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1.
吕伟 《地质与勘探》2023,59(6):1260-1270
为研究黑河地区金红石微量元素特征及榴辉岩型金红石矿床的成矿地质条件,本文选取滇西澜沧黑河地区榴辉岩、石榴多硅白云母片岩中的金红石进行LA-ICP-MS微量元素分析。结果表明金红石微量元素呈现阶梯式三级分布特征,最富集Nb、Ta,其次是Zr、Hf,含量较少的元素有Ba、Rb、Sr、Th、REE;榴辉岩、榴闪岩类原岩属于变质基性岩类,含蓝晶石榴闪岩原岩属于玄武质凝灰岩类,石榴多硅白云母片岩类原岩属于泥质岩类;榴辉岩中金红石Nb/Ta比值均要高于其全岩Nb/Ta比值,金红石Nb、Ta含量与变质作用过程中元素在各矿物间的分配系数有关;采用金红石Zr含量温度计获得黑河地区榴辉岩的峰期变质阶段金红石形成温度为578～605℃,峰期变质作用后的退变质流体会造成金红石中Zr的再平衡。此外,黑河地区具备榴辉岩型金红石矿床形成的成矿物源、成矿作用的物理化学条件以及成矿的物质基础,有一定的找矿潜力。  相似文献   

2.
根据矿物成分及其结构演变,将大别山榴辉岩的退变质过程分为三个阶段:贫流体阶段、弱流体阶段和富流体阶段。贫流体阶段发生于榴辉岩相环境中,其主要作用是柯石英-石英和文石- 方解石等同质多象转变、石榴子石和绿辉石等的重结晶,以及绿辉石中硬玉和钠长石的固溶体出溶等。弱流体阶段发生于榴辉岩相退变质的晚期,含水矿物闪石、绿帘石和云母,以及钠长石等低压矿物大量形成之前,其标志是蓝晶石变斑晶和金红石脉的形成,以及浸染状金红石的富集成矿。富流体阶段始于低级角闪岩相退变质环境,并可能一直持续到近地表处。该阶段以出现大量含水和挥发份的矿物(如闪石、绿帘石、多硅白云母、钠云母、黑云母、磷灰石和碳酸盐等)为特征。围绕石榴子石和绿辉石的闪石次变边、闪  相似文献   

3.
应用LA-ICP-MS方法对新疆西南天山高压-超高压变质带中的榴辉岩及其高压脉体中的金红石和榍石进行了Zr含量的检测和Zr温度计的计算。榴辉岩中位于石榴石幔部且与绿辉石共生的金红石包体Zr含量都集中于10~20μg/g;而基质金红石的Zr含量为30~50μg/g,高于包体金红石。榍石均为金红石退变质的产物,且各样品间的榍石Zr含量较均一,都集中在3~5μg/g之间。脉体金红石Zr含量则与榴辉岩中基质金红石的Zr含量相当甚至偏高一些,为30~60μg/g。金红石和榍石的Zr温度计研究也表明,榴辉岩石榴石中的金红石包体生长于压力峰期阶段,温压条件为480~540℃、2.7~3.0 GPa;基质金红石随温度增加达到退变质再平衡,记录了温度峰期的条件,约530~590℃、2.4~2.7 GPa;榴辉岩中高压脉体中的金红石则生长于退变质榴辉岩相阶段,金红石Zr温度计给出结果为540~580℃、1.5~2.1 GPa,记录了近等温降压的过程;榴辉岩中的榍石在1.0 GPa左右达到平衡,榍石Zr温度计给出的温度为540~560℃,记录了进一步的近等温降压的过程。根据以上4个阶段的分析结果,得出一个较完整的顺时针p-T轨迹,且与相平衡模拟所限定的p-T轨迹相一致。金红石的Zr含量可以作为压力的指示,表明压力校正在金红石Zr温度计中起到了重要作用。在对金红石和榍石Zr温度计进行应用时,要结合细致的岩相学观察,综合考虑压力、活度、扩散速率、退变质作用和流体影响等方面的因素,才能得到比较精确的温压估算结果和pT轨迹。  相似文献   

