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1.
《Applied Geochemistry》1998,13(7):861-884
Concentrations of the rare earth elements (REE), Th and U have been determined in thermal waters emerging from a number of locations in and around the Idaho Batholith. Previous investigators have suggested that the source of heat for the geothermal systems studied is the radioactive decay of K, Th and U which are enriched in the rocks through which the fluids flow. Thus, knowledge of the behavior of REE, Th and U in these systems may contribute to a better understanding of the potential consequences of the interaction of hydrothermal fluids with deeply buried nuclear waste. Such studies may also lead to the possible use of REE as an exploration tool for geothermal resources. The thermal waters investigated may be characterized as near-neutral to slightly alkaline, dilute, NaHCO3-dominated waters with relatively low temperatures of last equilibration with their reservoir rocks (<200°C). REE, Th and U concentrations were measured using Fe(OH)3 coprecipitation, followed by ICP-MS, which yielded detection limits of 0.01–0.003 μg/l for each element, depending on the volume of fluid sample taken. The concentrations of REE, Th and U measured (from <0.1 up to a few μg/l) are 3–5 orders of magnitude less than chondritic, in agreement with concentrations of these elements measured in other similar continental geothermal systems. The REE exhibit light REE-enriched patterns when normalized to chondrite, but when normalized to NASC or local granites, they exhibit flat or slightly heavy REE-enriched trends. These findings indicate that the REE are either taken up in proportion to their relative concentrations in the source rocks, or that the heavy REE are preferentially mobilized. Concentrations of REE and Th are often higher in unfiltered, compared to filtered samples, indicating an important contribution of suspended particulates, whereas U is apparently truly dissolved. In some of the hot springs the REE concentrations exhibit marked temporal variations, which are greater than the variations observed in major element concentrations, alkalinity and temperature. There are also variations in the fluid concentrations of REE, Th and U related to general location within the study area which may be reflective of variations in the concentrations of these elements in the reservoir rocks at depth. Thermal waters in the southern and central parts of the field area all contain ∑REE concentrations exceeding 0.1 μg/l (up to as high as 3 μg/l), Th exceeding 0.2 μg/l and U generally <0.4 μg/l. In contrast, thermal waters from the northern area contain lower ∑REE (<0.6 μg/l) and Th (<0.1 μg/l), but higher U (>3.0 μg/l). Using experimentally measured and theoretically estimated thermodynamic data, the distribution of species for La, Ce and Nd have been calculated and also the solubility of pure, endmember (La, Ce, Nd) phosphate phases of the monazite structure in selected hot spring fluids. These calculations indicate that, at the emergence temperatures, CO2−3 and OH− complexes of the REE are the predominant species in the thermal waters, whereas at the deep-aquifer temperatures, OH complexes predominate. In these thermal waters, monazite solubility is strongly prograde with respect to temperature, with solubility often decreasing several orders of magnitude upon cooling from the deep-aquifer to the emergence temperature. At the surface temperature, calculated monazite solubilities are, within the uncertainty of the thermodynamic data, comparable to the REE concentrations measured in the filtered samples, whereas at the deep-aquifer temperature, monazite solubilities are generally several orders of magnitude higher than the REE concentrations measured in the filtered or unfiltered samples. Therefore, a tentative model is suggested in which the thermal fluids become saturated with respect to a monazite-like phase (or perhaps an amorphous or hydrated phosphate) upon ascent and cooling, followed by subsequent precipitation of that phase. The temporal variations in REE content can then be explained as a result of sampling variable mixtures of particulate matter and fluid and/or variable degrees of attainment of equilibrium between fluid and solid phosphate.  相似文献   

2.
Monazite chemical composition: some implications for monazite geochronology   总被引：9，自引：1，他引：8  
An investigation of the chemical composition of monazite from a number of localities has been carried out. Samples used include monazites from metamorphic rocks, granitic rocks and a hydrothermal ore deposit. The REE distribution pattern of monazite varies greatly in accordance with its geological environment. A remarkable feature of the monazites studied is that their chondrite-normalised REE distribution patterns are mostly uniform between grains within the same sample, but differ significantly from sample to sample. This characteristic apparently indicates that there is an important effect on the REE distribution of monazite exerted by the host rock or source material from which monazite crystallised. Another important feature shown by the monazites studied is that monazites in rocks containing garnet as a major mineral show extreme depletion of HREE, whereas monazites in rocks without garnet or monazite that formed after the garnet breakdown contain significantly higher amounts of Y and HREE. This suggests that the phase assemblage, especially garnet, plays an important role in the REE distribution of monazites in these rocks. The value of REE distribution in monazite is exemplified with regard to the origin of monazite in the Lewisian metamorphic rocks, which is a fundamental issue in monazite geochronology. Received: 17 March 1999 / Accepted: 16 July 1999  相似文献   

