A two-stage evolution model for the Amantaytau orogenic-type gold deposit in Uzbekistan   总被引：4，自引：0，他引：4  

Jan Pasava  Hartwig Frimmel  Anna Vymazalová  Petr Dobes  Alexandr V. Jukov  Rustam I. Koneev 《Mineralium Deposita》2013,48(7):825-840

A lithogeochemical, mineral chemical, isotopic, and fluid inclusion study of barren, low-, and high-grade Au-mineralized samples from the shear zone-hosted Amantaytau gold deposit, Uzbekistan, shows that the local host rocks, Late Ordovician–Earlz Silurian carbonacous shales, are likely to have been an important source of Au, As, Ni, and S in the formation of the deposit. Syn-depositional pyrite in these shales contains on average 0.23 ppm Au, 1,083 ppm As, and 861 ppm Ni. The distribution of rare earth elements (REE) indicates a homogeneous source of light REE, whereas the heavy REE distribution reflects most likely primary variations in the sediments. The mineralized zone is marked by a positive Eu anomaly, which supports reducing conditions during the mineralization. A hydrothermal overprint by an aqueous–carbonic fluid is reflected in a high-grade Au-mineralized sample by δ¹³C values of ?13.0?‰ (V-PDB). The δ ³⁴S values in pyrite (?0.13 to +7.30?‰ CDT) from barren and mineralized samples are consistent with marine sulfate being the principal source of the ore sulfur. Assuming a formation temperature of between 300 and 400 °C for the main stage of mineralization, as indicated by the alteration mineral assemblage, the calculated δ ¹⁸O_fluid is between 9.5 and 13.4?‰ V-SMOW, which points at a metamorphic origin of the ore fluid.  相似文献   

Chemistry and isotope ratios of sulfur in basalts and volcanic gases at Kilauea volcano,Hawaii     

Hitoshi Sakai  Thomas J. Casadevall  James G. Moore 《Geochimica et cosmochimica acta》1982,46(5):729-738

Eighteen basalts and some volcanic gases from the submarine and subaerial parts of Kilauea volcano were analyzed for the concentration and isotope ratios of sulfur. By means of a newly developed technique, sulfide and sulfate sulfur in the basalts were separately but simultaneously determined. The submarine basalt has 700 ± 100 ppm total sulfur with δ³⁴S_Σs of $\text{0.7 ± 0.1 ‰}$. The sulfate/sulfide molar ratio ranges from 0.15 to 0.56 and the fractionation factor between sulfate and sulfide is $\text{+7.5 ± 1.5‰}$. On the other hand, the concentration and δ³⁴S_Σs values of the total sulfur in the subaerial basalt are reduced to 150 ± 50 ppm and $\text{?0.8 ± 0.2‰}$, respectively. The sulfate to sulfide ratio and the fractionation factor between them are also smaller, 0.01 to 0.25 and +3.0‰, respectively. Chemical and isotopic evidence strongly suggests that sulfate and sulfide in the submarine basalt are in chemical and isotopic equilibria with each other at magmatic conditions. Their relative abundance and the isotope fractionation factors may be used to estimate the $\text{?o}{}_2$ and temperature of these basalts at the time of their extrusion onto the sea floor. The observed change in sulfur chemistry and isotopic ratios from the submarine to subaerial basalts can be interpreted as degassing of the SO₂ from basalt thereby depleting sulfate and ³⁴S in basalt.The volcanic sulfur gases, predominantly SO₂, from the 1971 and 1974 fissures in Kilauea Crater have δ³⁴S values of 0.8 to 0.9%., slightly heavier than the total sulfur in the submarine basalts and definitely heavier than the subaerial basalts, in accord with the above model. However, the δ³⁴S value of sulfur gases (largely SO₂) from Sulfur Bank is 8.0%., implying a secondary origin of the sulfur. The δ³⁴S values of native sulfur deposits at various sites of Kilauea and Mauna Loa volcanos, sulfate ions of four deep wells and hydrogen sulfide from a geothermal well along the east rift zone are also reported. The high δ³⁴S values (+5 to +6%._o) found for the hydrogen sulfide might be an indication of hot basaltseawater reaction beneath the east rift zone.  相似文献   

Seawater contribution to polymetallic Ni–Mo–PGE–Au mineralization in Early Cambrian black shales of South China: Evidence from Mo isotope,PGE, trace element,and REE geochemistry     

《Ore Geology Reviews》2013

The Early Cambrian black shale sequence of the Niutitang Formation in South China hosts a synsedimentary, organic carbon-rich, polymetallic sulfide layer with extreme metal concentrations, locally mined as polymetallic Ni–Mo–PGE–Au ore. In combination with previously reported data, we present Mo isotope, platinum-group element (PGE), and trace and rare-earth element (REE) data for the polymetallic sulfide ores and host black shales from four mine sites (Dazhuliushui and Maluhe in Guizhou Province, and Sancha and Cili in Hunan Province, respectively), several hundred kilometers apart. The polymetallic sulfide ores have consistently heavy δ^98/95Mo values of 0.94 to 1.38‰ (avg. 1.13 ± 0.14‰, 1σ, n = 11), and the host black shale and phosphorite have slightly more variable δ^98/95Mo values of 0.81‰ to 1.70‰ (n = 14). This latter variation is due to variable paleoenvironmental conditions from suboxic to euxinic, and partly closed-system fractionation in isolated marine sedimentary basins. Both the polymetallic sulfides and host black shales show PGE distribution patterns similar to that of present-day seawater, but different from those of ancient submarine-hydrothermal deposits and modern submarine hydrothermal fluids. The polymetallic sulfide bed has a generally consistent metal enrichment by a factor of 10⁷ compared to present-day seawater. PAAS-normalized REE + Y patterns of the polymetallic sulfide bed are characterized by a remarkably positive Y anomaly, consistent with an origin of the REE predominantly from seawater. Small positive Eu anomalies in some of the sulfide ores could reflect minor hydrothermal components involved. The Mo isotope, PGE, and trace and rare-earth element geochemical data suggest that metals in the polymetallic Ni–Mo–PGE–Au sulfide ore layer were scavenged mostly from Early Cambrian seawater, by both in-situ precipitation and local re-deposition of sulfide clasts.  相似文献   

