Features of rare earth elements geochemistry in coals of Central Kazakhstan

This research presents the results of a comprehensive study of mineralogical and geochemical features of REE distribution in coals of Central Kazakhstan deposits—Karaganda coal basin and Shubarkol deposit,which have large hard coal reserves and are industrially important for the coal industry of Kazakhstan;the research is based on 205 samples of clayey interlayers and coal seams.It shows basic patterns of distribution and features of concentration for impurity elements,gives an estimate of the impurity elements concentration,including REE,defines conditions and factors of their accumulation,and studies features of their forms in coal and coal-bearing rocks,which allows estimating the mechanisms of their migration and conditions of accumulation.According to the results of geochemical indicators,the article establishes the factors of REE dislocation,reveals the composition of margin rocks that have influenced REE concentration in coal seams,and the presented latest data on mineralogy allowed to establish the ways of their transportation to the paleobasin during the synand epigenetic periods of formation of the coal deposits of Central Kazakhstan being researched.It was found that the coals are insignificantly enriched with heavy lanthanides from Ho to Lu.The distribution curves of UCC normalized REE values in the coals are similar and coincide,but they are less than the average value for world coal,and amount to only one-third of the UCC.It was found that the highest concentrations of all REE are characteristic of clayey interlayers and oxidized coals.The La/Yb ratio in this case increases upwards along the section,indicating mainly clastogenic mechanism of REE delivery to the coals.In coal and clay samples,the predominant mineral form of REE is light lanthanide phosphates.Identified particles of REE from minerals and their composition peculiarities suppose autigene nature of their formation.The formation of the bulk of autigene minerals occurred during the maturation of brown coals and their transformation into hard ones.

通化地区中生代大川花岗岩岩体成因与REE赋存状态——来自岩石地球化学、锆石U-Pb定年和Hf同位素制约

吉林南部地区位于华北克拉通北缘东段,是一个经历了太古宙、元古宙、古生代、中生代以及新生代漫长地质历史演化的地质构造区,广泛发育晚中生代富集稀土元素的碱长花岗岩。本文选取该区富集稀土元素的大川花岗岩体,开展岩相学、锆石U-Pb年代学与Hf同位素、岩石地球化学研究,结果表明:该岩体主要由细粒、中粒和粗粒黑云母碱长花岗岩所组成,其次是花岗伟晶岩;主量元素具有高硅(w(SiO_(2))=72.56%~84.09%)、低铝(w(Al_(2)O_(3))=8.15%~14.76%)、准铝—强过铝质(A/CNK=0.98~1.60)的特征,属于高钾钙碱性系列;样品稀土质量分数较高(w(ΣREE)=88.53×10^(-6)~839.95×10^(-6)),(La/Yb)_(N)=2.30~41.24,富集轻稀土元素,亏损重稀土元素,稀土配分模式为右倾型,Eu负异常比较明显,δEu值为0.05~0.60,分异指数(ID=86.72~97.69)较高,固结指数(IS=0.16~1.13)较低,显示在岩浆演化过程中经历了斜长石、黑云母、磷灰石等矿物不同程度的分离结晶作用,结合岩相学特征,初步认为大川碱长花岗岩为高分异花岗岩;粗粒黑云母碱长花岗岩单颗粒锆石U-Pb同位素年龄为(120.8±1.6)Ma;锆石ε_(Hf)(t)值全部为负值(-10.7~-5.2),对应的Hf同位素二阶段模式年龄为2 587~2 090 Ma;基于同位素与岩石地球化学数据,初始岩浆起源于新太古代—古元古代陆壳物质的部分熔融,岩体为同源岩浆房经岩浆结晶分异作用后岩浆上侵就位的产物。岩矿鉴定及全岩微量显示,随着岩浆的演化,石英含量逐渐升高,黑云母含量逐渐降低,稀土总量也逐渐降低,稀土主要富集在粗粒黑云母碱长花岗岩相中。

