Rare earth and other rare elements in uranium ores of paleovalley deposits in the Vitim district: Distribution,occurrence, and applied implications

The degree of concentration and REE and Zr distribution and occurrence in uranium ore samples from paleovalley deposits are considered. Various types of REE distribution in ores with variable uranium content has been revealed: the negative type with predominance of LREE in ordinary ore and the V-shaped type with significant growth of Y, MREE, and HREE contents in high-grade ore. In addition, the relationship between U, on the one hand, and MREE, HREE, Y, and Zr, on the other hand, has been established. Predominant isomorphic incorporation of these elements into various uranium constituents is suggested. The conclusion was arrived at about the most probable gain of REE and Zr along with U on various geochemical barriers from postvolcanic thermal carbonated and sulfuric-acid aqueous solutions enriched in these chemical elements. The significant enrichment of uranium ore in REE confirms the real possibility of recovery of them as a by-product from working solutions in the process of in situ uranium leaching.     

Geochemical signatures of uranium oxides in the Lufilian belt: From unconformity-related to syn-metamorphic uranium deposits during the Pan-African orogenic cycle

The Pan-African Lufilian belt (Zambia and Democratic Republic of Congo) is known for its world-class copper and cobalt deposits. In addition, the Lufilian Copperbelt hosts several uranium occurrences concentrated within deformed siliciclastic rocks of the basal Neoproterozoic Katanga Supergroup. We report LA-ICPMS and EMP analyses of the rare earth element (REE) and yttrium (Y) abundances (designated as the REY signatures) of uranium oxides from two uranium mineralizing events of the Lufilian belt previously dated at 652 ± 8 Ma and 530 ± 6 Ma by the U–Pb method on uraninite. Uranium oxides dated at ca. 650 Ma from the External fold-and-thrust belt are characterized by (i) bell shape REE patterns centered on middle REE (MREE), (ii) positive europium (Eu) anomalies and (iii) relatively low Y contents. In contrast, uranium oxides dated at ca. 530 Ma from the Domes region are characterized by (i) REE patterns but with a less pronounced light REE (LREE) fractionation, (ii) negative Eu anomalies and (iii) higher Y contents. Moreover, the External fold-and-thrust belt also contains uranium mineralization dated at ca. 530 Ma having the same characteristics as the ca. 530 Ma uranium oxides from the Domes region (a moderately fractionated REE pattern and a negative Eu anomaly).As REY signatures are known to reflect mineralizing processes, the distinct geochemical signatures of the two uranium oxide generations (ca. 650 Ma and ca. 530 Ma) provide meaningful information about the uranium cycle during the Pan-African orogeny. Compared to the REY signatures of the known worldwide uranium deposit types, the REY signature of uranium oxides dated at ca. 650 Ma of the External fold-and-thrust belt is similar to the REE patterns from unconformity-related U deposits (Athabasca in Canada and Kombolgie in Australia). Uranium oxides of the Domes region and some of the External fold-and-thrust belt display similar characteristics to syn-metamorphic U deposit (Mistamisk in Canada). Accordingly, we propose that the two stages of uranium oxide crystallizations within the Lufilian belt, at ca. 650 and ca. 530 Ma, occurred under distinct physico-chemical conditions. The first stage, at ca. 650 Ma, may be related to late diagenesis hydrothermal processes, at the basement/cover interface, with the circulation of highly saline basinal brines linked to evaporites of the Roan Group. This Pan-African unconformity-related uranium deposit is the youngest of this type described to date. The second stage may be connected to metamorphic fluid circulations, at about 530 Ma, during the Lufilian orogeny in the Domes region and also in the External fold-and-thrust belt.     

