Paleoproterozoic subduction-related metasomatic signatures in the lithospheric mantle beneath NE Brazil: inferences from trace element and Sr–Nd–Pb isotopic compositions of Neoproterozoic high-K igneous rocks

Late Neoproterozoic (ca. 580 Ma), high-K, mafic-intermediate rocks represent voluminous bimodal magmatism in the Borborema Province, northeast Brazil. These rocks show the following chemical signatures that reflect derivation from a subduction-modified lithospheric mantle source: (1) enrichment in large ion lithophile elements (Rb, Ba, K, Th) and light rare-earth elements (REE) (La/Yb_CN=11–70), (2) pronounced negative Nb anomalies, and (3) radiogenic Sr (0.71202–0.7059) and unradiogenic Nd (_Nd from −9.3–−20.1) isotopic compositions. T_DM model ages suggest that modification of the lithospheric mantle source (metasomatised garnet lherzolite) may have occurred in the Paleoproterozoic during the Transamazonian/Eburnean tectonics that affected the region. Interaction with asthenospheric fluids is believed to have partially melted this enriched source in the Neoproterozoic, probably as a result of asthenosphere-derived fluid percolation in the Brasiliano/Pan-African shear zones that controlled the emplacement of these mafic-intermediate magmas. The involvement of this asthenospheric component is supported by the nonradiogenic Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb=16–17.3, ²⁰⁷Pb/²⁰⁴Pb=15.1–15.6, ²⁰⁸Pb/²⁰⁴Pb=36–37.5), which contrast with the enriched Sr and Nd compositions and thereby suggest the decoupling of Rb–Sr, Sm–Nd, and U–Pb systems at the time of intrusion of the mafic-intermediate magmas in the crust.     

Lead isotopic evidence for interaction between plume and lower crust during emplacement of peralkaline Lovozero rocks and related rare-metal deposits,East Fennoscandia,Kola Peninsula,Russia

The Lovozero alkaline massif—an agpaitic nepheline syenite layered intrusion—is located in the central part of the Kola Peninsula, Russia, and belongs to the Kola ultramafic alkaline and carbonatitic province (KACP) of Devonian age. Associated loparite and eudialyte deposits, which contain immense resources of REE, Nb, Ta, and Zr, constitute a world class mineral district. Previous Sr, Nd, and Hf isotope investigations demonstrated that these rocks and mineral deposits were derived from a depleted mantle source. However, because the Sr, Nd, and Hf abundances in the Kola alkaline rocks are significantly elevated, their isotopic compositions were relatively insensitive to contamination by the underlying crustal rocks through which the intruding magmas passed. Pb occurring in relatively lower abundance in the KACP rocks, by contrast, would have been a more sensitive indicator of an acquired crustal component. Here, we investigate the lead isotopic signature of representative types of Lovozero rocks in order to further characterize their sources. The measured Pb isotopic composition was corrected using the determined U and Th concentrations to the age of the crystallization of the intrusion (376?±?28 Ma, based on a ²⁰⁶Pb/²⁰⁴Pb versus ²³⁸U/²⁰⁴Pb isochron and 373?±?9 Ma, from a ²⁰⁸Pb/²⁰⁴Pb versus ²³²Th/²⁰⁴Pb isochron). Unlike the previously investigated Sr, Nd, and Hf isotopes, the lead isotopic composition plot was well outside the FOZO field. The ²⁰⁶Pb/²⁰⁴Pb values fall within the depleted MORB field, with some rocks having lower ²⁰⁷Pb/²⁰⁴Pb but higher ²⁰⁸Pb/²⁰⁴Pb values. Together with other related carbonatites having both lower and higher ²⁰⁶Pb/²⁰⁴Pb values, the combined KACP rocks form an extended linear array defining either a?~2.5-Ga secondary isochron or a mixing line. The projection of this isotopic array toward the very unradiogenic composition of underlying 2.4–2.5-Ga basaltic rocks of the Matachewan superplume and associated Archean granulite facies country rock provides strong evidence that this old lower crust was the contaminant responsible for the deviation of the Lovozero rocks from a presumed original FOZO lead isotopic composition. Evaluating the presence of such a lower crustal component in the Lovozero rock samples suggests a 5–10% contamination by such rocks. Contamination by upper crustal rock is limited to only a negligible amount.     

Lead isotope systematics of the giant massive sulphide deposits in the Iberian Pyrite Belt

