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1.
张杰  张覃  陈代良 《矿物岩石》2003,23(3):35-38
对贵州织金新华含稀土磷矿床进行的稀土元素及微量元素分析结果表明,磷块岩中普遍富集稀土元素,稀土总量∑REE较高,并富集Y元素及La,Nd等轻稀土元素。LREE/HREE比值较高。含稀土磷块岩普遍具Ce负异常,显示其对源区的继承性。指示成磷环境处于氧化程度相对较高状态。稀土元素球粒陨石标准化模式曲线、北美页岩标准化模式曲线、Ce元素异常、LREE/HREE比值、微量元素特征及岩石矿物特征表明,织金新华含稀土磷矿床具以正常海相生物-化学沉积等为主伴有海相热水沉积混合成因的特征。在磷矿成矿过程中沉积物沉积时,活体生物及死亡残骸不同程度地摄取和富集了La,Nd,Ce等稀土元素、Y元素及其他微量元素,沉积在含磷层位,构成大量的含稀土、含生物碎屑白云质磷块岩。  相似文献   

2.
对采自羌塘盆地角木日地区的二叠系碳酸盐岩,包括下二叠统展金组白云岩和中二叠统龙格组灰岩进行了元素地球 化学分析,并讨论了其对古沉积环境的指示意义。结果表明,样品Y/Ho比值平均为45.14,Gd表现为轻微Gd正异常,符合 海相灰岩特征;SiO2和Al2O3的平均含量较低,反映研究区陆源物质的侵入较为有限。碳酸盐岩中ΣREE含量较低,稀土元 素分异程度整体较弱,轻稀土元素相对重稀土元素呈轻微富集特征,Ce,Eu均具有明显负异常,结合V/Cr,V/(V+Ni),Sr/ Ba及Sr/Ca等微量元素含量及比值特征认为,研究区早-中二叠世沉积期海水总体呈氧化环境。纵向上龙格组顶部表现出氧 化性增强、盐度增大的趋势,推测可能与当时水体变浅有关,与早二叠世晚期研究区构造应力由拉张向挤压的变化有密切 关系。  相似文献   

3.
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 NdSN/YbSN = 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 (NdSN/YbSN > 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.  相似文献   

4.
李莹  何保  滕寿仁  邓颖 《矿物岩石》2019,39(1):74-81
为探讨辽宁大台沟铁矿床的成矿物质来源及形成环境,选取典型铁矿石5块进行主量元素、微量元素和稀土元素分析测试。结果显示:大台沟铁矿床保存有明显的化学沉积特征,化学成分主要由Fe_2O_3,FeO和SiO_2组成(Fe_2O_3+FeO+SiO_2=87.33%~96%),其他组分(MnO,MgO,CaO,Na_2O,K_2O,TiO_2,P_2O_5,Al_2O_3)含量较低;页岩标准化后的稀土元素配分曲线显示为稀土总量低(ΣREE平均为19.65×10-6),轻稀土元素相对亏损,重稀土元素相对富集;且具有一定的Eu(Eu/Eu~*=1.52~2.72),Y(Y/Y~*=1.18~1.52),La(La/La~*=1.17~2.26)的正异常,弱的Ce(Ce/Ce~*=0.79~0.92)异常;Y/Ho值平均34.19接近于海水的分布范围;Sr/Ba值平均1.79,属于火山岩和海相沉积物;Ti/V值平均38.84,属于火山建造。这些特征表明:该矿床的形成可能与海相火山沉积物有关,属于火山沉积变质型铁矿范围;成矿物质来源于热水和海水的混合作用;矿床形成于相对于缺氧的环境。  相似文献   