3.
The Ross orogen of Antarctica is an extensive (>3000 km‐long) belt of deformed and metamorphosed sedimentary rocks and granitoid batholiths, which formed during convergence and subduction of palaeo‐Pacific lithosphere beneath East Gondwana in the Neoproterozoic–early Palaeozoic. Despite its prominent role in Gondwanan convergent tectonics, and a well‐established magmatic record, relatively little is known about the metamorphic rocks in the Ross orogen. A combination of garnet Lu–Hf and monazite U–Pb (measured by laser‐ablation split‐stream ICP‐MS) geochronology reveals a protracted metamorphic history of metapelites and garnet amphibolites from a major segment of the orogen. Additionally, direct dating of a common rock‐forming mineral (garnet) and accessory mineral (monazite) allows us to test assumptions that are commonly used when linking accessory mineral geochronology to rock‐forming mineral reactions. Petrography, mineral zoning, thermobarometry and pseudosection modelling reveal a Barrovian‐style prograde path, reaching temperatures of ~610–680 °C. Despite near‐complete diffusional resetting of garnet major element zoning, the garnet retains strong rare earth element zoning and preserves Lu–Hf dates that range from c. 616–572 Ma. Conversely, monazite in the rocks was extensively recrystallized, with concordant dates that span from c. 610–500 Ma, and retain only vestigial cores. Monazite cores yield dates that overlap with the garnet Lu–Hf dates and typically have low‐Y and heavy rare earth element (HREE) concentrations, corroborating interpretations of low‐Y and low‐HREE monazite domains as records of synchronous garnet growth. However, ratios of REE concentrations in garnet and monazite do not consistently match previously reported partition coefficients for the REE between these two minerals. High‐Y monazite inclusions within pristine, crack‐free garnet yield U–Pb dates significantly younger than the Lu–Hf dates for the same samples, indicating recrystallization of monazite within garnet. The recrystallization of high‐Y and high‐HREE monazite domains over >50 Ma likely records either punctuated thermal pulses or prolonged residence at relatively high temperatures (up to ~610–680 °C) driving monazite recrystallization. One c. 616 Ma garnet Lu–Hf date and several c. 610–600 Ma monazite U–Pb dates are tentatively interpreted as records of the onset of tectonism metamorphism in the Ross orogeny, with a more robust constraint from the other Lu–Hf dates (c. 588–572 Ma) and numerous c. 590–570 Ma monazite U–Pb dates. The data are consistent with a tectonic model that involves shortening and thickening prior to widespread magmatism in the vicinity of the study area. The early tectonic history of the Ross orogen, recorded in metamorphic rocks, was broadly synchronous with Gondwana‐wide collisional Pan‐African orogenies.  相似文献   

4.
宋天锐  石玉若  郑宁 《地质学报》2014,88(9):1638-1650
华北中、新元古代地层的年龄数据很混乱(表1),本文建议将北京十三陵地区新发现的稀土矿物用SHRIMP方法测年,有助于问题的解决。北京十三陵地区保存了新太古代五台群和新—中元古代较完整的地层,电子耦合等离子体分析(即原子收光谱分析)(ICP)的定量分析数据表明,在这些地层中,岩石中所含钾和稀土元素含量都比北美页岩(NASC)、欧洲页岩(ES)和澳大利亚后太古宙页岩(PAAS)高出很多,经电子扫描+能谱仪+波谱仪(SEM+EDS+WDS)分析证明,在岩石中包含独居石(碎屑的和自生-成岩的)和磷钇矿(自生-成岩的),并首次发现钍石-独居石环带状混合矿物(变质的)以及显微脉状稀土硅酸盐矿物(地下流体形成的)等稀土矿物。利用激光拉曼光谱鉴定发现稀土矿物的分布状态包括:1在太古宙五台群的片麻岩中,云母、石英和长石之间有非自形晶独居石,而且在石英单晶里还有独居石的自形晶包裹体;并发现独居石和钍石-独居石环带状混合矿物,这些稀土矿物都是变质成因的;2在新太古代五台群片麻岩的准平原化风化面上,沉积的元古宙常沟组的底砾岩中发现了碎屑的独居石,这些独居石的同位素年龄对于元古宇的底界定年意义重大;3在常州沟组下部压扁-透镜状层理的粉砂岩中,普遍发现碎屑锆石的外缘生长出自生-成岩磷钇矿,磷钇矿的同位素定年对于常州沟组的地层年代有代表性意义;4串岭沟组的粉砂岩中发现了无形晶状自生-成岩独居石和磷钇矿,并且较多出现在显微缝合线内外,可作为SHRIMP测年的对象;5大红峪组粉砂岩中除了发现碎屑独居石外还发现脉状硅-铝稀土矿物,可能与后元古宙热液活动有关。事实上这些自生-成岩的稀土矿物的形成,都是源自太古宙富含稀土元素的变质岩石,其形成机理也与地下流体活动有关。笔者认为北京十三陵以及至华北地区,前寒武系富稀土元素形成的自生-成岩的稀土矿物,有助于用SHRIMP方法对前寒武纪地层的同位素测年研究。  相似文献   

