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1.
Nb,Ta的硅酸盐地球质量不平衡问题争论由来已久,备受关注。近年来研究发现,含金红石的榴辉岩Nb/Ta往往高于球粒陨石值(Nb/Ta=17.5),暗示其可能是平衡地球Nb亏损的独立储库。而洋壳玄武岩部分熔融实验表明Ta比Nb更倾向进入金红石晶格,这意味着作为俯冲洋壳部分熔融残留相的榴辉岩Nb/Ta不可能高于原岩。为了解释地质观察和实验结果之间的矛盾,系统分析了中国大陆科学钻探工程(CCSD)主孔、先导孔及附近地表榴辉岩的矿物微量元素。结果发现:榴辉岩中的Nb,Ta主要存在于金红石之中,其他矿物中含量极少;Nb,Ta之间存在着强烈分异(Nb/Ta=5.3～96.2),并总体上具有超球粒陨石的特征;韭闪石和多硅白云母的Nb/Ta平均分别为48.6,21.8,显示了很强的Nb,Ta分异能力;其他矿物如石榴石、绿辉石、绿帘石、磷灰石等的Nb、Ta含量及Nb/Ta都很低,对Nb-Ta分异不造成影响。认为导致Nb-Ta分异的不是金红石,而应出现在洋壳俯冲过程中金红石相出现之前的脱水和部分熔融阶段。富含Ti的角闪石(韭闪石)和白云母可能对Nb-Ta分异起到了决定性的作用。等金红石相出现之后,由于其对Nb,Ta的绝对控制作用,此前阶段的分异结果便被固定在金红石中而继承下来。因此,含金红石的榴辉岩常常表现出超球粒陨石Nb/Ta的特征,与金红石不能有效地分异Na,Ta的实验结果之间并不矛盾。在不均匀的上地幔中含金红石的榴辉岩是可能的超球粒陨石Nb/Ta储库之一。  相似文献   

2.
This paper reports detailed analyses of Nb and Ta concentrations of 19 eclogite samples and their principal mineral constituents from the main drill hole of the Chinese Continental Scientific Drilling Project (CCSD) and nearby outcrops. We observe highly fractionated and overall suprachondritic Nb/Ta values in minerals, e.g., rutile (4.8–87), titanite (12–62) and amphibole (2.0–67). Amphiboles in amphibolites (retrograded from eclogite) can be classified into two groups: a low Nb/Ta group that bears higher Al contents and is thus of higher pressure origin, and a high Nb/Ta, lower pressure group. The former group was likely formed during subduction; the latter may have formed during exhumation in the presence of rutile and titanite. The significant Nb/Ta fractionation in rutile and other minerals may reflect early dehydration of the subducted slab at shallow depths before the formation of rutile, which occurs at depths ≥50 km. The dehydration, with amphiboles existing as the main Nb–Ta-bearing phase, would lead to Nb/Ta fractionation, i.e., forming subchondritic Nb/Ta ratios in the released fluids and, complementarily, suprachondritic Nb/Ta ratios in the residual phases. While a large proportion of the fluids may escape from the slab to the mantle wedge, considerable amounts of the fluids can be retained in hydrous minerals within the descending slab, thus forming hydrated cold eclogites with subchondritic Nb/Ta characteristics. As subduction continues to depths over 50 km, rutile appears and consequently controls the Nb–Ta budget. In the presence of rutile, melting of the hydrated cold eclogites with very low Nb/Ta ratios would form magmas with negative Nb, Ta anomalies and subchondritic Nb/Ta. Further dehydration of the continuously descending slab results in even more fractionated Nb/Ta ratios in subsequently released fluids and residues, providing a feasible explanation for the large Nb/Ta variation observed in the modern arc magmas and residual eclogites.  相似文献   

