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1.
The study of radioactive element distribution in the rocks of the Guli Complex revealed an increase of uranium and thorium contents in the final products of magmatic differentiation. In the carbonatite complex, the radioactive elements are mainly accumulated in the early rocks—phoscorites, while their contents in the late phases, dolomitic carbonatites, decrease. The Th/U ratio increases from near-chondritic values in the weakly differentiated highly-magnesian primary magmas to the late rocks—phoscorites, calcitic carbonatites, and dolomitic carbonatites. The majority of radioactive elements are hosted in rare-metal accessory minerals: perovskite, pyrochlore, calzirtite, and apatite. Rock-forming minerals are characterized by extremely low contents of radioactive elements.  相似文献   

2.
Carbonatites that are hosted in metamorphosed ultramafic massifs in the roof of miaskite intrusions of the Il’mensky-Vishnevogorsky alkaline complex are considered. Carbonatites have been revealed in the Buldym, Khaldikha, Spirikha, and Kagan massifs. The geological setting, structure of carbonatite bodies, distribution of accessory rare-metal mineralization, typomorphism of rock-forming minerals, geochemistry, and Sr and Nd isotopic compositions are discussed. Dolomite-calcite carbonatites hosted in ultramafic rocks contain tetraferriphlogopite, richterite, accessory zircon, apatite, magnetite, ilmenite, pyrrhotite, pyrite, and pyrochlore. According to geothermometric data and the composition of rock-forming minerals, the dolomite-calcite carbonatites were formed under K-feldspar-calcite, albite-calcite, and amphibole-dolomite-calcite facies conditions at 575–300°C. The Buldym pyrochlore deposit is related to carbonatites of these facies. In addition, dolomite carbonatites with accessory Nb and REE mineralization (monazite, aeschynite, allanite, REE-pyrochlore, and columbite) are hosted in ultramafic massifs. The dolomite carbonatites were formed under chlorite-sericite-ankerite facies conditions at 300–200°C. The Spirikha REE deposit is related to dolomite carbonatite and alkaline metasomatic rocks. It has been established that carbonatites hosted in ultramafic rocks are characterized by high Sr, Ba, and LREE contents and variable Nb, Zr, Ti, V, and Th contents similar to the geochemical attributes of calcio-and magnesiocarbonatites. The low initial 87Sr/86Sr = 0.7044?0.7045 and εNd ranging from 0.65 to ?3.3 testify to their derivation from a deep mantle source of EM1 type.  相似文献   

3.
The Khaluta carbonatite complex comprizes fenites, alkaline syenites and shonkinites, and calcite and dolomite carbonatites. Textural and compositional criteria, melt inclusions, geochemical and isotopic data, and comparisons with relevant experimental systems show that the complex formed by liquid immiscibility of a carbonate-saturated parental silicate melt. Mineral and stable isotope geothermometers and melt inclusion measurements for the silicate rocks and carbonatite all give temperatures of crystallization of 915–1,000°C and 890–470°C, respectively. Melt inclusions containing sulphate minerals, and sulphate-rich minerals, most notably apatite and monazite, occur in all of the lithologies in the Khaluta complex. All lithologies, from fenites through shonkinites and syenites to calcite and dolomite carbonatites, and to hydrothermal mineralisation are further characterized by high Ba and Sr activity, as well as that of SO3 with formation of the sulphate minerals baryte, celestine and baryte-celestine. Thus, the characteristic features of the Khaluta parental melt were elevated concentrations of SO3, Ba and Sr. In addition to the presence of SO3, calculated fO2 for magnetites indicate a high oxygen fugacity and that Fe+3>Fe+2 in the Khaluta parental melt. Our findings suggest that the mantle source for Khaluta carbonatite and associated rocks, as well as for other carbonatites of the West Transbaikalia carbonatite province, were SO3-rich and characterized by high oxygen fugacity.  相似文献   