5.
Major, trace and rare earth elements (REE) concentration of the Eocene limestones, Jaisalmer Basin, Rajasthan, India are analysed to reconstruct the depositional conditions and to identify sources of REEs. Among the major oxides, CaO is the dominant oxide followed by SiO2 in the studied limestones. Trace element Ba dominates over the other trace elements and it shows negative correlation with CaO. The Sr, occurring in small concentration, shows positive correlation with CaO. Other trace elements such as V, Zr, Sc, Y, Rb, Ni, Pb Co, Cu, U occur in small concentrations. The studied limestones show a positive correlation of ΣREE with Fe2O3, Ni, Th, Sc, and Y. These limestones possess sea-water like shale-normalized REE + Y pattern with light REE depletion, slight Gd enrichment, slightly positive La anomaly, positive Y anomaly, positive Eu anomaly, negative Ce anomaly and superchondritic Y/Ho ratio from 23.12 to 28.57. The dominance of CaO and low percentage of MgO suggest that mineral phase is calcite and there is absence of dolomitization. The occurrence of SiO2 and Al2O3 in appreciable percentages may be because of the siliciclastic input during the limestone precipiatetion. The low concentration of Uranium (0.4-3.7) and authigenic Uranium (Average Total U-Th/3 value = 0.74) indicate that the studied limestones were precipitated in oxic condition from seawater. The depletion of LREE suggests that the limestones were precipitated from the seawater. The positive correlation of ΣREE with Al2O3 Fe2O3, Ni, Th, Sc, and Y and negative correlation with CaO suggest an input of siliciclastic sediments from the land during limestone precipitation. The negative Ce anomaly, slightly positive La anomaly, slight Gd enrichment, positive Y anomaly, and positive Eu anomaly also suggest that the limestone was precipitated from the seawater with some siliciclastic input from continent. The low values of the Y/Ho ratio (23.12 to 28.57) in the studied limestones suggest some modification of the seawater by the input of freshwater in a coastal environment. The REEs of the studied limestones are correlable with the shallow sea water REEs with exception of a few elements. We envisage a coastal/shallow marine depositional environment where mixing of the continental material in sea water appears feasible.  相似文献   

6.
闫斌  朱祥坤  唐索寒  漆亮 《现代地质》2010,24(5):832-839
通过分析三峡地区九龙湾剖面新元古代盖帽碳酸盐岩的稀土元素和锶同位素组成,对新元古代“雪球地球”事件结束后水体的性质提供了制约。盖帽碳酸盐岩的REE配分模式具有轻重稀土元素亏损的特征,存在轻微Y正异常以及较高的Y/Ho值,没有明显的La异常。这些特征与受淡水影响的陆缘盆地、湖泊等沉积环境相似,而不同于正常海水。这表明盖帽碳酸盐岩不是正常的海相沉积物,而是发育在淡水与海水混合环境中的沉积物。盖帽碳酸盐岩具有较高的87Sr/86Sr值,这是由于新元古代“雪球地球”事件结束后大量陆源风化物的输入引起的。因此,盖帽碳酸盐岩较高的87Sr/86Sr值不能代表当时全球海水信息,只能反映局部混合水体的信息。轻微的Ce负异常显示陡山沱组早期水体处于弱氧化状态。盖帽碳酸盐岩的REE和Sr同位素综合特征表明在新元古代“雪球地球”事件结束后,陡山沱组早期水体是携带大量陆源风化物的冰融水与海水混合的水体,而且此时的混合水体处于弱氧化状态。  相似文献   

7.
Abstract The Zudong and Guanxi granites are original rocks of the ion adsorption-type HREE and LREE deposits in weathering crust of granites. The ∑REE 1 ∑REE=REE+Y.
value and LREE 2 LREE=∑(La-Eu) and HREE=∑(Gd-Lu)+Y.
/ HREE ratio of the Zudong granite are 264 ppm and 0.81-0.24 respectively, and the average Y/∑REE ratio is 35.8-54.5%. This is mainly due to magmatic crystallization and evolution and deuteric metasomatism (albitization, muscovitization and fluorite-doveritization). These alterations resulted in endogenic mineralizations of yttrium-group REE fluorine carbonates, silicates and arsenates. The Guanxi granite is characterized by LREE enrichment (the average LREE/HREE ratio is 2.43).  相似文献   

8.
《Organic Geochemistry》1987,11(2):83-89
Rare earth element and yttrium abundances in vitrain, xylain, liptain, fusain and whole coal samples from Bulgarian coal deposits have been studied. Vitrain, xylain, and liptain are depleted, while fusain is enriched in REE and Y as compared to the whole coal samples from which they were selected. Chondrite-normalized patterns show relative enrichment of light (LREE) against heavy (HREE) rare earth elements, negative Eu anomaly, and positive Lu anomaly. The shale-normalized patterns of the lithotypes reveal an increase from LREE to HREE, while those of the whole coal samples and mineral interlayers are less fractionated. The petrographic composition of the coals is of secondary importance for the concentration of the REE and Y. The main factors are the source area and the input of dissolved REE and Y into the coal depositional sites.  相似文献   

