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1.
Rare earth element (REE) geochemistry and mineralogy have been studied in the weathered crusts derived from the Early Yanshanian (Jurassic) biotite granites of Dabu and Dingnan, as well as in the Indosinian (Permian) muscovite–biotite granite of Aigao in southern Jiangxi province, China, and the weathered crusts and clay sediments on biotite granites in the Sanyo belt, SW Japan, that is, Okayama, Tanakami, and Naegi areas. In all of the weathered crusts, biotite and plagioclase commonly tend to decrease toward the upper part of the profile, whereas kaolinite and residual quartz and K‐feldspar increase. The weathered crusts of the Dingnan granites and some Naegi granites, which are characterized by the enrichment in light REE (LREE) in C horizons, have higher total REE (ΣREE) content than the parent REE‐enriched granites. Weathering of LREE‐bearing apatite and fluorocarbonates in the Dingnan granites and allanite and apatite in some Naegi granites may account for the leaching of LREE at the B horizons. The leached LREE must result in subsequent enrichment of LREE in the C horizons. The enrichment is probably associated with mainly adsorption onto kaolinite and partly formation of possible secondary LREE‐bearing minerals. In Japan it was found that REE mineralization occurs not in the weathered granitic crusts but in reworked clay sediments, especially kaolinite‐rich layers, derived mainly from the weathering materials of REE‐enriched granitic rocks. The clay sediments are more enriched in LREE, which likely adsorbed onto kaolinite. Concentration of heavy REE within almost all the weathered crusts and clay sediments, however, may reflect mainly residual REE‐bearing minerals such as zircon, which originated in the parent granitic rocks. The findings of the present study support the three processes for fractionation of the REE during weathering: (i) selective leaching of rocks containing both stable and unstable REE‐bearing minerals; (ii) adsorption onto clay minerals; and (iii) presence of possible secondary LREE‐bearing minerals.  相似文献   

2.
Lithium is an important geochemical tracer for fluids or solids. However, because the electron microprobe cannot detect Li, variations of Li abundance at the micrometric scale are most often estimated from bulk analyses. In this study, the Li intense emission line at 670.706 nm in optical emission spectroscopy was used to perfect the analysis of Li at the micrometric scale by means of laser-induced breakdown spectroscopy (LIBS). To estimate lithium content for different geological materials, LIBS calibration of the emission line at 670.706 nm was achieved by use of synthetic glasses and natural minerals. The detection limit for this method is ∼5 ppm Li. Three applications to geological materials show the potential of LIBS for lithium determination, namely for Li-bearing minerals, melt inclusions, quartz, and associated fluid inclusions.For spodumene and petalite from granite pegmatite dikes (Portugal), the Li2O concentrations are 7.6 ± 1.6 wt% and 6.3 ± 1.3 wt%, respectively, by use of LIBS. These values agree with ion microprobe analyses, bulk analyses, or both. For eucryptite crystals, the Li concentrations are scattered because grain size is smaller than the LIBS spatial resolution (6 to 8 μm). Lithium concentrations of melt inclusions from the Streltsovka U deposit (Siberia) are in the range of 2 to 6.2 wt% (Li2O) for Li-rich daughter minerals. Lithium estimations on silicate glasses display values between 90 and 400 ppm.Lithium was also analyzed as a trace element in quartz. Transverse profiles were performed in hydrothermal barren quartz veins from the Spanish Central System (Sierra de Guadarrama). The highest Li concentrations (250 to 370 ppm) were found in specific growth bands in conjunction with the observed variation in optical cathodoluminescence intensity. Considering the fluid inclusion analysis, the source of fluid responsible to the Li enrichment in quartz is probably high-salinity fluids derived from sedimentary basins.  相似文献   

