Lead isotope variability in olivine-hosted melt inclusions from Iceland

The lead isotope and trace element compositions of a suite of olivine-hosted melt inclusions in primitive lava flows from the Reykjanes Peninsula in Iceland show extreme variability. Much of this variability is present in the composition of inclusions from one hand specimen of Háleyjabunga, a depleted picrite lava shield that erupted 13 ka. ²⁰⁸Pb/²⁰⁶Pb compositions in this sample span 50-90% of the total range found in Atlantic MORB, indicating that high-amplitude compositional heterogeneity is present in the mantle source of melts that aggregated to form a single eruption. The trace element and isotopic trends in the melt inclusions are coincident with those in whole rock samples from young lava flows of the Reykjanes Peninsula, and extend the total range of variation towards more depleted compositions. The incompatible trace element and lead isotope compositions of the inclusions are strongly coupled and lie close to binary mixing trends between the extreme melt inclusion compositions. These relationships indicate that the trace element variation in the melt inclusions reflects heterogeneity in the composition of the mantle source entering the melting region under the Reykjanes Peninsula. Large positive Sr concentration anomalies are present in three of the inclusions, but do not correlate with indicators of mantle melting or source variations and are likely to arise by reaction with plagioclase during crustal storage. Fractional melting of heterogeneous mantle is predicted to generate melts with a wide range of compositions, filling a large volume in trace element-isotope space. However, the compositional variations observed in the melt inclusions lie close to binary mixing curves. These observations may be accounted for by a two-stage model of melt mixing. The first stage occurs in porous channels that transport melt in the mantle and takes place before inclusion entrapment. This mixing stage generates a bimodal distribution of melt compositions that is supplied from the channels to sub-Moho and lower crustal magma lenses. The second stage of mixing occurs in these chambers, producing the binary mixing trends recorded in the inclusion compositions. The distribution of isotopic compositions observed in the melt inclusions and whole rock samples from the Reykjanes Peninsula is therefore controlled by melt mixing. These results have important implications for the interpretation of basalt composition in terms of distinct compositional entities within the upwelling solid mantle under mid-ocean ridges and ocean islands.     

Platinum-group elements in porphyry copper deposits: a reconnaissance study

Summary Sulphide and flotation concentrates from 33 porphyry copper deposits have been investigated for platinum-group elements (PGE), Au, Cu and platinum-group minerals (PGM). The major sulphides in the samples studied are chalcopyrite and pyrite. Bornite is less frequent and molybdenite occurs in traces only. PGM (merenskyite, sperrylite and an unidentified Pd-Sb telluride) have been found as inclusions in chalcopyrite.Pd and Pt are present in concentrations above the analytical detection limit (> 8 ppb) in 70% respectively 30% of the deposits studied. The contents of Os, Ir, Ru and Rh are below detection limits in all samples. The analytical results show that 7 deposits (six of island arc and one of continental margin setting) reveal relatively high Pd contents (130–1900 ppb) which are associated with high Au contents (1–28 ppm). In five of them discrete PGM can be identified in accordance with elevated levels of Pd. Correlations of Au, Pd and Pt point towards a common origin.Even though the data base is relatively small, a trend is obvious, suggesting that Au-rich island arc porphyry copper deposits might host more Pd and Pt than the continental margin type ones. Other aspects of intrusive rocks, such as geological age, chemical composition and magma type do not seem to influence PGE contents.

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Platingruppen-Elemente in porphyrischen Kupfer Lagerstätten: eine Überblicksstudie

