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1.
本文通过对CCSD主孔100～1100m范围内榴辉岩中单矿物的LA-ICP-MS分析，探讨了榴辉岩中单矿物之间的微量元素分配，发现超高压变质作用中石榴石和绿辉石之间Ti和C0的分配显著受Mg控制（如DCo^Grt/Omp=3．43DMg^Grt/Omp-0．34），而REE、Sr和Y的分配则受Ca分配所控制。绿辉石中REE、Pb和Th的含量则明显受超高压副矿物磷灰石的出现与否所控制。结合岩石学特征，对角闪石和绿辉石中微量元素的研究表明角闪石主要是绿辉石退变质的产物。但退变质矿物的微量元素组成不仅受原矿物控制，而且受退变质矿物组合类型影响。绿帘石的出现会显著降低共生角闪石中LREE和Sr的含量，而多硅白云母的分解则会增加角闪石中的Rb、Ba含量。另外，退变质过程中的流体活动也会影响退变质矿物中的LREE、Sr和Pb等。结合REE在榴辉岩各主要矿物间分配系数随温度、压力的变化，我们推测部分石榴石边部MREE的富集特征可能反映榴辉岩在折返过程中经历了短时增温作用，这可能是引起苏鲁地区榴辉岩相向麻粒岩相转变叠加现象以及超高压岩石经历部分熔融作用的重要原因。此外，榴辉岩中金红石Nb和Ta组成的高度不均一性为金红石形成于超高压变质阶段富Ti磁铁矿相变作用的成因机制提供了佐证。  相似文献   

2.
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   

3.
The major and trace element compositions of nine eclogites from the Dabie–Sulu ultrahigh pressure (UHP) metamorphic terrane in eastern China were determined for both whole rock and the main constituent minerals, garnet and clinopyroxene. The results indicate that the eclogite protoliths originated from a basaltic magma, which formed in a continental setting as shown by isotopic and immobile element data. Based on the garnet REE characteristics, the eclogites can be roughly divided into two groups. Group 1 has LREE enrichment with no Eu anomaly for whole rock, and smooth LREE depletion but HREE enrichment pattern for garnet, whereas group 2 shows a depletion of LREE with a pronounced positive Eu anomaly and flat HREE pattern for both whole rock and garnet. From these features, we suggest that the protoliths for group 2 are Fe–Ti–gabbros with relatively high cumulus plagioclase and Fe–Ti oxide, whereas the group 1 eclogites are probably from basalts. Therefore, the unusual garnet REE pattern observed in group 2 can be considered as an important signature for identifying gabbro protoliths for eclogites. The identification of gabbro protoliths from the eclogites in the Dabie–Sulu terrane provides evidence for Neoproterozoic rift magmatism in the northern margin of the Yangtze craton. During ultrahigh pressure metamorphism in the Dabie–Sulu terrane, LILEs (including Ba, Rb, Th, U, K) had high mobility, but REEs and HFSEs were immobile, and trace element distribution equilibrium was approached between garnet and clinopyroxene. An estimate of mass balance indicates that garnet and clinopyroxene host the majority of HREEs and Y, and clinopyroxene is a significant host for Sr, but minor and accessory minerals predominantly account for LREEs, Th, U, and Zr.  相似文献   

4.
Hydrous high-pressure veins formed during dehydration of eclogites in two paleo-subduction zones (Trescolmen locality in the Adula nappe, central Alps and Münchberg Gneiss Massif, Variscan fold belt, Germany) constrain the major and trace element composition of solutes in fluids liberated during dehydration of eclogites. Similar initial isotopic compositions of veins and host eclogites at the time of metamorphism indicate that the fluids were derived predominantly from the host rocks. Quartz, kyanite, paragonite, phengite, zoisite and omphacite are the dominant minerals in the veins. The major element compositions of the veins are in agreement with experimental evidence indicating that the composition of solutes in such fluids is dominated by SiO2 and Al2O3. Relative to N-MORB, the veins show enrichments of Cs, Rb, Ba, Pb, and K, comparable or slightly lower abundances of Sr, U, and Th, and very low abundances of Nd, Sm, Zr, Nb, Ti and Y. The differential fractionation of highly incompatible elements such as K, U and Th in the veins, as well as the presence of hydrous minerals in the eclogites rule out partial melting as a cause for vein formation. These results confirm previous suggestions that fluids derived from subducted basalt may have low abundances of high field strength elements, rare earth elements and Y. Variable vein-eclogite enrichment factors of incompatible alkalis and to a lesser extent Pb appear to reflect mineralogical controls (phengite, epidote-group minerals) on partitioning of these elements during dehydration of eclogite in subduction zones. However, abundance variations of incompatible elements in minerals from eclogites suggest that the composition of fluids released from eclogites at temperatures <700°C may not reflect true equilibrium partitioning during dehydration. Simple models for the trace elements U and Th indicate the relative importance of the basaltic and sedimentary portions of subducted oceanic crust in producing the characteristic chemical signatures of these elements in convergent plate margin volcanism.  相似文献   