Lead isotope analyses were performed on 26 polymetallic massive sulphide deposits of the Iberian Pyrite Belt, as well as on overlying gossans and associated volcanic rocks. All the massive sulphide deposits (except for Neves-Corvo), and nearly all the volcanic rocks show very similar isotopic compositions grouped around 18.183 (²⁰⁶Pb/²⁰⁴Pb), 15.622 (²⁰⁷Pb/²⁰⁴Pb) and 38.191 (²⁰⁸Pb/²⁰⁴Pb), indicating that most of the ore deposit lead was derived from the same continental crust environment as the associated volcanic rocks. The isotopic compositions are representative of the average south Iberian crust during the Devonian to Early Carboniferous (Dinantian), and their constancy implies a homogenization of the mineralizing fluids before the deposition of the massive sulphides from hydrothermal fluids circulating through interconnected regional fracture systems. This isotopic constancy is incompatible with multiple, small, independent hydrothermal cells of the East Pacific Rise type, and fits much better with a model of hydrothermal convections driven by “magmatic floor heating”. Neves-Corvo is the only south Iberian massive sulphide deposit to have a heterogeneous isotopic composition with, in particular, a highly radiogenic stanniferous ore (²⁰⁶Pb/²⁰⁴Pb of the cassiterite is >18.40). A model of lead mixing with three components is proposed to explain these variations: (1) one derived from the Devonian to Early Carboniferous (Dinantian) continental crust that generated all the other massive ores; (2) an Eohercynian stanniferous mineralization partly remobilized during the formation of the massive sulphides, but independent of them; and (3) a Precambrian continental crust component. The juxtaposition of three different sources places Neves-Corvo in a specific paleogeographic situation that could also explain its mineralogical specificity. The geodynamic context that best explains all the obtained isotopic results is one of an accretionary prism. The fact that lead isotope signatures of the gossans are almost identical to those of the underlying massive sulphides means that this technique could be a useful exploration tool for the Iberian Pyrite Belt.     

Pb-Sr-Nd isotopic compositions and trace element geochemistry of megacrysts and melilitites from the Tertiary Urach volcanic field: source composition of small volume melts under SW Germany

 The Urach volcanic field is unique within the Tertiary–Quaternary European volcanic province (EVP) due to more than 350 tuffaceous diatremes and only sixteen localities with extremely undersaturated olivine melilitite. We report representative Pb-Sr-Nd isotopic compositions and incompatible trace element data for twenty-two pristine augite, Cr-diopside, hornblende, and phlogopite megacryst samples from the diatremes, and seven melilitite whole rocks. The Pb isotopic compositions for melilitites and comagmatic megacrysts have very radiogenic ²⁰⁶Pb/²⁰⁴Pb ratios of 19.4 to 19.9 and plot on the northern hemisphere mantle reference line (NHRL). The data indicate absence of an old crustal component as reflected in the high ²⁰⁷Pb/²⁰⁴Pb ratios of many basalts from the EVP. This inference is supported by ²⁰⁶Pb/²⁰⁴Pb ratios of ∼17.6 to 18.3 and ɛ_Nd of ∼−7.8 to +1.6 for five phlogopite xenocryst samples reflecting a distinct and variably rejuvenated lower Hercynian basement. The ⁸⁷Sr/⁸⁶Sr ratios of 0.7033 to 0.7035 in the comagmatic megacrysts are low relative to their moderately radiogenic Nd isotopic compositions (ɛ_Nd +2.2 to +5.1) and consistent with a long-term source evolution with a low Rb/Sr ratio and depletion in light rare-earth elements (LREE). The melilitite whole-rock data show a similar range in Nd isotopic ratios as determined for the megacrysts but their Sr isotopic compositions are often much more radiogenic due to surface alteration. The REE patterns and incompatible trace element ratios of the melilitites (e.g. Nb/Th, Nb/U, Sr/Nd, P/Nd, Ba/Th, Zr/Hf) are similar to those in ocean island basalts (OIB); negative anomalies for normalized K and Rb concentrations support a concept of melt evolution in the lithospheric mantle. Highly variable Ce/Pb ratios of 29 to 66 are positively correlated with La/Lu, La/K₂O, and Ba/Nd and interpreted to reflect melting in the presence of residual amphibole and phlogopite. The data suggest an origin of the melilitites from a chemical boundary layer very recently enriched by melts from old OIB sources. We suggest that the OIB-like mantle domains represent low-temperature melting heterogeneities in an upwelling asthenosphere under western Europe. Received: 9 March 1995/Accepted: 24 July 1995     

Metallogeny and lead isotopic composition of base metal sulfide deposits in the Rappen area,northern Sweden

Early Proterozoic volcanic and sedimentary rocks of the Rappen district in northern Sweden were deposited at a destructive plate margin to the south of the Archaean craton of the western Baltic Shield. The volcano-sedimentary suite was intruded by two generations of early Proterozoic granites at ca. 1.89–1.85 Ga and ca.1.82–1.78 Ga, respectively, and metamorphosed at upper amphibolite facies conditions. Small stratabound iron, copper, and zinc deposits occur in felsic to mafic tuffs and arkosic sediments. Small deposits of molybdenum, tungsten, and uranium formed during the emplacement of the younger granites. The lead isotopic compositions of sulfide trace lead from the various deposits are highly heterogeneous. In the ²⁰⁶Pb/²⁰⁴Pb–²⁰⁷Pb/²⁰⁴Pb diagram they fall on mixing arrays between little evolved early Proterozoic lead and highly radiogenic Caledonian lead. The least radiogenic lead isotopic compositions from the various deposits have a wide range of ²⁰⁷Pb/²⁰⁴Pb ratios and thus indicate variable involvement of Archaean crustal lead in the Proterozoic deposits. Deposits hosted by siliciclastic rocks have higher ²⁰⁷Pb/²⁰⁴Pb ratios than deposits hosted in mafic to felsic tuffites. The lead isotopic heterogeneity suggests that the lead in the various deposits was locally derived and, furthermore, that the sedimentary rocks in part originated from the Archaean craton to the north. Lead mixing arrays in the ²⁰⁶Pb/²⁰⁴Pb–²⁰⁷Pb/²⁰⁴Pb diagram demonstrate that in Paleozoic time radiogenic lead was mobilized and transported in the basement. Source ages calculated from the mixing arrays (ca.1.9 Ga and ca.1.8 Ga) correspond to the age of the Early Proterozoic volcanism and metamorphism respectively. One group of deposits includes lead from at least three sources and illustrates that radiogenic lead was multiply mobilized and transported in the Proterozoic basement. It occurs in deposits that occur in zones that became permeable during the reactivations of the basement.     