Zusammenfassung Es wurden Sulfid- und Flotationskonzentrate aus 33 Porphyry Kupfer Lagerstätten: auf Platingruppenelemente (PGE), Au, Cu and Platingruppenminerale (PGM) untersucht. Die Hauptsulfide im untersuchten Probenmaterial sind Chalkopyrit und Pyrit. Bornit ist weniger häufig and Molybdänit tritt nur in Spuren auf. An PGM wurden Merenskyit (in den Lagerstätten: Elacite, Majdanpek and Skouries), Sperrylith und ein nicht näher identifizierbares Pd-Sb- Tellurid (in der Lagerstätte Mamut) als Einschlüsse in Chalkopyrit festgestellt.Pd ist in 70% and Pt in 30% der untersuchten Lagerstätten: nachweisbar (> 8 ppb), während die Gehalte von Os, Ir, Ru and Rh in allen Proben unterhalb der Nachweisgrenze liegen. In 7 Lagerstätten: (davon sechs vom Inselbogen- und eine vom Kontinentalrandtyp) wurden relativ hohe Pd-Konzentrationen (130–1900 ppb) festgestellt, die auch durch hohe Au-Gehalte (1–28 ppm) gekennzeichnet sind. In 5 Lagerstätten: sind entsprechend den hohen Pd-Gehalten PGM nachweisbar.Geochemische Korrelationen zwischen Au, Pd and Pt weisen auf eine gemeinsame Herkunft dieser Metalle hin. Obwohl der Datenbestand noch relativ klein ist, ist ein Trend bereits sichtbar, daß Au-reiche Inselbogenporphyries Where Pd- und Pt- Gehalte erwarten lassen als der Kontinentalrand-Typ. Andere Aspekte wie geologisches Alter, Magmentyp and Chemismus der betreffenden Intrusivgesteine spielen bei der PGEFührung offensichtlich keine Rolle.

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With 8 Figures     

Boron isotope composition of geothermal fluids and borate minerals from salar deposits (central Andes/NW Argentina)

We have measured the boron concentration and isotope composition of regionally expansive borate deposits and geothermal fluids from the Cenozoic geothermal system of the Argentine Puna Plateau in the central Andes. The borate minerals borax, colemanite, hydroboracite, inderite, inyoite, kernite, teruggite, tincalconite, and ulexite span a wide range of δ¹¹B values from −29.5 to −0.3‰, whereas fluids cover a range from −18.3 to 0.7‰. The data from recent coexisting borate minerals and fluids allow for the calculation of the isotope composition of the ancient mineralizing fluids and thus for the constraint of the isotope composition of the source rocks sampled by the fluids. The boron isotope composition of ancient mineralizing fluids appears uniform throughout the section of precipitates at a given locality and similar to values obtained from recent thermal fluids. These findings support models that suggest uniform and stable climatic, magmatic, and tectonic conditions during the past 8 million years in this part of the central Andes. Boron in fluids is derived from different sources, depending on the drainage system and local country rocks. One significant boron source is the Paleozoic basement, which has a whole-rock isotopic composition of δ¹¹B=−8.9±2.2‰ (1 SD); another important boron contribution comes from Neogene-Pleistocene ignimbrites (δ¹¹B=−3.8±2.8‰, 1 SD). Cenozoic andesites and Mesozoic limestones (δ¹¹B≤+8‰) provide a potential third boron source.     

The fidelity of melt inclusions as records of melt composition

A series of experiments created melt inclusions in plagioclase and pyroxene crystals grown from a basaltic melt at 1,150°C, 1.0 GPa to investigate diffusive fractionation during melt inclusion formation; additionally, P diffusion in a basaltic melt was measured at 1.0 GPa. Melt inclusions and melts within a few 100 microns of plagioclase–melt interfaces were analyzed for comparison with melt compositions far from the crystals. Melt inclusions and melt compositions in the boundary layer close to the crystal–melt interface were similar, but both differ significantly in incompatible element concentrations from melt found greater than approximately 200 microns away from the crystals. The compositional profiles of S, Cl, P, Fe, and Al in the boundary layers were successfully reproduced by a two-step model of rapid crystal growth followed by diffusive relaxation toward equilibrium after termination of crystal growth. Applying this model to investigate possible incompatible element enrichment in natural melt inclusions demonstrated that at growth rates high enough to create the conditions for melt inclusion formation, ∼10⁻⁹–10⁻⁸ m s⁻¹, the concentration of water in the boundary layer near the crystal was similar to that of the bulk melt because of its high diffusion coefficient, but sulfur, with a diffusivity similar to major elements and CO₂, was somewhat enriched in the boundary layer melt, and phosphorus, with its low diffusion coefficient similar to other high-field strength elements and rare earth elements, was significantly enriched. Thus, the concentrations of sulfur and phosphorus in melt inclusions may over-estimate their values in the bulk melt, and other elements with similar diffusion coefficients may also be enriched in melt inclusions relative to the bulk melt. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Lead isotope composition of tree rings as bio-geochemical tracers of heavy metal pollution: a reconnaissance study from Firenze,Italy

