Lead-isotope evidence for a Hercynian origin of the Salsigne gold deposit (Southern Massif Central,France)

The Salsigne gold deposit contains a complex association of sulphide layers, gold-rich disseminations, quartz-bearing veins and flat reefs, which are hosted by folded and slightly metamorphosed Paleozoic sediments on both sides of a major thrust zone. It is demonstrated that these various Au-As ore types have similar lead-isotope compositions (²⁰⁶Pb/²⁰⁴Pb = 18.22–18.56), which are characteristic of Hercynian ore deposits in the southern Massif Central. The Lower Cambrian to Devonian host rocks and associated Pb-Zn-Ba occurrences display distinctly less radiogenic corrected isotopic signatures (²⁰⁶Pb/²⁰⁴Pb = 17.83–17.98), which are characteristic of Cambrian lead in the Montagne-Noire. Concerning the controversial origin of the Salsigne gold mineralization, these results disagree with the former syngenetic hypothesis and support a new model of Hercynian syntectonic gold concentration.This work was supported by BRGM'S scientific program: Le gisement de Salsigne: caractérisation du modèle et évaluation du potentiel aurifère du district     

Ore lead and sulphur isotope pattern from the low-temperature veins of the Catalonian Coastal Ranges (NE Spain)

The lead isotopic composition of galenas from low-temperature veins of the Catalonian Coastal Ranges (NE Spain) displays a small but distinct range of values: 18.318 ≤²⁰⁶Pb/²⁰⁴Pb ≤ 18.678; 15.678 ≤²⁰⁷Pb/²⁰⁴Pb ≤ 15.767 and 38.534 ≤ ²⁰⁸Pb/²⁰⁴Pb ≤ 39.189. The data define a linear trend in the ²⁰⁸Pb/²⁰⁴Pb versus ²⁰⁶Pb/²⁰⁴Pb diagram that can be interpreted in terms of mixing of lead from different reservoirs. The lead appears to be derived from a solution that preferentially leached granites of Late-Hercynian age. Sulphur isotopic compositions of the galenas range from −8.5 to + 7.3‰ but variations in a single deposit are small (1–2‰), pointing to different sources of sulphur. In a δ³⁴S versus ²⁰⁶Pb/²⁰⁴Pb plot no clear correlation trends appear. Lead isotope data from deposits of similar characteristics situated within the Hercynian orogenic belt as the Linares-La Carolina district (S Spain) and the Inglesiente-Sulcis area (Sardinia) show slight differences indicating a source area of similar lead isotopic composition. In the CCR and Linares-La Carolina districts, the main source of lead is related to the Hercynian granites of each area, although small contributions from metasediments cannot be ruled out. The contribution of lead from metasedimentary rocks is particularly seen in the Sardinian (Hercynian vein-type) ores. Received: 8 August 1996 / Accepted: 5 December 1996     

Lead isotope and Pb-Pb model age determinations of ores from Central Europe and their metallogenetic interpretation

The paper presents lead isotope data from 211 samples from Phanerozoic lead-bearing ore occurrences in Central Europe, particularly from the Southern part of the former German Democratic Republic. The data are interpreted in terms of Amov's dynamic model of continuous lead isotope evolution. The relationships between thoro-genic and urano-genic model ages and the source of lead in different regional units are discussed. We observed differences in lead isotope evolution in the Hercynian internides and externides. Within the Moldanubian and Saxothuringian zones we distinguish five main lead-bearing ore associations: (1) Cambrian, stratiform base metal (Hermsdorf-Waldsassen; ²⁰⁶Pb/ ²⁰⁴Pb=17.50–17.70), (2) Devonian, vein type Sb-bearing, metamorphogene (neumühle-Hartmannsdorf; 17.80–18.00), (3) Upper Carboniferous-Permian, polymetallic, including tin, vein type (Kutna hora-Freiberg-Altenberg; 18.00–18.20), (4) Triassic (-Jurassic), Pb–Ba, vein type (Stibro-Halsbrücke; 18.20–18.60), (5) Cenozoic, polymetallic, vein type, riftogene (Roztoky-Banska tiavnica; 18.80–19.10). Pb isotope characteristics from ores of the Montagne Noire and the Brioude-Massiac district correspond to this subdivision. Ore associations from the Rheno-Hercynian zone display higher ²⁰⁷Pb/²⁰⁴Pb ratios which can be explained by more evolved and less metamorphosed source rocks. Mineralizations of the eastern Harz (Straßberg-Neudorf) belong to the Permian association, those from the western Harz (Clausthal-Bad Grund) to the Triassic-Jurassic. Because of Pb isotope agreement the stratabound Rammelsberg and the vein bound Ramsbeck-I mineralization are presumed to be isogenetic. Pb isotope identity of distinct mineralizations in the basement zone (Halsbrücke-Bad Grund) and in the Triassic sediments (Gorny Slask-Mechernich-Bleiglanzbänke) suggests a strong genetic coherence. Pb isotope conformity between the Upper Carboniferous-Permian-Triassic ore associations and Hercynian postkinematic granitoids, and lamprophyric rocks, also favours a close relationship. Pb isotope and other data indicate crustal sources. As the age of the ore associations decreases, crustal influences generally increase, apart from the Roztoky mineralization.     