Depositional age and tectonic environment of the Gouap banded iron formations from the Nyong group,SW Cameroon:Insights from isotopic,geochemical and geochronological studies of drillcore samples     

Landry Soh Tamehe  Chongtao Wei  Sylvestre Ganno  Carlos Alberto Rosiere  Jean Paul Nzenti  Chesther Gatse Ebotehouna  Guanwen Lu 《地学前缘(英文版)》2021,12(2):549-572

The discovery of the Gouap banded iron formations(BIFs)-hosted iron mineralization in the northwestern of the Nyong Group(Ntem Complex)in southwestern Cameroon provides unique insights into the geology of this region.In this contribution,we firstly report detailed study of geochemistry,isotopic and geochronology of well preserved samples of the Gouap BIFs collected from diamond drillcores.The Gouap BIFs consist mainly of amphibole BIFs and amphibole-pyrite BIFs characterized by dominant Fe₂O₃+SiO₂contents and variable contents of CaO,MgO and SO₃,consistent with the presence of amphibole,chlorite,epidote and pyrite,formed during amphibolite facies metamorphism and overprinted hydrothermal event.The amphibole–pyrite BIFs are typically enriched in trace and rare earth elements(REE)compared to the amphibole BIFs,suggesting the influence of detrital materials as well as secondary hydrothermal alteration.The Post Archean Australian Shale(PAAS)-normalized REE–Y profiles of the Gouap BIFs display positive La,Eu anomalies,weak negative Ce anomalies,indicating a mixture of low-temperature hydrothermal fluids and relatively oxic conditions probably under relative shallow seawater.We present here the first isotopic data of BIFs within the Ntem Complex.Theδ³⁰Si_NBS28values of the quartz from the Gouap BIFs vary from-1.5‰to-0.3‰and from-0.8‰to-0.9‰for the amphibole BIFs and amphibole–pyrite BIFs,respectively.The quartz hasδ¹⁸OV-SMOW values of 6.8‰–9.5‰(amphibole BIFs)and 9.2‰–10.6‰(amphibole–pyrite BIFs).The magnetite from the Gouap BIFs showsδ¹⁸O values ranging from-3.5‰to-1.8‰and from-3‰to-1.7‰for the amphibole BIFs and amphibole–pyrite BIFs,respectively.Moreover,the pyrite grains in the amphibole–pyrite BIFs displayδ34S values of 1.1‰–1.8‰.All isotopic data of the Gouap BIFs confirm that they might have precipitated from low-temperature hydrothermal fluids with detrital input distant from the volcanic activity.According to their geochemical and isotopic characteristics,we propose that the Gouap BIFs belong to the Superior type.In situ U–Pb zircon dating of BIFs was conducted to assess the BIF depositional age based on strong evidence of zircon in thin section.The Gouap BIFs were probably deposited at 2422±50 Ma in a region where sediments extended from continental shelf to deep-water environments along craton margins like the Caue Formation of the Minas Supergroup,Brazil.The studied BIFs have experienced regional hydrothermal activity and metamorphism at 2089±8.3 Ma during the Eburnean–Transamazonian orogeny.These findings suggest a physical continuity between the protocratonic masses of both Sao Francisco and Congo continents in the Rhyacian Period.  相似文献   

Sulfur cycling at the Mid-Atlantic Ridge: A multiple sulfur isotope approach     

Marc Peters  Harald Strauss  James Farquhar  Charlotte Ockert  Benjamin Eickmann  Cristiane L. Jost 《Chemical Geology》2010,269(3-4):180-196