Geochemistry of rare-earth elements in shallow groundwater, northeastern Guangdong Province, China

Shallow groundwater and hot springs were collected from northeastern Guangdong Province, Southeast China, to determine the concentrations and fractionation patterns of rare-earth elements(REE). The results show that the La, Ce and Nd of REEs are abundant in groundwater and rock samples, and the ∑REE contents in groundwater and rock samples range from 126.5 to 2875.3 ng/L, and 79.44 to 385.85 mg/L, respectively. The shallow groundwater has slightly HREE-enriched PAAS-normalized patterns. However, the granitic rocks PAAS-normalized patterns, with remarkable negative Eu anomalies, are different from that of shallow groundwater. The enrichment of HREE is considered to be controlled by REE complexation and readsorption for most groundwater has Ce and Eu positive anomalies. The Ce and Eu anomalies in groundwater are controlled by redox conditions. Moreover, the Fe-contain sediments dissolution and/or the reduction of Fe oxyhydroxides are another factor contributing to Ce anomalies. The Eu anomalies in groundwater are controlled by the preferential mobilization of Eu2+ during water-rock interaction compared to Eu3+.

Rare-earth element geochemistry reveals the provenance of sediments on the southwestern margin of the Challenger Deep

The hadal zone represents one of the last great frontiers in modern marine science,and deciphering the provenance of sediment that is supplied to these trench settings remains a largely unanswered question.Here,we examine the mineralogical and geochemical composition of a sediment core(core CD-1)that was recovered from the southwestern margin of the Challenger Deep within the Mariana Trench.Major element abundances and rare-earth element patterns from these sediments require inputs from both terrigenous dust and locally sourced volcanic debris.We exploit a two-endmember mixing model to demonstrate that locally sourced volcanic material dominates the sediment supply to the Challenger Deep(averaging^72%).The remainder,however,is supplied by aeolian dust(averaging^28%),which is consistent with adjacent studies that utilized Sr-Nd isotopic data.Building on a growing database,we strengthen our understanding of Asian aeolian dust input into the northwestern Pacific,which ultimately improves our appreciation of sedimentation in,and around,the hadal zone.

Geochemical characteristics and their significances of rare-earth elements in deep-water well core at the Lingnan Low Uplift Area of the Qiongdongnan Basin

A geochemical analysis of rare-earth elements （REEs） in 97 samples collected from the core of deep-water Well LS-A located at the Lingnan Low Uplift Area of the Qiongdongnan Basin is conducted, with the pur-pose of revealing the changes of sedimentary source and environment in the study region since Oligocene and evaluating the response of geochemical characteristics of REEs to the tectonic evolution. In the core samples, both∑REE and∑LREE （LREE is short for light-group REEs） fluctuate in a relatively wide range, while∑HREE （HREE is short for heavy-group REEs） maintains a relatively stable level. With the stratigraphic chronology becoming newer, both∑REE and∑LREE show a gradually rising trend overall. The∑REE of the core is relatively high from the bottom of Yacheng Formation （at a well depth of 4 207 m） to the top of Ledong Formation, and the REEs show partitioning characteristics of the enrichment of LREE, the stable content of HREE, and the negative anomaly of Eu to varying degrees. Overall the geochemical characteristics of REEs are relatively approximate to those of China＇s neritic sediments and loess, with significant ＂continental ori-entation＂. The∑REE of the core is relatively low in the lower part of Yacheng Formation （at a well depth of 4 207-4 330 m）, as shown by the REEs partitioning characteristics of the depletion of LREE, the relative enrich-ment of HREE, and the positive anomaly of Eu; the geochemical characteristics of REEs are approximate to those of oceanic crust and basalt overall, indicating that the provenance is primarily composed of volcanic eruption matters. As shown by the analyses based on sequence stratigraphy and mineralogy, the provenance in study region in the early Oligocene mainly resulted from the volcanic materials of the peripheral uplift ar-eas; the continental margin materials from the north contributed only insignificantly; the provenance devel-oped to a certain extent in the late Oligocene. Since the Miocene, the provenance has ceaselessly expanded from proximal to distal realm, embodying a characteristic of multi-source sedimentation. In the core strata with 31.5, 28.4, 25.5, 23, and 16 Ma from today, the geochemical parameters of REEs and Th/Sc ratio have significant saltation, embodying the tectonic movement events in the evolution of the Qiongdongnan Basin. In the tectonic evolution history of the South China Sea, the South China Sea Movement （34-25 Ma BP, early expansion of the South China Sea）, Baiyun Movement （23 Ma BP）, late expansion movement （23.5-16.5 Ma BP）, expansion-settlement transition, and other important events are all clearly recorded by the geochemi-cal characteristics of REEs in the core.

