Nb–V-enriched sövites of the northeastern and eastern part of the Amba Dongar carbonatite ring dike,India – A reflection of post-emplacement hydrothermal overprint?

Wakefieldite-(Ce,La) and vanadinite in coarse-grained calciocarbonatites (sövites) are for the first time reported from the northeastern part of the worldwide largest fluorite deposit at the Amba Dongar carbonatite ring dike, India. Sövite in this part of the carbonatite ring dike is rich in pyrochlore, calcite and magnetite. Pyrochlore makes up almost 50% of some sövite samples and shows core-to-rim compositional changes. The core of pyrochlore consists of primary fluorcalciopyrochlore with high F and Na contents while the margins gained elevated amounts of Pb, La and Ce with the associated loss of F and Na due to circulation of hydrothermal solutions. The presence of wakefieldite-(Ce,La) and vanadinite points to an exceptionally high V abundance in hydrothermal solutions formed towards the end of the carbonatite magma activity. This investigation thus opens new promising areas for Nb and REE prospection in the eastern part of the Amba Dongar carbonatite body.     

白云鄂博碳酸岩墙的稀土和微量元素地球化学及对其成因的启示

根据矿物组成白云鄂博矿区的碳酸岩岩可墙可分为白云石型、白云石－方解石共存型和方解石型三种类型。REE和微量元素地球化学表明，这三类碳酸岩岩墙为碳酸岩浆演化不同阶段的产物，白云石型和白云石－方解石共存型对应于早期岩浆阶段，其（La/Nd)n、(La/Yb)n比值随稀土总量的增加而增大，方解石型则对应于碳酸岩浆演化的晚期热液阶段，其稀土总量明显富集，但其（La/Nd)n、(La/Y)n和（La/Yb)n比值随稀土总量的增加却有减小的趋势，热液阶段也是白云鄂博稀土矿化的主要阶段。     

The Paleoproterozoic Montviel carbonatite-hosted REE–Nb deposit,Abitibi, Canada: Geology,mineralogy, geochemistry and genesis

The Montviel 250 Mt carbonatite-hosted REE–Nb deposit is hosted in a Paleoproterozoic alkaline suite located in the Sub-Province of Abitibi, in the Archean Province of the Superior. The alkaline intrusion consists of biotite clinopyroxenites, melano- to leucosyenites, a melteigite–ijolite–urtite series, riebeckite granite, a series of carbonatites and a carbonatite polygenic breccia. The carbonatite series includes silicocarbonatites, calciocarbonatites, rare magnesiocarbonatites, ferrocarbonatites and mixed carbonatites and are cut by a late, high-energy carbonatite polygenic breccia. Diamond drill hole assays and microscope observations indicate that Nb is hosted in pyrochlore from silicocarbonatite whereas the REE mineralization is mainly hosted in ferrocarbonatite, late mixed carbonatites and polygenic breccia, in REE-bearing carbonates and fluorocarbonate minerals. Diamond drill hole underground mapping and systematic assays have shed light on zones enriched in Nd and LREE with preferential Ba and Sr hydrothermal precipitation and zones enriched in Dy, Y and HREE displaying preferential F and P bearing hydrothermal precipitation. Petrographic observations, electron microprobe analyses, LA-ICPMS and X-ray diffraction were used to study the mineralization processes and to identify and quantify the REE-bearing burbankite–(Ce), carbocernaite–(Ce), ewaldite–(Y), huanghoite–(Nd), cordylite–(Ce), cordylite–(Nd), kukharenkoite–(Ce) and synchysite–(Ce). Most minerals are enriched in total LREE with values around 19.3 wt.%, have total MREE values around 2.2 wt.% and extremely variable total HREE values, with very high contents of Dy and Y averaging around 0.3 wt.% and 1.0 wt.%, respectively, and with total HREE reaching up to 10.0 wt.%. A paragenetic sequence is proposed that consists of: (1) a silicocarbonatite Nb stage, and (2) a calciocarbonatite stage, dominated by magmatism but accompanied by hydrothermal fluids, (3) a main ferrocarbonatite stage, dominated by episodes of Ba- and Sr-hydrothermalism and LREE mineralization, F- and P-hydrothermalism and HREE mineralization and evolved ferrocarbonatitic magmatism, (4) a renewed, mixed carbonatite magmatic stage with minor but increasing hydrothermalism, and (5) a terminal stage of fluid pressure buildup and explosion, leading to the creation of a HREE-enriched polygenic breccia. Globular melt inclusions of Ba–Cl–F (± Si–O) may indicate the presence and contribution of barium-bearing chlorofluoride melts during hydrothermal activity and mineralization of the carbonatite.     