5.
The textural and chemical evolution of allanite and monazite along a well‐constrained prograde metamorphic suite in the High Himalayan Crystalline of Zanskar was investigated to determine the P–T conditions for the crystallization of these two REE accessory phases. The results of this study reveals that: (i) allanite is the stable REE accessory phase in the biotite and garnet zone and (ii) allanite disappears at the staurolite‐in isograd, simultaneously with the occurrence of the first metamorphic monazite. Both monazite and allanite occur as inclusions in staurolite, indicating that the breakdown of allanite and the formation of monazite proceeded during staurolite crystallization. Staurolite growth modelling indicates that staurolite crystallized between 580 and 610 °C, thus setting the lower temperature limit for the monazite‐forming reaction at ~600 °C. Preservation of allanite and monazite inclusions in garnet (core and rim) constrains the garnet molar composition when the first monazite was overgrown and subsequently encompassed by the garnet crystallization front. Garnet growth modelling and the intersection of isopleths reveal that the monazite closest to the garnet core was overgrown by the garnet advancing crystallization front at 590 °C, which establishes an upper temperature limit for monazite crystallization. Significantly, the substitution of allanite by monazite occurs in close spatial proximity, i.e. at similar P–T conditions, in all rock types investigated, from Al‐rich metapelites to more psammitic metasedimentary rocks. This indicates that major silicate phases, such as staurolite and garnet, do not play a significant role in the monazite‐forming reaction. Our data show that the occurrence of the first metamorphic monazite in these rocks was mainly determined by the P–T conditions, not by bulk chemical composition. In Barrovian terranes, dating prograde monazite in metapelites thus means constraining the time when these rocks reached the 600 °C isotherm.  相似文献   

6.
Textural relationships occurring in a range of settings from the Bayan Obo Fe-REE-Nb deposit, Inner Mongolia, China, indicate reaction between monazite [(REE)PO4], bastnäsite [(REE)(CO3)F] and apatite. Within dolomite marble-hosted ores monazite grains occur surrounded by zones of intergrown bastnäsite and apatite. In fluoritised dolomite marble-hosted amphibole-calcite veins, co-existing apatite and bastnäsite are separated by zones of monazite plus calcite, whilst in aegirine-apatite veins hosted by banded aegirine-fluorite-magnetite-bastnäsite rocks, they are separated by zones of monazite and fluorite. Modal proportions for minerals in the reaction zones have been used to derive reaction stoichiometries, and suggest the following reactions: Consideration of these reactions, along with published experimental data and other reported mineral assemblages, suggests that the factors controlling the relative stabilities of monazite and bastnäsite are the pH, and the activities of HF?°, CO3 2?, Ca2+ and PO4 3?. Textures indicating reaction between REE phosphates and fluorocarbonates have been reported from a number of other settings and are consistent with the controls on reaction inferred from this study. The range of assemblages seen at Bayan Obo is a result of the variation between relatively unbuffered fluid compositions, and those buffered by the fluoritisation of the carbonate host rock. Mass-balance calculations suggest some mobilisation of the REE into the fluid phase during reaction, although this did not significantly alter the REE distribution in monazite and bastnäsite. The mineral compositions also reveal variation in the REE distribution with different paragenetic settings indicating variation in the composition of the metasomatic fluids. These changes may be related to changes in the fluid source region, or to variations in the fluid chemistry, particularly X CO2, leading to different REE solubilities at different periods in the development of the deposit.  相似文献   