REE and Trace Element Geochemistry of Yinachang Fe-Cu-REE Deposit, Yunnan Province, China

REE and other trace elements in ores, wall rocks, alkaline volcanic rocks and diabase dikes have been determined in the Yinachang Fe-Cu-REE deposit. Comparative studies of REE and trace element geochemical characteristics of these geological bodies indicate that the ores and alkaline volcanic rocks contain abundant REE and Y ({65.9}-{4633})×10+{-6}, with higher abundances of As, Mo, Nb, Co and U than those of the crust. Their chondrite-normalized patterns show a strong enrichment of LREE and a positive Eu anomaly, in contrast to those of the dolomites which are characterized by slight LREE enrichment and moderate negative Eu anomaly. The REE patterns of ores are similar to those of hydrothermal sediment cores in the East Pacific Rise, whereas the REE patterns of dolomites are similar to those of PAAS (Post-Archean Average Shale). In combination with the geological setting of the deposit, the primary ore-forming fluids might have higher REE and volatile elements, and might have been derived from mantle degassing, or the alkaline volcanic magmas. The Yinachang Fe-Cu-REE ore deposit is considered to be of volcanic exhalation-hydrothermal sedimentary origin.

Rare-earth and trace elements and hydrogen and oxygen isotopic compositions of Cretaceous kaolinitic sediments from the Lower Benue Trough, Nigeria: provenance and paleoclimatic significance

This study evaluated the Cretaceous(Campanian–Maastrichtian) kaolinitic sediments of the Ajali/Mamu and Enugu/Nkporo Formations from the Lower Benue Trough of Nigeria. A combined method of inductively coupled plasma–mass spectrometry and isotope ratio mass spectrometry was used to investigate trace and rareearth element geochemistry and hydrogen and oxygen isotopic compositions. These data were then used to infer the sediments' provenance and paleoclimatic conditions during their deposition. The sediments contained low concentrations of most trace elements, with the exceptions of Zr(651–1352 ppm), Ba(56–157 ppm), V(38–90 ppm),and Sr(15.1–59.6 ppm). Average values of Co and Ni were1.5 and 0.7 ppm, respectively. Trace and rare earth element values were lower than corresponding values for upper continental crust and Post-Archean Australian Shale, with the exception of Zr. The samples showed only slight light rare-earth enrichment and nearly flat heavy rare-earth depletion patterns, with negative Eu and Tm anomalies,typical of felsic sources. Geochemical parameters such as La/Sc, Th/Sc, and Th/Co ratios support that the kaolinitic sediments were derived from a felsic rock source, likely deposited in an oxic environment.^(18 )O values ranged from+ 15.4 to + 21.2% for the investigated samples, consistent with a residual material derived from chemicalweathering of felsic rock and redeposited in a sedimentary basin(typical values of + 19 to + 21.2%). While in the basin, the sediments experienced extended interactions with meteoric water enriched in d D and d16 O. However,the variation in d D and d16 O values for the investigated samples is attributed to the high temperature of formation(54–91 °C). The d D and d^(18 )O values suggest that the sediments, although obtained from different localities within the Lower Benue Trough, formed under similar hot,tropical climatic conditions.