REE/trace element characteristics of sandstone-type uranium deposits in the Ordos Basin

1 Introduction The Ordos Basin is the second largest sedimentary basin in China. During the last 10 years, a great progress has been achieved in the aspects of tectonic evolution, dynamics process, inner and outer geological processes during Mesozoic-Cen…     

Anomalous rare earth element,yttrium and zirconium mobility associated with uranium mineralization

The mobility of REE, Y and Zr during the Variscan uranium mineralization event in high‐grade metasediments of the Bohemian Massif, Czech Republic has been investigated to understand their behaviour in alkaline hydrothermal alterations. The REE patterns together with high mobility of Y and Zr point to movement of REE, Y, Zr and U by highly mineralising, oxidising basinal fluids in the Permian. Their high mobility during the origin of an economically important uranium mineralization is supported by the occurrence of Y‐ and Zr‐rich coffinite.     

砂岩型铀矿床层间氧化带前锋区稀有元素富集机制

在深入研究砂岩型铀矿床层间氧化带各地球化学分带中铀及其伴生元素的分布规律时,发现一些单价态(不变价)元素也常常富集在层间氧化带前锋区,其典型代表是钪(Sc)、钇(Y)和稀土元素(REE)等。作者在综合分析前苏联众多砂岩型铀矿床各地球化学分带中各种元素大量测试数据的基础上,论述了层间氧化带前锋区Eh值和pH值的变化规律以及它们所导致的变价元素(U、Se、Mo和V)和不变价元素(Sc、Y和REE)的分布规律和富集机制。实际上,层间氧化带前锋区既是氧化-还原电位(Eh值)又是酸碱度(pH值)的急剧变化区,两者大致同步消长。层间氧化带前锋区有两类地球化学障:单纯的还原障和还原-碱性综合障。两种地球化学障的发育与强度取决于原始未氧化岩石中硫化物、有机质和碳酸盐的含量。     

川北砂岩型铀矿稀土元素特征及铀成矿作用

在大量取样分析的基础上 ,本文系统分析研究了围岩、矿石、方解石脉和铀矿物的稀土元素组成 ,讨论了岩石、矿石沉积和成岩过程中的稀土元素变化规律 ,总结了川北砂岩型铀矿床的稀土元素地球化学特征。通过与典型的火山岩型和变质岩型热液成因铀矿床进行对比 ,认为川北砂岩型铀矿具有热液 (水 )改造成矿作用的稀土元素地球化学特点 ;铀矿化经历了沉积成岩和热液改造富集两个阶段。     

Methodology for Rare Earth Element Determinations of Uranium Oxides by Ion Microprobe

A methodology for the determination of the rare earth elements in uranium oxides by ion microprobe has been set up on a Cameca ims-3f instrument. An uranium oxide reference material from a syn-metamorphic uranium deposit related to albitisation has also been developed for this type of analysis. Applications of the methodology are presented for a series of uranium oxides selected from some major uranium deposit types: from the world's highest grade unconformity-related uranium deposit from the Athabasca Basin (Saskatchewan, Canada; the Shea Creek and the McArthur River examples), a perigranitic vein-type deposit (Pen Ar Ran, Vendée, France) and a volcanic caldera-related deposit (Streltsovkoye, Transbaikalia, Russia). Each type of uranium deposit appears to have a specific REE signature. All REE patterns from the Shea Creek and the McArthur deposits are characterised by bell-shaped patterns centred on Tb-Dy and similar to those already published for uranium oxides from unconformity-related deposits from Australia. Such bell-shaped REE patterns centred on Tb-Dy may therefore be considered as a typical signature of uranium oxides from Mesoproterozoic unconformity-related deposits. A smoother bell shape pattern centred on Eu characterises the syn-metamorphic albitisation related deposit of Mistamisk selected for the reference material. The REE patterns from the Pen Ar Ran deposit show a fractionation from LREE to HREE with anomalously high abundances of Sm, Eu and Gd with respect to the other REEs, similar to the REE patterns of uranium oxides from the volcanic-related deposits of Streltsovkoye.     