Structural setting and genesis of ore bodies in carbonate rocks in the M.te Atzei-M.te Ega mining area (Sulcis,SW Sardinia)

At least seven different types of ore bodies, with an ore stock of Ba, F, Fe, Pb, Zn, Cu and Sb occur in Paleozoic rocks (Lower-Middle Cambrian and Ordovician) in an ?15 km² area north of the Narcao village (SW Sardinia, Italy). The ore bodies are related both to syngenetic accumulations, and later epigenetic recirculation of the primary ores. In the Lower Cambrian the area studied shows evidence of synsedimentary tectonic instability, probably related to carbonate shelf margin features. The Upper Cambrian is lacking and the transgressive Ordovician sediments cover large areas of the previously gently folded Cambrian rocks (Sardic phase of Caledonian orogenesis). The main Hercynian tectonic phases had a much stronger compressive folding that is mirrored in a sequence of tight folds and upthrusts. The geometric setting resulting from the tectonic frame of the Cambrian and Ordovician sediments must be taken into account to understand the distribution and the genesis of most of the ore bodies.     

Isotopes and Geochronology of the Meixian-type Pb-Zn-(Ag)Deposits,Central Fujian Rift,South China:Implications for Geological Events

Central Fujian Rift is another new and important volcanogenic massive sulfide Pb-Zn polymetallic metallogenetic belt. In order to find out the material genesis and mineralization period of Meixian-type Pb-Zn-Ag deposits, S and Pb isotope analysis and isotope geochronology of ores and wall rocks for five major deposits are discussed. It is concluded that the composition of sulfur isotope from sulfide ore vary slightly in different deposits and the mean value is close to zero with the 834S ranging from -3.5‰ to ＋5.6‰ averaging at ＋2.0‰, which indicates that the sulfur might originate from magma or possibly erupted directly from volcano or was leached from ore-hosted volcanic rock. The lead from ores in most deposits displays radioactive genesis character （206pb/204pb〉18.140, 207Pb/204pb〉15.584, 208pb/204pb〉38.569） and lead isotope values of ores are higher than those of wall rocks, which indicates that the lead was likely leached from the ore-hosted volcanic rocks. Based on isotope data, two significant Pb-Zn metallogenesis are delineated, which are Mid- and Late-Proterozoic sedimentary exhalative metailogenesis （The single zircon U-Pb, Sm-Nd isochronal and Ar-Ar dating ages of ore- hosted wall rocks are calculated to be among 933-1788 Ma.） and Yanshanian magmatic hydrothermal superimposed and alternated metallogenesis （intrusive SHRIMP zircon U-Pb and Rb-Sr isochronal ages between 127-154 Ma）.     

Sulfur, lead and helium isotopic compositions of sulfide minerals from the Dachang Sn-polymetallic ore district in South China: implication for ore genesis

Summary The Dachang Sn-polymetallic ore district is one of the largest tin producing districts in China. Its origin has long been in dispute between magmatic-hydrothermal replacement and submarine exhalative-hydrothermal origin. The Dachang ore district comprises several types of ore deposits, including the Lamo magmatogenic skarn deposit near a granite intrusion, the Changpo-Tongkeng bedded and vein-type sulfide deposit, and the Gaofeng massive sulfide deposit. Sulfide minerals from the Lamo skarn ores show δ³⁴S values in the range between −3 and +4‰ with a mean close to zero, suggesting a major magmatic sulfur source that likely was the intrusive Longxianggai granite. Sulfide minerals from the Gaofeng massive ores show higher δ³⁴S values between +5 and +12‰, whereas sulfide minerals from the Changpo-Tongkeng bedded ores display lighter δ³⁴S values between −7 and −0.2‰. The difference in the sulfur isotope ranges in the two deposits can be interpreted by different degrees of inorganic thermochemcial reduction of marine sulfate using a one-step batch separation fractionation model. Sulfur isotopic compositions from the vein-type ores at Changpo-Tongkeng vary widely from −8 to +4‰, but most of the data cluster around −2.9‰, which is close to that of bedded ores (−3.6‰). The sulfur in vein-type ores might be derived from bedded ores or it represents a mixture of magmatic- and sedimentary-derived sulfur. Pb isotopic compositions of sulfide minerals in the Dachang ore district reveal a difference between massive and bedded ores, with the massive ores displaying more radiogenic Pb isotope ratios. Correlations of ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁷Pb/²⁰⁴Pb or ²⁰⁸Pb/²⁰⁴Pb for the massive and bedded ores are interpreted as two-component mixing of Pb leached from sedimentary host rocks and from deep-seated Precambrian basement rocks composed of metamorphosed volcano-sedimentary rocks. Pb isotopic compositions of sulfide minerals from vein-type ores overlap with those of bedded sulfides. Similar to the sulfur, the lead in vein-type ores might be derived from bedded ores. Skarn ores at Lamo show very limited variations in Pb isotopic compositions, which may reflect a major magmatic-hydrothermal lead source. Helium isotope data of fluid inclusions trapped in sulfides indicate that He in the massive and bedded ores has a different origin than He in fluorite of granite-related veins. The ³He/⁴He ratios of 1.2–2.9 Ra of fluid inclusions from sulfides at Gaofeng and Changpo-Tongkeng imply a contribution of mantle-derived fluids. Overall our data support a submarine exhalative-hydrothermal origin for the massive and bedded ore types at Dachang. Supplementary material to this paper is available in electronic form at Appendix available as electronic supplementary material     