Trace and rare earth element geochemistry of the black and grey shales of the Calabar Flank, Southeastern Nigeria: constraints on the depositional environment and the degree of metal enrichment

This study focuses on the trace and rare earth elements(REE)geochemistry of the Nkporo and Ekenkpon Shales of the Calabar Flank.The main aim is to infer their depositional environment and the degree of their metal enrichment.The shale samples were analyzed using inductively coupled plasma mass spectrometry.The results indicated that the mean concentrations of K,Na,and Fe in Nkporo and Ekenkpon Shales are 1.45,0.4,and 4.17 wt%,and 1.11,0.44,and 5.42 wt%;respectively.The Nkporo Shale is enriched with the following trace elements;P>Mn>Sr>Ba>Zn>Ce>Rb>Zr>V>Cr>Ni and depleted in the following trace elements;Ta>Ge>Sb>Bi>Cd>Ag>Te>In>Hg.While the Ekenkpon Shale is enriched with the following trace elements;P>Mn>Ba>Sr>V>Ce>Zr>Rb>Cr>Zn>Ni and depleted in;Sb>Ge>Bi>Ag>Ce>Te>In>Hg.The concentration of redox-sensitive elements such as V,Ni,Mo,U,Cu,Cr,Re,Cd,Sb,Ti,Mn,and their ratio V/Mo and U/Mo in the black and grey shale samples show different patterns.The REE obtained from the Nkporo and Ekenkpon Shales were PAAS normalized.The Nkporo Shale showed a slightly flat light rare-earth element(LREE),middle rare-earth element(MREE),and heavy rare earth element(HREE)pattern enrichment.Ce/Ce*ranges from 0.95 to 1.09 in Nkporo Shale and 0.67 to 1.40 in Ekenkpon Shale.The Ekenkpon Shale showed a slight LREE,MREE enrichment,and depleted HREE patterns.The Mn contents and U/Mo ratio in Nkporo and Ekenkpon Shales suggests a poor oxygen transitional environment.The V/Mo and V/(V+Ni)ratios indicated that the Nkporo shales were deposited in an anoxic to suboxic conditions and Ekenkpon shales were also deposited under an anoxic to suboxic conditions.The V/Ni ratio indicated that the organic matter in the Nkporo shale is terrigenous while that of the Ekenkpon shales are both terrigenous and marine in origin.

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 determined by the hydrothermal solutions involved in the infiltration metasomatism. The hydrothermal fluids are characterized by having slightly right-hand dipping REE patterns, being enriched in LREE and having strongly negative Eu anomalies. The uptake of REE from hydrothermal fluids during the growth of garnet crystals resulted in the garnets having similar REE patterns to the hydrothermal fluids. Based on the spatial variation of REE in skarns and the structures of the hosting strata, we can get a better understanding of the transport path and pattern of the fluids involved in the formation of skarns and their related deposits. REE geochemistry investigation can help elucidate the genesis of skarns and skarn-related deposits.

Mechanism of interaction relation between the rare-earth element Ce and impurity elements Pb and Bi in Ag-based filler metal

The mechanism of interaction relation between the rare-earth element Ce and elements Pb and Bi in Ag-based filler metal has been studied. The results show that the compounds CePb and CeBi with high melting point can be easily produced between these three elements in the filler metal, which greatly limited the formation of the isolated phase Pb or Bi and also eliminated the bad effect of impurity elements Pb and Bi on the spreading property of Ag-based filler metal. The metallurgical and quantum-mechanical bond formation analysis show that a strong chemical affinity was existed between the rare-earth element Ce and impurity elements Pb and Bi, which was proved by the XRD analysis results.