Pb isotope composition of tree rings (Celtis Australis) and urban aerosols have been determined to assess whether arboreal species can be used as bio-geochemical tracers of the evolution of heavy metal pollution to the environment. Particular care was paid to setting up a high quality analytical technique to work with arboreal species with low Pb content. The Pb isotope composition of tree rings from 1950 to 1995 is within the range of European aerosols and is correlated with the temporal evolution of Pb isotopes measured in air particulates from Firenze. The entire data set (tree rings and air particulates) demonstrate that Pb isotope composition of tree rings can be used successfully as a proxy of the atmospheric Pb isotope composition of urban areas. This, in turn, suggests that tree rings are potentially a powerful bio-geochemical tracer for monitoring air pollution history due to human activities.     

Genesis of kalsilite melilitite at Cupaello,Central Italy: Evidence from melt inclusions

The paper presents data on primary carbonate–silicate melt inclusions hosted in diopside phenocrysts from kalsilite melilitite of Cupaello volcano in Central Italy. The melt inclusions are partly crystalline and contain kalsilite, phlogopite, pectolite, combeite, calcite, Ba–Sr carbonate, baryte, halite, apatite, residual glass, and a gas phase. Daughter pectolite and combeite identified in the inclusions are the first finds of these minerals in kamafugite rocks from central Italy. Our detailed data on the melt inclusions in minerals indicate that the diopside phenocrysts crystallized at 1170–1190°C from a homogeneous melilitite magma enriched in volatile components (CO₂, 0.5–0.6 wt % H₂O, and 0.1–0.2 wt % F). In the process of crystallization at the small variation in P-T parameters two-phase silicate-carbonate liquid immiscibility occurred at lower temperatures (below 1080–1150°C), when spatially separated melilitite silicate and Sr-Ba-rich alkalicarbonate melts already existed. The silicate–carbonate immiscibility was definitely responsible for the formation of the carbonatite tuff at the volcano. The melilitite melt was rich in incompatible elements, first of all, LILE and LREE. This specific enrichment of the melt in these elements and the previously established high isotopic ratios are common to all Italian kamafugites and seem to be related to the specific ITEM mantle source, which underwent metasomatism and enrichment in incompatible elements.     

Compositions of biotite,amphibole, apatite and silicate melt inclusions from the Tongchang mine,Dexing porphyry deposit,SE China: Implications for the behavior of halogens in mineralized porphyry systems

The Dexing deposit, located in the Circum-Pacific ore belt, is the largest porphyry copper deposit in eastern China. It is composed of 3 separate plutons, which host three mines: Tongchang, Fujiawu and Zhushahong mines. The porphyritic granodiorite samples studied in this investigation were collected from the Tongchang ore-forming pluton of this giant deposit. This paper presents electron microprobe analyses of biotite, apatite, amphibole, plagioclase, potassium feldspar and rehomogenized glassy melt inclusions from the Tongchang porphyritic granodiorites. Petrographic observations of the samples are consistent with portions of the granodioritic magma represented by our samples being overprinted by potassic hydrothermal fluid which variably altered these minerals.All of the studied micas are Mg-rich biotites. The biotites are separated into altered magmatic and secondary types based on their petrographic and geochemical characteristics. The phlogopite components of the secondary biotites are typically higher than those of the altered magmatic biotites, and the X_Mg values of all biotites correlate negatively with Cl contents, consistent with the Mg–Cl avoidance principle. The X_Mg values also correlate negatively with (K₂O + Na₂O + BaO), FeO and TiO₂ for both generations of biotites. The calculated log (fH₂O/fHCl) values (for 690 K) of the coexisting potassic fluids, which are determined from the altered magmatic biotite compositions, range from 4.43 to 4.67, and are very similar to those of other major porphyry deposits. However, the log(fH₂O/fHF) and log(fHF/fHCl) values for the same batch of hydrothermal fluids are significant higher and lower than those of these other porphyry deposits, respectively.The Cl concentrations of amphiboles and melt inclusions range from 0.18 to 0.32 wt.% and 0.15 to 0.44 wt.%, respectively. Most apatites trapped in biotite and plagioclase phenocrysts display a bimodal Cl distribution: 0.19 to 1.35 wt.% and 1.48 to 3.73 wt.%. Similarly, the S contents of the apatite also show a distinct bimodal distribution reflecting the effects of variable anhydrite saturation during evolution of the Tongchang melt and variable dissolution of anhydrite by saline aqueous fluids. The Cl contents of the apatites from the Tongchang system are typically higher than those of other studied porphyry deposits. Furthermore, the Cl contents of the melt inclusions are at or very near the Cl saturation levels (0.36 to 0.46 wt.% at 850 °C and 50 MPa and 0.42 to 0.54 wt.% at 850 °C and 200 MPa) for these melt compositions at shallow crustal pressures. These findings suggest that the area of the granodioritic magma represented by our samples, and perhaps the bulk of the Tongchang granodioritic magma was rich in Cl. The melt inclusion compositions are consistent with a high-salinity, hydrosaline liquid being exsolved directly from the granodioritic melt directly. This high-salinity hydrosaline liquid was likely very efficient at dissolving, transporting and precipitating ore metals in the mineralizing magmatic–hydrothermal system.     