A lead isotope study of mineralization in the Saudi Arabian Shield

New lead isotope data are presented for some late Precambrian and early Paleozoic vein and massive sulfide deposits in the Arabian Shield. Using the Stacey Kramers (1975) model for lead isotope evolution, isochron model ages range between 720 m.y. and 420 m.y. Most of the massive sulfide deposits in the region formed before 680 m.y. ago, during evolution of the shield. Vein type mineralization of higher lead content occurred during the Pan African event about 550 m.y. ago and continued through the Najd period of extensive faulting in the shield that ended about 530 m.y. ago. Late post-tectonic metamorphism may have been responsible for vein deposits that have model ages less than 500 m.y. Alternatively some of these younger model ages may be too low due to the mineralizing fluids acquiring radiogenic lead from appreciably older local crustal rocks at the time of ore formation.The low²⁰⁷Pb/²⁰⁴Pb ratios found for the deposits in the main part of the shield and for those in north-eastern Egypt, indicate that the Arabian craton was formed in an oceanic crustal environment during the late Precambrian. Involvement of older, upper-crustal material in the formation of the ore deposits in this part of the shield is precluded by their low²⁰⁷Pb/²⁰⁴Pb and²⁰⁸Pb/²⁰⁴Pb characteristics.In the eastern part of the shield, east of longitude 44°20E towards the Al Amar-Idsas fault region, lead data are quite different. They exhibit a linear²⁰⁷Pb/²⁰⁴Pb-²⁰⁶Pb/²⁰⁴Pb relationship together with distinctly higher²⁰⁸Pb/²⁰⁴Pb characteristics. These data imply the existence of lower crustal rocks of early Proterozoic age that apparently have underthrust the shield rocks from the east. If most of the samples we have analyzed from this easterly region were mineralized 530 m.y. ago, then the age of the older continental rocks is 2,100±300 m.y. (2).The presence of upper crustal rocks, possibly also of early Proterozoic age, is indicated by galena data from Hailan in South Yemen and also from near Muscat in Oman. These data are the first to indicate such old continental material in these regions.     

Geochronological framework and Pb, Sr isotope geochemistry of the Qingchengzi Pb–Zn–Ag–Au orefield, Northeastern China

