首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 46 毫秒
1.
Lithium-rich, rare-element pegmatites are characterized by high concentrations of B, P, and F. The interactions of these components with H2O and rare alkalis lower liquidas and solidus temperatures, enhance silicate liquid-H2O miscibility, and control partitioning and concentration of Group I elements and higher-field-strength cations. Boron, F, and perhaps P may form peralkaline Na- and Li-species that promote early saturation in mica + quartz. Activities of F, P, and especially B are largely unbuffered throughout crystallization. Concentration of these components through fractional crystallization involving muscovite generates a peralkaline, Na-aluminosilicate-rich melt or vapor from which albitites rich in tourmaline, phosphates, F-rich micas, beryl, zircon, and Nb-Ta-Sn oxides crystallize. Phase equilibrium experiments with peraluminous B-P-F-rich rhyolite obsidian (macusanite) simulate many features of rare-element pegmatites, especially at H2O-undersaturated conditions.  相似文献   

2.
Nodules (coarse-grain ??plutonic?? rocks) were collected from the ca. 20 ka Pomici di Base (PB)-Sarno eruption of Mt. Somma-Vesuvius, Italy. The nodules are classified as monzonite-monzogabbro based on their modal composition. The nodules have porphyrogranular texture, and consist of An-rich plagioclase, K-feldspar, clinopyroxene (ferroan-diopside), mica (phlogopite-biotite) ± olivine and amphibole. Aggregates of irregular intergrowths of mostly alkali feldspar and plagioclase, along with mica, Fe-Ti-oxides and clinopyroxene, in the nodules are interpreted as crystallized melt pockets. Crystallized silicate melt inclusions (MI) are common in the nodules, especially in clinopyroxenes. Two types of MI have been identified. Type I consists of mica, Fe-Ti-oxides and/or dark green spinel, clinopyroxene, feldspar and a vapor bubble. Volatiles (CO2, H2O) could not be detected in the vapor bubbles by Raman spectroscopy. Type II inclusions are generally lighter in color and contain subhedral feldspar and/or glass and several opaque phases, most of which are confirmed to be oxide minerals by SEM analysis. Some of the opaque-appearing phases that are below the surface may be tiny vapor bubbles. The two types of MI have different chemical compositions. Type I MI are classified as phono-tephrite ?? tephri-phonolite ?? basaltic trachy-andesite, while Type II MI have basaltic composition. The petrography and MI geochemistry led us to conclude that the nodules represent samples of the crystal mush zone in the active plumbing system of Mt. Somma-Vesuvius that were entrained into the upwelling magma during the PB-Sarno eruption.  相似文献   

3.
四川西部天全地区花岗岩属于扬子地块西缘岩浆岩带,是"康滇地轴"北段的重要组成部分。岩石形成年龄为851±15Ma(MSWD=0.7),属于新元古代花岗岩,与扬子地块西缘和北缘大量的中酸性侵入体和火山岩具有相近的形成年龄。火夹沟花岗闪长岩为过铝质、低Si O2、具有相对亏损的Sr-Nd-Pb同位素地球化学组成,结合岩石低的Al2O3/Ti O2和高的Ca O/Na2O比值,其应是在镁铁质岩浆底侵的条件下,成熟度较低的杂砂岩部分熔融形成的过铝质熔体,岩石较低的Si O2含量表明其同化了部分镁铁质熔体。而角脚坪花岗岩具有高的Si O2含量,为过铝质、富Na的熔体,而且具有极度亏损的Sr-Nd同位素组成,表明其应是亏损的玄武质岩石(洋壳或是与地幔柱有关的玄武岩)在H2O饱和条件下发生低程度部分熔融形成的过铝质熔体。结合扬子西缘其它新元古代火成岩的地球化学特征及区域构造资料,我们认为天全地区的Na质花岗闪长岩-花岗岩组合代表在高地温梯度条件下,玄武质岩石在H2O饱和条件下发生部分熔融形成的过铝质花岗岩。  相似文献   