4.
南迦巴瓦地区广泛出露的中下地壳变基性岩部分熔融形成的层状混合岩和淡色花岗岩，为研究部分熔融过程中榍石的地球化学行为对熔体的微量元素组成的影响提供了良好的机会。相对于源岩或熔融残留体，淡色体亏损Ti、V、REE、Y、Nb、Ta、U等元素，与混合岩中榍石的微量元素特征互补。混合岩、淡色体和榍石微量元素特征表明南迦巴瓦角闪岩部分熔融形成的淡色体的微量元素特征主要受控于榍石的地球化学行为。角闪岩脱水部分熔融过程中，由于长英质熔体的低Ti溶解度，榍石以未熔残留体形式存在于暗色体中，导致熔体亏损Ti、REE、Nb、Ta、V、U等元素和Sr/Y比值相对升高。关键元素在榍石和熔体之间的配分系数受熔体成分影响明显。角闪岩中变质榍石DNb/Ta<1，因此变质榍石残留导致熔体Nb/Ta相对于源岩升高；而高Si-Al花岗质熔体中榍石DNb/Ta>1，因此与高Si-Al熔体平衡的榍石的分离（转熔或结晶分异）将导致熔体Nb/Ta比值相对源岩降低。榍石在部分熔融过程中的微量元素效应为理解变基性岩部分熔融产生熔体的地球化学特征提供新的认识。  相似文献   

5.
利用LA-ICP-MS对CCSD-MH超高压榴辉岩中金红石进行了详细的原位微区微量元素组成分析.金红石中高场强元素Nb和Ta含量主要受全岩Nb、Ta和TiO2含量控制, Zr、Hf含量比较稳定基本不受全岩含量影响.粒间金红石中, 同一颗粒金红石核部Zr含量系统高于边部, 而边部则出现了明显的Pb和Sr富集特征.CCSD-MH榴辉岩中金红石与全岩的Nb/Ta比值呈现明显的不一致性.全岩Nb/Ta比值明显低于金红石且与全岩TiO2含量负相关, 而金红石的Nb/Ta比值与全岩Nb、Ta含量和Nb/Ta比值没有明显的相关关系.金红石和全岩之间非完全耦合的Nb/Ta组成表明, 金红石并非形成于原岩的结晶过程中而是在超高压变质作用过程中形成, 尽管金红石是榴辉岩中Nb、Ta含量的主要载体矿物, 但金红石的Nb/Ta比值并不一定能完全代表全岩的特征, 而与全岩Nb、Ta和TiO2的含量有关.粒间金红石核部Zr含量所记录的温度与粒径之间具有明显的正相关性, 反映金红石中的Zr在其形成后没有封闭.粒间金红石所表现出的明显的边部富集Pb和Sr的特征, 反映了后期流体活动对金红石组成的影响.这些研究结果为金红石中Zr在高温下的扩散作用和后期流体活动的影响提供了重要证据, 这可能是利用金红石Zr含量地质温度计计算的苏鲁-大别榴辉岩变质温度(598~827℃) 偏低的主要原因.   相似文献   

6.
对中国大陆科学钻探（CCSD）主孔200~1005m范围内8件榴辉岩样品的金红石进行了LA-ICPMS原位微区微量元素分析,结合前人已发表的全岩和金红石分析数据,研究结果发现：在不同类型榴辉岩中,金红石的微量元素与其全岩成分具有不同的相关关系。金红石中的Nb和Ta元素含量不同程度地受控于全岩Nb和Ta含量。在高钛和低镁钛榴辉岩中,金红石的Cr与全岩Cr/TiO2正相关;在富镁榴辉岩中,金红石的Cr含量受全岩MgO含量的控制;在高钛和富镁榴辉岩中,全岩成分明显影响着金红石的Zr含量,金红石Zr温度计可能不适用。低镁钛榴辉岩的金红石的平衡温度普遍低于榴辉岩峰期变质温度,可能是变质流体参与下的扩散作用和退变质作用所致;多数情况下,单个样品中大部分金红石颗粒的Zr含量是均匀的,金红石Zr温度计所给出的温度可能代表着退变质再平衡的温度;CCSD榴辉岩的全岩Nb/Ta比值普遍低于其中金红石的Nb/Ta比值,不支持金红石榴辉岩可能是地球上超球粒陨石Nb/Ta比值储库的观点。  相似文献   