Genesis of the South Zhuguang Uranium Ore Field,South China: Pb Isotopic Compositions and Mineralization Ages

U–Pb isotopic analyses indicate that ores from the South Zhuguang uranium ore field, south China, have high common (non‐radiogenic) Pb contents, with variable and relatively radiogenic initial Pb contents. The U–Pb isochron method was used to date these ores, with plots of ²⁰⁸Pb/²⁰⁴Pb and ²⁰⁷Pb/²⁰⁴Pb versus ²⁰⁶Pb/²⁰⁴Pb being used to identify sample suites with similar initial Pb isotopic ratios and to normalize variable initial Pb isotopic ratios. The resulting U–Pb isochrons indicate two substages of uranium mineralization at ~57 and 52 Ma, with a later hydrothermal reformation at ~49 Ma, which homogenized Pb isotopic compositions. Initial Pb isotopic systematics indicate that the ore‐forming fluid was characterized by high ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁷Pb/²⁰⁴Pb ratios and low ²⁰⁸Pb/²⁰⁴Pb ratios, suggesting that the ore‐forming fluid was sourced from Cretaceous–Paleogene red‐bed basins, rather than from magma or the mantle, with consideration of mineralization ages.     

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     

Origin of the Dexing Cu-bearing porphyries,SE China: elemental and Sr–Nd–Pb–Hf isotopic constraints

The Dexing porphyry copper deposit, part of the circum-Pacific porphyry copper ore belt, is the largest porphyry copper deposit in China. We present new LA–ICP–MS zircon U–Pb and molybdenite Re–Os dating, bulk-rock elemental and Sr–Nd–Pb isotopic as well as in situ zircon Hf isotopic geochemistry for these ore-bearing porphyries, in an attempt to better constrain their petrogenesis. LA–ICP–MS zircon U–Pb dating shows that the Dexing porphyries were emplaced in the early Middle Jurassic (～171 Ma); molybdenite Re–Os dating indicates that the associated Cu–Mo mineralization was contemporaneous (～171 Ma) with the igneous intrusion. The rocks are mainly high-K calc-alkaline and show adakitic affinities, including high Sr and low Y and Yb contents, high Sr/Y and La/Yb ratios, and high Mg# (higher than pure crustal melts). These porphyries have initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7044?0.7047, ?_Nd(T) values of –1.5 to?+0.6, and ?_Hf(T) (in situ zircon) values of?+2.6 to?+4.6. They show unusually radiogenic Pb isotopic compositions with initial ²⁰⁶Pb/²⁰⁴Pb ratios up to 18.41 and ²⁰⁷Pb/²⁰⁴Pb up to 15.61. These isotopic compositions are distinctly different from either Pacific MORB or Yangtze lower crust but are similar to the subducting sediments in the western Pacific trenches. Detailed elemental and isotopic data suggest that the Dexing porphyries were emplaced in a continental arc setting coupled with westward subduction of the palaeo-Pacific plate. Partial melting involved the subducted slab (mainly the overlying sediments), with generated melts interacting with the lithospheric mantle wedge, thereby forming the investigated high-K calc-alkaline porphyry magmas.     

Sr,Nd and Pb Isotopic Systematics of the Cenozoic Basalts of the Korean Peninsula and Their Implications for the Permo-Triassic Continental Collision Boundary

Sr, Nd and Pb isotopic compositions of the Cenozoic basalts were analyzed from Baengnyeongdo Island, Jeongok, Ganseong, and Jejudo Island of Korea. They reveal relatively enriched Sr and Nd isotopic compositions (⁸⁷Sr/⁸⁶Sr = 0.70330∼0.70555, ¹⁴³Nd/¹⁴⁴Nd = 0.51298∼0.51256) compared with MORB.²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb values of all the analyzed Korean basalts lie above the Northern Hemisphere Reference Line (NHRL) defined by Hart (1984). Pb isotopic compositions of basalts from Jejudo Islands (²⁰⁶Pb/²⁰⁴Pb = 18.61∼19.12, ²⁰⁷Pb/²⁰⁴Pb = 15.54∼15.69, ²⁰⁸Pb/²⁰⁴Pb = 38.98∼39.72) are significantly more radiogenic than the rest (²⁰⁶Pb/²⁰⁴Pb = 17.72∼18.03, ²⁰⁷Pb/²⁰⁴Pb = 15.44∼15.58, ²⁰⁸Pb/²⁰⁴Pb = 37.77∼38.64). The Cenozoic Korean basalts thus can be divided into two groups based on their Sr, Nd and Pb isotopic compositions. The north group reveals mixing between DMM and EM1 while the south group displays DMM-EM2 mixing. Such a distribution is the same as Chinese Cenozoic basalts and it can be interpreted that the subcontinental lithospheric mantle under Korea represents simple lateral continuation of the South and North China Blocks. We suggest that Korean continental collision zone cross the Korean Peninsula through the region between the north and south basalt groups of Korea.     

