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1.
埃达克岩的Na亏损及其对地幔Na交代的指示意义   总被引：1，自引：3，他引：1  
埃达克岩是玄武质洋壳部分熔融的产物。然而,与实验室玄武岩部分熔融产生的埃达克质熔体相比,天然埃达克岩明显地高Mg、Cr和Ni,这表明埃达克岩浆在上升过程中有地幔成分的加入。本文的观察结果表明,全球新生代埃达克岩的Na2O含量低于5.8%,大约95%的新生代埃达克岩样品Na2O含量小于5.0%。然而,在埃达克岩产生的压力范围(1.5～3.0GPa),实验的玄武岩部分熔体大多数Na2O含量超过5.0%,最高达到9.0%,显示埃达克岩具有明显的Na亏损现象。我们认为这是埃达克熔体在热的地幔楔中与地幔橄榄岩反应的结果。在俯冲带,大洋板片熔融产生的熔体(埃达克熔体)上升并与地幔橄榄岩发生反应,原始的埃达克熔体获得MgO、Cr及Ni等地幔组分,但其Na2O和SiO2等通过反应进入地幔,导致地幔交代作用。根据长英质熔体与橄榄岩反应体系的相关系,我们认为,地幔单斜辉石、橄榄石、尖晶石的混染作用以及钠质角闪石和斜方辉石的分离结晶作用,是改变埃达克熔体组成并导致其Na亏损的一个重要的过程。埃达克岩的Na亏损为地幔Na交代作用和一些富Na的弧岩浆成因提供了重要证据。  相似文献   

2.
深部过程对埃达克质岩石成分的制约   总被引：45，自引：18，他引：27  
埃达克岩、太古宙TTG和中国东部广泛出露的燕山期埃达克质中酸性火山-侵入岩在岩石地球化学特征方面有许多相似之处,也有一些显著的差异。与典型的埃达克岩相比,太古宙TTG具有相对高Si和低Mg^#的特点：中国东部埃达克质岩石多表现为低Mg^#贫A120,和高K特征。埃达克岩相对高Mg^#是由于俯冲洋壳部分熔融产生的原生埃达克岩熔体受到了地幔橄榄岩的混染,太古宙TTG多无明显的地幔混染印记,反映其可能主要形成于下地壳底侵玄武岩的部分熔融,而与洋壳俯冲没有直接联系。中国东部埃达克质岩石相对低Mg^#畜K,暗示其可能是下地壳底侵玄武岩部分熔融或拆沉-熔融的产物,而幔源富钾熔体的混合、壳内分异和混染过程都有可能影响其成分特征中国东部部分地区的高镁埃达克质岩石可能揭示了下地壳拆沉一熔融和地幔混染过程。钾质埃达克岩的源区可能是被小比例软流圈熔体交代富集的底侵玄武岩层(增厚的下地壳)。结合燕山期岩浆作用和构造转换的特点来看,埃达克岩的形成是中国东部晚中生代岩石圈强烈减薄和大规模岩浆作用产物的一部分,这一重大构造体制的转换可能与地幔柱上涌对岩石圈的侵蚀和导致的伸展作用有关。  相似文献   

3.
Manganese contents and the iron/manganese ratio of igneous rocks have been used as a method of probing the heterogeneity in the Earth’s mantle during melting of peridotite and pyroxenite lithologies. Most previous work has assumed that changes in these parameters require differences in either source lithology or composition based on experiments indicating that manganese is slightly incompatible during melting and that the iron/manganese ratio is fixed by the presence of olivine. However, the presence of volatiles in the mantle drives melting at lower temperatures and with different compositions than in volatile-free systems, and thus the partitioning of Fe and Mn may in fact vary. We have produced silicate liquids in equilibrium with a peridotite assemblage under hydrous conditions at 3 GPa that show that Mn can also be unexpectedly compatible in garnet at 1375 °C and that Mn partitioning between solids and liquids can be strongly affected by temperature and liquid composition. The compatibility of Mn in garnet provides a mechanism for large variations of Mn contents and the Fe/Mn ratio in silicate melts that solely involves melting of mantle peridotite with only small compositional changes. Correlations between Mn variations and other indices indicative of melting in the presence of garnet may provide a means of more completely understanding the role of garnet at high pressures in peridotite melting.  相似文献   