4.
The Burpala alkaline massif contains rocks with more than 50 minerals rich in Zr,Nb,Ti,Th,Be and rare earth elements(REE).The rocks vary in composition from shonkinite,melanocratic syenite,nepheline and alkali syenites to alaskite and alkali granite and contain up to 10%LILE and HSFE,3.6%of REE and varying amounts of other trace elements(4%Zr,0.5%Y,0.5%Nb,0.5%Th and 0.1%U).Geological and geochemical data suggest that all the rocks in the Burpala massif were derived from alkaline magma enriched in rare earth elements.The extreme products of magma fractionation are REE rich pegmatites,apatite-fiuorite bearing rocks and carbonatites.The Sr and Nd isotope data suggest that the source of primary melt is enriched mantle(EM-Ⅱ).We correlate the massif to mantle plume impact on the active margin of the Siberian continent.  相似文献   

5.
The Early Cretaceous Sung Valley Ultramafic-Alkaline-Carbonatite (SUAC) complex intruded the Proterozoic Shillong Group of rocks and located in the East Khasi Hills and West Jaintia Hills districts of Meghalaya. The SUAC complex is a bowl-shaped depression covering an area of about 26 km2 and is comprised serpentinised peridotite forming the core of the complex with pyroxenite rim. Alkaline rocks are dominantly ijolite and nepheline syenite, occur as ring-shaped bodies as well as dykes. Carbonatites are, the youngest intrusive phase in the complex, where they form oval-shaped bodies, small dykes and veins. During the course of large scale mapping in parts of the Sung Valley complex, eleven carbonatite bodies were delineated. These isolated carbonatite bodies have a general NW-SE and E-W trend and vary from 20–125 m long and 10–40 m wide. Calcite carbonatite is the dominant variety and comprises minor dolomite and apatite and accessory olivine, magnetite, pyrochlore and phlogopite. The REE-bearing minerals identified in the Sung Valley carbonatites are bastnäsite-(Ce), ancylite-(Ce), belovite-(Ce), britholite-(Ce) and pyrochlore that are associated with calcite and apatite. The presence of REE carbonates and phosphates associated with REE-Nb bearing pyrochlore enhances the economic potential of the Sung Valley carbonatites. Trace-element geochemistry also reveals an enrichment of LREEs in the carbonatites and average ΣREE value of 0.102% in 26 bed rock samples. Channel samples shows average ΣREE values of 0.103 wt%. Moreover, few samples from carbonatite bodies has indicated relatively higher values for Sn, Hf, Ta and U. Since the present study focuses surface evaluation of REE, therefore, detailed subsurface exploration will be of immense help to determine the REE and other associated mineralization of the Sung Valley carbonatite prospect.  相似文献   

6.
This paper reports a geochemical and mineralogical study on carbonatites from the Guli massif, which hosts rare-metal mineralization. The principal carriers of radioactive elements in the carbonatites are pyrochlore-group minerals, zirconolite, and thorianite, which are described here. They are characterized by elevated concentrations (wt %) of radioactive elements: up to 17.89 UO2 and 20.01 ThO2 in pyrochlore, up to 6.49 UO2 and 94.29 ThO2 in thorianite, and up to 6.74 ThO2 in zirconolite. The pyrochlore-group minerals, zirconolite, and thorianite from the early calcite carbonatites occur in intimate association with Ti-Zr oxides calzirtite, perovskite, and baddeleyite. Significant radioactive element fractionation in early-stage derivatives results in the depletion of the residual magmatic products in these elements. The dolomite carbonatites are reported to contain only trace amounts of pyrochlore-group minerals. It was shown that the distribution of U, Th, Nb, and Ta in the calcite and dolomite carbonatites is correlated with the evolutionary trends of pyrochlore composition. Typical schemes of isomorphic substitution are proposed for pyrochlore-group minerals and zirconolite. The pyrochlore-group minerals show an apparent evolutionary trend from U-rich towards more Th- and Ta-rich varieties, and Ba-Sr cation-deficient varieties originate during the latest stage of the evolution. The pyrochlore-group minerals, zirconolite, and thorianite may also accumulate in placers, together with gold. Because of the relative ease of extraction of the accessory minerals, the carbonatites of the Guli massif can be considered as commercial sources of radioactive raw materials.  相似文献   