3.
山东五莲七宝山地区早白垩世的碱性侵入岩位于火山机构的中央部位,该岩体具有高Ba-Sr含量、高Nb/Ta和Zr/Hf比、低Ti/Eu比等特征,前人的研究指出其起源于岩石圈地幔。然而,该侵入体中的岩性与成分变化所反映的深部动力学过程尚未理清。本文对七宝山二长辉长岩和两类辉石二长岩开展了详细的矿物学和岩石地球化学研究,识别出钠质和钾质两类钾玄质岩石系列。该套碱性中基性侵入岩具有富碱、富轻稀土和富大离子亲石元素的特征,同时具有高的(La/Yb)N和(Gd/Yb)N值。碱性侵入岩中两类单斜辉石和两类斜长石作为再循环晶,记录了不同批次岩浆/熔体的混合,这些矿物组分和全岩成分共同约束了岩浆的起源与演化过程。结合前人的地球化学资料,本文指出七宝山碱性侵入岩的源区是曾受到沉积物交代的富集地幔,源区存在金云母脉体和角闪石脉体。上述脉体连同周围的地幔橄榄岩共同发生部分熔融,形成原生的碱性熔体。七宝山碱性侵入岩显示高的Nb/Ta和Zr/Hf比、低的Ti/Eu比,同时在微量元素蜘蛛图上呈现Ti*和Hf*的负异常,结合高稀土单斜辉石平衡熔体的属性,共同指示了碳酸盐熔体组分对该套碱性侵入岩的形成发挥了重要作用。钠质系列与钾质系列岩石反映了源区富碱矿物相类型相对贡献量的差异,即钠质为主的碱性岩反映源区角闪石的贡献更大,而钾质为主的碱性岩反映源区金云母的贡献占优势。此外,碱性侵入岩中的钾质系列具有异常高的Rb-Zr-Hf-U含量,很可能反映了源区在部分熔融过程中热液锆石熔解后形成的熔体加入到了钾质岩浆房内。本研究强调了碳酸盐熔体组分对高Nb/Ta碱性中基性的形成发挥着重要作用,亦强调了热液锆石的熔解加入导致岩浆具有高Zr-Hf-U含量的特征。  相似文献   

4.
TTG的Nb/Ta比值以及Nb、Ta相对于La(代表LILE)的亏损取决于部分熔融体系中金红石、角闪石作为残留相矿物存在与否.本研究采用金红石和低Mg#角闪石的微量元素分配系数模拟部分熔融过程中Nb-Ta-La的分馏.模拟结果表明:如果与TTG熔体平衡的残留相是不含金红石的石榴角闪岩,熔体Nb/Ta比值低于源岩但Ta含...  相似文献   

5.
The formation of titanite coronae after rutile is common in retrograde high-to ultrahigh-pressure meta-mafic rocks, which provides a good opportunity to address the geochemical behavior of HFSE in crustal environments. In the Sumdo eclogite, titanite occurs either as a corona around rutile grains or as semi-continuous veins cross-cutting the major foliation, whereas rutile grains occur either as inclusions in garnet or omphacite or as a relict core surrounded by titanite. Textural relationships ...  相似文献   

6.
Subduction zone geochemistry   总被引：1，自引：0，他引：1  
Crustal recycling at convergent plate boundaries is essential to mantle heterogeneity.However,crustal signatures in the mantle source of basaltic rocks above subduction zones were primarily incorporated in the form of liquid rather than solid phases.The physicochemical property of liquid phases is determined by the dehydration behavior of crustal rocks at the slab-mantle interface in subduction channels.Because of the significant fractionation in incompatible trace elements but the full inheritance in radiogenic isotopes relative to their crustal sources,the production of liquid phases is crucial to the geochemical transfer from the subducting crust into the mantle.In this process,the stability of specific minerals in subducting crustal rocks exerts a primary control on the enrichment of given trace elements in the liquid phases.For this reason,geochemically enriched oceanic basalts can be categorized into two types in terms of their trace element distribution patterns in the primitive mantle-normalized diagram.One is island arc basalts(IAB),showing enrichment in LILE,Pb and LREE but depletion in HFSE such as Nb and Ta relative to HREE,The other is ocean island basalts(OIB),exhibiting enrichment in LILE and LREE,enrichment or non-depletion in HFSE but depletion in Pb relative to HREE.In either types,these basalts show the enhanced enrichment of LILE and LREE with increasing their incompatibility relative to normal mid-ocean ridge basalts(MORB).The thermal regime of subduction zones can be categorized into two stages in both time and space,The first stage is characterized by compressional tectonism at low thermal gradients.As a consequence,metamorphic dehydration of the subducting crust prevails at forearc to subarc depths due to the breakdown of hydrous minerals such as mica and amphibole in the stability field of garnet and rutile,resulting in the liberation of aqueous solutions with the trace element composition that is considerably enriched in LILE,Pb and LREE but depleted in HFSE and HREE relative to normal MORB.This provides the crustal signature for the mantle sources of IAB.The second stage is indicated by extensional tectonism at high thermal gradients,leading to the partial melting of metamorphically dehydrated crustal rocks at subarc to postarc depths.This involves not only the breakdown of hydrous minerals such as amphibole,phengite and allanite in the stability field of garnet but also the dissolution of rutile into hydrous melts.As such,the hydrous melts can acquire the trace element composition that is significantly enriched in LILE,HFSE and LREE but depleted in Pb and HREE relative to normal MORB,providing the crustal signature for the mantle sources of OIB.In either case,these liquid phases would metasomatize the overlying mantle wedge peridotite at different depths,generating ultramafic metasomatites such as serpentinized and chloritized peridotites,and olivine-poor pyroxenites and hornblendites.As a consequence,the crustal signatures are transferred by the liquid phases from the subducting slab into the mantle.  相似文献   

