吉林延边地区土壤稀土元素的活化特征及其影响因素

采用ICP--MS 方法对吉林延边地区土壤中的15 项稀土元素的全量和有效量进行分析,并研究了该地区土壤稀土元素的活化特征及土壤元素全量和土壤pH 值对稀土元素活化的影响。结果表明: 延边地区稀土元素总有效态含量的分布范围为18. 52 ～ 118. 02 mg /kg,平均含量为56. 75 mg /kg,稀土有效量空间分布存在明显差异; 土壤稀土元素的活化系数为0. 23 ～ 0. 46,环境因素对稀土元素的活化有着重要的影响; 稀土元素全量与有效量之间皆呈显著正相关,相关系数为0. 480 ～ 0. 779,土壤中稀土元素有效含量受全量控制; 部分土壤稀土元素的活化系数与土壤pH 值呈显著正相关。     

湘江悬浮物的稀土元素地球化学研究

在湘江及其支流采集了44件悬浮物样品进行稀土元素 ICP—MS分析。研究表明,湘江悬浮物中稀土总量(∑REE)、轻稀土(LREE) 和重稀土(HREE)含量分别为63～387 μg/g,58.2～353 μg/g和4.8～34μg/g。尽管湘江悬浮物中稀土分布不均匀,稀土含量相差很大,所有样品的球粒陨石标准化曲线均呈向右倾斜的富LREE的模式,北美页岩标准化模式为LREE稍富集的平坦型。湘江中下游河心与两岸水体悬浮物中稀土发生了明显分异。湘江悬浮颗粒物中REE受多方面因素控制,其源区控制了REE分配模式,而其稀土元素含量与颗粒中粘土矿物及重矿物有关。支流捞刀河悬浮物稀土的分布模式为Eu正异常型,与北美页岩有显著差别,捞刀河的悬浮物物源及成因有待进一步研究。     

Rare earth elements in groundwater from different Alpine aquifers

Rare earth elements (REE) were determined in 39 groundwater samples collected at 14 sites under low- and high-flow conditions. Water samples derived from aquifers hosted in crystalline, molasse, flysch, carbonate and evaporite rocks located in Western Switzerland. The concentration of REE in groundwater circulating in different rocks showed large variations: lowest concentrations (ΣREE≤10 ng/L) occurred in groundwater from evaporite aquifers; highest concentrations (ΣREE up to 516 ng/L) were observed in carbonate aquifers, although REE in these waters do vary under different hydrological conditions; groundwater from other aquifers had ΣREE from 10 to 100 ng/L. Distinct REE signatures were observed in waters draining specific rocks. The REE patterns in groundwater from crystalline, molasse and flysch aquifers showed heavy-REE enrichment at different degrees. Groundwaters circulating in crystalline rocks were distinguished by negative anomalies in Ce and Eu, whereas those from carbonate aquifers were nearly flat with ΣREE and the magnitude of negative anomaly in Ce is likely to be controlled by iron concentrations. The REE-Post-Archean Australian Shales (PAAS) normalized patterns appear useful to recognize the aquifer type and suggest the possibility to use the REE as geochemical tracers.     

黔西南晴隆锑矿区萤石的稀土元素地球化学特征

对与辉锑矿共生萤石的稀土元素地球化学特征研究表明，所有萤石均具有Ce负异常，其稀土配分模式存在3种类型：Eu弱亏损型、Eu正常型、Eu富集型。从成矿早期至晚期，萤石的稀土配分从Eu弱亏损型向富集型演化，稀土总量逐渐降低，并由中稀土富集向轻稀土富集演化。成矿流体可能主要属于盆地流体，具有十分低的稀土总量，在成矿作用过程中，成矿流体由早期的还原条件转化为晚期的氮化条件，由中稀土富集向轻稀土富集演化。     

Rare earth element geochemistry of Late Cenozoic alkaline lavas of the McMurdo Volcanic Group, Antarctica

Rare earth element (REE) concentrations were determined in 16 Ross Island and northern Victoria Land alkaline lava samples which were representative of four lava lineages of the McMurdo Volcanic Group, Antarctica. A kaersutite and two feldspar mineral separates were also analysed.

Two of the lava lineages, a basanite to nepheline benmoreite and a basanite to phonolite, have similar chondrite-normalized REE fractionation patterns, with a continuous enrichment of light and heavy REE and depletion of middle REE. The patterns result from the fractionation of olivine, clinopyroxene, spinels, feldspar, kaersutite and apatite. Kaersutite is an important fractionated phase responsible for the middle REE depletion.