The Qingchengzi orefield in northeastern China, is a concentration of several Pb–Zn, Ag, and Au ore deposits. A combination of geochronological and Pb, Sr isotopic investigations was conducted. Zircon SHRIMP U–Pb ages of 225.3 ± 1.8 Ma and 184.5 ± 1.6 Ma were obtained for the Xinling and Yaojiagou granites, respectively. By step-dissolution Rb–Sr dating, ages of 221 ± 12 Ma and 138.7 ± 4.1 Ma were obtained for the sphalerite of the Zhenzigou Zn–Pb deposit and pyrargyrite of the Ag ore in the Gaojiabaozi Ag deposit, respectively. Pb isotopic ratios of the Ag ore at Gaojiabaozi (²⁰⁶Pb/²⁰⁴Pb = 18.38 to 18.53) are higher than those of the Pb–Zn ores (²⁰⁶Pb/²⁰⁴Pb = 17.66 to 17.96; Chen et al. [Chen, J.F., Yu, G., Xue, C.J., Qian, H., He, J.F., Xing, Z., Zhang, X., 2005. Pb isotope geochemistry of lead, zinc, gold and silver deposit clustered region, Liaodong rift zone, northeastern China. Science in China Series D 48, 467–476.]). Triassic granites show low Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb = 17.12 to 17.41, ²⁰⁷Pb/²⁰⁴Pb = 15.47 to 15.54, ²⁰⁸Pb/²⁰⁴Pb = 37.51 to 37.89) and metamorphic rocks of the Liaohe Group have high ratios (²⁰⁶Pb/²⁰⁴Pb = 18.20 to 24.28 and 18.32 to 20.06, ²⁰⁷Pb/²⁰⁴Pb = 15.69 to 16.44 and 15.66 to 15.98, ²⁰⁸Pb/²⁰⁴Pb = 37.29 to 38.61 and 38.69 to 40.00 for the marble of the Dashiqiao Formation and schist of the Gaixian Formation, respectively).Magmatic activities at Qingchengzi and in adjacent regions took place in three stages, and each contained several magmatic pulses: ca. 220 to 225 Ma and 211 to 216 Ma in the Triassic; 179 to 185 Ma, 163 to 168 Ma, 155 Ma and 149 Ma in the Jurassic, as well as ca. 140 to 130 Ma in the Early Cretaceous. The Triassic magmatism was part of the Triassic magmatic belt along the northern margin of the North China Craton produced in a post-collisional extensional setting, and granites in it formed by crustal melting induced by mantle magma. The Jurassic and Early Cretaceous magmatism was related to the lithospheric delamination in eastern China. The Triassic is the most important metallogenic stage at Qingchengzi. The Pb–Zn deposits, the Pb–Zn–Ag ore at Gaojiabaozi, and the gold deposits were all formed in this stage. They are temporally and spatially associated with the Triassic magmatic activity. Mineralization is very weak in the Jurassic. Ag ore at Gaojiabaozi was formed in the Early Cretaceous, which is suggested by the young Rb–Sr isochron age, field relations, and significantly different Pb isotopic ratios between the Pb–Zn–Ag and Ag ores. Pb isotopic compositions of the Pb–Zn ores suggest binary mixing for the source of the deposits. The magmatic end-member is the Triassic granites and the other metamorphic rocks of the Liaohe Group. Slightly different proportions of the two end-members, or an involvement of materials from hidden Cretaceous granites with slightly different Pb isotopic ratios, is postulated to interpret the difference of Pb isotopic compositions between the Pb–Zn–(Ag) and Ag ores. Sr isotopic ratios support this conclusion. At the western part of the Qingchengzi orefield, hydrothermal fluid driven by the heat provided by the now exposed Triassic granites deposited ore-forming materials in the low and middle horizons of the marbles of the Dashiqiao Formation near the intrusions to form mesothermal Zn–Pb deposits. In the eastern part, hydrothermal fluids associated with deep, hidden Triassic intrusions moved upward along a regional fault over a long distance and then deposited the ore-forming materials to form epithermal Au and Pb–Zn–Ag ores. Young magmatic activities are all represented by dykes across the entire orefield, suggesting that the corresponding main intrusion bodies are situated in the deep part of the crust. Among these, only intrusions with age of ca. 140 Ma might have released sufficient amounts of fluid to be responsible for the formation of the Ag ore at Gaojiabaozi.Our age results support previous conclusions that sphalerite can provide a reliable Rb–Sr age as long as the fluid inclusion phase is effectively separated from the “sulfide” phase. Our work suggests that the separation can be achieved by a step-resolution technique. Moreover, we suggest that pyrargyrite is a promising mineral for Rb–Sr isochron dating.     

U-Pb age and lead isotopic characterization of Au-bearing skarn related to the Andorra granite (central Pyrenees,Spain)

Auriferous skarns are associated with post- and late-kinematic Hercynian granites that intruded into Cambro-Ordovician to Devonian sediments of the central Pyrenees. We determined the age of the Andorra granite and the associated skarn at 305 ± 3 Ma by U-Pb dating titanite from the endo-skarn. The sulfur isotopic composition from sulfides in the skarn (Cardellach et al. 1992) shows a significant variation with isotopically light sulfur (³⁴S +3) in the barren skarns and heavy sulfur (³⁴S +11) in the gold-bearing skarns. Outwards, it increasingly resembles sulfur from arsenopyrite disseminations in the Cambro-Ordovician sediments. The lead isotopic composition from sulfides of the skarns is very homogeneous (²⁰⁶Pb/²⁰⁴Pb = 18.410, ²⁰⁷Pb/²⁰⁴Pb = 15.699, ²⁰⁸Pb/²⁰⁴Pb = 38.574) in contrast to the one in gold-bearing arsenopyrite veins and in arsenopyrite disseminations in the sediments (e.g. ²⁰⁶Pb/²⁰⁴Pb varies from 18.54 to 30.36). Combined, sulfur and lead isotope data indicate that the lead in the skarn is dominantly derived from the granite, whereas the sulfur is derived at variable portions from both the granite and the sediments.     

Isotope composition of Medieval lead glasses reflecting early silver production in Central Europe

The lead isotope composition of 32 lead glasses excavated from strata of the twelfth to early fifteenth century in six countries of NW Europe made the predominance of the Harz Mountains in this period of the Medieval European lead and silver production highly probable. Post-Variscan vein type galena, Devonian syngenetic hydrothermal ore (Rammelsberg) and blended ore from both deposits in the Harz were used. Our evaluation of 200 mining sites in Germany, Britain and Ireland also demonstrated that minor lead sources for lead glass were located in Bavaria/Bohemia and England. Lead ores from the Rhenohercynian orogenic belt in Germany are derived from rock sources close to the upper continental crust composition in ²³⁸U/²⁰⁴Pb of about 10 and Th/U of about 4. The ores in Central England originated from rocks with ²³⁸U/²⁰⁴Pb of about 11. Received: 24 September 1996 / Accepted: 17 January 1997     

H,O,S and Pb isotope studies of uranium ore deposits in granitoid rocks of South China

Most altered clay minerals in uranium ore deposits in granites in the selected provinces of South China haveδ ¹⁸O _m values ranging from 6.22 to 7.24,δD_m from −60 to −70,δ ¹⁸O from +3.05 to −3.07, and from −20.2 to −37.5‰. Relative enrichment of³²S in the uranium ore deposits and greater variations in Pb isotopic composition of galenas from them show that uranium ores in the granites were formed in such a way that uranium in shallow-source granites had been mobilized by heated meteoric waters and then migrated to local favourable locations along great faults to form uranium ore deposits. Zhang Shaoli, Yang Wenjin, Tang Chunjing and Xu Wenxin did part of this work.     