7.
Based on the investigation of melt inclusions using electron and ion microprobe analysis, we estimated the composition, evolution, and formation conditions of magmas responsible for the calcite-bearing ijolites and carbonatites of the Belaya Zima alkaline carbonatite complex (eastern Sayan, Russia). Primary melt and coexisting crystalline inclusions were found in the nepheline and calcite of these rocks. Diopside, amphibole (?), perovskite, potassium feldspar, apatite, calcite, pyrrhotite, and titanomagnetite were identified among the crystalline inclusions. The melt inclusions in nepheline from the ijolites are completely crystallized. The crystalline daughter phases of these inclusions are diopside, phlogopite, apatite, calcite, magnetite, and cuspidine. During thermometric experiments with melt inclusions in nepheline, the complete homogenization of the inclusions was attained through the dissolution of a gas bubble at temperatures of 1120–1130°C. The chemical analysis of glasses from the homogenized melt inclusions in nepheline of the ijolites revealed significant variations in the content of components: from 36 to 48 wt % SiO2, from 9 to 21 wt % Al2O3, from 8 to 25 wt % CaO, and from 0.6 to 7 wt % MgO. All the melts show very high contents of alkalis, especially sodium. According to the results of ion microprobe analysis, the average content of water in the melts is no higher than a few tenths of a percent. The most salient feature of the melt inclusions is the extremely high content of Nb and Zr. The glasses of melt inclusions are also enriched in Ta, Th, and light rare earth elements but depleted in Ti and Hf. Primary melt inclusions in calcite from the carbonatites contain a colorless glass and daughter phlogopite, garnet, and diopside. The silicate glass from the melt inclusions in calcite of the carbonatite is chemically similar to the glasses of homogenized melt inclusions in nepheline from the ijolites. An important feature of melt inclusions in calcite of the carbonatites is the presence in the glass of carbonate globules corresponding to calcite in composition. The investigation of melt inclusions in minerals of the ijolites and carbonatites and the analysis of the alkaline and ore-bearing rocks of the Belaya Zima Massif provided evidence for the contribution of crystallization differentiation and silicate-carbonate liquid immiscibility to the formation of these rocks. Using the obtained trace-element compositions of glasses of homogenized melt inclusions and various alkaline rocks and carbonatites, we determined to a first approximation the compositions of mantle sources responsible for the formation of the rock association of the Belaya Zima alkaline-carbonatite complex. The alkaline rocks and carbonatites were derived from the depleted mantle affected by extensive metasomatism. It is supposed that carbonate melts enriched in sodium and calcium were the main agents of mantle metasomatism.  相似文献   

8.
The Newania carbonatite complex of Rajasthan, India is one of the few dolomite carbonatites of the world, and oddly, does not contain alkaline silicate rocks thus providing a unique opportunity to study the origin and evolution of a primary carbonatite magma. In an attempt to characterize the mantle source, the source of carbon, and the magmatic and post-magmatic evolution of Newania carbonatites, we have carried out a detailed stable carbon and oxygen isotopic study of the complex. Our results reveal that, in spite of being located in a metamorphic terrain, these rocks remarkably have preserved their magmatic signatures in stable C and O isotopic compositions. The δ13C and δ18O variations in the complex are found to be results of fractional crystallization and low temperature post-magmatic alteration suggesting that like other carbonatites, dolomite carbonatites too fractionate isotopes of both elements in a similar fashion. The major difference is that the fractional crystallization of dolomite carbonatites fractionates oxygen isotopes to a larger extent. The modes of δ13C and δ18O variations in the complex, ?4.5?±?1‰ and 7?±?1‰, respectively, clearly indicate its mantle origin. Application of a multi-component Rayleigh isotopic fractionation model to the correlated δ13C versus δ18O variations in unaltered carbonatites suggests that these rocks have crystallized from a CO2 + H2O fluid rich magma, and that the primary magma comes from a mantle source that had isotopic compositions of δ13C ~ ?4.6‰ and δ18O ~ 6.3‰. Such a mantle source appears to be a common peridotite mantle (δ13C = ?5.0?±?1‰) whose carbon reservoir has insignificant contribution from recycled crustal carbon. Other Indian carbonatites, except for Amba Dongar and Sung Valley that are genetically linked to Reunion and Kerguelen plumes respectively, also appear to have been derived from similar mantle sources. Through this study we establish that dolomite carbonatites are generated from similar mantle source like other carbonatites, have comparable evolutionary history irrespective of their association with alkaline silicate rocks, and may remain resistant to metamorphism.  相似文献   