Critical metals in the critical zone: controls,resources and future prospectivity of regolith-hosted rare earth elements

The rare earth elements (REE) are a group of 17 metals that include the lanthanides, Sc and Y, which are critical for many modern technologies including consumer electronics, medicine and communication. One of the major controls on the concentrations of the REE in regolith material (including soils) is the abundance of these elements in the parent material. It is known that REE concentrations are largely inherited from the protolith rather than acquired during pedogenic processes but our understanding of how pedogenesis affects fractionation and accumulation of REE to produce potentially economic deposits of these critical metals is limited. This study provides a review of (1) the biogeochemical controls on REE distribution and mobility during pedogenesis and (2) the potential for REE extraction from regolith material. Factors that control mobilisation of REE during weathering include (1) the initial distribution of the REE in protolith minerals and the resistivity of these phases to weathering, (2) adsorption and absorption of REE to Fe- and Mn oxides, clay minerals and organic matter and (3) variations in pH and Eh conditions. We also discuss the relative importance of biogeochemical controls on REE mobility in soils in southern Australia, where REE concentrations are demonstrated to be largely a function of weathering of REE-enriched protoliths, the sorption of REE to weathering products and the accumulation of resistant minerals in soils.     

相山铀矿田成矿流体特征:来自微量、稀土元素地球化学证据

相山铀矿田的成矿流体性质和来源存在争议,为进一步探讨相山铀矿田成矿流体的性质和来源,本文对相山铀矿田西部的居隆庵铀矿床和北部的沙洲铀矿床中的新鲜围岩、蚀变围岩及矿石的微量、稀土元素含量及其变化进行了研究。结果显示:在含较多热液成因萤石的居隆庵铀矿床中,从新鲜围岩到蚀变围岩到矿石,Zr、Hf含量先降低再升高;而在含少量热液萤石的沙洲铀矿床中,新鲜围岩、蚀变围岩和矿石的Zr、Hf含量基本一致。鉴于富F流体易汲取岩石中的Zr、Hf,因此,这两个矿床中不同类型样品Zr、Hf含量的不同变化趋势,可能与居隆庵铀矿床的成矿流体富F、而沙洲铀矿床的成矿流体相对贫F有关。这两个铀矿床中矿石的稀土配分曲线与其各自的新鲜及蚀变围岩的稀土配分曲线形态相似但又存在差异,说明每个矿床的新鲜围岩、蚀变围岩和矿石之间的稀土元素既具有继承性、又受到不同性质的流体的影响。居隆庵铀矿床中矿石显示Eu负异常,可能主要是继承了围岩的Eu负异常;沙洲铀矿床中矿石Eu显示弱负异常至弱正异常的特征,可能与围岩中斜长石因热液蚀变作用而释放出的Eu的进入流体有关。基于新鲜围岩、蚀变围岩及矿石的U和REE研究,推断居隆庵铀矿床成矿流体中U和REE均以F的络合物形式迁移;但沙洲铀矿床中铀矿石品位较低,可能是与流体中相对贫F有关。     

Reconstruction of phosphate formation environments (from data on distribution of lanthanides)

The criteria for the evaluation of the REE composition of phosphorites and sedimentary rocks have been determined. These data are required to reconstruct depositional environments. Literature data on the geochemistry of some phosphorite deposits of Eurasia are considered. The REE patterns of Mesozoic phosphorites of the East European Platform are studied. On the basis of REE contents, the ratios of lanthanides and fields on the La–(Nd + Sm)–(Y + Dy), La–(Ce + Nd + Sm)–(Y + Dy), and LREE–MREE–(HREE×10) diagrams have been determined as indicators of climate and the depth and facies conditions of sedimentation.     