Magma evolution and the formation of porphyry Cu–Au ore fluids: evidence from silicate and sulfide melt inclusions

Silicate and sulfide melt inclusions from the andesitic Farallón Negro Volcanic Complex in NW Argentina were analyzed by laser ablation ICPMS to track the behavior of Cu and Au during magma evolution, and to identify the processes in the source of fluids responsible for porphyry-Cu-Au mineralization at the 600 Mt Bajo de la Alumbrera deposit. The combination of silicate and sulfide melt inclusion data with previously published geological and geochemical information indicates that the source of ore metals and water was a mantle-derived mafic magma that contained approximately 6 wt.% H₂O and 200 ppm Cu. This magma and a rhyodacitic magma mixed in an upper-crustal magma chamber, feeding the volcanic systems and associated subvolcanic intrusions over 2.6 million years. Generation of the ore fluid from this magma occurred towards the end of this protracted evolution and probably involved six important steps: (1) Generation of a sulfide melt upon magma mixing in some parts of the magma chamber. (2) Partitioning of Cu and Au into the sulfide melt (enrichment factor of 10,000 for Cu) leading to Cu and Au concentrations of several wt.% or ppm, respectively. (3) A change in the tectonic regime from local extension to compression at the end of protracted volcanism. (4) Intrusion of a dacitic magma stock from the upper part of the layered magma chamber. (5) Volatile exsolution and resorption of the sulfide melt from the lower and more mafic parts of the magma chamber, generating a fluid with a Cu/Au ratio equal to that of the precursor sulfide. (6) Focused fluid transport and precipitation of the two metals in the porphyry, yielding an ore body containing Au and Cu in the proportions dictated by the magmatic fluid source. The Cu/S ratio in the sulfide melt inclusions requires that approximately 4,000 ppm sulfur is extracted from the andesitic magma upon mixing. This exceeds the solubility of sulfide or sulfate in either of the silicate melts and implies an additional source for S. The extra sulfur could be added in the form of anhydrite phenocrysts present in the rhyodacitic magma. It appears, thus, that unusually sulfur-rich, not Cu-rich magmas are the key to the formation of porphyry-type ore deposits. Our observations imply that dacitic intrusions hosting the porphyry–Cu–Au mineralization are not representative of the magma from which the ore-fluid exsolved. The source of the ore fluid is the underlying more mafic magma, and unaltered andesitic dikes emplaced immediately after ore formation are more likely to represent the magma from which the fluids were generated. At Alumbrera, these andesitic dikes carry relicts of the sulfide melt as inclusions in amphibole. Sulfide inclusions in similar dykes of other, less explored magmatic complexes may be used to predict the Au/Cu ratio of potential ore-forming fluids and the expected metal ratio in any undiscovered porphyry deposit.Editorial handling: B. Lehmann     

Controls on supergene enrichment of porphyry copper deposits in the Central Andes: A review and discussion