Geochemical survey of rare earth elements (REEs) in the concealed ore body of Hongcheon,Korea

Because of the risk of diminishing supplies of rare earth elements (REEs) worldwide due to China’s dominance over REE supply, the necessity of developing domestic resources of REE has been realized in other countries. To explore new ore bodies, a geochemical survey was conducted at one existing carbonatite REE deposit in the Hongcheon area of Korea. Proper sampling strategies and baseline data for the interpretation of the results were determined through a pilot study conducted in the area. Enrichment in the concentration of light REE (LREE) over that of heavy REE, which is typical in carbonatite-type deposits, was observed in stream sediments and heavy mineral samples collected during the geochemical survey. Maximum concentrations of LREE were 2,299 and 27,798 mg/kg for stream sediments and heavy minerals, respectively. Among LREEs, La and Ce are the dominant components of all REEs, comprising approximately 68 % of mean concentrations. Considering the distribution pattern of La + Ce contents and the associations with the existing outcropping ore bodies, the zone of prospective REE mineralization was determined to be in the south-western part of the area. A detailed follow-up soil survey of the zone found even higher concentrations of La and Ce (2,450 and 3,100 mg/kg, respectively), and suggested the possible extension of the existing ore bodies. Likewise, a systematic geochemical survey for REE is feasible for locating concealed ore bodies in the area, where the mineralization is mostly covered with soil, and rock outcrops are scarce.     

Nodular monazite from placers in the Kular Ridge (Arctic Siberia,Russia): Composition and age

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.     

http://www.sciencedirect.com/science/article/pii/S1674987115001310

Bayan Obo ore deposit is the largest rare-earth element(REE) resource,and the second largest niobium(Nb) resource in the world.Due to the complicated element/mineral compositions and involving several geological events,the REE enrichment mechanism and genesis of this giant deposit still remains intense debated.The deposit is hosted in the massive dolomite,and nearly one hundred carbonatite dykes occur in the vicinity of the deposit.The carbonatite dykes can be divided into three types from early to late:dolomite,co-existing dolomite-calcite and calcite type,corresponding to different evolutionary stages of carbonatite magmatism based on the REE and trace element data.The latter always has higher REE content.The origin of the ore-hosting dolomite at Bayan Obo has been addressed in various models,ranging from a normal sedimentary carbonate rocks to volcano-sedimentary sequence,and a large carbonatitic intrusion.More geochemical evidences show that the coarse-grained dolomite represents a Mesoproterozoic carbonatite pluton and the fine-grained dolomite resulted from the extensive REE mineralization and modification of the coarse-grained variety.The ore bodies,distributed along an E-W striking belt,occur as large lenses and underwent more intense fluoritization and fenitization.The first episode mineralization is characterized by disseminated mineralization in the dolomite.The second or main-episode is banded and/or massive mineralization,cut by the third episode consisting of aegirinerich veins.Various dating methods gave different mineralization ages at Bayan Obo,resulting in long and hot debates.Compilation of available data suggests that the mineralization is rather variable with two peaks at~1400 and 440 Ma.The early mineralization peak closes in time to the intrusion of the carbonatite dykes.A significant thermal event at ca.440 Ma resulted in the formation of late-stage veins with coarse crystals of REE minerals.Fluids involving in the REE-Nb-Fe mineralization at Bayan Obo might be REE-F-C02-NaCI-H20 system.The presence of REE-carbonates as an abundant solid in the ores shows that the original ore-forming fluids are very rich in REE,and therefore,have the potential to produce economic REE ores at Bayan Obo.the Bayan Obo deposit is a product of mantle-derived carbonatitic magmatism at ca.1400 Ma,which was likely related to the breakup of Columbia.Some remobilization of REE occurred due to subduction of the Palaeo-Asian oceanic plate during the Silurian,forming weak vein-like mineralization.     