The role of sulfur in two hydrothermal vent systems, the Logatchev hydrothermal field at 14°45′N/44°58′W and several different vent sites along the southern Mid-Atlantic Ridge (SMAR) between 4°48′S and 9°33′S and between 12°22′W and 13°12′W, is examined by utilizing multiple sulfur isotope and sulfur concentration data. Isotope compositions for sulfide minerals and vent H₂S from different SMAR sites range from + 1.5 to + 8.9‰ in δ³⁴S and from + 0.001 to + 0.051‰ in Δ³³S. These data indicate mixing of mantle sulfur with sulfur from seawater sulfate. Combined δ³⁴S and Δ³³S systematics reveal that vent sulfide from SMAR is characterized by a sulfur contribution from seawater sulfate between 25 and 33%. This higher contribution, compared with EPR sulfide, indicates increased seawater sulfate reduction at MAR, because of a deeper seated magma chamber and longer fluid upflow path length, and points to fundamental differences with respect to subsurface structures and fluid evolution at slow and fast spreading mid-ocean ridges.Additionally, isotope data uncover non-equilibrium isotopic exchange between dissolved sulfide and sulfate in an anhydrite bearing zone below the vent systems at fluid temperatures between 335 and 400 °C. δ³⁴S values between + 0.2 to + 8.8‰ for dissolved and precipitated sulfide from Logatchev point to the same mixing process between mantle sulfur and sulfur from seawater sulfate as at SMAR. δ³⁴S values between ? 24.5 and + 6.5‰ and Δ³³S values between + 0.001 and + 0.125‰ for sulfide-bearing sediments and mafic/ultramafic host rocks from drill cores taken in the region of Logatchev indicate a clear contribution of biogenic sulfides formed via bacterial sulfate reduction. Basalts and basaltic glass from SMAR sites with Δ³³S = ? 0.008‰ reveal lower Δ³³S lower values than suggested on the basis of previously published isotopic measurements of terrestrial materials.We conclude that the combined use of both δ³⁴S and Δ³³S provides a more detailed picture of the sulfur cycling in hydrothermal systems at the Mid-Atlantic Ridge and uncovers systematic differences to hydrothermal sites at different mid-ocean ridge sites. Multiple sulfur isotope measurements allow identification of incomplete isotope exchange in addition to isotope mixing as a second important factor influencing the isotopic composition of dissolved sulfide during fluid upflow. Furthermore, based on Δ³³S we are able to clearly distinguish biogenic from hydrothermal sulfides in sediments even when δ³⁴S were identical.  相似文献   

浙江八面山萤石矿床稀土元素地球化学特征及成因探讨   总被引：4，自引：2，他引：2  

夏学惠  韩豫川  连卫  袁从建  徐少康  阎飞  梁中朋 《化工矿产地质》2009,31(4):193-200

对浙江八面山萤石矿床中不同类型萤石矿石和围岩样品的稀土元素的系统分析表明,细粒萤石矿石的ΣREE〈39×10-6,LREE为14.36×10-6～34.24×10-6,HREE0.96×10-6～2.04×10-6,Y〈3×10-6;巨晶萤石矿石中的ΣREE3.62×10-6～20.81×10-6,LREE2.71×10-6～17.67×10-6,HREE0.24×10-6～1.49×10-6;而围岩花岗岩的ΣREE460.29×10-6,LREE225.97×10-6,HREE91.32×10-6,Y＆gt;140×10-6;沉积岩中的ΣREE20.22×10-6、LREE16.11×10-6、HREE1.61×10-6。矿石与围岩中沉积岩的稀土总量、轻稀土、重稀土和Y的含量接近,与花岗岩的稀土总量、轻稀土、重稀土和Y元素含量相差悬殊。萤石矿石的稀土分布型式主要为轻稀土富集型,（La/Yb）N通常多数大于8,在8.07～17.26间,δEu值在0.45～1.30,δCe在0.89～1.14间,Ce、Eu基本不显异常。矿石与围岩的稀土地球化学研究显示,八面山萤石矿床为受地层、岩体与断裂共同控制＂三位一体＂的低温热液型矿床。  相似文献   

Sources of environmental sulfur in the groundwater system,southern New Zealand     

《Applied Geochemistry》2016

Sulfide minerals commonly occur in sediments and basement rocks in southern New Zealand, as authigenic precipitates from groundwater below the oxygenated surface zone. There are two principal potential sources for sulfur in the groundwater system: weathering of sulfide minerals in the metamorphic basement and rainwater-derived marine aerosols. We present data for these two key sulfur sources: metamorphic sulfide and associated hydrothermal Au-bearing veins within the Otago Schist (average δ³⁴S = −1.8 ± 2.4‰), and an inland saline lake (S derived entirely from rainwater, δ³⁴S = 21.4 ± 0.8‰). We use these two end member δ³⁴S values to estimate the contributions of these sources of sulfur in authigenic groundwater sulfide minerals and in waters derived from oxidation of these sulfide minerals, across a range of environments. We show that authigenic groundwater pyrite along joints in the Otago schist is derived primarily from metamorphic basement sulfur. In contrast, authigenic groundwater pyrite cementing Miocene-Recent aquifers shows a substantial marine aerosol component, and represents a distinct hydrogeological system. We suggest that marine aerosols represent a significant flux to the terrestrial sulfur cycle that has been present through the groundwater system in Otago over the past 20 million years.  相似文献   

Fluid Inclusion, Rare-Earth Element and Stable Isotope Study of Carbonate Minerals from the Pongkor Epithermal Gold–Silver Deposit, West Java, Indonesia     

I Wayan Warmada    Bernd Lehmann    Marolop Simandjuntak  Herian Sudarman Hemes 《Resource Geology》2007,57(2):124-135

The Pongkor gold–silver deposit is the largest low‐sulfidation epithermal precious metal deposit in Indonesia, and is of Pliocene age. The deposit consists of nine major subparallel quartz–adularia–carbonate veins with very low sulfide content. Vein infill records five paragenetic sequences, dominated by calcite in the early stage and quartz in the later stage of the hydrothermal evolution. Fluid inclusions in hydrothermal calcite and quartz of all stages indicate a temperature ranging from 180 to 220°C and a meteoric water origin (very low salinity close to 0 wt% NaCl equivalent). Carbon isotope data on calcite display a narrow range from ?6.5 to ?3.0‰δ¹³C. The oxygen isotope values have a wider range of +4.6 to +10.1‰δ¹⁸O. The broadly positive correlation of the δ¹³C versus δ¹⁸O plot suggests that the carbon species, which equilibrated during the formation of calcite, is dominated by H₂CO₃ not far from equilibrium with HCO₃^?. The abundance of rare earth and yttrium (REY) in carbonate samples is very low (>REY mostly <2 ppm). However, there is always a positive Eu anomaly, which indicates a deeper fluid reservoir at >250°C.  相似文献   