The Central Andes host some of the world’s largest porphyry copper deposits. The economic viability of these deposits is dependent on the size and quality of their supergene enrichment blanket. Published models that have strongly influenced exploration policy suggest that supergene enrichment ceased at 14 Ma due to an increase in aridity. Here we discuss these models using published geochronological, geomorphological and geological data. Geochronological data indicate that supergene oxidation and enrichment has been active between 17 and 27°S across the forearc of northern Chile and southern Peru from 44 to 6 Ma, and on the Bolivian Altiplano and Eastern Cordillera of Argentina from 11 Ma to present. There is evidence for cessation at 20, 14 and 6 Ma. However, a major problem is that as more geochronological data become available the age ranges and periods of enrichment increase. This suggests that the full spectrum of enrichment ages may not have been sampled. The relationship between supergene enrichment and the age of regional pediplain surface development is not well constrained. Only in two areas have surfaces related to enrichment been directly dated (southern Peru and south of 26°S in Chile) and suggest formation post 14 Ma. Sedimentological data indicate that a fluctuating arid/semi-arid climate prevailed across the Atacama Desert until between 4 and 3 Ma, climatic conditions that are thought to be favourable for supergene enrichment. The balance between uplift, erosion, burial and sufficient water supply to promote enrichment is complex. This suggests that a simple model for controlling supergene enrichment is unlikely to be widely applicable in northern Chile. General models that involve climatic desiccation at 14 Ma related to rainshadow development and/or the presence of an ancestral cold-upwelling Humboldt Current are not supported by the available geological evidence. The integration of disparate sedimentological, geomorphological and supergene age data will be required to fully understand the controls on and distribution of supergene oxidation and enrichment in the Central Andes.     

中甸弧雪鸡坪斑岩铜矿含矿斑岩锆石SHRIMP U-Pb年代学及Hf同位素特征

长期以来,关于雪鸡坪斑岩铜矿的成岩成矿时代具有很大的争议。为了限定成矿作用开始的时限,本文选择代表成矿前岩浆岩的绢英岩化带内含矿斑岩进行锆石SHRIMP年代学测试,获得了215.2±1.9Ma的成岩年龄,说明雪鸡坪斑岩铜矿形成于215Ma之后。锆石Hf同位素测试结果显示岩浆主要来源于地幔源区,但是锆石Hf同位素分布不均匀,8颗锆石εHf（t）的结果分布于1.1～2.1,二阶段模式年龄平均值为1150Ma,两颗锆石εHf（t）值为7.4和6.0,对应的二阶段模式年龄分别为778Ma和869Ma,暗示存在两种不同的岩浆源区,可能发生过岩浆混合作用,但需进一步的研究证实。区域同位素年代学对比结果表明,215Ma左右的岩浆活动是中甸弧主要的控制斑岩铜矿成矿的热事件。     

Oxygen isotope composition of syngenetic inclusions in diamond from the Finsch Mine,RSA

Oxygen isotope data have been obtained for silicate inclusions in diamonds, and similar associated minerals in peridotitic and eclogitic xenoliths from the Finsch kimberlite by laser-fluorination. Oxygen isotope analyses of syngenetic inclusions weighing 20–400 μg have been obtained by laser heating in the presence of ClF₃. ¹⁸O/¹⁶O ratios are determined on oxygen converted to CO₂ over hot graphite and, for samples weighing less than 750 μg (producing <12 μmoles O₂) enhanced CO production in the graphite reactor causes a systematic shift in both δ¹³C and δ¹⁸O that varies as a function of sample weight. A “pressure effect” correction procedure, based on the magnitude of δ¹³C (CO₂) depletion relative to δ¹³C (graphite), is used to obtain corrected δ¹⁸O values for inclusions with an accuracy estimated to be ±0.3‰ for samples weighing 40 μg.Syngenetic inclusions in host diamonds with similar δ¹³C values (−8.4‰ to −2.7‰) have oxygen isotope compositions that vary significantly, with a clear distinction between inclusions of peridotitic (+4.6‰ to +5.6‰) and eclogitic paragenesis (+5.7‰ to +8.0‰). The mean δ¹⁸O composition of olivine inclusions is indistinguishable from that of typical peridotitic mantle (5.25 ± 0.22‰) whereas syngenetic purple garnet inclusions possess relatively low δ¹⁸O values (5.00 ± 0.33‰). Reversed oxygen isotope fractionation between olivine and garnet in both diamond inclusions and diamondiferous peridotite xenoliths suggests that garnet preserves subtle isotopic disequilibrium related to genesis of Cr-rich garnet and/or exchange with the diamond-forming fluid. Garnet in eclogite xenoliths in kimberlite show a range of δ¹⁸O values from +2.3‰ to +7.3‰ but garnets in diamondiferous eclogites and as inclusions in diamond all have values >4.7‰.     

