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1.
云南省澜沧县地处临沧花岗岩的中南段，在其境内发现多地与花岗岩风化壳有关的离子吸附型稀土矿床。文章通过对该区晚三叠世黑云母二长花岗岩风化壳全风化层的剖面及钻孔样品分析，对赋存于花岗岩风化壳离子吸附型稀土矿床的成矿地质地球化学特征进行研究，探讨其关键成矿过程并总结地形地貌与风化壳和矿体露头的关系。研究表明，黑云母二长花岗岩风化壳分层特征明显，离子吸附型稀土矿体规模及形态严格受风化壳发育程度及微地貌控制；花岗岩风化壳全风化层稀土元素配分曲线呈右倾平滑的浅“W”型，轻稀土元素的分异程度强于重稀土元素；除Ce元素外，轻稀土元素的浸出率略高于重稀土元素；矿石类型为以轻稀土元素为主、中重稀土元素配分齐全的混合型稀土矿。通过厘定离子吸附型稀土矿床的关键成矿过程，文章发现内应力、渗透能力、风化程度、黏土矿物含量在风化壳剖面中由上至下变化特征综合决定了稀土矿体主要定位于风化壳全风化层。 相似文献
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3.
摘要：运用岩石地球化学方法,对广东惠东地区离子吸附型稀土矿床的地球化学特征进行研究。结果显示,风化壳中元素含量及配分特点总体上取决于母岩,但稀土元素在继承母岩稀土元素的基础上含量进一步富集,且各风化层中元素含量变化与风化作用之间具有一定相关性。WIG指数相较于CIA指数能更有效地描述风化壳风化强度,风化壳中稀土元素迁出富集与WIG指数及元素迁移系数具有一定规律性,轻稀土元素多在全风化层上部富集,而重稀土元素在全风化层下部及半风化层明显迁入富集,Ce、Eu均具明显负异常。 相似文献
4.
近年来,临沧花岗岩体风化壳内离子吸附型稀土(IREE)矿床的找矿勘查取得重要进展,岔河IREE矿床是该区新发现的中大型矿床之一,为IREE矿床成矿预测提供了研究实例.文章对岔河IREE矿床11个探矿工程风化剖面样品和1370件土壤地球化学样品的稀土元素,以及Ce异常分布、迁移及富集等表生地球化学特征和规律进行研究,结合前人研究成果总结出该区找矿模型,实施工程验证并取得了找矿发现.研究表明,风化花岗岩稀土元素配分模式与母岩相似,风化过程中REE发生淋滤、富集作用(全风化层富集程度最高),LREE和HREE发生了分异作用(LREE分异程度相对较高).在风化过程中,Ce异常与稀土元素氧化物总量(ΣREO)呈负相关,且Ce异常存在明显的分异作用,如风化剖面中黏土层Ce正异常(1.69)与全风化层上部Ce负异常(0.75)数值具有明显差异,为Ce异常用于IREE矿床成矿预测成为可能(见矿率达90％).该研究不仅能定位、定量的圈定IREE矿床成矿预测区,而且完善了IREE矿床找矿模型,具有重要的推广和应用价值. 相似文献
5.
Paul-Désiré Ndjigui Paul Bilong Dieudonné Bitom 《Journal of African Earth Sciences》2009,53(1-2):59-69
Strong negative cerium anomalies are developed in the saprolite zone of two serpentinite lateritic profiles in the Mada region of the Kongo–Nkamouma massif in the Lomié ultramafic complex (South-East Cameroon).The total lanthanide contents increase strongly from the parent rock (1.328 ppm) to the weathered materials (ranging from 74.32 to 742.18 ppm); the highest value is observed in the black nodules from the western weathering profile and the lowest one in the top of the clayey surface soil from the same profile. The lanthanide contents, except cerium, are highest in the saprolite and decrease along the profile. The light REE contents are very high compared to those of the heavy REE (LREE/HREE ranging from 3.21 to 44.37). The lanthanides normalized with respect to the parent rock reveal: (i) strong negative Ce anomalies with [Ce/Ce1] ranging from 0.006 to 0.680 in the saprolite zone; (ii) strong positive Ce anomalies with [Ce/Ce1] ranging from 1.23 to 23.96 from the top of the saprolite to the clayey surface horizon; (iii) positive Eu anomalies with [Eu/Eu1] ranging from 2.09 to 2.41 in all the weathered materials.Mass balance evaluation shows that, except cerium, lanthanides have been highly accumulated in the saprolite zone and moderately concentrated in the upper part of both profiles. Cerium has been highly accumulated in the nodules of the West Mada profile. The presence of negative Ce anomalies is confirmed by its low degree of accumulation whereas the positive ones are related to its high degree of accumulation. 相似文献
6.