In Situ Quantitative Measurement of Rare Earth Elements in Uranium Oxides by Laser Ablation‐Inductively Coupled Plasma‐Mass Spectrometry

Advances in the quantification of rare earth elements (REE) at the micrometric scale in uranium oxides by laser ablation‐inductively coupled plasma‐mass spectrometry are described. The determination of the best analytical conditions was tested using a uranium oxide (Mistamisk) the concentrations of REE in which were previously estimated by other techniques. Comparison between the use of U or Pb as an internal standard clearly showed a diameter‐dependent fractionation effect related to Pb at small crater diameters (16 and 24 μm), which was not found for U. The quantification of REE contents in uranium oxide samples using both matrix‐matched (uranium oxide) and non‐matrix‐matched (NIST SRM 610 certified glass) external calibrators displayed no significant difference, demonstrating a limited matrix effect for REE determination by LA‐ICP‐MS. Moreover, no major interferences on REEs were detected. The proposed methodology (NIST SRM 610 as external calibrator and U as internal standard) was applied to samples from uranium deposits from around the world. The results showed that LA‐ICP‐MS is a suitable analytical technique to determine REE down to the μg g^?1 level in uranium oxides at the micrometre scale and that this technique can provide significant insights into uranium metallogeny.     

Geochemical zoning around the McClean uranium deposits, Saskatchewan, Canada

Some 3400 drill core samples of the Athabasca Group and underlying regolith have been obtained by sampling 8-m sections from 55 diamond drill holes in the McClean Lake Area, Saskatchewan. Forty eight holes are from sections over six areas known to contain uranium mineralization and 7 are from unmineralized areas. The uranium zones are covered by 30 to 180 m of Athabasca sandstones and conglomerates.The uranium mineralization of the McClean deposits can be described as belonging to two different facies; a more reduced sulphide-arsenide facies and a more oxidized hematite-“bleached” facies, superimposed on any one of three host rocks.The sulphide-arsenide facies is probably older and, except in one deposit, it forms a patchy distribution of relicts. The principal pattern is an upwards increase in sulphur/arsenic ratio. The hematite-“bleached” facies appears to be younger and may represent a reworking of the earlier sulphide-arsenide facies mineralization under more oxidizing conditions.The trace metals can be grouped according to their redox behaviour. Vanadium, Mo and U, occurring as oxides, form one group while Ni, Co, Zn, Cu and As, occurring as sulphides and/or arsenides, form intermediate and most reduced groups, respectively. Iron is concentrated in the most oxidized facies as hematite or goethite and in the most reduced facies as pyritebravoite, siderite and chlorite. Manganese follows the distribution of siderite.The ratio of oxidized to reduced minerals can be represented by the ratio of U/Ni. This ratio can be used to estimate the variation of redox potential in the deposit at the time of deposition or alteration. The principal pattern is one of systematic increase in U/Ni ratio or oxidation potential both upward and to the northeast in each of the hematite and bleached facies.A generalized Eh-pH diagram is used to qualitatively describe the significance of each mineral facies.The U/Ni ratio of the transition between the hematite and “bleached” facies increases upwards. The phase diagram suggests that a possible cause is an upward decrease in pH and increase in Eh.The overall distribution is compatible with the origin of the deposits due to reduction at the interface between a plume of reductant emanating from fractures in the sub-Athabasca basement and an oxidizing aquifer moving southwestward in the sandstone. This model does not accurately predict the distribution of elements among the seven McClean Lake pods. However, it explains the overall pattern. Local variations in metal ratios in solution either in time or reflecting local provenance could be adduced to explain local deviations from the overall pattern.Clay alteration, apparently largely contemporaneous with the earliest mineralization, is largely illitic but with sporadic occurrences of xenotime and goyazite. Thus K and to some extent P, Y and light REE's are also enriched to some degree in the deposits.Uranium analysis of the drill core shows that there is little movement of U into the overlying sandstones from basement rocks and regolith that contain no uranium deposits. Uranium in the Athabasca sandstone from these areas averages less than 1 ppm. However, where uranium zones have been found in the basement rocks, regolith and lower Athabasca sandstone, U values greater than 2–3 ppm consistently occur in the overlying sandstones at or near surface.There appear to be two types of U anomalies, those that flank the deposits and those that directly overlie them. Both types exhibit vertical and lateral continuity. They are associated with vertical to steeply dipping fracture systems that traverse the Athabasca sandstone from basement to surface. The fractures are thought to be related to diagenetic processes from compaction of the sedimentary rocks over basement irregularities as well as tectonic processes (i.e. re-adjustment along old basement structures).These results suggest that target areas containing deeply buried uranium deposits could be defined by U analyses of the Athabasca sandstone from quite widely spaced holes of limited depth. This conclusion can be compared to XRD and chemical studies of clay mineral distribution within the Athabasca sandstone about the deposits.     