9.
The Burpala alkaline massif is a unique geological object. More than 50 Zr, Nb, Ti, Th, Be, and REE minerals have been identified in rare-metal syenite of this massif. Their contents often reach tens of percent, and concentrations of rare elements in rocks are as high as 3.6% REE, 4% Zr, 0.5% Y, 0.5% Nb, 0.5% Th, and 0.1% U. Geological and geochemical data show that all rocks in the Burpala massif are derivatives of alkaline magma initially enriched in rare elements. These rocks vary in composition from shonkinite, melanocratic syenite, nepheline and alkali syenites to alaskite and alkali granite. The extreme products of magma fractionation are rare-metal pegmatites, apatite-fluorite rocks, and carbonatites. The primary melts were related to the enriched EM-2 mantle source. The U-Pb zircon ages of pulaskite (main intrusive phase) and rare-metal syenite (vein phase) are estimated at 294 ± 1 and 283 ± 8 Ma, respectively. The massif was formed as a result of impact of the mantle plume on the active continental margin of the Siberian paleocontinent.  相似文献   

10.
The magmatic heritage of carbonatites can be identified on the basis of a combination of geological criteria such as, their mode of occurrence, the nature of associated igneous rocks, the presence of minerals of igneous origin, fenitization, characteristic trace element contents and isotopic composition. Late Proterozoic Samalpatti carbonatites were studied in view of these criteria, and were found to contain metamorphic minerals that normally form under thermal metamorphic conditions and which have unusual chemical compositions. A combination of criteria points clearly to a magmatic origin for these carbonatites. Field relations indicate that the dominant modes of intrusion of carbonatite into the encompassing pyroxenites and syenites include small dykes, veins, or lenses. The igneous nature of these carbonatites has been described elsewhere and chemically they are classified as calico-carbonatites. Currently, very little is known about the metamorphic textures and mineralogy observed in the Samalpatti carbonatites. In this study, several metamorphic minerals are reported including diopside, grossularite, vesuvianite, K-feldspar and wollastonite, and a hornfelsic texture is described. These mineral phases and texture characterize thermal metamorphism under low pressure and high temperature (LP-HT) metamorphic conditions (650°_750°C) or metasomatism aided by hot-fluid advection. The metamorphic nature of minerals reported is also confirmed by electron microprobe study. The Samalpatti carbonatite samples show much lower values of characteristic trace elements (P, Sr, Ba, Zr, Nb, Th, Y and REEs) than average concentrations for magmatic carbonatite. Stable isotopic (d13C and d18O) compositions of Samalpatti carbonatites do not fall in the primary igneous carbonatite (PIC) domain. The petrological and chemical signatures of these carbonatites suggest metasomatism in conjunction with fluid advection. Such a metasomatic process may drastically change the chemistry of the rocks in addition to enrichment of heavier stable isotopes. During this metasomatic process, characteristic elements would be dissolved in the high d18O fluid, and together with Rayleigh fractionation would contribute to enhanced concentrations of 13C and 18O in Samalpatti carbonatites.  相似文献   