Veronique Kamgang Kabeyene Beyala Estelle Ndome Effoudou Priso Georges Emmanuel Ekodeck 《Chemie der Erde / Geochemistry》2009,69(1):61-13
An in situ weathering profile overlying chlorite schists in the Mbalmayo-Bengbis formations (South Cameroon) was chosen for the study of the behaviour of REE and the evaluation of geochemical mass balance. After physical and mineralogical studies, the chlorite schists and the undisturbed weathered materials were chemically analyzed for major elements (X-ray fluorescence and titrimetry) and REE (ICP-MS). The behaviour of the REE in the Mbalmayo weathering system was established in comparison with the REE of the reference parent rock. Mass balance calculations were applied to both major elements and REE. The mineralogy of the materials was determined with the aid of a Philips 1720, diffractometer. The chlorite schists of the Mbalmayo sector show low REE contents (Σ=153.44 ppm). These rocks are relatively rich in LREE (about 125 times the chondritic value) and relatively poor in HREE (about 20 times the chondritic value). The REE diagram normalized to chondrites shows a slightly split graph ((La/Yb)N=6.18) with marked enrichment in LREE (LREE/HREE=9.50) in relation to HREE. Moreover, these spectra do not present any Ce anomaly, but a slightly positive Eu anomaly. The imperfectly evolved profile, whose materials are genetically linked, shows an atypical behaviour of REE. In effect, the LREE are more mobile than the HREE during weathering ((La/Yb)NASC<1) with weak Ce anomalies. This has been rarely reported in lateritic profiles characterized by higher HREE mobility than LREE during weathering processes with high Ce anomalies. This is either due to the difference in the stability of REE-bearing minerals, or to the weak acidic to basic pH conditions (6.70<pH<7.80), or even due to the average evolution of the weathering materials. The pathway of the REE along the profile is as follows: (1) leaching in the saprolites and summit of the profile, except for Ce, which precipitates very weakly in the nodular materials and the coarse saprolite materials, (2) at the base of the profile, solutions come in contact with chlorite schist formations, at this level, the pH increases (pH=7.79), HREE and a part of LREE partially void of Ce precipitate and (3) the other part of LREE precipitates further up in the profile. The geochemical mass balance calculations reveal that these elements are leached in the same phases as the relatively high Si, Al, K and Fe2+ contents. 相似文献
7.
“寨背式”离子吸附型稀土矿床多类型稀土矿化及其成因 总被引：1，自引：0，他引：1
赣南寨背离子吸附型稀土矿床产于寨背复式花岗岩体的风化壳中,自20世纪80年代发现以来一直以轻稀土型开采,近年在轻稀土型花岗岩风化壳中发现了重稀土矿。为了探讨轻稀土型花岗岩风化过程中重稀土元素的迁移、分馏和富集机制,本文选择了区内三个具有代表性的风化壳钻孔(ZK1、ZK2和ZK4)对其进行了全相和离子交换相稀土元素地球化学研究。结果显示：钻孔ZK4中离子交换相稀土含量介于14.90×10-6～835.8×10-6之间,并富集轻稀土(LREE/HREE=2.28～10.78);钻孔ZK1中离子交换相稀土含量达1470×10-6(9件样品均值),具有从轻稀土型向重稀土型过渡的配分特征(LREE/HREE=1.30～1.65),并且剖面自上而下显示轻、重稀土逐渐富集的趋势;钻孔ZK2中离子交换相稀土含量为492.4×10-6(8件样品均值),自上而下稀土配分类型从轻稀土型过渡至重稀土型(LREE/HREE=0.43～2.25),且轻稀土富集在全风化层上部而重稀土则富集在下部。三个钻孔的Nb/Ta和Zr/Hf... 相似文献
8.