Another of the lava lineages is mildly potassic with trachyandesite to peralkaline K-trachyte lavas which have partly overlapping REE fractionation patterns. There is a depletion in REE from tristanite to K-trachyte. Fractionation of olivine, clinopyroxene, feldspar and apatite probably control the REE chemistry of the lineage, greater degrees of apatite fractionation deplete the K-trachyte in REE relative to the tristanite. Feldspar fractionation in the genesis of the peralkaline K-trachyte is shown by a large negative Eu anomaly (Eu/Eu* = 0.10).

A nepheline hawaiite to anorthoclase phonolite lava lineage from the Erebus Centre shows enrichment of REE, although minor overlapping in the middle REE does occur. Anorthoclase phonolite has a positive Eu anomaly (Eu/Eu* = 1.31), indicating possible accumulation of anorthoclase. The lineage resulted from fractionation of olivine, clinopyroxene, magnetite and apatite.     

川西前陆盆地上侏罗统—白垩系泥质岩稀土元素地球化学

为了探讨川西前陆盆地上侏罗统—白垩系的物源属性及源区构造背景,对该区上侏罗统—白垩系泥质岩的稀土元素(REE)地球化学特征进行系统分析,结果表明,构造区及沉积环境对泥质岩的REE特征及其沉积分异作用有一定的控制性。在沉积成岩过程中,泥质岩的REE特征在一定程度上受到沉积作用的改造;泥质岩具有明显的LREE富集、HREE丰度低、负Eu异常以及大多数样品具有较明显负Ce异常的特点;从J3到K2,泥质岩均具有较高的REE分异程度,不同阶段的REE平均分异程度相对稳定;泥质岩形成于一种总体偏氧化、局部具还原性质的沉积环境;源区母岩以沉积岩和花岗质岩石为主,也可能有玄武岩成分的混入;源区构造背景主要为大陆岛弧,也有来自被动大陆边缘的物源。     

Rare earth element geochemistry of dolomites in the Middle Devonian Presqu'ile barrier, Western Canada Sedimentary Basin: implications for fluid-rock ratios during dolomitization

Rare earth elements (REE) were determined in fine, medium and coarse crystalline replacement dolomites, and for saddle dolomite cements from the Middle Devonian Presqu'ile barrier from Pine Point and the subsurface of the Northwest Territories and north-eastern British Columbia. REE patterns of the fine crystalline dolomite are similar to those of Middle Devonian limestones from the Presqu'ile barrier. Fine crystalline dolomite occurs in the back-barrier facies and may represent penecontemporaneous dolomitization at, or just below, the sea floor. Medium crystalline dolomite is widespread in the lower southern and lower central barrier. Medium crystalline dolomite is slightly depleted in heavy REE compared with Devonian marine limestones and fine crystalline dolomite, and has negative Ce and Eu anomalies. Medium crystalline dolomites replaced pre-existing limestones or were recrystallized from earlier fine crystalline dolomites. During these processes, the REE patterns of their precursors were modified. Late stage, coarse crystalline replacement dolomite and saddle dolomite cements occur together in the upper barrier and have similar geochemical signatures. Coarse crystalline dolomites have negative Eu anomalies, and those from the Pine Point area also have positive La anomalies. Saddle dolomites are enriched in light REE and have positive La anomalies. The REE patterns of coarse crystalline dolomite and saddle dolomite differ from those of marine limestones and fine and medium crystalline dolomites, suggesting that different diagenetic fluids were responsible for these later dolomites. Although massive dolomitization requires relatively large volumes of fluids in order to provide the necessary amounts of Mg^2-. dolomitization and subsequent recrystallization may not necessarily modify the REE signatures of the precursor limestones because of the low concentrations of REE in most natural fluids. Thus, relative fluid-rock ratios during diagenesis may be estimated from REE patterns in the diagenetic and precursor minerals. Fine crystalline dolomites retain the REE patterns of their limestone precursors. In the medium and coarse crystalline dolomites the precursor REE patterns were apparently altered by large volumes of fluids involved during dolomitization. This study suggests that REE compositions of dolomites and their limestone precursors may provide important information about the relative amounts of fluids involved during diagenetic processes, such as dolomitization.     