11.
In most alkaline-ultrabasic-carbonatite ring complexes, the distribution of trace elements in the successive derivatives of mantle magmas is usually controlled by the Rayleigh equation of fractional crystallization in accordance with their partition coefficients, whereas, that of late derivatives, nepheline syenites and carbonatites, is usually consistent with trends characteristic of silicate-carbonate liquid immiscibility. In contrast to the carbonatites of ring complexes, carbonatites from deep-seated linear zones have no genetic relation with alkaline-ultrabasic magmatism, and the associated alkaline rocks are represented only by the nepheline syenite eutectic association. The geochemical study of magmatic rocks from the Vishnevye Gory nepheline syenite-carbonatite complex (Urals), which is assigned to the association of deep-seated linear zones, showed that neither differentiation of a parental melt nor liquid immiscibility could produce the observed trace element distribution (Sr, Rb, REE, and Nb) in miaskites and carbonatites. Judging from the available fragmentary experimental data, the distribution patterns can be regarded as possible indicators of element fractionation between alkaline carbonate fluid and alkaline melt. Such trace element distribution is presumably controlled by a fluid-melt interaction; it was also observed in carbonatites and alkaline rocks of some ring complexes, and its scarcity can be explained by the lower density of aqueous fluid released from magma at shallower depths.  相似文献   

12.
LA-ICP MS data are presented for ilmenites from different rocks of the alkaline complexes of the Ukrainian Shield (Chernigovka carbonatite, Oktyabr’skii, Malaya Tersa, and Southern Kal’chinskii gabbrosyenite massifs). Ilmenites from the early intrusive phases (alkaline pyroxenites, gabbroids, and ultramafic rocks) have the elevated contents of Cr, Co, Ni, and V, while ilmenites from later alkaline and nepheline syenites, monzonites, and carbonatites are significantly enriched in Nb and Ta, which is caused by change in the alkalinity of the mineral-forming medium. Zr shows the more intrinsic behavior: its content is higher in the ilmenites from basic and ultrabasic rocks than in those from the nepheline syenites and carbonatites. This is mainly caused by temperature conditions of the formation of differentiated alkaline complexes. The carbonatites contain magnesian ilmenite (up to 22 mol % MgTiO3). Variations of Mg contents in ilmentes are correlated with Mg number of mafic minerals and depend also on the iron oxidation state (amount of magnetite) in the carbonatites. In the alkaline massifs of the Ukrainian Shield, ilmenites usually have the low contents of hematite end member (3–7 mol %). Ilmenite serves as a sensitive indicator of temperature, oxygen fugacity, and alkalinity of the mineral-forming medium during crystallization.  相似文献   

13.
Summary The Shillong Plateau of northeastern India hosts four Early Cretaceous (105–107Ma) ultramafic-alkaline-carbonatite complexes (UACC), which have been associated with the Kerguelen plume igneous activity. Petrological and geochemical characteristics of one of these UACC, the Sung Valley, are presented. The Sung Valley UACC was emplaced in to the Proterozoic Shillong Group of rocks and consists of ultramafics (serpentinized peridotite, pyroxenite, and melilitolite), alkaline rocks (ijolite and nepheline syenite), and carbonatites. Serpentinized peridotite, pyroxenite, and ijolitic rocks form the major part of the complex, the others constitute less than 5% of the total volume. Ijolite and melilitolite intrude peridotite and pyroxenite, while nepheline syenite and carbonatite intrude the ultramafic rocks as well as ijolite. Mineralogically, the carbonatites are classified as calcite carbonatite with minor apatite, phlogopite, pyrochlore and ilmenite. The serpentinized peridotites are wehrlitic. Chemical compositions of the silicate rocks do not show a distinct co-genetic relationship amongst them, nor do they show any geochemical relationships with the carbonatites. No noticeable fractionation trend is observed on the chemical variation diagrams of these rocks. It is difficult to establish the genetic evolution of the Sung Valley UACC through fractional crystallization of nephelinitic magma or through immiscible liquids. On the basis of petrological and geochemical data and previously published isotopic results from these rocks, it is suggested that they have been derived from a primary carbonate magma generated by the low-degree melting of a metasomatized mantle peridotite.  相似文献   