7.
《International Geology Review》2012,54(12):1506-1522
Garnet orthopyroxenites from Maowu (Dabieshan orogen, eastern China) were formed from a refractory harzburgite/dunite protolith. They preserve mineralogical and geochemical evidence of hydration/metasomatism and dehydration at the lower edge of a cold mantle wedge. Abundant polyphase inclusions in the cores of garnet porphyroblasts record the earliest metamorphism and metasomatism in garnet orthopyroxenites. They are mainly composed of pargasitic amphibole, gedrite, chlorite, talc, phlogopite, and Cl-apatite, with minor anhydrous minerals such as orthopyroxene, sapphirine, spinel, and rutile. Most of these phases have high XMg, NiO, and Ni/Mg values, implying that they probably inherited the chemistry of pre-existing olivine. Trace element analyses indicate that polyphase inclusions are enriched in large ion lithophile elements (LILE), light rare earth elements (LREE), and high field strength elements (HFSE), with spikes of Ba, Pb, U, and high U/Th. Based on the P–T conditions of formation for the polyphase inclusions (?1.4 GPa, 720–850°C), we suggest that the protolith likely underwent significant hydration/metasomatism by slab-derived fluid under shallow–wet–cold mantle wedge corner conditions beneath the forearc. When the hydrated rocks were subducted into a deep–cold mantle wedge zone and underwent high-pressure–ultrahigh-pressure (HP–UHP) metamorphism, amphibole, talc, and chlorite dehydrated and garnet, orthopyroxene, Ti-chondrodite, and Ti-clinohumite formed during prograde metamorphism. The majority of LILE (e.g. Ba, U, Pb, Sr, and Th) and LREE were released into the fluid formed by dehydration reactions, whereas HFSE (e.g. Ti, Nb, and Ta) remained in the cold mantle wedge lower margin. Such fluid resembling the trace element characteristics of arc magmas evidently migrates into the overlying, internal, hotter part of the mantle wedge, thus resulting in a high degree of partial melting and the formation of arc magmas.  相似文献   

8.
金红石边缘形成榍石冠状边结构在变质中-基性岩中普遍存在,是金红石与退变质流体携带的SiO_2与CaO作用的结果,反应形成的榍石微量元素特征受到金红石和流体的共同影响。雅鲁藏布江缝合带中角闪岩LZ06-04在抬升过程经历近等温降压退变质作用,石榴子石分解导致同一样品中含石榴子石部分与不含石榴子石部分的退变质流体成分的差异。两种流体分别与金红石反应,对应形成的榍石具有相似的Nb、Ta含量和Nb/Ta比值特征,但截然不同的REE特征。榍石的Nb、Ta来源于金红石,残余金红石与含水流体再平衡Nb、Ta的分配系数增大,且D_(Nb)~(Rt/Fluid)≥D_(Ta)~(Rt/Fluid);虽然Nb和Ta在含水流体中都表现为不活动元素,但相对于Nb,Ta在含水流体中活动性较高。榍石的Zr-Hf体系特征受到锆石、石榴子石等矿物的综合影响,并且Zr-Hf在含水流体中表现出比Nb-Ta更高的活动性。榍石的REE特征受流体中REE特征、榍石与流体配分系数以及共生矿物的影响。在岩浆或变质体系,榍石形成过程中,REE富集矿物(如石榴子石、锆石、褐帘石、独居石、磷灰石等)形成或分解将影响榍石的REE分布特征或形成REE环带结构。含水流体中金红石退变质形成榍石反应的进行受流体中TiO_2、CaO和SiO_2活度的影响。因此榍石常见于钙碱性岩浆岩、富Ca基性变质岩和矽卡岩中。流体中CaO活度的变化影响榍石的形成,进而影响Ti、Nb、Ta在流体中的运移能力。俯冲板片产生流体在交代上覆富Ca地幔楔物质过程中形成榍石残留同样可以造成部分熔融体具有亏损HFSE特征。  相似文献   