4.
The addition of phosphorus to H2O-saturated and initially subaluminous haplogranitic (Qz–Ab–Or) compositions at 200 MPa(H2O) promotes expansion of the liquidus field of quartz, a marked decrease of the solidus temperature, increased solubility limits of H2O in melt at low phosphorus concentrations, and fractionation of melt out of the haplogranite plane (projected along an Or28 isopleth) toward a peralkaline, silica-poor but quartz-saturated minimum composition. The partition coefficient for P2O5 between aqueous vapor and melt with an ASI (aluminum saturation index, mol Al/[mol Na+K])=1 is negligible (0.06), and consequently so are the effects of phosphorus on other melt-vapor relations involving major components. Phosphorus becomes more soluble in vapor, however, as the concentration of a NaPO3 component increases via the fractionation of melt by crystallization of quartz and feldspar. The experimental results here corroborate existing concepts regarding the interaction of phosphorus with alkali aluminosilicate melt: phosphorus has an affinity for alkalis and Al, but not Si. Phosphorus is incorporated into alkali feldspars by the exchange component AlPSi-2. For subaluminous compositions (ASI=1), the distribution coefficient of phosphorus between alkali feldspar and melt, D[P]Af/m, is 0.3. This value increases to D[P]Af/m=1.0 at a melt ASI value of 1.3. The increase in D[P]Af/m with ASI is expected from the fact that excess Al promotes the AlPSi-2 exchange. With this experimental data, the P2O5 content of feldspars and whole rocks can reveal important facets of crystallization and phosphorus geochemistry in subaluminous to peraluminous granitic systems.  相似文献   

5.
Late Proterozoic rocks of Tanol Formation in the Lesser Himalayas of Neelum Valley area are largely green schist to amphibolite facies rocks intruded by early Cambrian Jura granite gneiss and Jura granite representing Pan-African orogeny event in the area. These rocks are further intruded by pegmatites of acidic composition, aplites, and dolerite dykes. Based on field observations, texture, and petrographic character, three different categories of granite gneiss (i.e., highly porphyritic, coarse-grained two micas granite gneiss, medium-grained two micas granite gneiss, and leucocratic tourmaline-bearing muscovite granite gneiss), and granites (i.e., highly porphyritic coarse-grained two micas granite, medium-grained two micas granite, and leucocratic tourmaline-bearing coarse-grained muscovite granite) were classified. Thin section studies show that granite gneiss and granite are formed due to fractional crystallization, as revealed by zoning in plagioclase. The Al saturation index indicates that granite gneiss and granite are strongly peraluminous and S-type. Geochemical analysis shows that all granite gneisses are magnesian except one which is ferroan whereas all granites are ferroan except one which is magnesian. The CaO/Na2O ratio (>0.3) indicates that granitic melt of Jura granite gneiss and granite is pelite-psammite derived peraluminous granitic melt formed due to partial melting of Tanol Formation. The rare earth element (REE) patterns of the Jura granite and Jura granite gneiss indicate that granitic magma of Jura granite and Jura granite gneiss is formed due to partial melting of rocks that are similar in composition to that of upper continental crust.  相似文献   

6.
David London   《Lithos》2005,80(1-4):281-303
Although many explanations have been proposed for the internal zonation of granitic pegmatites, the most widely accepted model is attributed to R.H. Jahns. Jahns and Burnham [Jahns, R.H., Burnham, C.W., 1969. Experimental studies of pegmatite genesis: I. A model for the derivation and crystallization of granitic pegmatites. Econ. Geol. 64, 843–864] said that pegmatites owe their distinctive textural and zonal characteristics to the buoyant separation of aqueous vapor from silicate melt, giving rise to K-rich pegmatitic upper portions and Na-rich aplitic lower zones of individual pegmatites. Jahns and Tuttle [Janhs, R.H., Tuttle, O.F., 1963. Layered pegmatite–aplite intrusives. Spec. Pap.-Miner. Soc. Am. 1, 78–92] cited experiments as confirmation of this effect, but several experimental studies contradict the partitioning behavior that was the premise of Jahns' model. More recent work indicates that pegmatite-forming melts should cool quickly, or in any case, more quickly than crystallization can keep pace with. The distinctive textural and zonal features of pegmatites have been replicated in experiments that employ constitutional zone refining of melts that are substantially undercooled before crystallization commences. Melt boundary layers formed by this process would represent the last silicate liquids to crystallize in pegmatites, which explains the tendency in pegmatites for abrupt transitions from simple to evolved mineral and rock compositions. The sources of pegmatite-forming melts and of the causes of regional zonation within pegmatite groups represent important directions for future research.  相似文献   