9.
陈松  桂和荣  孙林华  刘向红 《现代地质》2011,25(4):802-807,818
采取了皖北任楼煤矿太原组灰岩和灰岩水样品进行稀土元素测试分析,结果显示灰岩样品稀土总量较低,平均为36.947×10-6,灰岩样品稀土配分模式表现为轻稀土富集、重稀土亏损型;灰岩水样品稀土总量平均为0.052 6×10-6,灰岩水样品轻、重稀土均富集,轻、重稀土之间分异明显。对灰岩含水层水岩相互作用进行研究,结果表明:轻稀土表现稳定,重稀土分异明显,尤其在Y处有一个明显的峰值;Y元素与Ca元素呈正相关关系,相比石灰岩,灰岩水的Y/Ho、Y/Dy分异更为明显。研究认为,灰岩水中Y元素的峰值效应也可作为灰岩水源识别的依据。  相似文献   

10.
Banded iron formations (BIFs) within the Lvliang region of Shanxi Province, China, are hosted by sediments of the Yuanjiacun Formation, part of the Paleoproterozoic Lvliang Group. These BIFs are located in a zone where sedimentation changed from clastic to chemical deposition, indicating that these are Superior-type BIFs. Here, we present new major, trace, and rare earth element (REE) data, along with Fe, Si, and O isotope data for the BIFs in the Yuanjiacun within the Fe deposits at Yuanjiacun, Jianshan, and Hugushan. When compared with Post Archean Australian Shale (PAAS), these BIFs are dominated by iron oxides and quartz, contain low concentrations of Al2O3, TiO2, trace elements, and the REE, and are light rare earth element (LREE) depleted and heavy rare earth element (HREE) enriched. The BIFs also display positive La, Y, and Eu anomalies, high Y/Ho ratios, and contain 30Si depleted quartz, with high δ18O values that are similar to quartz within siliceous units formed during hydrothermal activity. These data indicate that the BIFs within the Yuanjiacun Formation were precipitated from submarine hydrothermal fluids, with only negligible detrital contribution. None of the BIF samples analyzed during this study have negative Ce anomalies, although a few have a positive Ce anomaly that may indicate that the BIFs within the Yuanjiacun Formation formed during the Great Oxidation Event (GOE) within a redox stratified ocean. The positive Ce anomalies associated with some of these BIFs are a consequence of oxidization and the formation of surficial manganese oxide that have preferentially adsorbed Ho, LREE, and Ce4 +; these deposits formed during reductive dissolution at the oxidation–reduction transition zone or in deeper-level reducing seawater. The loss of Ce, LREE, and Ho to seawater and the deposition of these elements with iron hydroxides caused the positive Ce anomalies observed in some of the BIF samples, although the limited oxidizing ability of surface seawater at this time meant that Y/Ho and LREE/HREE ratios were not substantially modified, unlike similar situations within stratified ocean water during the Late Paleoproterozoic. Magnetite and hematite within the BIFs in the study area contain heavy Fe isotopes (56Fe values of 0.24–1.27‰) resulting from the partial oxidation and precipitation of Fe2 + to Fe3 + in seawater. In addition, mass-independent fractionation of sulfur isotopes within pyrite indicates that these BIFs were deposited within an oxygen-deficient ocean associated with a similarly oxygen-deficient atmosphere, even though the BIFs within the Yuanjiacun Formation formed after initiation of the GOE.  相似文献   

11.
邹家山铀矿床伴生重稀土元素的赋存特征   总被引:1,自引:0,他引:1  
初步研究发现,相山矿田邹家山矿床中伴生有较高的重稀土元素,回收这些珍稀的资源和探索其成因具有重要的意义,而查明这些伴生稀土在铀矿床中的赋存特征是前期基础性工作。为此本文采用电子探针和激光剥蚀电感耦合等离子体质谱分析了邹家山铀矿床中稀土元素的赋存状态。结果显示:该矿床稀土矿物主要为独居石、氟碳钙铈矿和磷钇矿;独居石、氟碳钙铈矿的LREE/HREE>1,为轻稀土富集型;而磷钇矿的LREE/HREE<1,为重稀土富集型。沥青铀矿、钛铀矿、铀钍石、铀石、钍石、锆石等铀钍矿物的稀土特征为重稀土富集型;铀钍矿物稀土总量(∑REE+Y)较高,为(3 805.78~65 307.00)×10-6,LREE/HREE<1,为0.01~0.80,平均为0.29。其他伴生矿物磷灰石、钾长石为轻稀土富集型,萤石为轻、重稀土富集型两类都有,而伊利石、黄铁矿的轻重稀土无明显相对富集。重稀土在磷钇矿和铀钍矿物中以类质同象形式存在,少量赋存于伴生矿物。  相似文献   

