The Sr isotopic characterization and Pb-Pb age of carbonate rocks from the Satka formation,the Lower Riphean Burzyan Group of the southern Urals

The Rb-Sr and U-Pb systematics are studied in carbonate deposits of the Satka and Suran formations corresponding to middle horizons of the Lower Riphean Burzyan Group in the Taratash and Yamantau anticlinoria, respectively, the southern Urals. The least altered rock samples retaining the ⁸⁷Sr/⁸⁶Sr ratio of sedimentation basin have been selected for analysis using the original method of leaching the secondary carbonate phases and based on strict geochemical criteria of the retentivity (Mn/Sr < 0.2, Fe/Sr < 5 and Mg/Ca < 0.024). The stepwise dissolution in 0.5 N HBr has been used to enrich samples in the primary carbonate phase before the Pb-Pb dating. Three (L-4 to L-6) of seven consecutive carbonate fractions obtained by the step-wise leaching are most enriched in the primary carbonate (in terms of the U-Pb systematics). In the ²⁰⁶Pb/²⁰⁴Pb-²⁰⁷Pb/²⁰⁴Pb diagram, data points of these fractions plot along an isochron determining age of 1550 ± 30 Ma (MSWD = 0.7) for the upper member of the Satka Formation. The initial ⁸⁷Sr/⁸⁶Sr ratio in the least altered limestones of this formation is within the range of 0.70460–0.70480. Generalization of the Sr isotopic data published for the Riphean carbonates from different continents showed that 1650–1350 Ma ago the ⁸⁷Sr/⁸⁶Sr ratio in the world ocean was low, slightly ranging from 0.70456 to 0.70494 and suggesting the prevalent impact of mantle flux.     

内蒙古道伦达坝铜钨锡矿床LA-ICP-MS锆石和锡石U-Pb年龄及其地质意义

道伦达坝矿床位于大兴安岭南段,是一个铜钨锡矿床,其铜、钨、锡储量均达中型。矿体呈脉状,主要产于二叠系砂板岩中的断裂破碎带中,华力西期黑云母花岗岩中的断裂破碎带中亦赋存有矿体。文章选取2件石英-萤石-白云母-电气石-锡石-黑钨矿阶段的矿石样品对其中的进行了LA-ICP-MS U-Pb定年,获得2件样品的~(207)Pb/~(206)Pb-~(238)U/~(206)Pb谐和年龄分别为(134.7±6.6)Ma(MSWD=1.4)和(136.8±7.4)Ma(MSWD=1.7),~(206)Pb/~(207)Pb-~(238)U/~(207)Pb等时线年龄分别为(132±12)Ma(MSWD=0.76)和(135±13)Ma(MSWD=0.9)。锡石定年结果表明,道伦达坝矿床形成于早白垩世。对矿区外围张家营子岩体中的斑状细粒花岗岩进行了LA-ICP-MS锆石U-Pb测年,获得的~(206)Pb/~(238)U加权平均年龄为(135±1)Ma(MSWD=1.3),该岩体的形成年龄与道伦达坝矿床的成矿年龄在误差范围内一致。本次定年结果表明道伦达坝矿床形成于早白垩世,与同期的花岗质岩浆活动有密切的成因联系,该矿床属于与花岗岩有关的岩浆热液脉型矿床。     

U-Pb age and Sr-chemostratigraphy of limestone from the Sorna Formation,Azyr-Tal Range,Kuznetsk Alatau

The U-Pb(Pb-Pb) age was determined for limestone from member III of the Sorna Formation out- cropped on the Azyr-Tal Range, Kuznetsk Alatau. The weighted average value from three calculated values is 523 ± 5 Ma (MSWD = 0.02, 2σ). This age coincides with the Early Cambrian age interval determined with Sr isotopic chemostratigraphy (⁸⁷Sr/⁸⁶Sr ratio is 0.70850–0.70852). The low value of μ₂ = ²³⁸U/²⁰⁴Pb for limestone is due to the evolution of diagenetic fluid containing lead from the mantle reservoir into the Sorna sediments.     