3.
Geochemical and mineralogical studies were conducted on the 12-m-thick weathering profile of the Kata Beach granite in Phuket, Thailand, in order to reveal the transport and adsorption of rare earth elements (REE) related to the ion-adsorption type mineralization. The parent rock is ilmenite-series biotite granite with transitional characteristics from I type to S type, abundant in REE (592 ppm). REE are contained dominantly in fluorocarbonate as well as in allanite, titanite, apatite, and zircon. The chondrite-normalized REE pattern of the parent granite indicates enrichment of LREE relative to HREE and no significant Ce anomaly. The upper part of the weathering profile from the surface to 4.5 m depth is mostly characterized by positive Ce anomaly, showing lower REE contents ranging from 174 to 548 ppm and lower percentages of adsorbed REE from 34% to 68% compared with the parent granite. In contrast, the lower part of the profile from 4.5 to 12 m depth is characterized by negative Ce anomaly, showing higher REE contents ranging from 578 to 1,084 ppm and higher percentages from 53% to 85%. The negative Ce anomaly and enrichment of REE in the lower part of the profile suggest that acidic soil water in an oxidizing condition in the upper part mostly immobilized Ce4+ as CeO2 and transported REE3+ downward to the lower part of the profile. The transported REE3+ were adsorbed onto weathering products or distributed to secondary minerals such as rhabdophane. The immobilization of REE results from the increase of pH due to the contact with higher pH groundwater. Since the majority of REE in the weathered granite are present in the ion-adsorption fraction with negative Ce anomaly, the percentages of adsorbed REE are positively correlated with the whole-rock negative Ce anomaly. The result of this study suggests that the ion-adsorption type REE mineralization is identified by the occurrence of easily soluble REE fluorocarbonate and whole-rock negative Ce anomaly of weathered granite. Although fractionation of REE in weathered granite is controlled by the occurrence of REE-bearing minerals and adsorption by weathering products, the ion-adsorption fraction tends to be enriched in LREE relative to weathered granite.  相似文献   

4.
锂铍金属是世界关键金属资源,矿床类型多样,成矿作用发生在大陆地壳。但大陆地壳中锂铍元素的迁移-循环规律及不同锂铍矿床间的成因联系尚不清楚。本文系统地总结与梳理了大陆地壳结构与物质循环特征和不同类型锂铍金属矿床间的成因联系,提出大陆地壳锂铍循环-成矿系统的概念与模型,并将大陆地壳锂铍的迁移与循环划分为四个过程:变质过程、深熔过程、花岗岩浆过程、花岗质岩浆岩风化、淋滤与蚀变的浅-表生过程。沉积岩中锂铍元素在变质过程中可富集到一些变质矿物中,一些富锂铍黏土矿物也在变质过程转变成新的富锂铍变质矿物(如绿泥石、云母与堇青石);地壳深熔过程使得锂铍元素从变质矿物中释放出来并聚集在花岗岩浆中,麻粒岩相深熔(如黑云母脱水熔融与堇青石分解熔融)可能是锂铍大规模成矿的主要熔融方式;绝大多数锂铍矿床与花岗岩浆及其岩浆岩有关,是花岗岩浆与花岗质岩浆岩在不同演化阶段与不同方式富集成矿的结果;浅-表生过程对锂铍花岗岩-伟晶岩和流纹岩与流纹质凝灰岩的物理化学改造,可形成盐湖卤水型锂矿床、黏土型锂矿床以及各种次生锂铍矿床。变质过程中锂铍的迁移与富集机制,大型-超大型花岗岩-伟晶岩型锂铍矿床形成条件与关键控制因素等问题,是亟待研究与思考的科学问题。  相似文献   