7.
Our study of fluid and melt inclusions in quartz and feldspar from granite pegmatite from the Precambrian Rønne granite, Bornholm Island, Denmark revealed extremely alkali bicarbonate- and carbonate-rich inclusions. The solid phases (daughter crystals) are mainly nahcolite [NaHCO3], zabuyelite [Li2CO3], and in rare cases potash [K2CO3] in addition to the volatile phases CO2 and aqueous carbonate/bicarbonate solution. Rare melt inclusions contain nahcolite, dawsonite [NaAl(CO3)(OH)2], and muscovite. In addition to fluid and melt inclusions, there are primary CO2-rich vapor inclusions, which mostly contain small nahcolite crystals. The identification of potash as a naturally occurring mineral would appear to be the first recorded instance. From the appearance of high concentrations of these carbonates and bicarbonates, we suggest that the mineral-forming media were water- and alkali carbonate-rich silicate melts or highly concentrated fluids. The coexistence of silicate melt inclusions with carbonate-rich fluid and nahcolite-rich vapor inclusions indicates a melt-melt-vapor equilibrium during the crystallization of the pegmatite. These results are supported by the results of hydrothermal diamond anvil cell experiments in the pseudoternary system H2O–NaHCO3–SiO2. Additionally, we show that boundary layer effects were insignificant in the Bornholm pegmatites and are not required for the origin of primary textures in compositionally simple pegmatites at least.  相似文献   

8.
Fluorine-, boron- and phosphorus-rich pegmatites of the Variscan Ehrenfriedersdorf complex crystallized over a temperature range from about 700 to 500 °C at a pressure of about 1 kbar. Pegmatite quartz crystals continuously trapped two different types of melt inclusions during cooling and growth: a silicate-rich H2O-poor melt and a silicate-poor H2O-rich melt. Both melts were simultaneously trapped on the solvus boundaries of the silicate (+ fluorine + boron + phosphorus) − water system. The partially crystallized melt inclusions were rehomogenized at 1 kbar between 500 and 712 °C in steps of 50 °C by conventional rapid-quench hydrothermal experiments. Glasses of completely rehomogenized inclusions were analyzed for H2O by Raman spectroscopy, and for major and some trace elements by EMP (electron microprobe). Both types of melt inclusions define a solvus boundary in an XH2O–T pseudobinary system. At 500 °C, the silicate-rich melt contains about 2.5 wt% H2O, and the conjugate water-rich melt about 47 wt% H2O. The solvus closes rapidly with increasing temperature. At 650 °C, the water contents are about 10 and 32 wt%, respectively. Complete miscibility is attained at the critical point: 712 °C and 21.5 wt% H2O. Many pegmatites show high concentrations of F, B, and P, this is particularly true for those pegmatites associated with highly evolved peraluminous granites. The presence of these elements dramatically reduces the critical pressure for fluid–melt systems. At shallow intrusion levels, at T ≥ 720 °C, water is infinitely soluble in a F-, B-, and P-rich melt. Simple cooling induces a separation into two coexisting melts, accompanied with strong element fractionation. On the water-rich side of the solvus, very volatile-rich melts are produced that have vastly different physical properties as compared to “normal” silicate melts. The density, viscosity, diffusivity, and mobility of such hyper-aqueous melts under these conditions are more comparable to an aqueous fluid. Received: 15 September 1999 / Accepted: 10 December 1999  相似文献   