The source of sulfur in sulfide deposits in the Siberian Platform traps (from isotope data)     

V.V. Ryabov  O.N. Simonov  S.G. Snisar  A.A. Borovikov 《Russian Geology and Geophysics》2018,59(8):945-961

The source of sulfur in giant Norilsk-type sulfide deposits is discussed. A review of the state of the problem and a critical analysis of existing hypotheses are made. The distribution of δ³⁴S in sulfides of ore occurrences and small and large deposits and in normal sedimentary, metamorphogenic, and hypogene sulfates is considered. A large number of new δ³⁴S data for sulfides and sulfates in various deposits, volcanic and terrigenous rocks, coals, graphites, and metasomatites are presented. The main attention is focused on the objects of the Norilsk and Kureika ore districts. The δ³⁴S value varies from -14 to + 22.5‰ in sulfides of rocks and ores and from 15.3 to 33‰ in anhydrites. In sulfide-sulfate intergrowths and assemblages, δ³⁴S is within 4.2-14.6‰ in sulfides and within 15.3-21.3‰ in anhydrites. The most isotopically heavy sulfur was found in pyrrhotite veins in basalts (δ³⁴S = 21.6‰), in sulfate veins cutting dolomites (δ³⁴S = 33‰), and in subsidence caldera sulfates in basalts (δ³⁴S = 23.2-25.2‰). Sulfide ores of the Tsentral’naya Shilki intrusion have a heavy sulfur isotope composition (δ³⁴S = + 17.7‰ (n = 15)). Thermobarogeochemical studies of anhydrites have revealed inclusions of different types with homogenization temperatures ranging from 685 °C to 80 °C. Metamorphogenic and hypogene anhydrites are associated with a carbonaceous substance, and hypogene anhydrites have inclusions of chloride-containing salt melts. We assume that sulfur in the trap sulfide deposits was introduced with sulfates of sedimentary rocks (δ³⁴S = 22-24‰). No assimilation of sulfates by basaltic melt took place. The sedimentary anhydrites were “steamed” by hydrocarbons, which led to sulfate reduction and δ³⁴S fractionation. As a result, isotopically light sulfur accumulated in sulfides and hydrogen sulfide, isotopically heavy sulfur was removed by aqueous calcium sulfate solution, and “residual” metamorphogenic anhydrite acquired a lighter sulfur isotope composition as compared with the sedimentary one. The wide variations in δ³⁴S in sulfides and sulfates are due to changes in the physicochemical parameters of the ore-forming system (first of all, temperature and P_ch4) during the sulfate reduction. The regional hydrocarbon resources were sufficient for large-scale ore formation.  相似文献   

Geochemical Charactristics and Genesis of Topaz—Bearing Porphyries in Yangbin Area of Taishun County,Zhejiang Province     

Wang Dezi  Liu Changshi  Shen Weizhou  Min Maozhong  Ling Hongfei 《中国地球化学学报》1995,14(1):13-25

The host rocks of the porphyry tin deposits in the Yangbin area are principally topaz-bearing porphyry dikes about 2 km long and 2–20m wide. Three lithologie types are identified for the dikes: topaz-bearing potassium feldspar granitic porphyry, topaz-bearing monzonitic granitic porphyry and topaz-bearing quartz porphyry. The content of topaz in the rocks ranges from 10 to 20 vol.%. Porphyritic texture is characteristic, with quartz, potassium feldspar and albite as main phenocryst minerals. The phenocryst occupies 10–20 vol% of the rocks. The rock groundmass consists of subhedral topaz, quartz and protolithionite. Topaz has a unit-cell parameter b=8.797 (Å), and F:OH=1.92:0.18, indicating a F-rich variety formed at high temperature. The topaz-bearing porphyries occurring in this area are strongly peraluminous (A/NKC=1.574–12.94), with high ratios of F/Cl (146–303) and Rb/Sr (5–122). They are rich in incompatible elements (Sn, 313 × 10^?6–1042 × 10^?6; W, 6 × 10^?6–218 × 10^?6; Nb, 27 × 10^?6–54 × 10^?6), but poor in compatible elements (Sr, 10 × 10^?6–28 × 10^?6; Ba, 58 × 10^?6–73 × 10^?6; V, 3 × 10^?6–12 × 10^?6, Cl, 150 × 10^?6–226 × 10^?6). The rocks are also characterized by high total REE amount (281.69 × 10^?6–319.76 × 10^?6), with strong Eu depletion (δEu=0.01–0.03) and low ratio of LREE/HREE (0.78–0.84). In summary, the authors propose an idea of S-type genesis for the topaz-bearing porphyries with tin mineralization, instead of I-type.  相似文献   

Sulfur and lead isotopic compositions of massive sulfides from deep-sea hydrothermal systems: Implications for ore genesis and fluid circulation     