14.
The paper discusses the mineralogy and geochemistry of altered rocks associated with calcite and dolomite–ankerite carbonatites of the Onguren dyke–vein complex in the Western Transbaikal Region. The alteration processes in the Early Proterozoic metamorphic complex and synmetamorphic granite hosting carbonatite are areal microclinization and riebeckitization; carbonates, phlogopite, apatite, and aegirine occur in the near-contact zones of the dolomite–ankerite carbonatite veins; and silicification is displayed within separated zones adjacent to the veins. In aluminosilicate rocks, microclinization was accompanied by an increasing content of K, Fe3+, Ti, Nb (up to 460 ppm), Th, Cu, and REE; Na, Ti, Fe3+, Mg, Nb (up to 1500 ppm), Zr (up to 2800 ppm), Ta, Th, Hf, and REE accumulated in the inner zone of the riebeckitization column. High contents of Ln Ce (up to 11200 ppm), U (23 ppm), Sr (up to 7000 ppm), Li (up to 400 ppm), Zn (up to 600 ppm), and Th (up to 700 ppm) are typical of apatite–phlogopite–riebeckite altered rock; silicified rock contains up to (ppm): 2000 Th, 20 U, 13000 Ln Ce, and 5000 Ва. Ilmenite and later rutile are the major Nb carriers in alkali altered rocks. These minerals contain up to 2 and 7 wt % Nb2O5, respectively. In addition, ferrocolumbite and aeschynite-(Ce) occur in microcline and riebeckite altered rocks. Fluorapatite containing up to 2.7 wt % (Ln Ce)2O3, monazite-(Ce), cerite-(Ce), ferriallanite-(Ce), and aeschynite-(Ce) are the REE carriers in riebeckite altered rock. Bastnäsite-(Ce), rhabdophane-group minerals, and xenotime-(Y) are typical of silicified rock. Thorite, monazite-(Ce), and rhabdophane-group minerals are the Th carriers.  相似文献   

15.
Earlier, a belt of alkali-granite plutons and a carbonatite province were discovered in the South Gobi Desert, Mongolia. The Lugingol pluton of pseudoleucitic syenites with carbonatites was assigned to the alkali-granite belt. However, new dating showed that it is 40 Myr younger than the Khan-Bogdo pluton and a large fault separates it from the alkali-granite belt. In the same part of the South Gobi Desert, a dike series of alkaline K-shonkinites with a rare-metal carbonatite vein was found by V.I. Kovalenko west of the Lugingol pluton, near Mt. Baruun Hasar Uula, and a dike series of alkali and nepheline syenites was found by us northeast of the Lugingol pluton. These data give grounds to distinguish an intrusive complex of K-alkaline shonkinites and leucitic syenites with Late Paleozoic REE-bearing carbonatites. Thus, three alkaline-rock complexes of different ages are distinguished in the South Gobi Desert. We present refined geological maps of these complexes. The plutons of all three complexes are deposits of trace elements (REE, Nb, Zr, Y, P). The chemical composition of the silicate rocks of the complex, rare-metal agpaitic pegmatites, and carbonatite and apatite rare-metal ores was considered in detail. Shonkinites from Mt. Baruun Hasar Uula and the Mountain Pass mine (United States) and their carbonatites, along with the Lugingol carbonatites, belong to a single association of K-alkaline rocks and carbonatites, as evidenced by their identical chemical, mineral, and geochemical rare-metal compositions. Rare-earth element patterns and spidergrams show similarities and differences between the rare-metal rocks of three complexes as well as paragenetic differences between their rare-metal minerals. A rare process is described—the amorphization of rare-metal minerals, related to their high-temperature crystallization in a medium with abnormal silica contents of the Khan-Bogdo pegmatites. The parental magmas of the alkali-carbonatite complexes were generated from the EM-2 contaminated mantle that had undergone recycling, whereas the parental magmas of the Khan-Bogdo agpaitic alkali granites were produced from depleted mantle.  相似文献   

