite schist, biotite schist and the Arıkayası Formation, which is composed of marbles. Galena, sphalerite, chalcopyrite, pyrite and fahlore are the main minerals, and they are accompanied by small amounts of cerussite, anglesite, digenite, enargite, chalcocite, covellite, bornite, and Fe-oxides with gangue quartz. In addition to Pb, Zn, Cu, Ag, the ore samples contain substantial quantities of As, Cd and Bi and small amount of Au. Average contents of Cu, Pb, Zn and Ag are 77,400 ppm, 102,600 ppm, 6843 ppm and 203 ppm, respectively.The δ³⁴S values for galena, chalcopyrite and pyrite formed in the same stage vary in the range from − 1.7 to − 2.1‰ (average − 2.0), 0.1 to 0.3‰ (average 0.2) and − 1.5 to 2.6‰ (average + 1.5), respectively.δ³⁴S values for H₂S, representing the composition of the fluids responsible for the sulfide mineral formations and calculated from the δ³⁴S value are between − 2.77 and 1.33‰; it is consistent with the sulfur in sulfide minerals. δ¹⁸O_quartz values range from 11.3 to 16.4‰ and estimated δ¹⁸O_fluid values range from 5.4 to 10.6‰.Pyrite–galena and pyrite–chalcopyrite pairs calculated to determine equilibrium isotope temperatures based on δ³⁴S values are between 254.6 and 277.4 °C for pyrite–galena and 274.7 °C for pyrite–chalcopyrite. Sulfur and oxygen isotope values similar to the values for fluid equilibrated with an felsic magmatic source.Fluid inclusion studies on quartz of the same silicification stage coexisting with galena, sphalerite and chalcopyrite collected from the mineralized vein indicate that the temperature range of the fluids is 235 °C to 340 °C and that the salinities are 0.7 to 4.49 wt.% NaCl equivalent. The wide range of homogenization temperatures and relatively lower salinities of the fluid inclusions indicate that at least two different fluid generations were trapped in the quartz from only one fluid type. Also, lower salinities of fluid inclusion probably indicate mixing of meteoric water and magmatic fluid.The galena has ²⁰⁶Pb/²⁰⁴Pb values of 18.862–18.865, ²⁰⁷Pb/²⁰⁴Pb values of 15.707–15.711, and ²⁰⁸Pb/²⁰⁴Pb values of 39.033–39.042. The lead isotope values show a similarity with upper crustal values.     

Mobility of rare earth elements in the system soils–plants–groundwaters: a case study of an arid area (Oman)

Groundwater samples from six wells and various species of plants from soils developed on ophiolites were collected from an arid area (AlKhod area, Oman) and analyzed for trace elements including rare earth elements (REEs). The distribution patterns of REEs in plants indicated an enrichment in middle REEs (MREEs?=?Sm to Dy) and heavy REEs (HREEs?=?Ho to Lu), when they are normalized to the REE composition of the Post Archean Australian Shale (PAAS), with a significant negative anomaly in Ce and a positive anomaly in Eu. Compared to Oman ophiolites, the REEs in different species of plants are depleted in Ce and enriched in MREEs and slightly enriched in light REE (LREE?=?from La to Nd). Relative to PAAS, the distribution of REEs in groundwaters revealed similar patterns to the REE distribution in plants. The distribution patterns of REEs in plants relative to those in waters are nearly flat. These patterns suggest that the transfer of REEs from soil solutions to the groundwaters in Oman occurs without any significant fractionation.