4.
The influence of water on melting of mantle peridotite   总被引：47，自引：8，他引：39  
This experimental study examines the effects of variable concentrations of dissolved H2O on the compositions of silicate melts and their coexisting mineral assemblage of olivine + orthopyroxene ± clinopyroxene ± spinel ± garnet. Experiments were performed at pressures of 1.2 to 2.0 GPa and temperatures of 1100 to 1345 °C, with up to ∼12 wt% H2O dissolved in the liquid. The effects of increasing the concentration of dissolved H2O on the major element compositions of melts in equilibrium with a spinel lherzolite mineral assemblage are to decrease the concentrations of SiO2, FeO, MgO, and CaO. The concentration of Al2O3 is unaffected. The lower SiO2 contents of the hydrous melts result from an increase in the activity coefficient for SiO2 with increasing dissolved H2O. The lower concentrations of FeO and MgO result from the lower temperatures at which H2O-bearing melts coexist with mantle minerals as compared to anhydrous melts. These compositional changes produce an elevated SiO2/(MgO + FeO) ratio in hydrous peridotite partial melts, making them relatively SiO2 rich when compared to anhydrous melts on a volatile-free basis. Hydrous peridotite melting reactions are affected primarily by the lowered mantle solidus. Temperature-induced compositional variations in coexisting pyroxenes lower the proportion of clinopyroxene entering the melt relative to orthopyroxene. Isobaric batch melting calculations indicate that fluid-undersaturated peridotite melting is characterized by significantly lower melt productivity than anhydrous peridotite melting, and that the peridotite melting process in subduction zones is strongly influenced by the composition of the H2O-rich component introduced into the mantle wedge from the subducted slab. Received: 7 April 1997 / Accepted: 9 January 1998  相似文献   

5.
为完整了解华北克拉通的破坏程度和机制,加深对其西部陆块岩石圈地幔的研究十分重要,而位于华北克拉通西部集宁新生代碱性玄武岩中的地幔橄榄岩包体,为研究人员认识该地区的岩石圈地幔的性质和演化起到指示作用.运用LA-ICP-MS和LA-MC-ICP-MS对集宁地区橄榄岩矿物进行原位微区测试,获得其主量、微量元素和Sr同位素成分的数据.根据矿物组成,可以将集宁地区的橄榄岩分为两类:第一类为贫单斜辉石橄榄岩 (单斜辉石体积分数小于8%),它们经历了高程度的部分熔融,可能是古老难熔岩石圈地幔的残留;第二类为二辉橄榄岩 (单斜辉石体积分数大于13%),其熔融程度低,代表了新生饱满的岩石圈地幔.第一类橄榄岩中单斜辉石REE含量整体偏低且轻微富集LREE,第二类橄榄岩中单斜辉石具有LREE富集和轻微亏损两种配分模式,大部分样品的核边有一定的强不相容元素及Sr同位素组成变化.这些微量元素和同位素特征都表明集宁橄榄岩包体经历过交代作用.(La/Yb)N和Ti/Eu比值特征表明它们经历过多阶段的交代作用,交代介质有硅酸盐、碳酸盐熔/流体,这些交代介质可能为来源于古亚洲洋板块俯冲时释放的熔/流体.   相似文献   

6.
Carbon dioxide solubilities in H2O-free hydrous silicate melts of natural andesite (CA), tholeiite (K 1921), and olivine nephelinite (OM1) compositions have been determined employing carbon-14 beta-track mapping techniques. The CO2 solubility increases with increasing pressure, temperature, and degree of silica-undersaturation of the silicate melt. At 1650° C, CO2 solubility in CA increases from 1.48±0.05 wt % at 15 kbar to 1.95±0.03 wt % at 30 kbar. The respective solubilities in OM1 are 3.41±0.08 wt % and 7.11±0.10 wt %. The CO2 solubility in K1921 is intermediate between those of CA and OM1 compositions. At lower temperatures, the CO2 contents of these silicate melts are lower, and the pressure dependence of the solubility is less pronounced. The presence of H2O also affects the CO2 solubility (20–30% more CO2 dissolves in hydrous than in H2O-free silicate melts); the solubility curves pass through an isothermal, isobaric maximum at an intermediate CO2/(CO2+H2O) composition of the volatile phase. Under conditions within the upper mantle where carbonate minerals are not stable and CO2 and H2O are present a vapor phase must exist. Because the solubility of CO2 in silicate melts is lower than that of H2O, volatiles must fractionate between the melt and vapor during partial melting of peridotite. Initial low-temperature melts will be more H2O-rich than later high-temperature melts, provided vapor is present during the melting. Published phase equilibrium data indicate that the compositional sequence of melts from peridotite +H2O+CO2 parent will be andesite-tholeiite-nephelinite with increasing temperature at a pressure of about 20 kbar. Examples of this sequence may be found in the Lesser Antilles and in the Indonesian Island Arcs.  相似文献   