四川冕宁包子山稀土矿床富Sr碳酸岩的发现及意义

全球范围内出露的碳酸岩大多为钙质、镁质、铁质碳酸岩,少量为钠质和硅质碳酸岩,极少有富Sr碳酸岩的报道,其岩石成因、资源意义及对碳酸岩岩浆演化的指示意义尚不清楚。本次在四川省牦牛坪稀土矿区南部包子山稀土矿床的露天采坑中发现了超级富Sr的碳酸岩,其呈不规则的脉状侵入到构造角砾岩中。岩石呈紫色-淡紫色,微晶-斑状结构,斑晶主要为萤石,基质主要为菱锶矿、方解石、氟碳铈矿、氟碳钙铈矿、金云母、重晶石并含少量的金属硫化物和氧化物。全岩的微量元素分析表明,其稀土元素总量(∑REE)达3.5%～6.1%,Sr含量达19.0%～27.7%,已超过稀土矿床和锶矿床的工业品位要求。岩石中的中、重稀土元素含量占稀土元素总量的1.14%～1.77%,一些高价值稀土元素含量较高,如Pr(939×10~(-6)～1399×10~(-6))、Nd(2783×10~(-6)～3937×10~(-6))、Gd(237×10~(-6)～320×10~(-6)),因此除轻稀土元素外,中、重稀土和锶元素也具有重要的资源意义。岩石强烈富集REE、Sr、Ba,而明显亏损P、Nb、Ta、Zr、Hf元素,可能与岩浆演化过程中锆石和其它基性矿物的结晶分离有关。全岩的Sr-Nd同位素组成与牦牛坪、里庄稀土矿床的碳酸岩相似,表明它们为同源岩浆产物。笔者认为,富Sr的碳酸岩代表了碳酸岩岩浆演化晚期的产物,REE、Sr、Ba、F和S元素均在岩浆演化晚期的碳酸岩中高度富集。碳酸岩岩浆超浅成侵位至构造角砾岩中,并与下渗的大气水相遇导致岩浆的淬冷和微晶-斑状结构的形成。早期基性矿物(如霓辉石、黑云母)及碳酸盐矿物(如方解石、白云石等)的结晶分离是造成晚期碳酸岩中稀土元素富集的重要原因。富Sr碳酸岩中石英斑晶的发现和其较低的SiO_2含量表明碳酸岩岩浆演化晚期可能是硅饱和的,且这种岩浆具有很低的SiO_2溶解能力。以菱锶矿(体积分数 50%)为主要碳酸盐矿物的稀土碳酸岩可能代表了一种新的碳酸岩类型,明显不同于已知的钙质、镁质、铁质和钠质碳酸岩。     

Geochemical characteristics of the Bayan Obo giant REE–Nb–Fe deposit: Constraints on its genesis

Geochemical characteristics of different dolomites in the Bayan Obo giant REE–Nb–Fe deposit in Inner Mongolia have been studied. Intensively REE-mineralized dolomites (total REE over 800 ppm) show similar geochemical characteristics to associated carbonatite dykes, with Ba, Th, REE enrichments and Sr, Nb, Ti, Cu depletions, which is different from those of dolomites in the deposit with low REE contents (total REE less than 800 ppm). The low REE dolomites display some transitional characteristics between carbonatite dyke and sedimentary carbonate, with La depletion and Nb enrichment. This indicates that the genesis of the REE-mineralized dolomites might be related to both carbonatite magma and sedimentary carbonates. Sulfur isotope data indicates two sulfur sources, a mantle source (δ³⁴S c.a. 0‰) and seawater (δ³⁴S c.a. +25‰). It is proposed that mineralized dolomites in the Bayan Obo giant REE–Nb–Fe deposit are the product of sedimentary carbonate hydrothermally metasomatised by carbonatite magma and/or associated fluids. These dolomites formed the large-scale rare earth mineralization in the unique Bayan Obo REE–Nb–Fe deposit.     