9.
Vapor-saturated experiments at 200 MPa with peraluminous, lithophile-element-rich rhyolite obsidian from Macusani, Peru, reveal high miscibility of H2O and silicate melt components. The H2O content of melt at saturation (11.5+-0.5 wt.%) is almost twice that predicted by existing melt speciation models. The corresponding solubility of melt components in vapor decreases from 15 wt.% dissolved solids (750°–775° C) to 9 wt.% at 600° C. With regard to major and most minor components, macusanite melt dissolves congruently in vapor. Among the elements studied (B, P, F, Li, Rb, Cs, Be, Sr, Ba, Nb, Zr, Hf, Y, Pb, Th, U, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, and Tm), only boron has a vapor/melt partition coefficient (D[B]) consistently 1 at superliquidus temperatures (>645° C). Phosphorus and fluorine behave similarly, with D[P] and D[F]<0.5. Little or no significant vapor/melt fractionation is evident among most periodic groups (alkalis, alkaline earths, Zr/Hf, or the REE). The temperature dependence of vapor/melt partition coefficients is generally greatest for cations with charge +3 (except Nb and U); most vapor/melt partition coefficients for trace elements increase with decreasing temperature to the liquidus. Crystallization proceeds by condensation of crystalline phases from vapor; most coexisting melts are aphyric. Changes in the major element content of melt are dominated by the mineral assemblage crystallized from vapor, which includes subequal proportions of white mica, quartz, albite, and orthoclase. The volumetric proportion of (mica + or-thoclase)/albite increases slightly with decreasing T, creating a sodic, alkaline vapor. Vapor deposition of topaz (T500° C), which consumes F from melt, returns K/Na ratios of melt to near unity with the vapor-deposition of albite. The abundances of most trace elements in residual melt change little with the crystallization of major phases, but in some cases are strongly controlled by the deposition of accessory phases including apatite (T550° C), which depletes the melt in P and REE. Below the liquidus, boron increasingly favors the vapor over melt with decreasing temperatures.  相似文献   

10.
The South Platte pegmatite district is well known for its significant enrichment in the rare earth elements (REE), Y, Nb, F, and for the exceptionally well-developed internal zonation of the complex pegmatites located within a reversely zoned portion of the Pikes Peak batholith. Chemical trends both within and between pegmatites define the behavior of major and trace elements and the role of F in the fractionation of the granitic magma and pegmatitic fluids, suggesting a new model for the evolution of the granite-pegmatite system.Whole-rock XRF and INAA analyses of the host Pikes Peak granite and quartz monzonite and pegmatite wall zones provide strong evidence that all three are related by differentiation. With increasing SiO2, there is systematic enrichment in K2O, Na2O, and Rb, and depletion in CaO, MgO, FeO1, TiO2, P2O5, Ba, Sr, and Sc. REE, Y, Zr, and Th were strongly partitioned out of the wall zone into the final residual fluids where they were concentrated up to an order of magnitude over levels in the granite.Within the district, there is also chemical zonation of F, Nb, Th, U, and REE between groups of pegmatites. Polyzonal quartz-core types typically contain more fluorite, samarskite, HREE-zircon, and yttrian-fluorite than their bizonal composite-core counterparts, which contain only sparse fluorite and allanite.The sequence of magmatic evolution involved: (1) a process of diffusive differentiation and fractional crystallization which produced a chemically stratified magma chamber with a hotter more mafic quartz monzonitic base and a more felsic, granitic top enriched in H2O, F, HREE, Nb, and Y; (2) resurgence of the more mafic lower level crystal mush in to the upper more felsic part of the pluton; and (3) separation of pegmatitic fluids from the juxtaposed magmas giving rise to two compositionally distinct groups of pegmatites.  相似文献   

11.
孟恩  刘福来  刘建辉  施建荣 《岩石学报》2012,28(9):2793-2806
本文对辽东南长海地区花岗质片麻岩进行了系统的岩石学和地球化学研究,以便对其原岩性质及形成的构造环境给予制约。研究结果表明,研究区内花岗质片麻岩类可划分为富钠和富钾两类花岗质岩石,前者包括黑云二长花岗质片麻岩和花岗闪长质片麻岩,矿物组成主要包括斜长石、石英、黑云母及少量的钾长石等,后者则主要包括花岗质、二长花岗质和糜棱岩化花岗质片麻岩,其矿物组成以钾长石、斜长石、石英和次要的白云母和黑云母为主。地球化学分析结果显示,富钠花岗质片麻岩具有富硅、富钠、高铝、富集LREEs和LILEs、强烈亏损HREEs和HFSEs(Nb、Ta、P、Ti)、轻重稀土强烈分馏、并显示弱负Eu异常和Ba的相对亏损等特征;而富钾花岗质片麻岩则显示高硅、富钾、过铝质的地球化学属性、富集LREEs和LILEs、亏损HREEs和HFSEs,与富钠花岗质岩石相比,轻重稀土分馏程度相对较弱、HFSEs以及Ba相对于Rb和Th的亏损程度更强,并显示中等负Eu异常和强烈的Sr负异常等特征。上述特征表明,辽东南长海地区富钠花岗质片麻岩应起源于中酸性陆壳物质的部分熔融,并可能有玄武质物质的加入,原岩应为具有活动大陆边缘属性的花岗闪长岩,其形成应与狼林地块(或胶辽地块)东南及南部先存洋盆向陆块之下的俯冲作用相联系;而富钾花岗质片麻岩应形成于中酸性陆壳物质的部分熔融,原岩为具有碰撞型花岗岩属性的碱性花岗岩,其形成应与洋壳消减闭合、陆陆碰撞拼贴相联系。  相似文献   

