辽东湾东南部海域柱状沉积物稀土元素地球化学特征与物源识别

对辽东湾东南部海域LDC30孔沉积物稀土元素（REE）、粒度等指标进行了分析,研究了其沉积物中稀土元素组成特征及其控制因素,并对其物质来源进行了探讨。结果表明,LDC30孔沉积物ΣREE平均值为149.49 μg/g,略高于黄海和东海,但是低于渤海和南海,并且低于全球沉积物ΣREE的平均值。研究区沉积物REE配分模式表现为明显的轻稀土富集、重稀土相对亏损;δEu的平均值为0.71,为中度亏损,δCe无异常;轻稀土与重稀土之间的分异作用较强,且轻重稀土内部分异明显。根据沉积物REE垂向变化特征,可将LDC30岩芯以51cm为界划分为两段,上段（0~51 cm）ΣREE含量随着深度的减小而呈增加的趋势,下段（51~99 cm）ΣREE含量在垂向上没有明显的波动变化,并且上段较下段稀土分异明显。δCe整体上比较稳定,但是在上段（0~51 cm）呈现下降的趋势。δEu垂向上也相对稳定的趋势。该孔沉积物REE参数与粒度之间无明显的相关性,REE组成不受粒度的控制,但重矿物对REE的组成和分布状况有重要的影响。LDC30孔沉积物物质来源比较稳定,并且具有强烈的陆源特征,其沉积物主要来源于辽东湾北部河流（大辽河、小凌河、双台子河等）,同时辽东湾西部河流滦河可能对LDC30孔上段沉积物有一定贡献。     

Origin of rare earth element anomalies in mangrove sediments,Sepetiba Bay,SE Brazil: used as geochemical tracers of sediment sources

Elemental contents were determined in two mangrove habitats along Sepetiba Bay, SE Brazil, an area impacted by local industrial activities, as well as hinterland water diversion networks. This study demonstrates how specific REEs (La, Ce, Nd, Sm, Eu, Tb, Yb and Lu) may be used as a sediment source tracer to mangrove-dominated coastlines. From the two stations studied, a pair of cores was collected, one in the mangrove forest and the other in the tidal flat. Station 1 results show a general enrichment in most of the fractioned patterns of the REEs normalised by Post-Archean Australian Shale. The relatively light rare earth elements are similarly enriched in the generally more polluted Station 1. Despite the probable difference in background sediment characteristics, a common sharp increase in mud contents patterns in the upper part of the mangrove sediment core was related to a lower REE content as well as Eu anomalies. With existing knowledge of clockwise water circulation in the bay, these patterns can be explained by man-made water diversion from the São Francisco and Guandu rivers, initiated more than 30 years ago, whereby suspended matter with relatively large contents of REEs and material originating from industrial sources accumulate in the eastern sector of the bay. This is the first comprehensive assessment of REEs as sedimentary tracers in a mangrove ecosystem in Brazil.     

长江与黄河沉积物REE地球化学及示踪作用

长江与黄河沉积物的稀土元素（ＲＥＥ）组成特征不同。长江沉积物ＲＥＥ含量较高,元素含量变化也大于黄河样品;球粒陨石标准化模式表明长江沉积物的（Ｌａ／Ｌｕ）Ｎ、（Ｌａ／Ｙｂ）Ｎ、（Ｇｄ／Ｙｂ）Ｎ的值也相应地比黄河沉积物中的高１０％左右,分布曲线均呈明显的石倾状,轻重稀土分馏明显,相对富集ＬＲＥＥ。且长江样品比黄河样品更富集ＬＲＥＥ,但Ｅｕ亏损不及黄河样品;两者的北美页岩标准化曲线均呈平坦稍右倾状,具有     

REE Geochemistry of Surficial Sediments from the Yellow Sea of China

REE geochemical studies of surficial sediment samples from the Yellow Sea of China have shown:(1)The average content of RE2O3 in the Yellow Sea sediments is 175 ppm,close to that in the East China Sea sediments.The REE distribution patterns in the Yellow Sea sediments are also similar to anomalies.These REE characteristics are typical of the continental crust.(2)The contents of REE are controlled mainly by the sediment grain size,i.e.,REE contents increase gradually with decreasing sediment grain size.REE are present mainly in clay minerals.In addition,REE contents are controlled obviously by heavy minerals.REE abundances in heavy minerals are much greater than those in light minerals.(3)Correlation analysis shows that REE have a close relationship with siderophile elements,especially Ti,which has the largest correlation coefficient relative to REE.Terrigenous clastic materials subjected to weathering and transport are suggested to be the main source of REE in the Yellow Sea sediments.     