Uranium-lead isotope systematics of Mars inferred from the basaltic shergottite QUE 94201

Uranium-lead ratios (commonly represented as ²³⁸U/²⁰⁴Pb = μ) calculated for the sources of martian basalts preserve a record of petrogenetic processes that were active during early planetary differentiation and formation of martian geochemical reservoirs. To better define the range of μ values represented by the source regions of martian basalts, we completed U-Pb elemental and isotopic analyses on whole rock, mineral and leachate fractions from the martian meteorite Queen Alexandra Range 94201 (QUE 94201). The whole rock and silicate mineral fractions have unradiogenic Pb isotopic compositions that define a narrow range (²⁰⁶Pb/²⁰⁴Pb = 11.16-11.61). In contrast, the Pb isotopic compositions of weak HCl leachates are more variable and radiogenic. The intersection of the QUE 94201 data array with terrestrial Pb in ²⁰⁶Pb/²⁰⁴Pb-²⁰⁷Pb/²⁰⁴Pb-²⁰⁸Pb/²⁰⁴Pb compositional space is consistent with varying amounts of terrestrial contamination in these fractions. We calculate that only 1-7% contamination is present in the purified silicate mineral and whole rock fractions, whereas the HCl leachates contain up to 86% terrestrial Pb. This terrestrial Pb contamination generated a ²⁰⁶Pb-²⁰⁷Pb array in the QUE fractions that appears to represent an ancient age, which contrasts with a much younger crystallization age of 327 ± 10 Ma derived from Rb-Sr and Sm-Nd isochrons (Borg L. E., Nyquist L. E., Taylor L. A., Wiesmann H. and Shih C. -Y. (1997) Constraints on Martian differentiation processes from Rb-Sr and Sm-Nd isotopic analyses of the basaltic shergottite QUE 94201. Geochim. Cosmochim. Acta61, 4915-4931). Despite the contamination, and accepting 327 ± 10 Ma as the crystallization age, we use the U-Pb data to determine the initial ²⁰⁶Pb/²⁰⁴Pb of QUE 94201 to be 11.086 ± 0.008 and to calculate the μ value of its mantle source to be 1.82 ± 0.01. The μ value calculated for the QUE 94201 source is the lowest determined for any martian basalt source, and, when compared to the highest values determined for martian basalt sources, indicates that μ values in martian source reservoirs vary by at least a factor of two. Additionally, the range of source μ values indicates that the μ value of bulk silicate Mars is approximately three. The amount of variation in the μ values of the mantle sources (μ ∼ 2-4) is greater than can be explained by igneous processes involving silicate phases alone. We suggest the possibility that a small amount of sulfide crystallization may generate greater extents of U-Pb fractionation during formation of the mantle sources of martian basalts.     

Direct dating of hydrothermal W mineralization: U-Pb age for hübnerite (MnWO4), Sweet Home Mine, Colorado

We have investigated the potential of hübnerite for U-Pb dating. Hübnerite forms typically at medium to low-temperatures in a wide range of pneumatolytic-hydrothermal mineral deposits, particularly porphyry molybdenum and Sn-specialized granites. Hübnerite from the Sweet Home Mine (Alma, Colorado) formed in a Pb-rich, U-poor environment, but still developed relatively radiogenic Pb isotopic compositions. The low Pb_common contents in hübnerite (0.075 to 0.155 ppm) demonstrate that Pb is efficiently excluded from the crystal lattice. In contrast, U may substitute for Mn. The U-Pb data of hübnerite scatter. Most of the scatter originates from samples with ²⁰⁶Pb/²⁰⁴Pb values below 50, where Pb_blank contributes up to 30% to Pb_total. Using the least radiogenic galena Pb, samples with ²⁰⁶Pb/²⁰⁴Pb values above 70 have overlapping ²⁰⁶Pb∗/²³⁸U and ²⁰⁷Pb∗/²³⁵U values and yield a ²⁰⁶Pb/²³⁸U age of 25.7 ± 0.3 Ma (2σ). Late stage apatite from the Sweet Home Mine yields a ²⁰⁶Pb/²⁰⁴Pb-²³⁸U/²⁰⁴Pb isochron corresponding to an age of 24.8 ± 0.5 Ma (2σ). A comparison of the U-Pb hübnerite ages with literature ⁴⁰Ar/³⁹Ar ages on earlier sericite and the U-Pb age on later apatite suggests that (i) hübnerite yields accurate U-Pb ages and (ii) the evolution of the Sweet Home mineralization from greisen-type mineralization to medium-temperature hydrothermal vein mineralization took place in a few hundred thousand years at most. Aqueous low-N₂-bearing and aqueous inclusions in the dated hübnerite have homogenization temperatures between 325 and 356 °C and moderate salinity (up to 6.7 wt% NaCl equiv.). Thus, hübnerite represents one of the rare examples of a mineral that can be dated accurately and carries petrological information.     