Geochemical constraints on the genesis of the Bayan Obo Fe-Nb-REE deposit in Inner Mongolia, China

Trace element and isotopic compositions of carbonate from ore bodies, country rock which hosts the ore bodies (H8 dolomite), a carbonatite dyke exposed in Dulahala near Bayan Obo, and rare earth element (REE)-rich dolomite in Bayan Obo have been determined to understand the genesis of the Bayan Obo Fe-Nb-REE ore deposit, the world’s largest resource of REE. The REE and trace element distribution patterns of samples from the REE-rich carbonatite dykes are identical to those of mineralized carbonate rocks, indicating a genetic linkage between the REE-rich carbonatite and mineralization in this region. By contrast, carbon and oxygen isotopes in the mineralized carbonate varied significantly, δ¹³C = −7.98‰ to −1.12‰, δ¹⁸O = 8.60-25.69‰, which are distinctively different from those in mantle-derived carbonatite. Abnormal isotopic fractionations between dolomite and calcite suggest that these two minerals are in disequilibrium in the carbonatite dyke, ore bodies, and H8 marble from Bayan Obo. This isotopic characteristic is also found in mineralized sedimentary marine micrite from Heinaobao, ∼25 km southeast of the Bayan Obo Fe-Nb-REE ore deposit. These facts imply that the carbonate minerals in the Bayan Obo deposit have resulted from sedimentary carbonate rocks being metasomatised by mantle-derived fluids, likely derived from a REE-enriched carbonatitic magma. The initial Nd isotope values of ore bodies and carbonatite dykes are identical, indicating that ore bodies, carbonatite dykes and veins may have a similar REE source.     

New data on carbonatites of the Il’mensky-Vishnevogorsky alkaline complex,the southern Urals,Russia

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.     

白云鄂博主、东矿三个剖面地球化学特征及其研究意义

近年来关于白云鄂博Nb-REE-Fe矿床H8岩体火成水成归属的争论已渐息,而矿床成矿过程以及REE富集机制仍是学术界关注的热点。文章对白云鄂博矿床白云石碳酸岩体、霓长岩化蚀变带、尖山组板岩3个典型剖面开展系统的岩石地球化学工作,发现赋矿碳酸岩、霓长岩、铁矿石微量与稀土元素配分模式具有相似性,靠近H8岩体的尖山组板岩往往有着更高的稀土元素含量,以及与成矿碳酸岩相近的微量元素配分模式。区内各类岩石单元稀土元素分馏明显,全岩La_N/Nd_N比值的变化规律显示,H8岩体内部比边缘更富La,边缘比岩体内部更富Nd。通过岩（矿）石薄片BSE图像结合矿物电子探针分析显示,H8岩体内的稀土元素矿物（主要是独居石、氟碳铈矿等）可分为2组,一组相对富La,呈半自形-他形,星点状分布;另一组相对富Nd,呈他形细粒,脉状分布。两组矿物中不同元素的富集特征可能代表了结晶过程中流体环境的改变。上述实验结合地质勘查结果表明,白云鄂博矿床初始成矿物质的起源与H8碳酸岩一致,均来源于中元古代碳酸岩岩浆活动,而不同类型的稀土元素矿物对应了白云岩成岩阶段与萤石矿化阶段两个不同的稀土矿化阶段。     

Trace element and REE geochemistry of Sanshenjiang gold deposit, southeastern Guizhou Province, China

The Sanshenjiang gold deposit in southeastern Guizhou Province, China, is hosted by the Neoproterozoic metasedimentary rocks which experienced low-grade greenschist facies metamorphism. Gold mineralization occurs mainly in the ribbon chiltern slate of the first member of the Longli Formation and is controlled by both strata and faults. Ore bodies are characterized by abundant quartz-arsenopyrite-gold-pyrite-bedding veins, veinlets and small lenses within the shear zone. In this study, trace element and REE geochemistry was analyzed to constrain the origin and genesis of this deposit. The trace element signatures of wall rocks and veins display a basically similar tendency in the spider diagram, showing the genetic relationship. The values of Co/Ni, Y/Ho, Hf/Sm, Nb/La and Th/La reflect that the hydrothermal fluids of this deposit were derived from the mixture of multiple sources with marked enrichment of Cl and moderate to high temperature. There is a broad similarity in the chondrite-normalized patterns and REE fractionation between wall rocks and ore bodies, possibly reflecting their similar origin. Based on the difference in δCe and δEu, quartz veins and lenses can be subdivided into weakly negative Ce-anomalies (δCe=0.81 to 1.06) with slight Eu anomalies (δEu=0.81 to 1.06) type and the significant positive Ce-anomalies (δCe=1.13 to 1.97) with moderate negative Eu-anomalies type, probably suggesting physical-chemical changes in the evolution process of ore-forming fluids from the early to late stage. It can be concluded that the ore-forming process may have experienced three stages: formation of the original ore source bed, regional metamorphism and gold mineralization, on the basis of trace element and REE analysis and field observation.     