12.
Extreme enrichment in H2O, B, P and F is characteristic of many evolved granites and pegmatites. We report experimental phase relations of a synthetic peraluminous pegmatite spiked with P2O5, B2O3 and F (5 wt% of each), Rb2O, Cs2O (1 wt% of each) and Li2O (0.5 wt%). Experiments were carried out in H2O-saturated conditions in cold-seal rapid-quench pressure vessels at 0.1-0.2 GPa. Crystallisation starts at about 820 °C with berlinite and topaz. Quartz appears at 700-750 °C. Topaz is replaced by muscovite at about 600 °C. At near-solidus temperatures (450-500 °C) amblygonite, lacroixite and a Cs-bearing aluminosilicate crystallise. In all charges aluminosilicate melt coexists with low-density hydrous fluid and hydrosaline melt. The latter is strongly enriched in Na3AlF6 and H3BO3 components. Experimental evidence of the liquid immiscibility and mineral reactions documented in our study offers new explanations of many enigmatic features of natural pegmatites.  相似文献   

13.
We have studied the controls on the Aluminum Saturation Index (ASI = molec. Al2O3/[(CaO)+(Na2O)+(K2O)]) and the concentration of normative corundum of granitic liquids saturated in alumina by equilibrating peraluminous minerals with initially metaluminous haplogranitic minimum composition liquids at 700–800 °C and 200 MPa, at, and below H2O saturation. The ASI and normative corundum increase with increasing H2O concentration in the melt (0.04 to 0.10 moles excess Al2O3 per mole of H2O), temperature, and with addition of the non-haplogranitic components Fe, Mg, and B. The ASI parameter and concentration of normative corundum cannot be used to monitor aAl2O3 between different mineral assemblages and melt because other components that affect the solubility of alumina, including H2O, Fe, Mg, and B, do not appear in their formulations. ASI and normative corundum, however, provide petrogenetic information about magmas generated by partial melting of strongly peraluminous protoliths by virtue of their regular and predictable variation with melt composition (e.g., H2O concentration) and temperature. For the application of these data to natural rocks it is necessary to choose as an analogue system the ASI-solubility or normative corundum-solubility relations of the most chemically complex peraluminous mineral present in the rock. Comparison of ASI values of anatectic leucosomes and allochthonous leucogranites with experimentally predicted values suggests low H2O concentrations in melt during crustal partial melting. Rapid melt segregation before equilibration with restitic peraluminous phases is also suggested in some cases.Editorial responsibility: I. Carmichael  相似文献   

14.
We report results of experiments constraining oxygen isotope fractionations between CO2 vapor and Na-rich melilitic melt at 1 bar and 1250 and 1400°C. The fractionation factor constrained by bracketed experiments, 1000.lnαCO2-Na melilitic melt, is 2.65±0.25 ‰ (±2σ; n=92) at 1250°C and 2.16±0.16 ‰ (2σ; n=16) at 1400°C. These values are independent of Na content over the range investigated (7.5 to 13.0 wt. % Na2O). We combine these data with the known reduced partition function ratio of CO2 to obtain an equation describing the reduced partition function ratio of Na-rich melilite melt as a function of temperature. We also fit previously measured CO2-melt or -glass fractionations to obtain temperature-dependent reduced partition function ratios for all experimentally studied melts and glasses (including silica, rhyolite, albite, anorthite, Na-rich melilite, and basalt). The systematics of these data suggest that reduced partition function ratios of silicate melts can be approximated either by using the Garlick index (a measure of the polymerization of the melt) or by describing melts as mixtures of normative minerals or equivalent melt compositions. These systematics suggest oxygen isotope fractionation between basalt and olivine at 1300°C of approximately 0.4 to 0.5‰, consistent with most (but not all) basalt glass-olivine fractionations measured in terrestrial and lunar basalts.  相似文献   