《Ore Geology Reviews》2017

Studies of sulfur and lead isotopic compositions in hydrothermal deposits are an important tool to determine the source and processes of both sulfur and lead, and to understand the origin of hydrothermal ore deposits. Here, the sulfur and lead isotopic compositions of sulfide minerals have been studied for different hydrothermal fields in the East Pacific Rise (EPR), Mid-Atlantic Ridge (MAR), Central Indian Ridge (CIR), Southwest Indian Ridge (SWIR), and North Fiji Basin (NFB). The sulfur isotopic compositions of the studied sulfide samples are variable (δ³⁴S 0.0 to 9.6‰, avg. δ³⁴S 4.7‰; n = 60), being close to the associated igneous rocks (~ 0‰ for, e.g., basalt, serpentinized peridotite), which may reflect the S in the sulfide samples is derived mainly from the associated igneous rocks, and a relatively small proportion (< 36%) of seawater sulfur incorporated into these sulfides during mixing between seawater (δ³⁴S 21‰) and hydrothermal fluid. In contrast for a mixed origin for the source of S, the majority of the lead isotopic compositions (²⁰⁶Pb/²⁰⁴Pb 17.541 ± 0.004 to 19.268 ± 0.001, ²⁰⁷Pb/²⁰⁴Pb 15.451 ± 0.001 to 15.684 ± 0.001, ²⁰⁸Pb/²⁰⁴Pb 37.557 ± 0.008 to 38.988 ± 0.002, n = 21) of the sulfides possess a basaltic Pb isotopic composition, suggesting that the lead in the massive sulfide is mainly leached from local basaltic rocks that host the sub-seafloor hydrothermal systems in sediment-free mid-ocean ridges and mature back-arc basins. Furthermore, sulfide minerals in the super-fast and fast spreading mid-ocean ridges (MORs) exhibit less spread in their the δ³⁴S values compared to sulfides from super-slow, and slow spreading MORs, which is most easily explained as a lesser degree of fluid-rock interaction and hydrothermal fluid-seawater mixing during hydrothermal ore-forming process. Additionally, the S and Pb isotope compositions of sulfides are controlled by the fluid processes for forming seafloor massive sulfide deposits. We demonstrate that the variable sulfur and lead isotopic compositions exhibit a relationship with the sulfur and lead sources, fluid–rock interaction, and fluid–seawater mixing.  相似文献   

The Paleoarchean Northern Mundo Novo Greenstone Belt,São Francisco Craton: Geochemistry,U–Pb–Hf–O in zircon and pyrite δ34S-Δ33S-Δ36S signatures     

《地学前缘(英文版)》2022,13(5):101252

Greenstone belts contain several clues about the evolutionary history of primitive Earth. Here, we describe the volcano-sedimentary rock association exposed along the eastern margin of the Gavião Block, named the Northern Mundo Novo Greenstone Belt (N-MNGB), and present data collected with different techniques, including U–Pb–Hf–O isotopes of zircon and multiple sulfur isotopes (³²S, ³³S, ³⁴S, and ³⁶S) of pyrite from this supracrustal sequence. A pillowed metabasalt situated in the upper section of the N-MNGB is 3337 ± 25 Ma old and has zircon with ε_Hf(t) =  ?2.47 to ?1.40, Hf model ages between 3.75 Ga and 3.82 Ga, and δ¹⁸O = +3.6‰ to +7.3‰. These isotopic data, together with compiled whole-rock trace element data, suggest that the mafic metavolcanic rocks formed in a subduction-related setting, likely a back-arc basin juxtaposed to a continental arc. In this context, the magma interacted with older Eoarchean crustal components from the Gavião Block. Detrital zircons from the overlying quartzites of the Jacobina Group are sourced from Paleoarchean rocks, in accordance with previous studies, yielding a maximum depositional age of 3353 ± 22 Ma. These detrital zircons have ε_Hf(t) =  ?5.40 to ?0.84, Hf model ages between 3.66 Ga and 4.30 Ga, and δ¹⁸O = +4.8‰ to +6.4‰. The pyrite multiple sulfur isotope investigation of the 3.3 Ga supracrustal rocks from the N-MNGB enabled a further understanding of Paleoarchean sulfur cycling. The samples have diverse isotopic compositions that indicate sulfur sourced from distinct reservoirs. Significantly, they preserve the signal of the anoxic Archean atmosphere, expressed by MIF-S signatures (Δ³³S between ?1.3‰ to +1.4‰) and a Δ³⁶S/Δ³³S slope of ?0.81 that is indistinguishable from the so-called Archean array. A BIF sample has a magmatic origin of sulfur, as indicated by the limited δ³⁴S range (0 to +2‰), Δ³³S ~ 0‰, and Δ³⁶S ~ 0‰. A carbonaceous schist shows positive δ³⁴S (2.1‰–3.5‰) and elevated Δ³³S (1.2‰–1.4‰) values, with corresponding negative Δ³⁶S between ?1.2‰ to ?0.2‰, which resemble the isotopic composition of Archean black shales and suggest a source from the photolytic reduction of elemental sulfur. The pillowed metabasalt displays heterogeneous δ³⁴S, Δ³³S, and Δ³⁶S signatures that reflect assimilation of both magmatic sulfur and photolytic sulfate during hydrothermal seafloor alteration. Lastly, pyrite in a massive sulfide lens is isotopically similar to barite of several Paleoarchean deposits worldwide, which might indicate mass dependent sulfur processing from a global and well-mixed sulfate reservoir at this time.  相似文献   

Rare-earth elements as source indicators of Pan-African granites from Obudu Plateau,Southeastern Nigeria   总被引：1，自引：1，他引：0  