5.
Most rare-metal granites in South China host major W deposits with few or without Ta–Nb mineralization. However, the Yashan granitic pluton, located in the Yichun area of western Jiangxi province, South China, hosts a major Nb–Ta deposit with minor W mineralization. It is thus important for understanding the diversity of W and Nb–Ta mineralization associated with rare-metal granites. The Yashan pluton consists of multi-stage intrusive units, including the protolithionite (-muscovite) granite, Li-mica granite and topaz–lepidolite granite from the early to late stages. Bulk-rock REE contents and La/Yb ratios decrease from protolithionite granite to Li-mica granite to topaz–lepidolite granite, suggesting the dominant plagioclase fractionation. This variation, together with increasing Li, Rb, Cs and Ta but decreasing Nb/Ta and Zr/Hf ratios, is consistent with the magmatic evolution. In the Yashan pluton, micas are protolithionite, muscovite, Li-mica and lepidolite, and zircons show wide concentration ranges of ZrO2, HfO2, UO2, ThO2, Y2O3 and P2O5. Compositional variations of minerals, such as increasing F, Rb and Li in mica and increasing Hf, U and P in zircon are also in concert with the magmatic evolution from protolithionite granite to Li-mica granite to topaz–lepidolite granite. The most evolved topaz–lepidolite granite has the highest bulk-rock Li, Rb, Cs, F and P contents, consistent with the highest contents of these elements and the lowest Nb/Ta ratio in mica and the lowest Zr/Hf ratio in zircon. Ta–Nb enrichment was closely related to the enrichment of volatile elements (i.e. Li, F and P) in the melt during magmatic evolution, which raised the proportion of non-bridging oxygens (NBOs) in the melt. The rims of zoned micas in the Li-mica and topaz–lepidolite granites contain lower Rb, Cs, Nb and Ta and much lower F and W than the cores and/or mantles, indicating an exotic aqueous fluid during hydrothermal evolution. Some columbite-group minerals may have formed from exotic aqueous fluids which were originally depleted in F, Rb, Cs, Nb, Ta and W, but such fluids were not responsible for Ta–Nb enrichment in the Yashan granite. The interaction of hydrothermal fluids with previously existing micas may have played an important role in leaching, concentrating and transporting W, Fe and Ti. Ta–Nb enrichment was associated with highly evolved magmas, but W mineralization is closely related to hydrothermal fluid. Thus these magmatic and hydrothermal processes explain the diversity of W and Ta–Nb mineralizations in the rare-metal granites.  相似文献   

6.
This paper mainly describes mineralogy and geochemistry of coals from the Weibei coalfield in the southeastern Ordos Basin, North China. A number of Al-hydroxide/oxyhydroxide minerals were detected in the Late Carboniferous coals (Nos. 5, 10 and 11 coals), especially in the No. 10 coal. Aluminum-hydroxide/oxyhydroxide minerals (nordstrandite, boehmite and diaspore) in the No. 10 coal are associated with kaolinite, suggesting that these minerals are derived from the breakdown of kaolinite. A model in which Al-hydroxide/oxyhydroxide minerals form from the incongruent dissolution of kaolinite is presented. Nordstrandite and boehmite mainly occur as massive lenses (<500 μm in length). Diaspore appears as massive aggregates and as single euhedral crystals (<50 μm in length) in a kaolinite matrix. The presence of high temperature quartz, and zircon indicates that there was input of felsic volcanic debris during accumulation of the Late Carboniferous coals. These volcanic materials have also had a significant influence on the enrichment of certain trace elements including Li, Be, Ga, Zr, Nb, Mo, Sn, W and U in the Late Carboniferous coals (Nos. 5, 10, and 11 coals). SEM-EDX results show that Ga in the No. 10 coal (whole coal average 33.4 μg/g; n = 2) mainly occurs within Al-hydroxide/oxyhydroxide minerals (nordstrandite, boehmite, and diaspore), kaolinite and organic matter.  相似文献   