Effects of rare-earth elements on the glass-forming ability and mechanical properties of Cu_(46)Zr_(47-x)Al_7M_x(M = Ce,Pr,Tb,and Gd) bulk metallic glasses

Cu46Zr47-xA17Mx （M = Ce, Pr, Tb, and Gd） bulk metallic glassy （BMG） alloys were prepared by copper-mold vacuum suction casting. The effects of rare-earth elements on the glass-forming ability （GFA）, thermal stability, and mechanical properties of Cu46Zr47-xA17Mx were investigated. The GFA of Cu46Zr47-xA17Mx （M = Ce, Pr） alloys is dependent on the content of Ce and Pr, and the optimal content is 4 at.%. Cu46Zr47-xA17Thx（X = 2, 4, and 5） amorphous alloys with a diameter of 5 mm can be prepared. The GFA of Cu46Zr47-xA17Gdx（x = 2, 4, and 5） increases with increasing Gd. Tx and Tp of all decrease. Tg is dependent on the rare-earth element and its content. ATx for most of these alloys decreases except the Cu46Zra2Al7Gd5 alloy. The activation energies △Eg, △Ex, and △Ep for the Cu46Zr42A17Gd5 BMG alloy with Kissinger equations are 340.7, 211.3, and 211.3 kJ/mol, respectively. These values with Ozawa equations are 334.8, 210.3, and 210.3 kJ/mol, respec- tively. The Cu46Zr45Al7Tb2 alloy presents the highest microhardness, Hv 590, while the Cu46Zr43A17Pr4 alloy presents the least, Hv 479. The compressive strength （at.f.） of the Cu46Zra3A17Gd4 BMG alloy is higher than that of the Cu46Zr43Al7Tb4 BMG alloy.

Trace element and REE geochemistry of the Zhewang gold deposit, southeastern Guizhou Province, China

The quartz vein-type gold deposits are widely hosted by the Neoproterozoic(Xiajiang Group) epimetamorphic clastic rock series in southeastern Guizhou Province, China. The Zhewang gold deposit studied in this paper occurs in the second lithological member of the Pinglue Formation of the Xiajiang Group. Trace element geochemistry of host rocks, quartz veins and arsenopyrite has revealed that ore-forming fluid was enriched in sulphophile elements such as Au, Ag, As, Sb, Pb and Zn, and simultaneously concentrated some magmaphile elements such as W and Mo, which probably provides some evidence for multi-stage mineralization or overprinting of magmatic hydrotherm. Quartz veins and arsenopyrite were characterized by depletion in HFSE and enrichment in LREE. Hf/Sm, Nb/La and Th/La imply that the ore-forming fluid was probably a NaCl-H2O solution system enriched in more Cl than F; Th/U values reflect the strong reducibility of the ore-forming fluid, coincident with the sulfide assemblages. The values of Co/Ni reflect that magmatic fluids may have partly participated in the ore-forming process and Y/Ho values have proved that the ore-forming fluid was associated with metamorphism and exotic hydrotherm which has reformed former quartz veins during late mineralization. The concentrations of REE, Eu anomalies and Ce anomalies of this deposit display that ore-forming elements mainly were derived from host rocks and possibly from a mixed deep source, and the ore-forming fluid was mixed by dominant metamorphic fluid and minor other sources. The physical-chemical conditions of ore-forming fluid changed from the initial stage to the late stage. The metamorphic fluid is responsible for the mineralization. Therefore, the Zhewang gold deposit is classified as a quartz vein-type gold deposit which may have been reformed by magmatic fluids during the late stage.