都龙锡锌多金属矿床LA-MC-ICPMS锡石U-Pb测年及其意义

云南都龙锡锌多金属矿床是我国最大的锡石硫化物矿床之一。缺乏精确可靠的成矿年代学判据,是该矿床成因认识存在较大分歧的重要原因之一,严重制约了地质勘探工作的深入。本文应用LA-MC-ICP-MS微区原位U-Pb同位素测年技术,对都龙矿区曼家寨矿段的锡石样品进行了研究,获得DL12-716、DL12-722、DL12-740等三件样品的206Pb/207Pb-238U/207Pb等时线年龄分别为89.2±4.1Ma(N=22,MSWD=4.5)、88.0±1.6Ma(N=24,MSWD=2.3)和87.2±3.9Ma(N=31,MSWD=14),207Pb/206Pb-238U/206Pb谐和年龄分别为96.6±3.5Ma(MSWD=8.1)、93.6±1.6Ma(MSWD=5.8)和82.0±2.5Ma(MSWD=11)。结合矿床地质特征和前人成岩-成矿年代学成果,表明都龙矿区锡成矿作用主要发生在晚白垩纪,与燕山晚期岩浆热液活动关系密切,结合地质事实,表明燕山晚期岩浆热液活动是老君山矿集区锡钨多金属成矿的关键。通过区域地质及年代学对比,表明滇东南地区晚白垩世存在大规模花岗岩成岩-锡成矿事件。     

Geochemistry of Neogene magmatism at Spitsbergen Island

Petrological and geochemical data obtained on Neogene magmatism restricted to a deep fault in Andree Land at Spitsbergen Island, which was related to the overall restyling of the Arctic territory at 25–20 Ma, indicate that the derivation of the Neogene magmas was significantly affected by the continental pyroxenite mantle. The Neogene basalts are noted for a radiogenic isotopic composition of Pb (²⁰⁷Pb/²⁰⁴Pb= 15.5–15.55, ²⁰⁶Pb/²⁰⁴Pb = 18.4–18.6, ²⁰⁸Pb/²⁰⁴ Pb = 38.4–38.6) and Sr(⁸⁷Sr/⁸⁶Sr = 0.7038–0.7048) at low ¹⁴³Nd/¹⁴⁴Nd = 0.5129. Melts of this type are the extremely enriched end member of the isotopic mixing of a depleted and enriched sources and determine a geochemical trend that passes through the compositions of alkaline magmas from Quaternary volcanoes at Spitsbergen and weakly enriched tholeiites of the Knipovich Ridge, which started to develop simultaneously with the onset of Neogene magmatism in the western part of Spitsbergen. The composition of the liquidus olivine (which is rich in NiO) indicates that melting occurred in the olivine-free mantle. Our data thus testify that a significant role in the genesis of the Neogene magmas was played by continental pyroxenite mantle.     

Geochemistry of lamprophyres from the Western Alps,Italy: implications for the origin of an enriched isotopic component in the Italian mantle

Cenozoic lamprophyres (minettes, spessartites, kersantite) from the Western Alps, northern Italy, represent small volume, mafic melts with high Mg#s and high Ni and Cr contents. All the lamprophyres show light REE enrichment, high incompatible element contents, and Ta, Ti and Nb troughs on chondrite-normalized diagrams. Age-corrected ⁸⁷Sr/⁸⁶Sr isotopic ratios (assuming t = 30 Ma) are highly variable and range from 0.70590 to 0.71884; ¹⁴³Nd/¹⁴⁴Nd ratios range from 0.51203 to 0.51242. Pb isotopic ratios are: ²⁰⁶Pb/²⁰⁴Pb = 18.669–18.895, ²⁰⁷Pb/²⁰⁴Pb = 15.605–15.689 and ²⁰⁸Pb/²⁰⁴Pb = 38.224–39.134. ⁸⁷Sr/⁸⁶Sr ratios show a negative correlation with ¹⁴³Nd/¹⁴⁴Nd, and a positive correlation with K, Ba, and Rb as well as with Ti, Th, Ta, Nb and Zr abundances. The primitive nature of the lamprophyres, coupled with their enriched incompatible trace element and isotopic signatures, suggest derivation from a metasomatized upper mantle source. Linear arrays in isotope space and elemental data plots suggest mixing between two distinct end-members in the Italian mantle; an enriched end-member that is isotopically similar to pelagic sediments, and a significantly less enriched end-member that approaches Bulk Earth values. New isotopic data indicate that the mantle source(s) of the lamprophyres from the Western Alps contain a very high proportion of the enriched end-member. The geochemical signature of the enriched end-member is attributed to fluids or melts derived from pelagic sediments subducted during the closure of the Tethyan Ocean in the late Cretaceous to early Tertiary.     