Stable lead isotopes reveal a natural source of high lead concentrations to gasoline-contaminated groundwater

Concentrations of total lead as high as 1,600 g/L were detected in gasoline-contaminated and uncontaminated groundwater at three gasoline-release sites in South Carolina. Total lead concentrations were highest in turbid groundwater samples from gasoline-contaminated and uncontaminated wells, whereas lower turbidity groundwater samples (collected using low-flow methods) had lower total lead concentrations. Dissolved lead concentrations in all wells sampled, however, were less than 15 g total lead/L, the current United States Environmental Protection Agency (US EPA) maximum contaminant level (MCL). Because many total lead concentrations exceeded the MCL, the source of lead to the groundwater system at two of the three sites was investigated using a stable lead isotope ratio approach. Plots of the stable isotope ratios of lead (Pb) in groundwater as ²⁰⁷Pb/²⁰⁶Pb versus ²⁰⁸Pb/²⁰⁶Pb, and ²⁰⁸Pb/²⁰⁴Pb versus ²⁰⁶Pb/²⁰⁴Pb were similar to ratios characteristic of lead-based minerals in local rocks of the southeastern US, and were not similar to the stable lead isotopes ratios characteristic of distant lead ore deposits such as Broken Hill, Australia, used to produce tetraethyl lead in gasoline products prior to its phase-out and ban in the United States. Moreover, the isotopic composition of dissolved lead was equivalent to the isotopic composition of total lead in turbid samples collected from the same well, suggesting that the majority of the lead detected in the groundwater samples was associated with sediment particulates of indigenous aquifer material, rather than lead associated with spilled leaded gasoline. The results of this investigation indicate that (1) lead detected at some gasoline-release sites may be derived from the local aquifer material, rather than the gasoline release, and consequently may affect site-specific remediation goals; (2) non-low flow groundwater sampling methods, such as a disposable bailer, may result in turbid groundwater samples and high total lead concentrations, and; (3) stable lead isotopes can be used to clarify the source of lead detected above permissible levels in gasoline-contaminated groundwater systems.     

西秦岭降扎地区金、铀矿床年代学对比研究

西秦岭降扎地区寒武、志留系中的金、铀矿床,是我国相当重要的碳硅泥岩型矿床。根据金矿床中岩石和矿石异常铅模式年龄、氩-氩同位素年龄和钾-氩同位素年龄等,获得了一批有益的年代学信息。金矿床的各种同位素年龄数据主要有2组:(1)242-186Ma;(2)137-47Ma.结合区域地质发展史、成矿热液脉与岩脉的穿切关系以及矿床产出的其它宏观特征等,确定金矿床的成矿时代为137-47Ma,与区域铀矿床形成的主要时代(117-55Ma)相比,二者成矿时间大体相同。     

Lead isotope study of Zn-Pb ore deposits associated with the Basque-Cantabrian basin and Paleozoic basement, Northern Spain

A total of forty-three galena samples from syngenetic and epigenetic Pb-Zn mineralizations emplaced in the Lower Cretaceous Basque-Cantabrian basin and Paleozoic basement of the Cinco Villas massif in the western Pyrenees, have been analyzed for Pb-isotopic composition. Galena from sedex mineralizations hosted in Carboniferous clastic rocks in the Cinco Villas massif display an homogeneous lead isotopic signature (²⁰⁶Pb/²⁰⁴4Pb 18.43, ²⁰⁷Pb/²⁰⁴Pb 15.66, ²⁰⁸Pb/ ²⁰⁴Pb 38.69) suggesting a single lead reservoir. These values are slightly more radiogenic than lead from other European Hercynian deposits, possibly reflecting the influence of a more evolved upper crustal source. Underlying Paleozoic sediments are proposed as lead source for the Cinco Villas massif ores. Analyses from twenty-six galena samples from the four strata-bound ore districts hosted in Mesozoic rocks reveal the existence of two populations regarding their lead isotopic composition. Galena from the western Santander districts (e.g., Reocin) is characterized by more radiogenic isotope values (²⁰⁶Pb/²⁰⁴Pb 18.74, ²⁰⁷Pb/²⁰⁴Pb 15.67, ²⁰⁸Pb/ ²⁰⁴Pb 38.73) than those from the central and eastern districts (Troya-Legorreta, Central and Western Vizcaya, ²⁰⁶Pb/²⁰⁴Pb 18.59, ²⁰⁷Pb/²⁰⁴Pb 15.66, ²⁰⁸Pb/ ²⁰⁴Pb 38.73). In all districts, the most likely source for these mineralizations was the thick sequence of Lower Cretaceous clastic sediments. The existence of two separate lead isotopic populations could be the result of regional difference in the composition of the basement rocks and the clastic sediments derived of it or different evolution histories. In both sub-basins, isotopic ratios indicate an increase in crustal influence as the age of the ores decreases.     