V. U. Ukaegbu  F. T. Beka 《中国地球化学学报》2008,27(2):130-134

The rare-earth element （REE） concentrations of representative granite samples from the southeast of the Obudu Plateau, Nigeria, were analyzed with an attempt to determine the signatures of their source, evolutionary history and tectonic setting. Results indicated that the granites have high absolute REE concentrations （190×10^-6-1191×10^-6; av.=549×10^-6） with the chondrite-normalized REE patterns characterized by steep negative slopes and prominent to slight or no negative Eu anomalies. All the samples are also characterized by high and variable concentrations of the LREE （151×10^-6-1169×10^-6; av.= 466×10^-6）, while the HREE show low abundance （4×10^-6-107×10^-6; av.=28×10^-6）. These are consistent with the variable levels of REE fractionation, and differentiation of the granites. This is further supported by the range of REE contents, the chondrite-normalized patterns and the ratios of LaN/YbN （2.30-343.37）, CeN/YbN （5.94-716.87）, LaN/SmN （3.14-11.68） and TbN/YbN （0.58-1.65）. The general parallelism of the REE patterns, suggest that all the granites were comagmatic in origin, while the high Eu/Eu＊ ratios （0.085-2.807; av.=0.9398） indicate high fo2 at the source. Similarly, irregular variations in LaN/YbN, CeN/YbN and Eu/Eu＊ ratios and REE abundances among the samples suggest behaviors that are related to mantle and crustal sources.  相似文献   

Origin of the Oligocene Tuolangla porphyry-skarn Cu-W-Mo deposit in Lhasa terrane,southern Tibet     

《China Geology》2020,3(3):369-384

Although some porphyry-skarn deposits occur in post-collisional extensional settings, the post-collisional deposits remain poorly understood. Here the authors describe the igneous geology, and mineralization history of Tuolangla, a newly-discovered porphyry-skarn Cu-W-Mo deposit in southern Tibet that belongs to the post-collisional class. The deposit is associated with Lower Cretaceous Bima Formation. It was intruded by granodiorite porphyry intrusions at about 23.1 Ma. Field investigation indicated that mineralization is spatially and temporally associated with granodiorite porphyry. Molybdenite yielded a Re-Os weighted mean age of 23.5 ± 0.3 Ma and is considered to represent the age of skarn mineralization at the deposit. The δ³⁴S values of sulfides, concentrated in a range between 0.6‰ to 3.4‰, show that the sulfur has a homogeneous source with characteristics of magmatic sulfur. The Pb isotopic compositions of sulfides indicate that ore-forming metal materials were derived from the mantle and ancient crust. The granodiorite porphyry displays high SiO₂ (68.78%–69.75%) and K₂O (3.40%–3.56%) contents, and relatively lower Cr (2.4×10^-6–4.09×10^-6), Ni (2.79×10^-6–3.58×10^-6) contents, and positive ε_Hf(t) values (7.7–12.9) indicating that the mineralization porphyry was derived from the partial melting of juvenile lower crust. The Tuolangla deposit is located in the central part of Zedang terrane. This terrane was once considered an ancient terrane. This terrane is in tectonic contact with Cretaceous ophiolitic rocks to its south and Mesozoic continental margin arc volcanics and intrusions of the Gangdese batholith of the Lhasa terrane to its north. Thus, the authors proposed that the Oligocene porphyry skarn Cu-W-Mo mineralization is probably associated with the Zedang terrane. This finding may clarify why the Oligocene (about 23 Ma) deposits are found only in the Zedang area and why mineralization types of the Oligocene mineralization are considerably different from those of the Miocene (17–14 Ma) mineralization.  相似文献   

Intermediate sulfidation epithermal gold-base metal deposits in Tertiary subaerial volcanic rocks,Sahinli/Tespih Dere (Lapseki/Western Turkey)     

Huseyin Yilmaz  Tolga Oyman  F. Nuran Sonmez  Greg B. Arehart  Zeki Billor 《Ore Geology Reviews》2010,37(3-4):236-258

Gold in the Sahinli and Tespih Dere intermediate sulfidation gold-base metal deposits in Western Turkey occurs in relatively deep epithermal quartz veins along with base metal minerals which have epithermal textures, including plumose quartz, vug infills, comb and cockade textures and matrix-supported milled breccias. The total sulfide content of the veins in the area is variable ranging from < 1% to 60% and is dominated by pyrite, galena, sphalerite and chalcopyrite. Sphalerite is Fe-poor (0.6 to 1.4 mol% FeS). Minor amounts of Ag-rich tetrahedrite are present. Primary hydrothermal alteration minerals include illite/muscovite, mixed-layer illite/smectite (11.6 Å) and clinochlore towards the east and, alunite, dickite/nacrite and pyrophyllite towards the west at Sahinli; major illite/muscovite and dickite occur at Tespih Dere and Sarioluk, respectively.Fluid inclusions in main-stage quartz at Sahinli are only liquid-rich, with homogenization temperatures ranging from 220 to 322 °C and the majority of T_h values between 250 and 300 °C. Salinity ranges from 4.3 to 6.9 wt.% NaCl equiv. First ice-melting temperatures (T_mf) between ?24.5 and ?19.0 °C indicate that the fluids were dominated by NaCl – H₂O during mineralization. The relatively higher average T_h at the Tespih Dere deposit (295 °C) is attributed to a relatively deeper level of exposure.Calculated δ¹⁸O values indicate that ore-forming hydrothermal fluids in the study area had δ¹⁸O_H2O ranging from + 1.1 to + 9.7‰ (average = 3.8‰), strongly ¹⁸O-enriched compared with present-day hydrothermal meteoric water in the area (δ¹⁸O = ?8.5‰). δD values of fluid inclusions in quartz range from ?58 to ?93‰ and δD values of clay minerals and alunite from ?40 to ?119‰. δD values from intermediate argillic alteration (average = ?68‰) in the study area are very similar to δD values of the present-day local geothermal system (average δD = ?54‰) whereas δD values from advanced-argillic alteration (average δD = ?33‰) are very different from the present-day local geothermal system.The δ³⁴S values in samples from the Sahinli and Tespih Dere deposits average ?2.9‰ for pyrite; ?3.3‰ for chalcopyrite; ?5.4‰ for sphalerite and ?7.6‰ for galena. These data are consistent with derivation of the sulfur from either igneous rocks or possibly from local wallrock.  相似文献   