7.
CCSD主孔超高压榴辉岩金红石中的矿物包裹体研究   总被引：6，自引：0，他引：6  
金红石是榴辉岩中的主要含钛副矿物。中国大陆科学钻探工程（CCSD）主孔100～2000m岩心样品中，金红石榴辉岩、多硅白云母榴辉岩和蓝晶石榴辉岩中都程度不等地含有金红石。金红石既可以与其他矿物一起被石榴石、绿辉石等主要变质矿物包裹，也可以包裹其他矿物。本文利用电子探针技术，对CCSD所揭示的超高压榴辉岩的金红石中的矿物包裹体进行了鉴定和分析。结果显示，绿辉石、富铪锆石、高铝榍石、韭闪石和红闪石、斜黝帘石等矿物包裹体形成于榴辉岩相进变质至峰期变质阶段；随着超高压变质带快速折返，榴辉岩经受强烈的退变质作用，包括金红石、绿辉石在内的多种矿物都经受了退变质作用，与金红石共生的钛铁矿完全或者部分退变成含铁金红石和钛铁晶石。在退变的金红石中，还发现了透辉石＋斜长石后成合晶、低铝榍石、镁绿闪石等退变质矿物组合。  相似文献   

8.
金红石是榴辉岩中的主要含钛副矿物。中国大陆科学钻探工程主孔100-2000m岩心样品中,金红石榴辉岩、多硅白云母榴辉岩和蓝晶石榴辉岩中都程度不等地含有金红石。金红石既可以与其它矿物一起包裹在主要变质矿物中,也可以呈粒间矿物,但在榴辉岩经受角闪岩相退变质作用过程中,金红石亦会退变为榍石。本文利用电子探针除了分析了金红石的主要元素外,还仔细测量了Nb、Cr、Zr含量。结果显示,Nb平均含量为147ppm,最高含量为670ppm,Cr的平均含量为614ppm,最高含量为3630ppm,低Nb特征(<1000ppm)显示榴辉岩原岩为镁铁质岩石;此外,三类榴辉岩也具有不同的金红石Nb、Cr地球化学特征,即金红石榴辉岩中的金红石表现为低Cr(<500ppm)、Nb变化大(0-670ppm)的特征,多硅白云母榴辉岩中的金红石以中等Cr含量(500-1200ppm)、Nb变化较大(0-480ppm)为特征,而蓝晶石榴辉岩中的金红石显著富Cr(2000-3630ppm),而Nb则非常贫乏(<140ppm)。在总共289个金红石Zr含量数据中,大部分Zr含量分布在150-240ppm之间,均值约为200ppm;利用Zacketal.(2004)提出的金红石温度计,计算得到金红石的形成温度介于690℃和7870℃之间。研究结果表明,金红石的微量元素分析是研究榴辉岩原岩特征及其钛成矿作用的实用方法之一。  相似文献   

9.
鱼卡金红石矿床是青海省境内发现的第一个超大型榴辉岩型金红石矿床。笔者在总结前人基础资料及详细野外地质矿产调查的基础上,通过榴辉岩岩石学及金红石矿物学研究,利用LA-ICP-MS法对该矿床中的金红石进行原位微量元素分析等。结果表明:金红石赋存状态主要有五种,即包裹结构、粒间结构、串珠状结构、退变残余结构、丝缕状出溶结构,其中以粒间和串珠状赋存状态产出时,含矿性最好。同时,变质阶段的差异、流体活动的强弱将影响金红石的赋存状态。流体活动越弱时,野外表现为榴辉岩的新鲜程度越高、且少或不发育长英质脉体、矿物越自形,则越有利于形成粒间和串珠状金红石富矿;折返过程中流体或熔体作用过强、野外表现为广泛发育长英质脉体、榴辉岩中矿物呈他形产出时,则金红石已经退变为钛铁矿和榍石。总结前人的地球化学和年龄数据表明:富集地幔源区、演化程度高、陆壳混染程度低的富钛基性原岩是鱼卡榴辉岩型金红石矿床主要物质来源,高压(超高压)变质作用促进了钛的进一步富集成矿,成矿年代集中在440～430Ma。金红石锆温度计显示的成矿温度主要在570～671℃之间,金红石中高场强元素Ti、Nb、Ta、Zr、Hf等富集,表明其可能形成于俯冲带环境。这些成因认识等将为柴北缘成矿带榴辉岩型金红石矿床的进一步找矿工作部署、勘查评价及突破提供了重要的理论支撑与借鉴。  相似文献   