Trace element and REE geochemistry of Sanshenjiang gold deposit, southeastern Guizhou Province, China

The Sanshenjiang gold deposit in southeastern Guizhou Province, China, is hosted by the Neoproterozoic metasedimentary rocks which experienced low-grade greenschist facies metamorphism. Gold mineralization occurs mainly in the ribbon chiltern slate of the first member of the Longli Formation and is controlled by both strata and faults. Ore bodies are characterized by abundant quartz-arsenopyrite-gold-pyrite-bedding veins, veinlets and small lenses within the shear zone. In this study, trace element and REE geochemistry was analyzed to constrain the origin and genesis of this deposit. The trace element signatures of wall rocks and veins display a basically similar tendency in the spider diagram, showing the genetic relationship. The values of Co/Ni, Y/Ho, Hf/Sm, Nb/La and Th/La reflect that the hydrothermal fluids of this deposit were derived from the mixture of multiple sources with marked enrichment of Cl and moderate to high temperature. There is a broad similarity in the chondrite-normalized patterns and REE fractionation between wall rocks and ore bodies, possibly reflecting their similar origin. Based on the difference in δCe and δEu, quartz veins and lenses can be subdivided into weakly negative Ce-anomalies (δCe=0.81 to 1.06) with slight Eu anomalies (δEu=0.81 to 1.06) type and the significant positive Ce-anomalies (δCe=1.13 to 1.97) with moderate negative Eu-anomalies type, probably suggesting physical-chemical changes in the evolution process of ore-forming fluids from the early to late stage. It can be concluded that the ore-forming process may have experienced three stages: formation of the original ore source bed, regional metamorphism and gold mineralization, on the basis of trace element and REE analysis and field observation.

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

The major elements, trace elements and REEs were analyzed on the samples collected from the sandstone-type uranium deposits in the Ordos Basin to constrain the mechanism of uranium enrichment. The total REE amount ranges from 36.7 to 701.8 μg/g and the REE distribution patterns of the sandstone-type uranium samples are characterized by LREE enrichment and high REE depletion. The results also indicated a high Y abundance and Eu anomalies between 0.77-1.81. High-precision ICP-MS results showed that U abundances are within the range of 0.73-150 μg/g, showing some strong correlation between U enrichment and related elements such as Ti, V, Zr, Mo, and Au. In addition, Th abundance is correlated with ΣREE.

Rare earth element(REE) geochemistry of different colored fluorites from the Baoshan Cu–Pb–Zn deposit, Southern Hunan,South China

The Baoshan Cu–Pb–Zn deposit, located in the central part of the Qin–Hang belt in South China, is closely related to the granodiorite-porphyry. However, the characteristics and the source of the ore-forming fluid are still ubiquitous. According to the crosscutting relationships between veinlets and their mineral assemblages, three stages of hydrothermal mineralization in this deposit were previously distinguished. In this contribution, two different colored fluorites from the major sulfide mineralization stage are recognized:(1) green fluorites coexisting with Pb–Zn ores;and(2) violet fluorites coexisting with pyrite ores. Y/Ho ratios verify the green fluorites and violet fluorites were co-genetic. The fluorites display elevated(La/Yb)Nratios, which decrease from 1201 to 5710 for green fluorites to 689–1568 for violet fluorites, indicating that they precipitated at the early hydrothermal sulfide stage,and Pb–Zn ores crystallized earlier than pyrite ores. The similar Tb/La ratios of the fluorites also indicate that they precipitated at an early stage within a short time. From the green fluorites to violet fluorites, the total rare earth element(ΣREE)concentrationsdecreasefrom1052–1680 ppm to 148–350 ppm, indicating that the green fluorites precipitated from a more acidic fluid. The Eu/Eu*ratios increase from 0.17 to 0.30 for green fluorites to0.29–0.48 for violet fluorites, and the Ce/Ce* ratios decrease from 1.08–1.13 to 0.93–1.11, suggesting a gradual increase in oxygen fugacity(fO_(2)) and pH value of the mineralization fluid. Though the fluorites display similar REE patterns to the granodiorite-porphyry and limestone,the ΣREE concentrations of the fluorites are significantly higher than those of limestone and the granodiorite-porphyry, suggesting that an important undetected non-magmatic source is involved to provide sufficient REE for fluorites. The most plausible mechanism is fluid mixing between magma fluid and an undetected non-magmatic fluid.