湛江湾海域表层沉积物稀土元素特征及其物源指示意义

通过对湛江湾近海海域表层沉积物样品粒度和稀土元素(RE E)测试分析,系统地研究海域沉积物稀土元素地球化学特征并探讨其物质来源.结果表明,研究区沉积物的稀土元素含量变化较大,平均值为163.23μg/g,湾外的REE含量(168.61μg/g)高于湾内的REE含量(142.17μg/g);不同类型沉积物的稀土元素含量存...     

黔中小流域水体悬浮物与沉积物微量元素地球化学特征及物源指示

系统探讨了黔中小流域水体悬浮物和沉积物中微量及稀土元素地球化学特征。结果表明,元素含量在河流与湖泊、悬浮物与沉积物之间均存在明显差异。稀土元素北美页岩标准化分布模式大致为轻稀土相对富集的平坦模式,δEu为0.82～1.25,δCe为0.79～1.25,整体变化不大,均表现为弱异常。麦翁河稀土总量与分布模式均发生异常,主要受上游盘龙煤矿影响。悬浮物的∑REE与pH呈反相关关系,而沉积物的∑REE却与pH表现出正相关关系,表明悬浮物与沉积物中稀土元素行为的控制因素不同。元素相关分析、因子分析及微量元素图解均表明悬浮物与沉积物中的元素具有同源性,主要来源于流域岩石化学风化和土壤物理侵蚀的产物,而某些金属元素Zn、Co、Cu、Cr、Ni则来源于周边工矿企业、农业生产等人为排放。本研究丰富和发展了喀斯特地区水体元素地球化学,揭示了小流域化学风化与物理侵蚀过程中的元素特征和物质输送状况,并为该流域的生态环境现状、治理及管理提供了科学依据和基础资料。     

Geochemistry and biogeochemistry of rare earth elements in a surface environment (soil and plant) in South China

Plants and soils derived from different kinds of parent materials in South China were collected for analyses of rare earth elements (REEs) by inductively coupled plasma-mass spectrometry (ICP-MS). The distribution patterns and transportation characteristics of REEs in the soil–plant system were studied. The results show that geochemical characteristics of REEs depend on the types of soils, soils derived from granite being the highest in REE concentration. In a soil profile, REE concentrations are higher in B and C horizons than those in A horizon, with Eu negative anomaly and Ce positive anomaly. Plants of different genera growing in the same sampling site have quite similar REE distribution pattern, but plants of the same genera growing in different soils show considerable variation in characteristics of REEs. The patterns of the different parts of plant resemble each other, but the slope of the patterns becomes different. REEs have fractionated when they were transported and migrated from soil to plant root, stem and leaf, revealing that heavy REEs are relatively less available. REEs distributions in plants are influenced by the soil they grow in and also characterized by their individual biogeochemical characteristics. Biological absorption coefficients indicate difference of REE absorption capacity of plants. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Distribution of Rare—earth Elements in the Shenzhen Bay and Dapeng Bay Modern Sediments

The aim of this paper is to study the REE geochemistry of the Shenzhen Bay (SZB) and Dapeng Bay(DPB) modern sediments, discuss their REE distribution patterns, reveal the REE geochemical difference between the two bays which share the same material source but are deposited in different sedimentary environments, and expound their dynamic changes.It can be concluded that the SZB and DPB sediments are essentially of continental source.Their REE distribution patterns are quite different from those of Pacific pelagic sediments, but are very similar to those of South Chi-na granites.Because of different sedimentary environments prevailing in the SZB and DPB, some REE fractionation would have taken place in the sediments of the two bays.     