Pb-Pb age and Sr isotopic characteristic of the Middle Riphean phosphorite concretions: The Zigaza-Komarovo Formation of the South Urals

The Pb-Pb age of phosphorite concretions of the Zigaza-Komarovo Formation, which composes the intermediate horizons of the Riphean stratotype of the South Urals, was determined in fractions resulting from the stepwise dissolution of concretions in 0.1 N, 0.5 N, and 1 N HCl. The determination of the Sr isotopic composition in phosphate fractions was favorable for rejection the fractions polluted with extraneous material. On the ²⁰⁷Pb/²⁰⁴Pb-²⁰⁶Pb/²⁰⁴Pb diagram, the isochron based on 31 points corresponds to 1330 ± 20 Ma (MSWD = 1.12), which is in agreement with the stratigraphic position of the Zigaza-Komarovo Formation. The decreased μ₂ value of 9.57 for the phosphorite concretions relative to that of the average earthly lead based on the Stacey-Kramers model (9.74) is related to the rocks with an admixture of mantle lead, which occur in the run-off area of the Zigaza-Komarovo sediments.     

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.     

Nd, Pb, and Sr isotope composition of juvenile magmatism in the Mesozoic large magmatic province of northern Chile (18–27°S): indications for a uniform subarc mantle

The Jurassic to Early Cretaceous magmatic arc of the Andes in northern Chile was a site of major additions of juvenile magmas from the subarc mantle to the continental crust. The combined effect of extension and a near stationary position of the Jurassic to lower Cretaceous arc favoured the emplacement and preservation of juvenile magmatic rocks on a large vertical and horizontal scale. Chemical and Sr, Nd, and Pb isotopic compositions of mainly mafic to intermediate volcanic and intrusive rock units coherently indicate the generation of the magmas in a subduction regime and the dominance of a depleted subarc mantle source over contributions of the ambient Palaeozoic crust. The isotopic composition of the Jurassic (²⁰⁶Pb/²⁰⁴Pb: ∼ 18.2; ²⁰⁷Pb/²⁰⁴Pb: ∼ 15.55; ¹⁴³Nd/¹⁴⁴Nd: ∼ 0.51277; ⁸⁷Sr/⁸⁶Sr: ∼ 0.703–0.704) and Present (²⁰⁶Pb/²⁰⁴Pb: ∼ 18.5; ²⁰⁷Pb/²⁰⁴Pb: ∼ 15.57; 143Nd/144Nd: ∼ 0.51288; ⁸⁷Sr/⁸⁶Sr: ∼ 0.703–0.704) depleted subarc mantle beneath the Central and Southern Andes (18°–40°S) was likely uniform over the entire region. Small differences of isotope ratios between Jurassic and Cenozoic to Recent of subarc mantle-derived could be explained by radiogenic growth in a still uniform mantle source.Electronic Supplementary Material Supplementary material is available to authorised users in the online version of this article at .     

A Pb isotope investigation of the Guli massif, Maymecha-Kotuy alkaline-ultramafic complex, Siberian flood basalt province, Polar Siberia

Summary Covering a vast area of the northern Siberian platform are the Siberian flood basalts (SFB), which make up one of the world’s largest magmatic provinces. Along the northeastern margin of the SFB province lies the Maymecha-Kotuy alkaline-ultramafic complex, consisting of a large volume of alkaline lavas, numerous dykes, and the Guli massif together with numerous other, smaller alkaline plutons. The genetic link between the SFB and the Maymecha-Kotuy complex continues to be a subject of active debate. Although the rocks in both units have essentially the same age close to the Permian-Triassic boundary, questions remain as to the relative order of emplacement and the contributing source materials of each lithology. This study builds upon earlier petrologic, geochemical, and isotopic work to further an understanding of the relationship between SFB and alkaline rocks. A whole-rock U-Pb age of 250 ± 9 Ma was determined for the Guli massif, which lies within the range of ages previously reported for the SFB. The Pb isotopic composition of the Guli rocks plot mainly in the lower portion of the OIB field, and dunite and carbonatite extend downward into the MORB field suggesting for them a more depleted source than the one that produced the SFB. The combined Pb, Sr, and Nd isotopic systematics of the SFB and the Guli alkaline rocks enable the identification of several discrete source components. The first component dominates many of the Guli rocks and is characterized by low ⁸⁷Sr/⁸⁶Sr (0.7031 to 0.7038), high ε_Nd (+5.35 to +3.97), and relatively unradiogenic Pb (²⁰⁶Pb/²⁰⁴Pb = 17.88–18.31; ²⁰⁷Pb/²⁰⁴Pb = 15.38–15.46; ²⁰⁸Pb/²⁰⁴Pb = 37.33–37.70), which we associate with the depleted (MORB source) mantle. The second component representing most of the SFB demonstrates a notable chemical and isotopic uniformity with ⁸⁷Sr/⁸⁶Sr values of 0.7046 to 0.7052, ε_Nd values of 0 to +2.5, and an average Pb isotopic composition of ²⁰⁶Pb/²⁰⁴Pb = 18.3, ²⁰⁷Pb/²⁰⁴Pb = 15.5, and ²⁰⁸Pb/²⁰⁴Pb = 38.0. This component, making up the majority of SFB, is speculated to be a relatively primitive lower mantle plume with a near-chondritic signature. Contamination by upper and lower continental crustal material, designated as components 3 and 4, is postulated to explain the isotopic characteristics of some of the higher SiO₂ Guli rocks and SFB. Finally, metasomatic processes associated with the invasion of the Siberian super-plume add a fifth component responsible for the extreme enrichment in rare-earth and related elements found in some Guli rocks and SFB.     