5.
Microscopic melt inclusions found in magmatic minerals are undoubtedly one of the most important sources of information on the chemical composition of melts. This paper reports on the successful application of near-infrared (NIR) femtosecond laser ablation (LA) - inductively coupled plasma-mass spectrometry to in situ determination of incompatible trace elements (Li, Rb, Sr, Y, Zr, Nb, Cs, Ba, REE, Ta, Th, U) and ore metals (As, Mo, Pb) in individual melt inclusions hosted in quartz from the Mount Pinatubo dacites, Philippines. The determined elements cover a concentration range of five orders of magnitude. Femtosecond LA-ICP-MS analyses of twenty-eight individual melt inclusions demonstrate the efficiency of the microanalytical technique and suggests a spectacular homogeneity of the entrapped melt, at least with respect to the following incompatible trace elements: Rb, Sr, Nb, Cs, Ba, La, Ce, Pr, Nd, Pb, Th. The analytical precision (1s) for Na, Ca, Rb, Sr, Y, Nb, Ba and LREE ranged from 3 to 20%. Comparison of trace element concentrations in Mt. Pinatubo melt inclusions determined by femtosecond LA-ICP-MS with those of melt inclusions previously analysed by secondary ion mass spectrometry analysis (SIMS) and those of matrix glasses previously determined by nanosecond LA-ICP-MS showed an agreement typically within 30–40%. The homogeneity of trace element concentrations of the Mt. Pinatubo melt inclusions and the matrix glasses is consistent with the melt inclusion origin as homogeneous rhyolitic melt that was trapped in quartz phenocrysts at the final crystallisation stages of the host adakite (dacite) magma.  相似文献   

6.
The geochemical patterns of major and trace elements in zonal garnets and the mineral inclusions in them formed by progressive and regressive metamorphism of pelites are established. It is shown that an increase in temperature and pressure led to a decrease in the Y and HREE contents in garnets, and the increase in their contents is related to a decrease in the PT-parameters of their formation. A negative correlation between the CaO and REE contents in garnet indicates their isomorphism. The main reason for the sharp increase in the CaO content in garnets during collision metamorphism is mass transfer between the garnet and the plagioclase. The deviations from this situaiton, which are expressed in simultaneous increase in the grossular component in garnet and the anorthite component in plagioclase, are caused by metamorphic reactions related to the epidote decomposition. The mass transfer of major and trace elements between the reacting phases in metamorphic reactions mostly occurred with preservation of the balance of matter. The mirror shape and the character of the REE patterns of the rock-forming minerals relative to the composition of the rock indicate the equilibration of the HREE and Y contents between garnet, the major concentrator of these elements in the rock, and other phases. The balance between the LREEs and HREEs in the rock is achieved by the presence of variable amounts of monazite.  相似文献   