7.
侯江龙  李建康  张玉洁  李超 《地球科学》2018,43(6):2042-2054
四川康定甲基卡超大型锂矿是我国最大的硬岩型锂矿床之一,矿区中南部呈岩株状出露的二云母花岗岩常被认为是成矿伟晶岩的"矿源岩",对其开展Li同位素地球化学研究,对探讨矿区稀有金属的来源与演化具有重要意义.研究工作基于详细的野外地质调查,采用MC-ICP-MS方法对岩体锂同位素组成开展了研究.研究结果显示,岩体Li含量介于192×10-6~470×10-6,均值为309×10-6,δ7Li值介于-1.56‰~+0.90‰,均值为-0.24‰,与平均上地壳值基本一致,具有高Li低δ7Li的特征.δ7Li与Li、Rb、Ga、SiO2及εNd（t）不存在明显的相关性,岩体锂同位素组成反映了其形成时的源区特征,未受岩浆结晶分异作用和蚀变作用的影响.岩体岩石地球化学、同位素地球化学资料表明,岩浆来源以三叠系西康群砂泥岩的部分熔融为主,可能有部分深源物质的加入.此外,岩体Li同位素的变化规律表明伟晶岩的成矿流体来源于二云母花岗岩.岩体Li含量与Li同位素组合不仅可用来划分锂矿床类型,而且对稀有金属找矿具有一定的指导意义.   相似文献   

8.
《Chemical Geology》2003,193(3-4):273-293
The El Berrocal granite/U-bearing quartz vein (UQV) system has been studied as a natural analogue of a high-level radioactive waste repository. The main objective was to understand the geochemical behaviour of natural nuclides under different physicochemical conditions. Within this framework, the argillization processes related to fracturing and formation of the uranium–quartz vein were studied from a mineralogical and isotopic standpoint in order to establish their temperatures of formation and thus complete the geothermal history of the system. For this purpose, δ18O values were determined for pure mineral from the unaltered granite and quartz from the uranium–quartz vein, as well as for mixture samples from the hydrothermally altered granite (sericitised granite) and clayey samples from fracture fillings, including the clayey walls of the uranium–quartz vein. The isotopic signature of quartz from the uranium–quartz vein and the monophasic nature of its fluid inclusions led us to conclude that the isotopic signature of water in equilibrium with quartz was approximately in the range from −8.3‰ to −5.7‰ V-SMOV, its temperature of formation being around 85–120 °C. The δ18O values of pure sericite from the hydrothermally altered granite, calculated by means of the oxygen fraction molar method, indicate that its temperature of formation, in equilibrium with the aforementioned waters, is also in the range from 70 °C to approximately 120 °C. Clays from fracture fillings and clayey walls of the uranium–quartz vein are usually mixtures, in different proportions, of illite, approximately formed between 70 and 125 °C; two generations of kaolinite formed at approximately 90–130 °C and at around 25 °C, respectively; smectite, formed at ≤25 °C; and occasionally palygorskite, formed either between 30 and 45 °C or 19 and 32 °C, depending on the fractionation equation used. These data suggest that sericite from the hydrothermally altered granite, quartz from the uranium–quartz vein, illite and the first generation of kaolinite from the fracture fillings resulted from the same hydrothermal process affecting the El Berrocal granite in relation to fracturing. Under certain physicochemical conditions (T≈100 °C, pH≈8 and log [H4SiO4] between −4 and −3), illite and kaolinite can be paragenetic. As a result of weathering processes, smectite was formed from hydrothermal illite and inherited albite under alkaline weathering, while the second generation of kaolinite was formed from smectite, under acid conditions and close to the sulphide-rich uranium–quartz vein. Palygorskite is an occasional mineral formed probably either during the thermal tail of the above-described hydrothermal process or during weathering processes. In both cases, palygorskite must have formed from alkaline Si–Mg-rich solutions. Finally, these data and processes are discussed in terms of natural analogue processes, drawing some implications for the performance assessment of a deep geological radwaste repository (DGRR).  相似文献   

9.
Fluorine is in the dynamic balance of two geochemical processes, enrichment and leaching, reflecting the adsorption and desorption of fluoride by clay minerals, respectively. The two geochemical processes of fluorine in soil are influenced by factors including geochemical characteristics of soil and clay minerals, pH and sanity of soil solutions, climate, grazing and agriculture activities. Main factors controlling enrichment and leaching process of fluorine in soil can be found with interaction consideration.  相似文献   