7.
王强  许继峰  赵振华 《地学前缘》2003,10(4):561-572
文中概述了强烈亏损重稀土元素的中酸性火成岩(或埃达克质岩)的研究历史、现状和意义,列出了扬子地块东部、青藏高原以及新疆北部与铜金成矿有关的同类岩石的一些特征,重点分析了当前强烈亏损重稀土元素的中酸性火成岩(或埃达克质岩)的研究中所存在的问题,并提出了一些初步的设想。强烈亏损重稀土元素的中酸性火成岩(或埃达克质岩)不仅具有重要的地球动力学意义(可能与俯冲、拆沉、底侵、板片窗或地幔交代等深部过程有关),而且具有极其重要的Cu、Au成矿意义。俯冲洋壳熔融形成的埃达克岩及其成矿作用已有相当深入的研究,但是来自大陆内部的强烈亏损重稀土元素的中酸性火成岩的成因、岩石组合及其成矿作用是否类似于俯冲洋壳熔融形成的埃达克岩,还需要深入的研究。一些强烈亏损重稀土元素的中酸性火成岩(或埃达克质岩)的所表现出的高钾特征很可能与高压(>1 GPa)条件下的熔融或源岩的高钾有关。文中提出了一个有别于俯冲洋壳熔融+埃达克岩+Cu、Au成矿的新工作模型——拆沉洋壳或下地壳熔融+强烈亏损重稀土元素的中酸性火成岩(或埃达克质岩)+Cu、Au成矿。拆沉洋壳或下地壳熔融形成熔体的Fe_2O_3对地幔的交代(氧化)作用可能是Cu、Au从地幔迁出并最终成矿的一个重要原因,但是增厚下地壳环境中流体的作用也不?  相似文献   

8.
富铌玄武岩：板片熔体交代的地幔楔橄榄岩部分熔融产物   总被引：4，自引：0，他引：4  
富铌玄武岩是一类具有特殊地球化学特征的岛弧玄武岩。与正常岛弧玄武岩相比，它具有硅饱和并富钠的特征；同时具有相对高的Nb（一般>7×10-6）、TiO2（1%～2%）和P含量，以及低的LILE/HFSE和HREE/HFSE比值，并富集高场强元素；它的原始地幔标准化微量元素图显示了弱的Nb、Ta负异常（有时出现弱的正异常），原始地幔标准化La/Nb比值小于2（但很少小于0.7），它是由受埃达克质熔体交代过的地幔橄榄岩部分熔融形成的。由于富铌玄武岩与埃达克岩是大洋板片俯冲作用的直接产物，因此，通过对该岩石组合及与俯冲作用有关的流体和熔体的研究，不仅可以查明洋壳俯冲作用过程中的岩浆活动特征，还可以阐明洋壳俯冲及壳幔相互作用，具十分重要的地质意义。  相似文献   

9.
This experimental study examines the mineral/melt partitioning of incompatible trace elements among high-Ca clinopyroxene, garnet, and hydrous silicate melt at upper mantle pressure and temperature conditions. Experiments were performed at pressures of 1.2 and 1.6 GPa and temperatures of 1,185 to 1,370 °C. Experimentally produced silicate melts contain up to 6.3 wt% dissolved H 2O, and are saturated with an upper mantle peridotite mineral assemblage of olivine+orthopyroxene+clinopyroxene+spinel or garnet. Clinopyroxene/melt and garnet/melt partition coefficients were measured for Li, B, K, Sr, Y, Zr, Nb, and select rare earth elements by secondary ion mass spectrometry. A comparison of our experimental results for trivalent cations (REEs and Y) with the results from calculations carried out using the Wood-Blundy partitioning model indicates that H 2O dissolved in the silicate melt has a discernible effect on trace element partitioning. Experiments carried out at 1.2 GPa, 1,315 °C and 1.6 GPa, 1,370 °C produced clinopyroxene containing 15.0 and 13.9 wt% CaO, respectively, coexisting with silicate melts containing ~1–2 wt% H 2O. Partition coefficients measured in these experiments are consistent with the Wood-Blundy model. However, partition coefficients determined in an experiment carried out at 1.2 GPa and 1,185 °C, which produced clinopyroxene containing 19.3 wt% CaO coexisting with a high-H 2O (6.26±0.10 wt%) silicate melt, are significantly smaller than predicted by the Wood-Blundy model. Accounting for the depolymerized structure of the H 2O-rich melt eliminates the mismatch between experimental result and model prediction. Therefore, the increased Ca 2+ content of clinopyroxene at low-temperature, hydrous conditions does not enhance compatibility to the extent indicated by results from anhydrous experiments, and models used to predict mineral/melt partition coefficients during hydrous peridotite partial melting in the sub-arc mantle must take into account the effects of H 2O on the structure of silicate melts.  相似文献   