Pb-Pb age of sedimentary phosphorite reworking in Lower Riphean carbonate sediments,the Satka Formation of Southern Urals

The mineral composition and U-Pb and Rb-Sr systematics of phosphorites from the Satka Formation of Lower Riphean carbonates, the Burzyan Group of Southern Urals, are studied. Phosphorites occurring as small lenses between stromatolite layers are composed largely of fluorapatite with admixture of detrital quartz, feldspars, illite, and chlorite. Phosphorite samples have been subjected to stepwise dissolution in 1 N (fraction L-1) and 2 N (fraction L-2) HCl. As is established, the maximum apatite content is characteristic of fraction L-1, while fraction L-2 is enriched in products of dolomite and sulfide dissolution and in elements leached from siliciclastic components. The Sr content in the Satka apatites (280–560 ppm) is substantially lower as compared with that in unaltered marine apatite. The ⁸⁷Sr/⁸⁶Sr “initial ratio in the phosphorites studied (0.71705–0.72484) and host dolomites from the lower part of the Satka Formation is significantly higher than in the Early Riphean seawater that indicates a reset of the Rb-Sr original systems in sediments. The Pb-Pb age of 1340 ± 30 Ma (MSWD = 6.4) estimated based on 7 data points characterizing fractions L-1 and L-2 is younger than the formation time of overlying Burzyan sediments, being consistent, within the error range, with date of the Mashak rifting event recorded at the Early-Middle Riphean boundary. The comparative U-Pb characteristics of two soluble fractions (L-1 and L-2) and silicate residue of phosphorites show that epigenetic redistribution of Pb and U was characteristic of the phosphorite horizon only. The initial Pb isotope composition and μ (²³⁸U/²⁰⁴Pb) estimated according to model by Stacey and Kramers for the early diagenetic fluids in carbonate and phosphate sediments of the Satka Formation suggest that they were in isotopic equilibrium with erosion products of the Taratash crystalline complex.     

Origin of the absarokite–banakite association of the Damavand volcano (Iran): trace elements and Sr,Nd, Pb isotope constraints

The activity of the Damavand volcano (Central Alborz, northern Iran) began 1.8 Ma ago and continued up to 7 ka BP. Although the volcanic suite is clearly of shoshonitic affinity, only two petrographic types can be distinguished in the studied lavas: (1) weakly differentiated absarokites (49 < %SiO₂ < 51), scattered around the volcano but with a regional extension, (2) highly differentiated banakites (59 < %SiO₂ < 63), which form the bulk of the 4,000 m thick volcanic pile. All lavas are alkalic (3.7 < %K₂O < 5), REE and LILE-rich (e.g., 85 < La < 148 ppm; 9 < Th < 32 ppm) and show highly fractionated REE patterns (69 < La/Yb < 115) and pronounced Nb–Ta negative anomalies. The absarokites are characterised by Sr (0.7045–0.7046) and Nd (0.51266–0.51269) isotope compositions close to the Bulk Earth values, and distinct from those of the banakites (0.7047 < ⁸⁷Sr/⁸⁶Sr < 0.7049, 0.51258 < ¹⁴³Nd/¹⁴⁴Nd < 0.51262). The Pb isotope ratios are also slightly lower in the absarokites than in the banakites (18.71 < ²⁰⁶Pb/²⁰⁴Pb < 18.77, 15.62 < ²⁰⁷Pb/²⁰⁴Pb < 15.63, 38.85 < ²⁰⁸Pb/²⁰⁴Pb < 38.91, and 18.77 < ²⁰⁶Pb/²⁰⁴Pb < 18.84, 15.62 < ²⁰⁷Pb/²⁰⁴Pb < 15.64, 38.94 < ²⁰⁸Pb/²⁰⁴Pb < 39.06, respectively). Overall, there is a clear tendency towards higher Sr, Pb and lower Nd isotope ratios with increasing degree of differentiation. This study suggests that the absarokites result from a low degree of partial melting (∼5%) of a highly metasomatized mantle source, which inherited its characteristics from an old subduction setting. The initiation of volcanic activity 1.8 Ma ago results from variations in the lithospheric thermal regime, probably related to lithospheric delamination as proposed for Anatolia (Pearce et al. 1990). The banakites are mainly generated by extensive fractional crystallisation (∼70%) of the absarokitic magma, with a limited amount (a few percents) of assimilation of an old crustal component, in the form of bulk assimilation or AFC processes, which both can explain the Sr, Nd and Pb isotope data.     