10.
高岭石对重金属离子的吸附机理及其溶液的pH条件   总被引：14，自引：0，他引：14  
高岭石对Cu^2+,Pb^2+离子的吸附实验及高岭石的溶解实验表明,高岭石对重金属离子的吸附有别于石英单一表面配位模式,离子交换和表面配位模式并存,并随溶液pH由酸性往碱性的变化发生规律性的演替：pH<6.5时主要表现为外圈层配位的离子交换吸附,且在pH<4时由于受到高岭石表层中铝的高溶出及溶液中较高离子强度的影响,高岭石对Cu^2+,Pb^2+离子的吸附率较低,pH为5～6时由于高岭石端面的荷电性为近中性,吸附率则有明显的提升并且表现为一个吸附平台;pH>6.5时离子交换和表面配位均为重要吸附机制,pH再升高时沉淀机制则起着重要作用。研究表明,pH调控高岭石-水界面溶解与质子化-去质子化反应过程,并影响着Cu^2+,Pb^2+离子的吸附行为。最后采用Sverjensky(1993)表面配位的物理模型对吸附结果作了描述。  相似文献   

11.
《Applied Geochemistry》2002,17(7):885-902
An ancient saprolite has developed on the Palaeoproterozoic granulite, granite gneiss and amphibolite bedrock of the Vuotso–Tankavaara area of central Finnish Lapland. The present day climatic regime in Finnish Lapland lies within the northern boreal zone and so the saprolite there can be regarded as fossil. Cores of saprolite were collected from 4 sections (42 samples) and analyzed chemically and mineralogically. In the study area, progressive weathering of the rocks has been marked by gradual enrichment in Al, Fe and Ti; and depletion of Na, K and Ca. The higher concentration of Fe(III) and water and reduced Na and Ca in weathered bedrock in the 4 sections are indicative of oxidation, hydration and leaching processes involved during weathering. The primary minerals in the saprolite are plagioclase feldspar, K-feldspar, quartz, garnet (almandine) and hornblende; the common secondary minerals are kaolinite, halloysite, and vermiculite in addition to minor amounts of sericite. Intense weathering is indicated by: (1) the presence of kaolinite and halloysite in 4 sections of different bedrock types, and (2) the comparatively lower SiO2/Al2O3 (wt.%) ratio (2.30) of weathered granulites (3 sections) as compared to fresh granulite (4.33) and that of weathered amphibolite (2.68) as compared to fresh amphibolite (3.56). In general, kaolinite and halloysite have formed through the weathering of feldspars, garnet, and biotite. Vermiculite is the most probable alteration product of biotite. The formation of kaolinite and halloysite in Finnish Lapland indicates wetter and warmer climatic conditions during the time of their formation than at present. The possible time for formation of the saprolite is early Cretaceous–early Tertiary into Middle Miocene.  相似文献   

12.
The Penouta peraluminous low-phosphorous granite is the most important low-grade, high-tonnage Sn-Ta-Nb-bearing albite granite from the Iberian Massif. A sheet or laccolith shape, instead of a stock, is inferred for the Penouta granite, maybe in relation with the low viscosity and high mobility of a fluorine-bearing melt. Subhorizontal lateral extension of the magma is also inferred via vertical and horizontal geochemical variations. The absence of compositional gaps in variation diagrams, coupled with continuous evolutionary trends of compatible and incompatible elements with height, discard a multi-pulse intrusion and point to a single magma pulse. Mineral chemistry, trace element and least-squares mass balance modelling support a differentiation process from bottom to top in the emplacement place. The absence of switch from incompatible to compatible behaviour (bell-shaped trends) in Sn, Nb and Ta variation diagrams, coupled to experimental constraints on tantalite and cassiterite saturation, suggest that Nb-Ta oxides and probably cassiterite were not fractionated mineral phases, their crystallisation being related to concentration gradients within a trapped intercumulus melt. Major and trace element modelling support that the concentration upwards of Ta and the Ta/Nb ratio could be a consequence of mineral fractionation, with a key role of muscovite (mainly primary) for the Ta/Nb ratio, as this mineral has a higher partition coefficient for Nb than Ta. Our results suggest that fluorine and peraluminosity had a limited effect in the Ta/Nb ratio variations. Hence, Ta enrichment is mainly controlled by fractional crystallisation processes. In most cases, Sn enrichment was also concomitant with Ta, indicating that crystal-melt fractionation processes also played an important role in Sn concentration. Nevertheless, the strongest Sn enrichment in the granite (e.g., central part of the granite body) does not correspond to a significant Ta enrichment. The high affinity of Sn for fluids and the high partitioning of Ta for melt could explain this decoupling. Nevertheless, the magmatic signature of cassiterites in these strongly Sn-enriched zones (central part of the granite body) rules out a hydrothermal subsolidus origin for this fluid. By analogy with models carried out in sill-like bodies it seems likely that the Sn enrichment in the central part of the granite body is related to fluid saturation/degassing occurred in the lower margin, as a consequence of cooling and crystallisation of mostly anhydrous minerals (i.e. second boiling). The vapour exsolved migrated into the hotter melt up to the central part, where it probably was reabsorbed, yielding cassiterite with a magmatic signature. Moreover, we suggest that heat loss in the upper margin of the granite body might also contribute to the formation of a second fluid-saturated zone. As a result, pegmo-aplites and greisen were developed.  相似文献   