Tertiary basalts and peridotite xenoliths from the Hessian Depression (NW Germany), reflecting mantle compositions low in radiogenic Nd and Sr

A total of 17 alkali basalts (alkali olivine basalt, limburgite, olivine nephelinite) and quartz tholeiites, and of 10 peridotite xenoliths (or their clinopyroxenes) were analyzed for Nd and Sr isotopes. ¹⁴³Nd/¹⁴⁴Nd ratios and ⁸⁷Sr/⁸⁶Sr ratios of all basalts and of the majority of ultramafic xenoliths plot below the mantle array with a large variation in Nd isotopes and a smaller variation in Sr isotopes. The tholeiites were less radiogenic in Nd than the alkali basalts. Volcanics from the Eifel and Massif Central regions contain Nd and Sr, which is more radiogenic than that of the basalts from the Hessian Depression. Nd and Sr isotopic compositions of all rocks from the latter area, with the exception of one tholeiite and one peridotite plot in the same field of isotope ratios as the Ronda ultramafic tectonite (SW Spain), which ranges in composition from garnet to plagioclase peridotite. The alkali basaltic rocks are products of smaller degrees of partial melting of depleted peridotite, which has undergone a larger metasomatic alteration compared with the source rock of tholeiitic magmas. For the peridotite xenoliths such metasomatic alteration is indicated by the correlation of their K contents and isotopic compositions. We assume that the upper mantle locally can acquire isotopic signatures low in radiogenic Nd and Sr from the introduction of delaminated crust. Such granulites low in radiogenic Nd and Sr are products of early REE fractionation and granite (Rb) separation.     

A Study of REE and Pb,Sr and Nd Isotopes in Garnet—Lherzolite Xenoliths from Mingxi,Fujian Province

The REE and Pb, Sr, Nd isotopes in three xenoliths from limburgite and scoria-breccias, including spinel-lherzolite, spinel-garnet-lherzolite and phlogopite-gamet-lherzolite, were analysed. The REE contents of the xenoliths are 1.3 to 3.3 times those of the chondrites with their REE patterns characterized by weak LREE depletion. The¹⁴³Nd/¹⁴⁴Nd values of whole rocks and minerals range from 0.51306 to 0.51345 with εNd=+ 8.2− +15.8,²⁰⁶Pb/²⁰⁴ Pb < 18.673, and²⁰⁷Pb/²⁰⁴Pb < 15.574. All this goes to show that the upper mantle in Mingxi at the depth of 67–82 km is a depleted mantle of MORB type, with⁸⁷Sr/⁸⁶ Sr ratios 0.70237–0.70390. In Nd-Sr diagram the data points of whole rocks are all out of the mantle array, implying that the xenoliths from Mingxi have more radiogenic Sr isotopes than those of the mantle array.     

Controls on magmatism in an island arc environment: study of lavas and sub-arc xenoliths from the Tabar–Lihir–Tanga–Feni island chain, Papua New Guinea