Rare earth element geochemistry of potassic lavas from the Birunga and Toro-Ankole regions of Uganda,Africa

Neutron activation determination of La, Ce, Sm, Eu, Tb, Yb, Lu, Ta, Hf, Sc, Co and Th in potassic lavas from the Birunga and Toro-Ankole regions show that the rocks are characterized by high rare earth element (REE) contents (161–754 ppm) and form two groups based upon differing La/Yb ratios. One group is made up of katungite, ugandite and mafurite with La/Yb =146–312, and the other of rocks of the leucitite and phonolitic tephrite series, La/Yb =30–56. The trace element content of the ugandite group is similar to that of kimberlites. The data do not indicate any trends of differentiation or simple relationships between the two groups of rocks, although katungite is unlikely to be parental to rocks of lower La/Yb ratios. It is unlikely that in terms of La/Yb ratios that partial melting of mica-garnet-lherzolite mantle can form katungite because of the very small amounts of partial melting required (0.2%), although the La/Yb ratios of 150–200 (ugandites, mafurites) and 30–60 (leucitites, phonolitic tephrites) can be accounted for by 0.3–1.5% and 1–9% melting respectively, if the REE are then concentrated without further La and Yb fractionation. Partial melting of mantle which has been metasomatized by alkaline earths and REE bearing fluids or mixing of carbonatite and nephelenite are also compatable with the observed geochemistry of the lavas. It is considered that gas transfer processes which selectively enrich the light REE may have obscured REE evidence pertaining to early partial melting and/or differentiation processes and therefore that REE geochemistry is of little use in determining the petrogenetic processes involved in the formation of potassic lavas.     

REE fractionation,mineral speciation,and supergene enrichment of the Bear Lodge carbonatites,Wyoming, USA

The Eocene (ca. 55–38 Ma) Bear Lodge alkaline complex in the northern Black Hills region of northeastern Wyoming (USA) is host to stockwork-style carbonatite dikes and veins with high concentrations of rare earth elements (e.g., La: 4140–21000 ppm, Ce: 9220–35800 ppm, Nd: 4800–13900 ppm). The central carbonatite dike swarm is characterized by zones of variable REE content, with peripheral zones enriched in HREE including yttrium. The principle REE-bearing phases in unoxidized carbonatite are ancylite and carbocernaite, with subordinate monazite, fluorapatite, burbankite, and Ca-REE fluorocarbonates. In oxidized carbonatite, REE are hosted primarily by Ca-REE fluorocarbonates (bastnäsite, parisite, synchysite, and mixed varieties), with lesser REE phosphates (rhabdophane and monazite), fluorapatite, and cerianite. REE abundances were substantially upgraded (e.g., La: 54500–66800 ppm, Ce: 11500–92100 ppm, Nd: 4740–31200 ppm) in carbonatite that was altered by oxidizing hydrothermal and supergene processes. Vertical, near surface increases in REE concentrations correlate with replacement of REE(±Sr,Ca,Na,Ba) carbonate minerals by Ca-REE fluorocarbonate minerals, dissolution of matrix calcite, development of Fe- and Mn-rich gossan, crystallization of cerianite and accompanying negative Ce anomalies in secondary fluorocarbonates and phosphates, and increasing δ¹⁸O values. These vertical changes demonstrate the importance of oxidizing meteoric water during the most recent modifications to the carbonatite stockwork. Scanning electron microscopy, energy dispersive spectroscopy, and electron probe microanalysis were used to investigate variations in mineral chemistry controlling the lateral complex-wide geochemical heterogeneity. HREE-enrichment in some peripheral zones can be attributed to an increase in the abundance of secondary REE phosphates (rhabdophane group, monazite, and fluorapatite), while HREE-enrichment in other zones is a result of HREE substitution in the otherwise LREE-selective fluorocarbonate minerals. Microprobe analyses show that HREE substitution is most pronounced in Ca-rich fluorocarbonates (parisite, synchysite, and mixed syntaxial varieties). Peripheral, late-stage HREE-enrichment is attributed to: 1) fractionation during early crystallization of LREE selective minerals, such as ancylite, carbocernaite, and Ca-REE fluorocarbonates in the central Bull Hill dike swarm, 2) REE liberated during breakdown of primary calcite and apatite with higher HREE/LREE ratios, and 3) differential transport of REE in fluids with higher PO₄³⁻/CO₃²⁻ and F⁻/CO₃²⁻ ratios, leading to phosphate and pseudomorphic fluorocarbonate mineralization. Supergene weathering processes were important at the stratigraphically highest peripheral REE occurrence, which consists of fine, acicular monazite, jarosite, rutile/pseudorutile, barite, and plumbopyrochlore, an assemblage mineralogically similar to carbonatite laterites in tropical regions.     