Pb and Sr isotope and geochemical data from the Pb–Zn deposit Bleiberg (Austria): constraints on the age of mineralization

Summary The timing of Zn–Pb mineralization hosted by early dolomitized lagoonal limestones (Crest facies) at Bleiberg (Carinthia, Austria) has been constrained using Sr-isotopes. This late stage Zn–Pb mineralization is a special feature of the Bleiberg deposit. Samples of the mineralized Crest facies are characterized by higher concentrations of minor and trace elements (except Ba and Sr) compared to samples from the weakly mineralized Wetterstein limestone of the lagoonal facies. The samples from the Crest facies indicate that a fluid with a minimum ⁸⁷Sr/⁸⁶Sr ratio of 0.7083 reacted at 210±30 Ma with carbonate rocks having ⁸⁷Sr/⁸⁶Sr ratios of approximately 0.7077 during a late stage of ore formation. The ⁸⁷Sr/⁸⁶Sr ratios correlate with the Mn and Cl concentrations. Lead isotope data of whole rock samples of Bleiberg yielded an isochron age of 180±40 Ma. They furthermore confirm the presence of two types of common lead; an isotopically distinct ore lead component is present within and close to the ore bodies. The other common Pb component is present in host rocks and in gangue minerals and is distinguished from the ore lead by lower ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios. The Sr and the Pb ages are consistent with geological evidence indicating a Triassic age of Pb–Zn mineralization and support genetic models emphasizing the role of bacteriogenic sulfate reduction at low temperatures prior to subsidence and burial. Elevated ⁸⁷Sr/⁸⁶Sr values (>0.7080) of gangue minerals indicate an epigenetic origin of strontium. Our results are consistent with a genetic model postulating formation of the ore-bearing hydrothermal fluids “at depth” where they leached lead from pre-Upper Carboniferous basement rocks.     

U-Pb garnet chronometry in high-grade rocks—case studies from the central Damara orogen (Namibia) and implications for the interpretation of Sm-Nd garnet ages and the role of high U-Th inclusions

Garnets from different migmatites and granites from the Damara orogen (Namibia) were dated with the U-Pb technique after bulk dissolution of the material. Measured ²⁰⁶Pb/²⁰⁴Pb ratios are highly variable and range from ca. 21 to 613. Variations in isotope (²⁰⁸Pb/²⁰⁴Pb, ²⁰⁶Pb/²⁰⁴Pb) and trace element (Th/U, U/Nd, Sm/Nd) ratios of the different garnets show that some garnets contain significant amounts of monazite and zircon inclusions. Due to their very low ²⁰⁶Pb/²⁰⁴Pb ratios, garnets from pelitic migmatites from the Khan area yield Pb-Pb ages with large errors precluding a detailed evaluation. However, the ²⁰⁷Pb/²⁰⁶Pb ages (ca. 550–500 Ma) appear to be similar to or older than U-Pb monazite ages (530±1–517±1 Ma) and Sm-Nd garnet ages (523±4–512±3 Ma) from the same sample. It is reasonable to assume that the Pb-Pb garnet ages define growth ages because previous studies are consistent with a higher closure temperature for the U-Pb system in garnet relative to the U-Pb system in monazite and the Sm-Nd system in garnet. For igneous migmatites from Oetmoed, Pb-Pb garnet ages (483±15–492±16 Ma) and one Sm-Nd garnet whole rock age (487±8 Ma) are similar whereas the monazite from the same sample is ca. 30–40 Ma older (528±1 Ma). These monazite ages are, however, similar to monazite ages from nearby unmigmatized granite samples and constrain precisely the intrusion of the precursor granite in this area. Although there is a notable difference in closure temperature for the U-Pb and Sm-Nd system in garnet, the similarity of both ages indicate that both garnet ages record garnet growth in a migmatitic environment. Restitic garnet from an unmigmatized granite from Omaruru yields similar U-Pb (493±30–506±30 Ma) and Sm-Nd (493±6–488±7 Ma) garnet ages whereas the monazite from this rock is ca. 15–25 Ma older (516±1–514±1 Ma). Whereas the monazite ages define probably the peak of regional metamorphism in the source of the granite, the garnet ages may indicate the time of melt extraction. For igneous garnets from granites at Oetmoed, the similarity between Pb-Pb (483±34–474±17 Ma) and Sm-Nd (492±5–484±13 Ma) garnet ages is consistent with fast cooling rates of granitic dykes in the lower crust. Differences between garnet and monazite U-Pb ages can be explained by different reactions that produced these minerals at different times and by the empirical observation that monazite seems resistant to later thermal re-equilibration in the temperature range between 750 and 900 °C (e.g. Braun et al. 1998). For garnet analyses that have low ²⁰⁶Pb/²⁰⁴Pb ratios, the influence of high- inclusions is small. However, the relatively large errors preclude a detailed evaluation of the relationship between the different chronometers. For garnet with higher ²⁰⁶Pb/²⁰⁴Pb ratios, the overall similarity between the Pb-Pb and Sm-Nd garnet ages implies that the inclusions are not significantly older than the garnet and therefore do not induce a premetamorphic Pb signature upon the garnet. The results presented here show that garnet with low ²³⁸U/²⁰⁴Pb ratios together with Sm-Nd garnet data and U-Pb monazite ages from the same rock can be used to extract geologically meaningful ages that can help to better understand tectonometamorphic processes in high-grade terranes.Editorial responsibility: J. Hoefs     