10.
对华北克拉通北缘达里诺尔地区鸽子山附近玄武岩中的含金云母辉石岩捕虏体进行了岩石学、矿物学的研究,并对其中的单斜辉石、斜方辉石、金云母和粒间熔体进行了原位微区主、微量元素分析。结果显示,单斜辉石和斜方辉石具有低的Mg^#、Cr 2O 3和高的Al2O3含量,斜方辉石还具有高的MnO含量,这些特征表明辉石岩代表了交代熔体在地幔中冷却固结堆晶形成的岩脉。辉石岩中金云母、粒间熔体的出现及其不平衡的地球化学特征说明辉石岩形成以后又遭受到了多期次的硅酸盐熔体地幔交代作用。结晶出单斜辉石的母岩浆在蛛网图上具有K、Pb元素的弱负异常但不具有Nb、Ta、Ti元素的负异常,推测形成辉石岩的熔体可能来自软流圈地幔。粒间熔体的低SiO2,高MgO和FeO的特征指示其形成于地幔超基性岩的部分熔融,蛛网图上明显的K、Pb正异常以及Nb、Ta负异常说明其源区也存在俯冲沉积物的贡献。基于此,认为中国东部新生代岩石圈地幔经历了多期次地幔交代作用。  相似文献   

11.
Fluids and Melts in the Upper Mantle   总被引：3，自引：0，他引：3  
This paper presents a direct study of the fluids and melts in the upper mantle by examining the fluid inclusions, melt inclusions and glasses trapped in the mantle lherzolite xenoliths entrained by Cenozoic alkali basalts (basanite, olivine-nephelinite and alkali-olivine basalt) from eastern China. The study indicates that the volatile components, which are dissolved in high-pressure solid mineral phases of mantle peridotite at depths, may be exsolved under decompressive conditions of mantle plume upwelling to produce the initial free fluid phases in the upper mantle. The free fluid phases migrating in the upper mantle may result in lowering of the mantle solidus (and liquidus), thereby initiating partial melting of the upper mantle, and in the meantime, producing metasomatic effects on the latter.  相似文献   

12.
Crystalline and melt inclusions were studied in garnet,diopside,potassium feldspar,and sphene from the garnet syenite porphyry of the carbonatite-bearing complex Mushugai-Khuduk,southern Mongolia.Phlogopite,clinopyroxene,albite,potassium feldspar,spheric,wollastonite,magnetite,Ca and Sr sulfates,fluorite,and apatite were identified among the crystalline inclusions. The melt inclusions were homogenized at 1010～1080℃and analyzed on an electron microprobe.Silicate,salt,and combined silicate- salt melt inclusions were found.Silicate melts show considerable variations in SiO_2 concentration(56 to 66wt% ),high Na_2O K_2O (up to 17wt% ),and elevated Zr,F,and C1 contents.In terms of bulk rock chemistry,the silicate melts are alkali syenites.During thermometric experiments,salt melt inclusions quenched into homogeneous glasses of predominantly sulfate compositions containing no more than 1.3wt% SiO_2.These melts are enriched in alkalis,Ba,Sr,P,F,and C1.The investigation of the silicate and salt melt inclusions in minerals of the garnet syenite porphyries indicate that these rocks were formed under influence of the processes of crystallization differentiation and magma separation into immiscible silicate and salt(sulfate)liquids.  相似文献   