9.
A wide range of trace elements have been analysed in mantle xenoliths (whole rocks, clinopyroxene and amphibole separates) from alkaline lavas in the Eastern Carpathians (Romania), in order to understand the process of metasomatism in the subcontinental mantle of the Carpatho-Pannonian region. The xenoliths include spinel lherzolites, harzburgites and websterites, clinopyroxenites, amphibole veins and amphibole clinopyroxenites. Textures vary from porphyroclastic to granoblastic, or equigranular. Grain size increases with increasing equilibrium temperature of mineralogical assemblages and results from grain boundary migration. In peridotites, interstitial clinopyroxenes (cpx) and amphiboles resulted from impregnation and metasomatism of harzburgites or cpx-poor lherzolites by small quantities of a melt I with a melilitite composition. Clinopyroxenites, amphibole veins and amphibole clinopyroxenites are also formed by metasomatism as a result of percolation through fracture systems of large quantities of a melt II with a melanephelinite composition. These metasomatic events are marked by whole-rock enrichments, relative to the primitive mantle (PM), in Rb, Th and U associated in some granoblastic lherzolites and in clinopyroxene and amphibole veins with enrichments in LREE, Ta and Nb. Correlations between major element whole-rock contents in peridotites demonstrate that the formation of interstitial amphibole and clinopyroxene induced only a slight but variable increase of the Ca/Al ratio without apparent modifications of the initial mantle composition. Metasomatism is also traced by enrichments in the most incompatible elements and the LREE. The Ta, Nb, MREE and HREE contents remained unchanged and confirm the depleted state of the initial but heterogeneous mantle. Major and trace element signature of clinopyroxene suggests that amphibole clinopyroxenites and some granoblastic lherzolites have been metasomatized successively by melts I and II. Both melts I and II were Ca-rich and Si-poor, somewhat alkaline (Na > K). Melt I differed from melt II in having higher Mg and Cr contents offset by lower Ti, Al, Fe and K contents. Both were highly enriched in all incompatible trace elements relative to primitive mantle, showing positive anomalies in Rb, Ba, Th, Sr and Zr. They contrasted by their Ta, Nb and LREE contents, lower in melt I than in melt II. Melts I and II originate during a two-stage melting event from the same source at high pressure and under increasing temperature. The source assemblage could be that of a metasomatized carbonated mantle but was more likely that of an eclogite of crustal affinity. Genetic relationships between calc-alkaline and alkaline lavas from Eastern Carpathians and these melts are thought to be only indirect, the former originating from partial melting of mantle sources respectively metasomatized by the melts I and II. Received: 17 March 1997 / Accepted: 14 July 1997  相似文献   

10.
Fractionation between Nb and Ta, elements generally regarded as geochemical ‘identical twins’, is a key to deciphering the formation of the continental crust (CC). Here we show that Nb/Ta of rutile grains in eclogitic rocks from the Chinese Continental Scientific Drilling (CCSD) project are remarkably heterogeneous but overall subchondritic at core depths of 100–700 m, and are less variable and mainly suprachondritic at core depths of 700–3025 m, indicating clear Nb/Ta fractionation across a subducted slab. To understand the potential mechanism of Nb/Ta fractionation within the subducted plate, we analysed by laser ablation ICPMS a thermal migration experiment in which a wet andesite was placed in a large thermal gradient (300°C/cm with ends ranging from 950–350°C) at 0.5Gpa. Results show that Nb, Ta and Ti, driven by the thermal gradient, preferentially migrate by diffusion through supercritical fluids into the cooler end of the experiment (at 650–350°C). Due to contrasting Nb and Ta thermal migration patterns, dramatic fractionation between Nb, Ta, and Ti took place in the cooler end. Experimental results are consistent with the measured Nb, Ta in rutile from CCSD drillhole samples. We consider that major fractionation between Nb, Ta must occur before rutile appears, most likely during the prograde blueschist to amphibole–eclogite transformation, when Ti is also mobile. Before rutile appears, partitioning between Ti‐rich dominant minerals such as amphiboles and fluids in the hotter region where dehydration preferentially occurs, produces Nb–Ta–Ti‐rich fluids with subchondritic Nb/Ta, and dehydration residues with suprachondritic Nb/Ta. Meanwhile, owing to evolution of the thermal gradient within the subducting slab, thermal migration of Nb, Ta, and Ti in aqueous fluids result in Nb, Ta, and Ti enrichment in the cooler region and depletion in the hotter region. As a result of high‐pressure metamorphism, hydrous rutile‐rich eclogites with overall subchondritic Nb/Ta form in the cooler region, whereas relatively anhydrous rutile‐poor eclogites with suprachondritic Nb/Ta form in the hotter region. Subsequently, partial melting of hydrous rutile‐rich eclogites with initial subchondritic Nb/Ta at deeper levels transfers overall subchondritic Nb/Ta coupled with Nb, Ta, and Ti depletion characteristics to the CC, leaving dry rutile‐poor eclogites with suprachondritic Nb/Ta and rutile‐rich residual eclogites with overall, heterogeneous subchondritic Nb/Ta as a complementary reservoir to the CC.  相似文献   