为了解风化壳中离子交换相稀土元素的特征,对广西某地花岗岩风化壳剖面样品进行了X射线衍射及主量、稀土元素地球化学特征的研究.剖面自上而下可划分为腐殖土层(A1)、亚粘土层(A2)、网纹状风化层(B1)和全风化层(B2);自A1至B2,粘土矿物的含量和化学风化蚀变指数快速降低;与母岩相比A1、A2、B1中全相Ce、Nd和HREE相对富集,B2中全相稀土与母岩特征相似,所有样品的离子交换相HREE亏损,Y相对富集;离子交换相轻、重稀土一起富集在B2中.据此推测,花岗岩中褐帘石、榍石等易风化的稀土矿物为离子交换相稀土提供了主要的物源,锆石、磷钇矿等难风化的稀土矿物的残留及表生稀土矿物的形成使全相HREE相对富集;离子交换相轻、重稀土元素的分馏程度随风化程度的增加而变化. 相似文献
9.
Wendy J. Harrison 《Geochimica et cosmochimica acta》1981,45(9):1529-1544
Partition coefficients for the rare earth elements (REE) Ce, Sm and Tm between coexisting garnets and hydrous liquids have been determined at high pressure and temperatures (30 kbar and 1300 and 1500°C). Two synthetic systems were studied, Mg3Al2Si3O12-H2O and Ca3Al2Si3O12-H2O, in addition to a natural pyrope-bearing system.Deviations from Henry's Law behaviour occur at geologically relevant REE concentrations. At concentrations < 3 ppm Ce, < 12 ppm Sm, < 80 ppm Tm in pyrope and < 100 ppm Ce, < 250 ppm Sm, < 1000 ppm Tm in grossular (at 30 kbar and 1300°C), Dgarnet liquidREE increases as the REE concentration in the garnet decreases. At higher concentrations, DREE is constant. Dgrossular liquidREE also constant when the garnet contains less than about 2 ppm Sm or Tm. The REE concentration at which DREE becomes constant increases with increasing temperature, decreasing REE ionic radius and increasing Ca content of the garnet.Partitioning behaviour of Ce, Sm and Tm between a natural pyrope-rich garnet and hydrous liquid is analogous to that in the synthetic systems and substantiates the substitution model proposed by Harrison and Wood (1980).Values of DREEgarnet/liquid for which Henry's Law is obeyed are systematically higher for grossular than for pyrope (Dpyrope/liquid = 0.067(Ce), 0.108(Sm), 0.155(Tm) and Dgrossular/Liquid = 0.65(Ce), 0.75(Sm), 4.55(Tm).The implications of non-Henry's Law partitioning of REE for models of basalt petrogenesis involving garnet are far-ranging. Deviations from Henry's Law permit refinements to be made to calculated REE abundances once basic model parameters have been defined. 相似文献
10.
The results of REE leached by some organic acids with various concentrations and water/rock ratios for different durations from a mixed samples of the weathering crust of a granite in Gonghe,Guangdong,China,showed that:1)the contents of REE leached increase with increasing concentrations of the organic acids;2) the contents of REE leached by 0.01mol/L organic acids increase with increasing water/rock ration;3) the interaction between the organic acids and the samples enhances the pH value of the medium and the contents of REE leached tend to increase with decreasing pH value;and 4) compared with those leached by ammonia sulfate,the REE leached by the organic acids are characterized by a weaker negative C e anomaly,a stronger negative Eu anomaly,and lower(La/Sm)N and (Gd/Yb)N ratios,indicating that the organic acids have made contributions to the fractionation of REE in the weathering crust. 相似文献
11.
The behaviour of the rare-earth elements(REE)during the weathering of granites was studied in southern Guangxi,China.Based on the study of the weathering profiles,the soil,weathered and sub-weatereb zones are identified with different REE geochemical behaviours throug the weathering profiles of granite.The Ce anomalies of the weathering profiles cover a large range of values with most falling between 1.02 and 1.43in the soil zone and 0.16and 0.40in the weathered and sub-weathered zones.Light rare-earth elements(LREE) and heavy rare-earth elements(HREE)are enriched to varying degree in the weathering profiles as compared to host granites.In the soil zone,more HREEs are leached than LREEs,and HREEs are more enriched than LREE in the weathered and sub-weathered zones.It is considered that infiltration and adsorption on clays are two processes controlling the enrichment and formation of REE deposits in the weathering profiles of granite. 相似文献
12.