Zircon geochemistry and U–Pb age at rare metal deposits of syenite in the Ukrainian Shield

The distribution of rare and rare earth elements in zircon at the Yastrebets, Azov (Zr–REE–Y), and Perzhan (Be) rare metal deposits of the Ukrainian Shield was studied. Additional evidence for magmatic genesis of these deposits is obtained: unaltered zircon is characterized by a magmatic REE distribution spectrum with a somewhat higher δ¹⁸O value than that of the mantle (6.6‰ on average). The final formation stage of the deposit was marked by predominance of fluids enriched in Y, REE, Nb, and heavy oxygen, resulting in anomalous geochemical characteristics of zircon rims and alteration zones (up to 81500 Y ppm, over 10300 ppm Nb, and 13.9‰ δ¹⁸O). The age of zircon formed in ore-bearing Yastrebets and Azov nonnepheline syenite deposits was estimated at ~1770 Ma (U–Pb, SHRIMP-II).     

基于克里格法刻画砂岩型铀矿U、Ra和U-Ra平衡系数垂向分布规律——以二连盆地芒来铀矿床为例

砂岩型铀矿是绿色经济可采的重要能源矿种,目前是世界上重要的铀矿勘探类型之一。二连盆地芒来铀矿床、鄂尔多斯盆地纳岭沟铀矿床铀矿体多呈板状产出,板状铀矿体成因备受关注。为研究砂岩型铀矿内部U、Ra和铀镭平衡系数（Kp）分布的垂向分布规律,本文以二连盆地芒来铀矿床为例,采用具有网格精度高优点的克里格插值法研究U、Ra和Kp垂向分布规律,分别利用放射性样品分析数据和定量伽马测井五点式反褶积法反演U含量数据,通过克里格法精细刻画砂岩型矿体中U、Ra和Kp分布的垂向分布规律。研究发现,该矿床板状矿体内部具有卷状的特征,Kp分布形态可以用来判断含氧含铀水的运移方向以及氧化强弱。该方法对研究铀矿体形态、铀矿成矿规律和后续地浸开采具有重要意义。     

砂岩型铀矿的微生物成矿作用研究述评

目前,砂岩型铀矿是全球应用最为广泛和最有前景的铀矿类型,也是我国最主要的工业铀矿类型。本文展示了当今世界最新的铀资源分布和组成,强调了砂岩型铀矿在世界和中国铀矿资源中的重要性,梳理了实验室条件下微生物对U(VI)的还原性富集和非还原性富集机理,归纳了地质条件下微生物参与砂岩型铀矿的成矿证据。微生物对铀富集作用的实验研究,主要体现在还原性和非还原性富集两个方面。微生物对U(VI)的还原性富集研究最为深入,包括微生物的细胞色素、菌毛和电子穿梭体在U(VI)的还原过程中的作用。微生物对U(VI)的非还原性富集表现在微生物表面吸附、表面络合沉淀和细胞内积聚作用。微生物参与砂岩型铀矿成矿作用的证据,可分为直接证据和间接证据。直接证据主要有铀矿物形态学特征、P元素含量和矿物纳米晶体尺寸;间接证据主要有黄铁矿硫同位素和方解石碳同位素组成以及相应烃类包裹体特征。在未来的研究工作中,应重视微区实验方法在砂岩型铀矿中的应用,以及含油气/煤盆地上覆地层的砂岩型铀矿找矿工作,应探索更加适当的指标和评价体系以量化微生物对砂岩型铀矿的成矿作用。     