11.
Trace element partition coefficients (D's) for up to 13 REE, Nb, Ta, Zr, Hf, Sr and Y have been determined by SIMS analysis of seven garnets, four clinopyroxenes, one orthopyroxene and one phlogopite crystallized from an undoped basanite and a lightly doped (200 ppm Nb, Ta and Hf) quartz tholeiite. Experiments were conducted at 2–7.5 GPa, achieving near-liquidus crystallization at relatively low temperatures of 1080–1200°C under strongly hydrous conditions (5–27 wt.% added water). Garnet and pyroxene DREE show a parabolic pattern when plotted against ionic radius, and conform closely to the lattice strain model of Blundy and Wood (Blundy, J.D., Wood, B.J., 1994. Prediction of crystal–melt partition coefficients from elastic moduli. Nature 372, 452–454). Comparison, at constant pressure, between hydrous and anhydrous values of the strain-free partition coefficient (D0) for the large cation sites of garnet and clinopyroxene reveals the relative importance of temperature and melt water content on partitioning. In the case of garnet, the effect of lower temperature, which serves to increase D0, and higher water content, which serves to decrease D0, counteract each other to the extent that water has little effect on garnet–melt D0 values. In contrast, the effect of water on clinopyroxene–melt D0 overwhelms the effect of temperature, such that D0 is significantly lower under hydrous conditions. For both minerals, however, the lower temperature of the hydrous experiments tends to tighten the partitioning parabolas, increasing fractionation of light from heavy REE compared to anhydrous experiments.

Three sets of near-liquidus clinopyroxene–garnet two-mineral D values increase the range of published experimental determinations, but show significant differences from natural two-mineral D's determined for subsolidus mineral pairs. Similar behaviour is observed for the first experimental data for orthopyroxene–clinopyroxene two-mineral D's when compared with natural data. These differences are in large part of a consequence of the subsolidus equilibration temperatures and compositions of natural mineral pairs. Great care should therefore be taken when using natural mineral–mineral partition coefficients to interpret magmatic processes.

The new data for strongly hydrous compositions suggest that fractionation of Zr–Hf–Sm by garnet decreases with increasing depth. Thus, melts leaving a garnet-dominated residuum at depths of about 200 km or greater may preserve source Zr/Hf and Hf/Sm. This contrasts with melting at shallower depths where both garnet and clinopyroxene will cause Zr–Hf–Sm fractionation. Also, at shallower depths, clinopyroxene-dominated fractionation may produce a positive Sr spike in melts from spinel lherzolite, but for garnet lherzolite melting, no Sr spike will result. Conversely, clinopyroxene megacrysts with negative Sr spikes may crystallize from magmas without anomalous Sr contents when plotted on mantle compatibility diagrams. Because the characteristics of strongly hydrous silicate melt and solute-rich aqueous fluid converge at high pressure, the hydrous data presented here are particularly pertinent to modelling processes in subduction zones, where aqueous fluids may have an important metasomatic role.  相似文献   


12.
The transfer of fluid and elements from subducting crust to the overlying mantle wedge is a fundamental process affecting arc magmatism and the chemical differentiation of the Earth. While the production of fluid by breakdown of hydrous minerals is well understood, the liberation of trace elements remains generally unconstrained. In this paper, we evaluate the behaviour of trace elements during prograde metamorphism and dehydration using samples of high-pressure, low-temperature metamorphic rocks from New Caledonia. Samples examined include mafic and pelitic rock-types that range in grade from lawsonite blueschist to eclogite facies, and represent typical lithologies of subducting crust. Under lawsonite blueschist facies conditions, the low temperatures of metamorphism inhibit equilibrium partitioning between metamorphic minerals and allow for the persistence of igneous and detrital minerals. Despite this, the most important hosts for trace-elements include lawsonite, (REE, Pb, Sr), titanite (REE, Nb, Ta), allanite (LREE, U, Th), phengite (LILE) and zircon (Zr, Hf). At epidote blueschist to eclogite facies conditions, trace-element equilibrium may be attained and epidote (REE, Sr, Th, U, Pb), garnet (HREE), rutile (Nb, Ta), phengite (LILE) and zircon (Zr, Hf) are the major trace-element hosts. Chlorite, albite, amphibole and omphacite contain very low concentrations of the investigated trace elements. The comparison of mineral trace-element data and bulk-rock data at different metamorphic grades indicates that trace elements are not liberated in significant quantities by prograde metamorphism up to eclogite facies. Combining our mineral trace-element data with established phase equilibria, we show that the trace elements considered are retained by newly-formed major and accessory minerals during mineral breakdown reactions to depths of up to 150 km. In contrast, significant volumes of fluid are released by dehydration reactions. Therefore, there is a decoupling of fluid release and trace element release in subducting slabs. We suggest that the flux of trace elements from the slab is not simply linked to mineral breakdown, but results from complex fluid-rock interactions and fluid-assisted partial melting in the slab.Electronic Supplementary Material Supplementary material is available in the online version of this article at http://dx.doi.org/10.1007/s00410-003-0495-5.Editorial responsibility: J. Hoefs  相似文献   