10.
藏西北戈木日榴辉岩岩石学特征及其构造意义   总被引：1，自引：0，他引：1  
苑婷媛  赵中宝  曾庆高  刘焰 《岩石学报》2016,32(12):3729-3742
戈木日榴辉岩产出于羌塘中部龙木错-双湖古板块缝合带内,是羌塘中部高压变质岩带的重要组成部分,前人多认为其系洋壳冷俯冲的产物。该榴辉岩的矿物组合可分为四期:第一期为含Fe~(3+)的钙钠闪石+钠云母+钠长石+绿泥石+石英+富含LREE、Th和U的褐帘石+榍石±富Mn的石榴子石。富Mg的石榴子石+贫Fe的绿辉石+不含微量元素的黝帘石+石英+钠云母+金红石+黄铁矿则为第二期矿物组合。第三期为退变质组合,包括钠长石、绿泥石、榍石和阳起石。第四期为磁铁矿、新生绿帘石和针状钛铁矿。热力学半定量模拟表明,石榴子石核部形成于T=644℃,P=13.0kbar,lgfO_2=-16.3~-16.4,而石榴子石幔部则形成于T=695℃,P=16.6kbar,lgfO_2=-19.0~-19.5,表明该榴辉岩属中温榴辉岩,而不是前人所言的冷榴辉岩,这反映了羌塘中部古特提斯洋盆的构造演化历史比较复杂,不仅有冷俯冲的洋壳,还有中温俯冲的洋壳。该榴辉岩在进变质过程中经历了还原作用,早期含Fe~(3+)的钙钠闪石和褐帘石等形成于高氧逸度之下的含水矿物,转变为形成于低氧逸度条件下的石榴子石和贫Fe的绿辉石、黝帘石等矿物,释放出水和轻REE、Th、U、Ba等微量元素。折返阶段新生成的矿物均不含有这些微量元素,表明早期阶段释放的微量元素很可能离开了俯冲板片,随流体进入上覆地幔楔。本文的研究进一步证实了进变质与还原作用共同促进了物质从俯冲板片中活化、转移至上覆地幔楔,这有助于理解具有独特地球化学特征的岛弧岩浆的起源。  相似文献   

11.
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   

12.
Redistribution of HFSE elements during rutile replacement by titanite   总被引：2，自引：0，他引：2  
Titanite growth at the expense of rutile during retrograde hydration of eclogite into amphibolite is a common phenomenon. We investigated an amphibolite sample from the Tromsø eclogite facies terrain in Northern Norway to gain insight into the trace element distribution between rutile and titanite during incomplete resorption of the rutile by titanite. Patchy compositional zoning of Al, Ti, and F in titanite relates to the presence of a fluid with variable Ti/Al and/or F during its growth. Laser ablation ICP–MS and electron microprobe data for high field strength elements (HFSE: Nb, Zr, Ta, and Hf) of rutile resorbed by titanite indicate a pronounced enrichment of these elements in the rim of a large single rutile crystal (~8 mm) and a systematic decrease towards uniform HFSE contents in the large core. HFSE contents of smaller rutile grains (~0.5 mm) and rutile inclusions (<100 μm) in the titanite overgrowth are similar or higher than in the rims of large rutile crystals. Element profiles from the rim inward demonstrate that HFSE enrichment in rutile is controlled by diffusion. HFSE ratios in diffusion-altered rutile show systematic variations compared with the uniform core composition of the large rutile. Modelling of Zr and Nb diffusion in rutile indicates that diffusion coefficients in rutile in fluid-dominated natural systems must be considerably higher than those determined experimentally at 1 bar in dry systems. Variations of HFSE contents in the newly formed titanite show no systematic spatial distribution. HFSE ratios in titanite and the rims of rutile are different, indicating different solid/fluid distribution coefficients in these minerals. Element fractionation by diffusion into the relict rutile and during fluid-mediated growth of new titanite could substantially change the HFSE budget of these minerals and could affect their use for geochemical tracing and other applications, such as Zr-based geothermobarometry.  相似文献   