7.
Abstract: The North granitic body of the Miyako pluton is located in the Northern Kitakami belt, Northeast Japan. The formation of the scheelite–chalcopyrite–magnetite–bearing aplitic veins and scheelite–chalcopyrite–magnetite–bearing Yamaguchi skarn deposit was closely associated with the formation of the Miyako plutons. Petrographic facies of the North granitic body vary from quartz diorite in marginal zone (zone A), to tonalite and granodiorite (zone B), and to granite (zone C) in the central. The large numbers of aplitic veins distributed around the Yamaguchi mining area are divided into two groups: barren and scheelite–mag–netite–chalcopyrite–bearing aplitic veins. The latter cut massive clinopyroxene skarns of the Yamaguchi deposit, and are composed of plagioclase, K‐feldspar and titanite. Some plagioclase crystals have dusty cores with irregularly shaped K‐feldspar flakes, and clear rims of albite. Textures of plagioclase in the mineralized aplitic veins are different from the idiomorphic textures with sharp plagioclase crystal boundaries that occur in the North granitic body and barren aplitic veins. These textural data suggest that the mineralized aplitic veins were formed from hydrothermal fluid. Changes in the contents of major and minor (Rb, Sr, Sc, Co, Th, U) elements in the North Miyako granitic body are similar to those of zoned plutons formed by typical magmatic differentiation processes. On the other hand, concentrations of REE, especially middle to heavy REE, of granitic rocks in zone C and barren aplitic veins are significantly lower than those of granitic rocks in zones A and B. The hypothetical chondrite‐normalized REE patterns, calculated assuming fractional crystallization from zone B granitic melt, suggest that REE concentrations of the residual melt increased with the degree of fractional crystallization, and changed into a pattern with enriched LREE and strongly negative Eu anomaly. However, the REE patterns of granitic rocks in zone C are different from the hypothetical patterns. Moreover, the REE patterns of magnetite–scheelite–chalcopyrite aplitic veins are quite different from those of granitic rocks. The Cu contents of granitic rocks in the North Miyako body increase from zone A (5–26 ppm) to zone B (10–26 ppm), and then clearly decrease to zone C (5–7 ppm) and drastically increase to the barren aplitic veins (39–235 ppm). Concentrations of Cu in the mineralized aplitic veins are also higher than those of the granitic rocks in zone C. The decrease in REE and Cu contents of granitic rocks from zone B to zone C is not a result of simple magmatic fractional differentiation. Fluid inclusions in quartz from mineralized aplitic veins contain 3.3 wt% NaCl equivalent and 5.8 wt% CO2. It was also demonstrated experimentally that the removal of MREE and HREE by fluid from melt enabled the formation of complexes of REE and ligands of OH‐ and CO32‐. Based on the possibility that the melt of the granitic rocks of zone C and the mineralized aplitic veins coexisted with CO2‐bearing fluid, it is thought that REE were extracted from the melt to the CO2‐bearing fluid, and that the REE in the mineralized aplitic veins were transported by the CO2‐bearing fluid. It is likely that the low HREE and Cu contents of the granitic rocks in zone C could have been caused by the removal of those elements from the granitic melt by the fluid coexisting with the melt. The expelled materials could have been the sources of scheelite–magnetite–chalcopyrite–bearing aplitic veins and copper mineralization of the Yamaguchi Cu‐W skarn deposit.  相似文献   

8.
大连震旦系十三里台组首次发现自生稀土元素矿物独居石后 ,在北京十三陵中元古代长城系常州沟组、串岭沟组和大红峪组又发现了自生的独居石以及其他磷酸盐和硅酸盐稀土矿物。自生稀土矿物的形成和岩石中稀土元素含量较高有关 ;电子探针背散射图像和 P、Th、L a、Ce、Nd、Y等元素面分布图像研究表明 ,沉积岩中的自生稀土矿物与岩浆岩、变质岩和碎屑成因的截然不同。本文首次报道了元古宙长城系常州沟组沉积岩中碎屑锆石边部成岩过程中形成的自生磷钇矿。中国北方元古宙泥砂质碎屑沉积岩普遍具有高稀土组合 ,许多地区都可能存在独居石等自生稀土矿物 ,如天津蓟县、辽西、辽南和宣化等地 ,为利用离子探针 (SHRIMP)确定其同位素地质年代提供了可能。此外 ,本文对比了大连震旦系自生独居石和内蒙白云鄂博矿区东矿的独居石晶形和化学成分的相似性 ,再一次提出中国北方元古宙富稀土地层可能是内蒙古白云鄂博巨型稀土元素矿床的矿源层问题。  相似文献   