13.
Selective enrichment or depletion in either Zr and Hf (HFSE4+)or Nb and Ta (HFSE5+) is a feature commonly observed in manymantle-derived melts and amphiboles occurring as either disseminatedminerals in mantle xenoliths and peridotite massifs or in veinassemblages cutting these rocks. The fractionation of Nb fromZr seen in natural mantle amphiboles suggests that their incorporationis governed by different crystal-chemical mechanisms. An extensiveset of new partitioning experiments between pargasite–kaersutiteand melt under upper-mantle conditions shows that HFSE incorporationand fractionation depends on amphibole major-element compositionand the presence or absence of dehydrogenation. Multiple regressionanalysis shows that Amph/LDNb/Zr is strongly dependent on themg-number of the amphibole as a result of a combination of amphiboleand melt structure effects, so that the following generalizationsapply: (1) high-mg-number amphiboles crystallized from unmodifiedmantle melts more easily incorporate Zr relative to Nb leadingto an increase of the Nb/Zr ratio in the residual melt; (2)low-mg-number amphiboles, such as those found in veins cuttingperidotites, may strongly deplete the residual melt in Nb andcause very low Nb/Zr in residual melts. Implications and applicationsto mantle environments are discussed. KEY WORDS: trace elements; high field strength elements; partition coefficients; amphibole; upper mantle  相似文献   

14.
The Ulaan Tolgoi massif of rare-metal (Ta, Nb, and Zr) granites was formed at approximately 300Ma in the Eastern Sayan zone of rare-metal alkaline magmatism. The massif consists of alkaline salic rocks of various composition (listed in chronologic order of their emplacement): alkaline syenite → alkaline syenite pegmatite → pantellerite → alkaline granite, including ore-bearing alkaline granite, whose Ta and Nb concentrations reach significant values. The evolution of the massif ended with the emplacement of trachybasaltic andesite. The rocks of the massif show systematic enrichment in incompatible elements in the final differentiation products of the alkaline salic magmas. The differentiation processes during the early evolution of the massif occurred in an open system, with influx of melts that contained various proportions of incompatible elements. The magma system was closed during the origin of the ore-bearing granites. Rare-metal granitoids in the Eastern Sayan zone were produced by magmas formed by interaction between mantle melts (which formed the mafic dikes) with crustal material. The mantle melts likely affected the lower parts of the crust and either induced its melting, with later mixing the anatectic and mantle magmas, or assimilated crustal material and generated melts with crustal–mantle characteristics. The origin of the Eastern Sayan zone of rare-metal alkaline magmatism was related to rifting, which was triggered by interaction between the Tarim and Barguzin mantle plumes. The Eastern Sayan zone was formed in the marginal part of the Barguzin magmatic province, and rare-metal magmas in it were likely generated in relation with the activity of the Barguzin plume.  相似文献   