A Geochemical Study of an REE-rich Carbonatite Dyke at Bayan Obo, Inner Mongolia, Northern China

An REE-rich carbonatite dyke was found in Dulahala, close to the Bayan Obo superlarge REE-Nb-Fe mineral deposit in Inner Mongolia, northern China. The REE content in the dyke varies greatly, from 1% up to 20% (wt), which might constitute rich REE ores. Light REEs in the carbonatite are enriched and highly fractionated relative to heavy REEs and there is no Eu anomaly. The REE and trace element distribution patterns of the carbonatite are identical to those of fine-grained dolomite marble which is the host rock of the Bayan Obo REE-Nb-Fe superlarge mineral deposit. This indicates a petrogenetic linkage between the REE-rich carbonatite and the mineralizations in this region.     

Thorium-poor monazite and columbite-(Fe) mineralization in the Gleibat Lafhouda carbonatite and its associated iron-oxide-apatite deposit of the Ouled Dlim Massif,South Morocco

Recent exploration work in South Morocco revealed the occurrence of several carbonatite bodies, including the Paleoproterozoic Gleibat Lafhouda magnesiocarbonatite and its associated iron oxide mineralization, recognized here as iron-oxide-apatite (IOA) deposit type. The Gleibat Lafhouda intrusion is hosted by Archean gneiss and schist and not visibly associated with alkaline rocks. Metasomatized micaceous rocks occur locally at the margins of the carbonatite outcrop and were identified as glimmerite fenite type. Rare earth element (REE) and Nb mineralization is mainly linked to the associated IOA mineralization and is represented by monazite-(Ce) and columbite-(Fe) as major ore minerals. The IOA mineralization mainly consists of magnetite and hematite that usually contain large apatite crystals, quartz and some dolomite. Monazite-(Ce) is closely associated with fluorapatite and occurs as inclusions within the altered parts of apatite and along cracks or as separate phases near apatite. Monazite shows no zonation patterns and very low Th contents (<0.4 wt%), which would be beneficial for commercial extraction of the REE and which indicates monazite formation from apatite as a result of hydrothermal volatile-rich fluids. Similar monazite-apatite mineralization and chemistry also occurs at depth within the carbonatite, although the outcropping carbonatite is barren, suggesting an irregular REE ore distribution within the carbonatite body. The barren carbonatite contains some tiny unidentified secondary Nb-Ta-U phases, synchysite and monazite. Niobium mineralization is commonly represented by anhedral minerals of columbite-(Fe) which occur closely associated with magnetite-hematite and host up to 78 wt% Nb₂O₅, 7 wt% Ta₂O₅ and 1.6 wt% Sc₂O₃. This association may suggest that columbite-(Fe) precipitated by an interaction of Nb-rich fluids with pre-existing Fe-rich minerals or as pseudomorphs after pre-existing Nb minerals like pyrochlore. Our results most strongly suggest that the studied mineralization is economically important and warrants both, further research and exploration with the ultimate goal of mineral extraction.     