Genesis of the Jinding Zn-Pb deposit,northwest Yunnan Province,China: Constraints from rare earth elements and noble gas isotopes     

《Ore Geology Reviews》2017

The giant sediment-hosted Jinding zinc-lead deposit is located in the Lanping Basin, northwestern Yunnan Province, China. The genesis of the deposit has long been debated and the sources of the ore-forming fluids and metals are controversial. This study presents rare earth element (REE) and noble gas isotope data that constrain the origins of the ore fluids and the heat source driving the hydrothermal circulation. The early-stage sulfides are enriched in light REEs and have high ∑REE values (30.8–94.8 ppm) and weakly negative Eu (δEu 0.85–0.89) and Ce anomalies (δCe 0.84–0.95), suggesting that the fluids were likely derived from dissolution of Upper Triassic marine carbonates with input of REEs from aluminosilicate rocks in the basin. In contrast, the late-stage sulfides have irregular REE patterns, generally low ∑REE values (0.24–10.8 ppm) and positive Eu (δEu 1.22–10.9) and weakly negative Ce anomalies (δCe 0.53–0.90), which suggest that the ore-forming fluids interacted with evaporite minerals. The ³He/⁴He (0.01–0.04 R_a) and ⁴⁰Ar/³⁶Ar values (301–340) of the ore-forming fluids indicate crustal and atmospheric origins for these noble gases. These findings are in agreement with the published fluid inclusion microthermometry data and the results of H, O, C, S, Pb and Sr isotope studies. Our data, in combination with published results, support a two-stage hydrothermal mineralization model, involving early-stage basinal brines and late-stage meteoric water that acquired metals and heat from crustal sources.  相似文献   

Aubrites and diogenites: Trace element clues to their origin     

Rainer Wolf  Mitsuru Ebihara  Gerhard R. Richter  Edward Anders 《Geochimica et cosmochimica acta》1983,47(12):2257-2270

We have analyzed by RNAA 25 aubrite and 9 diogenite samples for 13 to 29 siderophile, volatile, and lithophile trace elements. Both meteorite classes show a typically igneous siderophile element pattern, with Ir, Os, Re, Ge more depleted than Au, Ni, Pd, Sb. But aubrites tend to have about 10 × higher abundances (10^?3 ? 10 ^{? 4} × Cl for the first 4 and 10^?2?10^?3 × Cl for the last 4 siderophiles), apparently reflecting smaller metal/silicate distribution coefficients at lowerf(O₂), or less complete segregation of metal. Se is surprisingly abundant in aubrites (up to 0.4 × Cl), but Te is less so ($\text{Se}\text{Te}\text{? 5 × Cl}$), apparently due to its stronger siderophile character. Other volatiles (Ag, Zn, In, Cd, Bi, T1) show depletions intermediate between lunar dunite and the Earth's mantle.Of 7 aubrites analyzed for REE (Ce, Nd, Eu, Tb, Yb, Lu), 6 are depleted in REE (0.08?0.5 × Cl) and 5 show negative Eu anomalies (the exceptions are Bishopville and Mt. Egerton silicate). This supports an igneous origin, as already noted by Boynton and Schmitt (1972). No samples of the complementary, basaltic and feldspathic rocks have been found thus far, but one of our samples of Khor Temiki dark is a candidate for the basalt. It is 5?7 × enriched in REE and only slightly less so in Rb, Cs, and U. Though shocked and enriched in siderophiles to ~0.05 × Cl, it apparently represents a new meteorite class.Three diogenites analyzed for REE show very diverse patterns, from strongly depleted in light REE for Tatahouine (Ce = 0.01 × Cl) to flat for Garland (~2.5 × Cl). The data confirm the trends found by Fukuokaet al. (1977) as well as their interpretations.Factor analysis shows several parallel groupings for aubrites and diogenites: siderophiles (Re, Ir, Os, Pd, Ge), chalcophiles (Se, Te), volatiles (Ag, In, Tl) and incompatibles (U, REE, and Cs or Rb). But there are some differences for elements such as Ni, Sb, Cd, Bi, Au, and Zn, most of which behave more sensibly in aubrites than in diogenites.Several element pairs that differ greatly in volatility (Cs-U, Ge-Ir) correlate closely in aubrites, in approximately Cl-chondrite proportions. These correlations, and other lines of evidence, suggest strongly that aubrites originated by igneous processes in their parent body, not by direct nebular condensation. The source material may have resembled EL chondrites in oxidation state and depletion of refractories, metal, and volatiles.  相似文献   