13.
We determined the melting phase relations, melt compositions, and melting reactions of carbonated peridotite on two carbonate-bearing peridotite compositions (ACP: alkali-rich peridotite + 5.0 wt % CO2 and PERC: fertile peridotite + 2.5 wt % CO2) at 10–20 GPa and 1,500–2,100 °C and constrain isopleths of the CO2 contents in the silicate melts in the deep mantle. At 10–20 GPa, near-solidus (ACP: 1,400–1,630 °C) carbonatitic melts with < 10 wt % SiO2 and > 40 wt % CO2 gradually change to carbonated silicate melts with > 25 wt % SiO2 and < 25 wt % CO2 between 1,480 and 1,670 °C in the presence of residual majorite garnet, olivine/wadsleyite, and clinoenstatite/clinopyroxene. With increasing degrees of melting, the melt composition changes to an alkali- and CO2-rich silicate melt (Mg# = 83.7–91.6; ~ 26–36 wt % MgO; ~ 24–43 wt % SiO2; ~ 4–13 wt % CaO; ~ 0.6–3.1 wt % Na2O; and ~ 0.5–3.2 wt % K2O; ~ 6.4–38.4 wt % CO2). The temperature of the first appearance of CO2-rich silicate melt at 10–20 GPa is ~ 440–470 °C lower than the solidus of volatile-free peridotite. Garnet + wadsleyite + clinoenstatite + carbonatitic melt controls initial carbonated silicate melting at a pressure < 15 GPa, whereas garnet + wadsleyite/ringwoodite + carbonatitic melt dominates at pressure > 15 GPa. Similar to hydrous peridotite, majorite garnet is a liquidus phase in carbonated peridotites (ACP and PERC) at 10–20 GPa. The liquidus is likely to be at ~ 2,050 °C or higher at pressures of the present study, which gives a melting interval of more than 670 °C in carbonated peridotite systems. Alkali-rich carbonated silicate melts may thus be produced through partial melting of carbonated peridotite to 20 GPa at near mantle adiabat or even at plume temperature. These alkali- and CO2-rich silicate melts can percolate upward and may react with volatile-rich materials accumulate at the top of transition zone near 410-km depth. If these refertilized domains migrate upward and convect out of the zone of metal saturation, CO2 and H2O flux melting can take place and kimberlite parental magmas can be generated. These mechanisms might be important for mantle dynamics and are potentially effective metasomatic processes in the deep mantle.  相似文献   

14.
Lithium elemental and isotopic disequilibrium has frequently been observed in the continental and oceanic mantle xenoliths, but its origin remains controversial. Here, we present a combined elemental and Li isotopic study on variably metasomatised peridotite xenoliths entrained in the Cenozoic basalts from Shangzhi in Northeast (NE) China that provides insight into this issue. Li concentration (0.3–2.7 ppm) and δ7Li (mostly 2‰–6‰) in olivine from the Shangzhi peridotites are similar to the normal mantle values and show roughly negative correlations with the indices of melt extraction (such as modal olivine and whole rock MgO). These features are consistent with variable degrees of partial melting. In contrast, clinopyroxene from the Shangzhi xenoliths shows significant Li enrichment (0.9–6.1 ppm) and anomalously light δ7Li (??13.8‰ to 7.7‰) relative to normal mantle values. Such features can be explained by Li diffusion from silicate melts or Li-rich fluids occurring over a very short time (several minutes to several hours). Moreover, the light Li isotopic compositions preserved in some bulk samples also indicate that these percolated melts/fluids have not had enough time to isotopically equilibrate with the bulk peridotite. We thus emphasize that Li isotopic fractionation in the Shangzhi mantle xenoliths is mainly related to Li diffusion from silicate melts or Li-rich fluids that took place shortly before or coincident with their entrainment into the host magmas.  相似文献   

15.
女山中更新世碧玄岩岩浆的起源和演化   总被引：9，自引：0，他引：9  
夏林圻  夏祖春 《岩石学报》1994,10(3):223-235
产于大陆板内环境的女山中更新世碧玄质火山岩及其所含幔源二辉橄榄岩捕虏体的研究结果揭示，在裂谷作用初始阶段，由于软流圈地幔柱上隆减压，造成深部溶解于地幔橄榄岩高压固体矿物相中的挥发组分出溶，这些出溶的初始地幔流体相在一定部位聚集，于３０Ｍａ前，大约３７ｋｍ之下，在地幔橄榄岩中诱发同步的部分熔融和交代作用，并相应产生原生碧玄质岩浆。后者上升速度较快，既未经历壳内高位岩浆房贮集，也没有遭受大陆地壳混染，只是在输送往地表的途中伴随结晶分离作用，发生一定程度演化。  相似文献   