12.
Carbon isotope (δ13C) and rare earth element (REE) concentrations in representative samples of the shallow marine Subathu Formation, explored from the Neelkanth and Dogadda sections of Northwestern Himalaya (India) were determined to infer the palaeo-environmental condition during the late Paleocene and middle Eocene. δ13C values show variation of ~5.0‰ with maximum excursion (?27.34‰) in calcareous sandstone at the basal part and minimum (?22‰) in red shale towards the terminal end. Total REE concentration varies (due to lithology) from 27.23?ppm to 564.35?ppm with an average of 187.60?ppm. The chondrite and PAAS normalized patterns exhibit positive Ce anomaly (0.95–4.45), enriched LREE, and depleted HREE, medium Y/Ho ratio (~30–45) along with positive correlation between Y/Dy and Y/Ho ratio. In addition, calcite veins present in some shale samples indicate redox sensitive trace elements. The overall REE abundance and distribution suggests highly oxygenated environment under the shallow marine regressive phase of deposition. The depositional setting, biostratigraphical constrained age along with δ13C values and lower TOC suggested an intense warm period, that might be coeval with the Paleocene-Eocene Thermal Maxima event (PETM).  相似文献   

13.
The distribution of rare earth elements (REE) in ferromanganese nodules from DOMES Site A has been determined by instrumental neutron activation methods. The concentrations of the REE vary markedly. Low concentrations characterize samples from a depression (the valley), in which Quaternary sediments are thin or absent; high concentrations are found in samples from the surrounding abyssal hills (the highlands) where the Quaternary sediment section is relatively thick. Moreover, the valley nodules are strongly depleted in the light trivalent REE (LREE) and Ce compared with nodules from the highlands, some of the former showing negative Ce anomalies.The REE abundances in the nodules are strongly influenced by the REE abundances in coexisting bottom water. Some controls on the REE chemistry of bottom waters include: a) the more effective removal of the LREE relative to the HREE from seawater because of the greater degree of complexation of the latter elements with seawater ligands, b) the very efficient oxidative scavenging of Ce on particle surfaces in seawater, and c) the strong depletion of both Ce and the LREE in, or a larger benthic flux of the HREE into, the Antarctic Bottom Water (AABW) which flows through the valley. The distinctive REE chemistry of valley nodules is a function of their growth from geochemically evolved AABW. In contrast, the REE chemistry of highland nodules indicates growth from a local, less evolved seawater source.  相似文献   

14.
研究了邹家山铀矿床原始矿石中的稀土元素含量特征及其在酸浸过程中的行为。结果表明:(1)该矿床矿石中伴生的稀土元素总含量很高,∑REE平均含量达3231.55×10-6,其中HREE达2933.39×10-6,属珍贵的重稀土元素富集型,具有负Eu异常、Ce无异常的特征。(2)在强酸及氧化剂浸泡条件下,轻、重稀土元素的浸出行为明显不同。重稀土元素更易被浸出,其浸出率是轻稀土元素的2倍左右。在强酸或强酸加氧化剂浸泡下,随原子序数的增加,轻稀土元素(La~Eu)的浸出率较明显增加,而重稀土元素(Gd~Lu-Y)的浸出率则小幅度递减;15种稀土元素中Gd的浸出率最高,La的浸出率最低。(3)初步获得邹家山铀矿床伴生稀土元素酸法浸出的最佳硫酸浓度和氧化剂用量,即在硫酸浓度为30g/L的条件下,100mL的浸泡液中含有2mL30%的过氧化氢时,稀土元素浸出率可达到最高值。  相似文献   