重庆高燕锰矿床含锰碳酸盐岩稀土元素特征   总被引：1，自引：0，他引：1       下载免费PDF全文

陈佳  朱明忠  董树义  张自贤  程文斌  曾敏  陈荣彬 《地质找矿论丛》2017,32(3):367-374

重庆城口高燕锰矿属于大型碳酸盐锰矿床。文章在系统野外地质调查及样品采集基础上,结合前人研究工作,采用等离子质谱仪(ICP-MS)分析了高燕矿区师家沟、板相沟及750平硐样品的稀土元素含量。分析结果显示,其稀土元素总量范围49.79×10~(-6)~281.24×10~(-6),平均含量125.92×10~(-6);轻重稀土比值范围1.79~3.58,显示轻稀土元素富集,且轻稀土元素之间的分馏程度高于重稀土元素;w(La)/w(Ce)=0.36~0.93,δEu=1.13~2.96,呈现弱正铕异常;δCe=2.09~5.84,有强的正铈异常。认为含锰碳酸盐岩形成于强还原的碱性环境沉积过程中,且有热水参与,成岩成矿的温度小于250℃,锰富集阶段处于滨岸的高能环境中。CeS10在本区具有示矿作用。  相似文献   

Fluid inclusion,rare earth element geochemistry,and isotopic characteristics of the eastern ore zone of the Baiyangping polymetallic Ore district,northwestern Yunnan Province,China     

《Journal of Asian Earth Sciences》2014

The Baiyangping Cu–Ag polymetallic ore district is located in the northern part of the Lanping–Simao foreland fold belt, which lies between the Jinshajiang–Ailaoshan and Lancangjiang faults in western Yunnan Province, China. The source of ore-forming fluids and materials within the eastern ore zone were investigated using fluid inclusion, rare earth element (REE), and isotopic (C, O, and S) analyses undertaken on sulfides, gangue minerals, wall rocks, and ores formed during the hydrothermal stage of mineralization. These analyses indicate: (1) The presence of five types of fluid inclusion, which contain various combinations of liquid (l) and vapor (v) phases at room temperature: (a) H₂O (l), (b) H₂O (l) + H₂O (v), (c) H₂O (v), (d) C_mH_n (v), and (e) H₂O (l) + CO₂ (l), sometimes with CO₂ (v). These inclusions have salinities of 1.4–19.9 wt.% NaCl equivalents, with two modes at approximately 5–10 and 16–21 wt.% NaCl equivalent, and homogenization temperatures between 101 °C and 295 °C. Five components were identified in fluid inclusions using Raman microspectrometry: H₂O, dolomite, calcite, CH₄, and N₂. (2) Calcite, dolomitized limestone, and dolomite contain total REE concentrations of 3.10–38.93 ppm, whereas wall rocks and ores contain REE concentrations of 1.21–196 ppm. Dolomitized limestone, dolomite, wall rock, and ore samples have similar chondrite-normalized REE patterns, with ores in the Huachangshan, Xiaquwu, and Dongzhiyan ore blocks having large negative δCe and δEu anomalies, which may be indicative of a change in redox conditions during fluid ascent, migration, and/or cooling. (3) δ³⁴S values for sphalerite, galena, pyrite, and tetrahedrite sulfide samples range from −7.3‰ to 2.1‰, a wide range that indicates multiple sulfur sources. The basin contains numerous sources of S, and deriving S from a mixture of these sources could have yielded these near-zero values, either by mixing of S from different sources, or by changes in the geological conditions of seawater sulfate reduction to sulfur. (4) The C–O isotopic analyses yield δ¹³C values from ca. zero to −10‰, and a wider range of δ¹⁸O values from ca. +6 to +24‰, suggestive of mixing between mantle-derived magma and marine carbonate sources during the evolution of ore-forming fluids, although potential contributions from organic carbon and basinal brine sources should also be considered. These data indicate that ore-forming fluids were derived from a mixture of organism, basinal brine, and mantle-derived magma sources, and as such, the eastern ore zone of the Baiyangping polymetallic ore deposit should be classified as a “Lanping-type” ore deposit.  相似文献   

Paleoclimatic interpretation of the past 30 ka from isotopic studies of the deep confined aquifer of the North China plain     

《Applied Geochemistry》2003,18(7):997-1009

The δ¹⁸O and δD values in the deep confined aquifer beneath the North China Plain which is located at 112°30′E–119°30′E and 34°46′N–40°25′N, reflect differences in paleoclimatic conditions between the Holocene and the late Pleistocene. Groundwater samples whose ¹⁴C ages are between 12 and 25 ka B.P have ranges of −9.4 to −11.7‰ for δ¹⁸O and −76‰ to −85‰ for δD values. These very negative δ¹⁸O and δD values reflect the cold and arid climate in the last glacial period. The temperature estimated in this period is 6–9 °C cooler than that of the present. The entire ranges of δ¹⁸O and δD values for samples with ¹⁴C dating from 7 ka B.P to present are −7.7‰ to −10.2‰ and −63‰ to −73‰, respectively. The greater δ¹⁸O and δD enrichments of these samples indicate a period of relatively humid and warm climate in the Holocene. However, the wide ranges of δ¹⁸O (−9.0‰ to −11.1‰) and δD (−66‰ to −80‰) values for samples with ¹⁴C age ranging from 12 to 7 ka B.P. imply an unstable climatic condition of rapidly increasing temperature, which marks the transition from the Pleistocene to the Holocene.  相似文献