7.
对松多榴辉岩中单矿物进行的LA-ICP-MS原位微区微量元素分析研究结果表明,石榴石主要富集中、重稀土元素和Y,同时具有高丰度的Sc、V、Cr和Co等元素;绿辉石中的微量元素以中稀土元素、Sr、Sc、V、Cr、Co、Ni和Ti为主,含有一定量的Zr、Hf等。石榴石、绿辉石、角闪石和绿帘石中均显示轻稀土元素亏损的特点,表明在退变质过程中没有发生明显的富轻稀土元素的外来流体交代作用,因而其微量元素矿物地球化学的某些特点不同于苏鲁地区的榴辉岩。石榴石变斑晶中某些元素(如Ti、Zr)的分带性暗示了榴辉岩在紧随峰期变质之后的折返过程中发生了降压增温过程。榴辉岩主要变质矿物中微量元素的分配显然受到矿物主量元素的分配所控制,如MgO在石榴石和绿辉石之间的分配对Ni、Co、Ti分配的控制以及CaO的分配对Sr、Y、REE分配的控制等。退变质过程中矿物的形成或分解以及物理化学条件的改变都可以引起矿物间微量元素的重新分配。由绿辉石退变质而形成的角闪石,较之原先的绿辉石,其微量元素配分曲线总体特征会发生变化,但元素总体丰度相近,某些元素特点相似,又反映了绿辉石和角闪石之间的成生联系。金红石是Ti、Nb、Ta、Zr、Hf的主要赋存矿物,而与之共生的绿帘石所表现出来的高场强元素的亏损特征表明了金红石的存在所带来的影响。  相似文献   

8.
Trace element concentrations of peridotitic garnet inclusions in diamonds from two Chinese kimberlite pipes were determined using the ion microprobe. Garnet xenocrysts from the same two kimberlite pipes were also analyzed for comparison. In contrast to their extremely refractory major element compositions, all harzburgitic garnets showed enrichment in light rare earth elements (REE) relative to chondrite, resulting in sinuous REE patterns. Both normal and sinuous REE patterns were observed from the lherzolitic garnets. Concentrations of REE in garnets changed significantly from diamond to diamond and no specific correlations were observed with their major element compositions. Analyses of randomly selected two to three points within every grain of a large number of garnet inclusions by the ion microprobe demonstrated that there was no evident compositional heterogeneity, and multiple grains of one phase from a single diamond host also exhibit very similar compositions. This implies that the trace element heterogeneity within one grain or among multiple inclusions from the same diamond host, as reported from Siberian diamonds, is not a common feature for these Chinese diamonds. Concentrations of Na, Ti, and Zr tend to decrease when garnets become more refractory, but variations of Sr and Li are more complex. Compositions rich in light REE and relatively poor in high field strength elements (HFSE) of the harzburgitic garnet inclusions in diamonds are generally consistent with metasomatism by carbonatite melts. The trace element features observed from the garnet inclusions in Chinese diamonds may be caused by carbonatite melt infiltration and partial melt extraction. Spatial and temporal gradients in melt/rock ratio and temperature are the main reasons for the large variations of REE patterns and other trace element concentrations. Received: 27 April 1999 / Accepted: 1 March 2000  相似文献   

9.
Development of several different microbeam techniques permits in situ analysis of trace elements in natural and synthetic mineral assemblages, which in turn makes possible determination of two-mineral partitioning behavior for trace elements (D-values). With the experimental approach, control of compositional and physical variables is possible, but equilibrium needs to be carefully assessed, and in some instances compositions and optimal experimental conditions are different from the natural situation. With the natural mineral approach, physical conditions must be assessed independently, accepting the uncertainties involved in geothermobarometric determinations based on coexisting mineral compositions. A potentially complex history of formation must be unravelled as well, with the attendant possibility of non-equilibrium.

Comparison of D-values determined for coexisting amphibole and Ca-clinopyroxene indicates overall good agreement for Sr, Zr, Hf, Y, and REE, but significant discrepancy for Rb, Ba, Nb, and Ta (experimental values much lower than natural values). For coexisting Ca-clinopyroxene and garnet, the spread of data is greater and fewer elements can be compared (Rb, Ba, Nb, and Ta data are not adequate). However Sr, Y, Zr, Hf, and Nd-Lu (of the rare-earth elements) agree reasonably well, but La and Ce experimental values for clinopyroxene/garnet are much lower than the natural values. These differences for both mineral pairs may be attributed in part to critical compositional differences between synthetic and natural minerals, where compositional factors play a key role in controlling accommodation of trace elements in the mineral structure. A second factor is the possibile existence of minute inclusions rich in trace elements trapped in the natural minerals. These inclusions may be submicroscopic and unavoidable, even by microbeam analysis. More work on both experimental and natural systems should resolve the discrepancies and help to realize the full potential for using trace elements to assess petrological processes in the mantle, where knowledge of D-value variation as a function of composition, pressure, and temperature is essential.  相似文献   