13.
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   

14.
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   

15.
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   

16.
The depleted mantle and the continental crust are generally thought to balance the budget of refractory and lithophile elements of the Bulk Silicate Earth (BSE), resulting in complementary trace element patterns. However, the two high field strength elements (HFSE) niobium and tantalum appear to contradict this mass balance. All reservoirs of the silicate Earth exhibit subchondritic Nb/Ta ratios, possibly as a result of Nb depletion.In this study a series of nineteen orogenic MORB-type eclogites from different localities was analyzed to determine their HFSE concentrations and to contribute to the question of whether subducted oceanic crust could form a hidden reservoir to account for the mass imbalance of Nb/Ta between BSE and the chondritic reservoir. Concentrations of HFSE were analyzed with isotope dilution (ID) techniques. Additionally, LA-ICPMS analyses of clinopyroxene, garnet and rutile have been performed. Rutile is by far the major host for Nb and Ta in all analyzed eclogites. However, many rutiles revealed zoning in Nb/Ta ratios, with cores being higher than rims. Accordingly, in situ analyses of rutiles have to be evaluated carefully and rutile cores do not necessarily reflect a bulk rock Nb and Ta composition, although over 90% of these elements reside in rutile.The HFSE concentration data in bulk rocks show that the orogenic eclogites have subchondritic Nb/Ta ratios and near chondritic Zr/Hf ratios. The investigated eclogites show neither enrichment of Nb compared to similarly incompatible elements (e.g. La), nor fractionation of Nb/Ta ratios relative to MOR-basalts, the likely precursor of these rocks. This indicates that during the conversion of the oceanic crust to eclogites in most cases, (1) HFSE and REE have similar mobility on average, possibly because both element groups remain in the down going slab, and (2) no significant fractionation of Nb/Ta occurs in subducted oceanic crust. With an average Nb/Ta ratio of 14.2 ± 1.4 (2s.e.), the investigated eclogites cannot balance the differences between BSE and chondrite. Additionally, as their average Nb/Ta is indistinguishable from the Nb/Ta of MORB, they are also an unlikely candidate to balance the potentially small differences in Nb/Ta between the continental crust and the mantle.  相似文献   

17.
The petrogenetic relations among Ti‐rich minerals in high‐grade metabasites is illuminated here through a detailed petrological investigation of an anatectic garnet–clinopyroxene granulite from the Grenville Province, Ontario, Canada containing rutile, titanite and ilmenite in distinct microtextural settings. Garnet porphyroblasts exhibit zoned Ti concentrations (up to 0.15 wt% TiO2 in their cores), as well as a variety of rutile inclusion types, including clusters of small, variably elongate grains and thin (≤1 μm) oriented needles. Calcite inclusions in garnet, commonly observed surrounding garnet cores containing quartz and clinozoisite, indicate the presence of evolving C–O–H fluids during garnet growth and suggest that the rutile clusters may have formed from subsequent Ti diffusion and rutile precipitation within existing fluid inclusions. Titanite forms large subhedral crystals and typically occurs where the primary garnet–clinopyroxene assemblage is in contact with leucosome containing megacrystic hornblende, silvialitic scapolite and calcic plagioclase. Many titanite crystals exhibit marginal subgrains that correspond with sharp changes in their major and trace element composition, likely related to a dissolution–precipitation or recrystallization process following primary crystallization. Clinopyroxene–ilmenite symplectite coronas surround titanite in most locations, likely forming from reaction with the hornblende‐plagioclase matrix (±fluids/melt). Integration of multi‐equilibria thermobarometry and Zr thermometry in rutile and titanite with phase equilibrium modelling allows definition of a clockwise P–T path evolving to peak pressures of ~1.5 GPa at ~750°C during garnet and rutile growth, followed by peak temperature conditions of ~1.2 GPa and ~820–880°C associated with melt‐present titanite growth, and finally cooling and decompression to regional amphibolite facies conditions (~1.0 GPa and ~750°C) associated with the formation of clinopyroxene–ilmenite symplectites surrounding titanite. P–T pseudosections calculated for the pristine (leucosome‐ and titanite ‐free) metabasite bulk composition reproduce much of the prograde phase relations, but predict rutile as the stable Ti‐rich mineral at the peak thermal conditions associated with melt‐present titanite growth. The P–M(CaO) and T–M(CaO) models show that bulk CaO concentrations have a significant effect on the stability ranges of titanite and rutile. Increased bulk CaO tends to stabilize titanite to higher pressure and temperature at the expense of rutile, with a ≥15% increase in CaO producing the observed titanite‐bearing assemblage at high‐P granulite facies conditions. Thus, the model results are consistent with the textural observations, which suggest that titanite stability is associated with a chemical exchange between the host metabasite and a Ca‐rich melt.  相似文献   