Rare earth elements in fine-grained sediments of major rivers from the high-standing island of Taiwan

Thirty-eight sediment samples from 15 primary rivers on Taiwan were retrieved to characterize the rare earth element (REE) signature of fluvial fine sediment sources. Compared to the three large rivers on the Chinese mainland, distinct differences were observed in the REE contents, upper continental crust normalized patterns and fractionation factors of the sediment samples. The average REE concentrations of the Taiwanese river sediments are higher than those of the Changjiang and Huanghe, but lower than the Zhujiang. Light rare earth elements (LREEs) are enriched relative to heavy rare earth elements (HREEs) with ratios from 7.48 to 13.03. We found that the variations in (La/Lu)_UCC–(Gd/Lu)_UCC and (La/Yb)_UCC–(Gd/Yb)_UCC are good proxies for tracing the source sediments of Taiwanese and Chinese rivers due to their distinguishable values. Our analyses indicate that the REE compositions of Taiwanese river sediments were primarily determined by the properties of the bedrock, and the intensity of chemical weathering in the drainage areas. The relatively high relief and heavy rainfall also have caused the REEs in the fluvial sediments from Taiwan to be transported to the estuaries down rivers from the mountains, and in turn delivered nearly coincidently to the adjacent seas by currents and waves. Our studies suggest that the REE patterns of the river sediments from Taiwan are distinguishable from those from the other sources of sediments transported into the adjacent seas, and therefore are useful proxies for tracing the provenances and dispersal patterns of sediments, as well as paleoenvironmental changes in the marginal seas.     

REE geochemistry of fine-grained sediments from major rivers around the Yellow Sea

To investigate the distribution pattern and controlling factors of rare earth elements (REEs) in riverine sediments, river mouth sediments were collected at five geographically different rivers around the Yellow Sea. Two- (1 M HCl leached and residual fractions) and five-step sequential extraction schemes (the SEDEX method) were applied to size-separated sediments < 20 µm. For the total REE composition, patterns normalized relative to the upper continental crust (UCC) showed light REE (LREE) and middle (MREE) enrichments in the Korean river sediments and MREE enrichment in the Chinese river sediments. LREE and MREE enrichments in 1 M HCl leached fractions played a major role in the distribution patterns of the total compositions in all the river sediments. About half of LREE enrichment in Korean river sediments was explained by the residual fraction. Comparison of the REE composition with major elements (Al, Fe, Ca, P) in each fraction of the SEDEX scheme revealed that MREE enrichment could be explained by reactive iron minerals, including goethite and hematite, although REE/Fe ratios showed different trends among the rivers due to different major REE-host iron minerals. After extracting reactive irons, authigenic phosphate, and carbonate, the sequential 1 M HCl fraction indicated that LREE enrichment in Korean river sediments may have originated from clay minerals, such as chlorite. These observations suggest that LREE enrichment may be a good tracer, while MREE enrichment should be used cautiously considering diagenetic modification, when using the REE composition to identify the sources of terrestrial materials.     

Rare Earth Element Patterns in the Karst Terrains of Guizhou Province, China: Implication for Water/Particle Interaction

The authors determine the concentrations of dissolved (<0.22 μm) rare earth elements (REE) and suspended particulate matter (SPM) of typical karst rivers in Guizhou Province, China during the high-flow period. The concentrations of acid-soluble REE extracted from SPM using diluted hydrochloric acid are also obtained to investigate water/particle interaction in the river water. The dissolved REE contents in the river water are extremely low in the rivers of the study. The dissolved REE distribution patterns normalized by the Post Archean Australia Shale (PAAS) in the karst rivers are not flat, show slight enrichment of heavy REE to light REE, and also have significant negative Ce and Eu anomalies. The acid-soluble REE appears to have similar distribution patterns as characterized by MREE enrichment and slight LREE depletion, with unremarkable Ce and Eu anomalies. The PAAS-normalized REE distribution patterns of SPM are flat with negative Eu anomalies. The contents and distribution patterns of REE in the SPM are closely related to the lithological character of the source rocks. The SPM contains almost all the REE produced in the process of surficial weathering. This demonstrates that particle-hosted REE are the most important form of REE occurrence. REE fractionation, which takes place during weathering and transport, leads to an obvious HREE enrichment in the dissolved loads relative to the SPM. Y/Ho ratio can be used to shed light on REE behaviors during water/particle interaction.     