Bayan Obo Controversy: Carbonatites versus Iron Oxide‐Cu‐Au‐(REE‐U)

The Bayan Obo Fe‐REE‐Nb deposit is the world’s largest rare earth element (REE) resource and its genesis has been the subject of much debate for many years. The most popular are the carbonatite‐related and hydrothermal Fe oxide‐Cu‐Au‐(REE‐U) genetic models. Comparisons of geologic setting, lithology, mineral assemblages, metal associations, geochemistry (particularly REE and light REE/heavy REE ratios), fluid chemistry and isotopics indicate that the Bayan Obo deposit shares features of both types, which are classified differently; that is, the carbonatites model is host‐rock based, while the Fe oxide‐Cu‐Au‐(REE‐U) model is essentially mineral assemblage and metal association based. A speculative classification scheme is tentatively put forward to link the two models, but many questions remain for further studies.     

碳酸岩岩浆演化过程中REE富集与分异的研究进展及碳酸岩中的矿物学分带

稀土元素(REE)作为"三稀资源"之一,是中国重要的战略性矿产资源,碳酸岩型稀土矿床是世界稀土的主要来源.成矿碳酸岩的岩浆演化以及稀土元素的富集和分异机理一直是碳酸岩型稀土矿床研究的热点和难点,国内外学者对碳酸岩的岩浆起源、岩浆演化过程中稀土元素富集与分异的机理进行了大量的研究与探讨,但仍存在较多的争议,限制了碳酸岩型稀土元素成矿理论的发展及国内外碳酸岩型稀土矿床的找矿勘查工作.文章重点对稀土成矿碳酸岩的起源、岩浆演化过程及在此过程中REE的富集与分异行为进行了详细的文献调研和评述,同时,基于笔者在冕宁牦牛坪稀土矿床前期的研究工作和最新发现,认为碳酸岩中普遍存在矿物学分带,它是岩浆演化过程的最佳记录,是不同成分矿物结晶分异作用的体现.对牦牛坪稀土矿床碳酸岩的矿物学分带特征及其中的熔体、熔流体和流体包裹体进行了初步描述与探讨,以期为研究碳酸岩的岩浆演化、岩浆-流体转化过程及稀土元素的富集与分异机理提供新的思路,促使对稀土碳酸岩矿物学分带及其对REE富集与分异的研究引起更多的关注和重视.     

REE mineralization in the carbonatites of the sung valley ultramafic-alkaline-carbonatite complex,Meghalaya, India

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.     

The Chemistry of Niobium Mineralisation at Bayan Obo, Inner Mongolia, China: Constraints on the Hydrothermal Precipitation and Alteration of Nb-Minerals

As well as world class Fe and REE resources the Bayan Obo mineral deposits also hosts significant niobium resources(estimated as 2.2 Mt Nb with an average grade of 0.13 wt% Nb).Niobium in this study is primarily hosted in aeschynite-(Ce) and(Nd),but with subsidiary amounts of pyrochlore,fergusonite-(Ce),fersmite and columbite.Here we report on the paragenetic and textural setting of aeschynite,pyrochlore and fergusonite in the main ore bodies and in a carbonatite dyke.Niobium in a carbonatite sample is hosted in a phase tentatively(due to significant Ca,Mn and Ti contents) identified as fergusonite-(Ce).Aeschynite occurs overgrowing foliation in banded ores,in fractures and vugs in aegirine-rich rocks and in calcite veins.The composition in all settings is similar,but some examples in banded ores develop significant zonation in Y,Th and the REE,inferred to relate to buffering of halogen acid species to low levels by dissolution and fluoritisation of calcite,and the preferential precipitation of LREE from solution due to lower mineral solubility products compared to the HREE.Although lower in total concentration the ratios of REE in pyrochlore are similar to those of aeschynite and suggest the same metal source.The crystallisation of pyrochlore probably relates to growth in paragenetic settings where carbonates had already been eliminated and hence the buffering of F-species activities in the hydrothermal fluid was reduced.Both aeschynite and pyrochlore show evidence of alteration.Primary alteration of aeschynite resulted in leaching of A-site cations(Ca,REE,Th) and Nb,addition of Fe,and ultimately replacement by Ba-Ti phases(baotite and bafertisite).Secondary,metamictisation enhanced,possibly supergene alteration of pyrochlore resulted in hydration,leaching of A-site cations leading to the development of lattice vacancies and increases in Si.The presence of hydrothermal Nb resources at Bayan Obo suggests there may be potential for further Nb discoveries in the area,whilst the trends in element mobility during alteration have significant implications for the utility of A-B oxides as components of materials for immobilisation of radionuclides.