Mineralization age and sources of ore‐forming material of the Nanmushu Zn‐Pb deposit in the Micangshan Tectonic Belt at the northern margin of the Yangtze Craton,China: Constraints from Rb‐Sr dating and Sr‐Pb isotopes

The Nanmushu Zn‐Pb deposit, hosted by the Neoproterozoic Dengying Formation dolostone, is located in the eastern part of the Micangshan tectonic belt at the northern margin of the Yangtze Craton, China. This study involves a systematic field investigation, detailed mineralogical study, and Rb‐Sr and Pb isotopic analyses of the deposit. The results of Rb‐Sr isotopic dating of coexisting sphalerite and galena yield an isochron age of 486.7 ± 3.1 Ma, indicating the deposit was formed during the Late Cambrian to Early Ordovician. This mineralization age is interpreted to be related to the timing of destruction of the paleo‐oil reservoir in the Micangshan tectonic belt. All initial ⁸⁷Sr/⁸⁶Sr ratios of sphalerite and galena (0.70955–0.71212) fall into the range of the Mesoproterozoic Huodiya Group basement rocks (0.70877–0.71997) and Dengying Formation sandstone (0.70927–0.71282), which are significantly higher than those of Cambrian Guojiaba Formation limestone (0.70750–0.70980), Cambrian Guojiaba Formation carbonaceous slate (0.70766–0.71012), and Neoproterozoic Dengying Formation dolostone (0.70835–0.70876). Such Sr isotope signatures suggest that the ore strontium was mainly derived from a mixed source, and both of the Huodiya Group basement rocks and Dengying Formation sandstone were involved in ore formation. Both sphalerite and galena are characterized by an upper‐crustal source of lead (²⁰⁶Pb/²⁰⁴Pb = 17.849–18.022, ²⁰⁷Pb/²⁰⁴Pb = 15.604–15.809, and ²⁰⁸Pb/²⁰⁴Pb = 37.735–38.402), and their Pb isotopes are higher than, but partly overlap with, those of the Huodiya Group basement rocks, but differ from those of the Guojiaba and Dengying Formations. This suggests that the lead also originated from a mixed source, and the Huodiya Group basement rocks played a significant role. The Sr and Pb isotopic results suggest that the Huodiya Group basement rocks were one of the most important sources of metallogenic material. The geological and geochemical characteristics show that the Nanmushu Zn‐Pb deposit is similar to typical Mississippi Valley type, and the fluid mixing may be a reasonable metallogenic mechanism for Nanmushu Zn‐Pb deposit.     

The geological and metallogenic setting of stratabound carbonate-hosted Zn-Pb mineralizations in the West Asturian Leonese Zone, NW Spain

Several carbonate-hosted stratabound zinc-lead ores in the Ponferrada-Caurel area (NW Spain) are hosted by the Lower to Middle Cambrian Vegadeo Formation. Two clearly distinct groups of mineralizations occur in different stratigraphic positions. The stratiform disseminated ore is located in the Lower Member as irregular and millimetre-thick layers of sphalerite and galena replacing earlier pyrite. The lack of hydrothermal alteration and the heavy C., O and S isotopic signatures suggest that this ore is of premetamorphic origin, the sulphur and fluids being derived from the host carbonates. The more likely source of the sulphide is the abiogenic thermal reduction of sulphate derived from sulphate beds intercalated with the carbonates. The second group of mineralizations is located at the top of the Vegadeo Fm, always along its contact with the overlaying shales and sandstones of the Cabos Series. This group is economically more important and include three styles of strata-bound mineralizations. The more common one is the silica ore, a hydrothermal rock that traces the contact between the carbonate and the detrital rocks along more than 50 km. Locally, a carbonate-rich ore is found along the contact between the silica ore and the Vegadeo Fm. Laterally to these rocks, there are large bodies of the breccia ore, made up of sulphides and calcite in a matrix of chlorite. The ore assemblage is composed of sphalerite and galena with minor amounts of chalcopyrite and pyrite. Co-Ni-As sulphides, bismuthinite, tetrahedrite and Pb-Bi sulphosalts are also found as trace minerals. The geological relationships and the isotopic signatures suggest that the three ores are synchronous and of late Hercynian age. They are interpreted as linked with a tectonically driven fluid flow along the stratigraphic contact between the carbonate and the detrital rocks.The model of ore genesis involves the circulation of fluids in likely equilibrium with the detrital rocks that react with the Vegadeo Fm leading to the metasomatic replacement of limestones by quartz with synchronous precipitation of sulphides. The genesis of breccias is probably due to the formation of overpressured zones. The hydrothermal alteration results in a systematic depletion in both ¹⁸O and ¹³C of the carbonates due to the infiltration of fluids, of likely mixed metamorphic and surface origin. Fluid inclusions in the chloritic breccia suggest that the ore formation took place at temperatures higher than 200 °C in relationship with low salinity (up to 1.2% wt. NaCl eq.) water-rich (H₂O>99%) fluids. Sulphur isotopes suggest that most of the sulphur has a common origin with the stratiform ores, but here there is a significant but variable input from the detrital rocks. Lead isotopes of the different ores are within the Cambrian signature of the southern Hercynian Belt, with a long crustal history. However, mixing with a minor juvenile component cannot be ruled out. The geographic and stratigraphic proximity and the similar lead signatures between the premetamorphic and the Hercynian mineralizations suggest that the latter was derived from the remobilization, in a lead frozen system, of the stratiform-disseminated ones. The premetamorphic mineralizations can be interpreted as similar to the widespread Mississippi Valley-type deposits found in the southern Hercynian Belt. The second group of deposits can be defined as synto postmetamorphic stratabound, carbonate-hosted Zn-Pb deposits, broadly similar to MVT but formed in an orogenic setting. Specific features such as the presence of chlorite, the fluid composition (low saline H₂O-NaCl fluids) and the temperatures of formation (above at 200 °C) are interpreted as characteristic of this tectonic setting.     