15.
王丹  郭敬辉  马旭东 《岩石学报》2021,37(2):341-355
英云闪长岩-奥长花岗岩-花岗闪长岩(TTG)是地球早期大陆地壳最重要的组成部分。TTG的Nb/Ta比值变化不仅与它的成因相关,而且与早期构造环境和地壳分异过程关系紧密。本文选择阴山地块出露的TTG片麻岩及下地壳斜长角闪岩/麻粒岩包体作为研究对象,开展了寄主花岗闪长岩和同源镁铁质包体中的角闪石和黑云母的原位微区矿物的微量元素分析工作,以及TTG与非同源斜长角闪岩包体的全岩主微量元素分析工作。矿物化学研究结果表明,花岗闪长岩和同源镁铁质包体的角闪石具有相似的Mg#值,但是两者具有明显不同的Nb/Ta比值。镁铁质包体中的角闪石更富Cr、Ta,Nb/Ta比值为30~50;TTG岩石中的角闪石Cr和Ta含量偏低,但具有更高的Nb/Ta比值(38~70)。TTG和镁铁质包体中的角闪石Cr含量与Nb/Ta具有较好的负相关关系。全岩地球化学分析结果揭示,TTG片麻岩的具有高Nb/Ta比值(13~65,平均值31),斜长角闪岩和麻粒岩包体具有变化的Nb/Ta比值(10~56)。太古宙绿岩带中玄武质岩石的Nb/Ta平均值为~15,阴山地块斜长角闪岩和麻粒岩包体具有高的Nb/Ta比值,反映了这些代表基性下地壳的岩石经历了部分熔融作用或后期的交代作用,使其Nb/Ta比值发生改变。研究区具有高Nb/Ta比值的TTG可能来源于高Nb/Ta比值基性下地壳部分熔融,并继承了源区高Nb/Ta比值的特征。通过本文研究揭示,高Nb/Ta比值的TTG并非一定形成于俯冲带洋壳榴辉岩相部分熔融,下地壳富角闪石和黑云母的岩石部分熔融是形成高Nb/Ta比值TTG的一种重要途径。  相似文献   

16.
During the evolution of the Earth, distinct geochemical reservoirs with different Nb/Ta ratios have developed. Archean granitoids of the tonalite–trondhjemite–granodiorite (TTG) suite, which represent the Earth’s early continental crust, show larger Nb/Ta variations than any other Earth reservoir. This implies that significant Nb–Ta fractionation must have occurred during early crust formation, while the underlying mechanism behind is still unclear. Here, we present a new model on how Nb may be fractionated from Ta during partial melting of subducted oceanic crust. Our data show that Nb/Ta ratios in melts derived from rutile- and titanite-bearing eclogite are largely controlled by the modal relative abundances of rutile and titanite in the source. High modal ratios of titanite over rutile generate melts with very high Nb/Ta (>60), whereas low modal titanite/rutile produces melts with much lower Nb/Ta (≤30). Very low Nb/Ta (<16) occur when all Ti-phases are consumed at very high degrees of melting. As the modal ratio of titanite to rutile is a function of pressure, the Nb/Ta of melts is a function of melting depth. Our new model helps to explain the extreme variation of Nb/Ta observed in many TTGs and thus how Nb and Ta were fractionated during the early evolution of the Earth. Furthermore, the model also indicates that simple one-stage melting models for mafic crust are not sufficient to explain the formation of TTGs.  相似文献   

17.
Radiogenic isotopic dating and Lu–Hf isotopic composition using laser ablation-inductively coupled plasma-mass spectrometry(LA-ICP-MS)of the Wude basalt in Yunnan province from the Emeishan large igneous province(ELIP)yielded timing of formation and post-eruption tectonothermal event.Holistic lithogeochemistry and elements mapping of basaltic rocks were further reevaluated to provide insights into crustal contamination and formation of the ELIP.A zircon U–Pb age of 251.3±2.0 Ma of the Wude basalt recorded the youngest volcanic eruption event and was consistent with the age span of 251-263 Ma for the emplacement of the ELIP.Such zircons hadεHf(t)values ranging from7.3 to+2.2,identical to those of magmatic zircons from the intrusive rocks of the ELIP,suggesting that crust-mantle interaction occurred during magmatic emplacement,or crust-mantle mixing existed in the deep source region prior to deep melting.The apatite U–Pb age at 53.6±3.4 Ma recorded an early Eocene magmatic superimposition of a regional tectonothermal event,corresponding to the Indian–Eurasian plate collision.Negative Nb,Ta,Ti and P anomalies of the Emeishan basalt may reflect crustal contamination.The uneven Nb/La and Th/Ta values distribution throughout the ELIP supported a mantle plume model origin.Therefore,the ELIP was formed as a result of a mantle plume which was later superimposed by a regional tectonothermal event attributed to the Indian–Eurasian plate collision during early Eocene.  相似文献   