10.
华北地块东南缘中生代侵入杂岩中所含榴辉岩类包体中矿物的分析结果表明, 组成榴辉岩类包体的各矿物之间元素的分配在榴辉岩相变质阶段已经达到了化学平衡;石榴石中Al、Fe、Mn, 单斜辉石中Na、Mg、Ca, 角闪石中Na、Mg、Fe等主量元素含量与其全岩之间均呈良好的正相关, 受全岩成分制约;石榴石明显富集HREE、贫LREE, 单斜辉石相对富集LREE、MREE、贫HREE, 两者轻、重稀土含量呈相互消长的互补关系, 石榴石和单斜辉石中分别富集Y、Sr, Ga和过渡族元素Sc、Ti、V、Cr、Co等含量较高, 其含量受全岩成分控制;金红石中稀土元素的含量很少, Fe、Al、Mg、Ca、Mn、Nb、Ta、Cr和Zr含量相对较高, Rb、Sr、Ba含量极低, 部分微量元素(如Nb、Cr、Fe、V、W等)含量与其原岩有继承和对应关系;部分原生或/和退变角闪石的REE配分模式分别与单斜辉石和石榴石相似, 过渡族金属元素等的含量与石榴石、单斜辉石和全岩具有一定的相关性, 角闪石容纳Na、K、Sr、Rb、Ba等元素的能力较强, 其成分除受全岩成分的制约外, 石榴石、单斜辉石对其形成也有影响。榴辉岩类包体与其寄主中生代侵入杂岩中部分高价态/高场强元素(HFSE)和重稀土元素(HREE)呈相互消长的关系。榴辉岩的形成与扬子地块和华北地块之间的俯冲-碰撞作用有关。  相似文献   

11.
The Burpala alkaline massif contains rocks with more than 50 minerals rich in Zr,Nb,Ti,Th,Be and rare earth elements(REE).The rocks vary in composition from shonkinite,melanocratic syenite,nepheline and alkali syenites to alaskite and alkali granite and contain up to 10%LILE and HSFE,3.6%of REE and varying amounts of other trace elements(4%Zr,0.5%Y,0.5%Nb,0.5%Th and 0.1%U).Geological and geochemical data suggest that all the rocks in the Burpala massif were derived from alkaline magma enriched in rare earth elements.The extreme products of magma fractionation are REE rich pegmatites,apatite-fiuorite bearing rocks and carbonatites.The Sr and Nd isotope data suggest that the source of primary melt is enriched mantle(EM-Ⅱ).We correlate the massif to mantle plume impact on the active margin of the Siberian continent.  相似文献   

12.
BEA  F. 《Journal of Petrology》1996,37(3):521-552
A systematic study with laser ablation—ICP-MS, scanningelectron microscopy and electron microprobe revealed that 70–95wt% of REE (except Eu), Y, Th and U in granite rocks and crustalprotoliths reside within REEYThU-rich accessories whose nature,composition and associations change with the rock aluminosity.The accessory assemblage of peraluminous granites, migmatitesand high-grade rocks is composed of monazite, xenotime (in low-Cavarieties), apatite, zircon, Thorthosilicate, uraninite andbetafite-pyrochlore. Metaluminous granites have allanite, sphene,apatite, zircon, monazite and Thorthosilicaie. Peralkaline graniteshave aeschinite, fergusonite, samarskite, bastnaesite, fluocerite,allanite, sphene, zircon, monazite, xenotime and Th-orthosilicate.Granulite-grade garnets are enriched in Nd and Sm by no lessthan one order of magnitude with respect to amphibolite-gradegarnets. Granulitegrade feldspars are also enriched in LREEwith respect to amphibolite-grade feldspars. Accessories causenon-Henrian behaviour of REE, Y, Th and U during melt—solidpartitioning. Because elevated fractions of monazite, xenotimeand zircon in common migmatites are included within major minerals,their behaviour during anatexis is controlled by that of theirhost. Settling curves calculated for a convecting magma showthat accessories are too small to settle appreciably, beingseparated from the melt as inclusions within larger minerals.Biotite has the greatest tendency to include accessories, therebyindirectly controlling the geochemistry of REE, Y, Th and U.We conclude that REE, Y, Th and U are unsuitable for petrogeneticalmodelling of granitoids through equilibrium-based trace-elementfractionation equations. KEY WORDS: accessory minerals; geochemical modelling; granitoids; REE, Y, Th, U  相似文献   