Controls of fluid chemistry and complexation on rare-earth element contents of anhydrite from the Pacmanus subseafloor hydrothermal system,Manus Basin,Papua New Guinea

Ocean Drilling Program (ODP) leg 193 successfully drilled four deep holes (126 to 386 m) into basement underlying the active dacite-hosted Pacmanus hydrothermal field in the eastern Manus Basin. Anhydrite is abundant in the drill core material, filling veins and vesicles, cementing breccias, and occasionally replacing igneous material. We report rare-earth element (REE) contents of anhydrite from a site of diffuse venting (Site 1188) which show extreme variability, in terms of both absolute concentrations (e.g., 0.08–28.3 ppm Nd) and pattern shape (La_N/Sm_N=0.08–3.78, Sm_N/Yb_N=0.48–23.1, Eu/Eu*=0.59–6.1). The range of REE patterns in anhydrite includes enrichments in the middle and heavy REEs and variable Eu anomalies. The patterns differ markedly from those of anhydrite recovered during ODP Leg 158 from the TAG hydrothermal system at the Mid-Atlantic Ridge which display uniform LREE-enriched patterns with positive Eu anomalies, very similar to TAG vent fluid patterns. As the system is active, the host-rock composition is uniform, and the anhydrite veins appear to relate to the same hydrothermal stage, we can rule out predominant host-rock and transport control. Instead, we propose that the variation in REE content reflects waxing and waning input of magmatic volatiles (HF, SO₂) and variable complexation of REEs in the fluids. REE speciation calculations suggest that increased fluoride and possibly sulfate concentrations at Pacmanus may affect REE complexation in fluids, whereas at TAG only chloride and hydroxide complexes play a significant role. The majority of the anhydrites do not show positive Eu anomalies, suggesting that the fluids were more oxidizing than in typical mid-ocean ridge hydrothermal systems. We use other hydrothermal fluids from the Manus Basin (Vienna Woods and Desmos), which bracket the Pacmanus fluids in terms of acidity and ligand concentrations, to examine the dependence of REE complexation on fluid composition. Geochemical modeling reveals that under the prevailing conditions at Pacmanus (pH~3.5, T=250–300 °C), Eu oxidation state and the relative importance of fluoride versus chloride complexing are very sensitive to small variations in oxygen fugacity, temperature, and pH. Patterns with extreme mid-REE enrichment may reflect speciation effects (free-ion abundance) coupled with crystal chemical control. We conclude that the great variability in REE concentrations and pattern shape is likely due to variable fluid composition and REE complexation in the fluids. Editorial handling: L. Meinert     

Geochemistry of rare earth elements in the mainstream of the Yangtze River,China

Water, suspended matter, and sediment samples were taken from 8 locations along the Yangtze River in 1992. The concentration and speciation (exchangeable, bound to carbonates, bound to Fe–Mn oxides, bound to organic matter, and residual forms) of rare earth elements (La, Ce, Nd, Sm, Eu, Tb, Yb, and Lu) were determined by instrumental neutron activation analysis (INAA).The contents of the soluble fraction of REEs in the river are low, and REEs mainly reside in particulate form. In the particles, the chondrite-normalized distribution patterns show significant LREE enrichment and Eu-depletion. While normalized to shales, both sediments and suspended matter samples show relative LREE enrichment and HREE depletion. REEs are relatively enriched in fine-grained fractions of the sediments.The speciation characteristics of REEs in the sediments and suspended matter are very similar. The amount of the five forms follows the order: residual>>bound to organic matter∼bound to Fe–Mn oxides>bound to carbonates>>exchangeable. About 65 to 85% of REEs in the particles exist in the residual form, and the exchangeable form is very low. High proportions of residual REEs reveal that REEs in sediments and suspended matter are controlled by their abundances in the earth's crust. Carbonate, Fe–Mn oxide and organic fractions of REEs in sediments account for 2.4–6.9%, 5.2–11.1%, and 7.3–14.0% of the total contents respectively. They are similar to those in the suspended matter. This shows that carbonates, Fe–Mn oxides and organic matter play important roles during the particle-water interaction processes. By normalization to shales, the 3 forms of REEs follow convex shapes according to atomic number with middle REE (Sm, Eu, and Tb) enrichment, while light REE and heavy REE are depleted.     