16.
白云鄂博碳酸岩型REE-Nb-Fe矿床是世界上最大的稀土矿床。稀土矿石产于整个白云石碳酸岩体和部分脉状碳酸岩中。对比世界上20余个火成碳酸岩地区的特征后发现,白云鄂博地区完全具备国外火成碳酸岩区的地质特征。在岩石、矿石组合上,本区也发育一套碳酸岩+超基性岩+碱性基性岩(含基性熔岩)+碱性岩+稀土矿石+铁矿石组合;在矿物组合上,以白云石为主,方解石次之,伴生一套碱性闪石、长石、霓石、磷灰石、萤石、磁铁矿、稀土矿物组合;在全岩化学成分、微量元素、稀土元素和Sr、Nd、Pb、C、O同位素上,这些岩石具有一定的亲缘关系,有着共同的来源;在岩体的形态与岩石组构上,它们以岩席、岩筒和脉岩的形式出现,并发育有强烈的熔离作用与流动构造;在区域构造上,发育隐伏穹窿构造、岩筒构造和巨型断裂汇聚构造。综合分析上述特征表明:白云鄂博地区具有中元古代破火山机构的痕迹,赋矿白云石碳酸岩体则是顺层侵入的火成碳酸岩体,东矿、主矿可能是一个火山颈构造控矿,而赋矿白云石碳酸岩体西南侧的苏木图矿床则是隐伏岩筒构造控矿。  相似文献   

17.
碳酸岩流体及其稀土成矿作用   总被引：12，自引：0，他引：12  
火成碳酸岩熔浆可侵入到大陆和洋壳构造环境 ,多数大陆构造环境下的碳酸岩在时间和空间上与地壳减薄事件有关 ,高温下它具有极强的搬运碱金属、大离子亲石元素和高场强元素的能力。碳酸岩中可能出现的原生包裹体有两相水溶液 (气 +液 )包裹体、含子矿物多相水溶液包裹体、含CO2 包裹体和CO2 +盐水溶液混合多相包裹体以及硅酸盐玻璃质熔融包裹体等。碳酸岩型稀土矿床中赋存的流体包裹体类型也可分为气液相、含碳水溶液相和气液固多相包裹体 ,包裹体中稀土子矿物的出现是该类矿床最显著的特征。富碱碳酸岩流体中REE ,Sr ,Th和Fe等都具有极高的溶解度 ,水岩反应和流体不混溶是造成成矿热液中REE及Fe等沉淀成矿的关键因素 ,REE的迁移沉淀可延续到低温、低盐度的成矿晚阶段  相似文献   

18.
http://www.sciencedirect.com/science/article/pii/S1674987110000125   总被引：3，自引：0，他引：3  
<正>Carbonatites are commonly related to the accumulation of economically valuable substances such as REE.Cu,and P.The debate over the origin of carbonatites and their relationship to associated silicate rocks has been ongoing for about 45 years.Worldwide,the rocks characteristically display more geochemical enrichments in Ba,Sr and REE than sedimentary carbonate rocks.However,carbonatite's geochemical features are disputed because of secondary mineral effects.Rock-forming carbonates from carbonatites at Qinling.Panxi region,and Bayan Obo in China show REE distribution patterns ranging from LREE enrichment to flat patterns.They are characterized by a Sr content more than 10 times higher than that of secondary carbonates.The coarse- and fine-grained dolomites from Bayan Obo H8 dolomite marbles also show similar high Sr abundance,indicating that they are of igneous origin.Some carbonates in Chinese carbonatites show REE(especially HREE) contents and distribution patterns similar to those of the whole rocks.These intrusive carbonatites display lower platinum group elements and stronger fractionation between Pt and Ir relative to high-Si extrusive carbonatite.This indicates that most intrusive carbonatites may be carbonate cumulates.Maoniuping and Daluxiang in Panxi region are large REE deposits.Hydrothermal fluorite ore veins occur outside of the carbonatite bodies and are emplaced in wallrock syenite.The fiuorite in Maoniuping has Sr and Nd isotopes similar to carbonatite.The Daluxiang fiuorite shows Sr and REE compositions different from those in Maoniuping.The difference is reflected by both the carbonatites and rock-forming carbonates,indicating that REE mineralization is related to carbonatites.The cumulate processes of carbonate minerals make fractionated fluids rich in volatiles and LREE as a result of low partition coefficients for REE between carbonate and carbonatite melt and an increase from LREE to HREE.The carbonatite-derived fluid has interacted with wallrock to form REE ore veins.The amount of carbonatite dykes occurring near the Bayan Obo orebodies may support the same mineralization model,i.e.that fluids evolved from the carbonatite dykes reacted with H8 dolomite marble,and thus the different REE and isotope compositions of coarse- and fine-grained dolomite may be related to reaction processes.  相似文献   