13.
本文以中国大陆科学钻探主孔0～2000m岩芯中的榴辉岩为对象,运用EMPA和LA-ICP-MS技术,系统测定了榴辉岩中石榴石和绿辉石的主量与微量元素组成,并据此讨论了它们的成岩成矿意义.研究结果表明,CCSD主孔榴辉岩中石榴石富重稀土和Sc、Y、Co,而绿辉石则富中稀土和Pb、Sr、V,石榴石和绿辉石的高场强元素(特别是Nb、Ta)含量均很低.石榴石存在不同程度的Ce负异常,指示榴辉岩的形成过程中卷入有地表氧化条件下形成的风化沉积物.石榴石具有低的Zr/Y比值,绿辉石普遍具有高的Sr含量,这些特征说明榴辉岩(特别是高钛榴辉岩)的原岩可能为遭受过壳源物质混染与交代的富集地幔部分熔融的产物.高钛与低钛榴辉岩中石榴石和绿辉石在主量及微量元素组成上存在一定差别,总体而言,高钛榴辉岩中石榴石具高的MgO含量和较高的MgO/TFeO比值,以及较高的稀土和Sc含量,而绿辉石则相对富TFeO、MnO,并具有较高的Sr、Zr、Hf含量.高钛榴辉岩中石榴石和绿辉石常出现不同程度的Eu正异常,Cr含量均显著低于低钛榴辉岩.综合分析表明,高钛榴辉岩的原岩最可能为富斜长石的辉长质侵入岩,原岩组成的差异应是导致二类榴辉岩中石榴石和绿辉石矿物化学组成存在差异的主要原因.  相似文献   

14.
对中国大陆科学钻探工程主孔榴辉岩退变质过程中的微量元素地球化学行为进行了研究。对退变质程度连续变化样品的不同部分的对比研究表明，流体作用下的退变质过程中大离子亲石元素（Cs、Rb、Ba、Sr、K、Th、U）和轻稀土元素表现出较大的活动性，重稀土元素和高场强元素变化相对较小。退变质后大离子亲石元素的显著增加和高场强元素、重稀土元素的轻微变化（甚至相对降低），表明与退变质作用有关的流体中的络阴离子含量很少，并不富集高场强元素和重稀土元素。退变质后总体上表现出的Si、大离子亲石元素和轻稀土元素的明显变化，表明外来流体参与了榴辉岩的退变质过程，带入和带出了一些元素。结合榴辉岩中单矿物微量元素组成以及前人对D^Mineral/Fluid的研究成果，对流体-榴辉岩作用形成的退变质分带（富石英条带→角闪岩→退变质榴辉岩→新鲜榴辉岩）的微量元素组成变化进行了详细研究。结果表明在流体作用下的榴辉岩退变质过程中，大离子亲石元素、轻稀土元素和高场强元素含量的变化除了受退变质流体性质的影响外，更大程度上取决于退变质过程中的矿物相（尤其是副矿物）的变化。  相似文献   

15.
Minerals occurring in dry and modally metasomatized spinel lherzolites from western Victoria have been analysed by proton microprobe for Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Ba, Pb, Br, rare-earth elements (REE), Th and U. Mass-balance calculations demonstrate that these trace elements are contained in specific acceptor minerals and do not occur in significant concentrations at clean grain boundaries. The level of particular trace elements in the rock depends on the presence of specific phases: for example high levels of REE, Sr (and U, Th, Br) require apatite, while Ba, Nb and Ta are strongly concentrated in amphibole±mica. Mantle metasomatism in these spinel lherzolites is inferred to result from an open-system process involving infiltration of fluids released by crystallizing silicate melts. This process produces metasomatic zones with different modal mineralogy and hence greatly different trace-element signatures. The data demonstrate that large-ion-lithophile (LIL) and high-field strength (HFS) elements in metasomatized spinel lherzolites are strongly concentrated in non-refractory phases, which will break down easily in heated volumes such as the walls of magma conduits. The heterogeneity observed in trace-element patterns of intraplate alkali basaltic rocks may not reflect source heterogeneity, but may result largely from contamination by metasomatized mantle wall rock. The KDs for most trace elements show little temperature dependence except for KDSr between orthopyroxene and clinopyroxene where KD decreases with increasing temperature. The generally uniform KDs can be used to test for disequilibrium in such assemblages.  相似文献   