REE geochemistry of sea-floor sediments of the continental shelf of the East China Sea

REE geochemistry has been studied of sea-floor sediments of the continental shelf of the East China Sea. The average content of RE₂O₃ is estimated at 175 ppm based on 68 sediment samples from the continental shelf. The absolute concentrations of Y and La-Lu in the sediments are shown in Table 3. The REE distribution patterns in the sediments demonstrate a distinct depletion in Eu and a negative slope. It is considered that the fragments of Mesozoie intermediate-acid igneous rocks widely distributed in southeastern China are the main source of REE in sea-floor sediments of the East China Sea continental shelf.     

鄱阳湖流域赣江北支水体和沉积物中稀土元素的含量和分异特征

稀土的开发和广泛应用使得人们倍加关注其在环境中的分布及其环境地球化学行为。赣江作为鄱阳湖流域五大入湖河之一,发源于稀土资源富集的赣南地区,而其下游水体及周边地下水中稀土元素的含量和分异特征目前尚不完全清楚。以赣江北支水体及沉积物为研究对象,开展了稀土元素地球化学研究。结果表明,赣江北支水体中稀土元素总量在地表水中为230~1 146 ng/L(均值458.85 ng/L),地下水中为284~1 498 ng/L(均值634.94 ng/L),沉积物中稀土元素总量为177.9~270.7 mg/kg(均值226.99 mg/kg)。PHREEQC模拟计算表明,水体中的稀土元素主要以碳酸根络合物(REEC0₃⁺)的形式存在。地表水和地下水总体上均表现为重稀土元素相较于轻、中稀土元素富集,沉积物未表现出明显的富集特性;水体具有Ce、Eu负异常特点,而沉积物表现为Ce正异常和Eu负异常,指示氧化还原环境和水岩相互作用对稀土元素在水-沉积物系统中迁移转化的影响。地下水中稀土元素的含量沿流向具有上升趋势,而水体中重稀土元素的富集程度不断减弱,同时碳酸根络合物(REEC0₃⁺)的占比不断降低,反映水体中稀土元素的含量受到pH、胶体吸附、络合作用以及地下水-地表水相互作用的影响。水体中重稀土元素的富集受到碳酸根络合反应的影响,Ce、Eu负异常与Ce氧化沉淀和母岩特性相关。Gd异常值表明,研究区中下游水体中的Gd元素受到人为输入的影响。     

Seawater-like trace element signatures (REE + Y) of Eoarchaean chemical sedimentary rocks from southern West Greenland,and their corruption during high-grade metamorphism