中国火山岩型铀矿的主要地质特征

火山岩型铀矿主要分布于环太平洋的中、新生代多金属成矿带,产于以酸性岩或碱性岩为主的陆相火山岩系中,据对火山岩的^87Sr／^88 Sr含量初始比值测定、火山岩的稀土元素分布模式和火山岩中的熔融包体测温研究,推测火山岩浆是硅铝壳高温大部分熔融的产物,并不同程度受到地幔物质的混染。火山喷发受区域大断裂带控制,形成喷发岩带。火山喷发岩带可进一步划分为几条喷发亚带,喷发亚带则由一系列的火山活动中心组成。火山岩型铀矿均产于断陷红盆旁侧,或在其附近存在基性脉岩群,显示铀矿化与深部构造岩浆活动存在成因联系,适中的剥蚀程度是重要的找矿前提。     

Trace and REE element geochemistry of fluorite and its relation to uranium mineralizations,Gabal Gattar Area,Northern Eastern Desert,Egypt

Uranium mineralizations occur and form in a broad range of geologic setting and age, including magmatic to surfacial conditions, and there are numerous controls on their transportation and deposition, such as redox, pH, ligand concentration, complexation, and temperature. These temporal and spatial variations have caused a range of ore deposit mineral assemblages. Consequently, understanding their conditions of formation is still in its infancy. This research reports rare earth elements (REE) and trace elements of fluorite associated with hexavalent uranium mineralizations and tests of genetic models for the deposits. These data contribute to a better understanding of the variables controlling fluorite formation and uranium ore composition through understanding the evolution of these ore-forming hydrothermal systems. Fluorite in Gabal Gattar granite occurs as disseminations and/or thin veinlets and encrustations filling some uranium mineralized fissures and fractures along the northern margin of host granite mass. In the U-poor samples, fluorite forms well-developed large crystals that are commonly zoned. The zones are represented by alternating colorless and violet zones, and the outer zones are frequently dark violet. In the U-rich samples, fluorite is usually anhedral, unzoned, and has a dark violet color. The results of analysis of REE and trace element contents of fluorites using laser ablation inductively coupled plasma mass spectrometry indicate that total REE in the anhedral unzoned fluorite are elevated compared to the well developed zoned fluorite, and also total REE in dark violet zones of zoned fluorite are elevated with respect to the colorless zones. The fluorites and host granite are generally characterized by strongly negative Eu anomalies and slightly negative or chondritic Ce anomalies. Accordingly, REE patterns of the fluorite and host granite are roughly alike, indicating that the source of REE and trace elements of hydrothermal fluids is the host granite leached by fluids. Y/Y*, Ce/Ce,* and Eu/Eu* patterns show that fluorite clearly records the compositional evolution of the hydrothermal solutions that have transferred trace and REE from host granite during the fluid–wall rocks interactions. The high uranium contents of fluorite in Gabal Gattar granite suggest that parent fluids bearing fluorine have interacted with host granite to leach uranium from the accessory minerals of granite and tetravalent uranium minerals in reduced or weakly oxidized zones.     

REE geochemical characteristics of the No. 302 uranium deposit in northern Guangdong, South China

The No. 302 uranium deposit, located in Guangdong Province, is a typical granite-type uranium ore deposit REE geochemical characteristics of the wall rocks, pitchblende, altered rocks, calcite and fluorite from this deposit have been systematically studied in this paper. The result showed that the alkali-metasomatic granites and other altered rocks have the same REE distribution patterns as Indosinian granites. It is indicated that the hydrothermal ore-forming solution had altered the Indosinian granites, and ore-forming materials may directly originate from the Indosinian granites. Calcite and fluorite of different stages are the products derived from the same source but different stages. The evolution and degassing of the mineralizing solution might induce LREE enrichment to varying degree. Mantle fluid and a large volume of mineralizer may be the crucial factors controlling uranium mineralization, and the hydrothermal solution with mineralizer played an important role in U transport and concentration. Meanwhile, the degassing of CO2 might promote U and REE precipitation.     