9.
The distribution of REE minerals in metasedimentary rocks was investigated to gain insight into the stability of allanite, monazite and xenotime in metapelites. Samples were collected in the central Swiss Alps, along a well‐established metamorphic field gradient that record conditions from very low grade metamorphism (250 °C) to the lower amphibolite facies (～600 °C). In the Alpine metapelites investigated, mass balance calculations show that LREE are mainly transferred between monazite and allanite during the course of prograde metamorphism. At very low grade metamorphism, detrital monazite grains (mostly Variscan in age) have two distinct populations in terms of LREE and MREE compositions. Newly formed monazite crystallized during low‐grade metamorphism (<440 °C); these are enriched in La, but depleted in Th and Y, compared with inherited grains. Upon the appearance of chloritoid (～440–450 °C, thermometry based on chlorite–choritoid and carbonaceous material), monazite is consumed, and MREE and LREE are taken up preferentially in two distinct zones of allanite distinguishable by EMPA and X‐ray mapping. Prior to garnet growth, allanite acquires two growth zones of clinozoisite: a first one rich in HREE + Y and a second one containing low REE contents. Following garnet growth, close to the chloritoid–out zone boundary (～556–580 °C, based on phase equilibrium calculations), allanite and its rims are partially to totally replaced by monazite and xenotime, both associated with plagioclase (± biotite ± staurolite ± kyanite ± quartz). In these samples, epidote relics are located in the matrix or as inclusions in garnet, and these preserve their characteristic chemical and textural growth zoning, indicating that they did not experience re‐equilibration following their prograde formation. Hence, the partial breakdown of allanite to monazite offers the attractive possibility to obtain in situ ages, representing two distinct crystallization stages. In addition, the complex REE + Y and Th zoning pattern of allanite and monazite are essential monitors of crystallization conditions at relatively low metamorphic grade.  相似文献   

10.
The paper presents mineralogical features and EPMA results of the Khamambettu carbonatites. The mineralogical data suggest that these rocks have been generated in magmatic and hydrothermal stages. Mineral geothermometer for carbonatite give temperatures of 790°–980°C. Fluid inclusion measurements in monazite (hydrothermal stage) give temperatures of 220°–290°C. One of the features of the carbonatites is high content of magnesia that is defined by the presence of dolomite, olivine, spinel, phlogopite, Mg-rich ilmenite. Chloritization, serpentinization, amphibolization, silicification processes and occurrence of barite, monazite-(Ce), strontianite, celestine are related to hydrothermal stage. Hydrothermal minerals at the Khamambettu were formed by recrystallization of primary carbonatite minerals in the presence of Ba, (SO4)2?, REE and Si carried in solution by the hydrothermal fluid.  相似文献   

11.
Upper Triassic-Jurassic black shale at Marvast, Iran, contains grey to green-grey ellipsoidal nodules of monazite ranging from 0.1 to 2?mm across. The presence of host-rock mineral inclusions within the monazite grains, low Th content in the monazite, lack of relict yellow cores (characteristic of igneous monazite), and the absence of monazite in the other sedimentary sequences in the Marvast area rule out a detrital origin for the monazite nodules and suggest authigenic crystallization during sediment compaction. Enrichment of the cores of the monazite grains in mid-range to heavy rare-earth elements (REE) and their rims in La + Ce point to variations in the degree of REE mobility and/or evolving composition of the diagenetic mineralizing fluid during nodule growth. The phosphorus and REE required for monazite crystallization were probably derived from seawater and adsorbed on clays and Fe-Mn hydroxides. The interstitial fluids expelled from the sediments during burial compaction and diagenesis became enriched in P and REE through complexing. The association of the Marvast monazite nodules with the black shale may indicate that organic complexes aided in the mobilization and transport of the REE into the pore fluids. Detailed field investigations in the study area and vicinity show that authigenic monazite in the upper Triassic-Jurassic shale sections is spatially associated with quartz lenses. It is likely that these lenses are surface expressions of shallow intrusive magmas, which provided the heat that promoted the mobilization and redistribution of the REE and P, and initiated precipitation of monazite in the overlying sediments.  相似文献   