Modern chemical sediments display a distinctive rare earth element + yttrium (REE + Y) pattern involving depleted LREE, positive La/La*_SN, Eu/Eu*_SN, and Y_SN anomalies (SN = shale normalised) that is related to precipitation from circumneutral to high pH waters with solution complexation of the REEs dominated by carbonate ions. This is often interpreted as reflecting precipitation from surface waters (usually marine). The oldest broadly accepted chemical sediments are c. 3,700 Ma amphibolite facies banded iron-formation (BIF) units in the Isua supracrustal belt, Greenland. Isua BIFs, including the BIF international reference material IF-G are generally considered to be seawater precipitates, and display these REE + Y patterns (Bolhar et al. in Earth Planet Sci Lett 222:43–60, 2004). Greenland Eoarchaean BIF metamorphosed up to granulite facies from several localities in the vicinity of Akilia (island), display REE + Y patterns identical to Isua BIF, consistent with an origin by chemical sedimentation from seawater and a paucity of clastic input. Furthermore, the much-debated magnetite-bearing siliceous unit of “earliest life” rocks (sample G91/26) from Akilia has the same REE + Y pattern. This suggests that sample G91/26 is also a chemical sediment, contrary to previous assertions (Bolhar et al. in Earth Planet Sci Lett 222:43–60, 2004), and including suggestions that the Akilia unit containing G91/26 consists entirely of silica-penetrated, metasomatised, mafic rock (Fedo and Whitehouse 2002a). Integration of our trace element data with those of Bolhar et al. (Earth Planet Sci Lett 222:43–60, 2004) demonstrates that Eoarchaean siliceous rocks in Greenland, with ages from 3.6 to 3.85 Ga, have diverse trace element signatures. There are now geographically-dispersed, widespread examples with Isua BIF-like REE + Y signatures, that are interpreted as chemically unaltered, albeit metamorphosed, chemical sediments. Other samples retain remnants of LREE depletion but are beginning to lose the distinct La, Eu and Y positive anomalies and are interpreted as metasomatised chemical sediments. Finally there are some siliceous samples with completely different trace element patterns that are interpreted as rocks of non-sedimentary origin, and include metasomatised mafic rocks. The positive La/La*_SN, Eu/Eu*_SN and Y_SN anomalies found in Isua BIFs and other Eoarchaean Greenland samples, such as G91/26 from Akilia, suggests that the processes of carbonate ion complexation controlling the REE − Y patterns were already established in the hydrosphere at the start of the sedimentary record 3,600–3,850 Ma ago. This is in accord with the presence of Eoarchaean siderite-bearing marbles of sedimentary origin, and suggests that CO₂ may have been a significant greenhouse gas at that time.     

北部湾东部海域表层沉积物稀土元素组成及物源指示意义

对北部湾东部海域70个表层沉积物样品的稀土元素(REE)分析结果表明,研究区沉积物 REE 呈现轻稀土元素(LREE)富集、重稀土元素(HREE)平坦以及中等程度的 Eu 异常等特征.REE 组成受沉积物粒度和生物碳酸盐含量的制约,具有典型风化上陆壳 REE 特征,其源岩以上陆壳的长英质岩石为主.根据研究区沉积物 REE 分布规律,研究区可划分为4个地球化学分区,各区域上陆壳标准化曲线明显的不同.物源判别显示研究区的西部、海南岛西南侧(Ⅰ区)呈多源沉积特征,来自以下几个物源区:(1)海南岛西南侧河流沉积物和沿岸侵蚀物;(2)由南向北输入的外海沉积物(冬季);(3)夏季或冬季由北部湾西北部和西部搬运来的沉积物.研究区中部粗粒沉积区(Ⅱ区)与北部湾西部沉积物来源是相同的,主要来源于红河输砂.东北部砂质区(Ⅲ区)沉积物可能来源于雷州半岛西北部近岸基岩侵蚀.研究区东北部(Ⅳ区)沉积物主要来自北部湾北部沿岸侵蚀、琼州海峡和雷州半岛西部的沿岸侵蚀.此外,部分沉积物还可能来自珠江流域以及南海北部陆架区和北部湾西北部     

REE and actinide microdistribution in Sahara 97072 and ALHA77295 EH3 chondrites: A combined cosmochemical and petrologic investigation