13.
The central trough of the Bolivian Altiplano is occupied by two wide salt crusts: the salar of Uyuni, which is probably the largest salt pan in the world (10,000 km2) and the salar of Coipasa (2,500 km2). Both crusts are essentially made of porous halite filled with an interstitial brine very rich in Li, K, Mg, B (up to 4.7 g/l Li, 4.3 g/l B, 30 g/l K and 75 g/l Mg). Lithium reserves are the highest known in the world, around 9 × 106 tons. Potassium, magnesium and boron reserves in brines are also important (around 194 × 106 tons K, 8 × 106 tons B and 211 × 106 tons Mg).

The crusts are the remnant of saline Lake Tauca (13,000–10,000 yr BP). Its salinity was estimated approximately at 80 g/l. Its paleochemistry was derived in two ways: (1) by dissolving the present amounts of all chemical components in the former lake volume, and (2) by simulating the evaporation of the major inflows to the basin. The resulting chemical compositions are quite different. The dissolution-derived one is 5 to 50 times less concentrated in Li, K, Mg, B than the evaporation-simulated ones. However all compositions present the same Na and Cl contents. This suggests either a removal of bittern salts or an enrichment of the former lake water in Na and Cl.

The most probable interpretation is that Lake Tauca redissolved a salt crust akin to that existing today. Several older lakes have been detected on the Altiplano. Nevertheless, such an explanation only pushes the problem back. It is likely that the anomaly was transferred from one lake to an other. Three hypotheses may be put forward: (1) bittern seepage through bottom sediments, (2) uptake of the missing components by minerals, and (3) leaching of ancient evaporites from the catchment area at the beginning of the lacustrine history of the basin. The excess halite could have been recycled from lake to lake. This latter process seems to be the most effective to explain the large excess of Na and Cl over the bittern solutes — Li, K, Mg and B. The occurrence of almost pure Na/1bCl saline springs flowing out from a gypsum diapir in the northern Altiplano gives substantial support to this hypothesis.  相似文献   


14.
作为一种“非传统稳定同位素”,锂同位素地球化学研究已经成为近年来国际上研究的热点之一.文章成功应用锂同位素对青藏高原西南部赛利普超钾质火山岩进行了示范研究.研究表明,赛利普超钾质火出岩的w(Li)为11.2×10-6～22.9× 10-6,同位素组成δ7Li为1.2‰～+3.5‰,平均值为0 2‰,与平均上地壳的相当.超钾质火山岩的锂同位素组成与岩浆结晶分异程度参数之间不存在任何相关性,这表明在超钾质火山岩结晶分异过程中没有发生明显的锂同位素分馏,锂同位素组成特征反映了其形成时的源区特征.超钾质火山岩的锂同位素组成变化范围达4.7‰,并且与pb-Sr-Nd同位素和岩浆结晶分异参数之间亦无任何相关性,表明锂同位素异常可能反映了不均匀源区岩石特征.通过计算模拟以及与前人的类似研究成果进行对比,笔者认为俯冲印度地壳而不是特提斯洋壳(包括沉积物)的流体/熔体参与了超钾质火山岩的源区富集,并在此基础上提出了超钾质火山岩成因模式.  相似文献   