The Tabar–Lihir–Tanga–Feni (TLTF) islands of Papua New Guinea mainly comprise high-K calc-alkaline and silica undersaturated alkaline rocks that have geochemical features typical for subduction-related magmatism. Numerous sedimentary, mafic, and ultramafic xenoliths recovered from Tubaf seamount, located on the flank of Lihir Island, provide a unique opportunity to study the elemental and isotopic composition of the crust and mantle wedge beneath the arc and to evaluate their relationships to the arc magmatism in the region. The sedimentary and mafic xenoliths show that the crust under the islands is composed of sedimentary sequences and oceanic crust with Pacific affinity. A majority of the ultramafic xenoliths contain features indicating wide spread metasomatism in the mantle wedge under the TLTF arc. Leaching experiments reveal that the metasomatized ultramafic xenoliths contain discrete labile phases that can account for up to 50% or more of elements such as Cu, Zn, Rb, U, Pb, and light REE (rare-earth elements), most likely introduced in the xenoliths via hydrous fluids released from a subducted slab. The leaching experiments demonstrated that the light REE enrichment pattern can be more or less removed from the metasomatized xenoliths and the residual phases exhibit REE patterns that range from flat to light REE depleted. Sr–Nd isotopic data for the ultramafic residues show a coupled behavior of increasing ⁸⁷Sr/⁸⁶Sr with decreasing ¹⁴³Nd/¹⁴⁴Nd ratios. The labile phases in the ultramafic xenoliths, represented by the leachates, show decoupling between Sr and Nd with distinctly more radiogenic ⁸⁷Sr/⁸⁶Sr than the residues. Both leachates and residues exhibit very wide range in their Pb isotopic compositions, indicating the involvement of three components in the mantle wedge under the TLTF islands. Two of the components can be identified as Pacific Oceanic mantle and Pacific sediments. Some of the ultramafic samples and clinopyroxene separates, however, exhibit relatively low ²⁰⁶Pb/²⁰⁴Pb at elevated ²⁰⁷Pb/²⁰⁴Pb suggesting that the third component is either Indian Ocean-type mantle or Australian subcontinental lithospheric mantle. Geochemical data from the ultramafic xenoliths indicate that although the mantle wedge in the area was extensively metasomatized, it did not significantly contribute to the isotopic and incompatible trace element compositions of TLTF lavas. Compared to the mantle samples, the TLTF lavas have very restricted Pb isotopic compositions that lie within the Pacific MORB range, indicating that magma compositions were dominated by melts released from a stalled subducted slab with Pacific MORB affinity. Interaction of slab melts with depleted peridotitic component in the mantle wedge, followed by crystal fractionation most likely generated the geochemical characteristics of the lavas in the area. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Lead sources in Mesozoic and Cenozoic Andean ore deposits,north-central Chile (30–34°S)

Mesozoic and Cenozoic ore deposits in the Chilean Andes between La Serena (~30°S) and Santiago (~34°S) include polymetallic vein, low- and high-sulfidation epithermal vein, skarn, porphyry copper-molybdenum and porphyry copper-gold. These deposits are associated with volcanic and plutonic complexes emplaced in eastward-migrating longitudinal arcs which formed during subduction along the continental margin of South America since the Middle Jurassic. Stratabound, but epigenetic, volcanic rock- and sedimentary rock-hosted manto deposits contain additional copper resources. Lead isotopic compositions in ore minerals from 29 deposits vary with age and geographic location, and hence with basement and host rocks. Lead in most ore deposits is derived from temporally related igneous rocks, except for the manto deposits whose lead is derived from host volcanic and sedimentary rock sequences. Lead in the ore deposits is dominated by two crustal sources. Low ²⁰⁷Pb/²⁰⁴Pb characterizes one source whereas high ²⁰⁷Pb/²⁰⁴Pb characterizes the second source. Lead isotopic compositions of Jurassic and Miocene ore minerals (²⁰⁶Pb/²⁰⁴Pb>18.50; ²⁰⁷Pb/²⁰⁴Pb>15.61) lie along the average crustal growth curve. By contrast, most Cretaceous deposits have ore minerals with lower ²⁰⁶Pb/²⁰⁴Pb (<18.39) and ²⁰⁷Pb/²⁰⁴Pb (<15.58) than Jurassic ore minerals. The shift in lead isotopic composition to lower lead isotopic values precludes derivation of lead from a source of similar composition to those in the Jurassic or Tertiary deposits. For Cretaceous deposits, polymetallic and low-sulfidation epithermal veins and a skarn have lower ²⁰⁶Pb/²⁰⁴Pb than a porphyry copper-gold system and peripheral gold veins at Andacollo (18.43-18.50). Late Cretaceous veins from the Bellavista deposit have the lowest ²⁰⁶Pb/²⁰⁴Pb (18.33) of all deposits. Ore minerals in Miocene and Pliocene porphyry copper-molybdenum deposits have higher ²⁰⁶Pb/²⁰⁴Pb (18.58-18.67) than Cretaceous deposits, consistent with their age being younger. The Miocene and Pliocene ore minerals also have higher ²⁰⁷Pb/²⁰⁴Pb (15.58-15.66) than Cretaceous ore minerals, thereby requiring an additional input from the high-²⁰⁷Pb/²⁰⁴Pb source into the younger deposits. Miocene auriferous deposits in the north have similar ²⁰⁶Pb/²⁰⁴Pb values as the Miocene and Pliocene porphyry copper-molybdenum deposits in the south, but they are distinguished by higher and variable ²⁰⁷Pb/²⁰⁴Pb (15.61-15.66) and ²⁰⁸Pb/²⁰⁴Pb (38.54-39.01), which are arrayed along steep mixing trends. These ore minerals have the largest input of high-²⁰⁷Pb/²⁰⁴Pb material in the deposits studied. By contrast, lead in the epigenetic manto deposits appears to be derived from the host volcanic or sedimentary rock-dominated sequences, and locally exhibits large-scale isotopic heterogeneity within a deposit. Overall, the lead isotopic compositions of ore minerals mimic the values and variations established in age-equivalent rock sequences. The low-²⁰⁷Pb/²⁰⁴Pb material in the deposits is derived from Cretaceous igneous rocks or their sources as they evolved with time; low ²⁰⁷Pb/²⁰⁴Pb characterizes these rocks. By contrast, high-²⁰⁷Pb/²⁰⁴Pb material is likely derived from Carboniferous to Triassic igneous rocks or their sources, as this lead isotopic characteristic dominates these rocks.     