12.
前寒武纪沉积岩中自生独居石的发现及其意义   总被引：5，自引：1，他引：5  
由于受到葛家屯组中发现自生方铅矿的启发 ,首次于大连前寒武纪震旦系十三里台组泥岩中发现了自生独居石 ,这一发现为在中国北方前寒武纪沉积岩中寻找自生独居石提供了重要的线索。它为进一步探索 U、Th- Pb同位素测年拓展了新的研究领域和提供了可能性。本文列举了中国北方前寒武纪沉积岩中 Ce元素异常以及 REE较高的例证 ,认为上述地区都有可能发现自生独居石。同时介绍了最近又在北京十三陵中元古代的常州沟组和串岭沟组所发现自生独居石的新资料。研究表明 ,自生独居石的电子探针扫描形态 ,与岩浆岩、变质岩及砂矿中截然不同。在地质年代分布上 ,元古宙 REE相对丰度较高 ,特别是 L REE较高的泥质岩多数来自古陆壳上。资料对比结果显示 :在 L a+Ce+Nd、Yb+Y、Sm+Gd+Dy三角图中 ,北京十三陵元古宙泥质岩、大连震旦系十三里台组泥岩和辽南 -辽西中元古代泥质岩都属于近古陆的沉积类型。首次提出 ,中国北方元古宙沉积与南方震旦系磷块岩沉积环境存在明显的不同并反映在三角图中 ,前者离 L a+Ce+Nd端点近 ,而后者由于成因上属于洋流上升沉积物而远离该端点。按照大连震旦系十三里台组沉积环境特点 ,自生独居石应为生物成矿作用的产物 ,含矿物泥岩形成于总体氧化环境中的局部还原亚环境中。基于此 ,建立了  相似文献   

13.
赣南新元古代变质岩稀土矿物及其地球化学特征   总被引：3，自引：2，他引：1  
近年来赣南地区首次报道了变质岩离子吸附型稀土矿床的发现,为离子吸附型稀土的找矿提供了新思路。赣南地区新元古代变质岩大面积分布,风化壳也广泛发育。文章对30件稀土元素含量(300×10~(-6))高的变质岩矿物样品进行了详细的电子探针分析,旨在查明赣南新元古代不同类型变质岩中的稀土矿物种类及特征,探讨其成因、对全岩稀土元素含量的贡献以及离子吸附型稀土元素的成矿潜力。研究表明,区域上变质岩可大致分为6类,分别是变质凝灰岩类、板岩类、千枚岩类、片岩类、变砂岩类和变粒岩类,不同类型变质岩的稀土矿物组合不同,除了普遍存在的、难风化的独居石、磷钇矿和锆石外,部分岩性中出现易风化的褐帘石、含稀土元素绿泥石和含稀土元素金红石,及表生的水磷酸盐和磷铝酸盐等矿物。这些富稀土矿物贡献了全岩中大部分稀土元素,且部分矿物成因与后期流体作用相关,为成矿提供了良好的条件。文章总结分析认为,赣南地区广泛分布的变质岩中,片岩类、变砂岩类和变质凝灰岩类均具有相对易风化的稀土矿物组合,尤其变质凝灰岩类和变砂岩类,能为离子吸附型稀土成矿提供充足的物质来源,具有可观的离子吸附型稀土成矿潜力。  相似文献   

14.
Rare earth element (REE) and yttrium concentrations of coexisting monazite and xenotime were determined from a suite of seven metapelites from the Variscan fold belt in NE Bavaria, Germany. The metapelites include a continuous prograde, mainly low-P (3–5 kbar) metamorphic profile from greenschist (c. 400 °C) to lower granulite facies conditions (c. 700 °C). The LREE (La–Sm) are incorporated preferentially in monoclinic monazite (REO9 polyhedron), whereas the HREE plus Y are concentrated in tetragonal xenotime (REO8 polyhedron). The major element concentrations of both phases in all rocks are very similar and do not depend on metamorphic grade. Monazite consists mainly of La, Ce and Nd (La0.20–0.23, Ce0.41–0.45, Nd0.15–0.18)PO4, all other elements are below 6 mol%. Likewise, xenotime consists mainly of YPO4 with some Dy and Gd solid solutions (Y0.76–0.80, Dy0.05–0.07, Gd0.04–0.06). In contrast, the minor HREE concentrations in monazite increase strongly with increasing metamorphic grade: Y, Dy and Gd increase by a factor of 3–5 from greenschist to granulite facies rocks. Monazite crystals often show zonation with cores low in HREE and rims high in HREE that is interpreted as growth zonation attained during prograde metamorphism. Similarly, Sm and Nd in xenotimes increase by a factor of 3–4 with increasing metamorphic grade. Prograde zonation in single crystals of xenotime was not observed. The XHREE+Y in monazite and XLREE in xenotime of the seven rocks define two limbs along the strongly asymmetric miscibility gap from c. 400 °C to 700 °C. The empirical calibration of the monazite miscibility gap limb coexisting with xenotime is appropriate for geothermometry. Due to its contents of U and Th, monazite has often been used for U–Pb age determination. The combination of our empirical thermometer on prograde zoned monazite along with possible age determination of zoned single crystals may provide information about prograde branches of temperature–time paths.  相似文献   