Mechanochemical-Assisted Leaching of Lamp Phosphors： A Green Engineering Approach for Rare-Earth Recovery

Rare-earth elements （REEs） are essential metals for the design and development of sustainable energy applications, Recycling these elements from waste streams enriched in them is crucial for securing an independent future supply for sustainable applications, This study compares the mechanisms of mechan- ical activation prior to a hydrometallurgical acid-leaching process and a solvometallurgical mechanochemical leaching process for the recovery of REEs from green lamp phosphor, LaPO4：Ce3＋, Th3＋, After 60 min of processing time, the REE leaching rates showed a significant enhancement of 60% after cycled mechanical activation, and 98% after the combined mechanochemical leaching process, High-resolution transmission electron microscopy （HR-TEM） imaging disclosed the cause for the improved REE leaching rates： The improved leaching and leaching patterns could he attributed to changes in the crystal morphology from monocrystalline to polycrystalline, Reduction of the crystallite size to the nanoscale in a polycrystalline material creates irregular packing of chemical units, resulting in an increase in defect-rich grain boundaries in the crystals, which enhances the leaching process, A solvometallurgical method was developed to combine the mechanical activation and leaching process into a single step, which is beneficial for operational cost, This results in an efficient and simple process that provides an alternative and greener recycling route for lamp phosphor waste,

Trace and rare-earth element geochemistry: A tool for petrogenetic and geotectonic modeling of ensimatic ortho-amphibolites from Pan-African belt of Obudu Plateau, Southeastern Nigeria

A model for the petrogenetic affinity and original geotectonic setting of ortho-amphibolites from the Obudu Plateau was tested using the distribution patterns of trace and rare-earth elements from the geochemical analyses of twelve representative amphibolite samples. Discrimination plots, normalized patterns of the incompatible trace elements against average MORB, low ratios of Ba/Nb (9–23) and Ba/Ta (130–327) and other geochemical characteristics suggest that the protoliths were dominantly of tholeiitic MORB composition. The values of the ratios of La/Ta (8.13–10.8), Rb/Sr (0.04–0.07), Th/U (mainly 4.43–5.43) and Hf/Ta (2.35–2.88) further indicate that the ortho-amphibolites demonstrate E-type MORB characteristics. These features are related to substantial ocean floor divergent tectonic boundary setting rather than marginal basin tectonic setting. This evolutionary pattern appears to be controlled by limited progressive partial melting and fractional crystallization of a single mantle source region, irrespective, however, of variations due to local source heterogeneities. The tholeiitic magmas were most probably generated by hotspot activities on the constructive plate margins and subsequently modified by subduction-related low-K tholeiitic chemistry due to narrowing of a proto oceanic basin between the West African craton and eastern Sahara plate. A likely model, therefore, is that the amphibolites of the Obudu Plateau represent ophiolitic suites with characteristics of enriched mid-ocean floor tholeiites, which were deformed and metamorphosed during a reversed plate motion involving subduction and collision within the Obudu Plateau in the Pan-African orogenic episode.

REE and Other Trace Element Chemistry of Oldhamite(CaS)in the Qingzhen Chondrite(EH3)and Their Genetic Implications

Instrumental neutron activation analysis(INAA) of 14 single oldhamite grains separated from the Qingzhen chondrite (EH3) for refractory(La,Ce,Sm ,Eu,Yb,Lu,Ca,Sc,Hf, and Th),volatile (Na,Cr,Zn,Se,Br,etc.)and siderophile elements (Fe,Ni,Co,Ir,Au ,and As) revealed that oldhamite is highly rich in refractory elements.The mineral serves as the principal carrier of REE and contains about 80% of the REEs in the Qingzhen enstatite chondrite .Furthermore, the large enrichment of LREE relative to HREE is noticed in oldhamite from the Qingzhen .In general, the oldhamite from metal-sulfide assemblages is richer in REE than that from the matrix,i.e.,the earlier the oldhamite grains condensed, the richer they are in REE. Meanwhile.oldhamite is also rich in vol-atile elements such as Se,Br, etc.In terms of the distribution of trace elements in oldhamitc from the Qingzhen ,the chondrite is srggested to have resulted from high-temperature condensation of solar nebula.