Isotopic systematics of He,Ar, S,Cu, Ni,Re, Os,Pb, U,Sm, Nd,Rb, Sr,Lu, and Hf in the rocks and ores of the Norilsk deposits

This paper reports the first results of a study of 11 isotope systems (³He/⁴He, ⁴⁰Ar/³⁶Ar, ³⁴S/³²S, ⁶⁵Cu/⁶³Cu, ⁶²Ni/⁶⁰Ni, ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd, ^206–208Pb/²⁰⁴Pb, Hf–Nd, U–Pb, and Re–Os) in the rocks and ores of the Cu–Ni–PGE deposits of the Norilsk ore district. Almost all the results were obtained at the Center of Isotopic Research of the Karpinskii All-Russia Research Institute of Geology. The use of a number of independent genetic isotopic signatures and comprehensive isotopic knowledge provided a methodic basis for the interpretation of approximately 5000 isotopic analyses of various elements. The presence of materials from two sources, crust and mantle, was detected in the composition of the rocks and ores. The contribution of the crustal source is especially significant in the paleofluids (gas–liquid microinclusions) of the ore-forming medium. Crustal solutions were probably a transport medium during ore formation. Air argon is dominant in the ores, which indicates a connection between the paleofluids and the atmosphere. This suggests intense groundwater circulation during the crystallization of ore minerals. The age of the rocks and ores of the Norilsk deposits was determined. The stage of orebody formation is restricted to a narrow age interval of 250 ± 10 Ma. An isotopic criterion was proposed for the ore-bearing potential of mafic intrusions in the Norilsk–Taimyr region. It includes several interrelated isotopic ratios of various elements: He, Ar, S, and others.     

The Pb-Sr-Nd isotope geochemistry of some recent circum-Mediterranean granites

Pb, Sr and Nd isotopic compositions have been analyzed in recent granites from Northern Africa, Northern Italy and Greece. Lead isotope compositions of K-feldspars are rather homogeneous, and cluster close to the modern lead of Stacey and Kramers (1975) but with slightly higher²⁰⁷Pb/²⁰⁴Pb and²⁰⁸Pb/²⁰⁴Pb ratios. The Cyclades samples, however, have higher²⁰⁶Pb/²⁰⁴Pb ratios. Addition of mantle-derived lead was probably very limited, which supports a quasi-closed system evolution of this element in the continental crust. The Sr, Nd data fall in the enriched part of the¹⁴³Nd/¹⁴⁴Nd vs.⁸⁷Sr/⁸⁶Sr diagram and define a smooth hyperbolic mixing curve. Over a wide area, straddling different orogens, most granites may be accounted for by a binary mixture between a recycled crustal component and a depleted mantle-like component. No correlation is observed between either Pb and Sr or Nd isotopic ratios, or any isotopic ratio and major element contents. Quantitative modelling suggests that two cases fit the Sr and Nd characteristics of these granites: they both require anatexis of the crust on a scale large enough to average the isotopic properties of heterogeneous terranes. In the first case, the mantle-derived component may be represented by differentiated Island Arc-type magmas, and the granites result from mixing these magmas with anatectic melts. In the second case, mantle-derived igneous rocks, such as obducted ophiolites, are part of the crustal source and their variable involvement in the anatectic process causes isotopic variations.CRPG Contribution n 630.     

Geochemistry of oceanic carbonatites compared with continental carbonatites: mantle recycling of oceanic crustal carbonate

Major and trace element and Sr-Nd-Pb-O-C isotopic compositions are presented for carbonatites from the Cape Verde (Brava, Fogo, Sáo Tiago, Maio and Sáo Vicente) and Canary (Fuerteventura) Islands. Carbonatites show pronounced enrichment in Ba, Th, REE, Sr and Pb in comparison to most silicate volcanic rocks and relative depletion in Ti, Zr, Hf, K and Rb. Calcio (calcitic)-carbonatites have primary (mantle-like) stable isotopic compositions and radiogenic isotopic compositions similar to HIMU-type ocean island basalts. Cape Verde carbonatites, however, have more radiogenic Pb isotope ratios (e.g. ²⁰⁶Pb/²⁰⁴Pb=19.3-20.4) than reported for silicate volcanic rocks from these islands (18.7-19.9; Gerlach et al. 1988; Kokfelt 1998). We interpret calcio-carbonatites to be derived from the melting of recycled carbonated oceanic crust (eclogite) with a recycling age of ~1.6 Ga. Because of the degree of recrystallization, replacement of calcite by secondary dolomite and elevated ‘¹³C and ‘¹⁸O, the major and trace element compositions of the magnesio (dolomitic)-carbonatites are likely to reflect secondary processes. Compared with Cape Verde calcio-carbonatites, the less radiogenic Nd and Pb isotopic ratios and the negative Ɨ/4 of the magnesio-carbonatites (also observed in silicate volcanic rocks from the Canary and Cape Verde Islands) cannot be explained through secondary processes or through the assimilation of Cape Verde crust. These isotopic characteristics require the involvement of a mantle component that has thus far only been found in the Smoky Butte lamproites from Montana, which are believed to be derived from subcontinental lithospheric sources. Continental carbonatites show much greater variation in radiogenic isotopic composition than oceanic carbonatites, requiring a HIMU-like component similar to that observed in the oceanic carbonatites and enriched components. We interpret the enriched components to be Phanerozoic through Proterozoic marine carbonate (e.g. limestone) recycled through shallow, subcontinental-lithospheric-mantle and deep, lower-mantle sources.     