K-Ar ages and Pb,Sr isotopic characteristics of Cenozoic volcanic rocks in Shandong Province,China

28 samples of Cenozoic volcanic rocks collected from Shandong Province have been dated by K-Ar method. They are mainly Neogene with an age range of 4–19 m. y. The basalts from Linqu and Yishui in west Shandong Province are Miocene and those from Penglai and Qixia in east Shandong Province are Miocene and Pliocene in age. The basalts from Wudi in north Shandong Province are Middle-Early Pleistocene in age. In each area the duration of volcanic eruption was estimated at about 2–3 m. y. Pb and Sr isotopic compositions and U, Th, Pb, Rb, Sr, and major elements in most of the samples were determined. The isotopic compositions are:²⁰⁶Pb/²⁰⁴Pb—16.92-18.48,²⁰⁷Pb/²⁰⁴Pb—15.30-15.59,²⁰⁸Pb/²⁰⁴Pb—37.83-38.54, and (⁸⁷Sr/⁸⁶Sr)_i—0.70327-0.70632. There are some positive or negative linear correlations between²⁰⁶Pb/²⁰⁴Pb and²⁰⁷Pb/²⁰⁴Pb, Pb isotopes and Pb content, Pb isotopes and Sr isotopes, and Sr isotopes and other elements. The basaltic rocks from east and west Shandong Province have somewhat differences in isotopic composition and element content. The basalts probably are products of multi-stage evolution of the mantle. They have preserved the primary features of the source, although they were influenced, to some extent, by the contamination of crustal materials.     

Petrogenesis of isotopically unusual Pliocene olivine leucitites from Deep Springs Valley, California