Multiple crustal sources for post-tectonic I-type granites in the Hercynian Iberian Belt

A post-tectonic plutonic array of felsic I-type granites crops out in the western Hercynian Iberian Belt. Isotope (Sr, Nd, Pb) data favour the absence of an important input of juvenile magmas in late- to post- tectonic Hercynian felsic magmatism in western Iberia, but suggest a reworking of different crustal protoliths, including oceanic metabasic rocks accreted to mid-to-lower crustal levels during the early stages of the collision. I-type granites were derived from different meta-igneous protoliths ranging from metabasic to felsic compositions depending on their geographical position from the external (e.g. Galicia—N Portugal, GNP) to the innermost continental areas (Spanish Central System and Los Pedroches Batholiths). The GNP I-type plutons related to eo-Hercynian accretional terranes have lower initial ⁸⁷Sr/⁸⁶Sr ratios, lower negative εNd values, and higher ²⁰⁶Pb/²⁰⁴Pb ratios than other I-type granites of the Central Iberian zone. These more isotopically primitive Hercynian I-type granites are important in tracking pre-Hercynian accreted oceanic lithosphere terranes.     

东秦岭钼矿带内碳酸岩脉型钼（铅）矿床地质 地球化学特征、成矿机制及成矿构造背景

东秦岭钼矿带位于华北板块南缘,NW-NWW向的固始―栾川深断裂带控制着钼矿床的空间分布.黄水庵碳酸岩脉型钼(铅)矿床的确定,为本矿带内已有碳酸岩脉型钼(铅)矿床(黄龙铺地区的大石沟、石家湾和桃园等)增添了又一新成员.本矿带不仅钼金属储量居世界已知单个钼矿带之首,而且碳酸岩脉和花岗斑岩两个成矿体系并存,亦是本区钼矿带的一大特色.业已查明,黄水庵和黄龙铺(大石沟)等碳酸岩脉型钼(铅)矿床的δ~(13)C=-5.3‰～-7.0‰,~(87)Sr/~(86)Sr=0.7049～0.7065.同时,方解石富含轻稀土(LREE/HREE=1.8～2.9).辉钼矿以富含Re(平均为110×10~(-6)～244×10~(-6))为特征.基于含矿碳酸岩脉方解石的Sr、Nd、Pb同位素比值(~(87)Sr/~(86)Sr对~(206)Pb/~(204)Pb、~(207)Pb/~(204)Pb对~(206)Pb/~(204)Pb和~(143)Nd/~(144)Nd对~(87)Sr/~(86)Sr)的关系图,我们初步判断本矿带区域陆壳之下可能存在有EMI(富集地幔Ⅰ),这些含矿碳酸岩脉是源于EMI的碱性硅酸盐-碳酸盐熔体-溶液结晶分异的产物,成矿金属Mo、Pb主要来自EMI.根据黄水庵和黄龙铺(大石沟)钼(铅)矿床的成矿年龄(Re-Os年龄分别为209.5 Ma和221 Ma),我们推断,碳酸岩脉型钼(铅)矿床形成于华北和扬子两大板块三叠纪碰撞造山后伸展阶段的晚三叠世时期,而在侏罗纪陆内造山晚期的伸展阶段,形成了晚侏罗-早白垩世的斑岩型和斑岩-矽卡岩型钼矿床(Re-Os年龄介于147～116 Ma).     