18.
Trace element compositions of submicroscopic inclusions in both the core and the coat of five coated diamonds from the Democratic Republic of Congo (DRC, formerly Zaire) have been analyzed by Laser Ablation Inductively Coupled Mass Plasma Spectrometry (LA-ICP-MS). Both the diamond core and coat inclusions show a general 2-4-fold enrichment in incompatible elements relative to major elements. This level of enrichment is unlikely to be explained by the entrapment of silicate mantle minerals (olivine, garnet, clinopyroxene, phlogopite) alone and thus submicroscopic fluid or glass inclusions are inferred in both the diamond coat and in the gem quality diamond core. The diamond core fluids have elevated High Field Strength Element (Ti, Ta, Zr, Nb) concentrations and are enriched in U relative to inclusions in the diamond coats and relative to chondrite. The core fluids are also moderately enriched in LILE (Ba, Sr, K). Therefore, we suggest that the diamond cores contain inclusions of silicate melt. However, the Ni content and Ni/Fe ratio of the trapped fluid are very high for a silicate melt in equilibrium with mantle minerals; high Ni and Co concentrations in the diamond cores are attributed to the presence of a sulfide phase coexisting with silicate melt in the diamond core inclusions. Inclusions in the diamond coat are enriched in LILE (U, Ba, Sr, K) and La over the diamond core fluids and to chondrite. The coats have incompatible element ratios similar to natural carbonatite (coat fluid: Na/Ba ≈0.66, La/Ta≈130). The coat fluid is also moderately enriched in HFSE (Ta, Nb, Zr) when normalized to chondritic Al. LILE and La enrichment is related to the presence of a carbonatitic fluid in the diamond coat inclusions, which is mixed with a HFSE-rich hydrous silicate fluid similar to that in the core. The composition of the coat fluid is consistent with a genetic link to group 1 kimberlite.  相似文献   

19.
对华北山东地区不同构造单元中生代白垩纪基性-中基性岩浆岩进行了系统的Re-Os同位素研究.侵入岩样品采自鲁西济南岩体、鲁中沂南岩体和胶东的观水岩墙群, 火山岩样品采自鲁西蒙阴、费县、方城青山群和鲁中安丘青山群.所有样品均以低Re(0.076×10-9~0.711×10-9)和Os(0.006×10-9~1.030×10-9)含量以及高放射成因Os同位素比值为特征, 其相应的初始187Os/188Os比值和γOs(t)值分别为0.131 6~0.529 1和4.30~319.00(安丘粗面安山岩分别高达1.463和1 060.000), 并具有较大变化范围(0.125~2.090 Ga)的Os同位素模式年龄.在Os-Nd和Os-Sr同位素关系图上, 这些样品分布于典型的岩石圈地幔与地壳端元组成之间, 显示壳-幔源岩浆混合特征.然而, 除1件观水岩体(MGS0610)和费县玄武岩之外, 各地质单元样品之间或所有的中生代岩浆岩作为整体, 样品的γOs(t)与(La/Ta)N和(Th/Nb)N比值间缺乏明显的相关关系, 说明样品的混源Os同位素并非来自岩浆作用过程中的地壳围岩混染.区内基性岩浆岩Os同位素模式年龄TMA明显小于古生代地幔橄榄岩包体的Re亏损模式年龄(TRD), 可能为地幔条件下源岩与再循环地壳物质发生交代作用后Re/Os比值升高所致.蒙阴高镁安山岩和沂南闪长岩在Yb-Re/Yb图解中大致位于中生代辉石岩包体与地壳端元之间, 也指示了下地壳拆沉后产生的熔体与地幔岩石可能发生了交代作用.蒙阴安山岩MMY-12(SiO2=56.4%)具有古老壳源特征的Os同位素模式年龄(2.090 Ga)、高Mg#(64.6)和高Os含量(0.089×10-9), 为这一解释提供了有力的佐证.   相似文献   

20.
Field evidence from the western Tianshan subduction complex in northwestern China indicates that the high field strength elements Ti, Nb, and Ta were mobilized and thereby fractionated from Zr and Hf during the dehydration process that transformed blueschist into eclogite. Both a segregation with a depletion halo, thought to represent initial mobilization during dehydration, and a transport vein, indicative of the long distance transport were investigated. In each case, centimeter-sized rutile grains grew as needle-like crystals in the segregation and as prismatic crystals in the vein. Within the host rock of the segregation, the Ti contents of garnet and omphacite, the modal abundances of rutile and titanite and the bulk rock Ti, Nb, and Ta contents decrease towards the segregation. These observations are consistent with transport of Ti, Nb, and Ta from the host rock into the segregation. Textural and geochemical data for the eclogite-facies vein minerals indicate that Ti-Nb-Ta-rich fluids were transported over long-distances (at minimum meter-scale) during fracture-controlled fluid flow. Complex forming ligands (e.g., Na-Si-Al polymers and F−) may have enhanced the solubility of Ti, Nb, and Ta in the fluid. Changes in fluid composition (e.g., XCO2) may both precipitate rutile and fractionate Ti, Nb, and Ta from LILE and REE.  相似文献   

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