Subduction cycling of volatiles and trace elements through the Central American volcanic arc: evidence from melt inclusions

Compositions of melt inclusions in olivine (Fo_90-64) from 11 localities in Guatemala, Nicaragua and Cost Rica along the Central American Volcanic Arc are used to constrain combined systematics of major and trace elements and volatile components (H₂O, S, Cl, F) in parental melts and to estimate volcanic fluxes of volatile elements. The melt inclusions cover the entire range of compositions reported for whole rocks from Central America. They point to large heterogeneity of magma sources on local and regional scales, related to variable contributions of diverse crustal (from the subducting and overriding plates) and mantle (from the wedge and incoming plate) components involved in magma genesis. Water in parental melts correlates inversely with Ti, Y and Na and positively with Ba/La and B/La (with the exception of Irazú Volcano), which indicates mantle melting fluxed by Ba-, B- and H₂O-rich, possibly, serpentinite-derived fluid beneath most parts of the arc. Different components with melt-like characteristics (high LREE, La/Nb and probably also Cl, S and F and low Ba/La) control the geochemical peculiarities of Guatemalan and Costa Rican magmas. The composition of parental magmas together with published data on volcanic volumes and total SO₂ flux from satellite measurements are used to constrain fluxes of volatile components and to estimate total magmatic flux in Central America. We found that volcanic flux accounts for only 13% of total magmatic and volatile fluxes. The remaining 87% of magmas remained in the lithosphere to form cumulates (∼39%) and intrusives (∼48%). The intrusive fraction of magmatic flux may be significantly larger beneath Nicaragua compared to Costa Rica. Interestingly, total fluxes of magmas and volatiles in Central America are quite similar to the global average estimates. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

西藏拉抗俄斑岩铜钼矿床流体包裹体研究

西藏冈底斯成矿带拉抗俄斑岩铜钼矿床位于西藏特提斯构造域拉萨地块东段中南部,是近年来青藏高原地质大调查项目评价的重点矿床之一。文章在钻孔地质编录的基础上,依据矿物组合、脉体穿切关系的不同,划分了3个成矿阶段:早阶段、中阶段以及晚阶段,成矿中阶段为主成矿阶段。根据包裹体室温下的相态充填度特征以及是否含有子矿物,可将其分为3大类:液相包裹体(Ⅰ)、气相包裹体(Ⅱ)和含子晶多相包裹体(Ⅲ)。成矿早阶段流体包裹体主要为Ⅰ、Ⅱ和Ⅲ类包裹体,均一温度集中在260~400℃之间,w(Na Cleq)为2.1%~39.4%;成矿中阶段的流体包裹体主要为Ⅰ、Ⅱ和Ⅲ类包裹体,具有典型的沸腾包裹体组合,均一温度集中在280~360℃,w(Na Cleq)为2.2%~37.1%;成矿晚阶段流体包裹体主要为Ⅰ类包裹体,均一温度集中在220~280℃,w(Na Cleq)为3.6%~5.6%,显示包裹体均一温度及盐度呈递减趋势。成矿流体是中高温、中高盐度,且富含成矿元素的Na Cl-H_2O体系流体。矿床形成的压力为(100±10)MPa,形成深度为(3.7±0.4)km。激光拉曼探针分析结果表明,流体包裹体液相成分主要为H_2O,气相成分含有CO_2;子矿物有黄铜矿、磁铁矿、赤铁矿、石膏、黄铁矿、金红石、长石等。成矿早阶段,岩浆房发生流体出溶;成矿中阶段,岩浆流体发生减压沸腾和不混溶作用。综上所述,温度降低、压力减小、pH值的增加以及氧化还原电位的变化是造成拉抗俄矿床成矿元素沉淀的主要因素。     