15.
The increasing strategic importance of Li- and Ta-ores during the last decades due to the strong consumption growth for rechargeable batteries and high temperature and corrosion resistant capacitors reactivated the interest of studies in pegmatite fields around the world, because these rocks supply respectively 25% and 100% of the world consumption in these elements. Research on petrogenetic issues and major and accessory mineral chemistry variations in rare element (REL)-pegmatites of the Borborema Pegmatite Province in Northeast Brazil were tested as tools for the diagnosis of the metallogenetic potential of rare metals in individual pegmatites and in the province as a whole along the last dozen of years. The results allowed to establish the nearly isobaric (3.8 kbar) crystallization conditions of the REL-pegmatites between approximately 580 °C (liquidus) and 400 °C (solidus) from a peraluminous melt saturated in an aquo-carbonic medium to low salinity volatile phase and an immiscible peralkaline flux-enriched (H2O, CO2, F, B, Li etc.) melt fraction, based on melt and fluid inclusion studies. Mineral-chemistry data from 30 selected REL-pegmatites in the province allowed to classify three of them as being of the complex-spodumene or -lepidolite subtype in Černý's classification. Both subtypes are supposed to be potentially fertile, (highly fractionated, and with good chances to bear Li- and Ta-ore concentrations). It was also possible to identify several pegmatitic granite intrusions with textural and lithogeochemical characteristics also found in source granites of REL-pegmatite provinces elsewhere. Preliminary chemical Pb/U/Th geochronological determinations in uraninite and xenotyme crystals of these granites indicate an age of 520 ± 10 Ma and match recently published Ar/Ar in mica and U/Pb ages in columbite-group minerals (CGM) of the REL-pegmatites between 509 and 525 Ma. Mineral-chemistry data from grains of the outer zones of the pegmatites do not allow to distinguish potentially fertile from barren pegmatites. This discrimination is possible only if samples of the inner intermediate zone, replacement pockets or quartz core are used. From the tested minerals trace-element determinations (mainly Li, Al, Ti, Ge, B among 14 tested elements) by LA-ICP-MS technique in quartz seem to be more efficient than the classical approach (of Rb, K, Cs, Ga, Sr Ta) in K-feldspar or micas, due to the susceptibility to hydrothermal or supergene alteration of the latter. Mineral-chemistry variations in CGM, tourmalines, garnet and gahnite turned out to be efficient discriminators but all of them have the disadvantage of an eventual and, if present, random distribution, typical for accessory minerals in pegmatites, not allowing a regular sampling in most cases. Additional tests are recommended to confirm respectively the preliminary results of mineral-chemistry as exploration tools on a larger number of pegmatites and geochronological data to confirm the existence of another, older, synorogenetic generation of REL-pegmatites in the BPP.  相似文献   

16.
Evidence of melting is presented from the Western Gneiss Region (WGR) in the core of the Caledonian orogen, Western Norway and the dynamic significance of melting for the evolution of orogens is evaluated. Multiphase inclusions in garnet that comprise plagioclase, potassic feldspar and biotite are interpreted to be formed from melt trapped during garnet growth in the eclogite facies. The multiphase inclusions are associated with rocks that preserve macroscopic evidence of melting, such as segregations in mafic rocks, leucosomes and pegmatites hosted in mafic rocks and in gneisses. Based on field studies, these lithologies are found in three structural positions: (i) as zoned segregations found in high‐P (ultra)mafic bodies; (ii) as leucosomes along amphibolite facies foliation and in a variety of discordant structures in gneiss; and (iii) as undeformed pegmatites cutting the main Caledonian structures. Segregations post‐date the eclogite facies foliation and pre‐date the amphibolite facies deformation, whereas leucosomes are contemporaneous with the amphibolite facies deformation, and undeformed pegmatites are post‐kinematic and were formed at the end of the deformation history. The geochemistry of the segregations, leucosomes and pegmatites in the WGR defines two trends, which correlate with the mafic or felsic nature of the host rocks. The first trend with Ca‐poor compositions represents leucosome and pegmatite hosted in felsic gneiss, whereas the second group with K‐poor compositions corresponds to segregation hosted in (ultra)mafic rocks. These trends suggest partial melting of two separate sources: the felsic gneisses and also the included mafic eclogites. The REE patterns of the samples allow distinction between melt compositions, fractionated liquids and cumulates. Melting began at high pressure and affected most lithologies in the WGR before or during their retrogression in the amphibolite facies. During this stage, the presence of melt may have acted as a weakening mechanism that enabled decoupling of the exhuming crust around the peak pressure conditions triggering exhumation of the upward‐buoyant crust. Partial melting of both felsic and mafic sources at temperatures below 800 °C implies the presence of an H2O‐rich fluid phase at great depth to facilitate H2O‐present partial melting.  相似文献   