16.
Over 700 apatite grains from a range of rock types have been analysed by laser-ablation microprobe ICPMS for 28 trace elements, to investigate the potential usefulness of apatite as an indicator mineral in mineral exploration. Apatites derived from different rock types have distinctive absolute and relative abundances of many trace elements (including rare-earth elements (REE), Sr, Y, Mn, Th), and chondrite-normalised trace-element patterns. The slope of chondrite-normalised REE patterns varies systematically from ultramafic through mafic/intermediate to highly fractionated granitoid rock types. (Ce/Yb)cn is very high in apatites from carbonatites and mantle-derived lherzolites (over 100 and over 200, respectively), while (Ce/Yb)cn values in apatites from granitic pegmatites are generally less than 1, reflecting both HREE enrichment and LREE depletion. Within a large suite of apatites from granitoid rocks, chemical composition is closely related to both the degree of fractionation and the oxidation state of the magma, two important parameters in determining the mineral potential of the magmatic system. Apatite can accept high levels of transition and chalcophile elements and As, making it feasible to recognise apatite associated with specific types of mineralisation. Multivariate statistical analysis has provided a user-friendly scheme to distinguish apatites from different rock types, based on contents of Sr, Y, Mn and total REE, the degree of LREE enrichment and the size of the Eu anomaly. The scheme can be used for the recognition of apatites from specific rock types or styles of mineralisation, so that the provenance of apatite grains in heavy mineral concentrates can be determined and used in geochemical exploration.  相似文献   

17.
碳酸岩流体及其稀土成矿作用   总被引：12，自引：0，他引：12  
火成碳酸岩熔浆可侵入到大陆和洋壳构造环境 ,多数大陆构造环境下的碳酸岩在时间和空间上与地壳减薄事件有关 ,高温下它具有极强的搬运碱金属、大离子亲石元素和高场强元素的能力。碳酸岩中可能出现的原生包裹体有两相水溶液 (气 +液 )包裹体、含子矿物多相水溶液包裹体、含CO2 包裹体和CO2 +盐水溶液混合多相包裹体以及硅酸盐玻璃质熔融包裹体等。碳酸岩型稀土矿床中赋存的流体包裹体类型也可分为气液相、含碳水溶液相和气液固多相包裹体 ,包裹体中稀土子矿物的出现是该类矿床最显著的特征。富碱碳酸岩流体中REE ,Sr ,Th和Fe等都具有极高的溶解度 ,水岩反应和流体不混溶是造成成矿热液中REE及Fe等沉淀成矿的关键因素 ,REE的迁移沉淀可延续到低温、低盐度的成矿晚阶段  相似文献   

18.
李双喜 《地质与勘探》2022,58(6):1196-1208
本文对苏北地区锦屏组磷矿石及地层样品进行了岩相学及地球化学分析,研究了磷矿初始沉积环境和源区特征。磷矿类微量元素富集Ba、Pb、U、Sr,贫Th、Ta、Nb、Ti;REE配分曲线为LREE富集型,Ce负异常,表明成矿环境为陆缘海,且成矿过程受深海热水沉积和生物作用影响。Sr、Nd同位素初始值判断磷灰岩物质来源为年轻的地壳物质。绿片岩类微量元素富集Rb、Th、K,贫Th、U、Ta、Nb、Sr、Ti;REE配分曲线为LREE富集型,判断其原岩为陆源碎屑岩。（混合）片麻岩类微量元素富集Pb、Th、K,亏损Ba、Ta、Nb、Sr、Ti;REE配分曲线为LREE富集型,具地幔源区特征。  相似文献   