18.
The complex vein associations hosted in southern Sulu ultrahigh-pressure (UHP) eclogites contain quartz ± omphacite (or jadeite) ± kyanite ± allanite ± zoisite ± rutile ± garnet. These minerals have chemical compositions similar to those of host eclogites. Inclusions of polycrystalline quartz pseudomorphs after coesite were identified in vein allanite and garnet, and coesite inclusions were found in vein zircon. These facts suggest that the veins together with host eclogites have been subjected to synchronous UHP metamorphism. The vein minerals contain relatively high concentrations of rare earth elements (REE), high-field-strength elements (HFSE) and transition metal elements (TME). A kyanite-quartz vein has a whole-rock composition similar to adjacent UHP metamorphic granitic gneisses. Abundant primary multi-solid fluid inclusions trapped within UHP vein minerals contain complex daughter minerals of muscovite, calcite, anhydrite, magnetite, pyrite, apatite, celestite and liquid and gas phase of H2O with solids up to 30-70% of the inclusion volume. The presence of daughter minerals anhydrite and magnetite indicates the subduction fluids were oxidizing, and provides a possible interpretation for the high oxygen fugacity of subduction zone magmas. These characteristics imply that the UHP vein minerals were crystallized from supercritical silicate-rich aqueous fluids that were in equilibrium with peak-UHP minerals, and that the fluids in deeply subducted continental crust may contain very high concentrations of silicate as well as HREE, HFSE and TME. Such fluids might have resulted in major fractionation between Nb and Ta, i.e. the UHP fluids have subchondritic Nb/Ta values, whereas the host eclogites after extraction of the fluids have suprachondritic Nb/Ta values. Therefore, voluminous residual eclogites with high Nb/Ta ratios may be the complementary suprachondritic reservoir capable of balancing the subchondritic depleted mantle and continental crust reservoirs.  相似文献   

19.
Trace element distribution in Central Dabie eclogites   总被引：16，自引：0，他引：16  
Coesite-bearing eclogites from Dabieshan (central China) have been studied by ion microprobe to provide information on trace element distributions in meta-basaltic mineral assemblages during high-pressure metamorphism. The primary mineralogy (eclogite facies) appears to have been garnet and omphacite, usually with coesite, phengite and dolomite, together with high-alumina titanite or rutile, or both titanite and rutile; kyanite also occurs occasionally as an apparently primary phase. It is probable that there was some development of quartz, epidote and apatite whilst the rock remained in the eclogite facies. A later amphibolite facies overprint led to partial replacement of some minerals and particularly symplectitic development after omphacite. They vary from very fine-grained dusty-looking to coarser grained Am + Di + Pl symplectites. The eclogite facies minerals show consistent trace element compositions and partition coefficients indicative of mutual equilibrium. Titanite, epidote and apatite all show high concentrations of REE relative to clinopyroxene. The compositions of secondary (amphibolite facies) minerals are clearly controlled by local rather than whole-rock equilibrium, with the composition of amphibole in particular depending on whether it is replacing clinopyroxene or garnet. REE partition coefficients for Cpx/Grt show a dependence on the Ca content of the host phases, with D REE Cpx/Grt decreasing with decreasing D Ca . This behaviour is very similar to that seen in mantle eclogites, despite differences in estimated temperatures of formation of 650–850 °C (Dabieshan) and 1000–1200 °C (mantle eclogites). With the exception of HREE in garnet, trace elements in the eclogites are strongly distributed in favour of minor or accessory phases. In particular, titanite and rutile strongly concentrate Nb and Zr, whilst LREE–MREE go largely into epidote, titanite and apatite. If these minor/accessory minerals behave in a refractory manner during melting or fluid mobilisation events and do not contribute to the melt/fluid, then the resultant melts and fluids will be strongly depleted in LREE–MREE. Received: 11 February 1999 / Accepted: 31 January 2000  相似文献   

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