Geochemical studies on REE and trace elements from several Cu-Au deposits along the lower Yangtze metallogenic valley, central-southern Anhui Province

The Yangtze Valley was one of the most important metallogenic regions during the Jurassic-Cretaceous period in East China, where more than 200 polymetallic Cu-Fe-Au, Mo, Zn, Pb, Ag deposits have been found. Trace elements were chemically analyzed and the relevant data were collected from literature for the Yanshanian (Mesozoic) igneous rocks which have close relationship with Cu-Au mineralization. Copper mineralization in the lower Yangtze Valley can be divided into three major types: skarn type, porphyry type and volcanic type. The porphyry type is of rare occurrence, such as the Shaxi porphyry copper deposit in the northern part of the lower Yangtze metallogenic valley. This paper focuses on the REE and trace element geochemistry of several Cu-Au deposits along the lower part of Yangtze metallogenic valley in Anhui. The results showed that there are differences in REE distribution for these four types of Cu-Au mineralization, which confine the sources of REE and trace elements as well as other mantle and transitional compatible elements. The results of both REE and trace element geochemical studies showed that these elements with different characteristics have different origins, probably representing different sources of Cu-Au deposits in the deep crust and upper mantle environments. The 40Ar/39Ar dating of one biotite sample gave an age of 131 Ma with a high level of confidence, which represents the age of formation of the Shaxi porphyrite intrusive with porphrytic Cu-Au mineralization, which is consistent with that of the majority of the adjacent acid intrusives with mass Cu-Au mineralization along the Yangtze metallogenic belt in the Yanshanian period (Mesozoic). This is the first attempt to use the high precision method to date the Shaxi porphyrite intrusive.

Variations of trace elements and rare earth elements(REEs)treated by two different methods for snow-pit samples on the Qinghai-Tibetan Plateau and their implications

Although previous investigations of the trace elements in snow and ice from the Qinghai-Tibetan Plateau obtained interesting information about pollution from human activities on the plateau, most were based on traditional acidification methods.To emphasize the influence of the different sample-preparation methods on the records of trace elements and rare earth elements, snow samples were collected from glaciers on the Qinghai-Tibetan Plateau in China and prepared using two methods: traditional acidification and total digestion. Concentrations of 18 trace elements(Al, Ti, Fe, Rb, Sr, Ba, V, Cr, Mn, Li,Cu, Co, Mo, Cs, Sb, Pb, Tl, and U), along with 14 rare earth elements(REEs: La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er,Tm, Yb, and Lu), Y, and Th in the snow samples, were measured using inductively coupled plasma-sector field mass spectrometry(ICP-SFMS). The results showed that the mass fraction of the trace elements(defined as ratio of concentration in the acid-leachable fraction to that in the digested sample) such as Mo, Ti, Al, Rb, and V, varied from 0.06 to 0.5. The mass fraction of other trace elements varied from about 0.6 to more than 0.9; those of the REEs, Y, and Th varied from 0.34 to0.75. Lower mass fractions will lead to an overestimated contribution of other sources, especially human activities, and the underestimated fluxes of these trace elements(especially REEs, Y, and Th, as well as dust) if the REEs are used as the proxy for the crust dust. The two sample-preparation methods exhibited different REE normalized distribution patterns,REE ratios, and provenance-tracing results. The REE normalized distribution patterns and proxies in the digested samples are more reliable and integrated than those found in traditional acidification method for dust-provenance tracing.