17.
Silicate melt inclusions (MI) commonly provide the best record of pre-eruptive H2O and CO2 contents of subvolcanic melts, but the concentrations of CO2 and H2O in the melt (glass) phase within MI can be modified by partitioning into a vapor bubble after trapping. Melt inclusions may also enclose vapor bubbles together with the melt (i.e., heterogeneous entrapment), affecting the bulk volatile composition of the MI, and its post-entrapment evolution. In this study, we use numerical modeling to examine the systematics of post-entrapment volatile evolution within MI containing various proportions of trapped vapor from zero to 95 volume percent. Modeling indicates that inclusions that trap only a vapor-saturated melt exhibit significant decrease in CO2 and moderate increase in H2O concentrations in the melt upon nucleation and growth of a vapor bubble. In contrast, inclusions that trap melt plus vapor exhibit subdued CO2 depletion at equivalent conditions. In the extreme case of inclusions that trap mostly the vapor phase (i.e., CO2–H2O fluid inclusions containing trapped melt), degassing of CO2 from the melt is negligible. In the latter scenario, the large fraction of vapor enclosed in the MI during trapping essentially serves as a buffer, preventing post-entrapment modification of volatile concentrations in the melt. Hence, the glass phase within such heterogeneously entrapped, vapor-rich MI records the volatile concentrations of the melt at the time of trapping. These numerical modeling results suggest that heterogeneously entrapped MI containing large vapor bubbles represent amenable samples for constraining pre-eruptive volatile concentrations of subvolcanic melts.  相似文献   

18.
Dehydration melting of muscovite in metasedimentary sequences is the initially dominant mechanism of granitic melt generation in orogenic hinterlands. In dry (vapour-absent) crust, muscovite reacts with quartz to produce K-feldspar, sillimanite, and monzogranitic melt. When water vapour is present in excess, sillimanite and melt are the primary products of muscovite breakdown, and any K-feldspar produced is due to melt crystallization. Here we document the reaction mechanisms that control nucleation and growth of K-feldspar, sillimanite, and silicate melt in the metamorphic core of the Himalaya, and outline the microstructural criteria used to distinguish peritectic K-feldspar from K-feldspar grains formed during melt crystallization. We have characterized four stages of microstructural evolution in selected psammitic and pelitic samples from the Langtang and Everest regions: (a) K-feldspar nucleates epitaxially on plagioclase while intergrowths of fibrolitic sillimanite and the remaining hydrous melt components replace muscovite. (b) In quartzofeldspathic domains, K-feldspar replaces plagioclase by K+–Na+ cation exchange, while melt and intergrowths of sillimanite+quartz form in the aluminous domains. (c) At 7–8 vol.% melt generation, the system evolves from a closed to open system and all phases coarsen by up to two orders of magnitude, resulting in large K-feldspar porphyroblasts. (d) Preferential crystallization of residual melt on K-feldspar porphyroblasts and coarsened quartz forms an augen gneiss texture with a monzogranitic-tonalitic matrix that contains intergrowths of sillimanite+tourmaline+muscovite+apatite. Initial poikiloblasts of peritectic K-feldspar trap fine-grained inclusions of quartz and biotite by replacement growth of matrix plagioclase. During subsequent coarsening, peritectic K-feldspar grains overgrow and trap fabric-aligned biotite, resulting in a core to rim coarsening of inclusion size. These microstructural criteria enable a mass balance of peritectic K-feldspar and sillimanite to constrain the amount of free H2O present during muscovite dehydration. The resulting modal proportion of K-feldspar in the Himalayan metamorphic core requires vapour-absent conditions during muscovite dehydration melting and leucogranite formation, indicating that the generation of large volumes of granitic melts in orogenic belts is not necessarily contingent on an external source of fluids.  相似文献   