15.
《Applied Geochemistry》2000,15(9):1369-1381
Thirty-eight samples of stream sediments draining high-grade metamorphic rocks in the Walawe Ganga (river) Basin, Sri Lanka, were analysed for their REE contents, together with samples of metamorphic suites from the source region. The metamorphic rocks are enriched in light REE (LREE) compared to heavy REE (HREE) and are characterised by high La/Lu ratios and negative Eu anomalies. The chondrite-normalised patterns for these granulite-grade rocks are similar to that of the average post-Archaean upper crust, but they are slightly enriched with La and Ce. The REE contents of the <63-μm fraction of the stream sediments are similar to the probable source rocks, but the other grain size fractions show more enriched patterns. The <63-μm stream sediments fraction contains lower total REE, more pronouncd negative Eu anomalies, higher EuN/SmN and lower La N/LuN ratios relative to other fractions. The lower La N/LuN ratio is related to the depletion of heavy minerals in the <63-μm fraction. The 63–125-μm and 125–177-μm grain size fractions of sediments are particularly enriched in LREE (average ΣLREE=2990 μg/g and 3410 μg/g, respectively). The total HREE contents are surprisingly uniform in all size fractions. However, the REE contents in the Walawe Ganga sediments are not comparable with those of the granulite-grade rocks from the source region of the sediments. The enrichment of REE is accounted for by the presence of REE containing accessory mineral phases such as zircon, monazite, apatite and garnet. These minerals are derived from an unknown source, presumably from scattered bodies of granitic pegmatites.  相似文献   

16.
Nodular monazite occurs in metamorphic rocks worldwide and has zonal REE patterns. This paper focuses on the composition of nodular monazite hosted by Permian black shales of the Kular Ridge in the Kular-Nera terrane. This monazite variety (called kularite in the Russian literature) reaches commercial amounts in placers of the area. The contents of Ce, Nd, and La in the analyzed monazite nodules show correlations at Ce/Nd = 14.39La + 0.0919 (in apfu) and Ce/Nd = 0.2318La + 0.1135 (in wt.%) and vary regularly from core to rim. All monazite compositions fall on this trend, but specific grains may plot in its different parts. Thermodynamic calculations indicate that monazite forms via an intermediate precursor (LnPO4·2H2O). The Ce:La:Nd changes in different grains record Eh-pH variations during nucleation and a gradual temperature increase during subsequent growth. The Ce:La:Nd ratio changes partly in grain rims as a result of oxidative dissolution. Judging by the tectonic setting, REE came to the Kular-Nera rocks from the weathered Tomtor Nb-REE deposit, being transported by the Paleo-Khatanga River with monazite nanoparticles bound to the surface of clay minerals.  相似文献   