19.
The Elchuru alkaline igneous intrusion is an arcuate-shaped ring complex, approximately 16 km2 in area, cropping out in the Eastern Ghats high grade metamorphic series. It is part of an alkaline province composed of a number of intrusions which range from ijolite-melteigite to alkali gabbro (viz. malignite, melalusitanite, shonkinite) and then to hypersolvus nepheline syenite followed by subsolvus nepheline syenite. The complex is cut by late lamprophyric dykes. A nephelinized alkaline gneiss, within the investigated complex, is the only deformed rock type and is regarded as an older unit not related to the comagmatic series. The remainder of the complex was emplaced post-tectonically. Sovitic carbonatite is a conspicuous Iithologic unit associated with the complex. Chemical analyses of 19 selected samples for 13 major oxides and 5 trace elements (Rb, Ba, Sr, Zr and Nb) are presented to establish a geochemical model for the investigated complex. The mineralogy, petrography and geochemistry of the rocks of the Elchuru Alkaline Complex suggest that it was formed by differentiation of an initially alkali-rich ijolitic magma as reflected in the crystallization of nepheline, kaersutitic amphibole and alkali feldspar. With progressive increase in alkali feldspar content (volume percentage) the ijolite passes to malignite and then nepheline syenites. Amphibole shows sodic enrichment from a dominant calcic variety. Pyroxene, likewise, shows sodic enrichment following the scheme salite-ferrosalite to aegirine-augite. The igneous cycle closes with the intrusion of biotite lamprophyre. There is a systematic increase in total alkalies (Na2O+K2O) and decrease in CaO from the early mafic rocks to the syenitic rocks. The alkali-lime index of the complex is 48 indicating its strongly alkaline nature (Peacock 1931), and they are miaskitic in character (agpaicity index <1, Currie 1976). Such miaskitic complexes are associated with carbonatites (Heinrich 1966).  相似文献   

20.
Summary Two bimodal carbonatite complexes in Namibia of Cretaceous age are explored as to the presence and composition of a coexisting carbonatitic fluid. The Kalkfeld and Ondurakorume complexes contain both Ca- and Mg/Fe-carbonatites, composed of calcite alone or calcite with ferroan dolomite, fluorapatite and strontianite. The major element evolution in the bulk rocks from s?vites to beforsites is due to crystallization of calcite and fluorapatite. All carbonatites show a negative Y anomaly in normalised REE plots. Fractionation is accompanied by successively lower HREE contents between Tb and Yb, expressed by the ratios Nd/Ho and Ho/Lu. The evolution of this downward-facing hump goes along with decreasing Y contents in bulk rocks and minerals. All this requires an additional phase coexisting with the carbonate liquid during fractionation. Comparison between the bulk rocks and the expelled fluid shows that the latter had preferentially accumulated the HREE and Y. Further evidence for this process are hydrothermal, HREE, Y-rich fluorites in other carbonatite complexes which reflect the composition of the expelled fluid. The high strength of fluoride complexes suggests that fluoride complexing in the carbonatitic fluid is the process responsible for extracting HREE and Y from the carbonatite magma, leaving fractionated carbonatite rocks depleted in these elements. The geochemical evolution of carbonatite magmas along fractionation has therefore to be considered in a melt-mineral-fluid system. Correspondence: B. Bühn, Instituto de Geociências, Universidade de Brasilia, Campus Universitário Darcy Ribeiro, Brasilia 70910-900, Brazil  相似文献   

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