15.
通过对6722铀矿床地质－地球化学特征及长英质隐爆角砾岩和围岩超微构造研究，结合U，Th等元素溶浸实验结果，得出“隐爆气热流体溶浸成矿富集机制”；来自深部的富含挥发组分（H2O、F、CO2等）的高热安粗岩浆，在早白垩世末（107Ma）沿富城花岗岩体西部蚀变带发育的火山机构中发生隐爆作用，致使围岩发生强烈脆性变形，生成长英质隐爆角砾岩带和震裂花岗岩带；压力、温度降低导致安粗岩浆中挥发组分逸出形成气热流进入稳隐爆裂隙中，并将蚀变花岗岩中的活动性成矿元素（U）浸出转移；成矿物质在物理化学条件（p,t,Eh,pH,化学组分等）急剧变化的部位（长英质隐爆角砾岩及碎裂花岗岩）沉淀富集。  相似文献   

16.
铌、钽矿产分布较广。内生铌钽矿成矿类型主要为伟晶岩型、稀有金属花岗岩型、碳酸岩型和碱性岩型;外生矿床多为内生矿床经过风化和沉积等外生作用发生二次富集的风化壳型和残坡积、冲积砂矿型。从成矿时代来看,伟晶岩型矿床成矿时代跨度较大,从3.08 Ga到0.19 Ga;碱性岩型矿床主要成矿期分别在2.25~1.35 Ga和0.75~0.19 Ga;碳酸岩型矿床成矿期主要分布在0.75~0.6 Ga和0.4~0.35 Ga;花岗岩型主要分布在0.75~0.19 Ga的中晚期。碳酸岩型铌矿床和伟晶岩型钽矿床是目前勘探的主要目标。  相似文献   

17.
A number of trace elements have been determined spectrographically in the rocks and minerals of the Skaergaard intrusion, East Greenland. The original basic magma from which the varied rocks of the complex were developed is shown to have had a normal trace element composition. The sorting out of the trace elements into the various mineral series produced by strong fractional crystallization of the original basic magma is traced in detail by means of analyses of the separated minerals. Certain of the trace elements (Cr, Ni) are shown to be strongly concentrated in the early rocks so that later fractions have little or none of them; other elements (P, V, Cu, Sc, Mn, S) reach maximum values in the middle, or late middle stages represented by certain olivine-free gabbros and ferrogabbros; other elements (Li, Zr, Y, La, Ba, Rb) tend to remain in the residual liquid during fractionation and are thus abundant in the latest granite fraction. Still other trace elements (Co, Sr, Ga, Mo) show only small changes in amount throughout the series. Of these Co is a little more abundant in the early and middle stages, Sr in the middle stages, Ga in the later stages and Mo in the early and later but not in the middle stages. The distribution of the trace elements in the rocks is considered in relation to the varying composition of the minerals produced by the fractional crystallization processes and an attempt is made to discuss the mineral compositions in terms of crystal chemical concepts.The Skaergaard sequence of differentiation from gabbros, through ferrogabbros, to granite is considered to be a common trend of fractionation of basic magma at high levels in the crust, and the observed changes in trace element composition are therefore regarded as having wide geochemical significance. The trace element composition of the intermediate Skaergaard differentiates is significantly different from that of diorites reported by other workers and suggests that diorites have had some other origin than by fractionation of basic magma. On the other hand the trace element composition of many granites resembles that of the granite fraction produced in the Skaergaard intrusion.  相似文献   