17.
U–Pb isotopic data from the northern Monashee complex, one of the deepest structural exposures in the southern Canadian Cordillera, indicate that the age of metamorphism varies according to structural position in a 6 km thick section. This metamorphism resulted in an unusual sequence in which rocks with the lowest-grade mineral assemblage (kyanite–sillimanite–staurolite–muscovite) are underlain and overlain by higher-grade rocks. Xenotime and monazite U–Pb dates vary progressively from 64 Ma in the structurally highest rocks to 49 Ma in the deepest rocks. Discordant U–Pb ages from Proterozoic and Cretaceous monazite and titanite are used to interpret the thermal significance of the early Tertiary dates. The discordant analyses define linear arrays with lower intercepts that broadly overlap with early Tertiary, and the amount of discordance varies with structural level; it is least in the deeper rocks and greatest in higher rocks. Electron microprobe work showed that the monazite discordance in the deeper rocks resulted from Tertiary mineral overgrowth and recrystallization rather than Pb diffusion. We use previous studies of Pb diffusion and the fact that Proterozoic monazite and titanite suffered only negligible to moderate amounts of diffusive Pb loss to contend that elevated temperatures (c. 600–650 °C are inferred from pelitic mineral assemblages) existed in the deeper rocks for a short duration, perhaps a few million years. The downwards younging 64–49 Ma U–Pb dates are interpreted as closely reflecting xenotime and monazite growth ages rather than cooling ages or substantially reset ages based on the lack of Pb diffusion in monazite and the previously obtained 40Ar/39Ar data which suggest that rapid cooling occurred immediately after the U–Pb dates. In addition, growth ages are interpreted as thermal peak ages based on U–Pb dates from coeval kyanite-bearing leucosomes, the consistent nature of the U–Pb dates throughout the study area, and petrographic relationships which suggest that monazite grew before or during development of the syn-metamorphic foliation. These interpretations lead us to conclude that metamorphism was diachronous according to structural level, with higher rocks attaining peak temperatures and cooling rapidly while deeper rocks were heating towards a thermal peak that was attained a few million years later. This thermal scenario requires that higher rocks cannot have been the heat source for the deeper metamorphism, as was previously proposed.  相似文献   

18.
This study is aimed at understanding the behavior of monazite, xenotime, apatite and zircon, and the redistribution of Zr, REE, Y, Th, and U among melt, rock-forming and accessory phases in a prograde metamorphic sequence, the Kinzigite Formation of Ivrea-Verbano, NW Italy, that may represent a section from the middle to lower continental crust. Metamorphism ranges from middle amphibolite to granulite facies and metapelites show evidence of intense partial melting and melt extraction. The appearance of melt controls the grain size, fraction of inclusions and redistribution of REE, Y, Th, and U among accessories and major minerals. The textural evolution of zircon and monazite follows, in general, the model of Watson et al. (1989). Apatite is extracted from the system dissolved into partial melts. Xenotime is consumed in garnet-forming reactions and is the first source for the elevated Y and HREE contents of garnet. Once xenotime is exhausted, monazite, apatite, zircon, K-feldspar, and plagioclase are progressively depleted in Y, HREE, and MREE as the modal abundance of garnet increases. Monazite is severely affected by two retrograde reactions, which may have consequences for U-Pb dating of this mineral. Granulite-grade metapelites (stronalites) are significantly richer in Ti, Al, Fe, Mg, Sc, V, Cr, Zn, Y, and HREE, and poorer in Li, Na, K, Rb, Cs, Tl, U, and P, but have roughly the same average concentration of Cu, Sr, Pb, Zr, Ba, LREE, and Th as amphibolite-grade metapelites (kinzigites). The kinzigite-stronalite transition is marked by the sudden change of Th/U from 5–6 to 14–15, the progressive increase of Nb/Ta, and the decoupling of Ho from Y. Leucosomes were saturated in zircon, apatite, and (except at the lowest degree of partial melting) monazite. Their REE patterns, especially the magnitude of the Eu anomaly, depend on the relative proportion of feldspars and monazite incorporated into the melt. The presence of monazite in the source causes an excellent correlation of LREE and Th, with nearly constant Nd/Th ≈ 2.5–3. The U depletion and increase in Th/U characteristic of granulite facies only happens in monazite-bearing rocks. It is attributed to enhancement of the U partitioning in the melt due to elevated Cl activity followed by the release of a Cl-rich F-poor aqueous fluid at the end of the crystallization of leucosomes. Halide activity in partial melts was buffered by monazite and apatite. Since the U (and K) depletion does not substantially affect the heat-production of metapelites, and mafic granulites maintain similar Th/U and abundance of U and Th as their unmetamorphosed equivalents, it seems that geochemical changes associated to granulitization have only a minor influence on heat-production in the lower crust.  相似文献   

19.
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   

20.
The distribution of REEs and some minor elements in tourmalines of different associations and deposits of the Russian Far East is studied by the methods of ICP-MS, ICP-MS with laser ablation and scanning electron microscopy. The duality of REE speciation in tourmaline is established: in high-temperature varieties, most REEs (mainly HREEs) are incorporated in rare minerals (monazite, xenotime, zircon, and F–Ce–Y carbonate), whereas hydrothermal ores are characterized by isomorphic incorporation of LREEs in the mineral structure, as well as by a fine admixture of zircon at the expense of detrital clasts in flyschoid rocks with the zones of tourmalinization.  相似文献   

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