15.
本文以弓长岭铁矿二矿区磁铁石英岩、磁铁富矿和蚀变围岩样品为研究对象,进行了主量元素、微量元素、稀土元素和Fe同位素的测试。结果表明:磁铁石英岩主要由TFe2O3和SiO2组成,Al2O3和TiO2质量分数较低,微量元素质量分数和稀土元素质量分数均较低;经澳大利亚后太古界平均页岩(PAAS)标准化的稀土配分模式呈现出轻稀土亏损和重稀土富集,La、Eu和Y的正异常明显,Ce的异常不明显,Y/Ho值较高;富集Fe的重同位素,且与海底喷发热液经过氧化沉淀后的Fe同位素特征一致。磁铁富矿与磁铁石英岩的地球化学特征有很好的一致性和继承性,但磁铁富矿的REE和Eu质量分数较高,且较磁铁石英岩富集Fe的轻同位素,范围更大,与蚀变岩的Fe同位素组成相近。弓长岭铁矿的磁铁石英岩是陆源物质加入很少的古海洋化学沉积岩,为喷出的海底热液与海水的混合条件下氧化沉淀形成的。磁铁富矿推测为富Fe的轻同位素热液对磁铁石英岩进行改造,经过去硅富铁作用形成的。  相似文献   

16.
碳酸盐岩是地球表层岩石圈的重要组成部分,其化学组成可提供沉积环境与海洋水体演化等信息,然而,前人对碳酸盐岩中稀土等元素的分布与变化特征关注不足。本文选择穿越中国东部6个一级大地构造单元的3条地球化学走廊带,系统采集了582件碳酸盐岩地层样品,并准确分析了包括稀土元素(REE)在内的81项指标的含量。结果表明,中国东部地球化学走廊带碳酸盐岩稀土元素(REE+Y)总量为(0.59~183)×10-6,均值为24.0×10-6,纯净碳酸盐岩(CMC含量≥99%)均值为4.80×10-6。PAAS标准化后其显示具有轻稀土相对于中稀土和重稀土略亏损、δEu轻微正异常、δCe中度负异常等特征。白云岩中稀土含量、LREE/HREE值一般低于石灰岩;砂泥质含量相近时,前中生代各时代碳酸盐岩稀土分布模式相差不大,各构造单元稀土分布特征基本相似;与其他时代相比,中生代及中新元古代碳酸盐岩具有相对较平坦的稀土分布模式。研究表明,碳酸盐岩中稀土分布受碎屑物质影响明显,表现为稀土元素含量与碳酸根负相关,与碎屑物质相关元素(Si、Ti、Rb、Cs、Th、Zr等)、黏土相关元素(Al、Fe、K等)等正相关。成岩过程及白云化过程对较纯净碳酸盐岩中稀土分布特征影响不明显。我国古生代纯净碳酸盐岩分布模式受控于海相环境,其分布模式与现今海水相近;中生代纯净石灰岩受到陆相或海陆交互相的影响,具有较平坦的稀土分布模式。氧化还原条件对δCe的影响较δEu更为明显,δCe值受海相环境控制,极端正异常值(δCe>1.3)受到还原环境或/和热液影响。若假定海水中REE自中元古代至今无太大变化,各时代稀土元素分配系数均值介于103.55~102.39,分配系数差异是造成碳酸盐岩中轻稀土亏损、Ce负异常及Y正异常的主要原因。微生物(席)可富集稀土等金属元素并改变沉积环境,这可能是造成中新元古界碳酸盐岩较平坦的稀土分布模式的主要原因。  相似文献   

17.
Rare Earth Element Geochemistry of Late Palaeozoic Coals in North China   总被引:7,自引:0,他引:7  
Instrumental Neutron Activation Analysis (INAA) was done to determine the abundances of rare earth elements (REE) of 58 samples of Late Palaeozoic Carboniferous-Permian coals and related rocks in North China. Detailed study of REE geochemistry shows that the ∑REE of most coals studied in this paper is in a normal range between 30×10-6 and 80×10-6 with a mean of 56×10-6. The REE in the Taiyuan Formation in the northern part of North China are much richer than those in the southern part. This is due to the shorter distance to the source area in the north. Moreover, the IREE is in positive correlation to coal ash, especially closely related to the content of clay minerals <2μm in size. This reveals that most REE were carried by terrigenous clastic materials, especially fine clay minerals. In the coals the light REE (LREE) are much richer than the heavy REE (HREE), and the LREE/HREE ratio in coals generally varies from 2 to 8. The LREE/HREE ratio of high-ash, low-sulphur coals is higher than that of lo  相似文献   