川西甲基卡花岗伟晶岩型锂矿床中熔体、流体包裹体固相物质研究

川西甲基卡二云母花岗岩和伟晶岩内发育大量原生熔体包裹体和富晶体流体包裹体。为了查明甲基卡成矿熔体、流体性质与演化特征,运用激光拉曼光谱和扫描电镜鉴定了甲基卡花岗伟晶岩型锂矿床中二云母花岗岩及伟晶岩脉不同结构带内的原生熔体、流体包裹体的固相物质。分析结果表明,甲基卡二云母花岗岩石英内熔体包裹体的矿物组合为磷灰石+白云母、白云母+钠长石、白云母+石墨;伟晶岩绿柱石内富晶体流体包裹体的矿物组合主要为刚玉、富铝铁硅酸盐+刚玉+锂辉石、锂辉石+石英+锂绿泥石;伟晶岩锂辉石内富晶体流体包裹体的矿物组合主要为磷灰石、锡石、磁铁矿、石英+钠长石+锂绿泥石、萤石、富钙镁硅酸盐+富铁铝硅酸盐+富铁硅酸盐+石英;花岗岩浆熔体与伟晶岩浆熔体(流体)具有一定的差异,成矿熔体、流体成分总体呈现出碱质元素(Na、Si、Al)、挥发分(F、P、CO_2)含量增高及基性元素(Fe、Mg、Ca)降低的特征;包裹体中子矿物与主矿物的化学成分具有一定的差别,揭示出伟晶岩熔体(流体)存在局部岩浆分异作用,具不混溶性及非均匀性。因此认为,伟晶岩熔浆(流体)为岩浆分异与岩浆不混溶共同作用的产物,挥发分含量的增高(F、P、CO_2)使伟晶岩能够与稀有金属组成各类络合物或化合物,这对于稀有金属成矿起到了至关重要的作用。     

黑龙江省岔路口斑岩钼矿床流体包裹体和稳定同位素特征

岔路口超大型斑岩钼矿床位于大兴安岭北部,是目前中国东北地区最大的钼矿床,矿体赋存于中酸性杂岩体及侏罗系火山-沉积岩内,其中花岗斑岩、石英斑岩、细粒花岗岩与钼矿化关系密切.流体包裹体研究表明,岔路口矿床主要发育富液两相包裹体、富气两相包裹体和含子矿物多相包裹体.花岗斑岩石英斑晶中流体包裹体的形成温度集中在230 ～ 440℃和470～510℃两个温度区间,盐度分别介于0.7％ ～ 53.7％ NaCl eqv和6.2％～61.3％ NaCl eqv两个区间;成矿早阶段钾长石-石英-磁铁矿脉中流体包裹体的形成温度集中在320～440℃、盐度介于4.2％ ～ 52.3％NaCl eqv;成矿中阶段石英-辉钼矿脉和角砾岩中流体包裹体的形成温度集中在260～410℃、盐度介于0.4％～52.3％ NaCleqv;成矿晚阶段石英-萤石-方铅矿-闪锌矿脉中流体包裹体的形成温度集中在170～320℃、盐度介于0.5％ ～ 11.1％ NaCleqv.成矿流体具高温、高盐度及高氧逸度的特征,总体上属于富F的H2O-NaCl±CO2体系.成矿流体的δ 18Ow值为-4.5‰～3.2‰,δDw值为-138‰～-122‰,表明成矿流体为岩浆水与雨水的混合流体.金属硫化物的δ34S值介于-1.9‰～+3.6‰,均值为+1.6‰,表明成矿物质主要来自深源岩浆.多期次的流体沸腾作用是该矿床的主要成矿机制.     

Genesis of melilitolite from Colle Fabbri: inferences from melt inclusions

Melilite and wollastonite from the Colle Fabbri stock contain silicate melt and silicate-carbonate inclusions. The homogenization temperatures of silicate inclusions are within the magmatic temperature range of mantle ultrabasic melts: about 1,320?±?15 °С. Their composition is melilititic and evolves to the composition of leucite tephrite and phonolite. The composition of silicate-carbonate inclusions are high SiO₂, Ca-rich, enriched in alkalies and are similar to that of inclusions of carbonatite melts in the minerals of melilitolites of other intrusive ultramafic complexes. They are also similar to the compositions of metasomatized travertine covering the melilitolite stock. The presence of primary silicate and silicate-carbonate inclusions evidences that the melilitite magma from which melilitolites of Colle Fabbri crystallized was associated with carbonatite liquid. This liquid was highly fluidized, mobile and aggressive. Actively interacting with overlying travertine, the liquid enriched them with alkalies, aluminosilicates and incompatible elements, which resulted in the equalization of their compositions. Heterogeneous compositional dominions were formed at the contact between melilitolite and wall pelites. In the minerals of these contact facies high-Si melt inclusions of varying composition have been observed. Their occurrence is related to the local assimilation by the high-temperature melilitite magma of pelitic country rocks. The content of incompatible elements in melilitite melts and melilitolites is higher than the mantle norm and they have peculiar indicator ratios, spectra, Eu/Eu^* ratio, which suggest a peculiar mantle source.     