碳酸盐岩风化形成的红土保存着喀斯特发展演化历史证据,同时也是喀斯特地区土壤研究的重要对象。文章选取云
南石林地区的两处典型碳酸盐岩剖面为研究对象,对主量元素,微量元素及稀土元素在风化层的迁移特征及分布规律进行
研究,为探究风化层的成因提供依据。结果显示：（1） 以Ti为参比元素的剖面迁移特征表明,两剖面的主量元素在成土过
程中有相似的迁移规律,多数表现为淋失;微量元素略有差异,富集淋失程度不一。（2） UCC 标准化蜘蛛图显示,相对于
基岩,风化层中的Ca和Sr均出现亏损;与UCC相比,Fe、Ti等元素轻微富集,Mg、Ca、Na、K、P等元素显示了强烈的亏
损特征。（3） 基岩与风化层的REE分布模式相似,但风化层的稀土相对富集,轻稀土元素间的分异较大而重稀土元素间的
分异较小,且SJC剖面的轻、重稀土元素比值大于QST剖面;稀土元素球粒陨石标准化后,SJC剖面的Eu为负异常,剖面
上部和下部出现Ce负异常;QST剖面Ce负异常,Eu明显负异常。（4） 元素含量变化和元素对Al-Ti、Al-Fe及Zr-Hf相关性
说明剖面上覆红土是下伏基岩风化的结果。研究结果显示,两个剖面的元素地球化学特征与基岩存在很好的继承性,风化
层是基岩原位风化的产物。 相似文献
13.
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. 相似文献
14.
Paul-Dsir Ndjigui Paul Bilong Dieudonn Bitom Abdoulaye Dia 《Journal of African Earth Sciences》2008,50(5):305-328
The behaviour of major and trace elements have been studied along two serpentinite weathering profiles located in the Kongo-Nkamouna and Mang North sites of the Lomié ultramafic complex.The serpentinites are characterized by high SiO2 and MgO contents, very low trace, rare earth and platinum-group element contents. Lanthanide and PGE contents are higher in the Nkamouna sample than in Mang North. Normalized REE patterns according to the CI chondrites reveal that: (i) all REE are below chondrites abundances in the Mang North sample; (ii) the (La/Yb)N ratio value is higher in the Nkamouna sample (23.72) than in the Mang one (1.78), this confirms the slightly more weathered nature of the Nkamouna sample. Normalized PGE patterns according to the same CI chondrites reveal a negative Pt anomaly in the Mang sample. The Nkamouna sample is characterized by a flat normalized PGE pattern.All element contents increase highly from the parent rock to the coarse saprolite.In the weathering profiles, Fe2O3 contents decrease from the bottom to the top contrarily to Al2O3, SiO2 and TiO2. The contents of alkali and alkaline oxides are under detection limit.Concerning trace elements, Cr, Ni, Co, Cu, Zn and Sc decrease considerably from the bottom to the top while Zr, Th, U, Be, Sb, Sn, W, Ta, Sr, Rb, Hf, Y, Li, Ga, Nb and Pb increase towards the clayey surface soil. Chromium, Ni and Co contents are high in the weathered materials in particular in the saprolite zone and in the nodules.REE contents are high in the weathered materials, particularly in Nkamouna. Their concentrations decrease along both profiles. Light REE are more abundant than heavy REE. Normalized REE patterns according to the parent rock reveal positive Ce anomalies in all the weathered materials and negative Eu anomalies only at the bottom of the coarse saprolite (Nkamouna site). Positive Ce anomalies are higher in the nodular horizon of both profiles. An additional calculation method of lanthanide anomalies, using NASC data, confirms positive Ce anomalies ([Ce/Ce*]NASC = 1.15 to 60.68) in several weathered materials except in nodules ([Ce/Ce*]NASC = 0.76) of the upper nodular horizon (Nkamouna profile). The (La/Yb)N ratios values are lower in the Nkamouna profile than in Mang site.PGE are more abundant in the weathered materials than in the parent rock. The highest contents are obtained in the coarse saprolite and in the nodules. The elements with high contents along both profiles are Pt (63–70 ppb), Ru (49–52 ppb) and Ir (41 ppb). Normalized PGE patterns show positive Pt anomalies and negative Ru anomalies.The mass balance evaluation, using thorium as immobile element, reveals that:
- – major elements have been depleted along the weathering profile, except for Fe, Mn and Ti that have been enriched even only in the coarse saprolite;
- – all the trace elements have been depleted along both profiles, except for Cr, Co, Zn, Sc, Cu, Ba, Y, Ga, U and Nb that have been enriched in the coarse saprolite;
- – rare earth elements have been abundantly accumulated in the coarse saprolite, before their depletion towards the top of the profiles;
- – platinum-group elements have been abundantly accumulated in the coarse saprolite but have been depleted towards the clayey surface soil.