We report the results of rare earth elements (REEs) and U-Th inventory of individual minerals (oldhamite, enstatite and niningerite) in two of the most unequilibrated and primitive EH3 known so far, ALHA77295 and Sahara 97072. Under the highly reducing condition that prevailed during the formation of enstatite chondrites, REEs are mainly chalcophile and concentrated in oldhamite. The study is guided by detailed petrographic investigations of the individual minerals in chondrules, complex sulfide-metal clasts and enstatite-dominated matrices.We developed two textural parameters in order to resolve the evolution of oldhamite condensates and their residence in the solar gas prior to their accretion in the individual objects or in matrices and relate these textural features to the measured REE patterns of the individual oldhamite crystals. These textural parameters are the crystal habit of oldhamite grains (idiomorphic or anhedral) and their host assemblages. REE concentrations were measured by SIMS and LA-ICPMS.Oldhamite grains display REE enrichments (10-100 × CI). Four types of REE patterns are encountered in oldhamite in ALHA77295. In general the REE distributions cannot be assigned to a specific oldhamite-bearing assemblage. The most represented REE pattern is characterized by both slight to large positive Eu and Yb anomalies and is enriched in light REEs relative to heavy REEs. This pattern is present in 97% of oldhamite in Sahara 97072, suggesting a different source region in the reduced part of the nebula or different parental EH asteroids for the two EH3 chondrites. Different parental asteroids are also supported by MgS-FeS zoning profiles in niningerite grains adjacent to troilite revealing both normal and reverse zoning trends and different MnS contents. The observed homogeneity of REE distribution in oldhamite grains in Sahara 97072 is not related to the mild metamorphic event identified in this meteorite that caused breakdown of the major K- and Rb-bearing sulfide (djerfisherite).REE concentrations in enstatite range between 0.2 and 8 × CI. Hence, enstatite is an important REE host next to oldhamite. Most patterns are characterized by negative Eu and Yb anomalies. Niningerites are negligible contributors to bulk EH3 REE inventory. Average positive Eu and Yb anomalies observed in most oldhamite are complimentary to the negative ones in enstatite thus explaining the flat patterns of the bulk meteorites. The condensation calculations based on cosmic abundances predict that the first oldhamite condensates should have flat REE patterns with Eu and Yb depletions since Eu and Yb condense at lower temperature than other REE. However, this pattern is seen in enstatite. Our findings are at odds with the predicted negative Eu and Yb anomalies in oldhamite earliest condensates from a closed system in a reduced solar source. Our petrographic, mineral chemistry and REE abundances of oldhamite, enstatite and niningerite discards an origin of oldhamite by impact melting (Rubin et al., 2009).Our results do not support in first order the scenario of the incorporation of REE in the Earth’s core to explain ¹⁴²Nd excess in terrestrial samples relative to chondrites because oldhamite is the major REE carrier phase and has super-chondritic Sm/Nd ratios.     

REE Geochemistry of Precambrian Metamorphic Rocks in Wutaishan Region

The metasedimentary-volcanic series of the Wutai and Hutuo groups experienced regional metamorphism and thus turned into moderate-to low-grade metamorphic rocks.REE abundances and REE distribution patterns in the Shizui and Taihuai Subgroup metasedimentary-volcanic rocks are typical of the Archean,whereas the Gaofan Subgroup and the Hutuo Group show post-Archean REE geochemical char-acteristics.Five types of REE distribution pattern are distinguished:(1)rightward inclined smooth curves with little REE anomaly(Eu/Eu*=0.73-0.95) and heavy REE depletion (e.g.the Late Archean metasedimentary rocks);(2)rightward inclined V-shaped curves with sharp Eu anoma-ly (Eu/Eu*=0.48-0.76) and slightly higher ∑REE (e.g.the post-Archean metasedimentary rocks);(3) rightward inclined steep curves with negative Eu anomaly(Eu/Eu*=0.73-0.76) and the lowest ∑REE (e.g.the post-Archean dolomites);(4)rightward inclined,nearly smooth curves with both positive Eu anomaly and unremarkable positive Eu anomaly(Eu/Eu*=0.95-1.25)(e.g.the meta-basic volcanic rocks);and (5) rightward inclined curves with Eu anomaly(Eu/Eu*=1.09-1.19)and heavy REE depletion(e.g.the meta-acid volcanic rocks).Strata of the two groups are considered to have been formed in an island-arc belt-an instable continental petrogenetic environment.     

Rare-earth elements in Luochuan loess section,Shaanxi province

TheΣ REE in loesses of different ages in the Luochuan section shows a narrow range of variation, indicating the homogeneity of loessic materials in chemical composition. The REEs in loess are concentrated mainly in silt-sized detrital minerals. Loesses and paleosols of different ages all are relatively enriched in rare-earth elements of the Ce family, and show similar REE distribution patterns. The fractionation among various REEs in the loess is different from that in morainic, marine and lacustrine sediments, but is similar to that in sand samples from deserts in Northwest China. The ratios of Ce/Ce* and Eu/Eu* reflect that the provenance of loessic materials and their accumulating area are all in an oxidation environment with weakly basic mediums under arid or semi-arid climate.