白云鄂博铁稀土矿床中稀土元素的分配特点

有关白云鄂博铁稀土矿床中稀土元素的组成特点和赋存形式,我所在六十年代曾作了大量工作,积累了大批数据。本文主要是利用这些数据,对该矿床中的稀土元素特别是其中的Nd、Sm、Eu的分配特点作初步阐述。     

长江中下游地区若干Cu(Au)、Cu-Fe(Au)和Fe矿床中钙质夕卡岩的稀土元素地球化学

本区夕卡岩的稀土元素（ＲＥＥ）分布模式表现为富集轻稀土元素（ＬＲＥＥ）的直线型和以Ｃｅ、Ｐｒ或Ｎｄ为峰值的折线型。夕卡岩全岩中ＲＥＥ分布模式基本上受石榴子石中ＲＥＥ的分配行为控制。石榴子石富集ＬＲＥＥ可能是承袭形成它们的初始物中ＲＥＥ丰度和分配行为的反映。石榴子石中ＲＥＥ（尤其是Ｌａ）分布的不均匀性、石榴子石微裂隙及包裹体中ＲＥＥ的丰度可能是导致直线型和过渡型ＲＥＥ分布模式的主要原因。石榴子石中折线型ＲＥＥ分布模式可能受石榴子石晶体化学和晶体结构的控制。具有这种ＲＥＥ分布模式的钙铁－钙铝榴石可能代表相对平衡条件下岩浆结晶分异产物。     

Rare earth element geochemistry of Late Devonian reefal carbonates, Canning Basin, Western Australia: confirmation of a seawater REE proxy in ancient limestones

Rare earth element and yttrium (REE+Y) concentrations were determined in 49 Late Devonian reefal carbonates from the Lennard Shelf, Canning Basin, Western Australia. Shale-normalized (SN) REE+Y patterns of the Late Devonian samples display features consistent with the geochemistry of well-oxygenated, shallow seawater. A variety of different ancient limestone components, including microbialites, some skeletal carbonates (stromatoporoids), and cements, record seawater-like REE+Y signatures. Contamination associated with phosphate, Fe-oxides and shale was tested quantitatively, and can be discounted as the source of the REE+Y patterns. Co-occurring carbonate components that presumably precipitated from the same seawater have different relative REE concentrations, but consistent REE+Y patterns. Clean Devonian early marine cements (n = 3) display REE+Y signatures most like that of modern open ocean seawater and the highest Y/Ho ratios (e.g., 59) and greatest light REE (LREE) depletion (average Nd_SN/Yb_SN = 0.413, SD = 0.076). However, synsedimentary cements have the lowest REE concentrations (e.g., 405 ppb). Non-contaminated Devonian microbialite samples containing a mixture of the calcimicrobe Renalcis and micritic thrombolite aggregates in early marine cement (n = 11) have the highest relative REE concentrations of tested carbonates (average total REE = 11.3 ppm). Stromatoporoid skeletons, unlike modern corals, algae and molluscs, also contain well-developed, seawater-like REE patterns. Samples from an estuarine fringing reef have very different REE+Y patterns with LREE enrichment (Nd_SN/Yb_SN > 1), possibly reflecting inclusion of estuarine colloidal material that contained preferentially scavenged LREE from a nearby riverine input source. Hence, Devonian limestones provide a proxy for marine REE geochemistry and allow the differentiation of co-occurring water masses on the ancient Lennard Shelf. Although appropriate partition coefficients for quantification of Devonian seawater REE concentrations from out data are unknown, hypothetical Devonian Canning Basin seawater REE patterns were obtained with coefficients derived from modern natural proxies and experimental values. Resulting Devonian seawater patterns are slightly enriched in LREE compared to most modern seawaters and suggest higher overall REE concentrations, but are very similar to seawaters from regions with high terrigenous inputs. Our results suggest that most limestones should record important aspects of the REE geochemistry of the waters in which they precipitated, provided they are relatively free of terrigenous contamination and major diagenetic alteration from fluids with high, non-seawater-like REE contents. Hence, we expect that many other ancient limestones will serve as seawater REE proxies, and thereby provide information on paleoceanography, paleogeography and geochemical evolution of the oceans.     

层控夕卡岩及有关矿床形成过程的稀土元素行为——以安徽冬瓜山矿床为例

对安徽省冬瓜山层控夕卡岩型铜（金）矿床中穿层方向上不同蚀变程度的大理岩，顺层方向上距岩体远近不同但垂向深度的块状石榴子石夕卡岩及其主矿物石榴子石，不同演化阶段的石英及矿石等到的REE特征进行了系统研究，结果显示，在穿层方向上，大理岩被交代的程度愈深其稀土总量（∑REE）愈高，Eu负异常愈显著，尽管，夕卡岩全岩的RE分布模式与原岩（大理岩）相似，但前者的稀土总量（∑REE）远高于后者，且Eu异常更为显著，显然不是继续承原岩的REE特征所致，而是受控于其主矿物石榴子石的REE特征，后者又由参与交代作用的岩浆热液REE所决定，热液中的REE具有缓和右倾型分布模式，LREE富集，较显著的Eu负异常等基本特征，石榴子石晶体基本承袭了热液的REE特征，REE的空间变化特征结果地层的构造特征可以揭示夕卡岩及相关矿体形成过程中流体的输运径及输运方式，REE的研究有助于深化对层控夕卡岩及其相关矿床形成过程的认识。     