Strontium and Lead Isotopic Study of the Carbonate‐hosted Xujiashan Antimony Deposit from Hubei Province,South China: Implications for its Origin

The Xujiashan antimony deposit is hosted by marine carbonates of the Upper Sinian Doushantuo and Dengying Formations in Hubei Province, South China. Our Sr isotopic data from pre‐ and syn‐mineralization calcites that host the mineralization show that the pre‐mineralization calcite displays a narrow range of ⁸⁷Sr/⁸⁶Sr ratios (0.7096 to 0.7097), similar to the ratios of the Sinian seawater, and high Sr concentrations (2645 to 8174 ppm). In contrast, the syn‐mineralization calcite exhibits low Sr concentrations (785 to 2563 ppm) and high ⁸⁷Sr/⁸⁶Sr ratios (0.7109 to 0.7154), which is interpreted as the result of addition of radiogenic strontium during the antimony mineralization. The study of Sr isotopes suggests that their Sr component to the pre‐mineralization calcite derived directly from the host rocks (i.e. the Sinian marine carbonates), while radiogenic ⁸⁷Sr for the syn‐mineralization calcite derived from the underlying Mesoproterozoic Lengjiaxi Group basement through hydrothermal fluid circulation along the major fault that hosts the mineralization. The Pb isotopic ratios of stibnite are subdivided into two groups (Group A and Group B), Group A is characterized by higher radiogenic lead, with ²⁰⁶Pb/²⁰⁴Pb = 18.874 to 19.288, ²⁰⁷Pb/²⁰⁴Pb = 15.708 to 15.805, and ²⁰⁸Pb/²⁰⁴Pb = 38.642 to 39.001. Group B shows lower lead isotope ratios (²⁰⁶Pb/²⁰⁴Pb = 17.882 to 18.171, ²⁰⁷Pb/²⁰⁴Pb = 15.555 to 15.686, and ²⁰⁸Pb/²⁰⁴Pb = 37.950 to 38.340). The single‐stage model ages of Group A are mainly negative or slightly positive values (‐258 to 3 Ma), while those of Group B range from 636 to 392 Ma, with an average of 495 ± 65 Ma. In addition, there are positive linear correlations among Pb isotopic ratios. These results suggest that the lead of Group A stibnite was mainly derived from the Sinian marine carbonates, and that of Group B stibnite from the underlying Lengjiaxi Group basement. This conclusion is consistent with the results of the Sr isotopes. These results indicate that the Xujiashan deposit is not syngenetic sedimentary and in situ reworked origin as previously considered. The metal (mainly Sb) of this deposit was not only derived from the Sinian host rocks, but also partly derived from the underlying Mesoproterozoic Lengjiaxi Group basement.     

Mechanisms for anhydrite and gypsum formation in the Kuroko massive sulfide–sulfate deposits,north Japan

The Sr, Ba, and rare earth elements (REEs) concentrations and Sr isotopic composition of anhydrite and gypsum have been determined for samples from the Matsumine, Shakanai, and Hanaoka Kuroko-type massive sulfide–sulfate deposits of northern Japan to evaluate the mechanisms of sekko (anhydrite and gypsum) ore formation. The Sr isotopic compositions of the samples fall in the range of 0.7077–0.7087, intermediate between that for middle Miocene (13–15 Ma) seawater (0.7088) (Peterman et al., Geochim Cosmochim Acta, 34:105–120, 1970) and that for country rocks (e.g., 0.7030–0.7050) (Shuto, Assn Geol Collab Japan Monograph 18:91–105, 1974). The Kuroko anhydrite samples exhibit two types of chondrite-normalized REE patterns: one with a decrease from light REEs (LREEs) to heavy REEs (HREEs) (type I), and another with a LREE-depleted pattern (type II). Based on the Sr content and isotopic ratio (assuming an Sr/Ca (mM/M) of 8.7 for seawater), anhydrite is considered to have formed by mixing of preheated seawater with a hydrothermal solution of Sr/Ca (mM/M) = ca. 0.59–1.36 under the condition in which the partition coefficient (Kd) ranges between ca. 0.5 and 0.7. This results in the formation of anhydrite with higher Sr content with an Sr isotopic value close to that of seawater under seawater-dominant conditions. Larger crystals of type II anhydrite are partly replaced by smaller ones, indicating that anhydrite dissolution and recrystallization occurred after or during the formation of sekko ore. Gypsum, which partially replaces anhydrite in the Kuroko deposits, also exhibits two distinct chondrite-normalized REE patterns. Because LREEs are likely to be more readily mobilized during dissolution and recrystallization, it is hypothesized that LREEs are leached from type I anhydrite, resulting in the formation of type II anhydrite with LREE-depleted profiles.     