16.
We performed modified iterative sandwich experiments (MISE) to determine the composition of carbonatitic melt generated near the solidus of natural, fertile peridotite + CO2 at 1,200–1,245°C and 6.6 GPa. Six iterations were performed with natural peridotite (MixKLB-1: Mg# = 89.7) and ∼10 wt% added carbonate to achieve the equilibrium carbonatite composition. Compositions of melts and coexisting minerals converged to a constant composition after the fourth iteration, with the silicate mineral compositions matching those expected at the solidus of carbonated peridotite at 6.6 GPa and 1,230°C, as determined from a sub-solidus experiment with MixKLB-1 peridotite. Partial melts expected from a carbonated lherzolite at a melt fraction of 0.01–0.05% at 6.6 GPa have the composition of sodic iron-bearing dolomitic carbonatite, with molar Ca/(Ca + Mg) of 0.413 ± 0.001, Ca# [100 × molar Ca/(Ca + Mg + Fe*)] of 37.1 ± 0.1, and Mg# of 83.7 ± 0.6. SiO2, TiO2 and Al2O3 concentrations are 4.1 ± 0.1, 1.0 ± 0.1, and 0.30 ± 0.02 wt%, whereas the Na2O concentration is 4.0 ± 0.2 wt%. Comparison of our results with other iterative sandwich experiments at lower pressures indicate that near-solidus carbonatite derived from mantle lherzolite become less calcic with increasing pressure. Thus carbonatitic melt percolating through the deep mantle must dissolve cpx from surrounding peridotite and precipitate opx. Significant FeO* and Na2O concentrations in near solidus carbonatitic partial melt likely account for the ∼150°C lower solidus temperature of natural carbonated peridotite compared to the solidus of synthetic peridotite in the system CMAS + CO2. The experiments demonstrate that the MISE method can determine the composition of partial melts at very low melt fraction after a small number of iterations.  相似文献   

17.
大兴安岭北部诺敏河地幔金云母及钾质地幔熔体研究   总被引：2，自引：1，他引：1  
隋建立  李霓  樊祺诚  徐义刚 《岩石学报》2014,30(12):3587-3594
在大兴安岭北部诺敏河第四纪钾质火山岩携带的地幔捕虏体中,发现少量金云母矿物和富钾地幔熔体。金云母颗粒大小1~5mm,呈网脉状充填在橄榄石和辉石、石榴子石等地幔矿物间隙。电子探针研究表明地幔橄榄石、单斜辉石、斜方辉石和石榴石等矿物几乎不含钾质成分(K2O0.01%),而金云母矿物成分具有高钾(K2O~10%)、高钛(Ti O25.41%~7.74%)的特点,暗示区域地幔钾的富集与金云母矿物有密切关系。地幔金云母的成因往往与富钾地幔流体/熔体的交代作用有关,在地幔捕虏体矿物反应边的硅酸盐熔体(囊体)中,发现富硅、富钾的熔体,K2O 4%~8%。结合前人地幔熔体研究,认为区域地幔经历了多期、不同成分地幔熔体的富集作用,其中富钾熔体对地幔钾质成分的富集起到重要作用。诺敏钾质火山正是富钾地幔部分熔融的产物,钾质熔体成分的来源可能与俯冲再循环的壳源物质有关。  相似文献   