晴隆锑矿床中萤石的稀土元素特征及其指示意义

本文系统地研究了黔西南晴隆锑矿床中萤石的稀土元素地球化学,表明不同颜色、不同矿物组合的萤石的稀土元素含量变化较大,但具有固定的REE分配模式,以明显的负Ce异常、富MREE、分配曲线相对平缓为特征;这种配分模式主要是受其晶体化学因素的控制,而与溶液中REE络合物的稳定性关系不大。萤石的稀土元素组成与其矿物共生组合关系不大,但与其颜色关系较密切。萤石的Ce、Eu异常主要是受氧逸度的控制,流体源区的氧逸度较高,矿物沉淀场所的氧逸度相对较低,从而导致该矿中萤石呈明显的负Ce异常,或正或负的Eu异常。晴隆锑矿床形成于开放体系条件下,水/岩反应很可能是导致萤石发生沉淀的主要机制。萤石中的Ca部分来自茅口组灰岩,部分来自大厂层玄武岩;而矿化剂F可能主要来自外部。     

REE patterns of eucrites and their genetic implications

Rare earth element (REE) abundances in eucrites were precisely determined on Juvinas, Pasamonte, Cachari, Stannem and Antarctic eucrites Y-74450,63,D+G; Y-75015,20,E+F; Y-75011,73; Y-790007,61,F; Y-75011,84,D-1 and Y-790007,61,E-4. The last two samples are eucrite clasts from polymict eucrites. The other Antarctic eucrite samples are matrix from polymict eucrites.Like the Stannern eucrite, all of the Antarctic eucrites have relatively high REE abundances. REE abundances in two clast samples are higher than those in the Stannern and matrix samples of the Antarctic eucrites. When REE abundances in the Antarctic eucrites and the Stannem eucrite are normalized by the REE abundance suite of the Juvinas or Pasamonte eucrites, highly linear REE patterns are obtained. For the Juvinas- or Pasamonte-normalized REE patterns of the Antarctic and Stannern eucrites, the inclination of the linear REE patterns increases with increasing REE abundances. These observations suggest that the eucrites with larger REE abundances such as the Stannern and Antarctic eucrites were produced as residual liquid in a fractional crystallization process from the main group of eucrites (e.g., the Juvinas eucrite). On the other hand, the Moore County cumulate eucrite is considered to be a solid phase formed in this process.     

800MPa下泥质岩部分熔融实验研究：残留相及熔体相REE地球化学特征

利用JL-3600t压机实验研究了800MPa、不同温度条件下泥质岩部分熔融过程,利用EMPA和LA-ICPMS分别测定了熔体相和残留相中主要化学组成以及微量元素（包括REE）组成。实验结果表明,泥质岩低程度部分熔融（〈25％）形成的熔体中REE含量分布于308．8-3565μg／g较大范围内,显示较大的不均匀性,其REE球粒陨石标准化分布模式显示弱的M型REE“四分组效应”,而残留相矿物石榴子石中REE含量变化于167．5—1008μg／g范围,也显示有明显的不均匀性,其REE球粒陨石标准化分布模式显示明显的W型REE“四分组效应”,尤以第一段La-Nd最为显著;随着部分熔融程度的增加（〉30％）,其形成的熔体中REE集中在523．2—1130μg／g范围,残留相石榴子石中BEE集中在288．6—512．7μg／g范围,均显示相对均匀;熔体相和残留相石榴子石矿物的REE球粒陨石标准化分布模式不发育REE“四分组效应”。实验前后Cl质量平衡计算的结果表明该实验过程中并没有产生岩浆挥发分相。上述特征表明S型花岗岩中的REE“四分组效应”现象很可能与泥质岩低程度部分熔融具有成因联系。     

内蒙古白云鄂博矿床的稀土矿化时代与期次

内蒙古白云鄂博REE-Fe-Nb矿床是世界罕见的超大型多金属矿床, 但矿床成因一直没有解决, 而年代学研究是解决矿床成因的基础。本文结合矿床地质特征, 系统地分析了前人的年代学研究成果, 并对白云鄂博矿床的Sm-Nd同位素体系进行了深入的分析和讨论。结果表明, 白云鄂博稀土的成矿时代约为1.3 Ga, 与碳酸岩墙的形成时间一致, 成矿物质来源于地幔。加里东期的热事件(约0.44 Ga)导致了白云鄂博矿床晚期稀土矿脉的形成和原有矿体中部分稀土矿物的重结晶, 但成矿物质主要来源于矿体内部的稀土再循环, 外源物质的贡献不明显。约1.3 Ga到约0.44 Ga间的一系列中间年龄为后期热扰动的结果, 并不代表成矿事件。简言之, 白云鄂博矿床只在中元古代发生过一次实质性的稀土矿化作用, 地幔是稀土物质的单一源区。     