U redox fronts and kaolinisation in basement-hosted unconformity-related U ores of the Athabasca Basin (Canada): late U remobilisation by meteoric fluids

Proterozoic basement-hosted unconformity-related uranium deposits of the Athabasca Basin (Saskatchewan, Canada) were affected by significant uranium redistribution along oxidation–reduction redox fronts related to cold and late meteoric fluid infiltration. These redox fronts exhibit the same mineralogical and geochemical features as the well-studied uranium roll-front deposits in siliclastic rocks. The primary hydrothermal uranium mineralisation (1.6–1.3 Ga) of basement-hosted deposits is strongly reworked to new disseminated ores comprising three distinctly coloured zones: a white-green zone corresponding to the previous clay-rich alteration halo contemporaneous with hydrothermal ores, a uranium front corresponding to the uranium deposition zone of the redox front (brownish zone, rich in goethite) and a hematite-rich red zone marking the front progression. The three zones directly reflect the mineralogical zonation related to uranium oxides (pitchblende), sulphides, iron minerals (hematite and goethite) and alumino-phosphate-sulphate (APS) minerals. The zoning can be explained by processes of dissolution–precipitation along a redox interface and was produced by the infiltration of cold (<50°C) meteoric fluids to the hydrothermally altered areas. U, Fe, Ca, Pb, S, REE, V, Y, W, Mo and Se were the main mobile elements in this process, and their distribution within the three zones was, for most of them, directly dependent on their redox potential. The elements concentrated in the redox fronts were sourced by the alteration of previously crystallised hydrothermal minerals, such as uranium oxides and light rare earth element (LREE)-rich APS. The uranium oxides from the redox front are characterised by LREE-enriched patterns, which differ from those of unconformity-related ores and clearly demonstrate their distinct conditions of formation. Uranium redox front formation is thought to be linked to fluid circulation episodes initiated during the 400–300 Ma period during uplift and erosion of the Athabasca Basin when it was near the Equator and to have been still active during the last million years. A major kaolinisation event was caused by changes in the fluid circulation regime, reworking the primary uranium redox fronts and causing the redistribution of elements originally concentrated in the uranium-enriched meteoric-related redox fronts.     

Hydrothermal mineralization in the sandstone–hosted Hangjinqi uranium deposit,North Ordos Basin,China

Tabular–type uranium ore deposits (the Hangjinqi and Daying deposits) have recently been found in the Middle Jurassic Zhiluo Formation, north of the Ordos Basin, China. Petrographic observations, the chemical composition of U minerals determined by EMPA and fs–LA–ICP–MS, whole rock geochemistry and the microthermometric study of fluid inclusions have been integrated to characterize the genetic conditions of the U mineralization in the Hangjinqi sandstone–hosted deposit. Two different groups of U minerals have been identified. One group includes coffinite(I) associated with vanadium–rich micas. Coffinite(I) is enriched in vanadium (V) and devoid of iron (Fe) and yttrium (Y) and has a LREE–enriched chondrite–normalized REE pattern. The U minerals of this group are similar to meteoric fluid infiltration related deposits. The second group has coeval coffinite(II) and coarsely crystalline calcite cement. Coffinite(II) is enriched in Y and Fe and depleted in V and is marked by a flat chondrite–normalized REE pattern, which is compatible with typical hydrothermal genetic deposits with high–salinity mineralizing fluids. The temperature and salinity of the primary aqueous inclusions in the ore–stage calcite are 120–180 °C and 8.00–16.34% (eq. wt% NaCl), respectively. These mineral assemblages, temperatures and salinities indicate that the Hangjinqi deposit was affected by two distinct types of ore–bearing fluids: low–salinity meteoric waters and high–salinity hydrothermal fluids. The meteoric fluids event began at 97 ± 5 Ma with the titling of the northern Ordos Basin and the uplift of the Hetao region to the north. Hydrothermal U mineralization occurred since 39 ± 2 Ma with the rifting of the Hetao graben. Thus, the previous biogenic model for the U mineralization should be modified in the uraniferous region of the north Ordos Basin.