18.
In this study we have used laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), to produce a high resolution coral record of rare earth elements (REE), Mn and Ba from coastal Porites corals from the Great Barrier Reef of Australia. Validation of the LA-ICP-MS technique indicated that the method provides accurate and reproducible (RSD = 13-18%) analysis of low concentration REE in corals (∼1 to 100 ppb). The REE composition in coral samples was found to closely reflect that of the surrounding seawater and distribution coefficients of ∼1-2 indicated minimal fractionation of the series during incorporation into coral carbonate. To explore the idea that coral records of REE can be used to investigate dissolved seawater composition, we analyzed two coastal corals representing a total of ∼30 yr of growth, including a 10-yr overlapping period. Comparable results were obtained from the two samples, particularly in terms of elemental ratios (Nd/Yb) and the Ce anomaly. Based on this evidence and results from the determination of distribution coefficients, we suggest that useful records of seawater REE composition can be obtained from coral carbonates. When compared to the REE composition of a mid shelf coral, coastal corals showed a significant terrestrial influence, characterized by higher REE concentrations (greater than 10 times) and light REE enrichment. The REE composition of coastal seawater inferred from the coral record was dependent on seasonal factors and the influence of flood waters. REE fractionation displayed a strong seasonal cycle that correlated closely with Mn concentration. We suggest that higher Nd/Yb ratios and higher Mn concentrations in summer result from scavenging of heavy REE by particulate organic ligands and Mn reductive dissolution respectively, both processes displaying higher rates during periods of high primary productivity. The Ce anomaly also displayed a strong seasonal cycle showing an enhanced anomaly during summer and during flood events. This is consistent with the Ce anomaly being primarily controlled by the abundance of Ce oxidizing bacteria. Based on these arguments, we suggest that the coral record of dissolved REE and Mn may be regarded as a useful proxy for biological activity in coastal seawater.  相似文献   

19.
我国东部苏鲁皖地区新生代碱性玄武岩中,除了含有大量地幔橄榄岩类捕虏体以外,尚含有一定数量的石榴石、普通辉石和歪长石巨晶。这些巨晶是在地幔不同深度上从玄武岩中晶出的。巨晶组合的分离结晶作用对熔体稀土元素含量有很大影响。赋存巨晶的碱性玄武岩所具有的LREE富集、HREE亏损的稀土元素分配型式是由地幔橄榄岩类部分熔融程度、石榴石巨晶和普通辉石巨晶的早期高压熔离和玄武岩的结晶分异作用等综合因素造成的。  相似文献   

20.
Settling particles were sampled monthly for 1 year using an automated time-series sediment trap positioned at similar depths at two sites of high diatomaceous productivity in the North Pacific Ocean and Bering Sea. The particles were analyzed for rare earth elements (REEs) by inductively coupled plasma mass spectrometry (ICP-MS) with and without chemical treatment of the bulk samples to isolate siliceous fractions. The REE composition of the bulk samples is explained largely by the contribution of two distinct components: (i) carbonate with a higher REE concentration, a negative Ce anomaly and lighter REE (LREE) enrichment; (ii) opal with a lower REE concentration, a weaker negative Ce anomaly and heavier REE (HREE) enrichment.The siliceous fractions of settling particles are characterized by high Si/Al ratios (30-190), reflecting high diatom productivity at the studied sites. The La/Al ratio of the siliceous fraction is close to that of the upper crust, but the Lu/Al and Lu/La ratios are significantly higher than those of the upper crust or airborne particles, indicating the presence of excess HREEs in the siliceous fraction. Diatoms are believed to be important carriers of HREEs.The Ce anomaly, Eu anomaly, slope of the REE pattern, and ΣREE of the siliceous fraction vary exponentially with decreasing total mass flux. They can be well-reproduced according to the differential dissolution kinetics of elements in the order of Ce < lighter REEs (LREEs) < Eu = heavier REEs (HREEs) < Si from settling particles, where the dissolution rate is critically reduced through particle aggregation. This order is consistent with the vertical distribution of dissolved REEs and Si in oceans. The differential dissolution kinetics leads to HREE enrichment of the original diatoms and REE enrichment of dissolved diatoms. The Lu/Si ratio of the siliceous fraction of settling particles recovered from some of the highest diatom fluxes is identical to that of the two elements dissolved in deep seawater, providing further evidence for the dissolution of siliceous matter in deep water.  相似文献   

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