15.
Mélanie Davranche Olivier Pourret Gérard Gruau Aline Dia Martine Le Coz-Bouhnik 《Geochimica et cosmochimica acta》2005,69(20):4825-4835
Experiments were conducted to evaluate the impact of organic complexation on the development of Ce anomalies and the lanthanide tetrad effect during the adsorption of rare-earth elements (REE) onto MnO2. Two types of aqueous solutions—NaCl and NaNO3—were tested at pH 5 and 7.5. Time-series experiments indicate that a steady-state is reached within less than 10 h when REE occur as free inorganic species, whereas steady state is not reached before 10 d when REE occur as REE-humate complexes. The distribution coefficients (KdREE) between suspended MnO2 and solution show no or only very weak positive Ce anomaly or lanthanide tetrad effect when REE occur as humate complexes, unlike the results obtained in experiments with REE occurring as free inorganic species. Monitoring of dissolved organic carbon (DOC) concentrations show that log KdREEorganic/KdDOC ratios are close to 1.0, implying that the REE and humate remain bound to each other upon adsorption. Most likely, the Ce anomaly reduction/suppression in the organic experiments arises from a combination of two processes: (i) inability of MnO2 to oxidize Ce(III) because of shielding of MnO2 surfaces by humate molecules and (ii) Ce(IV) cannot be preferentially removed from solution due to quantitative complexation of the REE by organic matter. We suggest that the lack of lanthanide tetrad effect arises because the adsorption of REE-humate complexes onto MnO2 occurs dominantly via the humate side of the complexes (anionic adsorption), thereby preventing expression of the differences in Racah parameters for 4f electron repulsion between REE and the oxide surface. The results presented here explain why, despite the development of strongly oxidizing conditions and the presence of MnO2 in the aquifer, no (or insignificant) negative Ce anomalies are observed in organic-rich waters. The present study demonstrates experimentally that the Ce anomaly cannot be used as a reliable proxy of redox conditions in organic-rich waters or in precipitates formed at equilibrium with organic-rich waters. 相似文献
16.
海南岛东部地区砖红壤中稀土元素含量及其纵向分异研究 总被引：7，自引：0，他引：7
对海南岛东部地区发育典型的5个砖红壤剖面的REE组成特征及其纵向变化规律进行研究发现,基岩与成土母质决定着土壤中稀土元素的最初含量,由花岗岩风化而成的砖红壤的REE含量大于砂页岩风化而成的砖红壤的REE含量,土壤表层强烈的淋溶作用又导致由土壤剖面深部至浅部∑REE逐步减少。基岩及成土母质决定了砖红壤中呈现的LREE富集及Eu亏损的特点,而土壤发育过程中REE分异作用又使这些特征在成土母岩的基础上发生了一定程度的叠加。砖红壤剖面表层氧化和水解作用导致Ce在土壤表层中的富集,并导致由剖面深部至浅部,Ce呈现出由负异常向正异常演化之趋势。 相似文献
17.