Temporal variation of isotope and rare earth element abundances in volcanic rocks from Guam: implications for the evolution of the Mariana Arc

Volcanic rocks exposed on Guam were erupted during the Late Middle Eocene (Facpi Fm.), Late Eocene-Oligocene (Alutom Fm.) and Miocene (Umatac Fm.). Four magma series are recognized: the boninite series (44 m.y.b.p.), the tholeiite and calc-alkaline series, which were erupted along with boninite series lavas at 32–36 m.y.b.p. and high-K lavas of the Umatac Fm. (14 m.y.b.p.). Isotope and and rare earth element (REE) characteristics of the four magma series are distinct. Boninite series lavas have U-shaped REE patterns, relatively low ¹⁴³Nd/¹⁴⁴Nd (0.51294–0.51298), and high ²⁰⁶Pb/²⁰⁴Pb (19.0–19.2). Tholeiite series lavas are LREE (light REE) depleted, and have high ¹⁴³Nd/¹⁴⁴Nd (0.51304–0.51306) and low ²⁰⁶Pb/²⁰⁴Pb (18.4–18.5). Calc-alkaline series lavas have Sr, Nd and Pb isotope ratios similar to tholeiite series lavas, but flat to U-shaped REE patterns. Umatac Fm. lavas are strongly LREE-enriched, and have higher ⁸⁷Sr/ ⁸⁶Sr (0.70375–0.70380) and ²⁰⁷Pb/²⁰⁴Pb relative to ²⁰⁶Pb/ ²⁰⁴Pb than Facpi and Alutom Fm. lavas. Boninite and tholeiite series magmas, erupted in the position of the Palau-Kyushu Ridge, were probably derived from distinct mantle sources having OIB and N-MORB-like isotopic characteristics, together with fluids derived from subducted Pacific plate basalt. Calc-alkaline series lavas were most likely derived from the tholeiite series by extensive crystal fractionation, wallrock contamination and magma mixing. Lavas of the Umatac Fm., erupted in the position of the West Mariana Ridge, may include up to 2–3% subducted sediment, similar to some active Mariana arc lavas.     

Lead Isotopic Composition and Lead Source of the Huogeqi Cu-Pb-Zn Deposit, Inner Mongolia, China

The Huogeqi orefield located on the northern side of Mt. Langshan, Inner Mongolia occurs in the Middle Proterozoic Langshan Group metamorphic rocks, and the orebodies arc stratiform. In the past twenty years, many Chinese geologists have conducted researches on the Huogeqi Cu-Pb-Zn deposit, but there has been still a controversy on its origin. Some advocate that the deposit is of sedimentary-metamorphic rcworking origin, some hold that it is of sea-floor SEDEX origin, and others have a preference for magmatic superimposition origin. The crux of the controversy is that there is no common understanding about the source of ore-forming materials. In this paper, the Pb isotopic compositions of regional Achaean-Early Proterozoic basement rocks, various types of sedimentary- metamorphic rocks and volcanic rocks in the mining district, Late Proterozoic and Hercynian magmatic rocks arc introduced and compared with the orc-lead composition, so as to constrain the source of the ore lead. The result indicates that （1） sulfides in the ores have homogeneous Pb isotopic compositions, showing a narrow variation range. Their ^206pb/^204pb ratios arc within a range of 17.027- 17.317; ^207Pb/^204pb ratios, 15.451-15.786 and ^208Pb/^204pb ratios, 36.747-37.669; （2） the Pb isotopic compositions of the regional Achaean-Early Proterozoic basement rocks arc characteristic of the old Pb isotopic composition at the early-stage evolution of the Earth, which varies over a wider range, reflecting significant differences in Pb isotopic compositions of the ores. All this indicates that the source of ore lead has no bearing on the basement rocks; （3） the sedimentary-metamorphic rocks in the mining district arc characterized by highly variable and more radiogenic Pb isotopic compositions and their Pb isotopic ratios arc obviously higher than those of ores, demonstrating that ore lead did not result from metamorphic rcworking of these rocks; （4） Pb isotopic compositions of Late Proterozoic diorite-gabbro and Hercynian granite are higher than those of ores. Meanwhile, the Pb isotopic compositions of sulfides in the small-sized strata-penetrating mineralized veinlets formed at later stages arc completely consistent with that of sulfides in stratiform-banded ores, suggesting that these veiniets arc the product of autochthonous rcworking of the stratiform-banded ores during the period of metamorphism and the late magmatic superimposition-mineralization can be excluded; （5） amphibolite, whose protolith is basic volcanic rocks, has the same Pb isotopic compositions as ores, implying that ore lead was derived probably from basic volcanism. So, the source of ore-forming materials for the Huogeqi deposit is like that of the volcanic massive sulfide （VMS） deposits. However, the orebodies do not occur directly within the volcanic rocks, and instead they overlie the volcanic rocks, showing some differences from those typical VMS-type deposits.