19.
Partitioning of F between H2O and CO2 fluids and topaz rhyolite melt   总被引：2，自引：0，他引：2  
Fluid/melt distribution coefficients for F have been determined in experiments conducted with peraluminous topaz rhyolite melts and fluids consisting of H2O and H2O+CO2 at pressures of 0.5 to 5 kbar, temperatures of 775°–1000°C, and concentrations of F in the melt ranging from 0.5 to 6.9 wt%. The major element, F, and Cl concentrations of the starting material and run product glasses were determined by electron microprobe, and the concentration of F in the fluid was calculated by mass balance. The H2O concentrations of some run product glasses were determined by ion microprobe (SIMS). The solubility of melt in the fluid phase increases with increasing F in the system; the solubility of H2O in the melt is independent of the F concentration of the system with up to 6.3 wt% F in the melt. No evidence of immiscible silica- and fluoriderich liquids was detected in the hydrous but water-undersaturated starting material glasses (8.5 wt% F in melt) or in the water-saturated run product glasses. F concentrates in topaz rhyolite melts relative to coexisting fluids at most conditions studied; however, DF (wt% F in fluid/wt% F in melt) increases strongly with increasing F in the system. Maximum values of DF in this study are significantly larger than those previously reported in the literature. Linear extrapolation of the data suggests that DF is greater than one for water-saturated, peraluminous granitic melts containing 8 wt% F at 800° C and 2 kbar. DF increases as temperature and as (H2O/H2O+CO2) of the fluid increase. For topaz rhyolite melts containing 1 wt% F and with H2O-rich fluids, DF is independent of changes in pressure from 2 to 5 kbar at 800° C; for melts containing 1 wt% F and in equilibrium with CO2-bearing fluids the concentrations of F in fluid increases with increasing pressure. F-and lithophile element-enriched granites may evolve to compositions containing extreme concentrations of F during the final stages of crystallization. If F in the melt exceeds 8 wt%, DF is greater than one and the associated magmatic-hydrothermal fluid contains >4 molal F. Such F-enriched fluids may be important in the mass transport of ore constituents, i.e., F, Mo, W, Sn, Li, Be, Rb, Cs, U, Th, Nb, Ta, and B, from the magma.  相似文献   

20.
Partition coefficients (DBemineral/melt) for beryllium between hydrous granitic melt and alkali feldspars, plagioclase feldspars, quartz, dark mica, and white mica were determined by experiment at 200 MPa H2O as a function of temperature (650-900°C), activity of Be in melt (trace levels to beryl saturation), bulk composition, and thermal run direction. At trace levels, Be is compatible in plagioclase of An31 (1.84 at 700°C) and muscovite (1.35 at 700°C) but incompatible in biotite (0.39-0.54 from 650-800°C), alkali feldspar (0.38-0.19 from 680-850°C), quartz (0.24 at 800°C), and albite (0.10 at 750°C). The partition coefficients are different at saturation of the melt in beryl: lower in the case of plagioclase of An31 (0.89 at 700°C), muscovite (0.87 at 700°C), biotite (0.18-0.08 from 675-800°C), alkali feldspar (0.18-0.14 from 680-700°C), and quartz (0.17-0.08 from 750-800°C), but higher in the case of albite (0.37 at 750°C).With other data sources, these new partition coefficients were utilized to track, first, the distribution of Be between aluminous quartzofeldspathic source rocks and their anatectic melts, and second, the dispersion or concentration of Be in melt through igneous crystal fractionation of different magma types (e.g., S-type, I-type) up to beryl-saturated granitic pegmatites and, finally, into their hydrothermal aureoles. Among the rock-forming minerals, cordierite, calcic oligoclase, and muscovite (in this order) control the fate of Be because of the compatibility of Be in these phases. In general, beryl-bearing pegmatites can arise only after extended crystal fractionation of large magma batches (to F, fraction of melt remaining, ≤0.05); granitic magmas that originate from cordierite-bearing protoliths or that contain large modal quantities of calcic oligoclase will not achieve beryl saturation at any point in their evolution.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号