Samira Mokhtari Asl Mohammadreza Jafari Reza Zarei Sahamiyeh Vahid Shahrokhi 《Arabian Journal of Geosciences》2015,8(9):7125-7139
Farsesh barite in the central part of Iranian Sanandaj-Sirjan zone is a sample of epigenetic hydrothermal mineralization in dolomitized limestone, which provides appropriate chemicophysical conditions making the passage of mineral-bearing fluids possible. Barite veins may range from a few centimeters to 2 m in thickness that increases downward. The microthermometry measurements obtained from more than 30 fluid inclusions show relative homogenization temperatures ranging from 125 to 200 °C with an average of 110 °C for Farsesh barite deposits. The mean salinity measured proves 16 times as much as weight percentage of NaCl for barite. Coexistence of liquid- and vapor-rich fluid inclusions in barite minerals may provide an evidence of boiling in ore veins. Moreover, occurrence of bladed calcite, high-grade ore zones, and presence of hydrothermal breccia are all consistent with boiling. Thermometric studies indicate that homogenization temperatures (Th) for primary and pseudosecondary fluid inclusions in barite range from 125 to 200 °C with an average of 1,100 °C. The δ34S values of barite also lie between 8.88 and 16.6 %. The relatively narrow spread in δ34S values may suggest uniform environmental conditions throughout the mineralization field. Thus, δ34S values are lower than those of contemporaneous seawater, which indicates a contribution of magmatic sulfur to the ore-forming solution. Barite is marked by total amounts of rare Earth elements (REEs) (6.25–17.39 ppm). Moreover, chondrite-normalized REE patterns of barite indicate a fractionation of light REEs (i.e., LREEs) from La to Sm, similar to those for barite from different origins. The LaCN/LuCN ratios and chondrite-normalized REE patterns reveal that barite in Farsesh deposit is enriched in LREEs compared with heavy rare Earth elements (HREEs). Similarity between Ce/La ratios in barite samples and those found in deep-sea barite supports its marine origin. Lanthanum and Gd exhibit positive anomalies, which are common features of chemical marine sediments. Cerium shows a negative anomaly in most samples inherited from the negative Ce anomaly of hydrothermal fluid that is mixed with seawater at barite precipitation. The available data including tectonic setting, host rock characteristics, REE geochemistry, and sulfur isotopic compositions may support a hydrothermal submarine origin for Farsesh barite deposit. 相似文献
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本区燕山早期花岗岩发育的风化壳中的粘土矿物以高岭石和埃洛石(7Å)为主;蒙脱石、三水铝石及其它为新查明矿物。据粘土矿物组合特征,自风化剖面深部到地表分为三个带:含蒙脱石带,高岭石和埃洛石(7Å)带,含三水铝石带。本文探讨了矿物在风化过程中的生成演化顺序,并进行了热力学的解释。据各带粘土物质的阳离子交换量与稀土含量变化的不一致关系认为,稀土在C带中的富集是化学风化的结果,与粘土矿物组合无关。 相似文献
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The total rare-earth element values(ΣREE)of loess in the Xinjiang region vary over a range of 128-200 ppm ,with an average of 153ppm .The average REE content of loess lies between the earth‘s crust (155ppm) and sedimentary rocks(151ppm).The Xinjiang loess,with the REE distribu-tion patterns characterized by negative slopes ,is rich in the Ce-family elements, and has a distribu-tion pattern characteristic of sedimentary rocks.The North Xinjiang loess is relatively depleted in Tb,but rich in Yb and Lu.The South Xinjiang loess is relatively rich in light rare-earth elements.This is full proof that the Xinjiang loess comes partly from weathered materials(clay rock,sandstone)in the region studied.The REE distribution patterns in the Xinjiang loess are similar to those in the precipitated dust and Aeolian sand,indicating the same material source.The REE distribution pat-terns in the Xinjiang loess are also similar to those in loess from the middle Yellow River Valley,China and Taskent,the former USSR.This implies that loesses of the three locations(Xinjiang,the mid-dle Yellow River Valley and Taskent) come from a common material source.But the REE patterns in the Xinjiang loess are different from those in wall rocks (volcanic rock,K-bearing volcanic rock).Generally ,LREE/HREE,Eu/Eu* and Ce/Ce* ratios reflect the features of parent materials of loess,indicating that the parent rocks were probably in the early stage of alkaline weathering and the weathered materials existed in an oxidation environment with basic mediums under arid-climatic conditions before transport.As a result,the migration ability of the REE is weak. 相似文献