High-K mafic alkalic lavas (5.4 to 3.2 wt% K₂O) from Deep Springs Valley, California define good correlations of increasing incompatible element (e.g., Sr, Zr, Ba, LREE) and compatible element contents (e.g., Ni, Cr) with increasing MgO. Strontium and Nd isotope compositions are also correlated with MgO; ⁸⁷Sr/⁸⁶Sr ratios decrease and ɛ_Nd values increase with decreasing MgO. The Sr and Nd isotope compositions of these lavas are extreme compared to most other continental and oceanic rocks; ⁸⁷Sr/⁸⁶Sr ratios range from 0.7121 to 0.7105 and ɛ_Nd values range from −16.9 to −15.4. Lead isotope ratios are relatively constant, ²⁰⁶Pb/²⁰⁴Pb ∼17.2, ²⁰⁷Pb/²⁰⁴Pb ∼15.5, and ²⁰⁸Pb/²⁰⁴Pb ∼38.6. Depleted mantle model ages calculated using Sr and Nd isotopes imply that the reservoir these lavas were derived from has been distinct from the depleted mantle reservoir since the early Proterozoic. The Sr-Nd-Pb isotope variations of the Deep Springs Valley lavas are unique because they do not plot along either the EM I or EM II arrays. For example, most basalts that have low ɛ_Nd values and unradiogenic ²⁰⁶Pb/²⁰⁴Pb ratios have relatively low ⁸⁷Sr/⁸⁶Sr ratios (the EM I array), whereas basalts with low ɛ_Nd values and high ⁸⁷Sr/⁸⁶Sr ratios have radiogenic ²⁰⁶Pb/²⁰⁴Pb ratios (the EM II array). High-K lavas from Deep Springs Valley have EM II-like Sr and Nd isotope compositions, but EM I-like Pb isotope compositions. A simple method for producing the range of isotopic and major- and trace-element variations in the Deep Springs Valley lavas is by two-component mixing between this unusual K-rich mantle source and a more typical depleted mantle basalt. We favor passage of MORB-like magmas that partially fused and were contaminated by potassic magmas derived from melting high-K mantle veins that were stored in the lithospheric mantle. The origin of the anomalously high ⁸⁷Sr/⁸⁶Sr and ²⁰⁸Pb/²⁰⁴Pb ratios and low ɛ_Nd values and ²⁰⁶Pb/²⁰⁴Pb ratios requires addition of an old component with high Rb/Sr and Th/Pb ratios but low Sm/Nd and U/Pb ratios into the mantle source region from which these basalts were derived. This old component may be sediments that were introduced into the mantle, either during Proterozoic subduction, or by foundering of Proterozoic age crust into the mantle at some time prior to eruption of the lavas. Received: 28 February 1997 / Accepted: 9 July 1998     

江西彭山锡多金属矿集区尖峰坡锡矿床LA-MC-ICP-MS锡石U-Pb测年及其地质意义

江西彭山锡多金属矿集区位于江西省德安县,处于钦杭成矿带东段靠扬子板块一侧,是扬子板块东南缘地区一个重要的锡多金属矿集区。目前该地区尚缺乏精确可靠的成矿年代学资料。本文应用LA-MC-ICP-MS微区原位U-Pb同位素测年技术,对矿集区内尖峰坡矿床中锡石样品进行了研究,获得尖峰坡锡矿的206Pb/207Pb-238U/207Pb等时线年龄129.7±2.5Ma(N=31,MSWD=5.5),207Pb/206Pb-238U/206Pb谐和年龄为128.3±2.5Ma(N=31,MSWD=7.6),表明尖峰坡矿区锡成矿作用主要发生在早白垩世,与已报道的彭山地区燕山期花岗岩的成岩年龄相一致。紧密的时间以及空间关系显示燕山晚期岩浆-热液活动对形成彭山锡多金属矿集区的大规模成矿作用至关重要。对华南地区锡钨区域成矿年代学对比表明,扬子板块东南缘的锡钨成矿带均形成于早白垩世(146~124Ma),这与其北侧的长江中下游成矿带九瑞-鄂东南铜多金属矿集区的成岩成矿时代相同,而明显不同于南岭地区晚侏罗世(160~150Ma)以及滇东南-桂西北地区晚白垩世(98~76Ma)的锡钨成矿作用,说明扬子板块东南缘具有与南岭以及滇东南-桂西北地区不同的锡钨成矿背景,而应与长江中下游地区的构造岩浆作用事件统一来开展深入研究。     

U-Pb age and Sr isotope signature of cap limestones from the Neoproterozoic Tsagaan Oloom Formation, Dzabkhan River Basin, Western Mongolia

The U-Pb and Pb-Pb methods were used for determining age of cap limestones from the Neoproterozoic Tsagaan Oloom Formation corresponding to the lower part of the sedimentary cover in the Dzabkahn microcontinent of Central Asia. The weighted average age value appeared to be equal to 632 ± 14 Ma (MSWD = 0.11, probability 0.74). This value allows the following assumptions: (1) the lower boundary of the Tsagaan Oloom Formation corresponds to the beginning of the Ediacaran; (2) Dzabkhan tillites are correlative with glacial sediments of the Marinoan Epoch. The low ²³⁸U/²⁰⁴Pb and ²³²Th/²³⁸U ratios observed in initial Pb sources of limestones from the Tsagaan Oloom Formation indicate that the Dzabkhan paleobasin received at its early development stages a bulk of material from eroded upper Riphean juvenile rocks. The ⁸⁷Sr/⁸⁶Sr ratio in fractions of Tsagaan Oloom limestones enriched with primary carbonate material and satisfying geochemical criteria of Rb-Sr systems retentivity (Mn/Sr < 0.20 and Fe/Sr < 1) varies from 0.70676 to 0.70691 and reflects this ratio in the World Ocean approximately 630 Ma ago.