Geology and Geochemistry of the Bianbianshan Au‐Ag‐Cu‐Pb‐Zn Deposit,Southern Da Hinggan Mountains,Northeastern China

The Bianbianshan deposit, the unique gold-polymetal (Au-Ag-Cu-Pb-Zn) veined deposit of the polymetal metallogenic belt of the southern segment of Da Hinggan Mountains mineral province, is located at the southern part of the Hercynian fold belt of the south segment of Da Hinggan Mountains mineral province, NE China. Ores at the Bianbianshan deposit occur within Cretaceous andesite and rhyolite in the form of gold-bearing quartz veins and veinlet groups containing native gold, electrum, pyrite, chalcopyrite, galena and sphalerite. The deposit is hosted by structurally controlled faults associated with intense hydrothermal alteration. The typical alteration assemblage is sericite + chlorite + calcite + quartz, with an inner pyrite - sericite - quartz zone and an outer seicite - chlorite - calcite - epidote zone between orebodies and wall rocks. δ34 S values of 17 sulfides from ores changing from –1.67 to +0.49‰ with average of –0.49‰, are similar to δ34 S values of magmatic or igneous sulfide sulfur. 206Pb/204Pb, 207Pb/204Pb and 208Pb/ 204Pb data of sulfide from ores range within 17.66–17.75, 15.50–15.60, and 37.64–38.00, respectively. These sulfur and lead isotope compositions imply that ore-forming materials might mainly originate from deep sources. H and O isotope study of quartz from ore-bearing veins indicate a mixed source of deep-seated magmatic water and shallower meteoric water. The ore formations resulted from a combination of hydrothermal fluid mixing and a structural setting favoring gold-polymetal deposition. Fluid mixing was possibly the key factor resulting in Au-Ag-Cu-Pb-Zn deposition in the deposit. The metallogenesis of the Bianbianshan deposit may have a relationship with the Cretaceous volcanic-subvolcanic magmatic activity, and formed during the late stage of the crust thinning of North China.     

Lead isotopes of the carbonate-hosted Kabwe, Tsumeb, and Kipushi Pb-Zn-Cu sulphide deposits in relation to Pan African orogenesis in the Damaran-Lufilian Fold Belt of Central Africa

Lead isotope ratios of galena from the carbonate-hosted massive sulphide deposits of Kabwe (Pb-Zn) and Tsumeb (Pb-Zn-Cu) in Zambia and Namibia, respectively, have been measured and found to be homogeneous and characteristic of upper crustal source rocks. Kabwe galena has average isotope ratios of ^206/204Pb = 17.997 ± 0.007, ^207/204Pb = 15.713 ± 0.010 and ^208/204Pb = 38.410 ± 0.033. Tsumeb galena has slightly higher ^206/204Pb (18.112 ± 0.035) and slightly lower ^207/204Pb (15.674 ± 0.016) and ^208/204Pb (38.276 ± 0.073) ratios than Kabwe galena. The isotopic differences are attributed to local differences in the age and composition of the respective source rocks for Kabwe and Tsumeb. The homogeneity of the ore lead in the two epigenetic deposits suggests lead sources of uniform isotopic composition or, alternatively, thorough mixing of lead derived from sources with relatively similar isotopic compositions. Both deposits have relatively high ²³⁸U/²⁰⁴Pb ratios of 10.31 and 10.09 for Kabwe and Tsumeb galenas, respectively. These isotope ratios are considered to be typical of the upper continental crust in the Damaran-Lufilian orogenic belt, as also indicated by basement rocks and Cu-Co sulphides in stratiform Katangan metasediments which have a mean μ-value of 10.25 ± 0.12 in the Copperbelt region of Zambia and the Democratic Republic of Congo (formerly Zaire). The ²³²Th/²⁰⁴Pb isotope ratios of 43.08 and 40.42 for Kabwe and Tsumeb suggest Th-enriched source regions with ²³²Th/²³⁵U (κ-values) of 4.18 and 4.01, respectively. Model isotopic ages determined for the Kabwe (680 Ma) and Tsumeb (530 Ma) deposits indicate that the timing of the mineralisation was probably related to phases of orogenic activity associated with the Pan-African Lufilian and Damaran orogenies, respectively. Galena from the carbonate-hosted Kipushi Cu-Pb-Zn massive sulphide deposit in the Congo also has homogeneous lead isotope ratios, but its isotopic composition is comparable to that of the average global lead evolution curve for conformable massive sulphide deposits. The μ (9.84) and κ (3.69) values indicate a significant mantle component, and the isotopic age of the Kipushi deposit (456 Ma) suggests that the emplacement of the mineralisation was related to a post-tectonic phase of igneous activity in the Lufilian belt. The isotope ratios (^206/204Pb, ^207/204Pb, ^208/204Pb) of the three deposits are markedly different from the heterogeneous lead ratios of the Katangan Cu-Co stratiform mineralisation of the Copperbelt as well as those of the volcanogenic Nampundwe massive pyrite deposit in the Zambezi belt which typically define radiogenic linear trends on lead-lead plots. The host-rock dolomite of the Kabwe deposit also has homogeneous lead isotope ratios identical to the ore galena. This observation indicates contamination of the Kabwe Dolomite Formation with ore lead during mineralisation. Received: 8 September 1997 / Accepted: 21 August 1998