西华山黑钨矿-石英脉绿柱石中熔融包裹体的成分

借助高温高压技术与电子探针分析,首次获得黑钨矿-石英脉绿柱石中晶质熔融包裹体的主要成分。熔融包裹体的成分主要是SiO2和Al2O3(分别平均为70.72%和13.94%)及少量K2O(2.0%),其他氧化物含量甚低,并且含有大量的挥发分(主要是H2O,达11.56%)。激光拉曼光谱分析表明,熔融包裹体液相中CO2、H2S等含量不高(分别为7.8%和4.3%),气相部分主要是一些还原性气体。熔融包裹体代表HF-H2O-花岗岩体系结晶分异最后阶段残余熔融体的成分,证实脉钨矿床的成矿流体不是单一的热水溶液,而是硅酸盐熔体与超临界流体共存的岩浆-热液过渡性流体,其成矿作用始于岩浆-热液过渡阶段。     

The late Cretaceous lithospheric mantle beneath the Central Andes: Evidence from phase equilibria and composition of mantle xenoliths

Temperature estimates and chemical composition of mantle xenoliths from the Cretaceous rift system of NW Argentina (26°S) constrain the rift evolution and chemical and physical properties of the lithospheric mantle at the eastern edge of the Cenozoic Andean plateau. The xenolith suite comprises mainly spinel lherzolite and subordinate pyroxenite and carbonatized lherzolite. The spinel lherzolite xenoliths equilibrated at high-T (most samples >1000 °C) and P below garnet-in. The Sm–Nd systematics of compositionally unzoned clino- and orthopyroxene indicate a Cretaceous minimum age for the high-T regime, i.e., the asthenosphere/lithosphere thermal boundary was at ca. 70 km depth in the Cretaceous rift. Major elements and Cr, Ni, Co and V contents of the xenoliths range between values of primitive and depleted mantle. Calculated densities based on the bulk composition of the xenoliths are <3280 kg/m³ for the estimated P–T conditions and indicate a buoyant, stable upper mantle lithosphere. The well-equilibrated metamorphic fabric and mineral paragenesis with the general lack of high-T hydrous phases did not preserve traces of metasomatism in the mantle xenoliths. Late Mesozoic metasomatism, however, is obvious in the gradual enrichment of Sr, U, Th and light to medium REE and changes in the radiogenic isotope composition of an originally depleted mantle. These changes are independent of the degree of depletion evidenced by major element composition. ¹⁴³Nd/¹⁴⁴Nd_i ratios of clinopyroxene from the main group of xenoliths decrease with increasing Nd content from >0.5130 (depleted samples) to ca. 0.5127 (enriched samples). ⁸⁷Sr/⁸⁶Sr_i ratios (0.7127–0.7131, depleted samples; 0.7130–0.7134, enriched samples) show no variation with variable Sr contents. Pb_i isotope ratios of the enriched samples are rather radiogenic (²⁰⁶Pb/²⁰⁴Pb_i 18.8–20.6, ²⁰⁷Pb/²⁰⁴Pb_i 15.6–15.7, ²⁰⁸Pb/²⁰⁴Pb_i 38.6–47) compared with the Pb isotope signature of the depleted samples. The large scatter and high values of ²⁰⁸Pb/²⁰⁴Pb_i ratios of many xenoliths indicates at least two Pb sources that are characterized by similar U/Pb but by different Th/Pb ratios. The dominant mantle type in the investigated system is depleted mantle according to its Sr and Nd isotopic composition with relatively radiogenic Pb isotope ratios. This mantle is different from the Pacific MORB source and old subcontinental mantle from the adjacent Brazilian Shield. Its composition probably reflects material influx into the mantle wedge during various episodes of subduction that commenced in early Paleozoic or even earlier. Old subcontinental mantle was already replaced in the Paleozoic, but some inheritance from old mantle lithosphere is represented by rare xenoliths with isotope signatures indicating a Proterozoic origin.