华南酸性岩类风化壳稀土元素的生物地球化学及矿体贫化问题探讨

本文简述了华南酸性岩类风化壳稀土元素生物地球化学研究现状。研 究了几种氨基酸对稀土元素从花岗岩中溶出和在花岗岩风化壳中迁移的作用,结果表明大多数氨基酸可以促使稀土元素从花岗岩中溶出和在风化壳中迁移,尤以长链酸的作用较为明显。对比研究了华南停采的风化壳稀土矿的矿体表层和内部的品位变化,显示了矿体表层发生了贫化,其结果会对矿山生态环境产生负面影响。     

Rare earth element distributions in some Precambrian rocks and their phyllosilicates,Numedal, Norway

Mass spectrometric analyses for rare earth elements (REE) have been carried out on some Precambrian mica schists, gneisses and granites from the Precambrian Numedal area, Norway and on their phyllosilicates. The rocks, which are metamorphosed in the upper greenschist to amphibolite facies, were originally partly sedimentary, partly magmatic.The total REE contents for rocks varies from 145 to 761 ppm. An average of 16 phyllosilicate samples gave 417 ppm REE (max. of 1809 ppm, min. of ca. 50 ppm). Coexisting light and dark phyllosilicates have similar abundances of REE. For the micas of high REE content most of the REE was extractable by rinsing with EDTA. The data thus support the possibility of an extensive adsorption of REE ions on micaceous minerals. The REE distribution patterns do not provide a clear distinction between the sedimentary and magmatic origin for the rocks examined.     

Geochemical Behaviors of REE and Other Trace Elements during the Formation of Strata-bound Skarns and Related Deposits: A Case Study of the Dongguashan Cu (Au) Deposit, Anhui Province, China

REE and other trace elements in the altered marbles, massive skarns and ores, as well as garnet and quartz were determined in order to examine the behaviors of trace elements during hydrothermal alteration. It is demonstrated that the high-field-strength (HFS) elements Zr, Hf, Th and Nb were immobile while other trace elements were mobile during the formation of skarns and related deposits. REE and ore-forming elements such as Cu and Ag in hydrothermally-altered marbles and skarns were provided primarily by hydrothermal fluids. In the direction transverse of the strata, the more deeply the marbles were altered, the higher the total REE abundance and the larger the negative Eu anomalies would be. The chondrite-normalized REE patterns of skarns are similar to those of the marbles, but the former are distinguished by much higher REE contents and more remarkable negative Eu anomalies. Those patterns were apparently not inherited from the marble protolith, but were controlled by garnets, which were determine     

Rare earth elements in Permian salts and brines,Thuringia, Germany

Salts and brines have very low rare earth element (REE, La-Lu) concentrations. Thus, there is less knowledge of possible transfer of REE patterns during salt dissolution in water-rock interaction. REE levels in both media are close to or rather below limit of detection of commonly used methods. By dissolving salt samples in water followed by REE pre-concentration, REE contents of about 6.2 to 322 ng g⁻¹ were measured for four samples from the Merkers salt mine, Germany. These salts previously were identified to consist mainly of carnallite, halite and/or sylvite. Assuming congruent dissolution, REE patterns of brines and salts differ. Thus, a more complex interaction with (secondary) phases and complexation of REE should be taken into account to explain REE patterns in brines.     

Rare Earth Elements in Manganese Nodules from the Central Pacific Ocean

Manganese nodules in areas CP and CC of the central Pacific are rich in REE. Comparatively speaking,the REE contents of nodules in area CP are hihger than those in area CC; and the REE contents of nodulesfrom seamounts are higher than those of nodules from sea-floor plains and hills. Within the nodules, the REEshow a zonal distribution. The REE distribution patterns of the nodules are similar to those of the sedimentsand have a mirror image relationship with those of the sea water. Trivalent REE were not obviously differenti-ated when they entered into the nodules from the sea water.A major factor causing the difference of REE abundances between nodules and sediments is the redoxconditions. The redox intensity of the ocean floor of the Pacific is controlled mainly by Antarctic Bottom Wat-er(AABW), The iron-bearing facies in the nodules is the main carrier of REE.