18.
We performed partial melting experiments at 1 and 1.5 GPa, and 1180–1400 °C, to investigate the melting under mantle conditions of an olivine-websterite (GV10), which represents a natural proxy of secondary (or stage 2) pyroxenite. Its subsolidus mineralogy consists of clinopyroxene, orthopyroxene, olivine and spinel (+garnet at 1.5 GPa). Solidus temperature is located between 1180 and 1200 °C at 1 GPa, and between 1230 and 1250 °C at 1.5 GPa. Orthopyroxene (±garnet), spinel and clinopyroxene are progressively consumed by melting reactions to produce olivine and melt. High coefficient of orthopyroxene in the melting reaction results in relatively high SiO2 content of low melt fractions. After orthopyroxene exhaustion, melt composition is controlled by the composition of coexisting clinopyroxene. At increasing melt fraction, CaO content of melt increases, whereas Na2O, Al2O3 and TiO2 behave as incompatible elements. Low Na2O contents reflect high partition coefficient of Na between clinopyroxene and melt (\(D_{{{\text{Na}}_{ 2} {\text{O}}}}^{{{\text{cpx}}/{\text{liquid}}}}\)). Melting of GV10 produces Quartz- to Hyperstene-normative basaltic melts that differ from peridotitic melts only in terms of lower Na2O and higher CaO contents. We model the partial melting of mantle sources made of different mixing of secondary pyroxenite and fertile lherzolite in the context of adiabatic oceanic mantle upwelling. At low potential temperatures (T P < 1310 °C), low-degree melt fractions from secondary pyroxenite react with surrounding peridotite producing orthopyroxene-rich reaction zones (or refertilized peridotite) and refractory clinopyroxene-rich residues. At higher T P (1310–1430 °C), simultaneous melting of pyroxenite and peridotite produces mixed melts with major element compositions matching those of primitive MORBs. This reinforces the notion that secondary pyroxenite may be potential hidden components in MORB mantle source.  相似文献   

19.
We have experimentally investigated the phase and melting relations of garnet + clinopyroxene + carbonate assemblages at 2.5–5.5 GPa, to assess the feasibility of carbonated eclogite as a source for some crustally emplaced carbonatites. The solidus of our composition was at 1,125 °C at 2.5 GPa, 1,225 °C at 3.5 GPa and 1,310 °C at 5.0 GPa. Melts were sodic calcio-dolomitic carbonatites, and were markedly more calcic than the dolomitic melts produced by partial melting of carbonated peridotite. Na contents of the experimental carbonatites decreased with increasing pressure when compared at similar degrees of melting, and SiO2 contents increased with degree of melting. Experiments on a second composition with enhanced Na2O demonstrated its strong effect in lowering melting temperatures in carbonate eclogite. Natural carbonated eclogite bodies in the peridotitic upper mantle will have a range of solidus temperatures. In many cases, carbonate will be molten in the upper 250 km. Carbonate melt would segregate from its source eclogite at very low melt fractions and infiltrate surrounding peridotitic wall rock. This would result in metasomatic enrichment of the peridotitic wall rock, but its exact nature will depend on the relative P–T positions of the eclogite + CO2 and peridotite + CO2 solidii. As a result of these inevitable metasomatic interactions, it is considered unlikely that carbonatite melts derived from carbonated eclogite in the upper mantle could be emplaced into the crust unmodified. However, they may have a role in metasomatically enriching and carbonating parts of the upper mantle, producing sources suitable for subsequent production of silica undersaturated silicate liquids and carbonatites ultimately emplaced in the crust.Editorial responsibility: J. Hoefs  相似文献   

20.
With aim of providing constraints on the Late Paleozoic tectonic evolution of the southern Central Asian Orogenic Belt(CAOB),an integrated study was conducted on the geochronological and geochemical data for dioritic,granitic and diabase dykes from the Aqishan-Yamansu belt in the eastern Tianshan,NW China.Zircon U-Pb dating indicates that the dioritic and granitic dykes were both emplaced in the Late Carboniferous(~311 Ma and^315 Ma).The dioritic dykes show adakitic characteristics and have high Na2 O and positiveεHf(t)values(+12 to+17),which suggest an origin from partial melts of a subducted oceanic slab.The granitic dykes have high SiO2 and K2 O contents and are characterized by en riched light rare earth elements(LREE)and slightly flat heavy rare earth elements(HREE),with negative Eu and Nb-Ta-Ti anomalies.These dykes are alkali-calcic and show geochemical features of highly fractionated Itype granites.Their positiveεHf(t)values(+16 to+17)suggest that they were derived from a juvenile accreted oceanic crustal sou rce.The coeval diabase dykes have low SiO2 and K2 O contents but high TiO2,MgO and Mg#(54-59).They are enriched in LREE and show characteristics of enriched mid-ocean ridge basalts(E-MORB).The relatively high Ba/Th,slightly low Th/Ta ratios,and negative Nb-Ta anomalies imply a mantle source metasomatised by slab-derived fluids.Thus,these basic dykes were generated likely by partial melting of the upwelling asthenosphere mantle with a slight influence of slab-derived fluids.Therefore,we suggest that the formation of these Late Carboniferous dykes were triggered by a post-collisional slab breakoff and the Aqishan-Yamansu belt was a continental arc formed by southdipping subduction of the Kangguer oceanic plate.  相似文献   

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