18.
在吉林东部花岗岩区地下水化学成分和化学类型研究的基础上,以Na作为参比元素,确定了花岗岩风化过程中22种主量元素和微量元素的相对活动顺序。花岗岩区地下水的地球化学类型属低矿化度(变化范围为69.51×10-6~386.49×10-6,平均值为199.48×10-6)的HCO3-Ca和HCO3-Na-Ca型。花岗岩风化过程中元素的活动性顺序(RM)从大到小依次为:B、Ca、Mo、Zn、Sr、Na、Mg、Cr、Cu、Ni、K、Co、Li、V、As、Ba、Si、Y、Fe、Ti、Al、Mn。风化产物中的粘土矿物主要为高岭土、蒙脱石,反映出本区花岗岩的风化淋滤程度较弱的特点。  相似文献   

19.
The chemistry and. mineralogy of calcretes and associated calcareous fine earth from the lower River Murray Basin and Yorke Peninsula in South Australia suggest that the carbonate material was deposited as a continuous unit and subsequently modified. At each site examined the Ca/Mg ratio progressively decreases with increasing depth, and where data are available, a similar decrease in the Ca/Sr ratio is observed. This sequence is independent of the hardness or physical condition of the carbonate. In some places the carbonate from the lowest horizons is nearly pure dolomite. The change in Ca/Mg ratio with depth is considered to be due to leaching, probably during periods of the past when the climate was less arid and the rainfall penetrated to about 2 m.

In the lower Murray Basin the Ca/Mg ratio of the surface calcrete horizon progressively increases from Tailetn Bend N to Sedan, and the silicate clay fraction changes from sepiolite at Tailem Bend, to palygorskite at Murray Bridge and illite at Sedan. The bedrock also varies, from magnesium‐rich amphibolites at Tailem Bend to granite at Sedan and, further, there is an apparent relation between the chemistry of the non‐carbonate fraction of the calcretes and the underlying rock. The original carbonate deposit probably formed in lakes of different chemistry, and has been modified by solution and precipitation.  相似文献   

20.
通过研究鲁西七星台地区新太古代变质辉长岩及相关岩石的锆石SHRIMP U-Pb年龄和地球化学组成.它们侵入新太古代表壳岩和TTG岩体.根据12个样品SHRIMP U-Pb锆石定年,可把形成时代划分为3期:2 662~>2 711 Ma、2 608~2 618 Ma和2 508~2 526 Ma.其他样品（进行地球化学分析）的形成时代是根据岩石空间分布、野外特征及与定年样品所代表岩石的关系来确定的.>2.65 Ga变质辉长岩既有来自于富集地幔源区也有来自亏损地幔源区.~2.6 Ga变质辉长岩具平坦型稀土模式,大离子亲石元素富集,Nb、Ta、P亏损,来自亏损地幔源区,可能遭受陆壳物质影响,~2.6 Ga变质辉石岩显示中稀土富集,与单斜辉石堆晶作用有关.~2.5 Ga变质辉长岩存在平坦型-轻微亏损轻稀土和轻稀土富集型两种类型稀土模式.与~2.5 Ga变质辉长岩相比,~2.5 Ga变质辉长闪长岩稀土含量更高,轻重稀土分异程度更高,大离子亲石元素更为富集,Nb、Ta亏损更为明显,是~2.5 Ga辉长质岩浆进一步结晶分异产物.结合前人研究,可得出如下结论.（1）七星台地区存在>2.65 Ga、~2.6 Ga和~2.5 Ga 3期变质辉长岩,其中~2.6 Ga变质辉长岩规模最大;（2）不同时代变质辉长岩地球化学组成特征不同,反映了源区组成和形成过程的复杂性;（3）鲁西地区在新太古代早期（>2.7~2.6 Ga）存在长期连续的基性岩浆作用,可能与地幔岩浆板底垫托有关;（4）在七星台地区首次发现~2.5 Ga辉长岩-辉长闪长岩,为鲁西地区A带广泛存在的~2.5 Ga深熔作用提供了热源来自地幔的直接证据.   相似文献   

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