19.
Major-, minor-, and trace-element zoning have been measuredin garnets from four samples of differing bulk composition fromthe east flank of the Shelburne Falls Dome, western Massachusetts,using ion and electron microprobes. The samples are differentiallyretrograded, so traditional techniques of rim geothermometryand geobarometry and P-T path analysis yield equivocal results. Trace-element abundances in garnets vary with those of majorelements, particularly calcium. Garnets exhibit several typesof Ca zoning, each accompanied by a distinct mode of trace-clementzoning. Garnets from low-Ca pelites in the Goshen Formationdecrease to low Ca abundances near their rims. This featureis coupled with a decrease in Na/Si and Ti/Si. The outermostfew microns of these garnets show a depletion in Sc/Si and anenrichment in Mn/Si, Y/Si, and rare earth element (REE) abundancescompared with the garnet core. These variations are ascribedto changes in intensive parameters during garnet growth/re-equilibration,probably a decrease in pressure (< 1 kb) accompanied by asmall temperature increase, which led to a decrease in XgrossularMuch of the variation in trace-element content may reflect crystal-chemicaleffects. In contrast, cores of garnets from intermediate-Capelites in the Waits River Formation initially display decreasesin grossular content, followed by Ca increases towards theirrims. The decrease in grossular content correlates with strongincreases in Y/Si, Zr/Si, and REE contents. The Ca ‘inflection’observed in these garnets coincides with the last appearanceof clinozoisite inclusions in garnet. Clinozoisite-compatibleelements (Y, Zr, and REE) may be released during breakdown ofclinozoisite in an internal metasomatic process, producing someof the trace-element enrichments. Garnets from clinozoisite-bearingpelites in the Waits River Formation exhibit zoning profileswith an increase in Ca towards the rim. An abrupt enrichmentin grossular content (Xgrossular = 0.06) occurs near garnetcores in these high-CaO, low-SiO2, high-FeO samples. The Caincrease accompanies small decreases in Li/Si and Na/Si, smallincreases in Ti/Si and V/Si, and large decreases in Y/Si, Zr/Si,and REE abundance. The large trace-element variations are probablydue to an interval of growth of clinozoisite accessory mineralsseparating two distinct garnet-growth events. This garnet alsoshows Co and Cr increases toward the rim, probably as a resultof breakdown of magnetite. Proton-probe microanalysis of minerals in these calc-pelitesshows strong affinities of specific trace elements for certainminerals: Y in garnet, Ga and Rb in biotite, Zn and Ga in staurolite,Rb and Sr in muscovite, Sr and Pb in plagioclase, and Nb inilmenite. Trace-element zoning is shown to be a useful monitor of reactionhistories and possibly P-T paths during garnet growth.  相似文献   

20.
The mineralogy and the trace element compositions of hydrothermally-altered volcanic materials collected from ash fall deposits and in four debris-avalanche deposits (DADs) at La Soufrière volcano in Guadeloupe have been determined. Phreatic explosions of the 1976 eruption and flank collapse events have sampled various parts of the active and ancient hydrothermal systems of the volcano. Hydrothermal mineral assemblages (smectite + silica polymorphs ± pyrite/jarosite ± gypsum) are typical of rock alteration by low-temperature acid-sulphate fluids. High-temperature mineral assemblages are rare, indicating that phreatic explosions and flank collapse events have sampled mainly the upper parts of the volcanic edifice.Andesitic eruptive products affected by shallow hydrothermal alteration are complex assemblages of volcanic materials (glass, phenocrysts and xenocrysts with complex magmatic histories) of different ages and compositions. The use of incompatible element ratios and REE compositions normalised to an unaltered reference material overcomes the interpretation difficulties related to mass balance effects of alteration processes and the petrologic heterogeneity of the initial material.REE and other incompatible elements (Th, U, Hf, Zr) are mainly concentrated in the glassy matrix of unaltered andesitic rocks. Secondary S-bearing mineral phases (e.g., gypsum, jarosite) that have precipitated from acid-sulphate fluids do not contain substantial incompatible elements (REE, U, Th, Hf, Zr). Compositional variations of incompatible elements in hydrothermally-altered andesitic materials reflect mainly volcanic glass–smectite transformation, which is characterised by (i) strong depletion of alkalis and alkaline earths (Ba, Sr) and first transition series elements (Zn, Cu, Cr, Co, Ni), (ii) immobility of highly incompatible elements (Th, Zr, Hf, LREE) and (iii) strong depletion of MREE and HREE. The sigmoid shape of normalised REE pattern is characteristic of glass–smectite transformation by low-temperature acid-sulphate fluids. This transformation also produces significant variations in U/Th values, which offer the opportunity to date the cessation of hydrothermal alteration and to reconstruct the evolution in space and time of hydrothermal activity in a volcanic edifice.  相似文献   

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